Morphology and Image Analysis Core (MIAC) The objectives of the core are to: 1. Provide consultation and training In microscopy and optical Image analysis for MDRC investigators Provide access to senior personnel highly skilled in microscopy and optical image analysis for MDRC Investigators 3. Provide access to state-of-the-art instrumentation for microscopy and optical image analysis for MDRC Investigators 4. Develop and/or implement new technologies for microscopy and optical Image analysis beneficial to MDRC Investigators. The MIAC remains focused on providing state-of-the-art quantitative morphological analysis of fixed and living cells for MDRC Investigators working on diabetes, its complications, and related endocrine and metabolic disorders. The Core provides service, consultation, collaboration and access to instrumentation for a variety of microscopic and analytic techniques. The Core focuses on light microscopic and confocal analysis of fixed and living cells using immunocyto-chemlstry, visualization of fluorescent proteins and use of fluorescent reporter probes such as Ca2+ and mitochondrial function. The Core's major instruments are three confocal microscopes and a widefield inverted fluorescence microscope, along with the Instrumentation and software to carry out quantitative and other. The capabilities of the MIAC have been substantially augmented during the current funding cycle.
The research supported by this Core is relevant to public health because it will increase our understanding of the cellular and morphologic events that underlie the development of diabetes and its complications, and hence will facilitate the development of improved diagnostic, prevention and treatment strategies.
|Hu, Fang; Knoedler, Joseph R; Denver, Robert J (2016) A Mechanism to Enhance Cellular Responsivity to Hormone Action: KrÃ¼ppel-Like Factor 9 Promotes Thyroid Hormone Receptor-Î² Autoinduction During Postembryonic Brain Development. Endocrinology 157:1683-93|
|Taylor, Veronica G; Bommarito, Paige A; Tesmer, John J G (2016) Structure of the Regulator of G Protein Signaling 8 (RGS8)-GÎ±q Complex: MOLECULAR BASIS FOR GÎ± SELECTIVITY. J Biol Chem 291:5138-45|
|Hrycaj, Steven M; Wellik, Deneen M (2016) Hox genes and evolution. F1000Res 5:|
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|Allen, Susan J; Garcia-Galiano, David; Borges, Beatriz C et al. (2016) Leptin receptor null mice with reexpression of LepR in GnRHR expressing cells display elevated FSH levels but remain in a prepubertal state. Am J Physiol Regul Integr Comp Physiol 310:R1258-66|
|Airik, Rannar; Schueler, Markus; Airik, Merlin et al. (2016) A FANCD2/FANCI-Associated Nuclease 1-Knockout Model Develops Karyomegalic Interstitial Nephritis. J Am Soc Nephrol 27:3552-3559|
|Fitzgerald, James T; Funnell, Martha M; Anderson, Robert M et al. (2016) Validation of the Revised Brief Diabetes Knowledge Test (DKT2). Diabetes Educ 42:178-87|
|Cras-MÃ©neur, Corentin; Elghazi, Lynda; Fort, Patrice et al. (2016) Noninvasive in vivo imaging of embryonic Î²-cell development in the anterior chamber of the eye. Islets 8:35-47|
|Korot, Edward; Comer, Grant; Steffens, Timothy et al. (2016) Algorithm for the Measure of Vitreous Hyperreflective Foci in Optical Coherence Tomographic Scans of Patients With Diabetic Macular Edema. JAMA Ophthalmol 134:15-20|
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