The new Image Analysis Core (IAC) of the Michigan Diabetes Research and Training Center (MDRTC) is a state-of-the-art facility, which was established at the University of Michigan in 1991. It is equipped with modern light and electron microscopic facilities which are interfaced with a powerful, computerized image analysis system. The Fluorescent Imaging Unit of the IAC is equipped with instruments for the visualization and quantification of various intracellular ions in living cells. The purpose of the IAC is to a) provide MDRTC investigators with morphometric analyses and quantitative cellular and subcellular localization of molecules and ions, using the techniques of quantitative histochemistry, in situ hybridization and fluorophotometric ion analysis, b) provide consultation to MDRTC investigators for the design and conduct of research projects using these techniques, c) initiate, implement and disseminate to MDRTC investigators new and innovative image analysis techniques to foster research on diabetes, metabolic and endocrine diseases, and d) demonstrate and teach the above techniques to MDRTC investigators, trainees and technicians. The major objective of the IAC will be to provide state-of-the-art quantitative morphological analyses using molecular probes, with quality and development having priority. The IAC is expected to enhance and stimulate diabetes and related endocrinology and metabolism research by providing scientific collaboration, expert assistance and special facilities that are essential for the research of Center investigators and trainees but that are beyond their individual capabilities.

Project Start
2001-12-01
Project End
2002-11-30
Budget Start
Budget End
Support Year
25
Fiscal Year
2002
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Jiang, Lin; Su, Haoran; Keogh, Julia M et al. (2018) Neural deletion of Sh2b1 results in brain growth retardation and reactive aggression. FASEB J 32:1830-1840
Yu, Sangho; Cheng, Helia; François, Marie et al. (2018) Preoptic leptin signaling modulates energy balance independent of body temperature regulation. Elife 7:
Rumora, Amy E; Lentz, Stephen I; Hinder, Lucy M et al. (2018) Dyslipidemia impairs mitochondrial trafficking and function in sensory neurons. FASEB J 32:195-207
Xiong, Yi; Torsoni, Adriana Souza; Wu, Feihua et al. (2018) Hepatic NF-kB-inducing kinase (NIK) suppresses mouse liver regeneration in acute and chronic liver diseases. Elife 7:
Tank, E M; Figueroa-Romero, C; Hinder, L M et al. (2018) Abnormal RNA stability in amyotrophic lateral sclerosis. Nat Commun 9:2845
Liu, Yan; Jiang, Lin; Sun, Chengxin et al. (2018) Insulin/Snail1 axis ameliorates fatty liver disease by epigenetically suppressing lipogenesis. Nat Commun 9:2751
Sheng, Liang; Ye, Lan; Zhang, Dong et al. (2018) New Insights Into the Long Non-coding RNA SRA: Physiological Functions and Mechanisms of Action. Front Med (Lausanne) 5:244
Zhao, Xu-Yun; Xiong, Xuelian; Liu, Tongyu et al. (2018) Long noncoding RNA licensing of obesity-linked hepatic lipogenesis and NAFLD pathogenesis. Nat Commun 9:2986
Dreffs, Alyssa; Henderson, Desmond; Dmitriev, Andrey V et al. (2018) Retinal pH and Acid Regulation During Metabolic Acidosis. Curr Eye Res 43:902-912
Kumar, Navasuja; Pop-Busui, Rodica; Musch, David C et al. (2018) Central Corneal Thickness Increase Due to Stromal Thickening With Diabetic Peripheral Neuropathy Severity. Cornea 37:1138-1142

Showing the most recent 10 out of 1081 publications