Publications of G. Allan Johnson    :chronological  by type listing:

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@article{fds132726,
   Author = {G.A. Johnson},
   Title = {1. C.F. Beaulieu, X. Zhou, G.P. Cofer, G.A. Johnson.
             Diffusion-Weighted MR Microscopy with Fast Spin-Echo.
             Magnetic Resonance in Medicine 30, 201-206
             (1993).},
   Year = {1994},
   Key = {fds132726}
}

@article{fds132716,
   Author = {G.A. Johnson},
   Title = {1. Cho ZH, Ro YM. Multipoint K-Space Mapping Technique.
             Reviewed for Magn Reson. in Med.},
   Year = {1994},
   Key = {fds132716}
}

@booklet{Mcadams85a,
   Author = {McAdams, HP and Johnson, GA and Suddarth, SA and Ravin,
             CE},
   Title = {105 Optimization of Adaptive Filtration for Digital Chest
             Imaging},
   Journal = {Investigative Radiology},
   Volume = {20},
   Number = {6},
   Pages = {S27-S27},
   Publisher = {Ovid Technologies (Wolters Kluwer Health)},
   Year = {1985},
   Month = {September},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1985ARG0500122&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Doi = {10.1097/00004424-198509000-00133},
   Key = {Mcadams85a}
}

@booklet{Godwin84,
   Author = {Godwin, JD and Pelc, NJ and Johnson, GA and Fram, EK and C,
             R},
   Title = {106. PROGRESS IN ECG-GATED CT},
   Journal = {Investigative Radiology},
   Volume = {19},
   Number = {5},
   Pages = {S27-S27},
   Publisher = {Ovid Technologies (Wolters Kluwer Health)},
   Year = {1984},
   Month = {September},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1984TL42800126&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Doi = {10.1097/00004424-198409000-00131},
   Key = {Godwin84}
}

@booklet{Blinder85,
   Author = {Blinder, RA and Herfkens, RJ and Johnson, GA and Coleman,
             RE},
   Title = {121 SURFACE COIL MOTION ARTIFACTS IN MR IMAGING},
   Journal = {Investigative Radiology},
   Volume = {20},
   Number = {6},
   Pages = {S31-S31},
   Publisher = {Ovid Technologies (Wolters Kluwer Health)},
   Year = {1985},
   Month = {September},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1985ARG0500138&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Doi = {10.1097/00004424-198509000-00149},
   Key = {Blinder85}
}

@booklet{Johnson84,
   Author = {Johnson, GA and Herfkens, RJ and MacFall, JR},
   Title = {129. IN VIVO FIELD DEPENDENCE OF TISSUE RELAXATION
             TIMES},
   Journal = {Investigative Radiology},
   Volume = {19},
   Number = {5},
   Pages = {S33-S33},
   Publisher = {Ovid Technologies (Wolters Kluwer Health)},
   Year = {1984},
   Month = {September},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1984TL42800149&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Doi = {10.1097/00004424-198409000-00154},
   Key = {Johnson84}
}

@booklet{Stude84,
   Author = {Stude, R and Hedlund, L and Johnson, GA and Thompson,
             WM},
   Title = {159. A CT EVALUATION OF THREE HEPATOBILIARY CONTRAST
             AGENTS},
   Journal = {Investigative Radiology},
   Volume = {19},
   Number = {5},
   Pages = {S40-S40},
   Publisher = {Ovid Technologies (Wolters Kluwer Health)},
   Year = {1984},
   Month = {September},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1984TL42800179&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Doi = {10.1097/00004424-198409000-00184},
   Key = {Stude84}
}

@booklet{Herfkens84,
   Author = {Herfkens, RJ and Johnson, GA and Glover, G},
   Title = {166. IN VIVO CHEMICAL SHIFT IMAGING OF HYDROGEN},
   Journal = {Investigative Radiology},
   Volume = {19},
   Number = {5},
   Pages = {S42-S42},
   Publisher = {Ovid Technologies (Wolters Kluwer Health)},
   Year = {1984},
   Month = {September},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1984TL42800185&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Doi = {10.1097/00004424-198409000-00191},
   Key = {Herfkens84}
}

@booklet{Hedlund87,
   Author = {Hedlund, L and Cofer, G and Suddarth, S and Johnson,
             GA},
   Title = {177. SMALL ANIMAL ANESTHESIA AND MONITORING DURING EXTENDED
             MR MICROSCOPY},
   Journal = {Investigative Radiology},
   Volume = {22},
   Number = {9},
   Pages = {S44-S44},
   Publisher = {Ovid Technologies (Wolters Kluwer Health)},
   Year = {1987},
   Month = {September},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1987K178300189&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Doi = {10.1097/00004424-198709000-00193},
   Key = {Hedlund87}
}

@booklet{Sherrier84,
   Author = {Sherrier, RH and Johnson, GA and Ravin, CE and Suddarth,
             SA},
   Title = {194. DIGITAL SYNTHESIS OF LUNG NODULES},
   Journal = {Investigative Radiology},
   Volume = {19},
   Number = {5},
   Pages = {S49-S49},
   Publisher = {Ovid Technologies (Wolters Kluwer Health)},
   Year = {1984},
   Month = {September},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1984TL42800213&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Doi = {10.1097/00004424-198409000-00219},
   Key = {Sherrier84}
}

@article{fds174087,
   Author = {GA Johnson and SJ Boukma and PA Platz},
   Title = {2-mercaptobenzothiazole, an inhibitor of dopamine
             beta-hydroxylase.},
   Journal = {The Journal of pharmacy and pharmacology},
   Volume = {22},
   Number = {9},
   Pages = {710-2},
   Year = {1970},
   Month = {September},
   ISSN = {0022-3573},
   Keywords = {Animals • Brain Chemistry • Dopamine • Heart
             • Metaraminol • Mice • Mixed Function
             Oxygenases • Motor Activity • Myocardium •
             Norepinephrine • Rats • Thiazoles • analysis
             • antagonists & inhibitors* • drug effects •
             pharmacology • pharmacology*},
   Language = {eng},
   Key = {fds174087}
}

@article{fds132727,
   Author = {G.A. Johnson},
   Title = {2. H. Benveniste, G. Johnson, in "Microcirculatory Stasis in
             the Brain" (M. Tomita, Mchedlishvili, W. Roseblum, W.D.
             Heiss, Y. Fukuuchi, Ed.), p. 369-376, Excerpta Medica,
             Amsterdam, 1993.},
   Year = {1994},
   Key = {fds132727}
}

@article{fds132717,
   Author = {G.A. Johnson},
   Title = {2. Hafner S, Kuhn W. NMR Imaging of Water Contentin Chips.
             Reviewed for Magn. Reson. Imaging.},
   Year = {1994},
   Key = {fds132717}
}

@booklet{Johnson86a,
   Author = {JOHNSON, GA and THOMPSON, MB and DRAYER, BP},
   Title = {3-DIMENSIONAL MRI MICROSCOPY OF THE RAT-BRAIN},
   Journal = {INVESTIGATIVE RADIOLOGY},
   Volume = {21},
   Number = {9},
   Pages = {S25-S25},
   Publisher = {LIPPINCOTT-RAVEN PUBL},
   Year = {1986},
   Month = {September},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1986E000900109&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Johnson86a}
}

@booklet{Macfall95,
   Author = {MACFALL, IS and JOHNSON, GA},
   Title = {3-DIMENSIONAL ROOT-GROWTH, TURNOVER AND TRANSPORT AS SEEN
             WITH MAGNETIC-RESONANCE MICROSCOPY},
   Journal = {PLANT PHYSIOLOGY},
   Volume = {108},
   Number = {2},
   Pages = {31-31},
   Publisher = {AMER SOC PLANT PHYSIOLOGISTS},
   Year = {1995},
   Month = {June},
   ISSN = {0032-0889},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1995RE28900117&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Macfall95}
}

@booklet{Lester99a,
   Author = {Lester, DS and Lyon, RC and McGregor, GN and Engelhardt, RT and Schmued,
             LC and Johnson, GA and Johannessen, JN},
   Title = {3-Dimensional visualization of lesions in rat brain using
             magnetic resonance imaging microscopy.},
   Journal = {Neuroreport},
   Volume = {10},
   Number = {4},
   Pages = {737-741},
   Year = {1999},
   Month = {March},
   ISSN = {0959-4965},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/10208540},
   Abstract = {High-resolution (< 50 microm) magnetic resonance imaging
             microscopy (MRM) has been used to identify brain regions and
             localization of excitotoxin-induced lesions in fixed rat
             brains, subsequently confirmed using standard histology. The
             anatomical extent of lesions identified by MRM was identical
             to that seen in histological sections and various
             histopathological changes could be visualized. In contrast
             to the time involved in preparing and examining histological
             sections, lesions in intact brains could be rapidly
             identified and visualized in three dimensions by examining
             digitally generated sections in any plane. This study shows
             that MRM has tremendous potential as a prescreening tool for
             neurotoxicity and neuropathology. These observations suggest
             that MRM has the potential to affect pathology much as
             conventional MRI has influenced clinical
             imaging.},
   Doi = {10.1097/00001756-199903170-00014},
   Key = {Lester99a}
}

@article{fds132794,
   Author = {DS Lester and RC Lyon and GN McGregor and RT Engelhardt and LC Schmued and GA Johnson and JN Johannessen},
   Title = {3-Dimensional visualization of lesions in rat brain using
             magnetic resonance imaging microscopy.},
   Journal = {Neuroreport, ENGLAND},
   Volume = {10},
   Number = {4},
   Pages = {737-41},
   Year = {1999},
   Month = {March},
   ISSN = {0959-4965},
   Keywords = {Animals • Brain • Brain Diseases •
             Histocytochemistry • Image Processing,
             Computer-Assisted • Kainic Acid • Magnetic
             Resonance Imaging • Microscopy • Neurotoxins
             • Rats • analogs & derivatives • chemically
             induced • pathology • pathology* •
             toxicity},
   Abstract = {High-resolution (< 50 microm) magnetic resonance imaging
             microscopy (MRM) has been used to identify brain regions and
             localization of excitotoxin-induced lesions in fixed rat
             brains, subsequently confirmed using standard histology. The
             anatomical extent of lesions identified by MRM was identical
             to that seen in histological sections and various
             histopathological changes could be visualized. In contrast
             to the time involved in preparing and examining histological
             sections, lesions in intact brains could be rapidly
             identified and visualized in three dimensions by examining
             digitally generated sections in any plane. This study shows
             that MRM has tremendous potential as a prescreening tool for
             neurotoxicity and neuropathology. These observations suggest
             that MRM has the potential to affect pathology much as
             conventional MRI has influenced clinical
             imaging.},
   Key = {fds132794}
}

@article{fds132714,
   Author = {G.A. Johnson},
   Title = {3. J.C.M. Hsu, G.A. Johnson, W.M. Smith K.A. Reimer, R.E.
             Ideker. Magnetic Resonance Imaging of Chronic Myocardial
             Infarcts in Formalin Fixed Human Autopsy Specimens.
             Circulation 89:2133-2140 (1993).},
   Year = {1994},
   Key = {fds132714}
}

@article{fds352911,
   Author = {Rushmore, RJ and Wilson-Braun, P and Papadimitriou, G and Ng, I and Rathi, Y and Zhang, F and O'Donnell, LJ and Kubicki, M and Bouix, S and Yeterian, E and Lemaire, J-J and Calabrese, E and Johnson, GA and Kikinis, R and Makris, N},
   Title = {3D Exploration of the Brainstem in 50-Micron Resolution
             MRI.},
   Journal = {Front Neuroanat},
   Volume = {14},
   Pages = {40},
   Year = {2020},
   url = {http://dx.doi.org/10.3389/fnana.2020.00040},
   Abstract = {The brainstem, a structure of vital importance in mammals,
             is currently becoming a principal focus in cognitive,
             affective, and clinical neuroscience. Midbrain, pontine and
             medullary structures serve as the conduit for signals
             between the forebrain and spinal cord, are the epicenter of
             cranial nerve-circuits and systems, and subserve such
             integrative functions as consciousness, emotional
             processing, pain, and motivation. In this study, we
             parcellated the nuclear masses and the principal fiber
             pathways that were visible in a high-resolution T2-weighted
             MRI dataset of 50-micron isotropic voxels of a postmortem
             human brainstem. Based on this analysis, we generated a
             detailed map of the human brainstem. To assess the validity
             of our maps, we compared our observations with histological
             maps of traditional human brainstem atlases. Given the
             unique capability of MRI-based morphometric analysis in
             generating and preserving the morphology of 3D objects from
             individual 2D sections, we reconstructed the motor, sensory
             and integrative neural systems of the brainstem and rendered
             them in 3D representations. We anticipate the utilization of
             these maps by the neuroimaging community for applications in
             basic neuroscience as well as in neurology, psychiatry, and
             neurosurgery, due to their versatile computational nature in
             2D and 3D representations in a publicly available
             capacity.},
   Doi = {10.3389/fnana.2020.00040},
   Key = {fds352911}
}

@article{fds268810,
   Author = {Liu, C and Li, W and Wu, B and Jiang, Y and Johnson,
             GA},
   Title = {3D fiber tractography with susceptibility tensor
             imaging.},
   Journal = {Neuroimage},
   Volume = {59},
   Number = {2},
   Pages = {1290-1298},
   Year = {2012},
   Month = {January},
   ISSN = {1095-9572},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/21867759},
   Keywords = {Algorithms* • Animals • Brain • Diffusion
             Tensor Imaging • Image Enhancement • Image
             Interpretation, Computer-Assisted • Imaging,
             Three-Dimensional • Mice • Mice, Inbred C57BL
             • Nerve Fibers, Myelinated • Pattern Recognition,
             Automated • Reproducibility of Results •
             Sensitivity and Specificity • cytology* • methods
             • methods* • ultrastructure*},
   Abstract = {Gradient-echo MRI has revealed anisotropic magnetic
             susceptibility in the brain white matter. This magnetic
             susceptibility anisotropy can be measured and characterized
             with susceptibility tensor imaging (STI). In this study, a
             method of fiber tractography based on STI is proposed and
             demonstrated in the mouse brain. STI experiments of
             perfusion-fixed mouse brains were conducted at 7.0T. The
             magnetic susceptibility tensor was calculated for each voxel
             with regularization and decomposed into its eigensystem. The
             major eigenvector is found to be aligned with the underlying
             fiber orientation. Following the orientation of the major
             eigenvector, we are able to map distinctive fiber pathways
             in 3D. As a comparison, diffusion tensor imaging (DTI) and
             DTI fiber tractography were also conducted on the same
             specimens. The relationship between STI and DTI fiber tracts
             was explored with similarities and differences identified.
             It is anticipated that the proposed method of STI
             tractography may provide a new way to study white matter
             fiber architecture. As STI tractography is based on physical
             principles that are fundamentally different from DTI, it may
             also be valuable for the ongoing validation of DTI
             tractography.},
   Language = {eng},
   Doi = {10.1016/j.neuroimage.2011.07.096},
   Key = {fds268810}
}

@article{fds268850,
   Author = {Driehuys, B and Walker, J and Pollaro, J and Cofer, GP and Mistry, N and Schwartz, D and Johnson, GA},
   Title = {3He MRI in mouse models of asthma.},
   Journal = {Magn Reson Med},
   Volume = {58},
   Number = {5},
   Pages = {893-900},
   Year = {2007},
   Month = {November},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/17969115},
   Keywords = {Animals • Asthma • Disease Models, Animal* •
             Helium • Magnetic Resonance Imaging • Mice •
             Mice, Inbred BALB C • Mice, Inbred C57BL •
             methods* • pathology*},
   Abstract = {In the study of asthma, a vital role is played by mouse
             models, because knockout or transgenic methods can be used
             to alter disease pathways and identify therapeutic targets
             that affect lung function. Assessment of lung function in
             rodents by available methods is insensitive because these
             techniques lack regional specificity. A more sensitive
             method for evaluating lung function in human asthma patients
             uses hyperpolarized (HP) (3)He MRI before and after
             bronchoconstriction induced by methacholine (MCh). We now
             report the ability to perform such (3)He imaging of MCh
             response in mice, where voxels must be approximately 3000
             times smaller than in humans and (3)He diffusion becomes an
             impediment to resolving the airways. We show
             three-dimensional (3D) images that reveal airway structure
             down to the fifth branching and visualize ventilation at a
             resolution of 125 x 125 x 1000 microm(3). Images of
             ovalbumin (OVA)-sensitized mice acquired after MCh show both
             airway closure and ventilation loss. To also observe the MCh
             response in naive mice, we developed a non-slice-selective
             2D protocol with 187 x 187 microm(2) resolution that was
             fast enough to record the MCh response and recovery with
             12-s temporal resolution. The extension of (3)He MRI to
             mouse models should make it a valuable translational tool in
             asthma research.},
   Doi = {10.1002/mrm.21306},
   Key = {fds268850}
}

@article{06059673317,
   Author = {Badea, CT and Fubara, B and Hedlund, LW and Johnson,
             GA},
   Title = {4-D micro-CT of the mouse heart.},
   Journal = {Mol Imaging},
   Volume = {4},
   Number = {2},
   Pages = {110-116},
   Year = {2005},
   ISSN = {1535-3508},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/16105509},
   Keywords = {Computerized tomography;Cardiology;Photons;Motion
             control;Biological organs;Optical resolving
             power;Blood;},
   Abstract = {PURPOSE: Demonstrate noninvasive imaging methods for in vivo
             characterization of cardiac structure and function in mice
             using a micro-CT system that provides high photon fluence
             rate and integrated motion control. MATERIALS AND METHODS:
             Simultaneous cardiac- and respiratory-gated micro-CT was
             performed in C57BL/6 mice during constant intravenous
             infusion of a conventional iodinated contrast agent
             (Isovue-370), and after a single intravenous injection of a
             blood pool contrast agent (Fenestra VC). Multiple phases of
             the cardiac cycle were reconstructed with contrast to noise
             and spatial resolution sufficient for quantitative
             assessment of cardiac function. RESULTS: Contrast
             enhancement with Isovue-370 increased over time with a
             maximum of approximately 500 HU (aorta) and 900 HU (kidney
             cortex). Fenestra VC provided more constant enhancement over
             3 hr, with maximum enhancement of approximately 620 HU
             (aorta) and approximately 90 HU (kidney cortex). The maximum
             enhancement difference between blood and myocardium in the
             heart was approximately 250 HU for Isovue-370 and
             approximately 500 HU for Fenestra VC. In mice with Fenestra
             VC, volumetric measurements of the left ventricle were
             performed and cardiac function was estimated by ejection
             fraction, stroke volume, and cardiac output. CONCLUSION:
             Image quality with Fenestra VC was sufficient for
             morphological and functional studies required for a
             standardized method of cardiac phenotyping of the
             mouse.},
   Doi = {10.1162/15353500200504187},
   Key = {06059673317}
}

@article{fds157102,
   Author = {CT Badea and B Fubara and LW Hedlund and GA Johnson},
   Title = {4-D micro-CT of the mouse heart.},
   Journal = {Molecular imaging : official journal of the Society for
             Molecular Imaging, United States},
   Volume = {4},
   Number = {2},
   Pages = {110-6},
   ISSN = {1535-3508},
   Keywords = {Animals • Contrast Media • Heart • Iodine
             • Iopamidol • Mice • Mice, Inbred C57BL
             • Tomography, X-Ray Computed* •
             radiography*},
   Abstract = {PURPOSE: Demonstrate noninvasive imaging methods for in vivo
             characterization of cardiac structure and function in mice
             using a micro-CT system that provides high photon fluence
             rate and integrated motion control. MATERIALS AND METHODS:
             Simultaneous cardiac- and respiratory-gated micro-CT was
             performed in C57BL/6 mice during constant intravenous
             infusion of a conventional iodinated contrast agent
             (Isovue-370), and after a single intravenous injection of a
             blood pool contrast agent (Fenestra VC). Multiple phases of
             the cardiac cycle were reconstructed with contrast to noise
             and spatial resolution sufficient for quantitative
             assessment of cardiac function. RESULTS: Contrast
             enhancement with Isovue-370 increased over time with a
             maximum of approximately 500 HU (aorta) and 900 HU (kidney
             cortex). Fenestra VC provided more constant enhancement over
             3 hr, with maximum enhancement of approximately 620 HU
             (aorta) and approximately 90 HU (kidney cortex). The maximum
             enhancement difference between blood and myocardium in the
             heart was approximately 250 HU for Isovue-370 and
             approximately 500 HU for Fenestra VC. In mice with Fenestra
             VC, volumetric measurements of the left ventricle were
             performed and cardiac function was estimated by ejection
             fraction, stroke volume, and cardiac output. CONCLUSION:
             Image quality with Fenestra VC was sufficient for
             morphological and functional studies required for a
             standardized method of cardiac phenotyping of the
             mouse.},
   Key = {fds157102}
}

@article{fds132728,
   Author = {G.A. Johnson},
   Title = {4. X. Zhou, G.P. Cofer S. A. Suddarth, G. A. Johnson. High
             Field MR Microscopy Using Fast Spin Echoes. Magn Reson Med
             30:60-67 (1993).},
   Year = {1994},
   Key = {fds132728}
}

@article{fds268820,
   Author = {Badea, CT and Johnston, SM and Qi, Y and Johnson,
             GA},
   Title = {4D micro-CT for cardiac and perfusion applications with view
             under sampling.},
   Journal = {Phys Med Biol},
   Volume = {56},
   Number = {11},
   Pages = {3351-3369},
   Year = {2011},
   Month = {June},
   ISSN = {1361-6560},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/21558587},
   Keywords = {Animals • Artifacts • Four-Dimensional Computed
             Tomography • Heart • Lung • Mice •
             Perfusion Imaging • Phantoms, Imaging • X-Ray
             Microtomography • methods* • radiography •
             radiography*},
   Abstract = {Micro-CT is commonly used in preclinical studies to provide
             anatomical information. There is growing interest in
             obtaining functional measurements from 4D micro-CT. We
             report here strategies for 4D micro-CT with a focus on two
             applications: (i) cardiac imaging based on retrospective
             gating and (ii) pulmonary perfusion using multiple contrast
             injections/rotations paradigm. A dual source micro-CT system
             is used for image acquisition with a sampling rate of 20
             projections per second. The cardiac micro-CT protocol
             involves the use of a liposomal blood pool contrast agent.
             Fast scanning of free breathing mice is achieved using
             retrospective gating. The ECG and respiratory signals are
             used to sort projections into ten cardiac phases. The
             pulmonary perfusion protocol uses a conventional contrast
             agent (Isovue 370) delivered by a micro-injector in four
             injections separated by 2 min intervals to allow for
             clearance. Each injection is synchronized with the rotation
             of the animal, and each of the four rotations is started
             with an angular offset of 22.5 from the starting angle of
             the previous rotation. Both cardiac and perfusion protocols
             result in an irregular angular distribution of projections
             that causes significant streaking artifacts in
             reconstructions when using traditional filtered
             backprojection (FBP) algorithms. The reconstruction involves
             the use of the point spread function of the micro-CT system
             for each time point, and the analysis of the distribution of
             the reconstructed data in the Fourier domain. This enables
             us to correct for angular inconsistencies via deconvolution
             and identify regions where data is missing. The missing
             regions are filled with data from a high quality but
             temporally averaged prior image reconstructed with all
             available projections. Simulations indicate that
             deconvolution successfully removes the streaking artifacts
             while preserving temporal information. 4D cardiac micro-CT
             in a mouse was performed with adequate image quality at
             isotropic voxel size of 88 µm and 10 ms temporal
             resolution. 4D pulmonary perfusion images were obtained in a
             mouse at 176 µm and 687 ms temporal resolution. Compared
             with FBP reconstruction, the streak reduction ratio is 70%
             and the contrast to noise ratio is 2.5 times greater in the
             deconvolved images. The radiation dose associated with the
             proposed methods is in the range of a typical micro-CT dose
             (0.17 Gy for the cardiac study and 0.21 Gy for the perfusion
             study). The low dose 4D micro-CT imaging presented here can
             be applied in high-throughput longitudinal studies in a wide
             range of applications, including drug safety and
             cardiopulmonary phenotyping.},
   Language = {eng},
   Doi = {10.1088/0031-9155/56/11/011},
   Key = {fds268820}
}

@article{fds268815,
   Author = {Guo, X and Johnston, SM and Qi, Y and Johnson, GA and Badea,
             CT},
   Title = {4D micro-CT using fast prospective gating.},
   Journal = {Phys Med Biol},
   Volume = {57},
   Number = {1},
   Pages = {257-271},
   Year = {2012},
   Month = {January},
   ISSN = {1361-6560},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/22156062},
   Keywords = {Animals • Cardiac-Gated Imaging Techniques •
             Four-Dimensional Computed Tomography • Heart •
             Mice • Phantoms, Imaging • Rats • Rats,
             Sprague-Dawley • Respiratory-Gated Imaging Techniques
             • Time Factors • methods* •
             radiography},
   Abstract = {Micro-CT is currently used in preclinical studies to provide
             anatomical information. But, there is also significant
             interest in using this technology to obtain functional
             information. We report here a new sampling strategy for 4D
             micro-CT for functional cardiac and pulmonary imaging. Rapid
             scanning of free-breathing mice is achieved with fast
             prospective gating (FPG) implemented on a field programmable
             gate array. The method entails on-the-fly computation of
             delays from the R peaks of the ECG signals or the peaks of
             the respiratory signals for the triggering pulses.
             Projection images are acquired for all cardiac or
             respiratory phases at each angle before rotating to the next
             angle. FPG can deliver the faster scan time of retrospective
             gating (RG) with the regular angular distribution of
             conventional prospective gating for cardiac or respiratory
             gating. Simultaneous cardio-respiratory gating is also
             possible with FPG in a hybrid retrospective/prospective
             approach. We have performed phantom experiments to validate
             the new sampling protocol and compared the results from FPG
             and RG in cardiac imaging of a mouse. Additionally, we have
             evaluated the utility of incorporating respiratory
             information in 4D cardiac micro-CT studies with FPG. A
             dual-source micro-CT system was used for image acquisition
             with pulsed x-ray exposures (80 kVp, 100 mA, 10 ms). The
             cardiac micro-CT protocol involves the use of a liposomal
             blood pool contrast agent containing 123 mg I ml(-1)
             delivered via a tail vein catheter in a dose of 0.01 ml
             g(-1) body weight. The phantom experiment demonstrates that
             FPG can distinguish the successive phases of phantom motion
             with minimal motion blur, and the animal study demonstrates
             that respiratory FPG can distinguish inspiration and
             expiration. 4D cardiac micro-CT imaging with FPG provides
             image quality superior to RG at an isotropic voxel size of
             88 μm and 10 ms temporal resolution. The acquisition time
             for either sampling approach is less than 5 min. The
             radiation dose associated with the proposed method is in the
             range of a typical micro-CT dose (256 mGy for the cardiac
             study). Ignoring respiration does not significantly affect
             anatomic information in cardiac studies. FPG can deliver
             short scan times with low-dose 4D micro-CT imaging without
             sacrificing image quality. FPG can be applied in
             high-throughput longitudinal studies in a wide range of
             applications, including drug safety and cardiopulmonary
             phenotyping.},
   Language = {eng},
   Doi = {10.1088/0031-9155/57/1/257},
   Key = {fds268815}
}

@article{fds268783,
   Author = {Badea, CT and Johnston, SM and Lin, M and Hedlund, LW and Johnson,
             GA},
   Title = {4D micro-CT-based perfusion imaging in small
             animals},
   Journal = {Progress in Biomedical Optics and Imaging - Proceedings of
             SPIE},
   Volume = {7258},
   Publisher = {SPIE},
   Year = {2009},
   Month = {June},
   ISBN = {9780819475091},
   ISSN = {1605-7422},
   url = {http://dx.doi.org/10.1117/12.811213},
   Abstract = {Quantitative in-vivo imaging of lung perfusion in rodents
             can provide critical information for preclinical studies.
             However, the combined challenges of high temporal and
             spatial resolution have made routine quantitative perfusion
             imaging difficult in rodents. We have recently developed a
             dual tube/detector micro-CT scanner that is well suited to
             capture first-pass kinetics of a bolus of contrast agent
             used to compute perfusion information. Our approach is based
             on the paradigm that the same time density curves can be
             reproduced in a number of consecutive, small (i.e. 50μL )
             injections of iodinated contrast agent at a series of
             different angles. This reproducibility is ensured by the
             high-level integration of the imaging components of our
             system, with a micro-injector, a mechanical ventilator, and
             monitoring applications. Sampling is controlled through a
             biological pulse sequence implemented in LabVIEW. Image
             reconstruction is based on a simultaneous algebraic
             reconstruction technique implemented on a GPU. The
             capabilities of 4D micro-CT imaging are demonstrated in
             studies on lung perfusion in rats. We report 4D micro-CT
             imaging in the rat lung with a heartbeat temporal resolution
             of 140 ms and reconstructed voxels of 88 μm. The approach
             can be readily extended to a wide range of important
             preclinical models, such as tumor perfusion and
             angiogenesis, and renal function. © 2009
             SPIE.},
   Doi = {10.1117/12.811213},
   Key = {fds268783}
}

@article{fds268700,
   Author = {Xie, L and Qi, Y and Subashi, E and Liao, G and Miller-DeGraff, L and Jetten, AM and Johnson, GA},
   Title = {4D MRI of polycystic kidneys from rapamycin-treated
             Glis3-deficient mice.},
   Journal = {NMR Biomed},
   Volume = {28},
   Number = {5},
   Pages = {546-554},
   Year = {2015},
   Month = {May},
   ISSN = {0952-3480},
   url = {http://dx.doi.org/10.1002/nbm.3281},
   Abstract = {Polycystic kidney disease (PKD) is a life-threatening
             disease that leads to a grotesque enlargement of the kidney
             and significant loss of function. Several imaging studies
             with MRI have demonstrated that cyst size in polycystic
             kidneys can determine disease severity and progression. In
             the present study, we found that, although kidney volume and
             cyst volume decreased with drug treatment, renal function
             did not improve with treatment. Here, we applied dynamic
             contrast-enhanced MRI to study PKD in a Glis3 (GLI-similar
             3)-deficient mouse model. Cysts from this model have a wide
             range of sizes and develop at an early age. To capture this
             crucial stage and assess cysts in detail, we imaged during
             early development (3-17 weeks) and applied high
             spatiotemporal resolution MRI (125 × 125 × 125 cubic
             microns every 7.7 s). A drug treatment with rapamycin
             (also known as sirolimus) was applied to determine whether
             disease progression could be halted. The effect and synergy
             (interaction) of aging and treatment were evaluated using an
             analysis of variance (ANOVA). Structural measurements,
             including kidney volume, cyst volume and cyst-to-kidney
             volume ratio, changed significantly with age. Drug treatment
             significantly decreased these metrics. Functional
             measurements of time-to-peak (TTP) mean and TTP variance
             were determined. TTP mean did not change with age, whereas
             TTP variance increased with age. Treatment with rapamycin
             generally did not affect these functional metrics.
             Synergistic effects of treatment and age were not found for
             any measurements. Together, the size and volume ratio of
             cysts decreased with drug treatment, whereas renal function
             remained the same. The quantification of renal structure and
             function with MRI can comprehensively assess the
             pathophysiology of PKD and response to treatment.},
   Doi = {10.1002/nbm.3281},
   Key = {fds268700}
}

@article{fds174275,
   Author = {GA Johnson and EG Kim and SJ Boukma},
   Title = {5-hydroxyindole levels in rat brain after inhibition of
             dopamine -hydroxylase.},
   Journal = {The Journal of pharmacology and experimental
             therapeutics},
   Volume = {180},
   Number = {3},
   Pages = {539-46},
   Year = {1972},
   Month = {March},
   ISSN = {0022-3565},
   Keywords = {Administration, Oral • Animals • Brain •
             Brain Chemistry • Circadian Rhythm • Disulfiram
             • Dopamine beta-Hydroxylase • Hydroxyindoleacetic
             Acid • Injections, Intraperitoneal • Male •
             Methyltyrosines • Mixed Function Oxygenases •
             Monoiodotyrosine • Norepinephrine • Pargyline
             • Rats • Rats, Inbred Strains • Serotonin
             • Thiazoles • Thiourea • Time Factors •
             administration & dosage • analysis • analysis*
             • antagonists & inhibitors • antagonists &
             inhibitors* • biosynthesis • drug effects •
             enzymology* • pharmacology • pharmacology*},
   Language = {eng},
   Key = {fds174275}
}

@article{fds132729,
   Author = {G.A. Johnson},
   Title = {5. X. Zhou, Z. P. Liang, G.P. Cofer, C.F. Beaulieu, S.A.
             Suddarth, G.A. Johnson. Reduction of Ringing and Blurring
             Artifacts in Fast Spin-Echo Images. J Magn Reson Imag
             3:803-807 (1993).},
   Year = {1994},
   Key = {fds132729}
}

@booklet{Hedlund86b,
   Author = {Hedlund, L and Johnson, GA},
   Title = {53 MAGNETIC RESONANCE IMAGING OF THE RAT THORAX AND
             ABDOMEN},
   Journal = {Investigative Radiology},
   Volume = {21},
   Number = {9},
   Pages = {S14-S14},
   Publisher = {Ovid Technologies (Wolters Kluwer Health)},
   Year = {1986},
   Month = {September},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1986E000900063&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Doi = {10.1097/00004424-198609000-00071},
   Key = {Hedlund86b}
}

@article{fds132715,
   Author = {G.A. Johnson},
   Title = {6. M.M. Henson, O.W. Henson, S.L. Gewalt, J.L. Wilson, G. A.
             Johnson. Imaging the Cochlea by MRM. Hearing Research
             75:75-80 (1994).},
   Year = {1994},
   Key = {fds132715}
}

@article{fds132730,
   Author = {G.A. Johnson},
   Title = {7. J. MacFall, P. Spaine, R. Doudrick, G. Johnson.
             Alterations in Growth and Water Transport Processes in
             Fusiform Rust Galls of Pine as Determined by Magnetic
             Resonance Microsopy. Phytopathology 84:288-293
             (1994).},
   Year = {1994},
   Key = {fds132730}
}

@booklet{Mcadams85,
   Author = {MCADAMS, HP and JOHNSON, GA and SUDDARTH, SA and RAVIN,
             CE},
   Title = {71 HISTOGRAM DIRECTED PROCESSING OF DIGITAL CHEST
             IMAGES},
   Journal = {Investigative Radiology},
   Volume = {20},
   Number = {6},
   Pages = {S18-S18},
   Publisher = {Ovid Technologies (Wolters Kluwer Health)},
   Year = {1985},
   Month = {September},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1985ARG0500088&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Doi = {10.1097/00004424-198509000-00099},
   Key = {Mcadams85}
}

@article{fds132731,
   Author = {G.A. Johnson},
   Title = {8. B.R. Smith, G.A. Johnson, E.V. Groman, E.A. Linney.
             Magnetic Resonance Microscopy of Mouse Embryos. Proc. Nat.
             Acad. Sci. USA 91:3530-3533 (1994).},
   Year = {1994},
   Key = {fds132731}
}

@article{fds174091,
   Author = {GA Johnson and AE Kimberly},
   Title = {A Comparative Review of Current Methods for the
             Determination of Organic Matter in Sewage.},
   Journal = {Public health papers and reports},
   Volume = {31},
   Number = {Pt 2},
   Pages = {97-108},
   Year = {1905},
   Language = {ENG},
   Key = {fds174091}
}

@article{fds174249,
   Author = {GA Johnson and AE Kimberly},
   Title = {A Comparative Review of Current Methods for the
             Determination of Organic Matter in Sewage.},
   Journal = {Public health papers and reports},
   Volume = {31},
   Number = {Pt 2},
   Pages = {97-108},
   Year = {1905},
   ISSN = {0737-8769},
   Language = {eng},
   Key = {fds174249}
}

@article{fds204264,
   Author = {GA Johnson and JN Bloom and L Szczotka-Flynn and D Zauner and RL
             Tomsak},
   Title = {A comparative study of resident performance on standardized
             training examinations and the american board of
             ophthalmology written examination.},
   Journal = {Ophthalmology},
   Volume = {117},
   Number = {12},
   Pages = {2435-9},
   Year = {2010},
   Month = {December},
   ISSN = {1549-4713},
   url = {http://dx.doi.org/10.1016/j.ophtha.2010.03.056},
   Keywords = {Adult • Certification • Clinical Competence •
             Cohort Studies • Education, Medical, Graduate •
             Educational Measurement* • Female • Humans •
             Internship and Residency • Licensure • Male •
             Ophthalmology • United States • Young Adult •
             education* • standards • standards*},
   Abstract = {OBJECTIVE: To investigate the relationships between
             ophthalmology resident performance on the United States
             Medical Licensing Examination (USMLE), the Ophthalmic
             Knowledge Assessment Program (OKAP) exam and the American
             Board of Ophthalmology written qualifying examination
             (ABO-WQE). METHODS: Cohort study. METHODS: We included 76
             residents from 15 consecutive training classes (1991-2006)
             at 1 ophthalmologic residency training program. METHODS:
             Numeric scores on the USMLE Step 1 and OKAP examinations
             during the 3 years of residency, and first attempt pass rate
             on the ABO-WQE were recorded for 76 residents. Age and
             gender were also noted. Spearman's rank correlations and
             univariate and multivariate logistic analyses were performed
             to determine relevant associations. METHODS: First-time
             attempt pass rate on the ABO-WQE and/or successful
             completion of the ABO-WQE within 3 years of graduation from
             the residency program. RESULTS: The ABO-WQE first-attempt
             pass rate was 72.6%, consistent with the national average.
             Resident USMLE scores were not significantly associated with
             ABO-WQE performance. The ABO-WQE pass rate was significantly
             associated with OKAP examination scores during the 3
             residency years (year 1: odds ratio [OR], 8.85 and 95%
             confidence interval [CI] 1.82-42.79; year 2: OR, 5.28 and
             95% CI, 1.15-25.27; year 3: OR, 11.08 and 95% CI,
             1.86-68.96). Passing the OKAP examinations in all 3 years
             during residency training was associated with 5.43-fold
             increased odds of passing the ABO-WQE and failing all 3 OKAP
             examinations was associated with >9-fold lower odds of
             passing the ABO-WQE on the first attempt. CONCLUSIONS: Our
             results suggest that OKAP examination performance is a
             predictor of a resident's success in passing the ABO-WQE on
             the first attempt, as well as within 3 years of graduation
             from an ophthalmologic training program. Awareness of this
             association may permit identification of residents at risk
             for failing the ABO-WQE and encourage educational
             remediation to prevent this failure.},
   Language = {eng},
   Doi = {10.1016/j.ophtha.2010.03.056},
   Key = {fds204264}
}

@article{fds268739,
   Author = {Subashi, E and Moding, EJ and Cofer, GP and MacFall, JR and Kirsch, DG and Qi, Y and Johnson, GA},
   Title = {A comparison of radial keyhole strategies for high spatial
             and temporal resolution 4D contrast-enhanced MRI in small
             animal tumor models.},
   Journal = {Med Phys},
   Volume = {40},
   Number = {2},
   Pages = {022304},
   Year = {2013},
   Month = {February},
   ISSN = {0094-2405},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/23387766},
   Abstract = {PURPOSE: Dynamic contrast-enhanced (DCE) MRI has been widely
             used as a quantitative imaging method for monitoring tumor
             response to therapy. The simultaneous challenges of
             increasing temporal and spatial resolution in a setting
             where the signal from the much smaller voxel is weaker have
             made this MR technique difficult to implement in
             small-animal imaging. Existing protocols employed in
             preclinical DCE-MRI acquire a limited number of slices
             resulting in potentially lost information in the third
             dimension. This study describes and compares a family of
             four-dimensional (3D spatial + time), projection
             acquisition, radial keyhole-sampling strategies that support
             high spatial and temporal resolution. METHODS: The 4D method
             is based on a RF-spoiled, steady-state, gradient-recalled
             sequence with minimal echo time. An interleaved 3D radial
             trajectory with a quasi-uniform distribution of points in
             k-space was used for sampling temporally resolved datasets.
             These volumes were reconstructed with three different
             k-space filters encompassing a range of possible radial
             keyhole strategies. The effect of k-space filtering on
             spatial and temporal resolution was studied in a 5 mM
             CuSO(4) phantom consisting of a meshgrid with 350-μm
             spacing and in 12 tumors from three cell lines (HT-29, LoVo,
             MX-1) and a primary mouse sarcoma model (three
             tumors∕group). The time-to-peak signal intensity was used
             to assess the effect of the reconstruction filters on
             temporal resolution. As a measure of heterogeneity in the
             third dimension, the authors analyzed the spatial
             distribution of the rate of transport (K(trans)) of the
             contrast agent across the endothelium barrier for several
             different types of tumors. RESULTS: Four-dimensional radial
             keyhole imaging does not degrade the system spatial
             resolution. Phantom studies indicate there is a maximum 40%
             decrease in signal-to-noise ratio as compared to a fully
             sampled dataset. T1 measurements obtained with the
             interleaved radial technique do not differ significantly
             from those made with a conventional Cartesian spin-echo
             sequence. A bin-by-bin comparison of the distribution of the
             time-to-peak parameter shows that 4D radial keyhole
             reconstruction does not cause significant temporal blurring
             when a temporal resolution of 9.9 s is used for the
             subsamples of the keyhole data. In vivo studies reveal
             substantial tumor heterogeneity in the third spatial
             dimension that may be missed with lower resolution imaging
             protocols. CONCLUSIONS: Volumetric keyhole imaging with
             projection acquisition provides a means to increase
             spatiotemporal resolution and coverage over that provided by
             existing 2D Cartesian protocols. Furthermore, there is no
             difference in temporal resolution between the higher spatial
             resolution keyhole reconstruction and the undersampled
             projection data. The technique allows one to measure complex
             heterogeneity of kinetic parameters with isotropic,
             microscopic spatial resolution.},
   Doi = {10.1118/1.4774050},
   Key = {fds268739}
}

@article{fds268786,
   Author = {Guo, X and Johnston, SM and Johnson, GA and Badea,
             CT},
   Title = {A comparison of sampling strategies for dual energy
             micro-CT},
   Journal = {Progress in Biomedical Optics and Imaging - Proceedings of
             SPIE},
   Volume = {8313},
   Publisher = {SPIE},
   Year = {2012},
   Month = {May},
   ISBN = {9780819489623},
   ISSN = {1605-7422},
   url = {http://dx.doi.org/10.1117/12.911548},
   Abstract = {Micro-CT has become a powerful tool for small animal
             research. Many micro-CT applications require exogenous
             contrast agents, which are most commonly based on iodine.
             Despite advancements in contrast agents, single-energy
             micro-CT is sometimes limited in the separation of two
             different materials that share similar grayscale intensity
             values as in the case of bone and iodine. Dual energy
             micro-CT offers a solution to this separation problem, while
             eliminating the need for pre-injection scanning. Various
             dual energy micro-CT sampling strategies are possible,
             including 1) single source sequential scanning, 2)
             simultaneous dual source acquisition, or 3) single source
             with kVp switching. But, no commercial micro-CT system
             exists in which all these sampling strategies have been
             implemented. This study reports on the implementation and
             comparison of these scanning techniques on the same small
             animal imaging system. Furthermore, we propose a new
             sampling strategy that combines dual source and kVp
             switching. Post-sampling and reconstruction, a simple
             two-material dual energy decomposition was applied to
             differentiate iodine from bone. The results indicate the
             time differences and the potential problems associated with
             each sampling strategy. Dual source scanning allows for the
             fastest acquisition, but is prone to errors in decomposition
             associated with scattering and imperfect geometric alignment
             of the two imaging chains. KVp switching prevents these
             types of artifacts, but requires more time for sampling. The
             novel combination between the dual source and kVp switching
             has the potential to reduce sampling time and provide better
             decomposition performance. © 2012 Copyright Society of
             Photo-Optical Instrumentation Engineers (SPIE).},
   Doi = {10.1117/12.911548},
   Key = {fds268786}
}

@article{fds174294,
   Author = {TL Rutledge and SA Kamelle and TD Tillmanns and NS Gould and JD Wright and DE Cohn and TJ Herzog and JS Rader and MA Gold and GA Johnson and JL
             Walker, RS Mannel and DS McMeekin},
   Title = {A comparison of stages IB1 and IB2 cervical cancers treated
             with radical hysterectomy. Is size the real
             difference?},
   Journal = {Gynecologic oncology},
   Volume = {95},
   Number = {1},
   Pages = {70-6},
   Year = {2004},
   Month = {October},
   ISSN = {0090-8258},
   url = {http://dx.doi.org/10.1016/j.ygyno.2004.07.027},
   Keywords = {Adult • Aged • Disease-Free Survival • Female
             • Follow-Up Studies • Humans • Hysterectomy
             • Lymph Node Excision • Lymph Nodes • Middle
             Aged • Neoplasm Recurrence, Local • Neoplasm
             Staging • Risk Factors • Treatment Outcome •
             Uterine Cervical Neoplasms • adverse effects •
             methods • pathology • pathology* • surgery
             • surgery*},
   Abstract = {OBJECTIVE: To compare stages IB1 and IB2 cervical cancers
             treated with radical hysterectomy (RH) and to define
             predictors of nodal status and recurrence. METHODS: Patients
             with stage IB cervical cancers undergoing RH between 1990
             and 2000 were evaluated and clinicopathological variables
             were abstracted. The perioperative complication rate,
             estimated blood loss (EBL), and OR time were also tabulated.
             Variables were analyzed using X(2) and t tests. Disease-free
             survival (DFS) was calculated by Kaplan-Meier method.
             Multivariate analysis was performed via stepwise logistic
             regression. Cox-proportional hazards were used to identify
             independent predictors of recurrence. RESULTS: RH was
             performed on 109 stage IB1 and 86 stage IB2 patients. Mean
             age, EBL, and perioperative complication rates were similar.
             Overall, 38 patients (14 IB1 vs. 24 IB2) had positive nodes
             (P = 0.01) including 9 patients with positive para-aortic
             nodes (2 IB1 and 7 IB2). Parametrial involvement (PI) and
             outer 2/3 depth of invasion (DOI) were significantly more
             common in the IB2 tumors as well. Patients with IB2 disease
             received adjuvant radiation more frequently than IB1
             patients (52% vs. 37%, P = 0.04). Univariate predictors of
             nodal status included lymphovascular space involvement
             (LVSI) (P = 0.001), DOI (P = 0.011), PI (P = 0.001), and
             stage (P = 0.011). Multivariate analysis identified only
             LVSI (OR 6.4, CI 2.4-17, P = 0. 0002) and PI (OR 8, CI
             3.1-20, P = 0. 0001) as independent predictors of positive
             nodes. With a median follow-up of 35 months, estimates of
             DFS revealed tumor size (P = 0.008), nodal status (P =
             0.0004), LVSI (P = 0.002), PI (P = 0.004), and DOI (P =
             0.0004) as significant univariate predictors. Neoadjuvant
             chemotherapy, age, grade, histology, and adjuvant radiation
             were not associated with recurrence. The significant
             independent predictors of DFS were LVSI (ROR 5.7, CI 2-16, P
             = 0.0064) and outer 2/3 DOI (OR 5.8, CI 2-20, P = 0.0029).
             Neither tumor size nor nodal status was a significant
             predictor of DFS. CONCLUSIONS: The prognosis in stage IB
             cervical cancer seems to be most influenced by presence of
             LVSI and DOI and not by tumor size as the staging criteria
             would suggest. These factors are best determined
             pathologically after radical hysterectomy. This report
             contains the largest comparison of IB1 and IB2 patients
             managed by RH. Tumor size failed to predict recurrence or
             nodal status when stratified by LVSI, DOI, and PI. Treatment
             decisions based on tumor size alone should be
             reconsidered.},
   Language = {eng},
   Doi = {10.1016/j.ygyno.2004.07.027},
   Key = {fds174294}
}

@booklet{Murad90,
   Author = {S. Murad and L. C. Walker and G. A. Johnson and S. R.
             Pinnell},
   Title = {A comparison of the inhibitory potential of minoxidil and
             its structural analogs toward lysyl hydroxylase in cultured
             fibroblasts},
   Journal = {Clinical Research},
   Volume = {38},
   Number = {2},
   Pages = {A667 -- A667},
   Year = {1990},
   Month = {April},
   Key = {Murad90}
}

@booklet{Murad90a,
   Author = {S. Murad and L. C. Walker and G. A. Johnson and S. R.
             Pinnell},
   Title = {A comparison of the inhibitory potential of minoxidil and
             its structural analogs toward lysyl hydroxylase in cultured
             fibroblasts},
   Journal = {Journal Of Investigative Dermatology},
   Volume = {94},
   Number = {4},
   Pages = {557 -- 557},
   Year = {1990},
   Month = {April},
   Key = {Murad90a}
}

@booklet{Rogers00,
   Author = {P. Rogers and P. A. Hailey and G. A. Johnson and V. A. Dight and C. Read and A. Shingler and P. Savage and T. Roche and J. Mondry},
   Title = {A comprehensive and flexible approach to the
             automated-dissolution testing of pharmaceutical drug
             products incorporating direct UV-vis fiber-optic analysis,
             on-line fluorescence analysis, and off-line storage
             options},
   Journal = {Laboratory Robotics And Automation},
   Volume = {12},
   Number = {1},
   Pages = {12 -- 22},
   Year = {2000},
   Month = {March},
   Key = {Rogers00}
}

@booklet{Hedlund81,
   Author = {Hedlund, LW and Jones, DP and Effmann, EL and Johnson, GA and Bates, WM and Beck, JW and Wolfe, W and Putman, CE},
   Title = {A computed tomographic study of the dog lung during
             hemorrhagic shock and after resuscitation.},
   Journal = {Invest Radiol},
   Volume = {16},
   Number = {6},
   Pages = {466-472},
   Year = {1981},
   ISSN = {0020-9996},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/7319752},
   Abstract = {A shock model was used to explore the capability of computed
             tomography (CT) to detect changes in lung density during
             hypovolemia and after resuscitation. The same level of the
             lower thorax was scanned repeatedly during base-line, shock
             (aortic pressure 60 mmHg), and after resuscitation with shed
             blood. The average baseline CT number (+/- SEM) for 5 areas
             of interest for four prone dogs was -754 +/- 16 (air =
             -1000, water = 0). This decreased 7.4% to -810 +/- 15 (P
             less than .05) during shock. After resuscitation CT density
             was -773 +/- 17 or 2.5% less than baseline (P greater than
             .1). A dorsal to ventral gradient of increasing CT density
             during baseline was maintained in all five areas during
             shock and post-resuscitation. From baseline to shock there
             were also significant changes in heart rate, mean aortic
             pressure, cardiac output, and vascular volume. Extravascular
             lung volume after resuscitation was equal to baseline
             volume. We conclude that CT is sufficiently sensitive to
             detect rapid physiological changes leading to increased or
             decreased lung density.},
   Doi = {10.1097/00004424-198111000-00003},
   Key = {Hedlund81}
}

@article{fds132854,
   Author = {LW Hedlund and DP Jones and EL Effmann and GA Johnson and WM Bates and JW
             Beck, W Wolfe and CE Putman},
   Title = {A computed tomographic study of the dog lung during
             hemorrhagic shock and after resuscitation.},
   Journal = {Investigative radiology, UNITED STATES},
   Volume = {16},
   Number = {6},
   Pages = {466-72},
   ISSN = {0020-9996},
   Keywords = {Animals • Dogs • Hemodynamic Processes • Lung
             • Resuscitation* • Shock, Hemorrhagic •
             Tomography, X-Ray Computed* • physiopathology •
             radiography*},
   Abstract = {A shock model was used to explore the capability of computed
             tomography (CT) to detect changes in lung density during
             hypovolemia and after resuscitation. The same level of the
             lower thorax was scanned repeatedly during base-line, shock
             (aortic pressure 60 mmHg), and after resuscitation with shed
             blood. The average baseline CT number (+/- SEM) for 5 areas
             of interest for four prone dogs was -754 +/- 16 (air =
             -1000, water = 0). This decreased 7.4% to -810 +/- 15 (P
             less than .05) during shock. After resuscitation CT density
             was -773 +/- 17 or 2.5% less than baseline (P greater than
             .1). A dorsal to ventral gradient of increasing CT density
             during baseline was maintained in all five areas during
             shock and post-resuscitation. From baseline to shock there
             were also significant changes in heart rate, mean aortic
             pressure, cardiac output, and vascular volume. Extravascular
             lung volume after resuscitation was equal to baseline
             volume. We conclude that CT is sufficiently sensitive to
             detect rapid physiological changes leading to increased or
             decreased lung density.},
   Key = {fds132854}
}

@article{fds268697,
   Author = {Calabrese, E and Badea, A and Cofer, G and Qi, Y and Johnson,
             GA},
   Title = {A Diffusion MRI Tractography Connectome of the Mouse Brain
             and Comparison with Neuronal Tracer Data.},
   Journal = {Cereb Cortex},
   Volume = {25},
   Number = {11},
   Pages = {4628-4637},
   Year = {2015},
   Month = {November},
   ISSN = {1047-3211},
   url = {http://hdl.handle.net/10161/10325 Duke open
             access},
   Abstract = {Interest in structural brain connectivity has grown with the
             understanding that abnormal neural connections may play a
             role in neurologic and psychiatric diseases. Small animal
             connectivity mapping techniques are particularly important
             for identifying aberrant connectivity in disease models.
             Diffusion magnetic resonance imaging tractography can
             provide nondestructive, 3D, brain-wide connectivity maps,
             but has historically been limited by low spatial resolution,
             low signal-to-noise ratio, and the difficulty in estimating
             multiple fiber orientations within a single image voxel.
             Small animal diffusion tractography can be substantially
             improved through the combination of ex vivo MRI with
             exogenous contrast agents, advanced diffusion acquisition
             and reconstruction techniques, and probabilistic fiber
             tracking. Here, we present a comprehensive, probabilistic
             tractography connectome of the mouse brain at microscopic
             resolution, and a comparison of these data with a neuronal
             tracer-based connectivity data from the Allen Brain Atlas.
             This work serves as a reference database for future
             tractography studies in the mouse brain, and demonstrates
             the fundamental differences between tractography and
             neuronal tracer data.},
   Doi = {10.1093/cercor/bhv121},
   Key = {fds268697}
}

@article{fds268695,
   Author = {Calabrese, E and Badea, A and Coe, CL and Lubach, GR and Shi, Y and Styner,
             MA and Johnson, GA},
   Title = {A diffusion tensor MRI atlas of the postmortem rhesus
             macaque brain.},
   Journal = {Neuroimage},
   Volume = {117},
   Pages = {408-416},
   Year = {2015},
   Month = {August},
   ISSN = {1053-8119},
   url = {http://dx.doi.org/10.1016/j.neuroimage.2015.05.072},
   Abstract = {The rhesus macaque (Macaca mulatta) is the most widely used
             nonhuman primate for modeling the structure and function of
             the brain. Brain atlases, and particularly those based on
             magnetic resonance imaging (MRI), have become important
             tools for understanding normal brain structure, and for
             identifying structural abnormalities resulting from disease
             states, exposures, and/or aging. Diffusion tensor imaging
             (DTI)-based MRI brain atlases are widely used in both human
             and macaque brain imaging studies because of the unique
             contrasts, quantitative diffusion metrics, and diffusion
             tractography that they can provide. Previous MRI and DTI
             atlases of the rhesus brain have been limited by low
             contrast and/or low spatial resolution imaging. Here we
             present a microscopic resolution MRI/DTI atlas of the rhesus
             brain based on 10 postmortem brain specimens. The atlas
             includes both structural MRI and DTI image data, a detailed
             three-dimensional segmentation of 241 anatomic structures,
             diffusion tractography, cortical thickness estimates, and
             maps of anatomic variability among atlas specimens. This
             atlas incorporates many useful features from previous work,
             including anatomic label nomenclature and ontology, data
             orientation, and stereotaxic reference frame, and further
             extends prior analyses with the inclusion of high-resolution
             multi-contrast image data.},
   Doi = {10.1016/j.neuroimage.2015.05.072},
   Key = {fds268695}
}

@article{fds268814,
   Author = {Badea, CT and Johnston, S and Johnson, B and Lin, M and Hedlund, LW and Johnson, GA},
   Title = {A dual micro-CT system for small animal imaging.},
   Journal = {Proc SPIE Int Soc Opt Eng},
   Volume = {6913},
   Pages = {691342},
   Year = {2008},
   Month = {April},
   ISSN = {0277-786X},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/22049304},
   Abstract = {Micro-CT is a non-invasive imaging modality usually used to
             assess morphology in small animals. In our previous work, we
             have demonstrated that functional micro-CT imaging is also
             possible. This paper describes a dual micro-CT system with
             two fixed x-ray/detectors developed to address such
             challenging tasks as cardiac or perfusion studies in small
             animals. A two-tube/detector system ensures simultaneous
             acquisition of two projections, thus reducing scanning time
             and the number of contrast injections in perfusion studies
             by a factor of two. The system is integrated with software
             developed in-house for cardio-respiratory monitoring and
             gating. The sampling geometry was optimized for 88 microns
             in such a way that the geometric blur of the focal spot
             matches the Nyquist sample at the detector. A geometric
             calibration procedure allows one to combine projection data
             from the two chains into a single reconstructed volume.
             Image quality was measured in terms of spatial resolution,
             uniformity, noise, and linearity. The modulation transfer
             function (MTF) at 10% is 3.4 lp/mm for single detector
             reconstructions and 2.3 lp/mm for dual tube/detector
             reconstructions. We attribute this loss in spatial
             resolution to the compounding of slight errors in the
             separate single chain calibrations. The dual micro-CT system
             is currently used in studies for morphological and
             functional imaging of both rats and mice.},
   Language = {ENG},
   Doi = {10.1117/12.772303},
   Key = {fds268814}
}

@article{fds132829,
   Author = {X Zhou and ZP Liang and SL Gewalt and GP Cofer and PC Lauterbur and GA
             Johnson},
   Title = {A fast spin echo technique with circular
             sampling.},
   Journal = {Magnetic resonance in medicine : official journal of the
             Society of Magnetic Resonance in Medicine / Society of
             Magnetic Resonance in Medicine, UNITED STATES},
   Volume = {39},
   Number = {1},
   Pages = {23-7},
   Year = {1998},
   Month = {January},
   ISSN = {0740-3194},
   Keywords = {Animals • Brain • Echo-Planar Imaging • Image
             Processing, Computer-Assisted • Magnetic Resonance
             Imaging • Models, Theoretical • Phantoms, Imaging*
             • Rats • Sensitivity and Specificity •
             anatomy & histology* • instrumentation • methods
             • methods*},
   Abstract = {This paper presents a fast spin echo (FSE) imaging method
             that employs circular sampling of k-space. The technique has
             been implemented on a 2 Tesla imaging system and validated
             on both phantoms and living animals. Experimental studies
             have shown that circular sampling can produce artifact-free
             FSE images without the need of phase correction. Although
             not fully explored, preliminary results also show that
             circular sampling may have advantages over the conventional
             rectilinear FSE in signal-to-noise ratio and imaging
             efficiency. A major disadvantage is the increased
             sensitivity to off-resonance effects. The authors expect
             that the FSE technique with circular sampling will find its
             applications in magnetic resonance microscopy,
             neuro-functional imaging, and real-time dynamic
             studies.},
   Key = {fds132829}
}

@booklet{Zhou98,
   Author = {Zhou, X and Liang, ZP and Gewalt, SL and Cofer, GP and Lauterbur, PC and Johnson, GA},
   Title = {A fast spin echo technique with circular
             sampling.},
   Journal = {Magn Reson Med},
   Volume = {39},
   Number = {1},
   Pages = {23-27},
   Year = {1998},
   Month = {January},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/9438433},
   Abstract = {This paper presents a fast spin echo (FSE) imaging method
             that employs circular sampling of k-space. The technique has
             been implemented on a 2 Tesla imaging system and validated
             on both phantoms and living animals. Experimental studies
             have shown that circular sampling can produce artifact-free
             FSE images without the need of phase correction. Although
             not fully explored, preliminary results also show that
             circular sampling may have advantages over the conventional
             rectilinear FSE in signal-to-noise ratio and imaging
             efficiency. A major disadvantage is the increased
             sensitivity to off-resonance effects. The authors expect
             that the FSE technique with circular sampling will find its
             applications in magnetic resonance microscopy,
             neuro-functional imaging, and real-time dynamic
             studies.},
   Doi = {10.1002/mrm.1910390106},
   Key = {Zhou98}
}

@booklet{Johnson82a,
   Author = {G. A. Johnson},
   Title = {A generalization of n-matrices},
   Journal = {Linear Algebra And Its Applications},
   Volume = {48},
   Number = {DEC},
   Pages = {201 -- 217},
   Year = {1982},
   Key = {Johnson82a}
}

@article{fds268872,
   Author = {de Lin, M and Ning, L and Badea, CT and Mistry, NN and Qi, Y and Johnson,
             GA},
   Title = {A high-precision contrast injector for small animal x-ray
             digital subtraction angiography.},
   Journal = {IEEE Trans Biomed Eng},
   Volume = {55},
   Number = {3},
   Pages = {1082-1091},
   Year = {2008},
   Month = {March},
   ISSN = {0018-9294},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/18334400},
   Keywords = {Angiography, Digital Subtraction • Animals •
             Contrast Media • Equipment Design • Equipment
             Failure Analysis • Iopamidol • Mice •
             Microinjections • Radiographic Image Enhancement •
             Reproducibility of Results • Sensitivity and
             Specificity • administration & dosage •
             administration & dosage* • instrumentation* •
             methods • veterinary*},
   Abstract = {The availability of genetically altered animal models of
             human disease for basic research has generated great
             interest in new imaging methodologies. Digital subtraction
             angiography (DSA) offers an appealing approach to functional
             imaging in small animals because of the high spatial and
             temporal resolution, and the ability to visualize and
             measure blood flow. The micro-injector described here meets
             crucial performance parameters to ensure optimal vessel
             enhancement without significantly increasing the total blood
             volume or producing overlap of enhanced structures. The
             micro-injector can inject small, reproducible volumes of
             contrast agent at high flow rates with computer-controlled
             timing synchronized to cardiopulmonary activity. Iterative
             bench-top and live animal experiments with both rat and
             mouse have been conducted to evaluate the performance of
             this computer-controlled micro-injector, a first
             demonstration of a new device designed explicitly for the
             unique requirements of DSA in small animals. Injection
             protocols were optimized and screened for potential
             physiological impact. For the optimized protocols, we found
             that changes in the time-density curves for representative
             regions of interest in the thorax were due primarily to
             physiological changes, independent of micro-injector
             parameters.},
   Doi = {10.1109/TBME.2007.909541},
   Key = {fds268872}
}

@article{fds268703,
   Author = {Angeli, S and Befera, N and Peyrat, J-M and Calabrese, E and Johnson,
             GA and Constantinides, C},
   Title = {A high-resolution cardiovascular magnetic resonance
             diffusion tensor map from ex-vivo C57BL/6 murine
             hearts.},
   Journal = {J Cardiovasc Magn Reson},
   Volume = {16},
   Number = {1},
   Pages = {77},
   Year = {2014},
   Month = {October},
   ISSN = {1097-6647},
   url = {http://dx.doi.org/10.1186/s12968-014-0077-x},
   Abstract = {BACKGROUND: The complex cardiac fiber structural
             organization and spatial arrangement of cardiomyocytes in
             laminar sheetlets contributes greatly to cardiac functional
             and contractile ejection patterns. This study presents the
             first comprehensive, ultra-high resolution, fully
             quantitative statistical tensor map of the fixed murine
             heart at isotropic resolution of 43 μm using diffusion
             tensor (DT) cardiovascular magnetic resonance (CMR).
             METHODS: Imaging was completed in approximately 12 hours
             using a six-directional encoding scheme, in five ex vivo
             healthy C57BL/6 mouse hearts. The tensor map constructed
             from this data provides an average description of the murine
             fiber architecture visualized with fiber tractography, and
             its population variability, using the latest advances in
             image tensor analysis and statistics. RESULTS: Results show
             that non-normalized cardiac tensor maps are associated with
             mean fractional anisotropy of 0.25 ± 0.07 and mean
             diffusivity of 8.9 ± 1.6 × 10⁻⁴mm²/s. Moreover,
             average mid-ventricular helical angle distributions ranged
             between -41 ± 3° and +52 ± 5° and were highly
             correlated with transmural depth, in agreement with prior
             published results in humans and canines. Calculated
             variabilities of local myocyte orientations were 2.0° and
             1.4°. Laminar sheet orientation variability was found to be
             less stable at 2.6°. Despite such variations, the murine
             heart seems to be highly structured, particularly when
             compared to canines and humans. CONCLUSIONS: This tensor map
             has the potential to yield an accurate mean representation
             and identification of common or unique features of the
             cardiac myocyte architecture, to establish a baseline
             standard reference of DTI indices, and to improve detection
             of biomarkers, especially in pathological states or
             post-transgenetic modifications.},
   Doi = {10.1186/s12968-014-0077-x},
   Key = {fds268703}
}

@article{fds356152,
   Author = {Adil, SM and Calabrese, E and Charalambous, LT and Cook, JJ and Rahimpour, S and Atik, AF and Cofer, GP and Parente, BA and Johnson, GA and Lad, SP and White, LE},
   Title = {A high-resolution interactive atlas of the human brainstem
             using magnetic resonance imaging.},
   Journal = {Neuroimage},
   Volume = {237},
   Pages = {118135},
   Year = {2021},
   Month = {August},
   url = {http://dx.doi.org/10.1016/j.neuroimage.2021.118135},
   Abstract = {Conventional atlases of the human brainstem are limited by
             the inflexible, sparsely-sampled, two-dimensional nature of
             histology, or the low spatial resolution of conventional
             magnetic resonance imaging (MRI). Postmortem high-resolution
             MRI circumvents the challenges associated with both
             modalities. A single human brainstem specimen extending from
             the rostral diencephalon through the caudal medulla was
             prepared for imaging after the brain was removed from a
             65-year-old male within 24 h of death. The specimen was
             formalin-fixed for two weeks, then rehydrated and placed in
             a custom-made MRI compatible tube and immersed in liquid
             fluorocarbon. MRI was performed in a 7-Tesla scanner with
             120 unique diffusion directions. Acquisition time for
             anatomic and diffusion images were 14 h and 208 h,
             respectively. Segmentation was performed manually.
             Deterministic fiber tractography was done using
             strategically chosen regions of interest and avoidance, with
             manual editing using expert knowledge of human neuroanatomy.
             Anatomic and diffusion images were rendered with isotropic
             resolutions of 50 μm and 200 μm, respectively. Ninety
             different structures were segmented and labeled, and 11
             different fiber bundles were rendered with tractography. The
             complete atlas is available online for interactive use at
             https://www.civmvoxport.vm.duke.edu/voxbase/login.php?return_url=%2Fvoxbase%2F.
             This atlas presents multiple contrasting datasets and
             selected tract reconstruction with unprecedented resolution
             for MR imaging of the human brainstem. There are immediate
             applications in neuroanatomical education, with the
             potential to serve future applications for neuroanatomical
             research and enhanced neurosurgical planning through "safe"
             zones of entry into the human brainstem.},
   Doi = {10.1016/j.neuroimage.2021.118135},
   Key = {fds356152}
}

@article{fds132839,
   Author = {SE Hurlston and WW Brey and SA Suddarth and GA Johnson},
   Title = {A high-temperature superconducting Helmholtz probe for
             microscopy at 9.4 T.},
   Journal = {Magnetic resonance in medicine : official journal of the
             Society of Magnetic Resonance in Medicine / Society of
             Magnetic Resonance in Medicine, UNITED STATES},
   Volume = {41},
   Number = {5},
   Pages = {1032-8},
   Year = {1999},
   Month = {May},
   ISSN = {0740-3194},
   Keywords = {Algorithms • Aluminum Oxide • Animals •
             Artifacts • Cold • Copper • Equipment Design
             • Heat • Helium • Image Processing,
             Computer-Assisted • Magnetic Resonance Imaging •
             Mice • Microscopy • Phantoms, Imaging • Radio
             Waves • Ruthenium Compounds • Sensitivity and
             Specificity • Signal Processing, Computer-Assisted
             • Thermal Conductivity • instrumentation •
             instrumentation*},
   Abstract = {The design and operation of a high-temperature
             superconducting (HTS) probe for magnetic resonance
             microscopy (MRM) at 400 MHz are presented. The design of the
             probe includes a Helmholtz coil configuration and a stable
             open-cycle cooling mechanism. Characterization of coil
             operating parameters is presented to demonstrate the
             suitability of cryo-cooled coils for MRM. Specifically, the
             performance of the probe is evaluated by comparison of
             signal-to-noise (SNR) performance with that of a copper
             Helmholtz pair, analysis of B1 field homogeneity, and
             quantification of thermal stability. Images are presented to
             demonstrate the SNR advantage of the probe for typical MRM
             applications.},
   Key = {fds132839}
}

@booklet{Hurlston99,
   Author = {Hurlston, SE and Brey, WW and Suddarth, SA and Johnson,
             GA},
   Title = {A high-temperature superconducting Helmholtz probe for
             microscopy at 9.4 T.},
   Journal = {Magn Reson Med},
   Volume = {41},
   Number = {5},
   Pages = {1032-1038},
   Year = {1999},
   Month = {May},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/10332887},
   Abstract = {The design and operation of a high-temperature
             superconducting (HTS) probe for magnetic resonance
             microscopy (MRM) at 400 MHz are presented. The design of the
             probe includes a Helmholtz coil configuration and a stable
             open-cycle cooling mechanism. Characterization of coil
             operating parameters is presented to demonstrate the
             suitability of cryo-cooled coils for MRM. Specifically, the
             performance of the probe is evaluated by comparison of
             signal-to-noise (SNR) performance with that of a copper
             Helmholtz pair, analysis of B1 field homogeneity, and
             quantification of thermal stability. Images are presented to
             demonstrate the SNR advantage of the probe for typical MRM
             applications.},
   Doi = {10.1002/(sici)1522-2594(199905)41:5<1032::aid-mrm23>3.0.co;2},
   Key = {Hurlston99}
}

@booklet{Black93,
   Author = {Black, RD and Early, TA and Roemer, PB and Mueller, OM and Mogro-Campero, A and Turner, LG and Johnson, GA},
   Title = {A high-temperature superconducting receiver for nuclear
             magnetic resonance microscopy.},
   Journal = {Science},
   Volume = {259},
   Number = {5096},
   Pages = {793-795},
   Year = {1993},
   Month = {February},
   ISSN = {0036-8075},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/8430331},
   Abstract = {A high-temperature superconducting-receiver system for use
             in nuclear magnetic resonance (NMR) microscopy is described.
             The scaling behavior of sources of sample and receiver-coil
             noise is analyzed, and it is demonstrated that Johnson, or
             thermal, noise in the receiver coil is the factor that
             limits resolution. The behavior of superconductors in the
             environment of an NMR experiment is examined, and a
             prototypical system for imaging biological specimens is
             discussed. Preliminary spin-echo images are shown, and the
             ultimate limits of the signal-to-noise ratio of the probe
             are investigated.},
   Doi = {10.1126/science.8430331},
   Key = {Black93}
}

@article{fds132865,
   Author = {RD Black and TA Early and PB Roemer and OM Mueller and A Mogro-Campero and LG Turner and GA Johnson},
   Title = {A high-temperature superconducting receiver for nuclear
             magnetic resonance microscopy.},
   Journal = {Science (New York, N.Y.), UNITED STATES},
   Volume = {259},
   Number = {5096},
   Pages = {793-5},
   Year = {1993},
   Month = {February},
   ISSN = {0036-8075},
   Keywords = {Animals • Humans • Magnetic Resonance Spectroscopy
             • Models, Theoretical • instrumentation* •
             methods},
   Abstract = {A high-temperature superconducting-receiver system for use
             in nuclear magnetic resonance (NMR) microscopy is described.
             The scaling behavior of sources of sample and receiver-coil
             noise is analyzed, and it is demonstrated that Johnson, or
             thermal, noise in the receiver coil is the factor that
             limits resolution. The behavior of superconductors in the
             environment of an NMR experiment is examined, and a
             prototypical system for imaging biological specimens is
             discussed. Preliminary spin-echo images are shown, and the
             ultimate limits of the signal-to-noise ratio of the probe
             are investigated.},
   Key = {fds132865}
}

@article{fds174305,
   Author = {SC Walker and T Shin and GM Zaunbrecher and JE Romano and GA Johnson and FW
             Bazer, JA Piedrahita},
   Title = {A highly efficient method for porcine cloning by nuclear
             transfer using in vitro-matured oocytes.},
   Journal = {Cloning and stem cells},
   Volume = {4},
   Number = {2},
   Pages = {105-12},
   Year = {2002},
   ISSN = {1536-2302},
   url = {http://dx.doi.org/10.1089/153623002320253283},
   Keywords = {Animals • Cloning, Organism • Culture Techniques
             • Embryo Transfer • Female • Microsatellite
             Repeats • Nuclear Transfer Techniques* • Oocytes
             • Pregnancy • Sex Ratio • Swine •
             cytology* • genetics • genetics* •
             methods*},
   Abstract = {To date, the efficiency of pig cloning by nuclear transfer
             of somatic cell nuclei has been extremely low, with less
             than 1% of transferred embryos surviving to term. Even the
             utilization of complex procedures such as two rounds of
             nuclear transfer has not resulted in greater overall
             efficiencies. As a result, the applicability of the
             technology for the generation of transgenic and cloned
             animals has not moved forward rapidly. We report here a
             simple nuclear transfer protocol, utilizing commercially
             available in vitro-matured oocytes, that results in greater
             than 5% overall cloning efficiency. Of five recipients
             receiving nuclear transfer embryos produced with a fetal
             fibroblast cell line as nuclear donor, all five established
             pregnancies by day 28 (100%), and 4/5 (80%) went to term.
             Efficiencies for each transfer were 7% (9 piglets/128
             doublets transferred), 5% (5/100), 12% (7/59), and 6.6%
             (7/106). The overall efficiency in all recipients was 5.5%
             and in pregnant recipients 7.7%, with a total of 28 cloned
             piglets produced. With the average fusion rate being 58%,
             the percentage of fused doublets producing a live piglet
             approached 12%. The method described here can be undertaken
             by a single micromanipulator at a reasonable cost, and
             should facilitate the broad utilization of porcine cloning
             technology in transgenic and nontransgenic
             applications.},
   Language = {eng},
   Doi = {10.1089/153623002320253283},
   Key = {fds174305}
}

@article{fds174077,
   Author = {DJ Waldon and MF Kubicek and GA Johnson and AE Buhl},
   Title = {A HPLC-based chloramphenicol acetyltransferase assay for
             assessing hair growth: comparison of the sensitivity of UV
             and fluorescence detection.},
   Journal = {European journal of clinical chemistry and clinical
             biochemistry : journal of the Forum of European Clinical
             Chemistry Societies},
   Volume = {31},
   Number = {1},
   Pages = {41-5},
   Year = {1993},
   Month = {January},
   ISSN = {0939-4974},
   Keywords = {Animals • Chloramphenicol O-Acetyltransferase •
             Chromatography, High Pressure Liquid* • Culture
             Techniques • Gene Expression • Hair •
             Keratins • Mice • Mice, Transgenic • Promoter
             Regions, Genetic • Sensitivity and Specificity •
             Spectrometry, Fluorescence • Spectrophotometry,
             Ultraviolet • analysis* • genetics •
             genetics* • growth & development*},
   Abstract = {In our attempt to measure hair growth by hair-specific
             markers, we used transgenic mice to express the
             chloramphenicol acetyltransferase gene under the control of
             an ultrahigh sulphur keratin gene promoter. To quantitate
             expression of the keratin gene, we required a
             chloramphenicol acetyltransferase assay which could measure
             enzyme activity in a single follicle and also could be used
             to assay a large number of samples without loss of
             sensitivity. We achieved this objective by utilizing a
             fluorescent substrate for chloramphenicol acetyltransferase.
             With HPLC-fluorescence detection, this substrate provides a
             sensitivity of less than 1 x 10(-13) mol, which is 1000
             times greater than that achievable with HPLC-UV detection in
             cultured follicles. Further, the assay was automated to
             facilitate the analysis of more than 100 samples/day. It
             should be possible to apply this fluorescent assay to a
             number of cell or tissue studies.},
   Language = {eng},
   Key = {fds174077}
}

@booklet{Waldon93a,
   Author = {D. J. Waldon and M. F. Kubicek and G. A. Johnson and A. E.
             Buhl},
   Title = {A hplc-based chloramphenicol acetyltransferase assay for
             assessing hair-growth - comparison of the sensitivity of uv
             and fluorescence detection},
   Journal = {European Journal Of Clinical Chemistry And Clinical
             Biochemistry},
   Volume = {31},
   Number = {1},
   Pages = {41 -- 45},
   Year = {1993},
   Month = {January},
   Key = {Waldon93a}
}

@article{fds312813,
   Author = {Badea, CT and Hedlund, LW and Johnson, GA},
   Title = {A LabVIEW Platform for Preclinical Imaging Using Digital
             Subtraction Angiography and Micro-CT.},
   Journal = {J Med Eng},
   Volume = {2013},
   Number = {581617},
   Pages = {581617},
   Year = {2013},
   url = {http://hdl.handle.net/10161/11992 Duke open
             access},
   Abstract = {CT and digital subtraction angiography (DSA) are ubiquitous
             in the clinic. Their preclinical equivalents are valuable
             imaging methods for studying disease models and treatment.
             We have developed a dual source/detector X-ray imaging
             system that we have used for both micro-CT and DSA studies
             in rodents. The control of such a complex imaging system
             requires substantial software development for which we use
             the graphical language LabVIEW (National Instruments,
             Austin, TX, USA). This paper focuses on a LabVIEW platform
             that we have developed to enable anatomical and functional
             imaging with micro-CT and DSA. Our LabVIEW applications
             integrate and control all the elements of our system
             including a dual source/detector X-ray system, a mechanical
             ventilator, a physiological monitor, and a power
             microinjector for the vascular delivery of X-ray contrast
             agents. Various applications allow cardiac- and
             respiratory-gated acquisitions for both DSA and micro-CT
             studies. Our results illustrate the application of DSA for
             cardiopulmonary studies and vascular imaging of the liver
             and coronary arteries. We also show how DSA can be used for
             functional imaging of the kidney. Finally, the power of 4D
             micro-CT imaging using both prospective and retrospective
             gating is shown for cardiac imaging.},
   Doi = {10.1155/2013/581617},
   Key = {fds312813}
}

@article{fds268870,
   Author = {Mukundan, S and Ghaghada, KB and Badea, CT and Kao, C-Y and Hedlund, LW and Provenzale, JM and Johnson, GA and Chen, E and Bellamkonda, RV and Annapragada, A},
   Title = {A liposomal nanoscale contrast agent for preclinical CT in
             mice.},
   Journal = {AJR Am J Roentgenol},
   Volume = {186},
   Number = {2},
   Pages = {300-307},
   Year = {2006},
   Month = {February},
   ISSN = {0361-803X},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/16423931},
   Keywords = {Animals • Contrast Media • Image Processing,
             Computer-Assisted • Liposomes • Mice •
             Radiography, Thoracic • Tomography, X-Ray Computed*
             • Triiodobenzoic Acids • chemistry •
             pharmacokinetics*},
   Abstract = {OBJECTIVE: The goal of this study was to determine if an
             iodinated, liposomal contrast agent could be used for
             high-resolution, micro-CT of low-contrast, small-size
             vessels in a murine model. MATERIALS AND METHODS: A
             second-generation, liposomal blood pool contrast agent
             encapsulating a high concentration of iodine (83-105 mg
             I/mL) was evaluated. A total of five mice weighing between
             20 and 28 g were infused with equivalent volume doses (500
             microL of contrast agent/25 g of mouse weight) and imaged
             with our micro-CT system for intervals of up to 240 min
             postinfusion. The animals were anesthetized, mechanically
             ventilated, and vital signs monitored allowing for
             simultaneous cardiac and respiratory gating of image
             acquisition. RESULTS: Initial enhancement of about 900 H in
             the aorta was obtained, which decreased to a plateau level
             of approximately 800 H after 2 hr. Excellent contrast
             discrimination was shown between the myocardium and cardiac
             blood pool (650-700 H). No significant nephrogram was
             identified, indicating the absence of renal clearance of the
             agent. CONCLUSION: The liposomal-based iodinated contrast
             agent shows long residence time in the blood pool, very high
             attenuation within submillimeter vessels, and no significant
             renal clearance rendering it an effective contrast agent for
             murine vascular imaging using a micro-CT
             scanner.},
   Doi = {10.2214/AJR.05.0523},
   Key = {fds268870}
}

@article{fds268784,
   Author = {Johnston, SM and Johnson, GA and Badea, CT},
   Title = {A material decomposition method for dual energy
             micro-CT},
   Journal = {Progress in Biomedical Optics and Imaging - Proceedings of
             SPIE},
   Volume = {7258},
   Publisher = {SPIE},
   Year = {2009},
   Month = {June},
   ISBN = {9780819475091},
   ISSN = {1605-7422},
   url = {http://dx.doi.org/10.1117/12.811673},
   Abstract = {The attenuation of x-rays in matter is dependent on the
             energy of the x-rays and the atomic composition of the
             matter. Attenuation measurements at multiple x-ray energies
             can be used to improve the identification of materials. We
             present a method to estimate the fractional composition of
             three materials in an object from x-ray CT measurements at
             two different energies. The energies can be collected from
             measurements from a single source-detector system at two
             points in time, or from a dual source-detector system at one
             point in time. This method sets up a linear system of
             equations from the measurements and finds the solution
             through a geometric construction of the inverse matrix
             equation. This method enables the estimation of the blood
             fraction within a region of living tissue in which blood
             containing an iodinated contrast agent is mixed with two
             other materials. We verified this method using x-ray CT
             simulations implemented in MATLAB, investigated the
             parameters needed to optimize the estimation, and then
             applied the method to a mouse model of lung cancer. A direct
             application of this method is the estimation of blood
             fraction in lung tumors in preclinical studies. This work
             was performed at the Duke Center for In Vivo Microscopy, an
             NCRR/NCI National Resource (P41 RR005959/U24 CA092656), and
             also supported by NCI R21 CA124584. ©2009
             SPIE.},
   Doi = {10.1117/12.811673},
   Key = {fds268784}
}

@article{fds359549,
   Author = {Feinberg, DA and Johnson, G},
   Title = {A methodology for co-registering abdominal MR images over
             multiple breath-holds.},
   Journal = {Magn Reson Med},
   Volume = {34},
   Number = {5},
   Pages = {770-774},
   Year = {1995},
   Month = {November},
   url = {http://dx.doi.org/10.1002/mrm.1910340517},
   Abstract = {Previous studies have demonstrated that the SNR of abdominal
             MR images can be increased by averaging images obtained in
             different breath-hold acquisitions. In this note, the
             authors present a simple new methodology for ensuring that
             images acquired in multiple breath-hold periods are
             accurately co-registered. Within each breath-hold, a quick
             coronal scout scan is followed by a longer axial scan. The
             scout is used to position the axial slices in a fixed
             position relative to the organ under examination. This MR
             technique can, in principle, be automated so as to add less
             than 1 s to the imaging time of the axial scan. The method
             can be used to increase SNR by signal averaging or to
             co-register images acquired during, for example, uptake of
             contrast agents. SNR improvement with negligible blurring is
             demonstrated in liver images acquired by this method from
             healthy volunteers.},
   Doi = {10.1002/mrm.1910340517},
   Key = {fds359549}
}

@article{fds268847,
   Author = {Shofer, S and Badea, C and Auerbach, S and Schwartz, DA and Johnson,
             GA},
   Title = {A micro-computed tomography-based method for the measurement
             of pulmonary compliance in healthy and bleomycin-exposed
             mice.},
   Journal = {Exp Lung Res},
   Volume = {33},
   Number = {3-4},
   Pages = {169-183},
   Year = {2007},
   ISSN = {0190-2148},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/17558678},
   Keywords = {Animals • Bleomycin • Disease Models, Animal
             • Female • Image Processing, Computer-Assisted
             • Lung • Lung Compliance* • Male • Mice
             • Mice, Inbred C57BL • Pulmonary Fibrosis •
             Reproducibility of Results • Time Factors •
             Tomography, X-Ray Computed • chemically induced •
             methods* • pathology • physiopathology •
             radiography*},
   Abstract = {Micro-computed tomography (microCT) is being increasingly
             used to examine small animal models of pulmonary injury. The
             authors have developed a microCT technique suitable for the
             determination of pulmonary compliance in injured mice. Lung
             volumes in normal mice were radiographically determined at
             end-inspiration and end-expiration and pulmonary compliance
             was calculated at 2 time points 2 weeks apart, whereas a
             second group of mice were given bleomycin and imaged 3 weeks
             following drug administration. Compliance measurements were
             validated using a commercially available ventilator system.
             MicroCT pulmonary compliance measurements are suitable for
             longitudinal measurements, and correlate with physiologic
             measurements of pulmonary compliance.},
   Doi = {10.1080/01902140701364458},
   Key = {fds268847}
}

@article{fds268854,
   Author = {Shofer, S and Badea, C and Qi, Y and Potts, E and Foster, WM and Johnson,
             GA},
   Title = {A micro-CT analysis of murine lung recruitment in
             bleomycin-induced lung injury.},
   Journal = {J Appl Physiol (1985)},
   Volume = {105},
   Number = {2},
   Pages = {669-677},
   Year = {2008},
   Month = {August},
   ISSN = {8750-7587},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/18566189},
   Keywords = {Animals • Antibiotics, Antineoplastic* •
             Bleomycin* • Collagen • Female • Image
             Processing, Computer-Assisted • Lung Compliance •
             Lung Diseases • Mice • Pulmonary Alveoli •
             Respiratory Function Tests • Respiratory Mechanics
             • Tidal Volume • Tomography, X-Ray Computed •
             chemically induced* • metabolism • pathology
             • pathology* • physiology •
             physiopathology},
   Abstract = {The effects of lung injury on pulmonary recruitment are
             incompletely understood. X-ray computed tomography (CT) has
             been a valuable tool in assessing changes in recruitment
             during lung injury. With the development of preclinical CT
             scanners designed for thoracic imaging in rodents, it is
             possible to acquire high-resolution images during the
             evolution of a pulmonary injury in living mice. We
             quantitatively assessed changes in recruitment caused by
             intratracheal bleomycin at 1 and 3 wk after administration
             using micro-CT in 129S6/SvEvTac mice. Twenty female mice
             were administered 2.5 U of bleomycin or saline and imaged
             with micro-CT at end inspiration and end expiration. Mice
             were extubated and allowed to recover from anesthesia and
             then reevaluated in vivo for quasi-static compliance
             measurements, followed by harvesting of the lungs for
             collagen analysis and histology. CT images were converted to
             histograms and analyzed for mean lung attenuation (MLA). MLA
             was significantly greater for bleomycin-exposed mice at week
             1 for both inspiration (P<0.0047) and exhalation (P<0.0377)
             but was not significantly different for week 3
             bleomycin-exposed mice. However, week 3 bleomycin-exposed
             mice did display significant increases in MLA shift from
             expiration to inspiration compared with either group of
             control mice (P<0.005), suggesting increased lung
             recruitment at this time point. Week 1 bleomycin-exposed
             mice displayed normal shifts in MLA with inspiration,
             suggesting normal lung recruitment despite significant
             radiographic and histological changes. Lung alveolar
             recruitment is preserved in a mouse model of
             bleomycin-induced parenchymal injury despite significant
             changes in radiographic and physiological
             parameters.},
   Doi = {10.1152/japplphysiol.00980.2007},
   Key = {fds268854}
}

@booklet{Johnson92b,
   Author = {G. A. Johnson and H. S. Borovetz and J. L.
             Anderson},
   Title = {A model of pulsatile flow in a uniform deformable
             vessel},
   Journal = {Journal Of Biomechanics},
   Volume = {25},
   Number = {1},
   Pages = {91 -- 100},
   Year = {1992},
   Month = {January},
   Key = {Johnson92b}
}

@article{fds174289,
   Author = {GA Johnson and HS Borovetz and JL Anderson},
   Title = {A model of pulsatile flow in a uniform deformable
             vessel.},
   Journal = {Journal of biomechanics},
   Volume = {25},
   Number = {1},
   Pages = {91-100},
   Year = {1992},
   Month = {January},
   ISSN = {0021-9290},
   Keywords = {Animals • Blood Circulation • Blood Flow Velocity
             • Blood Pressure • Blood Vessels • Carotid
             Arteries • Dogs • Models, Cardiovascular* •
             Movement • Regional Blood Flow • Rheology •
             Stress, Mechanical • anatomy & histology •
             physiology • physiology*},
   Abstract = {Simulations of blood flow in natural and artificial conduits
             usually require large computers for numerical solution of
             the Navier-Stokes equations. Often, physical insight into
             the fluid dynamics is lost when the solution is purely
             numerical. An alternative to solving the most general form
             of the Navier-Stokes equations is described here, wherein a
             functional form of the solution is assumed in order to
             simplify the required computations. The assumed forms for
             the axial pressure gradient and velocity profile are chosen
             such that conservation of mass is satisfied for fully
             established pulsatile flow in a straight, deformable vessel.
             The resulting equations are cast in finite-difference form
             and solved explicitly. Results for the limiting cases of
             rigid wall and zero applied pressure are found to be in good
             agreement with analytical solutions. Comparison with the
             experimental results of Klanchar et al. [Circ. Res. 66,
             1624-1635 (1990]) also shows good agreement. Application of
             the model to realistic physiological parameter values
             provides insight as to the influence of the pulsatile nature
             of the flow field on wall shear development in the presence
             of a moving wall boundary. Specifically, the model
             illustrates the dependence of flow rate and shear rate on
             the amplitude of the vessel wall motion and the phase
             difference between the applied pressure difference and the
             oscillations of the vessel radius. The present model can
             serve as a useful tool for experimentalists interested in
             quantifying the magnitude and character of velocity profiles
             and shearing forces in natural and artificial biologic
             conduits.},
   Language = {eng},
   Key = {fds174289}
}

@article{fds268709,
   Author = {Clark, DP and Johnson, GA and Badea, CT},
   Title = {A multi-resolution approach to retrospectively-gated cardiac
             micro-CT reconstruction},
   Journal = {Progress in Biomedical Optics and Imaging - Proceedings of
             SPIE},
   Volume = {9033},
   Publisher = {SPIE},
   Year = {2014},
   Month = {January},
   ISBN = {9780819498267},
   ISSN = {1605-7422},
   url = {http://dx.doi.org/10.1117/12.2043044},
   Abstract = {In preclinical research, micro-CT is commonly used to
             provide anatomical information; however, there is
             significant interest in using this technology to obtain
             functional information in cardiac studies. The fastest
             acquisition in 4D cardiac micro-CT imaging is achieved via
             retrospective gating, resulting in irregular angular
             projections after binning the projections into phases of the
             cardiac cycle. Under these conditions, analytical
             reconstruction algorithms, such as filtered back projection,
             suffer from streaking artifacts. Here, we propose a novel,
             multi-resolution, iterative reconstruction algorithm
             inspired by robust principal component analysis which
             prevents the introduction of streaking artifacts, while
             attempting to recover the highest temporal resolution
             supported by the projection data. The algorithm achieves
             these results through a unique combination of the split
             Bregman method and joint bilateral filtration. We illustrate
             the algorithm’s performance using a
             contrast-enhanced, 2D slice through the MOBY mouse phantom
             and realistic projection acquisition and reconstruction
             parameters. Our results indicate that the algorithm is
             robust to under sampling levels of only 34 projections per
             cardiac phase and, therefore, has high potential in reducing
             both acquisition times and radiation dose. Another potential
             advantage of the multi-resolution scheme is the natural
             division of the reconstruction problem into a large number
             of independent sub-problems which can be solved in parallel.
             In future work, we will investigate the performance of this
             algorithm with retrospectively-gated, cardiac micro-CT data.
             © 2014 SPIE.},
   Doi = {10.1117/12.2043044},
   Key = {fds268709}
}

@article{fds358783,
   Author = {Johnson, GA and Laoprasert, R and Anderson, RJ and Cofer, G and Cook, J and Pratson, F and White, LE},
   Title = {A multicontrast MR atlas of the Wistar rat
             brain.},
   Journal = {Neuroimage},
   Volume = {242},
   Pages = {118470},
   Year = {2021},
   Month = {November},
   url = {http://dx.doi.org/10.1016/j.neuroimage.2021.118470},
   Abstract = {We describe a multi-contrast, multi-dimensional atlas of the
             Wistar rat acquired at microscopic spatial resolution using
             magnetic resonance histology (MRH). Diffusion weighted
             images, and associated scalar images were acquired of a
             single specimen with a fully sampled Fourier reconstruction,
             61 angles and b=3000 s/mm2 yielding 50 um isotropic spatial
             resolution. The higher angular sampling allows use of the
             GQI algorithm improving the angular invariance of the scalar
             images and yielding an orientation distribution function to
             assist in delineating subtle boundaries where there are
             crossing fibers  and track density images providing insight
             into local fiber architecture.  A multigradient echo image
             of the same specimen was acquired at 25 um isotropic spatial
             resolution. A quantitative susceptibility map enhances fiber
             architecture relative to the magnitude images.  An
             accompanying multi-specimen atlas (n=6) was acquired with
             compressed sensing with the same diffusion protocol as used
             for the single specimen atlas.  An average was created
             using diffeomorphic mapping. Scalar volumes from the
             diffusion data, a T2* weighted volume, a quantitative
             susceptibility map, and a track density volume, all
             registered to the same space provide multiple contrasts to
             assist in anatomic delineation. The new template  provides
             significantly increased contrast in the scalar DTI images
             when compared to previous atlases. A compact interactive
             viewer based on 3D Slicer is provided to facilitate
             comparison among the contrasts in the multiple volumes. The
             single volume and average atlas with multiple 3D volumes
             provide an improved template for anatomic interrogation of
             the Wistar rat brain. The improved contrast to noise in the
             scalar DTI images and the addition of other volumes (eg.
             QA,QSM,TDI ) will facilitate automated label registration
             for MR histology and preclinical imaging.},
   Doi = {10.1016/j.neuroimage.2021.118470},
   Key = {fds358783}
}

@article{fds268795,
   Author = {Johnson, GA and Calabrese, E and Badea, A and Paxinos, G and Watson,
             C},
   Title = {A multidimensional magnetic resonance histology atlas of the
             Wistar rat brain.},
   Journal = {Neuroimage},
   Volume = {62},
   Number = {3},
   Pages = {1848-1856},
   Year = {2012},
   Month = {September},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/22634863},
   Abstract = {We have produced a multidimensional atlas of the adult
             Wistar rat brain based on magnetic resonance histology
             (MRH). This MR atlas has been carefully aligned with the
             widely used Paxinos-Watson atlas based on optical sections
             to allow comparisons between histochemical and immuno-marker
             data, and the use of the Paxinos-Watson abbreviation set.
             Our MR atlas attempts to make a seamless connection with the
             advantageous features of the Paxinos-Watson atlas, and to
             extend the utility of the data through the unique
             capabilities of MR histology: a) ability to view the brain
             in the skull with limited distortion from shrinkage or
             sectioning; b) isotropic spatial resolution, which permits
             sectioning along any arbitrary axis without loss of detail;
             c) three-dimensional (3D) images preserving spatial
             relationships; and d) widely varied contrast dependent on
             the unique properties of water protons. 3D diffusion tensor
             images (DTI) at what we believe to be the highest resolution
             ever attained in the rat provide unique insight into white
             matter structures and connectivity. The 3D isotropic data
             allow registration of multiple data sets into a common
             reference space to provide average atlases not possible with
             conventional histology. The resulting multidimensional atlas
             that combines Paxinos-Watson with multidimensional MRH
             images from multiple specimens provides a new, comprehensive
             view of the neuroanatomy of the rat and offers a
             collaborative platform for future rat brain
             studies.},
   Doi = {10.1016/j.neuroimage.2012.05.041},
   Key = {fds268795}
}

@article{fds132832,
   Author = {WL Hall and H Benveniste and LW Hedlund and GA Johnson},
   Title = {A new in vivo method for quantitative analysis of stroke
             lesions using diffusion-weighted magnetic resonance
             microscopy.},
   Journal = {NeuroImage, UNITED STATES},
   Volume = {3},
   Number = {3 Pt 1},
   Pages = {158-66},
   Year = {1996},
   Month = {June},
   ISSN = {1053-8119},
   Keywords = {Animals • Brain Ischemia • Disease Models, Animal
             • Female • Magnetic Resonance Imaging* •
             Microscopy • Models, Neurological • Rats •
             Rats, Inbred F344 • Stroke Volume • diagnosis
             • methods* • pathology* •
             physiopathology},
   Abstract = {Using three-dimensional diffusion-weighted MR microscopy and
             a rat model of focal cerebral ischemia, we evaluated the
             statistical characteristics of two parameters: absolute
             stroke volumes and change in stroke volumes over 6 h of
             middle cerebral artery (MCA) occlusion. In all rats, the
             absolute stroke volumes increased linearly over the 6-h MCA
             occlusion time period. On average, stroke volume growth rate
             was 2.1 +/- 0.5%/h. Sample size power analysis of our data
             demonstrated that to demonstrate a 10% reduction of the 6-h
             volumes, sample size per group would require 29 animals
             (these calculations are based on alpha = 0.05, beta = 0.20
             using normal approximation). A similar 30% reduction of
             stroke volume at 6 h poststroke (from approximately equal to
             200 to 140 mm3) would, in our "slope model," translate into
             a reduction of stroke growth rate from the normal + 11.25
             mm3/h (150 to 200 mm3 over 4 h) to 7 mm3/h (150 to 178 mm3
             over 4 h); power analysis in this case demonstrated that
             sample size is reduced to 15 animals per group (these
             calculations are based on alpha = 0.05, beta = 0.20 using
             normal approximation). We conclude that from a statistical
             standpoint our study demonstrates that stroke growth rate
             might be a more suitable parameter for evaluating the effect
             of treatment in both clinical and experimental stroke
             trials.},
   Key = {fds132832}
}

@booklet{Hall96,
   Author = {Hall, WL and Benveniste, H and Hedlund, LW and Johnson,
             GA},
   Title = {A new in vivo method for quantitative analysis of stroke
             lesions using diffusion-weighted magnetic resonance
             microscopy.},
   Journal = {Neuroimage},
   Volume = {3},
   Number = {3 Pt 1},
   Pages = {158-166},
   Year = {1996},
   Month = {June},
   ISSN = {1053-8119},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1996UQ76900002&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Abstract = {Using three-dimensional diffusion-weighted MR microscopy and
             a rat model of focal cerebral ischemia, we evaluated the
             statistical characteristics of two parameters: absolute
             stroke volumes and change in stroke volumes over 6 h of
             middle cerebral artery (MCA) occlusion. In all rats, the
             absolute stroke volumes increased linearly over the 6-h MCA
             occlusion time period. On average, stroke volume growth rate
             was 2.1 +/- 0.5%/h. Sample size power analysis of our data
             demonstrated that to demonstrate a 10% reduction of the 6-h
             volumes, sample size per group would require 29 animals
             (these calculations are based on alpha = 0.05, beta = 0.20
             using normal approximation). A similar 30% reduction of
             stroke volume at 6 h poststroke (from approximately equal to
             200 to 140 mm3) would, in our "slope model," translate into
             a reduction of stroke growth rate from the normal + 11.25
             mm3/h (150 to 200 mm3 over 4 h) to 7 mm3/h (150 to 178 mm3
             over 4 h); power analysis in this case demonstrated that
             sample size is reduced to 15 animals per group (these
             calculations are based on alpha = 0.05, beta = 0.20 using
             normal approximation). We conclude that from a statistical
             standpoint our study demonstrates that stroke growth rate
             might be a more suitable parameter for evaluating the effect
             of treatment in both clinical and experimental stroke
             trials.},
   Doi = {10.1006/nimg.1996.0017},
   Key = {Hall96}
}

@booklet{Johnson98,
   Author = {Allan Johnson and G and Hedlund, L and MacFall, J},
   Title = {A new window into the lung},
   Journal = {Physics World},
   Volume = {11},
   Number = {11},
   Pages = {35-38},
   Publisher = {IOP Publishing},
   Year = {1998},
   Month = {January},
   ISSN = {0953-8585},
   url = {http://dx.doi.org/10.1088/2058-7058/11/11/28},
   Doi = {10.1088/2058-7058/11/11/28},
   Key = {Johnson98}
}

@booklet{Todd01,
   Author = {M. D. Todd and G. A. Johnson and B. L. Althouse},
   Title = {A novel Bragg grating sensor interrogation system utilizing
             a scanning filter, a Mach-Zehnder interferometer and a 3 x 3
             coupler},
   Journal = {Measurement Science \& Technology},
   Volume = {12},
   Number = {7},
   Pages = {771 -- 777},
   Year = {2001},
   Month = {July},
   Key = {Todd01}
}

@article{fds161597,
   Author = {G.A. Johnson},
   Title = {A Petiet, GA Johnson, Active Staining of Mouse Embryos for
             Magnetic Resonance Microscopy. In: Hewitson Tim D & Darby
              Ian A (editors), Histology Protocols (Methods in Molecular
             Biology), Springer- Humana Press. Totowa, NJ. USA, in press,
             2009},
   Year = {2009},
   Key = {fds161597}
}

@booklet{Godwin84a,
   Author = {Godwin, JD and Johnson, GA and Fram, EK},
   Title = {A phantom for testing ECG-gated computed tomography of the
             heart.},
   Journal = {Invest Radiol},
   Volume = {19},
   Number = {4},
   Pages = {279-283},
   Year = {1984},
   ISSN = {0020-9996},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/6480305},
   Abstract = {A mechanical phantom has been built to evaluate
             electrocardiographically gated computed tomography of the
             heart. The phantom simulates the heart in terms of cyclic
             changes in chamber dimensions and wall thickness. Rate and
             excursion are variable, and the cavity of the chamber can be
             filled with liquid contrast media of different degrees of
             radio-opacity. Preliminary experiments with a prototypic
             gating system are described.},
   Doi = {10.1097/00004424-198407000-00008},
   Key = {Godwin84a}
}

@article{fds132753,
   Author = {JD Godwin and GA Johnson and EK Fram},
   Title = {A phantom for testing ECG-gated computed tomography of the
             heart.},
   Journal = {Investigative radiology, UNITED STATES},
   Volume = {19},
   Number = {4},
   Pages = {279-83},
   ISSN = {0020-9996},
   Keywords = {Electrocardiography* • Heart • Humans •
             Models, Structural* • Myocardial Contraction •
             Tomography, X-Ray Computed • methods* •
             radiography*},
   Abstract = {A mechanical phantom has been built to evaluate
             electrocardiographically gated computed tomography of the
             heart. The phantom simulates the heart in terms of cyclic
             changes in chamber dimensions and wall thickness. Rate and
             excursion are variable, and the cavity of the chamber can be
             filled with liquid contrast media of different degrees of
             radio-opacity. Preliminary experiments with a prototypic
             gating system are described.},
   Key = {fds132753}
}

@booklet{Look98,
   Author = {K. Y. Look and J. A. Blessing and B. E. Nelson and G. A.
             Johnson and W. C. Fowler and G. C. Reid},
   Title = {A phase II trial of isotretinoin and alpha interferon in
             patients with recurrent squamous cell carcinoma of the
             cervix - A Gynecologic Oncology Group Study},
   Journal = {American Journal Of Clinical Oncology-cancer Clinical
             Trials},
   Volume = {21},
   Number = {6},
   Pages = {591 -- 594},
   Year = {1998},
   Month = {December},
   Key = {Look98}
}

@article{fds174221,
   Author = {KY Look and JA Blessing and BE Nelson and GA Johnson and WC Fowler Jr and GC Reid},
   Title = {A phase II trial of isotretinoin and alpha interferon in
             patients with recurrent squamous cell carcinoma of the
             cervix: a Gynecologic Oncology Group study.},
   Journal = {American journal of clinical oncology},
   Volume = {21},
   Number = {6},
   Pages = {591-4},
   Year = {1998},
   Month = {December},
   ISSN = {0277-3732},
   Keywords = {Adult • Aged • Antineoplastic Agents •
             Carcinoma, Squamous Cell • Drug Therapy, Combination
             • Female • Humans • Interferon-alpha •
             Isotretinoin • Keratolytic Agents • Middle Aged
             • Neoplasm Recurrence, Local • Uterine Cervical
             Neoplasms • administration & dosage • drug
             therapy* • therapeutic use*},
   Abstract = {From January 1993 through January 1996, 37 patients with
             unresectable squamous carcinoma of the cervix were entered
             on study and scheduled to receive oral isotretinoin 1 mg/kg
             per day with subcutaneous alpha interferon 6,000,000
             units/day. A course was defined as 4 continuous weeks of
             therapy. The mean number of four-course cycles delivered was
             1.8. One patient was ineligible because of wrong cell type
             and two were never treated. Thus, 34 patients were evaluable
             for toxicity. Eight patients were inevaluable for response.
             Five did not receive a complete 4-week course and three did
             not have additional tumor measurements; thus 26 were
             evaluable for response. Prior radiotherapy had been given to
             25 patients and prior chemotherapy to 23 patients. There was
             no grade 4 neutropenia. The incidence of Gynecologic
             Oncology Group (GOG) grade 3 granulocytopenia and
             thrombocytopenia was 8.8% and 5.8%, respectively. Six
             patients (17.6%) developed grade 3 or worse nausea and
             vomiting. Four (11.7%) patients developed grade 3 neurologic
             symptoms. There were no complete responses and one partial
             response. The overall response rate was 3.8% (95% confidence
             interval, 0.1-19.6%). In this pretreated population,
             isotretinoin and alpha interferon in the dose and schedule
             employed exhibit minimal activity.},
   Language = {eng},
   Key = {fds174221}
}

@booklet{Johnson82f,
   Author = {JOHNSON, GA},
   Title = {A PRACTICAL APPROACH TO QUALITY ASSURANCE IN
             CT},
   Journal = {AMERICAN JOURNAL OF ROENTGENOLOGY},
   Volume = {139},
   Number = {2},
   Pages = {427-427},
   Year = {1982},
   ISSN = {0361-803X},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1982NY43600075&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Johnson82f}
}

@article{fds132799,
   Author = {ML Banson and GP Cofer and R Black and GA Johnson},
   Title = {A probe for specimen magnetic resonance microscopy.},
   Journal = {Investigative radiology, UNITED STATES},
   Volume = {27},
   Number = {2},
   Pages = {157-64},
   Year = {1992},
   Month = {February},
   ISSN = {0020-9996},
   Keywords = {Copper • Equipment Design • Evaluation Studies
             • Magnetic Resonance Spectroscopy • Microscopy
             • Polytetrafluoroethylene • Sensitivity and
             Specificity • instrumentation •
             methods*},
   Abstract = {One of the primary limits to spatial resolution in magnetic
             resonance (MR) microscopy is the limited signal. The purpose
             of this study is to build a radiofrequency (rf) probe for MR
             microscopy of fixed specimens at 300 MHz. The design
             criteria for the probe were (1) high sensitivity; (2) good
             rf homogeneity; (3) minimization of BO variations. All
             probes were Helmholtz pairs operating at 300 MHz. Coils were
             constructed from copper/Teflon/copper microwave substrate
             which eliminated susceptibility problems from solder and
             discrete capacitors. Signal-to-noise ratio (SNR) was
             compared with a conventional solenoid. Phantoms of agar gels
             and saline-filled tubes were used to characterize the SNR
             and homogeneity. SNR measurements of the coil pairs showed a
             marked improvement (up to 60%) over that of the reference
             solenoid. The region of homogeneity was defined as a 10%
             variation in signal intensity. This correlated with the
             coil's inner diameter. Graphs of SNR versus diameter,
             separation, and copper foil width allowed for optimization
             of the structure. Using this coil, MR microscopy is now
             possible on small, fixed specimens with pixels as small as
             20 x 20 x 30 microns. Work is currently under way exploiting
             the SNR and homogeneity provided by this probe to determine
             the degree to which MR microscopy might add to the
             pathologists' diagnostic tools.},
   Key = {fds132799}
}

@booklet{Banson92a,
   Author = {Banson, ML and Cofer, GP and Black, R and Johnson,
             GA},
   Title = {A probe for specimen magnetic resonance microscopy.},
   Journal = {Invest Radiol},
   Volume = {27},
   Number = {2},
   Pages = {157-164},
   Year = {1992},
   Month = {February},
   ISSN = {0020-9996},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/1601608},
   Abstract = {One of the primary limits to spatial resolution in magnetic
             resonance (MR) microscopy is the limited signal. The purpose
             of this study is to build a radiofrequency (rf) probe for MR
             microscopy of fixed specimens at 300 MHz. The design
             criteria for the probe were (1) high sensitivity; (2) good
             rf homogeneity; (3) minimization of BO variations. All
             probes were Helmholtz pairs operating at 300 MHz. Coils were
             constructed from copper/Teflon/copper microwave substrate
             which eliminated susceptibility problems from solder and
             discrete capacitors. Signal-to-noise ratio (SNR) was
             compared with a conventional solenoid. Phantoms of agar gels
             and saline-filled tubes were used to characterize the SNR
             and homogeneity. SNR measurements of the coil pairs showed a
             marked improvement (up to 60%) over that of the reference
             solenoid. The region of homogeneity was defined as a 10%
             variation in signal intensity. This correlated with the
             coil's inner diameter. Graphs of SNR versus diameter,
             separation, and copper foil width allowed for optimization
             of the structure. Using this coil, MR microscopy is now
             possible on small, fixed specimens with pixels as small as
             20 x 20 x 30 microns. Work is currently under way exploiting
             the SNR and homogeneity provided by this probe to determine
             the degree to which MR microscopy might add to the
             pathologists' diagnostic tools.},
   Doi = {10.1097/00004424-199202000-00013},
   Key = {Banson92a}
}

@article{fds268757,
   Author = {Calabrese, E and Badea, A and Watson, C and Johnson,
             GA},
   Title = {A quantitative magnetic resonance histology atlas of
             postnatal rat brain development with regional estimates of
             growth and variability.},
   Journal = {Neuroimage},
   Volume = {71},
   Pages = {196-206},
   Year = {2013},
   Month = {May},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/23353030},
   Abstract = {There has been growing interest in the role of postnatal
             brain development in the etiology of several neurologic
             diseases. The rat has long been recognized as a powerful
             model system for studying neuropathology and the safety of
             pharmacologic treatments. However, the complex
             spatiotemporal changes that occur during rat
             neurodevelopment remain to be elucidated. This work
             establishes the first magnetic resonance histology (MRH)
             atlas of the developing rat brain, with an emphasis on
             quantitation. The atlas comprises five specimens at each of
             nine time points, imaged with eight distinct MR contrasts
             and segmented into 26 developmentally defined brain regions.
             The atlas was used to establish a timeline of morphometric
             changes and variability throughout neurodevelopment and
             represents a quantitative database of rat neurodevelopment
             for characterizing rat models of human neurologic
             disease.},
   Doi = {10.1016/j.neuroimage.2013.01.017},
   Key = {fds268757}
}

@booklet{Solomon03,
   Author = {D. Solomon and M. Schiffman and R. Tarone and E. E.
             Partridge and L. Kilgore and S. Hester and J. L. Walker and G. A. Johnson and A. Yadack and R. S. Guido and K.
             Mcintyre-seltman and R. P. Edwards and J. Gruss and N. B.
             Kiviat and L. Koutsky and C. Mao a},
   Title = {A randomized trial on the management of low-grade squamous
             intraepithelial lesion cytology interpretations},
   Journal = {American Journal Of Obstetrics And Gynecology},
   Volume = {188},
   Number = {6},
   Pages = {1393 -- 1400},
   Year = {2003},
   Month = {June},
   Key = {Solomon03}
}

@article{fds373572,
   Author = {Tian, Y and Johnson, GA and Williams, RW and White,
             LE},
   Title = {A rapid workflow for neuron counting in combined light sheet
             microscopy and magnetic resonance histology.},
   Journal = {Front Neurosci},
   Volume = {17},
   Pages = {1223226},
   Year = {2023},
   url = {http://dx.doi.org/10.3389/fnins.2023.1223226},
   Abstract = {Information on regional variation in cell numbers and
             densities in the CNS provides critical insight into
             structure, function, and the progression of CNS diseases.
             However, variability can be real or a consequence of methods
             that do not account for technical biases, including
             morphologic deformations, errors in the application of cell
             type labels and boundaries of regions, errors of counting
             rules and sampling sites. We address these issues in a mouse
             model by introducing a workflow that consists of the
             following steps: 1. Magnetic resonance histology (MRH) to
             establish the size, shape, and regional morphology of the
             mouse brain in situ. 2. Light-sheet microscopy (LSM) to
             selectively label neurons or other cells in the entire brain
             without sectioning artifacts. 3. Register LSM volumes to MRH
             volumes to correct for dissection errors and both global and
             regional deformations. 4. Implement stereological protocols
             for automated sampling and counting of cells in 3D LSM
             volumes. This workflow can analyze the cell densities of one
             brain region in less than 1 min and is highly replicable in
             cortical and subcortical gray matter regions and structures
             throughout the brain. This method demonstrates the advantage
             of not requiring an extensive amount of training data,
             achieving a F1 score of approximately 0.9 with just 20
             training nuclei. We report deformation-corrected neuron
             (NeuN) counts and neuronal density in 13 representative
             regions in 5 C57BL/6J cases and 2 BXD strains. The data
             represent the variability among specimens for the same brain
             region and across regions within the specimen. Neuronal
             densities estimated with our workflow are within the range
             of values in previous classical stereological studies. We
             demonstrate the application of our workflow to a mouse model
             of aging. This workflow improves the accuracy of neuron
             counting and the assessment of neuronal density on a
             region-by-region basis, with broad applications for studies
             of how genetics, environment, and development across the
             lifespan impact cell numbers in the CNS.},
   Doi = {10.3389/fnins.2023.1223226},
   Key = {fds373572}
}

@booklet{Bazer99,
   Author = {F. W. Bazer and G. A. Johnson and A. G. Stagg and K. M.
             Taylor and E. Gootwine and A. Gertler and T. E.
             Spencer},
   Title = {A servomechanism in the ovine uterus regulates endometrial
             gene expression.},
   Journal = {Biology Of Reproduction},
   Volume = {60},
   Pages = {150 -- 150},
   Year = {1999},
   Key = {Bazer99}
}

@booklet{Johnson95a,
   Author = {G. A. Johnson and D. A. Mortensen and A. R.
             Martin},
   Title = {A simulation of herbicide use based on weed
             spatial-distribution},
   Journal = {Weed Research},
   Volume = {35},
   Number = {3},
   Pages = {197 -- 205},
   Year = {1995},
   Month = {June},
   Key = {Johnson95a}
}

@booklet{Johnson96d,
   Author = {G. A. Johnson and G. A. Livesay and S. L. Y. Woo and K. R.
             Rajagopal},
   Title = {A single integral finite strain viscoelastic model of
             ligaments and tendons},
   Journal = {Journal Of Biomechanical Engineering-transactions Of The
             Asme},
   Volume = {118},
   Number = {2},
   Pages = {221 -- 226},
   Year = {1996},
   Month = {May},
   Key = {Johnson96d}
}

@article{fds174112,
   Author = {GA Johnson and GA Livesay and SL Woo and KR Rajagopal},
   Title = {A single integral finite strain viscoelastic model of
             ligaments and tendons.},
   Journal = {Journal of biomechanical engineering},
   Volume = {118},
   Number = {2},
   Pages = {221-6},
   Year = {1996},
   Month = {May},
   ISSN = {0148-0731},
   Keywords = {Adult • Aged • Aged, 80 and over • Animals
             • Dogs • Elasticity • Humans • Ligaments
             • Middle Aged • Models, Biological* •
             Nonlinear Dynamics • Patella • Stress, Mechanical
             • Tendons • Viscosity • physiology •
             physiology*},
   Abstract = {A general continuum model for the nonlinear viscoelastic
             behavior of soft biological tissues was formulated. This
             single integral finite strain (SIFS) model describes finite
             deformation of a nonlinearly viscoelastic material within
             the context of a three-dimensional model. The specific form
             describing uniaxial extension was obtained, and the idea of
             conversion from one material to another (at a microscopic
             level) was then introduced to model the nonlinear behavior
             of ligaments and tendons. Conversion allowed different
             constitutive equations to be used for describing a single
             ligament or tendon at different strain levels. The model was
             applied to data from uniaxial extension of younger and older
             human patellar tendons and canine medial collateral
             ligaments. Model parameters were determined from
             curve-fitting stress-strain and stress-relaxation data and
             used to predict the time-dependent stress generated by
             cyclic extensions.},
   Language = {eng},
   Key = {fds174112}
}

@booklet{Johnson00c,
   Author = {G. A. Johnson and S. V. Mantha and T. A.
             Day},
   Title = {A spectrofluorometric survey of UV-induced blue-green
             fluorescence in foliage of 35 species},
   Journal = {Journal Of Plant Physiology},
   Volume = {156},
   Number = {2},
   Pages = {242 -- 252},
   Year = {2000},
   Month = {February},
   Key = {Johnson00c}
}

@article{fds132853,
   Author = {GA Johnson and CE Ravin},
   Title = {A survey of digital chest radiography.},
   Journal = {Radiologic clinics of North America, UNITED
             STATES},
   Volume = {21},
   Number = {4},
   Pages = {655-64},
   Year = {1983},
   Month = {December},
   ISSN = {0033-8389},
   Keywords = {Humans • Methods • Radiographic Image Enhancement
             • Radiography, Thoracic* • Subtraction Technique*
             • Technology, Radiologic • Tomography, X-Ray
             Computed*},
   Abstract = {The problems of chest radiography as they relate to digital
             systems are described, the current approaches to these
             problems are reviewed, and the utility of digital chest
             radiography is demonstrated.},
   Key = {fds132853}
}

@booklet{Johnson83a,
   Author = {Johnson, GA and Ravin, CE},
   Title = {A survey of digital chest radiography.},
   Journal = {Radiol Clin North Am},
   Volume = {21},
   Number = {4},
   Pages = {655-664},
   Year = {1983},
   Month = {December},
   ISSN = {0033-8389},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/6361846},
   Abstract = {The problems of chest radiography as they relate to digital
             systems are described, the current approaches to these
             problems are reviewed, and the utility of digital chest
             radiography is demonstrated.},
   Key = {Johnson83a}
}

@article{fds268817,
   Author = {Bowden, DM and Johnson, GA and Zaborsky, L and Green, WDK and Moore, E and Badea, A and Dubach, MF and Bookstein, FL},
   Title = {A symmetrical Waxholm canonical mouse brain for
             NeuroMaps.},
   Journal = {J Neurosci Methods},
   Volume = {195},
   Number = {2},
   Pages = {170-175},
   Year = {2011},
   Month = {February},
   ISSN = {1872-678X},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/21163300},
   Keywords = {Animals • Brain • Brain Mapping* • Functional
             Laterality • Image Processing, Computer-Assisted •
             Magnetic Resonance Imaging • Mice • Mice, Inbred
             C57BL • Models, Neurological • anatomy &
             histology* • methods • methods*},
   Abstract = {NeuroMaps (2010) is a Web-based application that enables
             investigators to map data from macaque studies to a
             canonical atlas of the macaque brain. It currently serves as
             an image processor enabling them to create figures suitable
             for publication, presentation and archival purposes.
             Eventually it will enable investigators studying any of
             several species to analyze the overlap between their data
             and multimodality data mapped by others. The purpose of the
             current project was to incorporate the Waxholm canonical
             mouse brain (Harwylycz, 2009) into NeuroMaps. An enhanced
             gradient echo (T2*) magnetic resonance image (MRI) of the
             Waxholm canonical brain (Johnson et al., 2010) was warped to
             bring the irregular biological midplane of the MRI into line
             with the mathematically flat midsagittal plane of the
             Waxholm space. The left hemisphere was deleted and the right
             hemisphere reflected to produce a symmetrical 3D MR image.
             The symmetrical T2* image was imported into NeuroMaps. The
             map executing this warp was applied to four other voxellated
             volumes based on the same canonical specimen and maintained
             at the Center for In-Vitro Microscopy (CIVM): a T2-weighted
             MRI, a T1-weighted MRI, a segmented image and an image
             reconstructed from Nissl-stained histological sections of
             the specimen. Symmetric versions of those images were
             returned to the CIVM repository where they are made
             available to other laboratories. Utility of the symmetric
             atlas was demonstrated by mapping and comparing a number of
             cortical areas as illustrated in three conventional mouse
             brain atlases. The symmetric Waxholm mouse brain atlas is
             now accessible in NeuroMaps where investigators can map
             image data to standard templates over the Web and process
             them for publication, presentation and archival purposes:
             http://braininfo.rprc.washington.edu/MapViewData.aspx.},
   Language = {eng},
   Doi = {10.1016/j.jneumeth.2010.11.028},
   Key = {fds268817}
}

@booklet{Johnson83,
   Author = {Johnson, GA and Suddarth, S and Dunnick, NR},
   Title = {A system for digital videodensitometry},
   Journal = {Proceedings of SPIE - The International Society for Optical
             Engineering},
   Volume = {419},
   Pages = {222-227},
   Year = {1983},
   Month = {December},
   url = {http://dx.doi.org/10.1117/12.936029},
   Doi = {10.1117/12.936029},
   Key = {Johnson83}
}

@booklet{Johnson83b,
   Author = {JOHNSON, GA and DANIELEY, N and SUDDARTH, S and DUNNICK,
             NR},
   Title = {A SYSTEM FOR DIGITAL VIDEODENSITOMETRY},
   Journal = {AMERICAN JOURNAL OF ROENTGENOLOGY},
   Volume = {141},
   Number = {6},
   Pages = {1360-1361},
   Year = {1983},
   ISSN = {0361-803X},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1983RT41800084&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Johnson83b}
}

@article{fds359544,
   Author = {Xiao, J and Hornburg, KJ and Cofer, G and Cook, JJ and Pratson, F and Qi,
             Y and Johnson, GA},
   Title = {A time-course study of actively stained mouse brains:
             Diffusion tensor imaging parameters and connectomic
             stability over 1 year.},
   Journal = {NMR Biomed},
   Volume = {35},
   Number = {1},
   Pages = {e4611},
   Year = {2022},
   Month = {January},
   url = {http://dx.doi.org/10.1002/nbm.4611},
   Abstract = {While the application of diffusion tensor imaging (DTI),
             tractography, and connectomics to fixed tissue is a common
             practice today, there have been limited studies examining
             the effects of fixation on brain microstructure over
             extended periods. This mouse model time-course study reports
             the changes of regional brain volumes and diffusion scalar
             parameters, such as fractional anisotropy, across 12
             representative brain regions as measures of brain structural
             stability. The scalar DTI parameters and regional volumes
             were highly variable over the first 2 weeks after fixation.
             The same parameters were consistent over a 2-8-week window
             after fixation, which means confounds from tissue stability
             over that scanning window were minimal. Quantitative
             connectomes were analyzed over the same time with extension
             out to 1 year. While there was some change in the scalar
             metrics at 1 year after fixation, these changes were
             sufficiently small, particularly in white matter, to support
             reproducible connectomes over a period ranging from 2-weeks
             to 1-year post-fixation. These findings delineate a scanning
             period, during which brain volumes, diffusion scalar
             metrics, and connectomes are remarkably consistent.},
   Doi = {10.1002/nbm.4611},
   Key = {fds359544}
}

@article{fds132740,
   Author = {G.A. Johnson},
   Title = {A. LeFurgey, S. Gewalt, N. Wallace, D. Kopf, G.A. Johnson,
             P. Ingram.   Magnetic Resonance Microscoopy of the Adult
             Barnacle.  in "Proc.,  MicroCosmopolitan (14th Australian
             Conference on Electron Microscopy,  1st Meeting,
             International Union of Microbeam Analysis Societies, 9th
              Symposium of the Microscopical Society of Australia).
              Syndey, Australia,  1996," p. 105.},
   Year = {1996},
   Key = {fds132740}
}

@booklet{Griffin98,
   Author = {W. P. Griffin and E. B. Savage and R. E. Clark and J. J.
             Pacella and G. A. Johnson and J. A. Magovern and G. J.
             Magovern},
   Title = {AB-180 circulatory support system - Summary of development
             and phase I clinical trial},
   Journal = {Asaio Journal},
   Volume = {44},
   Number = {5},
   Pages = {M719 -- M724},
   Year = {1998},
   Key = {Griffin98}
}

@article{fds174075,
   Author = {WP Griffin and EB Savage and RE Clark and JJ Pacella and GA Johnson and JA
             Magovern, GJ Magovern Sr},
   Title = {AB-180 circulatory support system: summary of development
             and phase I clinical trial.},
   Journal = {ASAIO journal (American Society for Artificial Internal
             Organs : 1992)},
   Volume = {44},
   Number = {5},
   Pages = {M719-24},
   Year = {1999},
   Month = {February},
   ISSN = {1058-2916},
   Keywords = {Feasibility Studies • Heart-Assist Devices* •
             Humans • Male • Middle Aged • Prosthesis
             Design},
   Abstract = {The AB-180 Circulatory Support System (AB-180 CSS; Cardiac
             Assist Technologies, Pittsburgh, PA) is a left ventricular
             assist system for investigational use in patients with
             postcardiotomy cardiogenic shock who are refractory to
             standard treatment with an intra-aortic balloon pump,
             pharmacologic treatment, or both. The intent of the AB-180
             CSS is to provide temporary (up to 14 days) mechanical
             circulatory support until the heart recovers adequate
             mechanical function. The system consists of a small
             implantable centrifugal pump and a controller. A unique
             infusion system produces a hydrodynamic bearing between
             rotational and stationary components of the AB-180 CSS pump.
             This infusion system also provides a source of heparin for
             localized anticoagulation. Extensive bench and animal work
             has illustrated anticoagulation requirements, established
             operating guidelines, and demonstrated safety and efficacy.
             An investigational device exemption has been granted for a
             Phase I, five patient feasibility study at Allegheny General
             Hospital in Pittsburgh, Pennsylvania. To date, the pump has
             been implanted in one patient. The results from this first
             case are presented here.},
   Language = {eng},
   Key = {fds174075}
}

@article{fds310029,
   Author = {Oliverio, MI and Delnomdedieu, M and Best, CF and Li, P and Morris, M and Callahan, MF and Johnson, GA and Smithies, O and Coffman,
             TM},
   Title = {Abnormal water metabolism in mice lacking the type 1A
             receptor for ANG II.},
   Journal = {Am J Physiol Renal Physiol},
   Volume = {278},
   Number = {1},
   Pages = {F75-F82},
   Year = {2000},
   Month = {January},
   ISSN = {1931-857X},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/10644657},
   Keywords = {Animals • Body Weight • Deamino Arginine
             Vasopressin • Female • Genotype • Kidney
             • Kidney Concentrating Ability • Losartan •
             Male • Mice • Osmolar Concentration •
             Receptor, Angiotensin, Type 1 • Receptors, Angiotensin
             • Urine • Urodynamics • Vasopressins •
             Water • Water Deprivation • anatomy & histology
             • antagonists & inhibitors • blood •
             chemistry • deficiency* • drug effects •
             genetics • metabolism* • pharmacology •
             physiology*},
   Abstract = {Mice lacking AT(1A) receptors for ANG II have a defect in
             urinary concentration manifested by an inability to increase
             urinary osmolality to levels seen in controls after
             thirsting. This defect results in extreme serum
             hypertonicity during water deprivation. In the basal state,
             plasma vasopressin levels are similar in wild-type controls
             and Agtr1a -/- mice. Plasma vasopressin levels increase
             normally in the AT(1A) receptor-deficient mice after 24 h of
             water deprivation, suggesting that the defect in urine
             concentration is intrinsic to the kidney. Using magnetic
             resonance microscopy, we find that the absence of AT(1A)
             receptors is associated with a modest reduction in the
             distance from the kidney surface to the tip of the papilla.
             However, this structural abnormality seems to play little
             role in the urinary concentrating defect in Agtr1a -/- mice
             since the impairment is largely reproduced in wild-type mice
             by treatment with an AT(1)-receptor antagonist. These
             studies demonstrate a critical role for the AT(1A) receptor
             in maintaining inner medullary structures in the kidney and
             in regulating renal water excretion.},
   Doi = {10.1152/ajprenal.2000.278.1.F75},
   Key = {fds310029}
}

@article{fds341986,
   Author = {Wang, N and Cofer, G and Anderson, RJ and Qi, Y and Liu, C and Johnson,
             GA},
   Title = {Accelerating quantitative susceptibility imaging acquisition
             using compressed sensing.},
   Journal = {Phys Med Biol},
   Volume = {63},
   Number = {24},
   Pages = {245002},
   Year = {2018},
   Month = {December},
   url = {http://dx.doi.org/10.1088/1361-6560/aaf15d},
   Abstract = {To evaluate the feasibility of compressed sensing (CS) for
             accelerating quantitative susceptibility mapping (QSM)
             acquisition in MR histology, control, demyelination, and
             remyelination mice were scanned using a modified 3D gradient
             echo (GRE) pulse sequence (allowing undersampling the
             k-space in two phase dimensions) at 9.4 T. Fully sampled and
             CS data at various acceleration factors (AF) (4.0-16.0) were
             acquired with high spatial resolution of 22.5 µm3
             isotropic. For prospective scans, the local phase was
             reconstructed slice-by-slice using a nonlinear
             reconstruction algorithm with phase cycling, and the QSM was
             calculated using the iLSQR method. Susceptibility values of
             major white matter tracts at various CS AF were compared
             with the fully sampled data as ground truth. The
             reconstructed QSM preserved major information with
             negligible artifacts, even at CS AF of 8.0 and 16.0. The
             maximum variation of susceptibility value of control mice
             was 5.8% in the fimbria (FI) area with the acceleration
             factor of 16.0, compared to the ground truth. The maximum
             variation was 9.5% in corpus callosum (CC) area of the
             demyelination mouse brain with the acceleration factor of
             8.0. The maximum variation was 8.2% in AC area of
             remyelination mouse brain with 16.0 acceleration factor.
             This preliminary study shows that CS can reduce the
             acquisition time of GRE MRI in MR histology without losing
             significant accuracy in quantitative susceptibility
             values.},
   Doi = {10.1088/1361-6560/aaf15d},
   Key = {fds341986}
}

@booklet{Scribner00,
   Author = {D. R. Scribner and J. Baldwin and G. A. Johnson},
   Title = {Actinomycosis mimicking a pelvic malignancy - A case
             report},
   Journal = {Journal Of Reproductive Medicine},
   Volume = {45},
   Number = {6},
   Pages = {515 -- 518},
   Year = {2000},
   Month = {June},
   Key = {Scribner00}
}

@article{fds174257,
   Author = {DR Scribner Jr and J Baldwin and GA Johnson},
   Title = {Actinomycosis mimicking a pelvic malignancy. A case
             report.},
   Journal = {The Journal of reproductive medicine},
   Volume = {45},
   Number = {6},
   Pages = {515-8},
   Year = {2000},
   Month = {June},
   ISSN = {0024-7758},
   Keywords = {Abdominal Pain • Actinomycosis • Colorectal
             Neoplasms • Diagnosis, Differential • Female
             • Humans • Middle Aged • Uterine Diseases
             • complications • diagnosis • diagnosis*
             • etiology* • pathology •
             surgery},
   Abstract = {BACKGROUND: Pelvic actinomycosis is difficult to diagnose
             preoperatively. The chronic infection is locally
             infiltrative and causes a profound induration of infected
             tissue planes. This induration, combined with absence of
             fever and leukocytosis, can mimic a pelvic malignancy. CASE:
             A 55-year-old woman was diagnosed with a pelvic mass after a
             two-month history of intermittent lower abdominal pain. The
             patient had had an intrauterine device for 12 years; it was
             removed two months prior to an exploratory laparotomy for
             the symptomatic mass. The mass was highly suggestive of
             colorectal cancer, with the rectosigmoid colon indurated and
             adherent to the uterus and sacrum. The induration of the
             colon extended caudally to within 3 cm of the anal verge. An
             abdominoperineal resection was performed along with a total
             abdominal hysterectomy, bilateral salpingo-oophorectomy and
             colostomy. Pathology revealed acute and chronic
             endometritis, left tuboovarian abscess and extensive, acute
             inflammation of the rectosigmoid colon without evidence of
             diverticuli. Actinomycosis was diagnosed based on the
             characteristic sulphur granules seen on hemotoxylin and
             eosin staining. CONCLUSION: Actinomycosis can mimic pelvic
             and abdominal malignancies. Surgeons should be aware of this
             infection to potentially spare women morbidity from
             excessive surgical procedures.},
   Language = {eng},
   Key = {fds174257}
}

@booklet{Jaeger00,
   Author = {L. A. Jaeger and R. C. Burghardt and G. A. Johnson and F. W.
             Bazer},
   Title = {Activation of conceptus and maternal integrins by
             transforming growth factor beta latency associated
             peptide.},
   Journal = {Biology Of Reproduction},
   Volume = {62},
   Pages = {281 -- 281},
   Year = {2000},
   Key = {Jaeger00}
}

@article{fds268838,
   Author = {Petiet, A and Johnson, GA},
   Title = {Active staining of mouse embryos for magnetic resonance
             microscopy.},
   Journal = {Methods Mol Biol},
   Volume = {611},
   Pages = {141-149},
   Year = {2010},
   ISSN = {1940-6029},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/19960328},
   Keywords = {Animals • Brain • Embryo, Mammalian •
             Formaldehyde • Magnetic Resonance Imaging • Mice
             • Microscopy • Staining and Labeling • Tissue
             Fixation • chemistry • metabolism •
             metabolism* • methods • methods*},
   Abstract = {Magnetic resonance histology (MRH) has found considerable
             application in structural phenotyping in the mouse embryo.
             MRH employs the same fundamental principles as clinical MRI,
             albeit with spatial resolution up to six orders of magnitude
             higher than that in clinical studies. Critical to obtaining
             this enormous gain in resolution is the need to enhance the
             weak signal from these microscopic voxels. This has been
             accomplished through the use of active staining, a method to
             simultaneously fix the embryonic/fetal tissues, while
             reducing the spin lattice relaxation time (T1). We describe
             here the methods that allow one to balance the fixation,
             which reduces the nuclear magnetic resonance (NMR) signal,
             with the enhancement of signal derived from the reduction in
             T1. Methods are included to cover the ranges of embryonic
             specimens from E10.5 through E19.5.},
   Language = {eng},
   Doi = {10.1007/978-1-60327-345-9_11},
   Key = {fds268838}
}

@article{fds268699,
   Author = {Papp, EA and Leergaard, TB and Calabrese, E and Johnson, GA and Bjaalie,
             JG},
   Title = {Addendum to “Waxholm Space atlas of the Sprague Dawley rat
             brain” [NeuroImage 97 (2014) 374-386].},
   Journal = {Neuroimage},
   Volume = {105},
   Pages = {561-562},
   Year = {2015},
   Month = {January},
   ISSN = {1053-8119},
   url = {http://dx.doi.org/10.1016/j.neuroimage.2014.10.017},
   Abstract = {The main focus of our original article was to describe the
             anatomical delineations constituting the first version of
             the WHS Sprague Dawley atlas, apply the Waxholm Space
             coordinate system, and publish the associated MRI/DTI
             template and segmentation volume in their original format.
             To increase usability of the dataset, we have recently
             shared an updated version of the volumetric image material
             (v1.01). The aims of this addendum are to inform about the
             improvements in the updated dataset, in particular related
             to navigation in the WHS coordinate system, and provide
             guidance for transforming coordinates acquired in the first
             version of the atlas.},
   Doi = {10.1016/j.neuroimage.2014.10.017},
   Key = {fds268699}
}

@booklet{Miyoshi89,
   Author = {K. Miyoshi and J. J. Pouch and S. A. Alterovitz and D. M.
             Pantic and G. A. Johnson},
   Title = {Adhesion, friction, and wear of plasma-deposited thin
             silicon-nitride films at temperatures to
             700-degrees-c},
   Journal = {Wear},
   Volume = {133},
   Number = {1},
   Pages = {107 -- 123},
   Year = {1989},
   Month = {September},
   Key = {Miyoshi89}
}

@article{fds311651,
   Author = {Vetreno, RP and Yaxley, R and Paniagua, B and Johnson, GA and Crews,
             FT},
   Title = {Adult rat cortical thickness changes across age and
             following adolescent intermittent ethanol
             treatment.},
   Journal = {Addict Biol},
   Volume = {22},
   Number = {3},
   Pages = {712-723},
   Year = {2017},
   Month = {May},
   ISSN = {1355-6215},
   url = {http://dx.doi.org/10.1111/adb.12364},
   Abstract = {Human studies have established that adolescence is a period
             of brain maturation that parallels the development of adult
             behaviors. However, little is known regarding cortical
             development in the adult rat brain. We used magnetic
             resonance imaging (MRI) and histology to assess the impact
             of age on adult Wistar rat cortical thickness on postnatal
             day (P)80 and P220 as well as the effect of adolescent binge
             ethanol exposure on adult (P80) cortical thickness. MRI
             revealed changes in cortical thickness between P80 and P220
             that differ across cortical region. The adult P220 rat
             prefrontal cortex increased in thickness whereas cortical
             thinning occurred in both the cingulate and parietal
             cortices relative to young adult P80 rats. Histological
             analysis confirmed the age-related cortical thinning. In the
             second series of experiments, an animal model of adolescent
             intermittent ethanol (AIE; 5.0 g/kg, intragastrically, 20
             percent ethanol w/v, 2 days on/2 days off from P25 to
             P55) was used to assess the effects of alcohol on cortical
             thickness in young adult (P80) rats. MRI revealed that AIE
             resulted in region-specific cortical changes. A small region
             within the prefrontal cortex was significantly thinner
             whereas medial cortical regions were significantly thicker
             in young adult (P80) AIE-treated rats. The observed increase
             in cortical thickness was confirmed by histology. Thus, the
             rat cerebral cortex continues to undergo cortical thickness
             changes into adulthood, and adolescent alcohol exposure
             alters the young adult cortex that could contribute to brain
             dysfunction in adulthood.},
   Doi = {10.1111/adb.12364},
   Key = {fds311651}
}

@article{fds174230,
   Author = {GA Johnson and VR Gutti and SK Loyalka and KA O'Beirne 2nd and SK
             Cochran, HM Dale and GR Kracke},
   Title = {Albuterol metered dose inhaler performance under hyperbaric
             pressures.},
   Journal = {Undersea & hyperbaric medicine : journal of the Undersea and
             Hyperbaric Medical Society, Inc},
   Volume = {36},
   Number = {1},
   Pages = {55-63},
   Year = {2009},
   Month = {April},
   ISSN = {1066-2936},
   Keywords = {Aerosols • Albuterol • Analysis of Variance •
             Asthma • Bronchial Spasm • Bronchodilator Agents
             • Diving • Humans • Hyperbaric Oxygenation
             • Metered Dose Inhalers • Nanoparticles •
             Particle Size • Pressure* • Weights and Measures
             • administration & dosage* • adverse effects
             • chemistry • contraindications • etiology
             • physiology • physiopathology • standards*
             • therapy},
   Abstract = {The weight change per actuation and aerosol particle size
             and number delivered by albuterol metered dose inhalers
             (MDIs) were measured in a multiplace hyperbaric chamber at
             pressures ranging from one atmosphere absolute (1 ATA, 0
             feet of seawater, fsw, 101 kPa) to three ATA (66 fsw, 304
             kPa). Weight change per actuation by CFC
             (chlorofluorocarbon) and long canister HFA
             (hydrofluoroalkane) powered MDIs was 13 +/- 1% and 12 +/- 1%
             less, respectively, at 3 ATA compared to 1 ATA. However,
             weight change per actuation by short canister HFA MDIs was
             not significantly changed with pressure. The geometric mean
             diameters of nano particles from the CFC and short canister
             HFA MDIs decreased from 50 nm at 0 fsw to 32 nm at 66 fsw
             whereas the long canister HFA aerosol diameters were not
             affected. The numbers of nanometer size particles delivered
             at 66 fsw were only 4-7% of those delivered at 0 fsw for the
             CFC and long canister HFA MDIs whereas for the short
             canister MDIs it was 26%. We conclude that the weight change
             per actuation of albuterol and the sizes and numbers of
             aerosol particles emitted from albuterol MDIs actuated in a
             hyperbaric environment vary by canister type.},
   Language = {eng},
   Key = {fds174230}
}

@booklet{Macfall94a,
   Author = {MacFall, JS and Spaine, P and Doudrick, R and Johnson,
             GA},
   Title = {Alterations in growth and water-transport processes in
             fusiform rust galls of pine, determined by magnetic
             resonance microscopy},
   Journal = {Phytopathology},
   Volume = {84},
   Number = {3},
   Pages = {288-293},
   Year = {1994},
   Month = {January},
   url = {http://dx.doi.org/10.1094/Phyto-84-288},
   Doi = {10.1094/Phyto-84-288},
   Key = {Macfall94a}
}

@article{fds343278,
   Author = {Antonsen, BT and Jiang, Y and Veraart, J and Qu, H and Nguyen, HP and Sijbers, J and Hörsten, SV and Johnson, GA and Leergaard,
             TB},
   Title = {Altered diffusion tensor imaging measurements in aged
             transgenic Huntington disease rats},
   Journal = {Brain Structure and Function},
   Volume = {218},
   Number = {3},
   Pages = {767-778},
   Year = {2013},
   url = {http://dx.doi.org/10.1007/s00429-012-0427-0},
   Abstract = {Rodent models of Huntington disease (HD) are valuable tools
             for investigating HD pathophysiology and evaluating new
             therapeutic approaches. Non-invasive characterization of
             HD-related phenotype changes is important for monitoring
             progression of pathological processes and possible effects
             of interventions. The first transgenic rat model for HD
             exhibits progressive late-onset affective, cognitive, and
             motor impairments, as well as neuropathological features
             reflecting observations from HD patients. In this report, we
             contribute to the anatomical phenotyping of this model by
             comparing high-resolution ex vivo DTI measurements obtained
             in aged transgenic HD rats and wild-type controls. By region
             of interest analysis supplemented by voxel-based statistics,
             we find little evidence of atrophy in basal ganglia regions,
             but demonstrate altered DTI measurements in the dorsal and
             ventral striatum, globus pallidus, entopeduncular nucleus,
             substantia nigra, and hippocampus. These changes are largely
             compatible with DTI findings in preclinical and clinical HD
             patients. We confirm earlier reports that HD rats express a
             moderate neuropathological phenotype, and provide evidence
             of altered DTI measures in specific HD-related brain
             regions, in the absence of pronounced morphometric changes.
             © 2012 The Author(s).},
   Doi = {10.1007/s00429-012-0427-0},
   Key = {fds343278}
}

@article{fds268771,
   Author = {Antonsen, BT and Jiang, Y and Veraart, J and Qu, H and Nguyen, HP and Sijbers, J and von Hörsten, S and Johnson, GA and Leergaard,
             TB},
   Title = {Altered diffusion tensor imaging measurements in aged
             transgenic Huntington disease rats.},
   Journal = {Brain Struct Funct},
   Volume = {218},
   Number = {3},
   Pages = {767-778},
   Year = {2013},
   Month = {May},
   ISSN = {1863-2653},
   url = {http://dx.doi.org/10.1007/s00429-012-0427-0},
   Abstract = {Rodent models of Huntington disease (HD) are valuable tools
             for investigating HD pathophysiology and evaluating new
             therapeutic approaches. Non-invasive characterization of
             HD-related phenotype changes is important for monitoring
             progression of pathological processes and possible effects
             of interventions. The first transgenic rat model for HD
             exhibits progressive late-onset affective, cognitive, and
             motor impairments, as well as neuropathological features
             reflecting observations from HD patients. In this report, we
             contribute to the anatomical phenotyping of this model by
             comparing high-resolution ex vivo DTI measurements obtained
             in aged transgenic HD rats and wild-type controls. By region
             of interest analysis supplemented by voxel-based statistics,
             we find little evidence of atrophy in basal ganglia regions,
             but demonstrate altered DTI measurements in the dorsal and
             ventral striatum, globus pallidus, entopeduncular nucleus,
             substantia nigra, and hippocampus. These changes are largely
             compatible with DTI findings in preclinical and clinical HD
             patients. We confirm earlier reports that HD rats express a
             moderate neuropathological phenotype, and provide evidence
             of altered DTI measures in specific HD-related brain
             regions, in the absence of pronounced morphometric
             changes.},
   Doi = {10.1007/s00429-012-0427-0},
   Key = {fds268771}
}

@article{fds174312,
   Author = {X Li and FW Bazer and H Gao and W Jobgen and GA Johnson and P Li, JR
             McKnight and MC Satterfield and TE Spencer and G Wu},
   Title = {Amino acids and gaseous signaling.},
   Journal = {Amino acids},
   Volume = {37},
   Number = {1},
   Pages = {65-78},
   Year = {2009},
   Month = {May},
   ISSN = {1438-2199},
   url = {http://dx.doi.org/10.1007/s00726-009-0264-5},
   Keywords = {Amino Acids • Animals • Carbon Monoxide •
             Cardiovascular Diseases • Energy Metabolism •
             Humans • Hydrogen Sulfide • Immune System Diseases
             • Nervous System Diseases • Nitric Oxide •
             Signal Transduction • Sulfur Dioxide •
             biosynthesis* • metabolism • metabolism* •
             physiology},
   Abstract = {Gases, such as nitric oxide (NO), carbon monoxide (CO),
             hydrogen sulfide (H(2)S), and sulfur dioxide (SO(2)) are
             known toxic pollutants in the air. However, they are now
             recognized as important signaling molecules synthesized in
             animals and humans from arginine, glycine (heme), and
             cysteine, respectively. At physiological levels, NO, CO, and
             SO(2) activate guanylyl cyclase to generate cGMP which
             elicits a variety of responses (including relaxation of
             vascular smooth muscle cells, hemodynamics,
             neurotransmission, and cell metabolism) via cGMP-dependent
             protein kinases. H(2)S is also a crucial regulator of both
             neurological function and endothelium-dependent relaxation
             through cGMP-independent mechanisms involving stimulation of
             membrane K(ATP) channels and intracellular cAMP signaling.
             Additionally, NO, CO, and H(2)S confer cytoprotective and
             immunomodulatory effects. Moreover, NH(3) is a major product
             of amino acid catabolism and profoundly affects the function
             of neurons and the vasculature through glutamine-dependent
             inhibition of NO synthesis. Emerging evidence shows that
             amino acids are not only precursors for these endogenous
             gases, but are also regulators of their production in a
             cell-specific manner. Thus, recent advances on gaseous
             signaling have greatly expanded our basic knowledge of amino
             acid biochemistry and nutrition. These exciting discoveries
             will aid in the design of new nutritional and
             pharmacological means to prevent and treat major health
             problems related to developmental biology and nutrient
             metabolism, including intrauterine growth restriction,
             preterm birth, aging, neurological disorders, cancer,
             obesity, diabetes, and cardiovascular disease.},
   Language = {eng},
   Doi = {10.1007/s00726-009-0264-5},
   Key = {fds174312}
}

@article{fds268720,
   Author = {Subashi, E and Choudhury, KR and Johnson, GA},
   Title = {An analysis of the uncertainty and bias in DCE-MRI
             measurements using the spoiled gradient-recalled echo pulse
             sequence.},
   Journal = {Med Phys},
   Volume = {41},
   Number = {3},
   Pages = {032301},
   Year = {2014},
   Month = {March},
   ISSN = {0094-2405},
   url = {http://dx.doi.org/10.1118/1.4865790},
   Abstract = {PURPOSE: The pharmacokinetic parameters derived from dynamic
             contrast-enhanced (DCE) MRI have been used in more than 100
             phase I trials and investigator led studies. A comparison of
             the absolute values of these quantities requires an
             estimation of their respective probability distribution
             function (PDF). The statistical variation of the DCE-MRI
             measurement is analyzed by considering the fundamental
             sources of error in the MR signal intensity acquired with
             the spoiled gradient-echo (SPGR) pulse sequence. METHODS:
             The variance in the SPGR signal intensity arises from
             quadrature detection and excitation flip angle
             inconsistency. The noise power was measured in 11 phantoms
             of contrast agent concentration in the range [0-1] mM (in
             steps of 0.1 mM) and in onein vivo acquisition of a
             tumor-bearing mouse. The distribution of the flip angle was
             determined in a uniform 10 mM CuSO4 phantom using the spin
             echo double angle method. The PDF of a wide range of T1
             values measured with the varying flip angle (VFA) technique
             was estimated through numerical simulations of the SPGR
             equation. The resultant uncertainty in contrast agent
             concentration was incorporated in the most common model of
             tracer exchange kinetics and the PDF of the derived
             pharmacokinetic parameters was studied numerically. RESULTS:
             The VFA method is an unbiased technique for measuringT1 only
             in the absence of bias in excitation flip angle. The
             time-dependent concentration of the contrast agent measured
             in vivo is within the theoretically predicted uncertainty.
             The uncertainty in measuring K(trans) with SPGR pulse
             sequences is of the same order, but always higher than, the
             uncertainty in measuring the pre-injection longitudinal
             relaxation time (T10). The lowest achievable
             bias/uncertainty in estimating this parameter is
             approximately 20%-70% higher than the bias/uncertainty in
             the measurement of the pre-injection T1 map. The fractional
             volume parameters derived from the extended Tofts model were
             found to be extremely sensitive to the variance in signal
             intensity. The SNR of the pre-injection T1 map indicates the
             limiting precision with which K(trans) can be calculated.
             CONCLUSIONS: Current small-animal imaging systems and pulse
             sequences robust to motion artifacts have the capacity for
             reproducible quantitative acquisitions with DCE-MRI. In
             these circumstances, it is feasible to achieve a level of
             precision limited only by physiologic variability.},
   Doi = {10.1118/1.4865790},
   Key = {fds268720}
}

@article{fds174264,
   Author = {GA Johnson and E Harrington},
   Title = {An apparatus for the simultaneous demineralization of
             fifty-four specimens.},
   Journal = {Stain technology},
   Volume = {52},
   Number = {3},
   Pages = {127-9},
   Year = {1977},
   Month = {May},
   ISSN = {0038-9153},
   Keywords = {Evaluation Studies as Topic • Formic Acids •
             Histological Techniques • Specimen Handling •
             instrumentation*},
   Abstract = {An apparatus designed to demineralize 54 specimens
             simultaneously is described. A drum with built-in specimen
             holders rotates continuously through a bath of acid,
             allowing a free exchange of demineralizing fluid over the
             specimens. Individual specimens can be easily introduced or
             withdrawn from the apparatus without disturbing
             others.},
   Language = {eng},
   Key = {fds174264}
}

@article{fds174195,
   Author = {GA JOHNSON},
   Title = {An arsine problem: engineering notes.},
   Journal = {American Industrial Hygiene Association quarterly},
   Volume = {14},
   Number = {3},
   Pages = {188-90},
   Year = {1953},
   Month = {September},
   ISSN = {0096-820X},
   Language = {eng},
   Key = {fds174195}
}

@article{fds268752,
   Author = {Johnson, GA and Cofer, GP and Gewalt, SL and Hedlund,
             LW},
   Title = {An engineering approach to image-based phenotyping},
   Journal = {2002 IEEE INTERNATIONAL SYMPOSIUM ON BIOMEDICAL IMAGING,
             PROCEEDINGS},
   Pages = {381-383},
   Publisher = {IEEE},
   Year = {2002},
   ISBN = {0-7803-7584-X},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000178000400095&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Doi = {10.1109/isbi.2002.1029273},
   Key = {fds268752}
}

@booklet{Halvorsen81,
   Author = {Halvorsen, RA and Woodfield, S and T., R and Allen, SM and Hedlung, LW and Johnson, GA and Thompson, WM},
   Title = {AN EVALUATION OF CONTRAST AGENTS FOR CT OF THE HEPATOBILIARY
             SYSTEM},
   Journal = {Investigative Radiology},
   Volume = {16},
   Number = {5},
   Pages = {387-387},
   Publisher = {Ovid Technologies (Wolters Kluwer Health)},
   Year = {1981},
   Month = {September},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1981MK56200053&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Doi = {10.1097/00004424-198109000-00053},
   Key = {Halvorsen81}
}

@booklet{Johnson81,
   Author = {JOHNSON, GA and KOROBKIN, M and HEINZ, R},
   Title = {AN EVALUATION OF MULTIPLANAR IMAGING CAPABILITIES OF 4
             CURRENT CT SCANNERS},
   Journal = {AMERICAN JOURNAL OF ROENTGENOLOGY},
   Volume = {136},
   Number = {6},
   Pages = {1279-1279},
   Year = {1981},
   ISSN = {0361-803X},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1981LU08900097&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Johnson81}
}

@article{fds268891,
   Author = {Johnson, GA and O'Foghludha, F},
   Title = {An experimental "trans-molybdenum" tube for
             mammography.},
   Journal = {Radiology},
   Volume = {127},
   Number = {2},
   Pages = {511-516},
   Year = {1978},
   Month = {May},
   ISSN = {0033-8419},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/644079},
   Keywords = {Fluorescence • Humans • Intubation •
             Mammography • Molybdenum • Radiation Dosage •
             instrumentation*},
   Abstract = {Possible mammographic advantages of "trans-molybdenum"
             anodes (atomic number greater than ZMo) are decreased dose
             because the fluorescent radiation is more penetrating, and
             increased useful output; contrast degradation is known to be
             tolerable. The output per mAs, the HVT in Al, and the
             penetration in Lucite were measured spectroscopically for an
             experimental Rh-anode tube and also for Mo- and W-anode
             mammographic tubes. The trans-molybdenum tube was shown to
             have output and dose advantages over Mo anodes, and output
             and contrast advantages over normal and selectively filtered
             W anodes. Possible applications in areas other than
             mammography are briefly discussed.},
   Doi = {10.1148/127.2.511},
   Key = {fds268891}
}

@booklet{Neiswanger87,
   Author = {L. Neiswanger and G. A. Johnson and V. P.
             Carey},
   Title = {An experimental-study of high rayleigh number mixed
             convection in a rectangular enclosure with restricted inlet
             and outlet openings},
   Journal = {Journal Of Heat Transfer-transactions Of The
             Asme},
   Volume = {109},
   Number = {2},
   Pages = {446 -- 453},
   Year = {1987},
   Month = {May},
   Key = {Neiswanger87}
}

@article{fds341989,
   Author = {Anderson, RJ and Cook, JJ and Delpratt, NA and Nouls, JC and Gu, B and McNamara, JO and Avants, BB and Johnson, GA and Badea,
             A},
   Title = {An HPC Pipeline with Validation Framework for Small Animal
             Multivariate Brain Analysis (SAMBA).},
   Journal = {CoRR},
   Volume = {abs/1709.10483},
   Year = {2017},
   Key = {fds341989}
}

@booklet{Johnson80d,
   Author = {JOHNSON, GA and FOGHLUDA, F},
   Title = {AN INVESTIGATION OF TRANSMOLYBDENUM FLUORESCENT ANODES FOR
             MAMMOGRAPHY},
   Journal = {AMERICAN JOURNAL OF ROENTGENOLOGY},
   Volume = {134},
   Number = {4},
   Pages = {855-855},
   Year = {1980},
   ISSN = {0361-803X},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1980JM11100062&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Johnson80d}
}

@book{fds292752,
   Author = {Paxinos, G and Watson, C and Calabrese, E and Badea, A and Johnson,
             G},
   Title = {An MRI/DTI Atlas of the Rat Brain},
   Pages = {224 pages},
   Publisher = {Elsevier, Academic Press},
   Year = {2015},
   Month = {May},
   ISBN = {978-0-12-417313-2},
   Abstract = {MRI/DTI Atlas of the Rat Brain offers two major enhancements
             when compared with earlier attempts to make MRI/DTI rat
             brain atlases. First, the spatial resolution at 25μm is
             considerably higher than previous data published. Secondly,
             the comprehensive set of MRI/DTI contrasts provided has
             enabled the authors to identify more than 80% of structures
             identified in The Rat Brain in Stereotaxic
             Coordinates.},
   Key = {fds292752}
}

@article{fds268756,
   Author = {Calabrese, E and Johnson, GA and Watson, C},
   Title = {An ontology-based segmentation scheme for tracking postnatal
             changes in the developing rodent brain with
             MRI.},
   Journal = {Neuroimage},
   Volume = {67},
   Pages = {375-384},
   Year = {2013},
   Month = {February},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/23246176},
   Abstract = {The postnatal period of neurodevelopment has been implicated
             in a number of brain disorders including autism and
             schizophrenia. Rodent models have proven to be invaluable in
             advancing our understanding of the human brain, and will
             almost certainly play a pivotal role in future studies on
             postnatal neurodevelopment. The growing field of magnetic
             resonance microscopy has the potential to revolutionize our
             understanding of neurodevelopment, if it can be successfully
             and appropriately assimilated into the vast body of existing
             neuroscience research. In this study, we demonstrate the
             utility of a developmental neuro-ontology designed
             specifically for tracking regional changes in MR biomarkers
             throughout postnatal neurodevelopment. Using this
             ontological classification as a segmentation guide, we track
             regional changes in brain volume in rats between postnatal
             day zero and postnatal day 80 and demonstrate differential
             growth rates in axial versus paraxial brain regions. Both
             the ontology and the associated label volumes are provided
             as a foundation for future MR-based studies of postnatal
             neurodevelopment in normal and disease states.},
   Doi = {10.1016/j.neuroimage.2012.11.037},
   Key = {fds268756}
}

@booklet{Pals86,
   Author = {D. T. Pals and S. Thaisrivongs and J. A. Lawson and W. M.
             Kati and S. R. Turner and G. L. Degraaf and D. W. Harris and G. A. Johnson},
   Title = {An orally active inhibitor of renin},
   Journal = {Hypertension},
   Volume = {8},
   Number = {12},
   Pages = {1105 -- 1112},
   Year = {1986},
   Month = {December},
   Key = {Pals86}
}

@article{fds174084,
   Author = {DT Pals and S Thaisrivongs and JA Lawson and WM Kati, SR Turner and GL
             DeGraaf, DW Harris and GA Johnson},
   Title = {An orally active inhibitor of renin.},
   Journal = {Hypertension},
   Volume = {8},
   Number = {12},
   Pages = {1105-12},
   Year = {1986},
   Month = {December},
   ISSN = {0194-911X},
   Keywords = {Administration, Oral • Animals • Blood Pressure
             • Dose-Response Relationship, Drug • Heart Rate
             • Humans • Macaca fascicularis • Male •
             Oligopeptides • Rats • Rats, Inbred Strains •
             Renin • Renin-Angiotensin System • Sodium •
             antagonists & inhibitors* • drug effects •
             pharmacology* • physiology},
   Abstract = {A potent renin inhibitor, U-71038 (Boc-Pro-Phe-N-MeHis-Leu
             psi[CHOHCH2]Val-Ile-Amp), was tested for oral effectiveness.
             Enzyme kinetic studies indicated that U-71038 was a
             competitive inhibitor of hog renin with an inhibitor
             constant (Ki) value of 12 nM. Intravenous as well as oral
             administration of U-71038 to anesthetized, ganglion-blocked
             rats infused with hog renin elicited dose-related
             hypotensive responses. Intravenous administration of U-71038
             to conscious, sodium-depleted monkeys caused dose-related
             decreases of blood pressure and plasma renin activity
             without affecting heart rate. Similarly, the oral
             administration of U-71038 at 50 mg/kg to conscious,
             sodium-depleted monkeys elicited a pronounced hypotension
             and decrease in plasma renin activity that persisted for 5
             hours. The hypotensive responses elicited by intravenous and
             oral administration of U-71038 to hog renin-infused rats and
             sodium-depleted monkeys were shown to be due entirely to
             inhibition of the renin-angiotensin system. A comparison of
             the results obtained after the intravenous administration of
             U-71038 with the results obtained after the oral
             administration of U-71038 implied that at least 10% of the
             orally administered U-71038 must have been absorbed to cause
             the observed effects in hog renin-infused rats and
             sodium-depleted monkeys. The studies demonstrated that an
             inhibitor of renin with a long duration of action and with
             oral effectiveness is a feasible entity.},
   Language = {eng},
   Key = {fds174084}
}

@booklet{Pals86a,
   Author = {D. T. Pals and S. Thaisrivongs and J. A. Lawson and W. M.
             Kati and S. R. Turner and G. L. Degraaf and D. W. Harris and G. A. Johnson},
   Title = {An orally-active inhibitor of renin},
   Journal = {Hypertension},
   Volume = {8},
   Number = {9},
   Pages = {833 -- 833},
   Year = {1986},
   Month = {September},
   Key = {Pals86a}
}

@booklet{Stafford80,
   Author = {M. L. Stafford and K. F. Guin and G. A. Johnson and L. A.
             Sanders and S. L. Rockey},
   Title = {Analysis of 1,4-dioxane in ethoxylated surfactants},
   Journal = {Journal Of The Society Of Cosmetic Chemists},
   Volume = {31},
   Number = {6},
   Pages = {281 -- 287},
   Year = {1980},
   Key = {Stafford80}
}

@booklet{Garlow02,
   Author = {J. E. Garlow and H. Ka and G. A. Johnson and R. C. Burghardt and L. A. Jaeger and F. W. Bazer},
   Title = {Analysis of osteopontin at the maternal-placental interface
             in pigs},
   Journal = {Biology Of Reproduction},
   Volume = {66},
   Number = {3},
   Pages = {718 -- 725},
   Year = {2002},
   Month = {March},
   Key = {Garlow02}
}

@article{fds174252,
   Author = {JE Garlow and H Ka and GA Johnson and RC Burghardt and LA Jaeger and FW
             Bazer},
   Title = {Analysis of osteopontin at the maternal-placental interface
             in pigs.},
   Journal = {Biology of reproduction},
   Volume = {66},
   Number = {3},
   Pages = {718-25},
   Year = {2002},
   Month = {March},
   ISSN = {0006-3363},
   Keywords = {Animals • Cell Membrane • Endometrium •
             Epithelial Cells • Female • Frozen Sections •
             In Situ Hybridization • Integrins • Oligopeptides
             • Osteopontin • Placenta • Pregnancy •
             RNA, Messenger • Sialoglycoproteins • Signal
             Transduction • Swine* • Trophoblasts • Uterus
             • analysis • analysis* • chemistry •
             chemistry* • genetics • metabolism •
             pharmacology • physiology},
   Abstract = {Noninvasive, epitheliochorial placentation in the pig
             follows a prolonged preimplantation period characterized by
             migration, spacing and elongation of conceptuses, and
             secretion of estrogen for maternal recognition of pregnancy.
             Osteopontin (OPN) is an extracellular matrix protein that
             binds integrins to promote cell-cell attachment and
             communication. OPN appears to play a key role in conceptus
             implantation and maintenance of pregnancy in sheep; however,
             a role for OPN in the porcine uterus has not been
             established. Therefore, this study examined OPN expression
             and function in the porcine uterus and conceptus
             (embryo/fetus and associated extraembryonic membranes).
             Northern and slot blot hybridization detected an increase in
             endometrial OPN expression between Days 25 and 30, and
             levels remained elevated through Day 85 of pregnancy. In
             situ hybridization localized OPN mRNA to discrete regions of
             the uterine luminal epithelium (LE) on Day 15 of pregnancy
             and to the entire LE thereafter. Glandular epithelial (GE)
             expression of OPN mRNA was first detected on Day 35 of
             pregnancy and increased through Day 85. Both 70- and 45-kDa
             forms of OPN protein were detected in cyclic and pregnant
             endometrium by Western blotting. OPN protein was localized
             to the LE and GE by immunofluorescence; however, only the
             70-kDa OPN was detected in uterine flushings. OPN protein
             was present along the entire uterine-placental interface
             after Day 30 of pregnancy. In addition, OPN mRNA and protein
             were localized to immune-like cells within the stratum
             compactum of the endometrium in both Day 9 cyclic and
             pregnant gilts. Incubation of OPN-coated microbeads with
             porcine trophectoderm and uterine luminal epithelial cells
             induced Arg-Gly-Asp (RGD)-dependent integrin activation and
             transmembrane accumulation of cytoskeletal molecules at the
             apical cell surface as assessed by immunofluorescence
             detection of talin or alpha-actinin as markers for focal
             adhesions. These results suggest that OPN, expressed by
             uterine epithelium and immune cells, may interact with
             receptors (i.e., integrins) on conceptus and uterus to
             promote conceptus development and signaling between these
             tissues as key contributors to attachment and placentation
             in the pig.},
   Language = {eng},
   Key = {fds174252}
}

@article{fds268721,
   Author = {Ashton, JR and Befera, N and Clark, D and Qi, Y and Mao, L and Rockman, HA and Johnson, GA and Badea, CT},
   Title = {Anatomical and functional imaging of myocardial infarction
             in mice using micro-CT and eXIA 160 contrast
             agent.},
   Journal = {Contrast Media Mol Imaging},
   Volume = {9},
   Number = {2},
   Pages = {161-168},
   Year = {2014},
   ISSN = {1555-4309},
   url = {http://dx.doi.org/10.1002/cmmi.1557},
   Abstract = {Noninvasive small animal imaging techniques are essential
             for evaluation of cardiac disease and potential
             therapeutics. A novel preclinical iodinated contrast agent
             called eXIA 160 has recently been developed, which has been
             evaluated for micro-CT cardiac imaging. eXIA 160 creates
             strong contrast between blood and tissue immediately after
             its injection and is subsequently taken up by the myocardium
             and other metabolically active tissues over time. We focus
             on these properties of eXIA and show its use in imaging
             myocardial infarction in mice. Five C57BL/6 mice were imaged
             ~2 weeks after left anterior descending coronary artery
             ligation. Six C57BL/6 mice were used as controls.
             Immediately after injection of eXIA 160, an enhancement
             difference between blood and myocardium of ~340 HU enabled
             cardiac function estimation via 4D micro-CT scanning with
             retrospective gating. Four hours post-injection, the healthy
             perfused myocardium had a contrast difference of ~140 HU
             relative to blood while the infarcted myocardium showed no
             enhancement. These differences allowed quantification of
             infarct size via dual-energy micro-CT. In vivo micro-SPECT
             imaging and ex vivo triphenyl tetrazolium chloride (TTC)
             staining provided validation for the micro-CT findings. Root
             mean squared error of infarct measurements was 2.7% between
             micro-CT and SPECT, and 4.7% between micro-CT and TTC. Thus,
             micro-CT with eXIA 160 can be used to provide both
             morphological and functional data for preclinical studies
             evaluating myocardial infarction and potential therapies.
             Further studies are warranted to study the potential use of
             eXIA 160 as a CT molecular imaging tool for other
             metabolically active tissues in the mouse.},
   Doi = {10.1002/cmmi.1557},
   Key = {fds268721}
}

@booklet{Bristow81,
   Author = {M. R. Bristow and W. A. Minobe and M. E. Billingham and J.
             B. Marmor and G. A. Johnson and B. M. Ishimoto and W. S.
             Sageman and J. R. Daniels},
   Title = {Anthracycline-associated cardiac and renal damage in rabbits
             - evidence for mediation by vasoactive substances},
   Journal = {Laboratory Investigation},
   Volume = {45},
   Number = {2},
   Pages = {157 -- 168},
   Year = {1981},
   Key = {Bristow81}
}

@article{fds174100,
   Author = {MR Bristow and WA Minobe and ME Billingham and JB Marmor and GA Johnson and BM Ishimoto and WS Sageman, JR Daniels},
   Title = {Anthracycline-associated cardiac and renal damage in
             rabbits. Evidence for mediation by vasoactive
             substances.},
   Journal = {Laboratory investigation; a journal of technical methods and
             pathology},
   Volume = {45},
   Number = {2},
   Pages = {157-68},
   Year = {1981},
   Month = {August},
   ISSN = {0023-6837},
   Keywords = {Animals • Arteries • Cardiomyopathies •
             Catecholamines • Doxorubicin • Female •
             Histamine Antagonists • Histamine Release • Kidney
             Diseases • Myocardium • Rabbits •
             Vasoconstrictor Agents • Vasodilator Agents •
             adverse effects* • blood • chemically induced*
             • metabolism • pharmacology •
             pharmacology*},
   Abstract = {We tested the hypothesis that anthracycline-induced cardiac
             and renal damage is mediated by vasoactive substances. A
             1-minute exposure to 5 micrograms per ml. of doxorubicin
             (DXR, Adriamycin) produced cardiac histamine release in
             isolated rabbit hearts. Under conditions in which histamine
             uptake and metabolism were impaired, the administration of
             DXR, 2 mg. per kg., over 1 minute was associated with
             elevations in arterial histamine and catecholamines. The
             chronic weekly administration of DXR produced severe cardiac
             and renal damage. The administration of combined histaminic
             and adrenergic blockade with diphenhydramine, cimetidine,
             phentolamine, and propranolol (DCPP) pre- and immediately
             post-DXR resulted in near total protection against
             DXR-mediated cardiac damage and prevented the majority of
             the renal lesions. The combined administration of
             diphenhydramine, cimetidine, phentolamine, and propranolol
             did not appear to be acting by mechanisms other than
             blockade of vasoactive amine receptors as cardiac uptake of
             DXR and the DXR antitumor response were not altered by
             diphenhydramine, cimetidine, phentolamine, and propranolol.
             This study demonstrates that anthracycline-associated
             cardiac and renal toxicity may be mediated by vasoactive
             substances and that anthracycline cardiomyopathy is
             potentially preventable.},
   Language = {eng},
   Key = {fds174100}
}

@booklet{Burvill95a,
   Author = {P. W. Burvill and G. A. Johnson and K. D. Jamrozik and C. S.
             Anderson and E. G. Stewartwynne and T. M. H.
             Chakera},
   Title = {Anxiety disorders after stroke - results from the perth
             community stroke study},
   Journal = {British Journal Of Psychiatry},
   Volume = {166},
   Pages = {328 -- 332},
   Year = {1995},
   Month = {March},
   Key = {Burvill95a}
}

@article{fds174259,
   Author = {PW Burvill and GA Johnson and KD Jamrozik and CS Anderson and EG
             Stewart-Wynne, TM Chakera},
   Title = {Anxiety disorders after stroke: results from the Perth
             Community Stroke Study.},
   Journal = {The British journal of psychiatry : the journal of mental
             science},
   Volume = {166},
   Number = {3},
   Pages = {328-32},
   Year = {1995},
   Month = {March},
   ISSN = {0007-1250},
   Keywords = {Adaptation, Psychological • Adult • Aged •
             Agoraphobia • Anxiety Disorders • Cerebrovascular
             Disorders • Comorbidity • Cross-Sectional Studies
             • Delirium, Dementia, Amnestic, Cognitive Disorders
             • Depressive Disorder • Female • Follow-Up
             Studies • Humans • Incidence • Male •
             Middle Aged • Sick Role • Western Australia •
             diagnosis • epidemiology • epidemiology* •
             psychology},
   Abstract = {BACKGROUND: The prevalence of anxiety disorders in 294
             patients who survived to four months in the Perth Community
             Stroke Study (Perth, Australia), and a follow-up of these
             patients at 12 months, are presented. METHOD: Diagnoses are
             described both in the usual DSM hierarchic format and by a
             non-hierarchic approach. Adoption of the hierarchic approach
             alone greatly underestimates the prevalence of anxiety
             disorders. RESULTS: Most cases were of agoraphobia, and the
             remainder were generalised anxiety disorder. The prevalence
             of anxiety disorders alone was 5% in men and 19% in women;
             in community controls, it was 5% in men and 8% in women.
             Adopting a non-hierarchic approach to diagnosis gave a
             prevalence of 12% in men and 28% in women. When those who
             showed evidence of anxiety disorder before stroke were
             subtracted, the latter prevalence was 9% in men and 20% in
             women. CONCLUSION: One-third of the men and half of the
             women with post-stroke anxiety disorders showed evidence of
             either depression or an anxiety disorder at the time of the
             stroke. At 12 month follow-up of 49 patients with
             agoraphobia by a non-hierarchic approach, 51% had recovered,
             and equal proportions of the remainder had died or still had
             agoraphobia. The only major difference in outcome between
             those with anxiety disorder alone and those with comorbid
             depression was the greater mortality in the
             latter.},
   Language = {eng},
   Key = {fds174259}
}

@booklet{Burg02,
   Author = {Burg, KJL and Delnomdedieu, M and Beiler, RJ and Culberson, CR and Greene, KG and Halberstadt, CR and Holder, WD and Loebsack, AB and Roland, WD and Johnson, GA},
   Title = {Application of magnetic resonance microscopy to tissue
             engineering: a polylactide model.},
   Journal = {J Biomed Mater Res},
   Volume = {61},
   Number = {3},
   Pages = {380-390},
   Year = {2002},
   Month = {September},
   ISSN = {0021-9304},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/12115463},
   Abstract = {Absorbable polymers are unique materials that find
             application as temporary scaffolds in tissue engineering.
             They are often extremely sensitive to histological
             processing and, for this reason, studying fragile,
             tissue-engineered constructs before implantation can be
             quite difficult. This research investigates the use of
             noninvasive imaging using magnetic resonance microscopy
             (MRM) as a tool to enhance the assessment of these cellular
             constructs. A series of cellular, polylactide constructs was
             developed and analyzed using a battery of tests, including
             MRM. Distribution of rat aortic smooth muscle cells within
             the scaffolds was compared as one example of a tissue
             engineering MRM application. Cells were loaded in varying
             amounts using static and dynamic methods. It was found that
             the cellular component was readily identified and the
             polymer microstructure readily assessed. Specifically, the
             MRM results showed a heterogeneous distribution of cells due
             to static loading and a homogenous distribution associated
             with dynamic loading, results that were not visible through
             biochemical tests, scanning electron microscopy, or
             histological evaluation independently. MRM also allowed
             differentiation between different levels of cellular
             loading. The current state of MRM is such that it is
             extremely useful in the refinement of polymer processing and
             cell seeding methods. This method has the potential, with
             technological advances, to be of future use in the
             characterization of cell-polymer interactions.},
   Doi = {10.1002/jbm.10146},
   Key = {Burg02}
}

@article{fds132755,
   Author = {KJ Burg and M Delnomdedieu and RJ Beiler and CR Culberson and KG Greene and CR Halberstadt and WD Holder and AB Loebsack and WD Roland and GA
             Johnson},
   Title = {Application of magnetic resonance microscopy to tissue
             engineering: a polylactide model.},
   Journal = {Journal of biomedical materials research, United
             States},
   Volume = {61},
   Number = {3},
   Pages = {380-90},
   Year = {2002},
   Month = {September},
   ISSN = {0021-9304},
   Keywords = {Absorbable Implants • Animals • Aorta •
             Biocompatible Materials • Cell Survival • Magnetic
             Resonance Imaging* • Materials Testing •
             Microscopy • Muscle, Smooth, Vascular • Polyesters
             • Porosity • Rats • Tissue Engineering •
             cytology • instrumentation • instrumentation*
             • methods • methods*},
   Abstract = {Absorbable polymers are unique materials that find
             application as temporary scaffolds in tissue engineering.
             They are often extremely sensitive to histological
             processing and, for this reason, studying fragile,
             tissue-engineered constructs before implantation can be
             quite difficult. This research investigates the use of
             noninvasive imaging using magnetic resonance microscopy
             (MRM) as a tool to enhance the assessment of these cellular
             constructs. A series of cellular, polylactide constructs was
             developed and analyzed using a battery of tests, including
             MRM. Distribution of rat aortic smooth muscle cells within
             the scaffolds was compared as one example of a tissue
             engineering MRM application. Cells were loaded in varying
             amounts using static and dynamic methods. It was found that
             the cellular component was readily identified and the
             polymer microstructure readily assessed. Specifically, the
             MRM results showed a heterogeneous distribution of cells due
             to static loading and a homogenous distribution associated
             with dynamic loading, results that were not visible through
             biochemical tests, scanning electron microscopy, or
             histological evaluation independently. MRM also allowed
             differentiation between different levels of cellular
             loading. The current state of MRM is such that it is
             extremely useful in the refinement of polymer processing and
             cell seeding methods. This method has the potential, with
             technological advances, to be of future use in the
             characterization of cell-polymer interactions.},
   Key = {fds132755}
}

@article{fds268871,
   Author = {De Lin and M and Toncheva, G and Nguyen, G and Kim, S and Anderson-Evans,
             C and Johnson, GA and Yoshizumi, TT},
   Title = {Application of MOSFET detectors for dosimetry in small
             animal radiography using short exposure times.},
   Journal = {Radiat Res},
   Volume = {170},
   Number = {2},
   Pages = {260-263},
   Year = {2008},
   Month = {August},
   ISSN = {0033-7587},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/18666818},
   Keywords = {Equipment Design • Equipment Failure Analysis •
             Radiation Dosage • Radiographic Image Enhancement
             • Radiometry • Sensitivity and Specificity •
             Transducers* • Transistors* • instrumentation*
             • methods},
   Abstract = {Digital subtraction angiography (DSA) X-ray imaging for
             small animals can be used for functional phenotyping given
             its ability to capture rapid physiological changes at high
             spatial and temporal resolution. The higher temporal and
             spatial requirements for small-animal imaging drive the need
             for short, high-flux X-ray pulses. However, high doses of
             ionizing radiation can affect the physiology. The purpose of
             this study was to verify and apply metal oxide semiconductor
             field effect transistor (MOSFET) technology to dosimetry for
             small-animal diagnostic imaging. A tungsten anode X-ray
             source was used to expose a tissue-equivalent mouse phantom.
             Dose measurements were made on the phantom surface and
             interior. The MOSFETs were verified with thermoluminescence
             dosimeters (TLDs). Bland-Altman analysis showed that the
             MOSFET results agreed with the TLD results (bias, 0.0625).
             Using typical small animal DSA scan parameters, the dose
             ranged from 0.7 to 2.2 cGy. Application of the MOSFETs in
             the small animal environment provided two main benefits: (1)
             the availability of results in near real-time instead of the
             hours needed for TLD processes and (2) the ability to
             support multiple exposures with different X-ray techniques
             (various of kVp, mA and ms) using the same MOSFET. This
             MOSFET technology has proven to be a fast, reliable small
             animal dosimetry method for DSA imaging and is a good system
             for dose monitoring for serial and gene expression
             studies.},
   Doi = {10.1667/RR1328.1},
   Key = {fds268871}
}

@article{fds268881,
   Author = {Maronpot, RR and Sills, RC and Johnson, GA},
   Title = {Applications of magnetic resonance microscopy.},
   Journal = {Toxicol Pathol},
   Volume = {32 Suppl 2},
   Pages = {42-48},
   Year = {2004},
   ISSN = {0192-6233},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/15503663},
   Keywords = {Animals • Brain • Fetus • Humans • Image
             Processing, Computer-Assisted • Imaging,
             Three-Dimensional • Magnetic Resonance Imaging* •
             Microscopy • Sulfur Oxides • Teratology •
             Urate Oxidase • genetics • metabolism •
             methods*},
   Abstract = {Magnetic resonance imaging (MRI) has enjoyed enormous
             clinical success since the first demonstration of the method
             more than 30 years ago. An increasing number of
             pharmaceutical manufacturers seeking new biomarkers for
             assessing drug efficacy and toxicity are turning to MRI. A
             specific application of MRI promises to revolutionize
             pathology for the basic scientist in the same way MRI has
             forever altered the standard of care in the clinical domain.
             More specifically, this application is the use of magnetic
             resonance microscopy (MRM) in conjunction with new staining
             methodologies that now make MRM routinely available to the
             widest range of investigators.},
   Doi = {10.1080/01926230490451707},
   Key = {fds268881}
}

@article{fds174168,
   Author = {RS Dhariwal and RK Fitch and CL Lavelle and GA Johnson},
   Title = {Artefacts observed on dental tissues during ion etching in a
             scanning electron microscope.},
   Journal = {Journal of anatomy},
   Volume = {122},
   Number = {Pt 1},
   Pages = {133-40},
   Year = {1976},
   Month = {September},
   ISSN = {0021-8782},
   Keywords = {Dental Amalgam • Dental Enamel • Dental Materials
             • Dentin • Histological Techniques • Humans
             • Ions • Microscopy, Electron, Scanning •
             Tooth • methods* • ultrastructure •
             ultrastructure*},
   Language = {eng},
   Key = {fds174168}
}

@booklet{Anderson93,
   Author = {C. S. Anderson and K. D. Jamrozik and P. W. Burvill and T.
             M. H. Chakera and G. A. Johnson and E. G.
             Stewartwynne},
   Title = {Ascertaining the true incidence of stroke - experience from
             the perth community stroke study, 1989-1990},
   Journal = {Medical Journal Of Australia},
   Volume = {158},
   Number = {2},
   Pages = {80 -- 84},
   Year = {1993},
   Month = {January},
   Key = {Anderson93}
}

@article{fds174290,
   Author = {CS Anderson and KD Jamrozik and PW Burvill and TM Chakera and GA
             Johnson, EG Stewart-Wynne},
   Title = {Ascertaining the true incidence of stroke: experience from
             the Perth Community Stroke Study, 1989-1990.},
   Journal = {The Medical journal of Australia},
   Volume = {158},
   Number = {2},
   Pages = {80-4},
   Year = {1993},
   Month = {January},
   ISSN = {0025-729X},
   Keywords = {Adolescent • Adult • Age Factors • Aged
             • Aged, 80 and over • Cerebrovascular Disorders
             • Confidence Intervals • Female • Follow-Up
             Studies • Humans • Incidence • Ischemic
             Attack, Transient • Male • Middle Aged • Sex
             Factors • Western Australia • epidemiology •
             epidemiology* • mortality},
   Abstract = {OBJECTIVE: To determine the age and sex specific incidence,
             and case fatality of stroke in Perth, Western Australia.
             DESIGN AND SETTING: A population-based descriptive
             epidemiological study. SUBJECTS: All residents of a
             geographically defined segment of the Perth metropolitan
             area (population 138,708) who had a stroke or transient
             ischaemic attack between 20 February 1989 and 19 August
             1990, inclusive. MAIN OUTCOME MEASURES: Definite acute
             "first-ever-in-a-lifetime" (first-ever) and recurrent stroke
             classified according to standard definitions and criteria.
             RESULTS: During the 18-month study period, 536 stroke events
             occurred among 492 patients, 69% of which were first-ever
             strokes. The crude annual event rate for all strokes was 258
             (95% confidence interval 231-285) per 100,000, and the
             overall case fatality at 28 days was 24% (95% CI, 20%-28%).
             The crude annual incidence for first-ever strokes was 178
             (95% CI, 156-200) per 100,000; 189 (95% CI, 157-221) per
             100,000 in males and 166 (95% CI, 136-196) per 100,000 in
             females. The corresponding rates, age-adjusted to the
             "world" population, were 132 (95% CI, 109-155) for males and
             77 (95% CI, 60-94) for females. CONCLUSIONS: In contrast to
             mortality rates for ischaemic heart disease, the incidence
             of stroke in Australia appears little different from that
             for several other Western countries. For both males and
             females the incidence of stroke rises exponentially with
             increasing age. Although the sex-dependent difference in the
             risk of stroke is greatest in middle age, males are at
             greater risk of stroke even among the most elderly. To
             determine the incidence of stroke accurately,
             population-based studies of stroke need exhaustive and
             overlapping sources of case ascertainment. If only cases
             admitted to hospital had been used, we would have
             underestimated the rate of stroke among the most elderly by
             almost 40%. We estimate that approximately 37,000 people,
             about 50% of whom are over the age of 75, suffer a stroke
             each year in Australia.},
   Language = {eng},
   Key = {fds174290}
}

@article{fds268719,
   Author = {Lee, C-L and Min, H and Befera, N and Clark, D and Qi, Y and Das, S and Johnson, GA and Badea, CT and Kirsch, DG},
   Title = {Assessing cardiac injury in mice with dual energy-microCT,
             4D-microCT, and microSPECT imaging after partial heart
             irradiation.},
   Journal = {Int J Radiat Oncol Biol Phys},
   Volume = {88},
   Number = {3},
   Pages = {686-693},
   Year = {2014},
   Month = {March},
   ISSN = {0360-3016},
   url = {http://dx.doi.org/10.1016/j.ijrobp.2013.11.238},
   Abstract = {PURPOSE: To develop a mouse model of cardiac injury after
             partial heart irradiation (PHI) and to test whether dual
             energy (DE)-microCT and 4-dimensional (4D)-microCT can be
             used to assess cardiac injury after PHI to complement
             myocardial perfusion imaging using micro-single photon
             emission computed tomography (SPECT). METHODS AND MATERIALS:
             To study cardiac injury from tangent field irradiation in
             mice, we used a small-field biological irradiator to deliver
             a single dose of 12 Gy x-rays to approximately one-third of
             the left ventricle (LV) of Tie2Cre; p53(FL/+) and Tie2Cre;
             p53(FL/-) mice, where 1 or both alleles of p53 are deleted
             in endothelial cells. Four and 8 weeks after irradiation,
             mice were injected with gold and iodinated
             nanoparticle-based contrast agents, and imaged with
             DE-microCT and 4D-microCT to evaluate myocardial vascular
             permeability and cardiac function, respectively.
             Additionally, the same mice were imaged with microSPECT to
             assess myocardial perfusion. RESULTS: After PHI with tangent
             fields, DE-microCT scans showed a time-dependent increase in
             accumulation of gold nanoparticles (AuNp) in the myocardium
             of Tie2Cre; p53(FL/-) mice. In Tie2Cre; p53(FL/-) mice,
             extravasation of AuNp was observed within the irradiated LV,
             whereas in the myocardium of Tie2Cre; p53(FL/+) mice, AuNp
             were restricted to blood vessels. In addition, data from
             DE-microCT and microSPECT showed a linear correlation (R(2)
             = 0.97) between the fraction of the LV that accumulated AuNp
             and the fraction of LV with a perfusion defect. Furthermore,
             4D-microCT scans demonstrated that PHI caused a markedly
             decreased ejection fraction, and higher end-diastolic and
             end-systolic volumes, to develop in Tie2Cre; p53(FL/-) mice,
             which were associated with compensatory cardiac hypertrophy
             of the heart that was not irradiated. CONCLUSIONS: Our
             results show that DE-microCT and 4D-microCT with
             nanoparticle-based contrast agents are novel imaging
             approaches complementary to microSPECT for noninvasive
             assessment of the change in myocardial vascular permeability
             and cardiac function of mice in whom myocardial injury
             develops after PHI.},
   Doi = {10.1016/j.ijrobp.2013.11.238},
   Key = {fds268719}
}

@article{fds132756,
   Author = {HH Qiu and GP Cofer and LW Hedlund and GA Johnson},
   Title = {Automated feedback control of body temperature for small
             animal studies with MR microscopy.},
   Journal = {IEEE transactions on bio-medical engineering, UNITED
             STATES},
   Volume = {44},
   Number = {11},
   Pages = {1107-13},
   Year = {1997},
   Month = {November},
   ISSN = {0018-9294},
   Keywords = {Animals • Body Temperature • Equipment Design
             • Feedback • Ferrets • Guinea Pigs •
             Magnetic Resonance Imaging • Mice • Microscopy
             • Models, Biological • Monitoring, Physiologic
             • Rats • Respiration, Artificial • Signal
             Processing, Computer-Assisted* • Thermometers* •
             instrumentation • methods • physiology*},
   Abstract = {A temperature control system consisting of a thermistor,
             signal processor, and computer algorithm was developed for
             magnetic resonance (MR) microscopy of small live animals.
             With control of body temperature within +/- 0.2 degree C of
             the set point, heart rate is stabilized and, in turn,
             repetition time (TR) during cardiac-gated studies is less
             variable. Thus, image quality and resolution are
             improved.},
   Key = {fds132756}
}

@booklet{Qiu97,
   Author = {Qiu, HH and Cofer, GP and Hedlund, LW and Johnson,
             GA},
   Title = {Automated feedback control of body temperature for small
             animal studies with MR microscopy.},
   Journal = {IEEE Trans Biomed Eng},
   Volume = {44},
   Number = {11},
   Pages = {1107-1113},
   Year = {1997},
   Month = {November},
   ISSN = {0018-9294},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/9353990},
   Abstract = {A temperature control system consisting of a thermistor,
             signal processor, and computer algorithm was developed for
             magnetic resonance (MR) microscopy of small live animals.
             With control of body temperature within +/- 0.2 degree C of
             the set point, heart rate is stabilized and, in turn,
             repetition time (TR) during cardiac-gated studies is less
             variable. Thus, image quality and resolution are
             improved.},
   Doi = {10.1109/10.641338},
   Key = {Qiu97}
}

@booklet{Sherrier85a,
   Author = {SHERRIER, RH and SUDDARTH, SA and JOHNSON, GA and RAVIN,
             CE},
   Title = {AUTOMATED OBSERVER STUDIES ON A DIGITAL CHEST
             SYSTEM},
   Journal = {INVESTIGATIVE RADIOLOGY},
   Volume = {20},
   Number = {6},
   Pages = {S18-S18},
   Publisher = {LIPPINCOTT-RAVEN PUBL},
   Year = {1985},
   Month = {January},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1985ARG0500090&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Sherrier85a}
}

@article{fds268883,
   Author = {Ali, AA and Dale, AM and Badea, A and Johnson, GA},
   Title = {Automated segmentation of neuroanatomical structures in
             multispectral MR microscopy of the mouse
             brain.},
   Journal = {Neuroimage},
   Volume = {27},
   Number = {2},
   Pages = {425-435},
   Year = {2005},
   Month = {August},
   ISSN = {1053-8119},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/15908233},
   Keywords = {Algorithms • Animals • Anisotropy • Bayes
             Theorem • Brain • Image Processing,
             Computer-Assisted • Magnetic Resonance Imaging •
             Male • Markov Chains • Mice • Mice, Inbred
             C57BL • Models, Statistical • Reproducibility of
             Results • anatomy & histology* • methods* •
             physiology* • statistics & numerical
             data*},
   Abstract = {We present the automated segmentation of magnetic resonance
             microscopy (MRM) images of the C57BL/6J mouse brain into 21
             neuroanatomical structures, including the ventricular
             system, corpus callosum, hippocampus, caudate putamen,
             inferior colliculus, internal capsule, globus pallidus, and
             substantia nigra. The segmentation algorithm operates on
             multispectral, three-dimensional (3D) MR data acquired at
             90-microm isotropic resolution. Probabilistic information
             used in the segmentation is extracted from training datasets
             of T2-weighted, proton density-weighted, and
             diffusion-weighted acquisitions. Spatial information is
             employed in the form of prior probabilities of occurrence of
             a structure at a location (location priors) and the pairwise
             probabilities between structures (contextual priors).
             Validation using standard morphometry indices shows good
             consistency between automatically segmented and manually
             traced data. Results achieved in the mouse brain are
             comparable with those achieved in human brain studies using
             similar techniques. The segmentation algorithm shows
             excellent potential for routine morphological phenotyping of
             mouse models.},
   Doi = {10.1016/j.neuroimage.2005.04.017},
   Key = {fds268883}
}

@article{fds268864,
   Author = {Sharief, AA and Badea, A and Dale, AM and Johnson,
             GA},
   Title = {Automated segmentation of the actively stained mouse brain
             using multi-spectral MR microscopy.},
   Journal = {Neuroimage},
   Volume = {39},
   Number = {1},
   Pages = {136-145},
   Year = {2008},
   Month = {January},
   ISSN = {1053-8119},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/17933556},
   Keywords = {Algorithms • Animals • Artificial Intelligence*
             • Brain • Image Enhancement • Image
             Interpretation, Computer-Assisted • Magnetic Resonance
             Imaging • Male • Mice • Mice, Inbred C57BL
             • Microscopy • Pattern Recognition, Automated
             • Reproducibility of Results • Sensitivity and
             Specificity • Staining and Labeling • Subtraction
             Technique • cytology* • methods •
             methods*},
   Abstract = {Magnetic resonance microscopy (MRM) has created new
             approaches for high-throughput morphological phenotyping of
             mouse models of diseases. Transgenic and knockout mice serve
             as a test bed for validating hypotheses that link genotype
             to the phenotype of diseases, as well as developing and
             tracking treatments. We describe here a Markov random fields
             based segmentation of the actively stained mouse brain, as a
             prerequisite for morphological phenotyping. Active staining
             achieves higher signal to noise ratio (SNR) thereby enabling
             higher resolution imaging per unit time than obtained in
             previous formalin-fixed mouse brain studies. The
             segmentation algorithm was trained on isotropic 43-mum T1-
             and T2-weighted MRM images. The mouse brain was segmented
             into 33 structures, including the hippocampus, amygdala,
             hypothalamus, thalamus, as well as fiber tracts and
             ventricles. Probabilistic information used in the
             segmentation consisted of (a) intensity distributions in the
             T1- and T2-weighted data, (b) location, and (c) contextual
             priors for incorporating spatial information. Validation
             using standard morphometric indices showed excellent
             consistency between automatically and manually segmented
             data. The algorithm has been tested on the widely used
             C57BL/6J strain, as well as on a selection of six
             recombinant inbred BXD strains, chosen especially for their
             largely variant hippocampus.},
   Doi = {10.1016/j.neuroimage.2007.08.028},
   Key = {fds268864}
}

@article{fds174293,
   Author = {GA Johnson and TR Hansen and KJ Austin and EA Van Kirk and WJ
             Murdoch},
   Title = {Baculovirus-insect cell production of bioactive
             choriogonadotropin-immunoglobulin G heavy-chain fusion
             proteins in sheep.},
   Journal = {Biology of reproduction},
   Volume = {52},
   Number = {1},
   Pages = {68-73},
   Year = {1995},
   Month = {January},
   ISSN = {0006-3363},
   Keywords = {Animals • Base Sequence • Cell Line •
             Chorionic Gonadotropin • DNA Primers • DNA,
             Complementary • Immunoglobulin G • Immunoglobulin
             Heavy Chains • Male • Mice • Molecular
             Sequence Data • Nucleopolyhedrovirus • Recombinant
             Fusion Proteins • Sheep • Spodoptera • Testis
             • Testosterone • Tumor Cells, Cultured •
             biosynthesis • biosynthesis* • blood • drug
             effects • genetics • pathology •
             pharmacology},
   Abstract = {A hybrid cDNA encoding a fusion protein between the beta
             subunit of hCG (beta hCG) and constant domains of a mouse
             IgG heavy chain (CH1-3) was inserted into a baculovirus
             expression vector. Insect cells transfected with foreign DNA
             synthesized multimeric forms of fusion protein that
             inhibited hCG-induced steroid hormone secretion by mouse
             Leydig tumor cells. Leydig cells were lysed by beta
             hCG-CH1-3 in the presence of complement. Intravenous
             injection of beta hCG-CH1-3 in rams was associated with
             testicular mononuclear leukocyte infiltration, interstitial
             tissue damage, and a transient depression in circulatory
             testosterone (levels returned to normal within 2 wk). It
             appears that targeted cell-killing can be mediated by
             recombinant proteins composed of the receptor-binding moiety
             of hormones and truncated effector (Fc) regions of lethal
             antibodies.},
   Language = {eng},
   Key = {fds174293}
}

@booklet{Johnson95c,
   Author = {G. A. Johnson and T. R. Hansen and K. J. Austin and E. A.
             Vankirk and W. J. Murdoch},
   Title = {Baculovirus-insect cell production of bioactive
             choriogonadotropin-immunoglobulin-g heavy-chain fusion
             proteins in sheep},
   Journal = {Biology Of Reproduction},
   Volume = {52},
   Number = {1},
   Pages = {68 -- 73},
   Year = {1995},
   Month = {January},
   Key = {Johnson95c}
}

@article{fds292756,
   Author = {Rajagopal, S and Kovacs, J and Badea, C and Johnson, GA and Rockman, HA and Piantadosi, CA and Lefkowitz, RJ},
   Title = {BETA-ARRESTINS REGULATE SIGNALING BY BONE MORPHOGENETIC
             PROTEIN TYPE II RECEPTOR IN PULMONARY ARTERIAL
             HYPERTENSION},
   Journal = {Journal of the American College of Cardiology},
   Volume = {57},
   Number = {14},
   Pages = {E2046-E2046},
   Publisher = {Elsevier BV},
   Year = {2011},
   Month = {April},
   ISSN = {0735-1097},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000291695102051&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Doi = {10.1016/s0735-1097(11)62046-9},
   Key = {fds292756}
}

@article{fds174135,
   Author = {BM Markaverich and RR Roberts and MA Alejandro and GA Johnson and BS
             Middleditch, JH Clark},
   Title = {Bioflavonoid interaction with rat uterine type II binding
             sites and cell growth inhibition.},
   Journal = {Journal of steroid biochemistry},
   Volume = {30},
   Number = {1-6},
   Pages = {71-8},
   Year = {1988},
   ISSN = {0022-4731},
   Keywords = {Animals • Binding, Competitive • Breast Neoplasms
             • Cell Division • Cell Line • Cell Nucleus
             • Cytosol • Female • Flavonoids • Humans
             • Kinetics • Rats • Receptors, Estradiol
             • Receptors, Estrogen • Uterus • cytology
             • drug effects • metabolism • metabolism*
             • pharmacology*},
   Abstract = {Competition analysis with a number of known bioflavonoids
             demonstrated that these compounds (luteolin, quercetin,
             pelargonin) compete for [3H]estradiol binding to cytosol and
             nuclear type II sites in rat uterine preparations. The
             inhibition of [3H]estradiol binding to type II sites was
             specific and these bioflavonoids did not interact with the
             rat uterine estrogen receptor. Since estradiol stimulation
             of nuclear type II sites in the rat uterus is highly
             correlated with cellular hypertrophy and hyperplasia, we
             assessed the effects of these compounds on the growth of
             MCF-7 human breast cancer cells in culture and on estradiol
             stimulation of uterine growth in the immature rat. The data
             demonstrated that addition of quercetin (5-10 micrograms/ml)
             to MCF-7 cell cultures resulted in a dose-dependent
             inhibition of cell growth (DNA/flask). This effect was
             reversible by removal of quercetin from the culture medium,
             or by the addition of 10 nM estradiol-17 beta to these cell
             cultures containing this bioflavonoid. Since estradiol-17
             beta (10 nM) stimulated nuclear type II sites and
             proliferation of MCF-7 cells, we believe bioflavonoid
             inhibition of MCF-7 cell growth may be mediated through an
             interaction with nuclear type II sites. This hypothesis was
             confirmed by in vivo studies which demonstrated that
             injection of luteolin or quercetin blocked estradiol
             stimulation of nuclear type II sites in the immature rat
             uterus and this correlated with an inhibition of uterine
             growth (wet and dry weight). These studies suggest
             bioflavonoids, through an interaction with type II sites,
             may be involved in cell growth regulation.},
   Language = {eng},
   Key = {fds174135}
}

@booklet{Markaverich88a,
   Author = {B. M. Markaverich and R. R. Roberts and M. A. Alejandro and G. A. Johnson and B. S. Middleditch and J. H.
             Clark},
   Title = {Bioflavonoid interaction with rat uterine type-ii
             binding-sites and cell-growth inhibition},
   Journal = {Journal Of Steroid Biochemistry And Molecular
             Biology},
   Volume = {30},
   Number = {1-6},
   Pages = {71 -- 78},
   Year = {1988},
   Key = {Markaverich88a}
}

@booklet{Spencer03,
   Author = {T. E. Spencer and R. C. Burghardt and G. A. Johnson and F.
             W. Bazer},
   Title = {Biology of progesterone and placental hormone actions on the
             uterus.},
   Journal = {Biology Of Reproduction},
   Volume = {68},
   Pages = {96 -- 97},
   Year = {2003},
   Key = {Spencer03}
}

@booklet{Teixeira97,
   Author = {M. G. Teixeira and K. J. Austin and D. J. Perry and V. D.
             Dooley and G. A. Johnson and B. R. Francis and T. R.
             Hansen},
   Title = {Bovine granulocyte chemotactic protein-2 is secreted by the
             endometrium in response to interferon-tau
             (IFN-tau)},
   Journal = {Endocrine},
   Volume = {6},
   Number = {1},
   Pages = {31 -- 37},
   Year = {1997},
   Month = {February},
   Key = {Teixeira97}
}

@article{fds174211,
   Author = {MG Teixeira and KJ Austin and DJ Perry and VD Dooley and GA Johnson and BR
             Francis, TR Hansen},
   Title = {Bovine granulocyte chemotactic protein-2 is secreted by the
             endometrium in response to interferon-tau
             (IFN-tau).},
   Journal = {Endocrine},
   Volume = {6},
   Number = {1},
   Pages = {31-7},
   Year = {1997},
   Month = {February},
   ISSN = {1355-008X},
   Keywords = {Amino Acid Sequence • Animals • Blotting, Western
             • Cattle • Chemokine CXCL6 • Chemokines
             • Chemokines, CXC* • Chromatography, Ion Exchange
             • Electrophoresis, Polyacrylamide Gel •
             Endometrium • Female • Interferon Type I •
             Molecular Sequence Data • Pregnancy Proteins •
             Sheep • immunology • metabolism*},
   Abstract = {Interferon-tau (IFN-tau) is secreted by the bovine conceptus
             and may regulate synthesis of uterine endometrial cytokines
             to provide an environment that is conductive to embryo
             development and implantation. Interferon-tau stimulates
             secretion of an 8-kDa uterine protein (P8) in the cow. P8
             was purified, digested to yield internal peptides, and
             partially sequenced to determine identity. Two internal
             peptides had 100% (13-mer) and 92% (12-mer) amino acid
             sequence identity with bovine granulocyte chemotactic
             protein-2 (bGCP-2). Bovine GCP-2 is an alpha-chemokine that
             acts primarily as a potent chemoattractant for granulocyte
             cells of the immune system. A peptide was synthesized based
             on a region of bGCP-2 that overlapped with a P8 peptide
             amino acid sequence, coupled to keyhole limpet hemocyanin,
             and used to generate high titer polyclonal antiserum in
             sheep. Western blots revealed that bGCP-2 was not released
             by endometrium from day 14 nonpregnant cows, but was
             released in response to 25 nM IFN-tau (p<0.05). Uterine
             GCP-2 exhibited high affinity to heparin agarose, a
             characteristic shared by all alpha chemokines. This is the
             first report describing presence of GCP-2 in the uterine
             endometrium and regulation by IFN-tau. The regulation of
             bGCP-2 by IFN-tau may have important implications for
             cytokine networking in the uterus during pregnancy. Also,
             the regulation of inflammation and angiogenesis by bGCP-2
             working together with other cytokines may be integral to
             establishing early pregnancy and implantation in the
             cow.},
   Language = {eng},
   Key = {fds174211}
}

@article{fds204273,
   Author = {M Glaucia Teixeira and KJ Austin and DJ Perry and VD Dooley and GA
             Johnson, BR Francis and TR Hansen},
   Title = {Bovine granulocyte chemotactic protein-2 is secreted by the
             endometrium in response to interferon-tau
             (IFN-τ).},
   Journal = {Endocrine},
   Volume = {6},
   Number = {1},
   Pages = {31-7},
   Year = {1997},
   Month = {February},
   ISSN = {1355-008X},
   url = {http://dx.doi.org/10.1007/BF02738799},
   Abstract = {Interferon-tau (IFN-τ) is secreted by the bovine conceptus
             and may regulate synthesis of uterine endometrial cytokines
             to provide an environment that is conducive to embryo
             development and implantation. Interferon-τ stimulates
             secretion of an 8-kDa uterine protein (P8) in the cow. P8
             was purified, digested to yield internal peptides, and
             partially sequenced to determine identity. Two internal
             peptides had 100% (13-mer) and 92% (12-mer) amino acid
             sequence identity with bovine granulocyte chemotactic
             protein-2 (bGCP-2). Bovine GCP-2 is an α-chemokine that
             acts primarily as a potent chemoattractant for granulocyte
             cells of the immune system. A peptide was synthesized based
             on a region of bGCP-2 that overlapped with a P8 peptide
             amino acid sequence, coupled to keyhole limpet hemocyanin,
             and used to generate high titer polyclonal antiserum in
             sheep. Western blots revealed that bGCP-2 was not released
             by endometrium from day 14 nonpregnant cows, but was
             released in response to 25 nM IFN-τ (p<0.05). Uterine GCP-2
             exhibited high affinity to heparin agarose, a characteristic
             shared by all α chemokines. This is the first report
             describing presence of GCP-2 in the uterine endometrium and
             regulation by IFN-τ. The regulation of bGCP-2 by IFN-τ may
             have important implications for cytokine networking in the
             uterus during pregnancy. Also, the regulation of
             inflammation and angiogenesis by bGCP-2 working together
             with other cytokines may be integral to establishing early
             pregnancy and implantation in the cow.},
   Language = {eng},
   Doi = {10.1007/BF02738799},
   Key = {fds204273}
}

@booklet{Binelli01,
   Author = {M. Binelli and P. Subramaniam and T. Diaz and G. A. Johnson and T. R. Hansen and L. Badinga and W. W.
             Thatcher},
   Title = {Bovine interferon-tau stimulates the Janus kinase-signal
             transducer and activator of transcription pathway in bovine
             endometrial epithelial cells},
   Journal = {Biology Of Reproduction},
   Volume = {64},
   Number = {2},
   Pages = {654 -- 665},
   Year = {2001},
   Month = {February},
   Key = {Binelli01}
}

@article{fds174175,
   Author = {M Binelli and P Subramaniam and T Diaz and GA Johnson and TR Hansen and L
             Badinga, WW Thatcher},
   Title = {Bovine interferon-tau stimulates the Janus kinase-signal
             transducer and activator of transcription pathway in bovine
             endometrial epithelial cells.},
   Journal = {Biology of reproduction},
   Volume = {64},
   Number = {2},
   Pages = {654-65},
   Year = {2001},
   Month = {February},
   ISSN = {0006-3363},
   Keywords = {Animals • Cattle • DNA-Binding Proteins •
             Dimerization • Electrophoresis • Endometrium
             • Epithelial Cells • Female • Immunoblotting
             • Immunohistochemistry • Interferon Type I •
             Janus Kinase 1 • Nuclear Proteins • Phenotype
             • Phosphorylation • Precipitin Tests •
             Pregnancy Proteins • Protein-Tyrosine Kinases •
             STAT1 Transcription Factor • Signal Transduction •
             Time Factors • Trans-Activators • cytology •
             drug effects • drug effects* • enzymology •
             genetics* • metabolism • metabolism* •
             pharmacology*},
   Abstract = {Trophoblastic bovine interferon-tau (bIFN-tau) suppresses
             luteolytic pulses of endometrial prostaglandin F(2alpha)
             (PGF(2alpha)) at the time of maternal recognition of
             pregnancy. This results in maintenance of the corpus luteum
             in cattle. The hypothesis that effects of bIFN-tau in the
             endometrium were through activation of the Janus kinase
             (JAK)-signal transducer and activator of transcription
             (STAT) pathway of signal transduction was tested. Whole
             cell, cytosolic, and nuclear extracts from bovine
             endometrial cells treated with bIFN-tau were analyzed by
             immunoprecipitation, immunoblotting, and electrophoretic
             mobility shift assays in a series of dose- and
             time-dependency experiments. Bovine IFN-tau stimulated
             tyrosine phosphorylation, homo- and heterodimer formation,
             nuclear translocation, and DNA binding of STAT proteins 1,
             2, and 3. Moreover, bIFN-tau induced synthesis of
             interferon-regulatory factor. In conclusion, bIFN-tau
             stimulates the JAK-STAT pathway in the bovine endometrium.
             It is proposed that activation of the JAK-STAT pathway is
             involved in regulating the antiluteolytic effects of
             bIFN-tau.},
   Language = {eng},
   Key = {fds174175}
}

@article{fds268766,
   Author = {Bug, W and Wong, WW and Gustafson, C and Johnson, GA and Martone, ME and Price, DL and Rosen, GD and Williams, RW and Zaslavsky, I and Nissanov,
             J},
   Title = {Brain atlasing tool interoperation: NeuroTerrain-Smart Atlas
             synergistic visualization and analysis environment},
   Journal = {Proceedings of the 3rd International IEEE EMBS Conference on
             Neural Engineering},
   Pages = {280-283},
   Publisher = {IEEE},
   Year = {2007},
   Month = {September},
   ISBN = {9781424407927},
   url = {http://dx.doi.org/10.1109/CNE.2007.369665},
   Abstract = {Many research efforts using anatomical image analysis have
             as their goal to identify biologically relevant objects
             present within the image data, to provide a means to
             quantitatively analyze these objects, to compare the
             distribution of those objects to other features, and finally
             to properly annotate the objects so as to be able share this
             analysis in an integrated informatics framework. The
             neuroinformatics tools designed to achieve these ends have
             been developed in a fragmented manner with each resource
             developing access to unique data sets and analytical
             capabilities, Their integration would enrich the
             neuroinformatic network enabling queries and analysis across
             a number of resources. A central objective of the Biomedical
             Informatics Research Network (BIRN) is to achieve this
             integration and we present here a demonstration of how two
             such tools - the NeuroTerrain Atlas/NetOStat client and the
             SMART Atlas - can expose their functionality via a re-usable
             interface, so as to promote interoperation of tools and
             data. © 2007 IEEE.},
   Doi = {10.1109/CNE.2007.369665},
   Key = {fds268766}
}

@article{fds357209,
   Author = {Blocker, SJ and Mowery, YM and Holbrook, MD and Qi, Y and Kirsch, DG and Johnson, GA and Badea, CT},
   Title = {Bridging the translational gap: Implementation of multimodal
             small animal imaging strategies for tumor burden assessment
             in a co-clinical trial.},
   Journal = {PLoS One},
   Volume = {14},
   Number = {4},
   Pages = {e0207555},
   Year = {2019},
   url = {http://dx.doi.org/10.1371/journal.pone.0207555},
   Abstract = {In designing co-clinical cancer studies, preclinical imaging
             brings unique challenges that emphasize the gap between man
             and mouse. Our group is developing quantitative imaging
             methods for the preclinical arm of a co-clinical trial
             studying immunotherapy and radiotherapy in a soft tissue
             sarcoma model. In line with treatment for patients enrolled
             in the clinical trial SU2C-SARC032, primary mouse sarcomas
             are imaged with multi-contrast micro-MRI (T1 weighted, T2
             weighted, and T1 with contrast) before and after immune
             checkpoint inhibition and pre-operative radiation therapy.
             Similar to the patients, after surgery the mice will be
             screened for lung metastases with micro-CT using respiratory
             gating. A systems evaluation was undertaken to establish a
             quantitative baseline for both the MR and micro-CT systems
             against which others systems might be compared. We have
             constructed imaging protocols which provide
             clinically-relevant resolution and contrast in a genetically
             engineered mouse model of sarcoma. We have employed tools in
             3D Slicer for semi-automated segmentation of both MR and
             micro-CT images to measure tumor volumes efficiently and
             reliably in a large number of animals. Assessment of tumor
             burden in the resulting images was precise, repeatable, and
             reproducible. Furthermore, we have implemented a publicly
             accessible platform for sharing imaging data collected
             during the study, as well as protocols, supporting
             information, and data analyses. In doing so, we aim to
             improve the clinical relevance of small animal imaging and
             begin establishing standards for preclinical imaging of
             tumors from the perspective of a co-clinical
             trial.},
   Doi = {10.1371/journal.pone.0207555},
   Key = {fds357209}
}

@article{fds132744,
   Author = {G.A. Johnson},
   Title = {C. Zimmer,  S.C.J. Wright, R.T. Engelhardt, G.A. Johnson,
             X.O. Breakefield,  R. Weissleder.  Tumor cell endocytosi
             (TCE) imaging facilitates delineation  of the glioma-brain
             interface. (1996).},
   Year = {1996},
   Key = {fds132744}
}

@booklet{Johnson03a,
   Author = {G. A. Johnson and M. M. Joyce and S. Lewis and J. F.
             Gonzalez and R. C. Burghardt and S. Woldesenbet and G. R.
             Newton},
   Title = {Caprine uterine and placental osteopontin (OPN) expression
             is distinct among epitheliochorial implanting
             species.},
   Journal = {Biology Of Reproduction},
   Volume = {68},
   Pages = {205 -- 206},
   Year = {2003},
   Key = {Johnson03a}
}

@article{fds174218,
   Author = {MM Joyce and JF González and S Lewis and S Woldesenbet and RC
             Burghardt, GR Newton and GA Johnson},
   Title = {Caprine uterine and placental osteopontin expression is
             distinct among epitheliochorial implanting
             species.},
   Journal = {Placenta},
   Volume = {26},
   Number = {2-3},
   Pages = {160-70},
   Year = {2005},
   Month = {July},
   ISSN = {0143-4004},
   url = {http://dx.doi.org/10.1016/j.placenta.2004.05.009},
   Keywords = {Animals • Epithelial Cells • Female •
             Gestational Age • Goats* • Molecular Probe
             Techniques • Nucleic Acid Hybridization •
             Osteopontin • Placenta • Pregnancy •
             Pregnancy, Animal • RNA, Messenger • Sheep •
             Sialoglycoproteins • Species Specificity • Swine
             • Uterus • genetics • metabolism •
             metabolism* • methods},
   Abstract = {Osteopontin (OPN) is the most highly up-regulated
             extracellular matrix/adhesion molecule in the uterus of
             humans and domestic animals as it becomes receptive to
             implantation. Studies in sheep and pigs have shown that OPN
             is a component of ovine and porcine histotroph characterized
             by a complex temporal and spatial pattern of uterine and
             conceptus expression involving immune, epithelial, and
             stromal cells. It is proposed that these expression events
             are orchestrated to contribute to conceptus attachment and
             placentation. However, differences in OPN expression between
             sheep and pigs have been detected that relate to differences
             in placentation. Therefore, this study examined OPN
             expression in the caprine uterus and conceptus to gain
             insight into mechanisms underlying OPN function(s) during
             pregnancy through comparative analysis of differences in
             placentation between pigs, sheep, and goats. Goats were
             hysterectomized (n = 5/day) on Days 5, 11, 13, 15, 17 or 19
             of the estrous cycle, and Days 5, 11, 13, 15, 17, 19 or 25
             of pregnancy. Slot-blot hybridization showed increases in
             endometrial OPN mRNA beginning on Day 17 of the estrous
             cycle and Day 19 of pregnancy. In situ hybridization
             localized OPN mRNA to endometrial glandular epithelium (GE),
             Day 25 myometrium, and cells scattered within the placenta
             hypothesized to be immune. Immunofluorescence microscopy
             detected OPN protein on the apical surface of endometrial
             lumenal epithelium (LE), in GE, and on conceptus (Tr).
             Western blot analysis detected primarily the native 70-kDa
             OPN protein in endometrial extracts from the estrous cycle
             and pregnancy, as well as in uterine flushings from pregnant
             goats. Co-induction of OPN and alpha-smooth muscle actin,
             but not desmin proteins, was observed in uterine stroma by
             Day 25 of pregnancy. OPN in cyclic GE, Day 25 myometrium,
             and desmin-negative endometrial stroma is unique and
             reflects subtle differences among superficial implanting
             species that correlate with the depth of Tr
             invasion.},
   Language = {eng},
   Doi = {10.1016/j.placenta.2004.05.009},
   Key = {fds174218}
}

@article{fds174300,
   Author = {TL Rutledge and MA Gold and DS McMeekin and WK Huh and MA Powell and SN
             Lewin, DG Mutch and GA Johnson and JL Walker and RS
             Mannel},
   Title = {Carcinosarcoma of the ovary-a case series.},
   Journal = {Gynecologic oncology},
   Volume = {100},
   Number = {1},
   Pages = {128-32},
   Year = {2006},
   Month = {January},
   ISSN = {0090-8258},
   url = {http://dx.doi.org/10.1016/j.ygyno.2005.07.119},
   Keywords = {Adult • Aged • Aged, 80 and over •
             Antineoplastic Combined Chemotherapy Protocols •
             Carboplatin • Carcinosarcoma • Chemotherapy,
             Adjuvant • Cisplatin • Doxorubicin • Female
             • Follow-Up Studies • Humans • Ifosfamide
             • Middle Aged • Ovarian Neoplasms •
             Paclitaxel • Proportional Hazards Models •
             Retrospective Studies • Treatment Outcome •
             administration & dosage • drug therapy* •
             pathology • surgery* • therapeutic
             use*},
   Abstract = {OBJECTIVE: To evaluate our experience with ovarian
             carcinosarcoma and identify prognostic factors. METHODS:
             Thirty-one cases of ovarian carcinosarcoma were identified
             over a 6-year time period through tumor registry and
             pathology records. Fisher exact test and log rank using
             Kaplan-Meier method (P < 0.05) were used to compare
             variables with outcome. RESULTS: All 31 patients underwent
             initial surgical treatment with an appropriate staging
             procedure. Stage distribution: 1 stage I, 6 stage II, 23
             stage III, and 1 stage IV. The median follow-up was 28
             months. The median survival for the entire group was 21
             months. Early vs. advanced stage significantly influenced
             progression-free interval, P = 0.05. Nineteen patients were
             found to have stage IIIC disease and required debulking
             procedures. In patients with stage IIIC disease, presence of
             residual disease was associated with decreased overall
             survival, P = 0.03. 29 patients received adjuvant
             chemotherapy with 11 patients receiving ifosfamide/cisplatin
             and 16 patients receiving carboplatin/taxol.
             Progression-free interval was improved with the use of
             ifosfamide/cisplatin vs. carboplatin/taxol. The median PFI
             was 12 months in the carbo/taxol group and has not been
             reached in the ifos/cisplatin group (P = 0.005). The overall
             survival was also significantly improved with the use of
             ifosfamide/cisplatin, P = 0.03. In advanced stage patients,
             overall survival was not significantly influenced by type of
             adjuvant chemotherapy administered, P = 0.13. CONCLUSIONS:
             Ovarian carcinosarcoma has a poor overall prognosis with
             median survival rates reported in the literature ranging
             from 7-10 months. Our series, although limited by a small
             number of patients, exhibits a more encouraging median
             survival of 21 months for the overall group. Aggressive
             debulking to eliminate residual disease and the use of
             ifosfamide/cisplatin chemotherapy seem to be factors in this
             improved outcome.},
   Language = {eng},
   Doi = {10.1016/j.ygyno.2005.07.119},
   Key = {fds174300}
}

@article{fds268856,
   Author = {Badea, CT and Hedlund, LW and Mackel, JFB and Mao, L and Rockman, HA and Johnson, GA},
   Title = {Cardiac micro-computed tomography for morphological and
             functional phenotyping of muscle LIM protein null
             mice.},
   Journal = {Mol Imaging},
   Volume = {6},
   Number = {4},
   Pages = {261-268},
   Year = {2007},
   ISSN = {1535-3508},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/17711781},
   Keywords = {Animals • Calibration • Diastole •
             Echocardiography • Heart Ventricles • Mice •
             Mice, Inbred C57BL • Mice, Knockout • Muscle
             Proteins • Myocardium • Phenotype •
             Tomography, X-Ray Computed • deficiency* •
             metabolism* • methods*},
   Abstract = {The purpose of this study was to investigate the use of
             micro-computed tomography (micro-CT) for morphological and
             functional phenotyping of muscle LIM protein (MLP) null mice
             and to compare micro-CT with M-mode echocardiography. MLP
             null mice and controls were imaged using both micro-CT and
             M-mode echocardiography. For micro-CT, we used a
             custom-built scanner. Following a single intravenous
             injection of a blood pool contrast agent (Fenestra VC, ART
             Advanced Research Technologies, Saint-Laurent, QC) and using
             a cardiorespiratory gating, we acquired eight phases of the
             cardiac cycle (every 15 ms) and reconstructed
             three-dimensional data sets with 94-micron isotropic
             resolution. Wall thickness and volumetric measurements of
             the left ventricle were performed, and cardiac function was
             estimated. Micro-CT and M-mode echocardiography showed both
             morphological and functional aspects that separate MLP null
             mice from controls. End-diastolic and -systolic volumes were
             increased significantly three- and fivefold, respectively,
             in the MLP null mice versus controls. Ejection fraction was
             reduced by an average of 32% in MLP null mice. The data
             analysis shows that two imaging modalities provided
             different results partly owing to the difference in
             anesthesia regimens. Other sources of errors for micro-CT
             are also analyzed. Micro-CT can provide the four-dimensional
             data (three-dimensional isotropic volumes over time)
             required for morphological and functional phenotyping in
             mice.},
   Doi = {10.2310/7290.2007.00022},
   Key = {fds268856}
}

@article{fds268829,
   Author = {Bucholz, E and Ghaghada, K and Qi, Y and Mukundan, S and Rockman, HA and Johnson, GA},
   Title = {Cardiovascular phenotyping of the mouse heart using a 4D
             radial acquisition and liposomal Gd-DTPA-BMA.},
   Journal = {Magn Reson Med},
   Volume = {63},
   Number = {4},
   Pages = {979-987},
   Year = {2010},
   Month = {April},
   ISSN = {1522-2594},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/20373399},
   Keywords = {Algorithms • Analysis of Variance • Animals •
             Cardiovascular Physiological Phenomena* • Contrast
             Media • Gadolinium DTPA • Imaging,
             Three-Dimensional • Liposomes • Magnetic Resonance
             Imaging • Mice • Mice, Inbred C57BL • Mice,
             Inbred DBA • Phenotype • chemistry •
             instrumentation • methods*},
   Abstract = {MR microscopy has enormous potential for small-animal
             cardiac imaging because it is capable of producing
             volumetric images at multiple time points to accurately
             measure cardiac function. MR has not been used as frequently
             as ultrasound to measure cardiac function in the small
             animal because the MR methods required relatively long scan
             times, limiting throughput. Here, we demonstrate
             four-dimensional radial acquisition in conjunction with a
             liposomal blood pool agent to explore functional differences
             in three populations of mice: six C57BL/6J mice, six DBA/2J
             mice, and six DBA/2J CSQ+ mice, all with the same
             gestational age and approximately the same weight.
             Cardiovascular function was determined by measuring both
             left ventricular and right ventricular end diastolic volume,
             end systolic volume, stroke volume, and ejection fraction.
             Statistical significance was observed in end diastolic
             volume, end systolic volume, and ejection fraction for left
             ventricular measurements between all three populations of
             mice. No statistically significant difference was observed
             in stroke volume in either the left or right ventricle for
             any of the three populations of mice. This study shows that
             MRI is capable of efficient, high-throughput,
             four-dimensional cardiovascular phenotyping of the
             mouse.},
   Language = {eng},
   Doi = {10.1002/mrm.22259},
   Key = {fds268829}
}

@booklet{Heinz84,
   Author = {HEINZ, ER and HERFKINS, R and JOHNSON, GA and DRAYER,
             BP},
   Title = {CAROTID-ARTERY IMAGING BY A 1.5-T MR SYSTEM},
   Journal = {AMERICAN JOURNAL OF NEURORADIOLOGY},
   Volume = {5},
   Number = {5},
   Pages = {670-670},
   Publisher = {AMER SOC NEURORADIOLOGY},
   Year = {1984},
   Month = {January},
   ISSN = {0195-6108},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1984TG20900067&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Heinz84}
}

@article{fds174172,
   Author = {G Song and DW Bailey and KA Dunlap and RC Burghardt and TE Spencer and FW
             Bazer, GA Johnson},
   Title = {Cathepsin B, cathepsin L, and cystatin C in the porcine
             uterus and placenta: potential roles in endometrial/placental
             remodeling and in fluid-phase transport of proteins secreted
             by uterine epithelia across placental areolae.},
   Journal = {Biology of reproduction},
   Volume = {82},
   Number = {5},
   Pages = {854-64},
   Year = {2010},
   Month = {May},
   ISSN = {1529-7268},
   url = {http://dx.doi.org/10.1095/biolreprod.109.080929},
   Abstract = {Cathepsins (CTSB and CTSL1) and their inhibitor, cystatin C
             (CST3), remodel uterine endometrium and placenta for
             transport of gases, micronutrients, and macromolecules
             essential for development and growth of the conceptus
             (embryo/fetus and placental membranes). We examined the
             temporal/spatial control of expression for CTSB, CTSL1, and
             CST3 mRNAs in endometria and placentae of pigs using three
             developmental models: 1) pigs were hysterectomized during
             the estrous cycle or pregnancy; 2) cyclic pigs were injected
             with estrogen to induce pseudopregnancy and were
             hysterectomized; and 3) pigs were ovariectomized, injected
             with progesterone, and hysterectomized. The abundance of
             CTSB, CTSL1, and CST3 mRNAs increased in endometrial
             epithelia during pregnancy and in response to exogenous
             progesterone but not estrogen. CST3 was also expressed in
             cells scattered within the stratum compactum stroma.
             Progesterone decreased epithelial but increased stromal
             compartment expression of CST3. CTSB increased in all
             chorionic epithelia, but CTSL1 was limited to chorionic
             epithelia that form areolae to absorb secretions from
             uterine glands. Based on the placental and endometrial
             distribution of CTSL1, we examined expression in the
             neonatal enterocytes known to transport immunoglobulins from
             colostrum. CTSL1 was also expressed in enterocytes of
             intestine from neonatal piglets. Therefore, CTSL1 is
             expressed by endometrial epithelia, placental areolae, and
             neonatal intestine, and it may function in the transport of
             macromolecules across these epithelia. Our results support
             the idea that reciprocal interactions between CSTL1, CTSB,
             and CST3 may be required to remodel endometrial and
             placental tissues for close apposition between maternal and
             fetal vasculatures and to facilitate transplacental
             transport of gases, micronutrients (amino acids, glucose),
             and macromolecules (proteins). Cysteine proteases and their
             inhibitors may also specifically modify proteins for
             successful utilization and fluid-phase transport across
             uterine, placental, and neonatal gut epithelia.},
   Language = {eng},
   Doi = {10.1095/biolreprod.109.080929},
   Key = {fds174172}
}

@booklet{Johnson87a,
   Author = {G. A. Johnson},
   Title = {Cbn wheel grinding},
   Journal = {Journal Of Metals},
   Volume = {39},
   Number = {9},
   Pages = {62 -- 63},
   Year = {1987},
   Month = {September},
   Key = {Johnson87a}
}

@booklet{Benveniste99,
   Author = {Benveniste, HD and Kim, KR and Hedlund, LW and Johnson, GA and Friedman,
             AH},
   Title = {Cerebral hemorrhage and edema following brain biopsy in
             rats: Significance of mean arterial blood
             pressure},
   Journal = {ANESTHESIOLOGY},
   Volume = {91},
   Number = {3A},
   Pages = {U371-U371},
   Publisher = {LIPPINCOTT WILLIAMS & WILKINS},
   Year = {1999},
   Month = {September},
   ISSN = {0003-3022},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000082480600839&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Benveniste99}
}

@article{fds174072,
   Author = {JD Tobias and GA Johnson and S Rehman and R Fisher and N
             Caron},
   Title = {Cerebral oxygenation monitoring using near infrared
             spectroscopy during one-lung ventilation in
             adults.},
   Journal = {Journal of minimal access surgery},
   Volume = {4},
   Number = {4},
   Pages = {104-107},
   Year = {2008},
   Month = {October},
   ISSN = {1998-3921},
   Abstract = {BACKGROUND: Changes in oxygenation occur during one-lung
             ventilation (OLV) due to intrapulmonary shunt. Although
             arterial oxygenation is generally adequate, there are no
             studies evaluating the effect of these changes on cerebral
             oxygenation. MATERIALS AND METHODS: Cerebral oxygenation
             (rSO(2)), heart rate (HR), blood pressure (BP), oxygen
             saturation (SaO(2)), and end-tidal carbon dioxide (ETCO(2))
             were prospectively monitored during OLV in adults. Cerebral
             oxygenation was monitored using near infrared spectroscopy.
             No clinical decisions were made based on the rSO2 value. BP
             and HR were the inspired oxygen concentration was adjusted
             as needed to maintain the SaO(2) >/= 95%. RESULTS: The study
             cohort included 40 adult patients. 18,562 rSO(2) values were
             collected during OLV. The rSO(2) was >/= baseline at 3,593
             of the 18,562 data points (19%). The rSO2 was 0-9 </=
             baseline in 7,053 (38%) of the readings, 10-19 </= baseline
             in 4,084 (22%) of the readings, and 20-29 </= baseline in
             3,898 (21%) of the readings. 2,599 (14%) of the rSO(2)
             values were less than 75% of the baseline value. Thirteen
             patients (32.5%) had at least one rSO2 value that was less
             than 75% of the baseline. Eight patients (20%) had rSO(2)
             values less than 75% of baseline for >/= 25% of the duration
             of OLV. These patients were older (63.7 +/- 10.2 vs 54.6 +/-
             9.8 years, P<0.025), weighed more (95.8 +/- 17.4 vs 82.6 +/-
             14.6 kgs, P=0.038), and were more likely to be ASA III vs II
             (7 of 8 versus 25 of 32, relative risk 1.75) than the
             remainder of the cohort. CONCLUSIONS: Significant changes in
             rSO2 occur during OLV for thoracic surgical procedures.
             Future studies are needed to determine the impact of such
             changes on the postoperative course of these
             patients.},
   Language = {ENG},
   Key = {fds174072}
}

@article{fds204262,
   Author = {GA Johnson},
   Title = {Changes imposed on GPs make it harder to respond to
             patients' needs.},
   Journal = {BMJ (Clinical research ed.)},
   Volume = {343},
   Pages = {d7700},
   Year = {2011},
   ISSN = {1468-5833},
   Keywords = {General Practice • Great Britain •
             Physician-Patient Relations* • Quality Assurance,
             Health Care* • State Medicine •
             standards*},
   Language = {eng},
   Key = {fds204262}
}

@article{fds204272,
   Author = {CL Gipson and GA Johnson and R Fisher and A Stewart and G Giles and JO
             Johnson, JD Tobias},
   Title = {Changes in cerebral oximetry during peritoneal insufflation
             for laparoscopic procedures.},
   Journal = {Journal of minimal access surgery},
   Volume = {2},
   Number = {2},
   Pages = {67-72},
   Year = {2006},
   Month = {June},
   ISSN = {0972-9941},
   Abstract = {BACKGROUND: Changes in cardiac output may occur during
             insufflation for laparoscopic procedures. However, there are
             limited data regarding its potential effects on cerebral
             oxygenation. METHODS: Cerebral oxygenation (ScO(2)), end
             tidal CO(2), heart rate, blood pressure and oxygen
             saturation by pulse oximetry were recorded every 5 minutes
             prior to insufflation, during insufflation and after
             desufflation. Minute ventilation was increased to maintain
             normocapnia and the depth of anesthesia was adjusted or
             fluids/phenylephrine administered to maintain the blood
             pressure within 20% of the baseline. RESULTS: The cohort for
             the study included 70 adults for laparoscopic herniorrhaphy,
             gastric bypass or cholecystectomy. A total of 1004 ScO(2)
             values were obtained during laparoscopy. The ScO(2)
             decreased from the baseline in 758 of the 1004 data points.
             The ScO(2) was 0-9 less than the baseline in 47.8% of the
             values, 10-19 less than the baseline in 24.9% of the values
             and 20-29 less than the baseline in 26 values (2.6%).
             Eighty-two (8.2%) of the values were less than 80% of the
             baseline value, while 25 values (2.5%) were less than 75% of
             the baseline value. Twelve patients had at least one ScO(2)
             value that was less than 80% of the baseline and 6 had at
             least one ScO(2) value that was less than 75% of the
             baseline. Four patients of the cohort had ScO(2) values less
             than 80% of the baseline for more than 50% of the
             laparoscopic procedure. CONCLUSIONS: Although relatively
             uncommon, significant changes in cerebral oxygenation do
             occur in some patients during insufflation for laparoscopic
             surgery.},
   Language = {eng},
   Key = {fds204272}
}

@article{fds357203,
   Author = {Wang, N and Mirando, AJ and Cofer, G and Qi, Y and Hilton, MJ and Johnson,
             GA},
   Title = {Characterization complex collagen fiber architecture in knee
             joint using high-resolution diffusion imaging.},
   Journal = {Magn Reson Med},
   Volume = {84},
   Number = {2},
   Pages = {908-919},
   Year = {2020},
   Month = {August},
   url = {http://dx.doi.org/10.1002/mrm.28181},
   Abstract = {PURPOSE: To evaluate the complex fiber orientations and 3D
             collagen fiber network of knee joint connective tissues,
             including ligaments, muscle, articular cartilage, and
             meniscus using high spatial and angular resolution diffusion
             imaging. METHODS: Two rat knee joints were scanned using a
             modified 3D diffusion-weighted spin echo pulse sequence with
             the isotropic spatial resolution of 45 μm at 9.4T. The b
             values varied from 250 to 1250 s/mm2 with 31 diffusion
             encoding directions for 1 rat knee. The b value was fixed to
             1000 s/mm2 with 147 diffusion encoding directions for the
             second knee. Both the diffusion tensor imaging (DTI) model
             and generalized Q-sampling imaging (GQI) method were used to
             investigate the fiber orientation distributions and
             tractography with the validation of polarized light
             microscopy. RESULTS: To better resolve the crossing fibers,
             the b value should be great than or equal to 1000 s/mm2 .
             The tractography results were comparable between the DTI
             model and GQI method in ligament and muscle. However, the
             tractography exhibited apparent difference between DTI and
             GQI in connective tissues with more complex collagen fibers
             network, such as cartilage and meniscus. In articular
             cartilage, there were numerous crossing fibers found in
             superficial zone and transitional zone. Tractography
             generated with GQI also resulted in more intact tracts in
             articular cartilage than DTI. CONCLUSION: High-resolution
             diffusion imaging with GQI method can trace the complex
             collagen fiber orientations and architectures of the knee
             joint at microscopic resolution.},
   Doi = {10.1002/mrm.28181},
   Key = {fds357203}
}

@article{fds268711,
   Author = {Lipinski, RJ and Holloway, HT and O'Leary-Moore, SK and Ament, JJ and Pecevich, SJ and Cofer, GP and Budin, F and Everson, JL and Johnson, GA and Sulik, KK},
   Title = {Characterization of subtle brain abnormalities in a mouse
             model of Hedgehog pathway antagonist-induced cleft lip and
             palate.},
   Journal = {PLoS One},
   Volume = {9},
   Number = {7},
   Pages = {e102603},
   Year = {2014},
   url = {http://hdl.handle.net/10161/11679 Duke open
             access},
   Abstract = {Subtle behavioral and cognitive deficits have been
             documented in patient cohorts with orofacial clefts (OFCs).
             Recent neuroimaging studies argue that these traits are
             associated with structural brain abnormalities but have been
             limited to adolescent and adult populations where brain
             plasticity during infancy and childhood may be a confounding
             factor. Here, we employed high resolution magnetic resonance
             microscopy to examine primary brain morphology in a mouse
             model of OFCs. Transient in utero exposure to the Hedgehog
             (Hh) signaling pathway antagonist cyclopamine resulted in a
             spectrum of facial dysmorphology, including unilateral and
             bilateral cleft lip and palate, cleft of the secondary
             palate only, and a non-cleft phenotype marked by midfacial
             hypoplasia. Relative to controls, cyclopamine-exposed
             fetuses exhibited volumetric differences in several brain
             regions, including hypoplasia of the pituitary gland and
             olfactory bulbs, hyperplasia of the forebrain septal region,
             and expansion of the third ventricle. However, in affected
             fetuses the corpus callosum was intact and normal division
             of the forebrain was observed. This argues that
             temporally-specific Hh signaling perturbation can result in
             typical appearing OFCs in the absence of
             holoprosencephaly--a condition classically associated with
             Hh pathway inhibition and frequently co-occurring with OFCs.
             Supporting the premise that some forms of OFCs co-occur with
             subtle brain malformations, these results provide a possible
             ontological basis for traits identified in clinical
             populations. They also argue in favor of future
             investigations into genetic and/or environmental modulation
             of the Hh pathway in the etiopathogenesis of orofacial
             clefting.},
   Doi = {10.1371/journal.pone.0102603},
   Key = {fds268711}
}

@booklet{Gerhards97,
   Author = {R. Gerhards and D. Y. Wysepester and D. Mortensen and G. A.
             Johnson},
   Title = {Characterizing spatial stability of weed populations using
             interpolated maps},
   Journal = {Weed Science},
   Volume = {45},
   Number = {1},
   Pages = {108 -- 119},
   Year = {1997},
   Key = {Gerhards97}
}

@article{fds174299,
   Author = {MC DODD and NJ BIGLEY and GA JOHNSON and RH MCCLUER},
   Title = {CHEMICAL ASPECTS ON INHIBITORS OF RH-O(D)
             ANTIBODY.},
   Journal = {Nature},
   Volume = {204},
   Pages = {549-52},
   Year = {1964},
   Month = {November},
   ISSN = {0028-0836},
   Keywords = {ANTIBODY FORMATION* • BRAIN CHEMISTRY* •
             CHEMISTRY* • EXPERIMENTAL LAB STUDY* •
             GANGLIOSIDES* • HEMAGGLUTINATION INHIBITION TESTS*
             • PEPTIDES* • PSEUDOMONAS* • RABBITS* •
             RH FACTORS*},
   Language = {eng},
   Key = {fds174299}
}

@article{fds132789,
   Author = {CH Maynor and HC Charles and RJ Herfkens and SA Suddarth and GA
             Johnson},
   Title = {Chemical shift imaging of atherosclerosis at 7.0
             Tesla.},
   Journal = {Investigative radiology, UNITED STATES},
   Volume = {24},
   Number = {1},
   Pages = {52-60},
   Year = {1989},
   Month = {January},
   ISSN = {0020-9996},
   Keywords = {Adipose Tissue • Aged • Aorta • Aortic
             Diseases • Arteriosclerosis • Cholesterol Esters
             • Female • Humans • Magnetic Resonance
             Spectroscopy • Male • Middle Aged •
             Triglycerides • diagnostic use* • metabolism
             • pathology • pathology*},
   Abstract = {Chemical shift imaging (CSI) was performed on cadaveric
             atherosclerotic fibrous plaques, periaortic adipose tissue,
             and cholesterol standards using a 7.0 Tesla horizontal bore
             prototype imaging spectrometer. Proton spectroscopy of
             intact tissue and deuterated chloroform extracted samples
             was done at the equivalent field strength of 7.0 Tesla on a
             vertical bore spectrometer, including studies of temperature
             dependence and T2 relaxation measurements. Spectra obtained
             using CSI on the imaging magnet were comparable with those
             from the conventional vertical spectrometer. Fibrous plaques
             and adipose tissue had unique spectral features, differing
             in the ratios of their water and various fat components.
             Chloroform extractions revealed a typical cholesteric ester
             spectrum for the fibrous plaque in contrast to the
             triglyceride spectrum of the adipose tissue. These two
             tissues also had different T2 relaxation measurements of
             their major fat resonances, with fibrous plaques having a
             short T2 compared to adipose tissue (15.9 milliseconds vs.
             46.2 milliseconds). Temperature dependence studies showed
             that spectral signal intensity of the fat resonance of the
             fibrous plaque increased while linewidth decreased with
             increasing temperature from 24 degrees C to 37 degrees C.
             Atherosclerotic lesions may be studied at 7.0 Tesla, and NMR
             parameters defined in the present study may be used for
             further studies at other magnetic field strengths.},
   Key = {fds132789}
}

@booklet{Maynor89,
   Author = {Maynor, CH and Charles, HC and Herfkens, RJ and Suddarth, SA and Johnson, GA},
   Title = {Chemical shift imaging of atherosclerosis at 7.0
             Tesla.},
   Journal = {Invest Radiol},
   Volume = {24},
   Number = {1},
   Pages = {52-60},
   Year = {1989},
   Month = {January},
   ISSN = {0020-9996},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/2917823},
   Abstract = {Chemical shift imaging (CSI) was performed on cadaveric
             atherosclerotic fibrous plaques, periaortic adipose tissue,
             and cholesterol standards using a 7.0 Tesla horizontal bore
             prototype imaging spectrometer. Proton spectroscopy of
             intact tissue and deuterated chloroform extracted samples
             was done at the equivalent field strength of 7.0 Tesla on a
             vertical bore spectrometer, including studies of temperature
             dependence and T2 relaxation measurements. Spectra obtained
             using CSI on the imaging magnet were comparable with those
             from the conventional vertical spectrometer. Fibrous plaques
             and adipose tissue had unique spectral features, differing
             in the ratios of their water and various fat components.
             Chloroform extractions revealed a typical cholesteric ester
             spectrum for the fibrous plaque in contrast to the
             triglyceride spectrum of the adipose tissue. These two
             tissues also had different T2 relaxation measurements of
             their major fat resonances, with fibrous plaques having a
             short T2 compared to adipose tissue (15.9 milliseconds vs.
             46.2 milliseconds). Temperature dependence studies showed
             that spectral signal intensity of the fat resonance of the
             fibrous plaque increased while linewidth decreased with
             increasing temperature from 24 degrees C to 37 degrees C.
             Atherosclerotic lesions may be studied at 7.0 Tesla, and NMR
             parameters defined in the present study may be used for
             further studies at other magnetic field strengths.},
   Doi = {10.1097/00004424-198901000-00012},
   Key = {Maynor89}
}

@article{fds132773,
   Author = {GA Johnson and GW Dewald and WR Strand and RK Winkelmann},
   Title = {Chromosome studies in 17 patients with the Sézary
             syndrome.},
   Journal = {Cancer, UNITED STATES},
   Volume = {55},
   Number = {10},
   Pages = {2426-33},
   Year = {1985},
   Month = {May},
   ISSN = {0008-543X},
   Keywords = {Adult • Aged • Chromosome Aberrations •
             Chromosomes • Female • Genetic Markers •
             Humans • Karyotyping • Male • Metaphase
             • Middle Aged • Sezary Syndrome • genetics*
             • mortality • pathology •
             ultrastructure*},
   Abstract = {Chromosome studies were done on phytohemagglutinin-stimulated
             peripheral blood from 17 patients with Sézary syndrome. A
             chromosomally abnormal clone was found in five patients:
             each patient had an abnormal chromosome 6 and four had an
             abnormal chromosome 1. Six patients without abnormal clones
             had more than 20% metaphases with random heteroploidy and
             sporadic structural anomalies. Only normal metaphases were
             seen in four patients, and no metaphases were found in two.
             Four of the five patients with an abnormal clone died, and
             their median survival from chromosome analysis was 6 months;
             only one of these patients died of lymphoma. The six
             patients with increased heteroploidy had long survivals and
             no apparent malignant process. Two of the four patients with
             normal metaphases died of malignant disease: one had
             lymphoma and the other squamous cell carcinoma. A third
             patient with normal chromosomes died of extensive visceral
             cutaneous T-cell lymphoma.},
   Key = {fds132773}
}

@booklet{Johnson85b,
   Author = {G. A. Johnson and G. W. Dewald and W. R. Strand and R. K.
             Winkelmann},
   Title = {Chromosome-studies in 17 patients with the sezary
             syndrome},
   Journal = {Cancer},
   Volume = {55},
   Number = {10},
   Pages = {2426 -- 2433},
   Year = {1985},
   Key = {Johnson85b}
}

@article{fds132907,
   Author = {AC Brau and LW Hedlund and GA Johnson},
   Title = {Cine magnetic resonance microscopy of the rat heart using
             cardiorespiratory-synchronous projection
             reconstruction.},
   Journal = {Journal of magnetic resonance imaging : JMRI, United
             States},
   Volume = {20},
   Number = {1},
   Pages = {31-8},
   Year = {2004},
   Month = {July},
   ISSN = {1053-1807},
   Keywords = {Animals • Artifacts • Female • Image
             Processing, Computer-Assisted* • Magnetic Resonance
             Imaging, Cine* • Microscopy • Myocardial
             Contraction* • Rats • Rats, Sprague-Dawley •
             Respiration* • methods},
   Abstract = {PURPOSE: To tailor a cardiac magnetic resonance (MR)
             microscopy technique for the rat that combines improvements
             in pulse sequence design and physiologic control to acquire
             high-resolution images of cardiac structure and function.
             MATERIALS AND METHODS: Projection reconstruction (PR) was
             compared to conventional Cartesian techniques in
             point-spread function simulations and experimental studies
             to evaluate its artifact sensitivity. Female Sprague-Dawley
             rats were imaged at 2.0 T using PR with direct encoding of
             the free induction decay. Specialized physiologic support
             and monitoring equipment ensured consistency of biological
             motion and permitted synchronization of imaging with the
             cardiac and respiratory cycles. RESULTS: The reduced
             artifact sensitivity of PR offered improved delineation of
             cardiac and pulmonary structures. Ventilatory
             synchronization further increased the signal-to-noise ratio
             by reducing inter-view variability. High-quality short-axis
             and long-axis cine images of the rat heart were acquired
             with 10-msec temporal resolution and microscopic spatial
             resolution down to 175 microm x 175 microm x 1 mm.
             CONCLUSION: Integrating careful biological control with an
             optimized pulse sequence significantly limits both the
             source and impact of image artifacts. This work represents a
             novel integration of techniques designed to support
             measurement of cardiac morphology and function in rodent
             models of cardiovascular disease.},
   Key = {fds132907}
}

@booklet{Brau04,
   Author = {Brau, ACS and Hedlund, LW and Johnson, GA},
   Title = {Cine magnetic resonance microscopy of the rat heart using
             cardiorespiratory-synchronous projection
             reconstruction.},
   Journal = {J Magn Reson Imaging},
   Volume = {20},
   Number = {1},
   Pages = {31-38},
   Year = {2004},
   Month = {July},
   ISSN = {1053-1807},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/15221806},
   Abstract = {PURPOSE: To tailor a cardiac magnetic resonance (MR)
             microscopy technique for the rat that combines improvements
             in pulse sequence design and physiologic control to acquire
             high-resolution images of cardiac structure and function.
             MATERIALS AND METHODS: Projection reconstruction (PR) was
             compared to conventional Cartesian techniques in
             point-spread function simulations and experimental studies
             to evaluate its artifact sensitivity. Female Sprague-Dawley
             rats were imaged at 2.0 T using PR with direct encoding of
             the free induction decay. Specialized physiologic support
             and monitoring equipment ensured consistency of biological
             motion and permitted synchronization of imaging with the
             cardiac and respiratory cycles. RESULTS: The reduced
             artifact sensitivity of PR offered improved delineation of
             cardiac and pulmonary structures. Ventilatory
             synchronization further increased the signal-to-noise ratio
             by reducing inter-view variability. High-quality short-axis
             and long-axis cine images of the rat heart were acquired
             with 10-msec temporal resolution and microscopic spatial
             resolution down to 175 microm x 175 microm x 1 mm.
             CONCLUSION: Integrating careful biological control with an
             optimized pulse sequence significantly limits both the
             source and impact of image artifacts. This work represents a
             novel integration of techniques designed to support
             measurement of cardiac morphology and function in rodent
             models of cardiovascular disease.},
   Doi = {10.1002/jmri.20089},
   Key = {Brau04}
}

@booklet{Fleming01,
   Author = {J. A. G. W. Fleming and Y. Choi and G. A. Johnson and T. E.
             Spencer and F. W. Bazer},
   Title = {Cloning of the ovine estrogen receptor-alpha promoter and
             functional regulation by ovine interferon-tau},
   Journal = {Endocrinology},
   Volume = {142},
   Number = {7},
   Pages = {2879 -- 2887},
   Year = {2001},
   Month = {July},
   Key = {Fleming01}
}

@article{fds174194,
   Author = {JA Fleming and Y Choi and GA Johnson and TE Spencer and FW
             Bazer},
   Title = {Cloning of the ovine estrogen receptor-alpha promoter and
             functional regulation by ovine interferon-tau.},
   Journal = {Endocrinology},
   Volume = {142},
   Number = {7},
   Pages = {2879-87},
   Year = {2001},
   Month = {July},
   ISSN = {0013-7227},
   Keywords = {Animals • Artificial Gene Fusion • Base Sequence
             • Cell Line, Transformed • Cloning, Molecular*
             • DNA-Binding Proteins • Electrophoresis •
             Endometrium • Enhancer Elements, Genetic •
             Epithelial Cells • Estrogen Receptor alpha •
             Female • Gene Deletion • Interferon Regulatory
             Factor-2 • Interferon Type I • Mutation •
             Pregnancy Proteins • Promoter Regions, Genetic •
             Receptors, Estrogen • Recombinant Proteins •
             Repressor Proteins* • Sheep • Thymidine Kinase
             • Transcription Factors* • Transcription, Genetic
             • cytology • drug effects • genetics •
             genetics* • metabolism • metabolism* •
             pharmacology • physiology*},
   Abstract = {Interferon-tau (IFNtau), the ruminant pregnancy recognition
             signal, inhibits transcription of the estrogen receptor
             alpha (ERalpha) gene in the endometrial lumenal epithelium
             of the sheep uterus, thereby abrogating production of
             luteolytic PGF(2alpha) pulses. The effects of IFNtau are
             mediated in part by IFN-stimulated response elements (ISREs)
             and IFN regulatory factor elements (IRFEs). The
             promoter/enhancer region of the ovine ERalpha gene was
             cloned, sequenced, and predicted to contain four IRFEs and
             one ISRE. Electrophoretic mobility shift assays indicated
             that the -2110 IRFE bound only IRF-1, whereas the -1877 IRFE
             and the -1284 ISRE were functional in binding IRF-1 and
             IRF-2. IFNtau inhibited transcriptional activity of the
             2.7-kb ovine ERalpha promoter in transfection assays using
             ovine lumenal epithelium cells. Analyses of sequential
             5'-deletion mutants of the ovine ERalpha promoter indicated
             that the effects of IFNtau may be mediated by IRFEs as well
             as other elements. Overexpression of ovine IRF-2, but not
             IRF-1, inhibited transcriptional activity of several regions
             of the ovine ERalpha promoter containing an IRFE or an ISRE
             as well as some, but not all, regions lacking these
             elements.},
   Language = {eng},
   Key = {fds174194}
}

@article{fds132916,
   Author = {GA Johnson and J Baker},
   Title = {Colonic perforation following mild trauma in a patient with
             Crohn's disease.},
   Journal = {The American journal of emergency medicine, UNITED
             STATES},
   Volume = {8},
   Number = {4},
   Pages = {340-1},
   Year = {1990},
   Month = {July},
   ISSN = {0735-6757},
   Keywords = {Adult • Colon • Crohn Disease • Humans •
             Intestinal Perforation • Male • complications*
             • etiology* • injuries* • pathology •
             surgery},
   Abstract = {A 26-year-old man with a history of Crohn's disease was
             struck in the abdomen by an opponent's shoulder while
             playing basketball. He presented to the emergency department
             3 hours later with the complaint of abdominal pain and was
             admitted to the hospital for observation. Nine hours after
             presentation a computed tomography scan showed he had
             pneumoperitoneum and then underwent laparotomy. A perforated
             segment of sigmoid colon with severe inflammatory disease
             was found and resected. The rest of his small and large
             bowels were otherwise unremarkable. His localized but severe
             inflammatory bowel disease predisposed him to bowel
             perforation with minimal trauma. This is the first report of
             a patient with inflammatory bowel disease and traumatic
             colon perforation; it is also the first report of a patient
             with a bowel perforation with minimal traumatic
             force.},
   Key = {fds132916}
}

@booklet{Johnson90a,
   Author = {G. A. Johnson and J. Baker},
   Title = {Colonic perforation following mild trauma in a patient with
             crohns-disease},
   Journal = {American Journal Of Emergency Medicine},
   Volume = {8},
   Number = {4},
   Pages = {340 -- 341},
   Year = {1990},
   Month = {July},
   Key = {Johnson90a}
}

@booklet{Fischer04,
   Author = {D. W. Fischer and R. G. Harvey and T. T. Bauman and S.
             Phillips and S. E. Hart and G. A. Johnson and J. J. Kells and P. Westra and J. Lindquist},
   Title = {Common lambsquarters (Chenopodium album) interference with
             corn across the northcentral United States},
   Journal = {Weed Science},
   Volume = {52},
   Number = {6},
   Pages = {1034 -- 1038},
   Year = {2004},
   Key = {Fischer04}
}

@article{fds174261,
   Author = {FW Bazer and TE Spencer and GA Johnson and RC Burghardt and G
             Wu},
   Title = {Comparative aspects of implantation.},
   Journal = {Reproduction (Cambridge, England)},
   Volume = {138},
   Number = {2},
   Pages = {195-209},
   Year = {2009},
   Month = {August},
   ISSN = {1741-7899},
   url = {http://dx.doi.org/10.1530/REP-09-0158},
   Keywords = {Animals • Blastocyst • Embryo Implantation •
             Endometrium • Female • Gene Expression Regulation,
             Developmental* • Interferons • Pregnancy •
             Pregnancy, Animal • Primates • Progesterone •
             Rats • Species Specificity • Swine •
             metabolism • physiology*},
   Abstract = {Uterine receptivity to implantation of blastocysts in
             mammals includes hatching from zona pellucida, precontact
             with uterine luminal (LE) and superficial glandular (sGE)
             epithelia and orientation of blastocyst, apposition between
             trophectoderm and uterine LE and sGE, adhesion of
             trophectoderm to uterine LE/sGE, and, in some species,
             limited or extensive invasion into the endometrial stroma
             and induction of decidualization of stromal cells. These
             peri-implantation events are prerequisites for pregnancy
             recognition signaling, implantation, and placentation
             required for fetal-placental growth and development through
             the remainder of pregnancy. Although there is a range of
             strategies for implantation in mammals, a common feature is
             the requirement for progesterone (P(4)) to downregulate
             expression of its receptors in uterine epithelia and P(4)
             prior to implantation events. P(4) then mediates its effects
             via growth factors expressed by stromal cells in most
             species; however, uterine luminal epithelium may express a
             growth factor in response to P(4) and/or estrogens in
             species with a true epitheliochorial placenta. There is also
             compelling evidence that uterine receptivity to implantation
             involves temporal and cell-specific expression of interferon
             (IFN)-stimulated genes that may be induced directly by an
             IFN or induced by P(4) and stimulated by an IFN. These genes
             have many roles including nutrient transport, cellular
             remodeling, angiogenesis and relaxation of vascular tissues,
             cell proliferation and migration, establishment of an
             antiviral state, and protection of conceptus tissues from
             challenges by the maternal immune cells.},
   Language = {eng},
   Doi = {10.1530/REP-09-0158},
   Key = {fds174261}
}

@article{fds174139,
   Author = {GA Johnson and EG Kim and PA Platz and MM Mickelson},
   Title = {Comparative aspects of tyrosine hydroxylase and tryptophan
             hydroxylase inhibition: arterenones and dihydroxyphenylacetamide
             (H 22-54).},
   Journal = {Biochemical pharmacology},
   Volume = {17},
   Number = {3},
   Pages = {403-10},
   Year = {1968},
   Month = {March},
   ISSN = {0006-2952},
   Keywords = {Acetophenones • Adrenal Medulla • Amides •
             Animals • Brain • Cattle • Iron •
             Mast-Cell Sarcoma • Methyltyrosines • Mice •
             Mixed Function Oxygenases* • Norepinephrine •
             Phenylacetates* • Phenylalanine • Sarcoma,
             Experimental • Tritium • Tryptophan •
             Tyrosine • antagonists & inhibitors • enzymology
             • enzymology* • metabolism • pharmacology
             • pharmacology*},
   Language = {eng},
   Key = {fds174139}
}

@article{fds174246,
   Author = {D Robertson and GA Johnson and RM Robertson and AS Nies and DG Shand and JA
             Oates},
   Title = {Comparative assessment of stimuli that release neuronal and
             adrenomedullary catecholamines in man.},
   Journal = {Circulation},
   Volume = {59},
   Number = {4},
   Pages = {637-43},
   Year = {1979},
   Month = {April},
   ISSN = {0009-7322},
   Keywords = {Adolescent • Adrenal Medulla • Adult • Blood
             Specimen Collection • Caffeine • Catecholamines
             • Epinephrine • Female • Humans •
             Isometric Contraction • Male • Middle Aged •
             Neurons • Norepinephrine • Physical Stimulation
             • Posture • Pressoreceptors • Valsalva
             Maneuver • blood • pharmacology •
             physiology*},
   Abstract = {We assessed the release of neuronal and adrenomedullary
             catecholamines in response to various stimuli of the
             sympathetic nervous system in normal subjects. Plasma
             catecholamines and their urinary metabolites,
             normetanephrine and metanephrine, were measured. Sodium
             restriction increased supine plasma norepinephrine by 37%
             and ambulatory plasma norepinephrine by 22%, with urinary
             normetanephrine excretion increased 29%. The sodium
             restriction did not elevate plasma epinephrine or urinary
             metanephrine. The most potent stimuli of norepinephrine were
             treadmill exercise, orthostasis, caffeine, the cold pressor
             test, sodium restriction and handgrip exercise, in
             descending order. Plasma epinephrine was increased by
             caffeine, treadmill exercise, the cold pressor test,
             handgrip exercise and the Valsalva maneuver, in that order.
             Syncope resulted in profound changes in plasma epinephrine
             but only modest changes in plasma norepinephrine. We
             conclude that in man, there is frequent dissociation between
             the effects of different stimuli on neuronal and
             adrenomedullary catecholamine release.},
   Language = {eng},
   Key = {fds174246}
}

@booklet{Macfall91,
   Author = {MACFALL, JS and JOHNSON, GA and KRAMER, PJ},
   Title = {Comparative water uptake by roots of different ages in
             seedlings of loblolly pine (Pinus taeda L.)},
   Journal = {New Phytologist},
   Volume = {119},
   Number = {4},
   Pages = {551-560},
   Publisher = {WILEY},
   Year = {1991},
   Month = {January},
   ISSN = {0028-646X},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1991HA17900010&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Abstract = {Magnetic resonance (MR) imaging was used to study water
             absorption from fine, moist sand by the taproot,
             first‐order lateral roots, and tine roots of
             9‐month‐old loblolly pine seedlings. Magnetic resonance
             imaging provides the opportunity for repeated
             non‐destructive measurements of water uptake by roots
             growing in a solid medium such as sand. Root systems of
             container‐grown seedlings were pruned to a taproot, one or
             two first‐order laterals and attached fine roots, and were
             planted in small containers. Reference tubes filled with a
             mixture of CuSO4/D2O were placed in each container in the
             field of view. Roots of individual seedlings were repeatedly
             imaged at approximately 3 h intervals. Water uptake by
             individual roots was measured and uptake was calculated
             based on biomass, root length, and surface area. Based on
             weight and surface area, but not on root length, fine roots
             were more efficient than the lateral or taproots in water
             uptake. Measurement of water content in MR images of wet
             sand was confirmed by the imaging of Sand phantoms. These
             phantoms were tubes filled with fine sand at varied water
             contents (5–25%). Additional tubes of CuSO4 with D2O were
             also imaged. A linear relationship between signal intensity
             of moist sand (normalized against the CuSO4/D2O) and water
             conteni was demonstrated (R2= 0.97). Fitting the normalized
             signal intensity of the sand to the calculated linear
             regression allowed calculation of the water content of the
             sand. Copyright © 1991, Wiley Blackwell. All rights
             reserved},
   Doi = {10.1111/j.1469-8137.1991.tb01047.x},
   Key = {Macfall91}
}

@booklet{Wong92,
   Author = {W. W. Wong and L. L. Clarke and G. A. Johnson and M.
             Llaurador and P. D. Klein},
   Title = {Comparison of 2 elemental-analyzer gas-isotope-ratio
             mass-spectrometer systems in the simultaneous measurement of
             c-13/c-12 ratios and carbon content in organic-samples},
   Journal = {Analytical Chemistry},
   Volume = {64},
   Number = {4},
   Pages = {354 -- 358},
   Year = {1992},
   Month = {February},
   Key = {Wong92}
}

@article{fds268729,
   Author = {Befera, NT and Badea, CT and Johnson, GA},
   Title = {Comparison of 4D-microSPECT and microCT for murine cardiac
             function.},
   Journal = {Mol Imaging Biol},
   Volume = {16},
   Number = {2},
   Pages = {235-245},
   Year = {2014},
   Month = {April},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/24037175},
   Abstract = {PURPOSE: The objective of this study was to compare a new
             generation of four-dimensional micro-single photon emission
             computed tomography (microSPECT) with microCT for the
             quantitative in vivo assessment of murine cardiac function.
             PROCEDURES: Four-dimensional isotropic cardiac images were
             acquired from anesthetized normal C57BL/6 mice with either
             microSPECT (n = 6) or microCT (n = 6). One additional mouse
             with myocardial infarction (MI) was scanned with both
             modalities. Prior to imaging, mice were injected with either
             technetium tetrofosmin for microSPECT or a liposomal blood
             pool contrast agent for microCT. Segmentation of the left
             ventricle (LV) was performed using Vitrea (Vital Images)
             software, to derive global and regional function. RESULTS:
             Measures of global LV function between microSPECT and
             microCT groups were comparable (e.g., ejection fraction = 71
             ± 6 % microSPECT and 68 ± 4 % microCT). Regional
             functional indices (wall motion, wall thickening, regional
             ejection fraction) were also similar for the two modalities.
             In the mouse with MI, microSPECT identified a large
             perfusion defect that was not evident with microCT.
             CONCLUSIONS: Despite lower spatial resolution, microSPECT
             was comparable to microCT in the quantitative evaluation of
             cardiac function. MicroSPECT offers an advantage over
             microCT in the ability to evaluate simultaneously myocardial
             radiotracer distribution and function, simultaneously.
             MicroSPECT should be considered as an alternative to microCT
             and magnetic resonance for preclinical cardiac imaging in
             the mouse.},
   Doi = {10.1007/s11307-013-0686-z},
   Key = {fds268729}
}

@booklet{Staggs98,
   Author = {K. L. Staggs and K. J. Austin and G. A. Johnson and M. G.
             Teixeira and C. T. Talbott and V. A. Dooley and T. R.
             Hansen},
   Title = {Complex induction of bovine uterine proteins by
             interferon-tau},
   Journal = {Biology Of Reproduction},
   Volume = {59},
   Number = {2},
   Pages = {293 -- 297},
   Year = {1998},
   Month = {August},
   Key = {Staggs98}
}

@article{fds132910,
   Author = {KL Staggs and KJ Austin and GA Johnson and MG Teixeira and CT Talbott and VA Dooley and TR Hansen},
   Title = {Complex induction of bovine uterine proteins by
             interferon-tau.},
   Journal = {Biology of reproduction},
   Volume = {59},
   Number = {2},
   Pages = {293-7},
   Year = {1998},
   Month = {August},
   ISSN = {0006-3363},
   Keywords = {Animals • Blotting, Western • Cattle • Cells,
             Cultured • Chemokine CXCL6 • Chemokines, CXC
             • Chromatography, Affinity • Endometrium •
             Epithelial Cells • Estrus • Female •
             Interferon Type I • Interferon Type I, Recombinant
             • Pregnancy • Pregnancy Proteins • Protein
             Biosynthesis* • Stimulation, Chemical • Ubiquitins
             • Uterus • biosynthesis • drug effects •
             metabolism • metabolism* • pharmacology •
             pharmacology* • physiology},
   Abstract = {Interferon-tau (IFN-tau) is released by the conceptus and
             induces two uterine proteins during early pregnancy:
             ubiquitin cross-reactive protein (UCRP) and granulocyte
             chemotactic protein-2 (GCP-2). The present experiments were
             designed to determine whether detection (Western blot) of
             cytosolic UCRP and release of GCP-2 could be used to examine
             IFN-tau signal transduction in cultured endometrial explants
             and primary epithelial cells. Recombinant (r) type 1 IFNs
             (rboIFN-tau and rboIFN-alpha; 5, 25, 100 nM) induced UCRP,
             but only rboIFN-tau induced GCP-2 in explant culture.
             Recombinant boIFN-tau and conceptus secretory proteins
             containing native IFN-tau induced UCRP and GCP-2 in cultured
             primary epithelial cells. All concentrations of rboIFN-alpha
             (25, 50, 100 nM) induced UCRP, but only the highest
             concentration induced GCP-2 in cultured primary epithelial
             cells. Interestingly, phorbol ester (100, 500, 1000 ng/ml)
             induced GCP-2, but it had no effect on UCRP. Because type 1
             IFNs induce UCRP, IFN-tau probably interacts with the janus
             kinase (Jak)-associated IFN-alpha receptor to phosphorylate
             signal transducers and activators of transcription (STAT)
             and/or interferon regulatory factor-1 (IRF-1). However,
             IFN-tau-specific induction of GCP-2 may involve a variant
             type 1 receptor subunit or activators of transcription that
             are associated with protein kinase C and the Jak/STAT/IRF-1
             pathway.},
   Language = {eng},
   Key = {fds132910}
}

@article{fds174148,
   Author = {B Govenar and M Freeman and DC Bergquist and GA Johnson and CR
             Fisher},
   Title = {Composition of a one-year-old Riftia pachyptila community
             following a clearance experiment: insight to succession
             patterns at deep-sea hydrothermal vents.},
   Journal = {The Biological bulletin},
   Volume = {207},
   Number = {3},
   Pages = {177-82},
   Year = {2004},
   Month = {December},
   ISSN = {0006-3185},
   Keywords = {Animals • Biomass • Ecosystem* • Environment*
             • Invertebrates • Pacific Ocean • Population
             Dynamics • Species Specificity • growth &
             development*},
   Language = {eng},
   Key = {fds174148}
}

@booklet{Brown87,
   Author = {Brown, JM and Fonteno, WC and Cassel, DK and Johnson,
             GA},
   Title = {COMPUTED TOMOGRAPHIC ANALYSES OF WATER DISTRIBUTION IN THREE
             POROUS FOAM MEDIA.},
   Journal = {Soil Science Society of America Journal},
   Volume = {51},
   Number = {5},
   Pages = {1121-1125},
   Publisher = {Soil Science Society of America},
   Year = {1987},
   Month = {January},
   url = {http://dx.doi.org/10.2136/sssaj1987.03615995005100050005x},
   Abstract = {Computer Assisted Tomography (CAT) is commonly used in
             diagnostic radiology to make nondestructive images and
             analyses of cross sections of the human body. CAT scanning
             may also be useful in imaging and measuring spatial
             distribution and changes in water distribution in porous
             media. The purpose of this paper is to review some of the
             details of CAT scanning that are of importance to the
             application of CAT scanning to porous media and to evaluate
             the use of the CAT scanner to measure the spatial
             distribution of water in three different porous media. The
             scanner's response to changes in the spatial distribution of
             water in three different porous phenolic foam materials
             after draining for 16 h was investigated. Water content
             distributions were successfully detected with good
             resolution on the x-ray image.},
   Doi = {10.2136/sssaj1987.03615995005100050005x},
   Key = {Brown87}
}

@article{fds268789,
   Author = {Badea, CT and Athreya, KK and Espinosa, G and Clark, D and Ghafoori, AP and Li, Y and Kirsch, DG and Johnson, GA and Annapragada, A and Ghaghada,
             KB},
   Title = {Computed tomography imaging of primary lung cancer in mice
             using a liposomal-iodinated contrast agent.},
   Journal = {PLoS One},
   Volume = {7},
   Number = {4},
   Pages = {e34496},
   Year = {2012},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/22485175},
   Abstract = {PURPOSE: To investigate the utility of a liposomal-iodinated
             nanoparticle contrast agent and computed tomography (CT)
             imaging for characterization of primary nodules in
             genetically engineered mouse models of non-small cell lung
             cancer. METHODS: Primary lung cancers with mutations in
             K-ras alone (Kras(LA1)) or in combination with p53
             (LSL-Kras(G12D);p53(FL/FL)) were generated. A
             liposomal-iodine contrast agent containing 120 mg Iodine/mL
             was administered systemically at a dose of 16 µl/gm body
             weight. Longitudinal micro-CT imaging with
             cardio-respiratory gating was performed pre-contrast and at
             0 hr, day 3, and day 7 post-contrast administration.
             CT-derived nodule sizes were used to assess tumor growth.
             Signal attenuation was measured in individual nodules to
             study dynamic enhancement of lung nodules. RESULTS: A good
             correlation was seen between volume and diameter-based
             assessment of nodules (R(2)>0.8) for both lung cancer
             models. The LSL-Kras(G12D);p53(FL/FL) model showed rapid
             growth as demonstrated by systemically higher volume changes
             compared to the lung nodules in Kras(LA1) mice (p<0.05).
             Early phase imaging using the nanoparticle contrast agent
             enabled visualization of nodule blood supply. Delayed-phase
             imaging demonstrated significant differential signal
             enhancement in the lung nodules of LSL-Kras(G12D);p53(FL/FL)
             mice compared to nodules in Kras(LA1) mice (p<0.05)
             indicating higher uptake and accumulation of the
             nanoparticle contrast agent in rapidly growing nodules.
             CONCLUSIONS: The nanoparticle iodinated contrast agent
             enabled visualization of blood supply to the nodules during
             the early-phase imaging. Delayed-phase imaging enabled
             characterization of slow growing and rapidly growing nodules
             based on signal enhancement. The use of this agent could
             facilitate early detection and diagnosis of pulmonary
             lesions as well as have implications on treatment response
             and monitoring.},
   Doi = {10.1371/journal.pone.0034496},
   Key = {fds268789}
}

@booklet{Cassel90,
   Author = {Cassel, DK and Brown, JM and Johnson, GA},
   Title = {Computer tomographic analysis of water distribution and flow
             in porous media},
   Journal = {Theoretical and Applied Climatology},
   Volume = {42},
   Number = {4},
   Pages = {223-228},
   Publisher = {Springer Nature},
   Year = {1990},
   Month = {December},
   ISSN = {0177-798X},
   url = {http://dx.doi.org/10.1007/BF00865982},
   Abstract = {Computer tomography (CT) is the reconstruction by computer
             of a tomographic plane (slice) of an object. The tomograph
             is developed from multiple X-ray absorption measurements
             (scans) made around the periphery of the object. Recent
             research in soil science indicates that CT, which has been
             used in the medical field for 17 years, may find
             applications in assessing the degree of uniformity, or lack
             thereof, of soils and other porous media, in determining the
             flow paths of water and solutes through soils and porous
             materials, and in determing the flow paths of water and
             solutes to roots of plants. This paper discusses the general
             concept of CT, some of the capabilities associated with
             software used to format the CT readings into the desired
             images, and presents some CT scan data for several draining
             porous media. © 1990 Springer-Verlag.},
   Doi = {10.1007/BF00865982},
   Key = {Cassel90}
}

@article{fds268746,
   Author = {HEDLUND, L and JONES, D and EFFMANN, E and JOHNSON, GA and BATES, W and WOLFE, W and PUTMAN, C},
   Title = {COMPUTERIZED TOMOGRAPHIC STUDY OF THE DOG LUNG DURING
             HEMORRHAGIC-SHOCK},
   Journal = {INVESTIGATIVE RADIOLOGY},
   Volume = {14},
   Number = {5},
   Pages = {369-369},
   Publisher = {LIPPINCOTT-RAVEN PUBL},
   Year = {1979},
   Month = {January},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1979HQ94500028&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {fds268746}
}

@booklet{Joyce04,
   Author = {M. M. Joyce and R. C. Burghardt and T. E. Spencer and G. A.
             Johnson},
   Title = {Conceptus secretory factors, other than estrogen, increase
             expression of interferon-stimulated genes in the porcine
             endometrium during pregnancy.},
   Journal = {Biology Of Reproduction},
   Pages = {211 -- 211},
   Year = {2004},
   Key = {Joyce04}
}

@article{fds157088,
   Author = {TE Spencer and RC Burghardt and GA Johnson and FW
             Bazer},
   Title = {Conceptus signals for establishment and maintenance of
             pregnancy.},
   Journal = {Animal reproduction science},
   Volume = {82-83},
   Pages = {537-50},
   Year = {2004},
   Month = {July},
   ISSN = {0378-4320},
   url = {http://dx.doi.org/10.1016/j.anireprosci.2004.04.014},
   Keywords = {Animals • Animals, Domestic • Corpus Luteum •
             Female • Fetus • Interferons • Pregnancy
             • Pregnancy Maintenance • Progesterone •
             Sheep • Signal Transduction* • Swine •
             Trophoblasts • metabolism • physiology •
             physiology*},
   Abstract = {Establishment and maintenance of pregnancy results from
             signaling by the conceptus (embryo/fetus and associated
             extraembryonic membranes) and requires progesterone produced
             by the corpus luteum. In most mammals, hormones produced by
             the trophoblast maintain progesterone production by acting
             directly or indirectly to maintain the corpus luteum. In
             domestic animals (ruminants and pigs), hormones from the
             trophoblast are antiluteolytic in that they act on the
             endometrium to prevent uterine release of luteolytic
             prostaglandin F2alpha. In cyclic and pregnant sheep,
             progesterone negatively autoregulates progesterone receptor
             gene expression in the endometrial luminal and superficial
             glandular epithelium. In cyclic sheep, loss of the
             progesterone receptor is closely followed by increases in
             epithelial estrogen receptors and then oxytocin receptors,
             allowing oxytocin to induce uterine release of luteolytic
             prostaglandin F2alpha pulses. In pregnant sheep, the
             conceptus trophoblast produces interferon tau that acts on
             the endometrium to inhibit transcription of the estrogen
             receptor alpha gene directly and the oxytocin receptor gene
             indirectly to abrogate development of the endometrial
             luteolytic mechanism. Subsequently, sequential, overlapping
             actions of progesterone, interferon tau, placental lactogen,
             and growth hormone comprise a hormonal servomechanism that
             regulates endometrial gland morphogenesis and terminal
             differentiated function to maintain pregnancy in sheep. In
             pigs, the conceptus trophoblast produces estrogen that
             alters the direction of prostaglandin F2alpha secretion from
             an endocrine to exocrine direction, thereby sequestering
             luteolytic prostaglandin F2alpha within the uterine lumen.
             Conceptus estrogen also increases expression of fibroblast
             growth factor 7 in the endometrial lumenal epithelium that,
             in turn, stimulates proliferation and differentiated
             functions of the trophectoderm, which expresses the
             fibroblast growth factor 7 receptor. Strategic manipulation
             of these physiological mechanisms may improve uterine
             capacity, conceptus survival, and reproductive
             health.},
   Language = {eng},
   Doi = {10.1016/j.anireprosci.2004.04.014},
   Key = {fds157088}
}

@article{fds174111,
   Author = {GA Johnson and FW Bazer and RC Burghardt and TE Spencer and G Wu and KJ
             Bayless},
   Title = {Conceptus-uterus interactions in pigs: endometrial gene
             expression in response to estrogens and interferons from
             conceptuses.},
   Journal = {Society of Reproduction and Fertility supplement},
   Volume = {66},
   Pages = {321-32},
   Year = {2009},
   Keywords = {Animals • Embryo Implantation • Embryo, Mammalian
             • Endometrium • Estrogens • Female •
             Gene Expression Regulation, Developmental • Interferons
             • Pregnancy • Swine • physiology •
             physiology*},
   Abstract = {This review highlights information on conceptus-uterus
             interactions in the pig with respect to uterine gene
             expression in response to estrogens and interferons (IFNs)
             secreted from elongating conceptuses. Pig conceptuses
             release estrogens for pregnancy recognition, but also
             secrete IFNs that do not appear to be antiluteolytic.
             Estrogens and IFNs induce expression of largely
             non-overlapping sets of genes, and evidence suggests that
             pig conceptuses orchestrate essential events of early
             pregnancy including pregnancy recognition signaling,
             implantation and secretion of histotroph by precisely
             controlling temporal and spatial (cell-specific) changes in
             uterine gene expression through initial secretion of
             estrogens, followed by cytokines including IFNG and IFND. By
             Day 12 of pregnancy, estrogens increase the expression of
             multiple genes in the uterine luminal epithelium including
             SPP1, STC1, IRF2 and STAT1 that likely have roles for
             implantation. By Day 15 of pregnancy, IFNs upregulate a
             large array of IFN responsive genes in the underlying stroma
             and glandular epithelium including ISG15, IRF1, STAT1, SLAs
             and B2M that likely have roles in uterine remodeling to
             support placentation.},
   Language = {eng},
   Key = {fds174111}
}

@article{fds204271,
   Author = {D Srinivasan and N Muthukrishnan and GA Johnson and A Erazo-Oliveras and J Lim and EE Simanek and JP Pellois},
   Title = {Conjugation to the cell-penetrating peptide TAT potentiates
             the photodynamic effect of carboxytetramethylrhodamine.},
   Journal = {PloS one},
   Volume = {6},
   Number = {3},
   Pages = {e17732},
   Year = {2011},
   ISSN = {1932-6203},
   url = {http://dx.doi.org/10.1371/journal.pone.0017732},
   Keywords = {Amino Acid Sequence • Animals • Carotenoids •
             Cell Death • Cell Line • Cell Membrane • Cell
             Membrane Permeability • Cell-Penetrating Peptides
             • Drug Synergism • Endocytosis • Endosomes
             • Humans • Light • Molecular Sequence Data
             • Photochemotherapy* • Photolysis • Protein
             Processing, Post-Translational • Rhodamines •
             Singlet Oxygen • chemistry • drug effects •
             metabolism • metabolism* • pharmacology •
             radiation effects • therapeutic use*},
   Abstract = {BACKGROUND: Cell-penetrating peptides (CPPs) can transport
             macromolecular cargos into live cells. However, the cellular
             delivery efficiency of these reagents is often suboptimal
             because CPP-cargo conjugates typically remain trapped inside
             endosomes. Interestingly, irradiation of fluorescently
             labeled CPPs with light increases the release of the peptide
             and its cargos into the cytosol. However, the mechanism of
             this phenomenon is not clear. Here we investigate the
             molecular basis of the photo-induced endosomolytic activity
             of the prototypical CPPs TAT labeled to the fluorophore
             5(6)-carboxytetramethylrhodamine (TMR). RESULTS: We report
             that TMR-TAT acts as a photosensitizer that can destroy
             membranes. TMR-TAT escapes from endosomes after exposure to
             moderate light doses. However, this is also accompanied by
             loss of plasma membrane integrity, membrane blebbing, and
             cell-death. In addition, the peptide causes the destruction
             of cells when applied extracellularly and also triggers the
             photohemolysis of red blood cells. These photolytic and
             photocytotoxic effects were inhibited by hydrophobic singlet
             oxygen quenchers but not by hydrophilic quenchers.
             CONCLUSIONS: Together, these results suggest that TAT can
             convert an innocuous fluorophore such as TMR into a potent
             photolytic agent. This effect involves the targeting of the
             fluorophore to cellular membranes and the production of
             singlet oxygen within the hydrophobic environment of the
             membranes. Our findings may be relevant for the design of
             reagents with photo-induced endosomolytic activity. The
             photocytotoxicity exhibited by TMR-TAT also suggests that
             CPP-chromophore conjugates could aid the development of
             novel Photodynamic Therapy agents.},
   Language = {eng},
   Doi = {10.1371/journal.pone.0017732},
   Key = {fds204271}
}

@booklet{Walker93a,
   Author = {L. C. Walker and S. Murad and A. G. Messenger and G. A.
             Johnson and S. R. Pinnell},
   Title = {Connective-tissue effects of minoxidil and its hydroxy
             derivatives on human dermal papilla cells in
             culture},
   Journal = {Clinical Research},
   Volume = {41},
   Number = {2},
   Pages = {A437 -- A437},
   Year = {1993},
   Month = {April},
   Key = {Walker93a}
}

@booklet{Walker93,
   Author = {L. C. Walker and S. Murad and A. G. Messenger and G. A.
             Johnson and S. R. Pinnell},
   Title = {Connective-tissue effects of minoxidil and its hydroxy
             derivatives on human dermal papilla cells in
             culture},
   Journal = {Journal Of Investigative Dermatology},
   Volume = {100},
   Number = {4},
   Pages = {552 -- 552},
   Year = {1993},
   Month = {April},
   Key = {Walker93}
}

@article{fds268730,
   Author = {Clark, D and Badea, A and Johnson, GA and Badea, CT},
   Title = {Constructing a 4D murine cardiac micro-CT atlas for
             automated segmentation and phenotyping applications},
   Journal = {Progress in Biomedical Optics and Imaging - Proceedings of
             SPIE},
   Volume = {8669},
   Publisher = {SPIE},
   Year = {2013},
   Month = {June},
   ISSN = {1605-7422},
   url = {http://dx.doi.org/10.1117/12.2007043},
   Abstract = {A number of investigators have demonstrated the potential of
             preclinical micro-CT in characterizing cardiovascular
             disease in mouse models. One major hurdle to advancing this
             approach is the extensive user interaction required to
             derive quantitative metrics from these 4D image arrays
             (space + time). In this work, we present: (1) a method for
             constructing an average anatomic cardiac atlas of the mouse
             based on 4D micro-CT images, (2) a fully automated approach
             for segmenting newly acquired cardiac data sets using the
             atlas, and (3) a quantitative characterization of atlasbased
             segmentation accuracy and consistency. Employing the
             deformable registration toolkit, ANTs, the construction of
             minimal deformation fields, and a novel adaptation of joint
             bilateral filtration, our atlas construction scheme was used
             to integrate 6, C57BL/6 cardiac micro-CT data sets, reducing
             the noise standard deviation from ~70 HU in the individual
             data sets to ~21 HU in the atlas data set. Using the
             segmentation tools in Atropos and our atlas-based
             segmentation, we were able to propagate manual labels to 5,
             C57BL/6 data sets not used in atlas construction. Average
             Dice coefficients and volume accuracies (respectively) over
             phases 1 (ventricular diastole), 3, and 5 (ventricular
             systole) of these 5 data sets were as follows: left
             ventricle, 0.96, 0.96; right ventricle, 0.89, 0.92; left
             atrium, 0.88, 0.89; right atrium, 0.86, 0.92; myocardium,
             0.90, 0.94. Once the atlas was constructed and segmented,
             execution of the proposed automated segmentation scheme took
             ~6.5 hours per data set, versus more than 50 hours required
             for a manual segmentation. © 2013 SPIE.},
   Doi = {10.1117/12.2007043},
   Key = {fds268730}
}

@booklet{Shengunther97,
   Author = {J. Shengunther and R. S. Mannel and J. L. Walker and G. A.
             Johnson},
   Title = {Construction of the ileocolonic continent urinary reservoir:
             Operative technique at the University of
             Oklahoma},
   Journal = {Journal Of Gynecologic Surgery},
   Volume = {13},
   Number = {2},
   Pages = {83 -- 88},
   Year = {1997},
   Key = {Shengunther97}
}

@article{fds268742,
   Author = {Peterson, RA and Gabrielson, KL and Allan Johnson and G and Pomper, MG and Coatney, RW and Winkelmann, CT},
   Title = {Continuing education course #1: non-invasive imaging as a
             problem-solving tool and translational biomarker strategy in
             toxicologic pathology.},
   Journal = {Toxicol Pathol},
   Volume = {39},
   Number = {1},
   Pages = {267-272},
   Year = {2011},
   Month = {January},
   ISSN = {0192-6233},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000293379600029&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Abstract = {The continuing education course "Non-Invasive Imaging as a
             Problem-Solving Tool and Translational Biomarker Strategy in
             Toxicologic Pathology" provided a thorough overview of
             commonly used imaging modalities and the logistics required
             for integration of small animal imaging into toxicologic
             pathology. Non-invasive imaging (NIN) is gaining acceptance
             as an important modality in toxicologic pathology. This
             technology allows nonterminal, time-course evaluation of
             functional and morphologic endpoints and can be used to
             translate biomarkers between preclinical animal models and
             human patients. NIN can support drug development as well as
             basic research in academic or industrial environments. An
             initial overview of theoretical principles was followed by
             focused presentations on magnetic resonance imaging
             (MRI)/magnetic resonance microscopy (MRM), positron emission
             tomography (PET)/single proton emission computed tomography
             (SPECT), ultrasonography (US, primarily focused on
             echocardiography), optical (bioluminescent) imaging, and
             computed tomography (CT). The choice of imaging modality
             will depend on the research question and the needed
             resolution.},
   Doi = {10.1177/0192623310390392},
   Key = {fds268742}
}

@article{fds268770,
   Author = {Bolon, B and Garman, RH and Gundersen, HJG and Allan Johnson and G and Kaufmann, W and Krinke, G and Little, PB and Makris, SL and Mellon, RD and Sulik, KK and Jensen, K},
   Title = {Continuing education course #3: current practices and future
             trends in neuropathology assessment for developmental
             neurotoxicity testing.},
   Journal = {Toxicol Pathol},
   Volume = {39},
   Number = {1},
   Pages = {289-293},
   Year = {2011},
   Month = {January},
   ISSN = {1533-1601},
   url = {http://dx.doi.org/10.1177/0192623310386247},
   Abstract = {The continuing education course on Developmental
             Neurotoxicity Testing (DNT) was designed to communicate
             current practices for DNT neuropathology, describe promising
             innovations in quantitative analysis and noninvasive
             imaging, and facilitate a discussion among experienced
             neuropathologists and regulatory scientists regarding
             suitable DNT practices. Conventional DNT neuropathology
             endpoints are qualitative histopathology and morphometric
             endpoints of particularly vulnerable sites (e.g., cerebral,
             cerebellar, or hippocampal thickness). Novel imaging and
             stereology measurements hold promise for automated analysis
             of factors that cannot be effectively examined in routinely
             processed specimens (e.g., cell numbers, fiber tract
             integrity). The panel recommended that dedicated DNT
             neuropathology data sets be acquired on a minimum of 8
             sections (for qualitative assessment) or 3 sections (for
             quantitative linear and stereological analyses) using a
             small battery of stains to examine neurons and myelin. Where
             guidelines permit discretion, immersion fixation is
             acceptable for younger animals (postnatal day 22 or
             earlier), and peripheral nerves may be embedded in paraffin.
             Frequent concerns regarding DNT data sets include
             false-negative outcomes due to processing difficulties
             (e.g., lack of concordance among sections from different
             animals) and insensitive analytical endpoints (e.g.,
             qualitative evaluation) as well as false-positive results
             arising from overinterpretation or misreading by
             inexperienced pathologists.},
   Doi = {10.1177/0192623310386247},
   Key = {fds268770}
}

@booklet{Halvorsen82,
   Author = {Halvorsen, RA and Woodfield, S and Hedlund, L and Johnson, GA and Thompson, WM},
   Title = {CONTRAST ENHANCEMENT OF THE HEPATOBILIARY SYSTEM DURING
             CT},
   Journal = {Investigative Radiology},
   Volume = {17},
   Number = {4},
   Pages = {S27-S27},
   Publisher = {Ovid Technologies (Wolters Kluwer Health)},
   Year = {1982},
   Month = {July},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1982PA96700126&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Doi = {10.1097/00004424-198207000-00134},
   Key = {Halvorsen82}
}

@booklet{Thompson83,
   Author = {Thompson, WM and Stude, R and Bates, M and Hedlund, L and Johnson,
             GA},
   Title = {CONTRAST ENHANCEMENT OF THE LIVER DURING
             CT},
   Journal = {Investigative Radiology},
   Volume = {18},
   Number = {4},
   Pages = {S11-S11},
   Publisher = {Ovid Technologies (Wolters Kluwer Health)},
   Year = {1983},
   Month = {July},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1983QZ74200056&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Doi = {10.1097/00004424-198307000-00064},
   Key = {Thompson83}
}

@booklet{Stude87,
   Author = {R. A. Stude and L. W. Hedlund and G. A. Johnson and W. M.
             Thompson},
   Title = {Contrast enhancement of the liver evaluation by automated
             contiguous pixel search},
   Journal = {Investigative Radiology},
   Volume = {22},
   Number = {2},
   Pages = {132 -- 136},
   Year = {1987},
   Month = {February},
   Key = {Stude87}
}

@article{fds268928,
   Author = {Stude, RA and Hedlund, LW and Johnson, GA and Thompson,
             WM},
   Title = {Contrast enhancement of the liver. Evaluation by automated
             contiguous pixel search.},
   Journal = {Invest Radiol},
   Volume = {22},
   Number = {2},
   Pages = {132-136},
   Year = {1987},
   Month = {February},
   ISSN = {0020-9996},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/3030962},
   Keywords = {Animals • Contrast Media* • Diatrizoate Meglumine
             • Dogs • Ethiodized Oil • Liver •
             Radiographic Image Enhancement* • Tomography, X-Ray
             Computed* • diagnostic use • radiography*},
   Abstract = {Eight dogs were infused with one of three different contrast
             agents: meglumine diatrizoate, iosulamide meglumine, or an
             ethiodized oil emulsion (EOE 13). Image intensity in the
             liver was evaluated globally and regionally by means of an
             automated pixel sampling method to determine differences in
             the rate of enhancement produced by the three agents. The
             results of the automated method were compared with those of
             the standard manual cursor method. The automated method
             showed that liver parenchyma was enhanced uniformly by all
             three contrast agents. The maximum degree of enhancement
             (Mean +/- SEM) for the three agents was diatrizoate, 12.0
             +/- 3.5 Hounsfield units (HU); iosluamide, 21.3 +/- 3.5 HU;
             and EOE 13, 37.2 +/- 4.25 HU. With the manual cursor method,
             contrast enhancement was about 20% more than estimated by
             the automated method. The automated method is better for
             evaluating the magnitude and pattern of contrast agent
             enhancement of the entire liver, since the currently
             employed cursor technique requires multiple evaluations to
             evaluate the entire liver.},
   Doi = {10.1097/00004424-198702000-00008},
   Key = {fds268928}
}

@article{fds268824,
   Author = {Howles, GP and Bing, KF and Qi, Y and Rosenzweig, SJ and Nightingale,
             KR and Johnson, GA},
   Title = {Contrast-enhanced in vivo magnetic resonance microscopy of
             the mouse brain enabled by noninvasive opening of the
             blood-brain barrier with ultrasound.},
   Journal = {Magn Reson Med},
   Volume = {64},
   Number = {4},
   Pages = {995-1004},
   Year = {2010},
   Month = {October},
   ISSN = {1522-2594},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/20740666},
   Keywords = {Animals • Blood-Brain Barrier • Brain •
             Contrast Media • Fluorocarbons • Gadolinium DTPA
             • Image Enhancement • Magnetic Resonance Imaging
             • Mice • Mice, Inbred C57BL • Microscopy
             • Sonication • anatomy & histology* •
             diagnostic use • diagnostic use* • metabolism*
             • methods • methods* • pharmacokinetics
             • pharmacokinetics* • radiation
             effects},
   Abstract = {The use of contrast agents for neuroimaging is limited by
             the blood-brain barrier (BBB), which restricts entry into
             the brain. To administer imaging agents to the brain of
             rats, intracarotid infusions of hypertonic mannitol have
             been used to open the BBB. However, this technically
             challenging approach is invasive, opens only a limited
             region of the BBB, and is difficult to extend to mice. In
             this work, the BBB was opened in mice, using unfocused
             ultrasound combined with an injection of microbubbles. This
             technique has several notable features: it (a) can be
             performed transcranially in mice; (b) takes only 3 min and
             uses only commercially available components; (c) opens the
             BBB throughout the brain; (d) causes no observed histologic
             damage or changes in behavior (with peak-negative acoustic
             pressures of 0.36 MPa); and (e) allows recovery of the BBB
             within 4 h. Using this technique, Gadopentetate Dimeglumine
             (Gd-DTPA) was administered to the mouse brain parenchyma,
             thereby shortening T(1) and enabling the acquisition of
             high-resolution (52 × 52 × 100 micrometers(3)) images in
             51 min in vivo. By enabling the administration of both
             existing anatomic contrast agents and the newer
             molecular/sensing contrast agents, this technique may be
             useful for the study of mouse models of neurologic function
             and pathology with MRI.},
   Language = {eng},
   Doi = {10.1002/mrm.22411},
   Key = {fds268824}
}

@booklet{Sills04,
   Author = {Sills, RC and Morgan, DL and Herr, DW and Little, PB and George, NM and Ton, TV and Love, NE and Maronpot, RR and Johnson,
             GA},
   Title = {Contribution of magnetic resonance microscopy in the 12-week
             neurotoxicity evaluation of carbonyl sulfide in Fischer 344
             rats.},
   Journal = {Toxicol Pathol},
   Volume = {32},
   Number = {5},
   Pages = {501-510},
   Year = {2004},
   url = {http://dx.doi.org/10.1080/01926230490493918},
   Abstract = {In this carbonyl sulfide (COS) study, magnetic resonance
             microscopy (MRM) and detailed light microscopic evaluation
             effectively functioned in parallel to assure that the
             distribution and degree of pathology in the brain was
             accurately represented. MRM is a powerful imaging modality
             that allows for excellent identification of neuroanatomical
             structures coupled with the ability to acquire 200 or more
             cross-sectional images of the brain, and the ability to
             display them in multiple planes. F344 rats were exposed to
             200-600 ppm COS for up to 12 weeks. Prior to MRM, rats were
             anesthetized and cardiac perfused with McDowell Trump's
             fixative containing a gadolinium MR contrast medium. Fixed
             specimens were scanned at the Duke Center for In Vivo
             Microscopy on a 9.4 Tesla magnetic resonance system adapted
             explicitly for microscopic imaging. An advantage of MRM in
             this study was the ability to identify lesions in rats that
             appeared clinically normal prior to sacrifice and the
             opportunity to identify lesions in areas of the brain which
             would not be included in conventional studies. Other
             advantages include the ability to examine the brain in
             multiple planes (transverse, dorsal, sagittal) and obtain
             and save the MRM images in a digital format that allows for
             postexperimental data processing and manipulation. MRM
             images were correlated with neuroanatomical and
             neuropathological findings. All suspected MRM images were
             compared to corresponding H&E slides. An important aspect of
             this study was that MRM was critical in defining our
             strategy for sectioning the brain, and for designing
             mechanistic studies (cytochrome oxidase evaluations) and
             functional assessments (electrophysiology studies) on
             specifically targeted anatomical sites following COS
             exposure.},
   Doi = {10.1080/01926230490493918},
   Key = {Sills04}
}

@article{fds132895,
   Author = {RC Sills and DL Morgan and DW Herr and PB Little and NM George and TV Ton and NE Love and RR Maronpot and GA Johnson},
   Title = {Contribution of magnetic resonance microscopy in the 12-week
             neurotoxicity evaluation of carbonyl sulfide in Fischer 344
             rats.},
   Journal = {Toxicologic pathology, United States},
   Volume = {32},
   Number = {5},
   Pages = {501-10},
   ISSN = {0192-6233},
   Keywords = {Administration, Inhalation • Air Pollutants •
             Animals • Brain • Dose-Response Relationship, Drug
             • Female • Image Processing, Computer-Assisted
             • Inhalation Exposure • Magnetic Resonance
             Imaging* • Male • Microscopy • Neurotoxicity
             Syndromes • Rats • Rats, Inbred F344 •
             Recovery of Function • Sulfur Oxides •
             administration & dosage • drug effects* •
             etiology* • methods • pathology •
             toxicity*},
   Abstract = {In this carbonyl sulfide (COS) study, magnetic resonance
             microscopy (MRM) and detailed light microscopic evaluation
             effectively functioned in parallel to assure that the
             distribution and degree of pathology in the brain was
             accurately represented. MRM is a powerful imaging modality
             that allows for excellent identification of neuroanatomical
             structures coupled with the ability to acquire 200 or more
             cross-sectional images of the brain, and the ability to
             display them in multiple planes. F344 rats were exposed to
             200-600 ppm COS for up to 12 weeks. Prior to MRM, rats were
             anesthetized and cardiac perfused with McDowell Trump's
             fixative containing a gadolinium MR contrast medium. Fixed
             specimens were scanned at the Duke Center for In Vivo
             Microscopy on a 9.4 Tesla magnetic resonance system adapted
             explicitly for microscopic imaging. An advantage of MRM in
             this study was the ability to identify lesions in rats that
             appeared clinically normal prior to sacrifice and the
             opportunity to identify lesions in areas of the brain which
             would not be included in conventional studies. Other
             advantages include the ability to examine the brain in
             multiple planes (transverse, dorsal, sagittal) and obtain
             and save the MRM images in a digital format that allows for
             postexperimental data processing and manipulation. MRM
             images were correlated with neuroanatomical and
             neuropathological findings. All suspected MRM images were
             compared to corresponding H&E slides. An important aspect of
             this study was that MRM was critical in defining our
             strategy for sectioning the brain, and for designing
             mechanistic studies (cytochrome oxidase evaluations) and
             functional assessments (electrophysiology studies) on
             specifically targeted anatomical sites following COS
             exposure.},
   Key = {fds132895}
}

@booklet{Sills04a,
   Author = {Sills, RC and Morgan, DL and Maronpot, RR and Johnson,
             GA},
   Title = {Contribution of magnetic resonance microscopy in the
             biologic and mechanistic assessment of carbonyl sulfide
             neurotoxicity in F344 rats},
   Journal = {TOXICOLOGY AND APPLIED PHARMACOLOGY},
   Volume = {197},
   Number = {3},
   Pages = {151-152},
   Publisher = {ACADEMIC PRESS INC ELSEVIER SCIENCE},
   Year = {2004},
   Month = {June},
   ISSN = {0041-008X},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000222348900052&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Sills04a}
}

@booklet{Shattuck97a,
   Author = {Shattuck, MD and Behringer, RP and Johnson, GA and Georgiadis,
             JG},
   Title = {Convection and flow in porous media. Part 1. Visualization
             by magnetic resonance imaging},
   Journal = {Journal of Fluid Mechanics},
   Volume = {332},
   Pages = {215-245},
   Publisher = {Cambridge University Press (CUP)},
   Year = {1997},
   Month = {February},
   url = {http://dx.doi.org/10.1017/s0022112096003990},
   Abstract = {We describe an experimental study of porous media convection
             (PMC) from onset to 8Rac. The goal of this work is to
             provide non-invasive imaging and high-precision heat
             transport measurements to test theories of convection in
             PMC. We obtain velocity information and visualize the
             convection patterns using magnetic resonance imaging (MRI).
             We study both ordered and disordered packings of
             mono-disperse spheres of diameter d = 3.204 ± 0.029 mm, in
             circular, rectangular, and hexagonal planforms. In general,
             the structure of the medium plays a role which is not
             predicted by theories which assume a homogeneous system.
             Disordered media are prepared by pouring mono-disperse
             spheres into the container. Large ordered regions of close
             packing for the spheres, with grain boundaries and isolated
             defects, characterize these media. The defects and grain
             boundaries play an important role in pattern formation in
             disordered media. Any deviation from close packing produces
             a region of larger porosity, hence locally larger
             permeability. The result is spatial variations in the
             Rayleigh number, Ra. We define the critical Ra, Rac, as the
             Rayleigh number at the onset of convection in the ordered
             regions. We find that stable localized convective regions
             exist around grain boundaries and defects at Ra < Rac. These
             remain as pinning sites for the convection patterns in the
             ordered regions as Ra increases above Rac up to 5Rac, the
             highest Ra studied in the disordered media. In ordered
             media, spheres are packed such that the only deviations from
             close packing occur within a thin (<d) region near the
             vertical walls. Stable localized convection begins at 0.5Rac
             in the wall regions but appears to play only a weak role in
             the pattern formation of the interior regions (bulk), since
             different stable patterns are observed in the bulk at the
             same Ra after each cycling of Ra below Rac, even for similar
             patterns of small rolls in the wall regions. The experiments
             provide a test of the following predictions for PMC: (i)
             that straight parallel rolls should be linearly stable for
             Rac < Ra < 5Rac; (ii) that at onset, the rolls should have a
             dimensionless wavevector qc = π; (iii) that at the upper
             end of this range rolls should lose stability to
             cross-rolls; (iv) that the initial slope of the Nusselt
             curve should be 2; (v) that there should be a rapid decay of
             vertical vorticity - hence no complex flows, such as those
             which occur for Rayleigh-Bénard convection (RBC) within the
             nominal regime of stable parallel rolls. These predictions
             are in partial agreement with our findings for the bulk
             convection in the ordered media. We observe roll-like
             structures which relax rapidly to stable patterns between
             Rac and 5Rac. However we find a wavenumber which is 0.7π
             compared to π derived from linear stability theory. We find
             an asymmetry between the size of the upflowing regions and
             downflowing regions as Ra grows above Rac. The ratio of the
             volume of the upflowing to the volume of the downflowing
             regions decreases as Ra increases and leads to a novel
             time-dependent state, which does not consist of cross-rolls.
             This time-dependent state begins at 6Rac and is observed up
             to 8Rac, the largest Ra which we studied. It seems likely
             that the occurrence of this state is linked to departures
             from the Boussinesq approximation at higher Ra. We also find
             that the slope of the Nusselt curve is 0.7, which does not
             agree with the predicted value of 2.},
   Doi = {10.1017/s0022112096003990},
   Key = {Shattuck97a}
}

@article{fds174234,
   Author = {S Banerjee and GA Johnson},
   Title = {Coregionalized single- and multiresolution spatially varying
             growth curve modeling with application to weed
             growth.},
   Journal = {Biometrics},
   Volume = {62},
   Number = {3},
   Pages = {864-76},
   Year = {2006},
   Month = {September},
   ISSN = {0006-341X},
   url = {http://dx.doi.org/10.1111/j.1541-0420.2006.00535.x},
   Keywords = {Bayes Theorem • Biometry • Markov Chains •
             Models, Biological* • Models, Statistical* • Monte
             Carlo Method • Normal Distribution • Setaria Plant
             • growth & development*},
   Abstract = {Modeling of longitudinal data from agricultural experiments
             using growth curves helps understand conditions conducive or
             unconducive to crop growth. Recent advances in Geographical
             Information Systems (GIS) now allow geocoding of
             agricultural data that help understand spatial patterns. A
             particularly common problem is capturing spatial variation
             in growth patterns over the entire experimental domain.
             Statistical modeling in these settings can be challenging
             because agricultural designs are often spatially replicated,
             with arrays of subplots, and interest lies in capturing
             spatial variation at possibly different resolutions. In this
             article, we develop a framework for modeling spatially
             varying growth curves as Gaussian processes that capture
             associations at single and multiple resolutions. We provide
             Bayesian hierarchical models for this setting, where
             flexible parameterization enables spatial estimation and
             prediction of growth curves. We illustrate using data from
             weed growth experiments conducted in Waseca, Minnesota, that
             recorded growth of the weed Setaria spp. in a spatially
             replicated design.},
   Language = {eng},
   Doi = {10.1111/j.1541-0420.2006.00535.x},
   Key = {fds174234}
}

@article{fds372233,
   Author = {G.A. Johnson},
   Title = {Correction for Johnson et al., Merged magnetic resonance and
             light sheet microscopy of the whole mouse
             brain.},
   Journal = {Proc Natl Acad Sci U S A},
   Volume = {120},
   Number = {25},
   Pages = {e2308718120},
   Year = {2023},
   Month = {June},
   url = {http://dx.doi.org/10.1073/pnas.2308718120},
   Doi = {10.1073/pnas.2308718120},
   Key = {fds372233}
}

@booklet{Monk94,
   Author = {B. J. Monk and J. A. Chapman and G. A. Johnson and B. K.
             Brightman and S. P. Wilczynski and M. J. Schell and H.
             Fan},
   Title = {Correlation of c-myc and her-2/neu amplification and
             expression with histopathologic variables in uterine corpus
             cancer},
   Journal = {American Journal Of Obstetrics And Gynecology},
   Volume = {171},
   Number = {5},
   Pages = {1193 -- 1198},
   Year = {1994},
   Month = {November},
   Key = {Monk94}
}

@article{fds174109,
   Author = {BJ Monk and JA Chapman and GA Johnson and BK Brightman and SP
             Wilczynski, MJ Schell and H Fan},
   Title = {Correlation of C-myc and HER-2/neu amplification and
             expression with histopathologic variables in uterine corpus
             cancer.},
   Journal = {American journal of obstetrics and gynecology},
   Volume = {171},
   Number = {5},
   Pages = {1193-8},
   Year = {1994},
   Month = {November},
   ISSN = {0002-9378},
   Keywords = {Adenocarcinoma • Aged • Autoradiography •
             Blotting, Northern • Blotting, Southern • Female
             • Gene Amplification* • Gene Expression* •
             Genes, erbB-2* • Genes, myc* • Humans •
             Middle Aged • Uterine Neoplasms • genetics* •
             pathology • pathology*},
   Abstract = {OBJECTIVE: Initial studies of protooncogenes in uterine
             corpus cancer have focused on a single aspect of the gene in
             question (deoxyribonucleic acid, ribonucleic acid, protein)
             or have studied a small number of patients. Therefore we
             evaluated c-myc and HER-2/neu gene amplification and
             ribonucleic acid overexpression in such malignancies and
             correlated these molecular changes with known pathologic
             risk factors. STUDY DESIGN: Quantitative Southern blot
             analysis for oncogene deoxyribonucleic acid was used to
             examine 37 tumors from patients with primary untreated
             uterine corpus cancer referred to the City of Hope National
             Medical Center. Six normal endometrial specimens were
             controls. Seventeen tumors were also examined by Northern
             blotting to assess increased ribonucleic expression.
             RESULTS: Histologic types included adenocarcinoma (n = 30),
             papillary serous adenocarcinoma (n = 2), adenosquamous
             carcinoma (n = 2), mixed mullerian sarcoma (n = 2), and
             leiomyosarcoma (n = 1). Carcinomas were stage I (n = 10), II
             (n = 18), or III (n = 6). Twenty-three had myometrial
             invasion of less than one third, six one third to two
             thirds, and eight deeper invasion (greater than two thirds).
             According to the criteria of the International Federation of
             Gynecology and Obstetrics stage was as follows: I (n = 22),
             II (n = 3), III (n = 7), and IV (n = 5). Ten (27%) and four
             (11%) tumors showed gene amplification of c-myc and
             HER-2/neu, respectively. Six demonstrated overexpression of
             either the c-myc or HER-2/neu gene. HER-2/neu gene
             amplification was associated more closely with
             overexpression. Stepwise logistic analysis demonstrated
             c-myc amplification to be associated with higher grade (p =
             0.01). CONCLUSION: In this referral population, c-myc
             activation is more common than HER-2/neu activation in
             uterine corpus cancer and is associated with tumors of
             higher grade.},
   Language = {eng},
   Key = {fds174109}
}

@booklet{Scribner99,
   Author = {D. R. Scribner and R. S. Mannel and J. L. Walker and G. A.
             Johnson},
   Title = {Cost analysis of laparoscopy versus laparotomy for early
             endometrial cancer},
   Journal = {Gynecologic Oncology},
   Volume = {75},
   Number = {3},
   Pages = {460 -- 463},
   Year = {1999},
   Month = {December},
   Key = {Scribner99}
}

@article{fds174313,
   Author = {DR Scribner Jr and RS Mannel and JL Walker and GA
             Johnson},
   Title = {Cost analysis of laparoscopy versus laparotomy for early
             endometrial cancer.},
   Journal = {Gynecologic oncology},
   Volume = {75},
   Number = {3},
   Pages = {460-3},
   Year = {1999},
   Month = {December},
   ISSN = {0090-8258},
   url = {http://dx.doi.org/10.1006/gyno.1999.5606},
   Keywords = {Aged • Costs and Cost Analysis • Endometrial
             Neoplasms • Female • Humans • Laparoscopy
             • Laparotomy • Lymph Node Excision • Neoplasm
             Staging • Retrospective Studies • economics*
             • pathology • surgery*},
   Abstract = {OBJECTIVE: The purpose of this study was to determine
             whether the cost associated with treatment of early stage
             endometrial cancer differs on the basis of the surgical
             approach. METHODS: A retrospective analysis was performed on
             a series of women with presumed early stage endometrial
             cancer treated between 5/96 and 1/99 at a single
             institution. The patients were grouped according to the
             surgical approach utilized. The first group consisted of 19
             patients who underwent laparoscopic assisted vaginal
             hysterectomy, bilateral salpingo-oophorectomy, and
             laparoscopic pelvic and paraaortic lymph node dissection.
             The second group consisted of 17 patients who underwent a
             total abdominal hysterectomy, bilateral salpingo-oophorectomy,
             and pelvic and paraaortic lymph node dissection. The two
             groups were compared with a two-tailed Student t test.
             Variables analyzed included age, Quetelet index (QI),
             surgical stage, number of lymph nodes, surgical time,
             estimated blood loss, postoperative complications, number of
             days in the hospital, and costs. The cost analysis was
             divided into room and board, pharmacy, ancillary services,
             operating room equipment, operating room services, and
             anesthesia. RESULTS: Both groups were similar in age, QI,
             and distribution of stage. The laparoscopic group required
             more OR time (237 vs 157 min, P < 0.001); however, the
             number of lymph nodes, estimated blood loss, and
             postoperative complications were not significantly different
             between the groups. The laparoscopic group required
             significantly shorter hospitalization than the laparotomy
             group (3.7 vs 5.2 days, P < 0.001) resulting in less room
             and board ($299 vs $454, P < 0.001) as well as pharmacy
             costs ($443 vs $625, P < 0.02). The cost of anesthesia was
             higher in the laparoscopic group ($696 vs $444, P < 0.001)
             but the costs of OR equipment, OR services, and total costs
             were not statistically different between the groups.
             CONCLUSION: Laparoscopic surgical management of early stage
             endometrial cancer is feasible with minimal morbidity. The
             cost savings of early hospital discharge is offset by longer
             surgical time and higher anesthetic costs. The total costs
             for each surgical approach are not statistically different.
             The presumed advantages of less pain, early resumption of
             normal activities, and overall improvement of quality of
             life await further investigation.},
   Language = {eng},
   Doi = {10.1006/gyno.1999.5606},
   Key = {fds174313}
}

@booklet{Johnson93a,
   Author = {G. A. Johnson and M. S. Defelice and Z. R.
             Helsel},
   Title = {Cover crop management and weed-control in corn
             (zea-mays)},
   Journal = {Weed Technology},
   Volume = {7},
   Number = {2},
   Pages = {425 -- 430},
   Year = {1993},
   Key = {Johnson93a}
}

@article{fds174145,
   Author = {GA Johnson and SJ Boukma and RA Lahti and J Mathews},
   Title = {Cyclic AMP and phosphodiesterase in synaptic vesicles from
             mouse brain.},
   Journal = {Journal of neurochemistry},
   Volume = {20},
   Number = {5},
   Pages = {1387-92},
   Year = {1973},
   Month = {May},
   ISSN = {0022-3042},
   Keywords = {Animals • Brain • Brain Chemistry* • Cattle
             • Cell Fractionation • Centrifugation, Density
             Gradient • Cyclic AMP • Male • Mice •
             Microscopy, Electron • Myocardium • Phosphoric
             Diester Hydrolases • Synaptic Vesicles • Tritium
             • analysis* • cytology • enzymology},
   Language = {eng},
   Key = {fds174145}
}

@article{fds349540,
   Author = {Wang, N and White, LE and Qi, Y and Cofer, G and Johnson,
             GA},
   Title = {Cytoarchitecture of the mouse brain by high resolution
             diffusion magnetic resonance imaging.},
   Journal = {Neuroimage},
   Volume = {216},
   Pages = {116876},
   Year = {2020},
   Month = {August},
   url = {http://dx.doi.org/10.1016/j.neuroimage.2020.116876},
   Abstract = {MRI has been widely used to probe the neuroanatomy of the
             mouse brain, directly correlating MRI findings to histology
             is still challenging due to the limited spatial resolution
             and various image contrasts derived from water relaxation or
             diffusion properties. Magnetic resonance histology has the
             potential to become an indispensable research tool to
             mitigate such challenges. In the present study, we acquired
             high spatial resolution MRI datasets, including diffusion
             MRI (dMRI) at 25 ​μm isotropic resolution and
             quantitative susceptibility mapping (QSM) at 21.5 ​μm
             isotropic resolution to validate with conventional mouse
             brain histology. Diffusion weighted images (DWIs) show
             better delineation of cortical layers and glomeruli in the
             olfactory bulb than fractional anisotropy (FA) maps.
             However, among all the image contrasts, including
             quantitative susceptibility mapping (QSM), T1/T2∗ images
             and DTI metrics, FA maps highlight unique laminar
             architecture in sub-regions of the hippocampus, including
             the strata of the dentate gyrus and CA fields of the
             hippocampus. The mean diffusivity (MD) and axial diffusivity
             (AD) yield higher correlation with DAPI (0.62 and 0.71) and
             NeuN (0.78 and 0.74) than with NF-160 (-0.34 and -0.49). The
             correlations between FA and DAPI, NeuN, and NF-160 are 0.31,
             -0.01, and -0.49, respectively. Our findings demonstrate
             that MRI at microscopic resolution deliver a
             three-dimensional, non-invasive and non-destructive platform
             for characterization of fine structural detail in both gray
             matter and white matter of the mouse brain.},
   Doi = {10.1016/j.neuroimage.2020.116876},
   Key = {fds349540}
}

@article{fds174238,
   Author = {GA Johnson and SM Jalal},
   Title = {DDT-induced chromosomal damage in mice.},
   Journal = {The Journal of heredity},
   Volume = {64},
   Number = {1},
   Pages = {7-8},
   Year = {1973},
   Month = {June},
   ISSN = {0022-1503},
   Keywords = {Animals • Chromatids • Chromosome Aberrations*
             • Chromosomes • DDT • Mice • Mice,
             Inbred BALB C • Mutagens • drug effects •
             drug effects* • pharmacology*},
   Language = {eng},
   Key = {fds174238}
}

@article{fds174292,
   Author = {LE Steadman and GA Johnson and EL Belden and WJ Murdoch},
   Title = {Decline in sialic acid composition of cellular membranes
             isolated from ovine corpora lutea during
             prostaglandin-induced luteolysis: apparent independence of
             autoimmune recognition.},
   Journal = {American journal of reproductive immunology (New York, N.Y.
             : 1989)},
   Volume = {19},
   Number = {1},
   Pages = {1-2},
   Year = {1989},
   Month = {January},
   ISSN = {1046-7408},
   Keywords = {Animals • Autoantibodies • Cell Membrane •
             Corpus Luteum • Dinoprost • Female •
             N-Acetylneuraminic Acid • Sheep • Sialic Acids
             • analysis • analysis* • drug effects •
             pharmacology* • physiology*},
   Abstract = {Sialic acid was quantified in plasma membranes of corpora
             lutea isolated during prostaglandin (PG) F2 alpha-induced
             luteolysis in sheep. Concentrations of sialic acid within
             membranes decreased after injection of PGF2 alpha, and
             before signs of luteal regression (i.e., a decline in tissue
             concentrations of progesterone) were manifested. Removal of
             residues of sialic acid from luteal membranes was not
             associated with cellular binding of gamma globulin, as
             monitored by indirect immunofluorescence microscopy. We
             suggest that desialylation of luteal membranes could be an
             important aspect of the mechanism of luteolysis. Such a
             process does not appear to involve participation of
             autoantibody.},
   Language = {eng},
   Key = {fds174292}
}

@booklet{Steadman89,
   Author = {L. E. Steadman and G. A. Johnson and E. L. Belden and W. J.
             Murdoch},
   Title = {Decline in sialic-acid composition of cellular membranes
             isolated from ovine corpora-lutea during
             prostaglandin-induced luteolysis - apparent independence of
             autoimmune recognition},
   Journal = {American Journal Of Reproductive Immunology},
   Volume = {19},
   Number = {1},
   Pages = {1 -- 2},
   Year = {1989},
   Month = {January},
   Key = {Steadman89}
}

@article{fds132725,
   Author = {G.A. Johnson},
   Title = {Delnomdedieu M, Hedlund LW, maronpot RR, Johson GA, MR
             microscopy and histopathology: Comparative approach to
             bromobenzene-induced hepatoxicity in the rat. hepatology 27;
             526-532 1998},
   Year = {1998},
   Key = {fds132725}
}

@article{fds268788,
   Author = {Clark, D and Johnson, GA and Badea, CT},
   Title = {Denoising of 4D Cardiac Micro-CT Data Using Median-Centric
             Bilateral Filtration.},
   Journal = {Proc SPIE Int Soc Opt Eng},
   Volume = {8314},
   Year = {2012},
   Month = {February},
   ISSN = {1605-7422},
   url = {http://dx.doi.org/10.1117/12.911478},
   Abstract = {Bilateral filtration has proven an effective tool for
             denoising CT data. The classic filter utilizes Gaussian
             domain and range weighting functions in 2D. More recently,
             other distributions have yielded more accurate results in
             specific applications, and the bilateral filtration
             framework has been extended to higher dimensions. In this
             study, brute-force optimization is employed to evaluate the
             use of several alternative distributions for both domain and
             range weighting: Andrew's Sine Wave, El Fallah Ford,
             Gaussian, Flat, Lorentzian, Huber's Minimax, Tukey's
             Bi-weight, and Cosine. Two variations on the classic
             bilateral filter which use median filtration to reduce bias
             in range weights are also investigated: median-centric and
             hybrid bilateral filtration. Using the 4D MOBY mouse phantom
             reconstructed with noise (stdev. ~ 65 HU), hybrid bilateral
             filtration, a combination of the classic and median-centric
             filters, with Flat domain and range weighting is shown to
             provide optimal denoising results (PSNRs: 31.69, classic;
             31.58 median-centric; 32.25, hybrid). To validate these
             phantom studies, the optimal filters are also applied to in
             vivo, 4D cardiac micro-CT data acquired in the mouse. In a
             constant region of the left ventricle, hybrid bilateral
             filtration with Flat domain and range weighting is shown to
             provide optimal smoothing (stdev: original, 72.2 HU;
             classic, 20.3 HU; median-centric, 24.1 HU; hybrid, 15.9 HU).
             While the optimal results were obtained using 4D filtration,
             the 3D hybrid filter is ultimately recommended for denoising
             4D cardiac micro-CT data because it is more computationally
             tractable and less prone to artifacts (MOBY PSNR: 32.05;
             left ventricle stdev: 20.5 HU).},
   Doi = {10.1117/12.911478},
   Key = {fds268788}
}

@booklet{Todd01a,
   Author = {M. D. Todd and G. A. Johnson and S. T. Vohra},
   Title = {Depolyment of a fiber Bragg grating-based measurement system
             in a structural health monitoring application},
   Journal = {Smart Materials \& Structures},
   Volume = {10},
   Number = {3},
   Pages = {534 -- 539},
   Year = {2001},
   Month = {June},
   Key = {Todd01a}
}

@booklet{Hayes84,
   Author = {HAYES, CE and JOHNSON, GA and HERFKENS, RJ},
   Title = {DESIGN CONSIDERATIONS FOR SMALL ANIMAL IMAGING IN A LARGE
             BORE MRI SYSTEM},
   Journal = {INVESTIGATIVE RADIOLOGY},
   Volume = {19},
   Number = {5},
   Pages = {S25-S25},
   Publisher = {LIPPINCOTT-RAVEN PUBL},
   Year = {1984},
   Month = {January},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1984TL42800118&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Hayes84}
}

@article{fds268848,
   Author = {Nouls, JC and Izenson, MG and Greeley, HP and Johnson,
             GA},
   Title = {Design of a superconducting volume coil for magnetic
             resonance microscopy of the mouse brain.},
   Journal = {J Magn Reson},
   Volume = {191},
   Number = {2},
   Pages = {231-238},
   Year = {2008},
   Month = {April},
   ISSN = {1090-7807},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/18221901},
   Keywords = {Animals • Brain • Electric Conductivity •
             Equipment Design • Equipment Failure Analysis •
             Magnetic Resonance Imaging • Magnetics • Mice
             • Microscopy • Transducers • cytology* •
             instrumentation* • methods* • veterinary •
             veterinary*},
   Abstract = {We present the design process of a superconducting volume
             coil for magnetic resonance microscopy of the mouse brain at
             9.4T. The yttrium barium copper oxide coil has been designed
             through an iterative process of three-dimensional
             finite-element simulations and validation against room
             temperature copper coils. Compared to previous designs, the
             Helmholtz pair provides substantially higher B(1)
             homogeneity over an extended volume of interest sufficiently
             large to image biologically relevant specimens. A
             custom-built cryogenic cooling system maintains the
             superconducting probe at 60+/-0.1K. Specimen loading and
             probe retuning can be carried out interactively with the
             coil at operating temperature, enabling much higher
             through-put. The operation of the probe is a routine,
             consistent procedure. Signal-to-noise ratio in a mouse brain
             increased by a factor ranging from 1.1 to 2.9 as compared to
             a room-temperature solenoid coil optimized for mouse brain
             microscopy. We demonstrate images encoded at 10x10x20mum for
             an entire mouse brain specimen with signal-to-noise ratio of
             18 and a total acquisition time of 16.5h, revealing
             neuroanatomy unseen at lower resolution. Phantom
             measurements show an effective spatial resolution better
             than 20mum.},
   Doi = {10.1016/j.jmr.2007.12.018},
   Key = {fds268848}
}

@article{fds132860,
   Author = {X Zhou and RR Maronpot and LW Hedlund and GP Cofer and GA
             Johnson},
   Title = {Detection of bromobenzene-induced hepatocellular necrosis
             using magnetic resonance microscopy.},
   Journal = {Magnetic resonance in medicine : official journal of the
             Society of Magnetic Resonance in Medicine / Society of
             Magnetic Resonance in Medicine, UNITED STATES},
   Volume = {34},
   Number = {6},
   Pages = {853-7},
   Year = {1995},
   Month = {December},
   ISSN = {0740-3194},
   Keywords = {Animals • Bromobenzenes • Dose-Response
             Relationship, Drug • Female • Image Processing,
             Computer-Assisted • Liver • Magnetic Resonance
             Spectroscopy • Necrosis • Rats • Rats, Inbred
             F344 • Sensitivity and Specificity • diagnostic
             use* • drug effects* • methods • pathology
             • toxicity*},
   Abstract = {The authors used magnetic resonance (MR) microscopy to
             assess hepatic tissue damage induced by bromobenzene both in
             living rats and in fixed rat liver tissues. Experiments were
             conducted at 7 Tesla on three groups of Fisher rats treated
             with bromobenzene at a single dose of 68, 135, and 269
             mg/kg, respectively. Optical microscopy of hematoxylin and
             eosin stained sections showed liver damage only at the
             highest dose, whereas with MR microscopy, tissue alterations
             were detected at all three doses both in vivo and ex vivo.
             The contrast mechanism of the superior sensitivity of MR
             microscopy is believed to be related to the changes in local
             diffusion coefficients that accompany cellular degeneration
             and death, although other contrast mechanisms may also be
             involved. The superior sensitivity of MR microscopy, as
             demonstrated in this study, has many implications for
             potential use of MR techniques to perform in vivo
             histology.},
   Key = {fds132860}
}

@booklet{Zhou95,
   Author = {Zhou, X and Maronpot, RR and Hedlund, LW and Cofer, GP and Johnson,
             GA},
   Title = {Detection of bromobenzene-induced hepatocellular necrosis
             using magnetic resonance microscopy.},
   Journal = {Magn Reson Med},
   Volume = {34},
   Number = {6},
   Pages = {853-857},
   Year = {1995},
   Month = {December},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/8598812},
   Abstract = {The authors used magnetic resonance (MR) microscopy to
             assess hepatic tissue damage induced by bromobenzene both in
             living rats and in fixed rat liver tissues. Experiments were
             conducted at 7 Tesla on three groups of Fisher rats treated
             with bromobenzene at a single dose of 68, 135, and 269
             mg/kg, respectively. Optical microscopy of hematoxylin and
             eosin stained sections showed liver damage only at the
             highest dose, whereas with MR microscopy, tissue alterations
             were detected at all three doses both in vivo and ex vivo.
             The contrast mechanism of the superior sensitivity of MR
             microscopy is believed to be related to the changes in local
             diffusion coefficients that accompany cellular degeneration
             and death, although other contrast mechanisms may also be
             involved. The superior sensitivity of MR microscopy, as
             demonstrated in this study, has many implications for
             potential use of MR techniques to perform in vivo
             histology.},
   Doi = {10.1002/mrm.1910340610},
   Key = {Zhou95}
}

@article{fds269111,
   Author = {Chen, XJ and Hedlund, LW and Möller, HE and Chawla, MS and Maronpot,
             RR and Johnson, GA},
   Title = {Detection of emphysema in rat lungs by using magnetic
             resonance measurements of 3He diffusion.},
   Journal = {Proc Natl Acad Sci U S A},
   Volume = {97},
   Number = {21},
   Pages = {11478-11481},
   Year = {2000},
   Month = {October},
   ISSN = {0027-8424},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/11027348},
   Keywords = {Animals • Emphysema • Helium • Humans •
             Lung • Magnetic Resonance Imaging • Male •
             Rats • Rats, Inbred F344 • diagnosis* •
             pathology*},
   Abstract = {Emphysema is a pulmonary disease characterized by alveolar
             wall destruction, resulting in enlargement of gas exchange
             spaces without fibrosis. This condition is a part of chronic
             obstructive pulmonary disease (COPD), which causes 3.5% of
             deaths worldwide [Anonymous (1990) World Health Stat. Q.
             Special, 1-51] and contributes greatly to the global burden
             of disease [Murray, C. J. & Lopez, A. D. (1996) Science 274,
             740-743]. Alveolar regeneration has been shown in animal
             models and could have potential for clinical treatment of
             early-stage emphysema. However, current techniques for
             detection of emphysema are not sensitive at the initial
             stages. Early-stage human panacinar emphysema is modeled in
             elastase-treated animals. Here, we provide an in vivo
             imaging method for differentiating normal and emphysematous
             rat lungs by measuring the apparent diffusion coefficient
             (ADC) of hyperpolarized (3)He by using magnetic resonance
             imaging. These data show that the ADC is significantly
             larger in elastase-treated rats, indicating alveolar
             expansion. Whereas these rats were clinically asymptomatic,
             conventional histology confirmed presence of injury. Our
             results indicate that measurement of the hyperpolarized
             (3)He ADC can be a valuable research tool and has potential
             application in the clinical setting.},
   Doi = {10.1073/pnas.97.21.11478},
   Key = {fds269111}
}

@booklet{Chen00,
   Author = {X. J. Chen and L. W. Hedlund and H. E. Moller and M. S.
             Chawla and R. R. Maronpot and G. A. Johnson},
   Title = {Detection of emphysema in rat lungs by using magnetic
             resonance measurements of He-3 diffusion},
   Journal = {Proceedings Of The National Academy Of Sciences Of The
             United States Of America},
   Volume = {97},
   Number = {21},
   Pages = {11478 -- 11481},
   Year = {2000},
   Month = {October},
   Key = {Chen00}
}

@article{fds268798,
   Author = {Smith, WM and Hsu, JCM and Johnson, GA and Reimer, KA and Ideker,
             RE},
   Title = {Detection of infarcted tissue the heart by magnetic
             resonance imaging},
   Journal = {Proceedings of the Annual Conference on Engineering in
             Medicine and Biology},
   Volume = {15},
   Number = {pt 1},
   Pages = {485-486},
   Year = {1993},
   Month = {December},
   Abstract = {Morphological analysis of myocardial infarct structure has
             demonstrated that there is probably an anatomical basis for
             the induction and maintenance of ventricular tachycardia.
             The further study of this phenomenon requires an efficient,
             accurate method for quantitative analysis of pathological
             anatomy. We have evaluated the ability of magnetic resonance
             imaging to distinguish between normal and infarcted tissue
             in formalin-fixed human hearts with distant myocardial
             infarctions.},
   Key = {fds268798}
}

@article{fds268897,
   Author = {Benveniste, H and Einstein, G and Kim, KR and Hulette, C and Johnson,
             GA},
   Title = {Detection of neuritic plaques in Alzheimer's disease by
             magnetic resonance microscopy.},
   Journal = {Proc Natl Acad Sci U S A},
   Volume = {96},
   Number = {24},
   Pages = {14079-14084},
   Year = {1999},
   Month = {November},
   ISSN = {0027-8424},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/10570201},
   Keywords = {Aged • Aged, 80 and over • Alzheimer Disease
             • Coloring Agents • Humans • Magnetic
             Resonance Imaging • Middle Aged • Protons •
             Senile Plaques • methods • pathology*},
   Abstract = {Magnetic resonance microscopy (MRM) theoretically provides
             the spatial resolution and signal-to-noise ratio needed to
             resolve neuritic plaques, the neuropathological hallmark of
             Alzheimer's disease (AD). Two previously unexplored MR
             contrast parameters, T2* and diffusion, are tested for
             plaque-specific contrast to noise. Autopsy specimens from
             nondemented controls (n = 3) and patients with AD (n = 5)
             were used. Three-dimensional T2* and diffusion MR images
             with voxel sizes ranging from 3 x 10(-3) mm(3) to 5.9 x
             10(-5) mm(3) were acquired. After imaging, specimens were
             cut and stained with a microwave king silver stain to
             demonstrate neuritic plaques. From controls, the alveus,
             fimbria, pyramidal cell layer, hippocampal sulcus, and
             granule cell layer were detected by either T2* or diffusion
             contrast. These structures were used as landmarks when
             correlating MRMs with histological sections. At a voxel
             resolution of 5.9 x 10(-5) mm(3), neuritic plaques could be
             detected by T2*. The neuritic plaques emerged as black,
             spherical elements on T2* MRMs and could be distinguished
             from vessels only in cross-section when presented in three
             dimension. Here we provide MR images of neuritic plaques in
             vitro. The MRM results reported provide a new direction for
             applying this technology in vivo. Clearly, the ability to
             detect and follow the early progression of amyloid-positive
             brain lesions will greatly aid and simplify the many
             possibilities to intervene pharmacologically in
             AD.},
   Doi = {10.1073/pnas.96.24.14079},
   Key = {fds268897}
}

@booklet{Anderson93a,
   Author = {C. S. Anderson and K. D. Jamrozik and P. W. Burvill and T.
             M. H. Chakera and G. A. Johnson and E. G.
             Stewartwynne},
   Title = {Determining the incidence of different subtypes of stroke -
             results from the perth community stroke study,
             1989-1990},
   Journal = {Medical Journal Of Australia},
   Volume = {158},
   Number = {2},
   Pages = {85 -- 89},
   Year = {1993},
   Month = {January},
   Key = {Anderson93a}
}

@article{fds174307,
   Author = {CS Anderson and KD Jamrozik and PW Burvill and TM Chakera and GA
             Johnson, EG Stewart-Wynne},
   Title = {Determining the incidence of different subtypes of stroke:
             results from the Perth Community Stroke Study,
             1989-1990.},
   Journal = {The Medical journal of Australia},
   Volume = {158},
   Number = {2},
   Pages = {85-9},
   Year = {1993},
   Month = {January},
   ISSN = {0025-729X},
   Keywords = {Adult • Aged • Aged, 80 and over • Cerebral
             Hemorrhage • Cerebral Infarction • Cerebrovascular
             Disorders • Female • Humans • Intracranial
             Embolism and Thrombosis • Male • Middle Aged
             • Western Australia • classification* •
             epidemiology • epidemiology*},
   Abstract = {OBJECTIVE: To determine the incidence and case fatality of
             seven distinct subtypes of stroke in Perth, Western
             Australia. DESIGN AND SETTING: A population-based
             descriptive epidemiological study. SUBJECTS: All residents
             of a geographically defined segment of the Perth
             metropolitan area (estimated population 138,708 persons) who
             had a stroke or transient ischaemic attack between 20
             February 1989 and 19 August 1990, inclusive. MAIN OUTCOME
             MEASURES: The following subtypes of stroke were classified
             according to standard clinical, radiological and
             pathological criteria: types of cerebral infarction, namely,
             large artery (thrombotic) occlusive infarction (LAOI),
             cerebral embolic infarction (EMBI), lacunar infarction
             (LACI) and boundary zone infarction (BZI); primary
             intracerebral haemorrhage (PICH); subarachnoid haemorrhage
             (SAH); and stroke of undetermined cause. RESULTS: Over the
             18-month study period 536 stroke events were registered, of
             which 86% (95% confidence interval, 83%-89%) had a defined
             "pathological" diagnosis on the basis of computed
             tomographic scanning, magnetic resonance imaging or
             necropsy. Cerebral infarction accounted for 71% of cases
             (95% CI, 68%-75%), PICH 11% (95% CI, 9%-14%) and SAH 4% (95%
             CI, 2%-5%). The 382 cases of cerebral infarction included
             LAOI (in approximately 71%), EMBI (15%), LACI (10%) and BZI
             (5%). While the incidence of all subtypes of stroke
             increased with age, there were age and sex differences in
             their proportional frequency, management and prognosis:
             patients with PICH, SAH and EMBI were more likely to be
             admitted to hospital, and these conditions carried the
             highest early case fatality. Over all, the 28-day case
             fatality was 24% (95% CI, 20%-28%), but varied from 0 for
             LACI and BZI, to 37% (95% CI, 15%-59%) for SAH and 35% (CI,
             23%-47%) for PICH. CONCLUSIONS: In this study, we found
             considerable differences in incidence rates, the effect of
             age and sex on incidence rates, and prognosis for the
             different subtypes of stroke. Hospital-based studies are
             likely to be selectively biased by emphasising strokes that
             are severe and require admission to hospital. These data
             have important implications in the design and evaluation of
             clinical trials of therapy for stroke.},
   Language = {eng},
   Key = {fds174307}
}

@booklet{Johnson99a,
   Author = {G. A. Johnson and R. C. Burghardt and G. R. Newton and F. W.
             Bazer and T. E. Spencer},
   Title = {Development and characterization of immortalized ovine
             endometrial cell lines},
   Journal = {Biology Of Reproduction},
   Volume = {61},
   Number = {5},
   Pages = {1324 -- 1330},
   Year = {1999},
   Month = {November},
   Key = {Johnson99a}
}

@article{fds174198,
   Author = {GA Johnson and RC Burghardt and GR Newton and FW Bazer and TE
             Spencer},
   Title = {Development and characterization of immortalized ovine
             endometrial cell lines.},
   Journal = {Biology of reproduction},
   Volume = {61},
   Number = {5},
   Pages = {1324-30},
   Year = {1999},
   Month = {November},
   ISSN = {0006-3363},
   Keywords = {Animals • Blotting, Western • Cell Line •
             Cell Nucleus • DNA-Binding Proteins • Endocrine
             System • Endometrium • Female • Fluorescent
             Antibody Technique, Direct • Interferon Regulatory
             Factor-1 • Interferon Type I • Microscopy,
             Fluorescence • Paracrine Communication •
             Phosphoproteins • Pregnancy Proteins • Receptors,
             Estrogen • Receptors, Progesterone • Recombinant
             Proteins • Sheep • Signal Transduction •
             Transcription Factors • Ubiquitins • analogs &
             derivatives • biosynthesis • cytology* •
             metabolism • physiology},
   Abstract = {The objective of this study was to generate immortalized
             endometrial epithelial and stromal cell lines from the ovine
             uterus. Luminal (LE) and glandular epithelial (GE) cells and
             stromal (ST) cells were enzymatically isolated from the
             uterus of a Day 5 cyclic ewe (estrus on Day 0), and primary
             cultures were immortalized by transduction with a retroviral
             vector (LXSN-16E6E7) packaged by the amphotropic fibroblast
             line PA-317. Cells having integrated the vector were
             selected by resistance to the neomycin analogue G418
             (0.6-0.8 mg/ml). Surviving cells were maintained in complete
             culture medium containing G418 (0.1 mg/ml) and subcultured
             for more than 40 passages. Phase-contrast microscopy
             revealed that LE and GE cells exhibited a cobblestone
             morphology whereas immortalized ST cells were spindle
             shaped. The epithelial origin of LE and GE was confirmed by
             positive cytokeratin immunostaining, and ST cells were
             vimentin positive. All cell lines were negative for smooth
             muscle alpha-actin staining. Western blot analyses of cell
             extracts revealed the presence of signal transducers and
             activators of transcription (STAT) proteins 1, 2, and 3. In
             the LE cells, interferon tau (IFNtau) induced nuclear
             translocation of STAT proteins 1 and 2 and up-regulated
             several IFN-inducible genes, including STATs 1, 2, and 3 and
             ubiquitin cross-reactive protein (UCRP/ISG17). In the LE
             cell line, IFN regulatory factor one was transiently
             up-regulated and then down-regulated by IFNtau.
             Immunostaining revealed the presence of nuclear estrogen
             receptor and progesterone receptor in all cell lines. These
             ovine endometrial cell lines provide useful in vitro model
             systems for the study of hormone and cytokine action, signal
             transduction pathways, cell-cell interactions, and gene
             expression in specific cell types of the ovine
             endometrium.},
   Language = {eng},
   Key = {fds174198}
}

@booklet{Spencer99b,
   Author = {T. E. Spencer and G. A. Johnson and R. C. Burghardt and J.
             A. G. W. Fleming and F. W. Bazer},
   Title = {Development and characterization of immortalized ovine
             endometrial cell lines.},
   Journal = {Biology Of Reproduction},
   Volume = {60},
   Pages = {142 -- 142},
   Year = {1999},
   Key = {Spencer99b}
}

@booklet{Stern88,
   Author = {STERN, RL and CLINE, HE and JOHNSON, GA and RAVIN,
             CE},
   Title = {DEVELOPMENT OF A 3D RECONSTRUCTED-IMAGE SURGICAL PLANNING
             STATION},
   Journal = {INVESTIGATIVE RADIOLOGY},
   Volume = {23},
   Number = {9},
   Pages = {S60-S60},
   Publisher = {LIPPINCOTT-RAVEN PUBL},
   Year = {1988},
   Month = {September},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1988Q574500240&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Stern88}
}

@booklet{Segars04,
   Author = {Segars, WP and Tsui, BMW and Frey, EC and Johnson, GA and Berr,
             SS},
   Title = {Development of a 4-D digital mouse phantom for molecular
             imaging research.},
   Journal = {Mol Imaging Biol},
   Volume = {6},
   Number = {3},
   Pages = {149-159},
   Year = {2004},
   ISSN = {1536-1632},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/15193249},
   Abstract = {PURPOSE: We develop a realistic and flexible 4-D digital
             mouse phantom and investigate its usefulness in molecular
             imaging research. METHODS: Organ shapes were modeled with
             non-uniform rational B-spline (NURBS) surfaces based on
             high-resolution 3-D magnetic resonance microscopy (MRM)
             data. Cardiac and respiratory motions were modeled based on
             gated magnetic resonance imaging (MRI) data obtained from
             normal mice. Pilot simulation studies in single-photon
             emission computed tomography (SPECT) and X-ray computed
             tomography (CT) were performed to demonstrate the utility of
             the phantom. RESULTS: NURBS are an efficient and flexible
             way to accurately model the anatomy and cardiac and
             respiratory motions for a realistic 4-D digital mouse
             phantom. The phantom is capable of producing realistic
             molecular imaging data from which imaging devices and
             techniques can be evaluated. CONCLUSION: The phantom
             provides a unique and useful tool in molecular imaging
             research. It can be used in the development of new imaging
             instrumentation, image acquisition strategies, and image
             processing and reconstruction methods.},
   Doi = {10.1016/j.mibio.2004.03.002},
   Key = {Segars04}
}

@article{fds132894,
   Author = {WP Segars and BM Tsui and EC Frey and GA Johnson and SS
             Berr},
   Title = {Development of a 4-D digital mouse phantom for molecular
             imaging research.},
   Journal = {Molecular imaging and biology : MIB : the official
             publication of the Academy of Molecular Imaging, United
             States},
   Volume = {6},
   Number = {3},
   Pages = {149-59},
   ISSN = {1536-1632},
   Keywords = {Animals • Image Processing, Computer-Assisted •
             Mice • Models, Anatomic* • Models, Animal* •
             Phantoms, Imaging* • Tomography, Emission-Computed,
             Single-Photon • Tomography, X-Ray Computed •
             anatomy & histology* • instrumentation •
             instrumentation* • physiology},
   Abstract = {PURPOSE: We develop a realistic and flexible 4-D digital
             mouse phantom and investigate its usefulness in molecular
             imaging research. METHODS: Organ shapes were modeled with
             non-uniform rational B-spline (NURBS) surfaces based on
             high-resolution 3-D magnetic resonance microscopy (MRM)
             data. Cardiac and respiratory motions were modeled based on
             gated magnetic resonance imaging (MRI) data obtained from
             normal mice. Pilot simulation studies in single-photon
             emission computed tomography (SPECT) and X-ray computed
             tomography (CT) were performed to demonstrate the utility of
             the phantom. RESULTS: NURBS are an efficient and flexible
             way to accurately model the anatomy and cardiac and
             respiratory motions for a realistic 4-D digital mouse
             phantom. The phantom is capable of producing realistic
             molecular imaging data from which imaging devices and
             techniques can be evaluated. CONCLUSION: The phantom
             provides a unique and useful tool in molecular imaging
             research. It can be used in the development of new imaging
             instrumentation, image acquisition strategies, and image
             processing and reconstruction methods.},
   Key = {fds132894}
}

@article{fds268840,
   Author = {Zhang, X and Badea, C and Jacob, M and Johnson, GA},
   Title = {Development of a noncontact 3-D fluorescence tomography
             system for small animal in vivo imaging.},
   Journal = {Proc SPIE Int Soc Opt Eng},
   Volume = {7191},
   Pages = {nihpa106691},
   Year = {2009},
   Month = {February},
   ISSN = {0277-786X},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/19587837},
   Abstract = {Fluorescence imaging is an important tool for tracking
             molecular-targeting probes in preclinical studies. It offers
             high sensitivity, but nonetheless low spatial resolution
             compared to other leading imaging methods such CT and MRI.
             We demonstrate our methodological development in small
             animal in vivo whole-body imaging using fluorescence
             tomography. We have implemented a noncontact fluid-free
             fluorescence diffuse optical tomography system that uses a
             raster-scanned continuous-wave diode laser as the light
             source and an intensified CCD camera as the photodetector.
             The specimen is positioned on a motorized rotation stage.
             Laser scanning, data acquisition, and stage rotation are
             controlled via LabVIEW applications. The forward problem in
             the heterogeneous medium is based on a normalized Born
             method, and the sensitivity function is determined using a
             Monte Carlo method. The inverse problem (image
             reconstruction) is performed using a regularized iterative
             algorithm, in which the cost function is defined as a
             weighted sum of the L-2 norms of the solution image, the
             residual error, and the image gradient. The relative weights
             are adjusted by two independent regularization parameters.
             Our initial tests of this imaging system were performed with
             an imaging phantom that consists of a translucent plastic
             cylinder filled with tissue-simulating liquid and two
             thin-wall glass tubes containing indocyanine green. The
             reconstruction is compared to the output of a finite element
             method-based software package NIRFAST and has produced
             promising results.},
   Doi = {10.1117/12.808199},
   Key = {fds268840}
}

@booklet{Ruwart90,
   Author = {M. J. Ruwart and S. K. Sharma and D. W. Harris and D. B.
             Lakings and B. D. Rush and K. F. Wilkinson and J. C.
             Cornette and D. B. Evans and J. M. Friis and K. J. Cook and G. A. Johnson},
   Title = {Development of a sensitive activity assay for high-volume
             evaluation of human renin inhibitory peptides in rat serum -
             results with u-71,038},
   Journal = {Pharmaceutical Research},
   Volume = {7},
   Number = {4},
   Pages = {407 -- 410},
   Year = {1990},
   Month = {April},
   Key = {Ruwart90}
}

@article{fds174226,
   Author = {M Zeiler and R Leiser and GA Johnson and HR Tinneberg and C
             Pfarrer},
   Title = {Development of an in vitro model for bovine placentation: a
             comparison of the in vivo and in vitro expression of
             integrins and components of extracellular matrix in bovine
             placental cells.},
   Journal = {Cells, tissues, organs},
   Volume = {186},
   Number = {4},
   Pages = {229-42},
   Year = {2007},
   ISSN = {1422-6421},
   url = {http://dx.doi.org/10.1159/000107947},
   Keywords = {Animals • Cattle • Cells, Cultured •
             Cytoskeleton • Embryo, Mammalian • Extracellular
             Matrix* • Female • Humans • Integrins •
             Placenta* • Pregnancy • Protein Subunits •
             Trophoblasts • Uterus • chemistry • cytology
             • genetics • metabolism • metabolism* •
             physiology},
   Abstract = {BACKGROUND/AIMS: Interaction of trophoblastic integrins with
             the extracellular matrix plays a role in embryo implantation
             and trophoblast invasion. The phenomenon of restricted
             trophoblast invasion, observed in the bovine
             epitheliochorial placenta offers intriguing conditions to
             study invasive processes. The migration of bovine
             trophoblast giant cells is accompanied by the expression of
             specific integrins and corresponding extracellular matrix
             ligands. METHODS: Primary cultures of different cell
             populations from cow placentomes were established and
             characterized, and in vitro phenotypes were compared with in
             vivo conditions by immunofluorescence. RESULTS: Propagated
             epithelial cells were positive for cytokeratin and vimentin,
             while fibroblasts contained alpha-smooth muscle actin,
             desmin and vimentin. Epithelial cells coexpressed integrin
             subunits alpha(6) and beta(1) with laminin, and fibroblast
             cells were positive for alpha(v), beta(3), fibronectin and
             laminin. In contrast to cells in vivo, cultured epithelial
             cells secreted fibronectin, while collagen IV was not
             detected. The occurrence of integrin subunits was confirmed
             at mRNA level by RT-PCR. CONCLUSION: We have established
             cell cultures isolated from maternal and fetal components of
             bovine placentomes expressing typical cytoskeletal filaments
             and integrin receptors also present in their in vivo
             counterparts. These bovine placentomal cells provide a
             suitable in vitro model for the study of cell-cell
             interactions.},
   Language = {eng},
   Doi = {10.1159/000107947},
   Key = {fds174226}
}

@booklet{Gray01,
   Author = {C. A. Gray and F. F. Bartol and B. J. Tarleton and A. A.
             Wiley and G. A. Johnson and F. W. Bazer and T. E.
             Spencer},
   Title = {Developmental biology of uterine glands},
   Journal = {Biology Of Reproduction},
   Volume = {65},
   Number = {5},
   Pages = {1311 -- 1323},
   Year = {2001},
   Month = {November},
   Key = {Gray01}
}

@article{fds174253,
   Author = {CA Gray and FF Bartol and BJ Tarleton and AA Wiley and GA Johnson and FW
             Bazer, TE Spencer},
   Title = {Developmental biology of uterine glands.},
   Journal = {Biology of reproduction},
   Volume = {65},
   Number = {5},
   Pages = {1311-23},
   Year = {2001},
   Month = {November},
   ISSN = {0006-3363},
   Keywords = {Animals • Endometrium • Estradiol • Female
             • Humans • Morphogenesis • Prolactin •
             Receptors, Estradiol • Receptors, Prolactin •
             Uterus • embryology • embryology* •
             physiology},
   Abstract = {All mammalian uteri contain endometrial glands that
             synthesize or transport and secrete substances essential for
             survival and development of the conceptus (embryo/fetus and
             associated extraembryonic membranes). In rodents, uterine
             secretory products of the endometrial glands are
             unequivocally required for establishment of uterine
             receptivity and conceptus implantation. Analyses of the
             ovine uterine gland knockout model support a primary role
             for endometrial glands and, by default, their secretions in
             peri-implantation conceptus survival and development.
             Uterine adenogenesis is the process whereby endometrial
             glands develop. In humans, this process begins in the fetus,
             continues postnatally, and is completed during puberty. In
             contrast, endometrial adenogenesis is primarily a postnatal
             event in sheep, pigs, and rodents. Typically, endometrial
             adenogenesis involves differentiation and budding of
             glandular epithelium from luminal epithelium, followed by
             invagination and extensive tubular coiling and branching
             morphogenesis throughout the uterine stroma to the
             myometrium. This process requires site-specific alterations
             in cell proliferation and extracellular matrix (ECM)
             remodeling as well as paracrine cell-cell and cell-ECM
             interactions that support the actions of specific hormones
             and growth factors. Studies of uterine development in
             neonatal ungulates implicate prolactin, estradiol-17 beta,
             and their receptors in mechanisms regulating endometrial
             adenogenesis. These same hormones appear to regulate
             endometrial gland morphogenesis in menstruating primates and
             humans during reconstruction of the functionalis from the
             basalis endometrium after menses. In sheep and pigs,
             extensive endometrial gland hyperplasia and hypertrophy
             occur during gestation, presumably to provide increasing
             histotrophic support for conceptus growth and development.
             In the rabbit, sheep, and pig, a servomechanism is proposed
             to regulate endometrial gland development and differentiated
             function during pregnancy that involves sequential actions
             of ovarian steroid hormones, pregnancy recognition signals,
             and lactogenic hormones from the pituitary or placenta. That
             disruption of uterine development during critical
             organizational periods can alter the functional capacity and
             embryotrophic potential of the adult uterus reinforces the
             importance of understanding the developmental biology of
             uterine glands. Unexplained high rates of peri-implantation
             embryonic loss in humans and livestock may reflect defects
             in endometrial gland morphogenesis due to genetic errors,
             epigenetic influences of endocrine disruptors, and
             pathological lesions.},
   Language = {eng},
   Key = {fds174253}
}

@booklet{Wu03,
   Author = {G. Y. Wu and J. T. Self and G. A. Johnson and F. W. Bazer and T. E. Spencer},
   Title = {Developmental changes in placental nitric oxide synthesis in
             pigs},
   Journal = {Biology Of Reproduction},
   Volume = {68},
   Pages = {153 -- 153},
   Year = {2003},
   Key = {Wu03}
}

@booklet{Kelly01,
   Author = {S. J. Kelly and M. Delnomdedieu and M. I. Oliverio and L. D.
             Williams and M. G. P. Saifer and M. R. Sherman and T. M.
             Coffman and G. A. Johnson and M. S. Hershfield},
   Title = {Diabetes insipidus in uricase-deficient mice: A model for
             evaluating therapy with poly(ethylene glycol)-modified
             uricase},
   Journal = {Journal Of The American Society Of Nephrology},
   Volume = {12},
   Number = {5},
   Pages = {1001 -- 1009},
   Year = {2001},
   Month = {May},
   Key = {Kelly01}
}

@article{fds269101,
   Author = {Kelly, SJ and Delnomdedieu, M and Oliverio, MI and Williams, LD and Saifer, MGP and Sherman, MR and Coffman, TM and Johnson, GA and Hershfield, MS},
   Title = {Diabetes insipidus in uricase-deficient mice: a model for
             evaluating therapy with poly(ethylene glycol)-modified
             uricase.},
   Journal = {J Am Soc Nephrol},
   Volume = {12},
   Number = {5},
   Pages = {1001-1009},
   Year = {2001},
   Month = {May},
   ISSN = {1046-6673},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/11316859},
   Keywords = {Animals • Body Water • Diabetes Insipidus •
             Disease Models, Animal • Gout • Humans •
             Kidney Concentrating Ability • Mice • Mice, Inbred
             C57BL • Mice, Knockout • Polyethylene Glycols
             • Recombinant Proteins • Urate Oxidase • Uric
             Acid • deficiency* • drug therapy • drug
             therapy* • enzymology* • genetics •
             metabolism • pathology • physiopathology •
             therapeutic use • therapeutic use* •
             urine},
   Abstract = {Uricase-deficient mice develop uric acid nephropathy, with
             high mortality rates before weaning. Urate excretion was
             quantitated and renal function was better defined in this
             study, to facilitate the use of these mice as a model for
             evaluating poly(ethylene glycol)-modified recombinant
             mammalian uricases (PEG-uricase) as a potential therapy for
             gout and uric acid nephropathy. The uric acid/creatinine
             ratio in the urine of uricase-deficient mice ranges from 10
             to >30; on a weight basis, these mice excrete 20- to 40-fold
             more urate than do human subjects. These mice consistently
             develop a severe defect in renal concentrating ability,
             resulting in an approximately sixfold greater urine volume
             and a fivefold greater fluid requirement, compared with
             normal mice. This nephrogenic diabetes insipidus leads to
             dehydration and death of nursing mice but, with adequate
             water replacement, high urine flow protects adults from
             progressive renal damage. Treatment of uricase-deficient
             mice with PEG-uricase markedly reduced urate levels and,
             when initiated before weaning, preserved the renal
             architecture (as evaluated by magnetic resonance
             micros-copy) and prevented the loss of renal concentrating
             function. PEG-uricase was far more effective and less
             immunogenic than unmodified uricase. Retention of uricase in
             most mammals and its loss in humans and some other primates
             may reflect the evolution of renal function under different
             environmental conditions. PEG-uricase could provide an
             effective therapy for uric acid nephropathy and refractory
             gout in human patients.},
   Doi = {10.1681/ASN.V1251001},
   Key = {fds269101}
}

@article{fds174151,
   Author = {X Li and FW Bazer and GA Johnson and RC Burghardt and DW Erikson and JW
             Frank, TE Spencer and I Shinzato and G Wu},
   Title = {Dietary Supplementation with 0.8% L-Arginine between Days 0
             and 25 of Gestation Reduces Litter Size in
             Gilts.},
   Journal = {The Journal of nutrition},
   Year = {2010},
   Month = {April},
   ISSN = {1541-6100},
   url = {http://dx.doi.org/10.3945/jn.110.121350},
   Abstract = {In this study, we determined the effects of l-arginine
             supplementation during early pregnancy on embryonic/fetal
             survival and growth in gilts. Gilts were housed individually
             in pens and fed twice daily 1 kg of a corn- and soybean
             meal-based diet supplemented with 0.0, 0.4, or 0.8%
             l-arginine (wt:wt) between d 0 and 25 of gestation (10
             gilts/treatment). The diets were made isonitrogenous by
             addition of appropriate amounts of l-alanine. At d 25 of
             gestation, gilts were fed l-alanine or l-arginine and
             hysterectomized 30 min later to obtain uteri and conceptuses
             (embryos and associated fetal membranes and fluids). Dietary
             supplementation with 0.4 or 0.8% l-arginine enhanced (P <
             0.05) its concentrations in maternal plasma (64 and 98%,
             respectively) as well as the vascularity of chorionic and
             allantoic membranes, compared with the control group.
             Reproductive performance [numbers of corpora lutea (CL) and
             fetuses, placental and fetal weights, and embryonic
             mortality] did not differ between the 0.4% Arg and control
             groups. However, supplementation with 0.8% l-arginine
             decreased (P < 0.05) uterine weight (-20%), total number of
             fetuses (-24%), CL number (-17%), total fetal weight (-34%),
             total volume of allantoic and amniotic fluids (-34 to 42%),
             concentrations of progesterone in maternal plasma (-33%), as
             well as total amounts of progesterone (-35%), estrone
             (-40%), and estrone sulfate (-37%) in allantoic fluid,
             compared with the control group. These results indicate that
             dietary supplementation with 0.8% l-arginine between d 0 and
             25 of gestation, while increasing placental vascularity,
             adversely affects the reproductive performance of
             gilts.},
   Language = {ENG},
   Doi = {10.3945/jn.110.121350},
   Key = {fds174151}
}

@article{fds174309,
   Author = {GA Johnson and EG Kim and W Veldkamp and R Russell},
   Title = {Difference in oral effectiveness of two tyrosine hydroxylase
             inhibitors.},
   Journal = {Biochemical pharmacology},
   Volume = {16},
   Number = {2},
   Pages = {401-3},
   Year = {1967},
   Month = {February},
   ISSN = {0006-2952},
   Keywords = {Animals • Body Weight • Brain • Brain
             Chemistry* • Dextroamphetamine • Diet •
             Dopamine • Eating • Enzymes • Male •
             Methyltyrosines • Mice • Movement •
             Norepinephrine • Oxidoreductases • Reserpine
             • Serotonin • Tyrosine • analysis • drug
             effects • pharmacology • pharmacology*},
   Language = {eng},
   Key = {fds174309}
}

@booklet{Spencer99a,
   Author = {T. E. Spencer and A. G. Stagg and T. L. Ott and G. A.
             Johnson and W. S. Ramsey and F. W. Bazer},
   Title = {Differential effects of intrauterine and subcutaneous
             administration of recombinant ovine interferon tau on the
             endometrium of cyclic ewes},
   Journal = {Biology Of Reproduction},
   Volume = {61},
   Number = {2},
   Pages = {464 -- 470},
   Year = {1999},
   Month = {August},
   Key = {Spencer99a}
}

@article{fds174157,
   Author = {TE Spencer and AG Stagg and TL Ott and GA Johnson and WS Ramsey and FW
             Bazer},
   Title = {Differential effects of intrauterine and subcutaneous
             administration of recombinant ovine interferon tau on the
             endometrium of cyclic ewes.},
   Journal = {Biology of reproduction},
   Volume = {61},
   Number = {2},
   Pages = {464-70},
   Year = {1999},
   Month = {August},
   ISSN = {0006-3363},
   Keywords = {Animals • Antiviral Agents • Carrier Proteins
             • Endometrium • Female • GTP
             Phosphohydrolases • GTP-Binding Proteins • Gene
             Expression Regulation, Developmental • In Situ
             Hybridization • Injections, Subcutaneous •
             Interferon Type I • Leucine Zippers • Pregnancy
             • Pregnancy Proteins • Protein Biosynthesis •
             Proteins • Receptors, Estrogen • Receptors,
             Oxytocin • Recombinant Proteins • Sheep •
             Ubiquitins • Uterus • administration & dosage
             • administration & dosage* • analogs & derivatives
             • biosynthesis • drug effects* • genetics
             • pharmacology • pharmacology*},
   Abstract = {Interferon tau (IFNtau) is the antiluteolytic signal
             produced by the conceptus of ruminants. Intrauterine
             administration of recombinant ovine IFNtau suppresses
             expression of endometrial estrogen receptor (ER) and
             oxytocin receptor (OTR) in the luminal and superficial
             glandular epithelia to abrogate the production of luteolytic
             prostaglandin F(2alpha) (PGF(2alpha)) pulses. Subcutaneous
             (s.c.) injections of recombinant ovine (o) IFNtau appear to
             extend the interestrous interval by altering uterine
             PGF(2alpha) response to oxytocin. The present study tested
             the hypothesis that antiluteolytic effects of roIFNtau
             injected into the uterine lumen (paracrine) or s.c.
             (endocrine) are equivalent in suppressing expression of
             endometrial ER and OTR and inducing uterine expression of
             type I IFN-regulated Mx and ubiquitin cross-reactive
             proteins (UCRP). Sixteen cyclic ewes were fitted with
             uterine catheters on Day 5 (Day 0 = estrus), were assigned
             randomly to receive treatment with control proteins or
             roIFNtau (2 x 10(7) antiviral units/day) by either
             intrauterine or s.c. injections from Days 11 to 15, and were
             ovariohysterectomized on Day 16. Results indicated that
             expression of ER and OTR mRNAs in endometrial epithelium was
             suppressed by intrauterine but not by s.c. injections of
             roIFNtau. Intrauterine injections of roIFNtau increased
             expression of Mx and UCRP mRNA in the endometrium.
             Subcutaneous injections of roIFNtau increased endometrial Mx
             mRNA levels but not UCRP mRNA. Unexpectedly, intrauterine
             and s.c. injections of roIFNtau were equally effective in
             inducing expression of Mx and UCRP mRNA in the corpus
             luteum. Although s.c. injections of roIFNtau induced Mx mRNA
             in the endometrial epithelium, s.c. injections of roIFNtau
             did not abrogate activation of the uterine luteolytic
             mechanism by suppressing epithelial ER and OTR expression.
             Therefore, results of this study failed to support the
             assumption that endocrine roIFNtau mimics antiluteolytic
             effects of paracrine IFNtau to improve pregnancy rates in
             sheep.},
   Language = {eng},
   Key = {fds174157}
}

@article{fds132763,
   Author = {RH Sherrier and C Chiles and GA Johnson and CE Ravin},
   Title = {Differentiation of benign from malignant pulmonary nodules
             with digitized chest radiographs.},
   Journal = {Radiology, UNITED STATES},
   Volume = {162},
   Number = {3},
   Pages = {645-9},
   Year = {1987},
   Month = {March},
   ISSN = {0033-8419},
   Keywords = {Coin Lesion, Pulmonary • Diagnosis, Differential •
             Humans • Lung Neoplasms • Radiographic Image
             Enhancement • methods* • radiography •
             radiography*},
   Abstract = {To assess whether it is possible to distinguish benign from
             malignant solitary pulmonary nodules with digital
             techniques, a retrospective study of 68 patients with proved
             solitary nodules was performed. The conventional chest
             radiograph for each patient was digitized to 2,048 X 2,048 X
             12 bits, and changes in the optical density within the
             nodule were analyzed. A number (the corrected gradient
             number) was then generated that reflected this variation.
             Striking differences were noted between 26 malignant nodules
             and 21 calcified granulomas. The technique was then applied
             to 21 benign nodules that had initially required thoracotomy
             or further study for diagnosis. In nine of these 21 patients
             (43%), the corrected gradient number allowed correct
             classification as a benign lesion.},
   Key = {fds132763}
}

@booklet{Sherrier87a,
   Author = {Sherrier, RH and Chiles, C and Johnson, GA and Ravin,
             CE},
   Title = {Differentiation of benign from malignant pulmonary nodules
             with digitized chest radiographs.},
   Journal = {Radiology},
   Volume = {162},
   Number = {3},
   Pages = {645-649},
   Year = {1987},
   Month = {March},
   ISSN = {0033-8419},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/3809476},
   Abstract = {To assess whether it is possible to distinguish benign from
             malignant solitary pulmonary nodules with digital
             techniques, a retrospective study of 68 patients with proved
             solitary nodules was performed. The conventional chest
             radiograph for each patient was digitized to 2,048 X 2,048 X
             12 bits, and changes in the optical density within the
             nodule were analyzed. A number (the corrected gradient
             number) was then generated that reflected this variation.
             Striking differences were noted between 26 malignant nodules
             and 21 calcified granulomas. The technique was then applied
             to 21 benign nodules that had initially required thoracotomy
             or further study for diagnosis. In nine of these 21 patients
             (43%), the corrected gradient number allowed correct
             classification as a benign lesion.},
   Doi = {10.1148/radiology.162.3.3809476},
   Key = {Sherrier87a}
}

@booklet{Macfall91b,
   Author = {J. R. Macfall and J. H. Maki and G. A. Johnson and L.
             Hedlund and H. Benveniste and G. Copher},
   Title = {Diffusion microcirculation mri in the rat-brain},
   Journal = {Magnetic Resonance In Medicine},
   Volume = {19},
   Number = {2},
   Pages = {305 -- 310},
   Year = {1991},
   Month = {June},
   Key = {Macfall91b}
}

@article{fds268743,
   Author = {O'Leary-Moore, SK and Johnson, GA and Calabrese, E and Budin, F and Oguz, I and Styner, MA and Parnell, SE and Sulik,
             KK},
   Title = {DIFFUSION TENSOR IMAGING (DTI)-BASED ANALYSIS OF FIBER TRACT
             ABNORMALITIES IN A MOUSE MODEL OF PRENATAL ALCOHOL
             EXPOSURE},
   Journal = {ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH},
   Volume = {36},
   Pages = {312A-312A},
   Year = {2012},
   ISSN = {0145-6008},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000304806002399&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {fds268743}
}

@article{fds268723,
   Author = {Calabrese, E and Du, F and Garman, RH and Johnson, GA and Riccio, C and Tong, LC and Long, JB},
   Title = {Diffusion tensor imaging reveals white matter injury in a
             rat model of repetitive blast-induced traumatic brain
             injury.},
   Journal = {J Neurotrauma},
   Volume = {31},
   Number = {10},
   Pages = {938-950},
   Year = {2014},
   Month = {May},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/24392843},
   Abstract = {Blast-induced traumatic brain injury (bTBI) is one of the
             most common combat-related injuries seen in U.S. military
             personnel, yet relatively little is known about the
             underlying mechanisms of injury. In particular, the effects
             of the primary blast pressure wave are poorly understood.
             Animal models have proven invaluable for the study of
             primary bTBI, because it rarely occurs in isolation in human
             subjects. Even less is known about the effects of repeated
             primary blast wave exposure, but existing data suggest
             cumulative increases in brain damage with a second blast.
             MRI and, in particular, diffusion tensor imaging (DTI), have
             become important tools for assessing bTBI in both clinical
             and preclinical settings. Computational statistical methods
             such as voxelwise analysis have shown promise in localizing
             and quantifying bTBI throughout the brain. In this study, we
             use voxelwise analysis of DTI to quantify white matter
             injury in a rat model of repetitive primary blast exposure.
             Our results show a significant increase in microstructural
             damage with a second blast exposure, suggesting that primary
             bTBI may sensitize the brain to subsequent
             injury.},
   Doi = {10.1089/neu.2013.3144},
   Key = {fds268723}
}

@article{fds336018,
   Author = {Nouls, JC and Badea, A and Anderson, RBJ and Cofer, GP and Allan
             Johnson, G},
   Title = {Diffusion tensor imaging using multiple coils for mouse
             brain connectomics.},
   Journal = {NMR Biomed},
   Volume = {31},
   Number = {6},
   Pages = {e3921},
   Year = {2018},
   Month = {June},
   url = {http://dx.doi.org/10.1002/nbm.3921},
   Abstract = {The correlation between brain connectivity and psychiatric
             or neurological diseases has intensified efforts to develop
             brain connectivity mapping techniques on mouse models of
             human disease. The neural architecture of mouse brain
             specimens can be shown non-destructively and
             three-dimensionally by diffusion tensor imaging, which
             enables tractography, the establishment of a connectivity
             matrix and connectomics. However, experiments on cohorts of
             animals can be prohibitively long. To improve throughput in
             a 7-T preclinical scanner, we present a novel two-coil
             system in which each coil is shielded, placed off-isocenter
             along the axis of the magnet and connected to a receiver
             circuit of the scanner. Preservation of the quality factor
             of each coil is essential to signal-to-noise ratio (SNR)
             performance and throughput, because mouse brain specimen
             imaging at 7 T takes place in the coil-dominated noise
             regime. In that regime, we show a shielding configuration
             causing no SNR degradation in the two-coil system. To
             acquire data from several coils simultaneously, the coils
             are placed in the magnet bore, around the isocenter, in
             which gradient field distortions can bias diffusion tensor
             imaging metrics, affect tractography and contaminate
             measurements of the connectivity matrix. We quantified the
             experimental alterations in fractional anisotropy and
             eigenvector direction occurring in each coil. We showed
             that, when the coils were placed 12 mm away from the
             isocenter, measurements of the brain connectivity matrix
             appeared to be minimally altered by gradient field
             distortions. Simultaneous measurements on two mouse brain
             specimens demonstrated a full doubling of the diffusion
             tensor imaging throughput in practice. Each coil produced
             images devoid of shading or artifact. To further improve the
             throughput of mouse brain connectomics, we suggested a
             future expansion of the system to four coils. To better
             understand acceptable trade-offs between imaging throughput
             and connectivity matrix integrity, studies may seek to
             clarify how measurement variability, post-processing
             techniques and biological variability impact mouse brain
             connectomics.},
   Doi = {10.1002/nbm.3921},
   Key = {fds336018}
}

@article{fds268736,
   Author = {Calabrese, E and Johnson, GA},
   Title = {Diffusion tensor magnetic resonance histology reveals
             microstructural changes in the developing rat
             brain.},
   Journal = {Neuroimage},
   Volume = {79},
   Pages = {329-339},
   Year = {2013},
   Month = {October},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/23648962},
   Abstract = {The postnatal period is a remarkably dynamic phase of brain
             growth and development characterized by large-scale
             macrostructural changes, as well as dramatic microstructural
             changes, including myelination and cortical layering. This
             crucial period of neurodevelopment is uniquely susceptible
             to a wide variety of insults that may lead to neurologic
             disease. MRI is an important tool for studying both normal
             and abnormal neurodevelopmental changes, and quantitative
             imaging strategies like diffusion tensor imaging (DTI) allow
             visualization of many of the complex microstructural changes
             that occur during postnatal life. Diffusion tensor magnetic
             resonance histology (DT-MRH) provides particularly unique
             insight into cytoarchitectural changes in the developing
             brain. In this study, we used DT-MRH to track
             microstructural changes in the rat brain throughout normal
             postnatal neurodevelopment. We provide examples of diffusion
             tensor parameter changes in both white matter and gray
             matter structures, and correlate these changes with changes
             in cytoarchitecture. Finally, we provide a comprehensive
             database of image sets as a foundation for future studies
             using DT-MRH to characterize abnormal neurodevelopment in
             rodent models of neurodevelopmental disease.},
   Doi = {10.1016/j.neuroimage.2013.04.101},
   Key = {fds268736}
}

@article{fds341985,
   Author = {Wang, N and Mirando, AJ and Cofer, G and Qi, Y and Hilton, MJ and Johnson,
             GA},
   Title = {Diffusion tractography of the rat knee at microscopic
             resolution.},
   Journal = {Magn Reson Med},
   Volume = {81},
   Number = {6},
   Pages = {3775-3786},
   Year = {2019},
   Month = {June},
   url = {http://dx.doi.org/10.1002/mrm.27652},
   Abstract = {PURPOSE: To evaluate whole knee joint tractography,
             including articular cartilage, ligaments, meniscus, and
             growth plate using diffusion tensor imaging (DTI) at
             microscopic resolution. METHODS: Three rat knee joints were
             scanned using a modified 3D diffusion-weighted spin echo
             pulse sequence with 90- and 45-μm isotropic spatial
             resolution at 9.4T. The b values varied from 250 to 1250
             s/mm2 with 4 times undersampling in phase directions.
             Fractional anisotropy (FA) and mean diffusivity (MD) were
             compared at different spatial resolution and b values.
             Tractography was evaluated at multiple b values and angular
             resolutions in different connective tissues, and compared
             with conventional histology. The mean tract length and tract
             volume in various types of tissues were also quantified.
             RESULTS: DTI metrics (FA and MD) showed consistent
             quantitative results at 90- and 45-μm isotropic spatial
             resolutions. Tractography of various connective tissues was
             found to be sensitive to the spatial resolution, angular
             resolution, and diffusion weightings. Higher spatial
             resolution (45 μm) supported tracking the cartilage
             collagen fiber tracts from the superficial zone to the deep
             zone, in a continuous and smooth progression in the
             transitional zone. Fiber length and fiber volume in the
             growth plate were strongly dependent on angular resolution
             and b values, whereas tractography in ligaments was found to
             be less dependent on spatial resolution. CONCLUSION: High
             spatial and angular resolution DTI and diffusion
             tractography can be valuable for knee joint research because
             of its visualization capacity for collagen fiber
             orientations and quantitative evaluation of tissue's
             microscopic properties.},
   Doi = {10.1002/mrm.27652},
   Key = {fds341985}
}

@article{fds132826,
   Author = {CF Beaulieu and X Zhou and GP Cofer and GA Johnson},
   Title = {Diffusion-weighted MR microscopy with fast
             spin-echo.},
   Journal = {Magnetic resonance in medicine : official journal of the
             Society of Magnetic Resonance in Medicine / Society of
             Magnetic Resonance in Medicine, UNITED STATES},
   Volume = {30},
   Number = {2},
   Pages = {201-6},
   Year = {1993},
   Month = {August},
   ISSN = {0740-3194},
   Keywords = {Animals • Diffusion • Image Processing,
             Computer-Assisted • Magnetic Resonance Imaging •
             Microscopy • Models, Structural • Rats •
             methods*},
   Abstract = {A diffusion-weighted fast spin-echo (FSE) imaging sequence
             for high-field MR microscopy was developed and
             experimentally validated in a phantom and in a live rat.
             Pulsed diffusion gradients were executed before and after
             the initial 180 degrees pulse in the FSE pulse train. This
             produced diffusion-related reductions in image signal
             intensity corresponding to gradient ("b") factors between
             1.80 and 1352 s/mm2. The degree of diffusion weighting was
             demonstrated to be independent of echo train length for
             experiments using trains up to 16 echoes long. Quantitative
             measurements on a phantom and on a live rat produced
             diffusion coefficients consistent with literature values.
             Importantly, the eight- to 16-fold increase in imaging
             efficiency with FSE was not accompanied by a significant
             loss of spatial resolution or contrast. This permits
             acquisition of in vivo three-dimensional data in time
             periods that are appropriate for evolving biological
             processes. The combination of accurate diffusion weighting
             and high spatial resolution provided by FSE makes the
             technique particularly useful for MR microscopy.},
   Key = {fds132826}
}

@booklet{Beaulieu93,
   Author = {Beaulieu, CF and Zhou, X and Cofer, GP and Johnson,
             GA},
   Title = {Diffusion-weighted MR microscopy with fast
             spin-echo.},
   Journal = {Magn Reson Med},
   Volume = {30},
   Number = {2},
   Pages = {201-206},
   Year = {1993},
   Month = {August},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/8366801},
   Abstract = {A diffusion-weighted fast spin-echo (FSE) imaging sequence
             for high-field MR microscopy was developed and
             experimentally validated in a phantom and in a live rat.
             Pulsed diffusion gradients were executed before and after
             the initial 180 degrees pulse in the FSE pulse train. This
             produced diffusion-related reductions in image signal
             intensity corresponding to gradient ("b") factors between
             1.80 and 1352 s/mm2. The degree of diffusion weighting was
             demonstrated to be independent of echo train length for
             experiments using trains up to 16 echoes long. Quantitative
             measurements on a phantom and on a live rat produced
             diffusion coefficients consistent with literature values.
             Importantly, the eight- to 16-fold increase in imaging
             efficiency with FSE was not accompanied by a significant
             loss of spatial resolution or contrast. This permits
             acquisition of in vivo three-dimensional data in time
             periods that are appropriate for evolving biological
             processes. The combination of accurate diffusion weighting
             and high spatial resolution provided by FSE makes the
             technique particularly useful for MR microscopy.},
   Doi = {10.1002/mrm.1910300208},
   Key = {Beaulieu93}
}

@article{fds269122,
   Author = {MacFall, JR and Maki, JH and Johnson, GA and Hedlund, L and Benveniste,
             H and Copher, G},
   Title = {Diffusion/microcirculation MRI in the rat
             brain.},
   Journal = {Magn Reson Med},
   Volume = {19},
   Number = {2},
   Pages = {305-310},
   Year = {1991},
   Month = {June},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/1908936},
   Keywords = {Animals • Brain • Carbon Dioxide •
             Cerebrovascular Circulation • Diffusion • Magnetic
             Resonance Imaging* • Microcirculation • Rats
             • Rats, Inbred Strains • administration & dosage
             • anatomy & histology • blood supply •
             metabolism • pharmacokinetics •
             physiology*},
   Abstract = {The CO2 fraction of an anesthetized rat's breathing mixture
             was changed (from 0 to 10%) to attempt to change the brain
             microcirculation and observe these changes in diffusion
             measurements of the neural tissue. Brain apparent diffusion
             coefficients were measured to be (0.71 +/- 0.01) X 10(-3)
             mm2/s before sacrifice and (0.39 +/- 0.01) X 10(-3) mm2/s
             after sacrifice. Multiple diffusion components were
             observed, consistent with flowing material, but the extra
             components did not increase with increased CO2. It is
             proposed that the additional components may be due to
             extracellular, extravascular water such as
             CSF.},
   Doi = {10.1002/mrm.1910190219},
   Key = {fds269122}
}

@article{fds268821,
   Author = {Hawrylycz, M and Baldock, RA and Burger, A and Hashikawa, T and Johnson,
             GA and Martone, M and Ng, L and Lau, C and Larson, SD and Nissanov, J and Puelles, L and Ruffins, S and Verbeek, F and Zaslavsky, I and Boline,
             J},
   Title = {Digital atlasing and standardization in the mouse
             brain.},
   Journal = {PLoS Comput Biol},
   Volume = {7},
   Number = {2},
   Pages = {e1001065},
   Year = {2011},
   Month = {February},
   ISSN = {1553-7358},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/21304938},
   Keywords = {Anatomy, Artistic • Animals • Atlases as Topic
             • Brain • Computational Biology • Male •
             Mice • Mice, Inbred C57BL • Models, Anatomic*
             • Models, Neurological • anatomy & histology*
             • standards • statistics & numerical
             data},
   Language = {eng},
   Doi = {10.1371/journal.pcbi.1001065},
   Key = {fds268821}
}

@article{fds174203,
   Author = {RM Vandemark and ME Fay and FR Porter and GA Johnson},
   Title = {Digital image-intensifier radiography at a level I trauma
             center.},
   Journal = {AJR. American journal of roentgenology},
   Volume = {168},
   Number = {4},
   Pages = {944-6},
   Year = {1997},
   Month = {April},
   ISSN = {0361-803X},
   Keywords = {Humans • Pelvis • Radiographic Image Enhancement
             • Radiography, Thoracic • Spinal Injuries •
             Spine • Trauma Centers • Wounds and Injuries
             • injuries • instrumentation* •
             radiography},
   Language = {eng},
   Key = {fds174203}
}

@booklet{Vandemark97,
   Author = {Vandemark, RM and Fay, ME and Porter, FR and Johnson,
             GA},
   Title = {Digital image-intensifier radiography at a level I trauma
             center.},
   Journal = {AJR Am J Roentgenol},
   Volume = {168},
   Number = {4},
   Pages = {944-946},
   Year = {1997},
   Month = {April},
   ISSN = {0361-803X},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/9124145},
   Doi = {10.2214/ajr.168.4.9124145},
   Key = {Vandemark97}
}

@booklet{Dunnick85,
   Author = {N. R. Dunnick and K. K. Ford and G. A. Johnson and J. C.
             Gunnells},
   Title = {Digital intravenous subtraction angiography for
             investigating renovascular hypertension - comparison with
             hypertensive urography},
   Journal = {Southern Medical Journal},
   Volume = {78},
   Number = {6},
   Pages = {690 -- 693},
   Year = {1985},
   Key = {Dunnick85}
}

@article{fds132748,
   Author = {NR Dunnick and KK Ford and GA Johnson and JC Gunnells},
   Title = {DIgital intravenous subtraction angiography for
             investigating renovascular hypertension: comparison with
             hypertensive urography.},
   Journal = {Southern medical journal, UNITED STATES},
   Volume = {78},
   Number = {6},
   Pages = {690-3},
   Year = {1985},
   Month = {June},
   ISSN = {0038-4348},
   Keywords = {Adolescent • Adult • Aged • Female •
             Humans • Hypertension • Hypertension, Renovascular
             • Male • Middle Aged • Renal Artery •
             Renin • Subtraction Technique* • Urography* •
             blood • diagnosis • radiography •
             radiography*},
   Abstract = {We used digital intravenous subtraction angiography (DSA) to
             evaluate 105 patients with suspected renovascular
             hypertension. Unilateral renal artery stenoses were
             identified in 14 patients, two of whom had previously had
             contralateral nephrectomy. In addition, one of three renal
             transplant recipients was found to have stenosis of the
             nutrient artery. Bilateral renal artery stenosis was
             demonstrated by DSA in three patients. Of the 88 patients
             who had concomitant minute sequence (hypertensive) urography
             (HIVP) delayed excretion suggested a renal artery lesion in
             only 8 patients. In the group of 88 patients, HIVP was able
             to detect renal artery stenosis in only 50% (eight of the
             16) of patients whose stenosis was detected by DSA. When the
             patients with a single kidney are excluded, HIVP showed 62%
             (eight of 13) of the lesions detected by DSA. There were no
             significant complications in the patients examined by either
             modality. DSA has replaced HIVP as the screening examination
             for renovascular causes of hypertension in our
             institution.},
   Key = {fds132748}
}

@booklet{Johnson81,
   Author = {Johnson, GA and Ford, K and Heinz, R},
   Title = {Digital radiography using the quantex ds-20},
   Journal = {Proceedings of SPIE - The International Society for Optical
             Engineering},
   Volume = {273},
   Pages = {114-119},
   Year = {1981},
   Month = {July},
   url = {http://dx.doi.org/10.1117/12.931792},
   Abstract = {The Quantex DS-20 digital image processor has been evaluated
             as a low cost alternative for digital vascular radiography.
             The processor is used in conjunction with a conventional
             remote radiographic/fluoroscopic system with no
             generator/processor interface required. (Use of a video-tape
             system reduces timing problems with minimal image
             degradation). Phantom studies indicate vessels as small as
             1.5 mm can be seen with concentrations of contrast as low as
             10 mgγ/ml. Animal studies show that subtraction images of
             diagnostic quality can be generated. © 1981
             SPIE.},
   Doi = {10.1117/12.931792},
   Key = {Johnson81}
}

@booklet{Johnson81e,
   Author = {JOHNSON, GA and FORD, KK and HEINZ, R},
   Title = {DIGITAL RADIOGRAPHY USING THE QUANTEX DS-20},
   Journal = {AMERICAN JOURNAL OF ROENTGENOLOGY},
   Volume = {136},
   Number = {6},
   Pages = {1274-1274},
   Year = {1981},
   ISSN = {0361-803X},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1981LU08900069&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Johnson81e}
}

@article{fds292751,
   Author = {Spiliopoulos, D and Kagadis, GC and Karnabatidis, D and Johnson, GA and Badea, CT},
   Title = {Digital Subtracted Angiography of Small Animals},
   Pages = {67-75},
   Booktitle = {Handbook of Small Animal Imaging: Preclinical Imaging,
             Therapy, and Applications},
   Publisher = {Taylor & Francis Books, Inc., CRC Press},
   Editor = {Kagadis, GC and Ford, NL and Loudos, GK and Karnabatidis,
             D},
   Year = {2016},
   Month = {March},
   ISBN = {978-1466555686},
   url = {http://dx.doi.org/10.1201/b19052-9},
   Doi = {10.1201/b19052-9},
   Key = {fds292751}
}

@article{fds132843,
   Author = {RH Sherrier and GA Johnson and SA Suddarth and C Chiles and C Hulka and CE
             Ravin},
   Title = {Digital synthesis of lung nodules.},
   Journal = {Investigative radiology, UNITED STATES},
   Volume = {20},
   Number = {9},
   Pages = {933-7},
   Year = {1985},
   Month = {December},
   ISSN = {0020-9996},
   Keywords = {Coin Lesion, Pulmonary • Humans • Lung Neoplasms
             • Radiography, Thoracic • Software • methods*
             • radiography*},
   Abstract = {Studies evaluating observer accuracy and visual perception
             of pulmonary nodules usually are based upon test films
             obtained from clinical practice in patients with proven
             pulmonary nodules. Unfortunately, such nodules do not always
             occur in the optimal size and location to facilitate
             testing. Such studies would be enhanced by the ability to
             place nodules of desired size and location on chest
             radiographs. This report describes a method of placing a
             computer-generated (synthesized) nodule on a digitized chest
             radiograph. To demonstrate the similarity of these
             synthesized nodules to real nodules, each digitized
             radiograph with a computer-generated nodule was paired with
             a digitized chest radiograph of a patient with a clinically
             proven pulmonary nodule. A total of 22 pairs of chest
             radiographs were then shown to 13 radiologists, who were
             asked to distinguish the synthesized nodule from the real
             nodule. With this two alternative forced-choice test, the
             radiologists were only able to distinguish the synthesized
             nodule in 51% of the cases, strongly suggesting that
             computer generated nodules may be used to simulate real
             pulmonary nodules in future tests of nodule
             detection.},
   Key = {fds132843}
}

@booklet{Sherrier85,
   Author = {Sherrier, RH and Johnson, GA and Suddarth, SA and Chiles, C and Hulka,
             C and Ravin, CE},
   Title = {Digital synthesis of lung nodules.},
   Journal = {Invest Radiol},
   Volume = {20},
   Number = {9},
   Pages = {933-937},
   Year = {1985},
   Month = {December},
   ISSN = {0020-9996},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/3841098},
   Abstract = {Studies evaluating observer accuracy and visual perception
             of pulmonary nodules usually are based upon test films
             obtained from clinical practice in patients with proven
             pulmonary nodules. Unfortunately, such nodules do not always
             occur in the optimal size and location to facilitate
             testing. Such studies would be enhanced by the ability to
             place nodules of desired size and location on chest
             radiographs. This report describes a method of placing a
             computer-generated (synthesized) nodule on a digitized chest
             radiograph. To demonstrate the similarity of these
             synthesized nodules to real nodules, each digitized
             radiograph with a computer-generated nodule was paired with
             a digitized chest radiograph of a patient with a clinically
             proven pulmonary nodule. A total of 22 pairs of chest
             radiographs were then shown to 13 radiologists, who were
             asked to distinguish the synthesized nodule from the real
             nodule. With this two alternative forced-choice test, the
             radiologists were only able to distinguish the synthesized
             nodule in 51% of the cases, strongly suggesting that
             computer generated nodules may be used to simulate real
             pulmonary nodules in future tests of nodule
             detection.},
   Doi = {10.1097/00004424-198512000-00008},
   Key = {Sherrier85}
}

@article{fds268753,
   Author = {Perez, BA and Ghafoori, AP and Johnston, SM and Jeffords, LB and Kim, Y and Badea, CT and Johnson, GA and Kirsch, DG},
   Title = {Dissecting the Mechanism of Tumor Response to Radiation
             Therapy with Primary Lung Cancers in Mice},
   Journal = {International Journal of Radiation Oncology*Biology*Physics},
   Volume = {75},
   Number = {3},
   Pages = {S537-S537},
   Publisher = {Elsevier BV},
   Year = {2009},
   Month = {November},
   ISSN = {0360-3016},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000270573602102&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Doi = {10.1016/j.ijrobp.2009.07.1227},
   Key = {fds268753}
}

@article{fds132824,
   Author = {JD Godwin and JM Speckman and EK Fram and GA Johnson and CE Putman and M
             Korobkin, RS Breiman},
   Title = {Distinguishing benign from malignant pulmonary nodules by
             computed tomography.},
   Journal = {Radiology, UNITED STATES},
   Volume = {144},
   Number = {2},
   Pages = {349-51},
   Year = {1982},
   Month = {July},
   ISSN = {0033-8419},
   Keywords = {Calcinosis • Coin Lesion, Pulmonary • Humans
             • Lung Neoplasms • Technology, Radiologic •
             Tomography, X-Ray Computed* • radiography*},
   Abstract = {Investigators have been able to distinguish benign pulmonary
             nodules from malignant ones in about two-thirds of the cases
             studied by detecting high computed tomography (CT) numbers
             (attributed to microscopic calcifications) within many
             benign nodules. This paper reports a similar analysis on a
             series of 22 benign and 14 malignant pulmonary nodules.
             Although about one-third of the benign nodules gave high CT
             numbers, all but one of the nodules diagnosed as benign by
             CT could also be diagnosed by detection of calcification on
             plain radiographs or conventional tomograms.},
   Key = {fds132824}
}

@booklet{Godwin82,
   Author = {Godwin, JD and Speckman, JM and Fram, EK and Johnson, GA and Putman, CE and Korobkin, M and Breiman, RS},
   Title = {Distinguishing benign from malignant pulmonary nodules by
             computed tomography.},
   Journal = {Radiology},
   Volume = {144},
   Number = {2},
   Pages = {349-351},
   Year = {1982},
   Month = {July},
   ISSN = {0033-8419},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/7089288},
   Abstract = {Investigators have been able to distinguish benign pulmonary
             nodules from malignant ones in about two-thirds of the cases
             studied by detecting high computed tomography (CT) numbers
             (attributed to microscopic calcifications) within many
             benign nodules. This paper reports a similar analysis on a
             series of 22 benign and 14 malignant pulmonary nodules.
             Although about one-third of the benign nodules gave high CT
             numbers, all but one of the nodules diagnosed as benign by
             CT could also be diagnosed by detection of calcification on
             plain radiographs or conventional tomograms.},
   Doi = {10.1148/radiology.144.2.7089288},
   Key = {Godwin82}
}

@booklet{Veres91,
   Author = {Veres, JS and Cofer, GP and Johnson, GA},
   Title = {Distinguishing Plant Tissues with Magnetic Resonance
             Microscopy},
   Journal = {American Journal of Botany},
   Volume = {78},
   Number = {12},
   Pages = {1704-1704},
   Publisher = {Wiley},
   Year = {1991},
   Month = {December},
   ISSN = {0002-9122},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1991GY25000009&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Doi = {10.2307/2444849},
   Key = {Veres91}
}

@article{fds325756,
   Author = {Wetzel, AW and Pomerantz, S and Nave, D and Meixner, W and Johnson,
             GA},
   Title = {Distributed multiuser visualization of time varying
             anatomical data},
   Journal = {Proceedings - Applied Imagery Pattern Recognition
             Workshop},
   Volume = {2001-January},
   Pages = {109-114},
   Publisher = {IEEE Comput. Soc},
   Year = {2001},
   Month = {January},
   ISBN = {0769512453},
   url = {http://dx.doi.org/10.1109/AIPR.2001.991211},
   Abstract = {We describe a networked environment for navigating and
             visualizing 3-dimensional anatomical data with extensions
             for time varying volumes. The Duke Center for In Vivo
             Microscopy (CIVM) has been capturing volumetric data of mice
             using magnetic resonance microscopy. Current data sets are
             51Z3 with 16 bit precision per voxel at an isotropic
             resolution of 50 microns. A new instrument will provide
             larger 512 ∗ 512 ∗ 2048 volumes. Because magnetic
             resonance imaging is nondestructive, both rapid time series
             and longer interval developmental series can be taken from
             living specimens. Our work builds on techniques put in place
             at the Pittsburgh Supercomputing Center and the University
             of Michigan for navigating Visible Human data using a
             client-server implementation, but applied to CIVM mouse
             data. Extension of the system to 4-dimensional data sets
             involves changes to compressed data representations and
             client viewing mechanisms. An essential aspect of the mouse
             studies is to facilitate comparison between different
             specimens, or even the same specimen over time, for studies
             of morphologic phenotype expression in gene
             knockouts.},
   Doi = {10.1109/AIPR.2001.991211},
   Key = {fds325756}
}

@booklet{Al-ramadan02,
   Author = {S. Y. Al-ramadan and G. A. Johnson and L. A. Jaeger and S.
             P. Brinsko and R. C. Burghardt},
   Title = {Distribution of integrin subunits, MUC-1, and osteopontin in
             equine uterine epithelium and conceptuses during early
             pregnancy.},
   Journal = {Biology Of Reproduction},
   Volume = {66},
   Pages = {323 -- 323},
   Year = {2002},
   Key = {Al-ramadan02}
}

@booklet{Helson80a,
   Author = {L. Helson and A. Majeranowski and C. Helson and M. Schwartz and G. A. Johnson and J. Nisselbaum},
   Title = {Dopa decarboxylase (ddc) and tryptophan decarboxylase(tdc)
             in neuroectodermal tumors - 2 separate enzymes},
   Journal = {Proceedings Of The American Association For Cancer
             Research},
   Volume = {21},
   Number = {MAR},
   Pages = {322 -- 322},
   Year = {1980},
   Key = {Helson80a}
}

@booklet{Helson80,
   Author = {L. Helson and G. A. Johnson and R. Smith},
   Title = {Dopa metabolism in neuro-blastoma},
   Journal = {Medical And Pediatric Oncology},
   Volume = {8},
   Number = {4},
   Pages = {317 -- 322},
   Year = {1980},
   Key = {Helson80}
}

@article{fds174104,
   Author = {L Helson and GA Johnson and R Smith},
   Title = {DOPA metabolism in neuroblastoma.},
   Journal = {Medical and pediatric oncology},
   Volume = {8},
   Number = {4},
   Pages = {317-22},
   Year = {1980},
   ISSN = {0098-1532},
   Keywords = {Adolescent • Bone Neoplasms • Brain Neoplasms
             • Child • Dihydroxyphenylalanine • False
             Negative Reactions • Female • Humans •
             Leukemia • Lymphoma • Neoplasm Recurrence, Local
             • Neuroblastoma • Time Factors •
             Vanilmandelic Acid • blood • cerebrospinal fluid
             • metabolism • metabolism* •
             urine},
   Abstract = {Blood plasma samples from 60 neuroblastoma patients prior
             to, during, and following treatment were studied for their
             content of circulating DOPA using a radioenzymatic assay.
             Normal values were established from children who were
             tumor-free or had other nonneurogenic tumors. The highest
             plasma DOPA concentration in tumor-free or nonneuroblastoma
             controls was 5.3 ng/ml with a mean of 2.15 ng/ml. Most
             neuroblastoma patients (28/31) with active disease had DOPA
             values above this level. Only one out of 30 "successfully"
             treated patients without evidence of disease was encountered
             with an abnormally high level. In treated patients, elevated
             values forewarned of impending clinical recurrence or
             persistent tumor. Cerebrospinal fluid DOPA levels in one
             patient with cerebral neuroblastoma were extraordinarily
             high and suggests that this assay may prove useful to
             distinguish neuroblastoma from other central neuroectodermal
             or metastatic tumors. Plasma DOPA appears to be a reliable
             predictive and diagnostic test for neuroblastoma.},
   Language = {eng},
   Key = {fds174104}
}

@article{fds174247,
   Author = {PF Von Voigtlander and SJ Boukma and GA Johnson},
   Title = {Dopaminergic denervation supersensitivity and dopamine
             stimulated adenyl cyclase activity.},
   Journal = {Neuropharmacology},
   Volume = {12},
   Number = {11},
   Pages = {1081-6},
   Year = {1973},
   Month = {November},
   ISSN = {0028-3908},
   Keywords = {Adenylate Cyclase • Animals • Apomorphine •
             Corpus Striatum • Cyclic AMP • Dopamine •
             Dose-Response Relationship, Drug • Hydroxydopamines
             • Male • Methyltyrosines • Mice • Nerve
             Endings • Receptors, Drug • Stimulation, Chemical
             • Sympathectomy • biosynthesis • drug effects
             • enzymology • metabolism • metabolism*
             • pharmacology • pharmacology* •
             physiology},
   Language = {eng},
   Key = {fds174247}
}

@article{fds268734,
   Author = {Bhavane, R and Badea, C and Ghaghada, KB and Clark, D and Vela, D and Moturu, A and Annapragada, A and Johnson, GA and Willerson, JT and Annapragada, A},
   Title = {Dual-energy computed tomography imaging of atherosclerotic
             plaques in a mouse model using a liposomal-iodine
             nanoparticle contrast agent.},
   Journal = {Circ Cardiovasc Imaging},
   Volume = {6},
   Number = {2},
   Pages = {285-294},
   Year = {2013},
   Month = {March},
   ISSN = {1941-9651},
   url = {http://dx.doi.org/10.1161/CIRCIMAGING.112.000119},
   Abstract = {BACKGROUND: The accumulation of macrophages in inflamed
             atherosclerotic plaques has long been recognized. In an
             attempt to develop an imaging agent for detection of
             vulnerable plaques, we evaluated the feasibility of a
             liposomal-iodine nanoparticle contrast agent for computed
             tomography imaging of macrophage-rich atherosclerotic
             plaques in a mouse model. METHODS AND RESULTS:
             Liposomal-iodine formulations varying in particle size and
             polyethylene glycol coating were fabricated and shown to
             stably encapsulate the iodine compound. In vitro uptake
             studies using optical and computed tomography imaging in the
             RAW 264.7 macrophage cell line identified the formulation
             that promoted maximal uptake. Dual-energy computed
             tomography imaging using this formulation in apolipoprotein
             E-deficient (ApoE(-/-)) mice (n=8) and control C57BL/6 mice
             (n=6) followed by spectral decomposition of the dual-energy
             images enabled imaging of the liposomes localized in the
             plaque. Imaging cytometry confirmed the presence of
             liposomes in the plaque and their colocalization with a
             small fraction (≈2%) of the macrophages in the plaque.
             CONCLUSIONS: The results demonstrate the feasibility of
             imaging macrophage-rich atherosclerotic plaques using a
             liposomal-iodine nanoparticle contrast agent and dual-energy
             computed tomography.},
   Doi = {10.1161/CIRCIMAGING.112.000119},
   Key = {fds268734}
}

@article{fds268806,
   Author = {Moding, EJ and Clark, DP and Qi, Y and Li, Y and Ma, Y and Ghaghada, K and Johnson, GA and Kirsch, DG and Badea, CT},
   Title = {Dual-energy micro-computed tomography imaging of
             radiation-induced vascular changes in primary mouse
             sarcomas.},
   Journal = {Int J Radiat Oncol Biol Phys},
   Volume = {85},
   Number = {5},
   Pages = {1353-1359},
   Year = {2013},
   Month = {April},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/23122984},
   Abstract = {PURPOSE: To evaluate the effects of radiation therapy on
             primary tumor vasculature using dual-energy (DE)
             micro-computed tomography (micro-CT). METHODS AND MATERIALS:
             Primary sarcomas were generated with mutant Kras and p53.
             Unirradiated tumors were compared with tumors irradiated
             with 20 Gy. A liposomal-iodinated contrast agent was
             administered 1 day after treatment, and mice were imaged
             immediately after injection (day 1) and 3 days later (day 4)
             with DE micro-CT. CT-derived tumor sizes were used to assess
             tumor growth. After DE decomposition, iodine maps were used
             to assess tumor fractional blood volume (FBV) at day 1 and
             tumor vascular permeability at day 4. For comparison, tumor
             vascularity and vascular permeability were also evaluated
             histologically by use of CD31 immunofluorescence and
             fluorescently-labeled dextrans. RESULTS: Radiation treatment
             significantly decreased tumor growth from day 1 to day 4
             (P<.05). There was a positive correlation between CT
             measurement of tumor FBV on day 1 and extravasated iodine on
             day 4 with microvascular density (MVD) on day 4 (R(2)=0.53)
             and dextran accumulation (R(2)=0.63) on day 4, respectively.
             Despite no change in MVD measured by histology, tumor FBV
             significantly increased after irradiation as measured by DE
             micro-CT (0.070 vs 0.091, P<.05). Both dextran and
             liposomal-iodine accumulation in tumors increased
             significantly after irradiation, with dextran fractional
             area increasing 5.2-fold and liposomal-iodine concentration
             increasing 4.0-fold. CONCLUSIONS: DE micro-CT is an
             effective tool for noninvasive assessment of vascular
             changes in primary tumors. Tumor blood volume and vascular
             permeability increased after a single therapeutic dose of
             radiation treatment.},
   Doi = {10.1016/j.ijrobp.2012.09.027},
   Key = {fds268806}
}

@article{fds268785,
   Author = {Badea, CT and Johnston, SM and Qi, Y and Ghaghada, K and Johnson,
             GA},
   Title = {Dual-energy micro-CT imaging for differentiation of iodine-
             and gold-based nanoparticles},
   Journal = {Progress in Biomedical Optics and Imaging - Proceedings of
             SPIE},
   Volume = {7961},
   Publisher = {SPIE},
   Year = {2011},
   Month = {May},
   ISBN = {9780819485038},
   ISSN = {1605-7422},
   url = {http://dx.doi.org/10.1117/12.878043},
   Abstract = {Spectral CT imaging is expected to play a major role in the
             diagnostic arena as it provides material decomposition on an
             elemental basis. One fascinating possibility is the ability
             to discriminate multiple contrast agents targeting different
             biological sites. We investigate the feasibility of dual
             energy micro-CT for discrimination of iodine (I) and gold
             (Au) contrast agents when simultaneously present in the
             body. Simulations and experiments were performed to measure
             the CT enhancement for I and Au over a range of voltages
             from 40-to-150 kVp using a dual source micro-CT system. The
             selected voltages for dual energy micro-CT imaging of Au and
             I were 40 kVp and 80 kVp. On a massconcentration basis, the
             relative average enhancement of Au to I was 2.75 at 40 kVp
             and 1.58 at 80 kVp. We have demonstrated the method in a
             preclinical model of colon cancer to differentiate vascular
             architecture and extravasation. The concentration maps of Au
             and I allow quantitative measure of the bio-distribution of
             both agents. In conclusion, dual energy micro-CT can be used
             to discriminate probes containing I and Au with immediate
             impact in pre-clinical research. © 2011
             SPIE.},
   Doi = {10.1117/12.878043},
   Key = {fds268785}
}

@article{fds268714,
   Author = {Badea, CT and Befera, N and Clark, D and Qi, Y and Johnson,
             GA},
   Title = {Dual-energy micro-CT imaging of pulmonary airway
             obstruction: Correlation with micro-SPECT},
   Journal = {Progress in Biomedical Optics and Imaging - Proceedings of
             SPIE},
   Volume = {9038},
   Publisher = {SPIE},
   Year = {2014},
   Month = {January},
   ISBN = {9780819498311},
   ISSN = {1605-7422},
   url = {http://dx.doi.org/10.1117/12.2043094},
   Abstract = {To match recent clinical dual energy (DE) CT studies
             focusing on the lung, similar developments for DE micro-CT
             of the rodent lung are required. Our group has been actively
             engaged in designing pulmonary gating techniques for micro-
             CT, and has also introduced the first DE micro-CT imaging
             method of the rodent lung. The aim of this study was to
             assess the feasibility of DE micro-CT imaging for the
             evaluation of airway obstruction in mice, and to compare the
             method with micro single photon emission computed tomography
             (micro-SPECT) using technetium-99m labeled macroaggregated
             albumin (99mTc-MAA). The results suggest that the induced
             pulmonary airway obstruction causes either atelectasis, or
             air-trapping similar to asthma or chronic bronchitis.
             Atelectasis could only be detected at early time points in
             DE micro-CT images, and is associated with a large increase
             in blood fraction and decrease in air fraction. Air trapping
             had an opposite effect with larger air fraction and
             decreased blood fraction shown by DE micro-CT. The decrease
             in perfusion to the hypoventilated lung (hypoxic
             vasoconstriction) is also seen in micro-SPECT. The proposed
             DE micro-CT technique for imaging localized airway
             obstruction performed well in our evaluation, and provides a
             higher resolution compared to micro-SPECT. Both DE micro-CT
             and micro-SPECT provide critical, quantitative lung
             biomarkers for image-based anatomical and functional
             information in the small animal. The methods are readily
             linked to clinical methods allowing direct comparison of
             preclinical and clinical results. © 2014
             SPIE.},
   Doi = {10.1117/12.2043094},
   Key = {fds268714}
}

@article{fds268698,
   Author = {Subashi, E and Qi, Y and Johnson, GA},
   Title = {Dynamic contrast-enhanced MR microscopy identifies regions
             of therapeutic response in a preclinical model of colorectal
             adenocarcinoma.},
   Journal = {Med Phys},
   Volume = {42},
   Number = {5},
   Pages = {2482-2488},
   Year = {2015},
   Month = {May},
   ISSN = {0094-2405},
   url = {http://dx.doi.org/10.1118/1.4917525},
   Abstract = {PURPOSE: A typical dynamic contrast-enhanced (DCE)-MRI study
             often compares the derived pharmacokinetic parameters on
             manually selected tumor regions or over the entire tumor
             volume. These measurements include domains where the
             interpretation of the biomarkers may be unclear (such as in
             necrotic areas). Here, the authors describe a technique for
             increasing the sensitivity and specificity of DCE-MRI by
             identifying tumor regions with a variable response to
             therapy. METHODS: Two cohorts (n = 8/group) of nu/nu mice
             with LS-174T implanted in the mammary fat pad were imaged at
             five time points over four weeks. The treatment/control
             group received bevacizumab/saline at a dose of 5 mg/kg or 5
             ml/kg twice weekly; imaging experiments were performed
             weekly. MR images were acquired at an isotropic resolution
             of 156 μm(3)(2.4 nl) and with a sampling rate of 9.9 s. The
             histogram of the time-to-peak (TTP) was used to identify two
             (fast- and slow-enhancing) regions based on a threshold of
             TTP = 1000 s. The regions were correlated with histology,
             and the effect of therapy was locally examined. RESULTS:
             Tumors in the treatment group had a significantly longer
             doubling time. The regions defined by thresholding the TTP
             histogram identified two distinct domains correlating
             significantly with tumor permeability and microvessel
             density. In the fast-enhancing region, the mean permeability
             constant (K(trans)) was significantly lower in the treatment
             group at day 9; in the slow-enhancing region, K(trans) was
             not different between the control and treatment groups. At
             day 9, the relative volume of the fast-enhancing region was
             significantly lower in the treatment group, while that of
             the slow-enhancing region was significantly higher.
             CONCLUSIONS: Two regions with distinct kinetic parameters
             were identified based on the histogram of TTP. The effect of
             bevacizumab, as measured by a decrease in K(trans), was
             confined to one of these regions. High spatiotemporal
             resolution MR studies may contribute unique insights into
             the response of the tumor microenvironment to
             therapy.},
   Doi = {10.1118/1.4917525},
   Key = {fds268698}
}

@article{fds341984,
   Author = {Privratsky, JR and Wang, N and Qi, Y and Ren, J and Morris, BT and Hunting,
             JC and Johnson, GA and Crowley, SD},
   Title = {Dynamic contrast-enhanced MRI promotes early detection of
             toxin-induced acute kidney injury.},
   Journal = {Am J Physiol Renal Physiol},
   Volume = {316},
   Number = {2},
   Pages = {F351-F359},
   Year = {2019},
   Month = {February},
   url = {http://dx.doi.org/10.1152/ajprenal.00416.2018},
   Abstract = {Acute kidney injury (AKI) is a common cause of morbidity and
             mortality in hospitalized patients. Nevertheless, there is
             limited ability to diagnose AKI in its earliest stages
             through the collection of structural and functional
             information. Magnetic resonance imaging (MRI) is
             increasingly being used to provide structural and functional
             data that characterize the injured kidney. Dynamic
             contrast-enhanced (DCE) MRI is an imaging modality with
             robust spatial and temporal resolution; however, its ability
             to detect changes in kidney function following AKI has not
             been determined. We hypothesized that DCE MRI would detect a
             prolongation in contrast transit time following
             toxin-induced AKI earlier than commonly used serum and
             tissue biomarkers. To test our hypothesis, we injected mice
             with either vehicle or cisplatin (30 mg/kg) and performed
             DCE MRI at multiple time points. We found that commonly used
             kidney injury biomarkers, including creatinine, blood urea
             nitrogen, and neutrophil gelatinase-associated lipocalin,
             did not rise until day 2 following cisplatin. Tissue levels
             of the proinflammatory cytokines and chemokines, tumor
             necrosis factor-α, interleukin (IL)-1β, IL-1α, IL-6, C-C
             motif chemokine ligand 2, and C-X-C motif chemokine ligand 2
             similarly did not upregulate until day 2 following
             cisplatin. However, the time to peak intensity of contrast
             in the renal collecting system was already prolonged at day
             1 following cisplatin compared with vehicle-treated mice.
             This intensity change mirrored changes in kidney injury as
             measured by histological analysis and in transporter
             expression in the proximal tubule. Taken together, DCE MRI
             is a promising preclinical imaging modality that is useful
             for assessing functional capacity of the kidney in the
             earliest stages following AKI.},
   Doi = {10.1152/ajprenal.00416.2018},
   Key = {fds341984}
}

@article{fds292754,
   Author = {Xie, L and Layton, AT and Wang, N and Larson, PEZ and Zhang, JL and Lee,
             VS and Liu, C and Johnson, GA},
   Title = {Dynamic contrast-enhanced quantitative susceptibility
             mapping with ultrashort echo time MRI for evaluating renal
             function.},
   Journal = {Am J Physiol Renal Physiol},
   Volume = {310},
   Number = {2},
   Pages = {F174-F182},
   Year = {2016},
   Month = {January},
   ISSN = {1931-857X},
   url = {http://dx.doi.org/10.1152/ajprenal.00351.2015},
   Abstract = {Dynamic contrast-enhanced (DCE) MRI can provide key insight
             into renal function. DCE MRI is typically achieved through
             an injection of a gadolinium (Gd)-based contrast agent,
             which has desirable T1 quenching and tracer kinetics.
             However, significant T2* blooming effects and signal voids
             can arise when Gd becomes very concentrated, especially in
             the renal medulla and pelvis. One MRI sequence designed to
             alleviate T2* effects is the ultrashort echo time (UTE)
             sequence. In the present study, we observed T2* blooming in
             the inner medulla of the mouse kidney, despite using UTE at
             an echo time of 20 microseconds and a low dose of 0.03
             mmol/kg Gd. We applied quantitative susceptibility mapping
             (QSM) and resolved the signal void into a positive
             susceptibility signal. The susceptibility values [in parts
             per million (ppm)] were converted into molar concentrations
             of Gd using a calibration curve. We determined the
             concentrating mechanism (referred to as the concentrating
             index) as a ratio of maximum Gd concentration in the inner
             medulla to the renal artery. The concentrating index was
             assessed longitudinally over a 17-wk course (3, 5, 7, 9, 13,
             17 wk of age). We conclude that the UTE-based DCE method is
             limited in resolving extreme T2* content caused by the
             kidney's strong concentrating mechanism. QSM was able to
             resolve and confirm the source of the blooming effect to be
             the large positive susceptibility of concentrated Gd. UTE
             with QSM can complement traditional magnitude UTE and offer
             a powerful tool to study renal pathophysiology.},
   Doi = {10.1152/ajprenal.00351.2015},
   Key = {fds292754}
}

@article{fds132914,
   Author = {BT Chen and GA Johnson},
   Title = {Dynamic lung morphology of methacholine-induced
             heterogeneous bronchoconstriction.},
   Journal = {Magnetic resonance in medicine : official journal of the
             Society of Magnetic Resonance in Medicine / Society of
             Magnetic Resonance in Medicine, United States},
   Volume = {52},
   Number = {5},
   Pages = {1080-6},
   Year = {2004},
   Month = {November},
   ISSN = {0740-3194},
   Keywords = {Animals • Bronchoconstriction* • Female •
             Helium • Injections, Intravenous • Isotopes •
             Magnetic Resonance Imaging • Methacholine Chloride
             • Rats • Rats, Sprague-Dawley • Respiratory
             System • administration & dosage • diagnostic use
             • drug effects* • methods* •
             pharmacology*},
   Abstract = {Hyperpolarized (HP) 3helium (3He) dynamic MRI was used to
             investigate airway response in rats following intravenous
             (i.v.) bolus administration of a contractile agent,
             methacholine (MCh). The method provides direct visualization
             of the ventilated regions within the lung. Heterogeneous
             bronchoconstriction following the i.v. MCh injection was
             evident using this technique. These 3He dynamic lung images
             revealed that the inspired fresh air was shunted to the
             less-constricted regions after the MCh challenge in a
             similar manner as described by Laplace's relationship for
             the stability between adjacent alveoli. The airways in the
             more-constricted regions became nearly closed, resulting in
             air trapping, while the airways in the less-constricted
             regions remained effectively open, leading to overinflation.
             These data suggest a lung model of airway constriction
             partitioned into ventilated and nonventilated regions. These
             nonventilated regions are heterogeneously distributed in the
             lung and this distribution cannot be deduced from
             spirometric measurement of the whole lung. We demonstrate
             that a combination of functional 3He images and anatomical
             1H images provide an effective method to diagnose regional
             lung abnormalities in rats.},
   Key = {fds132914}
}

@booklet{Chen04,
   Author = {Chen, BT and Johnson, GA},
   Title = {Dynamic lung morphology of methacholine-induced
             heterogeneous bronchoconstriction.},
   Journal = {Magn Reson Med},
   Volume = {52},
   Number = {5},
   Pages = {1080-1086},
   Year = {2004},
   Month = {November},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/15508158},
   Abstract = {Hyperpolarized (HP) 3helium (3He) dynamic MRI was used to
             investigate airway response in rats following intravenous
             (i.v.) bolus administration of a contractile agent,
             methacholine (MCh). The method provides direct visualization
             of the ventilated regions within the lung. Heterogeneous
             bronchoconstriction following the i.v. MCh injection was
             evident using this technique. These 3He dynamic lung images
             revealed that the inspired fresh air was shunted to the
             less-constricted regions after the MCh challenge in a
             similar manner as described by Laplace's relationship for
             the stability between adjacent alveoli. The airways in the
             more-constricted regions became nearly closed, resulting in
             air trapping, while the airways in the less-constricted
             regions remained effectively open, leading to overinflation.
             These data suggest a lung model of airway constriction
             partitioned into ventilated and nonventilated regions. These
             nonventilated regions are heterogeneously distributed in the
             lung and this distribution cannot be deduced from
             spirometric measurement of the whole lung. We demonstrate
             that a combination of functional 3He images and anatomical
             1H images provide an effective method to diagnose regional
             lung abnormalities in rats.},
   Doi = {10.1002/mrm.20251},
   Key = {Chen04}
}

@article{fds132844,
   Author = {GA Johnson and G Cates and XJ Chen and GP Cofer and B Driehuys and W
             Happer, LW Hedlund and B Saam, MD Shattuck and J
             Swartz},
   Title = {Dynamics of magnetization in hyperpolarized gas MRI of the
             lung.},
   Journal = {Magnetic resonance in medicine : official journal of the
             Society of Magnetic Resonance in Medicine / Society of
             Magnetic Resonance in Medicine, UNITED STATES},
   Volume = {38},
   Number = {1},
   Pages = {66-71},
   Year = {1997},
   Month = {July},
   ISSN = {0740-3194},
   Keywords = {Animals • Guinea Pigs • Helium • Isotopes
             • Lung • Magnetic Resonance Imaging • Male
             • Respiration • anatomy & histology* •
             diagnostic use* • methods*},
   Abstract = {The magnetization in hyperpolarized gas (HP) MRI is
             generated by laser polarization that is independent of the
             magnet and imaging process. As a consequence, there is no
             equilibrium magnetization during the image acquisition. The
             competing processes of gas inflow and depolarization of the
             spins lead to large changes in signal as one samples
             k-space. A model is developed of dynamic changes in
             polarization of hyperpolarized 3He during infusion and in
             vivo imaging of the lung and verified experimentally in a
             live guinea pig. Projection encoding is used to measure the
             view-to-view variation with temporal resolution < 4 ms.
             Large excitation angles effectively sample the magnetization
             in the early stages of inflow, highlighting larger airways,
             while smaller excitation angles produce images of the more
             distal spaces. The work provides a basis for pulse sequences
             designed to effectively exploit HP MRI in the
             lung.},
   Key = {fds132844}
}

@booklet{Johnson97b,
   Author = {Johnson, GA and Cates, G and Chen, XJ and Cofer, GP and Driehuys, B and Happer, W and Hedlund, LW and Saam, B and Shattuck, MD and Swartz,
             J},
   Title = {Dynamics of magnetization in hyperpolarized gas MRI of the
             lung.},
   Journal = {Magn Reson Med},
   Volume = {38},
   Number = {1},
   Pages = {66-71},
   Year = {1997},
   Month = {July},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/9211381},
   Abstract = {The magnetization in hyperpolarized gas (HP) MRI is
             generated by laser polarization that is independent of the
             magnet and imaging process. As a consequence, there is no
             equilibrium magnetization during the image acquisition. The
             competing processes of gas inflow and depolarization of the
             spins lead to large changes in signal as one samples
             k-space. A model is developed of dynamic changes in
             polarization of hyperpolarized 3He during infusion and in
             vivo imaging of the lung and verified experimentally in a
             live guinea pig. Projection encoding is used to measure the
             view-to-view variation with temporal resolution < 4 ms.
             Large excitation angles effectively sample the magnetization
             in the early stages of inflow, highlighting larger airways,
             while smaller excitation angles produce images of the more
             distal spaces. The work provides a basis for pulse sequences
             designed to effectively exploit HP MRI in the
             lung.},
   Doi = {10.1002/mrm.1910380111},
   Key = {Johnson97b}
}

@booklet{Kodali03,
   Author = {K. Kodali and C. M. Davitt and G. A. Johnson and T. L.
             Ott},
   Title = {Dynamin family member and antiviral protein, Mx,
             co-localizes with autocrine motility factor receptor in an
             ovine uterine lumenal epithelial cell line.},
   Journal = {Biology Of Reproduction},
   Volume = {68},
   Pages = {181 -- 181},
   Year = {2003},
   Key = {Kodali03}
}

@booklet{Lindquist98,
   Author = {J. L. Lindquist and J. A. Dieleman and D. A. Mortensen and G. A. Johnson and D. Y. Wyse-pester},
   Title = {Economic importance of managing spatially heterogeneous weed
             populations},
   Journal = {Weed Technology},
   Volume = {12},
   Number = {1},
   Pages = {7 -- 13},
   Year = {1998},
   Key = {Lindquist98}
}

@article{fds174258,
   Author = {GA Johnson and RA Lahti and TL Lemke and RV Heinzelman},
   Title = {Effect of alpha-methyl-5-hydroxytryptophan ethyl ester upon
             tissue norepinephrine levels in rats and
             mice.},
   Journal = {Biochemical pharmacology},
   Volume = {18},
   Number = {7},
   Pages = {1593-600},
   Year = {1969},
   Month = {July},
   ISSN = {0006-2952},
   Keywords = {5-Hydroxytryptophan • Adrenal Glands • Animals
             • Brain • Brain Chemistry • Esters •
             Mice • Mixed Function Oxygenases • Myocardium
             • Norepinephrine • Rats • Time Factors •
             Tyrosine • administration & dosage • analysis
             • analysis* • enzymology • metabolism •
             pharmacology • pharmacology*},
   Language = {eng},
   Key = {fds174258}
}

@booklet{Baker85,
   Author = {C. A. Baker and D. W. Harris and G. A. Johnson},
   Title = {Effect of atriopeptin-ii on cyclic-nucleotide production in
             tissue-culture cells},
   Journal = {Federation Proceedings},
   Volume = {44},
   Number = {4},
   Pages = {1108 -- 1108},
   Year = {1985},
   Key = {Baker85}
}

@article{fds174178,
   Author = {SA Warnke and SY Chen and DL Wyse and GA Johnson and PM
             Porter},
   Title = {Effect of Rotation Crops on Heterodera glycines Population
             Density in a Greenhouse Screening Study.},
   Journal = {Journal of nematology},
   Volume = {38},
   Number = {3},
   Pages = {391-8},
   Year = {2006},
   Month = {September},
   ISSN = {0022-300X},
   Abstract = {Crop rotation is a common means of reducing pathogen
             populations in soil. Several rotation crops have been shown
             to reduce soybean cyst nematode (Heterodera glycines)
             populations, but a comprehensive study of the optimal crops
             is needed. A greenhouse study was conducted to determine the
             effect of growth and decomposition of 46 crops on population
             density of H. glycines. Crops were sown in soil infested
             with H. glycines. Plants were maintained until 75 days after
             planting, when the soil was mixed, a sample of the soil
             removed to determine egg density, and shoots and roots
             chopped and mixed into the soil. After 56 days, soil samples
             were again taken for egg counts, and a susceptible soybean
             ('Sturdy') was planted in the soil as a bioassay to
             determine egg viability. Sunn hemp (Crotalaria juncea),
             forage pea (Pisum sativum), lab-lab bean (Lablab purpureus),
             Illinois bundleflower (Desman-thus illinoensis), and alfalfa
             (Medicago sativa) generally resulted in smaller egg
             population density in soil or number of cysts formed on
             soybean in the bioassay than the fallow control. Sunn hemp
             most consistently showed the lowest numbers of eggs and
             cysts. As a group, legumes resulted in lower egg population
             densities than monocots, Brassica species, and other
             dicots.},
   Language = {eng},
   Key = {fds174178}
}

@booklet{Johnson02b,
   Author = {G. A. Johnson and T. R. Hoverstad},
   Title = {Effect of row spacing and herbicide application timing on
             weed control and grain yield in corn (Zea
             mays)},
   Journal = {Weed Technology},
   Volume = {16},
   Number = {3},
   Pages = {548 -- 553},
   Year = {2002},
   Key = {Johnson02b}
}

@booklet{Stahl99,
   Author = {L. A. B. Stahl and G. A. Johnson and D. L. Wyse and D. D.
             Buhler and J. L. Gunsolus},
   Title = {Effect of tillage on timing of Setaria spp. emergence and
             growth},
   Journal = {Weed Science},
   Volume = {47},
   Number = {5},
   Pages = {563 -- 570},
   Year = {1999},
   Key = {Stahl99}
}

@article{fds132769,
   Author = {GA Johnson and CE Ravin},
   Title = {Effect of vertical cassette holder design and construction
             on scatter-to-primary radiation ratios.},
   Journal = {Radiology, UNITED STATES},
   Volume = {138},
   Number = {2},
   Pages = {461-4},
   Year = {1981},
   Month = {February},
   ISSN = {0033-8419},
   Keywords = {Humans • Radiography • Scattering, Radiation*
             • Technology, Radiologic • instrumentation*},
   Abstract = {This paper analyzes the contribution to scattered radiation
             at the film plane by individual components of a conventional
             wall-mounted cassette holder. With grid technique, scatter
             from the front panel of the cassette holder is effectively
             reduced, but considerable scatter reaches the film plane
             from the automatic exposure control pickup interposed
             between the grid and the film cassette. With air-gap
             technique (grid removed), the front panel of the cassette
             holder and the automatic exposure control pickup contribute
             equally to increased scattered radiation at the film plane.
             The contribution to the total scatter from the air-gap
             positioning plate is less significant.},
   Key = {fds132769}
}

@booklet{Johnson81a,
   Author = {Johnson, GA and Ravin, CE},
   Title = {Effect of vertical cassette holder design and construction
             on scatter-to-primary radiation ratios.},
   Journal = {Radiology},
   Volume = {138},
   Number = {2},
   Pages = {461-464},
   Year = {1981},
   Month = {February},
   ISSN = {0033-8419},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/7455131},
   Abstract = {This paper analyzes the contribution to scattered radiation
             at the film plane by individual components of a conventional
             wall-mounted cassette holder. With grid technique, scatter
             from the front panel of the cassette holder is effectively
             reduced, but considerable scatter reaches the film plane
             from the automatic exposure control pickup interposed
             between the grid and the film cassette. With air-gap
             technique (grid removed), the front panel of the cassette
             holder and the automatic exposure control pickup contribute
             equally to increased scattered radiation at the film plane.
             The contribution to the total scatter from the air-gap
             positioning plate is less significant.},
   Doi = {10.1148/radiology.138.2.7455131},
   Key = {Johnson81a}
}

@article{fds325755,
   Author = {O'Leary-Moore, SK and Godin, EA and Parnell, SE and Dehart, DB and Ament, JJ and Johnson, GA and Styner, M and Sulik,
             KK},
   Title = {EFFECTS OF ACUTE GESTATIONAL DAY 10 ETHANOL EXPOSURE ON THE
             DEVELOPING MOUSE BRAIN: A HIGH-RESOLUTION MAGNETIC RESONANCE
             MICROSCOPY STUDY},
   Journal = {ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH},
   Volume = {33},
   Number = {6},
   Pages = {132A-132A},
   Year = {2009},
   Key = {fds325755}
}

@article{8407765,
   Author = {Mai, W. and Badea, C.T. and Wheeler, C.T. and Hedlund, L.W. and Johnson, G.A.},
   Title = {Effects of breathing and cardiac motion on spatial
             resolution in the microscopic imaging of
             rodents},
   Journal = {Magn. Reson. Med. (USA)},
   Volume = {53},
   Number = {4},
   Pages = {858 - 65},
   Year = {2005},
   url = {http://dx.doi.org/10.1002/mrm.20400},
   Keywords = {biomedical MRI;cardiovascular system;diagnostic
             radiography;pneumodynamics;surgery;},
   Abstract = {One can acquire high-resolution pulmonary and cardiac images
             in live rodents with MR microscopy by synchronizing the
             image acquisition to the breathing cycle across multiple
             breaths, and gating to the cardiac cycle. The precision with
             which one can synchronize image acquisition to the motion
             defines the ultimate resolution limit that can be attained
             in such studies. The present work was performed to evaluate
             how reliably the pulmonary and cardiac structures return to
             the same position from breath to breath and beat to beat
             across the prolonged period required for MR microscopy.
             Radiopaque beads were surgically glued to the abdominal
             surface of the diaphragm and on the cardiac ventricles of
             anesthetized, mechanically ventilated rats. We evaluated the
             range of motion for the beads (relative to a reference
             vertebral bead) using digital microradiography with two
             specific biological gating methods: 1) ventilation
             synchronous acquisition, and 2) both ventilation synchronous
             and cardiac-gated acquisitions. The standard deviation (SD)
             of the displacement was &mu;m100 &mu;m, which is comparable
             to the resolution limit for in vivo MRI imposed by
             signal-to-noise ratio (SNR) constraints. With careful
             control of motion, its impact on resolution can be limited.
             This work provides the first quantitative measure of the
             motion-imposed resolution limits for in vivo
             imaging},
   Key = {8407765}
}

@article{fds268882,
   Author = {Maï, W and Badea, CT and Wheeler, CT and Hedlund, LW and Johnson,
             GA},
   Title = {Effects of breathing and cardiac motion on spatial
             resolution in the microscopic imaging of
             rodents.},
   Journal = {Magn Reson Med},
   Volume = {53},
   Number = {4},
   Pages = {858-865},
   Year = {2005},
   Month = {April},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/15799053},
   Keywords = {Animals • Cardiovascular Physiology* • Diaphragm
             • Magnetic Resonance Imaging • Male •
             Myocardial Contraction • Rats • Rats, Inbred F344
             • Reproducibility of Results • Tungsten •
             methods* • physiology* • radiography},
   Abstract = {One can acquire high-resolution pulmonary and cardiac images
             in live rodents with MR microscopy by synchronizing the
             image acquisition to the breathing cycle across multiple
             breaths, and gating to the cardiac cycle. The precision with
             which one can synchronize image acquisition to the motion
             defines the ultimate resolution limit that can be attained
             in such studies. The present work was performed to evaluate
             how reliably the pulmonary and cardiac structures return to
             the same position from breath to breath and beat to beat
             across the prolonged period required for MR microscopy.
             Radiopaque beads were surgically glued to the abdominal
             surface of the diaphragm and on the cardiac ventricles of
             anesthetized, mechanically ventilated rats. We evaluated the
             range of motion for the beads (relative to a reference
             vertebral bead) using digital microradiography with two
             specific biological gating methods: 1) ventilation
             synchronous acquisition, and 2) both ventilation synchronous
             and cardiac-gated acquisitions. The standard deviation (SD)
             of the displacement was < or =100 microm, which is
             comparable to the resolution limit for in vivo MRI imposed
             by signal-to-noise ratio (SNR) constraints. With careful
             control of motion, its impact on resolution can be limited.
             This work provides the first quantitative measure of the
             motion-imposed resolution limits for in vivo
             imaging.},
   Doi = {10.1002/mrm.20400},
   Key = {fds268882}
}

@article{fds268777,
   Author = {Mai, W and Badea, CT and Wheeler, CT and Hedlund, LW and Johnson,
             GA},
   Title = {Effects of breathing motion on the spatial resolution in
             microscopic imaging techniques of rodents},
   Journal = {2004 2nd IEEE International Symposium on Biomedical Imaging:
             Macro to Nano},
   Volume = {1},
   Pages = {472-475},
   Year = {2004},
   Month = {December},
   ISBN = {0780383885},
   Abstract = {Magnetic resonance microscopy is capable of producing
             high-resolution pulmonary images in live rodents by
             synchronizing the image acquisition across multiple breaths.
             The precision with which one can control motion will
             probably define the resolution limit that can be attained in
             such studies. This work was performed to evaluate how
             reliably the respiratory structures return to the same
             position from breath to breath each time data are acquired.
             Radio-opaque beads were surgically glued on the diaphragm of
             anesthetized, mechanically ventilated rats. Their range of
             motion (relative to a reference vertebral bead) was
             evaluated using digital micro-radiography with two specific
             biological pulse sequences: (1) ventilation synchronous
             acquisition, and (2) both ventilation synchronous and
             cardiac gated acquisition. The standard deviation of the
             displacement was on the order of, or less than 100 microns,
             which is comparable to the resolution limit for in vivo
             magnetic resonance imaging imposed by signal to noise
             constraints. With careful control of motion, its impact on
             resolution can be limited. This work provides the first
             quantitative measure of the motion imposed resolution limits
             for in vivo imaging. ©2004 IEEE.},
   Key = {fds268777}
}

@article{fds325752,
   Author = {Parnell, SE and Holloway, HT and Paniagua, B and Oguz, I and Styner, MA and Johnson, GA and Sulik, KK},
   Title = {EFFECTS OF CHRONIC EARLY GESTATIONAL ETHANOL EXPOSURE ON THE
             DEVELOPING BRAIN: A MAGNETIC RESONANCE MICROSCOPY
             STUDY},
   Journal = {ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH},
   Volume = {36},
   Pages = {279A-279A},
   Year = {2012},
   Key = {fds325752}
}

@article{fds132873,
   Author = {RH Sherrier and C Chiles and WE Wilkinson and GA Johnson and CE
             Ravin},
   Title = {Effects of image processing on nodule detection rates in
             digitized chest radiographs: ROC study of observer
             performance.},
   Journal = {Radiology, UNITED STATES},
   Volume = {166},
   Number = {2},
   Pages = {447-50},
   Year = {1988},
   Month = {February},
   ISSN = {0033-8419},
   Keywords = {Coin Lesion, Pulmonary • Filtration • Humans
             • Lung Neoplasms • ROC Curve* • Radiographic
             Image Enhancement • methods • methods* •
             radiography*},
   Abstract = {To evaluate the effects of image processing in digitized
             chest radiographs when high-resolution images are used, an
             examination was done in which the detection of pulmonary
             nodules in unprocessed digitized chest radiographs was
             compared with that in images that had undergone processing
             with two methods, adaptive filtration and histogram
             equalization. The processing techniques have been optimized
             in previous work to selectively enhance the retrocardiac and
             subdiaphragmatic areas without significant alteration of
             detail in the lung. Eight observers were shown 150 test
             radiographs (50 unprocessed, 50 processed with adaptive
             filtration, 50 processed with histogram equalization)
             containing 150 nodules. The results indicate a statistically
             significant (P less than .03) difference, with highest
             observer performance in the chest radiographs processed with
             adaptive filtration (median area under ROC curve = 0.78),
             compared with unprocessed images (median = 0.68) and chest
             radiographs processed with histogram equalization (median =
             0.62). Performance in the lung was not significantly
             different. Adaptive filtration applied to selectively
             enhance underexposed areas of film images may improve nodule
             detection. Histogram equalization provided no improvement in
             performance.},
   Key = {fds132873}
}

@booklet{Sherrier88a,
   Author = {Sherrier, RH and Chiles, C and Wilkinson, WE and Johnson, GA and Ravin,
             CE},
   Title = {Effects of image processing on nodule detection rates in
             digitized chest radiographs: ROC study of observer
             performance.},
   Journal = {Radiology},
   Volume = {166},
   Number = {2},
   Pages = {447-450},
   Year = {1988},
   Month = {February},
   ISSN = {0033-8419},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/3336719},
   Abstract = {To evaluate the effects of image processing in digitized
             chest radiographs when high-resolution images are used, an
             examination was done in which the detection of pulmonary
             nodules in unprocessed digitized chest radiographs was
             compared with that in images that had undergone processing
             with two methods, adaptive filtration and histogram
             equalization. The processing techniques have been optimized
             in previous work to selectively enhance the retrocardiac and
             subdiaphragmatic areas without significant alteration of
             detail in the lung. Eight observers were shown 150 test
             radiographs (50 unprocessed, 50 processed with adaptive
             filtration, 50 processed with histogram equalization)
             containing 150 nodules. The results indicate a statistically
             significant (P less than .03) difference, with highest
             observer performance in the chest radiographs processed with
             adaptive filtration (median area under ROC curve = 0.78),
             compared with unprocessed images (median = 0.68) and chest
             radiographs processed with histogram equalization (median =
             0.62). Performance in the lung was not significantly
             different. Adaptive filtration applied to selectively
             enhance underexposed areas of film images may improve nodule
             detection. Histogram equalization provided no improvement in
             performance.},
   Doi = {10.1148/radiology.166.2.3336719},
   Key = {Sherrier88a}
}

@booklet{Stewart00,
   Author = {M. D. Stewart and G. A. Johnson and R. C. Burghardt and C.
             A. Vyhlidal and S. H. Safe and F. W. Bazer and T. E.
             Spencer},
   Title = {Effects of interferon tau on short- and long-term activation
             of STAT proteins in immortalized ovine uterine luminal
             epithelial cells.},
   Journal = {Biology Of Reproduction},
   Volume = {62},
   Pages = {118 -- 118},
   Year = {2000},
   Key = {Stewart00}
}

@article{fds180938,
   Author = {DW Bailey and KA Dunlap and DW Erikson and AK Patel and FW Bazer and RC
             Burghardt, GA Johnson},
   Title = {Effects of long-term progesterone exposure on porcine
             uterine gene expression: progesterone alone does not induce
             secreted phosphoprotein 1 (osteopontin) in glandular
             epithelium.},
   Journal = {Reproduction (Cambridge, England)},
   Volume = {140},
   Number = {4},
   Pages = {595-604},
   Year = {2010},
   Month = {October},
   ISSN = {1741-7899},
   url = {http://dx.doi.org/10.1530/REP-10-0169},
   Abstract = {Pigs experience significant conceptus loss near
             mid-gestation, correlating with increasing glandular
             epithelial (GE) development and secretory activity. Secreted
             phosphoprotein 1 (SPP1, osteopontin) increases in GE between
             days 30 and 40 of pregnancy and is expressed in the GE of
             day 90 pseudopregnant pigs, suggesting that progesterone
             (P(4)) from corpora lutea is responsible for induction of
             SPP1 in GE. In this study, pigs were ovariectomized and
             treated daily with P(4) to assess effects of 40 days of P(4)
             exposure on SPP1, P(4) receptor (PGR), uteroferrin (ACP5),
             and fibroblast growth factor 7 (FGF7) expression in porcine
             endometria. PGR mRNA decreased in pigs injected with P(4)
             compared with pigs injected with corn oil (CO), and PGRs
             were downregulated in the luminal epithelium (LE) and GE.
             ACP5 mRNA increased in pigs injected with P(4) compared with
             pigs injected with CO, and ACP5 was induced in the GE of
             P(4)-treated pigs. FGF7 mRNA increased in pigs injected with
             P(4) compared with pigs injected with CO, and FGF7 was
             induced in the LE and GE of P(4)-treated pigs. SPP1 mRNA was
             not different between pigs injected with P(4) compared with
             pigs injected with CO, and SPP1 was not present in the GE of
             P(4)-treated pigs. Therefore, long-term P(4), in the absence
             of ovarian and/or conceptus factors, does not induce SPP1
             expression in GE. We hypothesize that a servomechanism
             involving sequential effects of multiple hormones and
             cytokines, similar to those for sheep and humans, is
             required for GE differentiation and function, including the
             synthesis and secretion of SPP1.},
   Language = {eng},
   Doi = {10.1530/REP-10-0169},
   Key = {fds180938}
}

@article{fds180940,
   Author = {DW Bailey and KA Dunlap and JW Frank and DW Erikson and BG White and FW
             Bazer, RC Burghardt and GA Johnson},
   Title = {Effects of long-term progesterone on developmental and
             functional aspects of porcine uterine epithelia and
             vasculature: progesterone alone does not support development
             of uterine glands comparable to that of pregnancy.},
   Journal = {Reproduction (Cambridge, England)},
   Volume = {140},
   Number = {4},
   Pages = {583-94},
   Year = {2010},
   Month = {October},
   ISSN = {1741-7899},
   url = {http://dx.doi.org/10.1530/REP-10-0170},
   Abstract = {In pigs, endometrial functions are regulated primarily by
             progesterone and placental factors including estrogen.
             Progesterone levels are high throughout pregnancy to
             stimulate and maintain secretion of histotroph from uterine
             epithelia necessary for growth, implantation, placentation,
             and development of the conceptus (embryo and its
             extra-embryonic membranes). This study determined effects of
             long-term progesterone on development and histoarchitecture
             of endometrial luminal epithelium (LE), glandular epithelium
             (GE), and vasculature in pigs. Pigs were ovariectomized
             during diestrus (day 12), and then received daily injections
             of either corn oil or progesterone for 28 days. Prolonged
             progesterone treatment resulted in increased weight and
             length of the uterine horns, and thickness of the
             endometrium and myometrium. Hyperplasia and hypertrophy of
             GE were not evident, but LE cell height increased,
             suggesting elevated secretory activity. Although GE
             development was deficient, progesterone supported increased
             endometrial angiogenesis comparable to that of pregnancy.
             Progesterone also supported alterations to the apical and
             basolateral domains of LE and GE. Dolichos biflorus
             agglutinin lectin binding and α(v) integrin were
             downregulated at the apical surfaces of LE and GE.
             Claudin-4, α(2)β(1) integrin, and vimentin were increased
             at basolateral surfaces, whereas occludins-1 and -2,
             claudin-3, and E-cadherin were unaffected by progesterone
             treatment indicating structurally competent trans-epithelial
             adhesion and tight junctional complexes. Collectively, the
             results suggest that progesterone affects LE, GE, and
             vascular development and histoarchitecture, but in the
             absence of ovarian or placental factors, it does not support
             development of GE comparable to pregnancy. Furthermore, LE
             and vascular development are highly responsive to the
             effects of progesterone.},
   Language = {eng},
   Doi = {10.1530/REP-10-0170},
   Key = {fds180940}
}

@booklet{Gibson83,
   Author = {J. K. Gibson and J. A. Gifford and P. F. Kane and G. L.
             Degraaf and F. G. Robinson and J. P. Hansen and D. W. Harris and G. A. Johnson and H. S. Greenberg and D. W.
             Ducharme},
   Title = {Effects of non-steroidal anti-inflammatory drugs on
             myocardial healing after myocardial-infarction},
   Journal = {Federation Proceedings},
   Volume = {42},
   Number = {3},
   Pages = {633 -- 633},
   Year = {1983},
   Key = {Gibson83}
}

@booklet{Spencer00,
   Author = {T. E. Spencer and G. A. Johnson and M. D. Stewart and M. M.
             Joyce and C. A. Gray and K. M. Taylor and A. Gertler and E.
             Gootwine and F. W. Bazer},
   Title = {Effects of ovine placental lactogen and growth hormone on
             ovine endometrial function.},
   Journal = {Biology Of Reproduction},
   Volume = {62},
   Pages = {264 -- 264},
   Year = {2000},
   Key = {Spencer00}
}

@booklet{Lee00,
   Author = {C. K. Lee and R. L. Weaks and G. A. Johnson and F. W. Bazer and J. A. Piedrahita},
   Title = {Effects of protease inhibitors and antioxidants on in vitro
             survival of porcine primordial germ cells},
   Journal = {Biology Of Reproduction},
   Volume = {63},
   Number = {3},
   Pages = {887 -- 897},
   Year = {2000},
   Month = {September},
   Key = {Lee00}
}

@article{fds174143,
   Author = {CK Lee and RL Weaks and GA Johnson and FW Bazer and JA
             Piedrahita},
   Title = {Effects of protease inhibitors and antioxidants on In vitro
             survival of porcine primordial germ cells.},
   Journal = {Biology of reproduction},
   Volume = {63},
   Number = {3},
   Pages = {887-97},
   Year = {2000},
   Month = {September},
   ISSN = {0006-3363},
   Keywords = {Acetylcysteine • Animals • Antioxidants •
             Apoptosis • Cell Survival • Cells, Cultured •
             DNA Fragmentation • Dose-Response Relationship, Drug
             • Fetus • Germ Cells • In Situ Nick-End
             Labeling • Microscopy, Electron • Protease
             Inhibitors • Swine • administration & dosage
             • alpha-Macroglobulins • cytology • drug
             effects • drug effects* • pharmacology •
             pharmacology* • physiology*},
   Abstract = {One of the problems associated with in vitro culture of
             primordial germ cells (PGCs) is the large loss of cells
             during the initial period of culture. This study
             characterized the initial loss and determined the
             effectiveness of two classes of apoptosis inhibitors,
             protease inhibitors, and antioxidants on the ability of
             porcine PGCs to survive in culture. Results from electron
             microscopic analysis and in situ DNA fragmentation assay
             indicated that porcine PGCs rapidly undergo apoptosis when
             placed in culture. Additionally, alpha(2)-macroglobulin, a
             protease inhibitor and cytokine carrier, and
             N:-acetylcysteine, an antioxidant, increased the survival of
             PGCs in vitro. While other protease inhibitors tested did
             not affect survival of PGCs, all antioxidants tested
             improved survival of PGCs (P: < 0.05). Further results
             indicated that the beneficial effect of the antioxidants was
             critical only during the initial period of culture. Finally,
             it was determined that in short-term culture, in the absence
             of feeder layers, antioxidants could partially replace the
             effect(s) of growth factors and reduce apoptosis.
             Collectively, these results indicate that the addition of
             alpha(2)-macroglobulin and antioxidants can increase the
             number of PGCs in vitro by suppressing apoptosis.},
   Language = {eng},
   Key = {fds174143}
}

@booklet{Spencer99,
   Author = {T. E. Spencer and A. Gray and G. A. Johnson and K. M. Taylor and A. Gertler and E. Gootwine and T. L. Ott and F. W.
             Bazer},
   Title = {Effects of recombinant ovine interferon tau, placental
             lactogen, and growth hormone on the ovine
             uterus},
   Journal = {Biology Of Reproduction},
   Volume = {61},
   Number = {6},
   Pages = {1409 -- 1418},
   Year = {1999},
   Month = {December},
   Key = {Spencer99}
}

@article{fds174304,
   Author = {TE Spencer and A Gray and GA Johnson and KM Taylor and A Gertler and E
             Gootwine, TL Ott and FW Bazer},
   Title = {Effects of recombinant ovine interferon tau, placental
             lactogen, and growth hormone on the ovine
             uterus.},
   Journal = {Biology of reproduction},
   Volume = {61},
   Number = {6},
   Pages = {1409-18},
   Year = {1999},
   Month = {December},
   ISSN = {0006-3363},
   Keywords = {Animals • Corpus Luteum • Endometrium •
             Female • Gene Expression • Glycoproteins •
             Growth Hormone • Interferon Type I • Ki-67 Antigen
             • Ovariectomy • Placental Lactogen •
             Pregnancy Proteins • RNA, Messenger • Receptors,
             Estrogen • Receptors, Oxytocin • Receptors,
             Progesterone • Recombinant Proteins • Serpins*
             • Sheep* • analysis • chemistry • drug
             effects • genetics • pharmacology •
             pharmacology* • physiology • physiology*},
   Abstract = {Studies were conducted to determine effects of intrauterine
             administration of recombinant ovine interferon tau (IFNtau),
             placental lactogen (PL), and growth hormone (GH) on
             endometrial function. In the first study, administration of
             IFNtau to cyclic ewes for one period (Days 11-15) resulted
             in an interestrous interval (IEI) of approximately 30 days,
             whereas administration for two periods (Days 11-15 and Days
             21-25) extended the IEI to greater than 50 days.
             Administration of IFNtau from Days 11 to 15 and of PL or GH
             from Days 21 to 25 failed to extend the IEI more than for
             IFNtau alone. In the second study, effects of IFNtau, PL,
             and GH on endometrial differentiation and function were
             determined in ovariectomized ewes receiving ovarian steroid
             replacement therapy. Endometrial expression of mRNAs for
             estrogen receptor (ER), progesterone receptor (PR), and
             oxytocin receptor (OTR) were not affected by PL or GH
             treatment; however, uterine milk protein mRNA levels and
             stratum spongiosum gland density were increased by both PL
             and GH treatments. Collectively, results indicated that 1)
             PL and GH do not regulate endometrial PR, ER, and OTR
             expression or affect corpus luteum life span; 2)
             down-regulation of epithelial PR expression is requisite for
             progesterone induction of secretory gene expression in
             uterine glandular epithelium; 3) effects of PL and GH on
             endometrial function require IFNtau; and 4) PL and GH
             regulate endometrial gland proliferation and perhaps
             differentiated function.},
   Language = {eng},
   Key = {fds174304}
}

@booklet{Johnson01b,
   Author = {G. A. Johnson and M. D. Stewart and C. A. Gray and Y. Choi and R. C. Burghardt and L. Y. Yu-lee and F. W. Bazer and T.
             E. Spencer},
   Title = {Effects of the estrous cycle, pregnancy, and interferon tau
             on 2 ',5 '-oligoadenylate synthetase expression in the ovine
             uterus},
   Journal = {Biology Of Reproduction},
   Volume = {64},
   Number = {5},
   Pages = {1392 -- 1399},
   Year = {2001},
   Month = {May},
   Key = {Johnson01b}
}

@article{fds174204,
   Author = {GA Johnson, MD Stewart and CA Gray and Y Choi and RC Burghardt and LY
             Yu-Lee, FW Bazer and TE Spencer},
   Title = {Effects of the estrous cycle, pregnancy, and interferon tau
             on 2',5'-oligoadenylate synthetase expression in the ovine
             uterus.},
   Journal = {Biology of reproduction},
   Volume = {64},
   Number = {5},
   Pages = {1392-9},
   Year = {2001},
   Month = {May},
   ISSN = {0006-3363},
   Keywords = {2',5'-Oligoadenylate Synthetase • Animals • Cell
             Line • Endometrium • Estrus • Female •
             Gene Expression* • Interferon Type I • Pregnancy
             • Pregnancy Proteins • Recombinant Proteins •
             Sheep • Uterus • administration & dosage •
             drug effects • genetics* • metabolism •
             metabolism* • pharmacology • pharmacology* •
             physiology*},
   Abstract = {The enzymes which comprise the 2',5'-oligoadenylate
             synthetase (OAS) family are interferon (IFN) stimulated
             genes which regulate ribonuclease L antiviral responses and
             may play additional roles in control of cellular growth and
             differentiation. This study characterized OAS expression in
             the endometrium of cyclic and pregnant ewes as well as
             determined effects of IFNtau and progesterone on OAS
             expression in cyclic or ovariectomized ewes and in
             endometrial epithelial and stromal cell lines. In cyclic
             ewes, low levels of OAS protein were detected in the
             endometrial stroma (S) and glandular epithelium (GE). In
             early pregnant ewes, OAS expression increased in the S and
             GE on Day 15. OAS expression in the lumenal epithelium (LE)
             was not detected in uteri from either cyclic or pregnant
             ewes. Intrauterine administration of IFNtau stimulated OAS
             expression in the S and GE, and this effect of IFNtau was
             dependent on progesterone. Ovine endometrial LE, GE, and S
             cell lines responded to IFNtau with induction of OAS
             proteins. In all three cell lines, the 40/46-kDa OAS forms
             were induced by IFNtau, whereas the 100-kDa OAS form
             appeared to be constitutively expressed and not affected by
             IFNtau. The 69/71-kDa OAS forms were induced by IFNtau in
             the S and GE cell lines, but not in the LE. Collectively,
             these results indicate that OAS expression in the
             endometrial S and GE of the early pregnant ovine uterus is
             directly regulated by IFNtau from conceptus and requires the
             presence of progesterone.},
   Language = {eng},
   Key = {fds174204}
}

@article{fds326004,
   Author = {Wolbarsht, ML and O'foghludha, FA and Sliney, DH and Guy, AW and Smith,
             AA and Johnson, GA},
   Title = {Electromagnetic emission from visual display units: A
             non-hazard},
   Journal = {Proceedings of SPIE - The International Society for Optical
             Engineering},
   Volume = {229},
   Pages = {187-195},
   Publisher = {SPIE},
   Year = {1980},
   Month = {October},
   url = {http://dx.doi.org/10.1117/12.958802},
   Abstract = {An analysis of the electromagnetic emissions of an IBM Model
             32772 visual display unit showed no hazardous levels in any
             portion of the spectrum. The actual level of emission was
             measured throughout the spectrum from low frequency radio
             waves through x-radiation, extending from 10 KHz through 10
             GHz, then 0.2 to 10 μm, and from 5 to over 40 keV. In many
             parts of the spectrum, the level of emission was below the
             sensitivity of available instrumentation. In the radio
             frequency range, including the microwave region,
             measurements were also made on black and white and color
             television sets for the purpose of comparison. © 1980,
             SPIE.},
   Doi = {10.1117/12.958802},
   Key = {fds326004}
}

@booklet{Johnson99d,
   Author = {G. A. Johnson and K. J. Austin and A. M. Collins and W. J.
             Murdoch and T. R. Hansen},
   Title = {Endometrial ISG17 mRNA and a related mRNA are induced by
             interferon-tau and localized to glandular epithelial and
             stromal cells from pregnant cows},
   Journal = {Endocrine},
   Volume = {10},
   Number = {3},
   Pages = {243 -- 252},
   Year = {1999},
   Month = {June},
   Key = {Johnson99d}
}

@article{fds174237,
   Author = {GA Johnson and KJ Austin and AM Collins and WJ Murdoch and TR
             Hansen},
   Title = {Endometrial ISG17 mRNA and a related mRNA are induced by
             interferon-tau and localized to glandular epithelial and
             stromal cells from pregnant cows.},
   Journal = {Endocrine},
   Volume = {10},
   Number = {3},
   Pages = {243-52},
   Year = {1999},
   Month = {June},
   ISSN = {1355-008X},
   url = {http://dx.doi.org/10.1007/BF02738623},
   Keywords = {Animals • Blotting, Northern • Cattle • Cell
             Line • Endometrium • Epithelial Cells •
             Female • In Situ Hybridization • Interferon Type I
             • Nuclear Proteins • Pregnancy • Pregnancy
             Proteins • RNA, Messenger • Recombinant Proteins
             • Stromal Cells • Tissue Distribution •
             analysis • biosynthesis* • chemistry •
             genetics* • metabolism* • pharmacology •
             pharmacology*},
   Abstract = {The interferon stimulated gene product, ISG17, conjugates to
             bovine uterine proteins in response to conceptus-derived
             interferon (IFN)-tau. The objectives of the present
             experiments were to examine induction of ISG17 (0.65 kb) and
             a related 2.5 kb mRNA in response to IFN-tau and pregnancy
             using Northern blotting procedures, and to determine cell
             types in the endometrium that expressed ISG17 mRNA using in
             situ hybridization. RNA was isolated from endometrial
             explants or from bovine endometrial (BEND) cells cultured in
             the absence (control) or presence of 25 nM recombinant (r)
             bolFN-tau for 0, 3, 6, 12, 24, or 48 h. The major ISG17 0.65
             kb mRNA and a minor 2.5 kb mRNA were induced (p<0.05) after
             6 h (explants) or 3 h (BEND cells) treatment with
             rboIFN-tau. Both mRNAs were present in endometrium from day
             18 pregnant cows, but were absent in endometrium from
             nonpregnant cows. The ISG17 mRNA was localized to stromal
             and glandular epithelial cells on d 18 of pregnancy. The 2.5
             kb mRNA may encode a novel ISG17 homolog, or a unique
             polyISG17 repeat that is similar in structure to the
             polyubiquitin genes. Because ISG17 mRNA is induced in
             stromal and glandular epithelial cells, it could be assumed
             that ISG17 has a role in regulating intracellular proteins
             in both cell types.},
   Language = {eng},
   Doi = {10.1007/BF02738623},
   Key = {fds174237}
}

@booklet{Ede01,
   Author = {P. N. Ede and G. A. Johnson},
   Title = {Energy relations of gas estimated from flare radiation in
             Nigeria},
   Journal = {International Journal Of Energy Research},
   Volume = {25},
   Number = {1},
   Pages = {85 -- 91},
   Year = {2001},
   Month = {January},
   Key = {Ede01}
}

@article{fds174233,
   Author = {RC Burghardt, JR Burghardt and JD Taylor 2nd and AT Reeder and BT
             Nguen, TE Spencer and KJ Bayless and GA Johnson},
   Title = {Enhanced focal adhesion assembly reflects increased
             mechanosensation and mechanotransduction at
             maternal-conceptus interface and uterine wall during ovine
             pregnancy.},
   Journal = {Reproduction (Cambridge, England)},
   Volume = {137},
   Number = {3},
   Pages = {567-82},
   Year = {2009},
   Month = {March},
   ISSN = {1741-7899},
   url = {http://dx.doi.org/10.1530/REP-08-0304},
   Keywords = {Animals • Cytoskeletal Proteins • Embryo
             Implantation • Extracellular Matrix Proteins •
             Female • Fluorescent Antibody Technique • Focal
             Adhesions • Integrins • Mechanotransduction,
             Cellular • Models, Animal • Pregnancy • Sheep
             • Trophoblasts • Uterus • analysis •
             metabolism* • physiology • physiology*},
   Abstract = {The integrity of the fetal-maternal interface is critical
             for proper fetal nourishment during pregnancy. Integrins are
             important adhesion molecules present at the interface during
             implantation; however, in vivo evidence for integrin
             activation and focal adhesion formation at the
             maternal-conceptus interface is limited. We hypothesized
             that focal adhesion assembly in uterine luminal epithelium
             (LE) and conceptus trophectoderm (Tr) results from integrin
             binding of extracellular matrix (ECM) at this interface to
             provide increased tensile forces and signaling to coordinate
             utero-placental development. An ovine model of unilateral
             pregnancy was used to evaluate mechanotransduction events
             leading to focal adhesion assembly at the maternal-conceptus
             interface and within the uterine wall. Animals were
             hysterectomized on days 40, 80, or 120 of pregnancy, and
             uteri immunostained for integrins (ITGAV, ITGA4, ITGA5,
             ITGB1, ITGB3, and ITGB5), ECM proteins (SPP1, LGALS15,
             fibronectin (FN), and vitronectin (VTN)), cytoskeletal
             molecules (ACTN and TLN1), and a signal generator (PTK2).
             Focal adhesion assembly in myometrium and stroma was also
             studied to provide a frame of reference for mechanical
             stretch of the uterine wall. Large focal adhesions
             containing aggregates of ITGAV, ITGA4, ITGA5, ITGB1, ITGB5,
             ACTN, and PTK2 were detected in interplacentomal uterine LE
             and Tr of gravid but not non-gravid uterine horns and
             increased during pregnancy. SPP1 and LGALS15, but not FN or
             VTN, were present along LE and Tr interfaces in both uterine
             horns. These data support the idea that focal adhesion
             assembly at the maternal-conceptus interface reflects
             adaptation to increasing forces caused by the growing fetus.
             Cooperative binding of multiple integrins to SPP1 deposited
             at the maternal-conceptus interface forms an adhesive mosaic
             to maintain a tight connection between uterine and placental
             surfaces along regions of epitheliochorial placentation in
             sheep.},
   Language = {eng},
   Doi = {10.1530/REP-08-0304},
   Key = {fds174233}
}

@article{fds174128,
   Author = {DJ Waldon and TT Kawabe and CA Baker and GA Johnson and AE
             Buhl},
   Title = {Enhanced in vitro hair growth at the air-liquid interface:
             minoxidil preserves the root sheath in cultured whisker
             follicles.},
   Journal = {In vitro cellular & developmental biology.
             Animal},
   Volume = {29A},
   Number = {7},
   Pages = {555-61},
   Year = {1993},
   Month = {July},
   ISSN = {1071-2690},
   Keywords = {Air • Animals • Cells, Cultured •
             Collagenases • Cysteine • Gelatin Sponge,
             Absorbable • Glycoproteins • Guanidines •
             Hair • Keratins • Mice • Minoxidil •
             Pyridines • Sulfotransferases • Tissue Inhibitor
             of Metalloproteinases • Vibrissae • analysis
             • antagonists & inhibitors • chemistry •
             cytology* • growth & development* • metabolism
             • pharmacology • pharmacology*},
   Abstract = {Inasmuch as hair follicles are difficult to maintain in
             culture, the study of hair biology using cultured hair
             follicles has met with only limited success. In our attempts
             to solve the problem of follicle degeneration, we cultured
             follicles at the air-surface interface on a modified
             collagen matrix (Gelfoam). In follicles cultured at the
             air-surface or submerged, we examined follicular morphology,
             hair shaft growth, sulfotransferase levels, cysteine
             incorporation, an expression of a tissue inhibitor of
             metalloproteinase (TIMP), and ultra-high sulfur keratin
             (UHSK). Follicles cultured at the air-liquid interface
             produced a 2.7-fold increase in hair growth and maintained
             an anagen-like morphology. Substrates such as nylon mesh
             seeded with fibroblasts, Full Thickness Skin, or 5-microns
             polycarbonate filter also supported hair growth, whereas
             Gelfilm, GF-A glass filter, filter paper, or 1-micron
             polycarbonate filter did not. The UHSK expression was
             significantly higher in the air-liquid interface cultures
             compared to the submerged culture. Several potassium channel
             openers, including minoxidil, a minoxidil analog, and the
             pinacidil analog (P-1075), all stimulated significant
             cysteine incorporation in follicles. Minoxidil and its
             analog specifically preserved the follicular root sheath, in
             contrast to P-1075 which did not, indicating a difference in
             the two drug types. The preservation of the root sheath was
             measured by increased TIMP expression and sulfotransferase
             activity and indicates that the root sheath is a target
             tissue for minoxidil. Our results show that follicles
             cultured at the air-liquid interface maintain a better
             morphology and produced greater hair growth than follicles
             cultured on tissue culture plastic.},
   Language = {eng},
   Key = {fds174128}
}

@booklet{Waldon93,
   Author = {D. J. Waldon and T. T. Kawabe and C. A. Baker and G. A.
             Johnson and A. E. Buhl},
   Title = {Enhanced in-vitro hair-growth at the air-liquid interface -
             minoxidil preserves the root sheath in cultured whisker
             follicles},
   Journal = {In Vitro Cellular \& Developmental Biology-animal},
   Volume = {29A},
   Number = {7},
   Pages = {555 -- 561},
   Year = {1993},
   Month = {July},
   Key = {Waldon93}
}

@article{fds157113,
   Author = {AA Sharief and GA Johnson},
   Title = {Enhanced T2 contrast for MR histology of the mouse
             brain.},
   Journal = {Magnetic resonance in medicine : official journal of the
             Society of Magnetic Resonance in Medicine / Society of
             Magnetic Resonance in Medicine, United States},
   Volume = {56},
   Number = {4},
   Pages = {717-25},
   Year = {2006},
   Month = {October},
   ISSN = {0740-3194},
   Keywords = {Animals • Brain Mapping • Contrast Media •
             Heterocyclic Compounds • Imaging, Three-Dimensional
             • Least-Squares Analysis • Magnetic Resonance
             Imaging • Male • Mice • Mice, Inbred C57BL
             • Organometallic Compounds • Staining and Labeling
             • methods*},
   Abstract = {A 3D Carr-Purcell-Meiboom-Gill (CPMG) sequence was
             implemented to obtain enhanced T(2) contrast in actively
             stained (perfusion with fixative and contrast agent) mouse
             brains at 9.4 T. Short interecho spacing was used to
             minimize diffusion and susceptibility losses. The sequence
             produced 16 3D volumes with an interecho spacing of 7 ms for
             isotropic 43-mu-resolution images of the mouse brains in a
             scan time of 4 hr. To enhance the signal-to-noise ratio
             (SNR) and contrast, the multiecho frequency domain image
             contrast (MEFIC) method was applied, resulting in a
             composite image with T(2)-weighted contrast. The high SNR
             and contrast thus achieved revealed aspects of mouse brain
             morphology, such as multiple cortical layers, groups of
             thalamic nuclei, layers of the inferior and superior
             colliculus, and molecular and granular layers of the
             cerebellum, with a high degree of definition and contrast
             that was not previously achieved in T(2)-weighted
             acquisitions at high fields.},
   Key = {fds157113}
}

@article{9150726,
   Author = {Sharief, AA and Johnson, GA},
   Title = {Enhanced T2 contrast for MR histology of the mouse
             brain.},
   Journal = {Magn Reson Med},
   Volume = {56},
   Number = {4},
   Pages = {717-725},
   Year = {2006},
   Month = {October},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/16964618},
   Keywords = {biomedical MRI;brain;data acquisition;image
             sequences;neurophysiology;},
   Abstract = {A 3D Carr-Purcell-Meiboom-Gill (CPMG) sequence was
             implemented to obtain enhanced T(2) contrast in actively
             stained (perfusion with fixative and contrast agent) mouse
             brains at 9.4 T. Short interecho spacing was used to
             minimize diffusion and susceptibility losses. The sequence
             produced 16 3D volumes with an interecho spacing of 7 ms for
             isotropic 43-mu-resolution images of the mouse brains in a
             scan time of 4 hr. To enhance the signal-to-noise ratio
             (SNR) and contrast, the multiecho frequency domain image
             contrast (MEFIC) method was applied, resulting in a
             composite image with T(2)-weighted contrast. The high SNR
             and contrast thus achieved revealed aspects of mouse brain
             morphology, such as multiple cortical layers, groups of
             thalamic nuclei, layers of the inferior and superior
             colliculus, and molecular and granular layers of the
             cerebellum, with a high degree of definition and contrast
             that was not previously achieved in T(2)-weighted
             acquisitions at high fields.},
   Doi = {10.1002/mrm.21026},
   Key = {9150726}
}

@booklet{Johnson02,
   Author = {G. A. Johnson and T. A. Day},
   Title = {Enhancement of photosynthesis in Sorghum bicolor by
             ultraviolet radiation},
   Journal = {Physiologia Plantarum},
   Volume = {116},
   Number = {4},
   Pages = {554 -- 562},
   Year = {2002},
   Month = {December},
   Key = {Johnson02}
}

@article{fds132898,
   Author = {KD Meisheri and GA Johnson and L Puddington},
   Title = {Enzymatic and non-enzymatic sulfation mechanisms in the
             biological actions of minoxidil.},
   Journal = {Biochemical pharmacology, ENGLAND},
   Volume = {45},
   Number = {2},
   Pages = {271-9},
   Year = {1993},
   Month = {January},
   ISSN = {0006-2952},
   Keywords = {Animals • Biotransformation • Humans •
             Minoxidil • Muscle, Smooth, Vascular • Potassium
             Channels • Proteins • Sulfotransferases •
             Triazines • Vasodilation • drug effects •
             metabolism • metabolism* • pharmacokinetics •
             pharmacology},
   Key = {fds132898}
}

@booklet{Meisheri93,
   Author = {K. D. Meisheri and G. A. Johnson and L. Puddington},
   Title = {Enzymatic and nonenzymatic sulfation mechanisms in the
             biological actions of minoxidil},
   Journal = {Biochemical Pharmacology},
   Volume = {45},
   Number = {2},
   Pages = {271 -- 279},
   Year = {1993},
   Month = {January},
   Key = {Meisheri93}
}

@booklet{Johnson97c,
   Author = {G. A. Johnson and R. Mannel and M. Khalifa and J. L. Walker and M. Wren and K. W. Min and D. M. Benbrook},
   Title = {Epidermal growth factor receptor in vulvar malignancies and
             its relationship to metastasis and patient
             survival},
   Journal = {Gynecologic Oncology},
   Volume = {65},
   Number = {3},
   Pages = {425 -- 429},
   Year = {1997},
   Month = {June},
   Key = {Johnson97c}
}

@article{fds174146,
   Author = {GA Johnson and R Mannel and M Khalifa and JL Walker and M Wren and KW Min and DM Benbrook},
   Title = {Epidermal growth factor receptor in vulvar malignancies and
             its relationship to metastasis and patient
             survival.},
   Journal = {Gynecologic oncology},
   Volume = {65},
   Number = {3},
   Pages = {425-9},
   Year = {1997},
   Month = {June},
   ISSN = {0090-8258},
   url = {http://dx.doi.org/10.1006/gyno.1997.4660},
   Keywords = {Carcinoma, Squamous Cell • Disease-Free Survival •
             Female • Humans • Lymphatic Metastasis •
             Receptor, Epidermal Growth Factor • Survival Rate
             • Vulvar Neoplasms • biosynthesis* •
             metabolism* • mortality • mortality* •
             pathology},
   Abstract = {OBJECTIVE: To evaluate the level of epidermal growth factor
             receptor (EGF-R) expression in vulvar malignancies and to
             determine if a correlation exists between EGF-R levels and
             metastasis or patient survival. METHODS: All patients with a
             diagnosis of invasive squamous cell carcinoma of the vulva
             who were treated at our institution with a primary radical
             vulvectomy and inguinal lymph node dissection from 1983 to
             1993 were eligible for the study. Sixty-one patients with
             available tissue blocks of benign vulvar epithelium, the
             primary malignant vulvar lesion, and groin node metastasis
             (when positive) were included in the study. Semiquantitative
             EGF-R expression was determined in a blinded fashion
             utilizing immunohistochemical staining of appropriate tissue
             samples. Survival was calculated utilizing Kaplan-Meier life
             table analysis based upon disease-free survival. RESULTS: A
             significant increase (P < 0.001) in mean EGF-R levels was
             demonstrated in the primary tumor (67%) versus benign vulvar
             epithelium (31%). In the 14 patients with lymph node
             metastasis, the mean EGF-R level in the primary tumor was
             65% versus 88% in the metastatic lesion (P < 0.001). The
             likelihood of lymph node metastasis was elevated in those
             patients with a benign tissue EGF-R level > or =40% (P <
             0.03) and in those patients with a primary tumor EGF-R level
             > or =90% (P < 0.025). Life table analysis revealed a
             cumulative disease-free survival of 45% for all patients.
             Disease-free survival in those patients with EGF-R levels >
             or =90% in the primary tumor was 25%, contrasting with a
             disease-free survival of 54% in those patients with EGF-R
             levels <90% (P < 0.05). CONCLUSIONS: There is a progressive
             increase in EGF-R expression from benign vulvar epithelium
             to primary malignant tissue to metastatic lesions within the
             same patient. Increased expression of EGF-R in the primary
             vulvar malignancy is significantly associated with lymph
             node metastasis and decreased patient survival. Increased
             expression of EGF-R in histologically benign vulvar
             epithelium has a significant association with lymph node
             metastasis and may predict decreased patient
             survival.},
   Language = {eng},
   Doi = {10.1006/gyno.1997.4660},
   Key = {fds174146}
}

@booklet{Choi01a,
   Author = {Y. Choi and G. A. Johnson and R. C. Burghardt and L. R.
             Berghman and M. M. Joyce and T. E. Spencer and F. W.
             Bazer},
   Title = {Epithelial expression of interferon regulatory factor two
             restricts expression of interferon tau-stimulated genes to
             the endometrial stroma and glandular epithelium of the ovine
             uterus.},
   Journal = {Biology Of Reproduction},
   Volume = {64},
   Pages = {108 -- 108},
   Year = {2001},
   Key = {Choi01a}
}

@article{fds268763,
   Author = {Smith, BR and Sattuck, MD and Hedlund, LW and Johnson,
             GA},
   Title = {Erratum: Time-course imaging of rat embryos in utero with
             magnetic resonance microscopy (Magnetic Resonance in
             Medicine (1998) 39 (673-677))},
   Journal = {Magnetic Resonance in Medicine},
   Volume = {39},
   Number = {6},
   Pages = {x},
   Year = {1998},
   Month = {January},
   Key = {fds268763}
}

@article{fds174255,
   Author = {BM Markaverich and RR Gregory and MA Alejandro and RS Varma and GA
             Johnson, BS Middleditch},
   Title = {Estrogen regulation of methyl p-hydroxyphenyllactate
             hydrolysis: correlation with estrogen stimulation of rat
             uterine growth.},
   Journal = {Journal of steroid biochemistry},
   Volume = {33},
   Number = {5},
   Pages = {867-76},
   Year = {1989},
   Month = {November},
   ISSN = {0022-4731},
   Keywords = {Animals • Cell Compartmentation • Chromatography
             • Cytosol • Esterases • Estrogens •
             Female • Hot Temperature • Kinetics •
             Lactates • Phenylpropionates • Rats •
             Substrate Specificity • Uterus • enzymology*
             • metabolism • metabolism* •
             physiology*},
   Abstract = {We have recently demonstrated that methyl
             p-hydroxyphenyllactate (MeHPLA) is the endogenous ligand for
             nuclear type II binding sites in the rat uterus and other
             estrogen target and non-target tissues. MeHPLA binds to
             nuclear type II binding sites with a very high binding
             affinity (Kd approximately 4-5 nM), blocks uterine growth in
             vivo, and inhibits MCF-7 human breast cancer cell growth in
             vitro. Conversely, the free acid (p-hydroxyphenyllactic
             acid, HPLA) interacts with type II binding sites with a much
             lower affinity (Kd approximately 200 nM) and does not
             inhibit estrogen-induced uterine growth in vivo or MCF-7
             cell growth in vitro. On the basis of these observations, we
             suggested that one way that estrogen may override MeHPLA
             inhibition of rat uterine growth may be to stimulate
             esterase hydrolysis of MeHPLA to HPLA. The present studies
             demonstrate that the rat uterus does contain an esterase
             (mol. wt approximately 50,000) which cleaves MeHPLA to HPLA,
             and that this enzyme is under estrogen regulation. This
             conclusion is supported by the observations that MeHPLA
             esterase activity is increased 2-3-fold above controls
             within 2-4 h following a single injection of estradiol, and
             is maintained at high levels for 16-24 h following hormone
             administration. This sustained elevation of MeHPLA esterase
             activity correlates with estradiol stimulation of true
             uterine growth and DNA synthesis.},
   Language = {eng},
   Key = {fds174255}
}

@booklet{Markaverich89,
   Author = {B. M. Markaverich and R. R. Gregory and M. A. Alejandro and R. S. Varma and G. A. Johnson and B. S. Middleditch},
   Title = {Estrogen regulation of methyl para-hydroxyphenylactate
             hydrolysis - correlation with estrogen stimulation of rat
             uterine growth},
   Journal = {Journal Of Steroid Biochemistry And Molecular
             Biology},
   Volume = {33},
   Number = {5},
   Pages = {867 -- 876},
   Year = {1989},
   Month = {November},
   Key = {Markaverich89}
}

@article{fds268774,
   Author = {Lipinski, RJ and Hammond, P and O'Leary-Moore, SK and Ament, JJ and Pecevich, SJ and Jiang, Y and Budin, F and Parnell, SE and Suttie, M and Godin, EA and Everson, JL and Dehart, DB and Oguz, I and Holloway, HT and Styner, MA and Johnson, GA and Sulik, KK},
   Title = {Ethanol-induced face-brain dysmorphology patterns are
             correlative and exposure-stage dependent.},
   Journal = {PLoS One},
   Volume = {7},
   Number = {8},
   Pages = {e43067},
   Year = {2012},
   ISSN = {1932-6203},
   url = {http://dx.doi.org/10.1371/journal.pone.0043067},
   Abstract = {Prenatal ethanol exposure is the leading preventable cause
             of congenital mental disability. Whereas a diagnosis of
             fetal alcohol syndrome (FAS) requires identification of a
             specific pattern of craniofacial dysmorphology, most
             individuals with behavioral and neurological sequelae of
             heavy prenatal ethanol exposure do not exhibit these
             defining facial characteristics. Here, a novel integration
             of MRI and dense surface modeling-based shape analysis was
             applied to characterize concurrent face-brain phenotypes in
             C57Bl/6J fetuses exposed to ethanol on gestational day (GD)7
             or GD8.5. The facial phenotype resulting from ethanol
             exposure depended upon stage of insult and was predictive of
             unique patterns of corresponding brain abnormalities.
             Ethanol exposure on GD7 produced a constellation of
             dysmorphic facial features characteristic of human FAS,
             including severe midfacial hypoplasia, shortening of the
             palpebral fissures, an elongated upper lip, and deficient
             philtrum. In contrast, ethanol exposure on GD8.5 caused mild
             midfacial hypoplasia and palpebral fissure shortening, a
             shortened upper lip, and a preserved philtrum. These
             distinct, stage-specific facial phenotypes were associated
             with unique volumetric and shape abnormalities of the septal
             region, pituitary, and olfactory bulbs. By demonstrating
             that early prenatal ethanol exposure can cause more than one
             temporally-specific pattern of defects, these findings
             illustrate the need for an expansion of current diagnostic
             criteria to better capture the full range of facial and
             brain dysmorphology in fetal alcohol spectrum
             disorders.},
   Doi = {10.1371/journal.pone.0043067},
   Key = {fds268774}
}

@booklet{Sherrier85b,
   Author = {SHERRIER, RH and CHILES, C and SUDDARTH, SA and JOHNSON, GA and RAVIN,
             CE},
   Title = {EVALUATION OF COMPUTER SYNTHESIZED PULMONARY
             NODULES},
   Journal = {INVESTIGATIVE RADIOLOGY},
   Volume = {20},
   Number = {6},
   Pages = {S27-S27},
   Publisher = {LIPPINCOTT-RAVEN PUBL},
   Year = {1985},
   Month = {January},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1985ARG0500124&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Sherrier85b}
}

@booklet{Johnson81a,
   Author = {Johnson, GA and Korobkin, M and Heinz, ER},
   Title = {Evaluation of multiplanar imaging capabilities of four
             current computed tomography (CT) scanners},
   Journal = {Proceedings of SPIE - The International Society for Optical
             Engineering},
   Volume = {273},
   Pages = {318-325},
   Publisher = {SPIE},
   Year = {1981},
   Month = {July},
   url = {http://dx.doi.org/10.1117/12.931819},
   Abstract = {Four state of the art CT scanners were evaluated with
             respect to optimal techniques for multiplanar imaging. The
             four scanners were a G. E. 8800, Pfizer 0^50, Picker
             Synerview 600 and Siemens Somatom 2. Patient movement
             artefacts can be minimized by choice of techniques that
             provide rapid data acquisition. By deferring reconstruction,
             using batch mode acquisition, suppressing screen display and
             operator interaction and minimizing tube loading as many as
             33 thin slices can be acquired in < 8 minutes. This rapid
             scan technique makes use of the narrow collimation over a
             large (5-0 cm) distance quite reasonable. A high contrast
             star resolution phantom was scanned using these rapid scan
             techniques. The multiplanar Images produced from narrow
             slices are much higher resolution than those created with
             more widely collimated slices. A low contrast (2.5%)
             resolution object scanned with the same rapid acquisition
             method shows improved resolution for the narrow collimation
             even in the presence of increased noise accompanying the
             narrow collimation. © 1981 SPIE.},
   Doi = {10.1117/12.931819},
   Key = {Johnson81a}
}

@article{fds268818,
   Author = {Ghaghada, KB and Badea, CT and Karumbaiah, L and Fettig, N and Bellamkonda, RV and Johnson, GA and Annapragada,
             A},
   Title = {Evaluation of tumor microenvironment in an animal model
             using a nanoparticle contrast agent in computed tomography
             imaging.},
   Journal = {Acad Radiol},
   Volume = {18},
   Number = {1},
   Pages = {20-30},
   Year = {2011},
   Month = {January},
   ISSN = {1878-4046},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/21145026},
   Keywords = {Animals • Contrast Media • Disease Models, Animal
             • Female • Imaging, Three-Dimensional •
             Mammary Neoplasms, Experimental • Mice • Mice,
             Inbred BALB C • Nanoparticles • Radiographic Image
             Enhancement • Reverse Transcriptase Polymerase Chain
             Reaction • Tomography, X-Ray Computed •
             Triiodobenzoic Acids • Tumor Microenvironment* •
             blood supply* • diagnostic use • diagnostic use*
             • methods • methods* • radiography*},
   Abstract = {RATIONALE AND OBJECTIVES: Non-invasive longitudinal imaging
             of tumor vasculature could provide new insights into the
             development of solid tumors, facilitating efficient delivery
             of therapeutics. In this study, we report three-dimensional
             imaging and characterization of tumor vascular architecture
             using a nanoparticle contrast agent and high-resolution
             computed tomography (CT) imaging. MATERIALS AND METHODS:
             Five Balb/c mice implanted with 4T1/Luc syngeneic breast
             tumors cells were used for the study. The nanoparticle
             contrast agent was systemically administered and
             longitudinal CT imaging was performed pre-contrast and at
             serial time points post-contrast, for up to 7 days for
             studying the characteristics of tumor-associated blood
             vessels. Gene expression of tumor angiogenic biomarkers was
             measured using quantitative real-time polymerase chain
             reaction. RESULTS: Early-phase imaging demonstrated the
             presence of co-opted and newly developed tumor vessels. The
             co-opted vessels demonstrated wall-permeability and
             "leakiness" characteristics evident by an increase in
             extravascular nanoparticle-based signal enhancement visible
             well beyond the margins of tumor. Diameters of
             tumor-associated vessels were larger than the contralateral
             normal vessels. Delayed-phase imaging also demonstrated
             significant accumulation of nanoparticle contrast agent both
             within and in areas surrounding the tumor. A heterogeneous
             pattern of signal enhancement was observed both within and
             among individual tumors. Gene-expression profiling
             demonstrated significant variability in several angiogenic
             biomarkers both within and among individual tumors.
             CONCLUSIONS: The nanoparticle contrast agent and
             high-resolution CT imaging facilitated visualization of
             co-opted and newly developed tumors vessels as well as
             imaging of nanoparticle accumulation within tumors. The use
             of this agent could provide novel insights into tumor
             vascular biology and could have implications on the
             monitoring of tumor status.},
   Language = {eng},
   Doi = {10.1016/j.acra.2010.09.003},
   Key = {fds268818}
}

@booklet{Muggia04,
   Author = {F. M. Muggia and J. A. Blessing and M. Method and D. S.
             Miller and G. A. Johnson and R. B. Lee and A.
             Menzin},
   Title = {Evaluation of vinorelbine in persistent or recurrent
             squamous cell carcinoma of the cervix: a Gynecologic
             Oncology Group study},
   Journal = {Gynecologic Oncology},
   Volume = {92},
   Number = {2},
   Pages = {639 -- 643},
   Year = {2004},
   Month = {February},
   Key = {Muggia04}
}

@article{fds174223,
   Author = {FM Muggia and JA Blessing and M Method and DS Miller and GA Johnson and RB
             Lee, A Menzin and Gynecologic Oncology Group
             study},
   Title = {Evaluation of vinorelbine in persistent or recurrent
             squamous cell carcinoma of the cervix: a Gynecologic
             Oncology Group study.},
   Journal = {Gynecologic oncology},
   Volume = {92},
   Number = {2},
   Pages = {639-43},
   Year = {2004},
   Month = {February},
   ISSN = {0090-8258},
   url = {http://dx.doi.org/10.1016/j.ygyno.2003.10.045},
   Keywords = {Adult • Aged • Antineoplastic Agents, Phytogenic
             • Carcinoma, Squamous Cell • Drug Administration
             Schedule • Female • Humans • Middle Aged
             • Uterine Cervical Neoplasms • Vinblastine •
             analogs & derivatives* • drug therapy* •
             therapeutic use*},
   Abstract = {PURPOSE: Vinorelbine is being explored by the Gynecologic
             Oncology Group (GOG) for its possible use in advanced or
             recurrent squamous cell carcinoma of the uterine cervix. The
             objective of this Phase II trial was to evaluate a days 1
             and 8 every-21-days schedule and determine its activity in
             patients who had failed standard chemotherapy. PATIENTS AND
             METHODS: Eligible patients with measurable disease and
             satisfactory baseline bone marrow, liver, and kidney
             functions were treated with vinorelbine 30 mg/m(2) given on
             days 1 and 8 every 21 days. A two-stage sampling design was
             used, proceeding to a second stage accrual if sufficient
             activity was documented in the first 25 patients. RESULTS:
             The study did proceed to the second stage and accrued 44
             patients. There were six objective responses (one complete,
             five partial) for a response rate of 13.7% (95% confidence
             interval: 5.2-27.4%). There were three patients with
             response in extra-pelvic sites (including the complete
             response) and three with response in the pelvis. The overall
             frequency of grades 3 and 4 neutropenia was 41%, whereas
             neuropathy was reported in 27% and was severe in three.
             Treatment-related pain, very severe in two instances, was
             also reported in 27%. CONCLUSION: Vinorelbine has moderate
             activity in a pretreated population with squamous cell
             carcinoma of the cervix. Accordingly, vinorelbine in this
             days 1 and 8 schedule is being studied further in
             combination with cisplatin by the GOG.},
   Language = {eng},
   Doi = {10.1016/j.ygyno.2003.10.045},
   Key = {fds174223}
}

@booklet{Joyce01,
   Author = {M. M. Joyce and T. E. Spencer and F. W. Bazer and R. C.
             Burghardt and C. Pfarrer and G. A. Johnson},
   Title = {Evidence for stromal decidualization in the pregnant ovine
             uterus.},
   Journal = {Biology Of Reproduction},
   Volume = {64},
   Pages = {317 -- 318},
   Year = {2001},
   Key = {Joyce01}
}

@booklet{Mantha01,
   Author = {S. V. Mantha and G. A. Johnson and T. A.
             Day},
   Title = {Evidence from action and fluorescence spectra that
             UV-induced violet-blue-green fluorescence enhances leaf
             photosynthesis},
   Journal = {Photochemistry And Photobiology},
   Volume = {73},
   Number = {3},
   Pages = {249 -- 256},
   Year = {2001},
   Month = {March},
   Key = {Mantha01}
}

@article{fds174166,
   Author = {SV Mantha and GA Johnson and TA Day},
   Title = {Evidence from action and fluorescence spectra that
             UV-induced violet-blue-green fluorescence enhances leaf
             photosynthesis.},
   Journal = {Photochemistry and photobiology},
   Volume = {73},
   Number = {3},
   Pages = {249-56},
   Year = {2001},
   Month = {March},
   ISSN = {0031-8655},
   Keywords = {Angiosperms • Photosynthesis • Plant Leaves •
             Spectrometry, Fluorescence • Ultraviolet Rays* •
             physiology • radiation effects*},
   Abstract = {We assessed the contribution of UV-induced violet-blue-green
             leaf fluorescence to photosynthesis in Poa annua, Sorghum
             halepense and Nerium oleander by measuring UV-induced
             fluorescence spectra (280-380 nm excitation, 400-550 nm
             emission) from leaf surfaces and determining the
             monochromatic UV action spectra for leaf photosynthetic
             O2-evolution. Peak fluorescence emission wavelengths from
             leaf surfaces ranged from violet (408 nm) to blue (448 nm),
             while excitation peaks for these maxima ranged from 333 to
             344 nm. Action spectra were developed by supplementing
             monochromatic radiation from 280 to 440 nm, in 20 nm
             increments, to a visible nonsaturating background of 500
             mumol m-2 s-1 photosynthetically active radiation and
             measuring photosynthetic O2-evolution rates. Photosynthetic
             rates tended to be higher with the 340 nm supplement than
             with higher or lower wavelength UV supplements. Comparing
             photosynthetic rates with the 340 nm supplement to those
             with the 400 nm supplement, the percentage enhancement in
             photosynthetic rates at 340 nm ranged from 7.8 to 9.8%. We
             suspect that 340 nm UV improves photosynthetic rates via
             fluorescence that provides violet-blue-green photons for
             photosynthetic energy conversion because (1) the peak
             excitation wavelength (340 nm) for violet-blue-green
             fluorescence from leaves was also the most effective UV
             wavelength at enhancing photosynthetic rates, and (2) the
             magnitude of photosynthetic enhancements attributable to
             supplemental 340 nm UV was well correlated (R2 = 0.90) with
             the apparent intensity of 340 nm UV-induced
             violet-blue-green fluorescence emission from
             leaves.},
   Language = {eng},
   Key = {fds174166}
}

@booklet{Gray02,
   Author = {C. A. Gray and R. C. Burghardt and G. A. Johnson and F. W.
             Bazer and T. E. Spencer},
   Title = {Evidence that absence of endometrial gland secretions in
             uterine gland knockout ewes compromises conceptus survival
             and elongation},
   Journal = {Reproduction},
   Volume = {124},
   Number = {2},
   Pages = {289 -- 300},
   Year = {2002},
   Month = {August},
   Key = {Gray02}
}

@article{fds174138,
   Author = {CA Gray and RC Burghardt and GA Johnson and FW Bazer and TE
             Spencer},
   Title = {Evidence that absence of endometrial gland secretions in
             uterine gland knockout ewes compromises conceptus survival
             and elongation.},
   Journal = {Reproduction (Cambridge, England)},
   Volume = {124},
   Number = {2},
   Pages = {289-300},
   Year = {2002},
   Month = {August},
   ISSN = {1470-1626},
   Keywords = {Animals • Blastocyst • Blotting, Western •
             Embryonic and Fetal Development • Endometrium •
             Female • Integrins • Interferon Type I •
             Mucin-1 • Mucins • Osteopontin • Pregnancy
             • Pregnancy Proteins • Pregnancy, Animal •
             Progesterone • Sheep • Sialoglycoproteins •
             Uterus • analysis • anatomy & histology •
             blood • chemistry • metabolism* • physiology*
             • secretion*},
   Abstract = {Endometrial glands are necessary for conceptus implantation
             and growth. In the ovine uterine gland knockout (UGKO)
             model, blastocysts hatch normally but fail to survive or
             elongate. This peri-implantation defect in UGKO ewes may be
             due to the absence of endometrial glands or, alternatively,
             to the lack of certain epithelial adhesion molecules or the
             inability of the endometrium to respond to signals from the
             conceptus. Two studies were performed to examine these
             hypotheses. In study one, normal (n = 8) and UGKO (n = 12)
             ewes were mated at oestrus (day 0) with intact rams and
             their uteri were flushed 14 days after oestrus. Normal ewes
             (n = 4) were also flushed on 14 days after oestrus. Uterine
             flushes from bred normal ewes contained filamentous
             conceptuses (n = 7 of 8), whereas those from UGKO ewes
             contained no conceptus (n = 5 of 12), a growth-retarded,
             tubular conceptus (n = 6 of 12), or a fragmented,
             filamentous conceptus (n = 1 of 12). In all groups,
             expression of mucin 1 and integrin alpha(v), alpha(5),
             beta(3) and beta(5) was localized at the apical surface of
             the endometrial luminal epithelium with no detectable
             differences between normal and UGKO ewes. Uterine flushes
             from pregnant ewes, but not cyclic or UGKO ewes, contained
             abundant immunoreactive interferon tau and the cell adhesion
             proteins, osteopontin and glycosylation-dependent cell
             adhesion molecule one. In study two, UGKO ewes were fitted
             with uterine catheters 5 days after oestrus, infused with
             recombinant ovine interferon tau or control proteins from 11
             to 15 days after oestrus, and underwent hysterectomy 16 days
             after oestrus. Expression of several interferon
             tau-stimulated genes (ISG17, STAT1, STAT2 and IRF-1) was
             increased in the endometrium from interferon tau-infused
             UGKO ewes. These results support the hypothesis that the
             defects in conceptus elongation and survival in UGKO ewes
             are due to the absence of endometrial glands and their
             secretions rather than to alterations in expression of
             anti-adhesive or adhesive molecules on the endometrial
             luminal epithelium or to the responsiveness of the
             endometrium to the conceptus pregnancy recognition
             signal.},
   Language = {eng},
   Key = {fds174138}
}

@article{fds357199,
   Author = {Blocker, SJ and Cook, J and Mowery, YM and Everitt, JI and Qi, Y and Hornburg, KJ and Cofer, GP and Zapata, F and Bassil, AM and Badea, CT and Kirsch, DG and Johnson, GA},
   Title = {Ex Vivo MR Histology and Cytometric Feature Mapping Connect
             Three-dimensional in Vivo MR Images to Two-dimensional
             Histopathologic Images of Murine Sarcomas.},
   Journal = {Radiol Imaging Cancer},
   Volume = {3},
   Number = {3},
   Pages = {e200103},
   Year = {2021},
   Month = {May},
   url = {http://dx.doi.org/10.1148/rycan.2021200103},
   Abstract = {Purpose To establish a platform for quantitative
             tissue-based interpretation of cytoarchitecture features
             from tumor MRI measurements. Materials and Methods In a
             pilot preclinical study, multicontrast in vivo MRI of murine
             soft-tissue sarcomas in 10 mice, followed by ex vivo MRI of
             fixed tissues (termed MR histology), was performed.
             Paraffin-embedded limb cross-sections were stained with
             hematoxylin-eosin, digitized, and registered with MRI.
             Registration was assessed by using binarized tumor maps and
             Dice similarity coefficients (DSCs). Quantitative cytometric
             feature maps from histologic slides were derived by using
             nuclear segmentation and compared with registered MRI,
             including apparent diffusion coefficients and transverse
             relaxation times as affected by magnetic field heterogeneity
             (T2* maps). Cytometric features were compared with each MR
             image individually by using simple linear regression
             analysis to identify the features of interest, and the
             goodness of fit was assessed on the basis of R2 values.
             Results Registration of MR images to histopathologic slide
             images resulted in mean DSCs of 0.912 for ex vivo MR
             histology and 0.881 for in vivo MRI. Triplicate repeats
             showed high registration repeatability (mean DSC, >0.9).
             Whole-slide nuclear segmentations were automated to detect
             nuclei on histopathologic slides (DSC = 0.8), and feature
             maps were generated for correlative analysis with MR images.
             Notable trends were observed between cell density and in
             vivo apparent diffusion coefficients (best line fit: R2 =
             0.96, P < .001). Multiple cytoarchitectural features
             exhibited linear relationships with in vivo T2* maps,
             including nuclear circularity (best line fit: R2 = 0.99, P <
             .001) and variance in nuclear circularity (best line fit: R2
             = 0.98, P < .001). Conclusion An infrastructure for
             registering and quantitatively comparing in vivo tumor MRI
             with traditional histologic analysis was successfully
             implemented in a preclinical pilot study of soft-tissue
             sarcomas. Keywords: MRI, Pathology, Animal Studies, Tissue
             Characterization Supplemental material is available for this
             article. © RSNA, 2021.},
   Doi = {10.1148/rycan.2021200103},
   Key = {fds357199}
}

@article{fds268744,
   Author = {BENVENISTE, H and JOHNSON, GA and KOZNIEWSKA, E and MAIESE, K and NARITOMI, H and POVLISHOCK, JT and HOSSMANN, KA},
   Title = {EXCITOTOXICITY AND ISCHEMIA IN THE RAT-BRAIN STUDIED IN-VIVO
             WITH HIGH-RESOLUTION MAGNETIC-RESONANCE-IMAGING},
   Journal = {MICROCIRCULATORY STASIS IN THE BRAIN},
   Volume = {1031},
   Pages = {369-376},
   Publisher = {ELSEVIER SCIENCE PUBL B V},
   Editor = {Tomita, M and Mchedlishvili, F and Rosenblum, W and Heiss, WD and Fukuuchi, Y},
   Year = {1993},
   Month = {January},
   ISBN = {0-444-89669-4},
   ISSN = {0531-5131},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1993BZ68Q00043&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {fds268744}
}

@article{fds174149,
   Author = {GA Johnson and TK Hung and AM Brant and HS Borovetz},
   Title = {Experimental determination of wall shear rate in canine
             carotid arteries perfused in vitro.},
   Journal = {Journal of biomechanics},
   Volume = {22},
   Number = {11-12},
   Pages = {1141-50},
   Year = {1989},
   ISSN = {0021-9290},
   Keywords = {Animals • Biomechanics • Carotid Arteries •
             Dogs • Endothelium, Vascular • Hemodynamics •
             Lipoproteins, LDL • Mathematical Computing •
             Models, Cardiovascular • metabolism • physiology*
             • physiopathology},
   Abstract = {The mathematical model of Hung (Tsai and Hung, 1984) is
             employed to determine the wall shear rate acting on canine
             carotid arteries perfused in vitro. Model equations for
             pulsatile flow in a deformable vessel are coupled with
             experimental data of dynamic pressure drop, flow rate,
             vessel radius and radial wall motion. Derived quantities,
             e.g. velocity profiles and wall shear, are obtained for
             vessels exposed to 'normotensive' hemodynamics,
             'hypertension' simulations and perfusions in which the
             compliance of the vessel wall is deliberately altered. Our
             results indicate that wall shear varies markedly as a
             function of the hemodynamic environment. The effects of
             vessel radius vs flow rate on the development of wall shear
             are also demonstrated. It is found that convective processes
             correlate with the magnitude of wall shear in the
             'hypertension' simulations. The present findings and
             complementary published data may explain, at least in part,
             the variations in vessel wall transport and endothelial cell
             biology we observe as a function of the hemodynamic
             environment. For example we have documented that the
             exposure of canine carotids to 'hypertensive' (vs
             'normotensive') hemodynamics is associated with an increased
             flux of lipoproteins (LDL) into the intima and luminal
             media. Alternations in wall compliance, on the other hand,
             profoundly influence endothelial shape, orientation and
             cytoskeletal array.},
   Language = {eng},
   Key = {fds174149}
}

@booklet{Johnson89,
   Author = {G. A. Johnson and T. K. Hung and A. M. Brant and H. S.
             Borovetz},
   Title = {Experimental-determination of wall shear rate in canine
             carotid arteries perfused invitro},
   Journal = {Journal Of Biomechanics},
   Volume = {22},
   Number = {11-12},
   Pages = {1141 -- 1150},
   Year = {1989},
   Key = {Johnson89}
}

@booklet{Johnson98a,
   Author = {G. A. Johnson and C. A. Gray and J. B. Word and T. L. Ott and T. E. Spencer and R. C. Burghardt and F. W.
             Bazer},
   Title = {Expression and secretion of osteopontin by ovine endometrium
             and conceptuses.},
   Journal = {Biology Of Reproduction},
   Volume = {58},
   Pages = {119 -- 119},
   Year = {1998},
   Key = {Johnson98a}
}

@booklet{Pfarrer02,
   Author = {C. D. Pfarrer and S. Hallack and G. A. Johnson and R. C.
             Burghardt and F. W. Bazer and R. Leiser},
   Title = {Expression of osteopontin in bovine placentomes and
             interplacentomal areas from early placentation until
             term.},
   Journal = {Biology Of Reproduction},
   Volume = {66},
   Pages = {229 -- 230},
   Year = {2002},
   Key = {Pfarrer02}
}

@article{fds174089,
   Author = {MD Ashworth and JW Ross and J Hu and FJ White and DR Stein and U Desilva and GA Johnson and TE Spencer and RD Geisert},
   Title = {Expression of porcine endometrial prostaglandin synthase
             during the estrous cycle and early pregnancy, and following
             endocrine disruption of pregnancy.},
   Journal = {Biology of reproduction},
   Volume = {74},
   Number = {6},
   Pages = {1007-15},
   Year = {2006},
   Month = {June},
   ISSN = {0006-3363},
   url = {http://dx.doi.org/10.1095/biolreprod.105.046557},
   Keywords = {Animals • Embryo Loss • Endometrium •
             Estrogens • Estrous Cycle • Female •
             Fertilization • Gene Expression Profiling • Gene
             Expression Regulation, Developmental • Gene Expression
             Regulation, Enzymologic • Interleukin-1 •
             Placentation • Pregnancy • Pregnancy, Animal
             • Prostaglandin-Endoperoxide Synthases • RNA,
             Messenger • Swine • Transcription, Genetic •
             analysis • drug effects • drug effects* •
             enzymology* • genetics • genetics* •
             metabolism* • pharmacology* • physiology •
             physiopathology • secretion},
   Abstract = {Porcine trophoblast attachment to the uterine surface is
             associated with increased conceptus and endometrial
             production of prostaglandins. Conceptus secretion of
             estrogen on Day 12 of gestation is important for
             establishment of pregnancy; however, early (Days 9 and 10)
             exposure to exogenous estrogens results in embryonic
             mortality. Present studies established the temporal and
             spatial pattern of endometrial PTGS1 (prostaglandin-endoperoxide
             synthase 1) and PTGS2 expression during the estrous cycle
             and early pregnancy and determined the effect of early
             estrogen treatment on endometrial PTGS expression in
             pregnant gilts. Endometrial PTGS1 mRNA expression increased
             2- to 3-fold after Day 10 of the estrous cycle and
             pregnancy, whereas PTGS2 mRNA expression increased 76-fold
             between Days 5 and 15 of the estrous cycle and pregnancy.
             Increased expression of the PTGS2 transcript was detected in
             the lumenal epithelium after Day 10 in both cyclic and
             pregnant gilts. There was a 10- and 20-fold increase in
             endometrial PTGS2 protein expression between Days 5 and 18
             of the estrous cycle and pregnancy respectively.
             Administration of estrogen on Days 9 and 10 of gestation
             increased endometrial PTGS2 mRNA and protein on Day 10, but
             decreased PTGS2 mRNA and protein in lumenal epithelium (LE)
             on Day 12 of gestation compared to vehicle-treated gilts.
             The present study demonstrates that an increase in uterine
             epithelial PTGS2 expression occurs after Day 10 of the
             estrous cycle and early pregnancy in the pig. The
             conceptus-independent increase in the uterine LE indicates
             that a novel pathway exists for endometrial induction PTGS2
             expression before conceptus elongation and attachment to the
             uterine surface. Epithelial expression of PTGS2 may serve as
             one of the signals for placental attachment and embryo
             survival in the pig. Early administration of estrogen on
             Days 9 and 10 of pregnancy alters endometrial PTGS2 mRNA and
             protein expression, which may, at least in part, represent a
             mechanism by which endocrine disruption of pregnancy causes
             total embryonic loss during implantation in the
             pig.},
   Language = {eng},
   Doi = {10.1095/biolreprod.105.046557},
   Key = {fds174089}
}

@booklet{Hicks00,
   Author = {B. A. Hicks and K. G. Carnahan and J. A. Baldock and S. J.
             Yankee and F. W. Bazer and G. A. Johnson and T. E. Spencer and T. L. Ott},
   Title = {Expression of the antiviral protein Mx in an immortalized
             ovine uterine glandular epithelial cell line.},
   Journal = {Biology Of Reproduction},
   Volume = {62},
   Pages = {288 -- 289},
   Year = {2000},
   Key = {Hicks00}
}

@booklet{Johnson99f,
   Author = {G. A. Johnson and T. E. Spencer and T. R. Hansen and K. J.
             Austin and R. C. Burghardt and F. W. Bazer},
   Title = {Expression of the interferon tau inducible ubiquitin
             cross-reactive protein in the ovine uterus},
   Journal = {Biology Of Reproduction},
   Volume = {61},
   Number = {1},
   Pages = {312 -- 318},
   Year = {1999},
   Month = {July},
   Key = {Johnson99f}
}

@article{fds174235,
   Author = {GA Johnson and TE Spencer and TR Hansen and KJ Austin and RC Burghardt and FW Bazer},
   Title = {Expression of the interferon tau inducible ubiquitin
             cross-reactive protein in the ovine uterus.},
   Journal = {Biology of reproduction},
   Volume = {61},
   Number = {1},
   Pages = {312-8},
   Year = {1999},
   Month = {July},
   ISSN = {0006-3363},
   Keywords = {Animals • Blotting, Northern • Blotting, Western
             • Cattle • Endometrium • Epithelium •
             Female • Gene Expression Regulation* • Gestational
             Age • In Situ Hybridization • Interferon Type I
             • Ovariectomy • Pregnancy • Pregnancy
             Proteins • RNA, Messenger • Recombinant Proteins
             • Sheep* • Stromal Cells • Ubiquitins •
             Uterus • analogs & derivatives* • analysis •
             chemistry • genetics • metabolism* •
             pharmacology • pharmacology*},
   Abstract = {Ubiquitin cross-reactive protein (UCRP) is a 17-kDa protein
             that shows cross-reactivity with ubiquitin antisera and
             retains the carboxyl-terminal Leu-Arg-Gly-Gly amino acid
             sequence of ubiquitin that ligates to, and directs
             degradation of, cytosolic proteins. It has been reported
             that bovine endometrial UCRP is synthesized and secreted in
             response to conceptus-derived interferon-tau (IFNtau). In
             the present studies, UCRP mRNA and protein were detected in
             ovine endometrium. Ovine UCRP mRNA was detectable on Day 13,
             peaked at Day 15, and remained high through Day 19 of
             pregnancy. The UCRP mRNA was localized to the luminal
             epithelium (LE), stromal cells (ST) immediately beneath the
             LE, and shallow glandular epithelium (GE) on Day 13, but it
             extended to the deep GE, deep ST, and myometrium of uterine
             tissues by Day 15 of pregnancy. Western blotting revealed
             induction of UCRP in the endometrial extracts from pregnant,
             but not cyclic, ewes. Ovine UCRP was also detected in
             uterine flushings from Days 15 and 17 of pregnancy and
             immunoprecipitated from Day 17 pregnant endometrial
             explant-conditioned medium. Treatment of immortalized ovine
             LE cells with recombinant ovine (ro) IFNtau induced
             cytosolic expression of UCRP, and intrauterine injection of
             roIFNtau into ovariectomized cyclic ewes induced endometrial
             expression of UCRP mRNA. These results are the first to
             describe temporal and spatial alterations in the cellular
             localization of UCRP in the ruminant uterus. Collectively,
             UCRP is synthesized and secreted by the ovine endometrium in
             response to IFNtau during early pregnancy. Because UCRP is
             present in the uterus and uterine flushings, it may regulate
             endometrial proteins associated with establishment and
             maintenance of early pregnancy in ruminants.},
   Language = {eng},
   Key = {fds174235}
}

@booklet{Hicks03,
   Author = {B. A. Hicks and S. J. Etter and K. G. Carnahan and M. M.
             Joyce and A. A. Assiri and S. J. Carling and K. Kodali and G. A. Johnson and T. R. Hansen and M. A. Mirando and G. L.
             Woods and D. K. Vanderwall and T. L. Ott},
   Title = {Expression of the uterine Mx protein in cyclic and pregnant
             cows, gilts, and mares},
   Journal = {Journal Of Animal Science},
   Volume = {81},
   Number = {6},
   Pages = {1552 -- 1561},
   Year = {2003},
   Month = {June},
   Key = {Hicks03}
}

@article{fds174174,
   Author = {BA Hicks and SJ Etter and KG Carnahan and MM Joyce and AA Assiri and SJ
             Carling, K Kodali and GA Johnson and TR Hansen and MA Mirando and GL
             Woods, DK Vanderwall and TL Ott},
   Title = {Expression of the uterine Mx protein in cyclic and pregnant
             cows, gilts, and mares.},
   Journal = {Journal of animal science},
   Volume = {81},
   Number = {6},
   Pages = {1552-61},
   Year = {2003},
   Month = {June},
   ISSN = {0021-8812},
   Keywords = {Animals • Blotting, Northern • Blotting, Western
             • Cattle • Estrus • Female • GTP-Binding
             Proteins • Gene Expression Regulation • Horses
             • In Situ Hybridization • Pregnancy •
             Pregnancy, Animal • Swine • Uterus •
             biosynthesis* • metabolism • metabolism* •
             physiology* • veterinary},
   Abstract = {Pregnancy and interferon-tau (IFN tau) upregulate uterine Mx
             gene expression in ewes; however, the only known role for Mx
             is in the immune response to viral infection. We hypothesize
             that Mx functions as a conceptus-induced component of the
             anti-luteolytic mechanism and/or regulator of endometrial
             secretion or uterine remodeling during early pregnancy. This
             study was conducted to determine the effects of early
             pregnancy on uterine Mx expression in domestic farm species
             with varied mechanisms of pregnancy recognition. Endometrium
             from cows, gilts, and mares was collected during the first
             20 d of the estrous cycle or pregnancy, and total messenger
             RNA (mRNA) and protein were analyzed for steady-state levels
             of Mx mRNA and protein. Northern blot analysis of Mx mRNA
             detected an approximately 2.5 Kb of mRNA in endometrium from
             each species. In pregnant cows, steady-state levels of Mx
             mRNA increased 10-fold (P < 0.05) above levels observed in
             cyclic cows by d 15 to 18. In cyclic gilts, slot blot
             analysis indicated that endometrial Mx mRNA levels did not
             change between d 5 and 18 of the cycle. However, in pregnant
             gilts, Mx levels tended (P = 0.06) to be elevated two-fold
             on d 16 only, and in situ hybridization indicated that this
             increase occurred in the stroma. In mares, Mx mRNA was low,
             but detectable, and did not change between ovulation (d 0)
             and d 20, regardless of reproductive status. Western blot
             analysis revealed multiple immunoreactive Mx protein bands
             in each species. One band was specific to pregnancy in cows.
             As in ewes, in situ hybridization analysis indicated that Mx
             mRNA was strongly expressed in the luminal epithelium,
             stroma, and myometrium by d 18 in cows. However, on d 14 in
             gilts, Mx was expressed primarily in the stroma, and on d 14
             in mares, low levels of Mx expression were confined largely
             to the luminal epithelium. The uteruses of cows, gilts, and
             mares express Mx, and expression is upregulated during
             pregnancy in cows and gilts--animals whose conceptuses
             secrete interferons during early pregnancy, but that possess
             different mechanisms for pregnancy recognition.},
   Language = {eng},
   Key = {fds174174}
}

@booklet{Spencer97,
   Author = {T. A. Spencer and D. S. Clark and G. A. Johnson and S. K.
             Erickson and L. K. Curtiss},
   Title = {Feasibility of an immunoassay for mevalonolactone},
   Journal = {Bioorganic \& Medicinal Chemistry},
   Volume = {5},
   Number = {5},
   Pages = {873 -- 882},
   Year = {1997},
   Month = {May},
   Key = {Spencer97}
}

@article{fds174267,
   Author = {TA Spencer and DS Clark and GA Johnson and SK Erickson and LK
             Curtiss},
   Title = {Feasibility of an immunoassay for mevalonolactone.},
   Journal = {Bioorganic & medicinal chemistry},
   Volume = {5},
   Number = {5},
   Pages = {873-82},
   Year = {1997},
   Month = {May},
   ISSN = {0968-0896},
   Keywords = {Animals • Antibody Formation • Haptens •
             Hemocyanin • Hydrogen-Ion Concentration •
             Immunoassay • Mevalonic Acid • Rabbits •
             Stereoisomerism • analogs & derivatives* •
             analysis • chemistry • immunology •
             methods*},
   Abstract = {Mevalonic acid is a key intermediate in a broad spectrum of
             cellular biological processes and their regulation.
             Availability of a rapid, sensitive and accurate method for
             its assay would be highly useful. Therefore, the feasibility
             of developing an immunoassay for mevalonic acid in
             biological samples was explored. The strategy employed was
             to synthesize several racemic haptens structurally
             resembling R-mevalonolactone, the cyclic form of mevalonic
             acid present at lower pH and presumed to be more antigenic.
             Two of these haptens were coupled to keyhole limpet
             hemocyanin, and the resulting conjugates were used
             successfully to generate antibodies in rabbits. The first
             antiserum bound to R,S-mevalonolactone much more effectively
             at pH 4.0 than at pH 6.0, consistent with the structural
             resemblance of the haptens to the lactone form. This
             antiserum also bound the free hapten from which it was
             generated and two others of different structure with
             comparable effectiveness; and slightly better than it bound
             R,S-mevalonolactone at pH 4.0. Similar results were obtained
             with the antiserum to the second hapten. The binding of
             either antiserum to the natural enantiomer,
             R-mevalonolactone, was 20 times weaker than to
             R,S-mevalonolactone, suggesting that the nonbiological
             enantiomer was more antigenic. Nevertheless, the results
             demonstrate that an immunochemical approach to accurate
             quantitation of mevalonic acid in biological samples is
             feasible.},
   Language = {eng},
   Key = {fds174267}
}

@article{fds174202,
   Author = {TE Spencer and GA Johnson and FW Bazer and RC Burghardt},
   Title = {Fetal-maternal interactions during the establishment of
             pregnancy in ruminants.},
   Journal = {Society of Reproduction and Fertility supplement},
   Volume = {64},
   Pages = {379-96},
   Year = {2007},
   Keywords = {Animals • Blastocyst • Embryo Implantation •
             Embryonic Development • Endometrium • Female
             • Hormones • Luteolysis • Pregnancy •
             Sheep • metabolism* • physiology •
             physiology*},
   Abstract = {This review integrates established information with new
             insights into molecular and physiological mechanisms
             responsible for events leading to pregnancy recognition,
             endometrial receptivity, and implantation with emphasis on
             sheep. After formation of the corpus luteum, progesterone
             acts on the endometrium and stimulates blastocyst growth and
             elongation to form a filamentous conceptus (embryo/fetus and
             associated extraembryonic membranes). Recurrent early
             pregnancy loss in the uterine gland knockout ewe model
             indicates that endometrial epithelial secretions are
             essential for peri-implantation blastocyst survival and
             growth. The elongating sheep conceptus secretes interferon
             tau (IFNT) that acts on the endometrium to inhibit
             development of the luteolytic mechanism by inhibiting
             transcription of the estrogen receptor alpha (ESR1) gene in
             the luminal (LE) and superficial ductal glandular (sGE)
             epithelia, which prevents estrogen-induction of oxytocin
             receptors (OXTR) and production of luteolytic prostaglandin
             F2-alpha pulses. Progesterone downregulates its receptors
             (PGR) in LE and then GE, correlating with a reduction of
             anti-adhesive MUC1 (mucin glycoprotein one) and induction of
             secreted LGALS15 (galectin 15) and SPP1 (secreted
             phosphoprotein one), that are proposed to regulate
             trophectoderm growth and adhesion. IFNT acts on the LE to
             induce WNT7A (wingless-type MMTV integration site family
             member 7A) and to stimulate LGALS15, CTSL (cathepsin L), and
             CST3 (cystatin C), which may regulate conceptus development
             and implantation. During the peri-implantation period,
             trophoblast giant binucleate cells (BNC) begin to
             differentiate from mononuclear trophectoderm cells, migrate
             and then fuse with the uterine LE as well as each other to
             form multinucleated syncytial plaques. Trophoblast giant BNC
             secrete chorionic somatomammotropin (CSH1 or placental
             lactogen) that acts on the endometrial glands to stimulate
             their morphogenesis and differentiated function. The
             interactive, coordinated and stage-specific effects of
             ovarian and placental hormones regulate endometrial events
             necessary for fetal-maternal interactions and successful
             establishment of pregnancy.},
   Language = {eng},
   Key = {fds174202}
}

@booklet{Jefferies01,
   Author = {B. Jefferies and G. A. Johnson},
   Title = {Feynman's operational calculi for noncommuting operators:
             Definitions and elementary properties},
   Journal = {Russian Journal Of Mathematical Physics},
   Volume = {8},
   Number = {2},
   Pages = {153 -- 171},
   Year = {2001},
   Key = {Jefferies01}
}

@booklet{Johnson00a,
   Author = {G. A. Johnson and M. D. Todd and B. L. Althouse and C. C.
             Chang},
   Title = {Fiber Bragg grating interrogation and multiplexing with a 3
             x 3 coupler and a scanning filter},
   Journal = {Journal Of Lightwave Technology},
   Volume = {18},
   Number = {8},
   Pages = {1101 -- 1105},
   Year = {2000},
   Month = {August},
   Key = {Johnson00a}
}

@booklet{Brau02,
   Author = {A. C. S. Brau and C. T. Wheeler and L. W. Hedlund and G. A.
             Johnson},
   Title = {Fiber-optic stethoscope: A cardiac monitoring and gating
             system for magnetic resonance microscopy},
   Journal = {Magnetic Resonance In Medicine},
   Volume = {47},
   Number = {2},
   Pages = {314 -- 321},
   Year = {2002},
   Month = {February},
   Key = {Brau02}
}

@article{fds269015,
   Author = {Brau, ACS and Wheeler, CT and Hedlund, LW and Johnson,
             GA},
   Title = {Fiber-optic stethoscope: a cardiac monitoring and gating
             system for magnetic resonance microscopy.},
   Journal = {Magn Reson Med},
   Volume = {47},
   Number = {2},
   Pages = {314-321},
   Year = {2002},
   Month = {February},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/11810675},
   Keywords = {Animals • Electrocardiography • Esophagoscopy*
             • Fiber Optics* • Heart Atria • Heart Rate
             • Heart Ventricles • Hemodynamic Processes •
             Magnetic Resonance Imaging • Mice • Mice, Inbred
             C57BL • Microscopy • Myocardial Contraction •
             Rats • Stethoscopes* • anatomy & histology* •
             instrumentation* • physiology},
   Abstract = {A fundamental problem associated with using the conventional
             electrocardiograph (ECG) to monitor a subject's cardiac
             activity during magnetic resonance imaging (MRI) is the
             distortion of the ECG due to electromagnetic interference.
             This problem is particularly pronounced in MR microscopy
             (MRI of small animals at microscopic resolutions (< 0.03
             mm(3))) because the strong, rapidly-switching magnetic field
             gradients induce artifacts in the animal's ECG that often
             mimic electrophysiologic activity, impairing the use of the
             ECG for cardiac monitoring and gating purposes. The
             fiber-optic stethoscope system offers a novel approach to
             measuring cardiac activity that, unlike the ECG, is immune
             to electromagnetic effects. The fiber-optic stethoscope is
             perorally inserted into the esophagus of small animals to
             optically detect pulsatile compression of the esophageal
             wall. The optical system is shown to provide a robust
             cardiac monitoring and gating signal in rats and mice during
             routine cardiac MR microscopy.},
   Doi = {10.1002/mrm.10049},
   Key = {fds269015}
}

@booklet{Sherrier88,
   Author = {Sherrier, RH and Suddarth, SA and Johnson, GA},
   Title = {Film-Based Digital Tomosynthesis Of The Chest},
   Journal = {Optical Engineering},
   Volume = {27},
   Number = {8},
   Pages = {691-695},
   Publisher = {SPIE-Intl Soc Optical Eng},
   Year = {1988},
   Month = {August},
   ISSN = {0091-3286},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1988P713200014&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Doi = {10.1117/12.7976742},
   Key = {Sherrier88}
}

@booklet{Todd98a,
   Author = {M. D. Todd and G. A. Johnson and B. A. Althouse and S. T.
             Vohra},
   Title = {Flexural beam-based fiber Bragg grating accelerometers},
   Journal = {Ieee Photonics Technology Letters},
   Volume = {10},
   Number = {11},
   Pages = {1605 -- 1607},
   Year = {1998},
   Month = {November},
   Key = {Todd98a}
}

@booklet{Todd98,
   Author = {M. D. Todd and G. A. Johnson and B. A. Althouse and S. T.
             Vohra},
   Title = {Flexural beam-based fiber Bragg grating accelerometers (vol
             10, pg 1605, 1998)},
   Journal = {Ieee Photonics Technology Letters},
   Volume = {10},
   Number = {12},
   Pages = {1799 -- 1799},
   Year = {1998},
   Month = {December},
   Key = {Todd98}
}

@booklet{Croft97,
   Author = {P. J. Croft and R. L. Pfost and J. M. Medlin and G. A.
             Johnson},
   Title = {Fog forecasting for the southern region: A conceptual model
             approach},
   Journal = {Weather And Forecasting},
   Volume = {12},
   Number = {3},
   Pages = {545 -- 556},
   Year = {1997},
   Month = {September},
   Key = {Croft97}
}

@article{fds268866,
   Author = {Bucholz, E and Ghaghada, K and Qi, Y and Mukundan, S and Johnson,
             GA},
   Title = {Four-dimensional MR microscopy of the mouse heart using
             radial acquisition and liposomal gadolinium contrast
             agent.},
   Journal = {Magn Reson Med},
   Volume = {60},
   Number = {1},
   Pages = {111-118},
   Year = {2008},
   Month = {July},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/18581419},
   Keywords = {Animals • Contrast Media • Gadolinium • Heart
             • Liposomes • Magnetic Resonance Imaging •
             Mice • Microscopy • anatomy & histology •
             diagnostic use • methods • methods* •
             physiology*},
   Abstract = {Magnetic resonance microscopy (MRM) has become an important
             tool for small animal cardiac imaging. In relation to
             competing technologies (microCT and ultrasound), MR is
             limited by spatial resolution, temporal resolution, and
             acquisition time. All three of these limitations have been
             addressed by developing a four-dimensional (4D) (3D plus
             time) radial acquisition (RA) sequence. The signal-to-noise
             ratio (SNR) has been optimized by minimizing the echo time
             (TE) (300 us). The temporal resolution and throughput have
             been improved by center-out trajectories resulting in
             repetition time (TR) <2.5 ms. The contrast has been enhanced
             through the use of a liposomal blood pool agent that reduces
             the T(1) of the blood to <400 ms. We have developed
             protocols for three specific applications: 1)
             high-throughput with spatial resolution of 87 x 87 x 352
             um(3) (voxel volume = 2.7 nL) and acquisition time of 16
             min; 2) high-temporal resolution with spatial resolution of
             87 x 87 x 352 um(3) (voxel volume = 2.7 nL) and temporal
             resolution at 4.8 ms and acquisition time of 32 minutes; and
             3) high-resolution isotropic imaging at 87 x 87 x 87 um(3)
             (voxel volume = 0.68 nL) and acquisition time of 31 min. The
             4D image arrays allow direct measure of cardiac functional
             parameters dependent on chamber volumes, e.g., ejection
             fraction (EF), end diastolic volume (EDV), and end systolic
             volume (ESV).},
   Doi = {10.1002/mrm.21618},
   Key = {fds268866}
}

@article{fds268710,
   Author = {Xie, L and Subashi, E and Qi, Y and Knepper, MA and Johnson,
             GA},
   Title = {Four-dimensional MRI of renal function in the developing
             mouse.},
   Journal = {NMR Biomed},
   Volume = {27},
   Number = {9},
   Pages = {1094-1102},
   Year = {2014},
   Month = {September},
   ISSN = {0952-3480},
   url = {http://dx.doi.org/10.1002/nbm.3162},
   Abstract = {The major roles of filtration, metabolism and high blood
             flow make the kidney highly vulnerable to drug-induced
             toxicity and other renal injuries. A method to follow kidney
             function is essential for the early screening of toxicity
             and malformations. In this study, we acquired high
             spatiotemporal resolution (four dimensional) datasets of
             normal mice to follow changes in kidney structure and
             function during development. The data were acquired with
             dynamic contrast-enhanced MRI (via keyhole imaging) and a
             cryogenic surface coil, allowing us to obtain a full
             three-dimensional image (isotropic resolution,
             125 microns) every 7.7 s over a 50-min scan. This time
             course permitted the demonstration of both contrast
             enhancement and clearance. Functional changes were measured
             over a 17-week course (at 3, 5, 7, 9, 13 and 17 weeks).
             The time dimension of the MRI dataset was processed to
             produce unique image contrasts to segment the four regions
             of the kidney: cortex (CO), outer stripe (OS) of the outer
             medulla (OM), inner stripe (IS) of the OM and inner medulla
             (IM). Local volumes, time-to-peak (TTP) values and decay
             constants (DC) were measured in each renal region. These
             metrics increased significantly with age, with the exception
             of DC values in the IS and OS. These data will serve as a
             foundation for studies of normal renal physiology and future
             studies of renal diseases that require early detection and
             intervention.},
   Doi = {10.1002/nbm.3162},
   Key = {fds268710}
}

@article{fds292760,
   Author = {Johnson, GA},
   Title = {Free radicals formed by exposure of pyrimidine solids to
             sodium atoms: an electron spin resonance
             study.},
   Journal = {Proc Natl Acad Sci U S A},
   Volume = {72},
   Number = {3},
   Pages = {974-978},
   Year = {1975},
   Month = {March},
   ISSN = {0027-8424},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/165496},
   Keywords = {Alloxan • Bromouracil • Cytosine • Electron
             Spin Resonance Spectroscopy • Fluorouracil • Free
             Radicals • Pyrimidines* • Sodium* • Thymine
             • Uracil • analogs & derivatives},
   Abstract = {Sodium atoms have been deposited on various pyrimidine
             powders under high vacuum at 77 degrees K and the electron
             spin resonance spectra of the resulting free radicals have
             been observed. Generally, the spectra show that the electron
             of the Na goes into a molecular orbital of the pyrimidine
             ring and the Na+ ions become attached to a carbonyl oxygen
             of the resulting pyrimidine anion. In 5-fluorouracil and
             5-chlorouracil, however, the halogen is evidently abstracted
             by the Na to form NaF or NaC1 and the neutral uracil
             radical. Thymine shows evidence for H-addition radicals as
             well as the Na+-[thymine]-complex. The H source for the
             addition radicals may be an H-2-0 impurity in the sample,
             with which the Na atoms combine to release the H atoms. In
             addition to a resonance with g equals 2.00 from the
             pyrimidine anion radical, broad resonances with g greater
             than 2 were observed for 5-bromouracil, 5-chlorouracil and
             5-iodouracil, as well as for alloxan and cytosine. These
             resonances, generally unstable at room temperature, are
             believed to arise from electrons trapped in interstitial
             sties or vacancies in the lattice.},
   Language = {eng},
   Doi = {10.1073/pnas.72.3.974},
   Key = {fds292760}
}

@article{fds268816,
   Author = {Zhang, X and Badea, CT and Hood, G and Wetzel, AW and Stiles, JR and Johnson, GA},
   Title = {Free-space fluorescence tomography with adaptive sampling
             based on anatomical information from microCT.},
   Journal = {Proc SPIE Int Soc Opt Eng},
   Volume = {7757},
   Number = {775706},
   Year = {2010},
   ISSN = {0277-786X},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/21743784},
   Abstract = {Image reconstruction is one of the main challenges for
             fluorescence tomography. For in vivo experiments on small
             animals, in particular, the inhomogeneous optical properties
             and irregular surface of the animal make free-space image
             reconstruction challenging because of the difficulties in
             accurately modeling the forward problem and the finite
             dynamic range of the photodetector. These two factors are
             fundamentally limited by the currently available forward
             models and photonic technologies. Nonetheless, both
             limitations can be significantly eased using a signal
             processing approach. We have recently constructed a
             free-space panoramic fluorescence diffuse optical tomography
             system to take advantage of co-registered microCT data
             acquired from the same animal. In this article, we present a
             data processing strategy that adaptively selects the optical
             sampling points in the raw 2-D fluorescent CCD images.
             Specifically, the general sampling area and sampling density
             are initially specified to create a set of potential
             sampling points sufficient to cover the region of interest.
             Based on 3-D anatomical information from the microCT and the
             fluorescent CCD images, data points are excluded from the
             set when they are located in an area where either the
             forward model is known to be problematic (e.g., large
             wrinkles on the skin) or where the signal is unreliable
             (e.g., saturated or low signal-to-noise ratio). Parallel
             Monte Carlo software was implemented to compute the
             sensitivity function for image reconstruction. Animal
             experiments were conducted on a mouse cadaver with an
             artificial fluorescent inclusion. Compared to our previous
             results using a finite element method, the newly developed
             parallel Monte Carlo software and the adaptive sampling
             strategy produced favorable reconstruction
             results.},
   Language = {ENG},
   Doi = {10.1117/12.841891},
   Key = {fds268816}
}

@booklet{Johnson85d,
   Author = {G. A. Johnson},
   Title = {From constant air to variable},
   Journal = {Ashrae Journal-american Society Of Heating Refrigerating And
             Air-conditioning Engineers},
   Volume = {27},
   Number = {1},
   Pages = {106 -- \&},
   Year = {1985},
   Key = {Johnson85d}
}

@booklet{Jaeger00a,
   Author = {L. A. Jaeger and L. S. Bustamante and G. A. Johnson and F.
             W. Bazer and R. C. Burghardt},
   Title = {Functional activation of conceptus and maternal
             integrins},
   Journal = {Faseb Journal},
   Volume = {14},
   Number = {4},
   Pages = {A783 -- A783},
   Year = {2000},
   Month = {March},
   Key = {Jaeger00a}
}

@article{fds174181,
   Author = {LA Jaeger and GA Johnson and H Ka and JG Garlow and RC Burghardt and TE
             Spencer, FW Bazer},
   Title = {Functional analysis of autocrine and paracrine signalling at
             the uterine-conceptus interface in pigs.},
   Journal = {Reproduction (Cambridge, England) Supplement},
   Volume = {58},
   Pages = {191-207},
   Year = {2001},
   ISSN = {1477-0415},
   Keywords = {Animals • Autocrine Communication • Blastocyst
             • Cell Communication • Cytokines • Embryo
             Implantation • Estrogens • Extracellular Matrix
             Proteins • Female • Growth Substances •
             Integrins • Paracrine Communication • Pregnancy
             • Progesterone • Receptors, Estrogen •
             Receptors, Progesterone • Swine • Uterus •
             metabolism • metabolism* • physiology •
             physiology*},
   Abstract = {The complexity of implantation necessitates intimate
             dialogue between conceptus and maternal cells, and precise
             coordination of maternal and conceptus signalling events.
             Maternal and conceptus-derived steroid hormones, growth
             factors and cytokines, as well as integrins and their
             ligands, have important and inter-related roles in mediating
             adhesion between apical aspects of conceptus trophectoderm
             and maternal uterine luminal epithelium that leads to
             formation of an epitheliochorial placenta. Integrin
             receptors appear to play fundamental roles in the
             implantation cascade and may interact with extracellular
             matrix molecules and other ligands to transduce cellular
             signals through autocrine and paracrine mechanisms.
             Functional in vitro analyses can be used to monitor
             individual contributions of specific integrin receptors and
             ligands to the signalling cascades of the maternal-conceptus
             interface. Integrative studies of implantation in pigs,
             using in vivo and in vitro approaches, are required to
             understand conceptus attachment and implantation in this
             species, and provide valuable opportunities to understand
             the fundamental mechanisms of implantation in all
             species.},
   Language = {eng},
   Key = {fds174181}
}

@article{fds174096,
   Author = {LA Jaeger and AK Spiegel and NH Ing and GA Johnson and FW Bazer and RC
             Burghardt},
   Title = {Functional effects of transforming growth factor beta on
             adhesive properties of porcine trophectoderm.},
   Journal = {Endocrinology},
   Volume = {146},
   Number = {9},
   Pages = {3933-42},
   Year = {2005},
   Month = {September},
   ISSN = {0013-7227},
   url = {http://dx.doi.org/10.1210/en.2005-0090},
   Keywords = {Animals • Blastocyst • Cell Adhesion • Cell
             Line, Transformed • Embryo Implantation •
             Endometrium • Female • Fibronectins •
             Integrins • Oligopeptides • RNA, Messenger •
             Signal Transduction • Swine • Talin •
             Transforming Growth Factor beta • Transforming Growth
             Factor beta1 • analysis • cytology* •
             genetics • metabolism • metabolism* •
             pharmacology • physiology • physiology*},
   Abstract = {In pigs, expression and amounts of biologically active
             TGFbetas at the conceptus-maternal interface increase
             significantly as conceptuses elongate and begin the
             implantation process. Before their activation, secreted
             TGFbetas are noncovalently associated with their respective,
             isoform-specific latency-associated peptides (LAPs), which
             contain the Arg-Gly-Asp (RGD) amino acid sequence that
             serves as a ligand for numerous integrins. Objectives of
             this study were to determine whether TGFbeta1 increases
             production of fibronectin by porcine trophectoderm, whether
             porcine trophectoderm adheres specifically to fibronectin
             and LAP, and whether functional interactions between porcine
             trophectoderm and the two TGFbeta-associated proteins,
             fibronectin and LAP, are integrin mediated. Porcine
             trophectoderm cells (pTr2) were cultured in presence of
             TGFbeta1, LAP, or pan-neutralizing anti-TGFbeta antibody;
             TGFbeta specifically increased (P < 0.05) fibronectin mRNA
             levels, as determined by Northern and slot blot analyses.
             Immunofluorescence microscopy demonstrated a TGFbeta-induced
             increase in fibronectin in pTr2 cells. In dispersed cell
             adhesion assays, adhesion of pTr2 cells to fibronectin was
             inhibited by an RGD-containing peptide (P < 0.05) and pTr2
             cells attached to recombinant LAP but not to an LAP mutant,
             which contained an RGE sequence rather than the RGD site (P
             < 0.05). Fibronectin- and LAP-coated microbeads induced
             integrin activation at apical surfaces of both trophectoderm
             and uterine luminal epithelial cells, as indicated by
             aggregation and transmembrane accumulation of talin detected
             with immunofluorescence microscopy. Cell surface
             biotinylation and immunoprecipitation revealed integrin
             subunits alphav and beta1 on apical membranes of pTr2 cells.
             These results suggest multiple effects of TGFbeta at the
             porcine conceptus-maternal interface, including
             integrin-mediated conceptus-maternal communication through
             LAP.},
   Language = {eng},
   Doi = {10.1210/en.2005-0090},
   Key = {fds174096}
}

@article{064610243504,
   Author = {Badea, CT and Hedlund, LW and Lin, MD and Boslego, JF and Johnson,
             GA},
   Title = {Functional imaging in small animals using tomographic
             digital subtraction angiography},
   Journal = {2006 3rd IEEE International Symposium on Biomedical Imaging:
             From Nano to Macro - Proceedings},
   Volume = {2006},
   Pages = {1208-1211},
   Address = {Arlington, VA, United States},
   Year = {2006},
   Month = {November},
   ISBN = {9780780395770},
   Keywords = {Imaging systems;Angiography;Computerized tomography;Optical
             resolving power;Algorithms;Data structures;},
   Abstract = {We propose the use of Tomographic Digital Subtraction
             Angiography (TDSA) for functional imaging in small animals.
             TDSA combines the advantages of high temporal resolution of
             digital subtraction angiography (DSA) and high spatial
             resolution of micro-computed tomography (CT). TDSA augments
             projection imaging methods such as DSA by providing
             three-dimensional information using tomosynthesis or CT
             reconstruction algorithms. Thus, four-dimensional (4D)
             datasets with a temporal resolution on the order of 100 ms
             and spatial resolution ranging from 100 microns to 1 mm,
             depending on the scanning angle, can be obtained. The
             approach is based on the novel paradigm that the same time
             density curves can be reproduced in a number of consecutive
             injections of microL volumes of contrast at a series of
             different angles of rotation. © 2006 IEEE.},
   Key = {064610243504}
}

@article{9054429,
   Author = {Badea, C.T. and Hedlund, L.W. and Ming De Lin and Boslego,
             J.F. and Johnson, G.A.},
   Title = {Functional imaging in small animals using tomographic
             digital subtraction angiography},
   Journal = {2006 3rd IEEE International Symposium on Biomedical Imaging:
             Macro to Nano (IEEE Cat. No.06EX1231C)},
   Pages = {1208 - 11},
   Address = {Arlington, VA, USA},
   Year = {2006},
   Keywords = {computerised tomography;diagnostic radiography;image
             reconstruction;image resolution;medical image
             processing;},
   Abstract = {We propose the use of tomographic digital subtraction
             angiography (TDSA) for functional imaging in small animals.
             TDSA combines the advantages of high temporal resolution of
             digital subtraction angiography (DSA) and high spatial
             resolution of micro-computed tomography (CT). TDSA augments
             projection imaging methods such as DSA by providing
             three-dimensional information using tomosynthesis or CT
             reconstruction algorithms. Thus, four-dimensional (4D)
             datasets with a temporal resolution on the order of 100 ms
             and spatial resolution ranging from 100 microns to 1 mm,
             depending on the scanning angle, can be obtained. The
             approach is based on the novel paradigm that the same time
             density curves can be reproduced in a number of consecutive
             injections of microL volumes of contrast at a series of
             different angles of rotation},
   Key = {9054429}
}

@article{fds132766,
   Author = {GA Johnson and LW Hedlund},
   Title = {Functional imaging of the lung.},
   Journal = {Nature medicine, UNITED STATES},
   Volume = {2},
   Number = {11},
   Pages = {1192},
   Year = {1996},
   Month = {November},
   ISSN = {1078-8956},
   Keywords = {Lung • Magnetic Resonance Imaging* •
             physiology*},
   Key = {fds132766}
}

@booklet{Johnson96,
   Author = {Johnson, GA and Hedlund, LW},
   Title = {Functional imaging of the lung.},
   Journal = {Nat Med},
   Volume = {2},
   Number = {11},
   Pages = {1192},
   Year = {1996},
   Month = {November},
   ISSN = {1078-8956},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/8898741},
   Doi = {10.1038/nm1196-1192},
   Key = {Johnson96}
}

@article{fds268976,
   Author = {Viallon, M and Cofer, GP and Suddarth, SA and Möller, HE and Chen, XJ and Chawla, MS and Hedlund, LW and Crémillieux, Y and Johnson,
             GA},
   Title = {Functional MR microscopy of the lung using hyperpolarized
             3He.},
   Journal = {Magn Reson Med},
   Volume = {41},
   Number = {4},
   Pages = {787-792},
   Year = {1999},
   Month = {April},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/10332855},
   Keywords = {Animals • Guinea Pigs • Helium • Isotopes
             • Lung • Magnetic Resonance Imaging, Cine •
             Microscopy • cytology • diagnostic use* •
             methods • methods* • physiology*},
   Abstract = {A new strategy designed to provide functional magnetic
             resonance images of the lung in small animals at microscopic
             resolution using hyperpolarized 3He is described. The pulse
             sequence is based on a combination of radial acquisition
             (RA) and CINE techniques, referred to as RA-CINE, and is
             designed for use with hyperpolarized 3He to explore lung
             ventilation with high temporal and spatial resolution in
             small animal models. Ventilation of the live guinea pig is
             demonstrated with effective temporal resolution of 50 msec
             and in-plane spatial resolution of <100 microm using
             hyperpolarized 3He. The RA-CINE sequence allows one to
             follow gas inflow and outflow in the airways as well as in
             the distal part of the lungs. Regional analysis of signal
             intensity variations can be performed and can help assess
             functional lung parameters such as residual gas volume and
             lung compliance to gas inflow.},
   Doi = {10.1002/(sici)1522-2594(199904)41:4<787::aid-mrm18>3.0.co;2-},
   Key = {fds268976}
}

@booklet{Viallon99,
   Author = {M. Viallon and G. P. Cofer and S. A. Suddarth and H. E.
             Moller and X. J. Chen and M. S. Chawla and L. W. Hedlund and Y. Cremillieux and G. A. Johnson},
   Title = {Functional MR microscopy of the lung using hyperpolarized
             He-3},
   Journal = {Magnetic Resonance In Medicine},
   Volume = {41},
   Number = {4},
   Pages = {787 -- 792},
   Year = {1999},
   Month = {April},
   Key = {Viallon99}
}

@article{fds319489,
   Author = {Howles, GP and Qi, Y and Rosenzweig, SJ and Nightingale, KR and Johnson,
             GA},
   Title = {Functional neuroimaging using ultrasonic blood-brain barrier
             disruption and manganese-enhanced MRI.},
   Journal = {Journal of visualized experiments : JoVE},
   Number = {65},
   Pages = {e4055},
   Year = {2012},
   Month = {October},
   url = {http://dx.doi.org/10.3791/4055},
   Abstract = {Although mice are the dominant model system for studying the
             genetic and molecular underpinnings of neuroscience,
             functional neuroimaging in mice remains technically
             challenging. One approach, Activation-Induced
             Manganese-enhanced MRI (AIM MRI), has been used successfully
             to map neuronal activity in rodents. In AIM MRI, Mn(2+) acts
             a calcium analog and accumulates in depolarized neurons.
             Because Mn(2+) shortens the T1 tissue property, regions of
             elevated neuronal activity will enhance in MRI. Furthermore,
             Mn(2+) clears slowly from the activated regions; therefore,
             stimulation can be performed outside the magnet prior to
             imaging, enabling greater experimental flexibility. However,
             because Mn(2+) does not readily cross the blood-brain
             barrier (BBB), the need to open the BBB has limited the use
             of AIM MRI, especially in mice. One tool for opening the BBB
             is ultrasound. Though potentially damaging, if ultrasound is
             administered in combination with gas-filled microbubbles
             (i.e., ultrasound contrast agents), the acoustic pressure
             required for BBB opening is considerably lower. This
             combination of ultrasound and microbubbles can be used to
             reliably open the BBB without causing tissue damage. Here, a
             method is presented for performing AIM MRI by using
             microbubbles and ultrasound to open the BBB. After an
             intravenous injection of perflutren microbubbles, an
             unfocused pulsed ultrasound beam is applied to the shaved
             mouse head for 3 minutes. For simplicity, we refer to this
             technique of BBB Opening with Microbubbles and UltraSound as
             BOMUS. Using BOMUS to open the BBB throughout both cerebral
             hemispheres, manganese is administered to the whole mouse
             brain. After experimental stimulation of the lightly sedated
             mice, AIM MRI is used to map the neuronal response. To
             demonstrate this approach, herein BOMUS and AIM MRI are used
             to map unilateral mechanical stimulation of the vibrissae in
             lightly sedated mice. Because BOMUS can open the BBB
             throughout both hemispheres, the unstimulated side of the
             brain is used to control for nonspecific background
             stimulation. The resultant 3D activation map agrees well
             with published representations of the vibrissae regions of
             the barrel field cortex. The ultrasonic opening of the BBB
             is fast, noninvasive, and reversible; and thus this approach
             is suitable for high-throughput and/or longitudinal studies
             in awake mice.},
   Doi = {10.3791/4055},
   Key = {fds319489}
}

@article{fds268772,
   Author = {Howles, GP and Qi, Y and Rosenzweig, SJ and Nightingale, KR and Johnson,
             GA},
   Title = {Functional neuroimaging using ultrasonic blood-brain barrier
             disruption and manganese-enhanced MRI.},
   Journal = {J Vis Exp},
   Number = {65},
   Pages = {e4055},
   Year = {2012},
   Month = {July},
   ISSN = {1940-087X},
   url = {http://dx.doi.org/10.3791/4055},
   Abstract = {Although mice are the dominant model system for studying the
             genetic and molecular underpinnings of neuroscience,
             functional neuroimaging in mice remains technically
             challenging. One approach, Activation-Induced
             Manganese-enhanced MRI (AIM MRI), has been used successfully
             to map neuronal activity in rodents. In AIM MRI, Mn(2+) acts
             a calcium analog and accumulates in depolarized neurons.
             Because Mn(2+) shortens the T1 tissue property, regions of
             elevated neuronal activity will enhance in MRI. Furthermore,
             Mn(2+) clears slowly from the activated regions; therefore,
             stimulation can be performed outside the magnet prior to
             imaging, enabling greater experimental flexibility. However,
             because Mn(2+) does not readily cross the blood-brain
             barrier (BBB), the need to open the BBB has limited the use
             of AIM MRI, especially in mice. One tool for opening the BBB
             is ultrasound. Though potentially damaging, if ultrasound is
             administered in combination with gas-filled microbubbles
             (i.e., ultrasound contrast agents), the acoustic pressure
             required for BBB opening is considerably lower. This
             combination of ultrasound and microbubbles can be used to
             reliably open the BBB without causing tissue damage. Here, a
             method is presented for performing AIM MRI by using
             microbubbles and ultrasound to open the BBB. After an
             intravenous injection of perflutren microbubbles, an
             unfocused pulsed ultrasound beam is applied to the shaved
             mouse head for 3 minutes. For simplicity, we refer to this
             technique of BBB Opening with Microbubbles and UltraSound as
             BOMUS. Using BOMUS to open the BBB throughout both cerebral
             hemispheres, manganese is administered to the whole mouse
             brain. After experimental stimulation of the lightly sedated
             mice, AIM MRI is used to map the neuronal response. To
             demonstrate this approach, herein BOMUS and AIM MRI are used
             to map unilateral mechanical stimulation of the vibrissae in
             lightly sedated mice. Because BOMUS can open the BBB
             throughout both hemispheres, the unstimulated side of the
             brain is used to control for nonspecific background
             stimulation. The resultant 3D activation map agrees well
             with published representations of the vibrissae regions of
             the barrel field cortex. The ultrasonic opening of the BBB
             is fast, noninvasive, and reversible; and thus this approach
             is suitable for high-throughput and/or longitudinal studies
             in awake mice.},
   Doi = {10.3791/4055},
   Key = {fds268772}
}

@booklet{Chen04a,
   Author = {Chen, BT and Yordanov, AT and Johnson, GA},
   Title = {Functional pulmonary MR microscopy in mice},
   Journal = {FASEB JOURNAL},
   Volume = {18},
   Number = {5},
   Pages = {A785-A785},
   Publisher = {FEDERATION AMER SOC EXP BIOL},
   Year = {2004},
   Month = {March},
   ISSN = {0892-6638},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000220470700119&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Chen04a}
}

@booklet{Pecora97,
   Author = {L. M. Pecora and T. L. Carroll and G. A. Johnson and D. J.
             Mar and J. F. Heagy},
   Title = {Fundamentals of synchronization in chaotic systems,
             concepts, and applications},
   Journal = {Chaos},
   Volume = {7},
   Number = {4},
   Pages = {520 -- 543},
   Year = {1997},
   Month = {December},
   Key = {Pecora97}
}

@article{fds174115,
   Author = {LM Pecora and TL Carroll and GA Johnson and DJ Mar and JF
             Heagy},
   Title = {Fundamentals of synchronization in chaotic systems,
             concepts, and applications.},
   Journal = {Chaos (Woodbury, N.Y.)},
   Volume = {7},
   Number = {4},
   Pages = {520-543},
   Year = {1997},
   Month = {December},
   ISSN = {1089-7682},
   url = {http://dx.doi.org/10.1063/1.166278},
   Abstract = {The field of chaotic synchronization has grown considerably
             since its advent in 1990. Several subdisciplines and
             "cottage industries" have emerged that have taken on bona
             fide lives of their own. Our purpose in this paper is to
             collect results from these various areas in a review article
             format with a tutorial emphasis. Fundamentals of chaotic
             synchronization are reviewed first with emphases on the
             geometry of synchronization and stability criteria. Several
             widely used coupling configurations are examined and, when
             available, experimental demonstrations of their success
             (generally with chaotic circuit systems) are described.
             Particular focus is given to the recent notion of
             synchronous substitution-a method to synchronize chaotic
             systems using a larger class of scalar chaotic coupling
             signals than previously thought possible. Connections
             between this technique and well-known control theory results
             are also outlined. Extensions of the technique are presented
             that allow so-called hyperchaotic systems (systems with more
             than one positive Lyapunov exponent) to be synchronized.
             Several proposals for "secure" communication schemes have
             been advanced; major ones are reviewed and their strengths
             and weaknesses are touched upon. Arrays of coupled chaotic
             systems have received a great deal of attention lately and
             have spawned a host of interesting and, in some cases,
             counterintuitive phenomena including bursting above
             synchronization thresholds, destabilizing transitions as
             coupling increases (short-wavelength bifurcations), and
             riddled basins. In addition, a general mathematical
             framework for analyzing the stability of arrays with
             arbitrary coupling configurations is outlined. Finally, the
             topic of generalized synchronization is discussed, along
             with data analysis techniques that can be used to decide
             whether two systems satisfy the mathematical requirements of
             generalized synchronization. (c) 1997 American Institute of
             Physics.},
   Language = {ENG},
   Doi = {10.1063/1.166278},
   Key = {fds174115}
}

@article{fds132720,
   Author = {G.A. Johnson},
   Title = {G.A. Johnson, G. Cates, X.J. Chen, G.P. Cofer,  B.
             Driehuys, W. Happer,  L.W. Hedlund, B. Saam, M. Shattuck,
             J. Swartz.  Dynamics of  magnetization in hyperpolarized
             gas MRI of the lung.  Magnetic Resonance  in Medicine
             submitted (1996).},
   Year = {1996},
   Key = {fds132720}
}

@article{fds132738,
   Author = {G.A. Johnson},
   Title = {G.A. Johnson, H. Beneveniste, R.T. Engelhardt, H. Qiu, L. W.
             Hedlund,  Magnetic resonance microscopy in basic studies of
             brain structure and  function.  New York Academy of
             Sciences.  In press (1996).},
   Year = {1996},
   Key = {fds132738}
}

@article{fds132721,
   Author = {G.A. Johnson},
   Title = {G.A. Johnson, L.W. Hedlund.  Functional imaging of the
             lung.  Nature  Medicine 2, 1192 (1996).},
   Year = {1996},
   Key = {fds132721}
}

@article{fds132739,
   Author = {G.A. Johnson},
   Title = {G.A. Johnson, R.D. Black, G.D. Cates, X.J. Chen, B.
             Driehuys, W. Happer,  L.W. Hedlund, H. Middleton, M.D.
             Shattuck, J. Swartz.  Polarization  dynamics of
             hyperpolarized 3He in lung imaging.  in "Proc., SMR 4th
             Annual  Scientific Meeting.  New York, NY, 1996," p.
             19.},
   Year = {1996},
   Key = {fds132739}
}

@article{fds174137,
   Author = {SK Lewis and JL Farmer and RC Burghardt and GR Newton and GA Johnson and DL
             Adelson, FW Bazer and TE Spencer},
   Title = {Galectin 15 (LGALS15): a gene uniquely expressed in the
             uteri of sheep and goats that functions in trophoblast
             attachment.},
   Journal = {Biology of reproduction},
   Volume = {77},
   Number = {6},
   Pages = {1027-36},
   Year = {2007},
   Month = {December},
   ISSN = {0006-3363},
   url = {http://dx.doi.org/10.1095/biolreprod.107.063594},
   Keywords = {Amino Acid Sequence • Animals • Cattle •
             Cells, Cultured • Embryo Implantation •
             Endometrium • Female • Galectins • Gene
             Expression • Goats • Molecular Sequence Data
             • Pregnancy • RNA, Messenger • Rabbits •
             Ruminants • Sheep • Swine • Trophoblasts
             • genetics • genetics* • metabolism •
             metabolism* • physiology • physiology*},
   Abstract = {Galectins are a family of secreted animal lectins with
             biological roles in cell adhesion and migration. In sheep,
             galectin 15 (LGALS15) is expressed specifically in the
             endometrial luminal (LE) and superficial glandular (sGE)
             epithelia of the uterus in concert with blastocyst
             elongation during the peri-implantation period. The present
             study examined LGALS15 expression in the uterus of cattle,
             goats, and pigs. Although the bovine genome contains an
             LGALS15-like gene, expressed sequence tags encoding LGALS15
             mRNA were found only for sheep, and full-length LGALS15
             cDNAs were cloned only from endometrial total RNA isolated
             from pregnant sheep and goats, but not pregnant cattle or
             pigs. Ovine and caprine LGALS15 were highly homologous at
             the mRNA (95%) and protein (91%) levels, and all contained a
             conserved carbohydrate recognition domain and RGD
             recognition sequence for integrin binding. Endometrial
             LGALS15 mRNA levels increased after Day 11 of both the
             estrous cycle and pregnancy, and were considerably increased
             after Day 15 of pregnancy in goats. In situ hybridization
             detected abundant LGALS15 mRNA in endometrial LE and sGE of
             early pregnant goats, but not in cattle or pigs.
             Immunoreactive LGALS15 protein was present in endometrial
             epithelia and conceptus trophectoderm of goat uteri and
             detected within intracellular crystal structures in
             trophectoderm and LE. Recombinant ovine and caprine LGALS15
             proteins elicited a dose-dependent increase in ovine
             trophectoderm cell attachment in vitro that was comparable
             to bovine fibronectin. These results support the hypothesis
             that LGALS15 is uniquely expressed in Caprinae endometria
             and functions as an attachment factor important for
             peri-implantation blastocyst elongation.},
   Language = {eng},
   Doi = {10.1095/biolreprod.107.063594},
   Key = {fds174137}
}

@booklet{Thompson82,
   Author = {W. M. Thompson and W. C. Meyers and M. Shaw and M. Bates and G. A. Johnson and L. W. Hedlund},
   Title = {Gallbladder density and iodine concentration in humans
             during oral cholecystography - a comparison of iopanoic acid
             and iopronic acid},
   Journal = {Investigative Radiology},
   Volume = {17},
   Number = {6},
   Pages = {621 -- 628},
   Year = {1982},
   Key = {Thompson82}
}

@booklet{Thompson80a,
   Author = {THOMPSON, WM and AMBERG, JR and LOWTHER, DT and SHAW, M and BATES, M and JOHNSON, GA},
   Title = {GALLBLADDER DENSITY AND IODINE CONCENTRATION IN HUMANS
             DURING ORAL CHOLECYSTOGRAPHY - A COMPARISON OF IOPANOIC ACID
             AND IOPRONIC ACID},
   Journal = {GASTROINTESTINAL RADIOLOGY},
   Volume = {5},
   Number = {1},
   Pages = {83-83},
   Publisher = {SPRINGER VERLAG},
   Year = {1980},
   Month = {January},
   ISSN = {0364-2356},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1980JN17700030&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Thompson80a}
}

@article{fds132888,
   Author = {WM Thompson and WC Meyers and M Shaw and M Bates and GA Johnson and LW
             Hedlund},
   Title = {Gallbladder density and iodine concentration in humans
             during oral cholecystography. A comparison of iopanoic acid
             and iopronic acid.},
   Journal = {Investigative radiology, UNITED STATES},
   Volume = {17},
   Number = {6},
   Pages = {621-8},
   ISSN = {0020-9996},
   Keywords = {Administration, Oral • Bile Acids and Salts •
             Cholecystography* • Clinical Trials • Contrast
             Media • Double-Blind Method • Gallbladder •
             Humans • Iodine • Iodobenzenes • Iopanoic
             Acid • administration & dosage* •
             analysis},
   Abstract = {A comparison of two oral cholecystopaques, iopanoic acid
             (Telepaque) and iopronic acid (Oravue), was performed using
             normal volunteers. Using a double-blind crossover design,
             comparisons were made between the degree of gallbladder
             opacification and the amount of iodine recovered from the
             gallbladder. Bile was collected via a double lumen
             intestinal tube before, during, and after stimulating
             gallbladder contraction. There were no differences between
             the two agents in terms of opacification or iodine
             concentration. Only 19% of the administered dose of either
             agent was recovered, and the maximum iodine concentration in
             bile was 10 mg I/ml. The results suggest that this technique
             has merit for future comparative studies of agents
             concentrated in the gallbladder.},
   Key = {fds132888}
}

@article{fds132816,
   Author = {GA Johnson and JD Godwin and EK Fram},
   Title = {Gated multiplanar cardiac computed tomography.},
   Journal = {Radiology, UNITED STATES},
   Volume = {145},
   Number = {1},
   Pages = {195-7},
   Year = {1982},
   Month = {October},
   ISSN = {0033-8419},
   Keywords = {Animals • Computers • Diatrizoate • Dogs
             • Electrocardiography* • Heart • Tomography,
             X-Ray Computed • diagnostic use • methods* •
             radiography*},
   Abstract = {Multiplanar reformatting was combined with
             electrocardiographically gated computed tomography (CT) to
             provide a three-dimensional assessment of the beating heart
             of a live dog. Separate systolic and diastolic images were
             made in transverse, sagittal, coronal, and paraxial views.
             Three-dimensional contour images that outlined the cardiac
             chambers and the myocardium were then made using a separate
             research computer. This three-dimensional appreciation of
             cardiac morphology could be extended to assess regional
             function. Practical problems that limit the application of
             these methods are discussed, along with the proposed
             solutions.},
   Key = {fds132816}
}

@booklet{Johnson82c,
   Author = {Johnson, GA and Godwin, JD and Fram, EK},
   Title = {Gated multiplanar cardiac computed tomography.},
   Journal = {Radiology},
   Volume = {145},
   Number = {1},
   Pages = {195-197},
   Year = {1982},
   Month = {October},
   ISSN = {0033-8419},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/7122877},
   Abstract = {Multiplanar reformatting was combined with
             electrocardiographically gated computed tomography (CT) to
             provide a three-dimensional assessment of the beating heart
             of a live dog. Separate systolic and diastolic images were
             made in transverse, sagittal, coronal, and paraxial views.
             Three-dimensional contour images that outlined the cardiac
             chambers and the myocardium were then made using a separate
             research computer. This three-dimensional appreciation of
             cardiac morphology could be extended to assess regional
             function. Practical problems that limit the application of
             these methods are discussed, along with the proposed
             solutions.},
   Doi = {10.1148/radiology.145.1.7122877},
   Key = {Johnson82c}
}

@booklet{Wang99,
   Author = {G. Y. Wang and G. A. Johnson and T. E. Spencer and F. W.
             Bazer},
   Title = {Generation of immortalized porcine uterine cell
             lines.},
   Journal = {Biology Of Reproduction},
   Volume = {60},
   Pages = {260 -- 261},
   Year = {1999},
   Key = {Wang99}
}

@article{fds268844,
   Author = {Badea, A and Johnson, GA and Williams, RW},
   Title = {Genetic dissection of the mouse brain using high-field
             magnetic resonance microscopy.},
   Journal = {Neuroimage},
   Volume = {45},
   Number = {4},
   Pages = {1067-1079},
   Year = {2009},
   Month = {May},
   ISSN = {1095-9572},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/19349225},
   Keywords = {Animals • Brain • Magnetic Resonance Imaging
             • Mice • Mice, Inbred C57BL • Mice, Inbred
             DBA • Mice, Inbred Strains • Microscopy •
             Species Specificity • anatomy & histology •
             cytology* • genetics* • methods* •
             physiology*},
   Abstract = {Magnetic resonance (MR) imaging has demonstrated that
             variation in brain structure is associated with differences
             in behavior and disease state. However, it has rarely been
             practical to prospectively test causal models that link
             anatomical and functional differences in humans. In the
             present study we have combined classical mouse genetics with
             high-field MR to systematically explore and test such
             structure-functional relations across multiple brain
             regions. We segmented 33 regions in two parental
             strains-C57BL/6J (B) and DBA/2J (D)-and in nine BXD
             recombinant inbred strains. All strains have been studied
             extensively for more than 20 years using a battery of
             genetic, functional, anatomical, and behavioral assays. We
             compared levels of variation within and between strains and
             sexes, by region, and by system. Average within-strain
             variation had a coefficient of variation (CV) of 1.6% for
             the whole brain; while the CV ranged from 2.3 to 3.6% for
             olfactory bulbs, cortex and cerebellum, and up to
             approximately 18% for septum and laterodorsal thalamic
             nucleus. Variation among strain averages ranged from 6.7%
             for cerebellum, 7.6% for whole brain, 9.0% for cortex, up to
             approximately 26% for the ventricles, laterodorsal thalamic
             nucleus, and the interpeduncular nucleus. Heritabilities
             averaged 0.60+/-0.18. Sex differences were not significant
             with the possible (and unexpected) exception of the pons (
             approximately 20% larger in males). A correlation matrix of
             regional volumes revealed high correlations among
             functionally related parts of the CNS (e.g., components of
             the limbic system), and several high correlations between
             regions that are not anatomically connected, but that may
             nonetheless be functionally or genetically
             coupled.},
   Doi = {10.1016/j.neuroimage.2009.01.021},
   Key = {fds268844}
}

@article{fds268843,
   Author = {Badea, A and Johnson, GA and Williams, RW},
   Title = {Genetic dissection of the mouse CNS using magnetic resonance
             microscopy.},
   Journal = {Curr Opin Neurol},
   Volume = {22},
   Number = {4},
   Pages = {379-386},
   Year = {2009},
   Month = {August},
   ISSN = {1473-6551},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/19542887},
   Abstract = {PURPOSE OF REVIEW: Advances in magnetic resonance microscopy
             (MRM) make it practical to map gene variants responsible for
             structural variation in brains of many species, including
             mice and humans. We review results of a systematic genetic
             analysis of MRM data using as a case study a family of well
             characterized lines of mice. RECENT ADVANCES: MRM has
             matured to the point that we can generate high contrast,
             high-resolution images even for species as small as a mouse,
             with a brain merely 1/3000th the size of humans. We
             generated 21.5-micron data sets for a diverse panel of BXD
             mouse strains to gauge the extent of genetic variation, and
             as a prelude to comprehensive genetic and genomic analyses.
             Here we review MRM capabilities and image segmentation
             methods; heritability of brain variation; covariation of the
             sizes of brain regions; and correlations between MRM and
             classical histological data sets. SUMMARY: The combination
             of high throughput MRM and genomics will improve our
             understanding of the genetic basis of structure-function
             correlations. Sophisticated mouse models will be critical in
             converting correlations into mechanisms and in determining
             genetic and epigenetic causes of differences in disease
             susceptibility.},
   Doi = {10.1097/WCO.0b013e32832d9b86},
   Key = {fds268843}
}

@article{fds268857,
   Author = {Johnston, SM and Johnson, GA and Badea, CT},
   Title = {Geometric calibration for a dual tube/detector micro-CT
             system.},
   Journal = {Med Phys},
   Volume = {35},
   Number = {5},
   Pages = {1820-1829},
   Year = {2008},
   Month = {May},
   ISSN = {0094-2405},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/18561657},
   Keywords = {Algorithms • Animals • Artifacts •
             Calibration • Equipment Design • Humans •
             Metals • Mice • Models, Statistical • Models,
             Theoretical • Phantoms, Imaging • Radiographic
             Image Interpretation, Computer-Assisted •
             Reproducibility of Results • Tomography Scanners, X-Ray
             Computed • Tomography, X-Ray Computed • X-Rays
             • instrumentation* • methods •
             methods*},
   Abstract = {The authors describe a dual tube/detector micro-computed
             tomography (micro-CT) system that has the potential to
             improve temporal resolution and material contrast in small
             animal imaging studies. To realize this potential, it is
             necessary to precisely calibrate the geometry of a dual
             micro-CT system to allow the combination of projection data
             acquired with each individual tube/detector in a single
             reconstructed image. The authors present a geometric
             calibration technique that uses multiple projection images
             acquired with the two imaging chains while rotating a
             phantom containing a vertical array of regularly spaced
             metallic beads. The individual geometries of the imaging
             chains are estimated from the phantom projection images
             using analytical methods followed by a refinement procedure
             based on nonlinear optimization. The geometric parameters
             are used to create the cone beam projection matrices
             required by the reconstruction process for each imaging
             chain. Next, a transformation between the two projection
             matrices is found that allows the combination of projection
             data in a single reconstructed image. The authors describe
             this technique, test it with a series of computer
             simulations, and then apply it to data collected from their
             dual tube/detector micro-CT system. The results demonstrate
             that the proposed technique is accurate, robust, and
             produces images free of misalignment artifacts.},
   Doi = {10.1118/1.2900000},
   Key = {fds268857}
}

@booklet{Middleditch89,
   Author = {B. S. Middleditch and G. A. Johnson and R. R. Gregory and M.
             A. Alejandro and B. M. Markaverich},
   Title = {Gingerol analysis without artifact formation},
   Journal = {Hrc-journal Of High Resolution Chromatography},
   Volume = {12},
   Number = {10},
   Pages = {677 -- 679},
   Year = {1989},
   Month = {October},
   Key = {Middleditch89}
}

@article{fds359545,
   Author = {Nair, KS and Srivastava, C and Brown, RV and Koli, S and Choquet, H and Kang, HS and Kuo, Y-M and Grimm, SA and Sutherland, C and Badea, A and Johnson, GA and Zhao, Y and Yin, J and Okamoto, K and Clark, G and Borrás,
             T and Zode, G and Kizhatil, K and Chakrabarti, S and John, SWM and Jorgenson, E and Jetten, AM},
   Title = {GLIS1 regulates trabecular meshwork function and intraocular
             pressure and is associated with glaucoma in
             humans.},
   Journal = {Nat Commun},
   Volume = {12},
   Number = {1},
   Pages = {4877},
   Year = {2021},
   Month = {August},
   url = {http://dx.doi.org/10.1038/s41467-021-25181-7},
   Abstract = {Chronically elevated intraocular pressure (IOP) is the major
             risk factor of primary open-angle glaucoma, a leading cause
             of blindness. Dysfunction of the trabecular meshwork (TM),
             which controls the outflow of aqueous humor (AqH) from the
             anterior chamber, is the major cause of elevated IOP. Here,
             we demonstrate that mice deficient in the Krüppel-like zinc
             finger transcriptional factor GLI-similar-1 (GLIS1) develop
             chronically elevated IOP. Magnetic resonance imaging and
             histopathological analysis reveal that deficiency in GLIS1
             expression induces progressive degeneration of the TM,
             leading to inefficient AqH drainage from the anterior
             chamber and elevated IOP. Transcriptome and cistrome
             analyses identified several glaucoma- and extracellular
             matrix-associated genes as direct transcriptional targets of
             GLIS1. We also identified a significant association between
             GLIS1 variant rs941125 and glaucoma in humans (P = 4.73 ×
             10-6), further supporting a role for GLIS1 into glaucoma
             etiology. Our study identifies GLIS1 as a critical regulator
             of TM function and maintenance, AqH dynamics, and
             IOP.},
   Doi = {10.1038/s41467-021-25181-7},
   Key = {fds359545}
}

@article{fds174286,
   Author = {JT Self and TE Spencer and GA Johnson and J Hu and FW Bazer and G
             Wu},
   Title = {Glutamine synthesis in the developing porcine
             placenta.},
   Journal = {Biology of reproduction},
   Volume = {70},
   Number = {5},
   Pages = {1444-51},
   Year = {2004},
   Month = {May},
   ISSN = {0006-3363},
   url = {http://dx.doi.org/10.1095/biolreprod.103.025486},
   Keywords = {3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide) •
             Alanine • Alanine Transaminase • Amino Acids
             • Amino Acids, Branched-Chain • Animals •
             Biological Transport • Female • Glutamate-Ammonia
             Ligase • Glutaminase • Glutamine • Placenta
             • Pregnancy • Swine • Transaminases •
             biosynthesis • biosynthesis* • enzymology •
             growth & development* • metabolism •
             metabolism*},
   Abstract = {Glutamine plays a vital role in fetal carbon and nitrogen
             metabolism and exhibits the highest fetal:maternal plasma
             ratio among all amino acids in pigs. Such disparate
             glutamine levels between mother and fetus suggest that
             glutamine may be actively synthesized and released into the
             fetal circulation by the porcine placenta. We hypothesized
             that branched-chain amino acid (BCAA) metabolism in the
             placenta plays an important role in placental glutamine
             synthesis. This hypothesis was tested by studying
             conceptuses from gilts on Days 20, 30, 35, 40, 45, 50, 60,
             90, or 110 of gestation (n = 6 per day). Placental tissue
             was analyzed for amino acid concentrations, BCAA transport,
             BCAA degradation, and glutamine synthesis as well as the
             activities of related enzymes (including BCAA transaminase,
             branched-chain alpha-ketoacid dehydrogenase, glutamine
             synthetase, glutamate-pyruvate transaminase, and
             glutaminase). On all days of gestation, rates of BCAA
             transamination were much greater than rates of
             branched-chain alpha-ketoacid decarboxylation. The glutamate
             generated from BCAA transamination was primarily directed to
             glutamine synthesis and, to a much lesser extent, alanine
             production. Placental BCAA transport, BCAA transamination,
             glutamine synthesis, and activities of related enzymes
             increased markedly between Days 20 and 40 of gestation, as
             did glutamine in fetal allantoic fluid. Accordingly,
             placental BCAA levels decreased after Day 20 of gestation in
             association with a marked increase in BCAA catabolism and
             concentrations of glutamine. There was no detectable
             catabolism of glutamine in pig placenta throughout
             pregnancy, which would ensure maximum output of glutamine by
             this tissue. These novel results demonstrate glutamine
             synthesis from BCAAs in pig placentae, aid in explaining the
             abundance of glutamine in the fetus, and provide valuable
             insight into the dynamic role of the placenta in fetal
             metabolism and nutrition.},
   Language = {eng},
   Doi = {10.1095/biolreprod.103.025486},
   Key = {fds174286}
}

@booklet{Self04,
   Author = {J. T. Self and T. E. Spencer and G. A. Johnson and J. B. Hu and F. W. Bazer and G. Y. Wu},
   Title = {Glutamine synthesis in the developing porcine
             placental},
   Journal = {Biology Of Reproduction},
   Volume = {70},
   Number = {5},
   Pages = {1444 -- 1451},
   Year = {2004},
   Month = {May},
   Key = {Self04}
}

@article{fds174092,
   Author = {JJ Muniz and MM Joyce and JD Taylor 2nd, JR Burghardt and RC
             Burghardt, GA Johnson},
   Title = {Glycosylation dependent cell adhesion molecule 1-like
             protein and L-selectin expression in sheep interplacentomal
             and placentomal endometrium.},
   Journal = {Reproduction (Cambridge, England)},
   Volume = {131},
   Number = {4},
   Pages = {751-61},
   Year = {2006},
   Month = {April},
   ISSN = {1470-1626},
   url = {http://dx.doi.org/10.1530/rep.1.00855},
   Keywords = {Actins • Animals • Blotting, Western •
             Endometrium • Female • Fluorescent Antibody
             Technique • Keratins • L-Selectin • Mucins
             • Placenta • Pregnancy • Pregnancy, Animal
             • Sheep • analysis • analysis* •
             chemistry* • metabolism* • methods},
   Abstract = {Glycosylation dependent cell adhesion molecule 1 (GlyCAM-1),
             a mucin component of sheep histotroph produced by glandular
             epithelium (GE) during early pregnancy, is hypothesized to
             function in implantation. However, GlyCAM-1 is present in
             uterine tissues subsequent to implantation suggesting
             additional functions of this l-selectin-binding ligand. This
             study focused on uterine GlyCAM-1 expression during
             placentome development in sheep. Western blot analysis of
             day 50 pregnant sheep identified 45, 40, and 25 kDa bands in
             interplacentomal endometrium, 40 and 25 kDa bands in
             placentomes, and 80 and 40 kDa bands in chorioallantois. The
             GlyCAM-1 proteins in interplacentomal regions were
             comparable to those detected in day 15-19 pregnant sheep,
             however, the 80 kDa form was unique to chorioallantois, and
             the absence of the 45 kDa GlyCAM-1 in placentomes indicated
             differences between interplacentomal and placentomal
             endometrium. Immunofluorescence identified GlyCAM-1 in
             lumenal epithelium (LE), stromal fibroblasts, and vascular
             smooth muscle cells. To better define its cellular
             distribution, GlyCAM-1 was co-localized with either
             epithelium-specific cytokeratin, smooth muscle-specific
             alpha-smooth muscle actin (alpha SMA), or stromal-specific
             vimentin. In interplacentomal endometrium, GlyCAM-1
             co-localized with cytokeratin in LE but not in GE. GlyCAM-1
             did not co-localize with alpha SMA, and was localized in the
             extracellular matrix of vimentin-positive stroma. In
             placentomes, GlyCAM-1 did not co-localize with cytokeratin,
             but did co-localize with alpha SMA and vimentin. Thus, in
             contrast to interplacentomal regions, GlyCAM-1 in
             placentomes was predominantly localized in vasculature
             rather than epithelial cells. Further, leukocytes expressing
             L-selectin were localized to the endothelial surface of
             GlyCAM-1-expressing vessels within placentomes. These data
             suggest that GlyCAM-1 assumes distinct functions in
             compartment-specific regions of the sheep
             uterus.},
   Language = {eng},
   Doi = {10.1530/rep.1.00855},
   Key = {fds174092}
}

@booklet{Muniz04,
   Author = {J. J. Muniz and M. M. Joyce and R. C. Burghardt and G. A.
             Johnson},
   Title = {Glycosylation-dependent cell adhesion molecule 1 (GlyCAM-1)
             expression in ovine placentomes implies roles in
             hematotrophic support for conceptus development.},
   Journal = {Biology Of Reproduction},
   Pages = {212 -- 212},
   Year = {2004},
   Key = {Muniz04}
}

@article{fds268722,
   Author = {Johnston, SM and Johnson, GA and Badea, CT},
   Title = {GPU-based iterative reconstruction with total variation
             minimization for micro-CT},
   Journal = {Progress in Biomedical Optics and Imaging - Proceedings of
             SPIE},
   Volume = {7622},
   Number = {PART 2},
   Year = {2010},
   ISBN = {9780819480231},
   ISSN = {1605-7422},
   url = {http://dx.doi.org/10.1117/12.844368},
   Abstract = {Dynamic imaging with micro-CT often produces
             poorly-distributed sets of projections, and reconstructions
             of this data with filtered backprojection algorithms (FBP)
             may be affected by artifacts. Iterative reconstruction
             algorithms and total variation (TV) denoising are promising
             alternatives to FBP, but may require running times that are
             frustratingly long. This obstacle can be overcome by
             implementing reconstruction algorithms on graphics
             processing units (GPU). This paper presents an
             implementation of a family of iterative reconstruction
             algorithms with TV denoising on a GPU, and a series of tests
             to optimize and compare the ability of different algorithms
             to reduce artifacts. The mathematical and computational
             details of the implementation are explored. The performance,
             measured by the accuracy of the reconstruction versus the
             running time, is assessed in simulations with a virtual
             phantom and in an in vivo scan of a mouse. We conclude that
             the simultaneous algebraic reconstruction technique with TV
             minimization (SART-TV) is a time-effective reconstruction
             algorithm for producing reconstructions with fewer artifacts
             than FBP. © 2010 SPIE.},
   Doi = {10.1117/12.844368},
   Key = {fds268722}
}

@booklet{Teixeira96,
   Author = {M. G. Teixeira and K. J. Austin and D. J. Perry and V. D.
             Dooley and G. A. Johnson and T. R. Hansen},
   Title = {Granulocyte chemotactic protein-2 (GCP-2) is a
             pregnancy-associated uterine chemokine.},
   Journal = {Biology Of Reproduction},
   Volume = {54},
   Pages = {190 -- 190},
   Year = {1996},
   Key = {Teixeira96}
}

@booklet{Newton99,
   Author = {G. R. Newton and S. Woldesenbet and T. Green and H. Powell and K. Sonnier and G. A. Johnson},
   Title = {H antigen expression by ovine endometrial
             cells.},
   Journal = {Biology Of Reproduction},
   Volume = {60},
   Pages = {120 -- 120},
   Year = {1999},
   Key = {Newton99}
}

@article{fds132743,
   Author = {G.A. Johnson},
   Title = {H. Qiu, L.W. Hedlund, H. Benveniste, S.L. Gewalt, G.A.
             Johnson.   Evaluation of a glycine antagonist in rat focal
             cerebral ischemia by  diffusion-weighted MR microscopy.
              in "Proc., SMR 4th Annual Scientific  Meeting.  New
             York, NY, 1996," p. 505.},
   Year = {1996},
   Key = {fds132743}
}

@article{fds174164,
   Author = {AR Diani and MJ Mulholland and KL Shull and MF Kubicek and GA Johnson and HJ Schostarez and MN Brunden and AE Buhl},
   Title = {Hair growth effects of oral administration of finasteride, a
             steroid 5 alpha-reductase inhibitor, alone and in
             combination with topical minoxidil in the balding stumptail
             macaque.},
   Journal = {The Journal of clinical endocrinology and
             metabolism},
   Volume = {74},
   Number = {2},
   Pages = {345-50},
   Year = {1992},
   Month = {February},
   ISSN = {0021-972X},
   Keywords = {Administration, Oral • Administration, Topical •
             Androstenes • Animals • Azasteroids •
             Chromatography, High Pressure Liquid •
             Dihydrotestosterone • Drug Interactions •
             Finasteride • Hair • Macaca • Male •
             Minoxidil • Reference Values • Testosterone •
             Testosterone 5-alpha-Reductase • administration &
             dosage • antagonists & inhibitors* • blood •
             drug effects* • pharmacology* • physiology •
             urine},
   Abstract = {A 5 alpha-reductase inhibitor, finasteride, was administered
             orally at 0.5 mg/day, alone or in combination with topical
             2% minoxidil, for 20 weeks to determine the effects on scalp
             hair growth in balding adult male stumptail macaque monkeys.
             A 7-day dose-finding study showed that both 0.5- and 2.0-mg
             doses of the drug produced a similar diminution in serum
             dihydrotestosterone (DHT) in male stumptails. Hair growth
             was evaluated by shaving and weighing scalp hair at baseline
             and at 4-week intervals during treatment to obtain
             cumulative delta hair weight (sum of the 4-week changes in
             hair weight from baseline) for the 20-week study. The
             activity of the 5 alpha-reductase enzyme was assessed by RIA
             of serum testosterone (T) and DHT at 4-week intervals. The
             combination of finasteride and minoxidil generated
             significant augmentation of hair weight (additive effect)
             compared to either drug alone. Finasteride increased hair
             weight in four of five monkeys. When the data of the one
             nonresponsive monkey were excluded, finasteride elicited a
             significant elevation in hair weight compared to topical
             vehicle alone. Minoxidil also evoked a significant increase
             in hair weight compared to vehicle alone. Serum T was
             unchanged, whereas serum DHT was significantly depressed in
             monkeys that received either finasteride or the combination
             of finasteride and minoxidil. These data suggest that
             inhibition of the conversion of T to DHT by this 5
             alpha-reductase inhibitor reverses the balding process and
             enhances hair regrowth by topical minoxidil in the male
             balding stumptail macaque.},
   Language = {eng},
   Key = {fds174164}
}

@booklet{Diani92,
   Author = {A. R. Diani and M. J. Mulholland and K. L. Shull and M. F.
             Kubicek and G. A. Johnson and H. J. Schostarez and M. N.
             Brunden and A. E. Buhl},
   Title = {Hair-growth effects of oral-administration of finasteride, a
             steroid 5-alpha-reductase inhibitor, alone and in
             combination with topical minoxidil in the balding stumptail
             macaque},
   Journal = {Journal Of Clinical Endocrinology And Metabolism},
   Volume = {74},
   Number = {2},
   Pages = {345 -- 350},
   Year = {1992},
   Month = {February},
   Key = {Diani92}
}

@article{fds268693,
   Author = {Johnston, SM and Johnson, GA and Badea, CT},
   Title = {Helical dual source cone-beam micro-CT},
   Journal = {2014 IEEE 11th International Symposium on Biomedical
             Imaging, ISBI 2014},
   Pages = {177-180},
   Year = {2014},
   Month = {July},
   ISBN = {9781467319591},
   url = {http://dx.doi.org/10.1109/isbi.2014.6867838},
   Abstract = {While helical scanning is well established in the clinical
             arena, most micro-CT scanners use circular cone beam
             trajectories and approximate reconstructions based on a
             filtered backprojection (FBP) algorithm. This may be
             sufficient for some applications, but in studies of larger
             animals, such as rats, the size of the detector can
             constrain the field of view and extend scan time. To address
             this problem, we have designed and implemented helical
             scanning and reconstruction procedures for an
             in-house-developed dual source cone-beam micro-CT system.
             The reconstruction uses a simultaneous algebraic
             reconstruction technique combined with total variation
             regularization (SART-TV). We implemented this algorithm on a
             graphics processing unit (GPU) to reduce run time. The
             results demonstrate the speed and accuracy of the GPU-based
             SART-TV algorithm. The helical scan enables the
             reconstruction of volumes with extended field of view for
             whole body micro-CT imaging of large rodents.},
   Doi = {10.1109/isbi.2014.6867838},
   Key = {fds268693}
}

@article{fds174225,
   Author = {DG Johnston and GA Johnson and KG Alberti and GH Millward-Sadler and J
             Mitchell, R Wright},
   Title = {Hepatic regeneration and metabolism after partial
             hepatectomy in diabetic rats: effects of insulin
             therapy.},
   Journal = {European journal of clinical investigation},
   Volume = {16},
   Number = {5},
   Pages = {384-90},
   Year = {1986},
   Month = {October},
   ISSN = {0014-2972},
   Keywords = {Adenine Nucleotides • Animals • DNA •
             Diabetes Mellitus, Experimental • Glucose •
             Hepatectomy* • Insulin • Lactates • Lactic
             Acid • Liver • Liver Glycogen • Liver
             Regeneration • Male • Organ Size • Pyruvates
             • Pyruvic Acid • Rats • Rats, Inbred Strains
             • Water • analysis • biosynthesis •
             blood • drug effects* • drug therapy •
             metabolism • metabolism* • therapeutic
             use*},
   Abstract = {The effect of insulin deficiency on liver regeneration has
             been assessed in untreated v. insulin-treated streptozotocin
             (65 mg kg-1) diabetic rats, 12, 24 and 48 h after partial
             hepatectomy. Dry weight of regenerating liver increased from
             12 to 48 h after partial hepatectomy and insulin treatment
             caused a further minor increase at 24 h. [6-3H]Thymidine
             uptake in untreated rats peaked at 24 h (12.5 +/- 3.4% of
             total cells labelled). Insulin therapy produced a delayed
             168% rise in uptake at 48 h. Insulin deficiency alone in
             sham-operated animals caused a 33% decrease in hepatic
             [ATP], while [ADP] rose by 43% and [AMP] by 86% at 12 h.
             Partial hepatectomy produced only minor further
             abnormalities in untreated animals. Insulin therapy
             increased hepatic [ATP] and decreased [ADP] and [AMP] 12 h
             after partial hepatectomy, but [ATP] remained decreased
             (15%) and [ADP] and [AMP] increased (45% and 73%
             respectively) compared with insulin-treated sham-operated
             controls. Metabolite changes observed after partial
             hepatectomy in untreated animals, including a decrease in
             hepatic [glycogen] and increases in [triglyceride] and the
             ratios of [lactate]:[pyruvate] and [3-hydroxybutyrate]:[acetoacetate],
             were partially reversed by insulin treatment. Insulin
             deficiency thus impairs regeneration after partial
             hepatectomy and magnifies the decline in hepatic
             intracellular energy state and the metabolite changes
             associated with liver regrowth.},
   Language = {eng},
   Key = {fds174225}
}

@article{fds161595,
   Author = {DG Johnston and GA Johnson and KG Alberti and GH Millward-Sadler and J
             Mitchell, R Wright},
   Title = {Hepatic regeneration and metabolism after partial
             hepatectomy in normal rats: effects of insulin
             therapy.},
   Journal = {European journal of clinical investigation,
             ENGLAND},
   Volume = {16},
   Number = {5},
   Pages = {376-83},
   Year = {1986},
   Month = {October},
   ISSN = {0014-2972},
   Keywords = {Adenine Nucleotides • Animals • DNA • Glucose
             • Glycogen • Hepatectomy* • Insulin •
             Liver • Liver Regeneration • Male • Organ
             Size • Rats • Rats, Inbred Strains •
             Thymidine • Water • analysis • biosynthesis
             • cytology • drug effects* • metabolism
             • metabolism* • therapeutic use*},
   Abstract = {The effect of insulin therapy on liver regeneration has been
             studied in normal fed rats 12, 24 and 48 h after partial
             hepatectomy. Dry weight of regenerating liver increased
             between 12 and 48 h after partial hepatectomy and was
             unaffected by insulin therapy. [6-3H] Thymidine uptake
             peaked at 24-h (24.7 +/- 2.4% of total liver cells) and
             insulin treatment had no additional effect. At 12-h after
             partial hepatectomy, hepatic [ATP] was decreased 15%, while
             [ADP] and [AMP] were increased 47% and 83% respectively
             compared with sham-operated animals. Partial hepatectomy
             also caused an increase in hepatic [triglyceride], a
             decrease in hepatic [glycogen] and an increase in the levels
             of glucose and several glycolytic intermediates. The hepatic
             redox ratios, [lactate]:[pyruvate] and [3-hydroxybutyrate]:[acetoacetate],
             were elevated. Insulin therapy had only minor effects on
             hepatic adenine nucleotide levels, intermediary metabolite
             concentrations or intrahepatic redox ratios after partial
             hepatectomy. These findings suggest a decreased hepatic
             intracellular energy state in regenerating liver; insulin
             therapy in normal rats does not influence this metabolic
             change nor the regenerative response.},
   Key = {fds161595}
}

@booklet{Johnston86a,
   Author = {D. G. Johnston and G. A. Johnson and K. G. M. M. Alberti and G. H. Millwardsadler and J. Mitchell and R.
             Wright},
   Title = {Hepatic regeneration and metabolism after
             partial-hepatectomy in diabetic rats - effects of insulin
             therapy},
   Journal = {European Journal Of Clinical Investigation},
   Volume = {16},
   Number = {5},
   Pages = {384 -- 390},
   Year = {1986},
   Month = {October},
   Key = {Johnston86a}
}

@booklet{Johnston86,
   Author = {D. G. Johnston and G. A. Johnson and K. G. M. M. Alberti and G. H. Millwardsadler and J. Mitchell and R.
             Wright},
   Title = {Hepatic regeneration and metabolism after
             partial-hepatectomy in normal rats - effects of insulin
             therapy},
   Journal = {European Journal Of Clinical Investigation},
   Volume = {16},
   Number = {5},
   Pages = {376 -- 383},
   Year = {1986},
   Month = {October},
   Key = {Johnston86}
}

@article{fds174120,
   Author = {J Shen-Gunther and JL Walker and GA Johnson and RS
             Mannel},
   Title = {Hepatic venoocclusive disease as a complication of whole
             abdominopelvic irradiation and treatment with the
             transjuglar intrahepatic portosystemic shunt: case report
             and literature review.},
   Journal = {Gynecologic oncology},
   Volume = {61},
   Number = {2},
   Pages = {282-6},
   Year = {1996},
   Month = {May},
   ISSN = {0090-8258},
   Keywords = {Abdomen • Adenocarcinoma • Ascites •
             Endometrial Neoplasms • Female • Hepatic
             Veno-Occlusive Disease • Humans • Jugular Veins
             • Middle Aged • Pelvis • Portasystemic Shunt,
             Surgical* • Radiotherapy • Randomized Controlled
             Trials as Topic • Stents • adverse effects* •
             complications • etiology* • instrumentation •
             radiotherapy • surgery},
   Abstract = {We report the novel use of the transjugular intrahepatic
             portosystemic shunt (TIPS) procedure for the treatment of
             intractable ascites due to hepatic venooclusive disease as a
             result of whole abdominopelvic radiotherapy. A patient with
             Stage III endometrioid carcinoma of the endometrium treated
             with postoperative whole abdominopelvic irradiation
             developed intractable ascites. Multiple paracenteses and
             computerized tomography were negative for recurrent
             carcinoma. Liver biopsy demonstrated hepatic venoocclusive
             disease, a rare complication of therapeutic radiation
             involving the liver. Successful relief of ascites and its
             adverse symptomology were achieved with the transjugular
             intrahepatic portosystemic shunt. Relevant literature
             regarding the pathogenesis, prognosis, and treatment of
             radiotherapy-related hepatic venoocclusive disease are
             reviewed.},
   Language = {eng},
   Key = {fds174120}
}

@booklet{Shengunther96,
   Author = {J. Shengunther and J. L. Walker and G. A. Johnson and R. S.
             Mannel},
   Title = {Hepatic venoocclusive disease as a complication of whole
             abdominopelvic irradiation and treatment with the
             transjugular intrahepatic portosystemic shunt: Case report
             and literature review},
   Journal = {Gynecologic Oncology},
   Volume = {61},
   Number = {2},
   Pages = {282 -- 286},
   Year = {1996},
   Month = {May},
   Key = {Shengunther96}
}

@article{fds371720,
   Author = {Johnston, DG and Johnson, GA and Alberti, KG},
   Title = {Hepatotrophic factors: implications for diabetes
             mellitus.},
   Journal = {Ciba Found Symp},
   Number = {55},
   Pages = {357-373},
   Year = {1977},
   ISSN = {0300-5208},
   url = {http://dx.doi.org/10.1002/9780470720363.ch18},
   Keywords = {Adenine Nucleotides • Animals • Diabetes
             Complications • Diabetes Mellitus • Diabetes
             Mellitus, Experimental • Dogs • Fatty Liver •
             Glucose • Humans • Injections, Subcutaneous •
             Insulin • Liver • Liver Cirrhosis • Liver
             Glycogen • Liver Regeneration • Portal Vein •
             Rats • administration & dosage* • analysis •
             drug therapy* • etiology • metabolism},
   Abstract = {In view of the importance of insulin in hepatic cell
             proliferation and regeneration, disturbances might be
             expected in these processes in diabetics. The relative
             importnace of insulin replacement given intraportally rather
             than subcutaneously is discussed. Results are presented
             showing that even when normoglycaemia is achieved with
             peripheral insulin infusion using the 'artificial pancreas'
             there are still abnormalities in intermediary metabolism.
             The incidence of cirrhosis in diabetes is reviewed and it is
             concluded that the evidence is poor for an increase in
             diabetics. Finally it is shown that in the normal diabetic
             rat changes are observed after partial hepatectomy
             consistent with an increase in redox potential within the
             regenerating liver. Insulin treatment improves redox status
             but does not completely reverse the changes
             shown.},
   Language = {eng},
   Doi = {10.1002/9780470720363.ch18},
   Key = {fds371720}
}

@booklet{Johnson99,
   Author = {G. A. Johnson and N. M. Ghoniem},
   Title = {Hierarchical modeling of C and Si nano-cluster nucleation
             utilizing quantum and statistical mechanics},
   Journal = {Journal Of Computer-aided Materials Design},
   Volume = {6},
   Number = {2-3},
   Pages = {337 -- 347},
   Year = {1999},
   Key = {Johnson99}
}

@booklet{Thompson83a,
   Author = {W. M. Thompson and R. A. Halvorsen and R. K. Gedgaudas and F. M. Kelvin and R. P. Rice and S. Woodfield and G. A.
             Johnson and L. W. Hedlund and D. B. Jorgensen},
   Title = {High kvp vs low kvp for t-tube and operative
             cholangiography},
   Journal = {Radiology},
   Volume = {146},
   Number = {3},
   Pages = {635 -- 642},
   Year = {1983},
   Key = {Thompson83a}
}

@article{fds268910,
   Author = {Thompson, WM and Halvorsen, RA and Gedgaudas, RK and Kelvin, FM and Rice, RP and Woodfield, S and Johnson, GA and Hedlund, LW and Jorgensen,
             DB},
   Title = {High kVp vs. low kVp for T-tube and operative
             cholangiography.},
   Journal = {Radiology},
   Volume = {146},
   Number = {3},
   Pages = {635-642},
   Year = {1983},
   Month = {March},
   ISSN = {0033-8419},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/6828675},
   Keywords = {Cholangiography • Cholecystectomy • Cholelithiasis
             • Diatrizoate • Diatrizoate Meglumine •
             Humans • Intraoperative Care • Models, Structural
             • Radiation Dosage • analogs & derivatives* •
             diagnostic use* • methods* • radiography*},
   Abstract = {Based on several considerations, high kVp and high contrast
             agent concentration should produce better-quality operative
             and T-tube cholangiograms than the currently recommended low
             kVp and low contrast agent concentration. To test this
             theory, two kinds of studies were performed. In a laboratory
             phantom, the influence of kVp and contrast agent
             concentration on detectability of different size phantom
             stones was evaluated. High kVp and high contrast agent
             concentration (110 kVp, 38% iodine) were also compared with
             low kVp and low contrast agent concentration (75 kVp, 15%
             iodine) in 62 patients undergoing operative or T-tube
             cholangiography. Almost all phantom stones were well shown
             with all kVps and iodine concentrations. As the kVp was
             raised there was a mild decrease in stone detectability but
             this decrease was partially corrected by raising the iodine
             concentration. Overall stone detectability with high kVp and
             high contrast agent concentration technique was better than
             or similar to the currently recommended low kVp and low
             contrast agent concentration technique. Evaluation of the
             direct cholangiograms by five radiologists revealed that the
             high kVp, high contrast agent concentration studies were
             superior or similar to the low kVp and low contrast agent
             concentration radiographs in 70% of the cases. Based on
             these results high kVp (100-110) and a high contrast agent
             concentration (38%) are recommended for direct
             cholangiography.},
   Doi = {10.1148/radiology.146.3.6828675},
   Key = {fds268910}
}

@booklet{Silverman82b,
   Author = {Silverman, PM and Johnson, GA and Korobkin, M and Thompson,
             WM},
   Title = {HIGH RESOLUTION MULTIPLANAR CT IMAGES OF THE
             LARYNX},
   Journal = {Investigative Radiology},
   Volume = {17},
   Number = {4},
   Pages = {S34-S34},
   Publisher = {Ovid Technologies (Wolters Kluwer Health)},
   Year = {1982},
   Month = {July},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1982PA96700153&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Doi = {10.1097/00004424-198207000-00161},
   Key = {Silverman82b}
}

@article{fds268808,
   Author = {Liu, C and Li, W and Johnson, GA and Wu, B},
   Title = {High-field (9.4 T) MRI of brain dysmyelination by
             quantitative mapping of magnetic susceptibility.},
   Journal = {Neuroimage},
   Volume = {56},
   Number = {3},
   Pages = {930-938},
   Year = {2011},
   Month = {June},
   ISSN = {1095-9572},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/21320606},
   Keywords = {Algorithms • Animals • Anisotropy • Axons
             • Brain • Brain Mapping • Demyelinating
             Diseases • Diffusion Tensor Imaging • Echo-Planar
             Imaging • Electromagnetic Fields* • Fourier
             Analysis • Image Processing, Computer-Assisted •
             Mice • Mice, Inbred C3H • Mice, Neurologic Mutants
             • Myelin Sheath • Tissue Fixation • methods*
             • pathology • pathology* •
             physiology},
   Abstract = {The multilayered myelin sheath wrapping around nerve axons
             is essential for proper functioning of the central nervous
             system. Abnormal myelination leads to a wide range of
             neurological diseases and developmental disorders.
             Non-invasive imaging of myelin content is of great clinical
             importance. The present work demonstrated that loss of
             myelin in the central nervous system of the shiverer mouse
             results in a dramatic reduction of magnetic susceptibility
             in white matter axons. The reduction resulted in a near
             extinction of susceptibility contrast between gray and white
             matter. Quantitative magnetic susceptibility imaging and
             diffusion tensor imaging were conducted on a group of
             control and shiverer mice at 9.4 T. We measured the
             resonance frequency distribution of the whole brain for each
             mouse. Magnetic susceptibility maps were computed and
             compared between the two groups. It was shown that the
             susceptibility contrast between gray and white matter was
             reduced by 96% in the shiverer compared to the controls.
             Diffusion measurements further confirmed intact fiber
             pathways in the shiverer mice, ruling out the possibility of
             axonal injury and its potential contribution to the altered
             susceptibility. As an autosomal recessive mutation, shiverer
             is characterized by an almost total lack of central nervous
             system myelin. Our data provide new evidences indicating
             that myelin is the predominant source of susceptibility
             differences between deep gray and white matter observed in
             magnetic resonance imaging. More importantly, the present
             study suggests that quantitative magnetic susceptibility is
             a potential endogenous biomarker for myelination.},
   Language = {eng},
   Doi = {10.1016/j.neuroimage.2011.02.024},
   Key = {fds268808}
}

@article{fds132762,
   Author = {X Zhou and GP Cofer and SA Suddarth and GA Johnson},
   Title = {High-field MR microscopy using fast spin-echoes.},
   Journal = {Magnetic resonance in medicine : official journal of the
             Society of Magnetic Resonance in Medicine / Society of
             Magnetic Resonance in Medicine, UNITED STATES},
   Volume = {30},
   Number = {1},
   Pages = {60-7},
   Year = {1993},
   Month = {July},
   ISSN = {0740-3194},
   Keywords = {Animals • Brain • Brain Neoplasms • Cerebral
             Cortex • Corpus Callosum • Humans • Image
             Enhancement • Image Processing, Computer-Assisted
             • Magnetic Resonance Imaging* • Melanoma •
             Microscopy* • Models, Structural • Rats •
             anatomy & histology • methods •
             pathology},
   Abstract = {Fast spin-echo imaging has been investigated with attention
             to the requirements and opportunities for high-field MR
             microscopy. Two- and three-dimensional versions were
             implemented at 2.0 T, 7.1 T, and 9.4 T. At these fields, at
             least eight echoes were collectable with a 10 ms TE from
             fixed tissue specimens and living animals, giving an
             eightfold improvement in imaging efficiency. To reduce the
             phase-encoding gradient amplitude and its duty cycle, a
             modified pulse sequence with phase accumulation was
             developed. Images obtained using this pulse sequence
             exhibited comparable signal-to-noise (SNR) to those obtained
             from the conventional fast spin-echo pulse sequences. Signal
             losses due to imperfections in RF pulses and lack of phase
             rewinders were offset in this sequence by reduced diffusion
             losses incurred with the gradients required for MR
             microscopy. Image SNR, contrast, edge effects and spatial
             resolution for three k-space sampling schemes were studied
             experimentally and theoretically. One method of sampling
             k-space, 4-GROUP FSE, was found particularly useful in
             producing varied T2 contrast at high field. Two-dimensional
             images of tissue specimens were obtained in a total
             acquisition time of 1 to 2 min with in-plane resolution
             between 30 to 70 microns, and 3D images with 256(3) arrays
             were acquired from fixed rat brain tissue (isotropic voxel =
             70 microns) and a living rat (isotropic voxel = 117 microns)
             in approximately 4.5 h.},
   Key = {fds132762}
}

@booklet{Zhou93a,
   Author = {Zhou, X and Cofer, GP and Suddarth, SA and Johnson,
             GA},
   Title = {High-field MR microscopy using fast spin-echoes.},
   Journal = {Magn Reson Med},
   Volume = {30},
   Number = {1},
   Pages = {60-67},
   Year = {1993},
   Month = {July},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/8371676},
   Abstract = {Fast spin-echo imaging has been investigated with attention
             to the requirements and opportunities for high-field MR
             microscopy. Two- and three-dimensional versions were
             implemented at 2.0 T, 7.1 T, and 9.4 T. At these fields, at
             least eight echoes were collectable with a 10 ms TE from
             fixed tissue specimens and living animals, giving an
             eightfold improvement in imaging efficiency. To reduce the
             phase-encoding gradient amplitude and its duty cycle, a
             modified pulse sequence with phase accumulation was
             developed. Images obtained using this pulse sequence
             exhibited comparable signal-to-noise (SNR) to those obtained
             from the conventional fast spin-echo pulse sequences. Signal
             losses due to imperfections in RF pulses and lack of phase
             rewinders were offset in this sequence by reduced diffusion
             losses incurred with the gradients required for MR
             microscopy. Image SNR, contrast, edge effects and spatial
             resolution for three k-space sampling schemes were studied
             experimentally and theoretically. One method of sampling
             k-space, 4-GROUP FSE, was found particularly useful in
             producing varied T2 contrast at high field. Two-dimensional
             images of tissue specimens were obtained in a total
             acquisition time of 1 to 2 min with in-plane resolution
             between 30 to 70 microns, and 3D images with 256(3) arrays
             were acquired from fixed rat brain tissue (isotropic voxel =
             70 microns) and a living rat (isotropic voxel = 117 microns)
             in approximately 4.5 h.},
   Doi = {10.1002/mrm.1910300110},
   Key = {Zhou93a}
}

@booklet{Drayer84,
   Author = {DRAYER, BP and HERFKENS, RJ and JOHNSON, GA and HEINZ, ER and YEATES,
             AE},
   Title = {HIGH-FIELD NMR IMAGING (1.5T) IN A HOSPITAL
             ENVIRONMENT},
   Journal = {AMERICAN JOURNAL OF NEURORADIOLOGY},
   Volume = {5},
   Number = {5},
   Pages = {669-669},
   Year = {1984},
   ISSN = {0195-6108},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1984TG20900058&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Drayer84}
}

@article{fds268875,
   Author = {Nahrendorf, M and Badea, C and Hedlund, LW and Figueiredo, J-L and Sosnovik, DE and Johnson, GA and Weissleder, R},
   Title = {High-resolution imaging of murine myocardial infarction with
             delayed-enhancement cine micro-CT.},
   Journal = {Am J Physiol Heart Circ Physiol},
   Volume = {292},
   Number = {6},
   Pages = {H3172-H3178},
   Year = {2007},
   Month = {June},
   ISSN = {0363-6135},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/17322414},
   Keywords = {Animals • Cineradiography • Contrast Media •
             Coronary Vessels • Disease Models, Animal •
             Feasibility Studies • Female • Iopamidol •
             Ligation • Mice • Mice, Inbred C57BL •
             Myocardial Infarction • Radiographic Image
             Interpretation, Computer-Assisted* • Reproducibility of
             Results • Time Factors • Tomography, X-Ray
             Computed* • Ventricular Function, Left •
             Ventricular Remodeling • diagnostic use • methods*
             • physiopathology • radiography* •
             surgery},
   Abstract = {The objective of this study was to determine the feasibility
             of delayed-enhancement micro-computed tomography (microCT)
             imaging to quantify myocardial infarct size in experimental
             mouse models. A total of 20 mice were imaged 5 or 35 days
             after surgical ligation of the left coronary artery or sham
             surgery (n=6 or 7 per group). We utilized a prototype
             microCT that covers a three-dimensional (3D) volume with an
             isotropic spatial resolution of 100 microm. A series of
             image acquisitions were started after a 200 microl bolus of
             a high-molecular-weight blood pool CT agent to outline the
             ventricles. CT imaging was continuously performed over 60
             min, while an intravenous constant infusion with iopamidol
             370 was started at a dosage of 1 ml/h. Thirty minutes after
             the initiation of this infusion, signal intensity in
             Hounsfield units was significantly higher in the infarct
             than in the remote, uninjured myocardium. Cardiac morphology
             and motion were visualized with excellent contrast and in
             fine detail. In vivo CT determination of infarct size at the
             midventricular level was in good agreement with ex vivo
             staining with triphenyltetrazolium chloride [5 days
             post-myocardial infarction (MI): r(2)=0.86, P<0.01; 35 days
             post-MI: r(2)=0.92, P<0.01]. In addition, we detected
             significant left ventricular remodeling consisting of left
             ventricular dilation and decreased ejection fraction. 3D
             cine microCT reliably and rapidly quantifies infarct size
             and assesses murine anatomy and physiology after coronary
             ligation, despite the small size and fast movement of the
             mouse heart. This efficient imaging tool is a valuable
             addition to the current phenotyping armamentarium and will
             allow rapid testing of novel drugs and cell-based
             interventions in murine models.},
   Doi = {10.1152/ajpheart.01307.2006},
   Key = {fds268875}
}

@article{fds268832,
   Author = {Howles, GP and Ghaghada, KB and Qi, Y and Mukundan, S and Johnson,
             GA},
   Title = {High-resolution magnetic resonance angiography in the mouse
             using a nanoparticle blood-pool contrast
             agent.},
   Journal = {Magn Reson Med},
   Volume = {62},
   Number = {6},
   Pages = {1447-1456},
   Year = {2009},
   Month = {December},
   ISSN = {1522-2594},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/19902507},
   Keywords = {Animals • Cerebral Arteries • Contrast Media
             • Gadolinium • Image Enhancement • Liposomes
             • Magnetic Resonance Angiography • Male •
             Mice • Mice, Inbred C57BL • Nanoparticles •
             anatomy & histology* • chemistry • chemistry*
             • diagnostic use* • methods*},
   Abstract = {High-resolution magnetic resonance angiography is already a
             useful tool for studying mouse models of human disease.
             Magnetic resonance angiography in the mouse is typically
             performed using time-of-flight contrast. In this work, a new
             long-circulating blood-pool contrast agent-a liposomal
             nanoparticle with surface-conjugated gadolinium (SC-Gd
             liposomes)-was evaluated for use in mouse neurovascular
             magnetic resonance angiography. A total of 12 mice were
             imaged. Scan parameters were optimized for both
             time-of-flight and SC-Gd contrast. Compared to
             time-of-flight contrast, SC-Gd liposomes (0.08 mmol/kg)
             enabled improved small-vessel contrast-to-noise ratio,
             larger field of view, shorter scan time, and imaging of
             venous structures. For a limited field of view,
             time-of-flight and SC-Gd were not significantly different;
             however, SC-Gd provided better contrast-to-noise ratio when
             the field of view encompassed the whole brain (P < 0.001) or
             the whole neurovascular axis (P < 0.001). SC-Gd allowed
             acquisition of high-resolution magnetic resonance
             angiography (52 x 52 x 100 micrometer(3) or 0.27 nL), with
             123% higher (P < 0.001) contrast-to-noise ratio in
             comparable scan time ( approximately 45 min). Alternatively,
             SC-Gd liposomes could be used to acquire high-resolution
             magnetic resonance angiography (0.27 nL) with 32% higher
             contrast-to-noise ratio (P < 0.001) in 75% shorter scan time
             (12 min).},
   Language = {eng},
   Doi = {10.1002/mrm.22154},
   Key = {fds268832}
}

@article{fds268873,
   Author = {Petiet, AE and Kaufman, MH and Goddeeris, MM and Brandenburg, J and Elmore, SA and Johnson, GA},
   Title = {High-resolution magnetic resonance histology of the
             embryonic and neonatal mouse: a 4D atlas and morphologic
             database.},
   Journal = {Proc Natl Acad Sci U S A},
   Volume = {105},
   Number = {34},
   Pages = {12331-12336},
   Year = {2008},
   Month = {August},
   ISSN = {1091-6490},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/18713865},
   Keywords = {Anatomy, Cross-Sectional • Animals • Animals,
             Newborn • Databases, Factual • Embryo, Mammalian
             • Embryonic Development* • Heart Septal Defects
             • Imaging, Three-Dimensional • Magnetic Resonance
             Imaging • Mice • Mice, Mutant Strains • Mice,
             Transgenic • Microscopy • Time Factors •
             anatomy & histology* • instrumentation •
             methods*},
   Abstract = {Engineered mice play an ever-increasing role in defining
             connections between genotype and phenotypic expression. The
             potential of magnetic resonance microscopy (MRM) for
             morphologic phenotyping in the mouse has previously been
             demonstrated; however, applications have been limited by
             long scan times, availability of the technology, and a
             foundation of normative data. This article describes an
             integrated environment for high-resolution study of normal,
             transgenic, and mutant mouse models at embryonic and
             neonatal stages. Three-dimensional images are shown at an
             isotropic resolution of 19.5 microm (voxel volumes of 8 pL),
             acquired in 3 h at embryonic days 10.5-19.5 (10 stages) and
             postnatal days 0-32 (6 stages). A web-accessible atlas
             encompassing this data was developed, and for critical
             stages of embryonic development (prenatal days 14.5-18.5),
             >200 anatomical structures have been identified and labeled.
             Also, matching optical histology and analysis tools are
             provided to compare multiple specimens at multiple
             developmental stages. The utility of the approach is
             demonstrated in characterizing cardiac septal defects in
             conditional mutant embryos lacking the Smoothened receptor
             gene. Finally, a collaborative paradigm is presented that
             allows sharing of data across the scientific community. This
             work makes magnetic resonance microscopy of the mouse embryo
             and neonate broadly available with carefully annotated
             normative data and an extensive environment for
             collaborations.},
   Doi = {10.1073/pnas.0805747105},
   Key = {fds268873}
}

@booklet{Blinder85a,
   Author = {BLINDER, RA and HERFKENS, RJ and COLEMAN, RE and JOHNSON, GA and SCHENCK, JF and HART, HR and FOSTER, TH and EDELSTEIN,
             WA},
   Title = {HIGH-RESOLUTION MRI IMAGING AT 1.5T USING SURFACE
             COILS},
   Journal = {JOURNAL OF NUCLEAR MEDICINE},
   Volume = {26},
   Number = {5},
   Pages = {P8-P8},
   Year = {1985},
   ISSN = {0161-5505},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1985AGS2100042&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Blinder85a}
}

@booklet{Silverman82,
   Author = {Silverman, PM and Johnson, GA and Korobkin, M and Thompson,
             WM},
   Title = {High-resolution multiplanar CT images of the
             larynx.},
   Journal = {Invest Radiol},
   Volume = {17},
   Number = {6},
   Pages = {634-637},
   Year = {1982},
   ISSN = {0020-9996},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/7152866},
   Abstract = {The standard technique for computed tomographic evaluation
             of the larynx utilizes 5-mm contiguous transaxial sections.
             Multiplanar images reformatted with these sections have not
             been of clinical use. We have evaluated the practicality of
             utilizing coronal and sagittal reformatted images produced
             from contiguous 1.5-mm transaxial sections. The technique of
             rapid sequential scanning with automatic table
             incrementation allows 36 contiguous thin section scans to be
             acquired in less than 9 minutes. Phantom studies showed a
             marked improvement in spatial resolution with thin section
             reconstructions. Preliminary clinical evaluation shows
             visualization of smaller structures with improved edge
             definition of both low- and high-contrast
             structures.},
   Doi = {10.1097/00004424-198211000-00019},
   Key = {Silverman82}
}

@article{fds132770,
   Author = {PM Silverman and GA Johnson and M Korobkin and WM
             Thompson},
   Title = {High-resolution multiplanar CT images of the
             larynx.},
   Journal = {Investigative radiology, UNITED STATES},
   Volume = {17},
   Number = {6},
   Pages = {634-7},
   ISSN = {0020-9996},
   Keywords = {Humans • Larynx • Models, Structural •
             Tomography, X-Ray Computed • methods* •
             radiography*},
   Abstract = {The standard technique for computed tomographic evaluation
             of the larynx utilizes 5-mm contiguous transaxial sections.
             Multiplanar images reformatted with these sections have not
             been of clinical use. We have evaluated the practicality of
             utilizing coronal and sagittal reformatted images produced
             from contiguous 1.5-mm transaxial sections. The technique of
             rapid sequential scanning with automatic table
             incrementation allows 36 contiguous thin section scans to be
             acquired in less than 9 minutes. Phantom studies showed a
             marked improvement in spatial resolution with thin section
             reconstructions. Preliminary clinical evaluation shows
             visualization of smaller structures with improved edge
             definition of both low- and high-contrast
             structures.},
   Key = {fds132770}
}

@article{fds268733,
   Author = {O'Leary-Moore, SK and Budin, F and Paniagua, B and Oguz, I and Johnson,
             GA and Sulik, KK},
   Title = {HIGH-RESOLUTION NEUROIMAGING REVEALS A RANGE OF CORPUS
             CALLOSUM INSULT INDUCED BY ETHANOL ON GESTATIONAL DAY 7
             INMICE},
   Journal = {ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH},
   Volume = {37},
   Pages = {167A-167A},
   Year = {2013},
   ISSN = {0145-6008},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000318998300625&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {fds268733}
}

@article{fds268813,
   Author = {Zhang, X and Badea, C and Hood, G and Wetzel, A and Qi, Y and Stiles, J and Johnson, GA},
   Title = {High-resolution reconstruction of fluorescent inclusions in
             mouse thorax using anatomically guided sampling and parallel
             Monte Carlo computing.},
   Journal = {Biomed Opt Express},
   Volume = {2},
   Number = {9},
   Pages = {2449-2460},
   Year = {2011},
   Month = {September},
   ISSN = {2156-7085},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/21991539},
   Abstract = {We present a method for high-resolution reconstruction of
             fluorescent images of the mouse thorax. It features an
             anatomically guided sampling method to retrospectively
             eliminate problematic data and a parallel Monte Carlo
             software package to compute the Jacobian matrix for the
             inverse problem. The proposed method was capable of
             resolving microliter-sized femtomole amount of quantum dot
             inclusions closely located in the middle of the mouse
             thorax. The reconstruction was verified against
             co-registered micro-CT data. Using the proposed method, the
             new system achieved significantly higher resolution and
             sensitivity compared to our previous system consisting of
             the same hardware. This method can be applied to any system
             utilizing similar imaging principles to improve imaging
             performance.},
   Language = {eng},
   Doi = {10.1364/BOE.2.002449},
   Key = {fds268813}
}

@article{fds132867,
   Author = {PM Silverman and GA Johnson and M Korobkin},
   Title = {High-resolution sagittal and coronal reformatted CT images
             of the larynx.},
   Journal = {AJR. American journal of roentgenology, UNITED
             STATES},
   Volume = {140},
   Number = {4},
   Pages = {819-22},
   Year = {1983},
   Month = {April},
   ISSN = {0361-803X},
   Keywords = {Computers • Humans • Laryngeal Neoplasms •
             Larynx • Time Factors • Tomography, X-Ray Computed
             • methods* • radiography* •
             radiotherapy},
   Key = {fds132867}
}

@booklet{Silverman83,
   Author = {Silverman, PM and Johnson, GA and Korobkin, M},
   Title = {High-resolution sagittal and coronal reformatted CT images
             of the larynx.},
   Journal = {AJR Am J Roentgenol},
   Volume = {140},
   Number = {4},
   Pages = {819-822},
   Year = {1983},
   Month = {April},
   ISSN = {0361-803X},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/6601398},
   Doi = {10.2214/ajr.140.4.819},
   Key = {Silverman83}
}

@article{fds268859,
   Author = {Johnson, GA and Ali-Sharief, A and Badea, A and Brandenburg, J and Cofer, G and Fubara, B and Gewalt, S and Hedlund, LW and Upchurch,
             L},
   Title = {High-throughput morphologic phenotyping of the mouse brain
             with magnetic resonance histology.},
   Journal = {Neuroimage},
   Volume = {37},
   Number = {1},
   Pages = {82-89},
   Year = {2007},
   Month = {August},
   ISSN = {1053-8119},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/17574443},
   Keywords = {Animals • Brain • Databases as Topic •
             Dominance, Cerebral • Image Enhancement • Image
             Processing, Computer-Assisted • Imaging,
             Three-Dimensional • Magnetic Resonance Imaging •
             Mice • Mice, Inbred C57BL • Phenotype* •
             Sensitivity and Specificity • Software* • anatomy
             & histology* • methods* • physiology},
   Abstract = {The Mouse Biomedical Informatics Research Network (MBIRN)
             has been established to integrate imaging studies of the
             mouse brain ranging from three-dimensional (3D) studies of
             the whole brain to focused regions at a sub-cellular scale.
             Magnetic resonance (MR) histology provides the entry point
             for many morphologic comparisons of the whole brain. We
             describe a standardized protocol that allows acquisition of
             3D MR histology (43-microm resolution) images of the fixed,
             stained mouse brain with acquisition times <30 min. A higher
             resolution protocol with isotropic spatial resolution of
             21.5 microm can be executed in 2 h. A third acquisition
             protocol provides an alternative image contrast (at
             43-microm isotropic resolution), which is exploited in a
             statistically driven algorithm that segments 33 of the most
             critical structures in the brain. The entire process, from
             specimen perfusion, fixation and staining, image acquisition
             and reconstruction, post-processing, segmentation,
             archiving, and analysis, is integrated through a structured
             workflow. This yields a searchable database for archive and
             query of the very large (1.2 GB) images acquired with this
             standardized protocol. These methods have been applied to a
             collection of both male and female adult murine brains
             ranging over 4 strains and 6 neurologic knockout models.
             These collection and acquisition methods are now available
             to the neuroscience community as a standard web-deliverable
             service.},
   Doi = {10.1016/j.neuroimage.2007.05.013},
   Key = {fds268859}
}

@article{fds132872,
   Author = {HP McAdams and GA Johnson and SA Suddarth and CE Ravin},
   Title = {Histogram-directed processing of digital chest
             images.},
   Journal = {Investigative radiology, UNITED STATES},
   Volume = {21},
   Number = {3},
   Pages = {253-9},
   Year = {1986},
   Month = {March},
   ISSN = {0020-9996},
   Keywords = {Computers • Humans • Lasers • Lung •
             Mediastinum • Radiographic Image Enhancement •
             Radiography, Thoracic • methods* •
             radiography},
   Abstract = {One of the potential advantages of digital chest imaging is
             the ability to process these images. However, such
             processing, when uniformly applied to the entire image, is
             often unsatisfactory due to the different processing
             requirements of lung field and mediastinum. Therefore, a
             method to selectively process these regions based upon the
             histogram of the original image has been developed. Thirteen
             conventional chest films were digitized with a laser film
             scanner. Analysis of individual lung field and mediastinum
             histograms showed that the chest image histogram is
             essentially bimodal with significant lung field-mediastinum
             histogram peak separation; overlap between these peaks is
             small (9% of the total histogram) and insensitive to minor
             pathologic change or radiographic technique. Using these
             histograms, a gray level threshold distinguishing
             mediastinum from lung field was selected and used to direct
             the regionally-selective processing of several chest images.
             This technique may prove especially useful for digital
             enhancement of the underexposed mediastinum often
             encountered on conventional chest radiographs.},
   Key = {fds132872}
}

@booklet{Mcadams86,
   Author = {McAdams, HP and Johnson, GA and Suddarth, SA and Ravin,
             CE},
   Title = {Histogram-directed processing of digital chest
             images.},
   Journal = {Invest Radiol},
   Volume = {21},
   Number = {3},
   Pages = {253-259},
   Year = {1986},
   Month = {March},
   ISSN = {0020-9996},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/3957599},
   Abstract = {One of the potential advantages of digital chest imaging is
             the ability to process these images. However, such
             processing, when uniformly applied to the entire image, is
             often unsatisfactory due to the different processing
             requirements of lung field and mediastinum. Therefore, a
             method to selectively process these regions based upon the
             histogram of the original image has been developed. Thirteen
             conventional chest films were digitized with a laser film
             scanner. Analysis of individual lung field and mediastinum
             histograms showed that the chest image histogram is
             essentially bimodal with significant lung field-mediastinum
             histogram peak separation; overlap between these peaks is
             small (9% of the total histogram) and insensitive to minor
             pathologic change or radiographic technique. Using these
             histograms, a gray level threshold distinguishing
             mediastinum from lung field was selected and used to direct
             the regionally-selective processing of several chest images.
             This technique may prove especially useful for digital
             enhancement of the underexposed mediastinum often
             encountered on conventional chest radiographs.},
   Doi = {10.1097/00004424-198603000-00011},
   Key = {Mcadams86}
}

@article{fds132878,
   Author = {GA Johnson and H Benveniste and RD Black and LW Hedlund and RR Maronpot and BR Smith},
   Title = {Histology by magnetic resonance microscopy.},
   Journal = {Magnetic resonance quarterly, UNITED STATES},
   Volume = {9},
   Number = {1},
   Pages = {1-30},
   Year = {1993},
   Month = {March},
   ISSN = {0899-9422},
   Keywords = {Animals • Histological Techniques • Histology*
             • Image Enhancement • Magnetic Resonance Imaging
             • Microscopy • Tissue Fixation •
             instrumentation • methods*},
   Abstract = {Magnetic resonance microscopy (MRM) has advanced from a
             technical challenge to a practical tool in a wide range of
             basic sciences. This article focuses on the use of MRM as a
             tool for histological studies. The technical challenges of
             limited signal to noise have been overcome by improved
             radio-frequency (rf) coil design and 3DFT encoding with
             large arrays. Resolution limits imposed by motion in in vivo
             studies have been overcome by improved physiologic
             monitoring and control and projection encoding. Integration
             of technologies now permits routine studies in vivo down to
             50 microns. MRM has also been applied to in vitro studies of
             fixed tissues where absence of motion allows studies down to
             10 microns. The nondestructive nature of the technique
             allows repeated studies of the same sample, retrospective
             studies through any arbitrary plane, registered studies
             using different contrast mechanisms, and examination of
             valuable specimens. The many and unique proton contrasts
             provided by MRM, i.e., T1, T2, and diffusion weighting,
             permit direct examination of the state of water in tissues,
             something not possible with other microscopic techniques.
             Finally, the inherent three-dimensional nature of MRM allows
             acquisition of perfectly registered isotropic 3D arrays
             that, when displayed with appropriate visualization tools,
             provide new perspectives to histologic examination. The
             technology of MRM continues to develop rapidly. New pulse
             sequences are reducing acquisition times. New computer
             architectures allow larger arrays. A new class of
             superconducting rf probe has increased the signal to noise
             ratio by 10 times. These developments promise routine use of
             MRM in histology studies with resolution to 1 micron in the
             near future.},
   Key = {fds132878}
}

@booklet{Johnson93,
   Author = {Johnson, GA and Benveniste, H and Black, RD and Hedlund, LW and Maronpot, RR and Smith, BR},
   Title = {Histology by magnetic resonance microscopy.},
   Journal = {Magn Reson Q},
   Volume = {9},
   Number = {1},
   Pages = {1-30},
   Year = {1993},
   Month = {March},
   ISSN = {0899-9422},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/8512830},
   Abstract = {Magnetic resonance microscopy (MRM) has advanced from a
             technical challenge to a practical tool in a wide range of
             basic sciences. This article focuses on the use of MRM as a
             tool for histological studies. The technical challenges of
             limited signal to noise have been overcome by improved
             radio-frequency (rf) coil design and 3DFT encoding with
             large arrays. Resolution limits imposed by motion in in vivo
             studies have been overcome by improved physiologic
             monitoring and control and projection encoding. Integration
             of technologies now permits routine studies in vivo down to
             50 microns. MRM has also been applied to in vitro studies of
             fixed tissues where absence of motion allows studies down to
             10 microns. The nondestructive nature of the technique
             allows repeated studies of the same sample, retrospective
             studies through any arbitrary plane, registered studies
             using different contrast mechanisms, and examination of
             valuable specimens. The many and unique proton contrasts
             provided by MRM, i.e., T1, T2, and diffusion weighting,
             permit direct examination of the state of water in tissues,
             something not possible with other microscopic techniques.
             Finally, the inherent three-dimensional nature of MRM allows
             acquisition of perfectly registered isotropic 3D arrays
             that, when displayed with appropriate visualization tools,
             provide new perspectives to histologic examination. The
             technology of MRM continues to develop rapidly. New pulse
             sequences are reducing acquisition times. New computer
             architectures allow larger arrays. A new class of
             superconducting rf probe has increased the signal to noise
             ratio by 10 times. These developments promise routine use of
             MRM in histology studies with resolution to 1 micron in the
             near future.},
   Key = {Johnson93}
}

@booklet{Green80,
   Author = {D. J. Green and G. A. Johnson and S. T. Hutchison},
   Title = {Hot-pressing sodium beta-alumina using solution spray-dried
             and freeze-dried powders},
   Journal = {Journal Of The Canadian Ceramic Society},
   Volume = {49},
   Pages = {7 -- 12},
   Year = {1980},
   Key = {Green80}
}

@article{fds174078,
   Author = {GA Johnson and PA Van Pernis},
   Title = {How pathology kept pace with expansion.},
   Journal = {Modern hospital},
   Volume = {105},
   Number = {5},
   Pages = {105-7},
   Year = {1965},
   Month = {November},
   ISSN = {0026-783X},
   Keywords = {Hospital Design and Construction* • Humans •
             Illinois • Laboratories* • Pathology*},
   Language = {eng},
   Key = {fds174078}
}

@article{fds132793,
   Author = {JR MacFall and HC Charles and RD Black and H Middleton and JC Swartz and B
             Saam, B Driehuys and C Erickson and W Happer and GD Cates and GA
             Johnson, CE Ravin},
   Title = {Human lung air spaces: potential for MR imaging with
             hyperpolarized He-3.},
   Journal = {Radiology, UNITED STATES},
   Volume = {200},
   Number = {2},
   Pages = {553-8},
   Year = {1996},
   Month = {August},
   ISSN = {0033-8419},
   Keywords = {Adult • Helium • Humans • Image Enhancement
             • Isotopes • Lung • Magnetic Resonance
             Imaging • Male • Middle Aged • anatomy &
             histology* • diagnostic use* • instrumentation
             • methods • methods*},
   Abstract = {Two healthy volunteers who had inhaled approximately 0.75 L
             of laser-polarized helium-3 gas underwent magnetic resonance
             imaging at 1.5 T with fast gradient-echo pulse sequences and
             small flip angles ( < 10 degrees). Thick-section (20 mm)
             coronal images, time-course data (30 images collected every
             1.8 seconds), and thin-section (6 mm) images were acquired.
             Subjects were able to breathe the gas (12% polarization)
             without difficulty. Thick-section images were of good
             quality and had a signal-to-noise ratio (S/N) of 32:1 near
             the surface coil and 16:1 farther away. The time images
             showed regional differences, which indicated potential value
             for quantitation. High-resolution images showed greater
             detail and a S/N of approximately 6:1.},
   Key = {fds132793}
}

@booklet{Macfall96,
   Author = {MacFall, JR and Charles, HC and Black, RD and Middleton, H and Swartz,
             JC and Saam, B and Driehuys, B and Erickson, C and Happer, W and Cates, GD and Johnson, GA and Ravin, CE},
   Title = {Human lung air spaces: potential for MR imaging with
             hyperpolarized He-3.},
   Journal = {Radiology},
   Volume = {200},
   Number = {2},
   Pages = {553-558},
   Year = {1996},
   Month = {August},
   ISSN = {0033-8419},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/8685356},
   Abstract = {Two healthy volunteers who had inhaled approximately 0.75 L
             of laser-polarized helium-3 gas underwent magnetic resonance
             imaging at 1.5 T with fast gradient-echo pulse sequences and
             small flip angles ( < 10 degrees). Thick-section (20 mm)
             coronal images, time-course data (30 images collected every
             1.8 seconds), and thin-section (6 mm) images were acquired.
             Subjects were able to breathe the gas (12% polarization)
             without difficulty. Thick-section images were of good
             quality and had a signal-to-noise ratio (S/N) of 32:1 near
             the surface coil and 16:1 farther away. The time images
             showed regional differences, which indicated potential value
             for quantitation. High-resolution images showed greater
             detail and a S/N of approximately 6:1.},
   Doi = {10.1148/radiology.200.2.8685356},
   Key = {Macfall96}
}

@booklet{Kudlacek95,
   Author = {P. E. Kudlacek and R. J. Anderson and D. K. Liebentritt and G. A. Johnson and C. J. Huerter},
   Title = {Human skin and platelet minoxidil sulfotransferase
             activities - biochemical-properties, correlations and
             contribution of thermolabile phenol sulfotransferase},
   Journal = {Journal Of Pharmacology And Experimental
             Therapeutics},
   Volume = {273},
   Number = {2},
   Pages = {582 -- 590},
   Year = {1995},
   Month = {May},
   Key = {Kudlacek95}
}

@article{fds174118,
   Author = {PE Kudlacek and RJ Anderson and DK Liebentritt and GA Johnson and CJ
             Huerter},
   Title = {Human skin and platelet minoxidil sulfotransferase
             activities: biochemical properties, correlations and
             contribution of thermolabile phenol sulfotransferase.},
   Journal = {The Journal of pharmacology and experimental
             therapeutics},
   Volume = {273},
   Number = {2},
   Pages = {582-90},
   Year = {1995},
   Month = {May},
   ISSN = {0022-3565},
   Keywords = {Arylsulfotransferase • Blood Platelets •
             Chromatography, High Pressure Liquid • Chromatography,
             Ion Exchange • Enzyme Stability • Humans •
             Minoxidil • Nitrophenols • Skin • Sodium
             Chloride • Substrate Specificity •
             Sulfotransferases • Temperature • antagonists &
             inhibitors • enzymology* • isolation &
             purification • metabolism* • pharmacology},
   Abstract = {Human scalp skin high speed supernatants were used to test
             whether minoxidil sulfotransferase (MNX-ST) and phenol
             sulfotransferase (PST) activities were present. Platelet
             homogenates from the same skin donors were used to test
             whether levels of sulfotransferase activities in the blood
             platelet would reflect levels of the enzyme activities in
             skin. Dopamine, p-nitrophenol and minoxidil were used as
             substrates for skin and platelet thermolabile (TL PST),
             thermostable (TS PST) and MNX-ST activities, respectively.
             Biochemical properties of each skin enzyme were the same as
             the platelet enzymes with respect to apparent Km values for
             substrates, pH optima, thermal stabilities and responses to
             inhibition by 2,6-dichloro-4-nitrophenol (DCNP). An
             unexpected finding was that skin and platelet MNX-ST thermal
             stabilities and responses to DCNP were more similar to TL
             PST than to TS PST, the enzyme reported to be responsible
             for MNX-ST activity. There were significant positive
             correlations of platelet sulfotransferases with the relative
             levels of activities of the same skin sulfotransferases.
             Unexpected findings were significant positive correlations
             of MNX-ST and TL PST activities. Partially purified platelet
             TS PST assayed with minoxidil as the substrate showed a
             response to DCNP and thermal stability that were the same as
             TS PST. Platelet TL PST assayed with minoxidil showed
             thermal stability and a response to DCNP that were
             essentially the same as TL PST. The results indicated that
             not only TS PST, but also TL PST activities in human skin
             and platelet contributed to MNX-ST activity. It will be
             feasible to test whether measures of platelet PST activities
             will predict physiologic responses to minoxidil.},
   Language = {eng},
   Key = {fds174118}
}

@article{fds132745,
   Author = {G.A. Johnson},
   Title = {Hurlston SE, Brey WW, Suddarth SA, Yap M, Johson GA. A high
             temperature superconducting Helmholtz probe for microscopy
             at 9.4 T Magn Res Med. In press 1998},
   Year = {1998},
   Key = {fds132745}
}

@article{fds269056,
   Author = {Chawla, MS and Chen, XJ and Cofer, GP and Hedlund, LW and Kerby, MB and Ottoboni, TB and Johnson, GA},
   Title = {Hyperpolarized 3He microspheres as a novel vascular signal
             source for MRI.},
   Journal = {Magn Reson Med},
   Volume = {43},
   Number = {3},
   Pages = {440-445},
   Year = {2000},
   Month = {March},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/10725887},
   Keywords = {Animals • Helium • Image Enhancement •
             Magnetic Resonance Angiography* • Male •
             Microscopy, Electron, Scanning • Microspheres •
             Pelvis • Phantoms, Imaging • Rats • blood
             supply • chemistry* • methods},
   Abstract = {Hyperpolarized (HP) 3He can be encapsulated within
             biologically compatible microspheres while retaining
             sufficient polarization to be used as a signal source for
             MRI. Two microsphere sizes were used, with mean diameters of
             5.3 +/- 1.3 microm and 10.9 +/- 3.0 microm. These
             suspensions ranged in concentration from 0.9-7.0% gas by
             volume. Spectroscopic measurements in phantoms at 2 T
             yielded 3He relaxation times that varied with gas
             concentration. At the highest 3He concentration, the
             spinlattice relaxation time, T1, was 63.8 +/- 9.4 sec, while
             the transverse magnetization decayed with a time constant of
             T2* = 11.0 +/- 0.4 msec. In vivo MR images of the pelvic
             veins in a rat were acquired during intravenous injection of
             3He microspheres (SNR approximately equal 15). Advantages
             such as intravascular confinement, lack of background
             signal, and limited recirculation indicate quantitative
             perfusion measurements may be improved using this novel
             signal source.},
   Doi = {10.1002/(sici)1522-2594(200003)43:3<440::aid-mrm16>3.0.co;2-},
   Key = {fds269056}
}

@article{fds269124,
   Author = {Chen, XJ and Chawla, MS and Cofer, GP and Hedlund, LW and Möller, HE and Johnson, GA},
   Title = {Hyperpolarized 3He NMR lineshape measurements in the live
             guinea pig lung.},
   Journal = {Magn Reson Med},
   Volume = {40},
   Number = {1},
   Pages = {61-65},
   Year = {1998},
   Month = {July},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/9660554},
   Keywords = {Animals • Guinea Pigs • Helium • Isotopes
             • Lung • Magnetic Resonance Spectroscopy •
             Pulmonary Gas Exchange • Reference Values •
             Respiratory Mechanics • Sensitivity and Specificity
             • anatomy & histology* • diagnostic use* •
             methods*},
   Abstract = {Spatially localized lineshapes of hyperpolarized (HP) 3He in
             guinea pig lungs have been measured in vivo. Three different
             axial slice locations, each containing different
             compositions of airway sizes and orientations, were studied.
             Gas peaks from major bronchi (2 ppm) and alveoli (-2 ppm)
             were distinguished. The gas phase spectra show structural
             features that are a result of frequency shifts caused by
             bulk magnetic susceptibility. For a given slice, the
             spectral lineshapes reflect the airway composition within
             the slice location, according to theory. The peak
             assignments given here also agree with previous studies done
             by Wagshul et al. with HP 129Xe. At each of the slice
             locations, data were acquired during two phases of the
             breathing cycle, resulting in a relative frequency shift of
             approximately 0.3 ppm in the superior slices. Spectra
             obtained over a number of breaths show the dynamics of the
             gas buildup in the lung and provide further evidence
             supporting the peak assignments.},
   Doi = {10.1002/mrm.1910400109},
   Key = {fds269124}
}

@booklet{Chawla00,
   Author = {M. S. Chawla and X. J. Chen and G. P. Cofer and L. W.
             Hedlund and M. B. Kerby and T. B. Ottoboni and G. A.
             Johnson},
   Title = {Hyperpolarized He-3 microspheres as a novel vascular signal
             source for MRI},
   Journal = {Magnetic Resonance In Medicine},
   Volume = {43},
   Number = {3},
   Pages = {440 -- 445},
   Year = {2000},
   Month = {March},
   Key = {Chawla00}
}

@booklet{Chen98,
   Author = {X. J. Chen and M. S. Chawla and G. P. Cofer and L. W.
             Hedlund and H. E. Moller and G. A. Johnson},
   Title = {Hyperpolarized He-3 NMR lineshape measurements in the live
             guinea pig lung},
   Journal = {Magnetic Resonance In Medicine},
   Volume = {40},
   Number = {1},
   Pages = {61 -- 65},
   Year = {1998},
   Month = {July},
   Key = {Chen98}
}

@article{fds174086,
   Author = {GA Johnson},
   Title = {HYPOCHLORITE TREATMENT OF PUBLIC WATER SUPPLIES: ITS
             ADAPTIBILITY AND LIMITATIONS.},
   Journal = {Journal. American Public Health Association},
   Volume = {1},
   Number = {8},
   Pages = {562-74},
   Year = {1911},
   Month = {August},
   ISSN = {0273-1975},
   Language = {eng},
   Key = {fds174086}
}

@article{fds174158,
   Author = {GA Johnson},
   Title = {HYPOCHLORITE TREATMENT OF PUBLIC WATER SUPPLIES: ITS
             ADAPTIBILITY AND LIMITATIONS.},
   Journal = {Journal. American Public Health Association},
   Volume = {1},
   Number = {8},
   Pages = {562-574},
   Year = {1911},
   Month = {August},
   Language = {ENG},
   Key = {fds174158}
}

@booklet{Spencer99c,
   Author = {T. E. Spencer and F. F. Bartol and F. W. Bazer and G. A.
             Johnson and M. M. Joyce},
   Title = {Identification and characterization of glycosylation-dependent
             cell adhesion molecule 1-like protein expression in the
             ovine uterus},
   Journal = {Biology Of Reproduction},
   Volume = {60},
   Number = {2},
   Pages = {241 -- 250},
   Year = {1999},
   Month = {February},
   Key = {Spencer99c}
}

@article{fds174088,
   Author = {TE Spencer and FF Bartol and FW Bazer and GA Johnson and MM
             Joyce},
   Title = {Identification and characterization of glycosylation-dependent
             cell adhesion molecule 1-like protein expression in the
             ovine uterus.},
   Journal = {Biology of reproduction},
   Volume = {60},
   Number = {2},
   Pages = {241-50},
   Year = {1999},
   Month = {February},
   ISSN = {0006-3363},
   Keywords = {Animals • Blotting, Western • Embryonic
             Development • Endometrium • Epithelium •
             Estrus • Female • Gestational Age •
             Immunosorbent Techniques • Mucins • Myometrium
             • Pregnancy • Sheep • Uterus • analysis*
             • chemistry • chemistry*},
   Abstract = {Glycosylation-dependent cell adhesion molecule 1 (GlyCAM-1)
             is an endothelial glycoprotein secreted in lymph nodes that
             serves as a ligand for leukocyte cell surface selectin and
             mediates lymphocyte extravasation. In the present studies,
             rabbit anti-rat GlyCAM-1 IgG was used in immunochemical
             analyses of GlyCAM-1-like protein in the ovine uterus. In
             cyclic ewes, GlyCAM-1 expression increased in the
             endometrial luminal epithelium (LE) and shallow glandular
             epithelium (cGE) between Days 1 and 5 and then decreased
             between Days 11 and 15. In pregnant ewes, GlyCAM-1 in the LE
             and cGE was low on Days 11 and 13, increased on Day 15, and
             was abundant on Days 17 and 19. Immunoreactive GlyCAM-1 was
             also detected in the conceptus trophectoderm on Days 13-19.
             Staining for GlyCAM-1 in the smooth muscle of the
             vasculature and myometrium was constitutive, and no staining
             was detected in the stroma. An immunoreactive protein of
             approximately 45 kDa was identified in endometrial extracts
             and uterine flushings from cyclic and pregnant ewes. In
             pregnant ewes, the relative amount of immunoreactive
             GlyCAM-1 in uterine flushings was low on Days 11 and 13 but
             high on Days 15 and 17. Results suggest that a GlyCAM-1-like
             protein may be a secretory product of the endometrial
             epithelium and/or conceptus trophectoderm. Patterns of
             distribution observed for immunoreactive GlyCAM-1-like
             protein in the endometrial epithelium, combined with
             proposed functions for lymphoid GlyCAM-1, suggest that this
             mucin glycoprotein may be involved in conceptus-maternal
             interactions during the periimplantation period of pregnancy
             in sheep.},
   Language = {eng},
   Key = {fds174088}
}

@article{fds357210,
   Author = {Badea, A and Wu, W and Shuff, J and Wang, M and Anderson, RJ and Qi, Y and Johnson, GA and Wilson, JG and Koudoro, S and Garyfallidis, E and Colton, CA and Dunson, DB},
   Title = {Identifying Vulnerable Brain Networks in Mouse Models of
             Genetic Risk Factors for Late Onset Alzheimer's
             Disease.},
   Journal = {Front Neuroinform},
   Volume = {13},
   Pages = {72},
   Year = {2019},
   url = {http://dx.doi.org/10.3389/fninf.2019.00072},
   Abstract = {The major genetic risk for late onset Alzheimer's disease
             has been associated with the presence of APOE4 alleles.
             However, the impact of different APOE alleles on the brain
             aging trajectory, and how they interact with the brain local
             environment in a sex specific manner is not entirely clear.
             We sought to identify vulnerable brain circuits in novel
             mouse models with homozygous targeted replacement of the
             mouse ApoE gene with either human APOE3 or APOE4 gene
             alleles. These genes are expressed in mice that also model
             the human immune response to age and disease-associated
             challenges by expressing the human NOS2 gene in place of the
             mouse mNos2 gene. These mice had impaired learning and
             memory when assessed with the Morris water maze (MWM) and
             novel object recognition (NOR) tests. Ex vivo MRI-DTI
             analyses revealed global and local atrophy, and areas of
             reduced fractional anisotropy (FA). Using tensor network
             principal component analyses for structural connectomes, we
             inferred the pairwise connections which best separate APOE4
             from APOE3 carriers. These involved primarily
             interhemispheric connections among regions of olfactory
             areas, the hippocampus, and the cerebellum. Our results also
             suggest that pairwise connections may be subdivided and
             clustered spatially to reveal local changes on a finer
             scale. These analyses revealed not just genotype, but also
             sex specific differences. Identifying vulnerable networks
             may provide targets for interventions, and a means to
             stratify patients.},
   Doi = {10.3389/fninf.2019.00072},
   Key = {fds357210}
}

@article{fds204260,
   Author = {C Abad and DF Antczak and J Carvalho and LW Chamley and Q Chen and S Daher and AE Damiano and V Dantzer and P Díaz and CE Dunk and E Daly and C Escudero and B Falcón and M Guillomot and YW Han and LK Harris and JP Huidobro-Toro and N Illsley and H Jammes and T Jansson and GA Johnson, JR Kfoury Jr and R
             Marín, P Murthi and B Novakovic and L Myatt and MG Petroff and FT
             Pereira, C Pfarrer and CW Redman and G Rice and R Saffery and JM Tolosa and C Vaillancourt and M Wareing and R Yuen and GE Lash},
   Title = {IFPA Meeting 2010 Workshop Report I: Immunology; ion
             transport; epigenetics; vascular reactivity;
             epitheliochorial placentation; proteomics.},
   Journal = {Placenta},
   Volume = {32 Suppl 2},
   Pages = {S81-9},
   Year = {2011},
   Month = {March},
   ISSN = {1532-3102},
   url = {http://dx.doi.org/10.1016/j.placenta.2010.12.019},
   Keywords = {Animals • Education • Epigenesis, Genetic •
             Female • Fetus • Humans • Ion Transport
             • Maternal-Fetal Exchange • Placenta •
             Placentation • Pregnancy • Proteomics •
             Trophoblasts • blood supply • cytology •
             immunology • methods • physiology •
             physiology*},
   Abstract = {Workshops are an important part of the IFPA annual meeting.
             At IFPA Meeting 2010 there were twelve themed workshops, six
             of which are summarized in this report. 1. The immunology
             workshop focused on normal and pathological functions of the
             maternal immune system in pregnancy. 2. The transport
             workshop dealt with regulation of ion and water transport
             across the syncytiotrophoblast of human placenta. 3. The
             epigenetics workshop covered DNA methylation and its
             potential role in regulating gene expression in placental
             development and disease. 4. The vascular reactivity workshop
             concentrated on methodological approaches used to study
             placental vascular function. 5. The workshop on
             epitheliochorial placentation covered current advances from
             in vivo and in vitro studies of different domestic species.
             6. The proteomics workshop focused on a variety of
             techniques and procedures necessary for proteomic analysis
             and how they may be implemented for placental
             research.},
   Language = {eng},
   Doi = {10.1016/j.placenta.2010.12.019},
   Key = {fds204260}
}

@booklet{Johnson02e,
   Author = {Johnson, GA and Hedlund, LW},
   Title = {Image based phenotyping: The visible mouse},
   Journal = {FASEB JOURNAL},
   Volume = {16},
   Number = {5},
   Pages = {A1091-A1091},
   Year = {2002},
   ISSN = {0892-6638},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000174593902021&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Johnson02e}
}

@article{fds268888,
   Author = {Sherrier, RH and Chotas, HG and Johnson, GA and Chiles, C and Ravin,
             CE},
   Title = {Image optimization in a computed-radiography/photostimulable-phosphor
             system.},
   Journal = {J Digit Imaging},
   Volume = {2},
   Number = {4},
   Pages = {212-219},
   Year = {1989},
   Month = {November},
   ISSN = {0897-1889},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/2488166},
   Keywords = {Humans • Image Processing, Computer-Assisted* •
             Radiography, Thoracic • Tomography, X-Ray Computed*
             • X-Ray Film},
   Abstract = {Photostimulable phosphor imaging is an exciting new
             technology that has several advantages over film/screen
             radiography, the most important of which is the linearity of
             the photostimulable phosphor system over a wide exposure
             latitude. The photostimulable phosphor image is digital, and
             as such, provides options of how the image is viewed by
             radiologists. This report discusses the various
             image-processing parameters available for a photostimulable
             phosphor system and describes a rational approach for
             selecting these parameters in portable chest radiography. As
             photostimulable phosphor imaging becomes more widely
             implemented, an understanding of the processing parameters
             will facilitate the production of images that take full
             advantage of the benefits of these systems.},
   Doi = {10.1007/BF03170408},
   Key = {fds268888}
}

@article{fds132851,
   Author = {GA Johnson and M Korobkin},
   Title = {Image techniques for multiplanar computed
             tomography.},
   Journal = {Radiology, UNITED STATES},
   Volume = {144},
   Number = {4},
   Pages = {829-34},
   Year = {1982},
   Month = {September},
   ISSN = {0033-8419},
   Keywords = {Humans • Models, Structural • Radiographic Image
             Enhancement • Technology, Radiologic • Tomography,
             X-Ray Computed • methods*},
   Abstract = {Hardware and software options of the GE 8800 CT scanner were
             analyzed with respect to their effect on image quality for
             multiplanar images. Phantom studies were undertaken to
             demonstrate the effect of collimation, thick pixel
             reconstruction, and interpolation of both high- and
             low-contrast multiplanar images. Noise and spatial
             resolution were measured. Thick pixel reconstruction was
             found to be most useful in aiding in the delineation of
             low-contrast lesion boundaries. In addition, this option
             permits use of lower techniques, thus speeding data
             acquisition and reducing patient dose. Clinical examples are
             included.},
   Key = {fds132851}
}

@booklet{Johnson82e,
   Author = {Johnson, GA and Korobkin, M},
   Title = {Image techniques for multiplanar computed
             tomography.},
   Journal = {Radiology},
   Volume = {144},
   Number = {4},
   Pages = {829-834},
   Year = {1982},
   Month = {September},
   ISSN = {0033-8419},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/7111733},
   Abstract = {Hardware and software options of the GE 8800 CT scanner were
             analyzed with respect to their effect on image quality for
             multiplanar images. Phantom studies were undertaken to
             demonstrate the effect of collimation, thick pixel
             reconstruction, and interpolation of both high- and
             low-contrast multiplanar images. Noise and spatial
             resolution were measured. Thick pixel reconstruction was
             found to be most useful in aiding in the delineation of
             low-contrast lesion boundaries. In addition, this option
             permits use of lower techniques, thus speeding data
             acquisition and reducing patient dose. Clinical examples are
             included.},
   Doi = {10.1148/radiology.144.4.7111733},
   Key = {Johnson82e}
}

@article{fds320200,
   Author = {Johnson, GA and Anderson, RJ and Cook, JJ and Long, C and Badea,
             A},
   Title = {Image-processing pipelines: Applications in magnetic
             resonance histology},
   Journal = {Progress in Biomedical Optics and Imaging - Proceedings of
             SPIE},
   Volume = {9784},
   Publisher = {SPIE},
   Year = {2016},
   Month = {January},
   ISBN = {9781510600195},
   url = {http://dx.doi.org/10.1117/12.2203525},
   Abstract = {Image processing has become ubiquitous in imaging research -
             so ubiquitous that it is easy to loose track of how diverse
             this processing has become. The Duke Center for In Vivo
             Microscopy has pioneered the development of Magnetic
             Resonance Histology (MRH), which generates large
             multidimensional data sets that can easily reach into the
             tens of gigabytes. A series of dedicated image-processing
             workstations and associated software have been assembled to
             optimize each step of acquisition, reconstruction,
             post-processing, registration, visualization, and
             dissemination. This talk will describe the image-processing
             pipelines from acquisition to dissemination that have become
             critical to our everyday work.},
   Doi = {10.1117/12.2203525},
   Key = {fds320200}
}

@booklet{Yelbuz03,
   Author = {Yelbuz, TM and Zhang, X and Choma, MA and Stadt, HA and Zdanowicz, M and Johnson, GA and Kirby, ML},
   Title = {Images in cardiovascular medicine. Approaching cardiac
             development in three dimensions by magnetic resonance
             microscopy.},
   Journal = {Circulation},
   Volume = {108},
   Number = {22},
   Pages = {e154-e155},
   Year = {2003},
   Month = {December},
   ISSN = {0009-7322},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000186894500017&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Doi = {10.1161/01.CIR.0000102940.17908.CA},
   Key = {Yelbuz03}
}

@article{fds268862,
   Author = {Driehuys, B and Cofer, GP and Pollaro, J and Mackel, JB and Hedlund, LW and Johnson, GA},
   Title = {Imaging alveolar-capillary gas transfer using hyperpolarized
             129Xe MRI.},
   Journal = {Proc Natl Acad Sci U S A},
   Volume = {103},
   Number = {48},
   Pages = {18278-18283},
   Year = {2006},
   Month = {November},
   ISSN = {0027-8424},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/17101964},
   Keywords = {Animals • Erythrocytes • Magnetic Resonance
             Imaging • Microcirculation • Oxygen • Rats
             • Rats, Inbred F344 • Respiration* • Xenon
             Isotopes • metabolism • metabolism* •
             methods*},
   Abstract = {Effective pulmonary gas exchange relies on the free
             diffusion of gases across the thin tissue barrier separating
             airspace from the capillary red blood cells (RBCs).
             Pulmonary pathologies, such as inflammation, fibrosis, and
             edema, which cause an increased blood-gas barrier thickness,
             impair the efficiency of this exchange. However, definitive
             assessment of such gas-exchange abnormalities is
             challenging, because no methods currently exist to directly
             image the gas transfer process. Here we exploit the
             solubility and chemical shift of (129)Xe, the magnetic
             resonance signal of which has been enhanced by 10(5) with
             hyperpolarization, to differentially image its transfer from
             the airspaces into the tissue barrier spaces and RBCs in the
             gas exchange regions of the lung. Based on a simple
             diffusion model, we estimate that this MR imaging method for
             measuring (129)Xe alveolar-capillary transfer is sensitive
             to changes in blood-gas barrier thickness of approximately 5
             microm. We validate the successful separation of tissue
             barrier and RBC images and show the utility of this method
             in a rat model of pulmonary fibrosis where (129)Xe
             replenishment of the RBCs is severely impaired in regions of
             lung injury.},
   Doi = {10.1073/pnas.0608458103},
   Key = {fds268862}
}

@article{fds132842,
   Author = {PJ Gareau and AC Wymore and GP Cofer and GA Johnson},
   Title = {Imaging inflammation: direct visualization of perivascular
             cuffing in EAE by magnetic resonance microscopy.},
   Journal = {Journal of magnetic resonance imaging : JMRI, United
             States},
   Volume = {16},
   Number = {1},
   Pages = {28-36},
   Year = {2002},
   Month = {July},
   ISSN = {1053-1807},
   Keywords = {Animals • Brain • Disease Models, Animal •
             Encephalomyelitis, Autoimmune, Experimental • Female
             • Guinea Pigs • Inflammation • Magnetic
             Resonance Imaging • Microscopy • Multiple
             Sclerosis • methods* • pathology •
             pathology*},
   Abstract = {PURPOSE: To determine if the architectural features revealed
             by magnetic resonance microscopy (MRM) allow one to detect
             microscopic abnormalities associated with neuroinflammation
             in fixed brain sections from animals with experimental
             allergic encephalomyelitis (EAE), an animal model for
             multiple sclerosis (MS). MATERIALS AND METHODS: Imaging was
             performed at the Center for In Vivo Microscopy (CIVM) using
             a 9.4-Tesla, 89-mm bore, superconducting magnet with
             actively shielded gradients capable of 850 mT/m. A number of
             MR contrasts and spatial resolutions were explored. RESULTS:
             The assessment of EAE brain showed that it is possible to
             visualize perivascular cuffing in vitro by MRM on
             three-dimensional T1 proton stains. CONCLUSION: Inflammatory
             cell infiltration is a prerequisite for the development of
             lesions in EAE and MS. Thus, the ability to directly detect
             individual perivascular cuffs of inflammation may provide a
             useful means of monitoring the time course of inflammatory
             events, as conventional histopathological scoring of
             perivascular cuffs is utilized, but in the absence of
             sectioning and staining.},
   Key = {fds132842}
}

@booklet{Gareau02,
   Author = {Gareau, PJ and Wymore, AC and Cofer, GP and Johnson,
             GA},
   Title = {Imaging inflammation: direct visualization of perivascular
             cuffing in EAE by magnetic resonance microscopy.},
   Journal = {J Magn Reson Imaging},
   Volume = {16},
   Number = {1},
   Pages = {28-36},
   Year = {2002},
   Month = {July},
   ISSN = {1053-1807},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/12112500},
   Abstract = {PURPOSE: To determine if the architectural features revealed
             by magnetic resonance microscopy (MRM) allow one to detect
             microscopic abnormalities associated with neuroinflammation
             in fixed brain sections from animals with experimental
             allergic encephalomyelitis (EAE), an animal model for
             multiple sclerosis (MS). MATERIALS AND METHODS: Imaging was
             performed at the Center for In Vivo Microscopy (CIVM) using
             a 9.4-Tesla, 89-mm bore, superconducting magnet with
             actively shielded gradients capable of 850 mT/m. A number of
             MR contrasts and spatial resolutions were explored. RESULTS:
             The assessment of EAE brain showed that it is possible to
             visualize perivascular cuffing in vitro by MRM on
             three-dimensional T1 proton stains. CONCLUSION: Inflammatory
             cell infiltration is a prerequisite for the development of
             lesions in EAE and MS. Thus, the ability to directly detect
             individual perivascular cuffs of inflammation may provide a
             useful means of monitoring the time course of inflammatory
             events, as conventional histopathological scoring of
             perivascular cuffs is utilized, but in the absence of
             sectioning and staining.},
   Doi = {10.1002/jmri.10136},
   Key = {Gareau02}
}

@booklet{Johnson81d,
   Author = {Johnson, GA and Nelson, CE and OʼFoghludha, F},
   Title = {IMAGING LIMITS IN DIGITAL RADIOGRAPHY},
   Journal = {Investigative Radiology},
   Volume = {16},
   Number = {5},
   Pages = {377-377},
   Publisher = {Ovid Technologies (Wolters Kluwer Health)},
   Year = {1981},
   Month = {September},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1981MK56200033&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Doi = {10.1097/00004424-198109000-00033},
   Key = {Johnson81d}
}

@article{fds268855,
   Author = {Badea, CT and Bucholz, E and Hedlund, LW and Rockman, HA and Johnson,
             GA},
   Title = {Imaging methods for morphological and functional phenotyping
             of the rodent heart.},
   Journal = {Toxicol Pathol},
   Volume = {34},
   Number = {1},
   Pages = {111-117},
   Year = {2006},
   ISSN = {0192-6233},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/16507552},
   Keywords = {Animals • Biological Markers • Heart •
             Magnetic Resonance Imaging • Mice •
             Microradiography • Myocardium • Rats •
             Tomography, X-Ray Computed • methods* • pathology*
             • radiography*},
   Abstract = {Small animal imaging has a critical role in phenotyping,
             drug discovery, and in providing a basic understanding of
             mechanisms of disease. Translating imaging methods from
             humans to small animals is not an easy task. The purpose of
             this work is to compare two cardiac imaging modalities,
             i.e., magnetic resonance microscopy (MRM) and microcomputed
             tomography (CT) for preclinical studies on rodents. We
             present the two technologies, the parameters that they can
             measure, the types of alterations that they can detect, and
             show how these imaging methods compare to techniques
             available in clinical medicine. While this paper does not
             refer per se to the cardiac risk assessment for drug or
             chemical development, we hope that the information will
             effectively address how MRM and micro-CT might be exploited
             to measure biomarkers critical for safety
             assessment.},
   Doi = {10.1080/01926230500404126},
   Key = {fds268855}
}

@article{fds268782,
   Author = {Johnson, K and Badea, C and Hedlund, L and Johnson,
             GA},
   Title = {Imaging techniques for small animal imaging models of
             pulmonary disease: Micro-CT (Toxicologic Pathology (2007)
             35, 5 (9-64))},
   Journal = {Toxicologic Pathology},
   Volume = {36},
   Number = {6},
   Pages = {895},
   Publisher = {SAGE Publications},
   Year = {2008},
   Month = {October},
   ISSN = {0192-6233},
   url = {http://dx.doi.org/10.1177/0192623308323921},
   Doi = {10.1177/0192623308323921},
   Key = {fds268782}
}

@article{fds132818,
   Author = {MM Henson and OW Henson and SL Gewalt and JL Wilson and GA
             Johnson},
   Title = {Imaging the cochlea by magnetic resonance
             microscopy.},
   Journal = {Hearing research, NETHERLANDS},
   Volume = {75},
   Number = {1-2},
   Pages = {75-80},
   Year = {1994},
   Month = {May},
   ISSN = {0378-5955},
   Keywords = {Animals • Chiroptera • Cochlea • Magnetic
             Resonance Imaging* • Scala Tympani • Spiral
             Ganglion • Tissue Fixation • Vestibular Nerve
             • Vestibulocochlear Nerve • anatomy & histology
             • anatomy & histology*},
   Abstract = {The isolated, fixed cochlea of the mustached bat was studied
             with three dimensional magnetic resonance (MR) microscopy.
             The cochlea of this animal is about 4 mm in diameter and its
             entire volume was imaged. With the field of view and matrix
             size used, the volume elements (voxels) making up the volume
             data set were isotropic 25 x 25 x 25 micron cubes. Three
             dimensional (3D) MR microscopy based on isotropic voxels has
             many advantages over commonly used light microscopy: 1) it
             is non destructive; 2) it is much less time consuming; 3) no
             dehydration is required and shrinkage is minimized; 4) the
             data set can be used to create sections in any desired
             plane; 5) the proper alignment of sections is inherent in
             the 3D acquisition so that no reference points are required;
             6) the entire data set can be viewed from any point of view
             in a volume rendered image; 7) the data is digital and
             features can be enhanced by computer image processing; and
             8) the isotropic dimensions of the voxels make the data
             well-suited for structural reconstructions and measurements.
             Good images of the osseous spiral lamina, spiral ligament,
             scala tympani, scala vestibuli, and nerve bundles were
             obtained. The vestibular (Reissner's) membrane was easily
             identified in the mustached bat and it appears to bulge into
             the scala vestibuli. The visibility of this structure
             suggests that MR microscopy would be well-suited for studies
             of endolymphatic hydrops.},
   Key = {fds132818}
}

@booklet{Henson94,
   Author = {Henson, MM and Henson, OW and Gewalt, SL and Wilson, JL and Johnson,
             GA},
   Title = {Imaging the cochlea by magnetic resonance
             microscopy.},
   Journal = {Hear Res},
   Volume = {75},
   Number = {1-2},
   Pages = {75-80},
   Year = {1994},
   Month = {May},
   ISSN = {0378-5955},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/8071156},
   Abstract = {The isolated, fixed cochlea of the mustached bat was studied
             with three dimensional magnetic resonance (MR) microscopy.
             The cochlea of this animal is about 4 mm in diameter and its
             entire volume was imaged. With the field of view and matrix
             size used, the volume elements (voxels) making up the volume
             data set were isotropic 25 x 25 x 25 micron cubes. Three
             dimensional (3D) MR microscopy based on isotropic voxels has
             many advantages over commonly used light microscopy: 1) it
             is non destructive; 2) it is much less time consuming; 3) no
             dehydration is required and shrinkage is minimized; 4) the
             data set can be used to create sections in any desired
             plane; 5) the proper alignment of sections is inherent in
             the 3D acquisition so that no reference points are required;
             6) the entire data set can be viewed from any point of view
             in a volume rendered image; 7) the data is digital and
             features can be enhanced by computer image processing; and
             8) the isotropic dimensions of the voxels make the data
             well-suited for structural reconstructions and measurements.
             Good images of the osseous spiral lamina, spiral ligament,
             scala tympani, scala vestibuli, and nerve bundles were
             obtained. The vestibular (Reissner's) membrane was easily
             identified in the mustached bat and it appears to bulge into
             the scala vestibuli. The visibility of this structure
             suggests that MR microscopy would be well-suited for studies
             of endolymphatic hydrops.},
   Doi = {10.1016/0378-5955(94)90058-2},
   Key = {Henson94}
}

@article{fds316054,
   Author = {Wei, H and Xie, L and Dibb, R and Li, W and Decker, K and Zhang, Y and Johnson, GA and Liu, C},
   Title = {Imaging whole-brain cytoarchitecture of mouse with MRI-based
             quantitative susceptibility mapping.},
   Journal = {Neuroimage},
   Volume = {137},
   Pages = {107-115},
   Year = {2016},
   Month = {August},
   ISSN = {1053-8119},
   url = {http://dx.doi.org/10.1016/j.neuroimage.2016.05.033},
   Abstract = {The proper microstructural arrangement of complex neural
             structures is essential for establishing the functional
             circuitry of the brain. We present an MRI method to resolve
             tissue microstructure and infer brain cytoarchitecture by
             mapping the magnetic susceptibility in the brain at high
             resolution. This is possible because of the heterogeneous
             magnetic susceptibility created by varying concentrations of
             lipids, proteins and irons from the cell membrane to
             cytoplasm. We demonstrate magnetic susceptibility maps at a
             nominal resolution of 10-μm isotropic, approaching the
             average cell size of a mouse brain. The maps reveal many
             detailed structures including the retina cell layers,
             olfactory sensory neurons, barrel cortex, cortical layers,
             axonal fibers in white and gray matter. Olfactory glomerulus
             density is calculated and structural connectivity is traced
             in the optic nerve, striatal neurons, and brainstem nerves.
             The method is robust and can be readily applied on MRI
             scanners at or above 7T.},
   Doi = {10.1016/j.neuroimage.2016.05.033},
   Key = {fds316054}
}

@article{fds174276,
   Author = {AL Asirvatham and GA Johnson and EL Belden and EA Van Kirk and GE Moss and WJ Murdoch},
   Title = {Immunization of mice against a synthetic N-terminal
             extracellular domain gonadotropin-releasing hormone receptor
             peptide: evidence for a direct uterine effect.},
   Journal = {American journal of reproductive immunology (New York, N.Y.
             : 1989)},
   Volume = {32},
   Number = {2},
   Pages = {95-100},
   Year = {1994},
   Month = {September},
   ISSN = {1046-7408},
   Keywords = {Amino Acid Sequence • Animals • Female •
             Immunization, Passive • Male • Mice • Mice,
             Inbred BALB C • Molecular Sequence Data • Peptide
             Fragments • Receptors, LHRH • Uterus •
             Vaccination • chemistry • immunology •
             immunology* • pathology},
   Abstract = {PROBLEM: Immature male and female mice were immunized with a
             synthetic peptide corresponding to amino acids 5-17
             (ASLEQDPNHCSAI) of the mouse hypophyseal
             gonadotropin-releasing hormone (GnRH) receptor. METHOD:
             Effect of immunization (postpuberal) was restricted to the
             uterus. Pituitary-gonadal functions were not altered.
             RESULTS: The endometrial lining of immunized females was
             thin and lacked glandular development. These observations
             were corroborated in actively immunized and passively
             immunized adult females. CONCLUSIONS: Apparently endometrial
             cells express a unique surface antigen, though reactive with
             antipeptide antibodies, that differs from the prototype
             pituitary GnRH receptor. Antibodies that selectively inhibit
             endometrial maturation might be used to treat proliferative
             diseases of the uterus.},
   Language = {eng},
   Key = {fds174276}
}

@booklet{Asirvatham94,
   Author = {A. L. Asirvatham and G. A. Johnson and E. L. Belden and E.
             A. Vankirk and G. E. Moss and W. J. Murdoch},
   Title = {Immunization of mice against a synthetic n-terminal
             extracellular domain gonadotropin-releasing-hormone receptor
             peptide - evidence for a direct uterine effect},
   Journal = {American Journal Of Reproductive Immunology},
   Volume = {32},
   Number = {2},
   Pages = {95 -- 100},
   Year = {1994},
   Month = {September},
   Key = {Asirvatham94}
}

@booklet{Zelei90,
   Author = {B. V. Zelei and C. J. Walker and G. A. Sawada and T. T.
             Kawabe and K. A. Knight and A. E. Buhl and G. A. Johnson and A. R. Diani},
   Title = {Immunohistochemical and autoradiographic findings suggest
             that minoxidil is not localized in specific cells of
             vibrissa, pelage, or scalp follicles},
   Journal = {Cell And Tissue Research},
   Volume = {262},
   Number = {3},
   Pages = {407 -- 413},
   Year = {1990},
   Month = {December},
   Key = {Zelei90}
}

@article{fds174107,
   Author = {BV Zelei and CJ Walker and GA Sawada and TT Kawabe and KA Knight and AE
             Buhl, GA Johnson and AR Diani},
   Title = {Immunohistochemical and autoradiographic findings suggest
             that minoxidil is not localized in specific cells of
             vibrissa, pelage, or scalp follicles.},
   Journal = {Cell and tissue research},
   Volume = {262},
   Number = {3},
   Pages = {407-13},
   Year = {1990},
   Month = {December},
   ISSN = {0302-766X},
   Keywords = {Animals • Autoradiography • Hair •
             Immunohistochemistry • Male • Melanins •
             Minoxidil • Rats • Scalp • Vibrissae •
             cytology* • metabolism • metabolism*},
   Abstract = {Immunohistochemistry with a minoxidil antibody suggested
             that minoxidil-immunoreactivity is associated with the root
             sheaths, laterally orientated differentiating matrix cells,
             and dividing epithelial cells of cultured vibrissa follicles
             of pigmented and albino neonatal mice. The dermal papilla
             and connective tissue sheath were devoid of
             minoxidil-immunoreactivity. To verify that
             minoxodil-immunoreactivity in the follicles was specific,
             immunostaining was conducted with dissected whisker pads,
             formalin-fixed "dead" follicles, and sections of spleen,
             liver and kidney (non-haired organs) cultured with
             minoxidil. Microscopic examination revealed
             minoxidil-immunoreactivity in all of these tissues.
             Follicles and whisker pads cultured with minoxidil, then
             washed for one h in media were devoid of
             minoxidil-immunoreactivity. These data suggest that
             minoxidil-immunoreactivity in cultured vibrissa follicles is
             probably non-specific. Sections of skin from C3H and CF1
             mice which were topically dosed with minoxidil (in vivo)
             showed no minoxidil-immunoreactivity. Autoradiography
             demonstrated that tritiated minoxidil was bound in vivo and
             in vitro only to melanin granules in pigmented follicles of
             rodent and human tissue. This is probably non-specific
             binding since melanin is known to accumulate several
             chemically and pharmacologically unrelated drugs. It is
             reasonable to conclude that, under the conditions of these
             experiments, minoxidil is not specifically localized in any
             cells of whisker, pelage or, scalp follicles.},
   Language = {eng},
   Key = {fds174107}
}

@booklet{Harris86,
   Author = {D. W. Harris and D. M. Sutter and G. A. Johnson and J. H.
             Ludens},
   Title = {Immunoreactive atrial natriuretic factors (ir-anf) in plasma
             of conscious, unperturbed doca-salt hypertensive
             rats},
   Journal = {Clinical Research},
   Volume = {34},
   Number = {2},
   Pages = {A479 -- A479},
   Year = {1986},
   Month = {April},
   Key = {Harris86}
}

@article{fds180932,
   Author = {G Wu and FW Bazer and RC Burghardt and GA Johnson and SW Kim and XL Li and MC
             Satterfield, TE Spencer},
   Title = {Impacts of amino acid nutrition on pregnancy outcome in
             pigs: mechanisms and implications for swine
             production.},
   Journal = {Journal of animal science},
   Volume = {88},
   Number = {13 Suppl},
   Pages = {E195-204},
   Year = {2010},
   Month = {April},
   ISSN = {1525-3163},
   url = {http://dx.doi.org/10.2527/jas.2009-2446},
   Keywords = {Adipose Tissue • Amino Acids • Animal Nutritional
             Physiological Phenomena • Animals • Diet •
             Female • Fetal Development • Fetal Growth
             Retardation • Litter Size • Muscle, Skeletal
             • Placenta • Pregnancy • Pregnancy Outcome
             • Swine • drug effects • embryology •
             growth & development • metabolism • physiology
             • physiology* • veterinary •
             veterinary*},
   Abstract = {Pigs suffer up to 50% embryonic and fetal loss during
             gestation and exhibit the most severe naturally occurring
             intrauterine growth retardation among livestock species.
             Placental insufficiency is a major factor contributing to
             suboptimal reproductive performance and reduced birth
             weights of pigs. Enhancement of placental growth and
             function through nutritional management offers an effective
             solution to improving embryonic and fetal survival and
             growth. We discovered an unusual abundance of the arginine
             family of AA in porcine allantoic fluid (a reservoir of
             nutrients) during early gestation, when placental growth is
             most rapid. Arginine is metabolized to ornithine, proline,
             and nitric oxide, and these compounds possess a plethora of
             physiological functions. Nitric oxide is a vasodilator and
             angiogenic factor, whereas both ornithine and proline are
             substrates for placental synthesis of polyamines, which are
             key regulators of protein synthesis and angiogenesis.
             Additionally, arginine, leucine, glutamine, and proline
             activate the mammalian target of rapamycin cell-signaling
             pathway to enhance protein synthesis and cell proliferation
             in placentae. To translate basic research on AA biochemistry
             and nutrition into application, dietary supplementation with
             0.83% l-arginine to gilts on d 14 to 28 or d 30 to 114 of
             gestation increased the number and litter birth weight of
             live-born piglets. In addition, supplementing the gestation
             diet with 0.4% l-arginine plus 0.6% l-glutamine enhanced the
             efficiency of nutrient utilization, reduced variation in
             piglet birth weight, and increased litter birth weight. By
             regulating syntheses of nitric oxide, polyamines, and
             proteins, functional AA stimulate placental growth and the
             transfer of nutrients from mother to embryo or fetus to
             promote conceptus survival, growth, and development.},
   Language = {eng},
   Doi = {10.2527/jas.2009-2446},
   Key = {fds180932}
}

@article{fds174076,
   Author = {TE Spencer and GA Johnson and FW Bazer and RC Burghardt},
   Title = {Implantation mechanisms: insights from the
             sheep.},
   Journal = {Reproduction (Cambridge, England)},
   Volume = {128},
   Number = {6},
   Pages = {657-68},
   Year = {2004},
   Month = {December},
   ISSN = {1470-1626},
   url = {http://dx.doi.org/10.1530/rep.1.00398},
   Keywords = {Animals • Blastocyst • Cell Adhesion Molecules
             • Embryo Implantation • Embryonic Development
             • Female • Gestational Age • Pregnancy •
             Sheep • Uterus • physiology •
             physiology*},
   Abstract = {Implantation in all mammals involves shedding of the zona
             pellucida, followed by orientation, apposition, attachment
             and adhesion of the blastocyst to the endometrium.
             Endometrial invasion does not occur in domestic ruminants;
             thus, definitive implantation is achieved by adhesion of the
             mononuclear trophoblast cells to the endometrial lumenal
             epithelium (LE) and formation of syncytia by the fusion of
             trophoblast binucleate cells with the LE. This review
             highlights new information on mechanisms regulating the
             implantation cascade in sheep. The embryo enters the uterus
             on day 4 at the morula stage of development and then
             develops into a blastocyst by day 6. The blastocyst sheds
             the zona pellucida (day 8), elongates to a filamentous form
             (days 11-16), and adheres to the endometrial LE (day 16).
             Between days 14 and 16, the binucleate cells begin to
             differentiate in the trophoblast and subsequently migrate
             and fuse with the endometrial LE to form syncytia.
             Continuous exposure of the endometrium to progesterone in
             early pregnancy downregulates the progesterone receptors in
             the epithelia, a process which is associated with loss of
             the cell-surface mucin MUC1 and induction of several
             secreted adhesion proteins. Recurrent early pregnancy loss
             in the uterine gland knockout ewe model indicates that
             secretions of the endometrial epithelia have a physiologic
             role in blastocyst elongation and implantation. A number of
             endometrial proteins have been identified as potential
             regulators of blastocyst development and implantation in
             sheep, including glycosylated cell adhesion molecule 1
             (GlyCAM-1), galectin-15, integrins and osteopontin. The
             epithelial derived secreted adhesion proteins (GlyCAM-1,
             galectin-15 and osteopontin) are expressed in a dynamic
             temporal and spatial manner and regulated by progesterone
             and/or interferon tau, which is the pregnancy recognition
             signal produced by the trophoblast during blastocyst
             elongation. The noninvasive and protracted nature of
             implantation in domestic animals provides valuable
             opportunities to investigate fundamental processes of
             implantation that are shared among all mammals.
             Understanding of the cellular and molecular signals that
             regulate uterine receptivity and implantation can be used to
             diagnose and identify causes of recurrent pregnancy loss and
             to improve pregnancy outcome in domestic animals and
             humans.},
   Language = {eng},
   Doi = {10.1530/rep.1.00398},
   Key = {fds174076}
}

@booklet{Farmer89,
   Author = {T. H. R. Farmer and G. A. Johnson and G. P. Cofer and R. R.
             Maronpot and D. Dixon and L. W. Hedlund},
   Title = {Implanted coil mr microscopy of renal pathology},
   Journal = {Magnetic Resonance In Medicine},
   Volume = {10},
   Number = {3},
   Pages = {310 -- 323},
   Year = {1989},
   Month = {June},
   Key = {Farmer89}
}

@article{fds269011,
   Author = {Farmer, TH and Johnson, GA and Cofer, GP and Maronpot, RR and Dixon, D and Hedlund, LW},
   Title = {Implanted coil MR microscopy of renal pathology.},
   Journal = {Magn Reson Med},
   Volume = {10},
   Number = {3},
   Pages = {310-323},
   Year = {1989},
   Month = {June},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/2733588},
   Keywords = {Animals • Electrodes, Implanted • Kidney •
             Kidney Diseases • Magnetic Resonance Imaging •
             Microscopy • Rats • Rats, Inbred Strains •
             chemically induced • metabolism • methods* •
             pathology*},
   Abstract = {Inductively coupled implanted coils have been shown to
             provide up to a 10-fold increase in signal-to-noise ratio
             when compared to whole-body imaging of small animals. The
             current study was designed to extend the implanted coil
             imaging technique to a rodent model of renal pathology.
             Resonant radiofrequency (RF) coils were implanted around the
             left kidney of four rats and inductively coupled from within
             a birdcage body coil. All images were acquired at 2 T using
             a T1-weighted spin-echo sequence with TR = 500 ms and TE =
             20 ms. In vivo MR microscopy with voxels of 117 x 117 x 2000
             microns demonstrated cortex, inner and outer medulla, and
             major vascular structures on baseline images. Mercuric
             chloride-induced nephrotoxic acute tubular necrosis (ATN)
             diminished cortico-medullary contrast at 24 h after dosing
             with pathologic evaluation demonstrating nephrotoxic changes
             in the inner cortex. The kidney regained a baseline MR
             appearance 360 h after dosing and resolution of the damage
             was confirmed with histology. T1 data were gathered on
             excised kidneys as an adjunct to the images to help
             correlate the loss and return of cortico-medullary contrast
             with the pathology and pathophysiology of nephrotoxic ATN.
             With implanted RF coils we were able to demonstrate renal
             pathology and follow its subsequent resolution.
             Specifically, loss and return of cortico-medullary contrast
             as a result of nephrotoxic ATN were serially documented in
             four rats. Such serial in vivo studies performed on single
             animals should further the use of MR microscopy by
             minimizing the number of animals required for adequate
             biostatistics.},
   Doi = {10.1002/mrm.1910100304},
   Key = {fds269011}
}

@booklet{Mcadams87,
   Author = {McAdams, HP and Johnson, GA and Suddarth, SA and Sherrier, RH and Ravin,
             CE},
   Title = {IMPLEMENTATION OF ADAPTIVE FILTRATION FOR DIGITAL CHEST
             IMAGING.},
   Journal = {Optical Engineering},
   Volume = {26},
   Number = {7},
   Pages = {669-674},
   Publisher = {SPIE-Intl Soc Optical Eng},
   Year = {1987},
   Month = {January},
   url = {http://dx.doi.org/10.1117/12.7974133},
   Abstract = {Previous work has demonstrated the potential for adaptive
             filtration in processing digital chest images. The technique
             uses the histogram of the image to determine the pixels (and
             regions) in which edge enhancement is applied. This paper
             extends that work by investigating the choice of parameters
             used in selectively enhancing the mediastinum. The image is
             separated into its low and high frequency components by
             convolution with a square kernel. The effect of kernel size
             was studied with a choice of 17 multiplied by 17 mm, which
             was found to be sufficient to include the frequencies of
             interest. A serious deficiency in previous implementations
             of this technique is the existence of ringing artifacts at
             the juncture of the lung and mediastinum. These result in
             part from the use of a step function to specify the low
             frequency image intensity above which high frequencies are
             amplified. By replacing this step with a smoother (cosine)
             function, the artifact can be removed.},
   Doi = {10.1117/12.7974133},
   Key = {Mcadams87}
}

@booklet{Zhang03,
   Author = {X. W. Zhang and T. M. Yelbuz and G. P. Cofer and M. A. Choma and M. L. Kirby and G. A. Johnson},
   Title = {Improved preparation of chick embryonic samples for magnetic
             resonance microscopy},
   Journal = {Magnetic Resonance In Medicine},
   Volume = {49},
   Number = {6},
   Pages = {1192 -- 1195},
   Year = {2003},
   Month = {June},
   Key = {Zhang03}
}

@article{fds269008,
   Author = {Zhang, X and Yelbuz, TM and Cofer, GP and Choma, MA and Kirby, ML and Johnson, GA},
   Title = {Improved preparation of chick embryonic samples for magnetic
             resonance microscopy.},
   Journal = {Magn Reson Med},
   Volume = {49},
   Number = {6},
   Pages = {1192-1195},
   Year = {2003},
   Month = {June},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/12768599},
   Keywords = {Animals • Chick Embryo • Contrast Media •
             Heart • Image Enhancement* • Magnetic Resonance
             Imaging* • Microscopy • anatomy & histology •
             embryology* • instrumentation*},
   Abstract = {Previous work demonstrated the power of three-dimensional
             (3D) magnetic resonance microscopy (MRM) to follow
             complicated morphologic development in the embryonic
             cardiovascular system. In this study we describe a new
             dual-contrast method for specimen preparation that combines
             perfusion fixation and immersion in fixative with macro- and
             small molecular gadolinium agents to provide enhanced
             definition of both the heart wall and chamber. MRM was
             performed at 9.4 T with image resolutions of 25, 31, and 50
             microm isotropic voxels for three stages of chick embryos
             (day 4, day 5.5, and day 9), and compared to histological
             sections of the same embryos. The results show considerable
             improvement of image quality over previous efforts, with
             better signal-to-noise ratio (SNR) and contrast between the
             cardiac chamber and myocardial wall. Excellent correlation
             was shown between the MRM images and histological sections.
             Thus, 3D high-resolution MRM in combination with the
             dual-contrast technique is useful for acquiring quantitative
             3D morphologic data regarding heart development.},
   Doi = {10.1002/mrm.10460},
   Key = {fds269008}
}

@article{fds268822,
   Author = {Brinegar, C and Schmitter, SS and Mistry, NN and Johnson, GA and Liang,
             Z-P},
   Title = {Improving temporal resolution of pulmonary perfusion imaging
             in rats using the partially separable functions
             model.},
   Journal = {Magn Reson Med},
   Volume = {64},
   Number = {4},
   Pages = {1162-1170},
   Year = {2010},
   Month = {October},
   ISSN = {1522-2594},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/20564601},
   Keywords = {Algorithms* • Animals • Blood Flow Velocity •
             Computer Simulation • Female • Image Enhancement
             • Image Interpretation, Computer-Assisted •
             Magnetic Resonance Angiography • Models,
             Cardiovascular* • Pulmonary Artery • Pulmonary
             Circulation • Rats • Rats, Inbred F344 •
             Reproducibility of Results • Sensitivity and
             Specificity • anatomy & histology • methods •
             methods* • physiology • physiology*},
   Abstract = {Dynamic contrast-enhanced MRI (or DCE-MRI) is a useful tool
             for measuring blood flow and perfusion, and it has found use
             in the study of pulmonary perfusion in animal models.
             However, DCE-MRI experiments are difficult in small animals
             such as rats. A recently developed method known as
             Interleaved Radial Imaging and Sliding window-keyhole (IRIS)
             addresses this problem by using a data acquisition scheme
             that covers (k,t)-space with data acquired from multiple
             bolus injections of a contrast agent. However, the temporal
             resolution of IRIS is limited by the effects of temporal
             averaging inherent in the sliding window and keyhole
             operations. This article describes a new method to cover
             (k,t)-space based on the theory of partially separable
             functions (PSF). Specifically, a sparse sampling of
             (k,t)-space is performed to acquire two data sets, one with
             high-temporal resolution and the other with extended k-space
             coverage. The high-temporal resolution training data are
             used to determine the temporal basis functions of the PSF
             model, whereas the other data set is used to determine the
             spatial variations of the model. The proposed method was
             validated by simulations and demonstrated by an experimental
             study. In this particular study, the proposed method
             achieved a temporal resolution of 32 msec.},
   Language = {eng},
   Doi = {10.1002/mrm.22500},
   Key = {fds268822}
}

@booklet{Cserhati89,
   Author = {A. F. Cserhati and V. K. Lucian and E. K. Austin and G. A.
             Johnson and P. D. Sarmiento and G. A. West and C.
             Magee},
   Title = {Impurity content, redistribution and interface topography in
             poly and amorphous-silicon based cobalt polycides},
   Journal = {Applied Surface Science},
   Volume = {38},
   Number = {1-4},
   Pages = {195 -- 195},
   Year = {1989},
   Month = {September},
   Key = {Cserhati89}
}

@article{fds132776,
   Author = {MD Hollett and GP Cofer and GA Johnson},
   Title = {In situ magnetic resonance microscopy.},
   Journal = {Investigative radiology, UNITED STATES},
   Volume = {22},
   Number = {12},
   Pages = {965-8},
   Year = {1987},
   Month = {December},
   ISSN = {0020-9996},
   Keywords = {Animals • Kidney • Magnetic Resonance Imaging
             • Models, Structural • Rats • anatomy &
             histology* • methods*},
   Abstract = {Recent developments in MR permit imaging at microscopic
             resolution. Efforts have focused on small samples that fit
             entirely in the imaging probe. Extension of the techniques
             to imaging of individual organs in small animals is
             complicated by both the need to acquire an excessive number
             of phase encodings and limited signal to noise. Implantable
             radiofrequency coils described in this work eliminate both
             problems, permitting MR microscopy in the kidney of a live
             200-g rat with spatial resolution of 117 X 117 X 1250 mu
             (.02 mm3). Inductive coupling permits complete freedom from
             external leads. A phantom designed to evaluate dielectric
             losses is described. Both phantom and in vivo comparison of
             live kidney images demonstrate the tenfold improvement in
             signal to noise obtained with the implantable
             coil.},
   Key = {fds132776}
}

@booklet{Hollett87,
   Author = {Hollett, MD and Cofer, GP and Johnson, GA},
   Title = {In situ magnetic resonance microscopy.},
   Journal = {Invest Radiol},
   Volume = {22},
   Number = {12},
   Pages = {965-968},
   Year = {1987},
   Month = {December},
   ISSN = {0020-9996},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/3440731},
   Abstract = {Recent developments in MR permit imaging at microscopic
             resolution. Efforts have focused on small samples that fit
             entirely in the imaging probe. Extension of the techniques
             to imaging of individual organs in small animals is
             complicated by both the need to acquire an excessive number
             of phase encodings and limited signal to noise. Implantable
             radiofrequency coils described in this work eliminate both
             problems, permitting MR microscopy in the kidney of a live
             200-g rat with spatial resolution of 117 X 117 X 1250 mu
             (.02 mm3). Inductive coupling permits complete freedom from
             external leads. A phantom designed to evaluate dielectric
             losses is described. Both phantom and in vivo comparison of
             live kidney images demonstrate the tenfold improvement in
             signal to noise obtained with the implantable
             coil.},
   Doi = {10.1097/00004424-198712000-00009},
   Key = {Hollett87}
}

@article{fds174140,
   Author = {CA Matyac and GP Cofer and JE Bailey and GA Johnson},
   Title = {In Situ Observations of Root-gall Formation Using Nuclear
             Magnetic Resonance Imaging.},
   Journal = {Journal of nematology},
   Volume = {21},
   Number = {1},
   Pages = {131-4},
   Year = {1989},
   Month = {January},
   ISSN = {0022-300X},
   Language = {eng},
   Key = {fds174140}
}

@booklet{Matyac89,
   Author = {Matyac, CA and Cofer, GP and Bailey, JE and Johnson,
             GA},
   Title = {In Situ Observations of Root-gall Formation Using Nuclear
             Magnetic Resonance Imaging.},
   Journal = {J Nematol},
   Volume = {21},
   Number = {1},
   Pages = {131-134},
   Year = {1989},
   Month = {January},
   ISSN = {0022-300X},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/19287587},
   Key = {Matyac89}
}

@article{fds132788,
   Author = {CT Huesgen and PC Burger and BJ Crain and GA Johnson},
   Title = {In vitro MR microscopy of the hippocampus in Alzheimer's
             disease.},
   Journal = {Neurology, UNITED STATES},
   Volume = {43},
   Number = {1},
   Pages = {145-52},
   Year = {1993},
   Month = {January},
   ISSN = {0028-3878},
   Keywords = {Aged • Aged, 80 and over • Alzheimer Disease
             • Fourier Analysis • Hippocampus • Humans
             • Magnetic Resonance Imaging* • Middle Aged •
             Neurofibrillary Tangles • pathology •
             pathology*},
   Abstract = {We used MR microscopy at 7 tesla to identify the anatomy of
             the degenerating hippocampus in Alzheimer's disease (AD),
             which we then correlated with the histopathologic findings
             in the same specimens. The specimens studied were resected
             postmortem from 13 patients with confirmed AD and from nine
             age-matched controls. We imaged the specimens in the coronal
             plane using either three-dimensional Fourier encoding or
             single-slice Carr, Purcell, Meiboom, Gill (CPMG) spin echo
             sequences. On all specimens imaged with the CPMG pulse
             sequence, we calculated the T2 relaxation times for
             subfields within the hippocampus. Histologic sections were
             taken from each specimen and compared with the corresponding
             MR image. Using histologic boundaries, we quantified the
             number of neuritic plaques and neurofibrillary tangles in
             each hippocampal subfield. We measured the area,
             morphometric characteristics, and width of identifiable
             signal variant regions on each image and compared these
             measurements with the histopathologic findings. The mean
             cross-sectional area of the hippocampus in AD was decreased
             by 31% compared with the control group. This atrophy was
             highly correlated with tangle counts within the hippocampus,
             but not with plaque counts. The width of the gray matter in
             hippocampal area CA1, as identified by MR, correlated with
             the total area of the hippocampus. An age-related decrease
             in the size of a low-signal region that corresponds
             histologically to input projections comprising part of the
             perforant pathway was identified. Measurements of the T2
             relaxation times of hippocampal subfields showed little
             regional variability and were not accurate indicators of
             disease presence or severity (p > 0.05).},
   Key = {fds132788}
}

@booklet{Huesgen93,
   Author = {Huesgen, CT and Burger, PC and Crain, BJ and Johnson,
             GA},
   Title = {In vitro MR microscopy of the hippocampus in Alzheimer's
             disease.},
   Journal = {Neurology},
   Volume = {43},
   Number = {1},
   Pages = {145-152},
   Year = {1993},
   Month = {January},
   ISSN = {0028-3878},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/8423879},
   Abstract = {We used MR microscopy at 7 tesla to identify the anatomy of
             the degenerating hippocampus in Alzheimer's disease (AD),
             which we then correlated with the histopathologic findings
             in the same specimens. The specimens studied were resected
             postmortem from 13 patients with confirmed AD and from nine
             age-matched controls. We imaged the specimens in the coronal
             plane using either three-dimensional Fourier encoding or
             single-slice Carr, Purcell, Meiboom, Gill (CPMG) spin echo
             sequences. On all specimens imaged with the CPMG pulse
             sequence, we calculated the T2 relaxation times for
             subfields within the hippocampus. Histologic sections were
             taken from each specimen and compared with the corresponding
             MR image. Using histologic boundaries, we quantified the
             number of neuritic plaques and neurofibrillary tangles in
             each hippocampal subfield. We measured the area,
             morphometric characteristics, and width of identifiable
             signal variant regions on each image and compared these
             measurements with the histopathologic findings. The mean
             cross-sectional area of the hippocampus in AD was decreased
             by 31% compared with the control group. This atrophy was
             highly correlated with tangle counts within the hippocampus,
             but not with plaque counts. The width of the gray matter in
             hippocampal area CA1, as identified by MR, correlated with
             the total area of the hippocampus. An age-related decrease
             in the size of a low-signal region that corresponds
             histologically to input projections comprising part of the
             perforant pathway was identified. Measurements of the T2
             relaxation times of hippocampal subfields showed little
             regional variability and were not accurate indicators of
             disease presence or severity (p > 0.05).},
   Doi = {10.1212/wnl.43.1_part_1.145},
   Key = {Huesgen93}
}

@booklet{Benveniste99a,
   Author = {Benveniste, H and Qui, H and Hedlund, LW and Hüttemeier, PC and Steele,
             SM and Johnson, GA},
   Title = {In vivo diffusion-weighted magnetic resonance microscopy of
             rat spinal cord: effect of ischemia and intrathecal
             hyperbaric 5% lidocaine.},
   Journal = {Reg Anesth Pain Med},
   Volume = {24},
   Number = {4},
   Pages = {311-318},
   Year = {1999},
   ISSN = {1098-7339},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/10445769},
   Abstract = {BACKGROUND AND OBJECTIVES: Pathophysiologic mechanisms
             underlying persistent neurologic deficits after continuous
             spinal anesthesia using hyperbaric 5% lidocaine are still
             not well understood. It has been suggested that high-dose
             intrathecal lidocaine induces irreversible conduction block
             and even ischemia in white matter tracts by breakdown of the
             blood-nerve barrier. In this study, we use
             diffusion-weighted magnetic resonance microscopy to
             characterize the effect of intrathecal hyperbaric 5%
             lidocaine in rat spinal cord. The parameter measured with
             DWM, is an "apparent diffusion coefficient," (ADC), which
             can be used to exclude the presence of ischemia. METHODS:
             Female Fischer CDF rats were used. Group 1 (n = 5) was
             exposed to ischemia, group 2 (n = 7) was exposed to
             intrathecal 5% hyperbaric lidocaine, and group 3 (n = 5) was
             exposed to intrathecal 7.5% glucose. Diffusion-weighted MR
             images in group 1 were acquired before and after ischemia
             induced by cardiac arrest and in groups 2 and 3 rats prior
             to and during perfusion of the spinal catheter with either
             5% hyperbaric lidocaine or 7.5% glucose. RESULTS: Ischemia
             decreased the ADC by 40% in gray matter and by 30% in white
             matter of spinal cord. Continuous intrathecal anesthesia
             with hyperbaric 5% lidocaine did not affect the spinal cord
             ADC. Further, 7.5% intrathecal glucose had no effect on ADCs
             in gray or white matter of spinal cord. CONCLUSIONS:
             Ischemia reduced the ADC in both spinal cord white and gray
             matter. Hyperbaric 5% lidocaine did not affect the spinal
             cord ADC during the first 1.5 hours. We suggest that 5%
             hyperbaric lidocaine does not induce irreversible neurologic
             deficits by causing spinal cord ischemia.},
   Doi = {10.1016/s1098-7339(99)90104-9},
   Key = {Benveniste99a}
}

@article{fds132840,
   Author = {H Benveniste and H Qui and LW Hedlund and PC Hüttemeier and SM Steele and GA Johnson},
   Title = {In vivo diffusion-weighted magnetic resonance microscopy of
             rat spinal cord: effect of ischemia and intrathecal
             hyperbaric 5% lidocaine.},
   Journal = {Regional anesthesia and pain medicine, UNITED
             STATES},
   Volume = {24},
   Number = {4},
   Pages = {311-8},
   ISSN = {1098-7339},
   Keywords = {Anesthetics, Local • Animals • Blood Pressure
             • Catheterization • Dose-Response Relationship,
             Drug • Female • Heart Rate • Injections,
             Spinal • Ischemia • Lidocaine • Magnetic
             Resonance Imaging • Microscopy • Rats • Rats,
             Inbred F344 • Spinal Cord • anatomy & histology*
             • blood supply* • chemically induced* •
             cytology • diagnosis* • drug effects •
             methods • pathology • physiopathology •
             toxicity*},
   Abstract = {BACKGROUND AND OBJECTIVES: Pathophysiologic mechanisms
             underlying persistent neurologic deficits after continuous
             spinal anesthesia using hyperbaric 5% lidocaine are still
             not well understood. It has been suggested that high-dose
             intrathecal lidocaine induces irreversible conduction block
             and even ischemia in white matter tracts by breakdown of the
             blood-nerve barrier. In this study, we use
             diffusion-weighted magnetic resonance microscopy to
             characterize the effect of intrathecal hyperbaric 5%
             lidocaine in rat spinal cord. The parameter measured with
             DWM, is an "apparent diffusion coefficient," (ADC), which
             can be used to exclude the presence of ischemia. METHODS:
             Female Fischer CDF rats were used. Group 1 (n = 5) was
             exposed to ischemia, group 2 (n = 7) was exposed to
             intrathecal 5% hyperbaric lidocaine, and group 3 (n = 5) was
             exposed to intrathecal 7.5% glucose. Diffusion-weighted MR
             images in group 1 were acquired before and after ischemia
             induced by cardiac arrest and in groups 2 and 3 rats prior
             to and during perfusion of the spinal catheter with either
             5% hyperbaric lidocaine or 7.5% glucose. RESULTS: Ischemia
             decreased the ADC by 40% in gray matter and by 30% in white
             matter of spinal cord. Continuous intrathecal anesthesia
             with hyperbaric 5% lidocaine did not affect the spinal cord
             ADC. Further, 7.5% intrathecal glucose had no effect on ADCs
             in gray or white matter of spinal cord. CONCLUSIONS:
             Ischemia reduced the ADC in both spinal cord white and gray
             matter. Hyperbaric 5% lidocaine did not affect the spinal
             cord ADC during the first 1.5 hours. We suggest that 5%
             hyperbaric lidocaine does not induce irreversible neurologic
             deficits by causing spinal cord ischemia.},
   Key = {fds132840}
}

@article{fds132806,
   Author = {RD Black and HL Middleton and GD Cates and GP Cofer and B Driehuys and W
             Happer, LW Hedlund and GA Johnson, MD Shattuck and JC
             Swartz},
   Title = {In vivo He-3 MR images of guinea pig lungs.},
   Journal = {Radiology, UNITED STATES},
   Volume = {199},
   Number = {3},
   Pages = {867-70},
   Year = {1996},
   Month = {June},
   ISSN = {0033-8419},
   Keywords = {Animals • Guinea Pigs • Helium • Lung •
             Magnetic Resonance Imaging • Male • Radioisotopes
             • anatomy & histology* • instrumentation •
             methods* • statistics & numerical data},
   Abstract = {The authors imaged the lungs of live guinea pigs with
             hyperpolarized (HP) helium-3 as a magnetic resonance (MR)
             signal source. HP He-3 gas produced through spin exchange
             with rubidium metal vapor was delivered through an
             MR-compatible, small-animal ventilator. Two- and
             three-dimensional lung images acquired with
             ventilation-gated, radial k-space sampling showed complete
             ventilation of both lungs. All images were of high quality,
             demonstrating that HP He-3 allows high-signal-intensity MR
             imaging in living systems.},
   Key = {fds132806}
}

@booklet{Black96,
   Author = {Black, RD and Middleton, HL and Cates, GD and Cofer, GP and Driehuys, B and Happer, W and Hedlund, LW and Johnson, GA and Shattuck, MD and Swartz,
             JC},
   Title = {In vivo He-3 MR images of guinea pig lungs.},
   Journal = {Radiology},
   Volume = {199},
   Number = {3},
   Pages = {867-870},
   Year = {1996},
   Month = {June},
   ISSN = {0033-8419},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/8638019},
   Abstract = {The authors imaged the lungs of live guinea pigs with
             hyperpolarized (HP) helium-3 as a magnetic resonance (MR)
             signal source. HP He-3 gas produced through spin exchange
             with rubidium metal vapor was delivered through an
             MR-compatible, small-animal ventilator. Two- and
             three-dimensional lung images acquired with
             ventilation-gated, radial k-space sampling showed complete
             ventilation of both lungs. All images were of high quality,
             demonstrating that HP He-3 allows high-signal-intensity MR
             imaging in living systems.},
   Doi = {10.1148/radiology.199.3.8638019},
   Key = {Black96}
}

@article{fds204265,
   Author = {CT Badea and LW Hedlund and Y Qi and B Berridge and GA
             Johnson},
   Title = {In vivo imaging of rat coronary arteries using bi-plane
             digital subtraction angiography.},
   Journal = {Journal of pharmacological and toxicological
             methods},
   Volume = {64},
   Number = {2},
   Pages = {151-7},
   Year = {2011},
   Month = {June},
   ISSN = {1873-488X},
   url = {http://dx.doi.org/10.1016/j.vascn.2011.05.008},
   Keywords = {Angiography, Digital Subtraction • Animals •
             Contrast Media • Coronary Angiography • Coronary
             Circulation • Male • Myocardial Perfusion Imaging
             • Nitroprusside • Rats • Rats, Sprague-Dawley
             • Time Factors • Vasodilator Agents •
             administration & dosage • drug effects* •
             instrumentation • methods* • pharmacology},
   Abstract = {BACKGROUND: X-ray based digital subtraction angiography
             (DSA) is a common clinical imaging method for vascular
             morphology and function. Coronary artery characterization is
             one of its most important applications. We show that
             bi-plane DSA of rat coronary arteries can provide a powerful
             imaging tool for translational safety assessment in drug
             discovery. METHODS: A novel, dual tube/detector system,
             constructed explicitly for preclinical imaging, supports
             image acquisition at 10 frames/s with 88-micron spatial
             resolution. Ventilation, x-ray exposure, and contrast
             injection are all precisely synchronized using a biological
             sequence controller implemented as a LabVIEW application. A
             set of experiments were performed to test and optimize the
             sampling and image quality. We applied the DSA imaging
             protocol to record changes in the visualization of
             coronaries and myocardial perfusion induced by a vasodilator
             drug, nitroprusside. The drug was infused into a tail vein
             catheter using a peristaltic infusion pump at a rate of 0.07
             mL/h for 3 min (dose: 0.0875 mg). Multiple DSA sequences
             were acquired before, during, and up to 25 min after drug
             infusion. Perfusion maps of the heart were generated in
             MATLAB to compare the drug effects over time. RESULTS: The
             best trade-off between the injection time, pressure, and
             image quality was achieved at 60 PSI, with the injection of
             150 ms occurring early in diastole (60 ms delay) and
             resulting in the delivery of 113 μL of contrast agent. DSA
             images clearly show the main branches of the coronary
             arteries in an intact, beating heart. The drug test
             demonstrated that DSA can detect relative changes in
             coronary circulation via perfusion maps. CONCLUSIONS: The
             methodology for DSA imaging of rat coronary arteries can
             serve as a template for future translational studies to
             assist in safety evaluation of new pharmaceuticals. Although
             x-ray imaging involves radiation, the associated dose (0.4
             Gy) is not a major limitation.},
   Language = {eng},
   Doi = {10.1016/j.vascn.2011.05.008},
   Key = {fds204265}
}

@article{fds268811,
   Author = {Badea, CT and Hedlund, LW and Qi, Y and Berridge, B and Johnson,
             GA},
   Title = {In vivo imaging of rat coronary arteries using bi-plane
             digital subtraction angiography.},
   Journal = {J Pharmacol Toxicol Methods},
   Volume = {64},
   Number = {2},
   Pages = {151-157},
   Year = {2011},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/21683146},
   Abstract = {INTRODUCTION: X-ray based digital subtraction angiography
             (DSA) is a common clinical imaging method for vascular
             morphology and function. Coronary artery characterization is
             one of its most important applications. We show that
             bi-plane DSA of rat coronary arteries can provide a powerful
             imaging tool for translational safety assessment in drug
             discovery. METHODS: A novel, dual tube/detector system,
             constructed explicitly for preclinical imaging, supports
             image acquisition at 10 frames/s with 88-micron spatial
             resolution. Ventilation, x-ray exposure, and contrast
             injection are all precisely synchronized using a biological
             sequence controller implemented as a LabVIEW application. A
             set of experiments were performed to test and optimize the
             sampling and image quality. We applied the DSA imaging
             protocol to record changes in the visualization of
             coronaries and myocardial perfusion induced by a vasodilator
             drug, nitroprusside. The drug was infused into a tail vein
             catheter using a peristaltic infusion pump at a rate of 0.07
             mL/h for 3 min (dose: 0.0875 mg). Multiple DSA sequences
             were acquired before, during, and up to 25 min after drug
             infusion. Perfusion maps of the heart were generated in
             MATLAB to compare the drug effects over time. RESULTS: The
             best trade-off between the injection time, pressure, and
             image quality was achieved at 60 PSI, with the injection of
             150 ms occurring early in diastole (60 ms delay) and
             resulting in the delivery of 113 μL of contrast agent. DSA
             images clearly show the main branches of the coronary
             arteries in an intact, beating heart. The drug test
             demonstrated that DSA can detect relative changes in
             coronary circulation via perfusion maps. CONCLUSIONS: The
             methodology for DSA imaging of rat coronary arteries can
             serve as a template for future translational studies to
             assist in safety evaluation of new pharmaceuticals. Although
             x-ray imaging involves radiation, the associated dose (0.4
             Gy) is not a major limitation.},
   Doi = {10.1016/j.vascn.2011.05.008},
   Key = {fds268811}
}

@article{fds174200,
   Author = {GA Johnson and SJ Boukma and EG Kim},
   Title = {In vivo inhibition of dopamine beta-hydroxylase by
             1-phenyl-3-(2-thiazolyl)-2-thiourea (U-14,624).},
   Journal = {The Journal of pharmacology and experimental
             therapeutics},
   Volume = {171},
   Number = {1},
   Pages = {80-7},
   Year = {1970},
   Month = {January},
   ISSN = {0022-3565},
   Keywords = {Adrenal Glands • Adrenalectomy • Animals •
             Brain • Brain Chemistry • Carbon Isotopes •
             Catecholamines • Disulfiram • Dopamine •
             Dopamine Antagonists* • Hydrolases • Male •
             Metaraminol • Mice • Monoamine Oxidase Inhibitors
             • Myocardium • Norepinephrine • Rats •
             Species Specificity • Thiazoles • Thiourea •
             Time Factors • Tritium • Tyrosine • analysis
             • antagonists & inhibitors* • biosynthesis •
             drug effects • enzymology • metabolism •
             metabolism* • pharmacology • pharmacology* •
             physiology},
   Language = {eng},
   Key = {fds174200}
}

@booklet{Veres91a,
   Author = {Veres, JS and Johnson, GA and Kramer, PJ},
   Title = {In vivo Magnetic Resonance Imaging of Blechnum Ferns:
             Changes in T1 and N (H) During Dehydration and
             Rehydration},
   Journal = {American Journal of Botany},
   Volume = {78},
   Number = {1},
   Pages = {80-80},
   Publisher = {Wiley},
   Year = {1991},
   Month = {January},
   ISSN = {0002-9122},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1991EW16700009&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Doi = {10.2307/2445231},
   Key = {Veres91a}
}

@article{fds132893,
   Author = {M Brouwer and DW Engel and J Bonaventura and GA Johnson},
   Title = {In vivo magnetic resonance imaging of the blue crab,
             Callinectes sapidus: effect of cadmium accumulation in
             tissues on proton relaxation properties.},
   Journal = {The Journal of experimental zoology, UNITED
             STATES},
   Volume = {263},
   Number = {1},
   Pages = {32-40},
   Year = {1992},
   Month = {August},
   ISSN = {0022-104X},
   Keywords = {Animals • Brachyura • Cadmium • Copper •
             Diet • Liver • Magnetic Resonance Imaging* •
             Male • Organ Specificity • Pancreas • Trace
             Elements • administration & dosage • analysis
             • anatomy & histology • anatomy & histology*
             • metabolism},
   Abstract = {Nuclear magnetic resonance imaging (MRI) has been used to
             visualize the internal anatomy of a living blue crab. The
             resolution obtained in these studies was sufficient to
             distinguish individual organs by the differences in their
             proton densities and proton relaxation properties. T1
             (spin-lattice relaxation time)-weighted imaging revealed the
             lipid-rich nature of the hepatopancreas and gonadal tissue.
             To evaluate the effect of metal-induced stress on the
             different organs, crabs were exposed to elevated levels of
             cadmium in their diet, which resulted in increased
             concentrations of both cadmium and copper in the
             hepatopancreas. The spin-spin relaxation time, T2, of mobile
             protons in the metal-exposed tissue was significantly
             greater than T2 in the control tissues. These measurements
             suggest that the excess copper in the exposed tissues was
             diamagnetic [Cu(I)], since the presence of paramagnetic
             copper [Cu(II)] would result in a decrease of observed T2
             values. We hypothesize that the increased T2 value is a
             reflection of increased free water in the hepatopancreas.
             These studies show that magnetic resonance imaging is an
             important nondestructive tool for the study of morphological
             and physiological changes that occur in marine invertebrates
             in response to anthropogenic and natural
             stresses.},
   Key = {fds132893}
}

@booklet{Brouwer92,
   Author = {Brouwer, M and Engel, DW and Bonaventura, J and Johnson,
             GA},
   Title = {In vivo magnetic resonance imaging of the blue crab,
             Callinectes sapidus: effect of cadmium accumulation in
             tissues on proton relaxation properties.},
   Journal = {J Exp Zool},
   Volume = {263},
   Number = {1},
   Pages = {32-40},
   Year = {1992},
   Month = {August},
   ISSN = {0022-104X},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/1645119},
   Abstract = {Nuclear magnetic resonance imaging (MRI) has been used to
             visualize the internal anatomy of a living blue crab. The
             resolution obtained in these studies was sufficient to
             distinguish individual organs by the differences in their
             proton densities and proton relaxation properties. T1
             (spin-lattice relaxation time)-weighted imaging revealed the
             lipid-rich nature of the hepatopancreas and gonadal tissue.
             To evaluate the effect of metal-induced stress on the
             different organs, crabs were exposed to elevated levels of
             cadmium in their diet, which resulted in increased
             concentrations of both cadmium and copper in the
             hepatopancreas. The spin-spin relaxation time, T2, of mobile
             protons in the metal-exposed tissue was significantly
             greater than T2 in the control tissues. These measurements
             suggest that the excess copper in the exposed tissues was
             diamagnetic [Cu(I)], since the presence of paramagnetic
             copper [Cu(II)] would result in a decrease of observed T2
             values. We hypothesize that the increased T2 value is a
             reflection of increased free water in the hepatopancreas.
             These studies show that magnetic resonance imaging is an
             important nondestructive tool for the study of morphological
             and physiological changes that occur in marine invertebrates
             in response to anthropogenic and natural
             stresses.},
   Doi = {10.1002/jez.1402630105},
   Key = {Brouwer92}
}

@booklet{Cofer89,
   Author = {Cofer, GP and Brown, JM and Allan Johnson and G},
   Title = {In vivo magnetic resonance microscopy at 5
             μm},
   Journal = {Journal of Magnetic Resonance (1969)},
   Volume = {83},
   Number = {3},
   Pages = {608-616},
   Publisher = {Elsevier BV},
   Year = {1989},
   Month = {January},
   ISSN = {0022-2364},
   url = {http://dx.doi.org/10.1016/0022-2364(89)90354-5},
   Doi = {10.1016/0022-2364(89)90354-5},
   Key = {Cofer89}
}

@article{fds157096,
   Author = {JM Brown and GA Johnson and PJ Kramer},
   Title = {In Vivo Magnetic Resonance Microscopy of Changing Water
             Content in Pelargonium hortorum Roots.},
   Journal = {Plant physiology},
   Volume = {82},
   Number = {4},
   Pages = {1158-1160},
   Year = {1986},
   Month = {December},
   ISSN = {0032-0889},
   Abstract = {Magnetic resonance imaging (MRI) was used to
             nondestructively observe changes in water content in roots
             of Pelargonium hortorum x Bailey during a period of
             relatively rapid transpiration. Anatomical regions of the
             root could be differentiated with a spatial resolution of
             0.1 x 0.1 mm. MRI shows great potential for study of
             plant-water relations.},
   Key = {fds157096}
}

@booklet{Brown86,
   Author = {Brown, JM and Johnson, GA and Kramer, PJ},
   Title = {In Vivo Magnetic Resonance Microscopy of Changing Water
             Content in Pelargonium hortorum Roots.},
   Journal = {Plant Physiol},
   Volume = {82},
   Number = {4},
   Pages = {1158-1160},
   Year = {1986},
   Month = {December},
   ISSN = {0032-0889},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/16665154},
   Abstract = {Magnetic resonance imaging (MRI) was used to
             nondestructively observe changes in water content in roots
             of Pelargonium hortorum x Bailey during a period of
             relatively rapid transpiration. Anatomical regions of the
             root could be differentiated with a spatial resolution of
             0.1 x 0.1 mm. MRI shows great potential for study of
             plant-water relations.},
   Doi = {10.1104/pp.82.4.1158},
   Key = {Brown86}
}

@article{fds269086,
   Author = {Chawla, MS and Chen, XJ and Möller, HE and Cofer, GP and Wheeler, CT and Hedlund, LW and Johnson, GA},
   Title = {In vivo magnetic resonance vascular imaging using
             laser-polarized 3He microbubbles.},
   Journal = {Proc Natl Acad Sci U S A},
   Volume = {95},
   Number = {18},
   Pages = {10832-10835},
   Year = {1998},
   Month = {September},
   ISSN = {0027-8424},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/9724790},
   Keywords = {Angiography • Animals • Helium • Lasers
             • Magnetic Resonance Imaging • Male • Rats
             • Rats, Sprague-Dawley • methods*},
   Abstract = {Laser-polarized gases (3He and 129Xe) are currently being
             used in magnetic resonance imaging as strong signal sources
             that can be safely introduced into the lung. Recently,
             researchers have been investigating other tissues using
             129Xe. These studies use xenon dissolved in a carrier such
             as lipid vesicles or blood. Since helium is much less
             soluble than xenon in these materials, 3He has been used
             exclusively for imaging air spaces. However, considering
             that the signal of 3He is more than 10 times greater than
             that of 129Xe for presently attainable polarization levels,
             this work has focused on generating a method to introduce
             3He into the vascular system. We addressed the low
             solubility issue by producing suspensions of 3He
             microbubbles. Here, we provide the first vascular images
             obtained with laser-polarized 3He. The potential increase in
             signal and absence of background should allow this technique
             to produce high-resolution angiographic images. In addition,
             quantitative measurements of blood flow velocity and tissue
             perfusion will be feasible.},
   Doi = {10.1073/pnas.95.18.10832},
   Key = {fds269086}
}

@booklet{Chawla98,
   Author = {M. S. Chawla and X. J. Chen and H. E. Moller and G. P. Cofer and C. T. Wheeler and L. W. Hedlund and G. A.
             Johnson},
   Title = {In vivo magnetic resonance vascular imaging using
             laser-polarized He-3 microbubbles},
   Journal = {Proceedings Of The National Academy Of Sciences Of The
             United States Of America},
   Volume = {95},
   Number = {18},
   Pages = {10832 -- 10835},
   Year = {1998},
   Month = {September},
   Key = {Chawla98}
}

@article{fds132790,
   Author = {GA Johnson and JH Maki},
   Title = {In vivo measurement of proton diffusion in the presence of
             coherent motion.},
   Journal = {Investigative radiology, UNITED STATES},
   Volume = {26},
   Number = {6},
   Pages = {540-5},
   Year = {1991},
   Month = {June},
   ISSN = {0020-9996},
   Keywords = {Acetone • Animals • Diffusion • Dimethyl
             Sulfoxide • Magnetic Resonance Imaging • Movement
             • Protons* • Rats • Water •
             methods*},
   Abstract = {Measurement of the self-diffusion coefficient D of water in
             tissue has been performed traditionally using the technique
             proposed by Stejskal and Tanner. A variant of that technique
             is shown here, employing flow-compensated gradients that
             significantly reduce the sensitivity to small coherent
             motions that are common in body imaging. An interleaved
             sequence with four values of diffusion-sensitizing gradient
             (b) minimizes registration errors. Eddy currents and other
             systematic errors are reduced, permitting the measurement of
             standards in an imaging context within 5% of nonimaging
             values in the literature. The flow-compensated sequence
             permits the measure of D for tissues in the abdominal cavity
             of the rat. We present in vivo measurements of D for the
             following rat tissues; liver, kidney (cortex), kidney
             (medulla) muscle, brain, fat.},
   Key = {fds132790}
}

@booklet{Johnson91a,
   Author = {Johnson, GA and Maki, JH},
   Title = {In vivo measurement of proton diffusion in the presence of
             coherent motion.},
   Journal = {Invest Radiol},
   Volume = {26},
   Number = {6},
   Pages = {540-545},
   Year = {1991},
   Month = {June},
   ISSN = {0020-9996},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/1650333},
   Abstract = {Measurement of the self-diffusion coefficient D of water in
             tissue has been performed traditionally using the technique
             proposed by Stejskal and Tanner. A variant of that technique
             is shown here, employing flow-compensated gradients that
             significantly reduce the sensitivity to small coherent
             motions that are common in body imaging. An interleaved
             sequence with four values of diffusion-sensitizing gradient
             (b) minimizes registration errors. Eddy currents and other
             systematic errors are reduced, permitting the measurement of
             standards in an imaging context within 5% of nonimaging
             values in the literature. The flow-compensated sequence
             permits the measure of D for tissues in the abdominal cavity
             of the rat. We present in vivo measurements of D for the
             following rat tissues; liver, kidney (cortex), kidney
             (medulla) muscle, brain, fat.},
   Doi = {10.1097/00004424-199106000-00006},
   Key = {Johnson91a}
}

@article{fds268853,
   Author = {Badea, CT and Drangova, M and Holdsworth, DW and Johnson,
             GA},
   Title = {In vivo small-animal imaging using micro-CT and digital
             subtraction angiography.},
   Journal = {Phys Med Biol},
   Volume = {53},
   Number = {19},
   Pages = {R319-R350},
   Year = {2008},
   Month = {October},
   ISSN = {0031-9155},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/18758005},
   Keywords = {Angiography, Digital Subtraction • Animals •
             Humans • X-Ray Microtomography • instrumentation
             • methods*},
   Abstract = {Small-animal imaging has a critical role in phenotyping,
             drug discovery and in providing a basic understanding of
             mechanisms of disease. Translating imaging methods from
             humans to small animals is not an easy task. The purpose of
             this work is to review in vivo x-ray based small-animal
             imaging, with a focus on in vivo micro-computed tomography
             (micro-CT) and digital subtraction angiography (DSA). We
             present the principles, technologies, image quality
             parameters and types of applications. We show that both
             methods can be used not only to provide morphological, but
             also functional information, such as cardiac function
             estimation or perfusion. Compared to other modalities, x-ray
             based imaging is usually regarded as being able to provide
             higher throughput at lower cost and adequate resolution. The
             limitations are usually associated with the relatively poor
             contrast mechanisms and potential radiation damage due to
             ionizing radiation, although the use of contrast agents and
             careful design of studies can address these limitations. We
             hope that the information will effectively address how x-ray
             based imaging can be exploited for successful in vivo
             preclinical imaging.},
   Doi = {10.1088/0031-9155/53/19/R01},
   Key = {fds268853}
}

@article{fds174241,
   Author = {CW Flanagan and RS Mannel and JL Walker and GA Johnson},
   Title = {Incidence and location of para-aortic lymph node metastases
             in gynecologic malignancies.},
   Journal = {Journal of the American College of Surgeons},
   Volume = {181},
   Number = {1},
   Pages = {72-4},
   Year = {1995},
   Month = {July},
   ISSN = {1072-7515},
   Keywords = {Abdomen • Endometrial Neoplasms • Female •
             Genital Neoplasms, Female • Humans • Lymph Node
             Excision • Lymphatic Metastasis* • Neoplasm
             Staging • Ovarian Neoplasms • Retrospective
             Studies • Uterine Cervical Neoplasms • pathology
             • pathology*},
   Abstract = {BACKGROUND: We sought to determine the location of
             metastases to para-aortic lymph nodes in patients with
             gynecologic malignancies. STUDY DESIGN: A retrospective
             chart review was performed for all cases of endometrial,
             ovarian, and cervical carcinoma in which right and left
             para-aortic lymph node dissection was done at our
             institution from 1985 to 1993. Records were assessed for
             tumor type as well as for presence and location of
             metastases to para-aortic lymph nodes. RESULTS: A total of
             315 patients had bilateral para-aortic lymphadenectomy
             performed at the time of laparotomy as part of staging or
             therapy for their gynecologic malignancies. A total of 47
             patients (15 percent) had metastasis to the para-aortic
             lymph nodes. Para-aortic metastasis were identified in 22
             (30 percent) of 73 patients with ovarian carcinoma, 11 (8
             percent) of 141 patients with cervical carcinoma, and 14 (14
             percent) of 101 patients sampled. Unilateral left-sided
             para-aortic node involvement was observed in 13 patients,
             unilateral right-sided involvement was present in 14
             patients, and bilateral involvement occurred in 20 patients.
             Regarding tumor type or origin, no significant difference
             was noted in right-sided compared with left-sided
             para-aortic metastases. CONCLUSIONS: Our data suggest no
             difference in the incidence of metastases to right-sided
             compared with left para-aortic lymph nodes in patients with
             gynecologic malignancies, emphasizing the need for bilateral
             evaluation of the para-aortic lymph nodes. This information
             is important in the clinical staging of gynecologic
             malignancies and in establishing protocols requiring
             para-aortic lymph node dissection.},
   Language = {eng},
   Key = {fds174241}
}

@booklet{Flanagan95,
   Author = {C. W. Flanagan and R. S. Mannel and J. L. Walker and G. A.
             Johnson},
   Title = {Incidence and location of paraaortic lymph-node metastases
             in gynecologic malignancies},
   Journal = {Journal Of The American College Of Surgeons},
   Volume = {181},
   Number = {1},
   Pages = {72 -- 74},
   Year = {1995},
   Month = {July},
   Key = {Flanagan95}
}

@article{fds174179,
   Author = {GA Johnson and EG Kim},
   Title = {Increase of brain levels of tryptophan induced by inhibition
             of dopamine beta-hydroxylase (EC 1.14.2.1).},
   Journal = {Journal of neurochemistry},
   Volume = {20},
   Number = {6},
   Pages = {1761-4},
   Year = {1973},
   Month = {June},
   ISSN = {0022-3042},
   Keywords = {Animals • Brain • Cresols • Disulfides •
             Dopamine beta-Hydroxylase • Hydroxyindoleacetic Acid
             • Imidazoles • Kinetics • Male •
             Norepinephrine • Oxazoles • Phenylthiourea •
             Rats • Serotonin • Thiazoles • Tryptophan
             • antagonists & inhibitors* • drug effects •
             metabolism • metabolism* • pharmacology},
   Language = {eng},
   Key = {fds174179}
}

@booklet{Johnson91b,
   Author = {G. A. Johnson and V. J. Kapoor and M. Shokrani and L. J.
             Messick and R. Nguyen and R. A. Stall and M. A.
             Mckee},
   Title = {Indium gallium-arsenide microwave-power transistors},
   Journal = {Ieee Transactions On Microwave Theory And
             Techniques},
   Volume = {39},
   Number = {7},
   Pages = {1069 -- 1076},
   Year = {1991},
   Month = {July},
   Key = {Johnson91b}
}

@article{fds132904,
   Author = {MJ Upfal and GA Johnson and AP Jacobson and PA Brady and JA
             Campbell},
   Title = {Indoor radon and lung cancer in China.},
   Journal = {Journal of the National Cancer Institute, UNITED
             STATES},
   Volume = {82},
   Number = {21},
   Pages = {1722-3},
   Year = {1990},
   Month = {November},
   ISSN = {0027-8874},
   Keywords = {Air Pollutants • Carcinogens • China • Dust
             • Female • Humans • Lung Neoplasms •
             Radon • adverse effects • epidemiology •
             etiology* • toxicity • toxicity*},
   Key = {fds132904}
}

@booklet{Upfal90,
   Author = {M. J. Upfal and G. A. Johnson and A. P. Jacobson and P. A.
             Brady and J. A. Campbell},
   Title = {Indoor radon and lung-cancer in china},
   Journal = {Journal Of The National Cancer Institute},
   Volume = {82},
   Number = {21},
   Pages = {1722 -- 1722},
   Year = {1990},
   Month = {November},
   Key = {Upfal90}
}

@article{fds174153,
   Author = {RC Ackerman and GA Johnson and EA Van Kirk and AL Asirvatham and WJ
             Murdoch},
   Title = {Induction of apoptotic or lytic death in an ovarian
             adenocarcinoma cell line by antibodies generated against a
             synthetic N-terminal extracellular domain
             gonadotropin-releasing hormone receptor peptide.},
   Journal = {Cancer letters},
   Volume = {81},
   Number = {2},
   Pages = {177-84},
   Year = {1994},
   Month = {June},
   ISSN = {0304-3835},
   Keywords = {Adenocarcinoma • Amino Acid Sequence • Animals
             • Apoptosis* • Cytotoxicity, Immunologic •
             Female • Humans • Immune Sera • Mice •
             Molecular Sequence Data • Ovarian Neoplasms •
             Peptide Fragments • Receptors, LHRH • Sheep •
             Tumor Cells, Cultured • immunology* •
             pathology*},
   Abstract = {A polyclonal antiserum was generated in ovariectomized sheep
             against a synthetic peptide corresponding to amino acids
             5-17 of the deduced mouse pituitary gonadotropin-releasing
             hormone (GnRH) receptor. Antipeptide antibodies did not bind
             native cells, but did react strongly with a human ovarian
             cancer cell line (OVCAR-3) reportedly sensitive to GnRH.
             Growth of cultured OVCAR-3 cells was specifically suppressed
             by antipeptide serum. This was attributed in part to
             programmed death (chromatin condensation and DNA
             fragmentation) of cells by antibody-induced apoptosis.
             Antibodies also exhibited a cytolytic effect (lactate
             dehydrogenase release) toward OVCAR-3 cells in the presence
             of the complement. Endometria of passively immunized mice
             lacked development; thus, antipeptide antibodies evidently
             recognize Mullerian duct derivatives. Experiments are in
             progress to determine whether the putative antigen is a
             variant of the pituitary GnRH receptor or a largely
             dissimilar protein. Effector-functional antibodies could be
             useful in the management of ovarian or uterine
             neoplasia.},
   Language = {eng},
   Key = {fds174153}
}

@booklet{Ackerman94,
   Author = {R. C. Ackerman and G. A. Johnson and E. A. Vankirk and A. L.
             Asirvatham and W. J. Murdoch},
   Title = {Induction of apoptotic or lytic death in an ovarian
             adenocarcinoma cell-line by antibodies generated against a
             synthetic n-terminal extracellular domain
             gonadotropin-releasing-hormone receptor peptide},
   Journal = {Cancer Letters},
   Volume = {81},
   Number = {2},
   Pages = {177 -- 184},
   Year = {1994},
   Month = {June},
   Key = {Ackerman94}
}

@booklet{Johnson91c,
   Author = {G. A. Johnson and C. A. Baker and K. A. Knight},
   Title = {Induction of minoxidil sulfotransferase (mst) activity
             during differentiation of normal human epidermal-keratinocytes
             (nheks)},
   Journal = {Faseb Journal},
   Volume = {5},
   Number = {6},
   Pages = {A1749 -- A1749},
   Year = {1991},
   Month = {March},
   Key = {Johnson91c}
}

@booklet{Johnson92a,
   Author = {G. A. Johnson and V. J. Kapoor and H. Jurgensen and D.
             Schmitz},
   Title = {Ingaas field-effect transistors with submicron gates for
             k-band applications},
   Journal = {Ieee Transactions On Microwave Theory And
             Techniques},
   Volume = {40},
   Number = {3},
   Pages = {429 -- 433},
   Year = {1992},
   Month = {March},
   Key = {Johnson92a}
}

@article{fds371722,
   Author = {Woods, HF and Stubbs, WA and Johnson, G and Alberti,
             KG},
   Title = {Inhibition by salicylate of gluconeogenesis in the isolated
             perfused rat liver.},
   Journal = {Clin Exp Pharmacol Physiol},
   Volume = {1},
   Number = {6},
   Pages = {535-540},
   Year = {1974},
   url = {http://dx.doi.org/10.1111/j.1440-1681.1974.tb00574.x},
   Doi = {10.1111/j.1440-1681.1974.tb00574.x},
   Key = {fds371722}
}

@article{fds174222,
   Author = {GA Johnson and EG Kim and SJ Boukma and D Lednicer and GA
             Youngdale},
   Title = {Inhibition of dopamine -hydroxylase by 5-phenoxymethyl-2-oxazolidinethiones.},
   Journal = {Journal of medicinal chemistry},
   Volume = {15},
   Number = {3},
   Pages = {327-9},
   Year = {1972},
   Month = {March},
   ISSN = {0022-2623},
   Keywords = {Adrenal Glands • Animals • Brain • Brain
             Chemistry • Cattle • Dopamine beta-Hydroxylase
             • Food Habits • Male • Mice • Mice,
             Inbred Strains • Mixed Function Oxygenases • Motor
             Activity • Norepinephrine • Oxazoles •
             Phenols • Structure-Activity Relationship •
             analysis • antagonists & inhibitors • antagonists
             & inhibitors* • drug effects • enzymology •
             pharmacology • pharmacology*},
   Language = {eng},
   Key = {fds174222}
}

@article{fds174273,
   Author = {GA Johnson and SJ Boukma and EG Kim},
   Title = {Inhibition of dopamine beta-hydroxylase by aromatic and
             alkyl thioureas.},
   Journal = {The Journal of pharmacology and experimental
             therapeutics},
   Volume = {168},
   Number = {2},
   Pages = {229-34},
   Year = {1969},
   Month = {August},
   ISSN = {0022-3565},
   Keywords = {Animals • Brain Chemistry • Disulfiram •
             Dopamine • Mice • Mixed Function Oxygenases •
             Norepinephrine • Rats • Thiourea • Tyramine
             • administration & dosage • analysis •
             antagonists & inhibitors* • metabolism •
             pharmacology • pharmacology*},
   Language = {eng},
   Key = {fds174273}
}

@booklet{Johnston81,
   Author = {D. G. Johnston and G. A. Johnson and H. Millwardsadler},
   Title = {Insulin and liver-regeneration after partial-hepatectomy
             (ph) in normal and diabetic rats},
   Journal = {Diabetologia},
   Volume = {21},
   Number = {3},
   Pages = {288 -- 288},
   Year = {1981},
   Key = {Johnston81}
}

@article{fds174127,
   Author = {RM Simmons and DW Erikson and J Kim and RC Burghardt and FW Bazer and GA
             Johnson, TE Spencer},
   Title = {Insulin-like growth factor binding protein-1 in the ruminant
             uterus: potential endometrial marker and regulator of
             conceptus elongation.},
   Journal = {Endocrinology},
   Volume = {150},
   Number = {9},
   Pages = {4295-305},
   Year = {2009},
   Month = {September},
   ISSN = {1945-7170},
   url = {http://dx.doi.org/10.1210/en.2009-0060},
   Keywords = {Animals • Cattle • Cell Movement • Cell
             Proliferation • Endometrium • Female •
             Insulin-Like Growth Factor Binding Protein 1 •
             Insulin-Like Growth Factor Binding Protein 3 •
             Interferon Type I • Pregnancy • Pregnancy Proteins
             • Progesterone • Sheep • Uterus • drug
             effects • metabolism • metabolism* •
             pharmacology • physiology*},
   Abstract = {Establishment of pregnancy in ruminants requires conceptus
             elongation and production of interferon-tau (IFNT), the
             pregnancy recognition signal that maintains ovarian
             progesterone (P4) production. These studies determined
             temporal and spatial alterations in IGF binding protein
             (IGFBP)-1 and IGFBP3 in the ovine and bovine uterus; effects
             of P4 and IFNT on their expression in the ovine uterus; and
             effects of IGFBP1 on ovine trophectoderm cell proliferation,
             migration, and attachment. IGFBP1 and IGFBP3 were studied
             because they are the only IGFBPs specifically expressed by
             the endometrial luminal epithelia in sheep. In sheep, IGFBP1
             and IGFBP3 expression was coordinate with the period of
             conceptus elongation, whereas only IGFBP1 expression was
             coordinate with conceptus elongation in cattle. IGFBP1 mRNA
             in the ovine endometria was between 5- and 29-fold more
             abundant between d 12 and 16 of pregnancy compared with the
             estrous cycle and greater on d 16 of pregnancy than
             nonpregnancy in the bovine uterus. In sheep, P4 induced and
             IFNT stimulated expression of IGFBP1 but not IGFBP3;
             however, the effect of IFNT did not mimic the abundant
             increase observed in pregnant ewes. Therefore, IGFBP1
             expression in the endometrium is regulated by another factor
             from the conceptus. IGFBP1 did not affect the proliferation
             of ovine trophectoderm cells in vitro but did stimulate
             their migration and mediate their attachment. These studies
             reveal that IGFBP1 is a common endometrial marker of
             conceptus elongation in sheep and cattle and most likely
             regulates conceptus elongation by stimulating migration and
             attachment of the trophectoderm.},
   Language = {eng},
   Doi = {10.1210/en.2009-0060},
   Key = {fds174127}
}

@article{fds174184,
   Author = {J Kim and G Song and H Gao and JL Farmer and MC Satterfield and RC
             Burghardt, G Wu and GA Johnson and TE Spencer and FW
             Bazer},
   Title = {Insulin-like growth factor II activates phosphatidylinositol
             3-kinase-protooncogenic protein kinase 1 and
             mitogen-activated protein kinase cell Signaling pathways,
             and stimulates migration of ovine trophectoderm
             cells.},
   Journal = {Endocrinology},
   Volume = {149},
   Number = {6},
   Pages = {3085-94},
   Year = {2008},
   Month = {June},
   ISSN = {0013-7227},
   url = {http://dx.doi.org/10.1210/en.2007-1367},
   Keywords = {Animals • Cell Differentiation • Cell Division
             • Cloning, Molecular • Female • Insulin-Like
             Growth Factor II • MAP Kinase Signaling System •
             Male • Pregnancy • Proto-Oncogene Proteins c-akt
             • RNA, Messenger • Ribosomal Protein S6 Kinases,
             90-kDa • Sheep • Uterus • Vasectomy •
             genetics • metabolism • p38 Mitogen-Activated
             Protein Kinases • physiology •
             physiology*},
   Abstract = {IGF-II, a potent stimulator of cellular proliferation,
             differentiation, and development, regulates uterine function
             and conceptus growth in several species. In situ
             hybridization analyses found that IGF-II mRNA was most
             abundant in the caruncular endometrial stroma of both
             cyclical and pregnant ewes. In the intercaruncular
             endometrium, IGF-II mRNA transitioned from stroma to luminal
             epithelium between d 14 and 20 of pregnancy. IGF-II mRNA was
             present in all cells of the conceptus but was particularly
             abundant in the yolk sac. Immunohistochemical analyses
             revealed that phosphorylated (p)-protooncogenic protein
             kinase 1, p-ribosomal protein S6 kinase, p-ERK1/2, and p-P38
             MAPK proteins were present at low levels in a majority of
             endometrial cells but were most abundant in the nuclei of
             endometrial luminal epithelium and conceptus trophectoderm
             of pregnant ewes. In mononuclear trophectoderm cells
             isolated from d-15 conceptuses, IGF-II increased the
             abundance of p-pyruvate dehydrogenase kinase 1,
             p-protooncogenic protein kinase 1, p-glycogen synthase
             kinase 3B, p-FK506 binding protein 12-rapamycin associated
             protein 1, and p-ribosomal protein S6 kinase protein within
             15 min, and the increase was maintained for 90 min. IGF-II
             also elicited a rapid increase in p-ERK1/2 and p-P38 MAPK
             proteins that was maximal at 15 or 30 min posttreatment.
             Moreover, IGF-II increased migration of trophectoderm cells.
             Collectively, these results support the hypothesis that
             IGF-II coordinately activates multiple cell signaling
             pathways critical to survival, growth, and differentiation
             of the ovine conceptus during early pregnancy.},
   Language = {eng},
   Doi = {10.1210/en.2007-1367},
   Key = {fds174184}
}

@article{fds268760,
   Author = {Johnson, GA and Chotas, HG and Suddarth, SA and Ziv, SB and Todd,
             BE},
   Title = {Integrated network for medical imaging research},
   Journal = {Proceedings of SPIE - The International Society for Optical
             Engineering},
   Volume = {1234 pt 1},
   Pages = {159-166},
   Year = {1990},
   Abstract = {There are a number of generic problems that researchers in
             medical imaging have in common. For example, researchers in
             MR, CT, PET, SPECT, DSA, and digital radiography all need to
             display and window digital images. We describe here an
             integrated with tools applicable to all of the current areas
             of medical imaging that enable researchers at Duke to share
             resources and solve software and hardware problems in a
             unified effort. We will show examples where efforts in a
             specific area of imaging research can be readily applied in
             new ways to different imaging modalities through the
             facilities provided in this integrated approach. We will
             point out some of the problems and opportunities in the
             research environment that are different from those
             encountered in clinical PACS system.},
   Key = {fds268760}
}

@booklet{Johnson98d,
   Author = {G. A. Johnson and T. R. Hoverstad and R. E.
             Greenwald},
   Title = {Integrated weed management using narrow corn row spacing,
             herbicides, and cultivation},
   Journal = {Agronomy Journal},
   Volume = {90},
   Number = {1},
   Pages = {40 -- 46},
   Year = {1998},
   Key = {Johnson98d}
}

@article{fds174274,
   Author = {PS Bridger and S Haupt and R Leiser and GA Johnson and RC Burghardt and HR
             Tinneberg, C Pfarrer},
   Title = {Integrin activation in bovine placentomes and in caruncular
             epithelial cells isolated from pregnant cows.},
   Journal = {Biology of reproduction},
   Volume = {79},
   Number = {2},
   Pages = {274-82},
   Year = {2008},
   Month = {August},
   ISSN = {0006-3363},
   url = {http://dx.doi.org/10.1095/biolreprod.108.067637},
   Keywords = {Animals • Cattle • Cell Proliferation • Cell
             Separation • Cells, Cultured • Epithelial Cells
             • Extracellular Matrix • Female •
             Fibronectins • Focal Adhesions • Integrins •
             Models, Biological • Placenta • Pregnancy •
             Pregnancy, Animal* • Trophoblasts • cytology
             • metabolism • metabolism* •
             physiology},
   Abstract = {In the bovine synepitheliochorial placenta, restricted
             trophoblast invasion requires complex interactions of
             integrin receptors with proteins of the extracellular matrix
             (ECM) and integrin receptors of neighboring cells. Activated
             integrins assemble to focal adhesions and are linked to the
             actin cytoskeleton via signaling molecules including
             alpha-actinin (ACTN), focal adhesion kinase (PTK2 or FAK),
             phosphotyrosine, and talin (TLN1). Aims of this study were
             to assess integrin activation and focal adhesion assembly
             within epithelial cells of bovine placentomes and
             low-passage (not transformed) placentomal caruncular
             epithelial cells cultured on dishes coated with ECM
             proteins. Immunofluorescence analysis was performed to
             colocalize the signaling molecules ACTN, PTK2,
             phosphotyrosine, and TLN1 with each other and with
             beta(1)-integrin (ITGB1) in placentomal cryosections
             throughout pregnancy and in caruncular epithelial cells in
             vitro. Antibody specificity was confirmed by Western blot.
             Cells were cultured on uncoated dishes, and the dishes were
             coated with fibronectin (FN), laminin (LAMA), and collagen
             type IV (COL4), thereby statistically assessing cell number
             and qualitatively assessing the expression pattern of ITGB1,
             phosphotyrosine, and TLN1. Results demonstrated integrin
             activation and focal adhesion assembly in the placentome and
             that low-passage caruncular epithelial cells maintain
             integrin-associated properties observed in vivo. Expression
             and/or colocalization of signaling molecules with ITGB1
             confirmed, for the first time, integrin activation and
             participation in "outside-in" and "inside-out" signaling
             pathways. The prominent role of ECM, and FN in particular,
             in integrin signaling is supported by the in vitro
             enhancement of proliferation and focal adhesion expression.
             Thus, this in vitro model provides excellent potential for
             further mechanistic studies designed to elucidate
             feto-maternal interactions in the bovine
             placentome.},
   Language = {eng},
   Doi = {10.1095/biolreprod.108.067637},
   Key = {fds174274}
}

@booklet{Burghardt02,
   Author = {R. C. Burghardt and G. A. Johnson and L. A. Jaeger and H. Ka and J. E. Garlow and T. E. Spencer and F. W.
             Bazer},
   Title = {Integrins and extracellular matrix proteins at the
             maternal-fetal interface in domestic animals},
   Journal = {Cells Tissues Organs},
   Volume = {172},
   Number = {3},
   Pages = {202 -- 217},
   Year = {2002},
   Key = {Burghardt02}
}

@article{fds174284,
   Author = {RC Burghardt and GA Johnson and LA Jaeger and H Ka and JE Garlow and TE
             Spencer, FW Bazer},
   Title = {Integrins and extracellular matrix proteins at the
             maternal-fetal interface in domestic animals.},
   Journal = {Cells, tissues, organs},
   Volume = {172},
   Number = {3},
   Pages = {202-17},
   Year = {2002},
   ISSN = {1422-6405},
   Keywords = {Animals • Embryo Implantation • Endometrium •
             Extracellular Matrix Proteins • Female • Humans
             • Integrins • Maternal-Fetal Exchange* •
             Osteopontin • Peptide Fragments • Placenta •
             Pregnancy • Protein Precursors • Sheep •
             Sialoglycoproteins • Swine • Transforming Growth
             Factor beta1 • cytology • genetics •
             metabolism • metabolism* • physiology •
             physiology*},
   Abstract = {Establishment of pregnancy in mammals requires coordinated
             conceptus-maternal interactions involving numerous hormones,
             growth factors and cytokines acting via specific receptors
             in the uterus. Uterine secretions play an important role in
             establishing synchrony between development of the conceptus
             and uterine receptivity, as well as in conceptus remodeling,
             adhesion, implantation and placentation in domestic species.
             Studies of non-invasive implantation in domestic livestock
             provide valuable opportunities to investigate fundamental
             processes of the initial events of apposition, attachment
             and adhesive interactions that are shared among species. In
             pigs and sheep, it appears that integrins play a dominant
             role in these fundamental processes via interactions with
             extracellular matrix molecules and other ligands to
             transduce cellular signals in uterine epithelial cells and
             conceptus trophectoderm. This review considers several of
             the potential integrin-binding ligands involved in the
             complex implantation adhesion cascade in pigs and sheep
             along with in vitro evidence for the transduction of
             cytoplasmic signals that may be required to sustain fetal
             and maternal contributions to the formation of the
             epitheliochorial placenta.},
   Language = {eng},
   Key = {fds174284}
}

@booklet{Buhl92,
   Author = {A. E. Buhl and T. T. Kawabe and D. K. Maccallum and D. J.
             Waldon and K. A. Knight and G. A. Johnson},
   Title = {Interaction of minoxidil with pigment in cells of the hair
             follicle - an example of binding without apparent biological
             effects},
   Journal = {Skin Pharmacology},
   Volume = {5},
   Number = {2},
   Pages = {114 -- 123},
   Year = {1992},
   Key = {Buhl92}
}

@article{fds174260,
   Author = {AE Buhl and TT Kawabe and DK MacCallum and DJ Waldon and KA Knight and GA
             Johnson},
   Title = {Interaction of minoxidil with pigment in cells of the hair
             follicle: an example of binding without apparent biological
             effects.},
   Journal = {Skin pharmacology : the official journal of the Skin
             Pharmacology Society},
   Volume = {5},
   Number = {2},
   Pages = {114-23},
   Year = {1992},
   ISSN = {1011-0283},
   Keywords = {Animals • Autoradiography • Cell Differentiation
             • Cell Division • Cysteine • Melanins •
             Melanocyte-Stimulating Hormones • Mice • Mice,
             Inbred C3H • Mice, Inbred C57BL • Mice, Inbred
             Strains • Minoxidil • Pigments, Biological •
             Protein Binding • Thymidine • Vibrissae •
             drug effects • metabolism • metabolism* •
             pharmacokinetics* • pharmacology},
   Abstract = {To identify minoxidil target cells in hair follicles we
             followed the uptake of radiolabeled drug in mouse vibrissae
             follicles both in vitro and in vivo. Autoradiography showed
             that both 3H-minoxidil and 3H-minoxidil sulfate accumulated
             in the differentiating epithelial matrix cells superior to
             the dermal papilla, a distribution similar to that of
             pigment. Minoxidil localized in melanocytes, melanocyte
             processes, and areas of greater melanin concentrations
             within the epithelial cells. Although uptake of minoxidil
             was significantly less in unpigmented follicles, the drug
             stimulated proliferation and differentiation of both
             pigmented and unpigmented follicles. Labeled minoxidil bound
             to Sepia melanin and was displaced with unlabeled minoxidil
             and other electron donor drugs. This interaction with
             melanin acts as a targeting mechanism of minoxidil to
             pigmented hair follicles but has no apparent functional
             significance in hair growth. This work illustrates how
             measurement of drugs in hair may be biased by
             pigmentation.},
   Language = {eng},
   Key = {fds174260}
}

@booklet{Choi01,
   Author = {Y. S. Choi and G. A. Johnson and R. C. Burghardt and L. R.
             Berghman and M. M. Joyce and K. M. Taylor and M. D. Stewart and F. W. Bazer and T. E. Spencer},
   Title = {Interferon regulatory factor-two restricts expression of
             interferon-stimulated genes to the endometrial stroma and
             glandular epithelium of the ovine uterus},
   Journal = {Biology Of Reproduction},
   Volume = {65},
   Number = {4},
   Pages = {1038 -- 1049},
   Year = {2001},
   Month = {October},
   Key = {Choi01}
}

@article{fds174124,
   Author = {Y Choi and GA Johnson and RC Burghardt and LR Berghman and MM Joyce and KM
             Taylor, MD Stewart and FW Bazer and TE Spencer},
   Title = {Interferon regulatory factor-two restricts expression of
             interferon-stimulated genes to the endometrial stroma and
             glandular epithelium of the ovine uterus.},
   Journal = {Biology of reproduction},
   Volume = {65},
   Number = {4},
   Pages = {1038-49},
   Year = {2001},
   Month = {October},
   ISSN = {0006-3363},
   Keywords = {Animals • DNA-Binding Proteins • Endometrium
             • Epithelium • Estrous Cycle • Female •
             Fluorescent Antibody Technique • Gene Expression*
             • Interferon Regulatory Factor-1 • Interferon
             Regulatory Factor-2 • Interferon Type I •
             Interferon-Stimulated Gene Factor 3 • Interferons
             • Phosphoproteins • Pregnancy Proteins •
             Promoter Regions, Genetic • RNA, Messenger •
             Recombinant Proteins • Repressor Proteins* • STAT1
             Transcription Factor • STAT2 Transcription Factor
             • Sheep* • Stromal Cells • Trans-Activators
             • Transcription Factors • Transcriptional
             Activation • Transfection • Uterus • analysis
             • drug effects • genetics • metabolism •
             metabolism* • pharmacology • pharmacology* •
             physiology • physiology*},
   Abstract = {Interferon tau (IFNtau) is the signal for maternal
             recognition of pregnancy in ruminants. The positive effects
             of IFNtau on IFN-stimulated gene (ISG) expression are
             mediated by ISG factor 3 (ISGF3), which is composed of
             signal transducer and activator of transcription (Stat) 1,
             Stat 2, and IFN regulatory factor-9 (IRF-9), and by
             gamma-activated factor (GAF), which is a Stat 1 homodimer.
             Induction of ISGs, such as ISG17 and 2',5'-oligoadenylate
             synthetase, by IFNtau during pregnancy is limited to the
             endometrial stroma (S) and glandular epithelium (GE) of the
             ovine uterus. The IRF-2, a potent transcriptional repressor
             of ISG expression, is expressed in the luminal epithelium
             (LE). This study determined effects of the estrous cycle,
             pregnancy, and IFNtau on expression of Stat 1, Stat 2,
             IRF-9, IRF-1, and IRF-2 genes in the ovine endometrium. In
             cyclic ewes, Stat 1, Stat 2, IRF-1, and IRF-9 mRNA and
             protein were detected at low levels in the S and GE. During
             pregnancy, expression of these genes increased only in the S
             and GE. Expression of IRF-2 was detected only in the LE and
             superficial GE (sGE) of both cyclic and pregnant ewes. In
             cyclic ewes, intrauterine administration of IFNtau
             stimulated Stat 1, Stat 2, IRF-9, and IRF-1 expression in
             the endometrium. Ovine IRF-2 repressed transcriptional
             activity driven by IFN-stimulated response elements that
             bind ISGF3, but not by gamma-activation sequences that bind
             GAF. These results suggest that IRF-2 in the LE and sGE
             restricts IFNtau induction of ISGs to the S and GE. In the S
             and GE, IFNtau hyperactivation of ISG expression likely
             involves formation and actions of the transcription factors
             ISGF3 and, perhaps, IRF-1.},
   Language = {eng},
   Key = {fds174124}
}

@article{fds174113,
   Author = {MM Joyce and FJ White and RC Burghardt and JJ Muñiz and TE Spencer and FW
             Bazer, GA Johnson},
   Title = {Interferon stimulated gene 15 conjugates to endometrial
             cytosolic proteins and is expressed at the uterine-placental
             interface throughout pregnancy in sheep.},
   Journal = {Endocrinology},
   Volume = {146},
   Number = {2},
   Pages = {675-84},
   Year = {2005},
   Month = {February},
   ISSN = {0013-7227},
   url = {http://dx.doi.org/10.1210/en.2004-1224},
   Keywords = {Animals • Blotting, Western • Cytokines •
             Cytosol • Endometrium • Female • Gene
             Expression • Immunohistochemistry • In Situ
             Hybridization • Interferon Type I • Male •
             Placenta • Pregnancy • Pregnancy Proteins •
             RNA, Messenger • Sheep • Ubiquitin • analogs
             & derivatives* • analysis • genetics •
             genetics* • metabolism • metabolism* •
             physiology*},
   Abstract = {Interferon-stimulated gene 15 (ISG15) is a ubiquitin homolog
             expressed in uteri of ruminants in response to interferon
             (IFN)-tau and is also induced during pregnancy in the uteri
             of mice, pigs, humans, and baboons. This study examined
             expression of ISG15 and its conjugation to target proteins
             in the ovine uterus beyond the period of IFNtau secretion by
             the conceptus. Although steady-state levels of ISG15 mRNA
             decreased after d 25 of pregnancy, ISG15 persisted in
             endometrium through d 120. In situ hybridization and
             immunocytochemistry localized ISG15 across the entire
             uterine wall through d 25, after which expression was
             restricted to endometrial stroma along the
             maternal-placental interface. Western blots revealed ISG15
             and ISG15-conjugated proteins in endometrium. Treatment of
             ovariectomized sheep with progesterone and IFNtau increased
             both free and conjugated ISG15. These results are the first
             to show in vivo regulation of ISG15 function (i.e.
             conjugation to target proteins) by a type I IFN in the
             uterus of any species and that ISG15 is expressed at
             contacts between the placenta and uterus when trophectoderm
             no longer produces IFNtau. Interestingly, mRNA for the type
             II IFNgamma was present in the endometrial stromal
             compartment on d 15-50, which may stimulate the synthesis of
             ISG15 through later pregnancy. We hypothesize that ISG15 is
             not merely a consequence of an antiviral state induced by
             trophoblast IFNtau but represents a critical component of
             the microenvironment at the uterine-placental interface
             during the progressive events of conceptus development,
             implantation, and placentation in sheep and perhaps other
             mammalian species.},
   Language = {eng},
   Doi = {10.1210/en.2004-1224},
   Key = {fds174113}
}

@booklet{Bazer00,
   Author = {F. W. Bazer and J. A. G. W. Fleming and G. A. Johnson and Y.
             S. Choi and M. D. Stewart and T. E. Spencer},
   Title = {Interferon tau inhibits transcription of the ovine estrogen
             receptor alpha gene: Involvement of STATs and
             IRFs.},
   Journal = {Biology Of Reproduction},
   Volume = {62},
   Pages = {292 -- 292},
   Year = {2000},
   Key = {Bazer00}
}

@booklet{Joyce02,
   Author = {M. M. Joyce and T. R. Hansen and G. A. Johnson},
   Title = {Interferon-stimulated gene 17 is expressed in the porcine
             uterus and may be critical to placental development across
             species.},
   Journal = {Biology Of Reproduction},
   Volume = {66},
   Pages = {185 -- 186},
   Year = {2002},
   Key = {Joyce02}
}

@booklet{Joyce03,
   Author = {M. M. Joyce and R. C. Burghardt and F. W. Bazer and G. M.
             Zaunbrecher and G. A. Johnson},
   Title = {Interferon-stimulated genes (ISGs) are induced in the
             endometrium of pregnant but not pseudopregnant
             pigs.},
   Journal = {Biology Of Reproduction},
   Volume = {68},
   Pages = {206 -- 206},
   Year = {2003},
   Key = {Joyce03}
}

@booklet{Stewart01,
   Author = {M. D. Stewart and G. A. Johnson and F. W. Bazer and T. E.
             Spencer},
   Title = {Interferon-tau (IFN tau) regulation of IFN-stimulated gene
             expression in cell lines lacking specific IFN-signaling
             components},
   Journal = {Endocrinology},
   Volume = {142},
   Number = {5},
   Pages = {1786 -- 1794},
   Year = {2001},
   Month = {May},
   Key = {Stewart01}
}

@article{fds174144,
   Author = {MD Stewart and GA Johnson and FW Bazer and TE Spencer},
   Title = {Interferon-tau (IFNtau) regulation of IFN-stimulated gene
             expression in cell lines lacking specific IFN-signaling
             components.},
   Journal = {Endocrinology},
   Volume = {142},
   Number = {5},
   Pages = {1786-94},
   Year = {2001},
   Month = {May},
   ISSN = {0013-7227},
   Keywords = {2',5'-Oligoadenylate Synthetase • Cell Line •
             DNA-Binding Proteins • Fibroblasts • Gene
             Expression Regulation • Humans • Interferon Type I
             • Interferon-Stimulated Gene Factor 3 •
             Interferon-Stimulated Gene Factor 3, gamma Subunit •
             Phosphorylation • Pregnancy Proteins • STAT1
             Transcription Factor • STAT2 Transcription Factor
             • STAT3 Transcription Factor • Trans-Activators
             • Transcription Factors • biosynthesis • drug
             effects* • genetics* • metabolism •
             pharmacology* • physiology},
   Abstract = {Interferon-tau (IFNtau) is a unique type I IFN secreted by
             the ruminant conceptus that acts in a paracrine manner on
             the endometrial epithelium to signal pregnancy recognition.
             In the ovine endometrium, IFNtau suppresses estrogen
             receptor alpha and oxytocin receptor gene expression, but
             increases or induces expression of IFN-simulated genes
             (ISGs), including signal transducer and activator of
             transcription-1 (STAT1), STAT2, ISG factor-3gamma
             (ISGF3gamma)/p48/IFN regulatory factor-9, and
             2',5'-oligoadenylate synthetase (OAS). Human fibroblast cell
             lines lacking specific IFN signaling components were
             employed to determine the roles of STAT1, STAT2, and
             ISGF3gamma in the effects of IFNtau on ISG protein
             expression. Results indicated that STAT1alpha or STAT1beta
             is required for IFNtau effects on STAT2, ISGF3gamma, and OAS
             (40/46, 69/71, and 100 kDa). STAT2 is required for effects
             on STAT1, ISGF3gamma, and all OAS forms. ISGF3gamma is
             required for effects of IFNtau on STAT2 and 40/46- and
             69/71-kDa OAS and plays a role in the effects of IFNtau on
             100-kDa OAS and STAT1. Mutation of Tyr(701), but not
             Ser(727), of STAT1 abolished the effects of IFNtau on ISG
             expression. Mutation of the SH2 domain of STAT1 abolished
             the effects of IFNtau on all ISGs and reduced increases in
             100-kDa OAS. These data illustrate the importance of
             transcription factors composed of STAT1, STAT2, and
             ISGF3gamma in the signaling pathway mediating the effects of
             IFNtau on ISG expression.},
   Language = {eng},
   Key = {fds174144}
}

@booklet{Stewart01a,
   Author = {D. M. Stewart and G. A. Johnson and C. A. Vyhlidal and R. C.
             Burghardt and S. H. Safe and L. Y. Yu-lee and F. W. Bazer and T. E. Spencer},
   Title = {Interferon-tau activates multiple signal transducer and
             activator of transcription proteins and has complex effects
             on interferon-responsive gene transcription in ovine
             endometrial epithelial cells},
   Journal = {Endocrinology},
   Volume = {142},
   Number = {1},
   Pages = {98 -- 107},
   Year = {2001},
   Month = {January},
   Key = {Stewart01a}
}

@article{fds174117,
   Author = {DM Stewart and GA Johnson and CA Vyhlidal and RC Burghardt and SH Safe and LY Yu-Lee and FW Bazer and TE Spencer},
   Title = {Interferon-tau activates multiple signal transducer and
             activator of transcription proteins and has complex effects
             on interferon-responsive gene transcription in ovine
             endometrial epithelial cells.},
   Journal = {Endocrinology},
   Volume = {142},
   Number = {1},
   Pages = {98-107},
   Year = {2001},
   Month = {January},
   ISSN = {0013-7227},
   Keywords = {Animals • Cell Nucleus • Cells, Cultured •
             DNA-Binding Proteins • Endometrium • Epithelial
             Cells • Female • Interferon Type I •
             Interferon-Stimulated Gene Factor 3 • Luciferases
             • Phosphorylation • Pregnancy Proteins •
             Promoter Regions, Genetic • Protein Transport •
             Recombinant Fusion Proteins • STAT1 Transcription
             Factor • STAT2 Transcription Factor • Sheep •
             Signal Transduction • Trans-Activators •
             Transcription Factors • Transcription, Genetic •
             Transfection • analysis • cytology • drug
             effects • genetics* • metabolism •
             metabolism* • pharmacology* • physiology •
             physiology*},
   Abstract = {Interferon-tau (IFNtau), a type I IFN produced by sheep
             conceptus trophectoderm, is the signal for maternal
             recognition of pregnancy. Although it is clear that IFNtau
             suppresses transcription of the estrogen receptor alpha and
             oxytocin receptor genes and induces expression of various
             IFN-stimulated genes within the endometrial epithelium,
             little is known of the signal transduction pathway activated
             by the hormone. This study determined the effects of IFNtau
             on signal transducer and activator of transcription (STAT)
             activation, expression, DNA binding, and transcriptional
             activation using an ovine endometrial epithelial cell line.
             IFNtau induced persistent tyrosine phosphorylation and
             nuclear translocation of STAT1 and -2 (10 min to 48 h), but
             transient phosphorylation and nuclear translocation of
             STAT3, -5a/b, and -6 (10 to <60 min). IFNtau increased
             expression of STAT1 and -2, but not STAT3, -5a/b, and -6.
             IFN-stimulated gene factor-3 and STAT1 homodimers formed and
             bound an IFN-stimulated response element (ISRE) and
             gamma-activated sequence (GAS) element, respectively. IFNtau
             increased transcription of GAS-driven promoters at 3 h, but
             suppressed their activity at 24 h. In contrast, the activity
             of an ISRE-driven promoter was increased at 3 and 24 h.
             These results indicate that IFNtau activates multiple STATs
             and has differential effects on ISRE- and GAS-driven gene
             transcription.},
   Language = {eng},
   Key = {fds174117}
}

@booklet{Johnson00d,
   Author = {G. A. Johnson and T. E. Spencer and R. C. Burghardt and M.
             M. Joyce and F. W. Bazer},
   Title = {Interferon-tau and progesterone regulate ubiquitin
             cross-reactive protein expression in the ovine
             uterus},
   Journal = {Biology Of Reproduction},
   Volume = {62},
   Number = {3},
   Pages = {622 -- 627},
   Year = {2000},
   Month = {March},
   Key = {Johnson00d}
}

@article{fds174133,
   Author = {GA Johnson and TE Spencer and RC Burghardt and MM Joyce and FW
             Bazer},
   Title = {Interferon-tau and progesterone regulate ubiquitin
             cross-reactive protein expression in the ovine
             uterus.},
   Journal = {Biology of reproduction},
   Volume = {62},
   Number = {3},
   Pages = {622-7},
   Year = {2000},
   Month = {March},
   ISSN = {0006-3363},
   Keywords = {Animals • Blotting, Western • Female •
             Hormone Antagonists • Hysterectomy • In Situ
             Hybridization • Interferon Type I • Pregnancy
             Proteins • Progesterone • Sheep • Ubiquitins
             • Uterus • analogs & derivatives* •
             antagonists & inhibitors • drug effects • genetics
             • metabolism • metabolism* • pharmacology
             • physiology},
   Abstract = {Ubiquitin cross-reactive protein (UCRP) is a functional
             ubiquitin homolog synthesized by the ruminant endometrium in
             response to conceptus-derived interferon-tau (IFNtau).
             Progesterone is required for IFNtau to exert antiluteolytic
             actions on the endometrium. Therefore, this study was
             designed to determine whether progesterone is requisite for
             IFNtau induction of UCRP expression within the ovine uterus.
             Cyclic ewes were ovariectomized and fitted with intrauterine
             (i.u.) catheters on Day 5 and treated daily with steroids
             (i.m.) and protein (i.u.) as follows: 1) progesterone (P,
             Days 5-24) and control serum proteins (CX, Days 11-24); 2) P
             and ZK 137.316 (ZK; progesterone receptor antagonist, Days
             11-24) and CX proteins; 3) P and recombinant ovine IFNtau
             (roIFNtau, Days 11-24); or 4) P and ZK and roIFNtau. All
             ewes were hysterectomized on Day 25. In P-treated ewes,
             roIFNtau increased endometrial UCRP mRNA and protein levels.
             However, administration of ZK to ewes ablated roIFNtau
             induction of UCRP. Recombinant ovine IFNtau induced
             expression of UCRP mRNA in progestinized endometrial luminal
             (LE) and glandular (GE) epithelium as well as in both
             stratum compactum and spongiosum layers of the stroma (ST).
             Progesterone receptor protein was located in endometrial ST,
             but not in LE and GE from these ewes. Results support the
             hypothesis that progesterone is required for IFNtau
             induction of type I IFN-responsive genes, such as UCRP, in
             the ruminant uterus.},
   Language = {eng},
   Key = {fds174133}
}

@booklet{Staggs97,
   Author = {K. L. Staggs and K. J. Austin and G. A. Johnson and C. T.
             Talbott and T. R. Hansen},
   Title = {Interferon-tau may elicit specific responses in the
             endometrium through signal transduction pathways other than
             the Jak/Stat system.},
   Journal = {Biology Of Reproduction},
   Volume = {56},
   Pages = {159 -- 159},
   Year = {1997},
   Key = {Staggs97}
}

@article{fds174185,
   Author = {FW Bazer and RC Burghardt and GA Johnson and TE Spencer and G
             Wu},
   Title = {Interferons and progesterone for establishment and
             maintenance of pregnancy: interactions among novel cell
             signaling pathways.},
   Journal = {Reproductive biology},
   Volume = {8},
   Number = {3},
   Pages = {179-211},
   Year = {2008},
   Month = {November},
   ISSN = {1642-431X},
   Keywords = {Animals • Embryo Implantation • Estrogens •
             Female • Humans • Interferon Type I •
             Interferons • Pregnancy • Pregnancy Maintenance
             • Pregnancy Proteins • Progesterone • Signal
             Transduction • Swine • Uterus • drug effects
             • physiology • physiology*},
   Abstract = {Type I and/or type II interferons (IFNs) are important in
             establishing uterine receptivity to implantation in mammals.
             Gene expression effected by IFNs may be induced, stimulated
             or inhibited, but most are IFN-stimulated genes (ISGs).
             Effects of IFNs range from pregnancy recognition signaling
             in ruminants by IFN tau (IFNT) to effects on cellular
             functions of the uterus and uterine vasculature. For most,
             if not all, actions of IFNs on the uterus, progesterone
             (P(4)) is permissive to ISG expression, with genes being
             induced by IFN or induced by P(4) and stimulated by IFN.
             Uterine receptivity to implantation is P(4)-dependent;
             however, implantation events are preceded by loss of
             expression of progesterone (PGR) and estrogen (ESR1)
             receptors by uterine epithelia. Thus, P4 likely stimulates
             PGR-positive stromal cells to express one or more
             progestamedins, e.g., fibroblast growth factors-7 and -10,
             and/or hepatocyte growth factor, that act via their
             respective receptors on uterine epithelia and trophectoderm
             to regulate expression of ISGs. FGF10 appears to be the most
             important progestamedin in sheep uteri during pregnancy.
             Sequential effects of P(4) to induce and IFNs to stimulate
             gene expression suggest that P(4) and IFNs activate
             complimentary cell signaling pathways to modulate expression
             of genes for attachment of trophectoderm to uterine lumenal
             and superficial glandular epithelia (LE/sGE), modify
             phenotype of uterine stromal cells, silence PGR and ESR1
             genes, signal pregnancy recognition, suppress genes for
             immune recognition, alter membrane permeability to enhance
             conceptus-maternal exchange of factors, increase endometrial
             vascularity and activate genes for transport of nutrients
             into the uterine lumen. In ewes, IFNT abrogrates the uterine
             luteolytic mechanism and stimulates expression of classical
             ISGs by GE and stromal cells, whereas LE/sGE express
             P(4)-induced and IFNT-stimulated genes important for uterine
             receptivity to implantation and conceptus development. These
             include wingless-type MMTV (mouse mammary tumor virus)
             integration site family member 7A (WNT7A) induced by IFNT,
             as well as galectin, proteases, protease inhibitors,
             transporters for glucose and amino acids, gastrin releasing
             polypeptide, insulin-like growth factor binding protein 1
             and a hypoxia inducible factor. The specific functions of
             IFNs and ISGs induced in primates, pigs and other mammals
             during pregnancy are not known, but likely are important in
             establishment of pregnancy. Understanding the roles of IFNs
             and ISGs in uterine receptivity for implantation is
             necessary to develop strategies to enhance reproductive
             health and fertility in humans and domestic animals. The
             magnitude of the LH surge was reduced in cows receiving
             endotoxin.},
   Language = {eng},
   Key = {fds174185}
}

@article{fds174306,
   Author = {FW Bazer and TE Spencer and GA Johnson},
   Title = {Interferons and uterine receptivity.},
   Journal = {Seminars in reproductive medicine},
   Volume = {27},
   Number = {1},
   Pages = {90-102},
   Year = {2009},
   Month = {January},
   ISSN = {1526-4564},
   url = {http://dx.doi.org/10.1055/s-0028-1108013},
   Keywords = {Animals • Embryo Implantation • Estrogens •
             Female • Interferons • Models, Biological •
             Pregnancy • Primates • Rodentia • Ruminants
             • Swine • Uterus • physiology •
             physiology*},
   Abstract = {This article focuses on the potential roles of interferons
             (IFNs) in establishing uterine receptivity to implantation.
             A common feature of the peri-implantation period of
             pregnancy in most mammals is production of type I and/or
             type II IFNs by trophoblasts that induce and/or stimulate
             expression of an array of IFN-stimulate genes (ISGs). These
             effects range from pregnancy recognition signaling in
             ruminants through IFN tau to effects on cellular functions
             of the uterus and uterine vasculature. For actions of IFNs,
             progesterone (P4) is permissive to the expression of many
             effects and to the expression of ISGs that are induced
             directly by an IFN or induced by P4 and stimulated by an IFN
             in a temporal and/or cell-specific manner. Uterine
             receptivity to implantation is P4 dependent; however,
             implantation events are preceded by loss of expression of
             progesterone (PGR) and estrogen (ESR1) receptors by uterine
             epithelia. Therefore, P4 likely acts via PGR-positive
             stromal cells to induce expression of fibroblast growth
             factors-7 and -10 and/or hepatocyte growth factor
             (progestamedins) that then act via their respective
             receptors on uterine epithelia and trophectoderm to affect
             expression of ISGs. The permissive effects of P4 on the
             expression of ISGs and the effects of P4 to induce and IFNs
             to stimulate gene expression raise the question of whether
             uterine receptivity to implantation requires P4 and IFN to
             activate unique, but complementary, cell signaling pathways.
             Uterine receptivity to implantation, depending on species,
             involves changes in the expression of genes for the
             attachment of trophectoderm to the uterine lumenal
             epithelium (LE) and superficial glandular epithelium (sGE),
             modification of the phenotype of uterine stromal cells, the
             silencing of PGR and ESR1 genes, the suppression of genes
             for immune recognition, alterations in membrane permeability
             to enhance conceptus-maternal exchange of factors, increased
             vascularity of the endometrium, activation of genes for
             transport of nutrients into the uterine lumen, and enhanced
             signaling for pregnancy recognition. Differential expression
             of genes by uterine LE/sGE, mid- to deep-glandular epithelia
             (GE), and stromal cells in response to P4 and IFNs is likely
             to influence uterine receptivity to implantation in most
             mammals. Understanding the roles of IFNs in uterine
             receptivity for implantation is necessary to develop
             approaches to enhance reproductive health and fertility in
             humans and domestic animals.},
   Language = {eng},
   Doi = {10.1055/s-0028-1108013},
   Key = {fds174306}
}

@article{fds268849,
   Author = {Goddeeris, MM and Rho, S and Petiet, A and Davenport, CL and Johnson,
             GA and Meyers, EN and Klingensmith, J},
   Title = {Intracardiac septation requires hedgehog-dependent cellular
             contributions from outside the heart.},
   Journal = {Development},
   Volume = {135},
   Number = {10},
   Pages = {1887-1895},
   Year = {2008},
   Month = {May},
   ISSN = {0950-1991},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/18441277},
   Keywords = {Animals • Fetal Heart • Heart Atria • Heart
             Septal Defects, Ventricular • Hedgehog Proteins •
             Mesoderm • Mice • Mice, Mutant Strains •
             Mutation • Signal Transduction • cytology •
             cytology* • embryology • genetics •
             metabolism*},
   Abstract = {Septation of the mammalian heart into four chambers requires
             the orchestration of multiple tissue progenitors.
             Abnormalities in this process can result in potentially
             fatal atrioventricular septation defects (AVSD). The
             contribution of extracardiac cells to atrial septation has
             recently been recognized. Here, we use a genetic marker and
             novel magnetic resonance microscopy techniques to
             demonstrate the origins of the dorsal mesenchymal protrusion
             in the dorsal mesocardium, and its substantial contribution
             to atrioventricular septation. We explore the functional
             significance of this tissue to atrioventricular septation
             through study of the previously uncharacterized AVSD
             phenotype of Shh(-/-) mutant mouse embryos. We demonstrate
             that Shh signaling is required within the dorsal mesocardium
             for its contribution to the atria. Failure of this addition
             results in severe AVSD. These studies demonstrate that AVSD
             can result from a primary defect in dorsal mesocardium,
             providing a new paradigm for the understanding of human
             AVSD.},
   Doi = {10.1242/dev.016147},
   Key = {fds268849}
}

@article{fds174231,
   Author = {DA Massuto and RN Hooper and EC Kneese and GA Johnson and NH Ing and BR
             Weeks, LA Jaeger},
   Title = {Intrauterine infusion of latency-associated peptide (LAP)
             during early porcine pregnancy affects conceptus elongation
             and placental size.},
   Journal = {Biology of reproduction},
   Volume = {82},
   Number = {3},
   Pages = {534-42},
   Year = {2010},
   Month = {March},
   ISSN = {1529-7268},
   url = {http://dx.doi.org/10.1095/biolreprod.109.081893},
   Abstract = {In the pig, transforming growth factor beta (TGFB), TGFB
             receptors (TGFBRs), and integrins are present during the
             peri-implantation period. Latency-associated peptide (LAP),
             a part of latent TGFB, can bind to integrin heterodimers via
             its Arg-Gly-Asp (RGD) sequence; therefore, ligand-receptor
             interactions between TGFB and TGFBRs, along with LAP and
             integrin heterodimers, may be functional in mediating events
             supporting conceptus elongation and attachment. With the use
             of surgically implantable osmotic pumps, we were able to
             maintain pregnancy with the aim of mechanistically altering
             in vivo receptor-ligand interactions involving TGFB with
             TGFBRs and LAP with integrins during porcine pregnancy. Day
             9 pregnant gilts received intrauterine infusions of LAP-RGD,
             a recombinant mutant of LAP (LAP-RGE), or vehicle control
             and were ovariohysterectomized on Day 13 or 24 of pregnancy.
             We hypothesized that intrauterine infusion of LAP-RGD would
             decrease downstream signaling of TGFB while increasing
             LAP-integrin interactions and that net effect would enhance
             conceptus survival and attachment early in the
             peri-implantation period but possibly increase the chance of
             abnormal placentation later in pregnancy. Additionally, we
             hypothesized that infusion of LAP-RGE would disrupt TGFB
             signals but not alter integrin signaling, and thus the net
             result would be decreased conceptus survival and abnormal
             development. Unexpectedly, LAP-RGD intrauterine infusions
             resulted in a reduction of conceptus elongation, whereas
             infusions of LAP-RGE permitted implantation and placentation
             but resulted in larger fetal weight, allantois length, and
             allantoic fluid volume. Results suggest TGFB and integrins
             are contributing factors in the regulation of conceptus
             elongation and placental and fetal size.},
   Language = {eng},
   Doi = {10.1095/biolreprod.109.081893},
   Key = {fds174231}
}

@booklet{Johnson85c,
   Author = {G. A. Johnson},
   Title = {Inverse no-matrices},
   Journal = {Linear Algebra And Its Applications},
   Volume = {64},
   Number = {JAN},
   Pages = {215 -- 222},
   Year = {1985},
   Key = {Johnson85c}
}

@article{fds268712,
   Author = {Calabrese, E and Badea, A and Coe, CL and Lubach, GR and Styner, MA and Johnson, GA},
   Title = {Investigating the tradeoffs between spatial resolution and
             diffusion sampling for brain mapping with diffusion
             tractography: time well spent?},
   Journal = {Hum Brain Mapp},
   Volume = {35},
   Number = {11},
   Pages = {5667-5685},
   Year = {2014},
   Month = {November},
   ISSN = {1065-9471},
   url = {http://dx.doi.org/10.1002/hbm.22578},
   Abstract = {Interest in mapping white matter pathways in the brain has
             peaked with the recognition that altered brain connectivity
             may contribute to a variety of neurologic and psychiatric
             diseases. Diffusion tractography has emerged as a popular
             method for postmortem brain mapping initiatives, including
             the ex-vivo component of the human connectome project, yet
             it remains unclear to what extent computer-generated tracks
             fully reflect the actual underlying anatomy. Of particular
             concern is the fact that diffusion tractography results vary
             widely depending on the choice of acquisition protocol. The
             two major acquisition variables that consume scan time,
             spatial resolution, and diffusion sampling, can each have
             profound effects on the resulting tractography. In this
             analysis, we determined the effects of the temporal tradeoff
             between spatial resolution and diffusion sampling on
             tractography in the ex-vivo rhesus macaque brain, a close
             primate model for the human brain. We used the wealth of
             autoradiography-based connectivity data available for the
             rhesus macaque brain to assess the anatomic accuracy of six
             time-matched diffusion acquisition protocols with varying
             balance between spatial and diffusion sampling. We show that
             tractography results vary greatly, even when the subject and
             the total acquisition time are held constant. Further, we
             found that focusing on either spatial resolution or
             diffusion sampling at the expense of the other is
             counterproductive. A balanced consideration of both sampling
             domains produces the most anatomically accurate and
             consistent results.},
   Doi = {10.1002/hbm.22578},
   Key = {fds268712}
}

@article{fds359552,
   Author = {Johnson, GA and O’Foghludha, F},
   Title = {Investigation of transmolybdenum fluorescent anodes for
             mammography},
   Journal = {Proceedings of SPIE - The International Society for Optical
             Engineering},
   Volume = {233},
   Pages = {158-163},
   Year = {1980},
   Month = {August},
   url = {http://dx.doi.org/10.1117/12.958917},
   Abstract = {Recent work has suggested a new approach to film/screen
             mammography through the use of transmolybdenum (Z > 42)
             fluorescent anodes. An experimental rhodium (Z = 45) anode
             with K emission at 20.0 - 23.2 keV has been compared to a
             conventional molybdenum anode. Previous spectral
             measurements have indicated a dose advantage for the Rh
             anode but no comparison of contrast has been made. A series
             of step wedges of different materials was imaged at several
             kVp and for several phantom thicknesses. The resulting data
             permits quantitative comparison of the radiographic
             contrast. At 40 kVp for an equivalent tissue thickness of
             4.8 cm the radiographic contrast provided by the Rh anode is
             at least equal to and under some conditions actually
             superior to that provided by a Mo anode. © 1980
             SPIE.},
   Doi = {10.1117/12.958917},
   Key = {fds359552}
}

@article{fds268787,
   Author = {Badea, CT and Stanton, IN and Johnston, SM and Johnson, GA and Therien,
             MJ},
   Title = {Investigations on X-ray luminescence CT for small animal
             imaging.},
   Journal = {Proc SPIE Int Soc Opt Eng},
   Volume = {8313},
   Pages = {83130T},
   Year = {2012},
   ISSN = {0277-786X},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/23227300},
   Abstract = {X-ray Luminescence CT (XLCT) is a hybrid imaging modality
             combining x-ray and optical imaging in which x-ray
             luminescent nanophosphors (NPs) are used as emissive imaging
             probes. NPs are easily excited using common CT energy x-ray
             beams, and the NP luminescence is efficiently collected
             using sensitive light based detection systems. XLCT can be
             recognized as a close analog to fluorescence diffuse optical
             tomography (FDOT). However, XLCT has remarkable advantages
             over FDOT due to the substantial excitation penetration
             depths provided by x-rays relative to laser light sources,
             long term photo-stability of NPs, and the ability to tune NP
             emission within the NIR spectral window. Since XCLT uses an
             x-ray pencil beam excitation, the emitted light can be
             measured and back-projected along the x-ray path during
             reconstruction, where the size of the X-ray pencil beam
             determines the resolution for XLCT. In addition, no
             background signal competes with NP luminescence (i.e., no
             auto fluorescence) in XLCT. Currently, no small animal XLCT
             system has been proposed or tested. This paper investigates
             an XLCT system built and integrated with a dual source
             micro-CT system. Two novel sampling paradigms that result in
             more efficient scanning are proposed and tested via
             simulations. Our preliminary experimental results in
             phantoms indicate that a basic CT-like reconstruction is
             able to recover a map of the NP locations and differences in
             NP concentrations. With the proposed dual source system and
             faster scanning approaches, XLCT has the potential to
             revolutionize molecular imaging in preclinical
             studies.},
   Doi = {10.1117/12.911465},
   Key = {fds268787}
}

@booklet{Maynor88,
   Author = {MAYNOR, CH and CHARLES, HC and HERFKENS, RJ and SUDDARTH, SA and JOHNSON, GA},
   Title = {INVITRO CHEMICAL-SHIFT IMAGING OF ATHEROSCLEROSIS AT
             7.0-TESLA},
   Journal = {INVESTIGATIVE RADIOLOGY},
   Volume = {23},
   Number = {9},
   Pages = {S3-S3},
   Publisher = {LIPPINCOTT-RAVEN PUBL},
   Year = {1988},
   Month = {September},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1988Q574500021&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Maynor88}
}

@booklet{Thompson80,
   Author = {Thompson, WM and Amberg, JR and Shaw, M},
   Title = {Iodine concentration and radiographic density during oral
             cholecystography},
   Journal = {Investigative Radiology},
   Volume = {15},
   Number = {5},
   Pages = {397},
   Publisher = {Ovid Technologies (Wolters Kluwer Health)},
   Year = {1980},
   Month = {January},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1980KK17000048&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Doi = {10.1097/00004424-198009000-00049},
   Key = {Thompson80}
}

@booklet{Waldon89,
   Author = {D. J. Waldon and A. E. Buhl and C. A. Baker and G. A.
             Johnson},
   Title = {Is minoxidil sulfate the active metabolite for
             hair-growth},
   Journal = {Clinical Research},
   Volume = {37},
   Number = {2},
   Pages = {A769 -- A769},
   Year = {1989},
   Month = {April},
   Key = {Waldon89}
}

@booklet{Waldon89a,
   Author = {D. J. Waldon and A. E. Buhl and C. A. Baker and G. A.
             Johnson},
   Title = {Is minoxidil sulfate the active metabolite for
             hair-growth},
   Journal = {Journal Of Investigative Dermatology},
   Volume = {92},
   Number = {3},
   Pages = {538 -- 538},
   Year = {1989},
   Month = {March},
   Key = {Waldon89a}
}

@article{fds174206,
   Author = {GA JOHNSON and RH MCCLUER},
   Title = {ISOLATION AND ANALYSIS OF MONO-, DI-, AND
             TRISIALOGANGLIOSIDES.},
   Journal = {Biochimica et biophysica acta},
   Volume = {70},
   Pages = {487-90},
   Year = {1963},
   Month = {August},
   ISSN = {0006-3002},
   Keywords = {BRAIN* • CHROMATOGRAPHY* • EXPERIMENTAL LAB STUDY*
             • GANGLIOSIDES* • HEXOSAMINES* • HEXOSES*
             • NEURAMINIC ACIDS* • NEUROCHEMISTRY*},
   Language = {eng},
   Key = {fds174206}
}

@booklet{Wang00,
   Author = {G. Y. Wang and G. A. Johnson and T. E. Spencer and F. W.
             Bazer},
   Title = {Isolation, immortalization, and initial characterization of
             uterine cell lines: An in vitro model system for the porcine
             uterus},
   Journal = {In Vitro Cellular \& Developmental Biology-animal},
   Volume = {36},
   Number = {10},
   Pages = {650 -- 656},
   Year = {2000},
   Key = {Wang00}
}

@article{fds174283,
   Author = {G Wang and GA Johnson and TE Spencer and FW Bazer},
   Title = {Isolation, immortalization, and initial characterization of
             uterine cell lines: an in vitro model system for the porcine
             uterus.},
   Journal = {In vitro cellular & developmental biology.
             Animal},
   Volume = {36},
   Number = {10},
   Pages = {650-6},
   Year = {2001},
   Month = {May},
   ISSN = {1071-2690},
   Keywords = {Animals • Blotting, Western • Cell Division •
             Cell Line, Transformed • Female • Models,
             Biological* • Swine • Uterus •
             cytology*},
   Abstract = {The aim of this study was to develop immortalized cell lines
             from porcine uterus. Endometrial cells including luminal
             epithelium (LE), glandular epithelium (GE), stroma (ST), and
             myometrium (MYO) were enzymatically isolated from the uterus
             of a day 12 pregnant gilt. Primary cultures were
             immortalized by transduction with a retroviral vector
             containing the E6 and E7 open reading frames of human
             papillomavirus type 16 (LXSN-16E6E7) packaged by the
             amphotropic fibroblast line PA-317. Cells having integrated
             the vector were selected by resistance to the neomycin
             analog G418 (0.4-1.5 mg/ml). Surviving cells were maintained
             in complete culture medium containing G418 (0.1 mg/ml) and
             subcultured for 1 yr. Expression of the E7 protein was
             confirmed in all cell lines by Western blotting. Phase
             contrast microscopy revealed that LE and GE cells exhibited
             cobblestone morphology, whereas ST and MYO cells exhibited
             spindle-shaped morphology. The epithelial origin of LE and
             GE was confirmed by positive immunostaining for cytokeratin.
             Stromal and MYO cells were vimentin-positive, but
             cytokeratin-negative. The MYO cell lines were positive for
             smooth muscle alpha-actin staining, whereas LE, GE, and ST
             cell lines were negative for alpha-actin. Western blotting
             indicated that all cell lines expressed both estrogen and
             progesterone receptors, but only GE cells secreted
             uteroferrin (UF). Collectively, these porcine uterine cell
             lines provide an in vitro model for studying cell
             type-specific actions of hormones and cytokines, signal
             transduction pathways, cell-cell interactions, and gene
             expression.},
   Language = {eng},
   Key = {fds174283}
}

@article{fds132741,
   Author = {G.A. Johnson},
   Title = {J.R. MacFall, H.C.Charles, R.D. Black, H. Middleton,
             J.Swartz, B. Saam,   B. Dreihuys, C. Erickson, W. Happer,
             G. Cates, G.A. Johnson, C.E. Ravin.   Human lung air
             spaces: potential for MR imaging with hyperpolarized He-3.
               Radiology 200, 553-558. (1996).},
   Year = {1996},
   Key = {fds132741}
}

@article{fds132742,
   Author = {G.A. Johnson},
   Title = {J.R. MacFall, H.C.Charles, R.D. Black, H. Middleton,
             J.Swartz, B. Saam,   W. Happer, G. Cates, G.A. Johnson,
             C.E. Ravin. MR imaging of lung air  spaces with
             hyperpolarized 3He.  in "Proc., SMR 4th Annual Scientific
              Meeting.  New York, NY, 1996," p. 21.},
   Year = {1996},
   Key = {fds132742}
}

@article{fds132722,
   Author = {G.A. Johnson},
   Title = {J.S. MacFall, G.A. Johnson, in "Encyclopedia of Nuclear
             Magnetic  Resonance" (D.M. Grant, R.K. Harris, Ed.), p.
             3633-3640, John Wiley &  Sons, London, 1996.},
   Year = {1996},
   Key = {fds132722}
}

@article{fds132746,
   Author = {G.A. Johnson},
   Title = {Johnson GA, Hedlund LW, MacFall JR. A new window into the
             lung. Physics in Medicine 35-38 1998},
   Year = {1998},
   Key = {fds132746}
}

@booklet{Ka01,
   Author = {H. Ka and L. A. Jaeger and G. A. Johnson and T. E. Spencer and F. W. Bazer},
   Title = {Keratinocyte growth factor is up-regulated by estrogen in
             the porcine uterine endometrium and functions in
             trophectoderm cell proliferation and differentiation},
   Journal = {Endocrinology},
   Volume = {142},
   Number = {6},
   Pages = {2303 -- 2310},
   Year = {2001},
   Month = {June},
   Key = {Ka01}
}

@article{fds174110,
   Author = {H Ka and LA Jaeger and GA Johnson and TE Spencer and FW
             Bazer},
   Title = {Keratinocyte growth factor is up-regulated by estrogen in
             the porcine uterine endometrium and functions in
             trophectoderm cell proliferation and differentiation.},
   Journal = {Endocrinology},
   Volume = {142},
   Number = {6},
   Pages = {2303-10},
   Year = {2001},
   Month = {June},
   ISSN = {0013-7227},
   Keywords = {Animals • Cell Differentiation • Cell Division
             • Culture Techniques • Endometrium • Enzyme
             Activation • Estradiol • Estrogens •
             Estrogens, Catechol • Female • Fibroblast Growth
             Factor 7 • Fibroblast Growth Factors • Gene
             Expression Regulation • Gestational Age •
             Mitogen-Activated Protein Kinase 1 • Mitogen-Activated
             Protein Kinase 3 • Mitogen-Activated Protein Kinases
             • Phosphorylation • Pregnancy • Progesterone
             • Proliferating Cell Nuclear Antigen • Receptor,
             Fibroblast Growth Factor, Type 2 • Receptors,
             Fibroblast Growth Factor* • Receptors, Growth Factor
             • Recombinant Proteins • Swine* •
             Trophoblasts • analysis • cytology • drug
             effects • genetics* • metabolism •
             metabolism* • pharmacology • pharmacology*},
   Abstract = {Keratinocyte growth factor (KGF) is expressed by uterine
             endometrial epithelial cells during the estrous cycle and
             during pregnancy in pigs, whereas KGF receptor is expressed
             in conceptus trophectoderm and endometrial epithelia. In
             particular, KGF expression in the endometrium is highest on
             day 12 of pregnancy. This corresponds to the period of
             maternal recognition of pregnancy in pigs, which is signaled
             by large amounts of estrogen secreted by conceptus
             trophectoderm acting on the endometrium. Our hypothesis is
             that estrogens of conceptus origin stimulate endometrial
             epithelial KGF expression, and, in turn, secreted KGF
             stimulates proliferation and differentiation of conceptus
             trophectoderm. To determine the factors affecting KGF
             expression in the uterus, endometrial explants from gilts on
             day 9 of the estrous cycle were cultured in the presence of
             17beta-estradiol, catechol estrogens, or progesterone.
             17beta-Estradiol stimulated the expression of KGF (P <
             0.05), whereas catechol estrogens had no effect (P > 0.05).
             Between days 9 and 15 of pregnancy, proliferating cell
             nuclear antigen was abundant in conceptuses, but was barely
             detectable in uterine endometrial epithelia. To determine
             the effects of KGF on conceptus trophectoderm, porcine
             trophectoderm (pTr) cells were treated with recombinant rat
             KGF (rKGF). rKGF increased the proliferation of pTr cells (P
             < 0.01) as measured by [(3)H]thymidine incorporation. rKGF
             elicited phosphorylation of KGF receptor and activated the
             mitogen-activated protein kinase (ERK1/2) cascade in pTr
             cells. pTr cell differentiation was affected by rKGF,
             because it increased expression of urokinase-type
             plasminogen activator, a marker for differentiation in pTr
             cells. Collectively, these results indicate that estrogen,
             the pregnancy recognition signal from the conceptus in pigs,
             increases uterine epithelial KGF expression, and, in turn,
             KGF stimulates the proliferation and differentiation of
             conceptus trophectoderm.},
   Language = {eng},
   Key = {fds174110}
}

@booklet{Ka00a,
   Author = {H. Ka and T. E. Spencer and G. A. Johnson and F. W.
             Bazer},
   Title = {Keratinocyte growth factor: Expression by endometrial
             epithelia of the porcine uterus},
   Journal = {Biology Of Reproduction},
   Volume = {62},
   Number = {6},
   Pages = {1772 -- 1778},
   Year = {2000},
   Month = {June},
   Key = {Ka00a}
}

@article{fds174080,
   Author = {H Ka and TE Spencer and GA Johnson and FW Bazer},
   Title = {Keratinocyte growth factor: expression by endometrial
             epithelia of the porcine uterus.},
   Journal = {Biology of reproduction},
   Volume = {62},
   Number = {6},
   Pages = {1772-8},
   Year = {2000},
   Month = {June},
   ISSN = {0006-3363},
   Keywords = {Animals • Blotting, Northern • Cloning, Molecular
             • DNA, Complementary • Endometrium •
             Epithelium • Estrus • Female • Fibroblast
             Growth Factor 10 • Fibroblast Growth Factor 7 •
             Fibroblast Growth Factors* • Gene Expression* •
             Growth Substances • In Situ Hybridization •
             Pregnancy • RNA, Messenger • Swine* •
             analysis • genetics* • metabolism •
             metabolism*},
   Abstract = {Keratinocyte growth factor/fibroblast growth factor-7
             (KGF/FGF-7) is an established paracrine mediator of
             hormone-regulated epithelial growth and differentiation. In
             all organs studied, KGF is uniquely expressed in cells of
             mesenchymal origin. To determine whether KGF and its
             receptor, keratinocyte growth factor receptor (KGFR) or
             fibroblast growth factor receptor-2IIIb, were expressed in
             the porcine uterus as a potential paracrine system mediating
             progesterone action, we cloned KGF and KGFR partial cDNAs
             from the porcine endometrium. KGF and KGFR expression was
             detected in endometrium by Northern blot hybridization.
             Interestingly, in situ hybridization results demonstrated
             that KGF was expressed by endometrial epithelia and was
             particularly abundant between Days 12 and 15 of the estrous
             cycle and pregnancy. KGF secretion into the lumen of the
             porcine uterus was also detected on Day 12 of the estrous
             cycle and pregnancy. KGFR was expressed in both endometrial
             epithelia and conceptus trophectoderm. These novel findings
             suggest that KGF may act on the uterine endometrial
             epithelium in an autocrine manner and on the conceptus
             trophectoderm in a paracrine manner in the pig, which is the
             only species possessing a true epitheliochorial type of
             placentation.},
   Language = {eng},
   Key = {fds174080}
}

@article{fds132719,
   Author = {G.A. Johnson},
   Title = {L.W. Hedlund, M.D. Shattuck, G.A. Johnson.
              Three-dimensional MR  microscopy of pulmonary dynamics.
              in "Proc., 1996.  New York, NY,  1996,"
             p.327.},
   Year = {1996},
   Key = {fds132719}
}

@article{fds132736,
   Author = {G.A. Johnson},
   Title = {L.W. Hedlund, S.L. Gewalt, G.P. Cofer, G.A. Johnson, in
             "Application of  Magnetic Resonance to the Study of the
             Lung" (A. Cutillo, Ed.), p. 401-415,  Futura Press, Mt.
             Kisko, NY, 1996.},
   Year = {1996},
   Key = {fds132736}
}

@booklet{Shen-gunther98,
   Author = {J. Shen-gunther and R. S. Mannel and J. L. Walker and G. A.
             Johnson and A. E. Sienko},
   Title = {Laparoscopic paraaortic lymphadenectomy using laparosonic
             coagulating shears},
   Journal = {Journal Of The American Association Of Gynecologic
             Laparoscopists},
   Volume = {5},
   Number = {1},
   Pages = {47 -- 50},
   Year = {1998},
   Month = {February},
   Key = {Shen-gunther98}
}

@article{fds174302,
   Author = {J Shen-Gunther and RS Mannel and JL Walker and GA Johnson and AE
             Sienko},
   Title = {Laparoscopic paraaortic lymphadenectomy using laparosonic
             coagulating shears.},
   Journal = {The Journal of the American Association of Gynecologic
             Laparoscopists},
   Volume = {5},
   Number = {1},
   Pages = {47-50},
   Year = {1998},
   Month = {February},
   ISSN = {1074-3804},
   Keywords = {Adult • Carcinoma, Squamous Cell • Female •
             Hemostasis, Surgical • Humans • Laparoscopes*
             • Laparoscopy • Lymph Node Excision • Middle
             Aged • Surgical Instruments • Time Factors •
             Ultrasonics • Uterine Cervical Neoplasms •
             instrumentation • methods • methods* •
             surgery},
   Abstract = {With marked innovations in endosurgical instrumentation,
             operative laparoscopy to include lymphadenectomy has become
             feasible and has a valuable role in the management of
             gynecologic malignancy. We used laparosonic coagulating
             shears (LCS) for laparoscopic paraaortic lymphadenectomy in
             two women with cervical carcinoma. Operating times for the
             laparoscopic portion were 55 and 65 minutes and blood loss
             was 20 and 30 ml, respectively. No surgical complications
             were encountered. Lymphatic tissues were evaluated
             histologically and no thermal artifacts were identified. The
             major advantage of the ultrasonically activated scalpel of
             the LCS is the ability to cut and coagulate tissues
             simultaneously without electrical current. The LCS may
             afford the surgeon a greater margin of safety than unipolar
             electrocoagulation scissors by eliminating potential thermal
             and electrical injury to vital structures.
             Ultrasonic-activated technology deserves extended clinical
             investigation in laparoscopic lymphadenectomy to
             substantiate our preliminary findings, as well as to explore
             its potential in gynecologic oncology.},
   Language = {eng},
   Key = {fds174302}
}

@booklet{Scribner02,
   Author = {D. R. Scribner and J. L. Walker and G. A. Johnson and D. S.
             Mcmeekin and M. A. Gold and R. S. Mannel},
   Title = {Laparoscopic pelvic and paraaortic lymph node dissection in
             the obese},
   Journal = {Gynecologic Oncology},
   Volume = {84},
   Number = {3},
   Pages = {426 -- 430},
   Year = {2002},
   Month = {March},
   Key = {Scribner02}
}

@article{fds174296,
   Author = {DR Scribner Jr and JL Walker and GA Johnson and DS McMeekin and MA Gold and RS Mannel},
   Title = {Laparoscopic pelvic and paraaortic lymph node dissection in
             the obese.},
   Journal = {Gynecologic oncology},
   Volume = {84},
   Number = {3},
   Pages = {426-30},
   Year = {2002},
   Month = {March},
   ISSN = {0090-8258},
   url = {http://dx.doi.org/10.1006/gyno.2001.6548},
   Keywords = {Adult • Aged • Aged, 80 and over • Aorta,
             Abdominal • Endometrial Neoplasms • Female •
             Humans • Laparoscopy • Lymph Node Excision •
             Lymphatic Metastasis • Middle Aged • Obesity
             • Pelvis • Retrospective Studies •
             complications • complications* • methods •
             methods* • pathology • surgery*},
   Abstract = {OBJECTIVE: The aim of this study was to determine the
             utility of laparoscopic pelvic and paraaortic lymph node
             dissection in obese women. METHODS: We performed a
             retrospective analysis from 1/8/96 to 1/14/01 at the
             University of Oklahoma Health Science Center, evaluating
             patients who had a Quetelet index (QI) > or =28 and had
             planned laparoscopic bilateral pelvic and paraaortic lymph
             node dissections (lnd) for their gynecologic cancer. This
             group was compared to a matched group of patients that had
             lnd done by laparotomy. Patients were identified by our
             institution's database and data were collected by review of
             their medical records. Data were collected regarding
             demographics, stage, histology, length of stay, and
             procedural information including completion rates, estimated
             blood loss (EBL), operating room (OR) time, lymph node
             count, assistant, and complications. Associations between
             variables were analyzed using Student t tests and chi(2)
             testing, Excel v9.0. RESULTS: Fifty-five patients had
             planned laparoscopic lnd (Group 1) and 45 patients had lnd
             via laparotomy (Group 2). All patients had the diagnosis of
             endometrial cancer. The percentage of stage I patients did
             not differ between groups (42/55, 71.2% versus 37/45, 82.2%,
             P = n.s.). Age and QI were also similar between groups,
             (64.6 versus 58.4, 40.0 versus 39.3, P = n.s.). Laparoscopy
             was completed in 35/55 (63.6%) cases. Reasons for conversion
             included obesity (23.6%), adhesions (1.8%), intraperitoneal
             cancer (5.5%), and bleeding (5.5%). QI > or =35 was
             associated with a decreased success rate compared to QI <35
             (44.4% versus 82.1%, P = 0.004). There was no difference in
             successful laparoscopy when the first assistant was a fellow
             or a community obstetrician/gynecologist (61.0% versus
             50.0%, P = n.s.). The patients in Group 1 who had
             laparoscopy completed had a longer OR time compared to those
             in Group 2 (265.3 versus 140.7 min, P < 0.0001), EBL and
             transfusion rates were equivalent (361.8 versus 344.2 ml,
             5.6% versus 6.7%, P = n.s.), and length of stay was shorter
             (2.8 versus 4.5 days, P = 0.0004). Group 1 had significantly
             fewer postoperative fevers (5.5% versus 31.1%, P = 0.0007),
             fewer postoperative ileus (0% versus 13.3%, P = 0.005), and
             a trend for fewer wound infections (9.0% versus 22.2%, P =
             0.07). CONCLUSIONS: Obesity is not a contraindication to
             laparoscopic pelvic and paraaortic lymph node dissection.
             The overall success rate was significantly higher in those
             patients with a QI <35. Advantages include shorter hospital
             stay, fewer postoperative fevers, fewer postoperative ileus,
             and possibly fewer wound infections.},
   Language = {eng},
   Doi = {10.1006/gyno.2001.6548},
   Key = {fds174296}
}

@booklet{Scribner01a,
   Author = {D. R. Scribner and J. L. Walker and G. A. Johnson and S. D.
             Mcmeekin and M. A. Gold and R. S. Mannel},
   Title = {Laparoscopic pelvic and paraaortic lymph node dissection:
             Analysis of the first 100 cases},
   Journal = {Gynecologic Oncology},
   Volume = {82},
   Number = {3},
   Pages = {498 -- 503},
   Year = {2001},
   Month = {September},
   Key = {Scribner01a}
}

@article{fds174212,
   Author = {DR Scribner Jr and JL Walker and GA Johnson and SD McMeekin and MA Gold and RS Mannel},
   Title = {Laparoscopic pelvic and paraaortic lymph node dissection:
             analysis of the first 100 cases.},
   Journal = {Gynecologic oncology},
   Volume = {82},
   Number = {3},
   Pages = {498-503},
   Year = {2001},
   Month = {September},
   ISSN = {0090-8258},
   url = {http://dx.doi.org/10.1006/gyno.2001.6314},
   Keywords = {Adult • Aged • Aged, 80 and over • Aorta,
             Thoracic • Endometrial Neoplasms • Female •
             Humans • Laparoscopy • Lymph Node Excision •
             Middle Aged • Neoplasm Staging • Ovarian Neoplasms
             • Pelvis • Retrospective Studies • adverse
             effects • methods* • pathology •
             surgery*},
   Abstract = {OBJECTIVE: The aim of this study was to analyze the first
             100 cases of planned laparoscopic pelvic and paraaortic
             lymph node dissection (LND) done for staging of gynecologic
             cancers. The goal of the study was to assess prognostic
             factors for conversion to laparotomy and document
             complications. METHODS: A retrospective review of patients
             who had planned laparoscopic bilateral pelvic and bilateral
             paraaortic LND for staging of their gynecologic cancer was
             performed. Patients were identified by our institutional
             database and data were collected by review of their medical
             records. Data were obtained regarding demographics, stage,
             histology, length of stay, and procedural information
             including completion rates, operating room time, estimated
             blood loss, assistant, lymph node count, and complications.
             Associations between variables were analyzed using Student t
             tests, analysis of variance, and chi(2) testing (Excel
             v7.0). RESULTS: A total of 103 patients were identified from
             12/15/95 to 8/28/00. Demographics included mean age of 66.2
             (25-92) and mean Quetelet index (QI) of 30.8 (15.9-56.1). A
             total of 34/103 (33.0%) had > or =1 previous laparotomy.
             Ninety-five patients had endometrial cancer and 8 had
             ovarian cancer. Eighty-six of 103 (83.5%) were stage I or
             II. The length of stay was shorter for those who had
             laparoscopy than for those who needed conversion to
             laparotomy (2.8 vs 5.6 days, P < 0.0001). Laparoscopy was
             completed in 73/103 (70.9%) of the cases. Completion rates
             were 62/76 (81.6%) with QI < 35 vs 11/27 (40.7%) with QI >
             or = 35, P < 0.001. Significantly more patients had their
             laparoscopy completed when an attending gynecologic
             oncologist was the first assistant compared to a fellow or a
             community obstetrician/gynecologist (92.9%, 69.0%, 64.5%, P
             < 0.0001). The top three reasons for conversion to
             laparotomy were obesity, 12/30 (29.1%), adhesions, 5/30
             (16.7%), and intraperitoneal disease, 5/30 (16.7%). Pelvic,
             common iliac, and paraaortic lymph node counts did not
             differ when compared to those of patients who had conversion
             to laparotomy (18.1, 5.1, 6.8 vs 17.3, 5.7, 6.8, P = ns).
             Complications included 2 urinary tract injuries, 2 pulmonary
             embolisms, and 6 wound infections (all in the laparotomy
             group). Two deaths occurred, 1 due to a vascular injury on
             initial trocar insertion and 1 due to a pulmonary embolism
             after a laparotomy for bowel herniation through a trocar
             incision. CONCLUSION: Laparoscopic bilateral pelvic and
             paraaortic LND can be completed successfully in 70.9% of
             patients. Age, obesity, previous surgery, and the need to
             perform this procedure in the community were not
             contraindications. Advantages include a shorter hospital
             stay, similar nodal counts, and acceptable
             complications.},
   Language = {eng},
   Doi = {10.1006/gyno.2001.6314},
   Key = {fds174212}
}

@article{fds268842,
   Author = {Song, J and Liu, Y and Gewalt, SL and Cofer, G and Johnson, GA and Liu,
             QH},
   Title = {Least-square NUFFT methods applied to 2-D and 3-D radially
             encoded MR image reconstruction.},
   Journal = {IEEE Trans Biomed Eng},
   Volume = {56},
   Number = {4},
   Pages = {1134-1142},
   Year = {2009},
   Month = {April},
   ISSN = {1558-2531},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/19174334},
   Keywords = {Animals • Computer Simulation • Image Processing,
             Computer-Assisted • Least-Squares Analysis* •
             Magnetic Resonance Imaging • Mice • Models,
             Statistical • Phantoms, Imaging •
             methods*},
   Abstract = {Radially encoded MRI has gained increasing attention due to
             its motion insensitivity and reduced artifacts. However,
             because its samples are collected nonuniformly in the
             k-space, multidimensional (especially 3-D) radially sampled
             MRI image reconstruction is challenging. The objective of
             this paper is to develop a reconstruction technique in high
             dimensions with on-the-fly kernel calculation. It implements
             general multidimensional nonuniform fast Fourier transform
             (NUFFT) algorithms and incorporates them into a k-space
             image reconstruction framework. The method is then applied
             to reconstruct from the radially encoded k-space data,
             although the method is applicable to any non-Cartesian
             patterns. Performance comparisons are made against the
             conventional Kaiser-Bessel (KB) gridding method for 2-D and
             3-D radially encoded computer-simulated phantoms and
             physically scanned phantoms. The results show that the NUFFT
             reconstruction method has better accuracy-efficiency
             tradeoff than the KB gridding method when the kernel weights
             are calculated on the fly. It is found that for a particular
             conventional kernel function, using its corresponding
             deapodization function as a scaling factor in the NUFFT
             framework has the potential to improve accuracy. In
             particular, when a cosine scaling factor is used, the NUFFT
             method is faster than KB gridding method since a closed-form
             solution is available and is less computationally expensive
             than the KB kernel (KB griding requires computation of
             Bessel functions). The NUFFT method has been successfully
             applied to 2-D and 3-D in vivo studies on small
             animals.},
   Doi = {10.1109/TBME.2009.2012721},
   Key = {fds268842}
}

@article{fds268861,
   Author = {Badea, CT and Wetzel, AW and Mistry, N and Pomerantz, S and Nave, D and Johnson, GA},
   Title = {Left ventricle volume measurements in cardiac micro-CT: the
             impact of radiation dose and contrast agent.},
   Journal = {Comput Med Imaging Graph},
   Volume = {32},
   Number = {3},
   Pages = {239-250},
   Year = {2008},
   Month = {April},
   ISSN = {0895-6111},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/18243656},
   Keywords = {Animals • Contrast Media • Heart Ventricles •
             Imaging, Three-Dimensional • Mice • Mice, Inbred
             C57BL • Radiation Dosage • Radiographic Image
             Interpretation, Computer-Assisted • Tomography, X-Ray
             Computed • administration & dosage • methods*
             • radiography*},
   Abstract = {Micro-CT-based cardiac function estimation in small animals
             requires measurement of left ventricle (LV) volume at
             multiple time points during the cardiac cycle. Measurement
             accuracy depends on the image resolution, its signal and
             noise properties, and the analysis procedure. This work
             compares the accuracy of the Otsu thresholding and a region
             sampled binary mixture approach, for live mouse LV volume
             measurement using 100 microm resolution datasets. We
             evaluate both analysis methods after varying the volume of
             injected contrast agent and the number of projections used
             for CT reconstruction with a goal of permitting reduced
             levels of both X-ray and contrast agent doses.},
   Doi = {10.1016/j.compmedimag.2007.12.004},
   Key = {fds268861}
}

@article{fds292761,
   Author = {Spielmann, AL and Nelson, RC and Lowry, CR and Johnson, GA and Sundaramoothy, G and Sheafor, DH and Paulson, EK},
   Title = {Liver: single breath-hold dynamic subtraction CT with
             multi-detector row helical technology feasibility
             study.},
   Journal = {Radiology},
   Volume = {222},
   Number = {1},
   Pages = {278-283},
   Year = {2002},
   Month = {January},
   ISSN = {0033-8419},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/11756737},
   Keywords = {Adult • Aged • Feasibility Studies • Female
             • Humans • Liver Neoplasms • Male •
             Middle Aged • Neovascularization, Pathologic •
             Prospective Studies • Subtraction Technique •
             Tomography, X-Ray Computed • methods* •
             radiography • radiography* • secondary},
   Abstract = {Fifty-two patients with known or suspected hypervascular
             malignancy were examined to determine the technical
             feasibility of performing single-breath-hold dynamic
             subtraction computed tomography (CT) of the liver with
             multi-detector row helical CT. The precontrast and hepatic
             arterial CT scans, which were acquired during the same
             breath hold, were subtracted. The mean liver-to-muscle
             contrast ratio on the precontrast, hepatic arterial, and
             subtracted images was 1.3, 1.4, and 2.3, respectively. In 13
             patients with lesions, the subtracted images showed a
             2.5-fold increase in mean lesion contrast compared with the
             hepatic arterial CT scans.},
   Language = {eng},
   Doi = {10.1148/radiol.2221010190},
   Key = {fds292761}
}

@article{fds268694,
   Author = {Borg, JS and Vu, M-A and Badea, C and Badea, A and Johnson, GA and Dzirasa,
             K},
   Title = {Localization of Metal Electrodes in the Intact Rat Brain
             Using Registration of 3D Microcomputed Tomography Images to
             a Magnetic Resonance Histology Atlas.},
   Journal = {eNeuro},
   Volume = {2},
   Number = {4},
   Pages = {e0017},
   Year = {2015},
   url = {http://hdl.handle.net/10161/10327 Duke open
             access},
   Abstract = {Simultaneous neural recordings taken from multiple areas of
             the rodent brain are garnering growing interest due to the
             insight they can provide about spatially distributed neural
             circuitry. The promise of such recordings has inspired great
             progress in methods for surgically implanting large numbers
             of metal electrodes into intact rodent brains. However,
             methods for localizing the precise location of these
             electrodes have remained severely lacking. Traditional
             histological techniques that require slicing and staining of
             physical brain tissue are cumbersome, and become
             increasingly impractical as the number of implanted
             electrodes increases. Here we solve these problems by
             describing a method that registers 3-D computerized
             tomography (CT) images of intact rat brains implanted with
             metal electrode bundles to a Magnetic Resonance Imaging
             Histology (MRH) Atlas. Our method allows accurate
             visualization of each electrode bundle's trajectory and
             location without removing the electrodes from the brain or
             surgically implanting external markers. In addition, unlike
             physical brain slices, once the 3D images of the electrode
             bundles and the MRH atlas are registered, it is possible to
             verify electrode placements from many angles by "re-slicing"
             the images along different planes of view. Further, our
             method can be fully automated and easily scaled to
             applications with large numbers of specimens. Our digital
             imaging approach to efficiently localizing metal electrodes
             offers a substantial addition to currently available
             methods, which, in turn, may help accelerate the rate at
             which insights are gleaned from rodent network
             neuroscience.},
   Doi = {10.1523/ENEURO.0017-15.2015},
   Key = {fds268694}
}

@booklet{Ford82a,
   Author = {Ford, KK and Heinz, ER and Johnson, GA and Drayer, BP and Dubois,
             PJ},
   Title = {Low-cost digital subtraction},
   Journal = {American Journal Of Neuroradiology},
   Volume = {3},
   Number = {1},
   Pages = {99-99},
   Year = {1982},
   Key = {Ford82a}
}

@booklet{Ford82,
   Author = {Ford, KK and Heinz, ER and Johnson, GA and Drayer, BD and Dubois,
             PJ},
   Title = {Low-cost digital subtraction angiography.},
   Journal = {AJNR Am J Neuroradiol},
   Volume = {3},
   Number = {4},
   Pages = {448-451},
   Year = {1982},
   ISSN = {0195-6108},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/6810680},
   Key = {Ford82}
}

@article{fds132892,
   Author = {KK Ford and ER Heinz and GA Johnson and BD Drayer and PJ
             Dubois},
   Title = {Low-cost digital subtraction angiography.},
   Journal = {AJNR. American journal of neuroradiology, UNITED
             STATES},
   Volume = {3},
   Number = {4},
   Pages = {448-51},
   ISSN = {0195-6108},
   Keywords = {Angiography • Humans • Radiographic Image
             Enhancement • Subtraction Technique • Videotape
             Recording • economics • methods*},
   Key = {fds132892}
}

@article{fds268830,
   Author = {Badea, CT and Johnston, SM and Subashi, E and Qi, Y and Hedlund, LW and Johnson, GA},
   Title = {Lung perfusion imaging in small animals using 4D micro-CT at
             heartbeat temporal resolution.},
   Journal = {Med Phys},
   Volume = {37},
   Number = {1},
   Pages = {54-62},
   Year = {2010},
   Month = {January},
   ISSN = {0094-2405},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/20175466},
   Keywords = {Animals • Cardiac-Gated Imaging Techniques •
             Contrast Media • Iopamidol • Lung •
             Microinjections • Perfusion Imaging • Radiographic
             Image Enhancement • Rats • Rats, Inbred F344
             • Reproducibility of Results • Sensitivity and
             Specificity • Tomography, X-Ray Computed •
             administration & dosage • diagnostic use* •
             methods • methods* • radiography* •
             veterinary • veterinary*},
   Abstract = {PURPOSE: Quantitative in vivo imaging of lung perfusion in
             rodents can provide critical information for preclinical
             studies. However, the combined challenges of high temporal
             and spatial resolution have made routine quantitative
             perfusion imaging difficult in small animals. The purpose of
             this work is to demonstrate 4D micro-CT for perfusion
             imaging in rodents at heartbeat temporal resolution and
             isotropic spatial resolution. METHODS: We have recently
             developed a dual tube/detector micro-CT scanner that is well
             suited to capture first pass kinetics of a bolus of contrast
             agent used to compute perfusion information. Our approach is
             based on the paradigm that similar time density curves can
             be reproduced in a number of consecutive, small volume
             injections of iodinated contrast agent at a series of
             different angles. This reproducibility is ensured by the
             high-level integration of the imaging components of our
             system with a microinjector, a mechanical ventilator, and
             monitoring applications. Sampling is controlled through a
             biological pulse sequence implemented in LABVIEW. Image
             reconstruction is based on a simultaneous algebraic
             reconstruction technique implemented on a graphic processor
             unit. The capabilities of 4D micro-CT imaging are
             demonstrated in studies on lung perfusion in rats. RESULTS:
             We report 4D micro-CT imaging in the rat lung with a
             heartbeat temporal resolution (approximately 150 ms) and
             isotropic 3D reconstruction with a voxel size of 88 microm
             based on sampling using 16 injections of 50 microL each. The
             total volume of contrast agent injected during the
             experiments (0.8 mL) was less than 10% of the total blood
             volume in a rat. This volume was not injected in a single
             bolus, but in multiple injections separated by at least 2
             min interval to allow for clearance and adaptation. We
             assessed the reproducibility of the time density curves with
             multiple injections and found that these are very similar.
             The average time density curves for the first eight and last
             eight injections are slightly different, i.e., for the last
             eight injections, both the maximum of the average time
             density curves and its area under the curve are decreased by
             3.8% and 7.2%, respectively, relative to the average time
             density curves based on the first eight injections. The
             radiation dose associated with our 4D micro-CT imaging is
             0.16 Gy and is therefore in the range of a typical micro-CT
             dose. CONCLUSIONS: 4D micro-CT-based perfusion imaging
             demonstrated here has immediate application in a wide range
             of preclinical studies such as tumor perfusion,
             angiogenesis, and renal function. Although our imaging
             system is in many ways unique, we believe that our approach
             based on the multiple injection paradigm can be used with
             the newly developed flat-panel slip-ring-based micro-CT to
             increase their temporal resolution in dynamic perfusion
             studies.},
   Language = {eng},
   Doi = {10.1118/1.3264619},
   Key = {fds268830}
}

@article{fds132734,
   Author = {G.A. Johnson},
   Title = {M. Delnomdedieu, L. W. Hedlund, R.R. Maronpot, G.A. Johnson.
             MR  microscopy to follow bromobenzene-induced hepatoxicity
             in the rat. in  "Proc., SMR 4th Annual Scientific Meeting.
              New York, NY, 1996," p.325.},
   Year = {1996},
   Key = {fds132734}
}

@article{fds132733,
   Author = {G.A. Johnson},
   Title = {M. Delnomdedieu, L.W. Hedlund, G.A. Johnson, R.R. Maronpot,
             Magnetic  Resonance Microscopy-A New Tool for the
             Toxicologic Pathologist.   Toxicologic Pathology 24, 36-44
             (1996).},
   Year = {1996},
   Key = {fds132733}
}

@article{fds132723,
   Author = {G.A. Johnson},
   Title = {M.D. Shattuck, G.P. Cofer, G.H. Glover, L.W. Hedlund, G.A.
             Johnson.    Three-dimensional projection microscopy of the
             lung. in "Proc., SMR 4th  Scientific Meeting.  New York,
             NY, 1996," p. 18.},
   Year = {1996},
   Key = {fds132723}
}

@article{fds268750,
   Author = {Sulik, KK and O'Leary-Moore, SK and Parnell, SE and Lipinski, RJ and Pecevich, S and Holloway, HT and Ament, J and Oguz, I and Budin, F and Jiang, Y and Dehart, DB and Styner, MA and Johnson,
             GA},
   Title = {Magnetic resonance and diffusion tensor imaging of pre- and
             postnatal brains in a mouse Fetal Alcohol Spectrum Disorders
             model},
   Journal = {ALCOHOL},
   Volume = {45},
   Number = {3},
   Pages = {282-282},
   Publisher = {ELSEVIER SCIENCE INC},
   Year = {2011},
   Month = {May},
   ISSN = {0741-8329},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000289538300070&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {fds268750}
}

@article{fds269032,
   Author = {Möller, HE and Chawla, MS and Chen, XJ and Driehuys, B and Hedlund, LW and Wheeler, CT and Johnson, GA},
   Title = {Magnetic resonance angiography with hyperpolarized 129Xe
             dissolved in a lipid emulsion.},
   Journal = {Magn Reson Med},
   Volume = {41},
   Number = {5},
   Pages = {1058-1064},
   Year = {1999},
   Month = {May},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/10332890},
   Keywords = {Abdomen • Animals • Artifacts • Blood Flow
             Velocity • Blood Volume • Contrast Media* •
             Electron Spin Resonance Spectroscopy • Fat Emulsions,
             Intravenous • Iliac Vein • Injections, Intravenous
             • Lasers • Magnetic Resonance Angiography •
             Magnetic Resonance Spectroscopy • Male • Pelvis
             • Rats • Renal Veins • Signal Processing,
             Computer-Assisted • Veins • Vena Cava, Inferior
             • Xenon Isotopes* • administration & dosage •
             anatomy & histology • blood supply • diagnostic
             use* • methods*},
   Abstract = {Hyperpolarized (HP) 129Xe can be dissolved in biologically
             compatible lipid emulsions while maintaining sufficient
             polarization for in vivo vascular imaging. For xenon in
             Intralipid 30%, in vitro spectroscopy at 2 T yielded a
             chemical shift of 197 +/- 1 ppm with reference to xenon gas,
             a spin-lattice relaxation time T1 = 25.3 +/- 2.1 sec, and a
             T2* time constant of 37 +/- 5 msec. Angiograms of the
             abdominal and pelvic veins in the rat obtained with 129Xe
             MRI after intravenous injection of HP 129Xe/Intralipid 30%
             into the tail demonstrated signal-to-noise ratios between 8
             and 29. An analysis of the inflow effect on time-of-flight
             images of two segments of the inferior vena cava yielded
             additional information. The mean blood flow velocity was
             34.7 +/- 1.0 mm/sec between the junction of the caudal veins
             and the kidneys and 13.3 +/- 0.8 mm/sec at the position of
             the diaphragm. The mean volume flow rates in these segments
             were 7.2 +/- 3.4 ml/min and 11.0 +/- 2.8 ml/min,
             respectively. Intravenous delivery of HP 129Xe dissolved in
             a carrier may lead to novel biomedical applications of
             laser-polarized gases.},
   Doi = {10.1002/(sici)1522-2594(199905)41:5<1058::aid-mrm26>3.0.co;2},
   Key = {fds269032}
}

@booklet{Moller99a,
   Author = {H. E. Moller and M. S. Chawla and X. J. Chen and B. Driehuys and L. W. Hedlund and C. T. Wheeler and G. A.
             Johnson},
   Title = {Magnetic resonance angiography with hyperpolarized Xe-129
             dissolved in a lipid emulsion},
   Journal = {Magnetic Resonance In Medicine},
   Volume = {41},
   Number = {5},
   Pages = {1058 -- 1064},
   Year = {1999},
   Month = {May},
   Key = {Moller99a}
}

@article{fds132780,
   Author = {GA Johnson and GP Cofer and B Fubara and SL Gewalt and LW Hedlund and RR
             Maronpot},
   Title = {Magnetic resonance histology for morphologic
             phenotyping.},
   Journal = {Journal of magnetic resonance imaging : JMRI, United
             States},
   Volume = {16},
   Number = {4},
   Pages = {423-9},
   Year = {2002},
   Month = {October},
   ISSN = {1053-1807},
   Keywords = {Animals • Magnetic Resonance Imaging* • Mice
             • Mice, Inbred C57BL • Phenotype •
             methods},
   Abstract = {Magnetic resonance histology (MRH) images of the whole mouse
             have been acquired at 100-micron isotropic resolution at 2.0
             T with image arrays of 256 x 256 x 1024. Higher resolution
             (50 x 50 x 50 microns) of limited volumes has been acquired
             at 7.1T with image arrays of 512 x 512 x 512. Even higher
             resolution images (20 x 20 x 20 microns) of isolated organs
             have been acquired at 9.4 T. The volume resolution
             represents an increase of 625000 x over conventional
             clinical MRI. The technological basis is summarized that
             will allow basic scientists to begin using MRH as a routine
             method for morphologcic phenotyping of the mouse. MRH
             promises four unique attributes over conventional histology:
             1). MRH is non-destructive; 2). MRH exploits the unique
             contrast mechanisms that have made MRI so successful
             clinically; 3). MRH is 3-dimensional; and 4). the data are
             inherently digital. We demonstrate the utility in
             morphologic phenotyping a whole C57BL/6J
             mouse.},
   Key = {fds132780}
}

@booklet{Johnson02a,
   Author = {Johnson, GA and Cofer, GP and Fubara, B and Gewalt, SL and Hedlund, LW and Maronpot, RR},
   Title = {Magnetic resonance histology for morphologic
             phenotyping.},
   Journal = {J Magn Reson Imaging},
   Volume = {16},
   Number = {4},
   Pages = {423-429},
   Year = {2002},
   Month = {October},
   ISSN = {1053-1807},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/12353257},
   Abstract = {Magnetic resonance histology (MRH) images of the whole mouse
             have been acquired at 100-micron isotropic resolution at 2.0
             T with image arrays of 256 x 256 x 1024. Higher resolution
             (50 x 50 x 50 microns) of limited volumes has been acquired
             at 7.1T with image arrays of 512 x 512 x 512. Even higher
             resolution images (20 x 20 x 20 microns) of isolated organs
             have been acquired at 9.4 T. The volume resolution
             represents an increase of 625000 x over conventional
             clinical MRI. The technological basis is summarized that
             will allow basic scientists to begin using MRH as a routine
             method for morphologcic phenotyping of the mouse. MRH
             promises four unique attributes over conventional histology:
             1). MRH is non-destructive; 2). MRH exploits the unique
             contrast mechanisms that have made MRI so successful
             clinically; 3). MRH is 3-dimensional; and 4). the data are
             inherently digital. We demonstrate the utility in
             morphologic phenotyping a whole C57BL/6J
             mouse.},
   Doi = {10.1002/jmri.10175},
   Key = {Johnson02a}
}

@article{fds268773,
   Author = {Xie, L and Cianciolo, RE and Hulette, B and Lee, HW and Qi, Y and Cofer, G and Johnson, GA},
   Title = {Magnetic resonance histology of age-related nephropathy in
             the Sprague Dawley rat.},
   Journal = {Toxicol Pathol},
   Volume = {40},
   Number = {5},
   Pages = {764-778},
   Year = {2012},
   Month = {July},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/22504322},
   Abstract = {Magnetic resonance histology (MRH) has become a valuable
             tool in evaluating drug-induced toxicity in preclinical
             models. However, its application in renal injury has been
             limited. This study tested the hypothesis that MRH could
             detect image-based biomarkers of chronic disease,
             inflammation, or age-related degeneration in the kidney,
             laying the foundation for more extensive use in evaluating
             drug toxicity. We examined the entire intact kidney in a
             spontaneous model of chronic progressive nephropathy.
             Kidneys from male Sprague Dawley rats were imaged at 8 weeks
             (n = 4) and 52 weeks (n =4) on a 9.4 T system dedicated to
             MR microscopy. Several potential contrast mechanisms were
             explored to optimize the scanning protocols. Full coverage
             of the entire kidney was achieved with isotropic spatial
             resolution at 31 microns (voxel volume = 30 pL) using a
             gradient recalled echo sequence. Isotropic spatial
             resolution of 15 microns (voxel volume < 4 pL) was achieved
             in a biopsy core specimen. Qualitative age-related
             structural changes, such as renal cortical microvasculature,
             tubular dilation, interstitial fibrosis, and glomerular
             architecture, were apparent. The nondestructive 3D images
             allowed measurement of quantitative differences of kidney
             volume, pelvis volume, main vessel volume, glomerular size,
             as well as thickness of the cortex, outer medulla, and inner
             medulla.},
   Doi = {10.1177/0192623312441408},
   Key = {fds268773}
}

@article{fds268706,
   Author = {Johnson, GA},
   Title = {Magnetic resonance histology.},
   Journal = {J Magn Reson Imaging},
   Volume = {42},
   Number = {1},
   Pages = {1-2},
   Year = {2015},
   Month = {July},
   ISSN = {1053-1807},
   url = {http://dx.doi.org/10.1002/jmri.24774},
   Doi = {10.1002/jmri.24774},
   Key = {fds268706}
}

@article{fds268728,
   Author = {Johnson, GA and Badea, A and Calabrese, E and Liu, C and Xie,
             L},
   Title = {Magnetic resonance histology: cool images- but who
             cares?},
   Journal = {TOXICOLOGY LETTERS},
   Volume = {221},
   Pages = {S50-S50},
   Publisher = {Elsevier BV},
   Year = {2013},
   ISSN = {0378-4274},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000323865800154&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Doi = {10.1016/j.toxlet.2013.06.183},
   Key = {fds268728}
}

@article{fds268705,
   Author = {Johnson, GA and Badea, A and Calabrese, E and Liu, C and Xie,
             L},
   Title = {Magnetic resonance histology—Applications in
             toxicology},
   Journal = {Toxicology Letters},
   Volume = {229},
   Pages = {S31-S32},
   Publisher = {Elsevier BV},
   Year = {2014},
   Month = {September},
   ISSN = {0378-4274},
   url = {http://dx.doi.org/10.1016/j.toxlet.2014.06.148},
   Doi = {10.1016/j.toxlet.2014.06.148},
   Key = {fds268705}
}

@booklet{Dixon88,
   Author = {Dixon, D and Johnson, GA and Cofer, GP and Hedlund, LW and Maronpot,
             RR},
   Title = {Magnetic resonance imaging (MRI): a new tool in experimental
             toxicologic pathology.},
   Journal = {Toxicol Pathol},
   Volume = {16},
   Number = {3},
   Pages = {386-391},
   Year = {1988},
   ISSN = {0192-6233},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/3194661},
   Abstract = {Magnetic Resonance Imaging (MRI) is a noninvasive imaging
             technique that provides multidimensional images of the soft
             tissues of the body. This imaging technique has proven to be
             an excellent diagnostic and experimental tool for the
             detection of pathologic alterations in soft tissues, as well
             as an adjunct screening method for following the genesis,
             progression, or regression of chemically induced lesions in
             the same live animal. Future applications of MRI technology
             in small animals include MRI microscopy, mapping of vascular
             or circulatory alterations, measurement of perfusion and
             diffusion rates of body fluids, and acquisition of cell
             metabolic states in combination with Nuclear Magnetic
             Resonance (NMR) spectroscopy, all of which will contribute
             immensely to the advancement of toxicologic and biomolecular
             research.},
   Doi = {10.1177/019262338801600311},
   Key = {Dixon88}
}

@article{fds132761,
   Author = {D Dixon and GA Johnson and GP Cofer and LW Hedlund and RR
             Maronpot},
   Title = {Magnetic resonance imaging (MRI): a new tool in experimental
             toxicologic pathology.},
   Journal = {Toxicologic pathology, UNITED STATES},
   Volume = {16},
   Number = {3},
   Pages = {386-91},
   Year = {1988},
   ISSN = {0192-6233},
   Keywords = {Animals • Magnetic Resonance Imaging* • Pathology*
             • Rats • Toxicology*},
   Abstract = {Magnetic Resonance Imaging (MRI) is a noninvasive imaging
             technique that provides multidimensional images of the soft
             tissues of the body. This imaging technique has proven to be
             an excellent diagnostic and experimental tool for the
             detection of pathologic alterations in soft tissues, as well
             as an adjunct screening method for following the genesis,
             progression, or regression of chemically induced lesions in
             the same live animal. Future applications of MRI technology
             in small animals include MRI microscopy, mapping of vascular
             or circulatory alterations, measurement of perfusion and
             diffusion rates of body fluids, and acquisition of cell
             metabolic states in combination with Nuclear Magnetic
             Resonance (NMR) spectroscopy, all of which will contribute
             immensely to the advancement of toxicologic and biomolecular
             research.},
   Key = {fds132761}
}

@article{fds268893,
   Author = {Herfkens, RJ and Johnson, GA},
   Title = {Magnetic resonance imaging at high-strength magnetic
             fields.},
   Journal = {Magn Reson Annu},
   Pages = {197-215},
   Year = {1985},
   ISSN = {8756-9787},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/3917235},
   Keywords = {Animals • Brain • Electromagnetic Fields •
             Heart • Humans • Magnetic Resonance Imaging •
             Magnetic Resonance Spectroscopy • anatomy & histology
             • instrumentation • methods*},
   Key = {fds268893}
}

@article{fds268898,
   Author = {Cyr, M and Caron, MG and Johnson, GA and Laakso, A},
   Title = {Magnetic resonance imaging at microscopic resolution reveals
             subtle morphological changes in a mouse model of
             dopaminergic hyperfunction.},
   Journal = {Neuroimage},
   Volume = {26},
   Number = {1},
   Pages = {83-90},
   Year = {2005},
   Month = {May},
   ISSN = {1053-8119},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/15862208},
   Abstract = {Structural abnormalities of the basal ganglia have been
             documented in several neuropsychiatric conditions associated
             with dysregulation of the dopamine system. However, the
             histological nature underlying these changes is largely
             unknown. Using magnetic resonance imaging at microscopic
             resolution (MRI, 9.4 T with 43 microm isotropic spatial
             resolution) and stereological techniques, we have
             investigated the effect of increased dopamine
             neurotransmission on brain morphology in mice with elevated
             extracellular dopamine, the dopamine transporter knockout
             (DAT-KO) mice. We first demonstrate the usefulness of MRI at
             microscopic resolution for the accurate identification and
             measurement of volumes of specific subregions, accounting
             for less than 0.03% (0.16 mm(3)) of the volume of a mouse
             brain. Furthermore, the MRI analysis reveals a significantly
             lower volume (-9%) of the anterior striatum of DAT-KO mice,
             while the volume of other dopamine-related structures such
             as the posterior striatum and the substantia nigra pars
             reticulata is unchanged in comparison to wild type
             littermates. Stereological analysis performed in the same
             brains reveals that one important structural factor
             accounting for this selective change in volume is a
             reduction of 18% in the absolute number of neuronal cell
             bodies. The feasibility of assessing accurately small
             morphological alterations in mouse models, where the
             molecular and histological pathologies can be easily
             compared in a controlled manner, provides a paradigm to
             examine the relevance of selective brain volumetric changes
             associated with a number of neuropathological
             conditions.},
   Doi = {10.1016/j.neuroimage.2005.01.039},
   Key = {fds268898}
}

@article{fds132905,
   Author = {M Cyr and MG Caron and GA Johnson and A Laakso},
   Title = {Magnetic resonance imaging at microscopic resolution reveals
             subtle morphological changes in a mouse model of
             dopaminergic hyperfunction.},
   Journal = {NeuroImage, United States},
   Volume = {26},
   Number = {1},
   Pages = {83-90},
   Year = {2005},
   Month = {May},
   ISSN = {1053-8119},
   Keywords = {Animals • Basal Ganglia • Brain • Cell Count
             • Dopamine • Dopamine Plasma Membrane Transport
             Proteins • Fluorescent Antibody Technique • Image
             Interpretation, Computer-Assisted • Magnetic Resonance
             Imaging • Male • Membrane Glycoproteins •
             Membrane Transport Proteins • Mice • Mice,
             Knockout • Models, Neurological • Neostriatum
             • Nerve Tissue Proteins • Neurons • anatomy &
             histology • anatomy & histology* • cytology •
             genetics • physiology • physiology*},
   Abstract = {Structural abnormalities of the basal ganglia have been
             documented in several neuropsychiatric conditions associated
             with dysregulation of the dopamine system. However, the
             histological nature underlying these changes is largely
             unknown. Using magnetic resonance imaging at microscopic
             resolution (MRI, 9.4 T with 43 microm isotropic spatial
             resolution) and stereological techniques, we have
             investigated the effect of increased dopamine
             neurotransmission on brain morphology in mice with elevated
             extracellular dopamine, the dopamine transporter knockout
             (DAT-KO) mice. We first demonstrate the usefulness of MRI at
             microscopic resolution for the accurate identification and
             measurement of volumes of specific subregions, accounting
             for less than 0.03% (0.16 mm(3)) of the volume of a mouse
             brain. Furthermore, the MRI analysis reveals a significantly
             lower volume (-9%) of the anterior striatum of DAT-KO mice,
             while the volume of other dopamine-related structures such
             as the posterior striatum and the substantia nigra pars
             reticulata is unchanged in comparison to wild type
             littermates. Stereological analysis performed in the same
             brains reveals that one important structural factor
             accounting for this selective change in volume is a
             reduction of 18% in the absolute number of neuronal cell
             bodies. The feasibility of assessing accurately small
             morphological alterations in mouse models, where the
             molecular and histological pathologies can be easily
             compared in a controlled manner, provides a paradigm to
             examine the relevance of selective brain volumetric changes
             associated with a number of neuropathological
             conditions.},
   Key = {fds132905}
}

@article{fds132879,
   Author = {BP Drayer and P Burger and B Hurwitz and D Dawson and J Cain and J Leong and R
             Herfkens, GA Johnson},
   Title = {Magnetic resonance imaging in multiple sclerosis: decreased
             signal in thalamus and putamen.},
   Journal = {Annals of neurology, UNITED STATES},
   Volume = {22},
   Number = {4},
   Pages = {546-50},
   Year = {1987},
   Month = {October},
   ISSN = {0364-5134},
   Keywords = {Humans • Magnetic Resonance Imaging* • Multiple
             Sclerosis • Putamen • Thalamus • diagnosis*
             • pathology*},
   Abstract = {High-field strength (1.5 Tesla) magnetic resonance imaging
             in 15 patients with multiple and extensive white-matter
             lesions and clinically definite multiple sclerosis
             delineated a previously undescribed finding of abnormally
             decreased signal intensity on T2-weighted images in the
             thalamus and putamen. The decreased signal intensity
             (preferential decreased T2 relaxation time) is most likely
             to be related to abnormally increased iron accumulation
             causing local magnetic field heterogeneities.},
   Key = {fds132879}
}

@booklet{Drayer87,
   Author = {Drayer, BP and Burger, P and Hurwitz, B and Dawson, D and Cain, J and Leong, J and Herfkens, R and Johnson, GA},
   Title = {Magnetic resonance imaging in multiple sclerosis: decreased
             signal in thalamus and putamen.},
   Journal = {Ann Neurol},
   Volume = {22},
   Number = {4},
   Pages = {546-550},
   Year = {1987},
   Month = {October},
   ISSN = {0364-5134},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/3435073},
   Abstract = {High-field strength (1.5 Tesla) magnetic resonance imaging
             in 15 patients with multiple and extensive white-matter
             lesions and clinically definite multiple sclerosis
             delineated a previously undescribed finding of abnormally
             decreased signal intensity on T2-weighted images in the
             thalamus and putamen. The decreased signal intensity
             (preferential decreased T2 relaxation time) is most likely
             to be related to abnormally increased iron accumulation
             causing local magnetic field heterogeneities.},
   Doi = {10.1002/ana.410220418},
   Key = {Drayer87}
}

@article{fds132827,
   Author = {JC Hsu and GA Johnson and WM Smith and KA Reimer and RE
             Ideker},
   Title = {Magnetic resonance imaging of chronic myocardial infarcts in
             formalin-fixed human autopsy hearts.},
   Journal = {Circulation, UNITED STATES},
   Volume = {89},
   Number = {5},
   Pages = {2133-40},
   Year = {1994},
   Month = {May},
   ISSN = {0009-7322},
   Keywords = {Algorithms • Formaldehyde • Fourier Analysis
             • Humans • Image Processing, Computer-Assisted
             • Magnetic Resonance Imaging • Magnetic Resonance
             Spectroscopy • Myocardial Infarction • Myocardium
             • Signal Processing, Computer-Assisted • Tissue
             Fixation • methods • methods* •
             pathology*},
   Abstract = {BACKGROUND: In post-myocardial infarction patients,
             three-dimensional structure of the infarct as well as
             infarct size are likely to be important factors affecting
             mortality, cardiac function, and arrhythmias. Current
             morphological methods for determining three-dimensional
             infarct structure in autopsied hearts are inexact and time
             consuming. The cardiac magnetic resonance imaging techniques
             used in living patients have shown potential in determining
             infarct size and structure but have limited resolution for
             morphometric postmortem studies. The recent development of
             magnetic resonance microscopy raises the possibility that
             three-dimensional infarct structure can be quantified at
             microscopic levels in autopsied hearts. The purpose of this
             study was to determine the ability of magnetic resonance
             imaging at different spatial resolutions to differentiate
             infarcted from noninfarcted myocardium. METHODS AND RESULTS:
             Magnetic resonance imaging was performed at 2.0 T on cross
             sections taken from 10 autopsied hearts containing old
             myocardial infarcts. T1 was derived from six images with
             repetition times (TRs) for each image ranging from 100 to
             3200 milliseconds. T2 was derived from multi-echo images
             with echo times (TEs) ranging from 10 to 60 milliseconds.
             Resolution was approximately 400 x 400 microns in 2-mm-thick
             slices. Sites of infarcted and noninfarcted tissue were
             identified from histological sections taken from each slice,
             and the T1 and T2 values of these sites were obtained.
             Microscopic images were acquired with voxels of 100 x 100 x
             625 microns, representing tissue volumes more than 1000-fold
             smaller than conventional clinical images. In all cases, T1
             of infarcted tissue (459 +/- 266 milliseconds, mean +/- SD)
             was greater than that of noninfarcted tissue (272 +/- 163
             milliseconds). Also, in all cases, T2 of infarcted tissue
             (49 +/- 14 milliseconds) was greater than that of
             noninfarcted tissue (35 +/- 8 milliseconds). CONCLUSIONS: T1
             and T2 values for infarcted tissue are significantly
             different from those of noninfarcted tissue (P < .001).
             Based on these findings, it should be possible to develop
             techniques to perform three-dimensional imaging and
             quantitation of infarcts with a resolution of 400 microns or
             less. When volumetric three-dimensional imaging was
             performed using a T1-weighted sequence, the resulting 256(3)
             arrays supported isotropic resolution at 400 microns (voxel
             volume, 0.064 mm3). Subsequent volume rendering using a
             compositing algorithm clearly shows the infarcted areas in
             three dimensions. The techniques demonstrate the potential
             for quantitative three-dimensional cardiac morphometry using
             magnetic resonance imaging.},
   Key = {fds132827}
}

@booklet{Hsu94,
   Author = {Hsu, JC and Johnson, GA and Smith, WM and Reimer, KA and Ideker,
             RE},
   Title = {Magnetic resonance imaging of chronic myocardial infarcts in
             formalin-fixed human autopsy hearts.},
   Journal = {Circulation},
   Volume = {89},
   Number = {5},
   Pages = {2133-2140},
   Year = {1994},
   Month = {May},
   ISSN = {0009-7322},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/8181138},
   Abstract = {BACKGROUND: In post-myocardial infarction patients,
             three-dimensional structure of the infarct as well as
             infarct size are likely to be important factors affecting
             mortality, cardiac function, and arrhythmias. Current
             morphological methods for determining three-dimensional
             infarct structure in autopsied hearts are inexact and time
             consuming. The cardiac magnetic resonance imaging techniques
             used in living patients have shown potential in determining
             infarct size and structure but have limited resolution for
             morphometric postmortem studies. The recent development of
             magnetic resonance microscopy raises the possibility that
             three-dimensional infarct structure can be quantified at
             microscopic levels in autopsied hearts. The purpose of this
             study was to determine the ability of magnetic resonance
             imaging at different spatial resolutions to differentiate
             infarcted from noninfarcted myocardium. METHODS AND RESULTS:
             Magnetic resonance imaging was performed at 2.0 T on cross
             sections taken from 10 autopsied hearts containing old
             myocardial infarcts. T1 was derived from six images with
             repetition times (TRs) for each image ranging from 100 to
             3200 milliseconds. T2 was derived from multi-echo images
             with echo times (TEs) ranging from 10 to 60 milliseconds.
             Resolution was approximately 400 x 400 microns in 2-mm-thick
             slices. Sites of infarcted and noninfarcted tissue were
             identified from histological sections taken from each slice,
             and the T1 and T2 values of these sites were obtained.
             Microscopic images were acquired with voxels of 100 x 100 x
             625 microns, representing tissue volumes more than 1000-fold
             smaller than conventional clinical images. In all cases, T1
             of infarcted tissue (459 +/- 266 milliseconds, mean +/- SD)
             was greater than that of noninfarcted tissue (272 +/- 163
             milliseconds). Also, in all cases, T2 of infarcted tissue
             (49 +/- 14 milliseconds) was greater than that of
             noninfarcted tissue (35 +/- 8 milliseconds). CONCLUSIONS: T1
             and T2 values for infarcted tissue are significantly
             different from those of noninfarcted tissue (P < .001).
             Based on these findings, it should be possible to develop
             techniques to perform three-dimensional imaging and
             quantitation of infarcts with a resolution of 400 microns or
             less. When volumetric three-dimensional imaging was
             performed using a T1-weighted sequence, the resulting 256(3)
             arrays supported isotropic resolution at 400 microns (voxel
             volume, 0.064 mm3). Subsequent volume rendering using a
             compositing algorithm clearly shows the infarcted areas in
             three dimensions. The techniques demonstrate the potential
             for quantitative three-dimensional cardiac morphometry using
             magnetic resonance imaging.},
   Doi = {10.1161/01.cir.89.5.2133},
   Key = {Hsu94}
}

@article{fds268762,
   Author = {Bcnveniste, H and Hüttemeier, PC and Qiu, H and Steele, S and Hedlund,
             LW and Allan Johnson and G},
   Title = {Magnetic resonance imaging of continuous spinal anesthesia
             with hyperbaric lidocaine: Root or white matter
             lesion?},
   Journal = {Regional Anesthesia},
   Volume = {22},
   Number = {2 SUPPL.},
   Pages = {15},
   Year = {1997},
   Month = {December},
   ISSN = {0146-521X},
   Abstract = {Introduction: Persistent neurologic deficits in patients
             after continuous spinal anesthesia with hyperbaric lidocaine
             may have been erroneously characterized as a cauda equina
             syndrome (1,2). First, clinical reports of symptoms rarely
             include pain (typical for cauda equina lesions) but most
             often consist of saddle anesthesia, paraplegia and sphincter
             dysfunction (typical for conus medullaris lesions).
             Secondly, spinal cord damage in dogs after intrathecal
             procaine (3) or lidocaine (4) is confined only to the myelin
             sheath beneath the pia mater and not nerve roots. In this
             study we use diffusion-weighted magnetic resonance imaging
             (DWI) to further characterize hyperbaric lidocaine-induced
             spinal cord damage. DWI measures diffusion of free protons
             and is a very sensitive detector of white or gray matter
             injury (5). Normal spinal cord gray and white matter as well
             as nerve roots are clearly visualized by DWI because the
             proton diffusion coefficient (DC) - the critical parameter
             measured with DWI - within these tissues differs. The effect
             of hyperbaric 5% lidocaine on the spinal cord diffusion
             coefficient will be compared with those found in ischémie
             conditions. Methods: The study was approved by the Duke
             University Animal Care Institutional Committee. Nine female
             adult Fisher rats (weighing 150-190g) were anesthetized with
             isoflurane, intubated and mechanically ventilated. Catheters
             were inserted into the right external jugular vein and
             carotid artery. Heart rate, arterial blood pressure and body
             temperature was monitored continuously. Diffusion-weighted
             MR images (DWI) were acquired at the level of C6 in five
             rats before and after ischemia induced by cardiac arrest. In
             another four rats catheters were first placed intrathecally
             via the atlanto-occipital membrane. Subsequently, DWI's were
             acquired at the level of C6 before and during 3 hr
             continuous intrathecal perfusion with 5% hyperbaric
             lidocaine. Hemodynamic stability during lidocaine
             administration was maintained with i.v. hydration, atropine
             and ephedrine as needed. All imaging was done on a 7 T
             magnet using a standard spin echo diffusion pulse sequence
             (5). Results: Ischemia reduced the diffusion coefficient
             (DC) of white matter by 25%, gray matter by 45% and nerve
             roots/dorsal root ganglia by 35%. Figure 1 shows that one
             hour of continuous intrathecal administration of 5%
             hyperbaric lidocaine reduces the DC of white matter by 15%
             and that the changes are not as profound as those found
             during ischemia (results are presented as mean ± SD).
             Figure 2 shows that in contrast to white matter, DCs of
             adjacent nerve roots are unaffected by 5 % hyperbaric
             lidocaine. Discussion: The present study has led to the
             following conclusion: (1) diffusion-weighted imaging of
             spinal cord in rats with indwelling intrathecal catheters is
             possible in vivo, (2) the diffusion coefficient of white
             matter is reduced by 15% after 1 hr of 5% hyperbaric
             lidocaine indicating onset of cytotoxic edema, (3) the
             lidocaine-induced changes in the white matter DC do not
             reach ischémie levels, (4) adjacent gray matter as well as
             nerve roots are unaffected. Ongoing work will provide
             information as to the exact pathophysiological sequence of
             events which lead to irreversible spinal cord damage during
             continuous spinal anesthesia with high dose hyperbaric 5%
             lidocaine. It is our goal that this research will be
             applicable to local anesthesia toxicity studies and useful
             as a future neurotoxicity screening tool for new intralhecal
             drugs designed for both anesthesia and analgesia.},
   Key = {fds268762}
}

@booklet{Smith99,
   Author = {Smith, BR and Huff, DS and Johnson, GA},
   Title = {Magnetic resonance imaging of embryos: an Internet resource
             for the study of embryonic development.},
   Journal = {Comput Med Imaging Graph},
   Volume = {23},
   Number = {1},
   Pages = {33-40},
   Year = {1999},
   ISSN = {0895-6111},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/10091866},
   Abstract = {The recent amassing of gene expression data to study
             development in mammals has led to an increased demand for
             access to human embryological data. The difficulty of
             obtaining well-preserved human embryos presents an important
             challenge to studying human development. The
             Multidimensional Human Embryo project is generating an image
             data set based on magnetic resonance microscopy of specimens
             from the highly respected Carnegie Collection of Human
             Embryos. The data are available from a web site to
             facilitate the work of clinicians, investigators, and
             students of human development. A consequence of the project
             will be to preserve a highly respected, yet impermanent,
             collection of human embryos and minimize the need for
             collecting new specimens.},
   Doi = {10.1016/s0895-6111(98)00061-5},
   Key = {Smith99}
}

@article{fds132767,
   Author = {BR Smith and DS Huff and GA Johnson},
   Title = {Magnetic resonance imaging of embryos: an Internet resource
             for the study of embryonic development.},
   Journal = {Computerized medical imaging and graphics : the official
             journal of the Computerized Medical Imaging Society, UNITED
             STATES},
   Volume = {23},
   Number = {1},
   Pages = {33-40},
   ISSN = {0895-6111},
   Keywords = {Embryo • Humans • Image Processing,
             Computer-Assisted* • Internet* • Magnetic
             Resonance Imaging* • anatomy & histology*},
   Abstract = {The recent amassing of gene expression data to study
             development in mammals has led to an increased demand for
             access to human embryological data. The difficulty of
             obtaining well-preserved human embryos presents an important
             challenge to studying human development. The
             Multidimensional Human Embryo project is generating an image
             data set based on magnetic resonance microscopy of specimens
             from the highly respected Carnegie Collection of Human
             Embryos. The data are available from a web site to
             facilitate the work of clinicians, investigators, and
             students of human development. A consequence of the project
             will be to preserve a highly respected, yet impermanent,
             collection of human embryos and minimize the need for
             collecting new specimens.},
   Key = {fds132767}
}

@article{fds268702,
   Author = {Cutlip, RG and Hollander, MS and Johnson, GA and Johnson, BW and Friend,
             SA and Baker, BA},
   Title = {Magnetic resonance imaging of graded skeletal muscle injury
             in live rats.},
   Journal = {Environ Health Insights},
   Volume = {8},
   Number = {Suppl 1},
   Pages = {31-39},
   Year = {2014},
   url = {http://hdl.handle.net/10161/10309 Duke open
             access},
   Abstract = {INTRODUCTION: Increasing number of stretch-shortening
             contractions (SSCs) results in increased muscle injury.
             METHODS: Fischer Hybrid rats were acutely exposed to an
             increasing number of SSCs in vivo using a custom-designed
             dynamometer. Magnetic resonance imaging (MRI) imaging was
             conducted 72 hours after exposure when rats were infused
             with Prohance and imaged using a 7T rodent MRI system (GE
             Epic 12.0). Images were acquired in the transverse plane
             with typically 60 total slices acquired covering the entire
             length of the hind legs. Rats were euthanized after MRI, the
             lower limbs removed, and tibialis anterior muscles were
             prepared for histology and quantified stereology. RESULTS:
             Stereological analyses showed myofiber degeneration, and
             cellular infiltrates significantly increased following 70
             and 150 SSC exposure compared to controls. MRI images
             revealed that the percent affected area significantly
             increased with exposure in all SSC groups in a graded
             fashion. Signal intensity also significantly increased with
             increasing SSC repetitions. DISCUSSION: These results
             suggest that contrast-enhanced MRI has the sensitivity to
             differentiate specific degrees of skeletal muscle strain
             injury, and imaging data are specifically representative of
             cellular histopathology quantified via stereological
             analyses.},
   Doi = {10.4137/EHI.S15255},
   Key = {fds268702}
}

@article{fds132815,
   Author = {GA Johnson and MB Thompson and GP Cofer and D Campen and RR
             Maronpot},
   Title = {Magnetic resonance imaging of hepatic neoplasms in the
             rat.},
   Journal = {Veterinary pathology, UNITED STATES},
   Volume = {26},
   Number = {4},
   Pages = {303-8},
   Year = {1989},
   Month = {July},
   ISSN = {0300-9858},
   Keywords = {Animals • Female • Liver Neoplasms, Experimental
             • Magnetic Resonance Imaging* • Ovariectomy •
             Rats • Rats, Inbred Strains • diagnosis •
             pathology* • veterinary},
   Abstract = {Magnetic resonance imaging (MRI) at microscopic resolution
             was done on a live rat that had chemically induced hepatic
             neoplasms. Beginning at the anterior aspect of the liver, 16
             contiguous transaxial slices (each 1.25 mm thick) were
             produced using three-dimensional Fourier transform
             sequences. The rat had been treated with diethylnitrosamine
             (200 mg/kg) at 70 days of age, and, subsequently, received
             periodic implants of 17a-ethynylestradiol for 60 weeks.
             Carr-Purcell-Meiboom-Gill (CPMG) sequences (repetition time
             = 2,000 and echo time = 20, 40, 60, 80 ms) were done to give
             quantitative measures of spin-spin relaxation times (T2).
             Pixel-by-pixel curve fitting from these multiple images
             yielded calculated T2 images. Histologic evaluation of three
             abnormal areas in the liver revealed solid and cystic
             hepatocellular adenomas. Although lesions were evident in
             early-echo images of the CPMG sequence, they were more
             apparent in the late-echo images. This was consistent with
             longer T2 relaxation times for the lesions. The voxels of
             dimensions (230 x 230 x 1,250 microns) permitted resolution
             of volume elements less than 0.07 mm3. This in turn
             permitted clear delineation of focal lesions less than 3 mm
             in diameter. The potential for MRI at microscopic resolution
             in toxicologic research is clearly demonstrated.},
   Key = {fds132815}
}

@booklet{Johnson89a,
   Author = {Johnson, GA and Thompson, MB and Cofer, GP and Campen, D and Maronpot,
             RR},
   Title = {Magnetic resonance imaging of hepatic neoplasms in the
             rat.},
   Journal = {Vet Pathol},
   Volume = {26},
   Number = {4},
   Pages = {303-308},
   Year = {1989},
   Month = {July},
   ISSN = {0300-9858},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/2763419},
   Abstract = {Magnetic resonance imaging (MRI) at microscopic resolution
             was done on a live rat that had chemically induced hepatic
             neoplasms. Beginning at the anterior aspect of the liver, 16
             contiguous transaxial slices (each 1.25 mm thick) were
             produced using three-dimensional Fourier transform
             sequences. The rat had been treated with diethylnitrosamine
             (200 mg/kg) at 70 days of age, and, subsequently, received
             periodic implants of 17a-ethynylestradiol for 60 weeks.
             Carr-Purcell-Meiboom-Gill (CPMG) sequences (repetition time
             = 2,000 and echo time = 20, 40, 60, 80 ms) were done to give
             quantitative measures of spin-spin relaxation times (T2).
             Pixel-by-pixel curve fitting from these multiple images
             yielded calculated T2 images. Histologic evaluation of three
             abnormal areas in the liver revealed solid and cystic
             hepatocellular adenomas. Although lesions were evident in
             early-echo images of the CPMG sequence, they were more
             apparent in the late-echo images. This was consistent with
             longer T2 relaxation times for the lesions. The voxels of
             dimensions (230 x 230 x 1,250 microns) permitted resolution
             of volume elements less than 0.07 mm3. This in turn
             permitted clear delineation of focal lesions less than 3 mm
             in diameter. The potential for MRI at microscopic resolution
             in toxicologic research is clearly demonstrated.},
   Doi = {10.1177/030098588902600403},
   Key = {Johnson89a}
}

@booklet{Levron98,
   Author = {Levron, D and Walter, DK and Appelt, S and Fitzgerald, RJ and Kahn, D and Korbly, SE and Sauer, KL and Happer, W and Earles, TL and Mawst, LJ and al,
             E},
   Title = {Magnetic resonance imaging of hyperpolarized 129Xe produced
             by spin exchange with diode-laser pumped
             Cs},
   Journal = {Applied Physics Letters},
   Volume = {73},
   Number = {18},
   Pages = {2666-2668},
   Publisher = {AIP Publishing},
   Year = {1998},
   url = {http://dx.doi.org/10.1063/1.122547},
   Abstract = {We report the results of experiments leading to the
             production of an image of a polarized 129Xe sample prepared
             by spin exchange with Cs, optically pumped with a spectrally
             narrowed 894.3 nm diode laser. Representative images of the
             average electron spin polarization are shown. Appreciable
             cesium electron polarization values were achieved, and a
             nuclear polarization of about 2.5% was measured for 129Xe.
             The absolute nuclear polarization was measured by
             water-calibrated free induction decay of the nuclear
             magnetic resonance signal, and the polarized xenon imaged
             using a 2 T magnetic resonance imaging system. © 1998
             American Institute of Physics.},
   Doi = {10.1063/1.122547},
   Key = {Levron98}
}

@article{fds268776,
   Author = {Shattuck, M and Behringer, R and Geordiadis, J and Johnson,
             GA},
   Title = {Magnetic resonance imaging of interstitial velocity
             distributions in porous media},
   Journal = {American Society of Mechanical Engineers, Fluids Engineering
             Division (Publication) FED},
   Volume = {125},
   Pages = {39-45},
   Year = {1991},
   Month = {December},
   Abstract = {In this article we report on a promising application of
             Magnetic Resonance Imaging (MRI), which can measure local
             interstitial velocity distributions inside fully-saturated
             porous media. We have extended the standard
             three-dimensional MRI sequence to include local velocity
             information. During flow, the moving spins of the fluid (in
             this case water) accumulate phase in the presence of
             magnetic field gradients. This phase is proportional to the
             local velocity. By repeating the measurement under the
             influence of different magnetic gradient strengths, we can
             reconstruct the velocity distribution in each volume element
             (voxel). Using this technique to study pressure-driven flow
             through a fully-saturated, cylindrical packed bed, we have
             observed flow channeling near the walls and an exponential
             distribution of velocities.},
   Key = {fds268776}
}

@article{fds343279,
   Author = {Shattuck, M and Behringer, R and Geordiadis, J and Johnson,
             GA},
   Title = {Magnetic resonance imaging of interstitial velocity
             distributions in porous media},
   Year = {1991},
   Month = {January},
   Abstract = {In this article we report on a promising application of
             Magnetic Resonance Imaging (MRI), which can measure local
             interstitial velocity distributions inside fully-saturated
             porous media. We have extended the standard
             three-dimensional MRI sequence to include local velocity
             information. During flow, the moving spins of the fluid (in
             this case water) accumulate phase in the presence of
             magnetic field gradients. This phase is proportional to the
             local velocity. By repeating the measurement under the
             influence of different magnetic gradient strengths, we can
             reconstruct the velocity distribution in each volume element
             (voxel). Using this technique to study pressure-driven flow
             through a fully-saturated, cylindrical packed bed, we have
             observed flow channeling near the walls and an exponential
             distribution of velocities. (A)},
   Key = {fds343279}
}

@article{fds340705,
   Author = {Shattuck, M and Behringer, R and Geordiadis, J and Johnson,
             GA},
   Title = {Magnetic resonance imaging of interstitial velocity
             distributions in porous media},
   Year = {1991},
   Month = {January},
   Abstract = {In this article we report on a promising application of
             Magnetic Resonance Imaging (MRI), which can measure local
             interstitial velocity distributions inside fully-saturated
             porous media. We have extended the standard
             three-dimensional MRI sequence to include local velocity
             information. During flow, the moving spins of the fluid (in
             this case water) accumulate phase in the presence of
             magnetic field gradients. This phase is proportional to the
             local velocity. By repeating the measurement under the
             influence of different magnetic gradient strengths, we can
             reconstruct the velocity distribution in each volume element
             (voxel). Using this technique to study pressure-driven flow
             through a fully-saturated, cylindrical packed bed, we have
             observed flow channeling near the walls and an exponential
             distribution of velocities. (A)},
   Key = {fds340705}
}

@booklet{Veres93,
   Author = {VERES, JS and COFER, GP and JOHNSON, GA},
   Title = {Magnetic resonance imaging of leaves},
   Journal = {New Phytologist},
   Volume = {123},
   Number = {4},
   Pages = {769-774},
   Publisher = {WILEY},
   Year = {1993},
   Month = {January},
   ISSN = {0028-646X},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1993LE53500015&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Abstract = {Several aspects of leaf anatomy and morphology make it
             difficult to image leaves with magnetic resonance imaging.
             Since most fully expanded leaves contain much intercellular
             air space and are often thin in one plane, relatively few
             water protons are available to provide signal. Their
             heterogeneous structure and the presence of many air‐water
             interfaces cause imaging problems as a result of differences
             in magnetic susceptibility of tissues and cells. Significant
             progress has been made in overcoming these difficulties,
             primarily by greatly reducing the echo time, permitting in
             vivo imaging of leaves at 7 and 9.4 Tesla with an in‐plane
             resolution of less than 15 μm2. Examples are shown and the
             potential for gaining information regarding in vivo water
             relations of leaves is discussed. Copyright © 1993, Wiley
             Blackwell. All rights reserved},
   Doi = {10.1111/j.1469-8137.1993.tb03788.x},
   Key = {Veres93}
}

@booklet{Stern90,
   Author = {Stern, RL and Johnson, GA and Ravin, CE},
   Title = {Magnetic resonance imaging of the thoracic cavity using a
             paused 3DFT acquisition technique.},
   Journal = {Magn Reson Imaging},
   Volume = {8},
   Number = {6},
   Pages = {747-753},
   Year = {1990},
   ISSN = {0730-725X},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/2266801},
   Abstract = {A new pulse sequence designed for magnetic resonance imaging
             of the entire thoracic cavity is described. This sequence,
             called 3DPAUSE, is a rapid three-dimensional Fourier
             transform (3DFT) sequences with periodic pauses for
             breathing and additional rf pulses after each pause to
             restore the magnetization to steady-state before data
             acquisition resumes. Cardiac motion artifacts are
             effectively removed by signal averaging. Respiratory motion
             artifacts are removed by breath hold. Image artifacts caused
             by an inadequate number of pauses or by inappropriate
             placement of the pauses within a scan are shown, and ways to
             avoid these artifacts are discussed. 3DPAUSE provides the
             ability to acquire three-dimensional arrays in the thoracic
             cavity with minimal artifacts from respiratory and cardiac
             motions in a clinically reasonable time.},
   Doi = {10.1016/0730-725x(90)90010-y},
   Key = {Stern90}
}

@article{fds132801,
   Author = {RL Stern and GA Johnson and CE Ravin},
   Title = {Magnetic resonance imaging of the thoracic cavity using a
             paused 3DFT acquisition technique.},
   Journal = {Magnetic resonance imaging, UNITED STATES},
   Volume = {8},
   Number = {6},
   Pages = {747-53},
   Year = {1990},
   ISSN = {0730-725X},
   Keywords = {Animals • Dogs • Humans • Magnetic Resonance
             Imaging • Thorax • anatomy & histology* •
             methods*},
   Abstract = {A new pulse sequence designed for magnetic resonance imaging
             of the entire thoracic cavity is described. This sequence,
             called 3DPAUSE, is a rapid three-dimensional Fourier
             transform (3DFT) sequences with periodic pauses for
             breathing and additional rf pulses after each pause to
             restore the magnetization to steady-state before data
             acquisition resumes. Cardiac motion artifacts are
             effectively removed by signal averaging. Respiratory motion
             artifacts are removed by breath hold. Image artifacts caused
             by an inadequate number of pauses or by inappropriate
             placement of the pauses within a scan are shown, and ways to
             avoid these artifacts are discussed. 3DPAUSE provides the
             ability to acquire three-dimensional arrays in the thoracic
             cavity with minimal artifacts from respiratory and cardiac
             motions in a clinically reasonable time.},
   Key = {fds132801}
}

@article{fds325754,
   Author = {Sulik, KK and O'Leary-Moore, SK and Parnell, SE and Godin, EA and Styner, MA and Lipinski, RJ and Johnson, GA},
   Title = {MAGNETIC RESONANCE IMAGING-BASED ANALYSES OF A FETAL ALCOHOL
             SPECTRUM DISORDERS MOUSE MODEL},
   Journal = {ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH},
   Volume = {34},
   Number = {8},
   Pages = {31A-31A},
   Year = {2010},
   Key = {fds325754}
}

@article{fds376637,
   Author = {Zhou, X and Johnson, GA},
   Title = {Magnetic resonance microscopy},
   Pages = {5-42-6-14},
   Booktitle = {Medical Imaging: Principles and Practices},
   Year = {2012},
   Month = {January},
   ISBN = {9781439871027},
   url = {http://dx.doi.org/10.1201/b12939},
   Abstract = {Visualization of internal structures of opaque biologic
             objects is essential in many biomedical studies. Limited by
             the penetration depth of the probing sources (photons and
             electrons) and the lack of endogenous contrast, conventional
             forms of microscopy such as optical microscopy and electron
             microscopy require tissues to be sectioned into thin slices
             and stained with organic chemicals or heavy-metal compounds
             prior to examination. These invasive and destructive
             procedures, as well as the harmful radiation in the case of
             electron microscopy, make it difficult to obtain
             three-dimensional information and virtually impossible to
             study biologic tissues in vivo.},
   Doi = {10.1201/b12939},
   Key = {fds376637}
}

@article{fds341990,
   Author = {Zhou, X and Johnson, GA},
   Title = {Magnetic resonance microscopy},
   Pages = {15-1-15-14},
   Booktitle = {Medical Devices and Systems},
   Year = {2006},
   Month = {January},
   ISBN = {9780849321221},
   Abstract = {Visualization of internal structures of opaque biologic
             objects is essential in many biomedical studies. Limited by
             the penetration depth of the probing sources (photons and
             electrons) and the lack of endogenous contrast, conventional
             forms of microscopy such as optical microscopy and electron
             microscopy require tissues to be sectioned into thin slices
             and stained with organic chemicals or heavy-metal compounds
             prior to examination. These invasive and destructive
             procedures, as well as the harmful radiation in the case of
             electron microscopy, make it difficult to obtain
             three-dimensional information and virtually impossible to
             study biologic tissues in vivo.},
   Key = {fds341990}
}

@article{fds342055,
   Author = {Zhou, X and Allan Johnson and G},
   Title = {Magnetic resonance microscopy},
   Pages = {13-1-13-14},
   Booktitle = {Biomedical Imaging},
   Year = {2003},
   Month = {January},
   ISBN = {9780849318108},
   Abstract = {Visualization of internal structures of opaque biologic
             objects is essential in many biomedical studies. Limited by
             the penetration depth of the probing sources (photons and
             electrons) and the lack of endogenous contrast, conventional
             forms of microscopy such as optical microscopy and electron
             microscopy require tissues to be sectioned into thin slices
             and stained with organic chemicals or heavy-metal compounds
             prior to examination. These invasive and destructive
             procedures, as well as the harmful radiation in the case of
             electron microscopy, make it difficult to obtain
             three-dimensional information and virtually impossible to
             study biologic tissues in vivo.},
   Key = {fds342055}
}

@article{fds268751,
   Author = {O'Leary-Moore, SK and Parnell, SE and Godin, EA and Johnson, GA and Styner, M and Oguz, I and Budin, F and Jiang, Y and Dehart, DB and Sulik,
             KK},
   Title = {MAGNETIC RESONANCE MICROSCOPY AND DIFFUSION TENSOR IMAGING
             DEFINE STAGE-DEPENDENT CHANGES IN BRAIN MORPHOLOGY AFTER
             PRENATAL ETHANOL EXPOSURE IN MICE},
   Journal = {ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH},
   Volume = {34},
   Number = {6},
   Pages = {298A-298A},
   Publisher = {WILEY-BLACKWELL},
   Year = {2010},
   Month = {June},
   ISSN = {0145-6008},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000291641500215&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {fds268751}
}

@booklet{Delnomdedieu98,
   Author = {M. Delnomdedieu and L. W. Hedlund and R. R. Maronpot and G.
             A. Johnson},
   Title = {Magnetic resonance microscopy and histopathology:
             Comparative approach of bromobenzene-induced hepatotoxicity
             in the rat},
   Journal = {Hepatology},
   Volume = {27},
   Number = {2},
   Pages = {526 -- 532},
   Year = {1998},
   Month = {February},
   Key = {Delnomdedieu98}
}

@article{fds269045,
   Author = {Delnomdedieu, M and Hedlund, LW and Maronpot, RR and Johnson,
             GA},
   Title = {Magnetic resonance microscopy and histopathology:
             comparative approach of bromobenzene-induced hepatotoxicity
             in the rat.},
   Journal = {Hepatology},
   Volume = {27},
   Number = {2},
   Pages = {526-532},
   Year = {1998},
   Month = {February},
   ISSN = {0270-9139},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/9462653},
   Keywords = {Animals • Bromobenzenes* • Female •
             Histocytochemistry • Liver Diseases • Microscopy
             • Rats • Rats, Inbred F344 • Reproducibility
             of Results • Sensitivity and Specificity •
             chemically induced • methods* •
             pathology*},
   Abstract = {The development of magnetic resonance (MR) microscopy has
             provided new approaches to histology and histopathology.
             Recent work has shown the promise of increased sensitivity
             in animal models of chemically induced hepatotoxicity.
             However, the field is so new that there is little experience
             to relate changes seen in MR micrographs to the more
             traditional optical images stained with hematoxylin and
             eosin. This work compares the sensitivity and
             reproducibility of MR microscopy with conventional
             histopathology in detecting bromobenzene-induced
             hepatotoxicity in the rat. A time-course study was
             undertaken to provide a range of histopathologies. Specimens
             were studied at 24, 48, 72, and 96 hours after exposure to
             10% of the median lethal dose of bromobenzene. Using 4
             animals per group (a total of 32 rats) added statistical
             significance to the study and defined a range of interanimal
             variability over 96 hours. This work shows that MR
             microscopy, besides being nondestructive and
             three-dimensional, is at least as sensitive as conventional
             hematoxylin-eosin staining in detecting bromobenzene-induced
             centrilobular lesions and recovery of the hepatocellular
             architecture in the rat. This study further suggests that,
             as we begin to understand the underlying mechanisms of
             contrast in MR histology, MR may, in fact, supply even
             higher specificity than more traditional studies: variations
             were observed in MR images of treated livers at a given time
             point that could be not be differentiated based on the
             grading of necrosis and inflammation on hematoxylin-eosin-stained
             sections.},
   Doi = {10.1002/hep.510270229},
   Key = {fds269045}
}

@article{fds268768,
   Author = {Godin, EA and O'Leary-Moore, SK and Khan, AA and Parnell, SE and Ament,
             JJ and Dehart, DB and Johnson, BW and Allan Johnson and G and Styner, MA and Sulik, KK},
   Title = {Magnetic resonance microscopy defines ethanol-induced brain
             abnormalities in prenatal mice: effects of acute insult on
             gestational day 7.},
   Journal = {Alcohol Clin Exp Res},
   Volume = {34},
   Number = {1},
   Pages = {98-111},
   Year = {2010},
   Month = {January},
   ISSN = {0145-6008},
   url = {http://dx.doi.org/10.1111/j.1530-0277.2009.01071.x},
   Abstract = {BACKGROUND: This magnetic resonance microscopy (MRM)-based
             report is the second in a series designed to illustrate the
             spectrum of craniofacial and central nervous system (CNS)
             dysmorphia resulting from single- and multiple-day maternal
             ethanol treatment. The study described in this report
             examined the consequences of ethanol exposure on gestational
             day (GD) 7 in mice, a time in development when gastrulation
             and neural plate development begins; corresponding to the
             mid- to late third week postfertilization in humans. Acute
             GD 7 ethanol exposure in mice has previously been shown to
             result in CNS defects consistent with holoprosencephaly
             (HPE) and craniofacial anomalies typical of those in Fetal
             Alcohol Syndrome (FAS). MRM has facilitated further
             definition of the range of GD 7 ethanol-induced defects.
             METHODS: C57Bl/6J female mice were intraperitoneally (i.p.)
             administered vehicle or 2 injections of 2.9 g/kg ethanol on
             day 7 of pregnancy. Stage-matched control and
             ethanol-exposed GD 17 fetuses selected for imaging were
             immersion fixed in a Bouins/Prohance solution. MRM was
             conducted at either 7.0 Tesla (T) or 9.4 T. Resulting 29
             microm isotropic spatial resolution scans were segmented and
             reconstructed to provide 3D images. Linear and volumetric
             brain measures, as well as morphological features, were
             compared for control and ethanol-exposed fetuses. Following
             MRM, selected specimens were processed for routine histology
             and light microscopic examination. RESULTS: Gestational day
             7 ethanol exposure resulted in a spectrum of median facial
             and forebrain deficiencies, as expected. This range of
             abnormalities falls within the HPE spectrum; a spectrum for
             which facial dysmorphology is consistent with and typically
             is predictive of that of the forebrain. In addition, other
             defects including median facial cleft, cleft palate,
             micrognathia, pituitary agenesis, and third ventricular
             dilatation were identified. MRM analyses also revealed
             cerebral cortical dysplasia/heterotopias resulting from this
             acute, early insult and facilitated a subsequent focused
             histological investigation of these defects. CONCLUSIONS:
             Individual MRM scans and 3D reconstructions of fetal mouse
             brains have facilitated demonstration of a broad range of GD
             7 ethanol-induced morphological abnormality. These results,
             including the discovery of cerebral cortical heterotopias,
             elucidate the teratogenic potential of ethanol insult during
             the third week of human prenatal development.},
   Doi = {10.1111/j.1530-0277.2009.01071.x},
   Key = {fds268768}
}

@article{fds268767,
   Author = {Parnell, SE and O'Leary-Moore, SK and Godin, EA and Dehart, DB and Johnson, BW and Allan Johnson and G and Styner, MA and Sulik,
             KK},
   Title = {Magnetic resonance microscopy defines ethanol-induced brain
             abnormalities in prenatal mice: effects of acute insult on
             gestational day 8.},
   Journal = {Alcohol Clin Exp Res},
   Volume = {33},
   Number = {6},
   Pages = {1001-1011},
   Year = {2009},
   Month = {June},
   ISSN = {0145-6008},
   url = {http://dx.doi.org/10.1111/j.1530-0277.2009.00921.x},
   Abstract = {BACKGROUND: Magnetic resonance microscopy (MRM), magnetic
             resonance imaging (MRI) at microscopic levels, provides
             unprecedented opportunities to aid in defining the full
             spectrum of ethanol's insult to the developing brain. This
             is the first in a series of reports that, collectively, will
             provide an MRM-based atlas of developmental stage-dependent
             structural brain abnormalities in a Fetal Alcohol Spectrum
             Disorders (FASD) mouse model. The ethanol exposure time and
             developmental stage examined for this report is gestational
             day (GD) 8 in mice, when the embryos are at early
             neurulation stages; stages present in humans early in the
             fourth week postfertilization. METHODS: For this study,
             pregnant C57Bl/6J mice were administered an ethanol dosage
             of 2.8 g/kg intraperitoneally at 8 days, 0 hour and again at
             8 days, 4 hours postfertilization. On GD 17, fetuses that
             were selected for MRM analyses were immersion fixed in a
             Bouin's/Prohance solution. Control fetuses from
             vehicle-treated dams were stage-matched to those that were
             ethanol-exposed. The fetal mice were scanned ex vivo at 7.0
             T and 512 x 512 x 1024 image arrays were acquired using 3-D
             spin warp encoding. The resulting 29 microm (isotropic)
             resolution images were processed using ITK-SNAP, a 3-D
             segmentation/visualization tool. Linear and volume
             measurements were determined for selected brain, head, and
             body regions of each specimen. Comparisons were made between
             control and treated fetuses, with an emphasis on determining
             (dis)proportionate changes in specific brain regions.
             RESULTS: As compared with controls, the crown-rump lengths
             of stage-matched ethanol-exposed GD 17 fetuses were
             significantly reduced, as were brain and whole body volumes.
             Volume reductions were notable in every brain region
             examined, with the exception of the pituitary and septal
             region, and were accompanied by increased ventricular
             volumes. Disproportionate regional brain volume reductions
             were most marked on the right side and were significant for
             the olfactory bulb, hippocampus, and cerebellum; the latter
             being the most severely affected. Additionally, the septal
             region and the pituitary were disproportionately large.
             Linear measures were consistent with those of volume. Other
             dysmorphologic features noted in the MR scans were choanal
             stenosis and optic nerve coloboma. CONCLUSIONS: This study
             demonstrates that exposure to ethanol occurring in mice at
             stages corresponding to the human fourth week
             postfertilization results in structural brain abnormalities
             that are readily identifiable at fetal stages of
             development. In addition to illustrating the utility of MR
             microscopy for analysis of an FASD mouse model, this work
             provides new information that confirms and extends human
             clinical observations. It also provides a framework for
             comparison of structural brain abnormalities resulting from
             ethanol exposure at other developmental stages and
             dosages.},
   Doi = {10.1111/j.1530-0277.2009.00921.x},
   Key = {fds268767}
}

@booklet{Johnson97a,
   Author = {Johnson, GA and Benveniste, H and Engelhardt, RT and Qiu, H and Hedlund,
             LW},
   Title = {Magnetic resonance microscopy in basic studies of brain
             structure and function.},
   Journal = {Ann N Y Acad Sci},
   Volume = {820},
   Series = {ANNALS OF THE NEW YORK ACADEMY OF SCIENCES},
   Pages = {139-147},
   Year = {1997},
   Month = {May},
   ISSN = {0077-8923},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/9237453},
   Doi = {10.1111/j.1749-6632.1997.tb46193.x},
   Key = {Johnson97a}
}

@article{fds132813,
   Author = {GA Johnson and H Benveniste and RT Engelhardt and H Qiu and LW
             Hedlund},
   Title = {Magnetic resonance microscopy in basic studies of brain
             structure and function.},
   Journal = {Annals of the New York Academy of Sciences, UNITED
             STATES},
   Volume = {820},
   Pages = {139-47; discussion 147-8},
   Year = {1997},
   Month = {May},
   ISSN = {0077-8923},
   Keywords = {Animals • Brain • Diagnostic Imaging • Humans
             • Microscopy • methods* • pathology •
             physiology • radiography*},
   Key = {fds132813}
}

@article{fds268884,
   Author = {Johnson, GA and Thompson, MB and Drayer, BP and Bone,
             SN},
   Title = {Magnetic resonance microscopy in neurologic
             models.},
   Journal = {Acta Radiol Suppl},
   Volume = {369},
   Pages = {267-268},
   Year = {1986},
   ISSN = {0365-5954},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/2980471},
   Keywords = {Animals • Brain • Chick Embryo • Magnetic
             Resonance Imaging • Rats • anatomy & histology*
             • cytology • methods*},
   Abstract = {Magnetic resonance imaging techniques have been developed to
             permit imaging with slice thickness less than 1 mm and
             pixels of 50 x 50 microns. Special purpose gradient and
             radiofrequency coils and three-dimensional imaging
             techniques enable acquisition of images with sufficient
             signal to noise to utilize these microscopic picture
             elements. Live 200 g rats were imaged enabling clear
             definition of gray and white matter structures. Examples
             include the Sylvian aqueduct and the substantia nigra.
             Three-dimensional microscopic images of live chick embryos
             enabled definition of ventricles and brain parenchyma as
             well as measurement of T1 over the set of 16 contiguous 1.2
             mm slices.},
   Key = {fds268884}
}

@article{fds268764,
   Author = {Benveniste, H and Einstein, G and Kim, KR and Allan Johnson,
             G},
   Title = {Magnetic resonance microscopy of Alzheimer's disease: Senile
             plaques - A whiter shade of pale?},
   Journal = {NeuroImage},
   Volume = {7},
   Number = {4 PART II},
   Pages = {S519},
   Year = {1998},
   Month = {January},
   url = {http://dx.doi.org/10.1016/s1053-8119(18)31352-1},
   Doi = {10.1016/s1053-8119(18)31352-1},
   Key = {fds268764}
}

@article{fds132845,
   Author = {GA Johnson and J Brown and PJ Kramer},
   Title = {Magnetic resonance microscopy of changes in water content in
             stems of transpiring plants.},
   Journal = {Proceedings of the National Academy of Sciences of the
             United States of America, UNITED STATES},
   Volume = {84},
   Number = {9},
   Pages = {2752-5},
   Year = {1987},
   Month = {May},
   ISSN = {0027-8424},
   Keywords = {Magnetic Resonance Spectroscopy • Plants • Water
             • metabolism*},
   Abstract = {Differences in water content and degree of binding in the
             various stem tissues of Pelargonium hortorum were observed
             by magnetic resonance imaging. 1H images were obtained with
             a resolution of 100 microns in the transverse plane and a
             slice thickness of 1250 microns. It was possible to
             distinguish the principal tissues of the stem by differences
             in their proton density or apparent water content and spin
             lattice relaxation time (T1) or degree of water binding.
             Measurements were made while the plant was slowly and
             actively transpiring. In the slowly transpiring plant, T1 of
             various tissues ranged from an average of 659 to 865 ms with
             a proton density variation of from 72 to 100%. In the
             actively transpiring plant, T1 ranged from an average of 511
             to 736 ms, and the proton density was reduced, ranging
             between 62 and 88% of the peak value found in the slowly
             transpiring plant. The fibrous sheath surrounding the
             vascular tissue and the epidermal region was found to have
             the highest spin density and T1. Both tissues are comprised
             of relatively small thick-walled cells. Cortical and pith
             parenchyma are composed of larger, thinner-walled cells with
             numerous intercellular spaces and lower spin density and T1.
             The differences are attributed to the higher water content
             by volume in the tissue composed of smaller, more compactly
             arranged cells. The resolution obtained in this work enables
             clear definition of tissues in the living plant and
             quantitative information concerning differences in the
             distribution and extent of binding of water.},
   Key = {fds132845}
}

@booklet{Johnson87d,
   Author = {Johnson, GA and Brown, J and Kramer, PJ},
   Title = {Magnetic resonance microscopy of changes in water content in
             stems of transpiring plants.},
   Journal = {Proc Natl Acad Sci U S A},
   Volume = {84},
   Number = {9},
   Pages = {2752-2755},
   Year = {1987},
   Month = {May},
   ISSN = {0027-8424},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/3472235},
   Abstract = {Differences in water content and degree of binding in the
             various stem tissues of Pelargonium hortorum were observed
             by magnetic resonance imaging. 1H images were obtained with
             a resolution of 100 microns in the transverse plane and a
             slice thickness of 1250 microns. It was possible to
             distinguish the principal tissues of the stem by differences
             in their proton density or apparent water content and spin
             lattice relaxation time (T1) or degree of water binding.
             Measurements were made while the plant was slowly and
             actively transpiring. In the slowly transpiring plant, T1 of
             various tissues ranged from an average of 659 to 865 ms with
             a proton density variation of from 72 to 100%. In the
             actively transpiring plant, T1 ranged from an average of 511
             to 736 ms, and the proton density was reduced, ranging
             between 62 and 88% of the peak value found in the slowly
             transpiring plant. The fibrous sheath surrounding the
             vascular tissue and the epidermal region was found to have
             the highest spin density and T1. Both tissues are comprised
             of relatively small thick-walled cells. Cortical and pith
             parenchyma are composed of larger, thinner-walled cells with
             numerous intercellular spaces and lower spin density and T1.
             The differences are attributed to the higher water content
             by volume in the tissue composed of smaller, more compactly
             arranged cells. The resolution obtained in this work enables
             clear definition of tissues in the living plant and
             quantitative information concerning differences in the
             distribution and extent of binding of water.},
   Doi = {10.1073/pnas.84.9.2752},
   Key = {Johnson87d}
}

@article{fds268758,
   Author = {Johnson, GA and Maronpot, RR},
   Title = {Magnetic resonance microscopy of chemically-induced liver
             foci.},
   Journal = {Toxicol Pathol},
   Volume = {17},
   Number = {4 Pt 1},
   Pages = {613-616},
   Year = {1989},
   ISSN = {0192-6233},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/2629098},
   Keywords = {Animals • Carcinogenicity Tests • Diet •
             Female • Liver • Liver Neoplasms, Experimental
             • Magnetic Resonance Imaging • Rats • Rats,
             Inbred F344 • chemically induced • pathology*
             • ultrastructure},
   Abstract = {Magnetic resonance imaging (MRI) is a new imaging technique
             used in clinical diagnosis. This paper describes extension
             of the technique to basic research applications--specifically
             detecting and characterizing chemically-induced liver
             neoplasms and foci of cellular alteration. Two systems have
             been built that allow spatial microscopic resolution--more
             than 100,000 x greater than that of earlier efforts. Use of
             spin-lattice (T1) and spin-spin (T2) relaxation times
             permits detailed characterization of the
             tissue.},
   Doi = {10.1177/0192623389017004106},
   Key = {fds268758}
}

@article{fds132781,
   Author = {EL Effmann and GA Johnson and BR Smith and GA Talbott and G
             Cofer},
   Title = {Magnetic resonance microscopy of chick embryos in
             ovo.},
   Journal = {Teratology, UNITED STATES},
   Volume = {38},
   Number = {1},
   Pages = {59-65},
   Year = {1988},
   Month = {July},
   ISSN = {0040-3709},
   Keywords = {Animals • Cardiovascular System • Chick Embryo
             • Magnetic Resonance Imaging • Nervous System
             • anatomy & histology* • embryology •
             methods*},
   Abstract = {Magnetic resonance imaging (MRI) of the live 11-day chick
             embryo with special radiofrequency coils and 3-D imaging
             methods has produced contiguous 1.25-mm-thick slices with
             200-microns pixel resolution, permitting definition of
             cardiac chambers, cerebral ventricles, spinal cord, liver,
             and lungs. It was the objective of this study to image
             younger chick embryos in ovo with higher spatial resolution
             through the application of implanted radiofrequency coils.
             Fertilized Arbor Acre eggs were windowed at 9, 6, and 4
             days. Circular coils 18 mm in diameter tuned to 85.5 MHz
             were suspended around the developing embryo. The eggs were
             sealed with tape and maintained at 37 degrees C during the
             imaging procedure. MRI was performed in a 2.0-Tesla GE
             system utilizing a 3-D Fourier transform acquisition in
             sagittal and axial planes with a partial saturation sequence
             (TR = 400 ms, TE = 27 ms). Approximately 1 hour of imaging
             time was required to obtain 16 contiguous 600-microns-thick
             slices with 50-microns pixel resolution. Embryos remained
             viable through the imaging procedure. Embryos were
             photographed, fixed, and cleared for correlative anatomical
             study. Vitelline vessels, dorsal aorta, aortic arches,
             cardinal veins, and cardiac chambers were identified as
             areas of decreased signal intensity. Cerebral ventricles and
             the vitreous portion of the eye have signal intensities that
             are less than adjacent neural, scleral, and lens tissue.
             Further refinements in MR instrumentation and imaging
             sequences promise improvements in resolution and offer the
             potential for sequential observations of the intact
             embryo.},
   Key = {fds132781}
}

@booklet{Effmann88,
   Author = {Effmann, EL and Johnson, GA and Smith, BR and Talbott, GA and Cofer,
             G},
   Title = {Magnetic resonance microscopy of chick embryos in
             ovo.},
   Journal = {Teratology},
   Volume = {38},
   Number = {1},
   Pages = {59-65},
   Year = {1988},
   Month = {July},
   ISSN = {0040-3709},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/3175940},
   Abstract = {Magnetic resonance imaging (MRI) of the live 11-day chick
             embryo with special radiofrequency coils and 3-D imaging
             methods has produced contiguous 1.25-mm-thick slices with
             200-microns pixel resolution, permitting definition of
             cardiac chambers, cerebral ventricles, spinal cord, liver,
             and lungs. It was the objective of this study to image
             younger chick embryos in ovo with higher spatial resolution
             through the application of implanted radiofrequency coils.
             Fertilized Arbor Acre eggs were windowed at 9, 6, and 4
             days. Circular coils 18 mm in diameter tuned to 85.5 MHz
             were suspended around the developing embryo. The eggs were
             sealed with tape and maintained at 37 degrees C during the
             imaging procedure. MRI was performed in a 2.0-Tesla GE
             system utilizing a 3-D Fourier transform acquisition in
             sagittal and axial planes with a partial saturation sequence
             (TR = 400 ms, TE = 27 ms). Approximately 1 hour of imaging
             time was required to obtain 16 contiguous 600-microns-thick
             slices with 50-microns pixel resolution. Embryos remained
             viable through the imaging procedure. Embryos were
             photographed, fixed, and cleared for correlative anatomical
             study. Vitelline vessels, dorsal aorta, aortic arches,
             cardinal veins, and cardiac chambers were identified as
             areas of decreased signal intensity. Cerebral ventricles and
             the vitreous portion of the eye have signal intensities that
             are less than adjacent neural, scleral, and lens tissue.
             Further refinements in MR instrumentation and imaging
             sequences promise improvements in resolution and offer the
             potential for sequential observations of the intact
             embryo.},
   Doi = {10.1002/tera.1420380109},
   Key = {Effmann88}
}

@booklet{Smith96,
   Author = {Smith, BR and Linney, E and Huff, DS and Johnson,
             GA},
   Title = {Magnetic resonance microscopy of embryos.},
   Journal = {Comput Med Imaging Graph},
   Volume = {20},
   Number = {6},
   Pages = {483-490},
   Year = {1996},
   ISSN = {0895-6111},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/9007215},
   Abstract = {We demonstrate that magnetic resonance (MR) microscopy
             provides a mechanism to investigate normal and abnormal
             developmental anatomy in a non-destructive and
             distortion-free manner. Techniques for the fixation,
             embedding, perfusion and image acquisition of embryos
             between 3 and 30 mm crown rump length are described. We
             describe the perfusion of a contrast agent to enhance images
             of the developing embryonic vasculature. Data are acquired
             as three-dimensional isotropic arrays which permit images to
             be reformatted retrospectively in any plane. The data are
             available for archiving, distributing and for
             post-acquisition manipulations. MR microscopy is a fast
             technique for producing three-dimensional reconstructions
             and is free from registration and sectioning
             artifacts.},
   Doi = {10.1016/s0895-6111(96)00046-8},
   Key = {Smith96}
}

@article{fds132819,
   Author = {BR Smith and E Linney and DS Huff and GA Johnson},
   Title = {Magnetic resonance microscopy of embryos.},
   Journal = {Computerized medical imaging and graphics : the official
             journal of the Computerized Medical Imaging Society, UNITED
             STATES},
   Volume = {20},
   Number = {6},
   Pages = {483-90},
   ISSN = {0895-6111},
   Keywords = {Anatomy, Artistic • Animals • Contrast Media
             • Databases, Factual • Embryo • Embryonic and
             Fetal Development* • Humans • Image Processing,
             Computer-Assisted • Magnetic Resonance Imaging* •
             Medical Illustration • Mice • Microscopy •
             anatomy & histology • anatomy & histology* •
             embryology},
   Abstract = {We demonstrate that magnetic resonance (MR) microscopy
             provides a mechanism to investigate normal and abnormal
             developmental anatomy in a non-destructive and
             distortion-free manner. Techniques for the fixation,
             embedding, perfusion and image acquisition of embryos
             between 3 and 30 mm crown rump length are described. We
             describe the perfusion of a contrast agent to enhance images
             of the developing embryonic vasculature. Data are acquired
             as three-dimensional isotropic arrays which permit images to
             be reformatted retrospectively in any plane. The data are
             available for archiving, distributing and for
             post-acquisition manipulations. MR microscopy is a fast
             technique for producing three-dimensional reconstructions
             and is free from registration and sectioning
             artifacts.},
   Key = {fds132819}
}

@booklet{Smith94,
   Author = {Smith, BR and Johnson, GA and Groman, EV and Linney,
             E},
   Title = {Magnetic resonance microscopy of mouse embryos.},
   Journal = {Proc Natl Acad Sci U S A},
   Volume = {91},
   Number = {9},
   Pages = {3530-3533},
   Year = {1994},
   Month = {April},
   ISSN = {0027-8424},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/8170941},
   Abstract = {The increased use of the mouse as a model for various
             aspects of mammalian biology has caused a renewed interest
             in developing strategies for examining and comparing normal
             and abnormal mouse embryonic development and anatomy. In
             this study, we have explored the use of magnetic resonance
             microscopy as a tool for these purposes. Techniques for the
             fixation, embedding, perfusion, and image acquisition of
             mouse embryos are described. The perfusion of bovine serum
             albumin-diethylenetriamine pentaacetic anhydride-gadolinium
             as a contrast agent enhances images of the developing
             embryonic vasculature during critical stages of
             organogenesis and allows for comparisons when embryos have
             been treated with teratogens such as retinoic acid. The
             acquired three-dimensional data sets are available for
             archiving, distributing, and postacquisition manipulations
             such as computer segmentation of anatomical
             structures.},
   Doi = {10.1073/pnas.91.9.3530},
   Key = {Smith94}
}

@article{fds132863,
   Author = {BR Smith and GA Johnson and EV Groman and E Linney},
   Title = {Magnetic resonance microscopy of mouse embryos.},
   Journal = {Proceedings of the National Academy of Sciences of the
             United States of America, UNITED STATES},
   Volume = {91},
   Number = {9},
   Pages = {3530-3},
   Year = {1994},
   Month = {April},
   ISSN = {0027-8424},
   Keywords = {Age Factors • Albumins • Animals • Contrast
             Media • Gadolinium DTPA* • Image Processing,
             Computer-Assisted • Mice • Organometallic
             Compounds • Pentetic Acid • analogs & derivatives
             • diagnostic use • embryology*},
   Abstract = {The increased use of the mouse as a model for various
             aspects of mammalian biology has caused a renewed interest
             in developing strategies for examining and comparing normal
             and abnormal mouse embryonic development and anatomy. In
             this study, we have explored the use of magnetic resonance
             microscopy as a tool for these purposes. Techniques for the
             fixation, embedding, perfusion, and image acquisition of
             mouse embryos are described. The perfusion of bovine serum
             albumin-diethylenetriamine pentaacetic anhydride-gadolinium
             as a contrast agent enhances images of the developing
             embryonic vasculature during critical stages of
             organogenesis and allows for comparisons when embryos have
             been treated with teratogens such as retinoic acid. The
             acquired three-dimensional data sets are available for
             archiving, distributing, and postacquisition manipulations
             such as computer segmentation of anatomical
             structures.},
   Key = {fds132863}
}

@booklet{Brown88,
   Author = {Brown, JM and Thomas, JF and Cofer, GP and Johnson,
             GA},
   Title = {Magnetic Resonance Microscopy of Stem Tissues of Pelargonium
             hortorum},
   Journal = {Botanical Gazette},
   Volume = {149},
   Number = {3},
   Pages = {253-259},
   Publisher = {University of Chicago Press},
   Year = {1988},
   Month = {September},
   ISSN = {0006-8071},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1988Q941300001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Doi = {10.1086/337713},
   Key = {Brown88}
}

@booklet{Benveniste00,
   Author = {Benveniste, H and Kim, K and Zhang, L and Johnson,
             GA},
   Title = {Magnetic resonance microscopy of the C57BL mouse
             brain.},
   Journal = {Neuroimage},
   Volume = {11},
   Number = {6 Pt 1},
   Pages = {601-611},
   Year = {2000},
   Month = {June},
   ISSN = {1053-8119},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000087963600003&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Abstract = {With the rapid progression in gene technologies, transgenic,
             targeted, and chemically induced mutations in mice are
             continually created. The major goal of these studies is to
             understand and characterize the effects of genotype on
             anatomy, physiology, and behavior and ultimately the role of
             genotype in development of disease. The demand for imaging
             techniques with high spatial resolution potential is rising
             because such imaging tools would expedite anatomical
             phenotyping in the genetically altered mice. Magnetic
             resonance microscopy (MRM) is a noninvasive, inherently
             three-dimensional (3D) imaging technique capable of
             visualizing several anatomical structures in the small
             mouse. The 3D nature of MRM also allows for interpretation
             of complex spatial relationships between substructures,
             which is important when phenotyping anatomically. The goal
             of this paper is to systematically describe three major
             brain regions in the C57BL/6J mouse at microanatomical
             spatial resolution ranges using in vitro MRM. We explore
             different MR contrast parameters, voxel sizes, and
             signal-to-noise ratios to best characterize C57BL/6J mouse
             brain microstructure by MRM. Further, we compare all MRM
             images with Nissl-stained brain sections. Major findings
             were as follows: T2* MR images visualized several gross
             anatomical regions in the mouse brain but not, for example,
             subregions within the hippocampus. Diffusion proton stains
             on the other hand were superior to T2* MR images and
             delineated many subregions within the hippocampus proper.
             Finally, contrast enhancement facilitated visualization of
             hippocampal anatomy on the T2* MR images. The results of
             this study are part of an ongoing initiative at our Center
             focused on creating a complete C57BL/6J mouse anatomical 3D
             image database by MRM.},
   Doi = {10.1006/nimg.2000.0567},
   Key = {Benveniste00}
}

@article{fds268911,
   Author = {Arnder, L and Zhou, X and Cofer, GP and Hedlund, LW and Johnson,
             GA},
   Title = {Magnetic resonance microscopy of the rat carotid artery at
             300 megahertz.},
   Journal = {Invest Radiol},
   Volume = {29},
   Number = {9},
   Pages = {822-826},
   Year = {1994},
   Month = {September},
   ISSN = {0020-9996},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/7995700},
   Keywords = {Angioplasty, Balloon • Animals • Arteriosclerosis
             • Carotid Arteries • Carotid Artery Diseases
             • Female • Magnetic Resonance Angiography •
             Microscopy • Rats • Rats, Sprague-Dawley •
             diagnosis • methods* • pathology* •
             therapy},
   Abstract = {RATIONALE AND OBJECTIVES: Magnetic resonance microscopy
             (MRM) has evolved from a technical curiosity to a tool with
             which researchers can study important disease models. But
             MRM is not simply an extension of clinical magnetic
             resonance imaging. In this article, the unique adaptations
             of MRM required in the study of carotid artery disease are
             outlined. The techniques of MRM are integrated into a
             specific model of carotid artery disease in the rat to allow
             in vivo studies of vascular wall thickening after removal of
             the vascular endothelium. METHODS: Imaging was performed at
             300 MHz in 250-gm Sprague-Dawley rats using surgically
             implanted radiofrequency coils to localize the region of
             interest and to provide an increase in the signal-to-noise
             ratio over that of volume or surface coils. A
             three-dimensional Fourier encoding sequence was modified
             with flow-dephasing gradients to minimize signal and
             artifacts from moving blood. RESULTS: In vivo images were
             acquired with spatial resolution of 25 x 25 x 400 microns
             and signal-to-noise ratio more than sufficient to define the
             morphology of the vascular wall. Significant changes in the
             intensity and distribution of signal were visible in the
             area surrounding the vessel after angioplasty. CONCLUSIONS:
             Signal-to-noise improvements from surgically implanted coils
             coupled to a three-dimensional radiofrequency-refocused
             sequence with flow-dephasing gradients were sufficient to
             define the wall of the carotid artery. The
             diffusion-weighted pulse sequence detects signal changes in
             the area surrounding the vessel after angioplasty. The MRM
             techniques described and the contrast observed allow us, for
             the first time to follow in vivo the early stage of
             developing atherosclerosis in the vessel wall and closely
             surrounding tissue.},
   Doi = {10.1097/00004424-199409000-00004},
   Key = {fds268911}
}

@article{fds268993,
   Author = {Hedlund, LW and Johnson, GA and Mills, GI},
   Title = {Magnetic resonance microscopy of the rat thorax and
             abdomen.},
   Journal = {Invest Radiol},
   Volume = {21},
   Number = {11},
   Pages = {843-846},
   Year = {1986},
   Month = {November},
   ISSN = {0020-9996},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/3781788},
   Keywords = {Abdomen • Animals • Magnetic Resonance
             Spectroscopy • Male • Myocardial Contraction
             • Rats • Rats, Inbred Strains • Respiration
             • Thorax • anatomy & histology* • diagnostic
             use},
   Abstract = {With magnetic resonance (MR) microscopy, high-resolution
             volumetric imaging (3DFT) of small animals is possible.
             Although these techniques are suitable for imaging the head
             and other small stationary objects, breathing and cardiac
             motion degrade the quality of body images. Scan synchronous
             ventilation and cardiac gating methods have been developed
             that permit acquisition of high-resolution images from
             anywhere in the body of small animals (150 to 400 g).
             Anesthetized rats were ventilated in synchrony with
             three-dimensional Fourier spin warp (3DFT) sequence (TR =
             400 to 1000 ms, TE = 20 ms). Eight or 16 slices (1.2 or 2.5
             mm thick) were acquired simultaneously. Effective pixel size
             was 200 X 200 mu. Imaging was performed in a 1.5 T, 1-m bore
             research system using a 28-cm diameter high field gradient
             coil and a 6-cm diameter radio frequency coil. For thoracic
             imaging, acquisitions were gated to the QRS of the ECG. Scan
             synchronous ventilation eliminated breathing motion
             artifacts and permitted visualization of peripheral vascular
             structures in the lung and liver. In images that were also
             cardiac gated, cardiac chambers and major thoracic vessels,
             including the coronary arteries, were well demonstrated.
             Thus, thoroughly characterized rodent models can now be
             studied with MR not only to explore noninvasively the
             intricacies of mammalian pathomorphology, but also to test
             the capabilities of MR and aid in interpreting MR
             data.},
   Doi = {10.1097/00004424-198611000-00002},
   Key = {fds268993}
}

@booklet{Hedlund91,
   Author = {Hedlund, LW and Maronpot, RR and Johnson, GA and Cofer, GP and Mills,
             GI and Wheeler, CT},
   Title = {Magnetic resonance microscopy of toxic renal injury induced
             by Bromoethylamine in rats},
   Journal = {Toxicological Sciences},
   Volume = {16},
   Number = {4},
   Pages = {787-797},
   Publisher = {Oxford University Press (OUP)},
   Year = {1991},
   Month = {January},
   ISSN = {0272-0590},
   url = {http://dx.doi.org/10.1093/toxsci/16.4.787},
   Abstract = {Magnetic Resonance Microscopy of Toxic Renal Injury Induced
             by Bromoethylamine in Rats. Hedlund, L. W., Maronpot, R. R.,
             Johnson, G. A., Cofer, G. P., Mills, G. I., and Wheeler, C.
             T. (1991). Fundam. Appl. Toxicol. 16, 787-797. The
             alkylhalide 2-bromoethylamine hydro-bromide (BEA) produces
             renal injury in rats that mimics analgesic-related renal
             injury in humans. Our purpose was to examine this injury, in
             vivo in rats, with magnetic resonance (MR) microscopy and
             correlate MR findings with findings from light microscopy of
             hematoxylin-eosin-stained sections. Rats (n = 48) were
             injected intravenously with BEA (150 mg/kg) or saline and
             imaged with MR 6, 48, and 336 hr later. The spin-spin
             relaxation time, T2, was measured from the cortex to the
             papilla. In other rats, we measured regional water content
             of the kidney. Renal injury was present 48 and 336 hr after
             BEA dosing based on increased renal organ weights, decreased
             urine specific gravity, and significant renal lesions (H &
             E). T2 was elevated in the inner stripe of the outer medulla
             in injured kidneys at 48 hr. The differences in T2 between
             cortex and outer medulla were also elevated 48 hr after BEA.
             In the inner medulla, there were no changes in T2 after BEA
             treatment. However, in all groups there were significant
             regional differences in T2. The value of T2 increased from
             outer to inner medulla and this gradient was directly
             correlated with water content. Thus, MR microscopy detected
             damage in the outer medulla after BEA injury but not the
             damage in the inner medulla. T2 appeared to reflect the
             water content in the different regions of the medulla. The
             noninvasive in vivo capability of MR microscopy, with its
             high sensitivity to tissue water, allows the toxicologist to
             monitor the progression and regression of toxic insult in
             the same animal. At present the technology is complicated.
             The precise and accurate measure of MR-sensitive parameters
             in live animals at microscopic resolution is difficult.
             However, as the technology matures, there will be
             significant improvements providing the toxicologist a unique
             in vivo tool. © 1991 by the Society of Toxicology.},
   Doi = {10.1093/toxsci/16.4.787},
   Key = {Hedlund91}
}

@article{fds269102,
   Author = {Hedlund, LW and Maronpot, RR and Johnson, GA and Cofer, GP and Mills,
             GI and Wheeler, CT},
   Title = {Magnetic resonance microscopy of toxic renal injury induced
             by bromoethylamine in rats.},
   Journal = {Fundam Appl Toxicol},
   Volume = {16},
   Number = {4},
   Pages = {787-797},
   Year = {1991},
   Month = {May},
   ISSN = {0272-0590},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/1884916},
   Keywords = {Animals • Ethylamines • Female • Kidney
             • Kidney Cortex • Kidney Diseases • Kidney
             Medulla • Magnetic Resonance Spectroscopy* •
             Microscopy • Organ Size • Rats • Rats, Inbred
             Strains • Specific Gravity • chemically induced*
             • methods* • pathology • pathology* •
             toxicity*},
   Abstract = {The alkylhalide 2-bromoethylamine hydrobromide (BEA)
             produces renal injury in rats that mimics analgesic-related
             renal injury in humans. Our purpose was to examine this
             injury, in vivo in rats, with magnetic resonance (MR)
             microscopy and correlate MR findings with findings from
             light microscopy of hematoxylin-eosin-stained sections. Rats
             (n = 48) were injected intravenously with BEA (150 mg/kg) or
             saline and imaged with MR 6, 48, and 336 hr later. The
             spin-spin relaxation time, T2, was measured from the cortex
             to the papilla. In other rats, we measured regional water
             content of the kidney. Renal injury was present 48 and 336
             hr after BEA dosing based on increased renal organ weights,
             decreased urine specific gravity, and significant renal
             lesions (H & E). T2 was elevated in the inner stripe of the
             outer medulla in injured kidneys at 48 hr. The differences
             in T2 between cortex and outer medulla were also elevated 48
             hr after BEA. In the inner medulla, there were no changes in
             T2 after BEA treatment. However, in all groups there were
             significant regional differences in T2. The value of T2
             increased from outer to inner medulla and this gradient was
             directly correlated with water content. Thus, MR microscopy
             detected damage in the outer medulla after BEA injury but
             not the damage in the inner medulla. T2 appeared to reflect
             the water content in the different regions of the medulla.
             The noninvasive in vivo capability of MR microscopy, with
             its high sensitivity to tissue water, allows the
             toxicologist to monitor the progression and regression of
             toxic insult in the same animal. At present the technology
             is complicated. The precise and accurate measure of
             MR-sensitive parameters in live animals at microscopic
             resolution is difficult. However, as the technology matures,
             there will be significant improvements providing the
             toxicologist a unique in vivo tool.},
   Doi = {10.1016/0272-0590(91)90164-y},
   Key = {fds269102}
}

@booklet{Tengowski00,
   Author = {Tengowski, MW and Hedlund, LW and Guyot, DJ and Burkhardt, JE and Johnson, GA},
   Title = {Magnetic resonance microscopy predicts findings in a
             theophylline-induced rat model of reproductive
             toxicity},
   Journal = {MOLECULAR BIOLOGY OF THE CELL},
   Volume = {11},
   Pages = {125A-125A},
   Publisher = {AMER SOC CELL BIOLOGY},
   Year = {2000},
   Month = {December},
   ISSN = {1059-1524},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000165525900655&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Tengowski00}
}

@booklet{Delnomdedieu96,
   Author = {Delnomdedieu, M and Hedlund, LW and Johnson, GA and Maronpot,
             RR},
   Title = {Magnetic resonance microscopy--a new tool for the
             toxicologic pathologist.},
   Journal = {Toxicol Pathol},
   Volume = {24},
   Number = {1},
   Pages = {36-44},
   Year = {1996},
   ISSN = {0192-6233},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/8839279},
   Abstract = {Parallel to its many applications in medical imaging,
             magnetic resonance (MR) microscopy is a potentially powerful
             tool in toxicologic pathology. Because of the intrinsic
             qualities of MR microscopy (noninvasiveness,
             3-dimensionality, and slicing in any chosen plane), the
             scientist has a new means by which to investigate different
             types of lesions based on differential contrast. By choosing
             appropriate proton stains to probe the state of the water in
             tissues, organ structure and vasculature can be seen and
             progressive lesion development can be followed in a given
             animal. This paper discusses toxicologic pathology
             applications for MR microscopy and compares MR microscopy
             with conventional histopathology using a time-course study
             of bromobenzene-induced hepatotoxicity in rats. Hematoxylin
             and eosin (H&E)-stained histological sections are compared
             with MR microscopy images from fixed tissue blocks to
             demonstrate one of the applications of MR microscopy to
             toxicologic pathology. The results indicate that MR
             microscopy is as sensitive as conventional H&E staining in
             detecting bromobenzene-induced hepatic lesions.},
   Doi = {10.1177/019262339602400106},
   Key = {Delnomdedieu96}
}

@article{fds132841,
   Author = {M Delnomdedieu and LW Hedlund and GA Johnson and RR
             Maronpot},
   Title = {Magnetic resonance microscopy--a new tool for the
             toxicologic pathologist.},
   Journal = {Toxicologic pathology, UNITED STATES},
   Volume = {24},
   Number = {1},
   Pages = {36-44},
   ISSN = {0192-6233},
   Keywords = {Animals • Brain Ischemia • Disease Models, Animal
             • Kidney • Liver • Magnetic Resonance Imaging
             • Microscopy • Rats • blood supply •
             drug effects • methods* • pathology •
             pathology*},
   Abstract = {Parallel to its many applications in medical imaging,
             magnetic resonance (MR) microscopy is a potentially powerful
             tool in toxicologic pathology. Because of the intrinsic
             qualities of MR microscopy (noninvasiveness,
             3-dimensionality, and slicing in any chosen plane), the
             scientist has a new means by which to investigate different
             types of lesions based on differential contrast. By choosing
             appropriate proton stains to probe the state of the water in
             tissues, organ structure and vasculature can be seen and
             progressive lesion development can be followed in a given
             animal. This paper discusses toxicologic pathology
             applications for MR microscopy and compares MR microscopy
             with conventional histopathology using a time-course study
             of bromobenzene-induced hepatotoxicity in rats. Hematoxylin
             and eosin (H&E)-stained histological sections are compared
             with MR microscopy images from fixed tissue blocks to
             demonstrate one of the applications of MR microscopy to
             toxicologic pathology. The results indicate that MR
             microscopy is as sensitive as conventional H&E staining in
             detecting bromobenzene-induced hepatic lesions.},
   Key = {fds132841}
}

@article{fds325753,
   Author = {Lipinski, RJ and Hammond, P and Ament, JJ and Pecevich, SJ and Jiang, Y and Dehart, DB and Johnson, GA and Sulik, KK},
   Title = {MAGNETIC RESONANCE MICROSCOPY-BASED 3D FACE-BRAIN
             CORRELATIONS IN AN FASD MOUSE MODEL},
   Journal = {ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH},
   Volume = {35},
   Number = {6},
   Pages = {266A-266A},
   Year = {2011},
   Key = {fds325753}
}

@article{fds268826,
   Author = {O'Leary-Moore, SK and Parnell, SE and Godin, EA and Dehart, DB and Ament, JJ and Khan, AA and Johnson, GA and Styner, MA and Sulik,
             KK},
   Title = {Magnetic resonance microscopy-based analyses of the brains
             of normal and ethanol-exposed fetal mice.},
   Journal = {Birth Defects Res A Clin Mol Teratol},
   Volume = {88},
   Number = {11},
   Pages = {953-964},
   Year = {2010},
   Month = {November},
   ISSN = {1542-0760},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/20842647},
   Keywords = {Abnormalities, Drug-Induced • Animals • Brain
             • Disease Models, Animal • Ethanol • Female
             • Fetal Alcohol Syndrome • Fetus •
             Gestational Age • Humans • Magnetic Resonance
             Imaging • Male • Mice • Mice, Inbred C57BL
             • Microscopy • Pregnancy • Prenatal Exposure
             Delayed Effects • abnormalities • chemically
             induced • drug effects* • embryology •
             methods • methods* • pathology •
             toxicity*},
   Abstract = {BACKGROUND: The application of magnetic resonance microscopy
             (MRM) to the study of normal and abnormal prenatal mouse
             development has facilitated discovery of dysmorphology
             following prenatal ethanol insult. The current analyses
             extend this work, providing a regional brain volume-based
             description of normal brain growth and illustrating the
             consequences of gestational day (GD) 10 ethanol exposure in
             the fetal mouse. METHODS: To assess normal growth, control
             C57Bl/6J fetuses collected on GD 16, GD 16.5, and GD 17 were
             scanned using a 9.4-T magnet, resulting in 29-μm isotropic
             resolution images. For the ethanol teratogenicity studies,
             C57Bl/6J dams were administered intraperitoneal ethanol (2.9
             g/kg) at 10 days, 0 hr, and 10 days, 4 hr, after
             fertilization, and fetuses were collected for analyses on GD
             17. From individual MRM scans, linear measurements and
             regional brain volumes were determined and compared.
             RESULTS: In control fetuses, each of the assessed brain
             regions increased in volume, whereas ventricular volumes
             decreased between GD 16 and GD 17. Illustrating a global
             developmental delay, prenatal ethanol exposure resulted in
             reduced body volumes, crown-rump lengths, and a generalized
             decrease in regional brain volumes compared with GD 17
             controls. However, compared with GD 16.5, morphologically
             matched controls, ethanol exposure resulted in volume
             increases in the lateral and third ventricles as well as a
             disproportionate reduction in cortical volume. CONCLUSIONS:
             The normative data collected in this study facilitate the
             distinction between GD 10 ethanol-induced developmental
             delay and frank dysmorphology. This work illustrates the
             utility of MRM-based analyses for developmental toxicology
             studies and extends our knowledge of the stage-dependency of
             ethanol teratogenesis.},
   Language = {eng},
   Doi = {10.1002/bdra.20719},
   Key = {fds268826}
}

@article{fds268727,
   Author = {Parnell, SE and Holloway, HT and O'Leary-Moore, SK and Dehart, DB and Paniaqua, B and Oguz, I and Budin, F and Styner, MA and Johnson, GA and Sulik, KK},
   Title = {Magnetic resonance microscopy-based analyses of the
             neuroanatomical effects of gestational day 9 ethanol
             exposure in mice.},
   Journal = {Neurotoxicol Teratol},
   Volume = {39},
   Pages = {77-83},
   Year = {2013},
   ISSN = {0892-0362},
   url = {http://dx.doi.org/10.1016/j.ntt.2013.07.009},
   Abstract = {Animal model-based studies have shown that ethanol exposure
             during early gestation induces developmental stage-specific
             abnormalities of the face and brain. The exposure
             time-dependent variability in ethanol's teratogenic outcomes
             is expected to contribute significantly to the wide spectrum
             of effects observed in humans with fetal alcohol spectrum
             disorder (FASD). The work presented here employs a mouse
             FASD model and magnetic resonance microscopy (MRM; high
             resolution magnetic resonance imaging) in studies designed
             to further our understanding of the developmental
             stage-specific defects of the brain that are induced by
             ethanol. At neurulation stages, i.e. at the beginning of
             gestational day (GD) 9 and again 4 hours later, time-mated
             C57Bl/6J dams were intraperitoneally administered 2.9 g/kg
             ethanol or vehicle. Ethanol-exposed fetuses were collected
             on GD 17, processed for MRM analysis, and results compared
             to comparably staged controls. Linear and volume
             measurements as well as shape changes for numerous
             individual brain regions were determined. GD 9 ethanol
             exposure resulted in significantly increased septal region
             width, reduction of cerebellar volume, and enlargement of
             all of the ventricles. Additionally, the results of shape
             analyses showed that many areas of the ethanol-exposed
             brains including the cerebral cortex, hippocampus and right
             striatum were significantly misshapen. These data
             demonstrate that ethanol can induce dysmorphology that may
             not be obvious based on volumetric analyses alone, highlight
             the asymmetric aspects of ethanol-induced defects, and add
             to our understanding of ethanol's developmental
             stage-dependent neuroteratogenesis.},
   Doi = {10.1016/j.ntt.2013.07.009},
   Key = {fds268727}
}

@article{fds304894,
   Author = {Badea, A and Johnson, GA},
   Title = {Magnetic resonance microscopy.},
   Journal = {Stud Health Technol Inform},
   Volume = {185},
   Pages = {153-184},
   Year = {2013},
   ISSN = {0926-9630},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/23542935},
   Abstract = {MRI, one of the major clinical imaging modalities, has
             gained an important role in studying small animal models,
             e.g., rats and mice. But imaging rodents comes with
             challenges, since the image resolution needs to be ~
             3000-times higher to resolve anatomical details at a level
             comparable to clinical imaging. A resolution on the order of
             100 microns or less redefines MR imaging as MR microscopy.
             We discuss in this chapter the basic components of the MR
             imaging chain, with a particular emphasis on small animal
             imaging demands: from hardware design to basic physical
             principles of MR image formation, and contrast mechanisms.
             We discuss special considerations of animal preparation for
             imaging, and staining methods to enhance contrast. Attention
             is given to factors that increase sensitivity, including
             exogenous contrast agents, high performance radiofrequency
             detectors, and advanced MR encoding sequences. Among these,
             diffusion tensor imaging and tractography add novel
             information on white matter tracts, helping to better
             understand important aspects of development and
             neurodegeneration. These developments open avenues for
             efficient phenotyping of small animal models, in vivo - to
             include anatomical as well as functional estimates, or
             ex-vivo - with exquisite anatomical detail. The need for
             higher resolution results in larger image arrays that need
             to be processed efficiently. We discuss image-processing
             approaches for quantitative characterization of animal
             cohorts, and building population atlases. High throughput is
             essential for these methods to become practical. We discuss
             current trends for increasing detector performance, the use
             of cryoprobes, as well as strategies for imaging multiple
             animals at the same time. Ultimately, the development of
             highly specific probes, with the possibility to be used in
             multimodal imaging, will offer new insights into histology.
             MRM, alone or in combination with other imaging modalities,
             will increase the knowledge of fundamental biological
             processes, help understanding the genetic basis of human
             diseases, and test pharmacological interventions.},
   Key = {fds304894}
}

@article{fds268793,
   Author = {Badea, A and Johnson, GA},
   Title = {Magnetic resonance microscopy.},
   Journal = {Anal Cell Pathol (Amst)},
   Volume = {35},
   Number = {4},
   Pages = {205-227},
   Booktitle = {Medical Imaging: Principles and Practices},
   Publisher = {IOS Press Ebooks},
   Year = {2012},
   ISBN = {9781439871027},
   ISSN = {0926-9630},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/22142643},
   Abstract = {Visualization of internal structures of opaque biologic
             objects is essential in many biomedical studies. Limited by
             the penetration depth of the probing sources (photons and
             electrons) and the lack of endogenous contrast, conventional
             forms of microscopy such as optical microscopy and electron
             microscopy require tissues to be sectioned into thin slices
             and stained with organic chemicals or heavy-metal compounds
             prior to examination. These invasive and destructive
             procedures, as well as the harmful radiation in the case of
             electron microscopy, make it difficult to obtain
             three-dimensional information and virtually impossible to
             study biologic tissues in vivo.},
   Doi = {10.3233/ACP-2011-0050},
   Key = {fds268793}
}

@booklet{Conner88,
   Author = {Conner, WE and Johnson, GA and Cofer, GP and Dittrich,
             K},
   Title = {Magnetic resonance microscopy: in vivo sectioning of a
             developing insect.},
   Journal = {Experientia},
   Volume = {44},
   Number = {1},
   Pages = {11-12},
   Year = {1988},
   Month = {January},
   ISSN = {0014-4754},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/3350110},
   Abstract = {The utility of magnetic resonance imaging vis-a-vis insect
             morphology and development was investigated. MRI is a
             noninvasive technique that distinguishes between tissues
             based on proton content and proton 'environment'. At present
             a resolution of 100 micron is achievable. The technique
             avoids fixation artifacts and allows the detection of motion
             within the organism.},
   Doi = {10.1007/BF01960223},
   Key = {Conner88}
}

@article{fds132771,
   Author = {WE Conner and GA Johnson and GP Cofer and K Dittrich},
   Title = {Magnetic resonance microscopy: in vivo sectioning of a
             developing insect.},
   Journal = {Experientia, SWITZERLAND},
   Volume = {44},
   Number = {1},
   Pages = {11-2},
   Year = {1988},
   Month = {January},
   ISSN = {0014-4754},
   Keywords = {Animals • Female • Lepidoptera • Magnetic
             Resonance Imaging* • Microscopy • Moths •
             Pupa • anatomy & histology • anatomy & histology*
             • growth & development},
   Abstract = {The utility of magnetic resonance imaging vis-a-vis insect
             morphology and development was investigated. MRI is a
             noninvasive technique that distinguishes between tissues
             based on proton content and proton 'environment'. At present
             a resolution of 100 micron is achievable. The technique
             avoids fixation artifacts and allows the detection of motion
             within the organism.},
   Key = {fds132771}
}

@article{fds268748,
   Author = {MACFALL, JS and SPAINE, PC and DOUDRICK, RE and JOHNSON,
             GA},
   Title = {MAGNETIC-RESONANCE MICROSCOPY (MRM) OF WATER TRANSPORT AND
             BINDING IN FUSIFORM RUST GALLS},
   Journal = {RESEARCH AND APPLICATIONS OF CHEMICAL SCIENCES IN
             FORESTRY},
   Volume = {104},
   Pages = {17-17},
   Publisher = {US DEPT AGR, FOREST SERV SO FOREST EXPT STN},
   Editor = {Vozzo, JA},
   Year = {1994},
   Month = {January},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1994BA75T00004&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {fds268748}
}

@booklet{Effmann87,
   Author = {EFFMANN, EL and JOHNSON, GA and SMITH, BR and TALBOTT, GA and COFER,
             G},
   Title = {MAGNETIC-RESONANCE MICROSCOPY OF LIVE CHICK-EMBRYOS IN
             OVO},
   Journal = {TERATOLOGY},
   Volume = {35},
   Number = {2},
   Pages = {A44-A44},
   Publisher = {WILEY-LISS},
   Year = {1987},
   Month = {April},
   ISSN = {0040-3709},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1987H226300076&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Effmann87}
}

@booklet{Arnder94,
   Author = {L. Arnder and X. H. Zhou and G. P. Cofer and L. W. Hedlund and G. A. Johnson},
   Title = {Magnetic-resonance microscopy of the rat carotid-artery at
             300-megahertz},
   Journal = {Investigative Radiology},
   Volume = {29},
   Number = {9},
   Pages = {822 -- 826},
   Year = {1994},
   Month = {September},
   Key = {Arnder94}
}

@booklet{Hedlund86a,
   Author = {L. W. Hedlund and G. A. Johnson and G. I.
             Mills},
   Title = {Magnetic-resonance microscopy of the rat thorax and
             abdomen},
   Journal = {Investigative Radiology},
   Volume = {21},
   Number = {11},
   Pages = {843 -- 846},
   Year = {1986},
   Month = {November},
   Key = {Hedlund86a}
}

@article{fds325757,
   Author = {SPAINE, P and MACFALL, JS and JOHNSON, GA},
   Title = {MAGNETIC-RESONANCE MICROSCOPY OF WATER-MOVEMENT THROUGH
             FUSIFORM RUST GALLS OF PINE},
   Journal = {RESEARCH AND APPLICATIONS OF CHEMICAL SCIENCES IN
             FORESTRY},
   Volume = {104},
   Pages = {11-16},
   Year = {1994},
   Key = {fds325757}
}

@booklet{Drayer86a,
   Author = {DRAYER, B and BURGER, P and DARWIN, R and RIEDERER, S and HERFKENS, R and JOHNSON, GA},
   Title = {MAGNETIC-RESONANCE-IMAGING OF BRAIN IRON},
   Journal = {AMERICAN JOURNAL OF NEURORADIOLOGY},
   Volume = {7},
   Number = {3},
   Pages = {373-380},
   Publisher = {AMER SOC NEURORADIOLOGY},
   Year = {1986},
   Month = {May},
   ISSN = {0195-6108},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1986C133300001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Drayer86a}
}

@booklet{Brown87a,
   Author = {BROWN, JM and KRAMER, PJ and COFER, GP and JOHNSON,
             GA},
   Title = {MAGNETIC-RESONANCE-IMAGING OF ROOT-WATER
             DISTRIBUTION},
   Journal = {HORTSCIENCE},
   Volume = {22},
   Number = {5},
   Pages = {1087-1087},
   Publisher = {AMER SOC HORTICULTURAL SCIENCE},
   Year = {1987},
   Month = {October},
   ISSN = {0018-5345},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1987K430400370&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Brown87a}
}

@article{fds357207,
   Author = {Sitek, KR and Gulban, OF and Calabrese, E and Johnson, GA and Lage-Castellanos, A and Moerel, M and Ghosh, SS and De Martino,
             F},
   Title = {Mapping the human subcortical auditory system using
             histology, postmortem MRI and in vivo MRI at
             7T.},
   Journal = {Elife},
   Volume = {8},
   Year = {2019},
   Month = {August},
   url = {http://dx.doi.org/10.7554/eLife.48932},
   Abstract = {Studying the human subcortical auditory system
             non-invasively is challenging due to its small, densely
             packed structures deep within the brain. Additionally, the
             elaborate three-dimensional (3-D) structure of the system
             can be difficult to understand based on currently available
             2-D schematics and animal models. Wfe addressed these issues
             using a combination of histological data, post mortem
             magnetic resonance imaging (MRI), and in vivo MRI at 7
             Tesla. We created anatomical atlases based on
             state-of-the-art human histology (BigBrain) and postmortem
             MRI (50 µm). We measured functional MRI (fMRI) responses to
             natural sounds and demonstrate that the functional
             localization of subcortical structures is reliable within
             individual participants who were scanned in two different
             experiments. Further, a group functional atlas derived from
             the functional data locates these structures with a median
             distance below 2 mm. Using diffusion MRI tractography, we
             revealed structural connectivity maps of the human
             subcortical auditory pathway both in vivo (1050 µm
             isotropic resolution) and post mortem (200 µm isotropic
             resolution). This work captures current MRI capabilities for
             investigating the human subcortical auditory system,
             describes challenges that remain, and contributes novel,
             openly available data, atlases, and tools for researching
             the human auditory system.},
   Doi = {10.7554/eLife.48932},
   Key = {fds357207}
}

@article{fds357198,
   Author = {Garrett, A and Rakhilin, N and Wang, N and McKey, J and Cofer, G and Anderson, RB and Capel, B and Johnson, GA and Shen,
             X},
   Title = {Mapping the peripheral nervous system in the whole mouse via
             compressed sensing tractography.},
   Journal = {J Neural Eng},
   Volume = {18},
   Number = {4},
   Year = {2021},
   Month = {June},
   url = {http://dx.doi.org/10.1088/1741-2552/ac0089},
   Abstract = {Objective.The peripheral nervous system (PNS) connects the
             central nervous system with the rest of the body to regulate
             many physiological functions and is therapeutically targeted
             to treat diseases such as epilepsy, depression, intestinal
             dysmotility, chronic pain, and more. However, we still lack
             understanding of PNS innervation in most organs because the
             large span, diffuse nature, and small terminal nerve bundle
             fibers have precluded whole-organism, high resolution
             mapping of the PNS. We sought to produce a comprehensive
             peripheral nerve atlas for use in future interrogation of
             neural circuitry and selection of targets for
             neuromodulation.Approach.We used diffusion tensor magnetic
             resonance imaging (DT-MRI) with high-speed compressed
             sensing to generate a tractogram of the whole mouse PNS. The
             tractography generated from the DT-MRI data is validated
             using lightsheet microscopy on optically cleared, antibody
             stained tissue.Main results.Herein we demonstrate the first
             comprehensive PNS tractography in a whole mouse. Using this
             technique, we scanned the whole mouse in 28 h and mapped PNS
             innervation and fiber network in multiple organs including
             heart, lung, liver, kidneys, stomach, intestines, and
             bladder at 70µm resolution. This whole-body PNS
             tractography map has provided unparalleled information; for
             example, it delineates the innervation along the
             gastrointestinal tract by multiple sacral levels and by the
             vagal nerves. The map enabled a quantitative tractogram that
             revealed relative innervation of the major organs by each
             vertebral foramen as well as the vagus nerve.Significance.This
             novel high-resolution nerve atlas provides a potential
             roadmap for future neuromodulation therapies and other
             investigations into the neural circuits which drive
             homeostasis and disease throughout the body.},
   Doi = {10.1088/1741-2552/ac0089},
   Key = {fds357198}
}

@article{fds174254,
   Author = {RD Geisert and JW Ross, MD Ashworth and FJ White and GA Johnson and U
             DeSilva},
   Title = {Maternal recognition of pregnancy signal or endocrine
             disruptor: the two faces of oestrogen during establishment
             of pregnancy in the pig.},
   Journal = {Society of Reproduction and Fertility supplement},
   Volume = {62},
   Pages = {131-45},
   Year = {2006},
   Keywords = {Animals • Endocrine Disruptors • Endometrium
             • Estrogens • Female • Pregnancy •
             Pregnancy Maintenance • Pregnancy, Animal •
             Receptors, Progesterone • Swine • metabolism
             • metabolism* • physiology*},
   Abstract = {Timing of conceptus growth and attachment to the uterine
             luminal epithelium is regulated by progesterone secretion
             from the corpus luteum and by expression of progesterone
             receptor in the uterine epithelia and stroma. Conceptus
             growth and uterine attachment are temporally associated with
             the disappearance of progesterone receptors from uterine
             epithelia. While the loss of progesterone receptor from the
             endometrial epithelia on day 10 of the oestrous cycle and
             pregnancy has been well documented, the factors involved
             with cell specific down-regulation of progesterone receptor
             are yet to be established. We propose that several
             progesterone stimulated factors activate nuclear factor
             kappa B (NF-kB) within the uterine epithelia, which leads to
             inhibition of progesterone receptor and concomitant
             stimulation of endometrial genes expressed during early
             conceptus development. Although oestrogens secreted by pig
             conceptuses function to establish pregnancy, timing of
             endometrial exposure to oestrogen is critical. Early
             oestrogen administration alters the pattern of gene
             expression through the NF-kB system desynchronising the
             uterine environment for conceptus implantation resulting in
             later embryonic loss.},
   Language = {eng},
   Key = {fds174254}
}

@article{fds174131,
   Author = {SL Woo and GA Johnson and BA Smith},
   Title = {Mathematical modeling of ligaments and tendons.},
   Journal = {Journal of biomechanical engineering},
   Volume = {115},
   Number = {4B},
   Pages = {468-73},
   Year = {1993},
   Month = {November},
   ISSN = {0148-0731},
   Keywords = {Animals • Biomechanics • Elasticity •
             Ligaments • Models, Biological* • Models,
             Structural • Reference Values • Stress,
             Physiological • Tendons • Viscosity •
             physiology* • physiopathology},
   Abstract = {Ligaments and tendons serve a variety of important functions
             in maintaining the structure of the human body. Although
             abundant literature exists describing experimental
             investigations of these tissues, mathematical modeling of
             ligaments and tendons also contributes significantly to
             understanding their behavior. This paper presents a survey
             of developments in mathematical modeling of ligaments and
             tendons over the past 20 years. Mathematical descriptions of
             ligaments and tendons are identified as either elastic or
             viscoelastic, and are discussed in chronological order.
             Elastic models assume that ligaments and tendons do not
             display time dependent behavior and thus, they focus on
             describing the nonlinear aspects of their mechanical
             response. On the other hand, viscoelastic models incorporate
             time dependent effects into their mathematical description.
             In particular, two viscoelastic models are discussed in
             detail; quasi-linear viscoelasticity (QLV), which has been
             widely used in the past 20 years, and the recently proposed
             single integral finite strain (SIFS) model.},
   Language = {eng},
   Key = {fds174131}
}

@booklet{Woo93,
   Author = {S. L. Y. Woo and G. A. Johnson and B. A.
             Smith},
   Title = {Mathematical-modeling of ligaments and tendons},
   Journal = {Journal Of Biomechanical Engineering-transactions Of The
             Asme},
   Volume = {115},
   Number = {4},
   Pages = {468 -- 473},
   Year = {1993},
   Month = {November},
   Key = {Woo93}
}

@booklet{Maki91a,
   Author = {Maki, JH and Benveniste, H and MacFall, JR and Johnson,
             GA},
   Title = {Maximization of contrast-to-noise ratio to distinguish
             diffusion and microcirculatory flow.},
   Journal = {J Magn Reson Imaging},
   Volume = {1},
   Number = {1},
   Pages = {39-46},
   Year = {1991},
   ISSN = {1053-1807},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/1802129},
   Abstract = {Optimization of the contrast-to-noise ratio (CNR) is
             described for microcirculation magnetic resonance (MR)
             imaging techniques based on flow-compensated/flow-dephased
             sequences, both with and without even-echo rephasing. The
             authors present the most advantageous manner of applying
             flow-dephased gradients, such that dephasing is maximal
             while diffusion losses are minimal. The theoretical
             considerations include phase, diffusion, echo time, and
             bandwidth in the determination of the optimal parameters for
             microcirculation imaging. Studies in phantoms consisting of
             stationary and flowing copper sulfate in Sephadex columns
             demonstrate the validity of the calculations. Optimized in
             vivo images of a rat stroke model demonstrate the potential
             of the flow-compensated/flow-dephased technique and the
             importance of optimizing CNR.},
   Doi = {10.1002/jmri.1880010105},
   Key = {Maki91a}
}

@article{fds132880,
   Author = {JH Maki and H Benveniste, JR MacFall and GA Johnson},
   Title = {Maximization of contrast-to-noise ratio to distinguish
             diffusion and microcirculatory flow.},
   Journal = {Journal of magnetic resonance imaging : JMRI, UNITED
             STATES},
   Volume = {1},
   Number = {1},
   Pages = {39-46},
   ISSN = {1053-1807},
   Keywords = {Animals • Cerebral Infarction • Diffusion* •
             Magnetic Resonance Imaging • Microcirculation* •
             Models, Structural • Rats • diagnosis* •
             methods* • physiopathology},
   Abstract = {Optimization of the contrast-to-noise ratio (CNR) is
             described for microcirculation magnetic resonance (MR)
             imaging techniques based on flow-compensated/flow-dephased
             sequences, both with and without even-echo rephasing. The
             authors present the most advantageous manner of applying
             flow-dephased gradients, such that dephasing is maximal
             while diffusion losses are minimal. The theoretical
             considerations include phase, diffusion, echo time, and
             bandwidth in the determination of the optimal parameters for
             microcirculation imaging. Studies in phantoms consisting of
             stationary and flowing copper sulfate in Sephadex columns
             demonstrate the validity of the calculations. Optimized in
             vivo images of a rat stroke model demonstrate the potential
             of the flow-compensated/flow-dephased technique and the
             importance of optimizing CNR.},
   Key = {fds132880}
}

@article{fds132831,
   Author = {TH Farmer and GP Cofer and GA Johnson},
   Title = {Maximizing contrast to noise with inductively coupled
             implanted coils.},
   Journal = {Investigative radiology, UNITED STATES},
   Volume = {25},
   Number = {5},
   Pages = {552-8},
   Year = {1990},
   Month = {May},
   ISSN = {0020-9996},
   Keywords = {Animals • Kidney • Magnetic Resonance Imaging
             • Microscopy • Models, Structural • Rats
             • Rats, Inbred Strains • anatomy & histology
             • instrumentation • instrumentation* •
             methods},
   Abstract = {Magnetic resonance (MR) microscopy with inductively coupled
             implanted coils has been used previously to follow loss and
             return of intra-medullary contrast as a result of
             nephrotoxic acute tubular necrosis with 117 microns
             resolution over a 2000 microns thick slice. The purpose of
             the current study was to further investigate the
             capabilities of in vivo MR microscopy by combining the
             implanted coil imaging technique with spin echo pulse
             sequence optimization done through signal-to-noise ratio
             (SNR) and contrast-to-noise ratio (CNR) modeling. These
             models included consideration of the effects of T2* and
             sampling time on signal-to-noise and contrast-to-noise
             ratios. They were initially tested with GdCl3 and agar gel
             phantoms constructed to the relaxation time and spin density
             specifications of the intra-medullary junction which bridges
             the outer and inner stripe of the outer medulla. In vivo
             microscopy was performed using single turn radiofrequency
             (RF) coils that were surgically implanted around the left
             kidney of two rats and inductively coupled to an external
             "birdcage" body coil. The models revealed maximum CNR per
             unit imaging time at a TR of 800 msec. A TE of 16 msec
             proved to be the best compromise between loss of transverse
             magnetization and decreased bandwidth. These CNR predictions
             were supported by the gel phantom and in vivo data.
             Maximizing the CNR in the current study enabled us to
             improve the resolution of in vivo MR microscopy to 78
             microns over a 1000 microns slice with an SNR of 40 and a
             CNR of eight in a total imaging time of 54
             minutes.},
   Key = {fds132831}
}

@booklet{Farmer90,
   Author = {Farmer, TH and Cofer, GP and Johnson, GA},
   Title = {Maximizing contrast to noise with inductively coupled
             implanted coils.},
   Journal = {Invest Radiol},
   Volume = {25},
   Number = {5},
   Pages = {552-558},
   Year = {1990},
   Month = {May},
   ISSN = {0020-9996},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/2345087},
   Abstract = {Magnetic resonance (MR) microscopy with inductively coupled
             implanted coils has been used previously to follow loss and
             return of intra-medullary contrast as a result of
             nephrotoxic acute tubular necrosis with 117 microns
             resolution over a 2000 microns thick slice. The purpose of
             the current study was to further investigate the
             capabilities of in vivo MR microscopy by combining the
             implanted coil imaging technique with spin echo pulse
             sequence optimization done through signal-to-noise ratio
             (SNR) and contrast-to-noise ratio (CNR) modeling. These
             models included consideration of the effects of T2* and
             sampling time on signal-to-noise and contrast-to-noise
             ratios. They were initially tested with GdCl3 and agar gel
             phantoms constructed to the relaxation time and spin density
             specifications of the intra-medullary junction which bridges
             the outer and inner stripe of the outer medulla. In vivo
             microscopy was performed using single turn radiofrequency
             (RF) coils that were surgically implanted around the left
             kidney of two rats and inductively coupled to an external
             "birdcage" body coil. The models revealed maximum CNR per
             unit imaging time at a TR of 800 msec. A TE of 16 msec
             proved to be the best compromise between loss of transverse
             magnetization and decreased bandwidth. These CNR predictions
             were supported by the gel phantom and in vivo data.
             Maximizing the CNR in the current study enabled us to
             improve the resolution of in vivo MR microscopy to 78
             microns over a 1000 microns slice with an SNR of 40 and a
             CNR of eight in a total imaging time of 54
             minutes.},
   Doi = {10.1097/00004424-199005000-00013},
   Key = {Farmer90}
}

@article{fds268781,
   Author = {Wetzel, AW and Badea, CT and Pomerantz, SM and Mistry, N and Nave, D and Johnson, GA},
   Title = {Measurement and modeling of 4D live mouse heart volumes from
             CT time series},
   Journal = {Proceedings of SPIE - The International Society for Optical
             Engineering},
   Volume = {6491},
   Publisher = {SPIE},
   Year = {2007},
   Month = {January},
   ISBN = {9780819466044},
   ISSN = {0277-786X},
   url = {http://dx.doi.org/10.1117/12.704792},
   Abstract = {In vivo quantitative studies of cardiac function in mouse
             models provide information about cardiac pathophysiology in
             more detail than can be obtained in humans. Quantitative
             measurements of left ventricular (LV) volume at multiple
             contractile phases are particularly important. However, the
             mouse heart's small size and rapid motion present challenges
             for precise measurement in live animals. Researchers at Duke
             University's Center for In Vivo Microscopy (CIVM) have
             developed noninvasive time-gated microcomputed tomography
             (micro-CT) techniques providing the temporal and spatial
             resolutions required for in vivo characterization of cardiac
             structure and function. This paper describes analysis of the
             resulting reconstructions to produce volume measurements and
             corresponding models of heart motion. We believe these are
             the most precise noninvasive estimates of in vivo LV volume
             currently available. Our technique uses binary mixture
             models to directly recover volume estimates from
             reconstructed datasets. Unlike methods using segmentation
             followed by voxel counting, this approach provides
             statistical error estimates and maintains good precision at
             high noise levels. This is essential for long term multiple
             session experiments that must simultaneously minimize
             contrast agent and x-ray doses. The analysis tools are built
             into the Pittsburgh Supercomputing Center's Volume Browser
             (PSC-VB) that provides networked multi-site data sharing and
             collaboration including analysis and visualization
             functions. © 2007 SPIE-IS&T.},
   Doi = {10.1117/12.704792},
   Key = {fds268781}
}

@article{fds132902,
   Author = {X Zhang and M Tengowski and L Fasulo and S Botts and SA Suddarth and GA
             Johnson},
   Title = {Measurement of fat/water ratios in rat liver using 3D
             three-point dixon MRI.},
   Journal = {Magnetic resonance in medicine : official journal of the
             Society of Magnetic Resonance in Medicine / Society of
             Magnetic Resonance in Medicine, United States},
   Volume = {51},
   Number = {4},
   Pages = {697-702},
   Year = {2004},
   Month = {April},
   ISSN = {0740-3194},
   Keywords = {Adipose Tissue • Animals • Biological Markers
             • Body Water • Carrier Proteins •
             Dose-Response Relationship, Drug • Drug Evaluation,
             Preclinical • Fatty Liver • Female • Humans
             • Image Enhancement • Imaging, Three-Dimensional
             • Liver • Magnetic Resonance Imaging •
             Microsomes, Liver • Rats • Rats, Inbred Strains
             • analysis • antagonists & inhibitors •
             chemically induced • chemistry* • diagnosis*
             • drug effects • methods • methods* •
             pathology • pathology*},
   Abstract = {Hepatic steatosis, or fatty liver, is commonly observed
             during the animal phase of drug safety studies. A
             noninvasive three-dimensional (3D) three-point Dixon method
             was used to quantitatively evaluate the fatty livers of rats
             induced by an experimental microsomal transfer protein (MTP)
             inhibitor, in an effort to develop a safety biomarker that
             could be translated to human studies. The method was
             implemented at 2.0 T for in vivo studies, and at 7.1 T for
             higher-resolution magnetic resonance (MR) histologic
             studies. In three separate protocols to study dose response
             and longitudinal evolution, intrahepatic fatty accumulation
             was detected by this method and confirmed by chemical and
             histologic assessments. Consistent with the pathologic
             changes, the fat/water ratios estimated by the MR technique
             increased significantly at doses of 1 mg/kg and 100 mg/kg of
             MTP inhibitor after 14 days of continuous administration.
             Among the more important findings were: 1). with the 3D
             three-point Dixon method, in vivo longitudinal studies of
             liver fat distribution can be conducted at significantly
             higher resolution than has previously been reported; 2). MR
             histology allows delineation of distribution at the
             microscopic scale of 0.0024 mm(3) resolution; and 3). the 3D
             three-point Dixon technique provides relative estimates of
             liver fat content and distribution at a high confidence
             level. This technique will be applicable in future studies
             in which fatty liver is a potential safety
             issue.},
   Key = {fds132902}
}

@booklet{Zhang04,
   Author = {Zhang, X and Tengowski, M and Fasulo, L and Botts, S and Suddarth, SA and Johnson, GA},
   Title = {Measurement of fat/water ratios in rat liver using 3D
             three-point dixon MRI.},
   Journal = {Magn Reson Med},
   Volume = {51},
   Number = {4},
   Pages = {697-702},
   Year = {2004},
   Month = {April},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/15065241},
   Abstract = {Hepatic steatosis, or fatty liver, is commonly observed
             during the animal phase of drug safety studies. A
             noninvasive three-dimensional (3D) three-point Dixon method
             was used to quantitatively evaluate the fatty livers of rats
             induced by an experimental microsomal transfer protein (MTP)
             inhibitor, in an effort to develop a safety biomarker that
             could be translated to human studies. The method was
             implemented at 2.0 T for in vivo studies, and at 7.1 T for
             higher-resolution magnetic resonance (MR) histologic
             studies. In three separate protocols to study dose response
             and longitudinal evolution, intrahepatic fatty accumulation
             was detected by this method and confirmed by chemical and
             histologic assessments. Consistent with the pathologic
             changes, the fat/water ratios estimated by the MR technique
             increased significantly at doses of 1 mg/kg and 100 mg/kg of
             MTP inhibitor after 14 days of continuous administration.
             Among the more important findings were: 1). with the 3D
             three-point Dixon method, in vivo longitudinal studies of
             liver fat distribution can be conducted at significantly
             higher resolution than has previously been reported; 2). MR
             histology allows delineation of distribution at the
             microscopic scale of 0.0024 mm(3) resolution; and 3). the 3D
             three-point Dixon technique provides relative estimates of
             liver fat content and distribution at a high confidence
             level. This technique will be applicable in future studies
             in which fatty liver is a potential safety
             issue.},
   Doi = {10.1002/mrm.20005},
   Key = {Zhang04}
}

@article{fds132882,
   Author = {BT Chen and AC Brau and GA Johnson},
   Title = {Measurement of regional lung function in rats using
             hyperpolarized 3helium dynamic MRI.},
   Journal = {Magnetic resonance in medicine : official journal of the
             Society of Magnetic Resonance in Medicine / Society of
             Magnetic Resonance in Medicine, United States},
   Volume = {49},
   Number = {1},
   Pages = {78-88},
   Year = {2003},
   Month = {January},
   ISSN = {0740-3194},
   Keywords = {Animals • Female • Helium • Image Processing,
             Computer-Assisted • Isotopes • Lung •
             Magnetic Resonance Imaging, Cine* • Phantoms, Imaging
             • Rats • Rats, Sprague-Dawley • Respiratory
             Mechanics* • Tidal Volume • anatomy & histology
             • diagnostic use • physiology*},
   Abstract = {Dynamic regional lung function was investigated in rats
             using a radial acquisition cine (RA-CINE) pulse sequence
             together with hyperpolarized (HP) (3)He gas delivered by a
             constant flow ventilator. Based on regional differences in
             the behavior of inspired air, the lung was conceptually
             divided into two regions (the major airways and the
             peripheral airspace) for purposes of functional analysis. To
             measure regional function in the major airways, a large RF
             flip angle (24 degrees) was applied to reduce (3)He
             magnetization in the peripheral airspace, and signal
             intensity (SI) was normalized with the projected airway
             diameter to estimate local airflow. Higher normalized signal
             intensity was observed in the left branch airway as compared
             to the right branch airway. To determine regional function
             in the peripheral airspace, a small RF flip angle (6
             degrees) was used. Incremental increases of peripheral SI in
             successive lung images were consistent with the increase in
             lung volume. A new "skipping" scanning strategy using dummy
             frames allows a trade-off between the number of frames
             acquired for dynamic information, the RF flip angle, and the
             penetration depth of (3)He magnetization into the lung. This
             work provides a novel approach to simultaneously assess
             dynamic regional function and morphology.},
   Key = {fds132882}
}

@booklet{Chen03,
   Author = {Chen, BT and Brau, ACS and Johnson, GA},
   Title = {Measurement of regional lung function in rats using
             hyperpolarized 3helium dynamic MRI.},
   Journal = {Magn Reson Med},
   Volume = {49},
   Number = {1},
   Pages = {78-88},
   Year = {2003},
   Month = {January},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/12509822},
   Abstract = {Dynamic regional lung function was investigated in rats
             using a radial acquisition cine (RA-CINE) pulse sequence
             together with hyperpolarized (HP) (3)He gas delivered by a
             constant flow ventilator. Based on regional differences in
             the behavior of inspired air, the lung was conceptually
             divided into two regions (the major airways and the
             peripheral airspace) for purposes of functional analysis. To
             measure regional function in the major airways, a large RF
             flip angle (24 degrees) was applied to reduce (3)He
             magnetization in the peripheral airspace, and signal
             intensity (SI) was normalized with the projected airway
             diameter to estimate local airflow. Higher normalized signal
             intensity was observed in the left branch airway as compared
             to the right branch airway. To determine regional function
             in the peripheral airspace, a small RF flip angle (6
             degrees) was used. Incremental increases of peripheral SI in
             successive lung images were consistent with the increase in
             lung volume. A new "skipping" scanning strategy using dummy
             frames allows a trade-off between the number of frames
             acquired for dynamic information, the RF flip angle, and the
             penetration depth of (3)He magnetization into the lung. This
             work provides a novel approach to simultaneously assess
             dynamic regional function and morphology.},
   Doi = {10.1002/mrm.10336},
   Key = {Chen03}
}

@article{fds268938,
   Author = {Möller, HE and Hedlund, LW and Chen, XJ and Carey, MR and Chawla, MS and Wheeler, CT and Johnson, GA},
   Title = {Measurements of hyperpolarized gas properties in the lung.
             Part III: (3)He T(1).},
   Journal = {Magn Reson Med},
   Volume = {45},
   Number = {3},
   Pages = {421-430},
   Year = {2001},
   Month = {March},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/11241699},
   Keywords = {Animals • Cardiac Output • Functional Residual
             Capacity • Guinea Pigs • Heart Arrest, Induced
             • Helium* • Image Enhancement* • Isotopes
             • Lung • Magnetic Resonance Spectroscopy* •
             Oxygen • Pulmonary Gas Exchange • blood •
             pathology • physiology • physiology*},
   Abstract = {Hyperpolarized (3)He spin-lattice relaxation was
             investigated in the guinea pig lung using spectroscopy and
             imaging techniques with a repetitive RF pulse series. T(1)
             was dominated by interactions with oxygen and was used to
             measure the alveolar O(2) partial pressure. In animals
             ventilated with a mixture of 79% (3)He and 21% O(2), T(1)
             dropped from 19.6 sec in vivo to 14.6 sec after cardiac
             arrest, reflecting the termination of the intrapulmonary gas
             exchange. The initial difference in oxygen concentration
             between inspired and alveolar air, and the temporal decay
             during apnea were related to functional parameters.
             Estimates of oxygen uptake were 29 +/- 11 mL min(-1) kg(-1)
             under normoxic conditions, and 9.0 +/- 2.0 mL min(-1) kg(-1)
             under hypoxic conditions. Cardiac output was estimated to be
             400 +/- 160 mL min(-1) kg(-1). The functional residual
             capacity derived from spirometric magnetic resonance
             experiments varied with body mass between 5.4 +/- 0.3 mL and
             10.7 +/- 1.1 mL. Magn Reson Med 45:421-430,
             2001.},
   Doi = {10.1002/1522-2594(200103)45:3<421::aid-mrm1055>3.0.co;2-k},
   Key = {fds268938}
}

@booklet{Moller01,
   Author = {H. E. Moller and L. W. Hedlund and X. J. Chen and M. R.
             Carey and M. S. Chawla and C. T. Wheeler and G. A.
             Johnson},
   Title = {Measurements of hyperpolarized gas properties in the lung.
             Part III: He-3 T-1},
   Journal = {Magnetic Resonance In Medicine},
   Volume = {45},
   Number = {3},
   Pages = {421 -- 430},
   Year = {2001},
   Month = {March},
   Key = {Moller01}
}

@article{fds367385,
   Author = {Nicholls, PJ and Pack, TF and Urs, NM and Kumar, S and Zhou, Y and Ichim,
             G and Ginzel, JD and Turu, G and Calabrese, E and Roberts, WL and Fan, P and Ostapchenko, VG and Guzman Lenis and MS and Beraldo, F and Hatina, J and Prado, VF and Prado, MAM and Spasojevic, I and Snyder, JC and Dzirasa,
             K and Johnson, GA and Caron, MG},
   Title = {Measuring Nonapoptotic Caspase Activity with a Transgenic
             Reporter in Mice.},
   Journal = {eNeuro},
   Volume = {9},
   Number = {5},
   Year = {2022},
   url = {http://dx.doi.org/10.1523/ENEURO.0147-21.2022},
   Abstract = {The protease caspase-3 is a key mediator of apoptotic
             programmed cell death. But weak or transient caspase
             activity can contribute to neuronal differentiation, axonal
             pathfinding, and synaptic long-term depression. Despite the
             importance of sublethal, or nonapoptotic, caspase activity
             in neurodevelopment and neural plasticity, there has been no
             simple method for mapping and quantifying nonapoptotic
             caspase activity (NACA) in rodent brains. We therefore
             generated a transgenic mouse expressing a highly sensitive
             and specific fluorescent reporter of caspase activity, with
             peak signal localized to the nucleus. As a proof of concept,
             we first obtained evidence that NACA influences
             neurophysiology in an amygdalar circuit. Then focusing on
             the amygdala, we were able to quantify a sex-specific
             persistent elevation in caspase activity in females after
             restraint stress. This simple in vivo caspase activity
             reporter will facilitate systems-level studies of apoptotic
             and nonapoptotic phenomena in behavioral and pathologic
             models.},
   Doi = {10.1523/ENEURO.0147-21.2022},
   Key = {fds367385}
}

@booklet{Qiu98,
   Author = {H. H. Qiu and L. W. Hedlund and M. R. Neuman and C. R.
             Edwards and R. D. Black and G. P. Cofer and G. A.
             Johnson},
   Title = {Measuring the progression of foreign-body reaction to
             silicone implants using in vivo MR microscopy},
   Journal = {Ieee Transactions On Biomedical Engineering},
   Volume = {45},
   Number = {7},
   Pages = {921 -- 927},
   Year = {1998},
   Month = {July},
   Key = {Qiu98}
}

@article{fds268995,
   Author = {Qiu, HH and Hedlund, LW and Neuman, MR and Edwards, CR and Black, RD and Cofer, GP and Johnson, GA},
   Title = {Measuring the progression of foreign-body reaction to
             silicone implants using in vivo MR microscopy.},
   Journal = {IEEE Trans Biomed Eng},
   Volume = {45},
   Number = {7},
   Pages = {921-927},
   Year = {1998},
   Month = {July},
   ISSN = {0018-9294},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/9644901},
   Keywords = {Animals • Female • Foreign-Body Reaction •
             Magnetic Resonance Imaging* • Microscopy • Neck
             • Prostheses and Implants • Rats • Rats,
             Sprague-Dawley • Silicones • adverse effects*
             • etiology • methods • pathology* •
             surgery},
   Abstract = {We used in vivo magnetic resonance (MR) microscopy to follow
             the growth of fibrous capsule as a foreign body reaction to
             silicone implants in rats. Anesthetized rats were imaged 1,
             7, 14, and 28 days after silicone-coated MR imaging coils
             were sutured to their neck muscles. On the twenty-eighth
             day, rats were sacrificed and coils and adjacent tissues
             were removed en bloc and fixed in formalin, reimaged with
             MR, and sectioned for conventional histology.
             Three-dimensional (3-D) spin-echo [3DFT] acquisition gave
             in-plane resolution of 32 x 32 microns in vivo and 16 x 16
             microns ex vivo. All MR images showed a diffuse band of
             elevated signal intensity between the silicone of the coil
             and adjacent tissue. The border of the hyperintense band was
             thin and not well defined at seven days post-implantation.
             From 7-28 days, the band showed relatively homogeneous
             signal intensity and its thickness increased 44% on the
             rectus muscle side and 78% on the subcutaneous side. The
             capsule thickness determined either by MR in vivo and ex
             vivo microscopy or conventional histology was not
             significantly different, and there was a significant
             correlation between thickness measurements among those
             methods. MR in vivo microscopy provides sufficient
             resolution and spatial information to serially evaluate the
             growth of the foreign body fibrous capsule over time, thus
             achieving greater accuracy and consistency in
             measurements.},
   Doi = {10.1109/10.686800},
   Key = {fds268995}
}

@article{fds268887,
   Author = {Hedlund, LW and Johnson, GA},
   Title = {Mechanical ventilation for imaging the small animal
             lung.},
   Journal = {ILAR J},
   Volume = {43},
   Number = {3},
   Pages = {159-174},
   Year = {2002},
   ISSN = {1084-2020},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/12105383},
   Keywords = {Anatomy, Cross-Sectional • Animals • Animals,
             Laboratory • Disease Models, Animal • Guinea Pigs
             • Lung* • Magnetic Resonance Imaging • Rats
             • Respiration, Artificial • anatomy & histology
             • instrumentation • methods* • physiology
             • physiology* • physiopathology},
   Abstract = {This review emphasizes some of the challenges and benefits
             of in vivo imaging of the small animal lung. Because
             mechanical ventilation plays a key role in high-quality,
             high-resolution imaging of the small animal lung, the
             article focuses particularly on the problems of ventilation
             support, control of breathing motion and lung volume, and
             imaging during different phases of the breathing cycle.
             Solutions for these problems are discussed primarily in
             relation to magnetic resonance imaging, both conventional
             proton imaging and the newer, hyperpolarized helium imaging
             of pulmonary airways. Examples of applications of these
             imaging solutions to normal and diseased lung are
             illustrated in the rat and guinea pig. Although difficult to
             perform, pulmonary imaging in the small animal can be a
             valuable source of information not only for the normal lung,
             but also for the lung challenged by disease.},
   Doi = {10.1093/ilar.43.3.159},
   Key = {fds268887}
}

@booklet{Hansen99,
   Author = {T. R. Hansen and K. J. Austin and D. J. Perry and J. K. Pru and M. G. Teixeira and G. A. Johnson},
   Title = {Mechanism of action of interferon-tau in the uterus during
             early pregnancy},
   Journal = {Journal Of Reproduction And Fertility},
   Pages = {329 -- 339},
   Year = {1999},
   Key = {Hansen99}
}

@article{fds174074,
   Author = {TR Hansen and KJ Austin and DJ Perry and JK Pru and MG Teixeira and GA
             Johnson},
   Title = {Mechanism of action of interferon-tau in the uterus during
             early pregnancy.},
   Journal = {Journal of reproduction and fertility. Supplement},
   Volume = {54},
   Pages = {329-39},
   Year = {1999},
   ISSN = {0449-3087},
   Keywords = {Amino Acid Sequence • Animals • Cattle •
             Chemokine CXCL2 • Chemokine CXCL6 • Chemokines
             • Chemokines, CXC • Corpus Luteum Maintenance
             • Dinoprost • Dinoprostone • Embryo,
             Mammalian • Female • Interferon Type I •
             Molecular Sequence Data • Pregnancy • Pregnancy
             Proteins • Pregnancy, Animal • Progesterone •
             Protein Binding • Receptors, Estradiol •
             Receptors, Interferon • Ubiquitins • genetics
             • metabolism • metabolism* •
             physiology*},
   Abstract = {Early pregnancy is maintained in ruminants through the
             actions of conceptus-derived interferon (IFN)-tau on the
             endometrium. IFN-tau alters uterine release of PGF2 alpha'
             which results in rescue of the corpus luteum and continued
             release of progesterone. The mechanism of action of IFN-tau
             includes inhibition of oestradiol receptors, consequent
             reduction in oxytocin receptors, activation of a
             cyclooxygenase inhibitor, and a shift in the PGs to favour
             PGE2 over PGF2 alpha' IFN-tau also induces several
             endometrial proteins that may be critical for survival of
             the developing embryo. One endometrial protein induced by
             pregnancy and IFN-tau has been identified as bovine
             granulocyte chemotactic protein-2 (bGCP-2). This chemotactic
             cytokine (chemokine) has been used as a marker to delineate
             IFN-tau from IFN-alpha responses in the endometrium. A
             second protein, called ubiquitin cross-reactive protein
             (UCRP), resembles a tandem ubiquitin repeat. UCRP becomes
             conjugated to cytosolic endometrial proteins in response to
             IFN-tau and pregnancy. Proteins conjugated to UCRP are
             either modulated or targeted for processing through the
             proteasome. The action of IFN-tau is mediated by induction
             of signal transducer and activator of transcription 1
             (STAT-1), STAT-2 and interferon regulatory factor 1 (IRF-1)
             transcription factors. Induction of these transcription
             factors, the alpha chemokines and UCRP is the prelude to
             maternal recognition of pregnancy in ruminants.},
   Language = {eng},
   Key = {fds174074}
}

@booklet{Mesfin87,
   Author = {G. M. Mesfin and G. A. Johnson and M. J. Higgins and D. F.
             Morris},
   Title = {Mechanism of anestrus in rats treated with an
             antihypertensive agent, losulazine hydrochloride},
   Journal = {Toxicology And Applied Pharmacology},
   Volume = {87},
   Number = {1},
   Pages = {91 -- 101},
   Year = {1987},
   Month = {January},
   Key = {Mesfin87}
}

@article{fds174220,
   Author = {GM Mesfin and GA Johnson and MJ Higgins and DF Morris},
   Title = {Mechanism of anestrus in rats treated with an
             antihypertensive agent, losulazine hydrochloride.},
   Journal = {Toxicology and applied pharmacology},
   Volume = {87},
   Number = {1},
   Pages = {91-101},
   Year = {1987},
   Month = {January},
   ISSN = {0041-008X},
   Keywords = {Anestrus • Animals • Antihypertensive Agents
             • Body Weight • Bromocriptine •
             Catecholamines • Dopamine • Estrus • Female
             • Follicle Stimulating Hormone • Genitalia, Female
             • Hypothalamus • Piperazines • Progesterone
             • Prolactin • Rats • Rats, Inbred Strains
             • blood • drug effects • drug effects* •
             metabolism • pharmacology • pharmacology*},
   Abstract = {The mechanism of anestrus in rats treated with losulazine, a
             peripheral sympatholytic antihypertensive agent, was
             investigated by determining its effect on hypothalamic
             catecholamines and serum sex hormones and by evaluating the
             influence of bromocriptine on the reproductive functions of
             rats treated with losulazine. Groups of six female Upjohn
             Sprague-Dawley rats were treated orally with 10 mg/kg/day of
             losulazine and/or 18.75 mg/kg/day of bromocriptine for 15 or
             27 days. Six rats were treated with losulazine plus 6.25
             mg/kg/day of bromocriptine for 16 days followed by
             losulazine alone for 11 days. Rats treated with losulazine
             only were depleted of hypothalamic catecholamines, were
             hyperprolactinemic, and had interrupted estrous cycles and
             attenuated vaginal mucosa. Treatment with bromocriptine, a
             dopamine receptor agonist, resulted in suppression of serum
             prolactin and normal estrous cycles. Rats reverted back to
             hyperprolactinemia and anestrus shortly after bromocriptine
             withdrawal. These results suggest that hyperprolactinemia
             mediated through hypothalamic dopamine depletion is the
             mechanism of anestrus in rats treated with
             losulazine.},
   Language = {eng},
   Key = {fds174220}
}

@article{fds132804,
   Author = {H Benveniste and LW Hedlund and GA Johnson},
   Title = {Mechanism of detection of acute cerebral ischemia in rats by
             diffusion-weighted magnetic resonance microscopy.},
   Journal = {Stroke; a journal of cerebral circulation, UNITED
             STATES},
   Volume = {23},
   Number = {5},
   Pages = {746-54},
   Year = {1992},
   Month = {May},
   ISSN = {0039-2499},
   Keywords = {Acute Disease • Animals • Brain • Brain
             Ischemia • Diffusion • Female • Glutamates
             • Glutamic Acid • Magnetic Resonance Imaging
             • N-Methylaspartate • Ouabain • Rats •
             Rats, Inbred Strains • Staining and Labeling •
             diagnosis* • drug effects • metabolism •
             methods* • pharmacology},
   Abstract = {BACKGROUND AND PURPOSE: The aim of this study was to measure
             apparent diffusion coefficients in rat brain tissue exposed
             to ouabain, glutamate, and N-methyl-D-aspartate and to
             compare them with apparent diffusion coefficients found in
             acute cerebral ischemia. METHODS: The apparent diffusion
             coefficient was measured using magnetic resonance microscopy
             in four groups of Sprague-Dawley rats after occlusion of the
             right middle cerebral artery and ipsilateral common carotid
             artery (n = 7), after ouabain exposure (n = 6), during
             glutamate exposure (n = 7), or during N-methyl-D-aspartate
             exposure (n = 3). Ouabain, glutamate, and
             N-methyl-D-aspartate were applied via an intracerebrally
             implanted microdialysis membrane. RESULTS: Three hours after
             the induction of focal cerebral ischemia, a 33% reduction in
             the apparent diffusion coefficient was observed in the right
             dorsolateral corpus striatum and olfactory cortex. After
             ouabain exposure, reductions in the apparent diffusion
             coefficient were observed within a 1,500-microns radius of
             the microdialysis membrane. Quantitative analysis revealed
             that apparent diffusion coefficient values in ischemic and
             ouabain-exposed tissue fell within the same range. Glutamate
             and N-methyl-D-aspartate reduced the brain tissue apparent
             diffusion coefficient by 35% and 40%, respectively.
             CONCLUSIONS: On the basis of these findings, we conclude
             that ischemia-induced apparent diffusion coefficient
             reductions are likely caused by a shift of extracellular to
             intracellular water.},
   Key = {fds132804}
}

@booklet{Benveniste92,
   Author = {Benveniste, H and Hedlund, LW and Johnson, GA},
   Title = {Mechanism of detection of acute cerebral ischemia in rats by
             diffusion-weighted magnetic resonance microscopy.},
   Journal = {Stroke},
   Volume = {23},
   Number = {5},
   Pages = {746-754},
   Year = {1992},
   Month = {May},
   ISSN = {0039-2499},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/1374575},
   Abstract = {BACKGROUND AND PURPOSE: The aim of this study was to measure
             apparent diffusion coefficients in rat brain tissue exposed
             to ouabain, glutamate, and N-methyl-D-aspartate and to
             compare them with apparent diffusion coefficients found in
             acute cerebral ischemia. METHODS: The apparent diffusion
             coefficient was measured using magnetic resonance microscopy
             in four groups of Sprague-Dawley rats after occlusion of the
             right middle cerebral artery and ipsilateral common carotid
             artery (n = 7), after ouabain exposure (n = 6), during
             glutamate exposure (n = 7), or during N-methyl-D-aspartate
             exposure (n = 3). Ouabain, glutamate, and
             N-methyl-D-aspartate were applied via an intracerebrally
             implanted microdialysis membrane. RESULTS: Three hours after
             the induction of focal cerebral ischemia, a 33% reduction in
             the apparent diffusion coefficient was observed in the right
             dorsolateral corpus striatum and olfactory cortex. After
             ouabain exposure, reductions in the apparent diffusion
             coefficient were observed within a 1,500-microns radius of
             the microdialysis membrane. Quantitative analysis revealed
             that apparent diffusion coefficient values in ischemic and
             ouabain-exposed tissue fell within the same range. Glutamate
             and N-methyl-D-aspartate reduced the brain tissue apparent
             diffusion coefficient by 35% and 40%, respectively.
             CONCLUSIONS: On the basis of these findings, we conclude
             that ischemia-induced apparent diffusion coefficient
             reductions are likely caused by a shift of extracellular to
             intracellular water.},
   Doi = {10.1161/01.str.23.5.746},
   Key = {Benveniste92}
}

@article{fds174270,
   Author = {GA Johnson and EG Kim and SJ Boukma},
   Title = {Mechanism of norepinephrine depletion by
             5-hydroxytryptophan.},
   Journal = {Proceedings of the Society for Experimental Biology and
             Medicine. Society for Experimental Biology and Medicine (New
             York, N.Y.)},
   Volume = {128},
   Number = {2},
   Pages = {509-12},
   Year = {1968},
   Month = {June},
   ISSN = {0037-9727},
   Keywords = {5-Hydroxytryptophan • Animals • Brain • Brain
             Chemistry • Carbon Isotopes • Injections,
             Intraperitoneal • Injections, Intravenous • Male
             • Methyltyrosines • Norepinephrine • Rats
             • Tyrosine • antagonists & inhibitors* •
             biosynthesis • metabolism • metabolism* •
             pharmacology • pharmacology*},
   Language = {eng},
   Key = {fds174270}
}

@article{fds204254,
   Author = {FW Bazer and G Song and J Kim and DW Erikson and GA Johnson and RC
             Burghardt, H Gao and M Carey Satterfield and TE Spencer and G
             Wu},
   Title = {Mechanistic mammalian target of rapamycin (MTOR) cell
             signaling: Effects of select nutrients and secreted
             phosphoprotein 1 on development of mammalian
             conceptuses.},
   Journal = {Molecular and cellular endocrinology},
   Year = {2011},
   Month = {September},
   ISSN = {1872-8057},
   url = {http://dx.doi.org/10.1016/j.mce.2011.08.026},
   Abstract = {Morphological differentiation of uterine glands in mammals
             is a postnatal event vulnerable to adverse effects of
             endocrine disruptors. Exposure of ewe lambs to a progestin
             from birth to postnatal day 56 prevents development of
             uterine glands and, as adults, the ewes are unable to
             exhibit estrous cycles or maintain pregnancy. Uterine
             epithelia secrete proteins and transport nutrients into the
             uterine lumen necessary for conceptus development, pregnancy
             recognition signaling and implantation, including arginine
             and secreted phosphoprotein 1 (SPP1). Arginine can be
             metabolized to nitric oxide and to polyamines or act
             directly to activate MTOR cell signaling to stimulate
             proliferation, migration, and mRNA translation in
             trophectoderm cells. SPP1 binds αvβ3 and α5β1 integrins
             and induces focal adhesion assembly, adhesion and migration
             of conceptus trophectoderm cells during implantation. Thus,
             arginine and SPP1 mediate growth, migration, cytoskeletal
             remodeling and adhesion of trophectoderm essential for
             pregnancy recognition signaling and implantation.},
   Language = {ENG},
   Doi = {10.1016/j.mce.2011.08.026},
   Key = {fds204254}
}

@booklet{Orlander02,
   Author = {J. D. Orlander and B. G. Fincke and D. Hermanns and G. A.
             Johnson},
   Title = {Medical residents' first clearly remembered experiences of
             giving bad news},
   Journal = {Journal Of General Internal Medicine},
   Volume = {17},
   Number = {11},
   Pages = {825 -- 840},
   Year = {2002},
   Month = {November},
   Key = {Orlander02}
}

@article{fds174101,
   Author = {JD Orlander and BG Fincke and D Hermanns and GA Johnson},
   Title = {Medical residents' first clearly remembered experiences of
             giving bad news.},
   Journal = {Journal of general internal medicine},
   Volume = {17},
   Number = {11},
   Pages = {825-31},
   Year = {2002},
   Month = {November},
   ISSN = {0884-8734},
   Keywords = {Adult • Communication • Female • Health
             Surveys • Humans • Internal Medicine* •
             Internship and Residency* • Male •
             Physician-Patient Relations*},
   Abstract = {CONTEXT: Communication of bad news to patients or families
             is a difficult task that requires skill and sensitivity.
             Little is known about doctors' formative experiences in
             giving bad news, what guidance they receive, or what lessons
             they learn in the process. OBJECTIVE: To learn the
             circumstances in which medical residents first delivered bad
             news to patients or families, the nature of their
             experience, and their opinions about how best to develop the
             needed skills. DESIGN: Confidential mailed survey. SETTING
             AND SUBJECTS: All medicine house officers at 2 urban,
             university-based residency programs in Boston. MAIN OUTCOME
             MEASURES: Details of medical residents' first clearly
             remembered experiences of giving bad news to a patient or
             family member; year in training; familiarity with the
             patient; information about any planning prior to,
             observation of, or discussion after their first experience;
             and the usefulness of such discussions. We also asked
             general questions about delivering bad news, such as how
             often this was done, as well as asking for opinions about
             actual and desired training. RESULTS: One hundred
             twenty-nine of two hundred thirteen surveys (61%) were
             returned. Most (73%) trainees first delivered bad news while
             a medical student or intern. For this first experience, most
             (61%) knew the patient for just hours or days. Only 59%
             engaged in any planning for the encounter. An attending
             physician was present in 6 (5%) instances, and a more-senior
             trainee in 14 (11%) others. Sixty-five percent of subjects
             debriefed with at least 1 other person after the encounter,
             frequently with a lesser-trained physician or a member of
             their own family. Debriefing focused on the reaction of
             those who were given the bad news and the reaction of the
             trainee. When there were discussions with more-senior
             physicians, before or after the encounter, these were judged
             to be helpful approximately 80% of the time. Most subjects
             had given bad news between 5 and 20 times, yet 10% had never
             been observed doing so. Only 81 of 128 (63%) had ever
             observed an attending delivering bad news, but those who did
             found it helpful 96% of the time. On 7-point scales,
             subjects rated the importance of skills in delivering bad
             news highly, (mean 6.8), believed such skill can be improved
             (mean 6.6), and thought that more guidance should be offered
             to them during such activity (mean 5.8). CONCLUSION: Medical
             students and residents frequently deliver bad news to
             patients and families. This responsibility begins early in
             training. In spite of their inexperience, many do not appear
             to receive adequate guidance or support during their
             earliest formative experiences.},
   Language = {eng},
   Key = {fds174101}
}

@booklet{Johnson97d,
   Author = {G. A. Johnson},
   Title = {Medicinal marijuana?},
   Journal = {New England Journal Of Medicine},
   Volume = {336},
   Number = {16},
   Pages = {1186 -- 1186},
   Year = {1997},
   Month = {April},
   Key = {Johnson97d}
}

@article{fds370388,
   Author = {Johnson, GA and Tian, Y and Ashbrook, DG and Cofer, GP and Cook, JJ and Gee, JC and Hall, A and Hornburg, K and Kaczorowski, CC and Qi, Y and Yeh,
             F-C and Wang, N and White, LE and Williams, RW},
   Title = {Merged magnetic resonance and light sheet microscopy of the
             whole mouse brain.},
   Journal = {Proc Natl Acad Sci U S A},
   Volume = {120},
   Number = {17},
   Pages = {e2218617120},
   Year = {2023},
   Month = {April},
   url = {http://dx.doi.org/10.1073/pnas.2218617120},
   Abstract = {We have developed workflows to align 3D magnetic resonance
             histology (MRH) of the mouse brain with light sheet
             microscopy (LSM) and 3D delineations of the same specimen.
             We start with MRH of the brain in the skull with gradient
             echo and diffusion tensor imaging (DTI) at 15 μm isotropic
             resolution which is ~ 1,000 times higher than that of most
             preclinical MRI. Connectomes are generated with
             superresolution tract density images of ~5 μm. Brains are
             cleared, stained for selected proteins, and imaged by LSM at
             1.8 μm/pixel. LSM data are registered into the reference
             MRH space with labels derived from the ABA common coordinate
             framework. The result is a high-dimensional integrated volume with registration
             (HiDiver) with alignment precision better than 50 µm.
             Throughput is sufficiently high that HiDiver is being used
             in quantitative studies of the impact of gene variants and
             aging on mouse brain cytoarchitecture and
             connectomics.},
   Doi = {10.1073/pnas.2218617120},
   Key = {fds370388}
}

@article{fds174269,
   Author = {GA JOHNSON and CR KISTLER and RH McCLUER},
   Title = {Metabolism of exogenous sialic acid in the
             rat.},
   Journal = {Proceedings of the Society for Experimental Biology and
             Medicine. Society for Experimental Biology and Medicine (New
             York, N.Y.)},
   Volume = {106},
   Pages = {124-7},
   Year = {1961},
   Month = {January},
   ISSN = {0037-9727},
   Language = {eng},
   Key = {fds174269}
}

@booklet{Korobkin81,
   Author = {KOROBKIN, M and JOHNSON, GA and BREIMAN, RS},
   Title = {METHODOLOGIC CONSIDERATIONS IN MULTIPLANAR REFORMATTING OF
             TRANSAXIAL CT IMAGES},
   Journal = {Investigative Radiology},
   Volume = {16},
   Number = {5},
   Pages = {374-374},
   Publisher = {Ovid Technologies (Wolters Kluwer Health)},
   Year = {1981},
   Month = {September},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1981MK56200027&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Doi = {10.1097/00004424-198109000-00027},
   Key = {Korobkin81}
}

@booklet{Macfall87,
   Author = {MacFall, JR and Wehrli, FW and Breger, RK and Johnson,
             GA},
   Title = {Methodology for the measurement and analysis of relaxation
             times in proton imaging.},
   Journal = {Magn Reson Imaging},
   Volume = {5},
   Number = {3},
   Pages = {209-220},
   Year = {1987},
   ISSN = {0730-725X},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/3041152},
   Abstract = {Measurements of proton T1 and T2 were performed on GdCl3
             solutions (20 less than T2 less than 500 msec, 90 less than
             T1 less than 1000 msec) on large-bore NMR imaging systems
             operating at 1.0T and 1.5T. CPMG multi-echo (ME), multiple
             saturation recovery (MSR) and modified fast inversion
             recovery (MFIR) pulse sequences as well as a sequence that
             combines and interleaves T1 and T2 weighted data acquisition
             (which we call "multiple saturation-recovery multiple-echo"
             (MSRME) were used. The relaxation data are compared to those
             obtained on a small bore NMR spectrometer operated at 1.5T.
             T1 and T2 values for the solutions were found to be the same
             within 10% for the two fields. Reproducibility of
             measurements of T1, T2 and the unnormalized spin density of
             the solutions was better than 5%. Systematic errors,
             amenable to correction through calibration, are noted in the
             imager T1 and T2 values. T1 and T2 values for some typical
             neural tissues at 1.5T and body tissue at 1.0T for human
             volunteers were obtained and are tabulated.},
   Doi = {10.1016/0730-725x(87)90022-1},
   Key = {Macfall87}
}

@article{fds132754,
   Author = {JR MacFall and FW Wehrli and RK Breger and GA Johnson},
   Title = {Methodology for the measurement and analysis of relaxation
             times in proton imaging.},
   Journal = {Magnetic resonance imaging, UNITED STATES},
   Volume = {5},
   Number = {3},
   Pages = {209-20},
   Year = {1987},
   ISSN = {0730-725X},
   Keywords = {Gadolinium • Magnetic Resonance Spectroscopy •
             Protons • Solutions • instrumentation •
             methods*},
   Abstract = {Measurements of proton T1 and T2 were performed on GdCl3
             solutions (20 less than T2 less than 500 msec, 90 less than
             T1 less than 1000 msec) on large-bore NMR imaging systems
             operating at 1.0T and 1.5T. CPMG multi-echo (ME), multiple
             saturation recovery (MSR) and modified fast inversion
             recovery (MFIR) pulse sequences as well as a sequence that
             combines and interleaves T1 and T2 weighted data acquisition
             (which we call "multiple saturation-recovery multiple-echo"
             (MSRME) were used. The relaxation data are compared to those
             obtained on a small bore NMR spectrometer operated at 1.5T.
             T1 and T2 values for the solutions were found to be the same
             within 10% for the two fields. Reproducibility of
             measurements of T1, T2 and the unnormalized spin density of
             the solutions was better than 5%. Systematic errors,
             amenable to correction through calibration, are noted in the
             imager T1 and T2 values. T1 and T2 values for some typical
             neural tissues at 1.5T and body tissue at 1.0T for human
             volunteers were obtained and are tabulated.},
   Key = {fds132754}
}

@article{fds174147,
   Author = {BM Markaverich and RR Gregory and MA Alejandro and JH Clark and GA
             Johnson, BS Middleditch},
   Title = {Methyl p-hydroxyphenyllactate. An inhibitor of cell growth
             and proliferation and an endogenous ligand for nuclear
             type-II binding sites.},
   Journal = {The Journal of biological chemistry},
   Volume = {263},
   Number = {15},
   Pages = {7203-10},
   Year = {1988},
   Month = {May},
   ISSN = {0021-9258},
   Keywords = {Animals • Breast Neoplasms • Cell Division •
             Cell Line • Cell Nucleus • Chromatography, Gel
             • Chromatography, High Pressure Liquid • Female
             • Humans • Lactates • Mass Spectrometry
             • Ovariectomy • Rats • Rats, Inbred Strains
             • Receptors, Estradiol • Receptors, Estrogen
             • drug effects* • isolation & purification •
             metabolism • metabolism* • pharmacology*},
   Abstract = {We previously described and partially characterized
             endogenous ligands for nuclear type II sites in normal and
             malignant tissues. Chromatography of these ligands on
             Sephadex LH-20 revealed that two peaks with binding activity
             (alpha and beta) could be resolved. The beta-peak component
             was present in all normal tissues that we examined, but not
             in malignant tissues, and it inhibited the growth of MCF-7
             human breast cancer cells in vitro. Conversely, the
             alpha-peak component was found to be present in both normal
             and malignant tissues, and did not inhibit MCF-7 cell
             growth. The present studies describe the purification and
             identification of the alpha-peak and beta-peak components in
             bovine serum and an assessment of the effects of these
             compounds on normal and malignant cell growth. Gas
             chromatography-mass spectroscopy analysis of the purified
             beta-peak component demonstrated that the compound was
             methyl p-hydroxyphenyllactate (MeHPLA). Competition analysis
             revealed that MeHPLA binds to nuclear type II sites with a
             high binding affinity, while physiological levels of this
             compound blocked estradiol stimulation of uterine growth in
             vivo and inhibited the growth of MCF-7 human breast cancer
             cells in vitro. The alpha-peak component was found to be the
             corresponding acid, p-hydroxyphenyllactic acid (HPLA). This
             compound interacted with nuclear type II sites with a
             relatively low affinity and did not block uterotropic
             response to estradiol or inhibit MCF-7 cell growth. These
             studies demonstrate that HPLA and MeHPLA are ligands for
             nuclear type II sites and that MeHPLA may be a very
             important regulator of normal and malignant cell
             growth.},
   Language = {eng},
   Key = {fds174147}
}

@booklet{Markaverich88b,
   Author = {B. M. Markaverich and R. R. Gregory and M. A. Alejandro and J. H. Clark and G. A. Johnson and B. S. Middleditch},
   Title = {Methyl para-hydroxyphenyllactate - an inhibitor of
             cell-growth and proliferation and an endogenous ligand for
             nuclear type-ii binding-sites},
   Journal = {Journal Of Biological Chemistry},
   Volume = {263},
   Number = {15},
   Pages = {7203 -- 7210},
   Year = {1988},
   Month = {May},
   Key = {Markaverich88b}
}

@booklet{Markaverich88,
   Author = {B. M. Markaverich and R. R. Gregory and M. A. Alejandro and G. A. Johnson and B. S. Middleditch},
   Title = {Methyl para-hydroxyphenyllactate - identification in
             rat-liver extracts},
   Journal = {Journal Of High Resolution Chromatography \& Chromatography
             Communications},
   Volume = {11},
   Number = {8},
   Pages = {605 -- 607},
   Year = {1988},
   Month = {August},
   Key = {Markaverich88}
}

@article{064610243353,
   Author = {De Lin and M and Hedlund, L and Johnson, GA},
   Title = {Micro radiography imaging of the rodent with phenylephrine
             induced vascular hypertension},
   Journal = {2006 3rd IEEE International Symposium on Biomedical Imaging:
             From Nano to Macro - Proceedings},
   Volume = {2006},
   Pages = {610-613},
   Address = {Arlington, VA, United States},
   Year = {2006},
   Month = {November},
   ISBN = {9780780395770},
   Keywords = {Medical imaging;Blood;Biological organs;Angiography;Data
             acquisition;Image analysis;},
   Abstract = {Vascular tonicity plays a major role in regulating the blood
             pressure and the perfusion of organs, and hypertension is a
             major cause of morbidity and mortality in humans. We use
             phenylephrine, a vasoconstrictor, to create a model of
             hypertension in the rat. This work demonstrates the use of a
             micro-X-ray digital subtraction angiography (DSA) system to
             image pharmacologically mediated changes in the vascular
             system of the rat. Imaging physiological function in the
             rodent calls for high spatial and temporal resolutions and
             the use of a reproducible image acquisition chain. Dynamic
             vascular images and quantitative perfusion metrics were
             acquired before and after a vasoconstrictor, phenylephrine
             drug injection. Dramatic effects of the vasoconstrictor on
             vascular dynamics are seen in the prolonged blood flow mean
             transit time, amount of ventricular filling, the size
             increase of the pulmonary arteries and aorta, and a
             substantial increase in mean arterial pressure. © 2006
             IEEE.},
   Key = {064610243353}
}

@article{9073128,
   Author = {Ming De Lin and Hedlund, L. and Johnson,
             G.A.},
   Title = {Micro radiography imaging of the rodent with phenylephrine
             induced vascular hypertension},
   Journal = {2006 3rd IEEE International Symposium on Biomedical Imaging:
             Macro to Nano (IEEE Cat. No.06EX1231C)},
   Pages = {610 - 13},
   Address = {Arlington, VA, USA},
   Year = {2006},
   Keywords = {blood vessels;diagnostic radiography;drugs;haemorheology;},
   Abstract = {Vascular tonicity plays a major role in regulating the blood
             pressure and the perfusion of organs, and hypertension is a
             major cause of morbidity and mortality in humans. We use
             phenylephrine, a vasoconstrictor, to create a model of
             hypertension in the rat. This work demonstrates the use of a
             micro-X-ray digital subtraction angiography (DSA) system to
             image pharmacologically mediated changes in the vascular
             system of the rat. Imaging physiological function in the
             rodent calls for high spatial and temporal resolutions and
             the use of a reproducible image acquisition chain. Dynamic
             vascular images and quantitative perfusion metrics were
             acquired before and after a vasoconstrictor, phenylephrine
             drug injection. Dramatic effects of the vasoconstrictor on
             vascular dynamics are seen in the prolonged blood flow mean
             transit time, amount of ventricular filling, the size
             increase of the pulmonary arteries and aorta, and a
             substantial increase in mean arterial pressure},
   Key = {9073128}
}

@article{fds268833,
   Author = {Badea, CT and Hedlund, LW and Cook, J and Berridge, BR and Johnson,
             GA},
   Title = {Micro-CT imaging assessment of dobutamine-induced cardiac
             stress in rats.},
   Journal = {J Pharmacol Toxicol Methods},
   Volume = {63},
   Number = {1},
   Pages = {24-29},
   Year = {2011},
   ISSN = {1873-488X},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/20399875},
   Keywords = {Animals • Cardiac Output • Dobutamine •
             Echocardiography • Electrocardiography • Heart
             • Heart Rate • Heart Ventricles • Magnetic
             Resonance Imaging • Male • Rats • Rats,
             Sprague-Dawley • Stress, Physiological • X-Ray
             Microtomography • administration & dosage • drug
             effects • drug effects* • methods* •
             pathology • pharmacology* • physiology •
             radiography*},
   Abstract = {INTRODUCTION: Dobutamine (DOB) stress in animal models of
             heart disease has been imaged so far using echocardiography
             and magnetic resonance imaging. The purpose of this study
             was to assess normal response to DOB stress in rats using
             anatomical and functional data using micro-computed
             tomography (CT). METHODS: Ten normal adult male rats were
             first injected with a liposomal-based blood pool contrast
             agent and next infused with DOB via a tail vein catheter.
             Using prospective gating, 5 pairs of systole/diastole
             micro-CT images were acquired (a) pre-infusion baseline; (b)
             at heart rate plateau during infusion of 10 μg/kg/min DOB;
             (c) at post-DOB infusion baseline; (d) at heart rate plateau
             during infusion of 30 μg/kg/min DOB; and (e) after
             post-infusion return to baseline. Heart rate, peripheral and
             breathing distensions were monitored by oximetry. Micro-CT
             images with 88-μm isotropic voxels were segmented to obtain
             cardiac function based on volumetric measurements of the
             left ventricle. RESULTS: DOB stress increased heart rate and
             cardiac output with both doses. Ejection fraction increased
             above baseline by an average of 35.9% with the first DOB
             dose and 18.4% with the second dose. No change was observed
             in the relative peripheral arterial pressures associated
             with the significant increases in cardiac output.
             DISCUSSION: Micro-CT proved to be a robust imaging method
             able to provide isotropic data on cardiac morphology and
             function. Micro-CT has the advantage of being faster and
             more cost-effective than MR and is able to provide higher
             accuracy than echocardiography. The impact of such an
             enabling technology can be enormous in evaluating
             cardiotoxic effects of various test drugs.},
   Language = {eng},
   Doi = {10.1016/j.vascn.2010.04.002},
   Key = {fds268833}
}

@article{fds132896,
   Author = {C Badea and LW Hedlund and GA Johnson},
   Title = {Micro-CT with respiratory and cardiac gating.},
   Journal = {Medical physics, United States},
   Volume = {31},
   Number = {12},
   Pages = {3324-9},
   Year = {2004},
   Month = {December},
   ISSN = {0094-2405},
   Keywords = {Animals • Artifacts • Electrocardiography •
             Equipment Design • Equipment Failure Analysis* •
             Heart • Lung • Mice • Mice, Inbred C57BL
             • Movement* • Radiographic Image Enhancement
             • Radiographic Image Interpretation, Computer-Assisted
             • Respiratory Mechanics • Tomography, X-Ray
             Computed • instrumentation* • methods •
             radiography* • veterinary},
   Abstract = {Cardiopulmonary imaging in rodents using micro-computed
             tomography (CT) is a challenging task due to both cardiac
             and pulmonary motion and the limited fluence rate available
             from micro-focus x-ray tubes of most commercial systems.
             Successful imaging in the mouse requires recognition of both
             the spatial and temporal scales and their impact on the
             required fluence rate. Smaller voxels require an increase in
             the total number of photons (integrated fluence) used in the
             reconstructed image for constant signal-to-noise ratio. The
             faster heart rates require shorter exposures to minimize
             cardiac motion blur imposing even higher demands on the
             fluence rate. We describe a system with fixed tube/detector
             and with a rotating specimen. A large focal spot x-ray tube
             capable of producing high fluence rates with short exposure
             times was used. The geometry is optimized to match focal
             spot blur with detector pitch and the resolution limits
             imposed by the reproducibility of gating. Thus, it is
             possible to achieve isotropic spatial resolution of 100
             microm with a fluence rate at the detector 250 times that of
             a conventional cone beam micro-CT system with rotating
             detector and microfocal x-ray tube. Motion is minimized for
             any single projection with 10 ms exposures that are
             synchronized to both cardiac and breathing motion. System
             performance was validated in vivo by studies of the
             cardiopulmonary structures in C57BL/6 mice, demonstrating
             the value of motion integration with a bright x-ray
             source.},
   Key = {fds132896}
}

@booklet{Badea04,
   Author = {Badea, C and Hedlund, LW and Johnson, GA},
   Title = {Micro-CT with respiratory and cardiac gating.},
   Journal = {Med Phys},
   Volume = {31},
   Number = {12},
   Pages = {3324-3329},
   Year = {2004},
   Month = {December},
   ISSN = {0094-2405},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/15651615},
   Abstract = {Cardiopulmonary imaging in rodents using micro-computed
             tomography (CT) is a challenging task due to both cardiac
             and pulmonary motion and the limited fluence rate available
             from micro-focus x-ray tubes of most commercial systems.
             Successful imaging in the mouse requires recognition of both
             the spatial and temporal scales and their impact on the
             required fluence rate. Smaller voxels require an increase in
             the total number of photons (integrated fluence) used in the
             reconstructed image for constant signal-to-noise ratio. The
             faster heart rates require shorter exposures to minimize
             cardiac motion blur imposing even higher demands on the
             fluence rate. We describe a system with fixed tube/detector
             and with a rotating specimen. A large focal spot x-ray tube
             capable of producing high fluence rates with short exposure
             times was used. The geometry is optimized to match focal
             spot blur with detector pitch and the resolution limits
             imposed by the reproducibility of gating. Thus, it is
             possible to achieve isotropic spatial resolution of 100
             microm with a fluence rate at the detector 250 times that of
             a conventional cone beam micro-CT system with rotating
             detector and microfocal x-ray tube. Motion is minimized for
             any single projection with 10 ms exposures that are
             synchronized to both cardiac and breathing motion. System
             performance was validated in vivo by studies of the
             cardiopulmonary structures in C57BL/6 mice, demonstrating
             the value of motion integration with a bright x-ray
             source.},
   Doi = {10.1118/1.1812604},
   Key = {Badea04}
}

@article{fds357200,
   Author = {Badea, A and Schmalzigaug, R and Kim, W and Bonner, P and Ahmed, U and Johnson, GA and Cofer, G and Foster, M and Anderson, RJ and Badea, C and Premont, RT},
   Title = {Microcephaly with altered cortical layering in GIT1
             deficiency revealed by quantitative neuroimaging.},
   Journal = {Magn Reson Imaging},
   Volume = {76},
   Pages = {26-38},
   Year = {2021},
   Month = {February},
   url = {http://dx.doi.org/10.1016/j.mri.2020.09.023},
   Abstract = {G Protein-Coupled Receptor Kinase-Interacting Protein-1
             (GIT1) regulates neuronal functions, including cell and axon
             migration and synapse formation and maintenance, and GIT1
             knockout (KO) mice exhibit learning and memory deficits. We
             noted that male and female GIT1-KO mice exhibit neuroimaging
             phenotypes including microcephaly, and altered cortical
             layering, with a decrease in neuron density in cortical
             layer V. Micro-CT and magnetic resonance microscopy (MRM)
             were used to identify morphometric phenotypes for the skulls
             and throughout the GIT1-KO brains. High field MRM of
             actively-stained mouse brains from GIT1-KO and wild type
             (WT) controls (n = 6 per group) allowed segmenting 37
             regions, based on co-registration to the Waxholm Space
             atlas. Overall brain size in GIT1-KO mice was ~32% smaller
             compared to WT controls. After correcting for brain size,
             several regions were significantly different in GIT1-KO mice
             relative to WT, including the gray matter of the ventral
             thalamic nuclei and the rest of the thalamus, the inferior
             colliculus, and pontine nuclei. GIT1-KO mice had reduced
             volume of white matter tracts, most notably in the anterior
             commissure (~26% smaller), but also in the cerebral
             peduncle, fornix, and spinal trigeminal tract. On the other
             hand, the basal ganglia appeared enlarged in GIT1-KO mice,
             including the globus pallidus, caudate putamen, and
             particularly the accumbens - supporting a possible
             vulnerability to addiction. Volume based morphometry based
             on high-resolution MRM (21.5 μm isotropic voxels) was
             effective in detecting overall, and local differences in
             brain volumes in GIT1-KO mice, including in white matter
             tracts. The reduced relative volume of specific brain
             regions suggests a critical, but not uniform, role for GIT1
             in brain development, conducive to brain microcephaly, and
             aberrant connectivity.},
   Doi = {10.1016/j.mri.2020.09.023},
   Key = {fds357200}
}

@article{fds268807,
   Author = {Jiang, Y and Johnson, GA},
   Title = {Microscopic diffusion tensor atlas of the mouse
             brain.},
   Journal = {Neuroimage},
   Volume = {56},
   Number = {3},
   Pages = {1235-1243},
   Year = {2011},
   Month = {June},
   ISSN = {1095-9572},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/21419226},
   Keywords = {Analysis of Variance • Animals • Atlases as Topic*
             • Brain • Databases, Factual • Diffusion
             Tensor Imaging • Image Processing, Computer-Assisted
             • Informatics • Internet • Male • Mice
             • Mice, Inbred C57BL • anatomy & histology* •
             methods*},
   Abstract = {Eight diffusion tensor imaging (DTI) datasets of normal
             adult C57BL/6J mouse brains were acquired with an isotropic
             Nyquist limited resolution of 43 μm (voxel volume ~80 pl).
             Each specimen was scanned with a b0 image and 6
             diffusion-weighted images. T1- and T2*-weighted data were
             acquired with each specimen to aid nonlinear registration of
             the data to a common reference space (called "Waxholm
             Space"). We identified 80 different discrete landmarks in
             Waxholm Space to provide the gold standard for measuring the
             registration quality. The accuracy of the registration was
             established by measuring displacement of the 80 landmarks in
             each registered brain from the same landmarks in the
             reference brain. The accuracy was better than 130 μm for
             95% of the landmarks (overall landmark displacement is
             65±40 μm, n=640). Mean and coefficient of variation
             atlases of DTI indices were generated with potential
             application for both voxel-based and region of
             interest-based analysis. To examine consistency of DTI data
             among individual subjects in this study and difference in
             diffusion indices between separate brain structures within
             each subject, averaged values of DTI indices (axial
             diffusivity, radial diffusivity, fractional anisotropy, and
             angular deviation of the primary eigenvector) were computed
             in 9 white matter structures in each brain. The variation of
             the DTI indices across the population was very small, e.g.,
             ~5% for axial diffusivity for each white matter structure,
             enabling confident differentiation of differences in these
             structures within each subject. ANOVA tests indicated that
             the current protocol is able to provide consistent DTI data
             of individual brains (p>0.25), and distinguish difference of
             diffusion indices between white matter structures (p<0.001).
             Power analysis was also performed to provide an estimate of
             the number of specimens required to detect a 10% change of
             the DTI indices in each white matter structure. The data
             provide a critical addition to Waxholm Space, the
             International Neuroinformatics Coordinating Facility
             (www.incf.org) online comprehensive atlas of the mouse
             brain.},
   Language = {eng},
   Doi = {10.1016/j.neuroimage.2011.03.031},
   Key = {fds268807}
}

@article{fds268837,
   Author = {Jiang, Y and Johnson, GA},
   Title = {Microscopic diffusion tensor imaging of the mouse
             brain.},
   Journal = {Neuroimage},
   Volume = {50},
   Number = {2},
   Pages = {465-471},
   Year = {2010},
   Month = {April},
   ISSN = {1095-9572},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/20034583},
   Keywords = {Animals • Anisotropy • Brain • Brain Mapping
             • Diffusion Tensor Imaging • Image Interpretation,
             Computer-Assisted • Mice • Staining and Labeling
             • Tissue Fixation • anatomy & histology* •
             methods • methods*},
   Abstract = {Diffusion tensor imaging (DTI) data at 43 mum isotropic
             resolution has been acquired on the intact adult mouse brain
             in 28-h scan time by using a streamlined protocol, including
             specimen fixation and staining, image acquisition,
             reconstruction, post-processing, and distribution. An
             intermediate registration of each component image is
             required to achieve the desired microscopic resolution.
             Multiple parameters have been derived, including fractional
             anisotropy, axial and radial diffusivity, and a color-coded
             orientation map of the primary eigenvector. Each DTI dataset
             was mapped to a common reference space to facilitate future
             standardized analysis. Fiber tracking has also been
             demonstrated, providing 3D connection information. This
             protocol to acquire high-resolution DTI data in a robust and
             repeatable fashion will serve as a foundation to
             quantitatively study mouse brain integrity and white matter
             architecture, at what we believe to be the highest spatial
             resolution yet attained.},
   Language = {eng},
   Doi = {10.1016/j.neuroimage.2009.12.057},
   Key = {fds268837}
}

@article{fds132747,
   Author = {G.A. Johnson},
   Title = {Miller JR, Hurlston SE, Face DW, Kountz DJ, MacFall JR,
             Hedlund LW, Ma QY, Johnson GA. Performance of a
             high-temperature superconducting probe for in vivo microsopy
             at 2.0 T Magn Reson Med. In press 1998},
   Year = {1998},
   Key = {fds132747}
}

@booklet{Johnson93b,
   Author = {G. A. Johnson and J. T. Handa and C. A. Baker and G. J.
             Jaffe},
   Title = {Minoxidil inhibits human rpe cell-growth by a mechanism
             dependent on the conversion to minoxidil
             sulfate},
   Journal = {Investigative Ophthalmology \& Visual Science},
   Volume = {34},
   Number = {4},
   Pages = {1426 -- 1426},
   Year = {1993},
   Month = {March},
   Key = {Johnson93b}
}

@booklet{Fiedlerweiss87,
   Author = {V. C. Fiedlerweiss and G. A. Johnson and C. M. Buys and C.
             A. Baker},
   Title = {Minoxidil sulfate and sulfotransferase activity in
             alopecia-areata},
   Journal = {Clinical Research},
   Volume = {35},
   Number = {3},
   Pages = {A682 -- A682},
   Year = {1987},
   Month = {April},
   Key = {Fiedlerweiss87}
}

@article{fds174250,
   Author = {AE Buhl and DJ Waldon and CA Baker and GA Johnson},
   Title = {Minoxidil sulfate is the active metabolite that stimulates
             hair follicles.},
   Journal = {The Journal of investigative dermatology},
   Volume = {95},
   Number = {5},
   Pages = {553-7},
   Year = {1990},
   Month = {November},
   ISSN = {0022-202X},
   Keywords = {Acetaminophen • Animals • Cells, Cultured •
             Chlorates • Diethylcarbamazine • Hair • Mice
             • Minoxidil • Sulfotransferases • Vibrissae
             • analogs & derivatives* • antagonists &
             inhibitors • cytology • drug effects • drug
             effects* • enzymology • metabolism •
             pharmacology},
   Abstract = {An important step in understanding minoxidil's mechanism of
             action on hair follicles was to determine the drug's active
             form. We used organ-cultured vibrissa follicles to test
             whether it is minoxidil or its sulfated metabolite,
             minoxidil sulfate, that stimulates hair growth. Follicles
             from neonatal mice were cultured with or without drugs and
             effects were assessed by measuring incorporation of
             radiolabeled cysteine in hair shafts of the treated
             follicles. Assays of minoxidil sulfotransferase activity
             indicated that vibrissae follicles metabolize minoxidil to
             minoxidil sulfate. Dose-response studies showed that
             minoxidil sulfate is 14 times more potent than minoxidil in
             stimulating cysteine incorporation in cultured follicles.
             Three drugs that block production of intrafollicular
             minoxidil sulfate were tested for their effects on
             drug-induced hair growth. Diethylcarbamazine proved to be a
             noncompetitive inhibitor of sulfotransferase and prevented
             hair growth stimulation by minoxidil but not by minoxidil
             sulfate. Inhibiting the formation of intracellular PAPS with
             chlorate also blocked the action of minoxidil but not of
             minoxidil sulfate. Acetaminophen, a potent sulfate scavenger
             blocked cysteine incorporation by minoxidil. It also blocked
             follicular stimulation by minoxidil sulfate apparently by
             directly removing the sulfate from the drug. Experiments
             with U-51,607, a potent minoxidil analog that also forms a
             sulfated metabolite, showed that its activity was inhibited
             by both chlorate and diethylcarbamazine. These studies show
             that sulfation is a critical step for hair-growth effects of
             minoxidil and that it is the sulfated metabolite that
             directly affects hair follicles.},
   Language = {eng},
   Key = {fds174250}
}

@booklet{Buhl90,
   Author = {A. E. Buhl and D. J. Waldon and C. A. Baker and G. A.
             Johnson},
   Title = {Minoxidil sulfate is the active metabolite that stimulates
             hair-follicles},
   Journal = {Journal Of Investigative Dermatology},
   Volume = {95},
   Number = {5},
   Pages = {553 -- 557},
   Year = {1990},
   Month = {November},
   Key = {Buhl90}
}

@booklet{Johnson83c,
   Author = {G. A. Johnson and K. J. Barsuhn and J. M.
             Mccall},
   Title = {Minoxidil sulfate, a metabolite of minoxidil},
   Journal = {Drug Metabolism And Disposition},
   Volume = {11},
   Number = {5},
   Pages = {507 -- 508},
   Year = {1983},
   Key = {Johnson83c}
}

@article{fds132908,
   Author = {GA Johnson and KJ Barsuhn and JM McCall},
   Title = {Minoxidil sulfate, a metabolite of minoxidil.},
   Journal = {Drug metabolism and disposition: the biological fate of
             chemicals, UNITED STATES},
   Volume = {11},
   Number = {5},
   Pages = {507-8},
   ISSN = {0090-9556},
   Keywords = {Animals • Bile • Chromatography, High Pressure
             Liquid • Female • Minoxidil • Pyrimidines
             • Rats • Rats, Inbred Strains • analogs &
             derivatives • metabolism • metabolism*},
   Key = {fds132908}
}

@booklet{Baker94,
   Author = {C. A. Baker and H. Uno and G. A. Johnson},
   Title = {Minoxidil sulfation in the hair follicle},
   Journal = {Skin Pharmacology},
   Volume = {7},
   Number = {6},
   Pages = {335 -- 339},
   Year = {1994},
   Key = {Baker94}
}

@article{fds174125,
   Author = {CA Baker and H Uno and GA Johnson},
   Title = {Minoxidil sulfation in the hair follicle.},
   Journal = {Skin pharmacology : the official journal of the Skin
             Pharmacology Society},
   Volume = {7},
   Number = {6},
   Pages = {335-9},
   Year = {1994},
   ISSN = {1011-0283},
   Keywords = {Animals • Female • Hair • Macaca •
             Minoxidil • Sulfates • Sulfotransferases •
             metabolism • metabolism*},
   Abstract = {The in vivo model which may be the most accurate for the
             ability to predict hair growth in humans, and which was
             utilized in the preclinical development of minoxidil, is the
             adult stumptailed macaque. Previous reports have suggested
             that the enzyme activity which accounts for the activation
             of minoxidil, i.e., minoxidil sulfotransferase, is present
             in skin. We have demonstrated that scalp skin from the
             stumptailed macaque contains minoxidil sulfotransferase
             activity, and further with dissection of that scalp skin
             into epidermis, dermis and hair follicle, most of
             sulfotransferase activity was present in the follicle.
             Sulfotransferase activity in the hair follicle in
             freeze-dried scalp skin sections from 9 stumptailed macaques
             ranged from 47 to 84% of the total (mean 61 +/- 12%). Much
             less minoxidil sulfotransferase activity was measured in the
             epidermis (mean 18 +/- 11%, with a range of 2-37%) and the
             dermis (mean 21 +/- 8%, with a range of 4-35%) of these
             scalp sections. These results indicate that the scalp skin
             from the stumptailed macaque contains minoxidil
             sulfotransferase activity and this activity is largely
             localized in the hair follicle which may account for its
             ability to stimulate hair growth in this animal
             model.},
   Language = {eng},
   Key = {fds174125}
}

@booklet{Baker91,
   Author = {C. A. Baker and H. Uno and G. A. Johnson},
   Title = {Minoxidil sulfotransferase activity in hair-follicles},
   Journal = {Clinical Research},
   Volume = {39},
   Number = {2},
   Pages = {A537 -- A537},
   Year = {1991},
   Month = {April},
   Key = {Baker91}
}

@booklet{Baker91a,
   Author = {C. A. Baker and H. Uno and G. A. Johnson},
   Title = {Minoxidil sulfotransferase activity in hair-follicles},
   Journal = {Journal Of Investigative Dermatology},
   Volume = {96},
   Number = {4},
   Pages = {576 -- 576},
   Year = {1991},
   Month = {April},
   Key = {Baker91a}
}

@booklet{Buhl94,
   Author = {A. E. Buhl and C. A. Baker and A. J. Dietz and F. T. Murray and G. A. Johnson},
   Title = {Minoxidil sulfotransferase activity influences the efficacy
             of rogaine(r) topical solutions (ts) - enzyme studies using
             scalp and platelets},
   Journal = {Journal Of Investigative Dermatology},
   Volume = {102},
   Number = {4},
   Pages = {534 -- 534},
   Year = {1994},
   Month = {April},
   Key = {Buhl94}
}

@booklet{Johnson92,
   Author = {G. A. Johnson and C. A. Baker and K. A. Knight},
   Title = {Minoxidil sulfotransferase, a marker of human keratinocyte
             differentiation},
   Journal = {Journal Of Investigative Dermatology},
   Volume = {98},
   Number = {5},
   Pages = {730 -- 733},
   Year = {1992},
   Month = {May},
   Key = {Johnson92}
}

@article{fds174244,
   Author = {GA Johnson and CA Baker and KA Knight},
   Title = {Minoxidil sulfotransferase, a marker of human keratinocyte
             differentiation.},
   Journal = {The Journal of investigative dermatology},
   Volume = {98},
   Number = {5},
   Pages = {730-3},
   Year = {1992},
   Month = {May},
   ISSN = {0022-202X},
   Keywords = {Biological Markers • Calcium • Cell
             Differentiation • Enzyme Induction • Humans •
             Keratinocytes • Sulfotransferases • Time Factors
             • Transglutaminases • cytology* • enzymology
             • metabolism • pharmacology •
             pharmacology*},
   Abstract = {The sulfation of minoxidil is catalyzed by a
             sulfotransferase activity in a number of tissues including
             skin. To investigate further the nature of the minoxidil
             sulfotransferase activity in epithelial tissue and to
             compare this activity to that of cholesterol
             sulfotransferase, which has already been shown to be induced
             during the differentiation of epithelial cells, we cultured
             normal human epidermal keratinocytes in a keratinocyte
             growth medium for 4 d, after which the media were replaced
             with either the same growth media or media with increasing
             Ca++ concentrations. Cholesterol sulfotransferase, minoxidil
             sulfotransferase, and transglutaminase were determined
             during the differentiation of the cells in the three media.
             Time-activity curves that suggested two different
             sulfotransferase activities were induced during the
             differentiation process. U-77581, a competitive inhibitor of
             minoxidil sulfotransferase activity, inhibited the sulfation
             of minoxidil sulfotransferase activity in the keratinocyte
             homogenates, but it did not inhibit the sulfation of
             cholesterol. These data indicate that at least two
             sulfotransferase activities are induced during the
             differentiation of epithelial keratinocytes and minoxidil
             sulfotransferase is an early marker of that
             differentiation.},
   Language = {eng},
   Key = {fds174244}
}

@article{fds268988,
   Author = {Hedlund, LW and Möller, HE and Chen, XJ and Chawla, MS and Cofer, GP and Johnson, GA},
   Title = {Mixing oxygen with hyperpolarized (3)He for small-animal
             lung studies.},
   Journal = {NMR Biomed},
   Volume = {13},
   Number = {4},
   Pages = {202-206},
   Year = {2000},
   Month = {June},
   ISSN = {0952-3480},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/10867697},
   Keywords = {Animals • Animals, Laboratory • Helium* •
             Intubation, Intratracheal • Isotopes • Lung •
             Magnetic Resonance Imaging • Oxygen* • Rats •
             Respiratory Function Tests • anatomy & histology •
             instrumentation • methods* • physiology*},
   Abstract = {Hyperpolarized helium (HP (3)He) is useful for direct MR
             imaging of the gas spaces of small animal lungs. Previously,
             breaths of 100% HP (3)He were alternated with breaths of air
             to maximize helium signal in the lungs and to minimize the
             depolarizing effects of O(2). However, for high-resolution
             imaging requiring many HP (3)He breaths (hundreds) and for
             pulmonary disease studies, a method was needed to
             simultaneously deliver O(2) and HP (3)He with each breath
             without significant loss of polarization. We modified our
             existing computer-controlled ventilator by adding a plastic
             valve, additional relays and a controller. O(2) and HP (3)He
             are mixed at the beginning of each breath within the body of
             a breathing valve, which is attached directly to the
             endotracheal tube. With this mixing method, we found that
             T(1) relaxation of HP (3)He in the guinea pig lung was about
             20 s compared to 30 s with alternate air/HP (3)He breathing.
             Because imaging times during each breath are short (about
             500 ms), the HP (3)He signal loss from O(2) contact is
             calculated to be less than 5%. We concluded that the
             advantages of mixing HP (3)He with O(2), such as shorter
             imaging times (reduced T(1) losses in reservoir) and
             improved physiologic stability, outweigh the small signal
             loss from the depolarizing effects of oxygen on HP
             (3)He.},
   Doi = {10.1002/1099-1492(200006)13:4<202::aid-nbm645>3.0.co;2-j},
   Key = {fds268988}
}

@booklet{Hedlund00a,
   Author = {L. W. Hedlund and H. E. Moller and X. J. Chen and M. S.
             Chawla and G. P. Cofer and G. A. Johnson},
   Title = {Mixing oxygen with hyperpolarized He-3 for small-animal lung
             studies},
   Journal = {Nmr In Biomedicine},
   Volume = {13},
   Number = {4},
   Pages = {202 -- 206},
   Year = {2000},
   Month = {June},
   Key = {Hedlund00a}
}

@booklet{Kim03,
   Author = {J. G. Kim and J. H. Song and J. L. Vallet and G. A. Rohrer and G. A. Johnson and M. M. Joyce and R. K.
             Christenson},
   Title = {Molecular characterization and expression of porcine bone
             morphogenetic protein receptor-IB in the uterus of cyclic
             and pregnant gilts},
   Journal = {Biology Of Reproduction},
   Volume = {68},
   Number = {3},
   Pages = {735 -- 743},
   Year = {2003},
   Month = {March},
   Key = {Kim03}
}

@article{fds174173,
   Author = {JG Kim and JH Song and JL Vallet and GA Rohrer and GA Johnson and MM Joyce and RK Christenson},
   Title = {Molecular characterization and expression of porcine bone
             morphogenetic protein receptor-IB in the uterus of cyclic
             and pregnant gilts.},
   Journal = {Biology of reproduction},
   Volume = {68},
   Number = {3},
   Pages = {735-43},
   Year = {2003},
   Month = {March},
   ISSN = {0006-3363},
   Keywords = {Amino Acid Sequence • Animals • Base Sequence
             • Blotting, Northern • Bone Morphogenetic Protein
             Receptors, Type I • Chromosome Mapping • Cloning,
             Molecular • Crosses, Genetic • DNA, Complementary
             • Endometrium • Expressed Sequence Tags •
             Female • Gene Expression Regulation • In Situ
             Hybridization • Male • Molecular Sequence Data
             • Point Mutation • Pregnancy • Pregnancy,
             Animal • Protein-Serine-Threonine Kinases • RNA,
             Messenger • Receptors, Growth Factor • Sequence
             Alignment • Sequence Analysis, DNA • Swine •
             biosynthesis • chemistry • genetics •
             genetics* • isolation & purification • metabolism
             • metabolism* • physiology •
             veterinary},
   Abstract = {Previous gene mapping analyses revealed a quantitative trait
             locus for uterine capacity on chromosome 8. Comparison of
             porcine and human genetic maps suggests that the bone
             morphogenetic protein receptor IB (BMPR-IB) gene may be
             located near this region. The objectives of this study were
             to 1) clone the full coding region for BMPR-IB, 2) examine
             BMPR-IB gene expression by the endometrium and its cellular
             localization in cyclic and pregnant gilts, and 3) map the
             BMPR-IB gene. By iterative screening of an expressed
             sequence tag library, we obtained a 3559-base pair cDNA
             clone including the full coding region of BMPR-IB.
             Endometrial BMPR-IB mRNA expression of White composite gilts
             was determined by Northern blotting in Days 10, 13, and 15
             cyclic and Days 10, 13, 15, 20, 30, and 40 pregnant gilts.
             In cyclic gilts, endometrial BMPR-IB mRNA expression was
             elevated on Days 13 and 15 (P < 0.01) compared with Day 10.
             Expression of BMPR-IB mRNA was localized in both luminal and
             glandular epithelium on Day 15. However, in pregnant gilts,
             BMPR-IB mRNA expression was not significantly different in
             the endometrium from Day 10 to Day 20, and it was
             significantly decreased on Days 30 and 40 (P = 0.011). The
             BMPR-IB gene was mapped to 108 cM on chromosome 8. These
             findings show that BMPR-IB mRNA expression is regulated
             differently in cyclic and pregnant gilts; this pattern of
             gene expression may be important for endometrial function
             during the luteal phase of the estrous cycle as compared
             with early pregnancy.},
   Language = {eng},
   Key = {fds174173}
}

@article{fds174228,
   Author = {E Asselin and GA Johnson and TE Spencer and FW Bazer},
   Title = {Monocyte chemotactic protein-1 and -2 messenger ribonucleic
             acids in the ovine uterus: regulation by pregnancy,
             progesterone, and interferon-tau.},
   Journal = {Biology of reproduction},
   Volume = {64},
   Number = {3},
   Pages = {992-1000},
   Year = {2001},
   Month = {March},
   ISSN = {0006-3363},
   Keywords = {Animals • Chemokine CCL2 • Chemokine CCL8 •
             Endometrium • Estrus • Female •
             Histocytochemistry • Image Processing,
             Computer-Assisted • Interferon Type I • Monocyte
             Chemoattractant Proteins • Nucleic Acid Hybridization
             • Pregnancy • Pregnancy Proteins • Pregnancy,
             Animal • Progesterone • RNA, Messenger •
             Random Allocation • Recombinant Proteins • Reverse
             Transcriptase Polymerase Chain Reaction • Sheep •
             Steroids • biosynthesis • cytology • genetics
             • genetics* • metabolism • metabolism* •
             pharmacology • pharmacology* • physiology* •
             veterinary},
   Abstract = {Endometrial leukocytes may play important roles during
             pregnancy. Because chemokines are regulators of immune cell
             activity and trafficking, this study determined if mRNAs for
             monocyte chemotactic proteins (MCP) were present in the
             ovine uterus and regulated by progesterone (P) and/or
             recombinant ovine interferon tau (roIFN-tau). Uteri of
             normal cycling and pregnant ewes (experiment 1) and uteri of
             ovariectomized ewes receiving intrauterine infusions of
             IFN-tau and/or i.m. injections of P (experiment 2) were used
             to detect MCP-1 and MCP-2 mRNA. In experiment 1, slot-blot
             hybridization analysis of endometrial total RNA revealed
             that MCP-1 and MCP-2 mRNA levels did not change during the
             estrous cycle but increased between Days 13 and 19 of
             pregnancy. Using in situ hybridization, MCP-1 and MCP-2 mRNA
             were localized to immune cells in the subepithelial compact
             stroma. Histomorphological studies and in situ hybridization
             for major basic protein (MBP) indicated that MCP-positive
             immune cells were eosinophils. In experiment 2, treatment
             with P and roIFN-tau increased (P < 0.05) the number of
             MCP-1- and MCP-2-expressing eosinophils in the endometrium
             compared to ewes treated with P alone. Injection of the P
             receptor antagonist (ZK 137,316) inhibited effects of P
             and/or roIFN-tau to recruit eosinophils expressing MCP-1 and
             MCP-2 mRNAs. Endometrial production of MCPs by eosinophils
             during early pregnancy may play a role(s) in central
             implantation and/or placentation in ewes that is crucial for
             successful establishment of pregnancy.},
   Language = {eng},
   Key = {fds174228}
}

@booklet{Asselin01,
   Author = {E. Asselin and G. A. Johnson and T. E. Spencer and F. W.
             Bazer},
   Title = {Monocyte chemotactic protein-1 and-2 messenger ribonucleic
             acids in the ovine uterus: Regulation by pregnancy,
             progesterone, and interferon-tau},
   Journal = {Biology Of Reproduction},
   Volume = {64},
   Number = {3},
   Pages = {992 -- 1000},
   Year = {2001},
   Month = {March},
   Key = {Asselin01}
}

@booklet{Johnson02g,
   Author = {G. A. Johnson and G. P. Cofer and S. L. Gewalt and L. W.
             Hedlund},
   Title = {Morphologic phenotyping with MR microscopy: The visible
             mouse},
   Journal = {Radiology},
   Volume = {222},
   Number = {3},
   Pages = {789 -- 793},
   Year = {2002},
   Month = {March},
   Key = {Johnson02g}
}

@article{fds268929,
   Author = {Johnson, GA and Cofer, GP and Gewalt, SL and Hedlund,
             LW},
   Title = {Morphologic phenotyping with MR microscopy: the visible
             mouse.},
   Journal = {Radiology},
   Volume = {222},
   Number = {3},
   Pages = {789-793},
   Year = {2002},
   Month = {March},
   ISSN = {0033-8419},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/11867802},
   Keywords = {Animals • Contrast Media • Gadolinium DTPA •
             Imaging, Three-Dimensional* • Magnetic Resonance
             Imaging • Male • Mice • Mice, Inbred C57BL
             • Mice, Knockout • Microscopy • Phenotype
             • Urate Oxidase • administration & dosage •
             anatomy & histology* • diagnostic use • genetics
             • methods*},
   Abstract = {A method for rapid morphologic phenotyping is demonstrated
             by using magnetic resonance microscopy. Whole fixed C57BL/6J
             mice were imaged at 110-microm isotropic resolution; limited
             volumes of the intact specimen, at 50-microm isotropic
             resolution; and isolated organs, at 25-microm isotropic
             resolution. The three-dimensional imaging technique was
             applied to uricase knockout mice to demonstrate the method
             for the evaluation of morphologic phenotype.},
   Doi = {10.1148/radiol.2223010531},
   Key = {fds268929}
}

@article{fds268812,
   Author = {Perperidis, D and Bucholz, E and Johnson, GA and Constantinides,
             C},
   Title = {Morphological studies of the murine heart based on
             probabilistic and statistical atlases.},
   Journal = {Comput Med Imaging Graph},
   Volume = {36},
   Number = {2},
   Pages = {119-129},
   Year = {2012},
   Month = {March},
   ISSN = {1879-0771},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/21820867},
   Keywords = {Algorithms* • Animals • Contrast Media • Data
             Interpretation, Statistical • Gadolinium DTPA •
             Heart • Image Enhancement • Image Interpretation,
             Computer-Assisted • Magnetic Resonance Imaging •
             Male • Mice • Mice, Inbred C57BL •
             Reproducibility of Results • Sensitivity and
             Specificity • Subtraction Technique* • anatomy &
             histology* • diagnostic use* • methods •
             methods*},
   Abstract = {This study directly compares morphological features of the
             mouse heart in its end-relaxed state based on constructed
             morphometric maps and atlases using principal component
             analysis in C57BL/6J (n=8) and DBA (n=5) mice. In
             probabilistic atlases, a gradient probability exists for
             both strains in longitudinal locations from base to apex.
             Based on the statistical atlases, differences in size
             (49.8%), apical direction (15.6%), basal ventricular blood
             pool size (13.2%), and papillary muscle shape and position
             (17.2%) account for the most significant modes of shape
             variability for the left ventricle of the C57BL/6J mice. For
             DBA mice, differences in left ventricular size and direction
             (67.4%), basal size (15.7%), and position of papillary
             muscles (16.8%) account for significant variability.},
   Language = {eng},
   Doi = {10.1016/j.compmedimag.2011.07.001},
   Key = {fds268812}
}

@article{fds268851,
   Author = {Hedlund, LW and Johnson, GA},
   Title = {Morphology of the small-animal lung using magnetic resonance
             microscopy.},
   Journal = {Proc Am Thorac Soc},
   Volume = {2},
   Number = {6},
   Pages = {481-502},
   Year = {2005},
   ISSN = {1546-3222},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/16352752},
   Keywords = {Animals • Artifacts • Image Processing,
             Computer-Assisted • Lung • Magnetic Resonance
             Imaging* • Mice • Microscopy* • Rats •
             pathology*},
   Abstract = {Small-animal imaging with magnetic resonance microscopy
             (MRM) has become an important tool in biomedical research.
             When MRM is used to image perfusion-fixed and "stained"
             whole mouse specimens, cardiopulmonary morphology can be
             visualized, nondestructively, in exquisite detail in all
             three dimensions. This capability can be a valuable tool for
             morphologic phenotyping of different mouse strains commonly
             used in genomics research. When these imaging techniques are
             combined with specialized methods for biological motion
             control and animal support, the lungs of the live, small
             animal can be imaged. Although in vivo imaging may not
             achieve the high resolution possible with a fixed specimen,
             dynamic functional studies and survival studies that follow
             the progression of pulmonary change related to disease or
             environmental exposure are possible. By combining
             conventional proton imaging with gas imaging, using
             hyperpolarized 3He, it is possible to image the tissue and
             gas compartments of the lung. This capability is illustrated
             in studies on an emphysema model in rats and on radiation
             damage of the lung. With further improvements in imaging and
             animal handling technology, we will be able to image faster
             and at higher resolutions, making MRM an even more valuable
             research tool.},
   Doi = {10.1513/pats.200507-074DS},
   Key = {fds268851}
}

@article{fds268869,
   Author = {Badea, A and Ali-Sharief, AA and Johnson, GA},
   Title = {Morphometric analysis of the C57BL/6J mouse
             brain.},
   Journal = {Neuroimage},
   Volume = {37},
   Number = {3},
   Pages = {683-693},
   Year = {2007},
   Month = {September},
   ISSN = {1053-8119},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/17627846},
   Keywords = {Animals • Anthropometry • Brain • Image
             Interpretation, Computer-Assisted • Imaging,
             Three-Dimensional • Magnetic Resonance Imaging •
             Mice • Mice, Inbred C57BL • Models, Anatomic*
             • Models, Neurological* • anatomy & histology*
             • methods*},
   Abstract = {Magnetic resonance microscopy (MRM), when used in
             conjunction with active staining, can produce
             high-resolution, high-contrast images of the mouse brain.
             Using MRM, we imaged in situ the fixed, actively stained
             brains of C57BL/6J mice in order to characterize the
             neuroanatomical phenotype and produce a digital atlas. The
             brains were scanned within the cranium vault to preserve the
             brain morphology, avoid distortions, and to allow an
             unbiased shape analysis. The high-resolution imaging used a
             T1-weighted scan at 21.5 microm isotropic resolution, and an
             eight-echo multi-echo scan, post-processed to obtain an
             enhanced T2 image at 43 microm resolution. The two image
             sets were used to segment the brain into 33 anatomical
             structures. Volume, area, and shape characteristics were
             extracted for all segmented brain structures. We also
             analyzed the variability of volumes, areas, and shape
             characteristics. The coefficient of variation of volume had
             an average value of 7.0%. Average anatomical images of the
             brain for both the T1-weighted and T2 images were generated,
             together with an average shape atlas, and a probabilistic
             atlas for 33 major structures. These atlases, with their
             associated meta-data, will serve as baseline for identifying
             neuroanatomical phenotypes of additional strains, and mouse
             models now under study. Our efforts were directed toward
             creating a baseline for comparison with other mouse strains
             and models of neurodegenerative diseases.},
   Doi = {10.1016/j.neuroimage.2007.05.046},
   Key = {fds268869}
}

@article{fds359547,
   Author = {Cody, D and Stickel, J and Johnson, G and Boone, J},
   Title = {MO‐D‐330D‐01: Molecular Imaging I: The Physics of
             Molecular Imaging},
   Journal = {Medical Physics},
   Volume = {33},
   Number = {6},
   Pages = {2160},
   Year = {2006},
   Month = {January},
   url = {http://dx.doi.org/10.1118/1.2241412},
   Abstract = {The first day of the Molecular Imaging Symposium (MI‐1)
             will focus on the technology aspects of molecular,
             functional, and small animal imaging. Modalities which will
             be discussed include micro‐CT, micro‐PET, and high
             resolution MRI for small animal imaging. The presentation on
             micro‐CT technology will include an introduction to the
             basic requirements of the scanner hardware, examples of the
             images and biological applications in which micro‐CT is
             useful, and the radiation dose to the small animal
             undergoing micro‐CT will also be discussed. Micro‐CT
             techniques require longer acquisition times than human
             scanners, and thus maintaining the animal in a viable but
             motionless state is of clear importance. Therefore, issues
             surrounding animal support including anesthesia and
             respiratory gating will also be presented. Micro‐PET
             systems are widely used in small animal imaging for genome
             research, and represent probably the mainstay of truly
             molecular imaging modalities at this point in time. The
             presentation on micro‐PET will include a description of
             micro‐PET scanner hardware, a discussion of
             PET‐radiotracers, and an overview of current small animal
             PET systems. The limitation of current micro‐PET system
             design will be discussed, and ideas for overcoming some of
             these limitations will be presented. High resolution MRI
             systems have the benefit of delivering exquisite contrast
             with excellent spatial resolution, with no ionizing
             radiation. The presentation on micro‐MRI techniques for
             phenotype imaging will describe the integration of physics,
             biology, chemistry, engineering, and computer science which
             is necessary to achieve state‐of‐the‐art small animal
             MRI imaging. The use of hyperpolarized gases for lung
             imaging and MR histology will be discussed as well. The
             availability of small animal imaging systems across a number
             of modalities has proved essential for a large number of
             research applications. The primary goal of MI‐1 is to help
             familiarize medical physicists with the technical design and
             capabilities of these high resolution small animal imaging
             systems, and to highlight research applications of their
             use. Different modalities are used to address different
             research questions, and this symposium will emphasize the
             strengths and weaknesses of each modality in regards to
             various research applications. Differences between animal
             imaging and human scanners will also be discussed. © 2006,
             American Association of Physicists in Medicine. All rights
             reserved.},
   Doi = {10.1118/1.2241412},
   Key = {fds359547}
}

@booklet{Hedlund86,
   Author = {Hedlund, LW and Johnson, GA and Karis, JP and Effmann,
             EL},
   Title = {MR "microscopy" of the rat thorax.},
   Journal = {J Comput Assist Tomogr},
   Volume = {10},
   Number = {6},
   Pages = {948-952},
   Year = {1986},
   ISSN = {0363-8715},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/3782566},
   Abstract = {High resolution images can be obtained from anywhere in the
             body of small animals with magnetic resonance combined with
             cardiac gating and scan synchronous ventilation. We used
             these methods to examine the intrathoracic anatomy of the
             rat. Anesthetized rats were intubated and ventilated in
             synchrony with imaging acquisition. Images were obtained in
             a 1 m bore, 1.5 T system fitted with a 28 cm diameter high
             field gradient coil and a 5 cm radio-frequency coil. We used
             cardiac gated, three-dimensional spin warp acquisitions.
             Eight contiguous slices (2.5 mm thick) were obtained
             simultaneously. In addition to visualizing major vessels and
             cardiac chambers, cardiac valves and papillary muscles were
             clearly demonstrated. Major pulmonary vessels and peripheral
             parenchyma were also seen. These results demonstrate MR
             "microscopy" can be used to image all major cardiopulmonary
             structures in the rat with respect to selected times of the
             cardiac cycle. This capability for noninvasive "microscopy"
             opens new avenues for cardiopulmonary research using well
             characterized rodent models.},
   Doi = {10.1097/00004728-198611000-00010},
   Key = {Hedlund86}
}

@article{fds132890,
   Author = {LW Hedlund and GA Johnson and JP Karis and EL Effmann},
   Title = {MR "microscopy" of the rat thorax.},
   Journal = {Journal of computer assisted tomography, UNITED
             STATES},
   Volume = {10},
   Number = {6},
   Pages = {948-52},
   ISSN = {0363-8715},
   Keywords = {Animals • Electrocardiography • Fourier Analysis
             • Magnetic Resonance Spectroscopy • Male •
             Rats • Rats, Inbred Strains • Thorax •
             anatomy & histology* • diagnostic use* •
             instrumentation • methods},
   Abstract = {High resolution images can be obtained from anywhere in the
             body of small animals with magnetic resonance combined with
             cardiac gating and scan synchronous ventilation. We used
             these methods to examine the intrathoracic anatomy of the
             rat. Anesthetized rats were intubated and ventilated in
             synchrony with imaging acquisition. Images were obtained in
             a 1 m bore, 1.5 T system fitted with a 28 cm diameter high
             field gradient coil and a 5 cm radio-frequency coil. We used
             cardiac gated, three-dimensional spin warp acquisitions.
             Eight contiguous slices (2.5 mm thick) were obtained
             simultaneously. In addition to visualizing major vessels and
             cardiac chambers, cardiac valves and papillary muscles were
             clearly demonstrated. Major pulmonary vessels and peripheral
             parenchyma were also seen. These results demonstrate MR
             "microscopy" can be used to image all major cardiopulmonary
             structures in the rat with respect to selected times of the
             cardiac cycle. This capability for noninvasive "microscopy"
             opens new avenues for cardiopulmonary research using well
             characterized rodent models.},
   Key = {fds132890}
}

@article{fds268759,
   Author = {MacFall, JR and Benveniste, H and Maki, J and Johnson, GA and Hedlund,
             L and Copher, G},
   Title = {MR diffusion measurements in stroke models in rat
             brains},
   Journal = {Proceedings of the Annual Conference on Engineering in
             Medicine and Biology},
   Number = {pt 1},
   Pages = {67-68},
   Year = {1990},
   Month = {December},
   Abstract = {It is shown that tissue self-diffusion coefficients can be
             calculated from a series of diffusion-weighted MR (magnetic
             resonance) images. By variation of the time between
             diffusion sensitizing gradient pulses, the motions of tissue
             water may be characterized on varying length scales from 10
             μm to 100 μm. Typically, the diffusion coefficient
             decreases as this diffusion time increases. Such
             characterization of tissue water properties may be of use in
             the study of the course of pathology in disease
             models.},
   Key = {fds268759}
}

@booklet{Drayer86b,
   Author = {DRAYER, B and BURGER, P and CAIN, J and LEONG, J and JOHNSON, GA and HEINZ,
             ER and RIEDERER, S and DJANG, W and HERFKENS, R},
   Title = {MR IMAGING AND PERLS STAIN OF BASAL GANGLIA IRON WITH NORMAL
             AGING},
   Journal = {AMERICAN JOURNAL OF NEURORADIOLOGY},
   Volume = {7},
   Number = {3},
   Pages = {554-555},
   Publisher = {AMER SOC NEURORADIOLOGY},
   Year = {1986},
   Month = {May},
   ISSN = {0195-6108},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1986C133300130&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Drayer86b}
}

@booklet{Maki91,
   Author = {Maki, JH and Benveniste, H and MacFall, JR and Piantadosi, CA and Johnson, GA},
   Title = {MR imaging of microcirculation in rat brain: correlation
             with carbon dioxide-induced changes in blood
             flow.},
   Journal = {J Magn Reson Imaging},
   Volume = {1},
   Number = {6},
   Pages = {673-681},
   Year = {1991},
   ISSN = {1053-1807},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/1823172},
   Abstract = {Considerable interest has been shown in developing a
             magnetic resonance (MR) imaging technique with quantitative
             capability in the evaluation of tissue microcirculation
             ("perfusion"). In the present study, the
             flow-dephased/flow-compensated (FD/FC) technique is
             evaluated for measuring rat cerebral blood flow (CBF) under
             nearly optimal laboratory conditions. Imaging was performed
             on a 2.0-T system equipped with shielded gradient coils. Rat
             CBF was varied by manipulating arterial carbon dioxide
             pressure (PaCO2). In parallel experiments, optimized MR
             imaging studies (seven rats) were compared with laser
             Doppler flowmetry (LDF) studies (nine rats). LDF values
             showed a high degree of correlation between CBF and PaCO2,
             agreeing with results in the literature. MR imaging values,
             while correlating with PaCO2, showed considerable scatter.
             The most likely explanation is unavoidable rat motion during
             the requisite long imaging times. Because of this motion
             sensitivity, the FD/FC technique cannot provide a
             quantitative measure of CBF. It can, however, provide a
             qualitative picture.},
   Doi = {10.1002/jmri.1880010609},
   Key = {Maki91}
}

@article{fds132785,
   Author = {JH Maki and H Benveniste, JR MacFall and CA Piantadosi and GA
             Johnson},
   Title = {MR imaging of microcirculation in rat brain: correlation
             with carbon dioxide-induced changes in blood
             flow.},
   Journal = {Journal of magnetic resonance imaging : JMRI, UNITED
             STATES},
   Volume = {1},
   Number = {6},
   Pages = {673-81},
   ISSN = {1053-1807},
   Keywords = {Animals • Artifacts • Brain • Carbon Dioxide
             • Cerebral Cortex • Cerebrovascular Circulation
             • Corpus Striatum • Female • Image
             Enhancement • Lasers • Linear Models •
             Magnetic Resonance Imaging • Microcirculation •
             Models, Structural • Motion • Rats • Rats,
             Inbred Strains • blood supply • blood supply*
             • blood* • diagnostic use • methods* •
             physiology*},
   Abstract = {Considerable interest has been shown in developing a
             magnetic resonance (MR) imaging technique with quantitative
             capability in the evaluation of tissue microcirculation
             ("perfusion"). In the present study, the
             flow-dephased/flow-compensated (FD/FC) technique is
             evaluated for measuring rat cerebral blood flow (CBF) under
             nearly optimal laboratory conditions. Imaging was performed
             on a 2.0-T system equipped with shielded gradient coils. Rat
             CBF was varied by manipulating arterial carbon dioxide
             pressure (PaCO2). In parallel experiments, optimized MR
             imaging studies (seven rats) were compared with laser
             Doppler flowmetry (LDF) studies (nine rats). LDF values
             showed a high degree of correlation between CBF and PaCO2,
             agreeing with results in the literature. MR imaging values,
             while correlating with PaCO2, showed considerable scatter.
             The most likely explanation is unavoidable rat motion during
             the requisite long imaging times. Because of this motion
             sensitivity, the FD/FC technique cannot provide a
             quantitative measure of CBF. It can, however, provide a
             qualitative picture.},
   Key = {fds132785}
}

@article{fds132757,
   Author = {CE Spritzer and JB Vogler and S Martinez and WE Garrett and GA Johnson and MJ McNamara and J Lohnes and RJ Herfkens},
   Title = {MR imaging of the knee: preliminary results with a 3DFT
             GRASS pulse sequence.},
   Journal = {AJR. American journal of roentgenology, UNITED
             STATES},
   Volume = {150},
   Number = {3},
   Pages = {597-603},
   Year = {1988},
   Month = {March},
   ISSN = {0361-803X},
   Keywords = {Adolescent • Adult • Arthroscopy • Female
             • Humans • Joint Diseases • Knee Injuries
             • Knee Joint • Magnetic Resonance Imaging* •
             Male • Middle Aged • anatomy & histology •
             diagnosis • methods • pathology*},
   Abstract = {The knees of 17 patients (18 extremities) with possible
             meniscal, cruciate ligament, and articular cartilage
             abnormalities were examined with a three-dimensional Fourier
             transform (3DFT), gradient-refocused acquisition in a steady
             state (GRASS) pulse sequence. Arthroscopic confirmation was
             available in all cases and was the standard for comparison.
             Thirteen of these extremities were also examined by using a
             two-dimensional Fourier transform spin-echo pulse sequence
             with a 2000-msec repetition time and 20- and 80-msec echo
             time. In these 13 cases, both pulse sequences correctly
             identified seven of eight meniscal abnormalities. However,
             interpretation of the 3DFT GRASS images resulted in fewer
             false-positive meniscal tears (three vs six). Cruciate
             ligament tears were detected more readily on the 3DFT GRASS
             images (six vs three with two possible tears on the
             spin-echo images). These preliminary findings suggest that
             the overall accuracy of MR imaging of the knee could be
             improved by including 3DFT gradient-refocused pulse
             sequences.},
   Key = {fds132757}
}

@booklet{Spritzer88,
   Author = {Spritzer, CE and Vogler, JB and Martinez, S and Garrett, WE and Johnson,
             GA and McNamara, MJ and Lohnes, J and Herfkens, RJ},
   Title = {MR imaging of the knee: preliminary results with a 3DFT
             GRASS pulse sequence.},
   Journal = {AJR Am J Roentgenol},
   Volume = {150},
   Number = {3},
   Pages = {597-603},
   Year = {1988},
   Month = {March},
   ISSN = {0361-803X},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/3257617},
   Abstract = {The knees of 17 patients (18 extremities) with possible
             meniscal, cruciate ligament, and articular cartilage
             abnormalities were examined with a three-dimensional Fourier
             transform (3DFT), gradient-refocused acquisition in a steady
             state (GRASS) pulse sequence. Arthroscopic confirmation was
             available in all cases and was the standard for comparison.
             Thirteen of these extremities were also examined by using a
             two-dimensional Fourier transform spin-echo pulse sequence
             with a 2000-msec repetition time and 20- and 80-msec echo
             time. In these 13 cases, both pulse sequences correctly
             identified seven of eight meniscal abnormalities. However,
             interpretation of the 3DFT GRASS images resulted in fewer
             false-positive meniscal tears (three vs six). Cruciate
             ligament tears were detected more readily on the 3DFT GRASS
             images (six vs three with two possible tears on the
             spin-echo images). These preliminary findings suggest that
             the overall accuracy of MR imaging of the knee could be
             improved by including 3DFT gradient-refocused pulse
             sequences.},
   Doi = {10.2214/ajr.150.3.597},
   Key = {Spritzer88}
}

@article{fds269110,
   Author = {Middleton, H and Black, RD and Saam, B and Cates, GD and Cofer, GP and Guenther, R and Happer, W and Hedlund, LW and Johnson, GA and Juvan,
             K},
   Title = {MR imaging with hyperpolarized 3He gas.},
   Journal = {Magn Reson Med},
   Volume = {33},
   Number = {2},
   Pages = {271-275},
   Year = {1995},
   Month = {February},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/7707920},
   Keywords = {Animals • Guinea Pigs • Helium • Image
             Enhancement • Lasers • Lung • Magnetic
             Resonance Imaging* • Magnetic Resonance Spectroscopy
             • Rubidium • Time Factors • anatomy &
             histology* • chemistry • diagnostic use* •
             metabolism • methods • radiation
             effects},
   Abstract = {Magnetic resonance images of the lungs of a guinea pig have
             been produced using hyperpolarized helium as the source of
             the MR signal. The resulting images are not yet sufficiently
             optimized to reveal fine structural detail within the lung,
             but the spectacular signal from this normally
             signal-deficient organ system offers great promise for
             eventual in vivo imaging experiments. Fast 2D and 3D GRASS
             sequences with very small flip angles were employed to
             conserve the norenewable longitudinal magnetization. We
             discuss various unique features associated with performing
             MRI with hyperpolarized gases, such as the selection of the
             noble gas species, polarization technique, and constraints
             on the MR pulse sequence.},
   Doi = {10.1002/mrm.1910330219},
   Key = {fds269110}
}

@article{fds132777,
   Author = {MD Shattuck and SL Gewalt and GH Glover and LW Hedlund and GA
             Johnson},
   Title = {MR microimaging of the lung using volume projection
             encoding.},
   Journal = {Magnetic resonance in medicine : official journal of the
             Society of Magnetic Resonance in Medicine / Society of
             Magnetic Resonance in Medicine, UNITED STATES},
   Volume = {38},
   Number = {6},
   Pages = {938-42},
   Year = {1997},
   Month = {December},
   ISSN = {0740-3194},
   Keywords = {Animals • Guinea Pigs • Lung • Magnetic
             Resonance Imaging • anatomy & histology* •
             methods*},
   Abstract = {Radial acquisition (RA) techniques have been extended to
             produce isotropic, three-dimensional images of lung in live
             laboratory animals at spatial resolution down to 0.013 mm3
             with a signal-to-noise ratio of 30:1. The pulse sequence and
             reconstruction algorithm have been adapted to allow
             acquisition of image matrices of up to 256(3) in less than
             15 min. Scan-synchronous ventilation has been incorporated
             to limit breathing motion artifacts. The imaging sequence
             permits randomizing and/or discarding selected views to
             minimize the consequences of breathing motion. The signal in
             lung parenchyma was measured as a function of flip angle
             (alpha) for different repetition times and found to follow
             the predictions for which there is an optimum excitation
             (Ernst) angle. A single T1 relaxation value of 780 +/- 54 ms
             fits all data from six guinea pigs at 2.0 T. This T1 value
             parameterizes the signal and allows for a priori
             optimization, such as calculation of the Ernst angle
             appropriate for lung imaging.},
   Key = {fds132777}
}

@booklet{Shattuck97,
   Author = {Shattuck, MD and Gewalt, SL and Glover, GH and Hedlund, LW and Johnson,
             GA},
   Title = {MR microimaging of the lung using volume projection
             encoding.},
   Journal = {Magn Reson Med},
   Volume = {38},
   Number = {6},
   Pages = {938-942},
   Year = {1997},
   Month = {December},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/9402195},
   Abstract = {Radial acquisition (RA) techniques have been extended to
             produce isotropic, three-dimensional images of lung in live
             laboratory animals at spatial resolution down to 0.013 mm3
             with a signal-to-noise ratio of 30:1. The pulse sequence and
             reconstruction algorithm have been adapted to allow
             acquisition of image matrices of up to 256(3) in less than
             15 min. Scan-synchronous ventilation has been incorporated
             to limit breathing motion artifacts. The imaging sequence
             permits randomizing and/or discarding selected views to
             minimize the consequences of breathing motion. The signal in
             lung parenchyma was measured as a function of flip angle
             (alpha) for different repetition times and found to follow
             the predictions for which there is an optimum excitation
             (Ernst) angle. A single T1 relaxation value of 780 +/- 54 ms
             fits all data from six guinea pigs at 2.0 T. This T1 value
             parameterizes the signal and allows for a priori
             optimization, such as calculation of the Ernst angle
             appropriate for lung imaging.},
   Doi = {10.1002/mrm.1910380613},
   Key = {Shattuck97}
}

@booklet{Malisch91,
   Author = {Malisch, TW and Hedlund, LW and Suddarth, SA and Johnson,
             GA},
   Title = {MR microscopy at 7.0 T: effects of brain
             iron.},
   Journal = {J Magn Reson Imaging},
   Volume = {1},
   Number = {3},
   Pages = {301-305},
   Year = {1991},
   ISSN = {1053-1807},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/1802143},
   Abstract = {The T2 of brain tissue is known to be field dependent,
             decreasing as B0 increases. Previous studies have attributed
             reduced T2 in the structures of the extrapyramidal motor
             system (EPMS) to high iron concentrations. The present study
             was designed to manipulate physiologic iron concentrations
             and study the effects on T2 and on the field dependence of
             T2 at 7.0 T in whole formalin-fixed brains. A rat model was
             devised in which iron concentrations in the structures of
             interest were altered by diet manipulation. Cerebral
             structures with different iron content were imaged and T2
             measured with MR microscopy at both 2.0 and 7.0 T. T2 of all
             tissues was shorter by 40%-60% at 7.0 T. Although some
             dependence of T2 on iron concentration was evident, it was
             less than expected. The strongest correlation was in the
             substantia nigra. The highest-resolution studies, at 30 x 30
             x 50 microns, show the myelin bundles in many of the EPMS
             structures but not in the substantia nigra. From these data,
             it appears that T2 at greater field strengths depends more
             on susceptibility-induced spin dephasing imposed by
             diffusion through the tissue microstructure than on the
             presence of iron.},
   Doi = {10.1002/jmri.1880010308},
   Key = {Malisch91}
}

@article{fds132810,
   Author = {TW Malisch and LW Hedlund and SA Suddarth and GA Johnson},
   Title = {MR microscopy at 7.0 T: effects of brain
             iron.},
   Journal = {Journal of magnetic resonance imaging : JMRI, UNITED
             STATES},
   Volume = {1},
   Number = {3},
   Pages = {301-5},
   ISSN = {1053-1807},
   Keywords = {Animals • Brain Chemistry • Extrapyramidal Tracts
             • Iron • Magnetic Resonance Imaging* • Rats
             • Rats, Inbred Strains • Substantia Nigra •
             anatomy & histology* • physiology*},
   Abstract = {The T2 of brain tissue is known to be field dependent,
             decreasing as B0 increases. Previous studies have attributed
             reduced T2 in the structures of the extrapyramidal motor
             system (EPMS) to high iron concentrations. The present study
             was designed to manipulate physiologic iron concentrations
             and study the effects on T2 and on the field dependence of
             T2 at 7.0 T in whole formalin-fixed brains. A rat model was
             devised in which iron concentrations in the structures of
             interest were altered by diet manipulation. Cerebral
             structures with different iron content were imaged and T2
             measured with MR microscopy at both 2.0 and 7.0 T. T2 of all
             tissues was shorter by 40%-60% at 7.0 T. Although some
             dependence of T2 on iron concentration was evident, it was
             less than expected. The strongest correlation was in the
             substantia nigra. The highest-resolution studies, at 30 x 30
             x 50 microns, show the myelin bundles in many of the EPMS
             structures but not in the substantia nigra. From these data,
             it appears that T2 at greater field strengths depends more
             on susceptibility-induced spin dephasing imposed by
             diffusion through the tissue microstructure than on the
             presence of iron.},
   Key = {fds132810}
}

@booklet{Smith92,
   Author = {Smith, BR and Effmann, EL and Johnson, GA},
   Title = {MR microscopy of chick embryo vasculature.},
   Journal = {J Magn Reson Imaging},
   Volume = {2},
   Number = {2},
   Pages = {237-240},
   Year = {1992},
   ISSN = {1053-1807},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/1562778},
   Abstract = {Six-day-old chick embryos were examined with magnetic
             resonance microscopy after vascular perfusion fixation and
             perfusion with gadolinium-doped gelatin to high-light the
             developing vascular anatomy. Gadolinium gelatin, with its
             short T1, provided a source of signal contrast within the
             vessels. The entire embryo was embedded in gelatin to
             minimize susceptibility artifacts that are prevalent at the
             high field strength (7.0 T) used. A series of single-section
             spin-echo images were acquired with various TRs to determine
             the optimal imaging sequence for a three-dimensional (3D)
             acquisition. The combination of gadolinium gelatin in the
             vascular spaces, gelatin embedding of the specimen, and
             optimal acquisition parameters yielded a 3D stack of
             high-resolution images that was readily reconstructed and
             rendered to effectively demonstrate the developing thoracic
             vessels in the embryo.},
   Doi = {10.1002/jmri.1880020220},
   Key = {Smith92}
}

@article{fds132846,
   Author = {BR Smith and EL Effmann and GA Johnson},
   Title = {MR microscopy of chick embryo vasculature.},
   Journal = {Journal of magnetic resonance imaging : JMRI, UNITED
             STATES},
   Volume = {2},
   Number = {2},
   Pages = {237-40},
   ISSN = {1053-1807},
   Keywords = {Animals • Blood Vessels • Chick Embryo •
             Magnetic Resonance Imaging • embryology* •
             methods*},
   Abstract = {Six-day-old chick embryos were examined with magnetic
             resonance microscopy after vascular perfusion fixation and
             perfusion with gadolinium-doped gelatin to high-light the
             developing vascular anatomy. Gadolinium gelatin, with its
             short T1, provided a source of signal contrast within the
             vessels. The entire embryo was embedded in gelatin to
             minimize susceptibility artifacts that are prevalent at the
             high field strength (7.0 T) used. A series of single-section
             spin-echo images were acquired with various TRs to determine
             the optimal imaging sequence for a three-dimensional (3D)
             acquisition. The combination of gadolinium gelatin in the
             vascular spaces, gelatin embedding of the specimen, and
             optimal acquisition parameters yielded a 3D stack of
             high-resolution images that was readily reconstructed and
             rendered to effectively demonstrate the developing thoracic
             vessels in the embryo.},
   Key = {fds132846}
}

@article{fds268952,
   Author = {Chen, XJ and Chawla, MS and Hedlund, LW and Möller, HE and MacFall, JR and Johnson, GA},
   Title = {MR microscopy of lung airways with hyperpolarized
             3He.},
   Journal = {Magn Reson Med},
   Volume = {39},
   Number = {1},
   Pages = {79-84},
   Year = {1998},
   Month = {January},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/9438440},
   Keywords = {Animals • Disease Models, Animal • Guinea Pigs
             • Helium • Humans • Image Enhancement •
             Isotopes • Lung • Magnetic Resonance Imaging
             • Male • Microscopy • Middle Aged •
             Pulmonary Gas Exchange • Reference Values •
             Sensitivity and Specificity • anatomy & histology*
             • diagnostic use* • methods • methods* •
             physiology},
   Abstract = {A technique using hyperpolarized (HP) 3He to image the small
             airways of the lung by using moderate flip angles and a
             short scanning period during early inspiration is
             demonstrated. Flip angles (alpha) ranging from 10-90 degrees
             were used in guinea pig experiments with scanning during the
             entire inspiration period. A second series acquired data
             throughout a short window of the ventilatory cycle with
             alpha = 45 degrees. The success of the animal studies has
             motivated implementation of similar imaging techniques in
             the clinical arena. Human studies involved imaging over the
             total inspiration period with alpha approximately 10
             degrees. The first series of guinea pig experiments
             demonstrated that larger flip angles (50-90 degrees) destroy
             the magnetization before it reaches the smaller airways. At
             moderate flip angles (20-40 degrees), airway branching down
             to the fourth generation was apparent. Fifth-order
             branchings were seen in the images of the second series. The
             trachea down to fourth generation pulmonary airway
             branching, along with some distal air spaces, was seen in
             the human lung images.},
   Doi = {10.1002/mrm.1910390113},
   Key = {fds268952}
}

@booklet{Chen98a,
   Author = {X. J. Chen and M. S. Chawla and L. W. Hedlund and H. E.
             Moller and J. R. Macfall and G. A. Johnson},
   Title = {MR microscopy of lung airways with hyperpolarized
             He-3},
   Journal = {Magnetic Resonance In Medicine},
   Volume = {39},
   Number = {1},
   Pages = {79 -- 84},
   Year = {1998},
   Month = {January},
   Key = {Chen98a}
}

@booklet{Farmer88,
   Author = {FARMER, THR and JOHNSON, GA and COFER, GP and MARONPOT, RR and HEDLUND,
             LW},
   Title = {MR MICROSCOPY OF NEPHROTOXIC ACUTE TUBULAR-NECROSIS IN THE
             RAT},
   Journal = {INVESTIGATIVE RADIOLOGY},
   Volume = {23},
   Number = {9},
   Pages = {S10-S10},
   Publisher = {LIPPINCOTT-RAVEN PUBL},
   Year = {1988},
   Month = {September},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1988Q574500048&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Farmer88}
}

@article{fds132862,
   Author = {RM Summers and LW Hedlund and GP Cofer and MB Gottsman and JF Manibo and GA
             Johnson},
   Title = {MR microscopy of the rat carotid artery after balloon injury
             by using an implanted imaging coil.},
   Journal = {Magnetic resonance in medicine : official journal of the
             Society of Magnetic Resonance in Medicine / Society of
             Magnetic Resonance in Medicine, UNITED STATES},
   Volume = {33},
   Number = {6},
   Pages = {785-9},
   Year = {1995},
   Month = {June},
   ISSN = {0740-3194},
   Keywords = {Angioplasty, Balloon • Animals • Carotid Artery
             Injuries • Carotid Artery, External • Carotid
             Stenosis • Female • Hyperplasia • Magnetic
             Resonance Imaging* • Microscopy • Rats •
             Rats, Sprague-Dawley • Tunica Intima • adverse
             effects* • pathology • pathology* •
             therapy},
   Abstract = {Neointimal hyperplasia after angioplasty was followed in
             vivo in rats by using MR microscopy and surgically implanted
             RF imaging coils. By using an inductively coupled pick-up
             coil, the arteries were imaged 4 days before and 3, 7, and
             14 days after angioplasty with a 3DFT spin echo sequence.
             Eight of 10 angioplastied rats showed moderate to severe
             stensois based MR measures of lumen diameter reduction from
             baseline images. There was a good correlation between total
             wall thickness between MR and hematoxylin and eosin
             (H&E)-stained sections obtained on the last day. Arteries in
             the intact and sham groups remained unchanged from baseline
             measurements. Because this imaging technique examines the
             artery under in vivo conditions of arterial pressure and
             flow, it promises to be a useful tool for evaluating
             pharmacological and mechanical methods of reducing the
             incidence of vascular stenosis.},
   Key = {fds132862}
}

@booklet{Summers95,
   Author = {Summers, RM and Hedlund, LW and Cofer, GP and Gottsman, MB and Manibo,
             JF and Johnson, GA},
   Title = {MR microscopy of the rat carotid artery after balloon injury
             by using an implanted imaging coil.},
   Journal = {Magn Reson Med},
   Volume = {33},
   Number = {6},
   Pages = {785-789},
   Year = {1995},
   Month = {June},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/7651114},
   Abstract = {Neointimal hyperplasia after angioplasty was followed in
             vivo in rats by using MR microscopy and surgically implanted
             RF imaging coils. By using an inductively coupled pick-up
             coil, the arteries were imaged 4 days before and 3, 7, and
             14 days after angioplasty with a 3DFT spin echo sequence.
             Eight of 10 angioplastied rats showed moderate to severe
             stensois based MR measures of lumen diameter reduction from
             baseline images. There was a good correlation between total
             wall thickness between MR and hematoxylin and eosin
             (H&E)-stained sections obtained on the last day. Arteries in
             the intact and sham groups remained unchanged from baseline
             measurements. Because this imaging technique examines the
             artery under in vivo conditions of arterial pressure and
             flow, it promises to be a useful tool for evaluating
             pharmacological and mechanical methods of reducing the
             incidence of vascular stenosis.},
   Doi = {10.1002/mrm.1910330607},
   Key = {Summers95}
}

@article{fds132886,
   Author = {SL Gewalt and GH Glover and LW Hedlund and GP Cofer, JR MacFall and GA
             Johnson},
   Title = {MR microscopy of the rat lung using projection
             reconstruction.},
   Journal = {Magnetic resonance in medicine : official journal of the
             Society of Magnetic Resonance in Medicine / Society of
             Magnetic Resonance in Medicine, UNITED STATES},
   Volume = {29},
   Number = {1},
   Pages = {99-106},
   Year = {1993},
   Month = {January},
   ISSN = {0740-3194},
   Keywords = {Animals • Female • Lung • Magnetic Resonance
             Imaging* • Microscopy • Rats • Rats,
             Sprague-Dawley • cytology*},
   Abstract = {Projection reconstruction has been implemented with
             self-refocused selection pulses on a small bore, 2.0 T MR
             microscope, to allow imaging of lung parenchyma. Scan
             synchronous ventilation and cardiac gating have been
             integrated with the sequence to minimize motion artifacts. A
             systematic survey of the pulse sequence parameters has been
             undertaken in conjunction with the biological gating
             parameters to optimize resolution and signal-to-noise (SNR).
             The resulting projection images with effective echo time of
             < 300 microseconds allow definition of lung parenchyma with
             an SNR improvement of approximately 15 x over a more
             conventional 2DFT short echo gradient sequence.},
   Key = {fds132886}
}

@booklet{Gewalt93,
   Author = {Gewalt, SL and Glover, GH and Hedlund, LW and Cofer, GP and MacFall, JR and Johnson, GA},
   Title = {MR microscopy of the rat lung using projection
             reconstruction.},
   Journal = {Magn Reson Med},
   Volume = {29},
   Number = {1},
   Pages = {99-106},
   Year = {1993},
   Month = {January},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/8419748},
   Abstract = {Projection reconstruction has been implemented with
             self-refocused selection pulses on a small bore, 2.0 T MR
             microscope, to allow imaging of lung parenchyma. Scan
             synchronous ventilation and cardiac gating have been
             integrated with the sequence to minimize motion artifacts. A
             systematic survey of the pulse sequence parameters has been
             undertaken in conjunction with the biological gating
             parameters to optimize resolution and signal-to-noise (SNR).
             The resulting projection images with effective echo time of
             < 300 microseconds allow definition of lung parenchyma with
             an SNR improvement of approximately 15 x over a more
             conventional 2DFT short echo gradient sequence.},
   Doi = {10.1002/mrm.1910290117},
   Key = {Gewalt93}
}

@booklet{Maki88a,
   Author = {MAKI, JH and COFER, GP and HEDLUND, LW and MACFALL, JR and JOHNSON,
             GA},
   Title = {MR MICROSCOPY USING DRIVEN EQUILIBRIUM (DEFT)},
   Journal = {INVESTIGATIVE RADIOLOGY},
   Volume = {23},
   Number = {9},
   Pages = {S21-S21},
   Publisher = {LIPPINCOTT-RAVEN PUBL},
   Year = {1988},
   Month = {September},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1988Q574500093&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Maki88a}
}

@booklet{Hedlund00,
   Author = {Hedlund, LW and Cofer, GP and Owen, SJ and Allan Johnson,
             G},
   Title = {MR-compatible ventilator for small animals:
             computer-controlled ventilation for proton and noble gas
             imaging.},
   Journal = {Magn Reson Imaging},
   Volume = {18},
   Number = {6},
   Pages = {753-759},
   Year = {2000},
   Month = {July},
   ISSN = {0730-725X},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/10930785},
   Abstract = {We describe an MR-compatible ventilator that is computer
             controlled to generate a variety of breathing patterns, to
             minimize image degrading effects of breathing motion, and to
             support delivery of gas anesthesia and experimental
             inhalational gases. A key feature of this ventilator is the
             breathing valve that attaches directly to the endotracheal
             tube to reduce dead volume and allows independent control of
             inspiratory and expiratory phases of ventilation. This
             ventilator has been used in a wide variety of MR and x-ray
             microscopy studies of small animals, especially for MR
             imaging the lungs with hyperpolarized gases ((3)He &
             (129)Xe).},
   Doi = {10.1016/s0730-725x(00)00154-5},
   Key = {Hedlund00}
}

@booklet{Middleton95,
   Author = {H. Middleton and R. D. Black and B. Saam and G. D. Cates and G. P. Cofer and R. Guenther and W. Happer and L. W. Hedlund and G. A. Johnson and K. Juvan and J. Swartz},
   Title = {Mr-imaging with hyperpolarized he-3 gas},
   Journal = {Magnetic Resonance In Medicine},
   Volume = {33},
   Number = {2},
   Pages = {271 -- 275},
   Year = {1995},
   Month = {February},
   Key = {Middleton95}
}

@booklet{Bone86a,
   Author = {BONE, SN and JOHNSON, GA and THOMPSON, MB},
   Title = {MRI MICROSCOPY OF THE DEVELOPING CHICK-EMBRYO},
   Journal = {INVESTIGATIVE RADIOLOGY},
   Volume = {21},
   Number = {9},
   Pages = {S34-S34},
   Publisher = {LIPPINCOTT-RAVEN PUBL},
   Year = {1986},
   Month = {September},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1986E000900143&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Bone86a}
}

@article{fds132822,
   Author = {B Drayer and P Burger and R Darwin and S Riederer and R Herfkens and GA
             Johnson},
   Title = {MRI of brain iron.},
   Journal = {AJR. American journal of roentgenology, UNITED
             STATES},
   Volume = {147},
   Number = {1},
   Pages = {103-10},
   Year = {1986},
   Month = {July},
   ISSN = {0361-803X},
   Keywords = {Adolescent • Adult • Aged • Aging •
             Brain • Brain Chemistry* • Brain Diseases •
             Child • Globus Pallidus • Humans • Iron
             • Magnetic Resonance Spectroscopy • Male •
             Middle Aged • Substantia Nigra • analysis •
             analysis* • diagnostic use* • metabolism •
             pathology},
   Abstract = {A prominently decreased signal intensity in the globus
             pallidum, reticular substantia nigra, red nucleus, and
             dentate nucleus was routinely noted in 150 consecutive
             individuals on T2-weighted images (SE 2000/100) using a high
             field strength (1.5 T)MR system. This MR finding correlated
             closely with the decreased estimated T2 relaxation times and
             the sites of preferential accumulation of ferric iron using
             the Perls staining method on normal postmortem brains. The
             decreased signal intensity on T2-weighted images thus
             provides an accurate in vivo map of the normal distribution
             of brain iron. Perls stain and MR studies in normal brain
             also confirm an intermediate level of iron distribution in
             the striatum, and still lower levels in the cerebral gray
             and white matter. In the white matter, iron concentration is
             (a) absent in the most posterior portion of the internal
             capsule and optic radiations, (b) higher in the frontal than
             occipital regions, and (c) prominent in the subcortical "U"
             fibers, particularly in the temporal lobe. There is no iron
             in the brain at birth; it increases progressively with
             aging. Knowledge of the distribution of brain iron should
             assist in elucidating normal anatomic structures and in
             understanding neurodegenerative, demyelinating, and
             cerebrovascular disorders.},
   Key = {fds132822}
}

@booklet{Drayer86,
   Author = {Drayer, B and Burger, P and Darwin, R and Riederer, S and Herfkens, R and Johnson, GA},
   Title = {MRI of brain iron.},
   Journal = {AJR Am J Roentgenol},
   Volume = {147},
   Number = {1},
   Pages = {103-110},
   Year = {1986},
   Month = {July},
   ISSN = {0361-803X},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/3487201},
   Abstract = {A prominently decreased signal intensity in the globus
             pallidum, reticular substantia nigra, red nucleus, and
             dentate nucleus was routinely noted in 150 consecutive
             individuals on T2-weighted images (SE 2000/100) using a high
             field strength (1.5 T)MR system. This MR finding correlated
             closely with the decreased estimated T2 relaxation times and
             the sites of preferential accumulation of ferric iron using
             the Perls staining method on normal postmortem brains. The
             decreased signal intensity on T2-weighted images thus
             provides an accurate in vivo map of the normal distribution
             of brain iron. Perls stain and MR studies in normal brain
             also confirm an intermediate level of iron distribution in
             the striatum, and still lower levels in the cerebral gray
             and white matter. In the white matter, iron concentration is
             (a) absent in the most posterior portion of the internal
             capsule and optic radiations, (b) higher in the frontal than
             occipital regions, and (c) prominent in the subcortical "U"
             fibers, particularly in the temporal lobe. There is no iron
             in the brain at birth; it increases progressively with
             aging. Knowledge of the distribution of brain iron should
             assist in elucidating normal anatomic structures and in
             understanding neurodegenerative, demyelinating, and
             cerebrovascular disorders.},
   Doi = {10.2214/ajr.147.1.103},
   Key = {Drayer86}
}

@article{fds132808,
   Author = {HE Möller and XJ Chen and B Saam and KD Hagspiel and GA Johnson and TA
             Altes, EE de Lange and HU Kauczor},
   Title = {MRI of the lungs using hyperpolarized noble
             gases.},
   Journal = {Magnetic resonance in medicine : official journal of the
             Society of Magnetic Resonance in Medicine / Society of
             Magnetic Resonance in Medicine, United States},
   Volume = {47},
   Number = {6},
   Pages = {1029-51},
   Year = {2002},
   Month = {June},
   ISSN = {0740-3194},
   Keywords = {Animals • Forecasting • Helium • Humans
             • Lung • Lung Diseases • Magnetic Resonance
             Imaging • Noble Gases • Pulmonary Gas Exchange
             • Xenon Radioisotopes • anatomy & histology*
             • diagnosis* • diagnostic use • diagnostic
             use* • methods* • physiology*},
   Abstract = {The nuclear spin polarization of the noble gas isotopes
             (3)He and (129)Xe can be increased using optical pumping
             methods by four to five orders of magnitude. This
             extraordinary gain in polarization translates directly into
             a gain in signal strength for MRI. The new technology of
             hyperpolarized (HP) gas MRI holds enormous potential for
             enhancing sensitivity and contrast in pulmonary imaging.
             This review outlines the physics underlying the optical
             pumping process, imaging strategies coping with the
             nonequilibrium polarization, and effects of the alveolar
             microstructure on relaxation and diffusion of the noble
             gases. It presents recent progress in HP gas MRI and
             applications ranging from MR microscopy of airspaces to
             imaging pulmonary function in patients and suggests
             potential directions for future developments.},
   Key = {fds132808}
}

@booklet{Moller02,
   Author = {Möller, HE and Chen, XJ and Saam, B and Hagspiel, KD and Johnson, GA and Altes, TA and de Lange, EE and Kauczor, H-U},
   Title = {MRI of the lungs using hyperpolarized noble
             gases.},
   Journal = {Magn Reson Med},
   Volume = {47},
   Number = {6},
   Pages = {1029-1051},
   Year = {2002},
   Month = {June},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/12111949},
   Abstract = {The nuclear spin polarization of the noble gas isotopes
             (3)He and (129)Xe can be increased using optical pumping
             methods by four to five orders of magnitude. This
             extraordinary gain in polarization translates directly into
             a gain in signal strength for MRI. The new technology of
             hyperpolarized (HP) gas MRI holds enormous potential for
             enhancing sensitivity and contrast in pulmonary imaging.
             This review outlines the physics underlying the optical
             pumping process, imaging strategies coping with the
             nonequilibrium polarization, and effects of the alveolar
             microstructure on relaxation and diffusion of the noble
             gases. It presents recent progress in HP gas MRI and
             applications ranging from MR microscopy of airspaces to
             imaging pulmonary function in patients and suggests
             potential directions for future developments.},
   Doi = {10.1002/mrm.10173},
   Key = {Moller02}
}

@article{fds320199,
   Author = {Xie, L and Bennett, KM and Liu, C and Johnson, GA and Zhang, JL and Lee,
             VS},
   Title = {MRI tools for assessment of microstructure and nephron
             function of the kidney.},
   Journal = {Am J Physiol Renal Physiol},
   Volume = {311},
   Number = {6},
   Pages = {F1109-F1124},
   Year = {2016},
   Month = {December},
   url = {http://dx.doi.org/10.1152/ajprenal.00134.2016},
   Abstract = {MRI can provide excellent detail of renal structure and
             function. Recently, novel MR contrast mechanisms and imaging
             tools have been developed to evaluate microscopic kidney
             structures including the tubules and glomeruli. Quantitative
             MRI can assess local tubular function and is able to
             determine the concentrating mechanism of the kidney
             noninvasively in real time. Measuring single nephron
             function is now a near possibility. In parallel to advancing
             imaging techniques for kidney microstructure is a need to
             carefully understand the relationship between the local
             source of MRI contrast and the underlying physiological
             change. The development of these imaging markers can impact
             the accurate diagnosis and treatment of kidney disease. This
             study reviews the novel tools to examine kidney
             microstructure and local function and demonstrates the
             application of these methods in renal pathophysiology.},
   Doi = {10.1152/ajprenal.00134.2016},
   Key = {fds320199}
}

@article{fds357205,
   Author = {Holbrook, MD and Blocker, SJ and Mowery, YM and Badea, A and Qi, Y and Xu,
             ES and Kirsch, DG and Johnson, GA and Badea, CT},
   Title = {MRI-Based Deep Learning Segmentation and Radiomics of
             Sarcoma in Mice.},
   Journal = {Tomography},
   Volume = {6},
   Number = {1},
   Pages = {23-33},
   Year = {2020},
   Month = {March},
   url = {http://dx.doi.org/10.18383/j.tom.2019.00021},
   Abstract = {Small-animal imaging is an essential tool that provides
             noninvasive, longitudinal insight into novel cancer
             therapies. However, considerable variability in image
             analysis techniques can lead to inconsistent results. We
             have developed quantitative imaging for application in the
             preclinical arm of a coclinical trial by using a genetically
             engineered mouse model of soft tissue sarcoma. Magnetic
             resonance imaging (MRI) images were acquired 1 day before
             and 1 week after radiation therapy. After the second MRI,
             the primary tumor was surgically removed by amputating the
             tumor-bearing hind limb, and mice were followed for up to
             6 months. An automatic analysis pipeline was used for
             multicontrast MRI data using a convolutional neural network
             for tumor segmentation followed by radiomics analysis. We
             then calculated radiomics features for the tumor, the
             peritumoral area, and the 2 combined. The first radiomics
             analysis focused on features most indicative of radiation
             therapy effects; the second radiomics analysis looked for
             features that might predict primary tumor recurrence. The
             segmentation results indicated that Dice scores were similar
             when using multicontrast versus single T2-weighted data
             (0.863 vs 0.861). One week post RT, larger tumor volumes
             were measured, and radiomics analysis showed greater
             heterogeneity. In the tumor and peritumoral area, radiomics
             features were predictive of primary tumor recurrence (AUC:
             0.79). We have created an image processing pipeline for
             high-throughput, reduced-bias segmentation of
             multiparametric tumor MRI data and radiomics analysis, to
             better our understanding of preclinical imaging and the
             insights it provides when studying new cancer
             therapies.},
   Doi = {10.18383/j.tom.2019.00021},
   Key = {fds357205}
}

@booklet{Johnson01,
   Author = {G. A. Johnson and F. W. Bazer and L. A. Jaeger and H. Ka and J. E. Garlow and C. Pfarrer and T. E. Spencer and R. C.
             Burghardt},
   Title = {Muc-1, integrin, and osteopontin expression during the
             implantation cascade in sheep},
   Journal = {Biology Of Reproduction},
   Volume = {65},
   Number = {3},
   Pages = {820 -- 828},
   Year = {2001},
   Month = {September},
   Key = {Johnson01}
}

@article{fds174103,
   Author = {GA Johnson and FW Bazer and LA Jaeger and H Ka and JE Garlow and C Pfarrer and TE Spencer and RC Burghardt},
   Title = {Muc-1, integrin, and osteopontin expression during the
             implantation cascade in sheep.},
   Journal = {Biology of reproduction},
   Volume = {65},
   Number = {3},
   Pages = {820-8},
   Year = {2001},
   Month = {September},
   ISSN = {0006-3363},
   Keywords = {Actinin • Animals • Cell Adhesion •
             Cytoskeleton • Embryo Implantation • Endometrium
             • Epithelium • Estrous Cycle • Female •
             Fluorescent Antibody Technique • Gestational Age •
             Immunohistochemistry • Integrins • Interferon Type
             I • Mucin-1 • Osteopontin • Pregnancy •
             Pregnancy Proteins • RNA, Messenger • Recombinant
             Proteins • Reverse Transcriptase Polymerase Chain
             Reaction • Sheep • Sialoglycoproteins • Talin
             • Trophoblasts • Uterus • analysis •
             analysis* • chemistry • genetics • genetics*
             • pharmacology • physiology •
             physiology*},
   Abstract = {The extracellular matrix protein osteopontin (OPN) is a
             component of histotroph that increases in uterine flushings
             from pregnant ewes during the peri-implantation period and
             is localized on the apical surfaces of the uterine luminal
             epithelium (LE) and conceptus trophectoderm (Tr). The
             potential involvement of OPN in the implantation adhesion
             cascade in sheep was investigated by examining temporal,
             spatial, and potential functional relationships between OPN,
             Muc-1, and integrin subunits during the estrous cycle and
             early pregnancy. Immunoreactive Muc-1 was highly expressed
             at the apical surfaces of uterine luminal (LE) and glandular
             epithelium (GE) in both cycling and pregnant ewes but was
             decreased dramatically on LE by Day 9 and was nearly
             undetectable by Day 17 of pregnancy when intimate contact
             between LE and Tr begins. In contrast, integrin subunits
             alpha(v), alpha(4), alpha(5), beta(1), beta(3), and beta(5)
             were constitutively expressed on conceptus Tr and at the
             apical surface of uterine LE and GE in both cyclic and early
             pregnant ewes. The apical expression of these subunits could
             contribute to the apical assembly of several OPN receptors
             including the alpha(v)beta(3), alpha(v)beta(1),
             alpha(v)beta(5), alpha(4)beta(1), and alpha(5)beta(1)
             heterodimers on endometrial LE and GE, and conceptus Tr in
             sheep. Functional analysis of potential OPN interactions
             with conceptus and endometrial integrins was performed on LE
             and Tr cells in vitro using beads coated with OPN,
             poly-L-lysine, or recombinant OPN in which the Arg-Gly-Asp
             sequence was replaced with RGE or RAD. Transmembrane
             accumulation of talin or alpha-actinin at the apical surface
             of uterine LE and conceptus Tr cells in contact with
             OPN-coated beads revealed functional integrin activation and
             cytoskeletal reorganization in response to OPN binding.
             These results provide a physiological framework for the role
             of OPN, a potential mediator of implantation in sheep, as a
             bridge between integrin heterodimers expressed by Tr and
             uterine LE responsible for adhesion for initial conceptus
             attachment.},
   Language = {eng},
   Key = {fds174103}
}

@booklet{Paulson01,
   Author = {Paulson, EK and Yoshizumi, TT and Frush, DP and Johnson,
             GA},
   Title = {Multi-detector vs single-detector CT: The organ doses are
             higher than you think},
   Journal = {RADIOLOGY},
   Volume = {221},
   Pages = {403-403},
   Publisher = {RADIOLOGICAL SOC NORTH AMERICA},
   Year = {2001},
   Month = {November},
   ISSN = {0033-8419},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000172126601192&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Paulson01}
}

@booklet{Nelson81,
   Author = {Nelson, CE and Johnson, GA and Bentel, G},
   Title = {MULTI-PLANAR RECONSTRUCTION–APPLICATIONS IN RADIATION
             ONCOLOGY TREATMENT PLANNING},
   Journal = {Investigative Radiology},
   Volume = {16},
   Number = {5},
   Pages = {417-417},
   Publisher = {Ovid Technologies (Wolters Kluwer Health)},
   Year = {1981},
   Month = {September},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1981MK56200113&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Doi = {10.1097/00004424-198109000-00113},
   Key = {Nelson81}
}

@article{064610243432,
   Author = {Mistry, N and De Lin and M and Hedlund, L and Johnson,
             GA},
   Title = {Multimodality imaging of pulmonary function in the
             rodent},
   Journal = {2006 3rd IEEE International Symposium on Biomedical Imaging:
             From Nano to Macro - Proceedings},
   Volume = {2006},
   Pages = {920-923},
   Address = {Arlington, VA, United States},
   Year = {2006},
   Month = {November},
   ISBN = {9780780395770},
   Keywords = {Medical imaging;Optical resolving power;Physiological
             models;Magnetic resonance imaging;Angiography;Imaging
             systems;},
   Abstract = {The high spatial and temporal resolution demands for imaging
             physiological function in the rodent call for the use of
             novel ways to combine information from different imaging
             modalities. This work describes ventilation imaging using
             hyperpolarized (HP) 3He magnetic resonance imaging (MRI) and
             perfusion imaging using X-ray digital subtraction
             angiography (DSA). We illustrate the key steps needed to
             combine the complementary data from the two modalities to
             provide qualitative and quantitative information on gas
             exchange in the lungs. The results indicate that
             multimodality imaging of pulmonary function in small animals
             can provide functional information at higher spatial and
             temporal resolution compared to many traditional imaging
             techniques. © 2006 IEEE.},
   Key = {064610243432}
}

@article{9054396,
   Author = {Mistry, N. and Ming De Lin and Hedlund, L. and Johnson,
             G.A.},
   Title = {Multimodality imaging of pulmonary function in the
             rodent},
   Journal = {2006 3rd IEEE International Symposium on Biomedical Imaging:
             Macro to Nano (IEEE Cat. No.06EX1231C)},
   Pages = {920 - 3},
   Address = {Arlington, VA, USA},
   Year = {2006},
   Keywords = {biomedical MRI;diagnostic radiography;haemorheology;image
             resolution;lung;medical image processing;pneumodynamics;},
   Abstract = {The high spatial and temporal resolution demands for imaging
             physiological function in the rodent call for the use of
             novel ways to combine information from different imaging
             modalities. This work describes ventilation imaging using
             hyperpolarized (HP) <sup>3</sup>He magnetic resonance
             imaging (MRI) and perfusion imaging using X-ray digital
             subtraction angiography (DSA). We illustrate the key steps
             needed to combine the complementary data from the two
             modalities to provide qualitative and quantitative
             information on gas exchange in the lungs. The results
             indicate that multimodality imaging of pulmonary function in
             small animals can provide functional information at higher
             spatial and temporal resolution compared to many traditional
             imaging techniques},
   Key = {9054396}
}

@booklet{Kamperschroer87,
   Author = {J. H. Kamperschroer and H. W. Kugel and M. A. Reale and S.
             L. Hayes and G. A. Johnson and J. L. Lowrance and P. A. Shah and P. Sichta and B. W. Sleaford and M. D. Williams and P.
             M. Zucchino},
   Title = {Multiple track doppler-shift spectroscopy system for tftr
             neutral beam injectors},
   Journal = {Review Of Scientific Instruments},
   Volume = {58},
   Number = {8},
   Pages = {1362 -- 1368},
   Year = {1987},
   Month = {August},
   Key = {Kamperschroer87}
}

@article{fds268799,
   Author = {Johnson, G and Thomson, DJ and Wu, EX and Williams,
             SCR},
   Title = {Multiple-window spectrum estimation applied to in vivo NMR
             spectroscopy},
   Journal = {Journal of Magnetic Resonance - Series B},
   Volume = {110},
   Number = {2},
   Pages = {138-149},
   Publisher = {Elsevier BV},
   Year = {1996},
   ISSN = {1064-1866},
   url = {http://dx.doi.org/10.1006/jmrb.1996.0023},
   Abstract = {Multiple-window spectrum estimation (MWSE) is a method of
             deriving frequency spectra from time series. A set of
             apodizing windows is applied to the time data and each
             windowed data set is Fourier transformed. The windows are
             prolate spheroidal sequences. These form the orthonormal set
             of functions that is maximally concentrated in both time and
             frequency domains. An iterative algorithm is then applied to
             the data set to find a leastsquares estimate of the power
             spectrum. In addition, statistical tests may be applied to
             determine the existence of periodic components at particular
             frequencies, their amplitudes, phases, and positions. The
             method is quantitative and makes no lineshape assumptions.
             Computer simulations were used to compare MWSE performance
             with that of conventional Fourier-transform processing with
             quantification by curve fitting. Signal-to-noise ratio,
             spectral resolution, linearity, and susceptibility to
             artifacts were compared. MWSE gives similar signal-to-noise
             ratio and spectral resolution to Fourier-transform data and
             is linear over three orders of magnitude but is much more
             robust with respect to artifacts. In particular, data
             truncation introduces no baseline distortion, broad baseline
             humps are removed automatically, and large solvent peaks may
             be easily removed without affecting adjacent lines. No
             separate phase correction is required. MWSE gives more
             accurate quantitative spectra, particularly when the time
             data are imperfect. The method is, therefore, particularly
             appropriate for processing in vivo data. The utility of the
             MWSE method is demonstrated on in vivo 'H, 31P, and 13C NMR
             spectroscopy data. e 1996 Academic Press,
             Inc.},
   Doi = {10.1006/jmrb.1996.0023},
   Key = {fds268799}
}

@article{fds268823,
   Author = {Pandit, P and Qi, Y and Story, J and King, KF and Johnson,
             GA},
   Title = {Multishot PROPELLER for high-field preclinical
             MRI.},
   Journal = {Magn Reson Med},
   Volume = {64},
   Number = {1},
   Pages = {47-53},
   Year = {2010},
   Month = {July},
   ISSN = {1522-2594},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/20572138},
   Keywords = {Animals • Disease Models, Animal • Female •
             Image Processing, Computer-Assisted • Liver Neoplasms,
             Experimental • Magnetic Resonance Imaging • Mice
             • Mice, Inbred C57BL • Radiography, Abdominal
             • diagnosis • methods*},
   Abstract = {With the development of numerous mouse models of cancer,
             there is a tremendous need for an appropriate imaging
             technique to study the disease evolution. High-field
             T(2)-weighted imaging using PROPELLER (Periodically Rotated
             Overlapping ParallEL Lines with Enhanced Reconstruction) MRI
             meets this need. The two-shot PROPELLER technique presented
             here provides (a) high spatial resolution, (b) high contrast
             resolution, and (c) rapid and noninvasive imaging, which
             enables high-throughput, longitudinal studies in
             free-breathing mice. Unique data collection and
             reconstruction makes this method robust against motion
             artifacts. The two-shot modification introduced here retains
             more high-frequency information and provides higher
             signal-to-noise ratio than conventional single-shot
             PROPELLER, making this sequence feasible at high fields,
             where signal loss is rapid. Results are shown in a liver
             metastases model to demonstrate the utility of this
             technique in one of the more challenging regions of the
             mouse, which is the abdomen.},
   Language = {eng},
   Doi = {10.1002/mrm.22376},
   Key = {fds268823}
}

@article{fds268874,
   Author = {Bucholz, EK and Song, J and Johnson, GA and Hancu,
             I},
   Title = {Multispectral imaging with three-dimensional rosette
             trajectories.},
   Journal = {Magn Reson Med},
   Volume = {59},
   Number = {3},
   Pages = {581-589},
   Year = {2008},
   Month = {March},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/18306410},
   Keywords = {Adipose Tissue • Algorithms • Artifacts •
             Body Water • Brain Mapping • Computer Simulation
             • Humans • Image Processing, Computer-Assisted*
             • Imaging, Three-Dimensional* • Magnetic Resonance
             Imaging • anatomy & histology •
             methods*},
   Abstract = {Two-dimensional intersecting k-space trajectories have
             previously been demonstrated to allow fast multispectral
             imaging. Repeated sampling of k-space points leads to
             destructive interference of the signal coming from the
             off-resonance spectral peaks; on-resonance data
             reconstruction yields images of the on-resonance peak, with
             some of the off-resonance energy being spread as noise in
             the image. A shift of the k-space data by a given
             off-resonance frequency brings a second frequency of
             interest on resonance, allowing the reconstruction of a
             second spectral peak from the same k-space data. Given the
             higher signal-to-noise per unit time characteristic of a 3D
             acquisition, we extended the concept of intersecting
             trajectories to three dimensions. A 3D, rosette-like pulse
             sequence was designed and implemented on a clinical 1.5T
             scanner. An iterative density compensation function was
             developed to weight the 3D intersecting trajectories before
             Fourier transformation. Three volunteers were scanned using
             this sequence and separate fat and water images were
             reconstructed from the same imaging dataset.},
   Doi = {10.1002/mrm.21551},
   Key = {fds268874}
}

@booklet{Sinor02,
   Author = {S. J. Sinor and M. M. Joyce and S. J. Yankey and A. M.
             Assiri and K. Kodali and L. S. Hartt and M. Robison and G.
             A. Johnson and T. L. Ott},
   Title = {Mx, estrogen receptor (ER), and progesterone receptor (PR)
             expression in ovine placentomal and interplacentomal
             endometrium during days 25 to 120 of pregnancy.},
   Journal = {Biology Of Reproduction},
   Volume = {66},
   Pages = {244 -- 244},
   Year = {2002},
   Key = {Sinor02}
}

@article{fds132909,
   Author = {TM Yelbuz and KL Waldo and X Zhang and M Zdanowicz and J Parker and TL
             Creazzo, GA Johnson and ML Kirby},
   Title = {Myocardial volume and organization are changed by failure of
             addition of secondary heart field myocardium to the cardiac
             outflow tract.},
   Journal = {Developmental dynamics : an official publication of the
             American Association of Anatomists, United
             States},
   Volume = {228},
   Number = {2},
   Pages = {152-60},
   Year = {2003},
   Month = {October},
   ISSN = {1058-8388},
   Keywords = {Animals • Cell Count • Cell Division • Cell
             Lineage • Cell Movement • Cell Size • Chick
             Embryo • Heart • Heart Atria • Heart Defects,
             Congenital • Heart Ventricles •
             Immunohistochemistry • Magnetic Resonance Imaging
             • Microscopy, Confocal • Myocardium •
             Myocytes, Cardiac • Neural Crest • Time Factors
             • cytology • cytology* • embryology •
             etiology* • pathology • surgery*},
   Abstract = {Cardiac neural crest ablation results in primary myocardial
             dysfunction and failure of the secondary heart field to add
             the definitive myocardium to the cardiac outflow tract. The
             current study was undertaken to understand the changes in
             myocardial characteristics in the heart tube, including
             volume, proliferation, and cell size when the myocardium
             from the secondary heart field fails to be added to the
             primary heart tube. We used magnetic resonance and confocal
             microscopy to determine that the volume of myocardium in the
             looped heart was dramatically reduced and the compact layer
             of myocardium was thinner after neural crest ablation,
             especially in the outflow tract and ventricular regions.
             Proliferation measured by 5-bromo-2'-deoxyuridine
             incorporation was elevated at only one stage during looping,
             cell death was normal and myocardial cell size was
             increased. Taken together, these results indicate that there
             are fewer myocytes in the heart. By incubation day 8 when
             the heart would have normally completed septation, the
             anterior (ventral) wall of the right ventricle and right
             ventricular outflow tract was significantly thinner in the
             neural crest-ablated embryos than normal, but the thickness
             of the compact myocardium was normal in all other regions of
             the heart. The decreased volume and number of myocardial
             cells in the heart tube after neural crest ablation most
             likely reflects the amount of myocardium added by the
             secondary heart field.},
   Key = {fds132909}
}

@booklet{Yelbuz03a,
   Author = {Yelbuz, TM and Waldo, KL and Zhang, X and Zdanowicz, M and Parker, J and Creazzo, TL and Johnson, GA and Kirby, ML},
   Title = {Myocardial volume and organization are changed by failure of
             addition of secondary heart field myocardium to the cardiac
             outflow tract.},
   Journal = {Dev Dyn},
   Volume = {228},
   Number = {2},
   Pages = {152-160},
   Year = {2003},
   Month = {October},
   ISSN = {1058-8388},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/14517987},
   Abstract = {Cardiac neural crest ablation results in primary myocardial
             dysfunction and failure of the secondary heart field to add
             the definitive myocardium to the cardiac outflow tract. The
             current study was undertaken to understand the changes in
             myocardial characteristics in the heart tube, including
             volume, proliferation, and cell size when the myocardium
             from the secondary heart field fails to be added to the
             primary heart tube. We used magnetic resonance and confocal
             microscopy to determine that the volume of myocardium in the
             looped heart was dramatically reduced and the compact layer
             of myocardium was thinner after neural crest ablation,
             especially in the outflow tract and ventricular regions.
             Proliferation measured by 5-bromo-2'-deoxyuridine
             incorporation was elevated at only one stage during looping,
             cell death was normal and myocardial cell size was
             increased. Taken together, these results indicate that there
             are fewer myocytes in the heart. By incubation day 8 when
             the heart would have normally completed septation, the
             anterior (ventral) wall of the right ventricle and right
             ventricular outflow tract was significantly thinner in the
             neural crest-ablated embryos than normal, but the thickness
             of the compact myocardium was normal in all other regions of
             the heart. The decreased volume and number of myocardial
             cells in the heart tube after neural crest ablation most
             likely reflects the amount of myocardium added by the
             secondary heart field.},
   Doi = {10.1002/dvdy.10364},
   Key = {Yelbuz03a}
}

@article{fds357208,
   Author = {Wang, N and Zhang, J and Cofer, G and Qi, Y and Anderson, RJ and White, LE and Allan Johnson and G},
   Title = {Neurite orientation dispersion and density imaging of mouse
             brain microstructure.},
   Journal = {Brain Struct Funct},
   Volume = {224},
   Number = {5},
   Pages = {1797-1813},
   Year = {2019},
   Month = {June},
   url = {http://dx.doi.org/10.1007/s00429-019-01877-x},
   Abstract = {Advanced biophysical models like neurite orientation
             dispersion and density imaging (NODDI) have been developed
             to estimate the microstructural complexity of voxels
             enriched in dendrites and axons for both in vivo and ex vivo
             studies. NODDI metrics derived from high spatial and angular
             resolution diffusion MRI using the fixed mouse brain as a
             reference template have not yet been reported due in part to
             the extremely long scan time required. In this study, we
             modified the three-dimensional diffusion-weighted spin-echo
             pulse sequence for multi-shell and undersampling acquisition
             to reduce the scan time. This allowed us to acquire several
             exhaustive datasets that would otherwise not be attainable.
             NODDI metrics were derived from a complex 8-shell diffusion
             (1000-8000 s/mm2) dataset with 384 diffusion
             gradient-encoding directions at 50 µm isotropic
             resolution. These provided a foundation for exploration of
             tradeoffs among acquisition parameters. A three-shell
             acquisition strategy covering low, medium, and high b values
             with at least angular resolution of 64 is essential for ex
             vivo NODDI experiments. The good agreement between neurite
             density index (NDI) and the orientation dispersion index
             (ODI) with the subsequent histochemical analysis of myelin
             and neuronal density highlights that NODDI could provide new
             insight into the microstructure of the brain. Furthermore,
             we found that NDI is sensitive to microstructural variations
             in the corpus callosum using a well-established
             demyelination cuprizone model. The study lays the ground
             work for developing protocols for routine use of
             high-resolution NODDI method in characterizing brain
             microstructure in mouse models.},
   Doi = {10.1007/s00429-019-01877-x},
   Key = {fds357208}
}

@article{fds268868,
   Author = {Badea, A and Nicholls, PJ and Johnson, GA and Wetsel,
             WC},
   Title = {Neuroanatomical phenotypes in the reeler
             mouse.},
   Journal = {Neuroimage},
   Volume = {34},
   Number = {4},
   Pages = {1363-1374},
   Year = {2007},
   Month = {February},
   ISSN = {1053-8119},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/17185001},
   Keywords = {Animals • Brain • Female • Heterozygote
             • Magnetic Resonance Imaging • Male • Mice
             • Mice, Neurologic Mutants • Mutation •
             Phenotype • anatomy & histology* •
             genetics},
   Abstract = {The reeler mouse (Reln) has been proposed as a
             neurodevelopmental model for certain neurological and
             psychiatric conditions and has been studied by qualitative
             histochemistry and electron microscopy. Using magnetic
             resonance microscopy (MRM), we have quantitated for the
             first time the neuromorphology of Reln mice at a resolution
             of 21.5 microm. The neuroanatomical phenotypes of
             heterozygous and homozygous mutant Reln mice were compared
             to those of wild type (WT) littermates using morphometry and
             texture analysis. The cortical, hippocampal, and cerebellar
             phenotypes of the heterozygous and homozygous mutant Reln
             mice were confirmed, and new features were revealed. The
             Reln(rl/rl) mice possessed a smaller brain, and both
             Reln(rl/+) and Reln(rl/rl) mice had increased ventricles
             compared to WT controls. Shape differences were found
             between WT and Reln(rl/rl) brains, specifically in
             cerebellum, olfactory bulbs, dorsomedial frontal and
             parietal cortex, certain regions of temporal and occipital
             lobes, as well as in the lateral ventricles and ventral
             hippocampus. These findings suggest that certain brain
             regions may be more severely impacted by the Reln mutation
             than others. Gadolinium-based active staining demonstrated
             that layers of the hippocampus were disorganized in
             Reln(rl/rl) mice and differences in thickness of these
             layers were identified between WT and Reln(rl/rl) mice. The
             intensity distributions characteristic to the dorsal,
             middle, and ventral hippocampus were altered in the
             Reln(rl/rl), especially in the ventral hippocampus. These
             differences were quantified using skewness and modeling the
             intensity distributions with a Gaussian mixture. Our results
             suggest that structural features of Reln(rl/rl) brain most
             closely phenocopy those of patients with Norman-Roberts
             lissencephaly.},
   Doi = {10.1016/j.neuroimage.2006.09.053},
   Key = {fds268868}
}

@booklet{Morgan04,
   Author = {Morgan, DL and Little, PB and Herr, DW and Moser, VC and Collins, B and Herbert, R and Johnson, GA and Maronpot, RR and Harry, GJ and Sills,
             RC},
   Title = {Neurotoxicity of carbonyl sulfide in F344 rats following
             inhalation exposure for up to 12 weeks.},
   Journal = {Toxicol Appl Pharmacol},
   Volume = {200},
   Number = {2},
   Pages = {131-145},
   Year = {2004},
   Month = {October},
   ISSN = {0041-008X},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/15476866},
   Abstract = {Carbonyl sulfide (COS), a high-priority Clean Air Act
             chemical, was evaluated for neurotoxicity in short-term
             studies. F344 rats were exposed to 75-600 ppm COS 6 h per
             day, 5 days per week for up to 12 weeks. In rats exposed to
             500 or 600 ppm for up to 4 days, malacia and microgliosis
             were detected in numerous neuroanatomical regions of the
             brain by conventional optical microscopy and magnetic
             resonance microscopy (MRM). After a 2-week exposure to 400
             ppm, rats were evaluated using a functional observational
             battery. Slight gait abnormality was detected in 50% of the
             rats and hypotonia was present in all rats exposed to COS.
             Decreases in motor activity, and forelimb and hindlimb grip
             strength were also detected. In rats exposed to 400 ppm for
             12 weeks, predominant lesions were in the parietal cortex
             area 1 (necrosis) and posterior colliculus (neuronal loss,
             microgliosis, hemorrhage), and occasional necrosis was
             present in the putamen, thalamus, and anterior olivary
             nucleus. Carbonyl sulfide specifically targeted the auditory
             system including the olivary nucleus, nucleus of the lateral
             lemniscus, and posterior colliculus. Consistent with these
             findings were alterations in the amplitude of the brainstem
             auditory evoked responses (BAER) for peaks N3, P4, N4, and
             N5 that represented changes in auditory transmission between
             the anterior olivary nucleus to the medial geniculate
             nucleus in animals after exposure for 2 weeks to 400 ppm
             COS. A concentration-related decrease in cytochrome oxidase
             activity was detected in the posterior colliculus and
             parietal cortex of exposed rats as early as 3 weeks.
             Cytochrome oxidase activity was significantly decreased at
             COS concentrations that did not cause detectable lesions,
             suggesting that disruption of the mitochondrial respiratory
             chain may precede these brain lesions. Our studies
             demonstrate that this environmental air contaminant has the
             potential to cause a wide spectrum of brain lesions that are
             dependent on the degree and duration of exposure.},
   Doi = {10.1016/j.taap.2004.04.013},
   Key = {Morgan04}
}

@article{fds132915,
   Author = {DL Morgan and PB Little and DW Herr and VC Moser and B Collins and R
             Herbert, GA Johnson and RR Maronpot and GJ Harry and RC
             Sills},
   Title = {Neurotoxicity of carbonyl sulfide in F344 rats following
             inhalation exposure for up to 12 weeks.},
   Journal = {Toxicology and applied pharmacology, United
             States},
   Volume = {200},
   Number = {2},
   Pages = {131-45},
   Year = {2004},
   Month = {October},
   ISSN = {0041-008X},
   Keywords = {Air Pollutants • Animals • Behavior, Animal •
             Blood Chemical Analysis • Brain Diseases •
             Electron Transport Complex IV • Evoked Potentials,
             Auditory, Brain Stem • Female • Histocytochemistry
             • Inhalation Exposure • Male • Motor Activity
             • Neurotoxins • Random Allocation • Rats
             • Rats, Inbred F344 • Sulfur Oxides •
             analysis • chemically induced* • drug effects
             • pathology • toxicity*},
   Abstract = {Carbonyl sulfide (COS), a high-priority Clean Air Act
             chemical, was evaluated for neurotoxicity in short-term
             studies. F344 rats were exposed to 75-600 ppm COS 6 h per
             day, 5 days per week for up to 12 weeks. In rats exposed to
             500 or 600 ppm for up to 4 days, malacia and microgliosis
             were detected in numerous neuroanatomical regions of the
             brain by conventional optical microscopy and magnetic
             resonance microscopy (MRM). After a 2-week exposure to 400
             ppm, rats were evaluated using a functional observational
             battery. Slight gait abnormality was detected in 50% of the
             rats and hypotonia was present in all rats exposed to COS.
             Decreases in motor activity, and forelimb and hindlimb grip
             strength were also detected. In rats exposed to 400 ppm for
             12 weeks, predominant lesions were in the parietal cortex
             area 1 (necrosis) and posterior colliculus (neuronal loss,
             microgliosis, hemorrhage), and occasional necrosis was
             present in the putamen, thalamus, and anterior olivary
             nucleus. Carbonyl sulfide specifically targeted the auditory
             system including the olivary nucleus, nucleus of the lateral
             lemniscus, and posterior colliculus. Consistent with these
             findings were alterations in the amplitude of the brainstem
             auditory evoked responses (BAER) for peaks N3, P4, N4, and
             N5 that represented changes in auditory transmission between
             the anterior olivary nucleus to the medial geniculate
             nucleus in animals after exposure for 2 weeks to 400 ppm
             COS. A concentration-related decrease in cytochrome oxidase
             activity was detected in the posterior colliculus and
             parietal cortex of exposed rats as early as 3 weeks.
             Cytochrome oxidase activity was significantly decreased at
             COS concentrations that did not cause detectable lesions,
             suggesting that disruption of the mitochondrial respiratory
             chain may precede these brain lesions. Our studies
             demonstrate that this environmental air contaminant has the
             potential to cause a wide spectrum of brain lesions that are
             dependent on the degree and duration of exposure.},
   Key = {fds132915}
}

@article{fds174295,
   Author = {AY Grahn and KS Bankiewicz and M Dugich-Djordjevic, JR Bringas and P
             Hadaczek, GA Johnson and S Eastman and M Luz},
   Title = {Non-PEGylated liposomes for convection-enhanced delivery of
             topotecan and gadodiamide in malignant glioma: initial
             experience.},
   Journal = {Journal of neuro-oncology},
   Volume = {95},
   Number = {2},
   Pages = {185-97},
   Year = {2009},
   Month = {November},
   ISSN = {1573-7373},
   url = {http://dx.doi.org/10.1007/s11060-009-9917-1},
   Keywords = {Animals • Antineoplastic Agents • Brain Neoplasms
             • Cell Survival • Contrast Media • Convection
             • Drug Delivery Systems* • Gadolinium DTPA •
             Glioblastoma • Humans • Liposomes • Male
             • Polyethylene Glycols • Rats • Rats,
             Sprague-Dawley • Survival Rate • Tissue
             Distribution • Topotecan • Tumor Cells, Cultured
             • Xenograft Model Antitumor Assays •
             administration & dosage • administration & dosage*
             • chemistry* • drug effects • drug therapy*
             • pathology • pharmacokinetics},
   Abstract = {Convection-enhanced delivery (CED) of highly stable
             PEGylated liposomes encapsulating chemotherapeutic drugs has
             previously been effective against malignant glioma
             xenografts. We have developed a novel, convectable
             non-PEGylated liposomal formulation that can be used to
             encapsulate both the topoisomerase I inhibitor topotecan
             (topoCED) and paramagnetic gadodiamide (gadoCED), providing
             an ideal basis for real-time monitoring of drug
             distribution. Tissue retention of topoCED following single
             CED administration was significantly improved relative to
             free topotecan. At a dose of 10 microg (0.5 mg/ml), topoCED
             had a half-life in brain of approximately 1 day and
             increased the area under the concentration-time curve (AUC)
             by 28-fold over free topotecan (153.8 vs. 5.5 microg day/g).
             The combination of topoCED and gadoCED was found to
             co-convect well in both naïve rat brain and malignant
             glioma xenografts (correlation coefficients 0.97-0.99). In a
             U87MG cell assay, the 50% inhibitory concentration (IC(50))
             of topoCED was approximately 0.8 microM at 48 and 72 h; its
             concentration-time curves were similar to free topotecan and
             unaffected by gadoCED. In a U87MG intracranial rat xenograft
             model, a two-dose CED regimen of topoCED co-infused with
             gadoCED greatly increased median overall survival at dose
             levels of 0.5 mg/ml (29.5 days) and 1.0 mg/ml (33.0 days)
             vs. control (20.0 days; P < 0.0001 for both comparisons).
             TopoCED at higher concentrations (1.6 mg/ml) co-infused with
             gadoCED showed no evidence of histopathological changes
             attributable to either agent. The positive results of tissue
             pharmacokinetics, co-convection, cytotoxicity, efficacy, and
             lack of toxicity of topoCED in a clinically meaningful dose
             range, combined with an ideal matched-liposome paramagnetic
             agent, gadoCED, implicates further clinical applications of
             this therapy in the treatment of malignant
             glioma.},
   Language = {eng},
   Doi = {10.1007/s11060-009-9917-1},
   Key = {fds174295}
}

@article{fds268745,
   Author = {MACFALL, JS and JOHNSON, GA},
   Title = {NONDESTRUCTIVE, 3-DIMENSIONAL STUDY OF ROOT-GROWTH WITH
             MAGNETIC-RESONANCE MICROSCOPY (MRM)},
   Journal = {RESEARCH AND APPLICATIONS OF CHEMICAL SCIENCES IN
             FORESTRY},
   Volume = {104},
   Pages = {18-18},
   Publisher = {US DEPT AGR, FOREST SERV SO FOREST EXPT STN},
   Editor = {Vozzo, JA},
   Year = {1994},
   Month = {January},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1994BA75T00005&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {fds268745}
}

@article{fds174193,
   Author = {FW Bazer and G Wu and TE Spencer and GA Johnson and RC Burghardt and K
             Bayless},
   Title = {Novel pathways for implantation and establishment and
             maintenance of pregnancy in mammals.},
   Journal = {Molecular human reproduction},
   Volume = {16},
   Number = {3},
   Pages = {135-52},
   Year = {2010},
   Month = {March},
   ISSN = {1460-2407},
   url = {http://dx.doi.org/10.1093/molehr/gap095},
   Keywords = {Animals • Embryo Implantation • Female •
             Humans • Pregnancy • Pregnancy, Animal* •
             Signal Transduction • Uterus • genetics •
             metabolism • physiology • physiology*},
   Abstract = {Uterine receptivity to implantation varies among species,
             and involves changes in expression of genes that are
             coordinate with attachment of trophectoderm to uterine
             lumenal and superficial glandular epithelia, modification of
             phenotype of uterine stromal cells, silencing of receptors
             for progesterone and estrogen, suppression of genes for
             immune recognition, alterations in membrane permeability to
             enhance conceptus-maternal exchange of factors, angiogenesis
             and vasculogenesis, increased vascularity of the
             endometrium, activation of genes for transport of nutrients
             into the uterine lumen, and enhanced signaling for pregnancy
             recognition. Differential expression of genes by uterine
             epithelial and stromal cells in response to progesterone,
             glucocorticoids, prostaglandins and interferons may
             influence uterine receptivity to implantation in mammals.
             Uterine receptivity to implantation is progesterone-dependent;
             however, implantation is preceded by loss of expression of
             receptors for progesterone (PGR) so that progesterone most
             likely acts via PGR-positive stromal cells throughout
             pregnancy. Endogenous retroviruses expressed by the uterus
             and/or blastocyst also affect implantation and placentation
             in various species. Understanding the roles of the variety
             of hormones, growth factors and endogenous retroviral
             proteins in uterine receptivity for implantation is
             essential to enhancing reproductive health and fertility in
             humans and domestic animals.},
   Language = {eng},
   Doi = {10.1093/molehr/gap095},
   Key = {fds174193}
}

@booklet{Johnson86b,
   Author = {Johnson, GA and Thompson, MB and Gewalt, SL and Hayes,
             CE},
   Title = {Nuclear magnetic resonance imaging at microscopic
             resolution},
   Journal = {Journal of Magnetic Resonance (1969)},
   Volume = {68},
   Number = {1},
   Pages = {129-137},
   Publisher = {Elsevier BV},
   Year = {1986},
   ISSN = {0022-2364},
   url = {http://dx.doi.org/10.1016/0022-2364(86)90322-7},
   Abstract = {Resolution limits in NMR imaging are imposed by bandwidth
             considerations, available magnetic gradients for spatial
             encoding, and signal to noise. This work reports
             modification of a clinical NMR imaging device with picture
             elements of 500 × 500 × 5000 μm to yield picture elements
             of 50 × 50 × 1000 μm. Resolution has been increased by
             using smaller gradient coils permitting gradient fields
             &gt;0.4 mT/cm. Significant improvements in signal to noise
             are achieved with smaller rf coils, close attention to
             choice of bandwidth, and signal averaging. These
             improvements permit visualization of anatomical structures
             in the rat brain with an effective diameter of 1 cm with the
             same definition as is seen in human imaging. The techniques
             and instrumentation should open a number of basic sciences
             such as embryology, plant sciences, and teratology to the
             potentials of NMR imaging. © 1986.},
   Doi = {10.1016/0022-2364(86)90322-7},
   Key = {Johnson86b}
}

@article{fds132791,
   Author = {JS MacFall and GA Johnson and PJ Kramer},
   Title = {Observation of a water-depletion region surrounding loblolly
             pine roots by magnetic resonance imaging.},
   Journal = {Proceedings of the National Academy of Sciences of the
             United States of America, United States},
   Volume = {87},
   Number = {3},
   Pages = {1203-7},
   Year = {1990},
   Month = {February},
   ISSN = {1091-6490},
   Abstract = {Magnetic resonance imaging was used to study sand containing
             various amounts of water and roots of loblolly pine planted
             into similar sand. Spin-lattice (T1) relaxation times of
             sand with water contents ranging from 0 to 25% (wt/wt)
             ranged from 472 to 1265 ms and increased with water content.
             Spin-spin (T2) relaxation times ranged from 54 to 76 ms and
             did not change in a discernible pattern with water content.
             Based on water content and measured T1 and T2 values, the
             signal intensity of sand/water images was predicted to
             increase with water content in a linear fashion, with the
             slope of the lines increasing with the time of acquisition
             repetition (TR). Measured signal intensity from images of
             sand with various water contents was found to follow a
             similar pattern. This allows interpretation of dark images
             of sand/water to be regions of low water content, and bright
             images to have comparatively greater water content. Images
             of loblolly pine seedling roots planted in identical sand
             showed the formation of a distinct water-depletion region
             first around the woody taproot and later showed the region
             extended and expanded around the lateral roots and clusters
             of mycorrhizal short roots. This observation strongly
             suggests that water uptake is occurring through the
             suberized region of the woody taproot.},
   Key = {fds132791}
}

@booklet{Macfall90,
   Author = {MacFall, JS and Johnson, GA and Kramer, PJ},
   Title = {Observation of a water-depletion region surrounding loblolly
             pine roots by magnetic resonance imaging.},
   Journal = {Proc Natl Acad Sci U S A},
   Volume = {87},
   Number = {3},
   Pages = {1203-1207},
   Year = {1990},
   Month = {February},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/11607063},
   Abstract = {Magnetic resonance imaging was used to study sand containing
             various amounts of water and roots of loblolly pine planted
             into similar sand. Spin-lattice (T1) relaxation times of
             sand with water contents ranging from 0 to 25% (wt/wt)
             ranged from 472 to 1265 ms and increased with water content.
             Spin-spin (T2) relaxation times ranged from 54 to 76 ms and
             did not change in a discernible pattern with water content.
             Based on water content and measured T1 and T2 values, the
             signal intensity of sand/water images was predicted to
             increase with water content in a linear fashion, with the
             slope of the lines increasing with the time of acquisition
             repetition (TR). Measured signal intensity from images of
             sand with various water contents was found to follow a
             similar pattern. This allows interpretation of dark images
             of sand/water to be regions of low water content, and bright
             images to have comparatively greater water content. Images
             of loblolly pine seedling roots planted in identical sand
             showed the formation of a distinct water-depletion region
             first around the woody taproot and later showed the region
             extended and expanded around the lateral roots and clusters
             of mycorrhizal short roots. This observation strongly
             suggests that water uptake is occurring through the
             suberized region of the woody taproot.},
   Doi = {10.1073/pnas.87.3.1203},
   Key = {Macfall90}
}

@article{fds157082,
   Author = {JS Macfall and PE Pfeffer and DB Rolin, JR Macfall and GA
             Johnson},
   Title = {Observation of the Oxygen Diffusion Barrier in Soybean
             (Glycine max) Nodules with Magnetic Resonance
             Microscopy.},
   Journal = {Plant physiology},
   Volume = {100},
   Number = {4},
   Pages = {1691-1697},
   Year = {1992},
   Month = {December},
   ISSN = {0032-0889},
   Abstract = {The effects of selected gas perfusion treatments on the
             spinlattice relaxation times (T(1)) of the soybean (Glycine
             max) nodule cortex and inner nodule tissue were studied with
             (1)H high resolution magnetic resonance microscopy. Three
             gas treatments were used: (a) perfusion with O(2) followed
             by N(2); (b) O(2) followed by O(2); and (c) air followed by
             N(2). Soybean plants with intact attached nodules were
             placed into the bore of a superconducting magnet and a
             selected root with nodules was perfused with the gas of
             interest. Magnetic resonance images were acquired with
             repetition times from 50 to 3200 ms. The method of partial
             saturation was used to calculate T(1) times on selected
             regions of the image. Calculated images based on T(1) showed
             longer T(1) values in the cortex than in the inner nodule
             during all of the gas perfusions. When nodules were perfused
             with O(2)-O(2), there was no significant change in the T(1)
             of the nodule between the two gas treatments. When the
             nodule was perfused with O(2)-N(2) or air-N(2), however, the
             T(1) of both the cortex and inner nodule increased. In these
             experiments, the increase in T(1) of the cortex was 2- to
             3-fold greater than the increase observed in the inner
             nodule. A similar change in T(1) was found in detached live
             nodules, but there was no change in T(1) with selective gas
             perfusion of detached dead nodules. These observations
             suggest that cortical cells respond differently to selected
             gas perfusion than the inner nodule, with the boundary of
             T(1) change sharply delineated at the interface of the inner
             nodule and the inner cortex.},
   Key = {fds157082}
}

@booklet{Macfall92,
   Author = {Macfall, JS and Pfeffer, PE and Rolin, DB and Macfall, JR and Johnson,
             GA},
   Title = {Observation of the Oxygen Diffusion Barrier in Soybean
             (Glycine max) Nodules with Magnetic Resonance
             Microscopy.},
   Journal = {Plant Physiol},
   Volume = {100},
   Number = {4},
   Pages = {1691-1697},
   Year = {1992},
   Month = {December},
   ISSN = {0032-0889},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/16653185},
   Abstract = {The effects of selected gas perfusion treatments on the
             spinlattice relaxation times (T(1)) of the soybean (Glycine
             max) nodule cortex and inner nodule tissue were studied with
             (1)H high resolution magnetic resonance microscopy. Three
             gas treatments were used: (a) perfusion with O(2) followed
             by N(2); (b) O(2) followed by O(2); and (c) air followed by
             N(2). Soybean plants with intact attached nodules were
             placed into the bore of a superconducting magnet and a
             selected root with nodules was perfused with the gas of
             interest. Magnetic resonance images were acquired with
             repetition times from 50 to 3200 ms. The method of partial
             saturation was used to calculate T(1) times on selected
             regions of the image. Calculated images based on T(1) showed
             longer T(1) values in the cortex than in the inner nodule
             during all of the gas perfusions. When nodules were perfused
             with O(2)-O(2), there was no significant change in the T(1)
             of the nodule between the two gas treatments. When the
             nodule was perfused with O(2)-N(2) or air-N(2), however, the
             T(1) of both the cortex and inner nodule increased. In these
             experiments, the increase in T(1) of the cortex was 2- to
             3-fold greater than the increase observed in the inner
             nodule. A similar change in T(1) was found in detached live
             nodules, but there was no change in T(1) with selective gas
             perfusion of detached dead nodules. These observations
             suggest that cortical cells respond differently to selected
             gas perfusion than the inner nodule, with the boundary of
             T(1) change sharply delineated at the interface of the inner
             nodule and the inner cortex.},
   Doi = {10.1104/pp.100.4.1691},
   Key = {Macfall92}
}

@article{fds174121,
   Author = {GA Johnson},
   Title = {Obstetric nursing is for men, too.},
   Journal = {The American journal of nursing},
   Volume = {66},
   Number = {12},
   Pages = {2714-5},
   Year = {1966},
   Month = {December},
   ISSN = {0002-936X},
   Keywords = {Female • Humans • Nurses, Male* • Obstetrical
             Nursing* • Pregnancy},
   Language = {eng},
   Key = {fds174121}
}

@article{fds174227,
   Author = {GW Fuller and GA Johnson},
   Title = {ON THE DIFFERENTIATION AND CLASSIFICATION OF WATER
             BACTERIA.},
   Journal = {The Journal of experimental medicine},
   Volume = {4},
   Number = {5-6},
   Pages = {609-626},
   Year = {1899},
   Month = {September},
   ISSN = {1540-9538},
   Language = {ENG},
   Key = {fds174227}
}

@article{fds174081,
   Author = {GW Fuller and GA Johnson},
   Title = {ON THE QUESTION OF STANDARD METHODS FOR THE DETERMINATION OF
             THE NUMBERS OF BACTERIA IN WATERS.},
   Journal = {Journal. Boston Society of Medical Sciences},
   Volume = {4},
   Number = {4},
   Pages = {85-86},
   Year = {1900},
   Month = {January},
   Language = {ENG},
   Key = {fds174081}
}

@article{fds174134,
   Author = {GW Fuller and GA Johnson},
   Title = {On the Question of Standard Methods for the Determination of
             the Numbers of Bacteria in Waters.},
   Journal = {Public health papers and reports},
   Volume = {25},
   Pages = {574-9},
   Year = {1899},
   ISSN = {0737-8769},
   Language = {eng},
   Key = {fds174134}
}

@article{fds174279,
   Author = {GW Fuller and GA Johnson},
   Title = {On the Question of Standard Methods for the Determination of
             the Numbers of Bacteria in Waters.},
   Journal = {Public health papers and reports},
   Volume = {25},
   Pages = {574-579},
   Year = {1899},
   Language = {ENG},
   Key = {fds174279}
}

@booklet{Shattuck95,
   Author = {Shattuck, MD and Behringer, RP and Johnson, GA and Georgiadis,
             JG},
   Title = {Onset and Stability of Convection in Porous Media:
             Visualization by Magnetic Resonance Imaging.},
   Journal = {Phys Rev Lett},
   Volume = {75},
   Number = {10},
   Pages = {1934-1937},
   Year = {1995},
   Month = {September},
   url = {http://dx.doi.org/10.1103/PhysRevLett.75.1934},
   Doi = {10.1103/PhysRevLett.75.1934},
   Key = {Shattuck95}
}

@article{fds132859,
   Author = {MD Shattuck and RP Behringer and GA Johnson and JG
             Georgiadis},
   Title = {Onset and Stability of Convection in Porous Media:
             Visualization by Magnetic Resonance Imaging.},
   Journal = {Phys Rev Lett},
   Volume = {75},
   Number = {10},
   Pages = {1934-1937},
   Year = {1995},
   Month = {September},
   ISSN = {0031-9007},
   Key = {fds132859}
}

@article{fds268775,
   Author = {Oldham, M and Sakhalkar, H and Oliver, T and Allan Johnson and G and Dewhirst, M},
   Title = {Optical clearing of unsectioned specimens for
             three-dimensional imaging via optical transmission and
             emission tomography.},
   Journal = {J Biomed Opt},
   Volume = {13},
   Number = {2},
   Pages = {021113},
   Year = {2008},
   ISSN = {1083-3668},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/18465962},
   Abstract = {Optical computed tomography (optical-CT) and optical
             emission computed tomography (optical-ECT) are new
             techniques that enable unprecedented high-resolution 3-D
             multimodal imaging of tissue structure and function.
             Applications include imaging macroscopic gene expression and
             microvasculature structure in unsectioned biological
             specimens up to 8 cm(3). A key requisite for these imaging
             techniques is effective sample preparation including optical
             clearing, which enables light transport through the sample
             while preserving the signal (either light absorbing stain or
             fluorescent proteins) in representative form. We review
             recent developments in optical-CT and optical-ECT, and
             compatible "fluorescence-friendly" optical clearing
             protocols.},
   Doi = {10.1117/1.2907968},
   Key = {fds268775}
}

@booklet{Gupta02,
   Author = {Gupta, AK and Johnson, GA and Nelson, RC},
   Title = {Optimization of eight-element multi-detector helical CT for
             imaging the abdomen},
   Journal = {Radiology},
   Volume = {222},
   Number = {2},
   Pages = {589-589},
   Year = {2002},
   Month = {February},
   Key = {Gupta02}
}

@article{fds132823,
   Author = {AK Gupta and RC Nelson and GA Johnson and EK Paulson and DM Delong and TT
             Yoshizumi},
   Title = {Optimization of eight-element multi-detector row helical CT
             technology for evaluation of the abdomen.},
   Journal = {Radiology, United States},
   Volume = {227},
   Number = {3},
   Pages = {739-45},
   Year = {2003},
   Month = {June},
   ISSN = {0033-8419},
   Keywords = {Artifacts • Humans • Phantoms, Imaging •
             Radiation Dosage • Radiography, Abdominal •
             Tomography Scanners, X-Ray Computed • Tomography,
             Spiral Computed* • methods • methods*},
   Abstract = {PURPOSE: To evaluate protocols for abdominal imaging with an
             eight-element multi-detector row computed tomographic (CT)
             scanner. MATERIALS AND METHODS: An eight-element helical CT
             scanner was used to acquire data in two phantoms with
             four-element (pitch, 0.75 and 1.5; section thickness, 1.25,
             2.5, and 5.0 mm) and eight-element (pitch, 0.625, 0.875,
             1.35 and 1.675; section thickness, 1.25 and 2.5 mm)
             protocols. One phantom was used for low-contrast
             detectability and streak artifact; the other, for
             high-contrast performance. Protocols included near constant
             radiation dose (140 kV and varied tube current, confirmed by
             using the above protocols to scan a dedicated radiation dose
             phantom). Data were analyzed by three blinded readers for
             streak artifacts, contrast-to-noise ratio, and z-axis
             resolution (contrast-transfer function). Statistical
             analysis included studentized range tests. RESULTS:
             Contrast-to-noise ratios for four and eight elements were
             not consistently different. Qualitative evaluation for
             streak artifacts revealed fewer artifacts for all
             eight-element 1.25-mm-thick section protocols, as compared
             with eight-element 2.5-mm protocols. All eight-element
             2.5-mm protocols except that with 27.0 mm per rotation had
             fewer streak artifacts than did four-element protocols (P
             =.02-.04). Contrast-transfer functions along the z axis for
             eight-element protocols were better than those for
             four-element protocols, demonstrating improved z-axis
             resolution (P <.05). CONCLUSION: Images acquired at eight
             sections per rotation demonstrated no sacrifice of
             contrast-to-noise ratio, improved z-axis resolution, and
             fewer streak artifacts, even when radiation dose was similar
             to that for four-element CT.},
   Key = {fds132823}
}

@booklet{Gupta03,
   Author = {Gupta, AK and Nelson, RC and Johnson, GA and Paulson, EK and Delong, DM and Yoshizumi, TT},
   Title = {Optimization of eight-element multi-detector row helical CT
             technology for evaluation of the abdomen.},
   Journal = {Radiology},
   Volume = {227},
   Number = {3},
   Pages = {739-745},
   Year = {2003},
   Month = {June},
   ISSN = {0033-8419},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/12702826},
   Abstract = {PURPOSE: To evaluate protocols for abdominal imaging with an
             eight-element multi-detector row computed tomographic (CT)
             scanner. MATERIALS AND METHODS: An eight-element helical CT
             scanner was used to acquire data in two phantoms with
             four-element (pitch, 0.75 and 1.5; section thickness, 1.25,
             2.5, and 5.0 mm) and eight-element (pitch, 0.625, 0.875,
             1.35 and 1.675; section thickness, 1.25 and 2.5 mm)
             protocols. One phantom was used for low-contrast
             detectability and streak artifact; the other, for
             high-contrast performance. Protocols included near constant
             radiation dose (140 kV and varied tube current, confirmed by
             using the above protocols to scan a dedicated radiation dose
             phantom). Data were analyzed by three blinded readers for
             streak artifacts, contrast-to-noise ratio, and z-axis
             resolution (contrast-transfer function). Statistical
             analysis included studentized range tests. RESULTS:
             Contrast-to-noise ratios for four and eight elements were
             not consistently different. Qualitative evaluation for
             streak artifacts revealed fewer artifacts for all
             eight-element 1.25-mm-thick section protocols, as compared
             with eight-element 2.5-mm protocols. All eight-element
             2.5-mm protocols except that with 27.0 mm per rotation had
             fewer streak artifacts than did four-element protocols (P
             =.02-.04). Contrast-transfer functions along the z axis for
             eight-element protocols were better than those for
             four-element protocols, demonstrating improved z-axis
             resolution (P <.05). CONCLUSION: Images acquired at eight
             sections per rotation demonstrated no sacrifice of
             contrast-to-noise ratio, improved z-axis resolution, and
             fewer streak artifacts, even when radiation dose was similar
             to that for four-element CT.},
   Doi = {10.1148/radiol.2273020591},
   Key = {Gupta03}
}

@article{fds268867,
   Author = {Jaffe, TA and Nelson, RC and Johnson, GA and Lee, ER and Yoshizumi, TT and Lowry, CR and Bullard, AB and DeLong, DM and Paulson,
             EK},
   Title = {Optimization of multiplanar reformations from isotropic data
             sets acquired with 16-detector row helical CT
             scanner.},
   Journal = {Radiology},
   Volume = {238},
   Number = {1},
   Pages = {292-299},
   Year = {2006},
   Month = {January},
   ISSN = {0033-8419},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/16373774},
   Keywords = {Adult • Aged • Equipment Design • Female
             • Humans • Image Processing, Computer-Assisted*
             • Male • Middle Aged • Phantoms, Imaging
             • Radiation Dosage • Radiography, Abdominal •
             Retrospective Studies • Tomography Scanners, X-Ray
             Computed* • Tomography, Spiral Computed* •
             instrumentation*},
   Abstract = {Institutional review board approval and waiver of consent
             were obtained for the patient component of this
             retrospective HIPAA-compliant study. By using an
             anthropomorphic phantom and metal oxide semiconductor field
             effect transistor detectors, radiation dose was determined
             for one eight-detector row and two 16-detector row computed
             tomographic (CT) protocols. A custom phantom was scanned by
             using the three protocols to identify isotropy.
             Contrast-to-noise ratios (CNRs) were determined for the same
             protocols by using a third phantom. Seven patients had
             undergone isotropic 16-detector row CT of the abdomen and
             pelvis. Anonymized coronal reformations at various
             thicknesses were ranked qualitatively by three radiologists.
             Effective dose equivalents were similar for the eight- and
             16-detector row protocols. When transverse and coronal
             reformations of data acquired in the custom phantom were
             compared, coronal reformations obtained with the 16-detector
             row and 0.625-mm section thickness protocol were found to be
             nearly identical to the transverse image for all sets of
             line pairs. CNRs were consistently highest on 5-mm-thick
             coronal reformations (CNR range, 1.2-3.3). For qualitative
             assessment, 2- and 3-mm-thick coronal reformations were
             consistently preferred.},
   Doi = {10.1148/radiol.2381050404},
   Key = {fds268867}
}

@booklet{Hurlston97,
   Author = {Hurlston, SE and Cofer, GP and Johnson, GA},
   Title = {Optimized radiofrequency coils for increased signal-to-noise
             ratio in magnetic resonance microscopy},
   Journal = {International Journal of Imaging Systems and
             Technology},
   Volume = {8},
   Number = {3},
   Pages = {277-284},
   Year = {1997},
   Month = {January},
   url = {http://dx.doi.org/10.1002/(SICI)1098-1098(1997)8:3<277::AID-IMA5>3.0.CO;2-7},
   Abstract = {The signal-to-noise ratio (SNR) is a major obstacle to
             achieving increased resolution in magnetic resonance
             microscopy (MRM). The SNR considerations for MRM are
             presented, with particular attention to the role of
             judicious receiver coil design in maximizing sensitivity and
             limiting noise contributions both from the sample and the
             coil. We present a number of different coil configurations
             that have been optimized for particular applications of MRM
             in the biological sciences. An overview of the literature
             regarding derivations of the SNR for birdcage-configuration
             volume coils, inductively coupled surface coils, and
             surgically implanted coils is presented in a unified
             fashion. Microscopy coils designed to reduce the total
             volume of excitation, thus coupling more closely to a given
             region of interest, are discussed. The volume coil is
             presented in terms of its application to lung imaging in
             small animals at 2 T and imaging of stroke at 7 T. The
             performance of traditional surface coils is demonstrated by
             application to spinal cord imaging in the rat. Finally,
             implanted coils are examined, as used in studies of the
             carotid arteries. © 1997 John Wiley & Sons,
             Inc.},
   Doi = {10.1002/(SICI)1098-1098(1997)8:3<277::AID-IMA5>3.0.CO;2-7},
   Key = {Hurlston97}
}

@article{fds268779,
   Author = {De Lin and M and Badea, CT and Johnson, GA},
   Title = {Optimized radiographic spectra for digital subtraction
             angiography in the mouse},
   Journal = {2004 2nd IEEE International Symposium on Biomedical Imaging:
             Macro to Nano},
   Volume = {2},
   Pages = {1412-1415},
   Year = {2004},
   Month = {December},
   ISBN = {9780780383883},
   Abstract = {The availability of genetically altered mouse models of
             human disease and the increasing use of small animals in
             basic research have spurred extraordinary interest in new
             imaging methodologies - particularly magnetic resonance
             microscopy, microCT, and microPET. To date, very little
             attention has been given to planar radiographic imaging. Yet
             there exists enormous potential for this modality given the
             ease of use and its potential speed. Functional imaging in
             mouse models can be addressed particularly well through the
             use of digital subtraction angiography. We describe here a
             system designed explicitly for digital subtraction
             angiography in the mouse and the optimization of acquisition
             parameters required to perform the highest quality
             functional subtraction angiograms. We focus on optimization
             of contrast using selective K-edge filters and the
             optimization of contrast agent though a carefully controlled
             biological pulse sequence. © 2004 IEEE.},
   Key = {fds268779}
}

@article{fds344782,
   Author = {De Lin and M and Samei, E and Badea, CT and Yoshizumi, TT and Allan
             Johnson, G},
   Title = {Optimized radiographic spectra for small animal digital
             subtraction angiography.},
   Journal = {Med Phys},
   Volume = {33},
   Number = {11},
   Pages = {4249-4257},
   Year = {2006},
   Month = {November},
   ISSN = {0094-2405},
   url = {http://dx.doi.org/10.1118/1.2356646},
   Keywords = {Algorithms* • Angiography, Digital Subtraction •
             Animals • Image Enhancement • Image
             Interpretation, Computer-Assisted • Rats •
             Reproducibility of Results • Sensitivity and
             Specificity • Spectrometry, X-Ray Emission •
             instrumentation • methods* • veterinary*},
   Abstract = {The increasing use of small animals in basic research has
             spurred interest in new imaging methodologies. Digital
             subtraction angiography (DSA) offers a particularly
             appealing approach to functional imaging in the small
             animal. This study examines the optimal x-ray, molybdenum
             (Mo) or tungsten (W) target sources, and technique to
             produce the highest quality small animal functional
             subtraction angiograms in terms of contrast and
             signal-difference-to-noise ratio squared (SdNR2). Two
             limiting conditions were considered-normalization with
             respect to dose and normalization against tube loading.
             Image contrast and SdNR2 were simulated using an established
             x-ray model. DSA images of live rats were taken at two
             representative tube potentials for the W and Mo sources.
             Results show that for small animal DSA, the Mo source
             provides better contrast. However, with digital detectors,
             SdNR2 is the more relevant figure of merit. The W source
             operated at kVps>60 achieved a higher SdNR2. The highest
             SdNR2 was obtained at voltages above 90kVp. However,
             operation at the higher potential results in significantly
             greater dose and tube load and reduced contrast
             quantization. A reasonable tradeoff can be achieved at tube
             potentials at the beginning of the performance plateau,
             around 70kVp, where the relative gain in SdNR2 is the
             greatest.},
   Doi = {10.1118/1.2356646},
   Key = {fds344782}
}

@article{fds357204,
   Author = {Anderson, RJ and Long, CM and Calabrese, ED and Robertson, SH and Johnson, GA and Cofer, GP and O'Brien, RJ and Badea,
             A},
   Title = {Optimizing Diffusion Imaging Protocols for Structural
             Connectomics in Mouse Models of Neurological
             Conditions.},
   Journal = {Front Phys},
   Volume = {8},
   Year = {2020},
   Month = {April},
   url = {http://dx.doi.org/10.3389/fphy.2020.00088},
   Abstract = {Network approaches provide sensitive biomarkers for
             neurological conditions, such as Alzheimer's disease (AD).
             Mouse models can help advance our understanding of
             underlying pathologies, by dissecting vulnerable circuits.
             While the mouse brain contains less white matter compared to
             the human brain, axonal diameters compare relatively well
             (e.g., ~0.6 μm in the mouse and ~0.65-1.05 μm in the human
             corpus callosum). This makes the mouse an attractive test
             bed for novel diffusion models and imaging protocols.
             Remaining questions on the accuracy and uncertainty of
             connectomes have prompted us to evaluate diffusion imaging
             protocols with various spatial and angular resolutions. We
             have derived structural connectomes by extracting gradient
             subsets from a high-spatial, high-angular resolution
             diffusion acquisition (120 directions, 43-μm-size voxels).
             We have simulated protocols with 12, 15, 20, 30, 45, 60, 80,
             100, and 120 angles and at 43, 86, or 172-μm voxel sizes.
             The rotational stability of these schemes increased with
             angular resolution. The minimum condition number was
             achieved for 120 directions, followed by 60 and 45
             directions. The percentage of voxels containing one dyad was
             exceeded by those with two dyads after 45 directions, and
             for the highest spatial resolution protocols. For the 86- or
             172-μm resolutions, these ratios converged toward 55% for
             one and 39% for two dyads, respectively, with <7% from
             voxels with three dyads. Tractography errors, estimated
             through dyad dispersion, decreased most with angular
             resolution. Spatial resolution effects became noticeable at
             172 μm. Smaller tracts, e.g., the fornix, were affected
             more than larger ones, e.g., the fimbria. We observed an
             inflection point for 45 directions, and an asymptotic
             behavior after 60 directions, corresponding to similar
             projection density maps. Spatially downsampling to 86 μm,
             while maintaining the angular resolution, achieved a
             subgraph similarity of 96% relative to the reference. Using
             60 directions with 86- or 172-μm voxels resulted in 94%
             similarity. Node similarity metrics indicated that major
             white matter tracts were more robust to downsampling
             relative to cortical regions. Our study provides guidelines
             for new protocols in mouse models of neurological
             conditions, so as to achieve similar connectomes, while
             increasing efficiency.},
   Doi = {10.3389/fphy.2020.00088},
   Key = {fds357204}
}

@booklet{Johnson81b,
   Author = {G. A. Johnson and J. J. Mcnamara},
   Title = {Organ ischemia after hemorrhagic-shock},
   Journal = {Surgical Forum},
   Volume = {32},
   Pages = {24 -- 26},
   Year = {1981},
   Key = {Johnson81b}
}

@article{fds174265,
   Author = {WL Dees and JK Hiney and NH McArthur and GA Johnson and GA Dissen, SR
             Ojeda},
   Title = {Origin and ontogeny of mammalian ovarian
             neurons.},
   Journal = {Endocrinology},
   Volume = {147},
   Number = {8},
   Pages = {3789-96},
   Year = {2006},
   Month = {August},
   ISSN = {0013-7227},
   url = {http://dx.doi.org/10.1210/en.2006-0394},
   Keywords = {Age Factors • Aging • Animals • Cell Count
             • Female • Ganglia, Sympathetic • Macaca
             mulatta • Mammals • Neural Crest • Neurons
             • Ovary • Receptor, Nerve Growth Factor •
             Sexual Maturation • Swine • Tyrosine
             3-Monooxygenase • cytology • cytology* •
             embryology • growth & development* • innervation*
             • metabolism • physiology},
   Abstract = {Mammalian ovaries contain sympathetic neurons expressing the
             low affinity neurotropin receptor (p75NTR). To date neither
             the role these neurons might play in ovarian physiology nor
             their embryological origin is known. Immunohistochemistry
             was used to detect postnatal changes in distribution and
             number of both p75NTR-positive and tyrosine
             hydroxylase-positive neurons in rhesus monkey ovaries. Pig
             fetuses were used to map the pathway of ovarian neuronal
             migration during embryonic development. Antiserum to p75NTR
             revealed the presence of isolated neurons and neurons
             clustered into ganglia in 2-month-old monkey ovaries. After
             8 months, the neurons exhibited well-developed processes,
             and other than being more extensively interlaced, the
             localization and morphology did not change after 2 yr of
             age. Total number of p75NTR-positive neurons present
             decreased gradually between 2 months and 12 yr of age and
             declined markedly with reproductive aging. Conversely, the
             subpopulation of neurons immunoreactive to anti-tyrosine
             hydroxylase increased significantly at puberty and then
             declined with the loss of reproductive capacity. By d 21 of
             fetal life in the pig, p75NTR neurons had migrated medially
             from the neural crest to form the paraaortic autonomic
             ganglia. Some neurons migrated ventrally from the ganglia
             and then continued ventrolaterally to enter the genital
             ridge. By d 27, neurons had entered the developing ovary,
             and by d 35, the migration was complete with neurons
             demonstrating immunoreactivity to NeuN, a neuron-specific
             marker. Results demonstrate that p75NTR-expressing ovarian
             neurons originate from the neural crest and that a
             catecholaminergic subset is associated with pubertal
             maturation of the ovary and subsequent reproductive
             function.},
   Language = {eng},
   Doi = {10.1210/en.2006-0394},
   Key = {fds174265}
}

@article{fds174280,
   Author = {MK Park and DH Lee and GA Johnson},
   Title = {Oscillometric blood pressures in the arm, thigh, and calf in
             healthy children and those with aortic coarctation.},
   Journal = {Pediatrics},
   Volume = {91},
   Number = {4},
   Pages = {761-5},
   Year = {1993},
   Month = {April},
   ISSN = {0031-4005},
   Keywords = {Adolescent • Aortic Coarctation • Arm •
             Arteries • Blood Pressure Determination • Blood
             Pressure* • Case-Control Studies • Child •
             Child, Preschool • Female • Humans • Leg
             • Male • Oscillometry • Reference Values
             • Thigh • blood supply • diagnosis •
             methods • physiology • physiopathology*},
   Abstract = {Comparing blood pressure (BP) obtained in the arm with that
             obtained in the thigh or calf is important in the diagnosis
             of aortic coarctation. However, normative mean and range of
             differences in BP between the arm and lower extremity sites
             are not available for normal children. It is also not known
             how accurately the differences in BP between the arm and the
             lower extremity sites predict the pulsed Doppler estimation
             of systolic pressure (SP) gradient across an aortic
             coarctation. To resolve these questions, the authors
             obtained two BP measurements by an oscillometric (Dinamap)
             method in the arm, thigh, and calf in 74 healthy children
             aged 4 to 16 years. Oscillometric BP was also obtained in 21
             children aged 3 to 17 years with preoperative or
             postoperative aortic coarctation and BP gradients were
             compared with that estimated by the pulsed Doppler method.
             Overall, SP was higher in the thigh and calf than in the
             arm. The gradients in SP expressed as arm SP minus calf SP
             [S(A-C)] and arm SP minus thigh SP [S(A-T)] were
             significantly greater in children 4 through 8 years old than
             in those 9 to 16 years old. The S(A-C) was -9.3 (+/- 7.4 SD)
             mm Hg in the 4- through 8-year group and -5.0 (+/- 6.9 SD)
             mm Hg in the 9- to 16-year group. The S(A-T) was -7.1 (+/-
             6.8 SD) mm Hg in the 4- through 8-year group and -2.4 (+/-
             7.7 SD) mm Hg in the 9- to 16-year group.(ABSTRACT TRUNCATED
             AT 250 WORDS)},
   Language = {eng},
   Key = {fds174280}
}

@booklet{Park93,
   Author = {M. K. Park and D. H. Lee and G. A. Johnson},
   Title = {Oscillometric blood pressures in the arm, thigh, and calf in
             healthy-children and those with aortic coarctation},
   Journal = {Pediatrics},
   Volume = {91},
   Number = {4},
   Pages = {761 -- 765},
   Year = {1993},
   Month = {April},
   Key = {Park93}
}

@booklet{Lee92,
   Author = {D. H. Lee and G. A. Johnson and M. K. Park},
   Title = {Oscillometric blood-pressure in the arm, thigh and calf in
             healthy-children and those with aortic coarctation},
   Journal = {Clinical Research},
   Volume = {40},
   Number = {4},
   Pages = {A834 -- A834},
   Year = {1992},
   Month = {December},
   Key = {Lee92}
}

@booklet{Johnson01a,
   Author = {G. A. Johnson and F. W. Bazer and J. E. Garlow and T. E.
             Spencer and C. T. Pfarrer and R. C. Burghardt},
   Title = {Osteopontin and activated alpha(v)beta(5) integrin receptors
             during implantation and placentation in sheep.},
   Journal = {Biology Of Reproduction},
   Volume = {64},
   Pages = {203 -- 203},
   Year = {2001},
   Key = {Johnson01a}
}

@booklet{Johnson03c,
   Author = {G. A. Johnson and R. C. Burghardt and M. M. Joyce and T. E.
             Spencer and F. W. Bazer and C. Pfarrer and C. A.
             Gray},
   Title = {Osteopontin expression in uterine stroma indicates a
             decidualization-like differentiation during ovine
             pregnancy},
   Journal = {Biology Of Reproduction},
   Volume = {68},
   Number = {6},
   Pages = {1951 -- 1958},
   Year = {2003},
   Month = {June},
   Key = {Johnson03c}
}

@article{fds174239,
   Author = {GA Johnson and RC Burghardt and MM Joyce and TE Spencer and FW Bazer and C
             Pfarrer, CA Gray},
   Title = {Osteopontin expression in uterine stroma indicates a
             decidualization-like differentiation during ovine
             pregnancy.},
   Journal = {Biology of reproduction},
   Volume = {68},
   Number = {6},
   Pages = {1951-8},
   Year = {2003},
   Month = {June},
   ISSN = {0006-3363},
   url = {http://dx.doi.org/10.1095/biolreprod.102.012948},
   Keywords = {Actins • Animals • Cell Differentiation •
             Decidua • Desmin • Embryo Implantation •
             Endometrium • Female • Fluorescent Antibody
             Technique • Genetic Markers • In Situ
             Hybridization • Keratins • Muscle, Smooth •
             Osteopontin • Pregnancy • RNA, Messenger •
             Sheep • Sialoglycoproteins • Stromal Cells •
             Swine • Uterus • Vimentin • biosynthesis
             • biosynthesis* • cytology • metabolism
             • metabolism* • physiology •
             physiology*},
   Abstract = {Osteopontin (OPN) is a component of the extracellular matrix
             that interacts with cell surface receptors, including
             integrins, to mediate cell adhesion, migration,
             differentiation, survival, and immune function. In pregnant
             mice and primates, OPN has been detected in decidualized
             stroma and is considered to be a gene marker for
             decidualization. Decidualization involves transformation of
             spindle-like fibroblasts into polygonal epithelial-like
             cells that are hypothesized to limit conceptus trophoblast
             invasion through the uterine wall during invasive
             implantation. Decidualization is not considered
             characteristic of species with noninvasive implantation,
             such as domestic animals. However, the extent of trophoblast
             invasion between sheep and pigs differs, with sheep
             exhibiting erosion of the uterine luminal epithelium (LE)
             and fusion of trophectoderm with LE to form syncytia, and
             pigs maintaining an intact LE throughout pregnancy.
             Therefore, the present study measured changes in the
             decidualization marker genes OPN, desmin, and alpha smooth
             muscle actin (alphaSMA) in ovine and porcine uterine stroma
             throughout pregnancy. The morphology of endometrial stromal
             cells in pregnant ewes changes following conceptus
             attachment, with cells increasing in size and becoming
             polyhedral in shape by Day 35 of pregnancy. Expression of
             OPN mRNA and protein, as well as desmin and alphaSMA
             proteins, was observed in this same uterine stromal
             compartment. In contrast, no morphological changes in
             uterine stroma nor induction of OPN mRNA and protein, or
             desmin protein, were detected during porcine pregnancy.
             Interestingly, alphaSMA protein was absent on Day 20, but
             prominent in uterine stroma of pregnant pigs on Day 45.
             Collectively, these results indicate that the uterine stroma
             of sheep undergoes a program of differentiation similar to
             decidualization in invasive implanting species, whereas
             porcine stroma exhibits differentiation that is more limited
             than that in sheep, rodents, or primates. Results suggest
             that uterine stromal decidualization is common to species
             with different types of placentation, but the extent is
             variable and correlates with the depth of trophoblast
             invasion during implantation.},
   Language = {eng},
   Doi = {10.1095/biolreprod.102.012948},
   Key = {fds174239}
}

@booklet{Johnson03b,
   Author = {G. A. Johnson and R. C. Burghardt and M. M. Joyce and T. E.
             Spencer and F. W. Bazer and C. A. Gray and C.
             Pfarrer},
   Title = {Osteopontin is synthesized by uterine glands and a 45-kDa
             cleavage fragment is localized at the uterine-placental
             interface throughout ovine pregnancy},
   Journal = {Biology Of Reproduction},
   Volume = {69},
   Number = {1},
   Pages = {92 -- 98},
   Year = {2003},
   Month = {July},
   Key = {Johnson03b}
}

@article{fds174310,
   Author = {GA Johnson and RC Burghardt and MM Joyce and TE Spencer and FW Bazer and CA
             Gray, C Pfarrer},
   Title = {Osteopontin is synthesized by uterine glands and a 45-kDa
             cleavage fragment is localized at the uterine-placental
             interface throughout ovine pregnancy.},
   Journal = {Biology of reproduction},
   Volume = {69},
   Number = {1},
   Pages = {92-8},
   Year = {2003},
   Month = {July},
   ISSN = {0006-3363},
   url = {http://dx.doi.org/10.1095/biolreprod.102.013573},
   Keywords = {Animals • Endometrium • Extracellular Matrix
             • Female • In Situ Hybridization • Molecular
             Weight • Osteopontin • Peptide Fragments •
             Placenta • Pregnancy • Pregnancy, Animal •
             RNA, Messenger • Sheep • Sialoglycoproteins •
             Uterus • biosynthesis* • chemistry • genetics
             • metabolism • metabolism*},
   Abstract = {Osteopontin (OPN) is a phosphorylated and glycosylated,
             secreted protein that is present in various epithelial cells
             and biological fluids. On freezing and thawing or treatment
             with proteases, the native 70-kDa protein gives rise to 45-
             and 24-kDa fragments. Secreted OPN functions as an
             extracellular matrix (ECM) protein that binds cell surface
             receptors to mediate cell-cell adhesion, cell-ECM
             communication, and cell migration. In sheep and humans, OPN
             is proposed to be a secretory product of uterine glandular
             epithelium (GE) that binds to uterine luminal epithelium
             (LE) and conceptus trophectoderm to mediate conceptus
             attachment, which is essential to maintain pregnancy through
             the peri-implantation period. Cell-cell adhesion,
             communication, and migration likely are important at the
             interface between uterus and placenta throughout pregnancy,
             but to our knowledge, endometrial and/or placental
             expression of OPN beyond the peri-implantation period has
             not been documented in sheep. Therefore, the present study
             determined temporal and spatial alterations in OPN mRNA and
             protein expression in the ovine uterus between Days 25 and
             120 of pregnancy. The OPN mRNA in total ovine endometrium
             increased 30-fold between Days 40 and 80 of gestation. In
             situ hybridization and immunofluorescence analyses revealed
             that the predominant source of OPN mRNA and protein
             throughout pregnancy was the uterine GE. Interestingly, the
             45-kDa form of OPN was detected exclusively, continuously,
             and abundantly along the apical surface of LE, on conceptus
             trophectoderm, and along the uterine-placental interface of
             both interplacentomal and placentomal regions through Day
             120 of pregnancy. The 45-kDa OPN is a proteolytic cleavage
             fragment of the native 70-kDa OPN, and it is the most
             abundant form in uterine flushes during early pregnancy. The
             45-kDa OPN is more stimulatory to cell attachment and cell
             migration than the native 70-kDa protein. Collectively, the
             present results support the hypothesis that ovine OPN is a
             component of histotroph secreted by the uterine GE that
             accumulates at the uterine-placental interface to influence
             maternal-fetal interactions throughout gestation in
             sheep.},
   Language = {eng},
   Doi = {10.1095/biolreprod.102.013573},
   Key = {fds174310}
}

@booklet{Johnson02d,
   Author = {G. A. Johnson and M. M. Joyce and R. C. Burghardt},
   Title = {Osteopontin/early T-cell activation factor-1 is expressed by
             fetal placental immune cells after day 20 of pregnancy in
             sheep but not pigs.},
   Journal = {Biology Of Reproduction},
   Volume = {66},
   Pages = {272 -- 273},
   Year = {2002},
   Key = {Johnson02d}
}

@booklet{Johnson03,
   Author = {G. A. Johnson and R. C. Burghardt and F. W. Bazer and T. E.
             Spencer},
   Title = {Osteopontin: Roles in implantation and placentation},
   Journal = {Biology Of Reproduction},
   Volume = {69},
   Number = {5},
   Pages = {1458 -- 1471},
   Year = {2003},
   Month = {November},
   Key = {Johnson03}
}

@article{fds174190,
   Author = {GA Johnson and RC Burghardt and FW Bazer and TE Spencer},
   Title = {Osteopontin: roles in implantation and placentation.},
   Journal = {Biology of reproduction},
   Volume = {69},
   Number = {5},
   Pages = {1458-71},
   Year = {2003},
   Month = {November},
   ISSN = {0006-3363},
   url = {http://dx.doi.org/10.1095/biolreprod.103.020651},
   Keywords = {Animals • Decidua • Embryo Implantation •
             Embryo, Mammalian • Endometrium • Female •
             Humans • Immunity, Cellular • Integrins •
             Osteopontin • Placenta • Placentation •
             Pregnancy • Progesterone • Sialoglycoproteins
             • Structure-Activity Relationship • Uterus •
             biosynthesis • chemistry • immunology •
             metabolism • physiology • physiology* •
             secretion},
   Abstract = {Osteopontin (OPN) is an acidic member of the small
             integrin-binding ligand N-linked glycoprotein (SIBLING)
             family of extracellular matrix proteins/cytokines that
             undergoes extensive posttranslational modification,
             including phosphorylation, glycosylation, and cleavage,
             yielding molecular mass variants ranging in size from 25 to
             75 kDa. The result is a versatile protein(s) with multiple
             functions arising from its role as a mediator of cell-cell
             and cell-extracellular matrix (ECM) communication that
             encompass both normal and tumorigenic developmental
             processes, immunological responses during inflammation and
             wound healing, and biomineralization. Studies in primates,
             pigs, sheep, and rodents have revealed that OPN is a major
             constituent of the uterine-placental microenvironment with
             influence as 1) a component of histotroph required for
             adhesion and signal transduction at the uterine-placental
             interface throughout pregnancy, 2) a gene product expressed
             by uterine stroma contributing to a decidualization-like
             transformation that correlates with the degree of conceptus
             invasiveness, and 3) a product of resident uterine and
             placental immune cells that may regulate their behavior and
             cytokine production. This minireview summarizes information
             regarding uterine and placental expression of OPN that has
             accumulated over the past 15 yr, and we briefly describe
             structural/functional properties of this protein that are
             likely relevant to its role(s) during pregnancy. Comparative
             studies have offered insights into the potential
             hormonal/cytokine, cellular, and molecular mechanisms
             underlying OPN-mediated adhesion, remodeling, and
             cell-cell/cell-ECM communication within the uterus and
             placenta. OPN has the potential to profoundly impact
             pregnancy, and investigators are now challenged to focus on
             the mechanistic nature of the functions of this multifaceted
             and major component of the uterine-placental
             microenvironment.},
   Language = {eng},
   Doi = {10.1095/biolreprod.103.020651},
   Key = {fds174190}
}

@booklet{Shen-gunther03,
   Author = {J. Shen-gunther and R. S. Mannel and J. L. Walker and M. A.
             Gold and G. A. Johnson},
   Title = {Outpatient implantation of a central venous access system in
             gynecologic oncology patients},
   Journal = {Journal Of Reproductive Medicine},
   Volume = {48},
   Number = {11},
   Pages = {875 -- 881},
   Year = {2003},
   Month = {November},
   Key = {Shen-gunther03}
}

@article{fds174236,
   Author = {J Shen-Gunther and RS Mannel and JL Walker and MA Gold and GA
             Johnson},
   Title = {Outpatient implantation of a central venous access system in
             gynecologic oncology patients.},
   Journal = {The Journal of reproductive medicine},
   Volume = {48},
   Number = {11},
   Pages = {875-81},
   Year = {2003},
   Month = {November},
   ISSN = {0024-7758},
   Keywords = {Adult • Aged • Aged, 80 and over • Ambulatory
             Care* • Catheterization, Central Venous •
             Catheters, Indwelling • Equipment Failure • Female
             • Genital Neoplasms, Female • Humans • Middle
             Aged • Oklahoma • Postoperative Complications
             • Prospective Studies • Subclavian Vein •
             drug therapy* • economics* • epidemiology •
             radiography • surgery • utilization*},
   Abstract = {OBJECTIVE: To determine the feasibility, accuracy,
             complications and cost of implantation of the PORT-A-CATH II
             Fluoro-Free venous access system (SIMS Deltec Inc., St.
             Paul, Minnesota) in the procedure room setting. STUDY
             DESIGN: A prospective study of 49 consecutive gynecologic
             oncology patients who underwent 53 PORT-A-CATH II System
             implantations was conducted. Local anesthesia and conscious
             sedation were used for the procedure. To localize and
             position the catheter tip, the CATH-FINDER (SIMS Deltec)
             electronic catheter sensing device was utilized. Demographic
             characteristics, operative data, complication rates, failure
             rates and itemized costs were collected and analyzed.
             RESULTS: For the 53 ports implanted, the mean operative time
             was 54 minutes (range, 39-74) and mean estimated blood loss
             was 17 mL (range, 7-50). Immediate complications included
             failure to thread the catheter or guidewire past the left
             subclavian vein (4 patients), pneumothorax (1) and
             electronic wire fracture (1). All catheter tips were
             positioned accurately, as confirmed by chest radiography.
             The procedural charge ranged from $1,946 to $2,042. The
             CATH-FINDER obviated the need for, and expenses of,
             fluoroscopy, operating room and anesthesia services,
             resulting in savings of approximately $2,000 per procedure.
             CONCLUSION: Implantation of the PORT-A-CATH II System was
             performed safely, accurately and cost effectively in the
             procedure room setting. The advantages of functional
             longevity, low complication rates and reduced cost of this
             port system offer an excellent option for long-term central
             venous access.},
   Language = {eng},
   Key = {fds174236}
}

@booklet{Johnson99b,
   Author = {G. A. Johnson and T. E. Spencer and R. C. Burghardt and F.
             W. Bazer},
   Title = {Ovine osteopontin: I. Cloning and expression of messenger
             ribonucleic acid in the uterus during the periimplantation
             period},
   Journal = {Biology Of Reproduction},
   Volume = {61},
   Number = {4},
   Pages = {884 -- 891},
   Year = {1999},
   Month = {October},
   Key = {Johnson99b}
}

@article{fds174150,
   Author = {GA Johnson and TE Spencer and RC Burghardt and FW
             Bazer},
   Title = {Ovine osteopontin: I. Cloning and expression of messenger
             ribonucleic acid in the uterus during the periimplantation
             period.},
   Journal = {Biology of reproduction},
   Volume = {61},
   Number = {4},
   Pages = {884-91},
   Year = {1999},
   Month = {October},
   ISSN = {0006-3363},
   Keywords = {Amino Acid Sequence • Animals • Base Sequence
             • Blotting, Western • Cloning, Molecular •
             Embryonic Development • Estrus • Female •
             Gene Expression Regulation, Developmental* • In Situ
             Hybridization • Molecular Sequence Data •
             Osteopontin • Pregnancy • Pregnancy, Animal •
             RNA, Messenger • Sheep • Sialoglycoproteins •
             Time Factors • Uterus • biosynthesis •
             biosynthesis* • genetics* • metabolism* •
             physiology • veterinary},
   Abstract = {Trophoblast-derived interferon tau (IFNtau) acts on the
             endometrium to increase secretion of several proteins during
             the pregnancy recognition period in ruminants. One of these
             is a 70-kDa acidic protein that has not been identified. Our
             hypothesis was that the 70-kDa acidic protein is osteopontin
             (OPN). OPN is an acidic glycoprotein that fragments upon
             freezing and thawing or treatment with proteases including
             thrombin. OPN contains a Gly-Arg-Gly-Asp-Ser (GRGDS)
             sequence that binds to cell surface integrins to promote
             cell-cell attachment and cell spreading. Using antisera to
             recombinant human OPN, both 70-kDa and 45-kDa proteins were
             identified in uterine flushings from pregnant ewes by
             Western blotting. A clone containing the entire ovine OPN
             cDNA coding sequence was isolated by screening a Day 15
             pregnant ovine endometrial cDNA library with a partial ovine
             OPN cDNA. In pregnant ewes, steady-state levels of OPN
             endometrial mRNA increased (P < 0. 01) after Day 17. In both
             cyclic and pregnant ewes, in situ hybridization analysis
             showed that OPN mRNA was localized on unidentified immune
             cells within the stratum compactum of the endometrium. In
             pregnant ewes, OPN mRNA was also expressed by the glandular
             epithelium. Results suggest that progesterone and/or IFNtau
             induce expression and secretion of OPN by uterine glands
             during the periimplantation period and that OPN may induce
             adhesion between luminal epithelium and trophectoderm to
             facilitate superficial implantation.},
   Language = {eng},
   Key = {fds174150}
}

@booklet{Johnson99c,
   Author = {G. A. Johnson and R. C. Burghardt and T. E. Spencer and G.
             C. R. Newton and T. L. Ott and F. W. Bazer},
   Title = {Ovine osteopontin: II. Osteopontin and alpha(v)beta(3)
             integrin expression in the uterus and conceptus during the
             periimplantation period},
   Journal = {Biology Of Reproduction},
   Volume = {61},
   Number = {4},
   Pages = {892 -- 899},
   Year = {1999},
   Month = {October},
   Key = {Johnson99c}
}

@article{fds174167,
   Author = {GA Johnson and RC Burghardt and TE Spencer and GR Newton and TL Ott and FW
             Bazer},
   Title = {Ovine osteopontin: II. Osteopontin and alpha(v)beta(3)
             integrin expression in the uterus and conceptus during the
             periimplantation period.},
   Journal = {Biology of reproduction},
   Volume = {61},
   Number = {4},
   Pages = {892-9},
   Year = {1999},
   Month = {October},
   ISSN = {0006-3363},
   Keywords = {Animals • Blotting, Western • Culture Media,
             Conditioned • Culture Techniques •
             Electrophoresis, Polyacrylamide Gel • Embryo, Mammalian
             • Embryonic Development* • Endometrium •
             Female • Osteopontin • Pregnancy • Pregnancy,
             Animal • Receptors, Vitronectin • Sheep •
             Sialoglycoproteins • Time Factors • Uterus •
             biosynthesis* • metabolism • metabolism* •
             veterinary},
   Abstract = {Osteopontin (OPN) is an acidic 70-kDa glycoprotein that is
             cleaved by proteases to yield 45-kDa and 24-kDa fragments.
             The 70-kDa and 45-kDa proteins contain a Gly-Arg-Gly-Asp-Ser
             (GRGDS) sequence that binds to cell surface integrins
             (primarily alpha(v)beta(3) heterodimer) to promote cell-cell
             attachment and cell spreading. A 70-kDa acidic protein was
             previously detected by two-dimensional (2D) PAGE in Day 17
             pregnant endometrial cytosolic extracts using Stainsall and
             identified as immunoreactive OPN using Western blotting.
             Three forms of immunoreactive OPN proteins (70, 45, and 24
             kDa) were detected by 1D PAGE and Western blot analysis of
             endometrial extracts. OPN protein in endometrial extracts
             did not differ between cyclic and pregnant ewes. However,
             the amount of 45-kDa OPN increased in uterine flushings from
             pregnant ewes between Days 11 and 17. Immunoreactive OPN was
             localized to luminal and glandular epithelia of both cyclic
             and pregnant ewes, and to trophectoderm of Day 19
             conceptuses. The alpha(v) and beta(3) integrins were
             detected on Day 19 endometrium and conceptuses by
             immunofluorescence. It was reported that OPN mRNA increases
             in the uterine glands of pregnant ewes and secretion of OPN
             protein into the uterine lumen increases during early
             pregnancy. The present results demonstrate accumulation of
             OPN protein on endometrial LE and conceptus trophectoderm.
             Therefore, it is hypothesized that progesterone and/or
             interferon-tau induce expression, secretion and/or
             proteolytic cleavage of OPN by uterine epithelium. Secreted
             OPN is then available as ligand for alpha(v)beta(3) integrin
             heterodimer on trophectoderm and uterus to 1) stimulate
             changes in morphology of conceptus trophectoderm and 2)
             induce adhesion between luminal epithelium and trophectoderm
             essential for implantation and placentation.},
   Language = {eng},
   Key = {fds174167}
}

@article{fds174188,
   Author = {S Noel and A Herman and GA Johnson and CA Gray, MD Stewart and FW Bazer and A Gertler and TE Spencer},
   Title = {Ovine placental lactogen specifically binds to endometrial
             glands of the ovine uterus.},
   Journal = {Biology of reproduction},
   Volume = {68},
   Number = {3},
   Pages = {772-80},
   Year = {2003},
   Month = {March},
   ISSN = {0006-3363},
   Keywords = {Animals • Binding Sites • Binding, Competitive
             • Blotting, Western • Endometrium • Female
             • Growth Hormone • Interferon Type I • Male
             • Placental Hormones • Placental Lactogen •
             Pregnancy Proteins • Prolactin • RNA • Random
             Allocation • Receptors, Prolactin • Receptors,
             Somatotropin • Reverse Transcriptase Polymerase Chain
             Reaction • Sheep • chemistry • genetics
             • metabolism • metabolism* • pharmacology
             • physiology • ultrastructure •
             veterinary},
   Abstract = {A hormonal servomechanism has been proposed to regulate
             differentiation and function of the endometrial glandular
             epithelium (GE) in the ovine uterus during pregnancy. This
             mechanism involves sequential actions of estrogen,
             progesterone, ovine interferon tau (IFNtau), placental
             lactogen (oPL), and placental growth hormone (oGH). The
             biological actions of oPL in vitro are mediated by
             homodimerization of the prolactin receptor (oPRLR) and
             heterodimerization of the oPRLR and oGH receptor. The
             objectives of the study were to determine the effects of
             intrauterine oPL, oGH, and their combination on endometrial
             histoarchitecture and gene expression and to localize and
             characterize binding sites for oPL in the ovine uterus in
             vivo using an in situ ligand binding assay. Intrauterine
             infusion of oPL and/or oGH following IFNtau into
             ovariectomized ewes treated with progesterone daily
             differentially affected endometrial gland number and
             expression of uterine milk proteins and osteopontin.
             However, neither hormone affected PRLR, insulin-like growth
             factor (IGF)-I, or IGF-II mRNA levels in the endometrium. A
             chimeric protein of placental secretory alkaline phosphatase
             (SEAP) and oPL was used to identify and characterize binding
             sites for oPL in frozen sections of interplacentomal
             endometrium from pregnant ewes. Specific binding of SEAP-oPL
             was detected in the endometrial GE on Days 30, 60, 90, and
             120 of pregnancy. In Day 90 endometrium, SEAP-oPL binding to
             the endometrial GE was displaced completely by oPL and
             prolactin (oPRL) but only partially by oGH. Binding
             experiments using the extracellular domain of the oPRLR also
             showed that iodinated oPL binding sites could be competed
             for by oPRL and oPL but not by oGH. Collectively, results
             indicate that oPL binds to receptors in the endometrial
             glands and that oPRL is more effective than oGH in competing
             for these binding sites. Thus, effects of oPL on the
             endometrial glands may be mediated by receptors for oPRL and
             oGH.},
   Language = {eng},
   Key = {fds174188}
}

@booklet{Noel03,
   Author = {S. Noel and A. Herman and G. A. Johnson and C. A. Gray and M. D. Stewart and F. W. Bazer and A. Gertler and T. E.
             Spencer},
   Title = {Ovine placental lactogen specifically rinds to endometrial
             glands of the ovine uterus},
   Journal = {Biology Of Reproduction},
   Volume = {68},
   Number = {3},
   Pages = {772 -- 780},
   Year = {2003},
   Month = {March},
   Key = {Noel03}
}

@booklet{Carroll99,
   Author = {T. L. Carroll and G. A. Johnson and L. M. Pecora and D. J.
             Mar},
   Title = {Parameter-insensitive and narrow-band synchronization of
             chaotic circuits},
   Journal = {International Journal Of Bifurcation And
             Chaos},
   Volume = {9},
   Number = {11},
   Pages = {2189 -- 2196},
   Year = {1999},
   Month = {November},
   Key = {Carroll99}
}

@booklet{Schuster96,
   Author = {H. G. Schuster and E. Niebur and E. R. Hunt and G. A.
             Johnson and M. Locher},
   Title = {Parametric feedback resonance in chaotic
             systems},
   Journal = {Physical Review Letters},
   Volume = {76},
   Number = {3},
   Pages = {400 -- 403},
   Year = {1996},
   Month = {January},
   Key = {Schuster96}
}

@article{fds132913,
   Author = {HG Schuster and E Niebur and ER Hunt and GA Johnson and M
             Löcher},
   Title = {Parametric feedback resonance in chaotic
             systems.},
   Journal = {Physical review letters},
   Volume = {76},
   Number = {3},
   Pages = {400-403},
   Year = {1996},
   Month = {January},
   ISSN = {1079-7114},
   Language = {ENG},
   Key = {fds132913}
}

@booklet{Johnson96b,
   Author = {G. A. Johnson and D. A. Mortensen and L. J. Young and A. R.
             Martin},
   Title = {Parametric sequential sampling based on multistage
             estimation of the negative binomial parameter
             k},
   Journal = {Weed Science},
   Volume = {44},
   Number = {3},
   Pages = {555 -- 559},
   Year = {1996},
   Key = {Johnson96b}
}

@article{fds132856,
   Author = {BP Drayer and W Olanow and P Burger and GA Johnson and R Herfkens and S
             Riederer},
   Title = {Parkinson plus syndrome: diagnosis using high field MR
             imaging of brain iron.},
   Journal = {Radiology, UNITED STATES},
   Volume = {159},
   Number = {2},
   Pages = {493-8},
   Year = {1986},
   Month = {May},
   ISSN = {0033-8419},
   Keywords = {Adult • Aged • Atrophy • Cerebellar Nuclei
             • Globus Pallidus • Humans • Iron •
             Magnetic Resonance Spectroscopy • Middle Aged •
             Parkinson Disease • Putamen • Substantia Nigra
             • analysis • analysis* • diagnosis* •
             diagnostic use* • pathology},
   Abstract = {The distribution of iron in the brain was analyzed using
             high field strength (1.5 T) magnetic resonance (MR) imaging
             in 14 healthy control individuals and six patients with
             Parkinson plus syndromes (multisystem atrophy and
             progressive supranuclear palsy) who were unresponsive to
             antiparkinsonian therapy. The normal topographic
             distribution of iron in the brain as indicated by high field
             MR images coincided precisely with the distribution of iron
             in the brain as determined by Perls staining for ferric
             iron. In Parkinson plus syndromes, there were abnormally
             increased concentrations of iron (decreased T2 relaxation
             times) in the putamen, and less prominent increases in the
             caudate nucleus and lateral pars compacta of the substantia
             nigra. In high field strength MR images of normal patients,
             the decreased signal intensity in the globus pallidus is
             more prominent than that of the putamen. In MR images of
             patients with Parkinson plus syndromes, the decreased signal
             intensity of the putamen is more prominent than that of the
             globus pallidus.},
   Key = {fds132856}
}

@booklet{Drayer86c,
   Author = {Drayer, BP and Olanow, W and Burger, P and Johnson, GA and Herfkens, R and Riederer, S},
   Title = {Parkinson plus syndrome: diagnosis using high field MR
             imaging of brain iron.},
   Journal = {Radiology},
   Volume = {159},
   Number = {2},
   Pages = {493-498},
   Year = {1986},
   Month = {May},
   ISSN = {0033-8419},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/3961182},
   Abstract = {The distribution of iron in the brain was analyzed using
             high field strength (1.5 T) magnetic resonance (MR) imaging
             in 14 healthy control individuals and six patients with
             Parkinson plus syndromes (multisystem atrophy and
             progressive supranuclear palsy) who were unresponsive to
             antiparkinsonian therapy. The normal topographic
             distribution of iron in the brain as indicated by high field
             MR images coincided precisely with the distribution of iron
             in the brain as determined by Perls staining for ferric
             iron. In Parkinson plus syndromes, there were abnormally
             increased concentrations of iron (decreased T2 relaxation
             times) in the putamen, and less prominent increases in the
             caudate nucleus and lateral pars compacta of the substantia
             nigra. In high field strength MR images of normal patients,
             the decreased signal intensity in the globus pallidus is
             more prominent than that of the putamen. In MR images of
             patients with Parkinson plus syndromes, the decreased signal
             intensity of the putamen is more prominent than that of the
             globus pallidus.},
   Doi = {10.1148/radiology.159.2.3961182},
   Key = {Drayer86c}
}

@booklet{Johnson84b,
   Author = {G. A. Johnson},
   Title = {Partitioned matrices satisfying certain null space
             properties},
   Journal = {Linear Algebra And Its Applications},
   Volume = {57},
   Number = {FEB},
   Pages = {75 -- 85},
   Year = {1984},
   Key = {Johnson84b}
}

@booklet{Todd99,
   Author = {M. D. Todd and G. A. Johnson and C. C. Chang},
   Title = {Passive, light intensity-independent interferometric method
             for fibre Bragg grating interrogation},
   Journal = {Electronics Letters},
   Volume = {35},
   Number = {22},
   Pages = {1970 -- 1971},
   Year = {1999},
   Month = {October},
   Key = {Todd99}
}

@booklet{Baxter89,
   Author = {Baxter, GW and Behringer, RP and Fagert, T and Johnson,
             GA},
   Title = {Pattern formation in flowing sand.},
   Journal = {Phys Rev Lett},
   Volume = {62},
   Number = {24},
   Pages = {2825-2828},
   Year = {1989},
   Month = {June},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/10040101},
   Doi = {10.1103/PhysRevLett.62.2825},
   Key = {Baxter89}
}

@article{fds132809,
   Author = {GW Baxter and RP Behringer and T Fagert and GA Johnson},
   Title = {Pattern formation in flowing sand.},
   Journal = {Phys Rev Lett},
   Volume = {62},
   Number = {24},
   Pages = {2825-2828},
   Year = {1989},
   Month = {June},
   ISSN = {0031-9007},
   Key = {fds132809}
}

@booklet{Miller99,
   Author = {J. R. Miller and S. E. Hurlston and Q. Y. Ma and D. W. Face and D. J. Kountz and J. R. Macfall and L. W. Hedlund and G.
             A. Johnson},
   Title = {Performance of a high-temperature superconducting probe for
             in vivo microscopy at 2.0 T},
   Journal = {Magnetic Resonance In Medicine},
   Volume = {41},
   Number = {1},
   Pages = {72 -- 79},
   Year = {1999},
   Month = {January},
   Key = {Miller99}
}

@article{fds268967,
   Author = {Miller, JR and Hurlston, SE and Ma, QY and Face, DW and Kountz, DJ and MacFall, JR and Hedlund, LW and Johnson, GA},
   Title = {Performance of a high-temperature superconducting probe for
             in vivo microscopy at 2.0 T.},
   Journal = {Magn Reson Med},
   Volume = {41},
   Number = {1},
   Pages = {72-79},
   Year = {1999},
   Month = {January},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/10025613},
   Keywords = {Animals • Artifacts • Brain • Female •
             Heat* • Image Processing, Computer-Assisted •
             Magnetic Resonance Imaging • Microscopy • Models,
             Theoretical • Rats • Rats, Inbred F344 •
             Thermal Conductivity • anatomy & histology •
             methods* • physiology*},
   Abstract = {The use of a high-temperature superconducting probe for in
             vivo magnetic resonance microscopy at 2 T is described. To
             evaluate the performance of the probe, a series of SNR
             comparisons are carried out. The SNR increased by a factor
             of 3.7 compared with an equivalent copper coil. Quantitative
             measures of the SNR gain are in good agreement with
             theoretical predictions. A number of issues that are unique
             to the application of HTS coils are examined, including the
             difficulty in obtaining homogenous excitation without
             degrading the SNR of the probe. The use of the HTS probe in
             transmit-receive mode is simple to implement but results in
             nonuniform excitation. The effect of using the probe in this
             mode of operation on the T1 and T2 contrast is investigated.
             Methods for improving homogeneity are explored, such as
             employing a transmit volume coil. It is found that the cost
             of using an external transmit coil is an increased probe
             noise temperature and a reduced SNR by approximately 30%.
             Other important aspects of the probe are considered,
             including the effect of temperature on probe stability.
             Three-dimensional in vivo imaging sets are acquired to
             assess the stability of the probe for long scans.
             High-resolution images of the rat brain demonstrate the
             utility of the probe for microscopy applications.},
   Doi = {10.1002/(sici)1522-2594(199901)41:1<72::aid-mrm11>3.0.co;2-a},
   Key = {fds268967}
}

@booklet{Black95,
   Author = {Black, RD and Early, TA and Johnson, GA},
   Title = {Performance of a High-Temperature Superconducting Resonator
             for High-Field Imaging},
   Journal = {Journal of Magnetic Resonance, Series A},
   Volume = {113},
   Number = {1},
   Pages = {74-80},
   Publisher = {Elsevier BV},
   Year = {1995},
   Month = {January},
   ISSN = {1064-1858},
   url = {http://dx.doi.org/10.1006/jmra.1995.1058},
   Abstract = {The practicalities involved with the use of a
             superconducting microimaging probe are outlined so that the
             power and problems associated with this technology can be
             assessed. The nonlinearity of the transmission
             characteristics of this class of probe, the intrinsic limits
             on bandwidth, the long ring-down times, the potential for
             spin damping, and the difficulties of suppressing Johnson
             noise are all discussed. Recent refinements that have
             delivered a factor of 30 gain in SNR (signal-to-noise ratio)
             relative to copper coils at room temperature are presented.
             Further reductions in noise sources should yield a gain of a
             factor of 60 in SNR. © 1995 Academic Press,
             Inc.},
   Doi = {10.1006/jmra.1995.1058},
   Key = {Black95}
}

@booklet{Suddarth87,
   Author = {Suddarth, SA and Johnson, GA and Sherrier, RH and Ravin,
             CE},
   Title = {Performance of high-resolution monitors for digital chest
             imaging.},
   Journal = {Med Phys},
   Volume = {14},
   Number = {2},
   Pages = {253-257},
   Year = {1987},
   ISSN = {0094-2405},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/3587149},
   Abstract = {High-resolution cathode-ray tubes (CRT's) are currently the
             most viable soft-copy display for digital radiography. We
             present here methods for measuring large-area contrast ratio
             and detail contrast ratio. A two-dimensional charge coupled
             device (ccd) array signal-averaged with a video frame buffer
             permits linear microradiometric measure of individual beam
             lines. Results from three different 1000-line monitors
             demonstrate the shift variance of resolution. The detail
             contrast ratio (or modulation depth) was found to vary from
             100% to less than 10% across the face of one CRT. Dynamic
             focus in both the horizontal and vertical deflection
             circuitry proved effective in reducing this shift variance.
             Comparisons of three phosphors demonstrate the utility of
             long persistence phosphors (P164) for static display in
             producing brighter images with less flicker. Recommendations
             for CRT design and selection for high-resolution digital
             radiography are included.},
   Doi = {10.1118/1.596079},
   Key = {Suddarth87}
}

@article{fds132798,
   Author = {SA Suddarth and GA Johnson and RH Sherrier and CE
             Ravin},
   Title = {Performance of high-resolution monitors for digital chest
             imaging.},
   Journal = {Medical physics, UNITED STATES},
   Volume = {14},
   Number = {2},
   Pages = {253-7},
   ISSN = {0094-2405},
   Keywords = {Computer Systems* • Humans • Radiographic Image
             Enhancement • Radiography, Thoracic •
             instrumentation*},
   Abstract = {High-resolution cathode-ray tubes (CRT's) are currently the
             most viable soft-copy display for digital radiography. We
             present here methods for measuring large-area contrast ratio
             and detail contrast ratio. A two-dimensional charge coupled
             device (ccd) array signal-averaged with a video frame buffer
             permits linear microradiometric measure of individual beam
             lines. Results from three different 1000-line monitors
             demonstrate the shift variance of resolution. The detail
             contrast ratio (or modulation depth) was found to vary from
             100% to less than 10% across the face of one CRT. Dynamic
             focus in both the horizontal and vertical deflection
             circuitry proved effective in reducing this shift variance.
             Comparisons of three phosphors demonstrate the utility of
             long persistence phosphors (P164) for static display in
             producing brighter images with less flicker. Recommendations
             for CRT design and selection for high-resolution digital
             radiography are included.},
   Key = {fds132798}
}

@article{fds204245,
   Author = {JD Tobias and GA Johnson and M Patel},
   Title = {Performance of the On-Q pain infusion device during
             hyperbaric therapy.},
   Journal = {Anesthesia and analgesia},
   Volume = {113},
   Number = {2},
   Pages = {275-7},
   Year = {2011},
   Month = {August},
   ISSN = {1526-7598},
   url = {http://dx.doi.org/10.1213/ANE.0b013e31821c4035},
   Keywords = {Air Pressure • Amides • Anesthesia, Conduction
             • Anesthetics, Local • Data Display • Diving
             • Fluid Therapy • Hyperbaric Oxygenation •
             Infusion Pumps* • Pain, Postoperative •
             Prospective Studies • administration & dosage •
             drug therapy • instrumentation • methods* •
             physiology},
   Abstract = {BACKGROUND: There are reports in the literature regarding
             the effects of hyperbaric conditions on various medical
             devices. In the current study we evaluated the performance
             of an elastomeric infusion device during exposure to a
             hyperbaric environment. METHODS: Nineteen disposable 400-mL
             On-Q pain ball infusion devices were filled with 0.2%
             ropivacaine and connected to an infusion catheter. The
             regulator of the device was set to deliver 14 mL/h.
             Hyperbaric oxygen therapy included 7 minutes to achieve the
             desired hyperbaric pressure level, 90 minutes at the
             specific pressure (atm), and 7 minutes to return to normal
             atmospheric pressure (1 atm), thereby resulting in a study
             interval or dive of 104 minutes. The trials were performed
             for the devices in the following sequence of dives with a
             return to 1 atm between: 1, 2, 2.4, 2.8, 3, and 1 atm. The
             fluid delivered during each dive was measured with a
             graduated column. Additionally, the collection device was
             weighed before and at the completion of each dive to
             determine the change in weight as a measure of the total
             amount of fluid infused. The output over 104 minutes was
             also studied in 5 infusion devices without hyperbaric
             pressure (control group). RESULTS: No difference in output
             of the devices was noted when comparing the study group and
             the control group. Although there was a decrease in the
             output of the devices over 8 to 9 hours, no difference
             between the 2 groups was noted. CONCLUSIONS: This
             preliminary investigation demonstrates no clinically
             significant change in the function of the On-Q pain device
             during exposure to a hyperbaric environment.},
   Language = {eng},
   Doi = {10.1213/ANE.0b013e31821c4035},
   Key = {fds204245}
}

@article{fds174183,
   Author = {GA JOHNSON and RH MCCLUER},
   Title = {PERIODATE OXIDATION STUDIES OF HUMAN BRAIN
             GANGLIOSIDES.},
   Journal = {Biochimica et biophysica acta},
   Volume = {84},
   Pages = {587-95},
   Year = {1964},
   Month = {October},
   ISSN = {0006-3002},
   Keywords = {CHROMATOGRAPHY* • GALACTOSE* • GANGLIOSIDES*
             • GLUCOSE* • NEURAMINIC ACIDS* •
             OXIDATION-REDUCTION* • PERIODIC ACIDS*},
   Language = {eng},
   Key = {fds174183}
}

@booklet{Fichter03,
   Author = {C. R. Fichter and G. A. Johnson and S. R. Braddock and J. D.
             Tobias},
   Title = {Perioperative care of the child with the Johanson-Blizzard
             syndrome},
   Journal = {Paediatric Anaesthesia},
   Volume = {13},
   Number = {1},
   Pages = {72 -- 75},
   Year = {2003},
   Month = {January},
   Key = {Fichter03}
}

@article{fds174068,
   Author = {CR Fichter and GA Johnson, SR Braddock and JD Tobias},
   Title = {Perioperative care of the child with the Johanson-Blizzard
             syndrome.},
   Journal = {Paediatric anaesthesia},
   Volume = {13},
   Number = {1},
   Pages = {72-5},
   Year = {2003},
   Month = {January},
   ISSN = {1155-5645},
   Keywords = {Abnormalities, Multiple • Anesthesia, Inhalation*
             • Anesthetics, Inhalation • Child, Preschool
             • Dwarfism • Female • Genes, Recessive •
             Humans • Methyl Ethers • Nose • Syndrome
             • abnormalities • complications •
             surgery*},
   Abstract = {The Johanson-Blizzard Syndrome (JBS) is an autosomal
             recessive disorder with a characteristic phenotype,
             including dwarfism, a beaked nose with aplastic alae nasi, a
             high forehead, mid-line ectodermal scalp defects with sparse
             hair and absent eyelashes/eyebrows, prominent scalp veins,
             low set ears, a large anterior fontanelle, micrognathia,
             thin lips, absent permanent dentition and microcephaly. In
             addition to the characteristic facial features, associated
             conditions include congenital heart disease,
             exocrine/endocrine pancreatic dysfunction, hypothyroidism,
             hypopituitarism, mental retardation, sensorineural hearing
             loss and vesico-ureteral reflux. A case is presented and the
             potential anaesthetic implications of this syndrome are
             discussed.},
   Language = {eng},
   Key = {fds174068}
}

@article{fds174311,
   Author = {W Veldkamp and HH Keasling and GA Johnson and WA Freyburger and RJ
             Collins},
   Title = {Pharmacologic studies with 3-(phenylpropoxy)guanidine
             cyclohexanesulfamate.},
   Journal = {Journal of pharmaceutical sciences},
   Volume = {56},
   Number = {7},
   Pages = {829-33},
   Year = {1967},
   Month = {July},
   ISSN = {0022-3549},
   Keywords = {Animals • Appetite • Appetite Depressants •
             Behavior, Animal • Blood Pressure • Body Weight
             • Brain • Cats • Cyclohexanes •
             Dextroamphetamine • Dogs • Drug Synergism •
             Electric Stimulation • Electrophysiology •
             Electroshock • Guanidines • Mice • Movement
             • Norepinephrine • Reserpine • Serotonin
             • Temperature • Tryptamines • drug effects
             • drug effects* • metabolism • pharmacology
             • pharmacology* • toxicity},
   Language = {eng},
   Key = {fds174311}
}

@article{fds204268,
   Author = {M Lin and Y Qi and AF Chen and CT Badea and GA Johnson},
   Title = {Phenylephrine-modulated cardiopulmonary blood flow measured
             with use of X-ray digital subtraction angiography.},
   Journal = {Journal of pharmacological and toxicological
             methods},
   Volume = {64},
   Number = {2},
   Pages = {180-6},
   Year = {2011},
   Month = {August},
   ISSN = {1873-488X},
   url = {http://dx.doi.org/10.1016/j.vascn.2011.08.001},
   Abstract = {BACKGROUND: Cardiopulmonary blood flow is an important
             indicator of organ function. Limitations in measuring blood
             flow in live rodents suggest that rapid physiological
             changes may be overlooked. For instance, relative
             measurements limit imaging to whole organs or large sections
             without adequately visualizing vasculature. Additionally,
             current methods use small samples and invasive techniques
             that often require killing animals, limiting sampling speed,
             or both. A recently developed high spatial- and
             temporal-resolution X-ray digital subtraction angiography
             (DSA) system visualizes vasculature and measures blood flow
             in rodents. This study was the first to use this system to
             measure changes in cardiopulmonary blood flow in rats after
             administering the vasoconstrictor phenylephrine. METHODS:
             Cardiopulmonary blood flow and vascular anatomy were
             assessed in 11 rats before, during, and after recovery from
             phenylephrine. After acquiring DSA images at 12 time points,
             a calibrated non-parametric deconvolution technique using
             singular value decomposition (SVD) was applied to calculate
             quantitative aortic blood flow in absolute metrics (mL/min).
             Trans-pulmonary transit time was calculated as the time
             interval between maximum signal enhancement in the pulmonary
             trunk and aorta. Pulmonary blood volume was calculated based
             on the central volume principle. Statistical analysis
             compared differences in trans-pulmonary blood volume and
             pressure, and aortic diameter using paired t-tests on
             baseline, peak, and late-recovery time points. RESULTS:
             Phenylephrine had dramatic qualitative and quantitative
             effects on vascular anatomy and blood flow. Major vessels
             distended significantly (aorta, ~1.2-times baseline) and
             mean arterial blood pressure increased ~2 times. Pulmonary
             blood volume, flow, pressure, and aortic diameter were not
             significantly different between baseline and late recovery,
             but differences were significant between baseline and peak,
             as well as peak and recovery time points. CONCLUSIONS: The
             DSA system with calibrated SVD technique acquired blood flow
             measurements every 30s with a high level of regional
             specificity, thus providing a new option for in vivo
             functional assessment in small animals.},
   Language = {eng},
   Doi = {10.1016/j.vascn.2011.08.001},
   Key = {fds204268}
}

@article{fds268809,
   Author = {Lin, M and Qi, Y and Chen, AF and Badea, CT and Johnson,
             GA},
   Title = {Phenylephrine-modulated cardiopulmonary blood flow measured
             with use of X-ray digital subtraction angiography.},
   Journal = {J Pharmacol Toxicol Methods},
   Volume = {64},
   Number = {2},
   Pages = {180-186},
   Year = {2011},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/21846505},
   Abstract = {INTRODUCTION: Cardiopulmonary blood flow is an important
             indicator of organ function. Limitations in measuring blood
             flow in live rodents suggest that rapid physiological
             changes may be overlooked. For instance, relative
             measurements limit imaging to whole organs or large sections
             without adequately visualizing vasculature. Additionally,
             current methods use small samples and invasive techniques
             that often require killing animals, limiting sampling speed,
             or both. A recently developed high spatial- and
             temporal-resolution X-ray digital subtraction angiography
             (DSA) system visualizes vasculature and measures blood flow
             in rodents. This study was the first to use this system to
             measure changes in cardiopulmonary blood flow in rats after
             administering the vasoconstrictor phenylephrine. METHODS:
             Cardiopulmonary blood flow and vascular anatomy were
             assessed in 11 rats before, during, and after recovery from
             phenylephrine. After acquiring DSA images at 12 time points,
             a calibrated non-parametric deconvolution technique using
             singular value decomposition (SVD) was applied to calculate
             quantitative aortic blood flow in absolute metrics (mL/min).
             Trans-pulmonary transit time was calculated as the time
             interval between maximum signal enhancement in the pulmonary
             trunk and aorta. Pulmonary blood volume was calculated based
             on the central volume principle. Statistical analysis
             compared differences in trans-pulmonary blood volume and
             pressure, and aortic diameter using paired t-tests on
             baseline, peak, and late-recovery time points. RESULTS:
             Phenylephrine had dramatic qualitative and quantitative
             effects on vascular anatomy and blood flow. Major vessels
             distended significantly (aorta, ~1.2-times baseline) and
             mean arterial blood pressure increased ~2 times. Pulmonary
             blood volume, flow, pressure, and aortic diameter were not
             significantly different between baseline and late recovery,
             but differences were significant between baseline and peak,
             as well as peak and recovery time points. DISCUSSION: The
             DSA system with calibrated SVD technique acquired blood flow
             measurements every 30s with a high level of regional
             specificity, thus providing a new option for in vivo
             functional assessment in small animals.},
   Doi = {10.1016/j.vascn.2011.08.001},
   Key = {fds268809}
}

@article{fds174245,
   Author = {MM Joyce, JR Burghardt and RC Burghardt and RN Hooper and LA Jaeger and TE Spencer and FW Bazer and GA Johnson},
   Title = {Pig conceptuses increase uterine interferon-regulatory
             factor 1 (IRF1), but restrict expression to stroma through
             estrogen-induced IRF2 in luminal epithelium.},
   Journal = {Biology of reproduction},
   Volume = {77},
   Number = {2},
   Pages = {292-302},
   Year = {2007},
   Month = {August},
   ISSN = {0006-3363},
   url = {http://dx.doi.org/10.1095/biolreprod.107.060939},
   Keywords = {Animals • Endometrium • Epithelium •
             Estradiol • Female • Fetus • Gene Expression
             • In Situ Hybridization • Interferon Regulatory
             Factor-1 • Interferon Regulatory Factor-2 •
             Interferons • Pregnancy • RNA, Messenger •
             Swine • Uterus • administration & dosage* •
             analysis • chemistry • chemistry* • drug
             effects • embryology* • genetics* •
             pharmacology • physiology*},
   Abstract = {Pig conceptuses secrete estrogen for pregnancy recognition,
             and they secrete interferons (IFNs) gamma and delta during
             the peri-implantation period. The uterine effects of pig
             IFNs are not known, although ruminant conceptuses secrete
             IFN tau for pregnancy recognition, and this increases the
             expression of IFN-stimulated genes (ISGs) in the
             endometrium. In sheep, the transcriptional repressor
             interferon-regulatory factor 2 (IRF2) is expressed in the
             endometrial luminal epithelium (LE) and appears to restrict
             IFN tau induction of most ISGs, including IRF1, to the
             stroma and glands. Interestingly, MX1, which is an ISG in
             sheep, is also expressed in the endometrial stroma of
             pregnant pigs. The objective of the present study was to
             determine if estrogen and/or conceptus secretory proteins
             (CSPs) that contain IFNs regulate IRF1 and IRF2 in pig
             endometria. The endometrial levels of IRF1 and IRF2 were low
             throughout the estrus cycle. After Day 12 of pregnancy, the
             levels of the classical ISGs, which include IRF1, STAT2,
             MIC, and B2M, increased in the overall endometrium, with
             expression of IRF1 and STAT2 being specifically localized to
             the stroma. IRF2 increased in the LE after Day 12. To
             determine the effects of estrogen, pigs were treated with 17
             beta-estradiol benzoate (E2). To determine the CSP effects,
             pigs were treated with E2 and implanted with mini-osmotic
             pumps that delivered control serum proteins (CX) to one
             ligated uterine horn and CSP to the other horn. Estrogen
             increased the level of IRF2 in the endometrial LE. The
             administration of E2 and infusion of CSP increased the level
             of IRF1 in the stroma. These results suggest that conceptus
             estrogen induces IRF2 in the LE and limits the induction of
             IRF1 by conceptus IFNs to the stroma. The cell-specific
             expression of IRF1 and IRF2 in the pig endometrium
             highlights the complex and overlapping events that are
             associated with gene expression during the peri-implantation
             period, when pregnancy recognition signaling and uterine
             remodeling for implantation and placentation are necessary
             for successful pregnancy.},
   Language = {eng},
   Doi = {10.1095/biolreprod.107.060939},
   Key = {fds174245}
}

@article{fds174271,
   Author = {MM Joyce and RC Burghardt and RD Geisert, JR Burghardt and RN Hooper and JW Ross, MD Ashworth and GA Johnson},
   Title = {Pig conceptuses secrete estrogen and interferons to
             differentially regulate uterine STAT1 in a temporal and cell
             type-specific manner.},
   Journal = {Endocrinology},
   Volume = {148},
   Number = {9},
   Pages = {4420-31},
   Year = {2007},
   Month = {September},
   ISSN = {0013-7227},
   url = {http://dx.doi.org/10.1210/en.2007-0505},
   Keywords = {Animals • Blastocyst • Embryo Implantation •
             Embryonic Development • Estradiol • Female •
             Gene Expression Regulation* • Pregnancy • STAT1
             Transcription Factor • Swine • Uterus •
             analogs & derivatives • cytology • cytology*
             • drug effects • genetics* • pharmacology
             • physiology • physiology*},
   Abstract = {Conceptus trophectoderm and uterine luminal epithelial cells
             interact via endocrine, paracrine, and autocrine modulators
             to mediate pregnancy recognition and implantation. Pig
             conceptuses not only release estrogens for pregnancy
             recognition but also secrete interferons during
             implantation. Because interferon-stimulated genes are
             increased by interferons secreted for pregnancy recognition
             in ruminants, we asked whether the interferon-stimulated
             gene, STAT1, is up-regulated in pig endometrium by conceptus
             estrogens and/or interferons. STAT1 expression in response
             to day of pregnancy, estrogen injection, and intrauterine
             infusion of conceptus secretory proteins in pigs indicated
             1) estrogen increases STAT1 in luminal epithelial cells, 2)
             conceptus secretory proteins that contain interferons
             increase STAT1 in stroma, 3) STAT1 increases in close
             proximity to the conceptus, and 4) early estrogen results in
             conceptus death and no STAT1 in stroma. The interactions of
             estrogen and interferons to regulate cell-type-specific
             expression of STAT1 highlight the complex interplay between
             endometrium and conceptus for pregnancy recognition and
             implantation.},
   Language = {eng},
   Doi = {10.1210/en.2007-0505},
   Key = {fds174271}
}

@booklet{Buhl89,
   Author = {A. E. Buhl and T. T. Kawabe and D. J. Waldon and K. A.
             Knight and G. A. Johnson and C. J. Walker and A. R.
             Diani},
   Title = {Pigmentation affects the distribution of mnx in
             hair-follicles but does not influence its
             activity},
   Journal = {Clinical Research},
   Volume = {37},
   Number = {2},
   Pages = {A745 -- A745},
   Year = {1989},
   Month = {April},
   Key = {Buhl89}
}

@booklet{Buhl89a,
   Author = {A. E. Buhl and T. T. Kawabe and D. J. Waldon and K. A.
             Knight and G. A. Johnson and C. J. Walker and A. R.
             Diani},
   Title = {Pigmentation affects the distribution of mnx in
             hair-follicles but does not influence its
             activity},
   Journal = {Journal Of Investigative Dermatology},
   Volume = {92},
   Number = {3},
   Pages = {409 -- 409},
   Year = {1989},
   Month = {March},
   Key = {Buhl89a}
}

@article{fds319488,
   Author = {Macfall, JS and Johnson, GA},
   Title = {Plants, seeds, roots, and soils as applications of magnetic
             resonance microscopy},
   Journal = {eMagRes},
   Volume = {1},
   Number = {1},
   Pages = {147-154},
   Publisher = {JOHN WILEY & SONS LTD},
   Year = {2012},
   Month = {January},
   url = {http://dx.doi.org/10.1002/9780470034590.emrstm0396},
   Abstract = {High-resolution magnetic resonance microscopy is discussed
             as a useful tool in the study of plant structure and
             physiology. In contrast to animals, plants have a relatively
             homogenous distribution of water throughout the tissues.
             High quality images highlighting both structural and
             physiological differences can be acquired of plant
             specimens, however, based on traditional MR parameters of
             T1, T2 and susceptibility effects from air filled spaces.
             Typical in plane resolutions of 5-40μm3 can be acquired,
             showing significant contrasts between tissues. Additionally,
             MR microscopy offers the ability to visualize and study
             plant roots in situ, without removal from the soil
             substrate. Applications of MR microscopy to plants includes
             studies of developmental anatomy, physiological changes with
             maturation, environmental physiology, pathologies, and the
             study of intact roots in soil.},
   Doi = {10.1002/9780470034590.emrstm0396},
   Key = {fds319488}
}

@booklet{Robinson81,
   Author = {D. S. Robinson and G. A. Johnson and J. Corcella and A. Nies and D. Howard and T. B. Cooper},
   Title = {Plasma 3,4-dihydroxyphenylglycol, catecholamines, and
             anti-depressant drug levels during treatment of
             depression},
   Journal = {Clinical Pharmacology \& Therapeutics},
   Volume = {29},
   Number = {2},
   Pages = {277 -- 277},
   Year = {1981},
   Key = {Robinson81}
}

@article{fds174189,
   Author = {DS Robinson and GA Johnson and A Nies and J Corcella and TB Cooper and D
             Albright, D Howard},
   Title = {Plasma levels of catecholamines and dihydroxyphenylglycol
             during antidepressant drug treatment.},
   Journal = {Journal of clinical psychopharmacology},
   Volume = {3},
   Number = {5},
   Pages = {282-7},
   Year = {1983},
   Month = {October},
   ISSN = {0271-0749},
   Keywords = {Adult • Aged • Amitriptyline • Antidepressive
             Agents • Blood Platelets • Catecholamines •
             Clinical Trials as Topic • Depressive Disorder •
             Double-Blind Method • Female • Glycols •
             Humans • Male • Methoxyhydroxyphenylglycol •
             Middle Aged • Monoamine Oxidase • Phenelzine
             • Psychiatric Status Rating Scales • Time Factors
             • analogs & derivatives • blood • blood*
             • drug therapy • enzymology • therapeutic use
             • therapeutic use*},
   Abstract = {Plasma norepinephrine, epinephrine, and 3,4-dihydroxyphenylglycol
             levels were measured in depressed outpatients treated in a
             double-blind controlled clinical trial with 150 mg/day of
             amitriptyline or 60 mg/day of phenelzine for 6 weeks. Both
             antidepressant drug treatments were associated with a
             significant decline in plasma dihydroxyphenylglycol
             concentrations, which was more pronounced with phenelzine.
             Plasma norepinephrine levels also declined during phenelzine
             but not amitriptyline treatment, and the posttreatment
             values correlated with clinical improvement with the
             monoamine oxidase inhibiting drug. Reductions in
             norepinephrine and dihydroxyphenylglycol correlated highly
             with the degree of platelet monoamine oxidase inhibition.
             Mechanisms of these antidepressant drug effects on amine
             metabolism and their implications are discussed.},
   Language = {eng},
   Key = {fds174189}
}

@booklet{Johnson87b,
   Author = {G. A. Johnson and V. J. Kapoor and P. G.
             Young},
   Title = {Plasma-deposited germanium nitride on indium-phosphide},
   Journal = {Journal Of The Electrochemical Society},
   Volume = {134},
   Number = {8B},
   Pages = {C430 -- C430},
   Year = {1987},
   Month = {August},
   Key = {Johnson87b}
}

@booklet{Robinson83,
   Author = {D. S. Robinson and G. A. Johnson and A. Nies and J. Corcella and T. B. Cooper and D. Albright and D. Howard},
   Title = {Plasma-levels of catecholamines and dihydroxyphenylglycol
             during anti-depressant drug-treatment},
   Journal = {Journal Of Clinical Psychopharmacology},
   Volume = {3},
   Number = {5},
   Pages = {282 -- 287},
   Year = {1983},
   Key = {Robinson83}
}

@article{fds174278,
   Author = {GA Johnson},
   Title = {Political Developments in Prehistory.},
   Journal = {Science (New York, N.Y.)},
   Volume = {216},
   Number = {4548},
   Pages = {867-869},
   Year = {1982},
   Month = {May},
   ISSN = {1095-9203},
   url = {http://dx.doi.org/10.1126/science.216.4548.867},
   Language = {ENG},
   Doi = {10.1126/science.216.4548.867},
   Key = {fds174278}
}

@article{fds174085,
   Author = {G Wu and FW Bazer and J Hu and GA Johnson and TE Spencer},
   Title = {Polyamine synthesis from proline in the developing porcine
             placenta.},
   Journal = {Biology of reproduction},
   Volume = {72},
   Number = {4},
   Pages = {842-50},
   Year = {2005},
   Month = {April},
   ISSN = {0006-3363},
   url = {http://dx.doi.org/10.1095/biolreprod.104.036293},
   Keywords = {1-Pyrroline-5-Carboxylate Dehydrogenase • Amniotic
             Fluid • Animals • Arginase • Carbon
             Radioisotopes • Female • Fetal Development •
             Male • Methionine • Ornithine •
             Oxidoreductases Acting on CH-NH Group Donors • Placenta
             • Polyamines • Pregnancy • Proline •
             Putrescine • S-Adenosylmethionine • Spermidine
             • Spermine • Sus scrofa • diagnostic use
             • growth & development* • metabolism •
             metabolism* • physiology*},
   Abstract = {Polyamines (putrescine, spermidine, and spermine) are
             essential for placental growth and angiogenesis. However,
             little is known about polyamine synthesis in the porcine
             placenta during conceptus development. The present study was
             conducted to test the hypothesis that arginine and proline
             are the major sources of ornithine for placental polyamine
             production in pigs. Placentae, amniotic fluid, and allantoic
             fluid were obtained from gilts on Days 20, 30, 35, 40, 45,
             50, 60, 90, and 110 of the 114-day gestation (n = 6 per
             day). Placentae as well as amniotic and allantoic fluids
             were analyzed for arginase, proline oxidase, ornithine
             aminotransferase (OAT), ornithine decarboxylase (ODC),
             proline transport, concentrations of amino acids and
             polyamines, and polyamine synthesis using established
             radiochemical and chromatographic methods. Neither arginase
             activity nor conversion of arginine into polyamines was
             detected in the porcine placenta. In contrast, both proline
             and ornithine were converted into putrescine, spermidine,
             and spermine in placental tissue throughout pregnancy. The
             activities of proline oxidase, OAT, and ODC as well as
             proline transport, polyamine synthesis from proline, and
             polyamine concentrations increased markedly between Days 20
             and 40 of gestation, declined between Days 40 and 90 of
             gestation, and remained at the reduced level through Day 110
             of gestation. Proline oxidase and OAT, but not arginase,
             were present in allantoic and amniotic fluids for the
             production of ornithine (the immediate substrate for
             polyamine synthesis). The activities of these two enzymes as
             well as the concentrations of ornithine and total polyamines
             in fetal fluids were highest at Day 40 but lowest at Days
             20, 90, and 110 of gestation. These results indicate that
             proline is the major amino acid for polyamine synthesis in
             the porcine placenta and that the activity of this synthetic
             pathway is maximal during early pregnancy, when placental
             growth is most rapid. Our novel findings provide a new base
             of information for future studies to define the role of
             proline in fetoplacental growth and development.},
   Language = {eng},
   Doi = {10.1095/biolreprod.104.036293},
   Key = {fds174085}
}

@booklet{Wu04,
   Author = {G. Y. Wu and T. E. Spencer and G. A. Johnson and F. W.
             Bazer},
   Title = {Polyamine synthesis from proline in the developing porcine
             placenta.},
   Journal = {Biology Of Reproduction},
   Pages = {158 -- 158},
   Year = {2004},
   Key = {Wu04}
}

@article{fds268819,
   Author = {Veraart, J and Leergaard, TB and Antonsen, BT and Van Hecke and W and Blockx, I and Jeurissen, B and Jiang, Y and Van der Linden and A and Johnson, GA and Verhoye, M and Sijbers, J},
   Title = {Population-averaged diffusion tensor imaging atlas of the
             Sprague Dawley rat brain.},
   Journal = {Neuroimage},
   Volume = {58},
   Number = {4},
   Pages = {975-983},
   Year = {2011},
   Month = {October},
   ISSN = {1095-9572},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/21749925},
   Keywords = {Algorithms • Animals • Atlases as Topic* •
             Brain • Brain Mapping • Diffusion Tensor Imaging
             • Magnetic Resonance Imaging • Male •
             Nonlinear Dynamics • Rats • Rats, Sprague-Dawley
             • anatomy & histology* • methods*},
   Abstract = {Rats are widely used in experimental neurobiological
             research, and rat brain atlases are important resources for
             identifying brain regions in the context of experimental
             microsurgery, tissue sampling, and neuroimaging, as well as
             comparison of findings across experiments. Currently, most
             available rat brain atlases are constructed from
             histological material derived from single specimens, and
             provide two-dimensional or three-dimensional (3D) outlines
             of diverse brain regions and fiber tracts. Important
             limitations of such atlases are that they represent
             individual specimens, and that finer details of tissue
             architecture are lacking. Access to more detailed 3D brain
             atlases representative of a population of animals is needed.
             Diffusion tensor imaging (DTI) is a unique neuroimaging
             modality that provides sensitive information about
             orientation structure in tissues, and is widely applied in
             basic and clinical neuroscience investigations. To
             facilitate analysis and assignment of location in rat brain
             neuroimaging investigations, we have developed a
             population-averaged three-dimensional DTI atlas of the
             normal adult Sprague Dawley rat brain. The atlas is
             constructed from high resolution ex vivo DTI images, which
             were nonlinearly warped into a population-averaged in vivo
             brain template. The atlas currently comprises a selection of
             manually delineated brain regions, the caudate-putamen
             complex, globus pallidus, entopeduncular nucleus, substantia
             nigra, external capsule, corpus callosum, internal capsule,
             cerebral peduncle, fimbria of the hippocampus, fornix,
             anterior commisure, optic tract, and stria terminalis. The
             atlas is freely distributed and potentially useful for
             several purposes, including automated and manual delineation
             of rat brain structural and functional imaging
             data.},
   Language = {eng},
   Doi = {10.1016/j.neuroimage.2011.06.063},
   Key = {fds268819}
}

@article{fds341988,
   Author = {Calabrese, E and Adil, SM and Cofer, G and Perone, CS and Cohen-Adad, J and Lad, SP and Johnson, GA},
   Title = {Postmortem diffusion MRI of the entire human spinal cord at
             microscopic resolution.},
   Journal = {Neuroimage Clin},
   Volume = {18},
   Pages = {963-971},
   Year = {2018},
   url = {http://dx.doi.org/10.1016/j.nicl.2018.03.029},
   Abstract = {The human spinal cord is a central nervous system structure
             that plays an important role in normal motor and sensory
             function, and can be affected by many debilitating
             neurologic diseases. Due to its clinical importance, the
             spinal cord is frequently the subject of imaging research.
             Common methods for visualizing spinal cord anatomy and
             pathology include histology and magnetic resonance imaging
             (MRI), both of which have unique benefits and drawbacks.
             Postmortem microscopic resolution MRI of fixed specimens,
             sometimes referred to as magnetic resonance microscopy
             (MRM), combines many of the benefits inherent to both
             techniques. However, the elongated shape of the human spinal
             cord, along with hardware and scan time limitations, have
             restricted previous microscopic resolution MRI studies (both
             in vivo and ex vivo) to small sections of the cord. Here we
             present the first MRM dataset of the entire postmortem human
             spinal cord. These data include 50 μm isotropic
             resolution anatomic image data and 100 μm isotropic
             resolution diffusion data, made possible by a 280 h long
             multi-segment acquisition and automated image segment
             composition. We demonstrate the use of these data for spinal
             cord lesion detection, automated volumetric gray matter
             segmentation, and quantitative spinal cord morphometry
             including estimates of cross sectional dimensions and gray
             matter fraction throughout the length of the
             cord.},
   Doi = {10.1016/j.nicl.2018.03.029},
   Key = {fds341988}
}

@article{fds292755,
   Author = {Calabrese, E and Hickey, P and Hulette, C and Zhang, J and Parente, B and Lad, SP and Johnson, GA},
   Title = {Postmortem Diffusion MRI of the Human Brainstem and Thalamus
             for Deep Brain Stimulator Electrode Localization},
   Journal = {MOVEMENT DISORDERS},
   Volume = {30},
   Number = {10},
   Pages = {E6-E6},
   Publisher = {WILEY-BLACKWELL},
   Year = {2015},
   Month = {September},
   ISSN = {0885-3185},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000360759500015&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {fds292755}
}

@article{fds268696,
   Author = {Calabrese, E and Hickey, P and Hulette, C and Zhang, J and Parente, B and Lad, SP and Johnson, GA},
   Title = {Postmortem diffusion MRI of the human brainstem and thalamus
             for deep brain stimulator electrode localization.},
   Journal = {Hum Brain Mapp},
   Volume = {36},
   Number = {8},
   Pages = {3167-3178},
   Year = {2015},
   Month = {August},
   ISSN = {1065-9471},
   url = {http://dx.doi.org/10.1002/hbm.22836},
   Abstract = {Deep brain stimulation (DBS) is an established surgical
             therapy for medically refractory tremor disorders including
             essential tremor (ET) and is currently under investigation
             for use in a variety of other neurologic and psychiatric
             disorders. There is growing evidence that the anti-tremor
             effects of DBS for ET are directly related to modulation of
             the dentatorubrothalamic tract (DRT), a white matter pathway
             that connects the cerebellum, red nucleus, and ventral
             intermediate nucleus of the thalamus. Emerging white matter
             targets for DBS, like the DRT, will require improved
             three-dimensional (3D) reference maps of deep brain anatomy
             and structural connectivity for accurate electrode
             targeting. High-resolution diffusion MRI of postmortem brain
             specimens can provide detailed volumetric images of
             important deep brain nuclei and 3D reconstructions of white
             matter pathways with probabilistic tractography techniques.
             We present a high spatial and angular resolution diffusion
             MRI template of the postmortem human brainstem and thalamus
             with 3D reconstructions of the nuclei and white matter
             tracts involved in ET circuitry. We demonstrate registration
             of these data to in vivo, clinical images from patients
             receiving DBS therapy, and correlate electrode proximity to
             tractography of the DRT with improvement of ET
             symptoms.},
   Doi = {10.1002/hbm.22836},
   Key = {fds268696}
}

@booklet{Gray03,
   Author = {C. A. Gray and M. D. Stewart and G. A. Johnson and T. E.
             Spencer},
   Title = {Postpartum uterine involution in sheep: histoarchitecture
             and changes in endometrial gene expression},
   Journal = {Reproduction},
   Volume = {125},
   Number = {2},
   Pages = {185 -- 198},
   Year = {2003},
   Month = {February},
   Key = {Gray03}
}

@article{fds174285,
   Author = {CA Gray, MD Stewart and GA Johnson and TE Spencer},
   Title = {Postpartum uterine involution in sheep: histoarchitecture
             and changes in endometrial gene expression.},
   Journal = {Reproduction (Cambridge, England)},
   Volume = {125},
   Number = {2},
   Pages = {185-98},
   Year = {2003},
   Month = {February},
   ISSN = {1470-1626},
   Keywords = {Animals • Apoptosis • B-Lymphocytes •
             Epithelium • Estradiol • Estrogen Receptor alpha
             • Female • Glycoproteins • Hysterectomy
             • Immunohistochemistry • In Situ Hybridization
             • Organ Size • Ovariectomy • Placenta •
             Postpartum Period • Pregnancy • Progesterone
             • RNA, Messenger • Receptors, Estrogen •
             Receptors, Oxytocin • Receptors, Progesterone •
             Receptors, Prolactin • Serpins* • Sheep •
             T-Lymphocytes • Uterus • analysis • anatomy &
             histology • anatomy & histology* • blood •
             cytology • genetics • immunology • metabolism
             • physiology*},
   Abstract = {After parturition, the uterus undergoes marked remodelling
             during involution; however, little is known of the hormonal,
             cellular and molecular mechanisms that regulate this
             process. The working hypothesis used in this study is that
             return of the ovine uterus to a non-pregnant state involves
             termination of a hormonal servomechanism that regulates
             endometrial gland morphogenesis and function during
             pregnancy. Suffolk ewes were ovariohysterectomized on
             postpartum days 1, 7, 14 or 28. Serum concentrations of
             oestradiol were high at parturition, declined to postpartum
             day 4, peaked on postpartum day 6, and then declined and
             remained low thereafter. Progesterone was undetectable in
             plasma from ewes post partum. Uterine wet mass and horn
             length decreased after postpartum day 1, but ovarian mass
             did not change. Residual placental cotyledons were present
             in the maternal caruncles on postpartum days 1 and 7 and
             were extruded by postpartum day 14 as plaques that were
             resorbed by postpartum day 28. The width of the total
             endometrium, stratum compactum, stratum spongiosum and
             myometrium, as well as endometrial gland density, decreased
             after parturition. Most apoptotic cells in the involuting
             uterus were large, vacuolated and located between the
             endometrial glandular epithelial cells on postpartum days 1
             and 7. Immunofluorescence analyses identified both T and B
             cells within the glandular epithelium on postpartum day 1.
             Cell proliferation was detected in the luminal epithelium
             and glandular epithelium on postpartum days 1 and 7. On
             postpartum day 1, expression of oestrogen receptor alpha
             (ERalpha) was not detected in luminal epithelium and was low
             in glandular epithelium, but ERalpha was present in
             epithelia thereafter. Progesterone receptor (PR) protein was
             not detected in endometrial epithelia on postpartum day 1,
             but was detected in the glandular epithelium thereafter.
             Between postpartum days 1 and 7, ERalpha and PR protein
             increased substantially in the endometrial glandular
             epithelium. On postpartum days 1-28, abundant expression of
             oxytocin receptor mRNA was detected in endometrial luminal
             epithelium and superficial to the middle glandular
             epithelium. Prolactin receptor (PRLR) mRNA was detected in
             glandular epithelium on all postpartum days, whereas mRNA
             for uterine milk protein (UTMP), an index of secretory
             capacity of glandular epithelium, was present only on
             postpartum day 1. Collectively, these results indicate that
             uterine involution in ewes involves remodelling of both
             caruncular and intercaruncular areas of the uterine wall and
             termination of differentiated uterine gland functions
             characteristic of pregnancy.},
   Language = {eng},
   Key = {fds174285}
}

@booklet{Buhl92a,
   Author = {A. E. Buhl and D. J. Waldon and S. J. Conrad and M. J.
             Mulholland and K. L. Shull and M. F. Kubicek and G. A.
             Johnson and M. N. Brunden and K. J. Stefanski and R. G.
             Stehle and R. C. Gadwood and B. V. Kamdar and L. M. Thomasco and H. J. Schostarez and T.},
   Title = {Potassium channel conductance - a mechanism affecting
             hair-growth both invitro and invivo},
   Journal = {Journal Of Investigative Dermatology},
   Volume = {98},
   Number = {3},
   Pages = {315 -- 319},
   Year = {1992},
   Month = {March},
   Key = {Buhl92a}
}

@article{fds174224,
   Author = {AE Buhl and DJ Waldon and SJ Conrad and MJ Mulholland and KL Shull and MF
             Kubicek, GA Johnson and MN Brunden and KJ Stefanski and RG
             Stehle},
   Title = {Potassium channel conductance: a mechanism affecting hair
             growth both in vitro and in vivo.},
   Journal = {The Journal of investigative dermatology},
   Volume = {98},
   Number = {3},
   Pages = {315-9},
   Year = {1992},
   Month = {March},
   ISSN = {0022-202X},
   Keywords = {Animals • Benzopyrans • Cells, Cultured •
             Cromakalim • Hair • Mice • Mice, Inbred C3H
             • Mice, Inbred C57BL • Minoxidil • Potassium
             Channels • Pyrroles • growth & development* •
             pharmacology • physiology*},
   Abstract = {The opening of intracellular potassium channels has been
             suggested as a mechanism regulating hair growth. Enhancing
             the flux of potassium ions is a mechanism shared by several
             structurally diverse antihypertensive agents including
             minoxidil sulfate (the active metabolite of minoxidil),
             pinacidil, P-1075 (a potent pinacidil analog), RP-49,356,
             diazoxide, cromakalim, and nicorandil. Of these drugs,
             minoxidil, pinacidil, and diazoxide have been reported to
             elicit hypertrichosis in humans. This potassium channel
             hypothesis was examined by testing these drugs for effects
             on hair growth both in vitro and in vivo. For the in vitro
             studies, mouse vibrissae follicles were cultured for 3 d
             with drug and the effects on hair growth were measured by
             metabolic labeling. All drugs, except diazoxide, enhanced
             cysteine incorporation into the hair shafts of the cultured
             vibrissae. Diazoxide was poorly soluble and thus was tested
             only at low doses. Minoxidil, P-1075, cromakalim, and
             RP-49,356 were also evaluated in vivo by measuring hair
             growth effects in balding stumptail macaque monkeys. The
             drugs were administered topically to defined sites on
             balding scalps once per day for 4-5 months and the amount of
             hair grown was determined by monthly measurements of shaved
             hair weight. Three of the drugs produced significant
             increases in hair weight whereas, the RP-49,356 had no
             effect. These studies provide correlative evidence that the
             opening of potassium channels is an important regulatory
             mechanism for hair growth. This provides the impetus for
             further studies on this potentially important mechanism
             affecting hair biology.},
   Language = {eng},
   Key = {fds174224}
}

@booklet{Johnson82,
   Author = {Johnson, GA},
   Title = {Practical approach to quality assurance in computed
             tomography},
   Journal = {Proceedings of SPIE - The International Society for Optical
             Engineering},
   Volume = {347},
   Pages = {148-154},
   Year = {1982},
   Month = {December},
   url = {http://dx.doi.org/10.1117/12.933821},
   Abstract = {The goal of tissue characterization via quantitative
             computed tomography can only be accomplished with careful
             control of certain parameters. A quality assurance program
             is described which includes daily measurement of certain
             essential elements e.g. Hounsfield conversion, linearity,
             noise and resolution. Secondary measurements of collimation,
             bed movement, dose, and sensitivity profiles are performed
             on a monthly basis. Daily measurements are accomplished in
             less than 15 minutes while monthly checks take less than 1.5
             hr thus minimizing conflict with a busy clinical routine.
             Examples of rapid recording methods and measurement
             techniques are included. © 1982 SPIE.},
   Doi = {10.1117/12.933821},
   Key = {Johnson82}
}

@booklet{Johnson80b,
   Author = {JOHNSON, GA and HOLT, DC and EFFMANN, EL},
   Title = {PRACTICAL GUIDELINES FOR SPECIMEN RADIOGRAPHY},
   Journal = {INVESTIGATIVE RADIOLOGY},
   Volume = {15},
   Number = {5},
   Pages = {377-377},
   Year = {1980},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1980KK17000009&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Johnson80b}
}

@booklet{Macfall91a,
   Author = {MacFall, JR and Maki, JH and Johnson, GA and Hedlund, LW and Cofer,
             GP},
   Title = {Pre- and postmortem diffusion coefficients in rat neural and
             muscle tissues.},
   Journal = {Magn Reson Med},
   Volume = {20},
   Number = {1},
   Pages = {89-99},
   Year = {1991},
   Month = {July},
   ISSN = {0740-3194},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1991FU08200009&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Abstract = {Pulsed gradient diffusion-weighted spin-echo images (7 to 11
             gradient strengths) were obtained in a coronal slice through
             the midbrain for five normal adult white rats before and
             after sacrifice in a 2-T CSI system with air temperature
             control. The pulse sequence was cardiac gated and
             respiratory synchronized in order to minimize motion
             artifacts (Tr greater than 2 s. Te = 30 ms). Diffusion
             coefficients reflecting several tissue compartments (D*) in
             brain and muscle were calculated and referenced to
             simultaneously imaged tubes of water. In the living animals,
             brain cortical matter had a value of D* = (0.82 +/- 0.02) x
             10(-3) mm2/s. deeper brain regions had a value of D* = (0.73
             +/- 0.02) x 10(-3) mm2/s, and the muscle had a value of D* =
             (1.4 +/- 0.1) x 10(-3) mm2/s. Postmortem the values in brain
             dropped by approximately 30%, while remaining constant in
             muscle. Signal intensity in the spin-echo images for muscle
             tissue rose by 50% over a 1- to 2-h interval after sacrifice
             while that of brain tissue remained relatively
             stable.},
   Doi = {10.1002/mrm.1910200110},
   Key = {Macfall91a}
}

@booklet{Winter85,
   Author = {WINTER, TC and JOHNSON, GA and MACFALL, JR},
   Title = {PRECISION AND ACCURACY IN THE MEASUREMENT OF T1 ON AN
             IMAGING-SYSTEM},
   Journal = {INVESTIGATIVE RADIOLOGY},
   Volume = {20},
   Number = {6},
   Pages = {S14-S14},
   Publisher = {LIPPINCOTT-RAVEN PUBL},
   Year = {1985},
   Month = {January},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1985ARG0500074&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Winter85}
}

@booklet{Micheli02,
   Author = {F. Micheli and C. H. Peterson and L. S. Mullineaux and C. R.
             Fisher and S. W. Mills and G. Sancho and G. A. Johnson and H. S. Lenihan},
   Title = {Predation structures communities at deep-sea hydrothermal
             vents},
   Journal = {Ecological Monographs},
   Volume = {72},
   Number = {3},
   Pages = {365 -- 382},
   Year = {2002},
   Month = {August},
   Key = {Micheli02}
}

@article{fds359546,
   Author = {Lu, H and Pollack, E and Young, R and Babb, JS and Johnson, G and Zagzag,
             D and Carson, R and Jensen, JH and Helpern, JA and Law,
             M},
   Title = {Predicting grade of cerebral glioma using vascular-space
             occupancy MR imaging.},
   Journal = {AJNR Am J Neuroradiol},
   Volume = {29},
   Number = {2},
   Pages = {373-378},
   Year = {2008},
   Month = {February},
   url = {http://dx.doi.org/10.3174/ajnr.A0794},
   Abstract = {BACKGROUND AND PURPOSE: MR imaging can measure tissue
             perfusion and the integrity of the blood-brain barrier. We
             hypothesize that a combined measure of cerebral blood volume
             and vascular permeability using vascular-space occupancy
             (VASO) MR imaging, a recently developed imaging technique,
             is of diagnostic value for predicting tumor grade. MATERIALS
             AND METHODS: Thirty-nine patients (9 World Health
             Organization [WHO] grade II, 20 grade III, and 10 grade IV
             as determined by histopathologic assessment) were examined
             using VASO MR imaging, and regions-of-interest analysis was
             performed in tumoral regions, as well as in regions
             contralateral to the tumor. A Mann-Whitney test was
             conducted on the resulting VASO indices for a pairwise
             comparison across tumor grades. Nominal logistic regression
             was used to evaluate the use of VASO parameters for
             predicting group membership (by the percentage of correct
             classifications). RESULTS: The ratio between tumor side and
             contralateral side, VASO(Ratio), showed significant
             differences in all 3 of the pairwise comparisons (P < .01).
             VASO values in the tumoral regions, VASO(Tumor), showed
             significant difference between grade II and III and between
             II and IV but not between III and IV. Both VASO(Tumor) and
             VASO(Ratio) were found to be significant predictors of tumor
             grade, giving diagnostic accuracies of 66.7% and 71.8%,
             respectively. When testing to discriminate grade II tumors
             from higher grade tumors, the areas under the receiver
             operating characteristic curve were found to be 0.974 and
             0.985 for VASO(Tumor) and VASO(Ratio), respectively.
             CONCLUSION: VASO MR imaging can be used for noninvasive
             tumor grade prediction based on cerebral blood volume and
             vascular permeability. VASO is more effective in separating
             WHO grade II from higher grades than in separating grade III
             from grade IV.},
   Doi = {10.3174/ajnr.A0794},
   Key = {fds359546}
}

@booklet{Choi03,
   Author = {Y. Choi and G. A. Johnson and T. E. Spencer and F. W.
             Bazer},
   Title = {Pregnancy and interferon tau regulate major
             histocompatibility complex class I and beta(2)-microglobulin
             expression in the ovine uterus},
   Journal = {Biology Of Reproduction},
   Volume = {68},
   Number = {5},
   Pages = {1703 -- 1710},
   Year = {2003},
   Month = {May},
   Key = {Choi03}
}

@article{fds174102,
   Author = {Y Choi and GA Johnson and TE Spencer and FW Bazer},
   Title = {Pregnancy and interferon tau regulate major
             histocompatibility complex class I and beta2-microglobulin
             expression in the ovine uterus.},
   Journal = {Biology of reproduction},
   Volume = {68},
   Number = {5},
   Pages = {1703-10},
   Year = {2003},
   Month = {May},
   ISSN = {0006-3363},
   url = {http://dx.doi.org/10.1095/biolreprod.102.012708},
   Keywords = {Animals • Endometrium • Estrous Cycle •
             Female • Fluorescent Antibody Technique • Gene
             Expression Regulation, Developmental • Genes, MHC Class
             I • In Situ Hybridization • Interferon Type I
             • Pregnancy • Pregnancy Proteins • Pregnancy,
             Animal • RNA, Messenger • Sheep • Uterus
             • beta 2-Microglobulin • biosynthesis •
             biosynthesis* • genetics • genetics* •
             metabolism • metabolism* • physiology •
             physiology*},
   Abstract = {Major histocompatibility complex (MHC) class I molecules,
             consisting of an alpha chain and beta2-microglobulin
             (beta2MG), play an important role in immune rejection
             responses by discriminating self and nonself and are
             increased by type I interferons during antiviral responses.
             Interferon tau (IFNtau), the pregnancy-recognition signal in
             ruminants, is a type I interferon produced by the ovine
             conceptus between Days 11 and 21 of gestation. In study 1,
             expression of MHC class I alpha chain and beta2MG mRNA and
             protein was detected primarily in endometrial luminal
             epithelium (LE) and glandular epithelium (GE) on Days 10 and
             12 of the estrous cycle and pregnancy. On Days 14-20 of
             pregnancy, MHC class I and beta2MG expression increased only
             in endometrial stroma and GE and, concurrently, was absent
             in LE and superficial ductal GE (sGE). Although neither MHC
             class I nor beta2MG proteins were detected in Day 20
             trophectoderm, beta2MG mRNA was detected in conceptus
             trophectoderm. In study 2, cyclic ewes were ovariectomized
             on Day 5, treated daily with progesterone to Day 16,
             received intrauterine infusions between Days 11 and 16 of
             either control serum proteins or recombinant ovine IFNtau,
             and were hysterectomized on Day 17. The IFNtau increased MHC
             class I and beta2MG expression only in endometrial stroma
             and GE. During pregnancy, MHC class I and beta2MG gene
             expression is inhibited in endometrial LE and sGE but,
             paradoxically, is stimulated by IFNtau in the stroma and GE.
             The silencing of MHC class I alpha chain and beta2MG genes
             in the endometrial LE and sGE during pregnancy recognition
             and establishment may be a critical mechanism preventing
             immune rejection of the conceptus allograft.},
   Language = {eng},
   Doi = {10.1095/biolreprod.102.012708},
   Key = {fds174102}
}

@booklet{Johnson98c,
   Author = {G. A. Johnson and K. J. Austin and E. A. van Kirk and T. R.
             Hansen},
   Title = {Pregnancy and interferon-tau induce conjugation of bovine
             ubiquitin cross-reactive protein to cytosolic uterine
             proteins},
   Journal = {Biology Of Reproduction},
   Volume = {58},
   Number = {4},
   Pages = {898 -- 904},
   Year = {1998},
   Month = {April},
   Key = {Johnson98c}
}

@article{fds174288,
   Author = {GA Johnson and KJ Austin and EA Van Kirk and TR Hansen},
   Title = {Pregnancy and interferon-tau induce conjugation of bovine
             ubiquitin cross-reactive protein to cytosolic uterine
             proteins.},
   Journal = {Biology of reproduction},
   Volume = {58},
   Number = {4},
   Pages = {898-904},
   Year = {1998},
   Month = {April},
   ISSN = {0006-3363},
   Keywords = {Amino Acid Sequence • Animals • Blotting, Western
             • Carrier Proteins • Cattle • Cytosol •
             Densitometry • Female • Interferon Type I •
             Molecular Sequence Data • Pregnancy • Pregnancy
             Proteins • Pregnancy, Animal • Proteins •
             Recombinant Proteins • Ubiquitins • Uterus •
             analogs & derivatives* • chemistry • chemistry*
             • metabolism • metabolism* • pharmacology
             • pharmacology* • physiology* •
             ultrastructure},
   Abstract = {Conceptus-derived interferon-tau (IFN-tau) induces bovine
             endometrial ubiquitin cross-reactive protein (UCRP) mRNA and
             protein on Days 15-21 of pregnancy. Bovine UCRP retains the
             Leu-Arg-Gly-Gly C-terminal sequence of ubiquitin that
             ligates to and directs degradation of cytosolic proteins.
             The objectives of the present experiments were to determine
             whether UCRP became conjugated to endometrial cytosolic
             proteins during early pregnancy and in response to
             recombinant bovine (rbo) IFN-tau. Ubiquitin (8 kDa), UCRP
             (17 kDa), and conjugates thereof (> or = 30 kDa) were
             quantitated using Western blotting and densitometry.
             Endometrial ubiquitin and its conjugates did not differ
             between Day 18 pregnant and nonpregnant cows, or between
             control and rboIFN-tau-treated (25 nM) explant cultures (Day
             14; nonpregnant). Bovine UCRP was induced in endometrium
             from pregnant as compared with nonpregnant cows. Conjugation
             of endometrial proteins to UCRP was induced in pregnant as
             compared to nonpregnant cows. Recombinant boIFN-tau induced
             UCRP and its conjugates in cultured endometrial explants
             from nonpregnant cows. It is concluded that UCRP, in
             response to rboIFN-tau, becomes conjugated to endometrial
             cytosolic proteins during early pregnancy. The regulation of
             uterine proteins by UCRP may be integral to the maintenance
             of early pregnancy in ruminants.},
   Language = {eng},
   Key = {fds174288}
}

@booklet{Johnson97,
   Author = {G. A. Johnson and K. J. Austin and E. A. Vankirk and T. R.
             Hansen},
   Title = {Pregnancy and interferon-tau induce conjugation of bovine
             ubiquitin cross-reactive protein to cytosolic uterine
             proteins.},
   Journal = {Biology Of Reproduction},
   Volume = {56},
   Pages = {160 -- 160},
   Year = {1997},
   Key = {Johnson97}
}

@article{fds174123,
   Author = {TE Spencer and GA Johnson and FW Bazer and RC Burghardt and M
             Palmarini},
   Title = {Pregnancy recognition and conceptus implantation in domestic
             ruminants: roles of progesterone, interferons and endogenous
             retroviruses.},
   Journal = {Reproduction, fertility, and development},
   Volume = {19},
   Number = {1},
   Pages = {65-78},
   Year = {2007},
   ISSN = {1031-3613},
   Keywords = {Animals • Cattle • Embryo Implantation* •
             Endogenous Retroviruses • Endometrium • Female
             • Gene Expression Regulation, Developmental •
             Interferons • Pregnancy • Pregnancy, Animal •
             Progesterone • Receptors, Progesterone • Ruminants
             • Sheep • Uterus • embryology •
             embryology* • metabolism • physiology •
             physiology*},
   Abstract = {The present review highlights new information on pregnancy
             recognition and conceptus development and implantation in
             sheep with respect to regulation by progesterone,
             interferons and endogenous retroviruses. After formation of
             the corpus luteum, progesterone acts on the endometrium and
             stimulates blastocyst growth and elongation to a filamentous
             conceptus (embryo/fetus and associated extra-embryonic
             membranes). The envelope of endogenous retroviruses related
             to Jaagsiekte sheep retroviruses appears to intrinsically
             regulate mononuclear trophectoderm cell proliferation and
             differentiation into trophoblast giant binucleate cells. The
             mononuclear trophectoderm cells of elongating sheep
             conceptuses secrete interferon-tau, which acts on the
             endometrium to prevent development of the luteolytic
             mechanism by inhibiting transcription of the gene for the
             oestrogen receptor alpha in the luminal and superficial
             ductal glandular epithelia. These actions prevent
             oestrogen-induced transcription of the oxytocin receptor
             gene and, therefore, oxytocin-induced luteolytic pulses of
             prostaglandin F2alpha. Progesterone down regulation of its
             receptors in luminal and glandular epithelia correlates
             temporally with a reduction in anti-adhesive mucin land
             induction of secreted galectin 15 (LGALSI5) and secreted
             phosphoprotein 1, which are proposed to regulate
             trophectoderm proliferation and adhesion. Interferon-c acts
             on the endometrial lumenal epithelium to induce WNT7A and to
             stimulate LGALS 15, cathepsin L and cystatin C, which are
             candidate regulators of conceptus development and
             implantation. The number of potential contributors to
             maternal recognition and establishment of pregnancy
             continues to grow and this highlights our limited
             appreciation of the complexity of the key molecules and
             signal transduction pathways that intersect during these key
             developmental processes. The goal of improving reproductive
             efficiency by preventing embryonic losses that occur during
             the peri-implantation period of pregnancy in domestic
             ruminants provides the challenge to increase our knowledge
             of endometrial function and conceptus development.},
   Language = {eng},
   Key = {fds174123}
}

@booklet{Johnson99g,
   Author = {G. A. Johnson and A. Calkins},
   Title = {Prehospital triage and communication performance in small
             mass casualty incidents: A gauge for disaster
             preparedness},
   Journal = {American Journal Of Emergency Medicine},
   Volume = {17},
   Number = {2},
   Pages = {148 -- 150},
   Year = {1999},
   Month = {March},
   Key = {Johnson99g}
}

@article{fds174119,
   Author = {GA Johnson and A Calkins},
   Title = {Prehospital triage and communication performance in small
             mass casualty incidents: a gauge for disaster
             preparedness.},
   Journal = {The American journal of emergency medicine},
   Volume = {17},
   Number = {2},
   Pages = {148-50},
   Year = {1999},
   Month = {March},
   ISSN = {0735-6757},
   Keywords = {Accidents, Traffic • Disaster Planning* •
             Emergency Medical Services* • Humans • New York
             • Outcome and Process Assessment (Health Care) •
             Prospective Studies • Quality Control • Relief
             Work* • Retrospective Studies • Triage* •
             Wounds and Injuries • etiology •
             therapy},
   Abstract = {Because of their infrequency, disasters are difficult to
             train for. Emergency prehospital personnel frequently
             participate in small mass casualty incidents (MCIs) (3 to 50
             victims). This study sought to examine prehospital
             performance in small MCIs in areas that are frequently
             mismanaged in disasters. Prospective data from the resource
             physician and retrospective data from tape recorded
             prehospital conversations were collected for a 9-month
             period. Clinical patient data, patient demographics,
             emergency medical services squad characteristics, and triage
             information were recorded. Forty-five consecutive MCIs were
             studied. Most of these were motor vehicle accidents.
             Prehospital providers included paid providers, nonpaid
             providers, and air and ground transport. The mean number of
             victims first identified (4.6%) was greatly different than
             the mean number of victims eventually transported from a
             scene (7.1%). Most patients were treated at a level 1 trauma
             center. Frequent errors included having multiple
             communicators on site (38%), misidentifying the number of
             victims (56%), and having unclear information for the
             resource physician (43%). Only 38% of events had prehospital
             triage information that was deemed appropriate in total.
             These results show that scene and triage errors are frequent
             in MCIs of small scale. This information can be used to
             assay a system's readiness for disasters.},
   Language = {eng},
   Key = {fds174119}
}

@article{fds174176,
   Author = {JW Ross, MD Ashworth and FJ White and GA Johnson and PJ Ayoubi and U
             DeSilva, KM Whitworth and RS Prather and RD Geisert},
   Title = {Premature estrogen exposure alters endometrial gene
             expression to disrupt pregnancy in the pig.},
   Journal = {Endocrinology},
   Volume = {148},
   Number = {10},
   Pages = {4761-73},
   Year = {2007},
   Month = {October},
   ISSN = {0013-7227},
   url = {http://dx.doi.org/10.1210/en.2007-0599},
   Keywords = {Abortion, Spontaneous • Aldehyde Reductase •
             Animals • Antigens, CD24 • Drug Administration
             Schedule • Embryo Loss • Endometrium •
             Epithelium • Estradiol • Female • Gene
             Expression • Gene Expression Profiling •
             Gestational Age • Neurokinin B • Oligonucleotide
             Array Sequence Analysis • Osteopontin • Pregnancy
             • Pregnancy, Animal • RNA, Messenger • Swine
             • Time Factors • Uterus • administration &
             dosage • analogs & derivatives • analogs &
             derivatives* • drug effects* • etiology* •
             genetics • metabolism • metabolism* •
             pharmacology},
   Abstract = {Establishment and maintenance of pregnancy in the pig
             involve intricate communication between the developing
             conceptuses and maternal endometrium. Conceptus synthesis
             and release of estrogen during trophoblastic elongation are
             essential factors involved with establishing
             conceptus-uterine communication. The present study
             identified endometrial changes in gene expression associated
             with implantation failure and complete pregnancy loss after
             premature exposure of pregnant gilts to exogenous estrogen.
             Gilts were treated with either 5 mg estradiol cypionate (EC)
             or corn oil on d-9 and -10 gestation, which was associated
             with complete conceptus degeneration by d-17 gestation.
             Microarray analysis of gene expression revealed that a total
             of eight, 32, and five genes were up-regulated in the EC
             endometrium, whereas one, 39, and 16 genes were
             down-regulated, on d 10, 13, and 15, respectively. Four
             endometrial genes altered by EC, aldose reductase (AKR1B1),
             secreted phosphoprotein 1 (SPP1), CD24 antigen (CD24), and
             neuromedin B (NMB), were evaluated using quantitative RT-PCR
             and in situ hybridization. In situ hybridization localized
             gene expression for NMB, CD24, AKR1B1, and SPP1 in the
             luminal epithelium, and confirmed the expression patterns
             from RT-PCR analysis. The aberrant expression patterns of
             endometrial AKR1B1, SPP1, CD24, and NMB 3-4 d after
             premature estrogen exposure to pregnant gilts may be
             involved with conceptus attachment failure to the uterine
             surface epithelium and induction of endometrial responses
             that disrupt the establishment of a viable
             pregnancy.},
   Language = {eng},
   Doi = {10.1210/en.2007-0599},
   Key = {fds174176}
}

@article{fds268704,
   Author = {Cao, W and Li, W and Han, H and O'Leary-Moore, SK and Sulik, KK and Allan
             Johnson, G and Liu, C},
   Title = {Prenatal alcohol exposure reduces magnetic susceptibility
             contrast and anisotropy in the white matter of mouse
             brains.},
   Journal = {Neuroimage},
   Volume = {102 Pt 2},
   Number = {0 2},
   Pages = {748-755},
   Year = {2014},
   Month = {November},
   ISSN = {1053-8119},
   url = {http://dx.doi.org/10.1016/j.neuroimage.2014.08.035},
   Abstract = {Prenatal alcohol exposure can result in long-term cognitive
             and behavioral deficits. Fetal alcohol spectrum disorder
             (FASD) refers to a range of permanent birth defects caused
             by prenatal alcohol exposure, and is the most common
             neurodevelopmental disorder in the US. Studies by autopsy
             and conventional structural MRI indicate that the midline
             structures of the brain are particularly vulnerable to
             prenatal alcohol exposure. Diffusion tensor imaging (DTI)
             has shown that abnormalities in brain white matter
             especially the corpus callosum are very common in FASD.
             Quantitative susceptibility mapping (QSM) is a novel
             technique that measures tissue's magnetic property. Such
             magnetic property is affected by tissue microstructure and
             molecular composition including that of myelin in the white
             matter. In this work, we studied three major white matter
             fiber bundles of a mouse model of FASD and compared it to
             control mice using both QSM and DTI. QSM revealed clear and
             significant abnormalities in anterior commissure, corpus
             callosum, and hippocampal commissure, which were likely due
             to reduced myelination. Our data also suggested that QSM may
             be even more sensitive than DTI for examining changes due to
             prenatal alcohol exposure. Although this is a preclinical
             study, the technique of QSM is readily translatable to human
             brain.},
   Doi = {10.1016/j.neuroimage.2014.08.035},
   Key = {fds268704}
}

@article{fds367905,
   Author = {Hornburg, KJ and Slosky, LM and Cofer, G and Cook, J and Qi, Y and Porkka,
             F and Clark, NB and Pires, A and Petrella, JR and White, LE and Wetsel, WC and Barak, L and Caron, MG and Johnson, GA},
   Title = {Prenatal heroin exposure alters brain morphology and
             connectivity in adolescent mice.},
   Journal = {NMR Biomed},
   Volume = {36},
   Number = {2},
   Pages = {e4842},
   Year = {2023},
   Month = {February},
   url = {http://dx.doi.org/10.1002/nbm.4842},
   Abstract = {The United States is experiencing a dramatic increase in
             maternal opioid misuse and, consequently, the number of
             individuals exposed to opioids in utero. Prenatal opioid
             exposure has both acute and long-lasting effects on health
             and wellbeing. Effects on the brain, often identified at
             school age, manifest as cognitive impairment, attention
             deficit, and reduced scholastic achievement. The
             neurobiological basis for these effects is poorly
             understood. Here, we examine how in utero exposure to heroin
             affects brain development into early adolescence in a mouse
             model. Pregnant C57BL/6J mice received escalating doses of
             heroin twice daily on gestational days 4-18. The brains of
             offspring were assessed on postnatal day 28 using 9.4 T
             diffusion MRI of postmortem specimens at 36 μm
             resolution. Whole-brain volumes and the volumes of 166
             bilateral regions were compared between heroin-exposed and
             control offspring. We identified a reduction in whole-brain
             volume in heroin-exposed offspring and heroin-associated
             volume changes in 29 regions after standardizing for
             whole-brain volume. Regions with bilaterally reduced
             standardized volumes in heroin-exposed offspring relative to
             controls include the ectorhinal and insular cortices.
             Regions with bilaterally increased standardized volumes in
             heroin-exposed offspring relative to controls include the
             periaqueductal gray, septal region, striatum, and
             hypothalamus. Leveraging microscopic resolution diffusion
             tensor imaging and precise regional parcellation, we
             generated whole-brain structural MRI diffusion connectomes.
             Using a dimension reduction approach with multivariate
             analysis of variance to assess group differences in the
             connectome, we found that in utero heroin exposure altered
             structure-based connectivity of the left septal region and
             the region that acts as a hub for limbic regulatory actions.
             Consistent with clinical evidence, our findings suggest that
             prenatal opioid exposure may have effects on brain
             morphology, connectivity, and, consequently, function that
             persist into adolescence. This work expands our
             understanding of the risks associated with opioid misuse
             during pregnancy and identifies biomarkers that may
             facilitate diagnosis and treatment.},
   Doi = {10.1002/nbm.4842},
   Key = {fds367905}
}

@article{fds174208,
   Author = {TD Tillmanns and CA Falkner and DB Engle and JY Wan and RS Mannel and JL
             Walker, GA Johnson and DS McMeekin and R Zuna and MA
             Gold},
   Title = {Preoperative predictors of positive margins after loop
             electrosurgical excisional procedure-Cone.},
   Journal = {Gynecologic oncology},
   Volume = {100},
   Number = {2},
   Pages = {379-84},
   Year = {2006},
   Month = {February},
   ISSN = {0090-8258},
   url = {http://dx.doi.org/10.1016/j.ygyno.2005.09.015},
   Keywords = {Adult • Cervical Intraepithelial Neoplasia •
             Conization • Electrosurgery • Female • Humans
             • Predictive Value of Tests • Preoperative Care
             • Retrospective Studies • Uterine Cervical
             Dysplasia • Uterine Cervical Neoplasms • methods*
             • pathology* • surgery*},
   Abstract = {OBJECTIVE: A LEEP-Cone may not be necessary for all patients
             with traditional cone indications. This study defines
             populations where a single pass technique with the LEEP is
             appropriate. METHODS: We retrospectively reviewed patients
             undergoing LEEP-Cone procedures performed at the University
             of Oklahoma Health Science Center from February of 1994 to
             July of 2002. Patients include those for LEEP-Cone with
             traditional excisional indications and those who underwent
             LEEP-Cone at the operating physician's discretion.
             Statistical analysis was used to compare preoperative
             factors with the resultant pathologic results. RESULTS: A
             total of 248 women underwent LEEP-Cone. 50.0% (33/66) of the
             patients with positive margins on the first pass had
             dysplasia or worse (CIN I-III or CA) in the second pass (top
             hat), compared to 6.6% (12/182) of the patients with a
             negative first pass (P < 0.0001). Univariate analysis found
             CIN III on histology and parity to be predictive of
             dysplasia in the top hat and two-step discrepancy to predict
             absence of dysplasia. On multivariate analysis, two-step
             discrepancy and parity remained predictive. Age >35 was the
             greatest percentile predictor of dysplasia in the top hat,
             and 91.5% of women <21 had normal top hat pathology.
             CONCLUSION: The retrospective data reported regarding
             LEEP-Cones reveal increased parity to predict dysplasia in
             the top hat and two-step discrepancy as a poor predictor of
             dysplasia in the top hat. Women under 21 years of age should
             have a single pass LEEP technique. The "top hat" is more
             appropriate as parity and age increase.},
   Language = {eng},
   Doi = {10.1016/j.ygyno.2005.09.015},
   Key = {fds174208}
}

@booklet{Burvill95,
   Author = {P. W. Burvill and G. A. Johnson and K. D. Jamrozik and C. S.
             Anderson and E. G. Stewartwynne and T. M. H.
             Chakera},
   Title = {Prevalence of depression after stroke - the perth community
             stroke study},
   Journal = {British Journal Of Psychiatry},
   Volume = {166},
   Pages = {320 -- 327},
   Year = {1995},
   Month = {March},
   Key = {Burvill95}
}

@article{fds174205,
   Author = {PW Burvill and GA Johnson and KD Jamrozik and CS Anderson and EG
             Stewart-Wynne, TM Chakera},
   Title = {Prevalence of depression after stroke: the Perth Community
             Stroke Study.},
   Journal = {The British journal of psychiatry : the journal of mental
             science},
   Volume = {166},
   Number = {3},
   Pages = {320-7},
   Year = {1995},
   Month = {March},
   ISSN = {0007-1250},
   Keywords = {Adaptation, Psychological • Adult • Aged •
             Aged, 80 and over • Cerebrovascular Disorders •
             Cohort Studies • Cross-Sectional Studies •
             Delirium, Dementia, Amnestic, Cognitive Disorders •
             Depressive Disorder • Female • Follow-Up Studies
             • Humans • Incidence • Male • Middle
             Aged • Recurrence • Sick Role • Western
             Australia • diagnosis • epidemiology •
             epidemiology* • psychology},
   Abstract = {BACKGROUND: The Perth Community Stroke Study (PCSS) was a
             population-based study of the incidence, cause, and outcome
             of acute stroke. METHOD: Subjects from the study were
             assessed initially, by examination and interview, and at
             four- and 12-month follow-ups to determine differences in
             prevalence of depression between the sexes and between
             patients with first-ever and recurrent strokes. RESULTS: The
             prevalence of depressive illness four months after stroke in
             294 patients from the PCSS was 23% (18-28%), 15% (11-19%)
             major depression and 8% (5-11%) minor depression. There were
             no significant differences between the sexes or between
             patients with first-ever and recurrent strokes. With a
             non-hierarchic approach to diagnosis of those with
             depression, 26% of men and 39% of women had an associated
             anxiety disorder, mainly agoraphobia. Nine per cent of male
             and 13% of female patients interviewed had evidence of
             depression at the time of the stroke. Twelve months after
             stroke 56% of the men were still depressed (40% major and
             16% minor), as were 30% of the women (12% major and 18%
             minor). CONCLUSION: The prevalence of depression after
             stroke was comparable with that reported from other studies,
             and considerably less than that reported from in-patient and
             rehabilitation units.},
   Language = {eng},
   Key = {fds174205}
}

@article{fds174095,
   Author = {TD Chinevere and CK Murray and E Grant Jr and GA Johnson and F Duelm and DR
             Hospenthal},
   Title = {Prevalence of glucose-6-phosphate dehydrogenase deficiency
             in U.S. Army personnel.},
   Journal = {Military medicine},
   Volume = {171},
   Number = {9},
   Pages = {905-7},
   Year = {2006},
   Month = {September},
   ISSN = {0026-4075},
   Keywords = {Adult • Endemic Diseases • Female •
             Glucosephosphate Dehydrogenase • Glucosephosphate
             Dehydrogenase Deficiency • Humans • Malaria •
             Male • Mass Screening • Military Medicine* •
             Military Personnel • Occupational Health* •
             Prevalence • Primaquine • Retrospective Studies
             • Risk Assessment • Risk Factors • United
             States • adverse effects • analysis • blood*
             • diagnosis • drug therapy • epidemiology
             • epidemiology* • statistics & numerical data*
             • therapeutic use},
   Abstract = {The U.S. Army recently mandated that soldiers undergo
             glucose-6-phosphate dehydrogenase (G6PD) testing before
             deployment to malarious regions. We retrospectively
             characterize the presence and degree of G6PD deficiency in
             U.S. military personnel by sex, self-reported ethnicity, and
             World Health Organization deficiency classification through
             test results obtained October 1, 2004 through January 17,
             2005. Data were available for 63,302 (54,874 males and 8,428
             females) subjects; 2.5% of males and 1.6% of females were
             deficient, with most having only moderate enzyme deficiency.
             African American males (12.2%) and females (4.1%), along
             with Asian males (4.3%), had the highest rates of G6PD
             deficiency. Most males were found to have class III variants
             while most females were class IV variants. The most severely
             deficient were Asian males (class II). These results suggest
             that universal screening for G6PD deficiency is clinically
             warranted, and particularly essential for those male service
             members who self-report ethnicity as African American,
             Asian, or Hispanic.},
   Language = {eng},
   Key = {fds174095}
}

@article{fds132752,
   Author = {GA Johnson and N Danieley and CE Ravin},
   Title = {Processing alternatives for digital chest
             imaging.},
   Journal = {Radiologic clinics of North America, UNITED
             STATES},
   Volume = {23},
   Number = {2},
   Pages = {335-40},
   Year = {1985},
   Month = {June},
   ISSN = {0033-8389},
   Keywords = {Humans • Radiographic Image Enhancement •
             Radiography, Thoracic • methods •
             methods*},
   Abstract = {Radiographic imaging of the chest remains one of the most
             important and most challenging problems in radiology. The
             wide range of information that results from the great
             variation of radiation behind the lungs compared with that
             behind the mediastinum creates a very difficult imaging
             problem. The introduction and continued investigation of
             digital techniques have presented a potential solution to
             this problem. In this article, the authors describe the
             image-processing techniques of histogram equalization and
             adaptive filtration in digital chest imaging.},
   Key = {fds132752}
}

@booklet{Johnson85a,
   Author = {Johnson, GA and Danieley, N and Ravin, CE},
   Title = {Processing alternatives for digital chest
             imaging.},
   Journal = {Radiol Clin North Am},
   Volume = {23},
   Number = {2},
   Pages = {335-340},
   Year = {1985},
   Month = {June},
   ISSN = {0033-8389},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/3991890},
   Abstract = {Radiographic imaging of the chest remains one of the most
             important and most challenging problems in radiology. The
             wide range of information that results from the great
             variation of radiation behind the lungs compared with that
             behind the mediastinum creates a very difficult imaging
             problem. The introduction and continued investigation of
             digital techniques have presented a potential solution to
             this problem. In this article, the authors describe the
             image-processing techniques of histogram equalization and
             adaptive filtration in digital chest imaging.},
   Key = {Johnson85a}
}

@booklet{Asselin99,
   Author = {E. Asselin and G. A. Johnson and T. E. Spencer and W. B.
             Fuller},
   Title = {Progesterone and interferon-tau regulate monocyte
             chemotactic protein-1 (MCP-1) in the ovine
             uterus.},
   Journal = {Biology Of Reproduction},
   Volume = {60},
   Pages = {95 -- 95},
   Year = {1999},
   Key = {Asselin99}
}

@article{fds174256,
   Author = {TE Spencer and GA Johnson and RC Burghardt and FW
             Bazer},
   Title = {Progesterone and placental hormone actions on the uterus:
             insights from domestic animals.},
   Journal = {Biology of reproduction},
   Volume = {71},
   Number = {1},
   Pages = {2-10},
   Year = {2004},
   Month = {July},
   ISSN = {0006-3363},
   url = {http://dx.doi.org/10.1095/biolreprod.103.024133},
   Keywords = {Animals • Animals, Domestic • Female •
             Placental Hormones • Pregnancy • Pregnancy, Animal
             • Progesterone • Sheep • Swine • Uterus
             • physiology • physiology*},
   Abstract = {Progesterone is unequivocally required for maternal support
             of conceptus (embryo/fetus and associated extraembryonic
             membranes) survival and development. In cyclic sheep,
             progesterone is paradoxically involved in suppressing and
             then initiating development of the endometrial luteolytic
             mechanism. In cyclic and pregnant sheep, progesterone
             negatively autoregulates progesterone receptor (PR) gene
             expression in the endometrial luminal (LE) and superficial
             glandular epithelium (GE). In cyclic sheep, PR loss is
             closely followed by increases in epithelial estrogen
             receptor (ERalpha) and then oxytocin receptor (OTR),
             allowing oxytocin to induce uterine release of luteolytic
             prostaglandin F2alpha pulses. In pregnant sheep, the
             conceptus produces interferon tau (IFNtau) that acts on the
             endometrium to inhibit transcription of the ERalpha gene and
             thus development of the endometrial luteolytic mechanism.
             After Day 13 of pregnancy, the endometrial epithelia do not
             express the PR, whereas the stroma and myometrium remain PR
             positive. The absence of PR in the endometrial GE is
             required for onset of differentiated function of the glands
             during pregnancy. The sequential, overlapping actions of
             progesterone, IFNtau, placental lactogen (PL), and growth
             hormone (GH) comprise a hormonal servomechanism that
             regulates endometrial gland morphogenesis and terminal
             differentiated function during gestation. In pigs, estrogen,
             the pregnancy-recognition signal, increases fibroblast
             growth factor 7 (FGF-7) expression in the endometrial LE
             that, in turn, stimulates proliferation and differentiated
             functions of the trophectoderm, which expresses the receptor
             for FGF-7. Strategic manipulation of these physiological
             mechanisms may offer therapeutic schemes to improve uterine
             capacity, conceptus survival, and reproductive health of
             domestic animals and humans.},
   Language = {eng},
   Doi = {10.1095/biolreprod.103.024133},
   Key = {fds174256}
}

@article{fds174106,
   Author = {KA Dunlap and DW Erikson and RC Burghardt and FJ White and KM Reed and JL
             Farmer, TE Spencer and RR Magness and FW Bazer and KJ Bayless and GA
             Johnson},
   Title = {Progesterone and placentation increase secreted
             phosphoprotein one (SPP1 or osteopontin) in uterine glands
             and stroma for histotrophic and hematotrophic support of
             ovine pregnancy.},
   Journal = {Biology of reproduction},
   Volume = {79},
   Number = {5},
   Pages = {983-90},
   Year = {2008},
   Month = {November},
   ISSN = {0006-3363},
   url = {http://dx.doi.org/10.1095/biolreprod.108.071068},
   Keywords = {Animals • Embryonic Development* • Female •
             Osteopontin • Pregnancy • Pregnancy, Animal •
             Progesterone • Sheep • Uterus • metabolism*
             • physiology*},
   Abstract = {Secreted phosphoprotein one (SPP1, osteopontin) may regulate
             conceptus implantation and placentation. We investigated
             effects of progesterone (P(4)) and the conceptus on
             expression and localization of SPP1 in the ovine uterus.
             Steady-state levels of SPP1 mRNA in the endometrium of
             unilaterally pregnant ewes did not differ significantly
             between nongravid and gravid horns within their respective
             days of pregnancy; however, levels did increase as pregnancy
             progressed. SPP1 mRNA was detectable in the glandular
             epithelium (GE) of both nongravid and gravid horns via in
             situ hybridization. SPP1 protein was localized to the apical
             surface of the luminal epithelium of both nongravid and
             gravid uterine horns. Gravid horns exhibited extensive
             stromal SPP1 on Days 40 through 120, whereas SPP1 was
             markedly lower in the stroma of nongravid uterine horns
             through Day 80 of pregnancy. By Day 120, stromal expression
             of SPP1 between nongravid and gravid horns was similar.
             Long-term P(4) treatment of ovariectomized ewes induced SPP1
             in the uterine stroma and GE. A bioactive 45-kDa SPP1
             fragment was purified from uterine secretions and promoted
             ovine trophectoderm cell attachment in vitro. Interestingly,
             increased stromal cell expression of SPP1 was positively
             associated with vascularization as assessed by von
             Willebrand factor staining. Finally, ovine uterine artery
             endothelial cells produced SPP1 during outgrowth into
             three-dimensional collagen matrices in an in vitro model
             system that recapitulates angiogenesis. Collectively, P(4)
             induces and the conceptus further stimulates SPP1 in uterine
             GE and stroma, where SPP1 likely influences histotrophic and
             hematotrophic support of conceptus development.},
   Language = {eng},
   Doi = {10.1095/biolreprod.108.071068},
   Key = {fds174106}
}

@booklet{Johnson99e,
   Author = {G. A. Johnson and T. E. Spencer and R. C. Burghardt and F.
             W. Bazer},
   Title = {Progesterone induces osteopontin expression in ovine
             endometrial glands.},
   Journal = {Biology Of Reproduction},
   Volume = {60},
   Pages = {210 -- 211},
   Year = {1999},
   Key = {Johnson99e}
}

@booklet{Johnson00b,
   Author = {G. A. Johnson and T. E. Spencer and R. C. Burghardt and K.
             M. Taylor and C. A. Gray and F. W. Bazer},
   Title = {Progesterone modulation of osteopontin gene expression in
             the ovine uterus},
   Journal = {Biology Of Reproduction},
   Volume = {62},
   Number = {5},
   Pages = {1315 -- 1321},
   Year = {2000},
   Month = {May},
   Key = {Johnson00b}
}

@article{fds174108,
   Author = {GA Johnson and TE Spencer and RC Burghardt and KM Taylor and CA Gray and FW
             Bazer},
   Title = {Progesterone modulation of osteopontin gene expression in
             the ovine uterus.},
   Journal = {Biology of reproduction},
   Volume = {62},
   Number = {5},
   Pages = {1315-21},
   Year = {2000},
   Month = {May},
   ISSN = {0006-3363},
   Keywords = {Animals • Blotting, Western • Endometrium •
             Epithelial Cells • Female • Fluorescent Antibody
             Technique • Gene Expression • In Situ
             Hybridization • Interferons • Osteopontin •
             Ovariectomy • Progesterone • Receptors,
             Progesterone • Recombinant Proteins • Sheep •
             Sialoglycoproteins • Uterus • antagonists &
             inhibitors • cytology • drug effects •
             genetics* • metabolism • metabolism* •
             pharmacology • physiology • physiology*},
   Abstract = {Osteopontin (OPN) is an acidic phosphorylated glycoprotein
             component of the extracellular matrix that binds to
             integrins at the cell surface to promote cell-cell
             attachment and cell spreading. This matrix constituent is a
             ligand that could potentially bind integrins on
             trophectoderm and endometrium to facilitate superficial
             implantation and placentation. OPN mRNA increases in the
             endometrial glandular epithelium (GE) of early-pregnant
             ewes, and OPN protein is secreted into the uterine lumen.
             Therefore, progesterone and/or interferon-tau (IFNtau) may
             regulate OPN expression in the uterine GE. Cyclic ewes were
             ovariectomized and fitted with intrauterine (i. u.)
             catheters on Day 5 and treated daily with steroids (i.m.)
             and protein (i.u.) as follows: 1) progesterone (P, Days
             5-24) and control serum proteins (CX, Days 11-24); 2) P and
             ZK 136.317 (ZK; progesterone receptor [PR] antagonist, Days
             11-24) and CX proteins; 3) P and recombinant ovine IFNtau
             (roIFNtau, Days 11-24); or 4) P and ZK and roIFNtau. All
             ewes were hysterectomized on Day 25. Progesterone induced
             the expression of endometrial OPN mRNA in the GE and
             increased secretion of a 45-kDa OPN protein from endometrial
             explants maintained in culture for 24 h. Administration of
             ZK ablated progesterone effects. Intrauterine infusion of
             roIFNtau did not affect OPN gene expression or secretion in
             any of the steroid treatments. Interestingly, OPN
             mRNA-positive GE cells lacked detectable PR expression,
             although PR were detected in the stroma. Results indicate
             that progesterone regulates OPN expression in GE through a
             complex mechanism that includes PR down-regulation, and we
             suggest the possible involvement of a progesterone-induced
             stromal cell-derived growth factor(s) that acts as a
             progestamedin.},
   Language = {eng},
   Key = {fds174108}
}

@booklet{Qiu97a,
   Author = {Qiu, H and Hedlund, LW and Gewalt, SL and Benveniste, H and Bare, TM and Johnson, GA},
   Title = {Progression of a focal ischemic lesion in rat brain during
             treatment with a novel glycine/NMDA antagonist: an in vivo
             three-dimensional diffusion-weighted MR microscopy
             study.},
   Journal = {J Magn Reson Imaging},
   Volume = {7},
   Number = {4},
   Pages = {739-744},
   Year = {1997},
   url = {http://dx.doi.org/10.1002/jmri.1880070421},
   Abstract = {Stroke was induced in two groups of anesthetized rats by
             occlusion of the middle cerebral artery (MCA) and
             ipsilateral common carotid artery. Group 1 (control)
             received vehicle and group 2 received the glycine
             N-methyl-D-aspartate (NMDA) antagonist ZD9379. Stroke volume
             was assessed by three-dimensional diffusion-weighted MR
             microscopy at 2.5 and 6 hours of MCA occlusion. At 2.5
             hours, stroke volumes were identical in the two groups. At 6
             hours, stroke volumes had increased by 15% in the control
             group; in contrast, the treated group showed a 40% reduced
             stroke volume. Conclusions from this in vivo study were as
             follows: (a) our technique allows more efficient and
             accurate measurement of stroke volume with an improvement in
             resolution over a previous method; (b) the ability to
             measure stroke volume at multiple time points shows volume
             change and assessment of time dependency of drug treatment;
             (c) at 6 hours, the glycine antagonist ZD9379 reduced stroke
             volume by 40%.},
   Doi = {10.1002/jmri.1880070421},
   Key = {Qiu97a}
}

@article{fds132877,
   Author = {H Qiu and LW Hedlund and SL Gewalt and H Benveniste and TM Bare and GA
             Johnson},
   Title = {Progression of a focal ischemic lesion in rat brain during
             treatment with a novel glycine/NMDA antagonist: an in vivo
             three-dimensional diffusion-weighted MR microscopy
             study.},
   Journal = {Journal of magnetic resonance imaging : JMRI, UNITED
             STATES},
   Volume = {7},
   Number = {4},
   Pages = {739-44},
   ISSN = {1053-1807},
   Keywords = {Animals • Brain • Brain Ischemia • Female
             • Image Processing, Computer-Assisted • Magnetic
             Resonance Imaging • Pyridazines • Quinolines
             • Rats • Rats, Inbred F344 • Receptors,
             Glycine • Time Factors • antagonists & inhibitors*
             • drug therapy* • methods • methods* •
             pathology • pathology* • therapeutic
             use*},
   Abstract = {Stroke was induced in two groups of anesthetized rats by
             occlusion of the middle cerebral artery (MCA) and
             ipsilateral common carotid artery. Group 1 (control)
             received vehicle and group 2 received the glycine
             N-methyl-D-aspartate (NMDA) antagonist ZD9379. Stroke volume
             was assessed by three-dimensional diffusion-weighted MR
             microscopy at 2.5 and 6 hours of MCA occlusion. At 2.5
             hours, stroke volumes were identical in the two groups. At 6
             hours, stroke volumes had increased by 15% in the control
             group; in contrast, the treated group showed a 40% reduced
             stroke volume. Conclusions from this in vivo study were as
             follows: (a) our technique allows more efficient and
             accurate measurement of stroke volume with an improvement in
             resolution over a previous method; (b) the ability to
             measure stroke volume at multiple time points shows volume
             change and assessment of time dependency of drug treatment;
             (c) at 6 hours, the glycine antagonist ZD9379 reduced stroke
             volume by 40%.},
   Key = {fds132877}
}

@booklet{Stewart00a,
   Author = {M. D. Stewart and G. A. Johnson and C. A. Gray and R. C.
             Burghardt and L. A. Schuler and M. M. Joyce and F. W. Bazer and T. E. Spencer},
   Title = {Prolactin receptor and uterine milk protein expression in
             the ovine endometrium during the estrous cycle and
             pregnancy},
   Journal = {Biology Of Reproduction},
   Volume = {62},
   Number = {6},
   Pages = {1779 -- 1789},
   Year = {2000},
   Month = {June},
   Key = {Stewart00a}
}

@article{fds174216,
   Author = {MD Stewart and GA Johnson and CA Gray and RC Burghardt and LA Schuler and MM Joyce and FW Bazer and TE Spencer},
   Title = {Prolactin receptor and uterine milk protein expression in
             the ovine endometrium during the estrous cycle and
             pregnancy.},
   Journal = {Biology of reproduction},
   Volume = {62},
   Number = {6},
   Pages = {1779-89},
   Year = {2000},
   Month = {June},
   ISSN = {0006-3363},
   Keywords = {Animals • Endometrium • Estrus • Female
             • Fluorescent Antibody Technique • Gene
             Expression* • Glycoproteins • Immunohistochemistry
             • In Situ Hybridization • Pregnancy • RNA,
             Messenger • Receptors, Prolactin • Reverse
             Transcriptase Polymerase Chain Reaction • Serpins*
             • Sheep* • analysis • genetics* •
             metabolism* • physiology*},
   Abstract = {Lactogenic hormones regulate epithelial proliferation,
             differentiation, and function in a variety of
             epitheliomesenchymal organs. During pregnancy, the ovine
             uterus is a potential site for endocrine and paracrine
             actions of lactogenic hormones in the form of pituitary
             prolactin (PRL) and placental lactogen (PL). These studies
             determined temporal and spatial alterations in PRL receptor
             (PRL-R) and expression of uterine milk proteins (UTMP), a
             marker of endometrial secretory activity, in the ovine
             endometrium during the estrous cycle and pregnancy.
             Slot-blot hybridization analysis indicated that steady-state
             levels of endometrial PRL-R mRNA increased during pregnancy.
             In situ hybridization and immunohistochemical analyses
             indicated that PRL-R mRNA and protein were exclusively
             expressed in the endometrial glandular epithelium (GE). No
             PRL-R mRNA expression was detected in luminal epithelium,
             stroma, myometrium, or conceptus trophectoderm. Reverse
             transcription-polymerase chain reaction analyses determined
             that the endometrial GE expressed both long and short
             alternative splice forms of the ovine PRL-R gene. Slot-blot
             hybridization analysis indicated that steady-state levels of
             intercaruncular endometrial UTMP mRNA increased about 3-fold
             between Days 20 and 60, increased another 3-fold between
             Days 60 and 80, and then declined slightly to Day 120. In
             pregnant ewes, UTMP mRNA expression was restricted to the
             endometrial GE in the stratum spongiosum (sGE), increased
             substantially between Days 15 and 17, and, between Days 17
             to 50 of gestation, was markedly higher in upper than lower
             sGE. After Day 50, hyperplasia of the sGE was accompanied by
             increased UTMP mRNA expression by all sGE. Collectively,
             results indicate that 1) endometrial sGE is a primary target
             for actions of lactogenic hormones and 2) UTMP mRNA
             expression is correlated with PL production by the
             trophectoderm and state of sGE differentiation during
             pregnancy. It is proposed that activation of PRL-R signal
             transduction pathways by PRL and PL plays a major role in
             endometrial GE remodeling and differentiated function during
             pregnancy in support of conceptus growth and
             development.},
   Language = {eng},
   Key = {fds174216}
}

@booklet{Stewart99,
   Author = {M. D. Stewart and G. A. Johnson and A. G. Stagg and R. C.
             Burghardt and L. A. Schuler and F. W. Bazer and T. E.
             Spencer},
   Title = {Prolactin receptor expression in the ovine
             uterus.},
   Journal = {Biology Of Reproduction},
   Volume = {60},
   Pages = {150 -- 150},
   Year = {1999},
   Key = {Stewart99}
}

@article{fds180931,
   Author = {G Wu and FW Bazer and RC Burghardt and GA Johnson and SW Kim and DA Knabe and P Li and X Li, JR McKnight and MC Satterfield and TE
             Spencer},
   Title = {Proline and hydroxyproline metabolism: implications for
             animal and human nutrition.},
   Journal = {Amino acids},
   Year = {2010},
   Month = {August},
   ISSN = {1438-2199},
   url = {http://dx.doi.org/10.1007/s00726-010-0715-z},
   Abstract = {Proline plays important roles in protein synthesis and
             structure, metabolism (particularly the synthesis of
             arginine, polyamines, and glutamate via pyrroline-5-carboxylate),
             and nutrition, as well as wound healing, antioxidative
             reactions, and immune responses. On a per-gram basis,
             proline plus hydroxyproline are most abundant in collagen
             and milk proteins, and requirements of proline for
             whole-body protein synthesis are the greatest among all
             amino acids. Therefore, physiological needs for proline are
             particularly high during the life cycle. While most mammals
             (including humans and pigs) can synthesize proline from
             arginine and glutamine/glutamate, rates of endogenous
             synthesis are inadequate for neonates, birds, and fish.
             Thus, work with young pigs (a widely used animal model for
             studying infant nutrition) has shown that supplementing 0.0,
             0.35, 0.7, 1.05, 1.4, and 2.1% proline to a proline-free
             chemically defined diet containing 0.48% arginine and 2%
             glutamate dose dependently improved daily growth rate and
             feed efficiency while reducing concentrations of urea in
             plasma. Additionally, maximal growth performance of chickens
             depended on at least 0.8% proline in the diet. Likewise,
             dietary supplementation with 0.07, 0.14, and 0.28%
             hydroxyproline (a metabolite of proline) to a plant
             protein-based diet enhanced weight gains of salmon. Based on
             its regulatory roles in cellular biochemistry, proline can
             be considered as a functional amino acid for mammalian,
             avian, and aquatic species. Further research is warranted to
             develop effective strategies of dietary supplementation with
             proline or hydroxyproline to benefit health, growth, and
             development of animals and humans.},
   Language = {ENG},
   Doi = {10.1007/s00726-010-0715-z},
   Key = {fds180931}
}

@article{fds174207,
   Author = {G Wu and FW Bazer and S Datta and GA Johnson and P Li and MC Satterfield and TE Spencer},
   Title = {Proline metabolism in the conceptus: implications for fetal
             growth and development.},
   Journal = {Amino acids},
   Volume = {35},
   Number = {4},
   Pages = {691-702},
   Year = {2008},
   Month = {November},
   ISSN = {1438-2199},
   url = {http://dx.doi.org/10.1007/s00726-008-0052-7},
   Keywords = {Amino Acids • Animals • Embryo, Mammalian •
             Female • Fetal Development* • Humans •
             Models, Biological • Placenta • Polyamines •
             Pregnancy • Pregnancy, Animal • Proline •
             Sheep • Swine • metabolism •
             metabolism*},
   Abstract = {Although there are published studies of proline biochemistry
             and nutrition in cultured cells and postnatal animals,
             little is known about proline metabolism and function in the
             conceptus (embryo/fetus, associated placental membranes, and
             fetal fluids). Because of the invasive nature of biochemical
             research on placental and fetal growth, animal models are
             often used to test hypotheses of biological importance.
             Recent evidence from studies with pigs and sheep shows that
             proline is a major substrate for polyamine synthesis via
             proline oxidase, ornithine aminotransferase, and ornithine
             decarboxylase in placentae. Both porcine and ovine placentae
             have a high capacity for proline catabolism and polyamine
             production. In addition, allantoic and amniotic fluids
             contain enzymes to convert proline into ornithine, which is
             delivered through the circulation to placental tissues.
             There is exquisite metabolic coordination among integrated
             pathways that support highest rates of polyamine synthesis
             and concentrations in placentae during early gestation when
             placental growth is most rapid. Interestingly, reduced
             placental and fetal growth are associated with reductions in
             placental proline transport, proline oxidase activity, and
             concentrations of polyamines in gestating dams with either
             naturally occurring or malnutrition-induced growth
             retardation. Conversely, increasing proline availability in
             maternal plasma through nutritional or pharmacological
             modulation in pigs and sheep enhances concentrations of
             proline and polyamines in placentae and fetal fluids, as
             well as fetal growth. These novel findings suggest an
             important role for proline in conceptus metabolism, growth
             and development, as well as a potential treatment for
             intrauterine growth restriction, which is a significant
             problem in both human medicine and animal
             agriculture.},
   Language = {eng},
   Doi = {10.1007/s00726-008-0052-7},
   Key = {fds174207}
}

@article{fds174186,
   Author = {GA Johnson},
   Title = {Psychological sequelae in stroke patients.},
   Journal = {Australian family physician},
   Volume = {20},
   Number = {11},
   Pages = {1605-7, 1610-1},
   Year = {1991},
   Month = {November},
   ISSN = {0300-8495},
   Keywords = {Anxiety Disorders • Cerebrovascular Disorders •
             Dementia • Depression • Humans • etiology
             • psychology* • therapy},
   Abstract = {The psychological sequelae of depression, anxiety and
             dementia are discussed as they affect the stroke sufferer.
             The author discusses the management options available to
             deal with these problems.},
   Language = {eng},
   Key = {fds174186}
}

@article{fds268858,
   Author = {Mistry, NN and Pollaro, J and Song, J and De Lin and M and Johnson,
             GA},
   Title = {Pulmonary perfusion imaging in the rodent lung using dynamic
             contrast-enhanced MRI.},
   Journal = {Magn Reson Med},
   Volume = {59},
   Number = {2},
   Pages = {289-297},
   Year = {2008},
   Month = {February},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/18228577},
   Keywords = {Animals • Contrast Media • Female •
             Gadolinium DTPA • Image Processing, Computer-Assisted
             • Lung • Magnetic Resonance Imaging •
             Phantoms, Imaging • Rats • Rats, Inbred F344
             • blood supply* • methods* •
             pharmacokinetics*},
   Abstract = {With the development of various models of pulmonary disease,
             there is tremendous interest in quantitative regional
             assessment of pulmonary function. While ventilation imaging
             has been addressed to a certain extent, perfusion imaging
             for small animals has not kept pace. In humans and large
             animals perfusion can be assessed using dynamic
             contrast-enhanced (DCE) MRI with a single bolus injection of
             a gadolinium (Gd)-based contrast agent. But the method
             developed for the clinic cannot be translated directly to
             image the rodent due to the combined requirements of higher
             spatial and temporal resolution. This work describes a novel
             image acquisition technique staggered over multiple,
             repeatable bolus injections of contrast agent using an
             automated microinjector, synchronized with image acquisition
             to achieve dynamic first-pass contrast enhancement in the
             rat lung. This allows dynamic first-pass imaging that can be
             used to quantify pulmonary perfusion. Further improvements
             are made in the spatial and temporal resolution by combining
             the multiple injection acquisition method with Interleaved
             Radial Imaging and "Sliding window-keyhole" reconstruction
             (IRIS). The results demonstrate a simultaneous increase in
             spatial resolution (<200 mum) and temporal resolution (<200
             ms) over previous methods, with a limited loss in
             signal-to-noise-ratio.},
   Doi = {10.1002/mrm.21353},
   Key = {fds268858}
}

@article{fds268841,
   Author = {MacKenzie-Graham, A and Tiwari-Woodruff, SK and Sharma, G and Aguilar, C and Vo, KT and Strickland, LV and Morales, L and Fubara, B and Martin, M and Jacobs, RE and Johnson, GA and Toga, AW and Voskuhl,
             RR},
   Title = {Purkinje cell loss in experimental autoimmune
             encephalomyelitis.},
   Journal = {Neuroimage},
   Volume = {48},
   Number = {4},
   Pages = {637-651},
   Year = {2009},
   Month = {December},
   ISSN = {1053-8119},
   url = {http://dx.doi.org/10.1016/j.neuroimage.2009.06.073},
   Abstract = {Gray matter atrophy observed by brain MRI is an important
             correlate to clinical disability and disease duration in
             multiple sclerosis. The objective of this study was to link
             brain atrophy visualized by neuroimaging to its underlying
             neuropathology using the MS model, experimental autoimmune
             encephalomyelitis (EAE). Volumetric changes in brains of EAE
             mice, as well as matched healthy normal controls, were
             quantified by collecting post-mortem high-resolution
             T2-weighted magnetic resonance microscopy and actively
             stained magnetic resonance histology images. Anatomical
             delineations demonstrated a significant decrease in the
             volume of the whole cerebellum, cerebellar cortex, and
             molecular layer of the cerebellar cortex in EAE as compared
             to normal controls. The pro-apoptotic marker caspase-3 was
             detected in Purkinje cells and a significant decrease in
             Purkinje cell number was found in EAE. Cross modality and
             temporal correlations revealed a significant association
             between Purkinje cell loss on neuropathology and atrophy of
             the molecular layer of the cerebellar cortex by
             neuroimaging. These results demonstrate the power of using
             combined population atlasing and neuropathology approaches
             to discern novel insights underlying gray matter atrophy in
             animal models of neurodegenerative disease.},
   Doi = {10.1016/j.neuroimage.2009.06.073},
   Key = {fds268841}
}

@booklet{Grist88,
   Author = {T. M. Grist and J. S. Hyde and A. Jesmanowicz and G. A.
             Johnson},
   Title = {Quadrature detection local coils for mri and
             mrs},
   Journal = {Investigative Radiology},
   Volume = {23},
   Number = {9},
   Pages = {S21 -- S21},
   Year = {1988},
   Month = {September},
   Key = {Grist88}
}

@article{fds357201,
   Author = {Sills, RC and Johnson, GA and Anderson, RJ and Johnson, CL and Staup, M and Brown, DL and Churchill, SR and Kurtz, DM and Cushman, JD and Waidyanatha, S and Robinson, VG and Cesta, MF and Andrews, DMK and Behl,
             M and Shockley, KR and Little, PB},
   Title = {Qualitative and Quantitative Neuropathology Approaches Using
             Magnetic Resonance Microscopy (Diffusion Tensor Imaging) and
             Stereology in a Hexachlorophene Model of Myelinopathy in
             Sprague-Dawley Rats.},
   Journal = {Toxicol Pathol},
   Volume = {48},
   Number = {8},
   Pages = {965-980},
   Year = {2020},
   Month = {December},
   url = {http://dx.doi.org/10.1177/0192623320968210},
   Abstract = {It is well established that hexachlorophene, which is used
             as an antibacterial agent, causes intramyelinic edema in
             humans and animal models. The hexachlorophene myelinopathy
             model, in which male Sprague-Dawley rats received 25 to 30
             mg/kg hexachlorophene by gavage for up to 5 days, provided
             an opportunity to compare traditional neuropathology
             evaluations with magnetic resonance microscopy (MRM)
             findings. In addition, stereology assessments of 3
             neuroanatomical sites were compared to quantitative
             measurements of similar structures by MRM. There were
             positive correlations between hematoxylin and eosin and
             luxol fast blue stains and MRM for identifying intramyelinic
             edema in the cingulum of corpus callosum, optic chiasm,
             anterior commissure (aca), lateral olfactory tracts,
             pyramidal tracts (py), and white matter tracts in the
             cerebellum. Stereology assessments were focused on the aca,
             longitudinal fasciculus of the pons, and py and demonstrated
             differences between control and treated rats, as was
             observed using MRM. The added value of MRM assessments was
             the ability to acquire qualitative 3-dimensional (3-D)
             images and obtain quantitative measurements of intramyelinic
             edema in 26 neuroanatomical sites in the intact brain. Also,
             diffusion tensor imaging (fractional anisotropy [FA])
             indicated that there were changes in the cytoarchitecture of
             the white matter as detected by decreases in the FA in the
             treated compared to the control rats. This study
             demonstrates creative strategies that are possible using
             qualitative and quantitative assessments of potential white
             matter neurotoxicants in nonclinical toxicity studies. Our
             results lead us to the conclusion that volumetric analysis
             by MRM and stereology adds significant value to the standard
             2-D microscopic evaluations.},
   Doi = {10.1177/0192623320968210},
   Key = {fds357201}
}

@booklet{Chotas96,
   Author = {Chotas, HG and Floyd, CE and Johnson, GA and Ravin,
             CE},
   Title = {Quality control phantom for digital chest
             radiography},
   Journal = {RADIOLOGY},
   Volume = {201},
   Pages = {685-685},
   Publisher = {RADIOLOGICAL SOC NORTH AMER},
   Year = {1996},
   Month = {November},
   ISSN = {0033-8419},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1996VP84300732&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Chotas96}
}

@article{fds132883,
   Author = {HG Chotas and CE Floyd and GA Johnson and CE Ravin},
   Title = {Quality control phantom for digital chest
             radiography.},
   Journal = {Radiology, UNITED STATES},
   Volume = {202},
   Number = {1},
   Pages = {111-6},
   Year = {1997},
   Month = {January},
   ISSN = {0033-8419},
   Keywords = {Humans • Phantoms, Imaging* • Quality Control
             • Radiographic Image Enhancement • Radiography,
             Thoracic • standards*},
   Abstract = {PURPOSE: To develop and test a chest phantom for routine
             quality control testing of digital radiography systems.
             MATERIALS AND METHODS: The phantom was constructed from
             sheets of copper, aluminum, and acrylic, which were cut and
             arranged to yield a radiographic projection resembling that
             of a human thorax. Regional test objects allowed
             quantitative assessment of optical density, contrast detail,
             and spatial resolution. Validation tests were performed to
             assess image stability in a stable imaging environment and
             sensitivity to changes in image quality when they occur.
             RESULTS: The phantom yielded consistent pseudoclinical
             images when used in a routine quality control program and
             facilitated detection of simulated problems that were
             induced in imaging system performance. CONCLUSION: The chest
             phantom enables quantitative, full-system testing of digital
             radiography system as they are used clinically for chest
             radiography.},
   Key = {fds132883}
}

@booklet{Chotas97,
   Author = {Chotas, HG and Floyd, CE and Johnson, GA and Ravin,
             CE},
   Title = {Quality control phantom for digital chest
             radiography.},
   Journal = {Radiology},
   Volume = {202},
   Number = {1},
   Pages = {111-116},
   Year = {1997},
   Month = {January},
   ISSN = {0033-8419},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/8988199},
   Abstract = {PURPOSE: To develop and test a chest phantom for routine
             quality control testing of digital radiography systems.
             MATERIALS AND METHODS: The phantom was constructed from
             sheets of copper, aluminum, and acrylic, which were cut and
             arranged to yield a radiographic projection resembling that
             of a human thorax. Regional test objects allowed
             quantitative assessment of optical density, contrast detail,
             and spatial resolution. Validation tests were performed to
             assess image stability in a stable imaging environment and
             sensitivity to changes in image quality when they occur.
             RESULTS: The phantom yielded consistent pseudoclinical
             images when used in a routine quality control program and
             facilitated detection of simulated problems that were
             induced in imaging system performance. CONCLUSION: The chest
             phantom enables quantitative, full-system testing of digital
             radiography system as they are used clinically for chest
             radiography.},
   Doi = {10.1148/radiology.202.1.8988199},
   Key = {Chotas97}
}

@article{fds268834,
   Author = {Mistry, NN and Thomas, A and Kaushik, SS and Johnson, GA and Driehuys,
             B},
   Title = {Quantitative analysis of hyperpolarized 3He ventilation
             changes in mice challenged with methacholine.},
   Journal = {Magn Reson Med},
   Volume = {63},
   Number = {3},
   Pages = {658-666},
   Year = {2010},
   Month = {March},
   ISSN = {1522-2594},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/20187176},
   Keywords = {Administration, Inhalation • Algorithms* • Animals
             • Asthma • Contrast Media • Helium •
             Image Enhancement • Isotopes • Magnetic Resonance
             Imaging • Methacholine Chloride • Mice •
             Mice, Inbred C57BL • Reproducibility of Results •
             Sensitivity and Specificity • administration & dosage
             • diagnosis* • diagnostic use • diagnostic
             use* • methods*},
   Abstract = {The capability to use high-resolution (3)He MRI to depict
             regional ventilation changes and airway narrowing in mice
             challenged with methacholine (MCh) offers the opportunity to
             gain new insights into the study of asthma. However, to
             fully exploit the value of this novel technique, it is
             important to move beyond visual inspection of the images
             toward automated and quantitative analysis. To address this
             gap, we describe a postprocessing approach to create
             ventilation difference maps to better visualize and quantify
             regional ventilation changes before and after MCh challenge.
             We show that difference maps reveal subtle changes in airway
             caliber, and highlight both focal and diffuse regional
             alterations in ventilation. Ventilation changes include both
             hypoventilation and compensatory areas of hyperventilation.
             The difference maps can be quantified by a histogram plot of
             the ventilation changes, in which the standard deviation
             increases with MCh dose (R(2) = 0.89). This method of
             analysis is shown to be more sensitive than simple
             threshold-based detection of gross ventilation
             defects.},
   Language = {eng},
   Doi = {10.1002/mrm.22311},
   Key = {fds268834}
}

@article{fds268828,
   Author = {Lin, M and Marshall, CT and Qi, Y and Johnston, SM and Badea, CT and Piantadosi, CA and Johnson, GA},
   Title = {Quantitative blood flow measurements in the small animal
             cardiopulmonary system using digital subtraction
             angiography.},
   Journal = {Med Phys},
   Volume = {36},
   Number = {11},
   Pages = {5347-5358},
   Year = {2009},
   Month = {November},
   ISSN = {0094-2405},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/19994543},
   Keywords = {Angiography, Digital Subtraction • Animals •
             Calibration • Heart • Lung • Male •
             Phantoms, Imaging • Rats • Rats, Inbred F344
             • Regional Blood Flow* • Thermodilution •
             anatomy & histology • methods* •
             physiology*},
   Abstract = {PURPOSE: The use of preclinical rodent models of disease
             continues to grow because these models help elucidate
             pathogenic mechanisms and provide robust test beds for drug
             development. Among the major anatomic and physiologic
             indicators of disease progression and genetic or drug
             modification of responses are measurements of blood vessel
             caliber and flow. Moreover, cardiopulmonary blood flow is a
             critical indicator of gas exchange. Current methods of
             measuring cardiopulmonary blood flow suffer from some or all
             of the following limitations--they produce relative values,
             are limited to global measurements, do not provide
             vasculature visualization, are not able to measure acute
             changes, are invasive, or require euthanasia. METHODS: In
             this study, high-spatial and high-temporal resolution x-ray
             digital subtraction angiography (DSA) was used to obtain
             vasculature visualization, quantitative blood flow in
             absolute metrics (ml/min instead of arbitrary units or
             velocity), and relative blood volume dynamics from discrete
             regions of interest on a pixel-by-pixel basis (100 x 100
             microm2). RESULTS: A series of calibrations linked the DSA
             flow measurements to standard physiological measurement
             using thermodilution and Fick's method for cardiac output
             (CO), which in eight anesthetized Fischer-344 rats was found
             to be 37.0 +/- 5.1 ml/min. Phantom experiments were
             conducted to calibrate the radiographic density to vessel
             thickness, allowing a link of DSA cardiac output
             measurements to cardiopulmonary blood flow measurements in
             discrete regions of interest. The scaling factor linking
             relative DSA cardiac output measurements to the Fick's
             absolute measurements was found to be 18.90 x CODSA =
             COFick. CONCLUSIONS: This calibrated DSA approach allows
             repeated simultaneous visualization of vasculature and
             measurement of blood flow dynamics on a regional level in
             the living rat.},
   Language = {eng},
   Doi = {10.1118/1.3231823},
   Key = {fds268828}
}

@article{fds268725,
   Author = {Argyridis, I and Li, W and Johnson, GA and Liu, C},
   Title = {Quantitative magnetic susceptibility of the developing mouse
             brain reveals microstructural changes in the white
             matter.},
   Journal = {Neuroimage},
   Volume = {88},
   Pages = {134-142},
   Year = {2014},
   Month = {March},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/24269576},
   Abstract = {Cerebral development involves a complex cascade of events
             which are difficult to visualize and quantify in vivo. In
             this study we combine information from Diffusion Tensor
             Imaging (DTI) and Quantitative Susceptibility Mapping (QSM)
             to analyze developing mouse brains at five stages up to
             56days postnatal. Susceptibility maps were calculated using
             frequency shifts in gradient echo MR images acquired at
             9.4T. The mean apparent magnetic susceptibility and magnetic
             susceptibility anisotropy of major white matter tracts were
             evaluated as a function of age. During the first two weeks,
             susceptibility of white matter appeared paramagnetic
             relative to surrounding gray matter; it then gradually
             became more diamagnetic. While diffusion anisotropy was
             already apparent and high at postnatal day 2, susceptibility
             anisotropy only became significant during the third week.
             This mismatch indicated different microstructural
             underpinnings for diffusion anisotropy and susceptibility
             anisotropy. Histological exams were also performed to
             evaluate myelin and iron content. It is confirmed that the
             main source of susceptibility contrast in WM is the myelin
             content. The ability to quantify the magnetic properties of
             white matter will provide valuable information on the
             architecture of the brain during development and potentially
             a more specific indicator for myelin degenerative
             diseases.},
   Doi = {10.1016/j.neuroimage.2013.11.026},
   Key = {fds268725}
}

@article{fds268718,
   Author = {Johnson, GA and Calabrese, E and Little, PB and Hedlund, L and Qi, Y and Badea, A},
   Title = {Quantitative mapping of trimethyltin injury in the rat brain
             using magnetic resonance histology.},
   Journal = {Neurotoxicology},
   Volume = {42},
   Pages = {12-23},
   Year = {2014},
   Month = {May},
   ISSN = {0161-813X},
   url = {http://hdl.handle.net/10161/10329 Duke open
             access},
   Abstract = {The growing exposure to chemicals in our environment and the
             increasing concern over their impact on health have elevated
             the need for new methods for surveying the detrimental
             effects of these compounds. Today's gold standard for
             assessing the effects of toxicants on the brain is based on
             hematoxylin and eosin (H&E)-stained histology, sometimes
             accompanied by special stains or immunohistochemistry for
             neural processes and myelin. This approach is time-consuming
             and is usually limited to a fraction of the total brain
             volume. We demonstrate that magnetic resonance histology
             (MRH) can be used for quantitatively assessing the effects
             of central nervous system toxicants in rat models. We show
             that subtle and sparse changes to brain structure can be
             detected using magnetic resonance histology, and correspond
             to some of the locations in which lesions are found by
             traditional pathological examination. We report for the
             first time diffusion tensor image-based detection of changes
             in white matter regions, including fimbria and corpus
             callosum, in the brains of rats exposed to 8 mg/kg and 12
             mg/kg trimethyltin. Besides detecting brain-wide changes,
             magnetic resonance histology provides a quantitative
             assessment of dose-dependent effects. These effects can be
             found in different magnetic resonance contrast mechanisms,
             providing multivariate biomarkers for the same spatial
             location. In this study, deformation-based morphometry
             detected areas where previous studies have detected cell
             loss, while voxel-wise analyses of diffusion tensor
             parameters revealed microstructural changes due to such
             things as cellular swelling, apoptosis, and inflammation.
             Magnetic resonance histology brings a valuable addition to
             pathology with the ability to generate brain-wide
             quantitative parametric maps for markers of toxic insults in
             the rodent brain.},
   Doi = {10.1016/j.neuro.2014.02.009},
   Key = {fds268718}
}

@article{fds268796,
   Author = {Badea, A and Gewalt, S and Avants, BB and Cook, JJ and Johnson,
             GA},
   Title = {Quantitative mouse brain phenotyping based on single and
             multispectral MR protocols.},
   Journal = {Neuroimage},
   Volume = {63},
   Number = {3},
   Pages = {1633-1645},
   Year = {2012},
   Month = {November},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/22836174},
   Abstract = {Sophisticated image analysis methods have been developed for
             the human brain, but such tools still need to be adapted and
             optimized for quantitative small animal imaging. We propose
             a framework for quantitative anatomical phenotyping in mouse
             models of neurological and psychiatric conditions. The
             framework encompasses an atlas space, image acquisition
             protocols, and software tools to register images into this
             space. We show that a suite of segmentation tools (Avants,
             Epstein et al., 2008) designed for human neuroimaging can be
             incorporated into a pipeline for segmenting mouse brain
             images acquired with multispectral magnetic resonance
             imaging (MR) protocols. We present a flexible approach for
             segmenting such hyperimages, optimizing registration, and
             identifying optimal combinations of image channels for
             particular structures. Brain imaging with T1, T2* and T2
             contrasts yielded accuracy in the range of 83% for
             hippocampus and caudate putamen (Hc and CPu), but only 54%
             in white matter tracts, and 44% for the ventricles. The
             addition of diffusion tensor parameter images improved
             accuracy for large gray matter structures (by >5%), white
             matter (10%), and ventricles (15%). The use of Markov random
             field segmentation further improved overall accuracy in the
             C57BL/6 strain by 6%; so Dice coefficients for Hc and CPu
             reached 93%, for white matter 79%, for ventricles 68%, and
             for substantia nigra 80%. We demonstrate the segmentation
             pipeline for the widely used C57BL/6 strain, and two test
             strains (BXD29, APP/TTA). This approach appears promising
             for characterizing temporal changes in mouse models of human
             neurological and psychiatric conditions, and may provide
             anatomical constraints for other preclinical imaging, e.g.
             fMRI and molecular imaging. This is the first demonstration
             that multiple MR imaging modalities combined with
             multivariate segmentation methods lead to significant
             improvements in anatomical segmentation in the mouse
             brain.},
   Doi = {10.1016/j.neuroimage.2012.07.021},
   Key = {fds268796}
}

@article{fds268792,
   Author = {Johnson, GA and Badea, A and Jiang, Y},
   Title = {Quantitative neuromorphometry using magnetic resonance
             histology.},
   Journal = {Toxicol Pathol},
   Volume = {39},
   Number = {1},
   Pages = {85-91},
   Year = {2011},
   Month = {January},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/21119052},
   Abstract = {Magnetic resonance imaging (MRI), now common in the clinical
             domain, has been adapted for use by the neuropathologist by
             increasing the spatial resolution over 100,000 times what is
             common in human clinical imaging. This increase in spatial
             resolution has been accomplished through a variety of
             technical advances-higher magnetic fields, more sensitive
             receivers, and clever encoding methods. Magnetic resonance
             histology (MRH), that is, the application of MRI to study
             tissue specimens, now makes three-dimensional imaging of the
             fixed brain in the cranium routine. Active staining
             (perfusion fixation with a paramagnetic contrast agent) has
             allowed us to reduce the scan time by more than 8 times over
             earlier methods. The result is a three-dimensional isotropic
             image array that can be viewed along any direction without
             loss of spatial resolution. Homologous slices can be chosen
             interactively. Since the tissue is still fully hydrated in
             the cranium, tissue shrinkage and distortion are virtually
             eliminated. Volume measurements of neural structures can be
             made with a high degree of precision and accuracy. MRH will
             not replace more traditional methods, but it promises
             enormous value in choosing particular areas and times for
             more traditional sectioning and assessment.},
   Doi = {10.1177/0192623310389622},
   Key = {fds268792}
}

@article{fds132838,
   Author = {H Benveniste and GP Cofer and CA Piantadosi and JN Davis and GA
             Johnson},
   Title = {Quantitative proton magnetic resonance imaging in focal
             cerebral ischemia in rat brain.},
   Journal = {Stroke; a journal of cerebral circulation, UNITED
             STATES},
   Volume = {22},
   Number = {2},
   Pages = {259-68},
   Year = {1991},
   Month = {February},
   ISSN = {0039-2499},
   Keywords = {Animals • Brain • Brain Ischemia • Cerebral
             Infarction • Diagnosis, Computer-Assisted •
             Magnetic Resonance Imaging* • Necrosis • Rats
             • Rats, Inbred Strains • Silver • diagnosis
             • diagnosis* • diagnostic use • pathology
             • pathology*},
   Abstract = {Proton magnetic resonance (MR) imaging has been recommended
             as a diagnostic tool for the detection of focal cerebral
             ischemia. We compared microscopic MR images of rat brains
             after focal cerebral ischemia with evidence of histological
             damage found on corresponding silver-impregnated or cresyl
             violet-stained brain sections. Ten male Wistar rats were
             subjected to permanent unilateral occlusions of the right
             middle cerebral and common carotid arteries under halothane
             anesthesia. Twenty-four hours later the area of injury on MR
             images amounted to 26% of the total slice area, whereas only
             9% of the total slice area was necrotic on histological
             sections from the same animals. The infarcted areas on
             tissue sections were surrounded by regions of selective
             neuronal injury in the cerebral cortex and occasionally in
             the hippocampus. The area of injury on MR images was larger
             than the combined areas of infarction and selective neuronal
             injury on histological sections. Areas of increased T2
             values on MR images extended medially into noninfarcted
             striatum and laterally and dorsally into noninfarcted
             cortex. The lateral and dorsal areas on MR images frequently
             coincided with cortical areas in which considerable
             selective neuronal injury was present in the upper cortical
             layers. We hypothesize that the abnormal areas on MR images
             above histologically normal brain tissue represent the
             ischemic penumbra. If true, this is the first demonstration
             of the ischemic penumbra by MR imaging and may reflect our
             use of Wistar rats, a new image analysis technique, and
             ultra-high resolution MR imaging.},
   Key = {fds132838}
}

@booklet{Benveniste91,
   Author = {Benveniste, H and Cofer, GP and Piantadosi, CA and Davis, JN and Johnson, GA},
   Title = {Quantitative proton magnetic resonance imaging in focal
             cerebral ischemia in rat brain.},
   Journal = {Stroke},
   Volume = {22},
   Number = {2},
   Pages = {259-268},
   Year = {1991},
   Month = {February},
   ISSN = {0039-2499},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/2003291},
   Abstract = {Proton magnetic resonance (MR) imaging has been recommended
             as a diagnostic tool for the detection of focal cerebral
             ischemia. We compared microscopic MR images of rat brains
             after focal cerebral ischemia with evidence of histological
             damage found on corresponding silver-impregnated or cresyl
             violet-stained brain sections. Ten male Wistar rats were
             subjected to permanent unilateral occlusions of the right
             middle cerebral and common carotid arteries under halothane
             anesthesia. Twenty-four hours later the area of injury on MR
             images amounted to 26% of the total slice area, whereas only
             9% of the total slice area was necrotic on histological
             sections from the same animals. The infarcted areas on
             tissue sections were surrounded by regions of selective
             neuronal injury in the cerebral cortex and occasionally in
             the hippocampus. The area of injury on MR images was larger
             than the combined areas of infarction and selective neuronal
             injury on histological sections. Areas of increased T2
             values on MR images extended medially into noninfarcted
             striatum and laterally and dorsally into noninfarcted
             cortex. The lateral and dorsal areas on MR images frequently
             coincided with cortical areas in which considerable
             selective neuronal injury was present in the upper cortical
             layers. We hypothesize that the abnormal areas on MR images
             above histologically normal brain tissue represent the
             ischemic penumbra. If true, this is the first demonstration
             of the ischemic penumbra by MR imaging and may reflect our
             use of Wistar rats, a new image analysis technique, and
             ultra-high resolution MR imaging.},
   Doi = {10.1161/01.str.22.2.259},
   Key = {Benveniste91}
}

@article{fds268726,
   Author = {Xie, L and Sparks, MA and Li, W and Qi, Y and Liu, C and Coffman, TM and Johnson, GA},
   Title = {Quantitative susceptibility mapping of kidney inflammation
             and fibrosis in type 1 angiotensin receptor-deficient
             mice.},
   Journal = {NMR Biomed},
   Volume = {26},
   Number = {12},
   Pages = {1853-1863},
   Year = {2013},
   Month = {December},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/24154952},
   Abstract = {Disruption of the regulatory role of the kidneys leads to
             diverse renal pathologies; one major hallmark is
             inflammation and fibrosis. Conventional magnitude MRI has
             been used to study renal pathologies; however, the
             quantification or even detection of focal lesions caused by
             inflammation and fibrosis is challenging. We propose that
             quantitative susceptibility mapping (QSM) may be
             particularly sensitive for the identification of
             inflammation and fibrosis. In this study, we applied QSM in
             a mouse model deficient for angiotensin receptor type 1
             (AT1). This model is known for graded pathologies, including
             focal interstitial fibrosis, cortical inflammation,
             glomerulocysts and inner medullary hypoplasia. We acquired
             high-resolution MRI on kidneys from AT1-deficient mice that
             were perfusion fixed with contrast agent. Two MR sequences
             were used (three-dimensional spin echo and gradient echo) to
             produce three image contrasts: T1, T2* (magnitude) and QSM.
             T1 and T2* (magnitude) images were acquired to segment major
             renal structures and to provide landmarks for the focal
             lesions of inflammation and fibrosis in the
             three-dimensional space. The volumes of major renal
             structures were measured to determine the relationship of
             the volumes to the degree of renal abnormalities and
             magnetic susceptibility values. Focal lesions were segmented
             from QSM images and were found to be closely associated with
             the major vessels. Susceptibilities were relatively more
             paramagnetic in wild-type mice: 1.46 ± 0.36 in the cortex,
             2.14 ± 0.94 in the outer medulla and 2.10 ± 2.80 in the
             inner medulla (10(-2) ppm). Susceptibilities were more
             diamagnetic in knockout mice: -7.68 ± 4.22 in the cortex,
             -11.46 ± 2.13 in the outer medulla and -7.57 ± 5.58 in the
             inner medulla (10(-2) ppm). This result was consistent with
             the increase in diamagnetic content, e.g. proteins and
             lipids, associated with inflammation and fibrosis. Focal
             lesions were validated with conventional histology. QSM was
             very sensitive in detecting pathology caused by small focal
             inflammation and fibrosis. QSM offers a new MR contrast
             mechanism to study this common disease marker in the
             kidney.},
   Doi = {10.1002/nbm.3039},
   Key = {fds268726}
}

@article{fds132732,
   Author = {G.A. Johnson},
   Title = {R.D. Black, H. Middleton, G.D. Cates, G.P. Cofer, B.
             Driehuys, W. Happer,   L. W. Hedlund, G.A. Johnson, M.D.
             Shattuck, J. Swartz, In vivo He-3 MR   Images of guinea pig
             lungs.  Radiology 199, 867-870 (1996).},
   Year = {1996},
   Key = {fds132732}
}

@article{fds132718,
   Author = {G.A. Johnson},
   Title = {R.T. Engelhardt, G.A. Johnson, T1r relaxation and its
             application to MR  histology.  Magnetic Resonance in
             Medicine 35, 781-786 (1996).},
   Year = {1996},
   Key = {fds132718}
}

@booklet{Frush01,
   Author = {Frush, DP and Yoshizumi, TT and Paulson, EK and Johnson,
             GA},
   Title = {Radiation dose from helical CT in children: Comparison of
             multi-slice and single-slice protocols},
   Journal = {RADIOLOGY},
   Volume = {221},
   Pages = {246-246},
   Publisher = {RADIOLOGICAL SOC NORTH AMERICA},
   Year = {2001},
   Month = {November},
   ISSN = {0033-8419},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000172126600589&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Frush01}
}

@article{8979178,
   Author = {Kelly, W.M. and Low, N.M. and Zillmer, A. and Johnson, G.A. and Normand, E.},
   Title = {Radiation environments and exposure considerations for the
             Multi-Mission Radioisotope Thermoelectric
             Generator},
   Journal = {AIP Conf. Proc. (USA)},
   Number = {813},
   Pages = {906 - 19},
   Year = {2006},
   Keywords = {electromagnetic shielding;magnetic fields;radiation;radioisotope
             thermoelectric generators;},
   Abstract = {The Multi-Mission Radioisotope Thermoelectric Generator
             (MMRTG) is the next generation (RTG) being developed by DOE
             to provide reliable, long-life electric power for NASA's
             planetary exploration programs. The MMRTG is being developed
             by Pratt &amp; Whitney Rocketdyne and Teledyne Energy
             Systems Incorporated (TESI) for use on currently planned and
             projected flyby, orbital and planet landing missions. This
             is a significant departure from the design philosophy of the
             past which was to match specific mission requirements to RTG
             design capabilities. Undefined mission requirements provide
             a challenge to system designers by forcing them to put a
             design envelope around "all possible missions". These
             multi-mission requirements include internal and external
             radiation sources. Internal sources include the particles
             ejected by decaying Pu-238 and its daughters plus particles
             resulting from the interaction of these particles with other
             MMRTG materials. External sources include the full spectrum
             of charged particle radiation surrounding planets with
             magnetic fields and the surfaces of extraterrestrial objects
             not shielded by magnetic fields. The paper presents the
             results of investigations into the environments outlined
             above and the impact of radiation exposure on potential
             materials to be used on MMRTG and ground support personnel.
             Mission requirements were also reviewed to evaluate total
             integrated dose and to project potential shielding
             requirements for materials. Much of the information on
             mission shielding requirements was provided by NASA's Jet
             Propulsion Laboratory. The primary result is an ionizing
             radiation design curve which indicates the limits to which a
             particular mission can take the MMRTG in terms of ionizing
             radiation exposure. Estimates of personnel radiation
             exposure during ground handling are also
             provided},
   Key = {8979178}
}

@article{fds174132,
   Author = {CA Baker and GA Johnson},
   Title = {Radioenzymatic assay of dihydroxyphenylglycol (DOPEG) and
             dihydroxyphenylethanol (DOPET) in plasma and cerebrospinal
             fluid.},
   Journal = {Life sciences},
   Volume = {29},
   Number = {2},
   Pages = {165-72},
   Year = {1981},
   Month = {July},
   ISSN = {0024-3205},
   Keywords = {Adult • Aged • Animals • Cats • Dogs
             • Ethanol • Female • Glycols • Humans
             • Infant • Male • Methoxyhydroxyphenylglycol
             • Middle Aged • Phenylethyl Alcohol •
             Radioisotope Dilution Technique • Rats •
             S-Adenosylmethionine • Tritium • analogs &
             derivatives • analogs & derivatives* • blood
             • blood* • cerebrospinal fluid},
   Language = {eng},
   Key = {fds174132}
}

@booklet{Baker81,
   Author = {C. A. Baker and G. A. Johnson},
   Title = {Radioenzymatic assay of dihydroxyphenylglycol (dopeg) and
             dihydroxyphenylethanol (dopet) in plasma and
             cerebrospinal-fluid},
   Journal = {Life Sciences},
   Volume = {29},
   Number = {2},
   Pages = {165 -- 172},
   Year = {1981},
   Key = {Baker81}
}

@article{fds174098,
   Author = {GA Johnson and JM Gren and R Kupiecki},
   Title = {Radioenzymatic assay of DOPA (3,4-dihydroxyphenylalanine).},
   Journal = {Clinical chemistry},
   Volume = {24},
   Number = {11},
   Pages = {1927-30},
   Year = {1978},
   Month = {November},
   ISSN = {0009-9147},
   Keywords = {Adult • Animals • Catechol O-Methyltransferase
             • Dihydroxyphenylalanine • Dopa Decarboxylase
             • Female • Humans • Male • analysis*
             • blood},
   Abstract = {We modified the single-isotope radioenzymatic assay for
             catecholamines [Life Sci. 21, 625 (1977)] to assay 3,
             4-dihydroxyphenylalanine (DOPA). DOPA decarboxylase is used
             to convert DOPA to dopamine, which concurrently is converted
             to [3H]-3-O-methyldopamine in the presence of
             catechol-O-methyltransferase and [methyl-3H]-S-adenosylmethionine
             and assayed radioenzymatically. For assay of plasma DOPA, 50
             microliter of untreated plasma is added directly into the
             incubation mixture. A duplicate mixture containing an
             internal standard requires a second 50-microliter aliquot of
             plasma. Because the assay measures both DOPA and endogenous
             dopamine, two additonal aliquots of plasma must be assayed
             for dopamine in the absence of the decarboxylase by the
             differential assay; DOPA is estimated by difference. The
             assay is sensitive to 25 pg (500 ng/liter of plasma).
             Analysis of DOPA (DOPA plus dopamine) and the concurrent
             differential assay of catecholamines in at least 10 samples
             can be done in a single working day. Plasma DOPA
             concentrations for 42 normotensive adults were 1430 +/- 19
             ng/liter (mean +/- SEM). In contrast, do-pamine
             concentrations for these same subjects averaged 23 +/- 20
             ng/liter. Values for the 24 women subjects (15 10 +/- 62
             ng/liter) significantly (P = 0.04) exceeded those for the
             men (1320 +/- 75 ng/liter).},
   Language = {eng},
   Key = {fds174098}
}

@booklet{Johnson80c,
   Author = {G. A. Johnson and C. A. Baker and R. T. Smith},
   Title = {Radioenzymatic assay of sulfate conjugates of catecholamines
             and dopa in plasma},
   Journal = {Life Sciences},
   Volume = {26},
   Number = {19},
   Pages = {1591 -- 1598},
   Year = {1980},
   Key = {Johnson80c}
}

@article{fds174262,
   Author = {GA Johnson and CA Baker and RT Smith},
   Title = {Radioenzymatic assay of sulfate conjugates of catecholamines
             and DOPA in plasma.},
   Journal = {Life sciences},
   Volume = {26},
   Number = {19},
   Pages = {1591-8},
   Year = {1980},
   Month = {May},
   ISSN = {0024-3205},
   Keywords = {Adolescent • Adult • Arylsulfatases •
             Catecholamines • Child • Child, Preschool •
             Dihydroxyphenylalanine • Dopamine • Epinephrine
             • Female • Humans • Infant • Male •
             Norepinephrine • Posture • Radioimmunoassay •
             Sulfuric Acid Esters • blood •
             blood*},
   Language = {eng},
   Key = {fds174262}
}

@booklet{Fram87,
   Author = {Fram, EK and Herfkens, RJ and Johnson, GA and Glover, GH and Karis, JP and Shimakawa, A and Perkins, TG and Pelc, NJ},
   Title = {Rapid calculation of T1 using variable flip angle gradient
             refocused imaging.},
   Journal = {Magn Reson Imaging},
   Volume = {5},
   Number = {3},
   Pages = {201-208},
   Year = {1987},
   ISSN = {0730-725X},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/3626789},
   Abstract = {We present a method for rapid measurement of T1 relaxation
             times using gradient refocused images at limited flip angles
             and short repetition times. This "variable nutation"
             techniques was investigated using a T1 phantom. There was a
             high correlation between measurements obtained with the
             variable nutation and partial saturation techniques. The
             ability of this method to create calculated T1 images is
             also demonstrated. We conclude that the variable nutation
             method may allow measurement of T1 relaxation times with a
             significant reduction in acquisition time compared to
             partial saturation techniques.},
   Doi = {10.1016/0730-725x(87)90021-x},
   Key = {Fram87}
}

@article{fds132800,
   Author = {EK Fram and RJ Herfkens and GA Johnson and GH Glover and JP Karis and A
             Shimakawa, TG Perkins and NJ Pelc},
   Title = {Rapid calculation of T1 using variable flip angle gradient
             refocused imaging.},
   Journal = {Magnetic resonance imaging, UNITED STATES},
   Volume = {5},
   Number = {3},
   Pages = {201-8},
   Year = {1987},
   ISSN = {0730-725X},
   Keywords = {Humans • Magnetic Resonance Spectroscopy •
             diagnostic use* • methods},
   Abstract = {We present a method for rapid measurement of T1 relaxation
             times using gradient refocused images at limited flip angles
             and short repetition times. This "variable nutation"
             techniques was investigated using a T1 phantom. There was a
             high correlation between measurements obtained with the
             variable nutation and partial saturation techniques. The
             ability of this method to create calculated T1 images is
             also demonstrated. We conclude that the variable nutation
             method may allow measurement of T1 relaxation times with a
             significant reduction in acquisition time compared to
             partial saturation techniques.},
   Key = {fds132800}
}

@article{fds268845,
   Author = {Howles, GP and Nouls, JC and Qi, Y and Johnson, GA},
   Title = {Rapid production of specialized animal handling devices
             using computer-aided design and solid freeform
             fabrication.},
   Journal = {J Magn Reson Imaging},
   Volume = {30},
   Number = {2},
   Pages = {466-471},
   Year = {2009},
   Month = {August},
   ISSN = {1053-1807},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/19629999},
   Abstract = {PURPOSE: To develop a process for rapidly and inexpensively
             producing customized animal handling devices for small
             animal imaging. MATERIALS AND METHODS: To meet the specific
             needs of a particular imaging experiment, measurements are
             taken from imaging data and the animal handling devices are
             designed using 3D computer-aided design (CAD) software.
             Parts are produced in a few days using solid freeform
             fabrication (SFF, a.k.a. rapid prototyping). RESULTS: This
             process is illustrated with the production of an animal
             handling system for stereotaxically prescribed therapeutic
             ultrasound and MRI of the mouse brain. The device provides
             integrated head-fixation, anesthesia delivery, and
             physiological monitoring in a modular system. Design and
             production took approximately 1 week and the cost was a
             small fraction of a traditional machine shop. CONCLUSION:
             Commercial animal handling products typically have limited
             functionality and are not integrated with other laboratory
             infrastructure. However, using CAD and SFF, sophisticated
             animal handling devices can be produced to meet the specific
             experimental needs. This process is typically faster and
             less expensive than using a traditional machine shop, and
             the products are more robust than typical homemade devices.
             Using high-quality purpose-built devices permits experiments
             to be executed with greater consistency and higher
             throughput.},
   Doi = {10.1002/jmri.21821},
   Key = {fds268845}
}

@booklet{Mermelstein01,
   Author = {M. D. Mermelstein and R. Posey and G. A. Johnson and S. T.
             Vohra},
   Title = {Rayleigh scattering optical frequency correlation in a
             single-mode optical fiber},
   Journal = {Optics Letters},
   Volume = {26},
   Number = {2},
   Pages = {58 -- 60},
   Year = {2001},
   Month = {January},
   Key = {Mermelstein01}
}

@article{fds174083,
   Author = {MD Mermelstein and R Posey Jr and GA Johnson and ST
             Vohra},
   Title = {Rayleigh scattering optical frequency correlation in a
             single-mode optical fiber.},
   Journal = {Optics letters},
   Volume = {26},
   Number = {2},
   Pages = {58-60},
   Year = {2001},
   Month = {January},
   ISSN = {0146-9592},
   Abstract = {The bichromatic optical frequency correlation function for
             Rayleigh backscattering from a pulse of laser light
             propagating along a single-mode optical fiber has been
             calculated and measured. It is shown that the optical
             correlation frequency, Dnu(c) , is equal to the reciprocal
             of pulse width T(w) . These results are important for the
             development of wavelength diversity techniques for the
             reduction of coherent Rayleigh noise in distributed Rayleigh
             backscattering single-mode optical fiber
             sensors.},
   Language = {eng},
   Key = {fds174083}
}

@article{fds268827,
   Author = {Pandit, P and Qi, Y and King, KF and Johnson, GA},
   Title = {Reduction of artifacts in T2 -weighted PROPELLER in
             high-field preclinical imaging.},
   Journal = {Magn Reson Med},
   Volume = {65},
   Number = {2},
   Pages = {538-543},
   Year = {2011},
   Month = {February},
   ISSN = {1522-2594},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/20928875},
   Keywords = {Animals • Artifacts* • Image Enhancement •
             Lung Neoplasms • Magnetic Resonance Imaging • Mice
             • Neoplasm Transplantation • Phantoms, Imaging
             • diagnosis • methods*},
   Abstract = {A simple technique is implemented for correction of
             artifacts arising from nonuniform T(2) -weighting of k-space
             data in fast spin echo-based PROPELLER (periodically rotated
             overlapping parallel lines with enhanced reconstruction). An
             additional blade with no phase-encoding gradients is
             acquired to generate the scaling factor used for the
             correction. Results from simulations and phantom
             experiments, as well as in vivo experiments in
             free-breathing mice, demonstrate the advantages of the
             proposed method. This technique is developed specifically
             for high-field imaging applications where T(2) decay is
             rapid.},
   Language = {eng},
   Doi = {10.1002/mrm.22624},
   Key = {fds268827}
}

@booklet{Zhou93,
   Author = {Zhou, X and Liang, ZP and Cofer, GP and Beaulieu, CF and Suddarth, SA and Johnson, GA},
   Title = {Reduction of ringing and blurring artifacts in fast
             spin-echo imaging.},
   Journal = {J Magn Reson Imaging},
   Volume = {3},
   Number = {5},
   Pages = {803-807},
   Year = {1993},
   ISSN = {1053-1807},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/8400569},
   Abstract = {A simple method was devised to reduce ringing and blurring
             artifacts caused by discontinuous T2 weighting of k-space
             data in fast spin-echo magnetic resonance (MR) imaging. The
             method demodulates the weighting function along the
             phase-encoding direction by using multiple T2 values derived
             from a set of non-phase-encoded echoes obtained from an
             extra excitation. The performance of this method was
             evaluated by computer simulations and experiments, which
             confirmed its capability of effectively reducing or, in some
             cases, even completely removing the ringing and blurring
             artifacts. The results also show that the proposed method
             produces better results than other artifact reduction
             methods. The method is particularly useful at high magnetic
             field strengths (7.1-9.4 T) and with strong gradients (> 20
             G/cm) used in MR microscopy, in which the apparent T2 values
             are short for most tissues. The authors expect that the
             proposed method will find useful applications in various
             fast spin-echo pulse sequences.},
   Doi = {10.1002/jmri.1880030518},
   Key = {Zhou93}
}

@article{fds132871,
   Author = {X Zhou and ZP Liang and GP Cofer and CF Beaulieu and SA Suddarth and GA
             Johnson},
   Title = {Reduction of ringing and blurring artifacts in fast
             spin-echo imaging.},
   Journal = {Journal of magnetic resonance imaging : JMRI, UNITED
             STATES},
   Volume = {3},
   Number = {5},
   Pages = {803-7},
   ISSN = {1053-1807},
   Keywords = {Artifacts* • Image Enhancement • Magnetic
             Resonance Imaging • Models, Structural • methods
             • methods*},
   Abstract = {A simple method was devised to reduce ringing and blurring
             artifacts caused by discontinuous T2 weighting of k-space
             data in fast spin-echo magnetic resonance (MR) imaging. The
             method demodulates the weighting function along the
             phase-encoding direction by using multiple T2 values derived
             from a set of non-phase-encoded echoes obtained from an
             extra excitation. The performance of this method was
             evaluated by computer simulations and experiments, which
             confirmed its capability of effectively reducing or, in some
             cases, even completely removing the ringing and blurring
             artifacts. The results also show that the proposed method
             produces better results than other artifact reduction
             methods. The method is particularly useful at high magnetic
             field strengths (7.1-9.4 T) and with strong gradients (> 20
             G/cm) used in MR microscopy, in which the apparent T2 values
             are short for most tissues. The authors expect that the
             proposed method will find useful applications in various
             fast spin-echo pulse sequences.},
   Key = {fds132871}
}

@booklet{Sherrier87,
   Author = {Sherrier, RH and Johnson, GA},
   Title = {Regionally adaptive histogram equalization of the
             chest.},
   Journal = {IEEE Trans Med Imaging},
   Volume = {6},
   Number = {1},
   Pages = {1-7},
   Year = {1987},
   ISSN = {0278-0062},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/18230420},
   Abstract = {Advances in the area of digital chest radiography have
             resulted in the acquisition of high-quality images of the
             human chest. With these advances, there arises a genuine
             need for image processing algorithms specific to the chest,
             in order to fully exploit this digital technology. We have
             implemented the well-known technique of histogram
             equalization, noting the problems encountered when it is
             adapted to chest images. These problems have been
             successfully solved with our regionally adaptive histogram
             equalization method. With this technique histograms are
             calculated locally and then modified according to both the
             mean pixel value of that region as well as certain
             characteristics of the cumulative distribution function.
             This process, which has allowed certain regions of the chest
             radiograph to be enhanced differentially, may also have
             broader implications for other image processing
             tasks.},
   Doi = {10.1109/TMI.1987.4307791},
   Key = {Sherrier87}
}

@article{fds292757,
   Author = {Sherrier, RH and Johnson, GA},
   Title = {REGIONALLY ADAPTIVE HISTOGRAM EQUALIZATION OF THE
             CHEST.},
   Journal = {IEEE Transactions on Medical Imaging},
   Volume = {MI-6},
   Number = {1},
   Pages = {1-7},
   Year = {1987},
   Abstract = {The authors have implemented the well-known technique of
             histogram equalization, noting the problems encountered when
             it is adapted to chest images. These problems have been
             successfully solved with a regionally adaptive histogram
             equalization method. With this technique, histograms are
             calculated locally and then modified according to both the
             mean pixel value of that region as well as certain
             characteristics of the cumulative distribution function.
             This process, which has allowed certain regions of the chest
             radiograph to be enhanced differentially, may also have
             broader implications for other image processing
             tasks.},
   Key = {fds292757}
}

@article{fds157104,
   Author = {RH Sherrier and GA Johnson},
   Title = {Regionally adaptive histogram equalization of the
             chest.},
   Journal = {IEEE transactions on medical imaging, United
             States},
   Volume = {6},
   Number = {1},
   Pages = {1-7},
   Year = {1987},
   ISSN = {0278-0062},
   Abstract = {Advances in the area of digital chest radiography have
             resulted in the acquisition of high-quality images of the
             human chest. With these advances, there arises a genuine
             need for image processing algorithms specific to the chest,
             in order to fully exploit this digital technology. We have
             implemented the well-known technique of histogram
             equalization, noting the problems encountered when it is
             adapted to chest images. These problems have been
             successfully solved with our regionally adaptive histogram
             equalization method. With this technique histograms are
             calculated locally and then modified according to both the
             mean pixel value of that region as well as certain
             characteristics of the cumulative distribution function.
             This process, which has allowed certain regions of the chest
             radiograph to be enhanced differentially, may also have
             broader implications for other image processing
             tasks.},
   Key = {fds157104}
}

@article{fds268912,
   Author = {Johnson, GA and Cofer, GP and Hedlund, LW and Maronpot, RR and Suddarth,
             SA},
   Title = {Registered (1)H and (3)He magnetic resonance microscopy of
             the lung.},
   Journal = {Magn Reson Med},
   Volume = {45},
   Number = {3},
   Pages = {365-370},
   Year = {2001},
   Month = {March},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/11241691},
   Keywords = {Animals • Anisotropy • Helium* • Hydrogen*
             • Image Enhancement* • Image Processing,
             Computer-Assisted • Imaging, Three-Dimensional •
             Isotopes • Lung • Magnetic Resonance Imaging
             • Male • Microscopy • Rats • Rats,
             Inbred F344 • Sensitivity and Specificity •
             methods* • pathology*},
   Abstract = {Using in vivo magnetic resonance microscopy, registered (1)H
             and hyperpolarized (3)He images of the rat lung were
             obtained with a resolution of 0.098 x 0.098 x 0.469 mm (4.5
             x 10(-3) mm(3)). The requisite stability and SNR was
             achieved through an integration of scan-synchronous
             ventilation, dual-frequency RF coils, anisotropic projection
             encoding, and variable RF excitation. The total acquisition
             time was 21 min for the (3)He images and 64 min for the (1)H
             image. Airways down to the 6th and 7th orders are clearly
             visible. Magn Reson Med 45:365-370, 2001.},
   Doi = {10.1002/1522-2594(200103)45:3<365::aid-mrm1047>3.0.co;2-0},
   Key = {fds268912}
}

@article{fds268794,
   Author = {Clark, D and Badea, A and Liu, Y and Johnson, GA and Badea,
             CT},
   Title = {Registration-based segmentation of murine 4D cardiac
             micro-CT data using symmetric normalization.},
   Journal = {Phys Med Biol},
   Volume = {57},
   Number = {19},
   Pages = {6125-6145},
   Year = {2012},
   Month = {October},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/22971564},
   Abstract = {Micro-CT can play an important role in preclinical studies
             of cardiovascular disease because of its high spatial and
             temporal resolution. Quantitative analysis of 4D cardiac
             images requires segmentation of the cardiac chambers at each
             time point, an extremely time consuming process if done
             manually. To improve throughput this study proposes a
             pipeline for registration-based segmentation and functional
             analysis of 4D cardiac micro-CT data in the mouse. Following
             optimization and validation using simulations, the pipeline
             was applied to in vivo cardiac micro-CT data corresponding
             to ten cardiac phases acquired in C57BL/6 mice (n = 5).
             After edge-preserving smoothing with a novel adaptation of
             4D bilateral filtration, one phase within each cardiac
             sequence was manually segmented. Deformable registration was
             used to propagate these labels to all other cardiac phases
             for segmentation. The volumes of each cardiac chamber were
             calculated and used to derive stroke volume, ejection
             fraction, cardiac output, and cardiac index. Dice
             coefficients and volume accuracies were used to compare
             manual segmentations of two additional phases with their
             corresponding propagated labels. Both measures were, on
             average, >0.90 for the left ventricle and >0.80 for the
             myocardium, the right ventricle, and the right atrium,
             consistent with trends in inter- and intra-segmenter
             variability. Segmentation of the left atrium was less
             reliable. On average, the functional metrics of interest
             were underestimated by 6.76% or more due to systematic label
             propagation errors around atrioventricular valves; however,
             execution of the pipeline was 80% faster than performing
             analogous manual segmentation of each phase.},
   Doi = {10.1088/0031-9155/57/19/6125},
   Key = {fds268794}
}

@article{fds174201,
   Author = {H Ka and S Al-Ramadan and DW Erikson and GA Johnson and RC Burghardt and TE
             Spencer, LA Jaeger and FW Bazer},
   Title = {Regulation of expression of fibroblast growth factor 7 in
             the pig uterus by progesterone and estradiol.},
   Journal = {Biology of reproduction},
   Volume = {77},
   Number = {1},
   Pages = {172-80},
   Year = {2007},
   Month = {July},
   ISSN = {0006-3363},
   url = {http://dx.doi.org/10.1095/biolreprod.106.056309},
   Keywords = {Animals • Estradiol • Female • Fibroblast
             Growth Factor 7 • Gene Expression Regulation •
             Progesterone • RNA, Messenger • Receptors,
             Estrogen • Receptors, Progesterone • Uterus •
             anatomy & histology • antagonists & inhibitors •
             drug effects* • metabolism • metabolism* •
             pharmacology*},
   Abstract = {Fibroblast growth factor 7 (FGF7) stimulates cell
             proliferation, differentiation, migration and angiogenesis.
             The consensus is that FGF7, expressed by mesenchymal cells,
             binds FGF receptor 2IIIb (FGFR2) on epithelia, thereby
             mediating epithelial-mesenchymal interactions. The pig
             uterus is unique in that FGF7 is expressed by the luminal
             epithelium (LE) and FGFR2 is expressed by the LE, glandular
             epithelium (GE), and trophectoderm to effect proliferation
             and differentiated cell functions during conceptus
             development and implantation. FGF7 expression by the uterine
             LE of pigs increases between Days 9 and 12 of the estrus
             cycle and pregnancy, as circulating concentrations of
             progesterone increase, progesterone receptors (PGR) in the
             uterine epithelia decrease, and the conceptuses secrete
             estradiol-17beta (E(2)), for pregnancy recognition.
             Furthermore, E(2) increases the expression of FGF7 in pig
             uterine explants. The present study investigates the
             relationships between progesterone, E(2), and their
             receptors and the expression of FGF7 in the pig uterus in
             vivo. Pigs were ovariectomized on Day 4 of the estrus cycle
             and injected i.m. daily from Day 4 to Day 12 with either
             corn oil (CO), progesterone (P4), P4 and ZK317,316 (PZK),
             E(2), P4 and E(2) (PE), or P4 and ZK and E(2) (PZKE). All
             gilts (n = 5/treatment) were hysterectomized on Day 12. The
             results suggest that: 1) P4 is permissive to FGF7 expression
             by down-regulating PGR in LE; 2) P4 stimulates PGR-positive
             uterine stromal cells to release an unidentified
             progestamedin that induces FGF7 expression by LE; 3) E(2)
             and P4 can induce FGF7 when PGR are rendered nonfunctional
             by ZK; and 4) E(2) from conceptuses interacts via estrogen
             receptor alpha, but not estrogen receptor beta in LE to
             induce maximal expression of FGF7 in LE on Day 12 of
             pregnancy in pigs.},
   Language = {eng},
   Doi = {10.1095/biolreprod.106.056309},
   Key = {fds174201}
}

@booklet{Ka00,
   Author = {H. H. Ka and L. A. Jaeger and G. A. Johnson and T. E.
             Spencer and F. W. Bazer},
   Title = {Regulation of keratinocyte growth factor expression and its
             function in the porcine uterus.},
   Journal = {Biology Of Reproduction},
   Volume = {62},
   Pages = {297 -- 297},
   Year = {2000},
   Key = {Ka00}
}

@booklet{Spencer03a,
   Author = {T. E. Spencer and G. A. Johnson and F. W. Bazer and G. Y.
             Wu},
   Title = {Regulation of placental nitric oxide synthesis by estrogen
             and progesterone in pigs.},
   Journal = {Biology Of Reproduction},
   Volume = {68},
   Pages = {363 -- 364},
   Year = {2003},
   Key = {Spencer03a}
}

@booklet{Zaunbrecher03,
   Author = {G. M. Zaunbrecher and T. E. Spencer and R. C. Burghardt and M. M. Joyce and F. W. Bazer and G. A. Johnson},
   Title = {Regulaton of glycosylation dependent cell adhesion molecule
             1 (GlyCAM-1) and l-selectin expression in the pregnant ovine
             uterus and placenta.},
   Journal = {Biology Of Reproduction},
   Volume = {68},
   Pages = {243 -- 243},
   Year = {2003},
   Key = {Zaunbrecher03}
}

@article{fds174287,
   Author = {GA JOHNSON and RH McCLUER},
   Title = {Relation of sialic acid to Rho (D) antigen.},
   Journal = {Proceedings of the Society for Experimental Biology and
             Medicine. Society for Experimental Biology and Medicine (New
             York, N.Y.)},
   Volume = {107},
   Pages = {692-4},
   Year = {1961},
   Month = {July},
   ISSN = {0037-9727},
   Keywords = {ANTIEMETICS/therapy* • CARBOHYDRASES/pharmacology*
             • NEURAMINIC ACIDS/pharmacology*},
   Language = {eng},
   Key = {fds174287}
}

@booklet{Baker84,
   Author = {C. A. Baker and J. P. Hansen and M. V. Williams and F. G.
             Robinson and J. E. Rogers and R. A. Zandt and M. G. Wendling and G. A. Johnson},
   Title = {Relationship between the physiologic activity of minoxidil
             and the plasma and tissue-levels of minoxidil and minoxidil
             sulfate},
   Journal = {Federation Proceedings},
   Volume = {43},
   Number = {3},
   Pages = {556 -- 556},
   Year = {1984},
   Key = {Baker84}
}

@article{fds132850,
   Author = {SE Dockery and SA Suddarth and GA Johnson},
   Title = {Relaxation measurements at 300 MHz using MR
             microscopy.},
   Journal = {Magnetic resonance in medicine : official journal of the
             Society of Magnetic Resonance in Medicine / Society of
             Magnetic Resonance in Medicine, UNITED STATES},
   Volume = {11},
   Number = {2},
   Pages = {182-92},
   Year = {1989},
   Month = {August},
   ISSN = {0740-3194},
   Keywords = {Animals • Kidney • Magnetic Resonance Imaging*
             • Microscopy • Rats • Rats, Inbred F344
             • anatomy & histology • methods},
   Abstract = {Previous data on changes in tissue T1 with field have
             suggested the convergence of tissue T1 values toward a
             common value at high (greater than 4.0 T) fields. Measures
             of T2 dependence have suggested reduction of T2 with field.
             The purpose of this study was to observe the T1 and T2 at
             85.5 and 300 MHz of microstructures in excised rat kidneys
             by employing MR microscopy. This study represents the first
             attempt of MR microscopy at 7.0 T with regard to the subject
             of magnetic field dependence of T1 and T2. As expected, T1
             did increase with increasing field strength but not as
             dramatically as might be expected. Subtle differences in the
             microstructures of the kidney and the binding of water in
             those structures were discernible on the basis of T1
             differences at 300 MHz. T2 values decreased, raising
             speculation concerning the mechanism for this dependence.
             The improved SNR permits smaller samples to be examined at
             much higher resolutions (greater than 30 X 30 X 200
             microns), further extending the potentials for MR
             microscopy.},
   Key = {fds132850}
}

@booklet{Dockery89,
   Author = {Dockery, SE and Suddarth, SA and Johnson, GA},
   Title = {Relaxation measurements at 300 MHz using MR
             microscopy.},
   Journal = {Magn Reson Med},
   Volume = {11},
   Number = {2},
   Pages = {182-192},
   Year = {1989},
   Month = {August},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/2779411},
   Abstract = {Previous data on changes in tissue T1 with field have
             suggested the convergence of tissue T1 values toward a
             common value at high (greater than 4.0 T) fields. Measures
             of T2 dependence have suggested reduction of T2 with field.
             The purpose of this study was to observe the T1 and T2 at
             85.5 and 300 MHz of microstructures in excised rat kidneys
             by employing MR microscopy. This study represents the first
             attempt of MR microscopy at 7.0 T with regard to the subject
             of magnetic field dependence of T1 and T2. As expected, T1
             did increase with increasing field strength but not as
             dramatically as might be expected. Subtle differences in the
             microstructures of the kidney and the binding of water in
             those structures were discernible on the basis of T1
             differences at 300 MHz. T2 values decreased, raising
             speculation concerning the mechanism for this dependence.
             The improved SNR permits smaller samples to be examined at
             much higher resolutions (greater than 30 X 30 X 200
             microns), further extending the potentials for MR
             microscopy.},
   Doi = {10.1002/mrm.1910110206},
   Key = {Dockery89}
}

@article{fds268831,
   Author = {Badea, A and Johnson, GA and Jankowsky, JL},
   Title = {Remote sites of structural atrophy predict later amyloid
             formation in a mouse model of Alzheimer's
             disease.},
   Journal = {Neuroimage},
   Volume = {50},
   Number = {2},
   Pages = {416-427},
   Year = {2010},
   Month = {April},
   ISSN = {1095-9572},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/20035883},
   Keywords = {Alzheimer Disease • Amyloid • Animals •
             Atrophy • Brain • Disease Models, Animal •
             Female • Image Interpretation, Computer-Assisted •
             Magnetic Resonance Imaging • Male • Mice •
             Mice, Transgenic • Plaque, Amyloid • metabolism
             • methods* • pathology • pathology*},
   Abstract = {Magnetic resonance (MR) imaging can provide a longitudinal
             view of neurological disease through repeated imaging of
             patients at successive stages of impairment. Until recently,
             the difficulty of manual delineation has limited volumetric
             analyses of MR data sets to a few select regions and a small
             number of subjects. Increased throughput offered by faster
             imaging methods, automated segmentation, and
             deformation-based morphometry have recently been applied to
             overcome this limitation with mouse models of neurological
             conditions. We use automated analyses to produce an unbiased
             view of volumetric changes in a transgenic mouse model for
             Alzheimer's disease (AD) at two points in the progression of
             disease: immediately before and shortly after the onset of
             amyloid formation. In addition to the cortex and
             hippocampus, where atrophy has been well documented in AD
             patients, we identify volumetric losses in the pons and
             substantia nigra where neurodegeneration has not been
             carefully examined. We find that deficits in cortical volume
             precede amyloid formation in this mouse model, similar to
             presymptomatic atrophy seen in patients with familial AD.
             Unexpectedly, volumetric losses identified by MR outside of
             the forebrain predict locations of future amyloid formation,
             such as the inferior colliculus and spinal nuclei, which
             develop pathology at very late stages of disease. Our work
             provides proof-of-principle that MR microscopy can expand
             our view of AD by offering a complete and unbiased
             examination of volumetric changes that guide us in
             revisiting the canonical neuropathology.},
   Language = {eng},
   Doi = {10.1016/j.neuroimage.2009.12.070},
   Key = {fds268831}
}

@booklet{Tenbrink88,
   Author = {R. E. Tenbrink and D. T. Pals and D. W. Harris and G. A.
             Johnson},
   Title = {Renin inhibitors containing psi-[ch2o] pseudopeptide
             inserts},
   Journal = {Journal Of Medicinal Chemistry},
   Volume = {31},
   Number = {3},
   Pages = {671 -- 677},
   Year = {1988},
   Month = {March},
   Key = {Tenbrink88}
}

@article{fds174116,
   Author = {RE TenBrink and DT Pals and DW Harris and GA Johnson},
   Title = {Renin inhibitors containing psi[CH2O] pseudopeptide
             inserts.},
   Journal = {Journal of medicinal chemistry},
   Volume = {31},
   Number = {3},
   Pages = {671-7},
   Year = {1988},
   Month = {March},
   ISSN = {0022-2623},
   Keywords = {Amino Acid Sequence • Angiotensinogen • Chemistry,
             Physical • Humans • Molecular Sequence Data •
             Physicochemical Phenomena • Renin •
             Structure-Activity Relationship • analogs &
             derivatives* • antagonists & inhibitors* •
             chemical synthesis • pharmacology},
   Abstract = {Renin inhibitors 2-4 with the D-Lys renin inhibitory peptide
             (RIP) sequence, but containing Leu psi[CH2O]Ala (2), Leu
             psi[CH2O]Val (3), and Leu psi[CH2O]Leu (4) at the P1-P1'
             site, were of a comparable potency to RIP. N-Terminal
             Boc-protected inhibitors containing Pro psi[CH2O]Phe in
             positions P4-P3 were potent inhibitors of renin, with
             Boc-Phe-Pro psi[CH2O]Phe-His-Leu psi[CH(OH)CH2]Val-Ile-(2-aminomethyl)
             pyridine (17) having an IC50 of 1.6 X 10(-9)
             M.},
   Language = {eng},
   Key = {fds174116}
}

@booklet{Scoggins91,
   Author = {J. R. Scoggins and J. Arellano and B. Esposito and G. A.
             Johnson and K. C. Brundidge},
   Title = {Report on a symposium on air-sea interaction and air-mass
             modification over the gulf of mexico 7-9 january 1991,
             galveston, texas},
   Journal = {Bulletin Of The American Meteorological Society},
   Volume = {72},
   Number = {6},
   Pages = {827 -- 832},
   Year = {1991},
   Month = {June},
   Key = {Scoggins91}
}

@article{fds174114,
   Author = {RS Dhariwal and GA Johnson and RM Browne and SL Rowles},
   Title = {Reprecipitation phenomena arising during the preparation of
             demineralised sections. III Scanning electron microscopic
             examinations of secondary calcium phosphate
             deposits.},
   Journal = {Stain technology},
   Volume = {51},
   Number = {6},
   Pages = {293-9},
   Year = {1976},
   Month = {November},
   ISSN = {0038-9153},
   Keywords = {Calcium Phosphates • Decalcification Technique* •
             Dentin • Humans • Microradiography •
             Microscopy, Electron, Scanning • Tooth • Tooth
             Calcification* • X-Ray Diffraction • radiography
             • ultrastructure*},
   Abstract = {Sections of teeth partly demineralized in 10% formic acid
             were examined by X-ray diffraction, microradiography and
             scanning electron microscopy. In the undemineralized
             circumpulpal dentin, the tubules were empty, lying in a
             matrix containing hydroxyapatite. In the "plume" areas of
             remineralisation, the tubules were filled with mineral
             deposits. X-ray diffraction revealed the presence of
             brushite and monetite in these areas. In the outer layers of
             dentin the tubules were empty, lying in a matrix containing
             some residual hydroxyapatite. These findings confirmed that
             the remineralisation process occurred within the dentinal
             tubules.},
   Language = {eng},
   Key = {fds174114}
}

@article{fds157079,
   Author = {MW Tengowski and P Sutovsky and LW Hedlund and DJ Guyot and JE
             Burkhardt, WE Thompson and M Sutovsky and GA Johnson},
   Title = {Reproductive cytotoxicity is predicted by magnetic resonance
             microscopy and confirmed by ubiquitin-proteasome
             immunohistochemistry in a theophylline-induced model of rat
             testicular and epididymal toxicity.},
   Journal = {Microscopy and microanalysis : the official journal of
             Microscopy Society of America, Microbeam Analysis Society,
             Microscopical Society of Canada, United States},
   Volume = {11},
   Number = {4},
   Pages = {300-12},
   Year = {2005},
   Month = {August},
   ISSN = {1431-9276},
   Keywords = {Animals • Apoptosis • Body Weight •
             Epididymis • Immunohistochemistry • In Situ
             Nick-End Labeling • Magnetic Resonance Spectroscopy
             • Male • Microscopy • Organ Size •
             Proteasome Endopeptidase Complex • Rats • Rats,
             Sprague-Dawley • Testis • Theophylline •
             Ubiquitin • chemistry • drug effects • drug
             effects* • metabolism* • physiology* •
             toxicity*},
   Abstract = {This study investigated the testicular changes in the rat
             induced by the nonspecific phosphodiesterase inhibitor,
             theophylline using magnetic resonance microscopy (MRM) and
             ubiquitin immunostaining techniques. In vivo T1- and
             T2-weighted images were acquired at 2 T under anesthesia.
             Increased signal observed in the theophylline-treated rats
             suggests that leakage of MRM contrast was occurring. In vivo
             MRM results indicate that day 16 testis displayed an
             increased T1-weighted water signal in the area of the
             seminiferous tubule that decreased by day 32. These findings
             were validated by histopathology, suggesting that in vivo
             MRM has the sensitivity to predict changes in testis and
             epididymal tissues. The participation of the ubiquitin
             system was investigated, using probes for various markers of
             the ubiquitin-proteasome pathway. MRM can be used to detect
             subtle changes in the vascular perfusion of organ systems,
             and the up-regulation/mobilization of ubiquitin-proteasome
             pathway may be one of the mechanisms used in
             theophylline-treated epididymis to remove damaged cells
             before storage in the cauda epididymis. The combined use of
             in vivo MRM and subsequent tissue or seminal analysis for
             the presence of ubiquitin in longitudinal studies may become
             an important biomarker for assessing testis toxicities drug
             studies.},
   Key = {fds157079}
}

@article{8754834,
   Author = {Tengowski, MW and Sutovsky, P and Hedlund, LW and Guyot, DJ and Burkhardt, JE and Thompson, WE and Sutovsky, M and Johnson,
             GA},
   Title = {Reproductive cytotoxicity is predicted by magnetic resonance
             microscopy and confirmed by ubiquitin-proteasome
             immunohistochemistry in a theophylline-induced model of rat
             testicular and epididymal toxicity.},
   Journal = {Microsc Microanal},
   Volume = {11},
   Number = {4},
   Pages = {300-312},
   Year = {2005},
   Month = {August},
   ISSN = {1431-9276},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/16079014},
   Keywords = {biochemistry;biological tissues;biomedical MRI;cellular
             biophysics;drugs;haemorheology;molecular
             biophysics;proteins;},
   Abstract = {This study investigated the testicular changes in the rat
             induced by the nonspecific phosphodiesterase inhibitor,
             theophylline using magnetic resonance microscopy (MRM) and
             ubiquitin immunostaining techniques. In vivo T1- and
             T2-weighted images were acquired at 2 T under anesthesia.
             Increased signal observed in the theophylline-treated rats
             suggests that leakage of MRM contrast was occurring. In vivo
             MRM results indicate that day 16 testis displayed an
             increased T1-weighted water signal in the area of the
             seminiferous tubule that decreased by day 32. These findings
             were validated by histopathology, suggesting that in vivo
             MRM has the sensitivity to predict changes in testis and
             epididymal tissues. The participation of the ubiquitin
             system was investigated, using probes for various markers of
             the ubiquitin-proteasome pathway. MRM can be used to detect
             subtle changes in the vascular perfusion of organ systems,
             and the up-regulation/mobilization of ubiquitin-proteasome
             pathway may be one of the mechanisms used in
             theophylline-treated epididymis to remove damaged cells
             before storage in the cauda epididymis. The combined use of
             in vivo MRM and subsequent tissue or seminal analysis for
             the presence of ubiquitin in longitudinal studies may become
             an important biomarker for assessing testis toxicities drug
             studies.},
   Doi = {10.1017/S143192760505021X},
   Key = {8754834}
}

@article{fds174170,
   Author = {GA Johnson},
   Title = {Research into psychiatric disorder after stroke: the need
             for further studies.},
   Journal = {The Australian and New Zealand journal of
             psychiatry},
   Volume = {25},
   Number = {3},
   Pages = {358-70},
   Year = {1991},
   Month = {September},
   ISSN = {0004-8674},
   Keywords = {Cerebrovascular Disorders • Delirium, Dementia,
             Amnestic, Cognitive Disorders • Depressive Disorder
             • Follow-Up Studies • Humans • Sick Role*
             • Social Environment • psychology*},
   Abstract = {Attention is drawn to some shortcomings of previous findings
             with regard to the nature, prevalence and aetiology of
             psychiatric disorder after stroke, and in particular
             post-stroke depression. Reasons for and drawbacks of the
             emphasis on depression in studies to date are discussed.
             Inconsistencies amongst previous findings are examined and
             it is suggested that many further studies in the area are
             warranted providing methodological difficulties are
             addressed adequately.},
   Language = {eng},
   Key = {fds174170}
}

@booklet{Johnson91,
   Author = {G. A. Johnson},
   Title = {Research into psychiatric-disorder after stroke - the need
             for further-studies},
   Journal = {Australian And New Zealand Journal Of Psychiatry},
   Volume = {25},
   Number = {3},
   Pages = {358 -- 370},
   Year = {1991},
   Month = {September},
   Key = {Johnson91}
}

@article{fds362951,
   Author = {Crater, S and Maharjan, S and Qi, Y and Zhao, Q and Cofer, G and Cook, JC and Johnson, GA and Wang, N},
   Title = {Resolution and b value dependent structural connectome in ex
             vivo mouse brain.},
   Journal = {Neuroimage},
   Volume = {255},
   Pages = {119199},
   Year = {2022},
   Month = {July},
   url = {http://dx.doi.org/10.1016/j.neuroimage.2022.119199},
   Abstract = {Diffusion magnetic resonance imaging has been widely used in
             both clinical and preclinical studies to characterize tissue
             microstructure and structural connectivity. The diffusion
             MRI protocol for the Human Connectome Project (HCP) has been
             developed and optimized to obtain high-quality,
             high-resolution diffusion MRI (dMRI) datasets. However, such
             efforts have not been fully explored in preclinical studies,
             especially for rodents. In this study, high quality dMRI
             datasets of mouse brains were acquired at 9.4T system from
             two vendors. In particular, we acquired a high-spatial
             resolution dMRI dataset (25 μm isotropic with 126
             diffusion encoding directions), which we believe to be the
             highest spatial resolution yet obtained; and a high-angular
             resolution dMRI dataset (50 μm isotropic with 384
             diffusion encoding directions), which we believe to be the
             highest angular resolution compared to the dMRI datasets at
             the microscopic resolution. We systematically investigated
             the effects of three important parameters that affect the
             final outcome of the connectome: b value (1000s/mm2 to
             8000 s/mm2), angular resolution (10 to 126), and spatial
             resolution (25 µm to 200 µm). The stability of
             tractography and connectome increase with the angular
             resolution, where more than 50 angles is necessary to
             achieve consistent results. The connectome and quantitative
             parameters derived from graph theory exhibit a linear
             relationship to the b value (R2 > 0.99); a single-shell
             acquisition with b value of 3000 s/mm2 shows comparable
             results to the multi-shell high angular resolution dataset.
             The dice coefficient decreases and both false positive rate
             and false negative rate gradually increase with coarser
             spatial resolution. Our study provides guidelines and
             foundations for exploration of tradeoffs among acquisition
             parameters for the structural connectome in ex vivo mouse
             brain.},
   Doi = {10.1016/j.neuroimage.2022.119199},
   Key = {fds362951}
}

@booklet{Johnson87c,
   Author = {JOHNSON, GA},
   Title = {RESOLUTION LIMITS IN MR - MR MICROSCOPY},
   Journal = {MEDICAL PHYSICS},
   Volume = {14},
   Number = {3},
   Pages = {499-499},
   Publisher = {AMER INST PHYSICS},
   Year = {1987},
   Month = {May},
   ISSN = {0094-2405},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1987H776800274&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Johnson87c}
}

@article{fds369118,
   Author = {Tian, Y and Cook, JJ and Johnson, GA},
   Title = {Restoring morphology of light sheet microscopy data based on
             magnetic resonance histology.},
   Journal = {Front Neurosci},
   Volume = {16},
   Pages = {1011895},
   Year = {2022},
   url = {http://dx.doi.org/10.3389/fnins.2022.1011895},
   Abstract = {The combination of cellular-resolution whole brain light
             sheet microscopy (LSM) images with an annotated atlas
             enables quantitation of cellular features in specific brain
             regions. However, most existing methods register LSM data
             with existing canonical atlases, e.g., The Allen Brain Atlas
             (ABA), which have been generated from tissue that has been
             distorted by removal from the skull, fixation and physical
             handling. This limits the accuracy of the regional
             morphologic measurement. Here, we present a method to
             combine LSM data with magnetic resonance histology (MRH) of
             the same specimen to restore the morphology of the LSM
             images to the in-skull geometry. Our registration pipeline
             which maps 3D LSM big data (terabyte per dataset) to MRH of
             the same mouse brain provides registration with low
             displacement error in ∼10 h with limited manual input. The
             registration pipeline is optimized using multiple stages of
             transformation at multiple resolution scales. A three-step
             procedure including pointset initialization, automated ANTs
             registration with multiple optimized transformation stages,
             and finalized application of the transforms on
             high-resolution LSM data has been integrated into a simple,
             structured, and robust workflow. Excellent agreement has
             been seen between registered LSM data and reference MRH data
             both locally and globally. This workflow has been applied to
             a collection of datasets with varied combinations of MRH
             contrasts from diffusion tensor images and LSM with varied
             immunohistochemistry, providing a routine method for
             streamlined registration of LSM images to MRH. Lastly, the
             method maps a reduced set of the common coordinate framework
             (CCFv3) labels from the Allen Brain Atlas onto the
             geometrically corrected full resolution LSM data. The
             pipeline maintains the individual brain morphology and
             allows more accurate regional annotations and measurements
             of volumes and cell density.},
   Doi = {10.3389/fnins.2022.1011895},
   Key = {fds369118}
}

@booklet{Johnson84a,
   Author = {G. A. Johnson},
   Title = {Retrofit control of a variable air volume system using
             variable speed drives},
   Journal = {Ashrae Journal-american Society Of Heating Refrigerating And
             Air-conditioning Engineers},
   Volume = {26},
   Number = {5},
   Pages = {44 -- 44},
   Year = {1984},
   Key = {Johnson84a}
}

@booklet{Hoverstad04,
   Author = {T. R. Hoverstad and J. L. Gunsolus and G. A. Johnson and R.
             R. King},
   Title = {Risk-efficiency criteria for evaluating economics of
             herbicide-based weed management systems in
             corn},
   Journal = {Weed Technology},
   Volume = {18},
   Number = {3},
   Pages = {687 -- 697},
   Year = {2004},
   Key = {Hoverstad04}
}

@article{fds268708,
   Author = {Clark, DP and Johnson, GA and Badea, CT},
   Title = {Robust material decomposition for spectral
             CT},
   Journal = {Progress in Biomedical Optics and Imaging - Proceedings of
             SPIE},
   Volume = {9038},
   Publisher = {SPIE},
   Year = {2014},
   Month = {January},
   ISBN = {9780819498311},
   ISSN = {1605-7422},
   url = {http://dx.doi.org/10.1117/12.2042546},
   Abstract = {There is ongoing interest in extending CT from anatomical to
             functional imaging. Recent successes with dual energy CT,
             the introduction of energy discriminating x-ray detectors,
             and novel, target-specific, nanoparticle contrast agents
             enable functional imaging capabilities via spectral CT.
             However, many challenges related to radiation dose, photon
             flux, and sensitivity still must be overcome. Here, we
             introduce a post-reconstruction algorithm called spectral
             diffusion that performs a robust material decomposition of
             spectral CT data in the presence of photon noise to address
             these challenges. Specifically, we use spectrally joint,
             piece-wise constant kernel regression and the split Bregman
             method to iteratively solve for a material decomposition
             which is gradient sparse, quantitatively accurate, and
             minimally biased relative to the source data. Spectral
             diffusion integrates structural information from multiple
             spectral channels and their corresponding material
             decompositions within the framework of diffusion-like
             denoising algorithms. Using a 3D, digital bar phantom and a
             material sensitivity matrix calibrated for use with a
             polychromatic x-ray source, we quantify the limits of
             detectability (CNR = 5) afforded by spectral diffusion in
             the triple-energy material decomposition of iodine (3.1
             mg/mL), gold (0.9 mg/mL), and gadolinium (2.9 mg/mL)
             concentrations. © 2014 SPIE.},
   Doi = {10.1117/12.2042546},
   Key = {fds268708}
}

@booklet{Johnson00,
   Author = {G. A. Johnson and F. W. Bazer and L. A. Jaeger and T. E.
             Spencer and C. Pfarrer and R. C. Burghardt},
   Title = {Role of MUC-1, integrins and extracellular matrix components
             in the implantation cascade in sheep.},
   Journal = {Biology Of Reproduction},
   Volume = {62},
   Pages = {281 -- 282},
   Year = {2000},
   Key = {Johnson00}
}

@booklet{Garlow00,
   Author = {J. E. Garlow and H. H. Ka and G. A. Johnson and L. A. Jaeger and R. C. Burghardt and F. W. Bazer},
   Title = {Role of osteopontin during early pregnancy in
             pigs.},
   Journal = {Biology Of Reproduction},
   Volume = {62},
   Pages = {282 -- 282},
   Year = {2000},
   Key = {Garlow00}
}

@article{fds204266,
   Author = {KJ Bayless and GA Johnson},
   Title = {Role of the cytoskeleton in formation and maintenance of
             angiogenic sprouts.},
   Journal = {Journal of vascular research},
   Volume = {48},
   Number = {5},
   Pages = {369-85},
   Year = {2011},
   ISSN = {1423-0135},
   url = {http://dx.doi.org/10.1159/000324751},
   Keywords = {Animals • Cytoskeleton • Humans •
             Neovascularization, Physiologic • Wound Healing •
             physiology*},
   Abstract = {Angiogenesis is the formation of new blood vessels from
             pre-existing structures, and is a key step in tissue and
             organ development, wound healing and pathological events.
             Changes in cell shape orchestrated by the cytoskeleton are
             integral to accomplishing the various steps of angiogenesis,
             and an intact cytoskeleton is also critical for maintaining
             newly formed structures. This review focuses on how the 3
             main cytoskeletal elements--microfilaments, microtubules,
             and intermediate filaments--regulate the formation and
             maintenance of angiogenic sprouts. Multiple classes of
             compounds target microtubules and microfilaments, revealing
             much about the role of actin and tubulin and their
             associated molecules in angiogenic sprout formation and
             maintenance. In contrast, intermediate filaments are much
             less studied, yet intriguing evidence suggests a vital, but
             unresolved, role in angiogenic sprouting. This review
             discusses evidence for regulatory molecules and
             pharmacological compounds that affect actin, microtubule and
             intermediate filament dynamics to alter various steps of
             angiogenesis, including endothelial sprout formation and
             maintenance.},
   Language = {eng},
   Doi = {10.1159/000324751},
   Key = {fds204266}
}

@booklet{Stewart02,
   Author = {M. D. Stewart and Y. S. Choi and G. A. Johnson and L. Y.
             Yu-lee and F. W. Bazer and T. E. Spencer},
   Title = {Roles of Stat1, Stat2, and interferon regulatory factor-9
             (IRF-9) in interferon tau regulation of IRF-1},
   Journal = {Biology Of Reproduction},
   Volume = {66},
   Number = {2},
   Pages = {393 -- 400},
   Year = {2002},
   Month = {February},
   Key = {Stewart02}
}

@article{fds174192,
   Author = {MD Stewart and Y Choi and GA Johnson and LY Yu-Lee and FW Bazer and TE
             Spencer},
   Title = {Roles of Stat1, Stat2, and interferon regulatory factor-9
             (IRF-9) in interferon tau regulation of IRF-1.},
   Journal = {Biology of reproduction},
   Volume = {66},
   Number = {2},
   Pages = {393-400},
   Year = {2002},
   Month = {February},
   ISSN = {0006-3363},
   Keywords = {Blotting, Western • Cell Line • Cells, Cultured
             • DNA-Binding Proteins • Fibroblasts • Humans
             • Indicators and Reagents • Interferon Regulatory
             Factor-1 • Interferon Type I •
             Interferon-Stimulated Gene Factor 3 •
             Interferon-Stimulated Gene Factor 3, gamma Subunit •
             Phosphoproteins • Phosphorylation • Pregnancy
             Proteins • RNA, Messenger • Reverse Transcriptase
             Polymerase Chain Reaction • STAT1 Transcription Factor
             • STAT2 Transcription Factor • Signal Transduction
             • Trans-Activators • Transcription Factors •
             Tyrosine • biosynthesis • genetics •
             metabolism • physiology • physiology*},
   Abstract = {Interferon tau (IFNtau) is the pregnancy recognition signal
             produced by the conceptus trophectoderm and acts in a
             paracine manner on the ovine endometrium to increase
             expression of IFN-stimulated genes primarily in the stroma
             and deep glandular epithelium, including IFN regulatory
             factor-1 (IRF-1). The roles of Stat1, Stat2, and IRF-9 in
             IFNtau regulation of IRF-1 expression were determined using
             human stromal fibroblasts lacking specific IFN signaling
             components or complemented with specific Stat1 mutants. In
             parental (2fTGH) cells treated with IFNtau, Stat1alpha/beta
             was tyrosine phosphorylated by 15 min, and IRF-1 mRNA and
             protein increased from 0 to 6 h, was maximal at 6 h, and
             decreased to 24 h. In contrast, IFNtau did not affect IRF-1
             expression in Stat1- and Stat2-deficient cells or in
             Stat1-deficient cells complemented with Stat1 Y701Q or Stat1
             R602L mutants. In Stat1-deficient cells complemented with
             the Stat1 S727A mutant, Stat1alpha, or Stat1beta and treated
             with IFNtau, IRF-1 increased from 0 to 6 h, was maximal at 6
             h, and decreased thereafter. In IRF-9-deficient cells
             stimulated with IFNtau, IRF-1 increased from 0 to 6 h but
             did not exhibit the sharp decline from 6 to 12 h observed in
             other cells. Collectively, results indicate that IFNtau
             effect on IRF-1 expression is primarily regulated by
             tyrosine-phosphorylated Stat1alpha or Stat1beta dimers,
             whereas the decline of IRF-1 after 6 h of IFNtau treatment
             is regulated by IRF-9.},
   Language = {eng},
   Key = {fds174192}
}

@booklet{Mcfall97,
   Author = {McFall, JS and Johnson, GA},
   Title = {Root form and function meshed by MRI.},
   Journal = {PLANT PHYSIOLOGY},
   Volume = {114},
   Number = {3},
   Pages = {20002-20002},
   Year = {1997},
   ISSN = {0032-0889},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1997XL11900006&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Mcfall97}
}

@article{06229906637,
   Author = {Miller, D.R. and Chen, S.Y. and Porter, P.M. and Johnson,
             G.A. and Wyse, D.L. and Stetina, S.R. and Klossner, L.D. and Nelson, G.A.},
   Title = {Rotation crop evaluation for management of the soybean cyst
             Nematode in Minnesota},
   Journal = {Agronomy Journal},
   Volume = {98},
   Number = {3},
   Pages = {569 - 578},
   Year = {2006},
   url = {http://dx.doi.org/10.2134/agronj2005.0185},
   Keywords = {Cultivation;},
   Abstract = {Crop rotation is an effective tactic for soybean cyst
             nematode (SCN) management. In the North Central region of
             the USA, corn is almost exclusively used as a nonhost
             rotation crop with soybean. This study was conducted to
             determine the effectiveness of crops common to or having
             potential use in the North Central region as rotation crops
             for managing SCN. Sixteen potential rotation crops and
             SCN-resistant and susceptible soybeans were grown along with
             six fallow controls in three commercial field sites near
             Waseca, Lamberton, and Morris, MN, in 2001, and
             SCN-susceptible soybean was grown on all plots in 2002.
             Nematode populations at planting, midseason, and harvest
             were measured both years; soybean yield was measured in
             2002. There was large variability in SCN populations and
             soybean yields at the three sites. Nevertheless, significant
             treatment effects were detected at all sites. While all of
             the rotation crops lowered SCN populations compared with
             SCN-susceptible soybean, there were only subtle differences
             among the individual rotation crops and among different
             groups of the crops. Leguminous nonhosts or poor hosts were
             best in reducing SCN population density. Corn, the most
             common rotation crop in Minnesota, was among the least
             effective in reducing nematode populations. There was an
             undetectable yield benefit from SCN management, although
             differences in yield were observed among the rotation crop
             treatments-probably due to agronomic factors. The data
             suggest that a single year of rotation of soybean with any
             of these crops before planting a susceptible soybean may not
             be sufficient in managing SCN. &copy; American Society of
             Agronomy.},
   Key = {06229906637}
}

@article{fds132737,
   Author = {G.A. Johnson},
   Title = {S. Hurlston, R.D. Black, W. Brey, X.J. Chen, L.W. Hedlund,
             R. Withers,  M.Yap, G.A. Johnson.  A superconducting
             surface coil for in vivo MR  microscopy. in "Proc., SMR 4th
             Annual Scientific Meeting.  New York, NY,  1996,"
             p.129.},
   Year = {1996},
   Key = {fds132737}
}

@article{fds371721,
   Author = {Johnson, G and Stubbs, WA and Woods, HF and Alberti,
             KGMM},
   Title = {Salicylate induced hypoglycaemia: a possible
             mechanism},
   Journal = {European Journal of Clinical Investigation},
   Volume = {4},
   Number = {5},
   Year = {1974},
   Month = {January},
   Key = {fds371721}
}

@booklet{Johnson80e,
   Author = {JOHNSON, GA and RAVIN, CE},
   Title = {SCATTERED RADIATION FROM THE FILM HOLDER IN CHEST
             RADIOGRAPHY},
   Journal = {AMERICAN JOURNAL OF ROENTGENOLOGY},
   Volume = {134},
   Number = {1},
   Pages = {201-201},
   Publisher = {AMER ROENTGEN RAY SOC},
   Year = {1980},
   Month = {January},
   ISSN = {0361-803X},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1980HZ88000054&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Johnson80e}
}

@article{fds174177,
   Author = {FJ White and RC Burghardt and J Hu and MM Joyce and TE Spencer and GA
             Johnson},
   Title = {Secreted phosphoprotein 1 (osteopontin) is expressed by
             stromal macrophages in cyclic and pregnant endometrium of
             mice, but is induced by estrogen in luminal epithelium
             during conceptus attachment for implantation.},
   Journal = {Reproduction (Cambridge, England)},
   Volume = {132},
   Number = {6},
   Pages = {919-29},
   Year = {2006},
   Month = {December},
   ISSN = {1470-1626},
   url = {http://dx.doi.org/10.1530/REP-06-0068},
   Keywords = {Animals • Embryo Implantation • Endometrium •
             Epithelium • Estrogens • Estrous Cycle •
             Female • Fluorescent Antibody Technique • In Situ
             Hybridization • Leukocytes • Macrophages •
             Mice • Osteopontin • Ovariectomy • Placenta
             • Pregnancy • Pregnancy, Animal •
             Progesterone • RNA, Messenger • analysis •
             chemistry • genetics • immunology •
             metabolism • metabolism* • pharmacology •
             physiology* • secretion*},
   Abstract = {Secreted phosphoprotein 1 (SPP1, osteopontin) is the most
             highly upregulated extracellular matrix/adhesion
             molecule/cytokine in the receptive phase human uterus, and
             Spp1 null mice manifest decreased pregnancy rates during
             mid-gestation as compared with wild-type counterparts. We
             hypothesize that Spp1 is required for proliferation,
             migration, survival, adhesion, and remodeling of cells at
             the conceptus-maternal interface. Our objective was to
             define the temporal/spatial distribution and steroid
             regulation of Spp1 in mouse uterus during estrous cycle and
             early gestation. In situ hybridization localized Spp1 to
             luminal epithelium (LE) and immune cells. LE expression was
             prominent at proestrus, decreased by estrus, and was nearly
             undetectable at diestrus. During pregnancy, Spp1 mRNA was
             not detected in LE until day 4.5 (day 1 = vaginal plug).
             Spp1-expressing immune cells were scattered within the
             endometrial stroma throughout the estrous cycle and early
             pregnancy. Immunoreactive Spp1 was prominent at the apical
             LE surface by day 4.5 of pregnancy and Spp1 protein was also
             co-localized with subsets of CD45-positive (leukocytes) and
             F4/80-positive (macrophages) cells. In ovariectomized mice,
             estrogen, but not progesterone, induced Spp1 mRNA, whereas
             estrogen plus progesterone did not induce Spp1 in LE. These
             results establish that estrogen regulates Spp1 in mouse LE
             and are the first to identify macrophages that produce Spp1
             within the peri-implantation endometrium of any species. We
             suggest that Spp1 at the apical surface of LE provides a
             mechanism to bridge conceptus to LE during implantation, and
             that Spp1-positive macrophages within the stroma may be
             involved in uterine remodeling for conceptus
             invasion.},
   Language = {eng},
   Doi = {10.1530/REP-06-0068},
   Key = {fds174177}
}

@article{fds174070,
   Author = {DW Erikson and RC Burghardt and KJ Bayless and GA
             Johnson},
   Title = {Secreted phosphoprotein 1 (SPP1, osteopontin) binds to
             integrin alpha v beta 6 on porcine trophectoderm cells and
             integrin alpha v beta 3 on uterine luminal epithelial cells,
             and promotes trophectoderm cell adhesion and
             migration.},
   Journal = {Biology of reproduction},
   Volume = {81},
   Number = {5},
   Pages = {814-25},
   Year = {2009},
   Month = {November},
   ISSN = {1529-7268},
   url = {http://dx.doi.org/10.1095/biolreprod.109.078600},
   Keywords = {Animals • Antigens, Neoplasm • Cattle • Cell
             Adhesion • Cell Line • Cell Movement • Cell
             Proliferation • Chromatography, Affinity •
             Dose-Response Relationship, Drug • Embryo Implantation
             • Epithelial Cells • Extracellular Matrix •
             Female • Fluorescent Antibody Technique • Integrin
             alphaVbeta3 • Integrins • Osteopontin •
             Pregnancy • Rats • Swine • Uterus • drug
             effects • metabolism • metabolism* •
             pharmacology • physiology*},
   Abstract = {Conceptus implantation involves pregnancy-specific
             alterations in extracellular matrix at the
             conceptus-maternal interface. Secreted phosphoprotein 1
             (SPP1, osteopontin) is induced just before implantation and
             is present at the conceptus-maternal interface in mammals.
             In the present study, we investigated mechanisms by which
             SPP1 facilitates porcine conceptus and uterine luminal
             epithelial cell attachment. Native bovine milk and wild-type
             rat recombinant SPP1 stimulated trophectoderm cell
             migration. Bovine milk SPP1, ovine uterine SPP1, and
             recombinant wild-type, but not mutated, rat SPP1 promoted
             dose- and cation-dependent attachment of porcine
             trophectoderm and uterine luminal epithelial cells, which
             was markedly reduced in the presence of a linear Arg-Gly-Asp
             integrin-blocking peptide. Affinity chromatography and
             immunoprecipitation experiments revealed direct binding of
             alpha v beta 6 trophectoderm and alpha v beta 3 uterine
             epithelial cell integrins to SPP1. Immunofluorescence
             microscopy using SPP1-coated microspheres revealed
             colocalization of the alpha v integrin subunit and talin at
             focal adhesions as well as at the apical domain of
             trophectoderm cells. Similarly, immunofluorescence staining
             of implantation sites in frozen gravid uterine cross
             sections localized SPP1 and alpha v integrin to the apical
             surfaces of trophectoderm and luminal epithelium and beta 3
             integrin to the apical surface of luminal epithelium. To our
             knowledge, the present study is the first to demonstrate
             functionally that SPP1 directly binds specific integrins to
             promote trophectoderm cell migration and attachment to
             luminal epithelium that may be critical to conceptus
             elongation and implantation.},
   Language = {eng},
   Doi = {10.1095/biolreprod.109.078600},
   Key = {fds174070}
}

@article{fds174171,
   Author = {J Kim and DW Erikson and RC Burghardt and TE Spencer and G Wu and KJ
             Bayless, GA Johnson and FW Bazer},
   Title = {Secreted phosphoprotein 1 binds integrins to initiate
             multiple cell signaling pathways, including FRAP1/mTOR, to
             support attachment and force-generated migration of
             trophectoderm cells.},
   Journal = {Matrix biology : journal of the International Society for
             Matrix Biology},
   Year = {2010},
   Month = {April},
   ISSN = {1569-1802},
   url = {http://dx.doi.org/10.1016/j.matbio.2010.04.001},
   Abstract = {Attachment and migration of trophectoderm (Tr) cells,
             hallmarks of blastocyst implantation in mammals, are unique
             uterine events. Secreted phosphoprotein 1 (SPP1) in the
             uterus binds integrins on conceptus Tr and uterine luminal
             epithelium (LE), affecting cell-cell and cell-matrix
             interactions. The signal transduction pathways activated by
             SPP1 and integrins in conceptuses have not been elucidated.
             Results of this study demonstrate that SPP1 binds
             alphavbeta3 and alpha5beta1 integrins to induce focal
             adhesion assembly, a prerequisite for adhesion and migration
             of Tr, through activation of: 1) P70S6K via crosstalk
             between FRAP1/mTOR and MAPK pathways; 2) mTOR, PI3K,
             MAPK3/MAPK1 (Erk1/2) and MAPK14 (p38) signaling to stimulate
             Tr cell migration; and 3) focal adhesion assembly and myosin
             II motor activity to induce migration of Tr cells. These
             cell signaling pathways, acting in concert, mediate
             adhesion, migration and cytoskeletal remodeling of Tr cells
             essential for expansion and elongation of conceptuses and
             attachment to uterine LE for implantation.},
   Language = {ENG},
   Doi = {10.1016/j.matbio.2010.04.001},
   Key = {fds174171}
}

@article{fds174298,
   Author = {FW Bazer and H Gao and GA Johnson and G Wu and DW Bailey and RC
             Burghardt},
   Title = {Select nutrients and glucose transporters in pig uteri and
             conceptuses.},
   Journal = {Society of Reproduction and Fertility supplement},
   Volume = {66},
   Pages = {335-6},
   Year = {2009},
   Keywords = {Amino Acids • Animals • Arginine • Embryo,
             Mammalian • Estradiol • Female • Glucose
             • Glucose Transport Proteins, Facilitative •
             Glutamine • Leucine • Pregnancy • Pregnancy,
             Animal • Pseudopregnancy • Swine • Uterus
             • analogs & derivatives • chemically induced
             • metabolism • metabolism*},
   Language = {eng},
   Key = {fds174298}
}

@article{fds174210,
   Author = {MC Satterfield and H Gao and X Li and G Wu and GA Johnson and TE Spencer and FW Bazer},
   Title = {Select nutrients and their associated transporters are
             increased in the ovine uterus following early progesterone
             administration.},
   Journal = {Biology of reproduction},
   Volume = {82},
   Number = {1},
   Pages = {224-31},
   Year = {2010},
   Month = {January},
   ISSN = {1529-7268},
   url = {http://dx.doi.org/10.1095/biolreprod.109.076729},
   Keywords = {Amino Acids • Animals • Blastocyst • Cationic
             Amino Acid Transporter 2 • Embryonic Development*
             • Endometrium • Female • Glucose •
             Glucose Transporter Type 1 • Mifepristone •
             Progesterone • RNA, Messenger • Sheep •
             Sodium-Glucose Transporter 1 • metabolism •
             metabolism* • pharmacology • pharmacology* •
             physiology*},
   Abstract = {The intrauterine milieu is a complex mixture of substances
             originating from serum and endometrium that support
             blastocyst growth and development. The present study
             identified alterations in glucose and amino acids in
             response to an early rise in progesterone (P4), which
             accelerates blastocyst growth and development. Bred ewes
             received daily injections of either corn oil (CO) vehicle or
             P4 from 36 h postmating (Day 0) to either Day 9 or Day 12.
             Another group of ewes received P4 to Day 8 and the
             antiprogestin mifepristone (RU486) from Day 8 to Day 12. The
             total amount of glucose, aspartate (acidic amino acid),
             arginine and lysine (basic amino acids), and citrulline,
             asparagine, serine, glutamine, beta-alanine, and alanine
             (neutral amino acids) was greater in uterine flushings from
             early P4- than CO-treated ewes on Day 9. On Day 12, only
             arginine and lysine were higher in uterine flushings from
             P4-treated ewes, whereas citrulline was reduced. Glucose
             transporters, SLC2A1 and SLC5A1, were increased in uterine
             luminal (LE) and superficial glandular (sGE) epithelia of
             early P4-treated ewes on Days 9 and 12 but were reduced in
             endometria from ewes treated with both P4 and RU486 (P4+RU).
             SLC7A2B, a transporter of basic amino acids, increased in
             LE/sGE of P4- versus CO-treated ewes on Day 12 but was
             reduced in P4+RU-treated ewes. Thus, select nutrients are
             increased in the uterine lumen by P4 concomitant with the
             upregulation of epithelial transporters for glucose and
             basic amino acids, suggesting that these nutrients stimulate
             blastocyst growth and development.},
   Language = {eng},
   Doi = {10.1095/biolreprod.109.076729},
   Key = {fds174210}
}

@article{fds174215,
   Author = {H Gao and G Wu and TE Spencer and GA Johnson and X Li and FW
             Bazer},
   Title = {Select nutrients in the ovine uterine lumen. I. Amino acids,
             glucose, and ions in uterine lumenal flushings of cyclic and
             pregnant ewes.},
   Journal = {Biology of reproduction},
   Volume = {80},
   Number = {1},
   Pages = {86-93},
   Year = {2009},
   Month = {January},
   ISSN = {0006-3363},
   url = {http://dx.doi.org/10.1095/biolreprod.108.071597},
   Keywords = {Amino Acids • Animals • Calcium • Estrous
             Cycle • Female • Glucose • Glutathione •
             Potassium • Pregnancy • Pregnancy, Animal •
             Sheep • Sodium • Uterus • metabolism •
             metabolism*},
   Abstract = {Nutrients in uterine secretions are essential for
             development and survival of conceptuses (embryo and
             associated extraembryonic membranes) during pregnancy;
             however, little is known about changes in the amounts of
             specific nutrients in the uterine fluids of cyclic and
             pregnant ruminants. This study determined quantities of
             glucose, amino acids, glutathione, calcium, sodium, and
             potassium in uterine lumenal fluid from cyclic (Days 3-16)
             and pregnant (Days 10-16) ewes. Total recoverable glucose,
             Arg, Gln, Leu, Asp, Glu, Asn, His, beta-Ala, Tyr, Trp, Met,
             Val, Phe, Ile, Lys, Cys, Pro, glutathione, calcium, and
             sodium were greater in the uterine fluid of pregnant
             compared with cyclic ewes between Days 10 and 16. In cyclic
             ewes, only modest changes in the total amounts of glucose,
             Asn, Cit, Tyr, Trp, Met, Val, Cys, glutathione, calcium, and
             potassium were detected between Days 3 and 16. However, in
             pregnant ewes, amounts of glucose, Arg, Gln, Glu, Gly, Cys,
             Leu, Pro, glutathione, calcium, and potassium in uterine
             fluids increased 3- to 23-fold between Days 10 and 14 and
             remained high to Day 16. Of particular interest were
             increases in glucose, Arg, Leu, and Gln in uterine flushings
             of pregnant ewes between Days 10 and 16 of pregnancy. Total
             amounts of His, ornithine, Lys, Ser, Thr, Ile, Phe, Trp,
             Met, and Cit in uterine fluids also increased, but to a
             lesser extent during early pregnancy. These novel results
             indicate activation of pregnancy-associated mechanisms for
             transport of nutrients into the uterine lumen, and they
             provide a framework for future studies of nutrients,
             including glucose, amino acids, and glutathione, required to
             activate nutrient-sensing cell signaling pathways for
             growth, development, and survival of conceptuses, as well as
             for optimization of culture media for in vitro studies of
             conceptus development.},
   Language = {eng},
   Doi = {10.1095/biolreprod.108.071597},
   Key = {fds174215}
}

@article{fds174079,
   Author = {H Gao and G Wu and TE Spencer and GA Johnson and FW Bazer},
   Title = {Select nutrients in the ovine uterine lumen. ii. glucose
             transporters in the uterus and peri-implantation
             conceptuses.},
   Journal = {Biology of reproduction},
   Volume = {80},
   Number = {1},
   Pages = {94-104},
   Year = {2009},
   Month = {January},
   ISSN = {0006-3363},
   url = {http://dx.doi.org/10.1095/biolreprod.108.071654},
   Keywords = {Animals • Blastocyst • Estrous Cycle • Female
             • Gene Expression Regulation, Developmental •
             Glucose Transport Proteins, Facilitative •
             Immunohistochemistry • In Situ Hybridization •
             Interferon Type I • Pregnancy • Pregnancy Proteins
             • Progesterone • RNA, Messenger • Random
             Allocation • Sheep • Uterus • antagonists &
             inhibitors • biosynthesis • genetics •
             metabolism* • pharmacology* • physiology •
             veterinary},
   Abstract = {Total glucose in ovine uterine lumenal fluid increases
             6-fold between Days 10 and 15 of gestation, but not the
             estrous cycle; however, mechanisms for glucose transport
             into the uterine lumen and uptake by conceptuses
             (embryo/fetus and associated membranes) are not established.
             This study determined the effects of the estrous cycle,
             pregnancy, progesterone (P4), and interferon tau (IFNT) on
             expression of both facilitative (SLC2A1, SLC2A3, and SLC2A4)
             and sodium-dependent (SLC5A1 and SLC5A11) glucose
             transporters in ovine uterine endometria from Days 10 to 16
             of the estrous cycle and Days 10 to 20 of pregnancy, as well
             as in conceptuses from Days 10 to 20 of pregnancy. The
             SLC2A1 and SLC5A1 mRNAs and proteins were most abundant in
             uterine luminal epithelia and superficial glandular
             epithelia (LE/sGE), whereas SLC2A4 was present in stromal
             cells and glandular epithelia (GE). SLC5A11 mRNA was most
             abundant in endometrial GE, whereas SLC2A3 mRNA was not
             detectable in endometria. SLC2A1, SLC2A3, SLC2A4, SLC5A1,
             and SLC5A11 were expressed in the trophectoderm and endoderm
             of conceptuses. Steady-state levels of SLC2A1, SLC5A1, and
             SLC5A11 mRNAs, but not SLC2A4 mRNA, were greater in
             endometria from pregnant than from cyclic ewes. Progesterone
             increased SLC2A1, SLC5A11, and SLC2A4 mRNAs in the LE/sGE
             and SLC5A1 in the GE of ovariectomized ewes. Expression of
             SLC5A1 was inhibited by ZK136,317 (progesterone receptor
             antagonist), and the combination of ZK136,317 and IFNT
             further decreased expression in GE. In constrast, P4 induced
             and IFNT stimulated expression of SLC2A1 and SLC5A11, and
             these effects were blocked by ZK136,317. Results of this
             study indicate differential expression of facilitative and
             sodium-dependent glucose transporters in ovine uteri and
             conceptuses for transport and uptake of glucose, and that P4
             or P4 and IFNT regulate their expression during the
             peri-implantation period of pregnancy.},
   Language = {eng},
   Doi = {10.1095/biolreprod.108.071654},
   Key = {fds174079}
}

@article{fds174130,
   Author = {H Gao and G Wu and TE Spencer and GA Johnson and FW Bazer},
   Title = {Select nutrients in the ovine uterine lumen. III. Cationic
             amino acid transporters in the ovine uterus and
             peri-implantation conceptuses.},
   Journal = {Biology of reproduction},
   Volume = {80},
   Number = {3},
   Pages = {602-9},
   Year = {2009},
   Month = {March},
   ISSN = {0006-3363},
   url = {http://dx.doi.org/10.1095/biolreprod.108.073890},
   Keywords = {Amino Acid Transport Systems, Basic • Animals •
             Arginine • Biological Transport • Blastocyst
             • Cationic Amino Acid Transporter 1 • Cationic
             Amino Acid Transporter 2 • Endometrium • Estrous
             Cycle • Female • Interferon Type I •
             Pregnancy • Pregnancy Proteins • Pregnancy, Animal
             • Progesterone • RNA, Messenger • Receptors,
             Progesterone • Sheep • Uterus • antagonists &
             inhibitors • metabolism • metabolism* •
             pharmacology • physiology},
   Abstract = {Arginine is an essential amino acid for conceptus
             (embryo/fetus and trophoblast/placenta) growth and
             development; however, the mechanisms for arginine transport
             into the uterine lumen and uptake by conceptuses are largely
             unknown. In this study, expression of System y(+) (SLC7A1,
             SLC7A2, and SLC7A3) cationic amino acid transporters in
             uteri of cyclic and pregnant ewes and conceptuses was
             studied, and effects of pregnancy, progesterone (P4), and
             interferon tau (IFNT) on their expression were investigated.
             SLC7A1 mRNA was most abundant in endometrial luminal (LE)
             and superficial glandular (sGE) epithelia on Day 16 of the
             estrous cycle and on Days 16-20 of pregnancy, whereas SLC7A2
             mRNA was most abundant in LE and mid to deep glandular (GE)
             epithelia on Days 14-20 of gestation. Expression of SLC7A1
             and SLC7A2 was enhanced in pregnant ewes in a cell-specific
             manner, but abundance of SLC7A3 was not affected by day of
             the estrous cycle or by pregnancy status. SLC7A1, SLC7A2,
             and SLC7A3 mRNAs were expressed in trophectoderm and
             endoderm of conceptuses. In ovariectomized ewes, short-term
             treatment of ewes with P4 and IFNT did not affect
             endometrial SLC7A1 mRNA, while long-term treatment with P4
             stimulated SLC7A1 in LE and GE, and IFNT tended to increase
             SLC7A1 abundance in LE. SLC7A2 mRNA abundance increased
             4.1-fold in response to short-term P4 treatment and an
             additional 1.7-fold by IFNT primarily in endometrial LE/sGE,
             and these effects were ablated by a P4 receptor antagonist.
             These results indicate that coordinate changes in SLC7A1,
             SLC7A2, and SLC7A3 expression in uterine endometria and
             conceptuses are likely important in transport of arginine
             that is critical to conceptus growth, development, and
             survival.},
   Language = {eng},
   Doi = {10.1095/biolreprod.108.073890},
   Key = {fds174130}
}

@article{fds174094,
   Author = {H Gao and G Wu and TE Spencer and GA Johnson and FW Bazer},
   Title = {Select nutrients in the ovine uterine lumen. IV. Expression
             of neutral and acidic amino acid transporters in ovine uteri
             and peri-implantation conceptuses.},
   Journal = {Biology of reproduction},
   Volume = {80},
   Number = {6},
   Pages = {1196-208},
   Year = {2009},
   Month = {June},
   ISSN = {0006-3363},
   url = {http://dx.doi.org/10.1095/biolreprod.108.075440},
   Keywords = {Amino Acid Transport Systems, Acidic • Amino Acid
             Transport Systems, Neutral • Animals • Corpus
             Luteum • Embryo, Mammalian • Endometrium •
             Estrous Cycle • Female • Interferon Type I •
             Pregnancy • Pregnancy Proteins • Pregnancy, Animal
             • Progesterone • RNA, Messenger • Sheep
             • metabolism • metabolism*},
   Abstract = {The availability of specific neutral and acidic amino acids
             in the uterine lumen of ewes increased significantly during
             the peri-implantation period, but mechanisms for their
             transport into the uterine lumen and uptake by conceptuses
             are not established in any species. In this study, effects
             of pregnancy, progesterone (P4), and interferon tau (IFNT)
             on expression of neutral and acidic amino acid transporters
             in uteri of cyclic and pregnant ewes and conceptuses were
             studied. SLC1A2, SLC1A3, SLC3A1, SLC6A14, SLC6A19, SLC7A6,
             SLC38A3, and SLC38A6 mRNAs were only weakly expressed in the
             ovine endometrium. However, SLC1A4, SLC1A5, SLC7A8, and
             SLC43A2 mRNAs were detectable in uterine luminal epithelia
             (LE), superficial glandular epithelia (sGE), and/or
             glandular epithelia (GE). SLC1A1 and SLC7A5 mRNAs were most
             abundant in LE/sGE and GE. SLC1A3 and SLC38A4 mRNAs were
             most abundant in uterine stroma. SLC38A6 mRNA was detected
             only in cells with a stromal distribution suggesting immune
             lineage. SLC1A5 mRNA was expressed primarily in LE/sGE and
             stromal cells, and it was more abundant in uteri of pregnant
             ewes (day x status interaction; P < 0.05). Furthermore, P4
             induced and IFNT further stimulated SLC1A5 expression in
             LE/sGE. Endometrial SLC1A1, SLC7A5, and SLC43A2 mRNAs
             demonstrated both temporal and cellSLC-specific changes.
             Several mRNAs were detectable in trophectoderm (SLC6A19,
             SLC7A5, SLC7A6, and SLC43A2), while others were more
             abundant in endoderm (SLC1A4, SLC1A5, SLC6A19, SLC7A5,
             SLC7A6, SLC7A8, and SLC43A2) of conceptuses. These results
             document coordinate changes in expression of transporters
             that are likely responsible for increases in amounts of
             neutral and acidic amino acids in the uterine lumen to
             support conceptus growth, development, and
             survival.},
   Language = {eng},
   Doi = {10.1095/biolreprod.108.075440},
   Key = {fds174094}
}

@article{fds204259,
   Author = {J Kim and RC Burghardt and G Wu and GA Johnson and TE Spencer and FW
             Bazer},
   Title = {Select nutrients in the ovine uterine lumen. IX.
             Differential effects of arginine, leucine, glutamine, and
             glucose on interferon tau, ornithine decarboxylase, and
             nitric oxide synthase in the ovine conceptus.},
   Journal = {Biology of reproduction},
   Volume = {84},
   Number = {6},
   Pages = {1139-47},
   Year = {2011},
   Month = {June},
   ISSN = {1529-7268},
   url = {http://dx.doi.org/10.1095/biolreprod.110.088153},
   Keywords = {Amino Acids • Animals • Arginine • Embryo,
             Mammalian • Embryonic Development • Female •
             Gene Expression Regulation, Developmental • Glucose
             • Glutamine • Interferon Type I • Leucine
             • Nitric Oxide Synthase • Ornithine Decarboxylase
             • Pregnancy • Pregnancy Proteins • RNA,
             Messenger • Sheep • Uterus • drug effects
             • genetics • metabolism • metabolism* •
             pharmacology • pharmacology* • physiology •
             physiology*},
   Abstract = {Nutrients are primary requirements for development of
             conceptuses (embryo and extraembryonic membranes), including
             protein synthesis. We have shown that arginine (Arg),
             leucine (Leu), and glucose stimulate protein synthesis
             through phosphorylation of MTOR signaling molecules, thereby
             increasing proliferation of ovine trophectoderm cells. This
             study determined whether Arg, Leu, glutamine (Gln), and
             glucose influence gene expression and protein synthesis in
             explant cultures of ovine conceptuses recovered from ewes on
             Day 16 of pregnancy. Conceptuses were deprived of select
             nutrients and then cultured with either Arg, Leu, Gln, or
             glucose for 18 h, after which they were analyzed for
             abundance of MTOR, RPS6K, RPS6, EIF4EBP1 (also known as
             4EBP1), IFNT, NOS2, NOS3, GCH1, and ODC1 mRNAs and proteins.
             Levels of MTOR, RPS6K, RPS6, and EIF4EBP1 mRNAs were not
             affected by treatment with any of the select nutrients.
             Similarly, expression of IFNT, NOS2, NOS3, and ODC1 mRNAs
             were not different. Interestingly, GCH1 mRNA levels
             increased in response to Arg treatment. Importantly, Arg,
             Leu, Gln, and glucose increased the abundance of
             phosphorylated MTOR, RPS6K, RPS6, and EIF4EBP1 proteins as
             well as NOS and ODC1 proteins, but only Arg increased the
             abundance of IFNT protein. These findings indicate that Arg,
             Leu, Gln, and glucose stimulate translation of mRNAs to
             increase synthesis of proteins through phosphorylation and
             activation of components of the MTOR signaling pathway.
             Increases in abundance of IFNT protein (the pregnancy
             recognition signal), NOS2, NOS3 and GCH1 for conversion of
             Arg to nitric oxide, and ODC1 for synthesis of polyamines
             are all important for growth and development of the ovine
             conceptus during pregnancy.},
   Language = {eng},
   Doi = {10.1095/biolreprod.110.088153},
   Key = {fds204259}
}

@article{fds174155,
   Author = {H Gao and G Wu and TE Spencer and GA Johnson and FW Bazer},
   Title = {Select nutrients in the ovine uterine lumen. V. Nitric oxide
             synthase, GTP cyclohydrolase, and ornithine decarboxylase in
             ovine uteri and peri-implantation conceptuses.},
   Journal = {Biology of reproduction},
   Volume = {81},
   Number = {1},
   Pages = {67-76},
   Year = {2009},
   Month = {July},
   ISSN = {0006-3363},
   url = {http://dx.doi.org/10.1095/biolreprod.108.075473},
   Keywords = {Animals • Embryo Implantation • Embryo, Mammalian
             • Estrous Cycle • Female • Food* • GTP
             Cyclohydrolase • Gene Expression Regulation,
             Developmental • Gene Expression Regulation, Enzymologic
             • Interferon Type I • Isoenzymes • Models,
             Biological • Nitric Oxide Synthase • Organ
             Specificity • Ornithine Decarboxylase • Pregnancy
             • Pregnancy Proteins • Progesterone • Sheep
             • Time Factors • Uterus • analysis •
             chemistry • drug effects • embryology •
             enzymology • genetics • genetics* •
             metabolism • metabolism* • pharmacology •
             physiology},
   Abstract = {Nitric oxide (NO) and polyamines are critical for
             implantation and development of conceptuses (embryo and
             extraembryonic membranes), but mechanisms regulating their
             biosynthesis in uteri and conceptuses are largely unknown.
             This study determined the effects of the estrous cycle,
             pregnancy, progesterone, and interferon tau (IFNT) on
             expression of NO synthases (NOS1, NOS2, and NOS3), guanosine
             triphosphate (GTP) cyclohydrolase (GCH1, the key enzyme in
             de novo synthesis of tetrahydrobiopterin, a cofactor for NO
             production), and ornithine decarboxylase (ODC1) in uterine
             endometria in cyclic ewes (Days 10-16) and pregnant ewes
             (Days 10-20). The mRNAs and proteins for NOS1 and ODC1 were
             most abundant in uterine luminal (LE) and superficial
             glandular (sGE) epithelia, and abundance was affected by day
             of estrous cycle and early pregnancy. NOS2, GCH1, and NOS3
             mRNAs were detected in very low abundance in uterine
             epithelia and stromal cells in both cyclic and pregnant
             ewes. NOS1 mRNA also was expressed very weakly in
             conceptuses, whereas NOS3 mRNA was abundant in the
             trophectoderm and endoderm of conceptuses, as were total
             NOS1 and NOS3 proteins, inhibitory p-NOS1 protein, and
             stimulatory p-NOS3 protein. GCH1 mRNA was abundant in the
             trophectoderm and endoderm of conceptuses between Days 13
             and 15 of pregnancy and then decreased thereafter, whereas
             ODC1 mRNA abundance increased in conceptuses between Days 13
             and 18 of pregnancy. GCH1 protein was localized primarily in
             the nuclei of trophectoderm and endoderm, and its abundance
             decreased after Day 14 of pregnancy, whereas ODC1 protein
             was more abundant in the trophectoderm than in the endoderm
             between Days 13 and 18 of pregnancy. Progesterone stimulated
             NOS1 and GCH1 expression in LE/sGE and glandular epithelia,
             whereas IFNT inhibited NOS1 expression in these cell types.
             Thus, biosynthesis of NO and polyamines in ovine uterine
             endometria and conceptuses is potentially regulated at
             transcriptional, translational, and posttranslational levels
             to favor conceptus development and implantation.},
   Language = {eng},
   Doi = {10.1095/biolreprod.108.075473},
   Key = {fds174155}
}

@article{fds174196,
   Author = {H Gao and G Wu and TE Spencer and GA Johnson and FW Bazer},
   Title = {Select nutrients in the ovine uterine lumen. VI. Expression
             of FK506-binding protein 12-rapamycin complex-associated
             protein 1 (FRAP1) and regulators and effectors of mTORC1 and
             mTORC2 complexes in ovine uteri and conceptuses.},
   Journal = {Biology of reproduction},
   Volume = {81},
   Number = {1},
   Pages = {87-100},
   Year = {2009},
   Month = {July},
   ISSN = {0006-3363},
   url = {http://dx.doi.org/10.1095/biolreprod.109.076257},
   Keywords = {Animals • Carrier Proteins • Embryo Implantation
             • Embryo, Mammalian • Estrous Cycle •
             Eukaryotic Initiation Factors • Female • Food*
             • Gene Expression Regulation • Gestational Age
             • Interferon Type I • Models, Biological •
             Organ Specificity • Pregnancy • Pregnancy Proteins
             • Pregnancy, Animal • Progesterone • Protein
             Kinases • Protein Multimerization • Sheep •
             Transcription Factors • Uterus • drug effects
             • embryology • genetics • genetics* •
             metabolism • metabolism* • pharmacology •
             physiology},
   Abstract = {FRAP1 (FK506-binding protein 12-rapamycin complex-associated
             protein 1), a component of the nutrient-sensing cell
             signaling pathway, is critical for cell growth and
             metabolism. The present study determined expression of FRAP1
             and associated members of the mTORC1 and mTORC2 cell
             signaling pathways in uteri of cyclic and pregnant ewes and
             conceptuses, as well as effects of pregnancy, progesterone
             (P4), and interferon tau (IFNT) on their expression. The
             mRNAs for FRAP1, LST8, MAPKAP1, RAPTOR, RICTOR, TSC1, TSC2,
             RHEB, and EIF4EBP1 were localized to luminal, superficial
             glandular, and glandular epithelia and stromal cells of
             uteri from cyclic and pregnant ewes, as well as
             trophectoderm and endoderm of conceptuses between Days 13
             and 18 of pregnancy. The abundance of FRAP1, RAPTOR, RICTOR,
             TSC1, and TSC2 mRNAs in endometria was unaffected by
             pregnancy status or by day of the estrous cycle or
             pregnancy; however, levels of LST8, MAPKAP1, RHEB, and
             EIF4EBP1 mRNA increased in endometria during early
             pregnancy. In ovariectomized ewes, P4 and IFNT stimulated
             expression of RHEB and EIF4EBP1 in uterine endometria. Total
             endometrial FRAP1 protein and phosphorylated FRAP1 protein
             levels were affected by pregnancy status and by day after
             onset of estrus, and phosphorylated FRAP1 protein was
             detected in nuclei of uterine epithelia and conceptuses. In
             endometria of pregnant ewes, increases in abundance of mRNAs
             for RICTOR, RHEB, and EIF4EBP1, as well as RHEB protein,
             correlated with rapid conceptus growth and development
             during the peri-implantation period. These results suggest
             that the FRAP1 cell signaling pathway mediates interactions
             between the maternal uterus and peri-implantation
             conceptuses and that P4 and IFNT affect this pathway by
             regulating expression of RHEB and EIF4EBP1.},
   Language = {eng},
   Doi = {10.1095/biolreprod.109.076257},
   Key = {fds174196}
}

@article{fds180937,
   Author = {JY Kim and RC Burghardt and G Wu and GA Johnson and TE Spencer and FW
             Bazer},
   Title = {Select Nutrients in the Ovine Uterine Lumen. VII. Effects of
             Arginine, Leucine, Glutamine, and Glucose on Trophectoderm
             Cell Signaling, Proliferation, and Migration.},
   Journal = {Biology of reproduction},
   Year = {2010},
   Month = {September},
   ISSN = {1529-7268},
   url = {http://dx.doi.org/10.1095/biolreprod.110.085738},
   Abstract = {Histotroph is required for survival and development of ovine
             conceptuses (embryo and extra-embryonic membranes). Results
             from our laboratory indicate that arginine (Arg), leucine
             (Leu), glutamine (Gln) and glucose increase in the uterine
             lumen between Days 10 and 15 of pregnancy, coincident with
             increases in expression of amino acid and glucose
             transporters by uterine epithelia, as well as trophectoderm
             and yolk sac of conceptuses, and elongation of the conceptus
             trophectoderm. Therefore, we hypothesized that Arg, Leu, Gln
             and glucose have differential effects on hypertrophy,
             hyperplasia and differentiated functions of trophectoderm
             cells that are critical to conceptus development. Primary
             ovine trophectoderm (oTr) cells isolated from Day 15
             conceptuses were serum-starved for 24h in a customized
             medium, deprived of select nutrients and then treated with
             either Arg, Leu, Gln or glucose. Western blot analyses of
             whole oTr cell extracts revealed that Arg, Leu and glucose,
             but not Gln, increased phosphorylated AKT1 (pAKT1) 2.8-,
             2.5-, and 1.8-fold, respectively, within 15 min and the
             increase was maintained to 60 min. Arg, Leu and glucose also
             stimulated 4.2-, 4.7-, and 2.3-fold increases in
             phosphorylated RPS6K (pRPS6K) within 15 min, as well as
             increases in pRPS6 protein between 0 and 30 min
             post-treatment that were sustained to 60 min. When oTr cells
             were treated with Arg, pRPS6K protein increased in nuclei,
             but this was not observed in nuclei of oTr cells treated
             with Leu and glucose. Immunocytochemical analyses also
             revealed abundant amounts of phosphorylated RPS6 protein in
             the cytoplasm of oTr cells treated with Arg, Leu and
             glucose. Further, Arg and Leu increased proliferation and
             migration of oTr cells. Collectively, these results indicate
             that Arg, Leu and glucose, but not Gln, in histotroph
             coordinately activate AKT1-MTOR and RPS6K-RPS6 cell
             signaling pathways to stimulate hypertrophy, hyperplasia,
             and migration of oTr cells.},
   Language = {ENG},
   Doi = {10.1095/biolreprod.110.085738},
   Key = {fds180937}
}

@article{fds180933,
   Author = {JY Kim and RC Burghardt and G Wu and GA Johnson and TE Spencer and FW
             Bazer},
   Title = {Select Nutrients in the Ovine Uterine Lumen. VIII. Arginine
             Stimulates Proliferation of Ovine Trophectoderm Cells
             Through MTOR-RPS6K-RPS6 Signaling Cascade and Synthesis of
             Nitric Oxide and Polyamines.},
   Journal = {Biology of reproduction},
   Year = {2010},
   Month = {September},
   ISSN = {1529-7268},
   url = {http://dx.doi.org/10.1095/biolreprod.110.085753},
   Abstract = {During the peri-implantation period in sheep, L-arginine
             (L-Arg) in the uterine lumen is an essential substrate for
             synthesis of nitric oxide (NO) by nitric oxide synthase
             (NOS) and polyamines via arginase and ornithine
             decarboxylase (ODC1) required for survival and development
             of ovine conceptuses (embryo and its extra-embryonic
             membranes). L-Arg can stimulate hypertrophy, hyperplasia and
             differentiation of the ovine conceptus trophectoderm;
             however, the responsible signal transduction cascade has not
             been determined. Therefore, this study examined possible
             signaling pathways mediated by L-Arg, as well as effects of
             two NO donors, SNAP and DETA, and putrescine (precursor for
             spermidine and spermine) on oTr cell proliferation. Further,
             the inhibition of these effects by L-NAME (an inhibitor of
             NOS) and Nor-NOHA (an inhibitor of arginase) was assessed.
             L-Arg treatment increased the abundance of phosphorylated
             MTOR, RPS6K and EIF4EBP1 in oTr cells. Consistent with
             activation of these cell signaling molecules, L-Arg
             increased protein synthesis and reduced protein degradation
             in oTr cells. Both NO and polyamines enhanced cell
             proliferation in a dose-dependent manner. The effects of
             L-Arg were partially inhibited by both L-NAME and Nor-NOHA.
             These results indicate that L-Arg enhances production of
             polyamines and NO and activates the MTOR/FRAP1-RPS6K-RPS6
             signaling pathway to stimulate proliferation and migration
             of oTr cells.},
   Language = {ENG},
   Doi = {10.1095/biolreprod.110.085753},
   Key = {fds180933}
}

@article{05149022881,
   Author = {Sancho, G. and Fisher, C.R. and Mills, S. and Micheli, F. and Johnson, G.A. and Lenihan, H.S. and Peterson, C.H. and Mullineaux, L.S.},
   Title = {Selective predation by the zoarcid fish Thermarces cerberus
             at hydrothermal vents},
   Journal = {Deep-Sea Research Part I: Oceanographic Research
             Papers},
   Volume = {52},
   Number = {5},
   Pages = {837 - 844},
   Year = {2005},
   url = {http://dx.doi.org/10.1016/j.dsr.2004.12.002},
   Keywords = {Tissue;Ecosystems;Biodiversity;Oceanography;},
   Abstract = {This study investigates predation by the vent zoarcid fish
             Thermarces cerberus through gastrointestinal analyses of 27
             specimens collected with the submersible ALVIN at vents at
             9&deg;50 prime N on the East Pacific Rise. T. cerberus fed
             most frequently on gastropod mollusks (mainly Lepetodrilus
             elevatus) and amphipod crustaceans (mainly Ventiella
             sulfuris). Species found occasionally in high abundance
             included the swarming amphipod Halice hesmonectes and the
             snail Cyathermia naticoides. Other items also found in
             gastrointestinal tracts, but in very low numbers, included
             polychaete worms, crustaceans and unidentified tissue
             clumps. The comparison between the size distribution of L.
             elevatus limpets ingested by T. cerberus and those found
             attached to vestimentiferan tubes suggest that the fish may
             selectively prey on large limpets. If the selective removal
             of large Lepetodrilus spp. limpets by T. cerberus does
             occur, then it would have potential community-level
             consequences at hydrothermal vents, since these mobile
             gastropods appear to inhibit the settlement of sessile vent
             species, including tube-building worms. Our results suggest
             possible direct and indirect effects of T. cerberus on
             benthic community structure at hydrothermal vents on the
             East Pacific Rise. &copy; 2005 Elsevier Ltd. All rights
             reserved.},
   Key = {05149022881}
}

@article{fds268737,
   Author = {Gyengesi, E and Calabrese, E and Sherrier, MC and Johnson, GA and Paxinos, G and Watson, C},
   Title = {Semi-automated 3D segmentation of major tracts in the rat
             brain: comparing DTI with standard histological
             methods.},
   Journal = {Brain Struct Funct},
   Volume = {219},
   Number = {2},
   Pages = {539-550},
   Year = {2014},
   Month = {March},
   ISSN = {1863-2653},
   url = {http://dx.doi.org/10.1007/s00429-013-0516-8},
   Abstract = {Researchers working with rodent models of neurological
             disease often require an accurate map of the anatomical
             organization of the white matter of the rodent brain. With
             the increasing popularity of small animal MRI techniques,
             including diffusion tensor imaging (DTI), there is
             considerable interest in rapid segmentation methods of
             neurological structures for quantitative comparisons.
             DTI-derived tractography allows simple and rapid
             segmentation of major white matter tracts, but the anatomic
             accuracy of these computer-generated fibers is open to
             question and has not been rigorously evaluated in the rat
             brain. In this study, we examine the anatomic accuracy of
             tractography-based segmentation in the adult rat brain. We
             analysed 12 major white matter pathways using semi-automated
             tractography-based segmentation alongside manual
             segmentation of Gallyas silver-stained histology sections.
             We applied four fiber-tracking algorithms to the DTI
             data-two integration methods and two deflection methods. In
             many cases, tractography-based segmentation closely matched
             histology-based segmentation; however different tractography
             algorithms produced dramatically different results. Results
             suggest that certain white matter pathways are more amenable
             to tractography-based segmentation than others. We believe
             that these data will help researchers decide whether it is
             appropriate to use tractography-based segmentation of white
             matter structures for quantitative DTI-based analysis of
             neurologic disease models.},
   Doi = {10.1007/s00429-013-0516-8},
   Key = {fds268737}
}

@article{fds132779,
   Author = {HE Möller and XJ Chen and MS Chawla and GP Cofer and B Driehuys and LW
             Hedlund, SA Suddarth and GA Johnson},
   Title = {Sensitivity and resolution in 3D NMR microscopy of the lung
             with hyperpolarized noble gases.},
   Journal = {Magnetic resonance in medicine : official journal of the
             Society of Magnetic Resonance in Medicine / Society of
             Magnetic Resonance in Medicine, UNITED STATES},
   Volume = {41},
   Number = {4},
   Pages = {800-8},
   Year = {1999},
   Month = {April},
   ISSN = {0740-3194},
   Keywords = {Animals • Guinea Pigs • Lung • Magnetic
             Resonance Imaging • Microscopy • Models,
             Theoretical • Noble Gases • Sensitivity and
             Specificity • cytology* • diagnostic use* •
             methods*},
   Abstract = {Three-dimensional magnetic resonance images of the guinea
             pig lung were acquired in vivo using hyperpolarized (HP)
             noble gases and radial projection encoding (PE). Results
             obtained with 3He (voxel size 17 microl) demonstrated high
             image quality showing airway structure down to the 5th or
             6th generations. Signal-to-noise ratios (SNRs) of 129Xe
             images (voxel size 40 microl) were lower by about 1 order of
             magnitude as a consequence of the smaller gyromagnetic
             ratio, a more rapid relaxation in the gas reservoir, and
             lower polarization and isotope abundance. Comparison between
             experimentally obtained SNRs and results from calculations
             based on a model that accounts for the three-dimensional PE
             acquisition scheme and the non-equilibrium situation in HP
             gas imaging yielded excellent agreement for small flip
             angles. A theoretical examination of the potential
             resolution in HP gas MR microscopy of the lungs suggests
             that in vivo visualization of alveolar clusters distal to
             respiratory bronchioles may be possible.},
   Key = {fds132779}
}

@booklet{Moller99,
   Author = {Möller, HE and Chen, XJ and Chawla, MS and Cofer, GP and Driehuys, B and Hedlund, LW and Suddarth, SA and Johnson, GA},
   Title = {Sensitivity and resolution in 3D NMR microscopy of the lung
             with hyperpolarized noble gases.},
   Journal = {Magn Reson Med},
   Volume = {41},
   Number = {4},
   Pages = {800-808},
   Year = {1999},
   Month = {April},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/10332857},
   Abstract = {Three-dimensional magnetic resonance images of the guinea
             pig lung were acquired in vivo using hyperpolarized (HP)
             noble gases and radial projection encoding (PE). Results
             obtained with 3He (voxel size 17 microl) demonstrated high
             image quality showing airway structure down to the 5th or
             6th generations. Signal-to-noise ratios (SNRs) of 129Xe
             images (voxel size 40 microl) were lower by about 1 order of
             magnitude as a consequence of the smaller gyromagnetic
             ratio, a more rapid relaxation in the gas reservoir, and
             lower polarization and isotope abundance. Comparison between
             experimentally obtained SNRs and results from calculations
             based on a model that accounts for the three-dimensional PE
             acquisition scheme and the non-equilibrium situation in HP
             gas imaging yielded excellent agreement for small flip
             angles. A theoretical examination of the potential
             resolution in HP gas MR microscopy of the lungs suggests
             that in vivo visualization of alveolar clusters distal to
             respiratory bronchioles may be possible.},
   Doi = {10.1002/(sici)1522-2594(199904)41:4<800::aid-mrm20>3.0.co;2-},
   Key = {Moller99}
}

@booklet{Bazer01,
   Author = {F. W. Bazer and T. E. Spencer and G. A. Johnson and R. C.
             Burghardt and L. A. Jaeger},
   Title = {Servomechanism in the ovine uterus for establishment and
             maintenance of pregnancy.},
   Journal = {Biology Of Reproduction},
   Volume = {64},
   Pages = {90 -- 90},
   Year = {2001},
   Key = {Bazer01}
}

@article{fds174229,
   Author = {GA Johnson},
   Title = {Settlement Patterns and Their Meaning.},
   Journal = {Science (New York, N.Y.)},
   Volume = {213},
   Number = {4503},
   Pages = {126-127},
   Year = {1981},
   Month = {July},
   ISSN = {1095-9203},
   url = {http://dx.doi.org/10.1126/science.213.4503.126},
   Language = {ENG},
   Doi = {10.1126/science.213.4503.126},
   Key = {fds174229}
}

@article{fds174159,
   Author = {P Riddle and GA Johnson},
   Title = {Sexual harassment: what role should health educators
             play?},
   Journal = {Health education},
   Volume = {14},
   Number = {1},
   Pages = {20-3},
   Year = {1990},
   Month = {April},
   ISSN = {0097-0050},
   Keywords = {Adaptation, Psychological • Employee Grievances •
             Female • Health Education* • Humans • Male
             • Sexual Behavior* • Social Behavior*},
   Language = {eng},
   Key = {fds174159}
}

@article{fds174268,
   Author = {GA Johnson},
   Title = {SHELLFISH CONSERVATION AND SEWAGE DISPOSAL.},
   Journal = {American journal of public health (New York, N.Y. :
             1912)},
   Volume = {4},
   Number = {11},
   Pages = {965-8},
   Year = {1914},
   Month = {November},
   ISSN = {0271-4353},
   Language = {eng},
   Key = {fds174268}
}

@article{8979156,
   Author = {Johnson, G.A.},
   Title = {Shield design for lunar surface applications},
   Journal = {AIP Conf. Proc. (USA)},
   Number = {813},
   Pages = {701 - 6},
   Year = {2006},
   Keywords = {electric generators;fission reactors;lunar surface;nuclear
             power;power conversion;radiation protection;},
   Abstract = {A shielding concept for lunar surface applications of
             nuclear power is presented herein. The reactor, primary
             shield, reactor equipment and power generation module are
             placed in a cavity in the lunar surface. Support structure
             and heat rejection radiator panels are on the surface,
             outside the cavity. The reactor power of 1,320
             kW<sub>t</sub> was sized to deliver 50 kW<sub>c</sub> from a
             thermoelectric power conversion subsystem. The dose rate on
             the surface is less than 0.6 mRem/hr at 100 meters from the
             reactor. Unoptimized shield mass is 1,020 kg which is much
             lighter than a comparable &pi; shield weighing in at 17,000
             kg},
   Key = {8979156}
}

@booklet{Wang01,
   Author = {G. Wang and K. Pran and G. Sagvolden and G. B. Havsgard and A. E. Jensen and G. A. Johnson and S. T.
             Vohra},
   Title = {Ship hull structure monitoring using fibre optic
             sensors},
   Journal = {Smart Materials \& Structures},
   Volume = {10},
   Number = {3},
   Pages = {472 -- 478},
   Year = {2001},
   Month = {June},
   Key = {Wang01}
}

@booklet{Moller98,
   Author = {H. E. Moller and X. J. Chen and M. S. Chawla and B. Driehuys and L. W. Hedlund and G. A. Johnson},
   Title = {Signal dynamics in magnetic resonance imaging of the lung
             with hyperpolarized noble gases},
   Journal = {Journal Of Magnetic Resonance},
   Volume = {135},
   Number = {1},
   Pages = {133 -- 143},
   Year = {1998},
   Month = {November},
   Key = {Moller98}
}

@article{fds269039,
   Author = {Möller, HE and Chen, XJ and Chawla, MS and Driehuys, B and Hedlund, LW and Johnson, GA},
   Title = {Signal dynamics in magnetic resonance imaging of the lung
             with hyperpolarized noble gases.},
   Journal = {J Magn Reson},
   Volume = {135},
   Number = {1},
   Pages = {133-143},
   Year = {1998},
   Month = {November},
   ISSN = {1090-7807},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/9799687},
   Keywords = {Animals • Guinea Pigs • Image Enhancement* •
             Lung • Magnetic Resonance Imaging* • Magnetics
             • Models, Theoretical • Noble Gases •
             Reproducibility of Results • anatomy & histology*
             • diagnostic use* • methods},
   Abstract = {The nonequilibrium bulk magnetic moment of hyperpolarized
             (HP) noble gases generated by optical pumping has unique
             characteristics. Based on the Bloch equations, a model was
             developed describing the signal dynamics of HP gases used in
             magnetic resonance imaging (MRI) of the lung with special
             consideration to the breathing cycle. Experimental
             verification included extensive investigations with HP 3He
             and 129Xe during both inspiration and held breath in live
             guinea pigs. Radial acquisition was used to investigate the
             view variations with a temporal resolution of 5 ms.
             Agreement between theoretical predictions and in vivo
             results was excellent. Additionally, information about
             effects from noble gas diffusion and spin-lattice relaxation
             was obtained. In vivo results for T1 were 28.8 +/- 1.8 s for
             3He and 31.3 +/- 1.8 s for 129Xe. Comparison with in vitro
             data indicated that relaxation in the pulmonary gas space is
             dominated by dipolar coupling with molecular oxygen. The
             results provide a quantitative basis for optimizing pulse
             sequence design in HP gas MRI of the lung.},
   Doi = {10.1006/jmre.1998.1563},
   Key = {fds269039}
}

@booklet{Karis87,
   Author = {Karis, JP and Allan Johnson and G and Glover, GH},
   Title = {Signal-to-noise improvements in three-dimensional NMR
             microscopy using limited-angle excitation},
   Journal = {Journal of Magnetic Resonance (1969)},
   Volume = {71},
   Number = {1},
   Pages = {24-33},
   Publisher = {Elsevier BV},
   Year = {1987},
   Month = {January},
   ISSN = {0022-2364},
   url = {http://dx.doi.org/10.1016/0022-2364(87)90124-7},
   Abstract = {The 3D FT variant of spin-echo imaging has previously been
             successfully used to yield images at microscopic resolution.
             In obtaining such high resolution, optimization of signal to
             noise for a given acquisition time is crucial. Using a
             limited-angle (<60) slice-selective pulse one can improve
             the effective signal to noise or reduce the experimental
             time. The spin echo is generated through gradient
             refocusing. A phantom with T1 of 800 and 1200 ms was used to
             simulate white and gray matter. Signal intensity was modeled
             by the expression M= M0sinθ[1-exp(- TR T1)] 1-exp(- TR
             T1)cosθ For TR < 200 ms, limited-angle excitation can yield
             improvements in signal to noise by greater than a factor of
             two. These results were experimentally verified on a 1.5 T
             prototype system (General Electric, Milwaukee, Wis.)
             configured with gradient and rf coils designed for NMR
             microscopy. In those cases where signal-to-noise concerns do
             not require signal averaging beyond that which is inherent
             in the 3D FT technique, the limited-angle approach can
             reduce the acquisition time by as much as a factor of four.
             These results were verified in small animal studies of the
             brain of a 200 g rat. © 1987.},
   Doi = {10.1016/0022-2364(87)90124-7},
   Key = {Karis87}
}

@article{fds292759,
   Author = {Johnson, GA and Manson, EL and O'Foghludha, F},
   Title = {Simple method of obtaining Si(Li) detector
             efficiency},
   Journal = {Nuclear Instruments and Methods},
   Volume = {151},
   Number = {1-2},
   Pages = {217-220},
   Publisher = {Elsevier BV},
   Year = {1978},
   Month = {May},
   ISSN = {0029-554X},
   url = {http://dx.doi.org/10.1016/0029-554X(78)90491-3},
   Abstract = {The efficiency of a semi-conductor detector is measured by
             compairing its response with that of an NaI(Tl) detector of
             known efficiency when both are exposed to the same flux of
             gamma-excited fluorescent X-rays. The experimental procedure
             is outlined and corrections and limitations are discussed.
             The technique is an inexpensive and convenient way of
             determining semi-conductor efficiency up to about 100 keV
             using a single radionuclide source of modest activity and
             readily-available fluorescers. © 1978.},
   Doi = {10.1016/0029-554X(78)90491-3},
   Key = {fds292759}
}

@booklet{Johnson80,
   Author = {Johnson, GA and O'Foghludha, F},
   Title = {Simulation of mammographic x-ray spectra.},
   Journal = {Med Phys},
   Volume = {7},
   Number = {3},
   Pages = {189-195},
   Year = {1980},
   ISSN = {0094-2405},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/7393143},
   Abstract = {Attempts to simulate Mo-anode spectra for film mammography
             by using Mo filters with W-anode tubes have been reported by
             several workers, and others have generated W-like continua
             for xeromammographic purposes by heavy Al filtration of
             Mo-anode tubes. In the present work the success of these
             simulations was tested by Si(Li) spectrometric methods that
             measured the spectral shapes and the exposure levels.
             Comparisons of Mo-anode/Al-filter with W-anode/Al-filter
             combinations were made, and also of W-anode/M-filter with
             Mo-anode/Mo-folter combinations. In certain circumstance the
             spectral shape is moderately well simulated but in all cases
             the useful output is less in the simulations than in the
             original spectra. The general conclusion is that simulation
             is always less attractive than direct use of the desired
             anode.},
   Doi = {10.1118/1.594684},
   Key = {Johnson80}
}

@article{fds132812,
   Author = {GA Johnson and F O'Foghludha},
   Title = {Simulation of mammographic x-ray spectra.},
   Journal = {Medical physics, UNITED STATES},
   Volume = {7},
   Number = {3},
   Pages = {189-95},
   ISSN = {0094-2405},
   Keywords = {Computers • Female • Humans • Mammography
             • Spectrometry, X-Ray Emission • Xeromammography
             • instrumentation • instrumentation* •
             methods},
   Abstract = {Attempts to simulate Mo-anode spectra for film mammography
             by using Mo filters with W-anode tubes have been reported by
             several workers, and others have generated W-like continua
             for xeromammographic purposes by heavy Al filtration of
             Mo-anode tubes. In the present work the success of these
             simulations was tested by Si(Li) spectrometric methods that
             measured the spectral shapes and the exposure levels.
             Comparisons of Mo-anode/Al-filter with W-anode/Al-filter
             combinations were made, and also of W-anode/M-filter with
             Mo-anode/Mo-folter combinations. In certain circumstance the
             spectral shape is moderately well simulated but in all cases
             the useful output is less in the simulations than in the
             original spectra. The general conclusion is that simulation
             is always less attractive than direct use of the desired
             anode.},
   Key = {fds132812}
}

@article{fds174277,
   Author = {JD Peuler and GA Johnson},
   Title = {Simultaneous single isotope radioenzymatic assay of plasma
             norepinephrine, epinephrine and dopamine.},
   Journal = {Life sciences},
   Volume = {21},
   Number = {5},
   Pages = {625-36},
   Year = {1977},
   Month = {September},
   ISSN = {0024-3205},
   Keywords = {Catechol O-Methyltransferase • Dopamine •
             Epinephrine • Humans • Methods •
             Norepinephrine • blood* • cerebrospinal fluid
             • metabolism},
   Language = {eng},
   Key = {fds174277}
}

@booklet{Nelson99,
   Author = {Nelson, RC and Johnson, GA and Spielman, AL and Lowry, CR and Sundaramoorthy, G and Sheafor, DH},
   Title = {Single breath-hold dynamic subtraction CT of the liver
             using-multidetector helical technology},
   Journal = {Radiology},
   Volume = {213P},
   Pages = {125-125},
   Year = {1999},
   Month = {November},
   Key = {Nelson99}
}

@booklet{Johnson80a,
   Author = {G. A. Johnson and R. M. Kupiecki and C. A.
             Baker},
   Title = {Single isotope derivative (radioenzymatic) methods in the
             measurement of catecholamines},
   Journal = {Metabolism-clinical And Experimental},
   Volume = {29},
   Number = {11},
   Pages = {1106 -- 1113},
   Year = {1980},
   Key = {Johnson80a}
}

@article{fds174243,
   Author = {GA Johnson and RM Kupiecki and CA Baker},
   Title = {Single isotope derivative (radioenzymatic) methods in the
             measurement of catecholamines.},
   Journal = {Metabolism: clinical and experimental},
   Volume = {29},
   Number = {11 Suppl 1},
   Pages = {1106-13},
   Year = {1980},
   Month = {November},
   ISSN = {0026-0495},
   Keywords = {Catechol O-Methyltransferase* • Catecholamines •
             Chemical Phenomena • Chemistry • Chromatography,
             Thin Layer • Dopa Decarboxylase • Humans •
             Methods • Phenylethanolamine N-Methyltransferase*
             • S-Adenosylmethionine* • Tritium • analysis*
             • cerebrospinal fluid},
   Language = {eng},
   Key = {fds174243}
}

@article{fds341778,
   Author = {Anderson, RJ and Cook, JJ and Delpratt, N and Nouls, JC and Gu, B and McNamara, JO and Avants, BB and Johnson, GA and Badea,
             A},
   Title = {Small Animal Multivariate Brain Analysis (SAMBA) - a High
             Throughput Pipeline with a Validation Framework.},
   Journal = {Neuroinformatics},
   Volume = {17},
   Number = {3},
   Pages = {451-472},
   Year = {2019},
   Month = {July},
   url = {http://dx.doi.org/10.1007/s12021-018-9410-0},
   Abstract = {While many neuroscience questions aim to understand the
             human brain, much current knowledge has been gained using
             animal models, which replicate genetic, structural, and
             connectivity aspects of the human brain. While voxel-based
             analysis (VBA) of preclinical magnetic resonance images is
             widely-used, a thorough examination of the statistical
             robustness, stability, and error rates is hindered by high
             computational demands of processing large arrays, and the
             many parameters involved therein. Thus, workflows are often
             based on intuition or experience, while preclinical
             validation studies remain scarce. To increase throughput and
             reproducibility of quantitative small animal brain studies,
             we have developed a publicly shared, high throughput VBA
             pipeline in a high-performance computing environment, called
             SAMBA. The increased computational efficiency allowed large
             multidimensional arrays to be processed in 1-3 days-a task
             that previously took ~1 month. To quantify the variability
             and reliability of preclinical VBA in rodent models, we
             propose a validation framework consisting of morphological
             phantoms, and four metrics. This addresses several sources
             that impact VBA results, including registration and template
             construction strategies. We have used this framework to
             inform the VBA workflow parameters in a VBA study for a
             mouse model of epilepsy. We also present initial efforts
             towards standardizing small animal neuroimaging data in a
             similar fashion with human neuroimaging. We conclude that
             verifying the accuracy of VBA merits attention, and should
             be the focus of a broader effort within the community. The
             proposed framework promotes consistent quality assurance of
             VBA in preclinical neuroimaging, thus facilitating the
             creation and communication of robust results.},
   Doi = {10.1007/s12021-018-9410-0},
   Key = {fds341778}
}

@article{fds132870,
   Author = {HG Chotas and RL Van Metter and GA Johnson and CE
             Ravin},
   Title = {Small object contrast in AMBER and conventional chest
             radiography.},
   Journal = {Radiology, UNITED STATES},
   Volume = {180},
   Number = {3},
   Pages = {853-9},
   Year = {1991},
   Month = {September},
   ISSN = {0033-8419},
   Keywords = {Diaphragm • Humans • Lung • Mediastinum
             • Models, Structural • Radiography, Thoracic*
             • Technology, Radiologic • methods •
             radiography},
   Abstract = {The ability of a commercially available scanning
             equalization system for chest radiography to render small
             object contrast in the lung-, mediastinum-, and
             subdiaphragm-equivalent regions of an acrylic chest phantom
             was quantitatively evaluated. Images from nine chest
             phantoms that represented a wide range of patient sizes and
             dynamic ranges of x-ray transmittance were analyzed. Subject
             contrast was measured with a photostimulable phosphor
             detector, and images were acquired in both equalized and
             nonequalized (conventional) imaging modes. Available subject
             contrast in the lung-equivalent region was 8%-15% lower in
             the equalized images compared with the nonequalized images
             in all phantoms (patient types); contrast in the
             mediastinum-, retro-cardiac-, and subdiaphragm-equivalent
             regions was 11%-63% higher in the equalized images, with the
             degree of improvement increasing as patient size and dynamic
             range increased. Images of each phantom were also acquired
             with the screen-film systems currently in use at the
             authors' institution, permitting an assessment of the
             relative performance (in terms of radiographic contrast) of
             these imagers with and without use of equalization.},
   Key = {fds132870}
}

@booklet{Chotas91,
   Author = {Chotas, HG and Van Metter and RL and Johnson, GA and Ravin,
             CE},
   Title = {Small object contrast in AMBER and conventional chest
             radiography.},
   Journal = {Radiology},
   Volume = {180},
   Number = {3},
   Pages = {853-859},
   Year = {1991},
   Month = {September},
   ISSN = {0033-8419},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/1871306},
   Abstract = {The ability of a commercially available scanning
             equalization system for chest radiography to render small
             object contrast in the lung-, mediastinum-, and
             subdiaphragm-equivalent regions of an acrylic chest phantom
             was quantitatively evaluated. Images from nine chest
             phantoms that represented a wide range of patient sizes and
             dynamic ranges of x-ray transmittance were analyzed. Subject
             contrast was measured with a photostimulable phosphor
             detector, and images were acquired in both equalized and
             nonequalized (conventional) imaging modes. Available subject
             contrast in the lung-equivalent region was 8%-15% lower in
             the equalized images compared with the nonequalized images
             in all phantoms (patient types); contrast in the
             mediastinum-, retro-cardiac-, and subdiaphragm-equivalent
             regions was 11%-63% higher in the equalized images, with the
             degree of improvement increasing as patient size and dynamic
             range increased. Images of each phantom were also acquired
             with the screen-film systems currently in use at the
             authors' institution, permitting an assessment of the
             relative performance (in terms of radiographic contrast) of
             these imagers with and without use of equalization.},
   Doi = {10.1148/radiology.180.3.1871306},
   Key = {Chotas91}
}

@booklet{Maki88,
   Author = {Maki, JH and Johnson, GA and Cofer, GP and MacFall,
             JR},
   Title = {SNR improvement in NMR microscopy using DEFT},
   Journal = {Journal of Magnetic Resonance (1969)},
   Volume = {80},
   Number = {3},
   Pages = {482-492},
   Publisher = {Elsevier BV},
   Year = {1988},
   Month = {January},
   ISSN = {0022-2364},
   url = {http://dx.doi.org/10.1016/0022-2364(88)90243-0},
   Abstract = {This paper examines the use of a driven equilibrium Fourier
             transform (DEFT) pulse sequence for improving the signal per
             unit time and hence image resolution in NMR microscopy. DEFT
             vs partial saturation (PS) is modeled and it is shown that
             DEFT is most useful in physiologic materials provided short
             TE values (TE ≪ T2) and short TR values (TR < T1) are
             used. Under these conditions, DEFT can yield up to a
             fourfold signal increase compared to PS. It is shown that
             DEFT can provide spin density and T1/T2-ratio-weighted
             images. DEFT is also shown to have SNR advantages as T1
             increases-an important consideration at higher magnetic
             fields. Experimental data that verify the theoretical
             predictions and the functioning of a DEFT pulse sequence to
             produce high-quality 2D spin-warp images of a phantom are
             presented. Studies performed on small animals demonstrate
             the utility of the DEFT sequence in MR microscopy by
             providing increased SNR and new contrast mechanisms over
             limited fields of view. © 1988.},
   Doi = {10.1016/0022-2364(88)90243-0},
   Key = {Maki88}
}

@article{fds174242,
   Author = {GW Fuller and GA Johnson},
   Title = {SOME POINTS OF THE DIFFERENTIATION AND CLASSIFICATION OF
             WATER BACTERIA.},
   Journal = {Journal. Boston Society of Medical Sciences},
   Volume = {4},
   Number = {4},
   Pages = {83-84},
   Year = {1900},
   Month = {January},
   Language = {ENG},
   Key = {fds174242}
}

@article{fds174152,
   Author = {GW Fuller and GA Johnson},
   Title = {Some Points on the Differentiation and Classification of
             Water Bacteria.},
   Journal = {Public health papers and reports},
   Volume = {25},
   Pages = {580-6},
   Year = {1899},
   ISSN = {0737-8769},
   Language = {eng},
   Key = {fds174152}
}

@article{fds174297,
   Author = {GW Fuller and GA Johnson},
   Title = {Some Points on the Differentiation and Classification of
             Water Bacteria.},
   Journal = {Public health papers and reports},
   Volume = {25},
   Pages = {580-586},
   Year = {1899},
   Language = {ENG},
   Key = {fds174297}
}

@article{fds268865,
   Author = {Song, J and Liu, QH and Johnson, GA and Badea, CT},
   Title = {Sparseness prior based iterative image reconstruction for
             retrospectively gated cardiac micro-CT.},
   Journal = {Med Phys},
   Volume = {34},
   Number = {11},
   Pages = {4476-4483},
   Year = {2007},
   Month = {November},
   ISSN = {0094-2405},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/18072512},
   Keywords = {Algorithms • Animals • Heart • Humans •
             Image Processing, Computer-Assisted • Imaging,
             Three-Dimensional • Least-Squares Analysis • Mice
             • Mice, Inbred C57BL • Models, Statistical •
             Myocardium • Phantoms, Imaging • Scattering,
             Radiation • Time Factors • Tomography, X-Ray
             Computed • X-Rays • metabolism • methods*
             • physiology},
   Abstract = {Recent advances in murine cardiac studies with
             three-dimensional (3D) cone beam micro-CT used a
             retrospective gating technique. However, this sampling
             technique results in a limited number of projections with an
             irregular angular distribution due to the temporal
             resolution requirements and radiation dose restrictions.
             Both angular irregularity and undersampling complicate the
             reconstruction process, since they cause significant
             streaking artifacts. This work provides an iterative
             reconstruction solution to address this particular
             challenge. A sparseness prior regularized weighted l2 norm
             optimization is proposed to mitigate streaking artifacts
             based on the fact that most medical images are compressible.
             Total variation is implemented in this work as the
             regularizer for its simplicity. Comparison studies are
             conducted on a 3D cardiac mouse phantom generated with
             experimental data. After optimization, the method is applied
             to in vivo cardiac micro-CT data.},
   Doi = {10.1118/1.2795830},
   Key = {fds268865}
}

@booklet{Johnson96c,
   Author = {G. A. Johnson and D. A. Mortensen and C. A.
             Gotway},
   Title = {Spatial and temporal analysis of weed seedling populations
             using geostatistics},
   Journal = {Weed Science},
   Volume = {44},
   Number = {3},
   Pages = {704 -- 710},
   Year = {1996},
   Key = {Johnson96c}
}

@booklet{Colbach00,
   Author = {N. Colbach and F. Forcella and G. A. Johnson},
   Title = {Spatial and temporal stability of weed populations over five
             years},
   Journal = {Weed Science},
   Volume = {48},
   Number = {3},
   Pages = {366 -- 377},
   Year = {2000},
   Key = {Colbach00}
}

@article{fds132869,
   Author = {XJ Chen and HE Möller and MS Chawla and GP Cofer and B Driehuys and LW
             Hedlund, GA Johnson},
   Title = {Spatially resolved measurements of hyperpolarized gas
             properties in the lung in vivo. Part I: diffusion
             coefficient.},
   Journal = {Magnetic resonance in medicine : official journal of the
             Society of Magnetic Resonance in Medicine / Society of
             Magnetic Resonance in Medicine, UNITED STATES},
   Volume = {42},
   Number = {4},
   Pages = {721-8},
   Year = {1999},
   Month = {October},
   ISSN = {0740-3194},
   Keywords = {Animals • Guinea Pigs • Helium • Isotopes
             • Lung • Magnetic Resonance Imaging •
             Pulmonary Diffusing Capacity • Xenon Isotopes •
             anatomy & histology* • diagnostic use •
             methods*},
   Abstract = {In imaging of hyperpolarized noble gases, a knowledge of the
             diffusion coefficient (D) is important both as a contrast
             mechanism and in the design of pulse sequences. We have made
             diffusion coefficient maps of both hyperpolarized (3)He and
             (129)Xe in guinea pig lungs. Along the length of the
             trachea, (3)He D values were on average 2.4 cm(2)/sec,
             closely reproducing calculated values for free gas (2.05
             cm(2)/sec). The (3)He D values measured perpendicular to the
             length of the trachea were approximately a factor of two
             less, indicating restriction to diffusion. Further evidence
             of restricted diffusion was seen in the distal pulmonary
             airspaces as the average (3)He D was 0.16 cm(2)/sec. An
             additional cause for the smaller (3)He D in the lung was due
             to the presence of air, which is composed of heavier and
             larger gases. The (129)Xe results show similar trends, with
             the trachea D averaging 0.068 cm(2)/sec and the lung D
             averaging 0.021 cm(2)/sec. Magn Reson Med 42:721-728,
             1999.},
   Key = {fds132869}
}

@booklet{Chen99,
   Author = {Chen, XJ and Möller, HE and Chawla, MS and Cofer, GP and Driehuys, B and Hedlund, LW and Johnson, GA},
   Title = {Spatially resolved measurements of hyperpolarized gas
             properties in the lung in vivo. Part I: diffusion
             coefficient.},
   Journal = {Magn Reson Med},
   Volume = {42},
   Number = {4},
   Pages = {721-728},
   Year = {1999},
   Month = {October},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/10502761},
   Abstract = {In imaging of hyperpolarized noble gases, a knowledge of the
             diffusion coefficient (D) is important both as a contrast
             mechanism and in the design of pulse sequences. We have made
             diffusion coefficient maps of both hyperpolarized (3)He and
             (129)Xe in guinea pig lungs. Along the length of the
             trachea, (3)He D values were on average 2.4 cm(2)/sec,
             closely reproducing calculated values for free gas (2.05
             cm(2)/sec). The (3)He D values measured perpendicular to the
             length of the trachea were approximately a factor of two
             less, indicating restriction to diffusion. Further evidence
             of restricted diffusion was seen in the distal pulmonary
             airspaces as the average (3)He D was 0.16 cm(2)/sec. An
             additional cause for the smaller (3)He D in the lung was due
             to the presence of air, which is composed of heavier and
             larger gases. The (129)Xe results show similar trends, with
             the trachea D averaging 0.068 cm(2)/sec and the lung D
             averaging 0.021 cm(2)/sec. Magn Reson Med 42:721-728,
             1999.},
   Doi = {10.1002/(sici)1522-2594(199910)42:4<721::aid-mrm14>3.0.co;2-},
   Key = {Chen99}
}

@article{fds269070,
   Author = {Chen, XJ and Möller, HE and Chawla, MS and Cofer, GP and Driehuys, B and Hedlund, LW and MacFall, JR and Johnson, GA},
   Title = {Spatially resolved measurements of hyperpolarized gas
             properties in the lung in vivo. Part II: T
             *(2).},
   Journal = {Magn Reson Med},
   Volume = {42},
   Number = {4},
   Pages = {729-737},
   Year = {1999},
   Month = {October},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/10502762},
   Keywords = {Animals • Guinea Pigs • Helium • Humans
             • Isotopes • Lung • Magnetic Resonance
             Imaging • Male • Middle Aged • Pulmonary
             Diffusing Capacity • Trachea • Xenon Isotopes
             • anatomy & histology • anatomy & histology*
             • diagnostic use • methods*},
   Abstract = {The transverse relaxation time, T *(2), of hyperpolarized
             (HP) gas in the lung in vivo is an important parameter for
             pulse sequence optimization and image contrast. We obtained
             T *(2) maps of HP (3)He and (129)Xe in guinea pig lungs (n =
             17) and in human lungs. Eight different sets of (3)He guinea
             pig studies were acquired, with variation of slice
             selection, tidal volume, and oxygen level. For example, for
             a (3)He tidal volume of 3 cm(3) and no slice selection, the
             average T *(2) in the trachea was 14.7 ms and 8.0 ms in the
             intrapulmonary airspaces. The equivalent (129)Xe experiment
             yielded an average T *(2) of 40.8 ms in the trachea and 18.5
             ms in the intrapulmonary airspaces. The average (3)He T *(2)
             in the human intrapulmonary airspaces was 9.4 ms. The
             relaxation behavior was predicted by treating the lung as a
             porous medium, resulting in good agreement between estimated
             and measured T *(2) values in the intrapulmonary airspaces.
             Magn Reson Med 42:729-737, 1999.},
   Doi = {10.1002/(sici)1522-2594(199910)42:4<729::aid-mrm15>3.0.co;2-},
   Key = {fds269070}
}

@booklet{Chen99a,
   Author = {X. J. Chen and H. E. Moller and M. S. Chawla and G. P. Cofer and B. Driehuys and L. W. Hedlund and J. R. Macfall and G.
             A. Johnson},
   Title = {Spatially resolved measurements of hyperpolarized gas
             properties in the lung in vivo. Part II:
             T-2*},
   Journal = {Magnetic Resonance In Medicine},
   Volume = {42},
   Number = {4},
   Pages = {729 -- 737},
   Year = {1999},
   Month = {October},
   Key = {Chen99a}
}

@booklet{Locher96,
   Author = {M. Locher and G. A. Johnson and E. R. Hunt},
   Title = {Spatiotemporal stochastic resonance in a system of coupled
             diode resonators},
   Journal = {Physical Review Letters},
   Volume = {77},
   Number = {23},
   Pages = {4698 -- 4701},
   Year = {1996},
   Month = {December},
   Key = {Locher96}
}

@article{fds132911,
   Author = {M Löcher and GA Johnson and ER Hunt},
   Title = {Spatiotemporal Stochastic Resonance in a System of Coupled
             Diode Resonators.},
   Journal = {Physical review letters},
   Volume = {77},
   Number = {23},
   Pages = {4698-4701},
   Year = {1996},
   Month = {December},
   ISSN = {1079-7114},
   Language = {ENG},
   Key = {fds132911}
}

@article{fds268747,
   Author = {JOHNSON, GA and OFOGHLUDHA, F},
   Title = {SPECTROMETRIC STUDIES OF WAVEFORM AND FILTRATION EFFECTS IN
             MAMMOGRAPHY},
   Journal = {PHYSICS IN MEDICINE AND BIOLOGY},
   Volume = {22},
   Number = {3},
   Pages = {593-593},
   Year = {1977},
   ISSN = {0031-9155},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1977DH45600190&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {fds268747}
}

@booklet{Benveniste98,
   Author = {Benveniste, H and Qui, H and Hedlund, LW and D'Ercole, F and Johnson,
             GA},
   Title = {Spinal cord neural anatomy in rats examined by in vivo
             magnetic resonance microscopy.},
   Journal = {Reg Anesth Pain Med},
   Volume = {23},
   Number = {6},
   Pages = {589-599},
   Year = {1998},
   ISSN = {1098-7339},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/9840856},
   Abstract = {BACKGROUND AND OBJECTIVES: Magnetic resonance microscopy
             (MRM) is a technique that is worthwhile for
             anesthesiologists because it allows spinal cord and plexus
             anatomy to be visualized three dimensionally and followed
             over time in the same animal. For example, the long-term
             effect of indwelling intrathecal or plexus catheters can be
             studied in situ, and convective and diffusive forces within
             intrathecal, epidural, or nerve sheath spaces can be
             investigated. Further, diffusion-weighted MRM, which
             measures an "apparent diffusion coefficient" (ADC), can be
             used to track the presence of ischemia, hypoperfusion, or
             cytotoxic edema. This study investigates problems associated
             with the use of in vivo MRM for spinal cord and peripheral
             nerve studies in the rat. METHODS: Twenty-one anesthetized
             female Fisher CDF rats were used. Group 1 (n=7) was used for
             anatomic three-dimensional studies. Groups 2 (n=4), 3 (n=4),
             and 4 (n=6) were used for measurements of the ADC. Group 2
             served as controls, group 3 received lumbar intrathecal
             catheters, and group 4 received cervical intrathecal
             catheters. RESULTS: Cervical spine, lumbar spine, and spinal
             nerves and ganglia were accurately visualized with MRM. As a
             rule, spinal cord gray and white matter were better
             demonstrated using diffusion-weighted proton stains. By
             contrast, T2-weighted proton staining superiorly
             demonstrated structures surrounding the spinal cord. In
             groups 3 and 4, indwelling intrathecal catheters did not
             affect the spinal cord ADC, indicating normal blood flow and
             no cytotoxic edema. Contrast studies revealed nonhomogeneous
             distribution of contrast predominately in the lateral and
             ventral intrathecal space. CONCLUSION: Three-dimensional
             diffusion-weighted MRM displays cervical and lumbar spine
             anatomy accurately in vivo. Apparent diffusion coefficients
             measurements are feasible in rat cervical spinal cord with
             intrathecal catheters. Spinal cord ADCs are unaffected by
             intrathecal catheters, indicating normal spinal cord
             perfusion.},
   Doi = {10.1016/s1098-7339(98)90087-6},
   Key = {Benveniste98}
}

@article{fds132858,
   Author = {H Benveniste and H Qui and LW Hedlund and F D'Ercole and GA
             Johnson},
   Title = {Spinal cord neural anatomy in rats examined by in vivo
             magnetic resonance microscopy.},
   Journal = {Regional anesthesia and pain medicine, UNITED
             STATES},
   Volume = {23},
   Number = {6},
   Pages = {589-99},
   ISSN = {1098-7339},
   Keywords = {Animals • Biomechanics • Catheters, Indwelling
             • Cervical Vertebrae • Coloring Agents •
             Contrast Media • Diffusion • Edema • Epidural
             Space • Feasibility Studies • Female •
             Follow-Up Studies • Injections, Spinal • Ischemia
             • Longitudinal Studies • Lumbar Vertebrae •
             Magnetic Resonance Imaging • Microscopy •
             Neurilemma • Peripheral Nervous System Diseases •
             Rats • Rats, Inbred F344 • Regional Blood Flow
             • Spinal Cord • Spinal Cord Diseases • Spinal
             Nerves • anatomy & histology • anatomy &
             histology* • blood supply • diagnosis •
             diagnostic use • instrumentation • methods* •
             pathology • physiology},
   Abstract = {BACKGROUND AND OBJECTIVES: Magnetic resonance microscopy
             (MRM) is a technique that is worthwhile for
             anesthesiologists because it allows spinal cord and plexus
             anatomy to be visualized three dimensionally and followed
             over time in the same animal. For example, the long-term
             effect of indwelling intrathecal or plexus catheters can be
             studied in situ, and convective and diffusive forces within
             intrathecal, epidural, or nerve sheath spaces can be
             investigated. Further, diffusion-weighted MRM, which
             measures an "apparent diffusion coefficient" (ADC), can be
             used to track the presence of ischemia, hypoperfusion, or
             cytotoxic edema. This study investigates problems associated
             with the use of in vivo MRM for spinal cord and peripheral
             nerve studies in the rat. METHODS: Twenty-one anesthetized
             female Fisher CDF rats were used. Group 1 (n=7) was used for
             anatomic three-dimensional studies. Groups 2 (n=4), 3 (n=4),
             and 4 (n=6) were used for measurements of the ADC. Group 2
             served as controls, group 3 received lumbar intrathecal
             catheters, and group 4 received cervical intrathecal
             catheters. RESULTS: Cervical spine, lumbar spine, and spinal
             nerves and ganglia were accurately visualized with MRM. As a
             rule, spinal cord gray and white matter were better
             demonstrated using diffusion-weighted proton stains. By
             contrast, T2-weighted proton staining superiorly
             demonstrated structures surrounding the spinal cord. In
             groups 3 and 4, indwelling intrathecal catheters did not
             affect the spinal cord ADC, indicating normal blood flow and
             no cytotoxic edema. Contrast studies revealed nonhomogeneous
             distribution of contrast predominately in the lateral and
             ventral intrathecal space. CONCLUSION: Three-dimensional
             diffusion-weighted MRM displays cervical and lumbar spine
             anatomy accurately in vivo. Apparent diffusion coefficients
             measurements are feasible in rat cervical spinal cord with
             intrathecal catheters. Spinal cord ADCs are unaffected by
             intrathecal catheters, indicating normal spinal cord
             perfusion.},
   Key = {fds132858}
}

@booklet{Locher97,
   Author = {M. Locher and G. A. Johnson and E. R. Hunt},
   Title = {Stability analysis of fixed points via chaos
             control},
   Journal = {Chaos},
   Volume = {7},
   Number = {4},
   Pages = {590 -- 596},
   Year = {1997},
   Month = {December},
   Key = {Locher97}
}

@article{fds174169,
   Author = {M Locher and GA Johnson and ER Hunt},
   Title = {Stability analysis of fixed points via chaos
             control.},
   Journal = {Chaos (Woodbury, N.Y.)},
   Volume = {7},
   Number = {4},
   Pages = {590-596},
   Year = {1997},
   Month = {December},
   ISSN = {1089-7682},
   url = {http://dx.doi.org/10.1063/1.166258},
   Abstract = {This paper reviews recent advances in the application of
             chaos control techniques to the stability analysis of
             two-dimensional dynamical systems. We demonstrate how the
             system's response to one or multiple feedback controllers
             can be utilized to calculate the characteristic multipliers
             associated with an unstable periodic orbit. The experimental
             results, obtained for a single and two coupled diode
             resonators, agree well with the presented theory. (c) 1997
             American Institute of Physics.},
   Language = {ENG},
   Doi = {10.1063/1.166258},
   Key = {fds174169}
}

@article{fds132901,
   Author = {P Parmananda and MA Rhode and GA Johnson and RW Rollins and HD Dewald and AJ Markworth},
   Title = {Stabilization of unstable steady states in an
             electrochemical system using derivative control.},
   Journal = {Phys Rev E Stat Phys Plasmas Fluids Relat Interdiscip
             Topics},
   Volume = {49},
   Number = {6},
   Pages = {5007-5011},
   Year = {1994},
   Month = {June},
   ISSN = {1063-651X},
   Key = {fds132901}
}

@booklet{Parmananda94,
   Author = {P. Parmananda and M. A. Rhode and G. A. Johnson and R. W.
             Rollins and H. D. Dewald and A. J. Markworth},
   Title = {Stabilization of unstable steady-states in an
             electrochemical system using derivative control},
   Journal = {Physical Review E},
   Volume = {49},
   Number = {6},
   Pages = {5007 -- 5013},
   Year = {1994},
   Month = {June},
   Key = {Parmananda94}
}

@booklet{Johnson95b,
   Author = {G. A. Johnson and M. Locher and E. R. Hunt},
   Title = {Stabilized spatiotemporal waves in a convectively unstable
             open flow system - coupled diode resonators},
   Journal = {Physical Review E},
   Volume = {51},
   Number = {3},
   Pages = {R1625 -- R1628},
   Year = {1995},
   Month = {March},
   Key = {Johnson95b}
}

@article{fds132912,
   Author = {GA Johnson and M Löcher and ER Hunt},
   Title = {Stabilized spatiotemporal waves in a convectively unstable
             open flow system: coupled diode resonators.},
   Journal = {Phys Rev E Stat Phys Plasmas Fluids Relat Interdiscip
             Topics},
   Volume = {51},
   Number = {3},
   Pages = {R1625-R1628},
   Year = {1995},
   Month = {March},
   ISSN = {1063-651X},
   Key = {fds132912}
}

@booklet{Locher97a,
   Author = {M. Locher and G. A. Johnson and E. R. Hunt},
   Title = {Stabilizing spatiotemporal patterns in a convectively
             unstable open flow system via kink-antikink
             pairs},
   Journal = {Chaos Solitons \& Fractals},
   Volume = {8},
   Number = {9},
   Pages = {1523 -- 1532},
   Year = {1997},
   Month = {September},
   Key = {Locher97a}
}

@booklet{Johnson96a,
   Author = {G. A. Johnson and M. Locher and E. R. Hunt},
   Title = {Stable states and kink dynamics in a system of coupled diode
             resonators},
   Journal = {Physica D},
   Volume = {96},
   Number = {1-4},
   Pages = {367 -- 374},
   Year = {1996},
   Month = {September},
   Key = {Johnson96a}
}

@article{fds268852,
   Author = {Petiet, A and Hedlund, L and Johnson, GA},
   Title = {Staining methods for magnetic resonance microscopy of the
             rat fetus.},
   Journal = {J Magn Reson Imaging},
   Volume = {25},
   Number = {6},
   Pages = {1192-1198},
   Year = {2007},
   Month = {June},
   ISSN = {1053-1807},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/17520739},
   Keywords = {Animals • Contrast Media • Fetus • Magnetic
             Resonance Imaging • Rats • Rats, Sprague-Dawley
             • Staining and Labeling • administration & dosage*
             • embryology* • methods*},
   Abstract = {PURPOSE: To develop a magnetic resonance histology (MRH)
             staining and fixation method by immersion to enhance the
             signal-to-noise ratio (SNR) with a paramagnetic contrast
             agent permitting microscopic acquisition within a 3-hour
             scan time. MATERIALS AND METHODS: Methods were optimized for
             embryonic day 18.5 (E18.5) rat fetuses and imaging at 9.4T
             with an RF refocused spin-echo pulse sequence (TR/TE = 75
             msec/5.2 msec). Fixation/staining was performed by immersion
             in Bouin's fixative containing varied concentrations of
             ProHance (from 10:1 to 500:1 Bouin's:ProHance) and for
             varied immersion durations (up to 24 hours). RESULTS: The
             results showed a significant change in T1 and T2 relaxation
             times as a function of concentration of contrast agent and
             immersion duration. As the contrast agent penetrated the
             tissues, T1 was reduced as desired (typically by 10x), but
             at the same time T2 was profoundly reduced (typically by 3x)
             due to both protein cross-linking from the fixative and the
             high concentration of contrast agent. A systematic
             assessment of this staining protocol showed an increased SNR
             (by 5x) over that in unstained specimens. CONCLUSION: This
             staining protocol reduced scan time for very-high-resolution
             images (19.5 microm) to only 3 hours, making MRH a routine
             tool for evaluating fetal development.},
   Doi = {10.1002/jmri.20932},
   Key = {fds268852}
}

@article{fds174126,
   Author = {G Song and KA Dunlap and J Kim and DW Bailey and TE Spencer and RC
             Burghardt, GF Wagner and GA Johnson and FW Bazer},
   Title = {Stanniocalcin 1 is a luminal epithelial marker for
             implantation in pigs regulated by progesterone and
             estradiol.},
   Journal = {Endocrinology},
   Volume = {150},
   Number = {2},
   Pages = {936-45},
   Year = {2009},
   Month = {February},
   ISSN = {1945-7170},
   url = {http://dx.doi.org/10.1210/en.2008-1026},
   Keywords = {Animals • Biological Markers • Embryo Implantation
             • Endometrium • Epithelial Cells • Estradiol
             • Female • Gene Expression Regulation •
             Glycoproteins • Organ Specificity • Pregnancy
             • Pregnancy, Animal* • Progesterone •
             Pseudopregnancy • RNA, Messenger • Swine •
             Time Factors • Uterus • drug effects • drug
             effects* • genetics • genetics* • metabolism
             • pharmacology* • physiology*},
   Abstract = {Stanniocalcin 1 (STC1) is a glycoprotein that decreases
             calcium and increases phosphate in cells/tissues. This
             investigation examined endocrine regulation of STC1 in
             endometria of pigs during the estrous cycle and pregnancy.
             STC1 mRNA was present exclusively in luminal epithelium (LE)
             between d 12 and 15 of the estrous cycle, increased between
             d 12 and d 20, and was not detectable by d 30 of pregnancy.
             STC1 protein was also detected in uterine flushings. To
             determine effects of estrogen and progesterone, pigs were
             ovariectomized and treated with these hormones alone or
             together. Progesterone, but not estrogen, induced STC1 in
             LE. Cotreatment with progesterone and estrogen further
             stimulated STC1 over progesterone alone. To determine
             effects of pseudopregnancy, nonpregnant gilts were given
             daily injections of estradiol benzoate from d 11 to d 14.
             STC1 was not expressed in LE on d 90 of pseudopregnancy,
             suggesting that the estradiol given to induce
             pseudopregnancy and/or long-term exposure to progesterone
             are required for down-regulation of STC1. To determine
             effects of long-term progesterone, without effects of
             estradiol, pigs were ovariectomized on d 12, given daily
             injections of progesterone through d 39, and hysterectomized
             on d 40 after estrus. STC1 was expressed in LE of
             progesterone-treated pigs, suggesting that estrogen is
             involved in down-regulation of STC1. We conclude that STC1
             is induced in LE by progesterone and further stimulated by
             estrogen, and its down-regulation in LE by d 25 likely
             requires exposure of the progestinized uterus to estrogen.
             The temporal and cell type-specific expression of STC1 makes
             this gene a unique marker for implantation in
             pigs.},
   Language = {eng},
   Doi = {10.1210/en.2008-1026},
   Key = {fds174126}
}

@article{fds268769,
   Author = {Constantinides, C and Aristokleous, N and Johnson, GA and Perperides,
             D},
   Title = {Static and dynamic cardiac modelling: Initial strides and
             results towards a quantitatively accurate mechanical heart
             model},
   Journal = {2010 7th IEEE International Symposium on Biomedical Imaging:
             From Nano to Macro, ISBI 2010 - Proceedings},
   Pages = {496-499},
   Publisher = {IEEE},
   Year = {2010},
   Month = {August},
   ISBN = {9781424441266},
   url = {http://dx.doi.org/10.1109/ISBI.2010.5490300},
   Abstract = {Magnetic Resonance Imaging (MRI) has exhibited significant
             potential for quantifying cardiac function and dysfunction
             in the mouse. Recent advances in highresolution cardiac MR
             imaging techniques have contributed to the development of
             acquisition approaches that allow fast and accurate
             description of anatomic structures, and accurate surface and
             finite element (FE) mesh model constructions for study of
             global mechanical function in normal and transgenic mice.
             This study presents work in progress for construction of
             quantitatively accurate threedimensional (3D) and 4D dynamic
             surface and FE models of murine left ventricular (LV) muscle
             in C57BL/6J (n=10) mice. Constructed models are subsequently
             imported into commercial software packages for the solution
             of the constitutive equations that characterize mechanical
             function, including computation of the stress and strain
             fields. They are further used with solid-free form
             fabrication processes to construct model-based material
             renditions of the human and mouse hearts. ©2010
             IEEE.},
   Doi = {10.1109/ISBI.2010.5490300},
   Key = {fds268769}
}

@article{fds174082,
   Author = {FJ White and JW Ross and MM Joyce and RD Geisert and RC Burghardt and GA
             Johnson},
   Title = {Steroid regulation of cell specific secreted phosphoprotein
             1 (osteopontin) expression in the pregnant porcine
             uterus.},
   Journal = {Biology of reproduction},
   Volume = {73},
   Number = {6},
   Pages = {1294-301},
   Year = {2005},
   Month = {December},
   ISSN = {0006-3363},
   url = {http://dx.doi.org/10.1095/biolreprod.105.045153},
   Keywords = {Animals • Corpus Luteum • Endometrium •
             Epithelial Cells • Female • Fertilization •
             Gene Expression Regulation, Developmental • Osteopontin
             • Pregnancy • Pregnancy, Animal •
             Progesterone • Pseudopregnancy • RNA, Messenger
             • Sialoglycoproteins • Steroids • Sus scrofa
             • Uterus • cytology • genetics* •
             metabolism • metabolism* • physiology •
             physiology* • secretion*},
   Abstract = {Secreted phosphoprotein 1 (SPP1, commonly referred to as
             osteopontin and formerly known as bone sialoprotein 1, early
             T-lymphocyte activation 1) is an extracellular
             matrix/adhesion molecule that is upregulated in the pregnant
             uterus of all mammals examined to date. This study focused
             on the pig, which has true epitheliochorial placentation and
             exhibits induction of SPP1 mRNA in luminal epithelium (LE)
             just before conceptus attachment and in glandular epithelium
             (GE) after Day 30 of pregnancy. The objective of this study
             was to determine steroid regulation of SPP1 mRNA and protein
             in porcine uterine epithelium. To examine the effect of
             estrogen, cyclic gilts were treated daily (Days 11-14) with
             5 mg estradiol benzoate (i.m.) and hysterectomized on Day
             15. To evaluate the long-term effect of pseudopregnancy,
             cyclic gilts were given daily injections (Days 11-15) with
             steroid as above and hysterectomized on Day 90. In situ
             hybridization showed high expression of SPP1 mRNA only in LE
             contiguous with apposing conceptus tissue on Day 15 of
             pregnancy. In contrast, estrogen injection resulted in
             moderate but uniform SPP1 mRNA in all LE of Day 15
             nonpregnant gilts, with expression maintained through Day 90
             of pseudopregnancy. SPP1 mRNA also localized to the GE of
             Day 90 pseudopregnant gilts, similar to expression in late
             gestation. Consistent with in situ hybridization results,
             SPP1 protein localized to the apical surface of LE in all
             estrogen-treated gilts and in the GE on Day 90 of
             pseudopregnancy. We conclude that, in pregnant pigs, SPP1 is
             induced by conceptus estrogen in uterine LE and is regulated
             in GE in a manner coincident with CL/placental progesterone
             production.},
   Language = {eng},
   Doi = {10.1095/biolreprod.105.045153},
   Key = {fds174082}
}

@article{fds174129,
   Author = {DW Harris and CA Baker and HH Saneii and GA Johnson},
   Title = {Stimulation of cyclic GMP formation in smooth muscle cells
             by atriopeptin II.},
   Journal = {Life sciences},
   Volume = {37},
   Number = {7},
   Pages = {591-7},
   Year = {1985},
   Month = {August},
   ISSN = {0024-3205},
   Keywords = {Animals • Atrial Natriuretic Factor • Carbachol
             • Cell Line • Cyclic GMP • Diterpenes •
             Female • Forskolin • Humans • Kidney •
             Lung • Muscle Proteins • Muscle, Smooth, Vascular
             • Nitroprusside • Pregnancy • Rabbits •
             biosynthesis* • drug effects • embryology •
             metabolism • metabolism* • pharmacology •
             pharmacology*},
   Abstract = {Addition of synthesized atriopeptin II (AP-2), a 23 amino
             acid peptide of rat atria, to rat thoracic aorta smooth
             muscle cells results in the stimulation of cyclic GMP
             production by the cells. The EC50 for the effect is 81 nM
             and a 7 fold increase occurs at 10 microM AP-2. Cyclic GMP
             levels increased within 15 seconds after the addition of
             AP-2 and were maximal at 5 minutes. Cyclic GMP levels in
             primary rabbit kidney cells were increased 15 fold by 10
             microM AP-2. However, no increase in cyclic GMP was detected
             in WI-38 fibroblast cells after the addition of 10 microM
             AP-2. Cyclic AMP levels were not affected by AP-2 in any of
             these cell systems. The effect upon cyclic GMP accumulation
             was specific for AP-2; none of the other compounds or
             peptides tested affected cyclic GMP levels.},
   Language = {eng},
   Key = {fds174129}
}

@booklet{Harris85,
   Author = {D. W. Harris and C. A. Baker and H. H. Saneii and G. A.
             Johnson},
   Title = {Stimulation of cyclic-gmp formation in smooth-muscle cells
             by atriopeptin-ii},
   Journal = {Life Sciences},
   Volume = {37},
   Number = {7},
   Pages = {591 -- 597},
   Year = {1985},
   Key = {Harris85}
}

@booklet{Locher98,
   Author = {M. Locher and D. Cigna and E. R. Hunt and G. A. Johnson and F. Marchesoni and L. Gammaitoni and M. E. Inchiosa and A. R.
             Bulsara},
   Title = {Stochastic resonance in coupled nonlinear dynamic
             elements},
   Journal = {Chaos},
   Volume = {8},
   Number = {3},
   Pages = {604 -- 615},
   Year = {1998},
   Month = {September},
   Key = {Locher98}
}

@article{fds174073,
   Author = {M Locher and D Cigna and ER Hunt and GA Johnson and F Marchesoni and L
             Gammaitoni, ME Inchiosa and AR Bulsara},
   Title = {Stochastic resonance in coupled nonlinear dynamic
             elements.},
   Journal = {Chaos (Woodbury, N.Y.)},
   Volume = {8},
   Number = {3},
   Pages = {604-615},
   Year = {1998},
   Month = {September},
   ISSN = {1089-7682},
   url = {http://dx.doi.org/10.1063/1.166342},
   Abstract = {We investigate the response of a linear chain of diffusively
             coupled diode resonators under the influence of thermal
             noise. We also examine the connection between spatiotemporal
             stochastic resonance and the presence of kink-antikink pairs
             in the array. The interplay of nucleation rates and kink
             speeds is briefly addressed. The experimental results are
             supplemented with simulations on a coupled map lattice. We
             furthermore present analytical results for the
             synchronization and signal processing properties of a Phi(4)
             field theory and explore the effects of various forms of
             nonlinear coupling. (c) 1998 American Institute of
             Physics.},
   Language = {ENG},
   Doi = {10.1063/1.166342},
   Key = {fds174073}
}

@booklet{Posey00,
   Author = {R. Posey and G. A. Johnson and S. T. Vohra},
   Title = {Strain sensing based on coherent Rayleigh scattering in an
             optical fibre},
   Journal = {Electronics Letters},
   Volume = {36},
   Number = {20},
   Pages = {1688 -- 1689},
   Year = {2000},
   Month = {September},
   Key = {Posey00}
}

@article{fds363003,
   Author = {Sitek, KR and Calabrese, E and Johnson, GA and Ghosh, SS and Chandrasekaran, B},
   Title = {Structural Connectivity of Human Inferior Colliculus
             Subdivisions Using in vivo and post mortem Diffusion MRI
             Tractography.},
   Journal = {Front Neurosci},
   Volume = {16},
   Pages = {751595},
   Year = {2022},
   url = {http://dx.doi.org/10.3389/fnins.2022.751595},
   Abstract = {Inferior colliculus (IC) is an obligatory station along the
             ascending auditory pathway that also has a high degree of
             top-down convergence via efferent pathways, making it a
             major computational hub. Animal models have attributed
             critical roles for the IC in in mediating auditory
             plasticity, egocentric selection, and noise exclusion. IC
             contains multiple functionally distinct subdivisions. These
             include a central nucleus that predominantly receives
             ascending inputs and external and dorsal nuclei that receive
             more heterogeneous inputs, including descending and
             multisensory connections. Subdivisions of human IC have been
             challenging to identify and quantify using standard brain
             imaging techniques such as MRI, and the connectivity of each
             of these subnuclei has not been identified in the human
             brain. In this study, we estimated the connectivity of human
             IC subdivisions with diffusion MRI (dMRI) tractography,
             using both anatomical-based seed analysis as well as
             unsupervised k-means clustering. We demonstrate sensitivity
             of tractography to overall IC connections in both high
             resolution post mortem and in vivo datasets. k-Means
             clustering of the IC streamlines in both the post mortem and
             in vivo datasets generally segregated streamlines based on
             their terminus beyond IC, such as brainstem, thalamus, or
             contralateral IC. Using fine-grained anatomical
             segmentations of the major IC subdivisions, the post mortem
             dataset exhibited unique connectivity patterns from each
             subdivision, including commissural connections through
             dorsal IC and lateral lemniscal connections to central and
             external IC. The subdivisions were less distinct in the
             context of in vivo connectivity, although lateral lemniscal
             connections were again highest to central and external IC.
             Overall, the unsupervised and anatomically driven methods
             provide converging evidence for distinct connectivity
             profiles for each of the IC subdivisions in both post mortem
             and in vivo datasets, suggesting that dMRI tractography with
             high quality data is sensitive to neural pathways involved
             in auditory processing as well as top-down control of
             incoming auditory information.},
   Doi = {10.3389/fnins.2022.751595},
   Key = {fds363003}
}

@article{fds357206,
   Author = {Atik, AF and Calabrese, E and Gramer, R and Adil, SM and Rahimpour, S and Pagadala, P and Johnson, GA and Lad, SP},
   Title = {Structural mapping with fiber tractography of the human
             cuneate fasciculus at microscopic resolution in cervical
             region.},
   Journal = {Neuroimage},
   Volume = {196},
   Pages = {200-206},
   Year = {2019},
   Month = {August},
   url = {http://dx.doi.org/10.1016/j.neuroimage.2019.04.030},
   Abstract = {Human spinal white matter tract anatomy has been mapped
             using post mortem histological information with the help of
             molecular tracing studies in animal models. This study used
             7 Tesla diffusion MR tractography on a human cadaver that
             was harvested 24 hours post mortem to evaluate cuneate
             fasciculus anatomy in cervical spinal cord. Based on this
             method, for the first time much more nuanced tractographic
             anatomy was used to investigate possible new routes for
             cuneate fasciculus in the posterior and lateral funiculus.
             Additionally, current molecular tracing studies were
             reviewed, and confirmatory data was presented along with our
             radiological results. Both studies confirm that upon entry
             to the spinal cord, upper cervical level tracts (C1-2-3)
             travel inside lateral funiculus and lower level tracts
             travel medially inside the posterior funiculus after entry
             at posterolateral sulcus which is different than traditional
             knowledge of having cuneate fasciculus tracts concentrated
             in the lateral part of posterior funiculus.},
   Doi = {10.1016/j.neuroimage.2019.04.030},
   Key = {fds357206}
}

@booklet{Johnson86,
   Author = {JOHNSON, GA and BAILEY, JE and BRUCK, RI and MATYAC,
             CA},
   Title = {STUDIES OF DISEASED ROOT-TISSUE USING NUCLEAR-MAGNETIC-RESONANCE
             IMAGING},
   Journal = {PHYTOPATHOLOGY},
   Volume = {76},
   Number = {10},
   Pages = {1067-1067},
   Publisher = {AMER PHYTOPATHOLOGICAL SOC},
   Year = {1986},
   Month = {October},
   ISSN = {0031-949X},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1986F034600096&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Johnson86}
}

@article{fds269021,
   Author = {Zhou, X and Maronpot, RR and Cofer, GP and Hedlund, LW and Johnson,
             GA},
   Title = {Studies on bromobenzene-induced hepatotoxicity using in vivo
             MR microscopy with surgically implanted RF
             coils.},
   Journal = {Magn Reson Med},
   Volume = {31},
   Number = {6},
   Pages = {619-627},
   Year = {1994},
   Month = {June},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/8057814},
   Keywords = {Animals • Bromobenzenes • Electromagnetics •
             Equipment Design • Female • Image Enhancement
             • Liver • Magnetic Resonance Imaging •
             Microscopy • Necrosis • Prostheses and Implants
             • Rats • Rats, Inbred F344 • adverse effects*
             • drug effects* • instrumentation • methods
             • methods* • pathology},
   Abstract = {Using surgically implanted RF coils at 300 MHz,
             three-dimensional microscopic MR images of rat liver were
             obtained in vivo to follow the development of pathology
             induced by bromobenzene exposure. Formalin fixed specimens
             of liver from these animals were also imaged using in vitro
             MR microscopy, followed by conventional optical microscopy.
             All MR images were acquired using a spin-warp pulse sequence
             with TR = 950 ms and TE = 23 ms. The in vivo images were
             reconstructed as 256(2) x 32 arrays with a voxel size of (50
             microns)2 x 219 microns, while the in vitro images were
             reconstructed as 256(2) x 128 arrays, giving an isotropic
             resolution at (39 microns)3. Based on results from six
             animals, we have found in all animals exposed to
             bromobenzene, image intensity decreased in specific hepatic
             tissue regions. These regions were well correlated to low
             signal intensity areas observed in in vitro MR images at
             higher resolution. Conventional optical microscopy indicated
             that the low signal intensity regions corresponded to areas
             of necrosis. The decrease in signal intensity is consistent
             with increased local diffusion coefficients as a result of
             necrosis. This study demonstrates that MR microscopy with
             implanted RF coils can be successfully used to follow tissue
             pathological changes in living tissues.},
   Doi = {10.1002/mrm.1910310607},
   Key = {fds269021}
}

@booklet{Zhou94,
   Author = {X. H. Zhou and R. R. Maronpot and G. P. Cofer and L. W.
             Hedlund and G. A. Johnson},
   Title = {Studies on bromobenzene-induced hepatotoxicity using in-vivo
             mr microscopy with surgically implanted rf
             coils},
   Journal = {Magnetic Resonance In Medicine},
   Volume = {31},
   Number = {6},
   Pages = {619 -- 627},
   Year = {1994},
   Month = {June},
   Key = {Zhou94}
}

@article{fds174136,
   Author = {W Veldkamp and GA Johnson and HH Keasling},
   Title = {Studies on the effects of reserpine in mice as influenced by
             its diluent.},
   Journal = {Journal of pharmaceutical sciences},
   Volume = {57},
   Number = {4},
   Pages = {613-7},
   Year = {1968},
   Month = {April},
   ISSN = {0022-3549},
   Keywords = {Amines • Animals • Appetite Depressants •
             Benzphetamine • Blepharoptosis • Brain •
             Citrates • Dextroamphetamine • Drug Antagonism
             • Hydrogen-Ion Concentration • Locomotion •
             Male • Methylcellulose • Mice •
             Norepinephrine • Phenethylamines • Propylamines
             • Reserpine • Serotonin • Sulfates •
             Suspensions • Time Factors • Vehicles* •
             administration & dosage* • chemically induced •
             drug effects • metabolism • pharmacology •
             pharmacology*},
   Language = {eng},
   Key = {fds174136}
}

@article{fds132848,
   Author = {GA Johnson and CA Baker},
   Title = {Sulfation of minoxidil by human platelet
             sulfotransferase.},
   Journal = {Clinica chimica acta; international journal of clinical
             chemistry, NETHERLANDS},
   Volume = {169},
   Number = {2-3},
   Pages = {217-27},
   Year = {1987},
   Month = {November},
   ISSN = {0009-8981},
   Keywords = {Adolescent • Adult • Arylsulfotransferase •
             Blood Platelets • Chromatography, High Pressure Liquid
             • Humans • Hydrogen-Ion Concentration • Male
             • Middle Aged • Minoxidil • Platelet Count
             • Sulfurtransferases • blood* • enzymology*
             • metabolism*},
   Abstract = {In an attempt to determine whether (1) sulfotransferase
             activity in human platelets would convert minoxidil to
             minoxidil sulfate and (2) inter-subject variations in this
             sulfotransferase activity could be noted, platelet
             homogenates were incubated with minoxidil and 35S-PAPS in
             HEPES buffer at 37 degrees C for 30 min. Radioactivity which
             was extracted into ethyl acetate and shown by HPLC to elute
             with authentic minoxidil sulfate was counted by
             scintillation counting. Aliquots of the platelet homogenates
             were also preincubated at 43 degrees C for 15 min to
             determine the thermal stability of the sulfotransferase
             activity. Sulfotransferase activity in platelets from 48
             adult males ranged from 0.9-13.2 pmol minoxidil sulfate
             produced/10(7) platelets per 30 min (mean 4.91 +/- 2.84
             pmol/10(7) platelets per 30 min +/- SD). Thermal stable
             sulfotransferase activity ranged from 0.2-7.6 pmol minoxidil
             produced/10(7) platelets per 30 min and varied from 15 to
             57% of the total sulfotransferase activity. Thus, the
             results indicate that human platelets can effect the
             sulfation of minoxidil and that sulfotransferase activity
             does show inter-subject variation.},
   Key = {fds132848}
}

@booklet{Kudlacek94,
   Author = {P. E. Kudlacek and R. J. Anderson and G. A.
             Johnson},
   Title = {Sulfation of minoxidil by human platelet thermolabile phenol
             sulfotransferase (tl pst)},
   Journal = {Clinical Research},
   Volume = {42},
   Number = {3},
   Pages = {A394 -- A394},
   Year = {1994},
   Month = {October},
   Key = {Kudlacek94}
}

@booklet{Johnson87,
   Author = {G. A. Johnson and C. A. Baker},
   Title = {Sulfation of minoxidil by human-platelet
             sulfotransferase},
   Journal = {Clinica Chimica Acta},
   Volume = {169},
   Number = {2-3},
   Pages = {217 -- 227},
   Year = {1987},
   Month = {November},
   Key = {Johnson87}
}

@booklet{Baker86,
   Author = {C. A. Baker and G. A. Johnson},
   Title = {Sulfation of minoxidil by human-platelet
             sulfotransferase},
   Journal = {Federation Proceedings},
   Volume = {45},
   Number = {3},
   Pages = {445 -- 445},
   Year = {1986},
   Month = {March},
   Key = {Baker86}
}

@booklet{Johnson82d,
   Author = {G. A. Johnson and K. J. Barsuhn and J. M.
             Mccall},
   Title = {Sulfation of minoxidil by liver sulfotransferase},
   Journal = {Biochemical Pharmacology},
   Volume = {31},
   Number = {18},
   Pages = {2949 -- 2954},
   Year = {1982},
   Key = {Johnson82d}
}

@article{fds174214,
   Author = {GA Johnson and KJ Barsuhn and JM McCall},
   Title = {Sulfation of minoxidil by liver sulfotransferase.},
   Journal = {Biochemical pharmacology},
   Volume = {31},
   Number = {18},
   Pages = {2949-54},
   Year = {1982},
   Month = {September},
   ISSN = {0006-2952},
   Keywords = {Animals • Biotransformation • Liver • Male
             • Minoxidil • Pyrimidines • Rats • Rats,
             Inbred Strains • Sulfurtransferases • enzymology*
             • metabolism*},
   Abstract = {The 100,000 g supernatant fraction of rat liver homogenate
             contains a sulfotransferase activity which catalyzes the
             sulfation of minoxidil. Synthetic minoxidil N-O sulfate and
             the enzyme synthesized product had identical chromatographic
             characteristics on high pressure liquid chromatography.
             Minoxidil sulfate, which yields minoxidil when treated with
             sulfatase, was slowly hydrolyzed in water. Several N-oxides
             of other heterocycles, including several other pyrimidines,
             triazines and imidazoles, were also substrates for this
             sulfotransferase.},
   Language = {eng},
   Key = {fds174214}
}

@article{fds268846,
   Author = {Rice, HE and Hsu, EW and Sheng, H and Evenson, DA and Freemerman, AJ and Safford, KM and Provenzale, JM and Warner, DS and Johnson,
             GA},
   Title = {Superparamagnetic iron oxide labeling and transplantation of
             adipose-derived stem cells in middle cerebral artery
             occlusion-injured mice.},
   Journal = {AJR Am J Roentgenol},
   Volume = {188},
   Number = {4},
   Pages = {1101-1108},
   Year = {2007},
   Month = {April},
   ISSN = {1546-3141},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/17377054},
   Keywords = {Adipose Tissue • Animals • Brain Ischemia •
             Contrast Media* • Infarction, Middle Cerebral Artery
             • Iron • Magnetic Resonance Imaging* • Mice
             • Mice, Inbred C57BL • Oxides • Stem Cell
             Transplantation • complications* • cytology*
             • diagnosis* • diagnostic use* • etiology
             • methods* • surgery*},
   Abstract = {OBJECTIVE: Adipose-derived stem cells are an alternative
             stem cell source for CNS therapies. The goals of the current
             study were to label adipose-derived stem cells with
             superparamagnetic iron oxide (SPIO) particles, to use MRI to
             guide the transplantation of adipose-derived stem cells in
             middle cerebral artery occlusion (MCAO)-injured mice, and to
             localize donor adipose-derived stem cells in the injured
             brain using MRI. We hypothesized that we would successfully
             label adipose-derived stem cells and image them with MRI.
             MATERIALS AND METHODS: Adipose-derived stem cells harvested
             from mice inbred for green fluorescent protein were labeled
             with SPIO ferumoxide particles through the use of
             poly-L-lysine. Adipose-derived stem cell viability, iron
             staining, and proliferation were measured after SPIO
             labeling, and the sensitivity of MRI in the detection of
             SPIO-labeled adipose-derived stem cells was assessed ex
             vivo. Adult mice (n = 12) were subjected to unilateral MCAO.
             Two weeks later, in vivo 7-T MRI was performed to guide
             stereotactic transplantation of SPIO-labeled adipose-derived
             stem cells into brain tissue adjacent to the infarct. After
             24 hours, the mice were sacrificed for high-resolution ex
             vivo 7-T or 9.4-T MRI and histologic study. RESULTS:
             Adipose-derived stem cells were efficiently labeled with
             SPIO particles without loss of cell viability or
             proliferation. Using MRI, we guided precise transplantation
             of adipose-derived stem cells. MR images of mice given
             injections of SPIO-labeled adipose-derived stem cells had
             hypointense regions that correlated with the histologic
             findings in donor cells. CONCLUSION: MRI proved useful in
             transplantation of adipose-derived stem cells in vivo. This
             imaging technique may be useful for studies of CNS stem cell
             therapies.},
   Doi = {10.2214/AJR.06.0663},
   Key = {fds268846}
}

@article{fds268922,
   Author = {Banson, ML and Cofer, GP and Hedlund, LW and Johnson,
             GA},
   Title = {Surface coil imaging of rat spine at 7.0
             T.},
   Journal = {Magn Reson Imaging},
   Volume = {10},
   Number = {6},
   Pages = {929-934},
   Year = {1992},
   ISSN = {0730-725X},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/1461090},
   Keywords = {Animals • Equipment Design • Magnetic Resonance
             Imaging • Rats • Rats, Sprague-Dawley • Spine
             • anatomy & histology* • instrumentation},
   Abstract = {An inductively coupled surface coil for imaging the rat
             spine at 7 T is described. This planar circular probe was
             made from microwave substrate to limit the size of the coil
             and to minimize the magnetic susceptibility. The surface
             coil was used as a single transmit/receive coil and as a
             receive-only coil with a birdcage body coil for excitation.
             The signal-to-noise ratio (SNR) of the probe was compared to
             a 5-cm birdcage coil and exceeded the birdcage coil's SNR by
             three to six times at superficial structures. The main
             advantages of the probe are an improved SNR for superficial
             structures and a simple design and use. Images with 50 x 50
             x 500 micron voxels were obtained of the rat spine with
             excellent anatomical detail.},
   Doi = {10.1016/0730-725x(92)90447-8},
   Key = {fds268922}
}

@booklet{Banson92,
   Author = {M. L. Banson and G. P. Cofer and L. W. Hedlund and G. A.
             Johnson},
   Title = {Surface coil imaging of rat spine at 7.0-t},
   Journal = {Magnetic Resonance Imaging},
   Volume = {10},
   Number = {6},
   Pages = {929 -- 934},
   Year = {1992},
   Key = {Banson92}
}

@booklet{Scribner01,
   Author = {D. R. Scribner and J. L. Walker and G. A. Johnson and S. D.
             Mcmeekin and M. A. Gold and R. S. Mannel},
   Title = {Surgical management of early-stage endometrial cancer in the
             elderly: Is laparoscopy feasible?},
   Journal = {Gynecologic Oncology},
   Volume = {83},
   Number = {3},
   Pages = {563 -- 568},
   Year = {2001},
   Month = {December},
   Key = {Scribner01}
}

@article{fds174187,
   Author = {DR Scribner Jr and JL Walker and GA Johnson and SD McMeekin and MA Gold and RS Mannel},
   Title = {Surgical management of early-stage endometrial cancer in the
             elderly: is laparoscopy feasible?},
   Journal = {Gynecologic oncology},
   Volume = {83},
   Number = {3},
   Pages = {563-8},
   Year = {2001},
   Month = {December},
   ISSN = {0090-8258},
   url = {http://dx.doi.org/10.1006/gyno.2001.6463},
   Keywords = {Aged • Aged, 80 and over • Endometrial Neoplasms
             • Female • Humans • Hysterectomy, Vaginal
             • Laparoscopy • Lymph Node Excision •
             Neoplasm Staging • Retrospective Studies •
             methods* • pathology • surgery*},
   Abstract = {OBJECTIVE: To give insight into the utility of laparoscopic
             staging of endometrial cancer in the elderly population by
             reviewing the surgical management of clinically stage I
             endometrial cancer patients. METHODS: A retrospective
             analysis evaluating patients that were > or =65 years old
             and had planned laparoscopic staging, traditional staging
             via a laparotomy, or a transvaginal hysterectomy as
             management of their early endometrial cancer. The
             laparoscopic group had complete staging with bilateral
             pelvic and paraaortic lymph node dissections and was
             compared to the group who had staging performed via
             laparotomy. Patients were identified by our institution's
             database and data were collected by review of their medical
             records. Data were collected on demographics, pathology, and
             procedural information including completion rates, operating
             room (OR) time, estimated blood loss (EBL), transfusions,
             lymph node count, complications, and length of stay.
             Associations between variables were analyzed by Student's t
             tests and chi(2) testing using Excel v. 9.0. RESULTS: From
             February 25, 1994, through December 21, 2000, 125 elderly
             patients were identified. Sixty-seven patients had planned
             laparoscopic staging (Group 1), 45 patients had staging via
             planned laparotomy (Group 2), and 13 patients had a
             transvaginal hysterectomy (Group 3). Group 1 and Group 2
             were compared regarding surgical and postoperative data. Age
             was not different between these groups (75.9 vs 74.7 years,
             P = NS). Quetelet index was also similar (29.4 vs 29.9, P =
             NS) 32.8% of Group 1 had > or =1 previous laparotomy
             compared to 51.1% in Group 2 (P = NS). In Group 1, 53/67
             (79.1%) had stage I or II disease compared to 29/45 (64.4%)
             in Group 2 (P = NS). Laparoscopy was completed in 52/67
             (77.6%) attempted procedures. The reasons for conversion to
             laparotomy were obesity 7/67 (10.4%), bleeding 4/67 (6.0%),
             intraperitoneal cancer 3/67 (4.5%), and adhesions 1/67
             (1.5%). OR time was significantly longer in successful Group
             1 patients compared to Group 2 patients (236 vs 148 min, p =
             0.0001). EBL was similar between these groups (298 vs 336
             ml, P = NS). Ten of 52 (19.2%) of successful Group 1
             patients received a blood transfusion compared to 1/45
             (2.2%) of Group 2 patients (P < 0.0001). Pelvic, common
             iliac, and paraaortic lymph node counts were similar between
             successful Group 1 patients and those in Group 2 combined
             with those that received a laparotomy in Group 1 (17.8, 5.2,
             6.6 vs 19.1, 5.1, 5.2, P = NS). Length of stay (LOS) was
             significantly shorter in Group 1 versus Group 2 (3.0 vs 5.8
             days, P < 0.0001). There were less fevers (6.0 vs 15.6%, P =
             0.01), less postoperative ileus's (0 vs 15.6%, P < 0.001),
             and less wound complications (6.0 vs 26.7%, P = 0.002) in
             Group 1 compared to Group 2. Group 3 average age was 77.5
             years. Concurrent medical comorbidities were the main reason
             for the transvaginal approach. OR time averaged 104.5 min.
             The average length of stay was 2.1 days with no procedural
             or postoperative complications. CONCLUSIONS: The favorable
             results from this retrospective study refute the bias that
             age is a relative contraindication to laparoscopic surgery.
             Laparoscopic staging was associated with an increased OR
             time and an increased rate of transfusion but equivalent
             blood loss and lymph node counts. Possible advantages are
             decreased length of stay, less postoperative ileus, and less
             infections complications. Transvaginal hysterectomy still
             remains a proven option for women with serious comorbid
             medical problems with short OR times, minimal complications,
             and short lengths of stay.},
   Language = {eng},
   Doi = {10.1006/gyno.2001.6463},
   Key = {fds174187}
}

@article{fds174105,
   Author = {SA Kamelle and TL Rutledge and TD Tillmanns and NS Gould and DE Cohn and J
             Wright, TJ Herzog and JS Rader and MA Gold and GA Johnson and JL Walker and RS Mannel and DS McMeekin},
   Title = {Surgical-pathological predictors of disease-free survival
             and risk groupings for IB2 cervical cancer: do the
             traditional models still apply?},
   Journal = {Gynecologic oncology},
   Volume = {94},
   Number = {2},
   Pages = {249-55},
   Year = {2004},
   Month = {August},
   ISSN = {0090-8258},
   url = {http://dx.doi.org/10.1016/j.ygyno.2004.05.038},
   Keywords = {Adult • Aged • Disease-Free Survival • Female
             • Humans • Hysterectomy • Lymph Node Excision
             • Lymphatic Metastasis • Lymphatic System •
             Middle Aged • Neoplasm Staging • Retrospective
             Studies • Risk Factors • Uterine Cervical
             Neoplasms • methods • pathology • pathology*
             • surgery*},
   Abstract = {OBJECTIVE: To evaluate how the independent predictors of
             recurrence for stage IB2 cervical cancers treated with
             up-front radical hysterectomy apply to established risk
             models. METHODS: Patients with IB2 cervical cancers
             diagnosed from 1990 to 2000 were identified from tumor
             registries of two institutions. Patients were classified
             into risk groups: high-risk (HR) (positive nodes,
             parametria, or margins), intermediate-risk (IR) (positive
             lymph vascular space involvement (LVSI) with any cervical
             stromal invasion (CSI), or (-) LVSI and > middle- CSI), or
             low-risk (LR) (absence of HR or IR characteristics).
             Disease-free survival (DFS) was estimated by Kaplan-Meier
             method and comparisons between subgroups were studied by log
             rank. A Cox proportional hazards model was used to determine
             independent predictors of recurrence. RESULTS: We identified
             86 patients with stage IB2 tumors treated by RH. We found
             34% of patients to be HR, 60% IR, and 6% LR. Of the 52 IR
             patients, 28 had (+) LVSI with superficial, middle, and
             outer 1/3 CSI, and 24 had (-) LVSI with middle or outer 1/3
             invasion. Overall, postoperative adjuvant radiation (PRT)
             was used in 52% of the 86 patients, including 0/5 LR, 16/52
             IR, and 29/29 HR patients. Univariate predictors of
             recurrence were pelvic nodal disease, (+) LVSI, (+)
             parametria, outer 1/3 CSI, and tumor size > 6 cm. Age,
             grade, histology, and the use of postoperative radiation
             were not associated with recurrence. Multivariate analysis
             identified LVSI as the only independent predictor of
             recurrence (RR 5.2, P = 0.03). Two-year DFS for LR, IR, and
             HR patients was 100%, 83%, and 60%, respectively. Only 4/24
             (17%) IR patients with (-) LVSI got PRT compared with 12/28
             (43%) of IR patients with (+) LVSI. The 2-year DFS for IR
             patients with (-) LVSI was 96%. IR (+) patients recurred
             more frequently with a 2-year DFS of 71%. CONCLUSIONS:
             Overall, 66% of patients with IB2 disease were classified as
             having low or intermediate-risk disease. IR patients with
             (-) LVSI and all LR patients did well with surgery alone.
             This study defines the independent importance of LVSI and
             questions the utility of published IR models when applied to
             stage IB2 cervical cancer.},
   Language = {eng},
   Doi = {10.1016/j.ygyno.2004.05.038},
   Key = {fds174105}
}

@article{fds329027,
   Author = {Wei, H and Gibbs, E and Zhao, P and Wang, N and Cofer, GP and Zhang, Y and Johnson, GA and Liu, C},
   Title = {Susceptibility tensor imaging and tractography of collagen
             fibrils in the articular cartilage.},
   Journal = {Magn Reson Med},
   Volume = {78},
   Number = {5},
   Pages = {1683-1690},
   Year = {2017},
   Month = {November},
   url = {http://dx.doi.org/10.1002/mrm.26882},
   Abstract = {PURPOSE: To investigate the B0 orientation-dependent
             magnetic susceptibility of collagen fibrils within the
             articular cartilage and to determine whether susceptibility
             tensor imaging (STI) can detect the 3D collagen network
             within cartilage. METHODS: Multiecho gradient echo datasets
             (100-μm isotropic resolution) were acquired from fixed
             porcine articular cartilage specimens at 9.4 T. The
             susceptibility tensor was calculated using phase images
             acquired at 12 or 15 different orientations relative to B0 .
             The susceptibility anisotropy of the collagen fibril was
             quantified and diffusion tensor imaging (DTI) was compared
             against STI. 3D tractography was performed to visualize and
             track the collagen fibrils with DTI and STI. RESULTS: STI
             experiments showed the distinct and significant anisotropic
             magnetic susceptibility of collagen fibrils within the
             articular cartilage. STI can be used to measure and quantify
             susceptibility anisotropy maps. Furthermore, STI provides
             orientation information of the underlying collagen network
             via 3D tractography. CONCLUSION: The findings of this study
             demonstrate that STI can characterize the orientation
             variation of collagen fibrils where diffusion anisotropy
             fails. We believe that STI could serve as a sensitive and
             noninvasive marker to study the collagen fibrils
             microstructure. Magn Reson Med 78:1683-1690, 2017. © 2017
             International Society for Magnetic Resonance in
             Medicine.},
   Doi = {10.1002/mrm.26882},
   Key = {fds329027}
}

@article{fds268717,
   Author = {Xie, L and Dibb, R and Cofer, GP and Li, W and Nicholls, PJ and Johnson,
             GA and Liu, C},
   Title = {Susceptibility tensor imaging of the kidney and its
             microstructural underpinnings.},
   Journal = {Magn Reson Med},
   Volume = {73},
   Number = {3},
   Pages = {1270-1281},
   Year = {2015},
   Month = {March},
   ISSN = {0740-3194},
   url = {http://dx.doi.org/10.1002/mrm.25219},
   Abstract = {PURPOSE: The purpose of this study was to determine whether
             susceptibility tensor imaging (STI) could overcome
             limitations of current techniques to detect tubules
             throughout the kidney. METHODS: Normal mouse kidneys
             (n = 4) were imaged at 9.4T using a three-dimensional
             gradient multi-echo sequence (55-micron isotropic
             resolution). Phase images from 12 orientations were obtained
             to compute the susceptibility tensor. Diffusion tensor
             imaging (DTI) with 12 encoding directions was compared with
             STI. Tractography was performed to visualize and track the
             course of tubules with DTI and STI. Confocal microscopy was
             used to identify which tubular segments of the nephron were
             detected by DTI and STI. RESULTS: Diffusion anisotropy was
             limited to the inner medulla of the kidney. DTI did not find
             a significant number of coherent tubular tracks in the outer
             medulla or cortex. With STI, we found strong susceptibility
             anisotropy and many tracks in the inner and outer medulla
             and in limited areas of the cortex. CONCLUSION: STI was able
             to track tubules throughout the kidney, whereas DTI was
             limited to the inner medulla. STI provides a novel contrast
             mechanism related to local tubule microstructure and may
             offer a powerful method to study the nephron.},
   Doi = {10.1002/mrm.25219},
   Key = {fds268717}
}

@booklet{Johnson98b,
   Author = {G. A. Johnson and D. J. Mar and T. L. Carroll and L. M.
             Pecora},
   Title = {Synchronization and imposed bifurcations in the presence of
             large parameter mismatch},
   Journal = {Physical Review Letters},
   Volume = {80},
   Number = {18},
   Pages = {3956 -- 3959},
   Year = {1998},
   Month = {May},
   Key = {Johnson98b}
}

@booklet{Carroll98,
   Author = {T. L. Carroll and G. A. Johnson},
   Title = {Synchronizing broadband chaotic systems to narrow-band
             signals},
   Journal = {Physical Review E},
   Volume = {57},
   Number = {2},
   Pages = {1555 -- 1558},
   Year = {1998},
   Month = {February},
   Key = {Carroll98}
}

@booklet{Schostarez93,
   Author = {H. J. Schostarez and J. M. Fisher and A. R. Diani and M. J.
             Mulholland and K. L. Schull and M. J. Zaya and T. J. Vidmar and G. A. Johnson and M. F. Kubicek and S. J. Humphrey and M. P. Smith},
   Title = {Synthesis and hair-growth stimulatory activity of
             5-fluoro-6-(1-piperidinyl)-2,4-pyrimidinediamine, 3-oxide
             (u-83,868)},
   Journal = {Abstracts Of Papers Of The American Chemical
             Society},
   Volume = {205},
   Pages = {131 -- MEDI},
   Year = {1993},
   Month = {March},
   Key = {Schostarez93}
}

@booklet{Johnson82b,
   Author = {G. A. Johnson},
   Title = {Synthesized signal generator sets phase-noise
             standard},
   Journal = {Microwaves \& Rf},
   Volume = {21},
   Number = {12},
   Pages = {110 -- 111},
   Year = {1982},
   Key = {Johnson82b}
}

@booklet{Johnson83d,
   Author = {G. A. Johnson},
   Title = {Synthesizer adjustments},
   Journal = {Microwaves \& Rf},
   Volume = {22},
   Number = {1},
   Pages = {15 -- 15},
   Year = {1983},
   Key = {Johnson83d}
}

@article{fds174303,
   Author = {AJ Roberts and AP Niarchos and VA Subramanian and RM Abel and SD Herman and JE Sealey and DB Case and RP White and GA Johnson and JH Laragh and WA Gay
             Jr},
   Title = {Systemic hypertension associated with coronary artery bypass
             surgery. Predisposing factors, hemodynamic characteristics,
             humoral profile, and treatment.},
   Journal = {The Journal of thoracic and cardiovascular
             surgery},
   Volume = {74},
   Number = {6},
   Pages = {846-59},
   Year = {1977},
   Month = {December},
   ISSN = {0022-5223},
   Keywords = {Adult • Aged • Blood Pressure •
             Catecholamines • Coronary Artery Bypass • Coronary
             Vessels • Dopamine beta-Hydroxylase • Female
             • Hemodynamics • Humans • Hypertension •
             Male • Middle Aged • Nitroprusside • Renin
             • Vascular Resistance • adverse effects* •
             blood • drug therapy • etiology* • pathology
             • therapeutic use},
   Abstract = {Systemic hypertension occurs in more than one third of
             patients having coronary artery bypass graft (CABG)
             operations. This report describes our studies in 100
             consecutive patients undergoing CABG. We found that certain
             preoperative clinical, angiographic, and biochemical factors
             predispose to the development of perioperative hypertension.
             These included a well-documented history of hypertension, an
             elevated blood pressure the day prior to operation, greater
             than 50 percent obstruction of the left main coronary
             artery, and increased levels of dopamine beta hydroxylase
             (DBH). The hemodynamic pattern of perioperative hypertension
             was that of an increased systemic vascular resistance which
             was associated with increased levels of plasma
             catecholamines and plasma renin activity (PRA).
             Nitroprusside was shown to be effective in managing CABG
             hypertension, although other, more specific therapy may be
             preferable.},
   Language = {eng},
   Key = {fds174303}
}

@article{fds132833,
   Author = {RT Engelhardt and GA Johnson},
   Title = {T1 rho relaxation and its application to MR
             histology.},
   Journal = {Magnetic resonance in medicine : official journal of the
             Society of Magnetic Resonance in Medicine / Society of
             Magnetic Resonance in Medicine, UNITED STATES},
   Volume = {35},
   Number = {5},
   Pages = {781-6},
   Year = {1996},
   Month = {May},
   ISSN = {0740-3194},
   Keywords = {Animals • Embryo • Female • Histological
             Techniques • Image Enhancement • Magnetic
             Resonance Imaging • Magnetic Resonance Spectroscopy
             • Mice • Microscopy • Phantoms, Imaging
             • anatomy & histology • diagnostic use •
             instrumentation • methods • methods*},
   Abstract = {The application of T1 rho an an alternative contrast
             parameter in high-field magnetic resonance histology (MRH)
             has been investigated. Spectroscopic measurements of T1 rho
             were performed on 5.75% agar and 1.0 mM MnCI2 phantoms at
             9.4 T to validate the accuracy of the imaging measurements.
             Image studies were performed at 2.0 and 9.4 T on
             perfusion-fixed 17.5-day-old mouse embryos. T1, T2, and T1
             rho relaxation times were calculated for the phantoms and
             muscle, diencephalon, and liver tissues. The 5.75% agar
             phantom and all tissues showed T1 rho dispersion with B1L,
             whereas the 1.0 mM MnCI2 phantom showed no significant B1L
             dependence. T1 rho dispersion with B(O) was observed arising
             from the effects of diffusion through susceptibility-induced
             gradients. T1 rho shows promise as a contrast parameter in
             high-field MRH because it is capable of producing T2-like
             contrast without the susceptibility artifacts associated
             with T2-weighted images.},
   Key = {fds132833}
}

@booklet{Engelhardt96,
   Author = {Engelhardt, RT and Johnson, GA},
   Title = {T1 rho relaxation and its application to MR
             histology.},
   Journal = {Magn Reson Med},
   Volume = {35},
   Number = {5},
   Pages = {781-786},
   Year = {1996},
   Month = {May},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/8722830},
   Abstract = {The application of T1 rho an an alternative contrast
             parameter in high-field magnetic resonance histology (MRH)
             has been investigated. Spectroscopic measurements of T1 rho
             were performed on 5.75% agar and 1.0 mM MnCI2 phantoms at
             9.4 T to validate the accuracy of the imaging measurements.
             Image studies were performed at 2.0 and 9.4 T on
             perfusion-fixed 17.5-day-old mouse embryos. T1, T2, and T1
             rho relaxation times were calculated for the phantoms and
             muscle, diencephalon, and liver tissues. The 5.75% agar
             phantom and all tissues showed T1 rho dispersion with B1L,
             whereas the 1.0 mM MnCI2 phantom showed no significant B1L
             dependence. T1 rho dispersion with B(O) was observed arising
             from the effects of diffusion through susceptibility-induced
             gradients. T1 rho shows promise as a contrast parameter in
             high-field MRH because it is capable of producing T2-like
             contrast without the susceptibility artifacts associated
             with T2-weighted images.},
   Doi = {10.1002/mrm.1910350520},
   Key = {Engelhardt96}
}

@article{fds132847,
   Author = {AC Nugent and GA Johnson},
   Title = {T1rho imaging using magnetization-prepared projection
             encoding (MaPPE).},
   Journal = {Magnetic resonance in medicine : official journal of the
             Society of Magnetic Resonance in Medicine / Society of
             Magnetic Resonance in Medicine, UNITED STATES},
   Volume = {43},
   Number = {3},
   Pages = {421-8},
   Year = {2000},
   Month = {March},
   ISSN = {0740-3194},
   Keywords = {Animals • Image Enhancement • Magnetic Resonance
             Spectroscopy • Magnetics • Mathematics • Mice
             • Phantoms, Imaging • Time Factors •
             methods*},
   Abstract = {T1rho contrast weighting using a magnetization-prepared
             projection encoding (MaPPE) pulse sequence was investigated.
             Fast radial imaging was implemented by applying
             magnetization preparation pulses, each followed by multiple
             RF alpha pulses encoding radial trajectories of k-space.
             Acquiring multiple views per preparatory pulse imposes
             view-to-view variation; the resultant distortion of the
             point-spread function is examined. The issue of maximizing
             signal while preserving the intended contrast weighting is
             addressed. Under modification of repetition time and flip
             angle (alpha), three distinct behavior regimes of the
             sequence are identified. The utility of the pulse sequence
             as a quantitative relaxation measurement tool is also
             examined by comparing imaging and spectroscopy experiments.
             A mouse was imaged in vitro to demonstrate the viability of
             application to MR histology. These images exhibit the
             utility of spinlocking and projection encoding as an
             aftemative contrast source to both T2-weighted MaPPE images
             and conventional T2-weighted spin-echo images.},
   Key = {fds132847}
}

@booklet{Nugent00,
   Author = {Nugent, AC and Johnson, GA},
   Title = {T1rho imaging using magnetization-prepared projection
             encoding (MaPPE).},
   Journal = {Magn Reson Med},
   Volume = {43},
   Number = {3},
   Pages = {421-428},
   Year = {2000},
   Month = {March},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/10725885},
   Abstract = {T1rho contrast weighting using a magnetization-prepared
             projection encoding (MaPPE) pulse sequence was investigated.
             Fast radial imaging was implemented by applying
             magnetization preparation pulses, each followed by multiple
             RF alpha pulses encoding radial trajectories of k-space.
             Acquiring multiple views per preparatory pulse imposes
             view-to-view variation; the resultant distortion of the
             point-spread function is examined. The issue of maximizing
             signal while preserving the intended contrast weighting is
             addressed. Under modification of repetition time and flip
             angle (alpha), three distinct behavior regimes of the
             sequence are identified. The utility of the pulse sequence
             as a quantitative relaxation measurement tool is also
             examined by comparing imaging and spectroscopy experiments.
             A mouse was imaged in vitro to demonstrate the viability of
             application to MR histology. These images exhibit the
             utility of spinlocking and projection encoding as an
             aftemative contrast source to both T2-weighted MaPPE images
             and conventional T2-weighted spin-echo images.},
   Doi = {10.1002/(sici)1522-2594(200003)43:3<421::aid-mrm14>3.0.co;2-},
   Key = {Nugent00}
}

@article{fds357202,
   Author = {Halem, HA and Hochgeschwender, U and Rih, JK and Nelson, R and Johnson,
             GA and Thiagalingam, A and Culler, MD},
   Title = {TBR-760, a Dopamine-Somatostatin Compound, Arrests Growth of
             Aggressive Nonfunctioning Pituitary Adenomas in
             Mice.},
   Journal = {Endocrinology},
   Volume = {161},
   Number = {8},
   Year = {2020},
   Month = {August},
   url = {http://dx.doi.org/10.1210/endocr/bqaa101},
   Abstract = {TBR-760 (formerly BIM-23A760) is a chimeric dopamine
             (DA)-somatostatin (SST) compound with potent agonist
             activity at both DA type 2 (D2R) and SST type 2 (SSTR2)
             receptors. Studies have shown that chimeric DA-SST compounds
             are more efficacious than individual DA and/or SST
             analogues, either alone or combined, in inhibiting secretion
             from primary cultures of human somatotroph and lactotroph
             tumor cells. Nonfunctioning pituitary adenomas (NFPAs)
             express both D2R and SSTR2 and, consequently, may respond to
             TBR-760. We used a mouse model with the pro-opiomelanocortin
             (POMC) gene knocked out that spontaneously develops
             aggressive NFPAs. Genomic microarray and DA and SST receptor
             messenger RNA expression analysis indicate that POMC KO
             mouse tumors and human NFPAs have similar expression
             profiles, despite arising from different cell lineages,
             establishing POMC KO mice as a model for study of NFPAs.
             Treatment with TBR-760 for 8 weeks resulted in nearly
             complete inhibition of established tumor growth, whereas
             tumors from vehicle-treated mice increased in size by 890 ±
             0.7%. Comparing TBR-760 with its individual DA and SST
             components, TBR-760 arrested tumor growth. Treatment with
             equimolar or 10×-higher doses of the individual SST or DA
             agonists, either alone or in combination, had no significant
             effect. One exception was the lower dose of DA agonist that
             induced modest suppression of tumor growth. Only the
             chimeric compound TBR-760 arrested tumor growth in this
             mouse model of NFPA. Further, significant tumor shrinkage
             was observed in 20% of the mice treated with TBR-760. These
             results support the development of TBR-760 as a therapy for
             patients with NFPA.},
   Doi = {10.1210/endocr/bqaa101},
   Key = {fds357202}
}

@article{fds174141,
   Author = {LS Hartt and SJ Carling and MM Joyce and GA Johnson and DK Vanderwall and TL Ott},
   Title = {Temporal and spatial associations of oestrogen receptor
             alpha and progesterone receptor in the endometrium of cyclic
             and early pregnant mares.},
   Journal = {Reproduction (Cambridge, England)},
   Volume = {130},
   Number = {2},
   Pages = {241-50},
   Year = {2005},
   Month = {August},
   ISSN = {1470-1626},
   url = {http://dx.doi.org/10.1530/rep.1.00596},
   Keywords = {Animals • Blotting, Northern • Endometrium •
             Estrogen Receptor alpha • Estrous Cycle • Female
             • Horses • Immunohistochemistry • In Situ
             Hybridization • Pregnancy • Pregnancy, Animal
             • RNA, Messenger • Receptors, Progesterone •
             analysis • analysis* • chemistry* • genetics
             • metabolism* • methods},
   Abstract = {Uterine function is primarily controlled by the combined
             actions of oestrogen and progesterone working through their
             cognate nuclear receptors. The mechanism of establishment of
             pregnancy in the mare is of interest because it involves
             prolonged pre-attachment and conceptus migration phases, and
             both invasive and non-invasive placental cell types, and as
             such has been an important comparative model. This study
             characterised regulation of oestrogen (ER) and progesterone
             (PR) receptors in the endometrium of the mare during the
             oestrous cycle and early pregnancy. Endometrial tissues
             collected during the oestrous cycle and early pregnancy were
             analysed for steady-state levels of ER and PR mRNA and
             protein. Steady-state levels of ER and PR mRNA were highest
             on days 0, 17 and 20 in cyclic mares and lowest on days 11
             and 14. A day-by-status interaction was detected, indicating
             that day 17 and day 20 pregnant mares exhibited low levels
             of ER and PR compared with the corresponding days of the
             oestrous cycle. In situ hybridisation analyses showed
             receptor mRNA localisation primarily in the luminal
             epithelium (LE), glandular epithelium (GE) and stroma around
             oestrus. During dioestrus and early pregnancy, receptors
             were not detected in the LE, and were lower in the stroma
             and deeper GE. Changes in hybridisation intensity in these
             cell types were consistent with changes in mRNA levels
             detected by slot-blot hybridisation. ER and PR proteins were
             detected in the nuclei of LE, GE and stromal cells.
             Consistent with results from in situ hybridisation, levels
             of ER and PR immunoreactivity were higher around oestrus,
             declined to low levels during dioestrus and remained low
             during early pregnancy. Results described here for temporal
             and spatial changes in steroid receptor gene expression in
             mares show the greatest similarities with those described
             for cattle and sheep.},
   Language = {eng},
   Doi = {10.1530/rep.1.00596},
   Key = {fds174141}
}

@booklet{White04,
   Author = {F. J. White and M. M. Joyce and J. B. Hu and T. E. Spencer and R. C. Burghardt and G. A. Johnson},
   Title = {Temporal and spatial expression of uterine osteopontin
             during the murine estrous cycle and pregnancy.},
   Journal = {Biology Of Reproduction},
   Pages = {153 -- 154},
   Year = {2004},
   Key = {White04}
}

@booklet{Hartt02,
   Author = {L. S. Hartt and M. M. Joyce and S. J. Sinor and H. Z. Liu and G. A. Johnson and D. K. Vanderwall and T. L.
             Ott},
   Title = {Temporal and spatial regulation of estrogen receptor a (ER)
             and progesterone receptor (PR) expression in the endometrium
             of nonpregnant and early pregnant mares.},
   Journal = {Biology Of Reproduction},
   Volume = {66},
   Pages = {316 -- 316},
   Year = {2002},
   Key = {Hartt02}
}

@article{fds268790,
   Author = {Johnston, SM and Johnson, GA and Badea, CT},
   Title = {Temporal and spectral imaging with micro-CT.},
   Journal = {Med Phys},
   Volume = {39},
   Number = {8},
   Pages = {4943-4958},
   Year = {2012},
   Month = {August},
   ISSN = {0094-2405},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/22894420},
   Abstract = {PURPOSE: Micro-CT is widely used for small animal imaging in
             preclinical studies of cardiopulmonary disease, but further
             development is needed to improve spatial resolution,
             temporal resolution, and material contrast. We present a
             technique for visualizing the changing distribution of
             iodine in the cardiac cycle with dual source micro-CT.
             METHODS: The approach entails a retrospectively gated dual
             energy scan with optimized filters and voltages, and a
             series of computational operations to reconstruct the data.
             Projection interpolation and five-dimensional bilateral
             filtration (three spatial dimensions + time + energy) are
             used to reduce noise and artifacts associated with
             retrospective gating. We reconstruct separate volumes
             corresponding to different cardiac phases and apply a linear
             transformation to decompose these volumes into components
             representing concentrations of water and iodine. Since the
             resulting material images are still compromised by noise, we
             improve their quality in an iterative process that minimizes
             the discrepancy between the original acquired projections
             and the projections predicted by the reconstructed volumes.
             The values in the voxels of each of the reconstructed
             volumes represent the coefficients of linear combinations of
             basis functions over time and energy. We have implemented
             the reconstruction algorithm on a graphics processing unit
             (GPU) with CUDA. We tested the utility of the technique in
             simulations and applied the technique in an in vivo scan of
             a C57BL∕6 mouse injected with blood pool contrast agent at
             a dose of 0.01 ml∕g body weight. Postreconstruction, at
             each cardiac phase in the iodine images, we segmented the
             left ventricle and computed its volume. Using the maximum
             and minimum volumes in the left ventricle, we calculated the
             stroke volume, the ejection fraction, and the cardiac
             output. RESULTS: Our proposed method produces
             five-dimensional volumetric images that distinguish
             different materials at different points in time, and can be
             used to segment regions containing iodinated blood and
             compute measures of cardiac function. CONCLUSIONS: We
             believe this combined spectral and temporal imaging
             technique will be useful for future studies of
             cardiopulmonary disease in small animals.},
   Doi = {10.1118/1.4736809},
   Key = {fds268790}
}

@booklet{Johnson94,
   Author = {G. A. Johnson and D. M. Tramaglini and R. E. Levine and K.
             Ohno and N. Y. Choi and S. L. Y. Woo},
   Title = {Tensile and viscoelastic properties of human patellar
             tendon},
   Journal = {Journal Of Orthopaedic Research},
   Volume = {12},
   Number = {6},
   Pages = {796 -- 803},
   Year = {1994},
   Month = {November},
   Key = {Johnson94}
}

@article{fds174213,
   Author = {GA Johnson and DM Tramaglini and RE Levine and K Ohno and NY Choi and SL
             Woo},
   Title = {Tensile and viscoelastic properties of human patellar
             tendon.},
   Journal = {Journal of orthopaedic research : official publication of
             the Orthopaedic Research Society},
   Volume = {12},
   Number = {6},
   Pages = {796-803},
   Year = {1994},
   Month = {November},
   ISSN = {0736-0266},
   url = {http://dx.doi.org/10.1002/jor.1100120607},
   Keywords = {Adult • Aged • Aged, 80 and over • Aging
             • Elasticity • Humans • Middle Aged •
             Muscle Contraction* • Muscle Relaxation • Patella
             • Stress, Mechanical • Tendons • Viscosity
             • physiology • physiology*},
   Abstract = {The tensile and viscoelastic properties of fresh-frozen,
             nonirradiated human patellar tendon were investigated in two
             groups of 15 specimens: one group was from individuals 29-50
             years old and the other group was from individuals 64-93
             years old. The central portion of each patella-patellar
             tendon-tibia complex was subjected to cyclic
             preconditioning, stress-relaxation, cyclic
             stress-relaxation, and load to failure tests. For each age
             group, stress-relaxation and stress-strain curves were
             obtained, from which percentage relaxation, ultimate tensile
             strength, strain at failure, modulus, and strain energy
             density were determined. Viscoelastic behavior was described
             with use of quasilinear viscoelasticity. The younger group
             showed a 46 +/- 9% (mean +/- SD) decrease in stress after 15
             minutes, whereas the older group exhibited a 50 +/- 6%
             decrease. The values for ultimate tensile strength and
             strain at failure, respectively, were 64.7 +/- 15.0 MPa and
             14 +/- 6% for the younger group and 53.6 +/- 10.0 MPa and 15
             +/- 5% for the older group. Modulus values were 660 +/- 266
             MPa for the younger group and 504 +/- 222 MPa for the older
             group. Except for ultimate tensile strength, which was 17%
             less for the older group than for the younger one, no
             statistically significant differences were found in tensile
             or viscoelastic properties. This study indicated that there
             were minimal differences in biomechanical properties of the
             substance of the patellar tendon between younger and older
             age groups.},
   Language = {eng},
   Doi = {10.1002/jor.1100120607},
   Key = {fds174213}
}

@booklet{Godwin83,
   Author = {Godwin, JD and Johnson, GA and Fram, EK},
   Title = {Testing electrocardiographically-gated ct of the heart with
             a motion phantom},
   Journal = {Investigative Radiology},
   Volume = {18},
   Number = {4},
   Pages = {S33-S33},
   Year = {1983},
   Key = {Godwin83}
}

@booklet{Kamperschroer89,
   Author = {J. H. Kamperschroer and L. R. Grisham and L. E. Dudek and G.
             M. Gammel and G. A. Johnson and H. W. Kugel and L. Lagin and T. E. Oconnor and P. A. Shah and P. Sichta and T. N.
             Stevenson and A. Vonhalle and M. D. Williams and R.
             Bastasz},
   Title = {Tftr neutral beam injected power measurement},
   Journal = {Review Of Scientific Instruments},
   Volume = {60},
   Number = {11},
   Pages = {3377 -- 3385},
   Year = {1989},
   Month = {November},
   Key = {Kamperschroer89}
}

@booklet{Ravin83,
   Author = {Ravin, CE and Johnson, GA},
   Title = {The 'optimal' chest radiograph},
   Journal = {Seminars in Respiratory Medicine},
   Volume = {5},
   Number = {1},
   Pages = {1-14},
   Publisher = {Georg Thieme Verlag KG},
   Year = {1983},
   Month = {January},
   url = {http://dx.doi.org/10.1055/s-2007-1011430},
   Doi = {10.1055/s-2007-1011430},
   Key = {Ravin83}
}

@article{fds174209,
   Author = {P Luly and GA Johnson and L Bolis and BA Pethica},
   Title = {The agglutination of erythrocytes by calcium phosphate
             sols.},
   Journal = {Biochimica et biophysica acta},
   Volume = {233},
   Number = {3},
   Pages = {730-3},
   Year = {1971},
   Month = {June},
   ISSN = {0006-3002},
   Keywords = {Animals • Calcium Chloride • Calcium Phosphates*
             • Cattle • Chemistry, Physical • Colloids
             • Electrophoresis • Erythrocytes* •
             Hemagglutination • Humans • Phosphates •
             Physicochemical Phenomena • Rats • Salmonidae
             • Sodium • Spectrophotometry},
   Language = {eng},
   Key = {fds174209}
}

@booklet{Macfall94,
   Author = {MacFall, JS and Johnson, GA},
   Title = {The architecture of plant vasculature and transport as seen
             with magnetic resonance microscopy},
   Journal = {Canadian Journal of Botany},
   Volume = {72},
   Number = {11},
   Pages = {1561-1573},
   Publisher = {Canadian Science Publishing},
   Year = {1994},
   Month = {January},
   url = {http://dx.doi.org/10.1139/b94-193},
   Doi = {10.1139/b94-193},
   Key = {Macfall94}
}

@booklet{Gray01a,
   Author = {C. A. Gray and G. A. Johnson and R. C. Burghardt and F. W.
             Bazer and T. E. Spencer},
   Title = {The defect in conceptus elongation in uterine gland knockout
             (UGKO) ewes is due to an absence of endometrial glands, but
             not differences in expression of lumenal epithelial adhesion
             molecules.},
   Journal = {Biology Of Reproduction},
   Volume = {64},
   Pages = {188 -- 188},
   Year = {2001},
   Key = {Gray01a}
}

@article{fds268731,
   Author = {Clark, D and Johnston, SM and Johnson, GA and Badea,
             CT},
   Title = {The effect of scatter correction on dual energy
             micro-CT},
   Journal = {Progress in Biomedical Optics and Imaging - Proceedings of
             SPIE},
   Volume = {8668},
   Publisher = {SPIE},
   Year = {2013},
   Month = {June},
   ISBN = {9780819494429},
   ISSN = {1605-7422},
   url = {http://dx.doi.org/10.1117/12.2006904},
   Abstract = {Dual energy (DE) CT imaging is expected to play a major role
             in the diagnostic arena as it provides a quantitative
             decomposition of basis materials, opening the door for new
             clinical applications without significantly increasing dose
             to the patient. DE-CT provides a particularly unique
             opportunity in preclinical CT where new elemental contrast
             agents are providing novel approaches for quantitative
             tissue characterization. We have implemented DE-CT imaging
             with a preclinical dual source micro-CT scanner. With this
             configuration, both forward and cross-scatter can
             substantially degrade image quality. This work investigated
             the effect of scatter correction on the accuracy of
             post-reconstruction iodine and calcium decomposition.
             Scatter has been estimated using a lead beam stop technique.
             Our approach involves noise reduction in the scatter
             corrected images using bilateral filtering. The scatter
             correction has been quantitatively evaluated using phantom
             experiments and in vivo cancer imaging. As shown by our
             measurements, the dual source scanning is affected more by
             the cross-scatter from the high energy to the low energy
             imaging chain. The scatter correction reduced the presence
             of cupping artifacts and increased both the accuracy and
             precision of dual energy decompositions of calcium and
             iodine. On average, the root mean square errors in
             retrieving true iodine and calcium concentrations via dual
             energy were reduced by 32%. As a result of scatter
             corrections, we expect more accurate quantification of
             important vascular biomarkers such as fractional blood
             volume and vascular permeability in preclinical cancer
             studies. © 2013 SPIE.},
   Doi = {10.1117/12.2006904},
   Key = {fds268731}
}

@booklet{Johnson02f,
   Author = {G. A. Johnson and L. Pipas and N. B. Newman-palmer and L. H.
             Brown},
   Title = {The emergency medicine rotation: A unique experience for
             medical students},
   Journal = {Journal Of Emergency Medicine},
   Volume = {22},
   Number = {3},
   Pages = {307 -- 311},
   Year = {2002},
   Month = {April},
   Key = {Johnson02f}
}

@article{fds174191,
   Author = {GA Johnson and L Pipas and NB Newman-Palmer and LH
             Brown},
   Title = {The emergency medicine rotation: a unique experience for
             medical students.},
   Journal = {The Journal of emergency medicine},
   Volume = {22},
   Number = {3},
   Pages = {307-11},
   Year = {2002},
   Month = {April},
   ISSN = {0736-4679},
   Keywords = {Clinical Clerkship • Curriculum •
             Diagnosis-Related Groups • Emergency Medicine •
             Emergency Service, Hospital • Hospitals, Teaching
             • Humans • Internal Medicine • New York
             • Program Evaluation • Prospective Studies •
             education • education* • methods* •
             statistics & numerical data},
   Abstract = {The objective of this study was to determine if an Emergency
             Medicine (EM) rotation for medical students offers a unique
             educational opportunity, and to document those experiences.
             Thirty-three medical students at one teaching hospital
             recorded in a computer database information about their
             patient encounters during EM and Internal Medicine (IM)
             rotations. Data collected included the types of patients
             seen, the level of participation in patient care and
             decision making, and procedures performed. A total of 2740
             patient encounters were recorded, 1564 EM and 1176 IM.
             Students on EM rotations were more likely than students on
             IM rotations to be involved in the initial evaluation (93.1%
             vs. 47.0%, respectively), diagnosis (93.5% vs. 44.7%,
             respectively), and decision making (93.3% vs. 43.5%,
             respectively); they were also more likely to perform
             procedures (31.7% vs. 8.5%, respectively). There were
             significant differences in the patient populations and
             disease processes encountered on the two rotations as
             well.},
   Language = {eng},
   Key = {fds174191}
}

@booklet{Nielsen94,
   Author = {C. H. Nielsen and G. A. Johnson},
   Title = {The experience of complete neuromuscular blockade in awake
             patients},
   Journal = {Journal Of Clinical Anesthesia},
   Volume = {6},
   Number = {5},
   Pages = {450 -- 450},
   Year = {1994},
   Key = {Nielsen94}
}

@article{fds174162,
   Author = {CH Nielsen and GA Johnson},
   Title = {The experience of complete neuromuscular blockade in awake
             patients.},
   Journal = {Journal of clinical anesthesia},
   Volume = {6},
   Number = {5},
   Pages = {450},
   Year = {1995},
   Month = {January},
   ISSN = {0952-8180},
   Keywords = {Awareness* • Humans • Ketamine • Lung •
             Neuromuscular Blocking Agents • Oxygen •
             Positive-Pressure Respiration • Pulmonary Atelectasis
             • Tidal Volume • administration & dosage •
             administration & dosage* • blood* • chemically
             induced • drug effects • pharmacology •
             physiopathology},
   Language = {eng},
   Key = {fds174162}
}

@booklet{Dockery88,
   Author = {DOCKERY, S and SUDDARTH, SA and COFER, GP and JOHNSON,
             GA},
   Title = {THE IMPACT OF INCREASED SPIN-LATTICE RELAXATION-TIME
             MICROSCOPY AT 7.0T},
   Journal = {INVESTIGATIVE RADIOLOGY},
   Volume = {23},
   Number = {9},
   Pages = {S20-S20},
   Publisher = {LIPPINCOTT-RAVEN PUBL},
   Year = {1988},
   Month = {September},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1988Q574500089&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Dockery88}
}

@article{fds174160,
   Author = {A Banerjee and R Rose and GA Johnson and RC Burghardt and SK
             Ramaiah},
   Title = {The influence of estrogen on hepatobiliary osteopontin
             (SPP1) expression in a female rodent model of alcoholic
             steatohepatitis.},
   Journal = {Toxicologic pathology},
   Volume = {37},
   Number = {4},
   Pages = {492-501},
   Year = {2009},
   ISSN = {1533-1601},
   url = {http://dx.doi.org/10.1177/0192623309335633},
   Keywords = {Alanine Transaminase • Analysis of Variance •
             Animals • Disease Models, Animal • Dose-Response
             Relationship, Drug • Estradiol • Estrous Cycle
             • Ethanol • Fatty Liver, Alcoholic • Female
             • Gene Expression • In Situ Hybridization •
             Liver • Neutrophil Infiltration • Osteopontin
             • Ovariectomy • Rats • Rats, Sprague-Dawley
             • administration & dosage • drug effects •
             genetics • immunology • metabolism •
             metabolism* • pathology • pharmacology •
             pharmacology*},
   Abstract = {Our recent studies suggest that higher neutrophil
             infiltration in females correlates with increased
             hepatobiliary expression of osteopontin (OPN) in alcoholic
             steatohepatitis (ASH). The objective of this study was to
             understand the role of alcohol in altering estrogen levels
             in females by examining the effect of ethanol (EtOH) on the
             estrous cycle and then investigate the potential
             relationship between estradiol (E2) and hepatobiliary OPN
             expression in a female rat ASH model. Ovariectomized (OVX)
             and E2-implanted OVX rats in the ASH group were evaluated
             for OPN mRNA and protein expression. Low doses of E2
             resulted in significant down-regulation of OPN protein and
             mRNA as compared to the OVX group. However, with increasing
             doses of E2, there was up-regulation of both OPN mRNA and
             protein. Osteopontin was localized primarily to the biliary
             epithelium. Liver injury assessed by serum ALT and
             histopathology revealed a pattern similar to OPN expression.
             In all groups, hepatic neutrophilic infiltration correlated
             positively with OPN expression. Based on these data, we
             conclude that in our ASH model, low doses of E2 appear to be
             hepatoprotective, whereas the protective effect appears to
             diminish with increasing doses of E2, although additional
             cause and effect studies are needed for confirmation.},
   Language = {eng},
   Doi = {10.1177/0192623309335633},
   Key = {fds174160}
}

@booklet{Johnson02c,
   Author = {G. A. Johnson and M. M. Joyce and S. J. Yankey and T. R.
             Hansen and T. L. Ott},
   Title = {The interferon stimulated genes (ISG) 17 and Mx have
             different temporal and spatial expression in the ovine
             uterus suggesting more complex regulation of the Mx
             gene},
   Journal = {Journal Of Endocrinology},
   Volume = {174},
   Number = {2},
   Year = {2002},
   Month = {August},
   Key = {Johnson02c}
}

@article{fds174163,
   Author = {GA Johnson and MM Joyce and SJ Yankey and TR Hansen and TL
             Ott},
   Title = {The Interferon Stimulated Genes (ISG) 17 and Mx have
             different temporal and spatial expression in the ovine
             uterus suggesting more complex regulation of the Mx
             gene.},
   Journal = {The Journal of endocrinology},
   Volume = {174},
   Number = {2},
   Pages = {R7-R11},
   Year = {2002},
   Month = {August},
   ISSN = {0022-0795},
   Keywords = {Animals • Estrous Cycle • Female •
             GTP-Binding Proteins* • Gene Expression Regulation
             • Gestational Age • Immunohistochemistry • In
             Situ Hybridization • Pregnancy • Pregnancy
             Proteins • Pregnancy, Animal • Proteins •
             RNA, Messenger • Random Allocation • Sheep •
             Uterus • analysis* • chemistry* • genetics*
             • metabolism* • methods},
   Abstract = {Interferon stimulated gene 17 (ISG17) and Mx are
             up-regulated in the ruminant uterus in response to
             interferon-tau (IFNtau) during early pregnancy. Recent
             evidence strongly indicates that expression of ISGs occur
             only in stroma (ST) and glandular epithelium (GE) during
             this time as a result of transcriptional repression by
             interferon regulatory factor two (IRF-2) expression in the
             LE. The present report tested this hypothesis by examining
             mRNA and protein expression of ISG17 and Mx in serial
             uterine cross-sections obtained from cyclic and early
             pregnant ewes. In situ and immunocytochemical analysis
             revealed that ISG17 mRNA and protein were low to
             undetectable, whereas Mx mRNA was expressed in the lumenal
             (LE) and superficial GE at all days of the estrous cycle
             examined. Both ISG17 and Mx mRNA increased in the stratum
             compactum ST between Days 11 and 13, and expression extended
             into the deep GE and stratum spongiosum ST on Days 15
             through 17 in pregnant ewes. Interestingly the Mx gene
             continued to be strongly expressed in LE and superficial GE
             through Day 17 of pregnancy, whereas ISG17 remained low to
             undetectable in these cells. Collectively, this study
             highlights the complexity of the uterine environment by
             unequivocally illustrating differential temporal and spatial
             expression of the IFN-responsive genes ISG17 and
             Mx.},
   Language = {eng},
   Key = {fds174163}
}

@article{fds174232,
   Author = {GA Johnson},
   Title = {The interview workshop.},
   Journal = {Journal of medical education},
   Volume = {49},
   Number = {1},
   Pages = {75-7},
   Year = {1974},
   Month = {January},
   ISSN = {0022-2577},
   Keywords = {Education, Continuing* • Family Practice • Female
             • Humans • Interview, Psychological* • Male
             • Michigan • Minority Groups • Primary Health
             Care • Rural Population • Schools, Medical* •
             Social Problems • Students, Medical • Videotape
             Recording},
   Language = {eng},
   Key = {fds174232}
}

@article{fds174272,
   Author = {GA Johnson and KG Alberti},
   Title = {The metabolic effects of sodium dichloroacetate in
             experimental hepatitis in the rat [proceedings]},
   Journal = {Biochemical Society transactions},
   Volume = {5},
   Number = {5},
   Pages = {1387-9},
   Year = {1977},
   ISSN = {0300-5127},
   Keywords = {Acetic Acids • Animals • Blood Glucose •
             Dichloroacetate • Fructose • Galactosamine •
             Hepatitis, Animal • Ketone Bodies • Lactates
             • Rats • blood • blood* • metabolism
             • pharmacology • pharmacology*},
   Language = {eng},
   Key = {fds174272}
}

@booklet{Cardina97,
   Author = {J. Cardina and G. A. Johnson and D. H. Sparrow},
   Title = {The nature and consequence of weed spatial
             distribution},
   Journal = {Weed Science},
   Volume = {45},
   Number = {3},
   Pages = {364 -- 373},
   Year = {1997},
   Key = {Cardina97}
}

@booklet{Diani91,
   Author = {A. R. Diani and D. J. Waldon and S. J. Conrad and M. J.
             Mulholland and K. L. Shull and M. F. Kubicek and G. A.
             Johnson and M. N. Brunden and A. E. Buhl},
   Title = {The opening of potassium channels - a mechanism for
             hair-growth},
   Journal = {Annals Of The New York Academy Of Sciences},
   Volume = {642},
   Pages = {504 -- 504},
   Year = {1991},
   Month = {December},
   Key = {Diani91}
}

@article{fds174199,
   Author = {GA Johnson and DW Baldridge},
   Title = {The orthodontic gospel according to Begg.},
   Journal = {Journal of the Louisiana Dental Association},
   Volume = {24},
   Number = {1},
   Pages = {5-8},
   Year = {1966},
   ISSN = {0024-6786},
   Keywords = {Dentistry • Orthodontics, Corrective},
   Language = {eng},
   Key = {fds174199}
}

@booklet{Burvill96,
   Author = {P. W. Burvill and G. A. Johnson and T. M. H. Chakera and E.
             G. Stewartwynne and C. S. Anderson and K. D.
             Jamrozik},
   Title = {The place of site of lesion in the aetiology of post-stroke
             depression},
   Journal = {Cerebrovascular Diseases},
   Volume = {6},
   Number = {4},
   Pages = {208 -- 215},
   Year = {1996},
   Key = {Burvill96}
}

@article{fds174069,
   Author = {GA Johnson and WR Copeland and AE Kimberly},
   Title = {The Relative Applicability of Current Methods for the
             Determination of Putrescibility in Sewage
             Effluents.},
   Journal = {Public health papers and reports},
   Volume = {31},
   Number = {Pt 2},
   Pages = {80-96},
   Year = {1905},
   Language = {ENG},
   Key = {fds174069}
}

@article{fds174197,
   Author = {GA Johnson and WR Copeland and AE Kimberly},
   Title = {The Relative Applicability of Current Methods for the
             Determination of Putrescibility in Sewage
             Effluents.},
   Journal = {Public health papers and reports},
   Volume = {31},
   Number = {Pt 2},
   Pages = {80-96},
   Year = {1905},
   ISSN = {0737-8769},
   Language = {eng},
   Key = {fds174197}
}

@article{fds174154,
   Author = {HE Williams and GA Johnson and LH Smith Jr},
   Title = {The renal clearance of oxalate in normal subjects and
             patients with primary hyperoxaluria.},
   Journal = {Clinical science},
   Volume = {41},
   Number = {3},
   Pages = {213-8},
   Year = {1971},
   Month = {September},
   ISSN = {0009-9287},
   Keywords = {Adult • Carbon Isotopes • Creatinine • Humans
             • Kidney • Male • Metabolism, Inborn Errors
             • Oxalates • blood • metabolism •
             metabolism* • urine*},
   Language = {eng},
   Key = {fds174154}
}

@article{fds174156,
   Author = {KA Dunlap and HI Kwak and RC Burghardt and FW Bazer and RR Magness and GA
             Johnson, KJ Bayless},
   Title = {The sphingosine 1-phosphate (S1P) signaling pathway is
             regulated during pregnancy in sheep.},
   Journal = {Biology of reproduction},
   Volume = {82},
   Number = {5},
   Pages = {876-87},
   Year = {2010},
   Month = {May},
   ISSN = {1529-7268},
   url = {http://dx.doi.org/10.1095/biolreprod.109.081604},
   Abstract = {Because sphingosine 1-phosphate (S1P) is a potent stimulator
             of angiogenesis, we hypothesized that the S1P pathway is
             activated to stimulate endometrial/placental angiogenesis
             during pregnancy. We initially localized S1P signaling
             pathway members in the gravid and nongravid uterine horns of
             unilaterally pregnant ewes. Sphingosine kinase-1 expression
             was greater in gravid compared to nongravid horns. In situ
             hybridization revealed elevated expression of sphingosine
             1-phosphate phosphatase (SGPP1) in gravid interplacentomal
             endometrial stroma on Days 20 and 40 compared to the
             nongravid uterine horn, but expression increased in
             endometrium of the nongravid uterine horn between Days 40
             and 120. SGPP1 expression increased in placentomes late in
             gestation. Sphingosine 1-phosphate lyase mRNA was modestly
             expressed at Day 20 and then decreased. In contrast,
             sphingosine 1-phosphate receptor 1 (S1PR1) mRNA increased in
             endometrium and caruncular stroma of the gravid uterine
             horn. Treatment with FTY720 and VPC23019, S1P receptor
             antagonists, blocked human and ovine endothelial cell
             invasion using an in vitro model of sprouting angiogenesis.
             Knockdown of S1PR1 with siRNA reduced invasion responses as
             well. We previously reported that delta-like 4 (DLL4) and A
             disintegrin and metalloproteinase with thrombospondin-like
             repeats 1 (ADAMTS1) participate in endothelial cell invasion
             stimulated by S1P and growth factors in vitro, and thus
             investigated whether their expression correlated with areas
             undergoing angiogenesis in vivo. DLL4 expression was similar
             to S1PR1, while ADAMTS1 mRNA was expressed by endometria of
             both nongravid and gravid horns, as well as conceptus and
             placentomes. These results establish that S1P signaling
             pathway members and S1P- and growth factor-regulated genes
             are prominent in uterine and placental tissue and in some
             cases are correlated with areas undergoing angiogenesis.
             Thus, S1P signaling may be crucial for proper
             fetal-placental development.},
   Language = {eng},
   Doi = {10.1095/biolreprod.109.081604},
   Key = {fds174156}
}

@booklet{Johnson95,
   Author = {G. A. Johnson and D. A. Mortensen and L. J. Young and A. R.
             Martin},
   Title = {The stability of weed seedling population-models and
             parameters in eastern nebraska corn (zea-mays) and soybean
             (glycine-max) fields},
   Journal = {Weed Science},
   Volume = {43},
   Number = {4},
   Pages = {604 -- 611},
   Year = {1995},
   Key = {Johnson95}
}

@article{fds174251,
   Author = {A Banerjee and RC Burghardt and GA Johnson and FJ White and SK
             Ramaiah},
   Title = {The temporal expression of osteopontin (SPP-1) in the rodent
             model of alcoholic steatohepatitis: a potential
             biomarker.},
   Journal = {Toxicologic pathology},
   Volume = {34},
   Number = {4},
   Pages = {373-84},
   Year = {2006},
   ISSN = {0192-6233},
   url = {http://dx.doi.org/10.1080/01926230600806543},
   Keywords = {Alanine Transaminase • Animals • Aspartate
             Aminotransferases • Biological Markers • Disease
             Models, Animal • Fatty Liver, Alcoholic • Gene
             Expression • Immunohistochemistry • In Situ
             Hybridization • Inflammation • Lipopolysaccharides
             • Liver Function Tests • Male • Neutrophil
             Infiltration • Osteopontin • RNA, Messenger •
             Rats • Rats, Sprague-Dawley • Sialoglycoproteins
             • Time Factors • blood • chemically induced
             • drug effects • etiology • genetics •
             metabolism • metabolism* • pathology •
             pathology* • pharmacology},
   Abstract = {Previous studies from our laboratory have shown that
             osteopontin (OPN) mediates neutrophil infiltration into the
             liver in a rodent model of alcoholic steatohepatitis (ASH).
             The objective of this study was to investigate the temporal
             and spatial pattern of hepatic OPN mRNA and protein
             expression during the progression of alcoholic liver
             disease. OPN mRNA and protein expression were evaluated
             using real time PCR, in situ hybridization, Western blot and
             immunohistochemistry respectively. ASH was induced in male
             Sprague-Dawley rats by feeding EtOH-containing
             Lieber-DeCarli diet for 6 weeks, followed by a single
             injection of lipopolysaccharide (LPS, 10 mg/kg, ip). Rats
             were sacrificed 2-, 12-and 24-hour post LPS injection. A
             progressive induction of OPN mRNA was observed that preceded
             hepatic neutrophil infiltration and the increase in OPN mRNA
             correlated with increases in OPN protein expression. OPN
             mRNA was localized primarily to the biliary epithelium. The
             data indicates that OPN is transcribed and translated within
             the biliary epithelium. These findings suggest a potential
             role of OPN as an early biomarker in predicting inflammatory
             liver diseases such as ASH.},
   Language = {eng},
   Doi = {10.1080/01926230600806543},
   Key = {fds174251}
}

@article{fds174099,
   Author = {AH Fishel and GA Johnson},
   Title = {The three-way conference -- nursing student, nursing
             supervisor and nursing educator.},
   Journal = {The Journal of nursing education},
   Volume = {20},
   Number = {6},
   Pages = {18-23},
   Year = {1981},
   Month = {June},
   ISSN = {0148-4834},
   Keywords = {Communication* • Education, Nursing, Baccalaureate*
             • Humans • Interpersonal Relations • Nursing,
             Supervisory* • Psychiatric Nursing • Students,
             Nursing* • Teaching* • education},
   Language = {eng},
   Key = {fds174099}
}

@article{fds132760,
   Author = {JH Maki, JR MacFall and GA Johnson},
   Title = {The use of gradient flow compensation to separate diffusion
             and microcirculatory flow in MRI.},
   Journal = {Magnetic resonance in medicine : official journal of the
             Society of Magnetic Resonance in Medicine / Society of
             Magnetic Resonance in Medicine, UNITED STATES},
   Volume = {17},
   Number = {1},
   Pages = {95-107},
   Year = {1991},
   Month = {January},
   ISSN = {0740-3194},
   Keywords = {Acetone • Animals • Brain • Dextrans •
             Diffusion • Edetic Acid • Female • Gadolinium
             • Gels • Image Enhancement • Magnetic
             Resonance Imaging • Microcirculation • Models,
             Biological • Models, Structural • Rats •
             Rats, Inbred F344 • Reproducibility of Results •
             Rheology • Water • blood supply • chemistry
             • instrumentation • methods* •
             physiology*},
   Abstract = {This paper describes a new MR imaging technique termed
             Modified Stejskal Tanner versus Flow Compensation (MST/FC)
             for the separation of diffusion and microcirculatory flow.
             The theory behind the sequence is explained, along with a
             five-component model of microcirculation applicable to any
             "perfusion" imaging technique. Phantom data is presented
             showing that (1) diffusion effects can be matched between
             MST and FC (suggesting the possibility of flow-compensated
             diffusion imaging), and (2) the technique is a quantitative
             method of separating diffusion and slow (less than 0.25
             mm/s) tortuous flow through a Sephadex column. Furthermore,
             animal images show the technique to be feasible and
             quantitative in measuring rat brain microcirculation under
             normal, vasodilated (hypercarbia), and no-flow (post mortem)
             conditions.},
   Key = {fds132760}
}

@booklet{Maki91b,
   Author = {Maki, JH and MacFall, JR and Johnson, GA},
   Title = {The use of gradient flow compensation to separate diffusion
             and microcirculatory flow in MRI.},
   Journal = {Magn Reson Med},
   Volume = {17},
   Number = {1},
   Pages = {95-107},
   Year = {1991},
   Month = {January},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/1712421},
   Abstract = {This paper describes a new MR imaging technique termed
             Modified Stejskal Tanner versus Flow Compensation (MST/FC)
             for the separation of diffusion and microcirculatory flow.
             The theory behind the sequence is explained, along with a
             five-component model of microcirculation applicable to any
             "perfusion" imaging technique. Phantom data is presented
             showing that (1) diffusion effects can be matched between
             MST and FC (suggesting the possibility of flow-compensated
             diffusion imaging), and (2) the technique is a quantitative
             method of separating diffusion and slow (less than 0.25
             mm/s) tortuous flow through a Sephadex column. Furthermore,
             animal images show the technique to be feasible and
             quantitative in measuring rat brain microcirculation under
             normal, vasodilated (hypercarbia), and no-flow (post mortem)
             conditions.},
   Doi = {10.1002/mrm.1910170114},
   Key = {Maki91b}
}

@article{fds268740,
   Author = {Pandit, P and Johnston, SM and Qi, Y and Story, J and Nelson, R and Johnson, GA},
   Title = {The utility of micro-CT and MRI in the assessment of
             longitudinal growth of liver metastases in a preclinical
             model of colon carcinoma.},
   Journal = {Acad Radiol},
   Volume = {20},
   Number = {4},
   Pages = {430-439},
   Year = {2013},
   Month = {April},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/23498983},
   Abstract = {RATIONALE AND OBJECTIVES: Liver is a common site for distal
             metastases in colon and rectal cancer. Numerous clinical
             studies have analyzed the relative merits of different
             imaging modalities for detection of liver metastases.
             Several exciting new therapies are being investigated in
             preclinical models. But, technical challenges in preclinical
             imaging make it difficult to translate conclusions from
             clinical studies to the preclinical environment. This study
             addresses the technical challenges of preclinical magnetic
             resonance imaging (MRI) and micro-computed tomography (CT)
             to enable comparison of state-of-the-art methods for
             following metastatic liver disease. MATERIALS AND METHODS:
             We optimized two promising preclinical protocols to enable a
             parallel longitudinal study tracking metastatic human colon
             carcinoma growth in a mouse model: T2-weighted MRI using
             two-shot PROPELLER (Periodically Rotated Overlapping
             ParallEL Lines with Enhanced Reconstruction) and
             contrast-enhanced micro-CT using a liposomal contrast agent.
             Both methods were tailored for high throughput with
             attention to animal support and anesthesia to limit
             biological stress. RESULTS AND CONCLUSIONS: Each modality
             has its strengths. Micro-CT permitted more rapid acquisition
             (<10 minutes) with the highest spatial resolution (88-micron
             isotropic resolution). But detection of metastatic lesions
             requires the use of a blood pool contrast agent, which could
             introduce a confound in the evaluation of new therapies. MRI
             was slower (30 minutes) and had lower anisotropic spatial
             resolution. But MRI eliminates the need for a contrast agent
             and the contrast-to-noise between tumor and normal
             parenchyma was higher, making earlier detection of small
             lesions possible. Both methods supported a relatively
             high-throughput, longitudinal study of the development of
             metastatic lesions.},
   Doi = {10.1016/j.acra.2012.09.030},
   Key = {fds268740}
}

@booklet{Mellin94,
   Author = {Mellin, AF and Cofer, GP and Smith, BR and Suddarth, SA and Hedlund, LW and Johnson, GA},
   Title = {Three dimensional magnetic resonance microangiography of rat
             neurovasculature.},
   Journal = {Magn Reson Med},
   Volume = {32},
   Number = {2},
   Pages = {199-205},
   Year = {1994},
   Month = {August},
   ISSN = {0740-3194},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1994NZ79300007&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Abstract = {Techniques are described to perform three dimensional (3D)
             MR microangiography. We have combined the use of a blood
             pool agent (Gd-DTPA-complexed with bovine serum albumin),
             three dimensional Fourier encoding, careful animal
             stabilization, and volume rendering to permit imaging with
             voxels of 60 x 60 x 60 microns. 3DFT encoding has been
             performed at 7.1 T with very large arrays (256 x 512 x 512).
             Interactive volume rendering allows a number of unique
             display opportunities that effectively exploit these
             isotropic 3D arrays.},
   Doi = {10.1002/mrm.1910320208},
   Key = {Mellin94}
}

@booklet{Stern89,
   Author = {Stern, RL and Cline, HE and Johnson, GA and Ravin,
             CE},
   Title = {Three-dimensional imaging of the thoracic
             cavity.},
   Journal = {Invest Radiol},
   Volume = {24},
   Number = {4},
   Pages = {282-288},
   Year = {1989},
   Month = {April},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1989U232200004&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Abstract = {Three-dimensional (3D) surface reconstruction techniques
             were applied to sets of computed tomographic (CT) images of
             the thoracic cavity. Emphasis was placed on extracting lung
             images. High quality, detailed 3D images of the lung surface
             and internal bronchial and vascular structures were
             produced.},
   Doi = {10.1097/00004424-198904000-00005},
   Key = {Stern89}
}

@article{9082523,
   Author = {Oldham, M. and Sakhalkar, H. and Oliver, T. and Ying Min
             Wang and Kirpatrick, J. and Yiting Cao and Badea, C. and Johnson, G.A. and Dewhirst, M.},
   Title = {Three-dimensional imaging of xenograft tumors using optical
             computed and emission tomography},
   Journal = {Med. Phys. (USA)},
   Volume = {33},
   Number = {9},
   Pages = {3193 - 202},
   url = {http://dx.doi.org/10.1118/1.2217109},
   Keywords = {bio-optics;biomedical optical imaging;cancer;cellular
             biophysics;computerised tomography;image
             reconstruction;proteins;tumours;},
   Abstract = {The physical basis and preliminary applications of optical
             computed tomography (optical-CT) and optical emission
             computed tomography (optical-ECT) are introduced, as new
             techniques with potential to provide unique 3D information
             on a variety of aspects of tumor structure and function. A
             particular focus here is imaging tumor micro-vasculature,
             and the spatial distribution of viable tumor cells, although
             the techniques have the potential for much wider
             application. The principle attractiveness of optical-CT and
             optical-ECT are that high resolution (&lt;20 &mu;m) and high
             contrast co-registered 3D images of structure and function
             can be acquired for relatively large intact samples. The
             unique combination of high contrast and resolution offers
             advantages over micro-CT and micro-MRI, and the lack of
             requirement for sectioning offers advantages over confocal
             microscopy, conventional microscopy, and histological
             sectioning techniques. Optical-CT/ECT are implemented using
             in-house custom apparatus and a commercial dissecting
             microscope capable of both transmission and fluorescence
             imaging. Basic studies to characterize imaging performance
             are presented. Negligible geometrical distortion and
             accurate reconstruction of relative attenuation coefficients
             was observed. Optical-CT and optical-ECT are investigated
             here by application to high resolution imaging of HCT116
             xenograft tumors, about 1 cc in dimension, which were
             transfected with constitutive red fluorescent protein (RFP).
             Tumor microvasculature was stained in vivo by tail vein
             injection of either passive absorbing dyes or active
             fluorescent markers (FITC conjugated lectin). Prior to
             imaging, the tumors were removed (ex vivo) and optically
             cleared in a key process to make the samples amenable to
             light transmission. The cleared tumors were imaged in three
             modes (i) optical-CT to image the 3D distribution of
             microvasculature as indicated by absorbing dye, (ii)
             optical-ECT using the FITC excitation and emission filter
             set, to determine microvasculature as indicated by
             lectin-endothelial binding, and (iii) optical-ECT using the
             DSRed2 filter set to determine the 3D distribution of viable
             tumor as indicated by RFP emission. A clear correlation was
             observed between the independent vasculature imaging modes
             (i) and (ii) and postimaging histological sections,
             providing substantial validation of the optical-CT and
             optical-ECT techniques. Strong correlation was also observed
             between the RFP imaging of mode iii, and modes i and ii,
             supporting the intuitive conclusion that well-perfused
             regions contain significant viable tumor. In summary,
             optical-CT and optical-ECT, when combined with new optical
             clearing techniques, represent powerful new imaging
             modalities with potential for providing unique information
             on the structure and function of tumors},
   Key = {9082523}
}

@article{fds268877,
   Author = {Oldham, M and Sakhalkar, H and Oliver, T and Wang, YM and Kirpatrick, J and Cao, Y and Badea, C and Johnson, GA and Dewhirst,
             M},
   Title = {Three-dimensional imaging of xenograft tumors using optical
             computed and emission tomography.},
   Journal = {Med Phys},
   Volume = {33},
   Number = {9},
   Pages = {3193-3202},
   Year = {2006},
   Month = {September},
   ISSN = {0094-2405},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/17022212},
   Keywords = {Animals • Cell Line, Tumor • Colonic Neoplasms
             • Humans • Image Enhancement • Image
             Interpretation, Computer-Assisted • Imaging,
             Three-Dimensional • Mice • Microscopy •
             Reproducibility of Results • Sensitivity and
             Specificity • Subtraction Technique* • Tomography,
             Emission-Computed, Single-Photon • Tomography, Optical
             • Tomography, X-Ray Computed • instrumentation
             • methods* • pathology*},
   Abstract = {The physical basis and preliminary applications of optical
             computed tomography (optical-CT) and optical emission
             computed tomography (optical-ECT) are introduced, as new
             techniques with potential to provide unique 3D information
             on a variety of aspects of tumor structure and function. A
             particular focus here is imaging tumor micro-vasculature,
             and the spatial distribution of viable tumor cells, although
             the techniques have the potential for much wider
             application. The principle attractiveness of optical-CT and
             optical-ECT are that high resolution (<20 microm) and high
             contrast co-registered 3D images of structure and function
             can be acquired for relatively large intact samples. The
             unique combination of high contrast and resolution offers
             advantages over micro-CT and micro-MRI, and the lack of
             requirement for sectioning offers advantages over confocal
             microscopy, conventional microscopy, and histological
             sectioning techniques. Optical-CT/ECT are implemented using
             in-house custom apparatus and a commercial dissecting
             microscope capable of both transmission and fluorescence
             imaging. Basic studies to characterize imaging performance
             are presented. Negligible geometrical distortion and
             accurate reconstruction of relative attenuation coefficients
             was observed. Optical-CT and optical-ECT are investigated
             here by application to high resolution imaging of HCT116
             xenograft tumors, about 1 cc in dimension, which were
             transfected with constitutive red fluorescent protein (RFP).
             Tumor microvasculature was stained in vivo by tail vein
             injection of either passive absorbing dyes or active
             fluorescent markers (FITC conjugated lectin). Prior to
             imaging, the tumors were removed (ex vivo) and optically
             cleared in a key process to make the samples amenable to
             light transmission. The cleared tumors were imaged in three
             modes (i) optical-CT to image the 3D distribution of
             microvasculature as indicated by absorbing dye, (ii)
             optical-ECT using the FITC excitation and emission filter
             set, to determine microvasculature as indicated by
             lectin-endothelial binding, and (iii) optical-ECT using the
             DSRed2 filter set to determine the 3D distribution of viable
             tumor as indicated by RFP emission. A clear correlation was
             observed between the independent vasculature imaging modes
             (i) and (ii) and postimaging histological sections,
             providing substantial validation of the optical-CT and
             optical-ECT techniques. Strong correlation was also observed
             between the RFP imaging of mode iii, and modes i and ii,
             supporting the intuitive conclusion that well-perfused
             regions contain significant viable tumor. In summary,
             optical-CT and optical-ECT, when combined with new optical
             clearing techniques, represent powerful new imaging
             modalities with potential for providing unique information
             on the structure and function of tumors.},
   Doi = {10.1118/1.2217109},
   Key = {fds268877}
}

@booklet{Bone86,
   Author = {Bone, SN and Johnson, GA and Thompson, MB},
   Title = {Three-dimensional magnetic resonance microscopy of the
             developing chick embryo.},
   Journal = {Invest Radiol},
   Volume = {21},
   Number = {10},
   Pages = {782-787},
   Year = {1986},
   Month = {October},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1986E347800003&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Abstract = {Magnetic resonance imaging microscopy was performed on live
             chick embryos. A combination of high gradient strength (0.47
             mT/cm), special purpose radiofrequency coils and
             3-dimensional Fourier imaging was used to obtain images with
             effective thickness of 1.25 mm and pixel dimensions as small
             as 200 mu in the live chick embryo. The signal-to-noise
             ratio was sufficient to allow unequivocal identification of
             the individual chambers of the heart, spinal cord,
             ventricles in the brain, and vascular structures in the
             liver of a live 11-day embryo. Anatomical assignment was
             accomplished with the aid of correlated histologic sections.
             Because there are no external landmarks, the plane of
             imaging is frequently oblique, making the 3-dimensional
             acquisition particularly useful.},
   Doi = {10.1097/00004424-198610000-00003},
   Key = {Bone86}
}

@booklet{Suddarth91,
   Author = {Suddarth, SA and Johnson, GA},
   Title = {Three-dimensional MR microscopy with large
             arrays.},
   Journal = {Magn Reson Med},
   Volume = {18},
   Number = {1},
   Pages = {132-141},
   Year = {1991},
   Month = {March},
   ISSN = {0740-3194},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1991EZ54700013&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Abstract = {MR microscopy of fixed specimens is described using large
             (256(3] arrays. Images are acquired at 7.0 T with voxels as
             small as 70 x 70 x 70 microns (3.4 x 10(-4) mm3), more than
             25,000 times smaller than routine clinical body imaging.
             Separation of the acquisition, reconstruction, archival, and
             analysis onto networked workstations provides flexibility
             and efficiency in handling the large data sets. The
             isotropic data can be interactively displayed through any
             plane without loss of in-plane resolution. The potential for
             applications of MR microscopy in clinical pathology is
             addressed.},
   Doi = {10.1002/mrm.1910180114},
   Key = {Suddarth91}
}

@booklet{Johnson87e,
   Author = {Johnson, GA and Thompson, MB and Drayer, BP},
   Title = {Three-dimensional MRI microscopy of the normal rat
             brain.},
   Journal = {Magn Reson Med},
   Volume = {4},
   Number = {4},
   Pages = {351-365},
   Year = {1987},
   Month = {April},
   ISSN = {0740-3194},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1987G775900005&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Abstract = {Magnetic resonance imaging techniques have been developed to
             enable imaging of the live rat brain with thin (1.2-mm)
             slices and microscopic pixels (115 X 115 microns).
             Signal-to-noise ratios high enough to realize the
             microscopic resolution are obtained with rf coils designed
             for the subject and through the use of three-dimensional
             Fourier spin warp imaging. The technique yields 16
             contiguous slices. Correlation with fixed pathologic
             specimens enables unequivocal identification of gray and
             white matter structures in the brain of a live 200-g rat.
             Structures clearly visible in the MR images include Ammon's
             horn, the hypothalamus, corpus callosum and substantia
             nigra, as well as a number of brainstem nuclei.},
   Doi = {10.1002/mrm.1910040406},
   Key = {Johnson87e}
}

@article{fds268835,
   Author = {Zhang, X and Badea, CT and Johnson, GA},
   Title = {Three-dimensional reconstruction in free-space whole-body
             fluorescence tomography of mice using optically
             reconstructed surface and atlas anatomy.},
   Journal = {J Biomed Opt},
   Volume = {14},
   Number = {6},
   Pages = {064010},
   Year = {2009},
   ISSN = {1560-2281},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/20059248},
   Keywords = {Algorithms* • Animals • Image Processing,
             Computer-Assisted • Imaging, Three-Dimensional •
             Mice • Mice, Nude • Phantoms, Imaging •
             Spectrometry, Fluorescence • Thermography •
             Tomography • Whole Body Imaging • X-Ray
             Microtomography • methods • methods*},
   Abstract = {We present a 3-D image reconstruction method for free-space
             fluorescence tomography of mice using hybrid anatomical
             prior information. Specifically, we use an optically
             reconstructed surface of the experimental animal and a
             digital mouse atlas to approximate the anatomy of the animal
             as structural priors to assist image reconstruction.
             Experiments are carried out on a cadaver of a nude mouse
             with a fluorescent inclusion (2.4-mm-diam cylinder)
             implanted in the chest cavity. Tomographic fluorescence
             images are reconstructed using an iterative algorithm based
             on a finite element method. Coregistration of the
             fluorescence reconstruction and micro-CT (computed
             tomography) data acquired afterward show good localization
             accuracy (localization error 1.2+/-0.6 mm). Using the
             optically reconstructed surface, but without the atlas
             anatomy, image reconstruction fails to show the fluorescent
             inclusion correctly. The method demonstrates the utility of
             anatomical priors in support of free-space fluorescence
             tomography.},
   Language = {eng},
   Doi = {10.1117/1.3258836},
   Key = {fds268835}
}

@booklet{Johnson81c,
   Author = {G. A. Johnson and J. J. Mcnamara},
   Title = {Thromboxane-a2 - a vital mediator in the acute response to
             hemorrhage},
   Journal = {Circulation},
   Volume = {64},
   Number = {4},
   Pages = {290 -- 290},
   Year = {1981},
   Key = {Johnson81c}
}

@booklet{Sostman85,
   Author = {Sostman, HD and Gore, JC and Flye, MW and Johnson, GA and Herfkens,
             RJ},
   Title = {Time course and mechanism of alterations in proton
             relaxation during liver regeneration in the
             rat.},
   Journal = {Hepatology},
   Volume = {5},
   Number = {4},
   Pages = {538-543},
   Year = {1985},
   ISSN = {0270-9139},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/2991104},
   Abstract = {We studied the proton T1 and T2, water and lipid content of
             regenerating rat liver from 1 to 7 days after 70%
             hepatectomy. Liver from normal and sham-operated animals and
             splenic tissue from all animals were studied as controls. In
             vivo proton spectroscopy and imaging of liver was performed
             in a separate group of control and posthepatectomy rats. The
             T2 of regenerating liver, but not of sham or normal control
             liver, was prolonged. Changes in T1, relative to normal
             tissue, were found in liver and spleen of both operated
             groups. Lipid content, assessed both by extraction of tissue
             samples and by in vivo spectroscopy, was increased in
             regenerating tissue but not in controls. Water content was
             similarly increased in regenerating liver tissue. Changes in
             water and lipid content appeared to contribute to the
             alterations in proton relaxation which we
             observed.},
   Doi = {10.1002/hep.1840050403},
   Key = {Sostman85}
}

@article{fds132783,
   Author = {HD Sostman and JC Gore and MW Flye and GA Johnson and RJ
             Herfkens},
   Title = {Time course and mechanism of alterations in proton
             relaxation during liver regeneration in the
             rat.},
   Journal = {Hepatology (Baltimore, Md.), UNITED STATES},
   Volume = {5},
   Number = {4},
   Pages = {538-43},
   ISSN = {0270-9139},
   Keywords = {Animals • Body Water • Lipids • Liver •
             Liver Regeneration* • Magnetic Resonance Spectroscopy
             • Male • Protons • Rats • Rats, Inbred
             Strains • Spectrum Analysis • Spleen • Time
             Factors • analysis • anatomy & histology •
             anatomy & histology* • diagnostic use* •
             methods},
   Abstract = {We studied the proton T1 and T2, water and lipid content of
             regenerating rat liver from 1 to 7 days after 70%
             hepatectomy. Liver from normal and sham-operated animals and
             splenic tissue from all animals were studied as controls. In
             vivo proton spectroscopy and imaging of liver was performed
             in a separate group of control and posthepatectomy rats. The
             T2 of regenerating liver, but not of sham or normal control
             liver, was prolonged. Changes in T1, relative to normal
             tissue, were found in liver and spleen of both operated
             groups. Lipid content, assessed both by extraction of tissue
             samples and by in vivo spectroscopy, was increased in
             regenerating tissue but not in controls. Water content was
             similarly increased in regenerating liver tissue. Changes in
             water and lipid content appeared to contribute to the
             alterations in proton relaxation which we
             observed.},
   Key = {fds132783}
}

@booklet{Smith98a,
   Author = {B. R. Smith and M. D. Shattuck and L. W. Hedlund and G. A.
             Johnson},
   Title = {Time-course imaging of rat embryos in utero with magnetic
             resonance microscopy},
   Journal = {Magnetic Resonance In Medicine},
   Volume = {39},
   Number = {4},
   Pages = {673 -- 677},
   Year = {1998},
   Month = {April},
   Key = {Smith98a}
}

@booklet{Smith98,
   Author = {Smith, BR and Sattuck, MD and Hedlund, LW and Johnson,
             GA},
   Title = {Time-course imaging of rat embryos in utero with magnetic
             resonance microscopy (vol 39, pg 673, 1998)},
   Journal = {Magnetic Resonance In Medicine},
   Volume = {39},
   Number = {6},
   Pages = {CP2-CP2},
   Year = {1998},
   Month = {June},
   Key = {Smith98}
}

@article{fds268905,
   Author = {Smith, BR and Shattuck, MD and Hedlund, LW and Johnson,
             GA},
   Title = {Time-course imaging of rat embryos in utero with magnetic
             resonance microscopy.},
   Journal = {Magn Reson Med},
   Volume = {39},
   Number = {4},
   Pages = {673-677},
   Year = {1998},
   Month = {April},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/9543433},
   Keywords = {Animals • Embryo • Embryonic and Fetal Development
             • Female • Fetus • Follow-Up Studies •
             Gestational Age • Image Processing, Computer-Assisted
             • Magnetic Resonance Imaging • Pregnancy •
             Rats • Rats, Sprague-Dawley • Time Factors •
             Uterus • anatomy & histology • anatomy &
             histology* • methods*},
   Abstract = {Magnetic resonance (MR) microscopy was used to noninvasively
             investigate the development of live rat embryos in utero.
             The difficulty in making sequential observations of a
             developing mammalian embryo has frustrated developmental
             biologists for many years. Most current technologies analyze
             normal and abnormal development by observing end point
             phenotypes (in fixed specimens) rather than investigating
             the live embryo. MR microscopy was adapted to allow rat
             litters to be scanned three times each (at 1- to 3-day
             intervals) and has produced images of live developing
             embryos. It was demonstrated that repeated anesthesia and
             imaging protocols produced no gross malformations in the rat
             pups that were subsequently delivered and observed.
             Three-dimensional projection encoding with phase rewinders
             produced isotropic [256(3)] image data sets in about 30
             minutes with excellent tissue contrast arising from
             steady-state effects in the amniotic fluid.},
   Doi = {10.1002/mrm.1910390424},
   Key = {fds268905}
}

@booklet{Baxter91,
   Author = {BAXTER, GW and LEONE, R and JOHNSON, GA and BEHRINGER,
             RP},
   Title = {TIME-DEPENDENCE, SCALING AND PATTERN-FORMATION FOR FLOWING
             SAND},
   Journal = {EUROPEAN JOURNAL OF MECHANICS B-FLUIDS},
   Volume = {10},
   Number = {2},
   Pages = {181-186},
   Publisher = {GAUTHIER-VILLARS},
   Year = {1991},
   Month = {January},
   ISSN = {0997-7546},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1991FR81800029&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Baxter91}
}

@article{fds132807,
   Author = {GA Johnson and RJ Herfkens and MA Brown},
   Title = {Tissue relaxation time: in vivo field dependence.},
   Journal = {Radiology, UNITED STATES},
   Volume = {156},
   Number = {3},
   Pages = {805-10},
   Year = {1985},
   Month = {September},
   ISSN = {0033-8419},
   Keywords = {Adipose Tissue • Animals • Dogs • Electron
             Spin Resonance Spectroscopy* • Kidney Cortex •
             Magnetic Resonance Spectroscopy* • Muscles •
             Spleen • anatomy & histology},
   Abstract = {Relaxation times (T1 and T2) were measured in vivo in
             mongrel dogs at fields of 0.3, 0.5, 1.0, 1.35, and 1.5 tesla
             (T). T1 was measured using nine values of inversion time
             ranging from 10 to 1,280 msec. T2 was measured with a
             four-point multiple spin-echo sequence. Relaxation times
             were calculated for muscle, kidney cortex, spleen, and
             adipose tissue. T2 is independent of field. A linear fit to
             the field dependence of T1 yields slopes of 400-500 msec/T
             for tissues in which the primary source of protons is water.
             The lower slope of adipose (approximately 150 msec/T)
             reflects the different mechanism of spin-lattice relaxation
             of the -CH2 protons.},
   Key = {fds132807}
}

@booklet{Johnson85,
   Author = {Johnson, GA and Herfkens, RJ and Brown, MA},
   Title = {Tissue relaxation time: in vivo field dependence.},
   Journal = {Radiology},
   Volume = {156},
   Number = {3},
   Pages = {805-810},
   Year = {1985},
   Month = {September},
   ISSN = {0033-8419},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/2991980},
   Abstract = {Relaxation times (T1 and T2) were measured in vivo in
             mongrel dogs at fields of 0.3, 0.5, 1.0, 1.35, and 1.5 tesla
             (T). T1 was measured using nine values of inversion time
             ranging from 10 to 1,280 msec. T2 was measured with a
             four-point multiple spin-echo sequence. Relaxation times
             were calculated for muscle, kidney cortex, spleen, and
             adipose tissue. T2 is independent of field. A linear fit to
             the field dependence of T1 yields slopes of 400-500 msec/T
             for tissues in which the primary source of protons is water.
             The lower slope of adipose (approximately 150 msec/T)
             reflects the different mechanism of spin-lattice relaxation
             of the -CH2 protons.},
   Doi = {10.1148/radiology.156.3.2991980},
   Key = {Johnson85}
}

@article{fds268863,
   Author = {Badea, CT and Hedlund, LW and De Lin and M and Mackel, JSB and Samei, E and Johnson, GA},
   Title = {Tomographic digital subtraction angiography for lung
             perfusion estimation in rodents.},
   Journal = {Med Phys},
   Volume = {34},
   Number = {5},
   Pages = {1546-1555},
   Year = {2007},
   Month = {May},
   ISSN = {0094-2405},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/17555236},
   Keywords = {Angiography, Digital Subtraction • Animals •
             Female • Lung • Magnetic Resonance Angiography
             • Perfusion • Radiographic Image Enhancement
             • Rats • Rats, Inbred F344 • Tomography,
             X-Ray Computed • blood supply • methods •
             methods* • radiography*},
   Abstract = {In vivo measurements of perfusion present a challenge to
             existing small animal imaging techniques such as magnetic
             resonance microscopy, micro computed tomography, micro
             positron emission tomography, and microSPECT, due to
             combined requirements for high spatial and temporal
             resolution. We demonstrate the use of tomographic digital
             subtraction angiography (TDSA) for estimation of perfusion
             in small animals. TDSA augments conventional digital
             subtraction angiography (DSA) by providing three-dimensional
             spatial information using tomosynthesis algorithms. TDSA is
             based on the novel paradigm that the same time density
             curves can be reproduced in a number of consecutive
             injections of microL volumes of contrast at a series of
             different angles of rotation. The capabilities of TDSA are
             established in studies on lung perfusion in rats. Using an
             imaging system developed in-house, we acquired data for
             four-dimensional (4D) imaging with temporal resolution of
             140 ms, in-plane spatial resolution of 100 microm, and slice
             thickness on the order of millimeters. Based on a structured
             experimental approach, we optimized TDSA imaging providing a
             good trade-off between slice thickness, the number of
             injections, contrast to noise, and immunity to artifacts.
             Both DSA and TDSA images were used to create parametric maps
             of perfusion. TDSA imaging has potential application in a
             number of areas where functional perfusion measurements in
             4D can provide valuable insight into animal models of
             disease and response to therapeutics.},
   Doi = {10.1118/1.2717384},
   Key = {fds268863}
}

@article{064710257107,
   Author = {Johnson, G.A. and Davis, J.G. and Qian, Y.L. and Doesken,
             K.C.},
   Title = {Topdressing turf with composted manure improves soil quality
             and protects water quality},
   Journal = {Soil Science Society of America Journal},
   Volume = {70},
   Number = {6},
   Pages = {2114 - 2121},
   Year = {2006},
   url = {http://dx.doi.org/10.2136/sssaj2005.0287},
   Keywords = {Manures;Hydraulic conductivity;Sediments;},
   Abstract = {Compost can improve soil properties when incorporated into
             soil; however, little information is available regarding
             impacts of compost topdressing. Objectives of this study
             were to evaluate the effects that topdressing composted
             dairy manure onto Kentucky bluegrass (Poa pratensis L.) has
             on: (i) soil physical properties, (ii) soil chemical
             properties, (iii) soil nitrate (NOs-N) and P concentrations
             below the rootzone, (iv) total runoff and sediment losses,
             and (v) N and P concentrations in runoff. Plots were
             topdressed with compost at 0, 33, 66, and 99 m<sup>3</sup>
             ha<sup>-1</sup>. Saturated hydraulic conductivity, bulk
             density, water retention, and soil nutrient levels were
             measured. A rainfall simulation was conducted, and runoff
             was collected and analyzed for total nitrogen (TN), nitrate
             nitrogen (NO<sub>3</sub>-N), ammonium nitrogen
             (NH<sub>4</sub>-N), total phosphorus (TP), total dissolved P
             (TDP), and orthophosphate (OP). Compost application of 99
             m<sup>3</sup> ha<sup>-1</sup> reduced bulk density, and
             increased water retention and P, K, Fe, and Mn
             concentrations in the surface soil. Compost applications of
             66 m<sup>3</sup> ha<sup>-1</sup> or greater raised soil
             electrical conductivity (EC); however, this increase i n
             soil EC did not negatively impact turf quality. Rates of
             runoff and erosion and concentrations of TN,
             NO<sub>3</sub>-N, TP, TDP, and OP in runoff were not
             different among treatments. However, all compost treatments
             did increase NH<sub>4</sub>-N concentrations in runoff.
             There were no differences in soil NO<sub>3</sub>-N or
             available P levels below the root zone. Topdressing
             composted manure onto established turf improved soil
             physical properties and nutrient concentrations without
             increasing nutrient runoff, with the exception of increased
             NH<sub>4</sub>-N levels in runoff. &copy; Soil Science
             Society of America.},
   Key = {064710257107}
}

@article{fds174217,
   Author = {GA Johnson and C Wilken and EA Van Kirk and EL Belden and WJ
             Murdoch},
   Title = {Toward regulation of gonadal function by a synthetic hybrid
             molecule composed of gonadotropin and Fc fragment of
             immunoglobulin G.},
   Journal = {American journal of reproductive immunology (New York, N.Y.
             : 1989)},
   Volume = {23},
   Number = {1},
   Pages = {22-5},
   Year = {1990},
   Month = {May},
   ISSN = {1046-7408},
   Keywords = {Animals • Cell Survival • Chorionic Gonadotropin
             • Cross-Linking Reagents • Immunoglobulin Fc
             Fragments • Immunoglobulin G • Leydig Cells •
             Luteinizing Hormone • Male • Reproduction •
             Sheep • Testis • Testosterone • Tumor Cells,
             Cultured • blood • drug effects • drug
             effects* • immunology • metabolism •
             pharmacology*},
   Abstract = {A conjugate of human chorionic gonadotropin (HCG) and Fc
             fragment of immunoglobulin G was prepared by covalent
             cross-linking using the heterobifunctional reagent,
             N-succinimidyl 3-(2-pyridyldithio) propionate. Mouse Leydig
             tumor cells expressing receptors for luteinizing hormone
             were specifically lysed in vitro as a consequence of
             complement fixation via the Fc component of the hybrid
             molecule. Furthermore, administration of HCG-Fc to rams
             caused an acute depression in circulatory testosterone. This
             novel concept of targeted inhibition of gonadal function
             could prove to have future applications in control of
             reproductive processes.},
   Language = {eng},
   Key = {fds174217}
}

@booklet{Johnson90,
   Author = {G. A. Johnson and C. Wilken and E. A. Vankirk and E. L.
             Belden and W. J. Murdoch},
   Title = {Toward regulation of gonadal-function by a synthetic hybrid
             molecule composed of gonadotropin and fc fragment of
             immunoglobulin-g},
   Journal = {American Journal Of Reproductive Immunology},
   Volume = {23},
   Number = {1},
   Pages = {22 -- 25},
   Year = {1990},
   Month = {May},
   Key = {Johnson90}
}

@article{fds364084,
   Author = {Shen, J and Zhao, Q and Qi, Y and Cofer, G and Johnson, GA and Wang,
             N},
   Title = {Tractography of Porcine Meniscus Microstructure Using
             High-Resolution Diffusion Magnetic Resonance
             Imaging.},
   Journal = {Front Endocrinol (Lausanne)},
   Volume = {13},
   Pages = {876784},
   Year = {2022},
   url = {http://dx.doi.org/10.3389/fendo.2022.876784},
   Abstract = {To noninvasively evaluate the three-dimensional collagen
             fiber architecture of porcine meniscus using diffusion MRI,
             meniscal specimens were scanned using a 3D
             diffusion-weighted spin-echo pulse sequence at 7.0 T. The
             collagen fiber alignment was revealed in each voxel and the
             complex 3D collagen network was visualized for the entire
             meniscus using tractography. The proposed automatic
             segmentation methods divided the whole meniscus to different
             zones (Red-Red, Red-White, and White-White) and different
             parts (anterior, body, and posterior). The diffusion tensor
             imaging (DTI) metrics were quantified based on the
             segmentation results. The heatmap was generated to
             investigate the connections among different regions of
             meniscus. Strong zonal-dependent diffusion properties were
             demonstrated by DTI metrics. The fractional anisotropy (FA)
             value increased from 0.13 (White-White zone) to 0.26
             (Red-Red zone) and the radial diffusivity (RD) value changed
             from 1.0 × 10-3 mm2/s (White-White zone) to 0.7 × 10-3
             mm2/s (Red-Red zone). Coexistence of both radial and
             circumferential collagen fibers in the meniscus was evident
             by diffusion tractography. Weak connections were found
             between White-White zone and Red-Red zone in each part of
             the meniscus. The anterior part and posterior part were less
             connected, while the body part showed high connections to
             both anterior part and posterior part. The tractography
             based on diffusion MRI may provide a complementary method to
             study the integrity of meniscus and nondestructively
             visualize the 3D collagen fiber architecture.},
   Doi = {10.3389/fendo.2022.876784},
   Key = {fds364084}
}

@booklet{Gunderson94,
   Author = {R. O. Gunderson and M. Oprisan and G. A. Johnson and E. C.
             Pfeiffer and D. L. Smith and A. W. Schneider and H. Volpe and B. Silverstein and R. J. Ringlee and T. E. Mcdermott and V. S. Rashkes and R. B. Adler and C. R. Heising and T. S.
             White and M. G. Lau},
   Title = {Transformer magnetizing current and iron-core losses in
             harmonic power-flow - discussion},
   Journal = {Ieee Transactions On Power Delivery},
   Volume = {9},
   Number = {1},
   Pages = {34 -- 39},
   Year = {1994},
   Month = {January},
   Key = {Gunderson94}
}

@article{fds174066,
   Author = {DA Massuto and EC Kneese and GA Johnson and RC Burghardt and RN Hooper and NH Ing and LA Jaeger},
   Title = {Transforming growth factor beta (TGFB) signaling is
             activated during porcine implantation: proposed role for
             latency-associated peptide interactions with integrins at
             the conceptus-maternal interface.},
   Journal = {Reproduction (Cambridge, England)},
   Volume = {139},
   Number = {2},
   Pages = {465-78},
   Year = {2010},
   Month = {February},
   ISSN = {1741-7899},
   url = {http://dx.doi.org/10.1530/REP-09-0447},
   Keywords = {Animals • Antigens, CD29 • Biotinylation •
             Cell Line • Embryo Implantation* • Female •
             Gestational Age • Immunohistochemistry • Integrin
             beta Chains • Integrin beta3 • Integrins •
             Peptides • Phosphorylation • Pregnancy •
             Protein Binding • Protein Precursors • Receptors,
             Transforming Growth Factor beta • Recombinant Proteins
             • Signal Transduction* • Smad2 Protein •
             Smad3 Protein • Swine • Transforming Growth Factor
             beta • Trophoblasts • Uterus • metabolism
             • metabolism*},
   Abstract = {The process of implantation is mediated by a complex network
             of signaling and adhesive factors. In the pig, latent and
             active transforming growth factor beta (TGFB), TGFB
             receptors (TGFBR), and integrins (ITGs) are present during
             the peri-implantation period. TGFB signals via TGFBR and
             activates downstream effector SMAD proteins 2 and 3
             (p-SMAD2/3). Latency-associated peptide (LAP), part of the
             latent TGFB complex, is known to bind to ITG heterodimers
             and activate TGFB. We hypothesize that active TGFBs and
             TGFBRs along with LAP and ITGs functionally interact at the
             conceptus-maternal interface to mediate events essential for
             conceptus development and attachment in pigs. Uteri and
             conceptuses from days 10, 12, 16, 20, and 24 pregnant gilts
             were immunostained for TGFB, LAP, and ITG subunits (ITGAV,
             ITGB1, ITGB3, ITGB5, ITGB6, and ITGB8). Activation of TGFBRs
             was evaluated by the presence of phosphorylated downstream
             effector SMAD2/3. Binding of LAP to ITGs was also evaluated
             using porcine trophectoderm cells. Abundant active TGFB was
             detected at the apical surfaces of epithelia at the
             conceptus-maternal interface, and p-SMAD2/3 was detected at
             both conceptus attachment and nonattachment sites during
             implantation. Separate aggregates of LAP, ITGB1, ITGB5, and
             later ITGB3 were detected at the porcine conceptus-maternal
             interface, and binding of LAP to ITGs on apical surfaces was
             demonstrated. Results suggest that functional LAP-ITG
             adhesion complexes support conceptus attachment and promote
             TGFB activation leading to TGFB interaction with TGFBR
             supporting events of porcine implantation.},
   Language = {eng},
   Doi = {10.1530/REP-09-0447},
   Key = {fds174066}
}

@booklet{Hansen97,
   Author = {T. R. Hansen and K. J. Austin and G. A. Johnson},
   Title = {Transient ubiquitin cross-reactive protein gene expression
             in the bovine endometrium},
   Journal = {Endocrinology},
   Volume = {138},
   Number = {11},
   Pages = {5079 -- 5082},
   Year = {1997},
   Month = {November},
   Key = {Hansen97}
}

@article{fds174248,
   Author = {TR Hansen and KJ Austin and GA Johnson},
   Title = {Transient ubiquitin cross-reactive protein gene expression
             in the bovine endometrium.},
   Journal = {Endocrinology},
   Volume = {138},
   Number = {11},
   Pages = {5079-82},
   Year = {1997},
   Month = {November},
   ISSN = {0013-7227},
   Keywords = {Animals • Blotting, Northern • Cattle •
             Endometrium • Estrus • Female • Gene
             Expression* • Glyceraldehyde-3-Phosphate Dehydrogenases
             • Interferon Type I • Pregnancy • Pregnancy
             Proteins • RNA, Messenger • Time Factors •
             Transcription, Genetic • Ubiquitins • analogs &
             derivatives* • drug effects • genetics •
             metabolism • pharmacology • physiology*},
   Abstract = {Bovine ubiquitin cross-reactive protein (boUCRP) is secreted
             by the endometrium from days 15 to 26 of pregnancy in
             response to conceptus-derived interferon-tau (IFN-tau). We
             hypothesized that the gene encoding boUCRP was under
             transcriptional control by the conceptus and IFN-tau.
             Northern blots using radiolabeled UCRP cDNA revealed a
             single UCRP transcript of approximately 700 b that was
             present (P < 0.05) in endometrial cells cultured with 25 nM
             rboIFN-tau. The UCRP mRNA was not detected in endometrium on
             days 15, 17, 18 or 19 of the estrous cycle (n = 4 cows on
             each day) or in spleen, kidney, liver, corpus luteum or
             muscle. Bovine UCRP mRNA was detectable (P < 0.05) in
             endometrium from pregnant cows by day 15, reached highest
             levels by day 17, remained elevated on days 18, 19 and 21,
             and then declined to amounts on day 26 that were not
             detectable. Northern blot using radiolabeled ubiquitin cDNA
             revealed presence of the two major ubiquitin transcripts UbB
             (1.2 Kb) and UbC (2.6 Kb) in all tissues examined. The
             bovine UCRP cDNA did not cross-hybridize with these
             ubiquitin transcripts. We conclude that transcription of the
             UCRP gene is transient during early pregnancy and regulated
             by IFN-tau.},
   Language = {eng},
   Key = {fds174248}
}

@booklet{Brown84a,
   Author = {Brown, MA and Johnson, GA},
   Title = {Transition metal-chelate complexes as relaxation modifiers
             in nuclear magnetic resonance.},
   Journal = {Med Phys},
   Volume = {11},
   Number = {1},
   Pages = {67-72},
   Year = {1984},
   ISSN = {0094-2405},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/6422223},
   Abstract = {Studies are reported of relaxation modifiers for use in
             nuclear magnetic resonance (NMR) imaging systems. Chelate
             complexes of transition metal salts are under investigation
             to determine their ability to reduce the spin-lattice
             relaxation time (T1) of the nucleus under observation and to
             reduce the toxicity of the metal ion. The
             ethylenediaminetetraacetate (EDTA) complexes of FeCl3,
             GdCl3, and MnCl2 are not as effective as the respective
             salts in reducing T1 of water protons at 90 MHz. For Mn,
             this diminution in ability is offset by a significant
             reduction in toxicity. Explanations for this loss of
             effectiveness are discussed.},
   Doi = {10.1118/1.595455},
   Key = {Brown84a}
}

@article{fds132821,
   Author = {MA Brown and GA Johnson},
   Title = {Transition metal-chelate complexes as relaxation modifiers
             in nuclear magnetic resonance.},
   Journal = {Medical physics, UNITED STATES},
   Volume = {11},
   Number = {1},
   Pages = {67-72},
   ISSN = {0094-2405},
   Keywords = {Chlorides* • Edetic Acid • Ferric Compounds •
             Gadolinium • Magnetic Resonance Spectroscopy* •
             Manganese • Manganese Compounds*},
   Abstract = {Studies are reported of relaxation modifiers for use in
             nuclear magnetic resonance (NMR) imaging systems. Chelate
             complexes of transition metal salts are under investigation
             to determine their ability to reduce the spin-lattice
             relaxation time (T1) of the nucleus under observation and to
             reduce the toxicity of the metal ion. The
             ethylenediaminetetraacetate (EDTA) complexes of FeCl3,
             GdCl3, and MnCl2 are not as effective as the respective
             salts in reducing T1 of water protons at 90 MHz. For Mn,
             this diminution in ability is offset by a significant
             reduction in toxicity. Explanations for this loss of
             effectiveness are discussed.},
   Key = {fds132821}
}

@article{fds204248,
   Author = {G Wu and FW Bazer and GA Johnson and DA Knabe and RC Burghardt and TE
             Spencer, XL Li and JJ Wang},
   Title = {Triennial Growth Symposium: important roles for L-glutamine
             in swine nutrition and production.},
   Journal = {Journal of animal science},
   Volume = {89},
   Number = {7},
   Pages = {2017-30},
   Year = {2011},
   Month = {July},
   ISSN = {1525-3163},
   url = {http://dx.doi.org/10.2527/jas.2010-3614},
   Keywords = {Animal Feed • Animal Nutritional Physiological
             Phenomena* • Animals • Diet • Dietary
             Supplements • Female • Glutamine • Lactation
             • Pregnancy • Swine • blood • growth &
             development* • metabolism* • pharmacology •
             veterinary*},
   Abstract = {L-Glutamine (Gln) has traditionally not been considered a
             nutrient needed in diets for livestock species or even
             mentioned in classic animal nutrition textbooks. This is due
             to previous technical difficulties in Gln analysis and the
             unsubstantiated assumption that animals can synthesize
             sufficient amounts of Gln to meet their needs. Consequently,
             the current (1998) version of NRC does not recommend dietary
             Gln requirements for swine. This lack of knowledge about Gln
             nutrition has contributed to suboptimal efficiency of global
             pig production. Because of recent advances in research, Gln
             is now known to be an abundant AA in physiological fluids
             and proteins and a key regulator of gene expression.
             Additionally, Gln can regulate cell signaling via the
             mammalian target of rapamycin pathway, adenosine
             monophosphate-activated protein kinase, extracellular
             signal-related kinase, Jun kinase, mitogen-activated protein
             kinase, and nitric oxide. The exquisite integration of
             Gln-dependent regulatory networks has profound effects on
             cell proliferation, differentiation, migration, metabolism,
             homeostasis, survival, and function. As a result of
             translating basic research into practice, dietary
             supplementation with 1% Gln maintains gut health and
             prevents intestinal dysfunction in low-birth-weight or
             early-weaned piglets while increasing their growth
             performance and survival. In addition, supplementing 1% Gln
             to a corn- and soybean-meal-based diet between d 90 and 114
             of gestation ameliorates fetal growth retardation in gilts
             and reduces preweaning mortality of piglets. Furthermore,
             dietary supplementation with 1% Gln enhances milk production
             by lactating sows. Thus, adequate amounts of dietary Gln, a
             major nutrient, are necessary to support the maximum growth,
             development, and production performance of
             swine.},
   Language = {eng},
   Doi = {10.2527/jas.2010-3614},
   Key = {fds204248}
}

@article{fds132759,
   Author = {C Zimmer and SC Wright Jr and RT Engelhardt and GA Johnson and C Kramm and XO Breakefield and R Weissleder},
   Title = {Tumor cell endocytosis imaging facilitates delineation of
             the glioma-brain interface.},
   Journal = {Experimental neurology},
   Volume = {143},
   Number = {1},
   Pages = {61-9},
   Year = {1997},
   Month = {January},
   ISSN = {0014-4886},
   url = {http://dx.doi.org/10.1006/exnr.1996.6350},
   Keywords = {Animals • Biological Markers • Brain Neoplasms
             • Endocytosis* • Glioma • Image Processing,
             Computer-Assisted • Rats • Tumor Cells, Cultured
             • pathology*},
   Abstract = {We describe a method for measuring tumor cell endocytosis in
             vivo and provide the anatomic correlate of this tumor cell
             function using a superparamagnetic and histologically
             detectable marker for cell uptake (MION). Rats (n = 22) were
             intrahemispherically implanted with a thymidine kinase
             (TK)-positive 9L gliosarcoma cell line, where TK served as
             the tumor marker. Twenty-four hours after intravenous
             injection of 10 mg Fe/kg of MION, rat brains were removed
             and underwent MR imaging ex vivo at near-microscopic
             resolution (isotropic voxel size of 86 microm, 9.4 T) prior
             to histologic processing. The imaging probe accumulated
             within tumor cells adjacent to the hyperpermeable
             tumor-brain interface including microscopic deposits and
             along finger-like invasions of the tumor into brain,
             facilitating the demarcation of the true histologic tumor
             border in three dimensions by MR microscopy. The method has
             potential research and clinical implications for delineating
             the tumor-brain interface prior to therapy and/or for
             providing a rational basis for imaging nanocolloid drug
             delivery to solid tumors.},
   Language = {eng},
   Doi = {10.1006/exnr.1996.6350},
   Key = {fds132759}
}

@booklet{Zimmer97,
   Author = {Zimmer, C and Wright, SC and Engelhardt, RT and Johnson, GA and Kramm,
             C and Breakefield, XO and Weissleder, R},
   Title = {Tumor cell endocytosis imaging facilitates delineation of
             the glioma-brain interface.},
   Journal = {Exp Neurol},
   Volume = {143},
   Number = {1},
   Pages = {61-69},
   Year = {1997},
   Month = {January},
   ISSN = {0014-4886},
   url = {http://dx.doi.org/10.1006/exnr.1996.6350},
   Abstract = {We describe a method for measuring tumor cell endocytosis in
             vivo and provide the anatomic correlate of this tumor cell
             function using a superparamagnetic and histologically
             detectable marker for cell uptake (MION). Rats (n = 22) were
             intrahemispherically implanted with a thymidine kinase
             (TK)-positive 9L gliosarcoma cell line, where TK served as
             the tumor marker. Twenty-four hours after intravenous
             injection of 10 mg Fe/kg of MION, rat brains were removed
             and underwent MR imaging ex vivo at near-microscopic
             resolution (isotropic voxel size of 86 microm, 9.4 T) prior
             to histologic processing. The imaging probe accumulated
             within tumor cells adjacent to the hyperpermeable
             tumor-brain interface including microscopic deposits and
             along finger-like invasions of the tumor into brain,
             facilitating the demarcation of the true histologic tumor
             border in three dimensions by MR microscopy. The method has
             potential research and clinical implications for delineating
             the tumor-brain interface prior to therapy and/or for
             providing a rational basis for imaging nanocolloid drug
             delivery to solid tumors.},
   Doi = {10.1006/exnr.1996.6350},
   Key = {Zimmer97}
}

@article{fds268860,
   Author = {Badea, CT and Hedlund, LW and De Lin and M and Boslego Mackel and JF and Johnson, GA},
   Title = {Tumor imaging in small animals with a combined
             micro-CT/micro-DSA system using iodinated conventional and
             blood pool contrast agents.},
   Journal = {Contrast Media Mol Imaging},
   Volume = {1},
   Number = {4},
   Pages = {153-164},
   Year = {2006},
   ISSN = {1555-4317},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/17193692},
   Keywords = {Angiography, Digital Subtraction • Animals •
             Contrast Media • Fibrosarcoma • Iodine • Rats
             • Rats, Inbred F344 • Tomography, X-Ray Computed
             • analysis • blood supply* • chemistry*
             • instrumentation* • methods* •
             radiography*},
   Abstract = {X-ray based micro-computed tomography (CT) and micro-digital
             subtraction angiography (DSA) are important non-invasive
             imaging modalities for following tumorogenesis in small
             animals. To exploit these imaging capabilities further, the
             two modalities were combined into a single system to provide
             both morphological and functional data from the same tumor
             in a single imaging session. The system is described and
             examples are given of imaging implanted fibrosarcoma tumors
             in rats using two types of contrast media: (a) a new
             generation of blood pool contrast agent containing iodine
             with a concentration of 130 mg/mL (Fenestratrade mark VC,
             Alerion Biomedical, San Diego, CA, USA) for micro-CT and (b)
             a conventional iodinated contrast agent (Isovue(R)-370 mg/mL
             iodine, trademark of Bracco Diagnostics, Princeton, NJ, USA)
             for micro-DSA. With the blood pool contrast agent, the 3D
             vascular architecture is revealed in exquisite detail at 100
             microm resolution. Micro-DSA images, in perfect registration
             with the 3D micro-CT datasets, provide complementary
             functional information such as mean transit times and
             relative blood flow through the tumor. This imaging approach
             could be used to understand tumor angiogenesis better and be
             the basis for evaluating anti-angiogenic
             therapies.},
   Doi = {10.1002/cmmi.103},
   Key = {fds268860}
}

@article{fds292753,
   Author = {Subashi, E and Cordero, FJ and Halvorson, KG and Qi, Y and Nouls, JC and Becher, OJ and Johnson, GA},
   Title = {Tumor location, but not H3.3K27M, significantly influences
             the blood-brain-barrier permeability in a genetic mouse
             model of pediatric high-grade glioma.},
   Journal = {J Neurooncol},
   Volume = {126},
   Number = {2},
   Pages = {243-251},
   Year = {2016},
   Month = {January},
   ISSN = {0167-594X},
   url = {http://dx.doi.org/10.1007/s11060-015-1969-9},
   Abstract = {Pediatric high-grade gliomas (pHGGs) occur with strikingly
             different frequencies in infratentorial and supratentorial
             regions. Although histologically these malignancies appear
             similar, they represent distinct diseases. Recent genomic
             studies have identified histone K27M H3.3/H3.1 mutations in
             the majority of brainstem pHGGs; these mutations are rarely
             encountered in pHGGs that arise in the cerebral cortex.
             Previous research in brainstem pHGGs suggests a restricted
             permeability of the blood-brain-barrier (BBB). In this work,
             we use dynamic contrast-enhanced (DCE) MRI to evaluate BBB
             permeability in a genetic mouse model of pHGG as a function
             of location (cortex vs. brainstem, n = 8 mice/group) and
             histone mutation (mutant H3.3K27M vs. wild-type H3.3, n = 8
             mice/group). The pHGG models are induced either in the
             brainstem or the cerebral cortex and are driven by PDGF
             signaling and p53 loss with either H3.3K27M or wild-type
             H3.3. T2-weighted MRI was used to determine tumor
             location/extent followed by 4D DCE-MRI for estimating the
             rate constant (K (trans) ) for tracer exchange across the
             barrier. BBB permeability was 67 % higher in cortical pHGGs
             relative to brainstem pHGGs (t test, p = 0.012) but was not
             significantly affected by the expression of mutant H3.3K27M
             versus wild-type H3.3 (t-test, p = 0.78). Although mice
             became symptomatic at approximately the same time, the mean
             volume of cortical tumors was 3.6 times higher than the mean
             volume of brainstem tumors. The difference between the mean
             volume of gliomas with wild-type and mutant H3.3 was
             insignificant. Mean K (trans) was significantly correlated
             to glioma volume. These results present a possible
             explanation for the poor response of brainstem pHGGs to
             systemic therapy. Our findings illustrate a potential role
             played by the microenvironment in shaping tumor growth and
             BBB permeability.},
   Doi = {10.1007/s11060-015-1969-9},
   Key = {fds292753}
}

@booklet{Utz87,
   Author = {Utz, JA and Herfkens, RJ and Johnson, CD and Shimakawa, A and Pelc, N and Glover, G and Johnson, GA and Spritzer, CE},
   Title = {Two-second MR images: comparison with spin-echo images in 29
             patients.},
   Journal = {AJR Am J Roentgenol},
   Volume = {148},
   Number = {3},
   Pages = {629-633},
   Year = {1987},
   Month = {March},
   ISSN = {0361-803X},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1987G131300036&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Abstract = {MR images can be obtained with a 2-sec scan time when an
             extremely short repetition rate (22 msec), limited flip
             angle (30 degrees), and gradient refocused echoes are used.
             Comparison of 415 such images obtained in 29 patients with
             routine T1-weighted (TR 500, TE 25) and T2-weighted (TR
             2000, TE 80) images showed that images free of respiratory
             artifacts could be obtained in all patients. Although
             abdominal organs were well seen with 2-sec scan time,
             overall evaluation of these organs was better on routine
             T1-weighted images. Vascular structures, however, were seen
             as well or better on the 2-sec images in 60% of cases. The
             images were extremely sensitive to field nonhomogeneity, and
             metallic artifact was exaggerated in five patients with
             surgical clips. Two-sec MR images provide a rapid method of
             localizing abdominal organs for further evaluation. The
             sensitivity to blood flow may assist in the assessment of
             vascular patency.},
   Doi = {10.2214/ajr.148.3.629},
   Key = {Utz87}
}

@booklet{Wendling83,
   Author = {M. G. Wendling and D. W. Ducharme and G. A. Johnson and R.
             B. Mccall and D. T. Pals},
   Title = {U-54,669f - a novel hypotensive agent},
   Journal = {Federation Proceedings},
   Volume = {42},
   Number = {2},
   Pages = {162 -- 166},
   Year = {1983},
   Key = {Wendling83}
}

@article{fds174067,
   Author = {MG Wendling and DW DuCharme and GA Johnson and RB McCall and DT
             Pals},
   Title = {U-54,669F: a novel hypotensive agent.},
   Journal = {Federation proceedings},
   Volume = {42},
   Number = {2},
   Pages = {162-6},
   Year = {1983},
   Month = {February},
   ISSN = {0014-9446},
   Keywords = {Angiotensin II • Animals • Antihypertensive
             Agents* • Blood Pressure • Cats •
             Dose-Response Relationship, Drug • Electric Stimulation
             • Female • Heart Rate • Macaca fascicularis
             • Male • Norepinephrine • Piperazines •
             Rats • Rats, Inbred Strains • blood • drug
             effects • drug effects* • pharmacology •
             pharmacology*},
   Abstract = {U-54,669F, a new antihypertensive agent, administered orally
             was associated with dose-related hypotensive responses in
             conscious, spontaneously hypertensive, and normotensive rats
             (0.015-0.5 mg/kg) and in supine conscious monkeys (1-10
             mg/kg). No loss of hypotensive efficacy of U-54,669F was
             observed after 1 wk of daily repetitive treatment. U-54,669F
             did not alter electrical postganglionic sympathetic nerve
             activity or postsynaptic sympathetic function. Hypotensive
             responses to U-54,669F were blunted in spinal cats.
             U-54,669F was associated with dose-related decreases in
             norepinephrine (NE) levels in plasma and in cardiac and
             splenic tissue, whereas brain NE was unaltered. U-54,669F
             attenuated vascular responses associated with electrical
             stimulation of sympathetic nerves. However, at hypotensive
             doses, U-54,669F did not impair the ability of monkeys to
             withstand orthostatic stress, or contraction of the
             nictitating membrane secondary to sympathetic stimulation in
             the cat. U-54,669F appears to alter peripheral sympathetic
             neurogenic function, but apparently does not enter the
             central nervous system and does not impair the ability to
             withstand orthostatic stress at effective hypotensive
             doses.},
   Language = {eng},
   Key = {fds174067}
}

@article{fds268839,
   Author = {Howles, GP and Qi, Y and Johnson, GA},
   Title = {Ultrasonic disruption of the blood-brain barrier enables in
             vivo functional mapping of the mouse barrel field cortex
             with manganese-enhanced MRI.},
   Journal = {Neuroimage},
   Volume = {50},
   Number = {4},
   Pages = {1464-1471},
   Year = {2010},
   Month = {May},
   ISSN = {1095-9572},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/20096789},
   Keywords = {Animals • Blood-Brain Barrier • Brain Mapping
             • Cerebral Cortex • Conscious Sedation •
             Imaging, Three-Dimensional • Magnetic Resonance Imaging
             • Manganese • Mice • Mice, Inbred C57BL
             • Microbubbles • Physical Stimulation • Touch
             Perception • Ultrasonics • Ultrasonography,
             Doppler, Transcranial • Vibrissae • metabolism
             • metabolism* • methods* • physiology •
             physiology*},
   Abstract = {Though mice are the dominant model system for studying the
             genetic and molecular underpinnings of neuroscience,
             functional neuroimaging in mice remains technically
             challenging. One approach, Activation-Induced
             Manganese-enhanced MRI (AIM MRI), has been used successfully
             to map neuronal activity in rodents. In AIM MRI,
             manganese(2+) acts a calcium analog and accumulates in
             depolarized neurons. Because manganese(2+) shortens T1,
             regions of elevated neuronal activity enhance in MRI.
             However, because manganese does not cross the blood-brain
             barrier (BBB), the need to osmotically disrupt the BBB has
             limited the use of AIM MRI, particularly in mice. In this
             work, the BBB was opened in mice using unfocused,
             transcranial ultrasound in combination with gas-filled
             microbubbles. Using this noninvasive technique to open the
             BBB bilaterally, manganese could be quickly administered to
             the whole mouse brain. With this approach, AIM MRI was used
             to map the neuronal response to unilateral mechanical
             stimulation of the vibrissae in lightly sedated mice. The
             resultant 3D activation map agreed well with published
             representations of the vibrissae regions of the barrel field
             cortex. The anterior portions of the barrel field cortex
             corresponding to the more rostral vibrissae showed greater
             activation, consistent with previous literature. Because the
             ultrasonic opening of the BBB is simple, fast, and
             noninvasive, this approach is suitable for high-throughput
             and longitudinal studies in awake mice. This approach
             enables a new way to map neuronal activity in mice with
             manganese.},
   Language = {eng},
   Doi = {10.1016/j.neuroimage.2010.01.050},
   Key = {fds268839}
}

@article{fds174097,
   Author = {GA Johnson and D Robinson and M Hornung},
   Title = {Unique bedrock and soils associated with the Teesdale
             flora.},
   Journal = {Nature},
   Volume = {232},
   Number = {5311},
   Pages = {453-6},
   Year = {1971},
   Month = {August},
   ISSN = {0028-0836},
   url = {http://dx.doi.org/10.1038/232453a0},
   Language = {eng},
   Doi = {10.1038/232453a0},
   Key = {fds174097}
}

@article{fds174219,
   Author = {TT Kawabe and MF Kubicek and GA Johnson and AE Buhl},
   Title = {Use of gamma-glutamyl transpeptidase activity as a marker of
             hair cycle and anagen induction in mouse hair
             follicles.},
   Journal = {The Journal of investigative dermatology},
   Volume = {103},
   Number = {1},
   Pages = {122-6},
   Year = {1994},
   Month = {July},
   ISSN = {0022-202X},
   Keywords = {Animals • Biological Markers • Cell Cycle •
             Dose-Response Relationship, Drug • Female • Hair
             • Histocytochemistry • Male • Mice •
             Minoxidil • analysis • analysis* • cytology*
             • drug effects • enzymology* •
             gamma-Glutamyltransferase • pharmacology •
             physiology},
   Abstract = {gamma-glutamyl transpeptidase activity was monitored in
             cycling mice by histologic localization and biochemical
             assay. Our objective for this study is to establish the
             relationship between gamma-glutamyl transpeptidase activity
             and hair growth and to determine whether its activity can be
             correlated to induced hair growth. In cycling mouse skin,
             gamma-glutamyl transpeptidase activity is pronounced during
             anagen and greatly diminished during telogen. In the skin,
             the enzyme is present exclusively in the outer and inner
             root sheaths of hair follicles. gamma-glutamyl
             transpeptidase is limited to the follicle below the level of
             the sebaceous gland and is completely absent in the follicle
             above the sebaceous gland level. During anagen, the outer
             root sheath in the hypodermis is intensely positive for
             gamma-glutamyl transpeptidase activity whereas the hair
             matrix cells and dermal papillar are negative. The inner
             root sheath above the bulb shows distinctive membrane
             staining for gamma-glutamyl transpeptidase. gamma-glutamyl
             transpeptidase activity can be seen to vary only in cycling
             follicles. Inducing anagen by plucking hair shafts results
             in an increase in gamma-glutamyl transpeptidase activity
             directly correlated to hair regrowth. In a similar manner,
             mice were plucked and treated with a daily dose of 2%
             minoxidil. A slight difference in cycle lengths was seen in
             animals treated with minoxidil when compared to vehicle
             control. Minoxidil treatment may cause an early initiation
             of anagen, but both the minoxidil-treated skin and the
             vehicle-treated skin entered telogen at the same time.
             Together, these studies indicate that gamma-glutamyl
             transpeptidase is a specific marker of anagen in growing
             hair.},
   Language = {eng},
   Key = {fds174219}
}

@booklet{Kawabe94,
   Author = {T. T. Kawabe and M. F. Kubicek and G. A. Johnson and A. E.
             Buhl},
   Title = {Use of gamma-glutamyl-transpeptidase activity as a marker of
             hair cycle and anagen induction in mouse
             hair-follicles},
   Journal = {Journal Of Investigative Dermatology},
   Volume = {103},
   Number = {1},
   Pages = {122 -- 126},
   Year = {1994},
   Month = {July},
   Key = {Kawabe94}
}

@article{fds268749,
   Author = {MacFall, JS and Johnson, GA},
   Title = {Use of magnetic resonance imaging in the study of plants and
             soils},
   Volume = {36},
   Number = {36},
   Pages = {99-113},
   Publisher = {SOIL SCIENCE SOC AMER},
   Editor = {Anderson, SH and Hopmans, JW},
   Year = {2015},
   Month = {October},
   ISBN = {9780891188087},
   ISSN = {0081-1904},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1994BB18K00009&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Abstract = {The nondestructive study of plants and soils in situ has
             historically been difficult due to the inherently opaque
             nature of the system. Repeated study of root growth and
             physiological processes in bulk soil has been impossible
             without techniques for remote sensing, such as x-ray,
             computed tomography, rhizotrons, or magnetic resonance
             imaging (MRI). Magnetic resonance imaging techniques are now
             providing tools for the direct, nondestructive study of
             plants and soils. New smaller bore, high field MRI scanners
             can provide resolutions (10-100 μm) far superior to
             resolutions provided by clinical scanners (>1 mm), and can
             truly be considered magnetic resonance microscopy (MRM).
             Images can be repeatedly acquired over time, providing both
             spatial and temporal information. The technique has provided
             information on water extraction by roots, root growth and
             function, flow of water through porous media, water
             distribution, and binding patterns in sand-sandstone and in
             planta, and plant physiological processes. The chemical
             environment can also be probed by examinations of relaxation
             times and diffusion coefficients measured by MRI. As the
             technique is further developed, many new and unique
             applications will be found.},
   Doi = {10.2136/sssaspecpub36.c9},
   Key = {fds268749}
}

@booklet{Brown90,
   Author = {Brown, JM and Kramer, PJ and Cofer, GP and Johnson,
             GA},
   Title = {Use of nuclear magnetic resonance microscopy for noninvasive
             observations of root-soil water relations},
   Journal = {Theoretical and Applied Climatology},
   Volume = {42},
   Number = {4},
   Pages = {229-236},
   Publisher = {Springer Nature},
   Year = {1990},
   Month = {December},
   ISSN = {0177-798X},
   url = {http://dx.doi.org/10.1007/BF00865983},
   Abstract = {As part of our strategy to study root-soil water
             relationships, it was necessary to develop a nondestructive
             technique to detect small changes in water distribution in
             and near the root. Nuclear magnetic resonance imaging (MRI),
             clinically used to nondestructively and noninvasively
             acquire anatomical information, can also be used to observe
             water distribution in roots, soils and other plant tissues.
             In MRI, a sample is placed in a strong magnetic field and a
             sequence of radio frequency (rf) pulses and magnetic field
             gradients is used to measure the concentration and
             relaxation properties of protons, chiefly those associated
             with water. This information is then reconstructed into a
             digital image representing the spatial distribution of water
             in plant tissues and soil. Today, intact roots less than 1
             mm in diameter growing in soil or synthetic media can be
             clearly imaged in less than 4 minutes at resolutions
             typically less than 30μm. This permits rapid production of
             images that simultaneously distinguish temporal changes in
             water distribution in root tissue, the rhizosphere and the
             adjacent soil at microscopic levels. Applications of this
             technique for investigating plant-soil water relationships
             will be discussed. © 1990 Springer-Verlag.},
   Doi = {10.1007/BF00865983},
   Key = {Brown90}
}

@booklet{Tengowski01,
   Author = {Tengowski, MW and Suddarth, SA and Cofer, GP and Wheeler, CT and Botts,
             S and Fasulo, LM and Jeffries-Griffor, JL and Amacher, DE and Lawton,
             MP and Hedlund, LW and Zhang, XW and Burkhardt, JE and Johnson,
             GA},
   Title = {Using technology to develop a hepatic lipidosis blomarker in
             the rat},
   Journal = {MOLECULAR BIOLOGY OF THE CELL},
   Volume = {12},
   Pages = {261A-261A},
   Publisher = {AMER SOC CELL BIOLOGY},
   Year = {2001},
   Month = {November},
   ISSN = {1059-1524},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000172372501425&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Tengowski01}
}

@article{fds204261,
   Author = {FW Bazer and G Wu and GA Johnson and J Kim and G Song},
   Title = {Uterine histotroph and conceptus development: select
             nutrients and secreted phosphoprotein 1 affect mechanistic
             target of rapamycin cell signaling in ewes.},
   Journal = {Biology of reproduction},
   Volume = {85},
   Number = {6},
   Pages = {1094-107},
   Year = {2011},
   Month = {December},
   ISSN = {1529-7268},
   url = {http://dx.doi.org/10.1095/biolreprod.111.094722},
   Abstract = {Interferon tau (IFNT), the pregnancy recognition signal in
             ruminants, abrogates the uterine luteolytic mechanism to
             ensure maintenance of function for the corpora lutea to
             produce progesterone (P4). IFNT also suppresses expression
             of classical IFN-stimulated genes by uterine lumenal
             epithelium (LE) and superficial glandular (sGE) epithelium
             but, acting in concert with progesterone, affects expression
             of a multitude of genes critical to growth and development
             of the conceptus. The LE and sGE secrete proteins and
             transport nutrients into the uterine lumen necessary for
             conceptus development, pregnancy recognition signaling, and
             implantation. Secretions include arginine and secreted
             phosphoprotein 1 (SPP1). Arginine can be metabolized to
             nitric oxide and to polyamines or act directly to activate
             the mechanistic target of rapamycin cell signaling pathway
             to stimulate proliferation, migration, and mRNA translation
             in trophectoderm cells. SPP1 binds alphavbeta3 and
             alpha5beta1 integrins to induce focal adhesion assembly,
             adhesion, and migration of conceptus trophectoderm cells
             during implantation. Thus, arginine and SPP1 mediate growth,
             migration, cytoskeletal remodeling, and adhesion of
             trophectoderm essential for pregnancy recognition signaling
             and implantation. This minireview focuses on components of
             histotroph that affect conceptus development in the
             ewe.},
   Language = {eng},
   Doi = {10.1095/biolreprod.111.094722},
   Key = {fds204261}
}

@article{fds174090,
   Author = {MM Joyce, JR Burghardt and RC Burghardt and RN Hooper and FW Bazer and GA Johnson},
   Title = {Uterine MHC class I molecules and beta 2-microglobulin are
             regulated by progesterone and conceptus interferons during
             pig pregnancy.},
   Journal = {Journal of immunology (Baltimore, Md. : 1950)},
   Volume = {181},
   Number = {4},
   Pages = {2494-505},
   Year = {2008},
   Month = {August},
   ISSN = {1550-6606},
   Keywords = {Animals • Embryo Implantation • Endometrium •
             Female • Histocompatibility Antigens Class I •
             Interferon Type I • Interferon-gamma • Interferons
             • Maternal-Fetal Exchange • Pregnancy •
             Pregnancy Proteins • Progesterone • RNA, Messenger
             • Random Allocation • Swine • Uterus •
             beta 2-Microglobulin • biosynthesis •
             biosynthesis* • embryology • genetics •
             immunology • immunology* • metabolism •
             metabolism* • physiology • physiology* •
             secretion • secretion*},
   Abstract = {MHC class I molecules and beta(2)-microglobulin (beta(2)m)
             are membrane glycoproteins that present peptide Ags to TCRs,
             and bind to inhibitory and activating receptors on NK cells
             and other leukocytes. They are involved in the
             discrimination of self from non-self. Modification of these
             molecules in the placenta benefits pregnancy, but little is
             known about their genes in the uterus. We examined the
             classical class I swine leukocyte Ags (SLA) genes SLA-1,
             SLA-2, and SLA-3, the nonclassical SLA-6, SLA-7, and SLA-8
             genes, and the beta(2)m gene in pig uterus during pregnancy.
             Uterine SLA and beta(2)m increased in luminal epithelium
             between days 5 and 9, then decreased between days 15 and 20.
             By day 15 of pregnancy, SLA and beta(2)m increased in stroma
             and remained detectable through day 40. To determine effects
             of estrogens, which are secreted by conceptuses to prevent
             corpus luteum regression, nonpregnant pigs were treated with
             estradiol benzoate, which did not affect the SLA or beta(2)m
             genes. In contrast, progesterone, which is secreted by
             corpora lutea, increased SLA and beta(2)m in luminal
             epithelium, whereas a progesterone receptor antagonist
             (ZK137,316) ablated this up-regulation. To determine effects
             of conceptus secretory proteins (CSP) containing IFN-delta
             and IFN-gamma, nonpregnant pigs were implanted with
             mini-osmotic pumps that delivered CSP to uterine horns. CSP
             increased SLA and beta(2)m in stroma. Cell-type specific
             regulation of SLA and beta(2)m genes by progesterone and
             IFNs suggests that placental secretions control expression
             of immune regulatory molecules on uterine cells to provide
             an immunologically favorable environment for survival of the
             fetal-placental semiallograft.},
   Language = {eng},
   Key = {fds174090}
}

@article{fds204263,
   Author = {FW Bazer and TE Spencer and GA Johnson and RC Burghardt},
   Title = {Uterine receptivity to implantation of blastocysts in
             mammals.},
   Journal = {Frontiers in bioscience (Scholar edition)},
   Volume = {3},
   Pages = {745-67},
   Year = {2011},
   ISSN = {1945-0524},
   Keywords = {Animals • Embryo Implantation • Endometrium •
             Female • Humans • Pregnancy • Receptors,
             Steroid • Species Specificity • Trophoblasts
             • Uterus • metabolism • metabolism* •
             physiology*},
   Abstract = {Reproduction in mammals is a highly complex biological
             process. The critical importance of reproduction to
             propagation of species required the natural evolution of
             various strategies that vary considerably across species.
             Regardless of species, a dialogue between the developing
             conceptus (embryo-fetus and associated placental membranes)
             and maternal uterus must be established during the
             peri-implantation period. The uterus must provide a
             microenvironment that supports growth and development of the
             conceptus and is receptive to implantation. During the same
             period, the conceptus must provide its pregnancy recognition
             signaling to sustain the functional life of corpora lutea
             for production of progesterone which is essential for
             implantation and placentation; critical events for
             successful pregnancy. However, it is within the
             peri-implantation period that most embryonic deaths occur
             due to deficiencies attributed to uterine functions or to
             the failure of the conceptus to develop appropriately,
             signal pregnancy recognition and/or undergo implantation and
             placentation. The challenge is to understand the complexity
             of key mechanisms that are characteristic of successful
             reproduction in humans and animals and to use that knowledge
             to enhance fertility and reproductive health or to establish
             acceptable methods for control of fertility.},
   Language = {eng},
   Key = {fds204263}
}

@article{fds157077,
   Author = {OB Boyko, SR Alston and GN Fuller and CM Hulette and GA Johnson and PC
             Burger},
   Title = {Utility of postmortem magnetic resonance imaging in clinical
             neuropathology.},
   Journal = {Archives of pathology & laboratory medicine, UNITED
             STATES},
   Volume = {118},
   Number = {3},
   Pages = {219-25},
   Year = {1994},
   Month = {March},
   ISSN = {0003-9985},
   Keywords = {Autopsy • Brain • Central Nervous System •
             Central Nervous System Neoplasms • Cerebrovascular
             Disorders • Humans • Magnetic Resonance Imaging*
             • Multiple Sclerosis • Nervous System Diseases
             • injuries • methods* • pathology •
             pathology*},
   Abstract = {Over 200 brains were examined by postmortem magnetic
             resonance imaging to determine the utility of this imaging
             procedure as an adjunct to the standard postmortem
             examination of the brain and spinal cord. One unembalmed
             cadaver was also studied using a conventional 1.5-tesla (T)
             field-strength unit, and three formalin-fixed sections of
             the hippocampus were imaged using a high field-strength
             (7.0-T) prototype imaging system. The postmortem magnetic
             resonance images proved to be an invaluable aid that
             complemented the standard pathologic examination of the
             brain and spinal cord. The compelling advantages of this
             postmortem radiographic procedure included the
             three-dimensional aspects of the images; the ability to
             detect mineral (ie, iron) deposits; small focal lesions such
             as hemorrhages or infarcts; and the ability to evaluate the
             extent of cerebral edema. For the same reasons, as well as
             its archival potential for documenting the topographic
             distribution of pathologic processes, this technique has
             great promise for forensic cases. High field-strength
             (7.0-T) imaging brought the resolution of magnetic resonance
             to the microscopic level and reaffirmed the potential value
             of magnetic resonance imaging for diagnostic and
             investigative studies in which both the histologic and fine
             radiologic features of lesions are of interest.},
   Key = {fds157077}
}

@booklet{Boyko94,
   Author = {Boyko, OB and Alston, SR and Fuller, GN and Hulette, CM and Johnson, GA and Burger, PC},
   Title = {Utility of postmortem magnetic resonance imaging in clinical
             neuropathology.},
   Journal = {Arch Pathol Lab Med},
   Volume = {118},
   Number = {3},
   Pages = {219-225},
   Year = {1994},
   Month = {March},
   ISSN = {0003-9985},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/8135623},
   Abstract = {Over 200 brains were examined by postmortem magnetic
             resonance imaging to determine the utility of this imaging
             procedure as an adjunct to the standard postmortem
             examination of the brain and spinal cord. One unembalmed
             cadaver was also studied using a conventional 1.5-tesla (T)
             field-strength unit, and three formalin-fixed sections of
             the hippocampus were imaged using a high field-strength
             (7.0-T) prototype imaging system. The postmortem magnetic
             resonance images proved to be an invaluable aid that
             complemented the standard pathologic examination of the
             brain and spinal cord. The compelling advantages of this
             postmortem radiographic procedure included the
             three-dimensional aspects of the images; the ability to
             detect mineral (ie, iron) deposits; small focal lesions such
             as hemorrhages or infarcts; and the ability to evaluate the
             extent of cerebral edema. For the same reasons, as well as
             its archival potential for documenting the topographic
             distribution of pathologic processes, this technique has
             great promise for forensic cases. High field-strength
             (7.0-T) imaging brought the resolution of magnetic resonance
             to the microscopic level and reaffirmed the potential value
             of magnetic resonance imaging for diagnostic and
             investigative studies in which both the histologic and fine
             radiologic features of lesions are of interest.},
   Key = {Boyko94}
}

@article{fds268791,
   Author = {Bowsher, JE and Yuan, H and Hedlund, LW and Turkington, TG and Akabani,
             G and Badea, A and Kurylo, WC and Ted Wheeler and C and Cofer, GP and Dewhirst, MW and Allan Johnson and G},
   Title = {Utilizing MRI information to estimate F18-FDG distributions
             in rat flank tumors},
   Journal = {IEEE Nuclear Science Symposium Conference
             Record},
   Volume = {4},
   Pages = {2488-2492},
   Year = {2004},
   Month = {December},
   ISSN = {1095-7863},
   Abstract = {This paper investigates the potential of magnetic resonance
             imaging (MRI) to improve the estimation of within-tumor
             variations in F18-FDG concentration. An image model is
             described for incorporating MRI images into positron
             emission tomography (PET) and single photon emission
             computed tomog-raphy (SPECT) radiotracer image
             reconstruction. The model promotes greater smoothing, of
             estimated radiotracer concentration, among nearby voxels
             that have more nearly similar MRI signals. R3230 mammary
             adenocarcinomas are grown on rat flanks. Autoradiography,
             histology, and T2-weighted MRI are used to demonstrate that
             the above image model accurately reflects true F18-FDG
             distributions in R3230 tumors. In vivo F18-FDG distributions
             are then reconstructed from PET projection data, with and
             without incorporating MRI. The F18-FDG images reconstructed
             with MRI show greater detail, and this additional detail is
             consistent with the results of the autoradiography and
             histology studies. © 2004 IEEE.},
   Key = {fds268791}
}

@booklet{Walsh01,
   Author = {B. Walsh and G. A. Johnson},
   Title = {Validation: Never an endpoint: A systems development life
             cycle approach to good clinical practice},
   Journal = {Drug Information Journal},
   Volume = {35},
   Number = {3},
   Pages = {809 -- 817},
   Year = {2001},
   Key = {Walsh01}
}

@article{fds351448,
   Author = {Wang, N and Anderson, RJ and Ashbrook, DG and Gopalakrishnan, V and Park, Y and Priebe, CE and Qi, Y and Laoprasert, R and Vogelstein, JT and Williams, RW and Johnson, GA},
   Title = {Variability and heritability of mouse brain structure:
             Microscopic MRI atlases and connectomes for diverse
             strains.},
   Journal = {Neuroimage},
   Volume = {222},
   Pages = {117274},
   Year = {2020},
   Month = {November},
   url = {http://dx.doi.org/10.1016/j.neuroimage.2020.117274},
   Abstract = {Genome-wide association studies have demonstrated
             significant links between human brain structure and common
             DNA variants. Similar studies with rodents have been
             challenging because of smaller brain volumes. Using high
             field MRI (9.4 T) and compressed sensing, we have achieved
             microscopic resolution and sufficiently high throughput for
             rodent population studies. We generated whole brain
             structural MRI and diffusion connectomes for four diverse
             isogenic lines of mice (C57BL/6J, DBA/2J, CAST/EiJ, and
             BTBR) at spatial resolution 20,000 times higher than human
             connectomes. We measured narrow sense heritability (h2) I.e.
             the fraction of variance explained by strains in a simple
             ANOVA model for volumes and scalar diffusion metrics, and
             estimates of residual technical error for 166 regions in
             each hemisphere and connectivity between the regions.
             Volumes of discrete brain regions had the highest mean
             heritability (0.71 ± 0.23 SD, n = 332), followed by
             fractional anisotropy (0.54 ± 0.26), radial diffusivity
             (0.34 ± 0.022), and axial diffusivity (0.28 ± 0.19).
             Connection profiles were statistically different in 280 of
             322 nodes across all four strains. Nearly 150 of the
             connection profiles were statistically different between the
             C57BL/6J, DBA/2J, and CAST/EiJ lines. Microscopic whole
             brain MRI/DTI has allowed us to identify significant
             heritable phenotypes in brain volume, scalar DTI metrics,
             and quantitative connectomes.},
   Doi = {10.1016/j.neuroimage.2020.117274},
   Key = {fds351448}
}

@booklet{Brown84,
   Author = {BROWN, MA and JOHNSON, GA},
   Title = {VARIABLE FIELD STUDIES OF POTENTIAL PARAMAGNETIC NMR
             CONTRAST AGENTS},
   Journal = {MAGNETIC RESONANCE IN MEDICINE},
   Volume = {1},
   Number = {2},
   Pages = {119-120},
   Year = {1984},
   ISSN = {0740-3194},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1984TF94000037&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Brown84}
}

@booklet{Karis86,
   Author = {KARIS, JP and GLOVER, GH and JOHNSON, GA},
   Title = {VARIANT ANGLE GRADIENT REFOCUSING IN 3-DIMENSIONAL MRI
             MICROSCOPY},
   Journal = {INVESTIGATIVE RADIOLOGY},
   Volume = {21},
   Number = {9},
   Pages = {S34-S34},
   Publisher = {LIPPINCOTT-RAVEN PUBL},
   Year = {1986},
   Month = {September},
   ISSN = {0020-9996},
   url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1986E000900141&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
   Key = {Karis86}
}

@booklet{Cline89,
   Author = {Cline, HE and Lorensen, WE and Herfkens, RJ and Johnson, GA and Glover,
             GH},
   Title = {Vascular morphology by three-dimensional magnetic resonance
             imaging.},
   Journal = {Magn Reson Imaging},
   Volume = {7},
   Number = {1},
   Pages = {45-54},
   Year = {1989},
   ISSN = {0730-725X},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/2918818},
   Abstract = {A three-dimensional examination of blood vessels is provided
             using MR data from seven cases. The vascular surfaces are
             constructed with an algorithm that automatically follows the
             selected artery or vein and generates a projected
             three-dimensional gradient shaded image. Fast 3DFT pulse
             sequences were optimized to enhance the time-of-flight
             contrast of the intravascular region. By increasing the
             surface threshold value in a three-dimensional head study,
             the flesh of a patient's face was peeled away to demonstrate
             the superfacial temporal artery. Gated cardiac images show
             the great vessels and cardiac chambers. A three-dimensional
             view of the aorta shows an irregular surface in the vicinity
             of an adrenal tumor. 3D MR exams provide a non-invasive
             technique for assessing vascular morphology in a clinical
             setting.},
   Doi = {10.1016/0730-725x(89)90323-8},
   Key = {Cline89}
}

@article{fds132805,
   Author = {HE Cline and WE Lorensen and RJ Herfkens and GA Johnson and GH
             Glover},
   Title = {Vascular morphology by three-dimensional magnetic resonance
             imaging.},
   Journal = {Magnetic resonance imaging, UNITED STATES},
   Volume = {7},
   Number = {1},
   Pages = {45-54},
   ISSN = {0730-725X},
   Keywords = {Adult • Algorithms* • Animals • Blood Vessels
             • Dogs • Head and Neck Neoplasms • Heart
             • Humans • Image Processing, Computer-Assisted
             • Magnetic Resonance Imaging • Male • anatomy
             & histology • anatomy & histology* • diagnosis
             • methods • methods*},
   Abstract = {A three-dimensional examination of blood vessels is provided
             using MR data from seven cases. The vascular surfaces are
             constructed with an algorithm that automatically follows the
             selected artery or vein and generates a projected
             three-dimensional gradient shaded image. Fast 3DFT pulse
             sequences were optimized to enhance the time-of-flight
             contrast of the intravascular region. By increasing the
             surface threshold value in a three-dimensional head study,
             the flesh of a patient's face was peeled away to demonstrate
             the superfacial temporal artery. Gated cardiac images show
             the great vessels and cardiac chambers. A three-dimensional
             view of the aorta shows an irregular surface in the vicinity
             of an adrenal tumor. 3D MR exams provide a non-invasive
             technique for assessing vascular morphology in a clinical
             setting.},
   Key = {fds132805}
}

@booklet{Aiken84,
   Author = {J. W. Aiken and D. W. Harris and G. A. Johnson and J. H.
             Ludens and C. J. Taylor and E. O. Weselcouch and G. J.
             Wilson},
   Title = {Vasodilator and natriuretic activity extracted from rat
             atria},
   Journal = {Federation Proceedings},
   Volume = {43},
   Number = {3},
   Pages = {453 -- 453},
   Year = {1984},
   Key = {Aiken84}
}

@article{fds132903,
   Author = {BT Chen and AT Yordanov and GA Johnson},
   Title = {Ventilation-synchronous magnetic resonance microscopy of
             pulmonary structure and ventilation in mice.},
   Journal = {Magnetic resonance in medicine : official journal of the
             Society of Magnetic Resonance in Medicine / Society of
             Magnetic Resonance in Medicine, United States},
   Volume = {53},
   Number = {1},
   Pages = {69-75},
   Year = {2005},
   Month = {January},
   ISSN = {0740-3194},
   Keywords = {Anesthesia • Animals • Contrast Media •
             Imaging, Three-Dimensional • Lung • Magnetic
             Resonance Imaging • Magnetic Resonance Spectroscopy
             • Male • Mice • Mice, Inbred C57BL •
             Pulmonary Ventilation • Respiration, Artificial •
             Ventilation-Perfusion Ratio • anatomy & histology*
             • diagnostic use* • methods* • physiology
             • physiology*},
   Abstract = {Increasing use of transgenic animal models for pulmonary
             disease has raised the need for methods to assess pulmonary
             structure and function in a physiologically stable mouse. We
             report here an integrated protocol using magnetic resonance
             microscopy with gadolinium (Gd)-labeled starburst dendrimer
             (G6-1B4M-Gd, MW = 192 +/- 1 kDa, R(h) = 5.50 +/- 0.04 nm)
             and hyperpolarized (3)helium ((3)He) gas to acquire images
             that demonstrate pulmonary vasculature and ventilated
             airways in live mice (n = 9). Registered three-dimensional
             images of (1)H and (3)He were acquired during breath-hold at
             2.0 T using radial acquisition (total acquisition time of 38
             and 25 min, respectively). The macromolecular Gd-labeled
             dendrimer (a half-life of approximately 80 min) increased
             the signal-to-noise by 81 +/- 30% in the left ventricle, 43
             +/- 22% in the lung periphery, and -4 +/- 5% in the chest
             wall, thus increasing the contrast of these structures
             relative to the less vascular surrounding tissues. A
             constant-flow ventilator was developed for the mouse to
             deliver varied gas mixtures of O(2) and N(2) (or (3)He)
             during imaging. To avoid hypoxemia, instrumental dead space
             was minimized and corrections were made to tidal volume lost
             due to gas compression. The stability of the physiologic
             support was assessed by the lack of spontaneous breathing
             and maintenance of a constant heart rate. We were able to
             stabilize the mouse for >8 hr using ventilation of 105
             breath/min and approximately 0.2 mL/breath. The feasibility
             of acquiring both pulmonary vasculature and ventilated
             airways was demonstrated in the mouse lung with in-plane
             spatial resolution of 70 x 70 microm(2) and slice thickness
             of 800 microm.},
   Key = {fds132903}
}

@booklet{Chen05,
   Author = {Chen, BT and Yordanov, AT and Johnson, GA},
   Title = {Ventilation-synchronous magnetic resonance microscopy of
             pulmonary structure and ventilation in mice.},
   Journal = {Magn Reson Med},
   Volume = {53},
   Number = {1},
   Pages = {69-75},
   Year = {2005},
   Month = {January},
   ISSN = {0740-3194},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/15690504},
   Abstract = {Increasing use of transgenic animal models for pulmonary
             disease has raised the need for methods to assess pulmonary
             structure and function in a physiologically stable mouse. We
             report here an integrated protocol using magnetic resonance
             microscopy with gadolinium (Gd)-labeled starburst dendrimer
             (G6-1B4M-Gd, MW = 192 +/- 1 kDa, R(h) = 5.50 +/- 0.04 nm)
             and hyperpolarized (3)helium ((3)He) gas to acquire images
             that demonstrate pulmonary vasculature and ventilated
             airways in live mice (n = 9). Registered three-dimensional
             images of (1)H and (3)He were acquired during breath-hold at
             2.0 T using radial acquisition (total acquisition time of 38
             and 25 min, respectively). The macromolecular Gd-labeled
             dendrimer (a half-life of approximately 80 min) increased
             the signal-to-noise by 81 +/- 30% in the left ventricle, 43
             +/- 22% in the lung periphery, and -4 +/- 5% in the chest
             wall, thus increasing the contrast of these structures
             relative to the less vascular surrounding tissues. A
             constant-flow ventilator was developed for the mouse to
             deliver varied gas mixtures of O(2) and N(2) (or (3)He)
             during imaging. To avoid hypoxemia, instrumental dead space
             was minimized and corrections were made to tidal volume lost
             due to gas compression. The stability of the physiologic
             support was assessed by the lack of spontaneous breathing
             and maintenance of a constant heart rate. We were able to
             stabilize the mouse for >8 hr using ventilation of 105
             breath/min and approximately 0.2 mL/breath. The feasibility
             of acquiring both pulmonary vasculature and ventilated
             airways was demonstrated in the mouse lung with in-plane
             spatial resolution of 70 x 70 microm(2) and slice thickness
             of 800 microm.},
   Doi = {10.1002/mrm.20307},
   Key = {Chen05}
}

@article{fds268836,
   Author = {Mistry, NN and Qi, Y and Hedlund, LW and Johnson,
             GA},
   Title = {Ventilation/perfusion imaging in a rat model of airway
             obstruction.},
   Journal = {Magn Reson Med},
   Volume = {63},
   Number = {3},
   Pages = {728-735},
   Year = {2010},
   Month = {March},
   ISSN = {1522-2594},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/20146375},
   Keywords = {Administration, Inhalation • Airway Obstruction •
             Algorithms* • Animals • Disease Models, Animal*
             • Female • Helium • Humans • Image
             Enhancement • Isotopes • Magnetic Resonance
             Imaging • Perfusion Imaging • Rats • Rats,
             Inbred F344 • Reproducibility of Results •
             Sensitivity and Specificity • administration & dosage
             • diagnosis* • diagnostic use • diagnostic
             use* • methods*},
   Abstract = {The global increase in asthma, chronic obstructive pulmonary
             disease, and other pulmonary diseases has stimulated
             interest in preclinical rat models of pulmonary disease.
             Imaging methods for study of these models is particularly
             appealing since the results can be readily translated to the
             clinical setting. Comprehensive understanding of lung
             function can be achieved by performing registered pulmonary
             ventilation and perfusion imaging studies in the same
             animal. While ventilation imaging has been addressed for
             small animals, quantitative pulmonary perfusion imaging has
             not been feasible until recently, with our proposed
             technique for quantitative perfusion imaging using multiple
             contrast-agent injections and a view-sharing radial imaging
             technique. Here, we combine the method with registered
             ventilation imaging using hyperpolarized (3)He in an airway
             obstruction rodent model. To our knowledge, this is the
             first comprehensive quantitative assessment of lung function
             in small animals at high spatial resolution. Standard
             deviation of the log (V/Q) is used as a quantitative
             biomarker to differentiate heterogeneity between the control
             and treatment group. The estimated value of the biomarker
             lies within the normal range of values reported in the
             literature. The biomarker that was extracted using the
             imaging technique described in this work showed
             statistically significant differences between the control
             rats and those with airway obstruction.},
   Language = {eng},
   Doi = {10.1002/mrm.22221},
   Key = {fds268836}
}

@article{fds132724,
   Author = {G.A. Johnson},
   Title = {Viallon M, Cofer GP, Suddarth SA, Msller H, Chen XJ, Chawla
             MS, Hedlund LW, Cr Millieux Y, Johson GA. Functional MR
             microscopy of the lung with hyperpolarized 3He. Mag Reson
             Med. In press 1998},
   Year = {1998},
   Key = {fds132724}
}

@booklet{Lester99,
   Author = {Lester, DS and Johannessen, JN and Pine, PS and McGregor, GN and Johnson, GA},
   Title = {Virtual neuropathology: A new approach to preclinical
             pathology using magnetic resonance imaging
             microscopy},
   Journal = {Spectroscopy (Santa Monica)},
   Volume = {14},
   Number = {7},
   Pages = {17-22},
   Year = {1999},
   Month = {December},
   ISSN = {0887-6703},
   Key = {Lester99}
}

@booklet{Lester00,
   Author = {Lester, DS and Pine, PS and Delnomdedieu, M and Johannessen, JN and Johnson, GA},
   Title = {Virtual neuropathology: three-dimensional visualization of
             lesions due to toxic insult.},
   Journal = {Toxicol Pathol},
   Volume = {28},
   Number = {1},
   Pages = {100-104},
   Year = {2000},
   ISSN = {0192-6233},
   url = {http://dx.doi.org/10.1177/019262330002800112},
   Abstract = {A first-pass approach incorporating high-field magnetic
             resonance imaging (MRI) was used for rapid detection of
             neuropathologic lesions in fixed rat brains. This inherently
             3-dimensional and nondestructive technique provides
             high-resolution, high-contrast images of fixed neuronal
             tissue in the absence of sectioning or staining. This
             technique, magnetic resonance microscopy (MRM), was used to
             identify diverse lesions in 2 well-established rat
             neurotoxicity models. The intrinsic contrast in the images
             delineated lesions that were identified using a battery of
             histologic stains, some of which would not be used in
             routine screening. Furthermore, the MRM images provided the
             locations of lesions, which were verified upon subsequent
             sectioning and staining of the same samples. The inherent
             contrast generated by water properties is exploited in MRM
             by choosing suitable pulse sequences, or proton stains. This
             approach provides the potential for a comprehensive initial
             MRM screen for neurotoxicity in preclinical models with the
             capability for extrapolation to clinical analyses using
             classical MRI.},
   Doi = {10.1177/019262330002800112},
   Key = {Lester00}
}

@article{fds132837,
   Author = {DS Lester and PS Pine and M Delnomdedieu and JN Johannessen and GA
             Johnson},
   Title = {Virtual neuropathology: three-dimensional visualization of
             lesions due to toxic insult.},
   Journal = {Toxicologic pathology, UNITED STATES},
   Volume = {28},
   Number = {1},
   Pages = {100-4},
   ISSN = {0192-6233},
   Keywords = {Animals • Brain • Image Processing,
             Computer-Assisted • Kainic Acid • Magnetic
             Resonance Imaging • Microscopy • Nervous System
             Diseases • Neurotoxicity Syndromes • Neurotoxins
             • Oxidopamine • Parkinson Disease, Secondary
             • Rats • Sympatholytics • analogs &
             derivatives • chemically induced • methods* •
             pathology • pathology* • toxicity},
   Abstract = {A first-pass approach incorporating high-field magnetic
             resonance imaging (MRI) was used for rapid detection of
             neuropathologic lesions in fixed rat brains. This inherently
             3-dimensional and nondestructive technique provides
             high-resolution, high-contrast images of fixed neuronal
             tissue in the absence of sectioning or staining. This
             technique, magnetic resonance microscopy (MRM), was used to
             identify diverse lesions in 2 well-established rat
             neurotoxicity models. The intrinsic contrast in the images
             delineated lesions that were identified using a battery of
             histologic stains, some of which would not be used in
             routine screening. Furthermore, the MRM images provided the
             locations of lesions, which were verified upon subsequent
             sectioning and staining of the same samples. The inherent
             contrast generated by water properties is exploited in MRM
             by choosing suitable pulse sequences, or proton stains. This
             approach provides the potential for a comprehensive initial
             MRM screen for neurotoxicity in preclinical models with the
             capability for extrapolation to clinical analyses using
             classical MRI.},
   Key = {fds132837}
}

@article{fds132887,
   Author = {F O'Foghludha and GA Johnson},
   Title = {Voltage waveform effects on output and penetration of W- and
             Mo-anode mammographic tubes.},
   Journal = {Physics in medicine and biology, ENGLAND},
   Volume = {26},
   Number = {2},
   Pages = {291-303},
   Year = {1981},
   Month = {March},
   ISSN = {0031-9155},
   Keywords = {Electrodes • Female • Humans • Mammography
             • Molybdenum • Tungsten • instrumentation
             • methods*},
   Abstract = {The output and half-value thickness (HVT) for arbitrary
             voltage waveforms can be calculated if the variation of both
             quantities with voltage is known under constant-potential
             (ripple-free) conditions. An apparatus to study this
             variation is described. It permits measurements of output
             and HVT with a Si(Li) spectrometer under conditions
             equivalent to constant-potential operation; it uses
             mechanical or electronic gating to limit observations to
             constant-potential operation; it uses mechanical or
             electronic gating to limit observations to short periods
             near the peaks of a sinusoidal waveform. For W anodes both
             HVT and output are found to follow simple power laws, while
             polynomial functions of voltage are needed for Mo anodes.
             Calculations based on these data agree well with experiments
             in which various ripples are simulated by altering the
             gating interval. For Mo anodes, the output increases as the
             ripple decreases, but the HVT changes very little. For W
             anodes both quantities decrease when the ripple increases.
             The implications in mammography are briefly
             discussed.},
   Key = {fds132887}
}

@booklet{Ofoghludha81,
   Author = {O'Foghludha, F and Johnson, GA},
   Title = {Voltage waveform effects on output and penetration of W- and
             Mo-anode mammographic tubes.},
   Journal = {Phys Med Biol},
   Volume = {26},
   Number = {2},
   Pages = {291-303},
   Year = {1981},
   Month = {March},
   ISSN = {0031-9155},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/7220605},
   Abstract = {The output and half-value thickness (HVT) for arbitrary
             voltage waveforms can be calculated if the variation of both
             quantities with voltage is known under constant-potential
             (ripple-free) conditions. An apparatus to study this
             variation is described. It permits measurements of output
             and HVT with a Si(Li) spectrometer under conditions
             equivalent to constant-potential operation; it uses
             mechanical or electronic gating to limit observations to
             constant-potential operation; it uses mechanical or
             electronic gating to limit observations to short periods
             near the peaks of a sinusoidal waveform. For W anodes both
             HVT and output are found to follow simple power laws, while
             polynomial functions of voltage are needed for Mo anodes.
             Calculations based on these data agree well with experiments
             in which various ripples are simulated by altering the
             gating interval. For Mo anodes, the output increases as the
             ripple decreases, but the HVT changes very little. For W
             anodes both quantities decrease when the ripple increases.
             The implications in mammography are briefly
             discussed.},
   Doi = {10.1088/0031-9155/26/2/008},
   Key = {Ofoghludha81}
}

@article{fds368127,
   Author = {Du, EY and Ortega, BK and Ninoyu, Y and Williams, RW and Cofer, GP and Cook, JJ and Hornburg, KJ and Qi, Y and Johnson, GA and Friedman,
             RA},
   Title = {Volumetric analysis of the aging auditory pathway using high
             resolution magnetic resonance histology.},
   Journal = {Front Aging Neurosci},
   Volume = {14},
   Pages = {1034073},
   Year = {2022},
   url = {http://dx.doi.org/10.3389/fnagi.2022.1034073},
   Abstract = {Numerous shown consequences of age-related hearing loss have
             been unveiled; however, the relationship of the cortical and
             subcortical structures of the auditory pathway with aging is
             not well known. Investigations into neural structure
             analysis remain sparse due to difficulties of doing so in
             animal models; however, recent technological advances have
             been able to achieve a resolution adequate to perform such
             studies even in the small mouse. We utilize 12 members of
             the BXD family of recombinant inbred mice and aged separate
             cohorts. Utilizing novel magnetic resonance histology
             imaging techniques, we imaged these mice and generated high
             spatial resolution three dimensional images which were then
             comprehensively labeled. We completed volumetric analysis of
             12 separate regions of interest specific to the auditory
             pathway brainstem nuclei and cortical areas with focus on
             the effect of aging upon said structures. Our results showed
             significant interstrain variation in the age-related effect
             on structure volume supporting a genetic influence in this
             interaction. Through multivariable modeling, we observed
             heterogenous effects of aging between different structures.
             Six of the 12 regions of interests demonstrated a
             significant age-related effect. The auditory cortex and
             ventral cochlear nucleus were found to decrease in volume
             with age, while the medial division of the medial geniculate
             nucleus, lateral lemniscus and its nucleus, and the inferior
             colliculus increased in size with age. Additionally, no
             sex-based differences were noted, and we observed a negative
             relationship between auditory cortex volume and mouse
             weight. This study is one of the first to perform
             comprehensive magnetic resonance imaging and quantitative
             analysis in the mouse brain auditory pathway
             cytoarchitecture, offering both novel insights into the
             neuroanatomical basis of age-related changes in hearing as
             well as evidence toward a genetic influence in this
             interaction. High resonance magnetic resonance imaging
             provides a promising efficacious avenue in future mouse
             model hearing loss investigations.},
   Doi = {10.3389/fnagi.2022.1034073},
   Key = {fds368127}
}

@article{fds268778,
   Author = {Badea, CT and Hedlund, LW and Wheeler, CT and Mai, W and Johnson,
             GA},
   Title = {Volumetric micro-CT system for in vivo microscopy},
   Journal = {2004 2nd IEEE International Symposium on Biomedical Imaging:
             Macro to Nano},
   Volume = {2},
   Pages = {1377-1380},
   Year = {2004},
   Month = {December},
   ISBN = {0780383885},
   Abstract = {Two of the major barriers to improved image quality in
             micro-CT are the reduced signal to noise imposed by the
             smaller voxels and the effects of physiologic motion. The
             most direct approach to increase the signal to noise ratio
             (SNR) is to increase the flux. This is not possible in most
             of laboratory and commercial micro-CT systems that are
             currently in use. We adopted a design that allows the use of
             high instantaneous X-ray flux combined with synchronization
             to physiologic motion. High quality imaging of moving organs
             such as the heart or the lungs is directly dependent on
             appropriate gating techniques. For this purpose, we acquired
             X-ray projections using a flexible controller to enable
             sophisticated biological pulse sequences to minimize the
             effects of motion. This paper reports on the development of
             a volumetric micro-CT scanner dedicated to structural and
             functional phenotyping of the live mouse. © 2004
             IEEE.},
   Key = {fds268778}
}

@article{fds132735,
   Author = {G.A. Johnson},
   Title = {W. L. Hall, H. Benveniste, L.W. Hedlund, G.A. Johnson, A new
             in vivo  method for quantitative analysis of stroke lesions
             using MR microscopy.   NeuroImage 3, 158-166
             (1996).},
   Year = {1996},
   Key = {fds132735}
}

@article{fds268716,
   Author = {Papp, EA and Leergaard, TB and Calabrese, E and Johnson, GA and Bjaalie,
             JG},
   Title = {Waxholm Space atlas of the Sprague Dawley rat
             brain.},
   Journal = {Neuroimage},
   Volume = {97},
   Pages = {374-386},
   Year = {2014},
   Month = {August},
   ISSN = {1053-8119},
   url = {http://dx.doi.org/10.1016/j.neuroimage.2014.04.001},
   Abstract = {Three-dimensional digital brain atlases represent an
             important new generation of neuroinformatics tools for
             understanding complex brain anatomy, assigning location to
             experimental data, and planning of experiments. We have
             acquired a microscopic resolution isotropic MRI and DTI
             atlasing template for the Sprague Dawley rat brain with 39
             μm isotropic voxels for the MRI volume and 78 μm isotropic
             voxels for the DTI. Building on this template, we have
             delineated 76 major anatomical structures in the brain.
             Delineation criteria are provided for each structure. We
             have applied a spatial reference system based on internal
             brain landmarks according to the Waxholm Space standard,
             previously developed for the mouse brain, and furthermore
             connected this spatial reference system to the widely used
             stereotaxic coordinate system by identifying cranial sutures
             and related stereotaxic landmarks in the template using
             contrast given by the active staining technique applied to
             the tissue. With the release of the present atlasing
             template and anatomical delineations, we provide a new tool
             for spatial orientation analysis of neuroanatomical
             location, and planning and guidance of experimental
             procedures in the rat brain. The use of Waxholm Space and
             related infrastructures will connect the atlas to
             interoperable resources and services for multi-level data
             integration and analysis across reference
             spaces.},
   Doi = {10.1016/j.neuroimage.2014.04.001},
   Key = {fds268716}
}

@article{fds268825,
   Author = {Johnson, GA and Badea, A and Brandenburg, J and Cofer, G and Fubara, B and Liu, S and Nissanov, J},
   Title = {Waxholm space: an image-based reference for coordinating
             mouse brain research.},
   Journal = {Neuroimage},
   Volume = {53},
   Number = {2},
   Pages = {365-372},
   Year = {2010},
   Month = {November},
   ISSN = {1095-9572},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/20600960},
   Keywords = {Animals • Atlases as Topic • Brain •
             Databases, Factual • Histology • Image Processing,
             Computer-Assisted • Imaging, Three-Dimensional •
             Magnetic Resonance Imaging • Male • Mice •
             Mice, Inbred C57BL • Reference Standards •
             Staining and Labeling • Thalamus • anatomy &
             histology • anatomy & histology* • methods •
             standards*},
   Abstract = {We describe an atlas of the C57BL/6 mouse brain based on MRI
             and conventional Nissl histology. Magnetic resonance
             microscopy was performed on a total of 14 specimens that
             were actively stained to enhance tissue contrast. Images
             were acquired with three different MR protocols yielding
             contrast dependent on spin lattice relaxation (T1), spin
             spin relaxation (T2), and magnetic susceptibility (T2*).
             Spatial resolution was 21.5 mum (isotropic). Conventional
             histology (Nissl) was performed on a limited set of these
             same specimens and the Nissl images were registered
             (3D-to-3D) to the MR data. Probabilistic atlases for 37
             structures are provided, along with average atlases. The
             availability of three different MR protocols, the Nissl
             data, and the labels provides a rich set of options for
             registration of other atlases to the same coordinate system,
             thus facilitating data-sharing. All the data is available
             for download via the web.},
   Language = {eng},
   Doi = {10.1016/j.neuroimage.2010.06.067},
   Key = {fds268825}
}

@article{fds204250,
   Author = {GA Johnson},
   Title = {Ways to communicate the threat of climate change to
             health.},
   Journal = {BMJ (Clinical research ed.)},
   Volume = {343},
   Pages = {d7376},
   Year = {2011},
   ISSN = {1468-5833},
   Keywords = {Climate Change* • Communication* • Greenhouse
             Effect • Humans • Public Health* • Social
             Behavior},
   Language = {eng},
   Key = {fds204250}
}

@article{fds341987,
   Author = {Allan Johnson and G and Wang, N and Anderson, RJ and Chen, M and Cofer, GP and Gee, JC and Pratson, F and Tustison, N and White,
             LE},
   Title = {Whole mouse brain connectomics.},
   Journal = {J Comp Neurol},
   Volume = {527},
   Number = {13},
   Pages = {2146-2157},
   Year = {2019},
   Month = {September},
   url = {http://dx.doi.org/10.1002/cne.24560},
   Abstract = {Methods have been developed to allow quantitative
             connectivity of the whole fixed mouse brain by means of
             magnetic resonance imaging (MRI). We have translated what we
             have learned in clinical imaging to the very special domain
             of the mouse brain. Diffusion tensor imaging (DTI) of
             perfusion fixed specimens can now be performed with spatial
             resolution of 45 μm3 , that is, voxels that are 21,000
             times smaller than the human connectome protocol. Specimen
             preparation has been optimized through an active staining
             protocol using a Gd chelate. Compressed sensing has been
             integrated into high performance reconstruction and post
             processing pipelines allowing acquisition of a whole mouse
             brain connectome in <12 hr. The methods have been
             validated against retroviral tracer studies. False positive
             tracts, which are especially problematic in clinical
             studies, have been reduced substantially to ~28%. The
             methods have been streamlined to provide high-fidelity,
             whole mouse brain connectomes as a routine study. The data
             package provides holistic insight into the mouse brain with
             anatomic definition at the meso-scale, quantitative volumes
             of subfields, scalar DTI metrics, and quantitative
             tractography.},
   Doi = {10.1002/cne.24560},
   Key = {fds341987}
}

@article{fds338016,
   Author = {Wang, N and Anderson, RJ and Badea, A and Cofer, G and Dibb, R and Qi, Y and Johnson, GA},
   Title = {Whole mouse brain structural connectomics using magnetic
             resonance histology.},
   Journal = {Brain Struct Funct},
   Volume = {223},
   Number = {9},
   Pages = {4323-4335},
   Year = {2018},
   Month = {December},
   url = {http://dx.doi.org/10.1007/s00429-018-1750-x},
   Abstract = {Diffusion tensor histology holds great promise for
             quantitative characterization of structural connectivity in
             mouse models of neurological and psychiatric conditions.
             There has been extensive study in both the clinical and
             preclinical domains on the complex tradeoffs between the
             spatial resolution, the number of samples in diffusion
             q-space, scan time, and the reliability of the resultant
             data. We describe here a method for accelerating the
             acquisition of diffusion MRI data to support quantitative
             connectivity measurements in the whole mouse brain using
             compressed sensing (CS). The use of CS allows substantial
             increase in spatial resolution and/or reduction in scan
             time. Compared to the fully sampled results at the same scan
             time, the subtle anatomical details of the brain, such as
             cortical layers, dentate gyrus, and cerebellum, were better
             visualized using CS due to the higher spatial resolution.
             Compared to the fully sampled results at the same spatial
             resolution, the scalar diffusion metrics, including
             fractional anisotropy (FA) and mean diffusivity (MD), showed
             consistently low error across the whole brain (< 6.0%)
             even with 8.0 times acceleration. The node properties of
             connectivity (strength, cluster coefficient, eigenvector
             centrality, and local efficiency) demonstrated correlation
             of better than 95.0% between accelerated and fully sampled
             connectomes. The acceleration will enable routine
             application of this technology to a wide range of mouse
             models of neurologic diseases.},
   Doi = {10.1007/s00429-018-1750-x},
   Key = {fds338016}
}

@article{fds174266,
   Author = {K Hayashi and DW Erikson and SA Tilford and BM Bany and JA Maclean 2nd and EB Rucker 3rd and GA Johnson and TE Spencer},
   Title = {Wnt genes in the mouse uterus: potential regulation of
             implantation.},
   Journal = {Biology of reproduction},
   Volume = {80},
   Number = {5},
   Pages = {989-1000},
   Year = {2009},
   Month = {May},
   ISSN = {0006-3363},
   url = {http://dx.doi.org/10.1095/biolreprod.108.075416},
   Keywords = {Animals • Base Sequence • Cloning, Molecular
             • DNA Primers • DNA, Complementary • Embryo
             Implantation • Estradiol • Female • Frizzled
             Receptors • Gene Expression • Mice •
             Ovariectomy • Ovary • Pregnancy •
             Progesterone • RNA, Messenger • Signal
             Transduction • Uterus • Wnt Proteins • drug
             effects • genetics • genetics* • metabolism
             • metabolism* • pharmacology},
   Abstract = {Wnt genes are involved in critical developmental and growth
             processes. The present study comprehensively analyzed
             temporal and spatial alterations in Wnt and Fzd gene
             expression in the mouse uterus during peri-implantation of
             pregnancy. Expression of Wnt4, Wnt5a, Wnt7a, Wnt7b, Wnt11,
             Wnt16, Fzd2, Fzd4, and Fzd6 was detected in the uterus
             during implantation. Wnt4 mRNA was most abundant in the
             decidua, whereas Wnt5a mRNA was restricted to the
             mesometrial decidua during decidualization. Wnt7a, Wnt7b,
             and Wnt11 mRNAs were abundantly detected in the endometrial
             epithelia. The expression of Wnt7b was robust in the luminal
             epithelium (LE) at the implantation site on Gestational Day
             5, whereas Wnt11 mRNA disappeared in the LE adjacent to the
             embryo in the antimesometrial implantation chamber but
             remained abundant in the LE. Wnt16 mRNA was localized to the
             stroma surrounding the LE on Day 4 and remained in the
             stroma adjacent to the LE but not in areas undergoing the
             decidual reaction. Fzd2 mRNA was detected in the decidua,
             Fzd4 mRNA was in the vessels and stroma surrounding the
             embryo, and Fzd6 mRNA was observed in the endometrial
             epithelia, stroma, and some blood vessels during
             implantation. Ovarian steroid hormone treatment was found to
             regulate Wnt genes and Fzd receptors in ovariectomized mice.
             Especially, single injections of progesterone stimulated
             Wnt11 mRNA, and estrogen stimulated Wnt4 and Wnt7b. The
             temporal and spatial alterations in Wnt genes likely play a
             critical role during implantation and decidualization in
             mice.},
   Language = {eng},
   Doi = {10.1095/biolreprod.108.075416},
   Key = {fds174266}
}

@booklet{Silverman82a,
   Author = {P. M. Silverman and M. Korobkin and W. M. Thompson and G. A.
             Johnson and T. B. Cole and S. R. Fisher},
   Title = {Work in progress - high-resolution, thin-section
             computed-tomography of the larynx},
   Journal = {Radiology},
   Volume = {145},
   Number = {3},
   Pages = {723 -- 725},
   Year = {1982},
   Key = {Silverman82a}
}

@article{fds269036,
   Author = {Silverman, PM and Korobkin, M and Thompson, WM and Johnson, GA and Cole,
             TB and Fisher, SR},
   Title = {Work in progress: high-resolution, thin-section computed
             tomography of the larynx.},
   Journal = {Radiology},
   Volume = {145},
   Number = {3},
   Pages = {723-725},
   Year = {1982},
   Month = {December},
   ISSN = {0033-8419},
   url = {http://www.ncbi.nlm.nih.gov/pubmed/7146403},
   Keywords = {Humans • Laryngeal Neoplasms • Time Factors •
             Tomography, X-Ray Computed • methods* •
             radiography*},
   Doi = {10.1148/radiology.145.3.7146403},
   Key = {fds269036}
}