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Chaodong Wu

Wu , Chaodong
Chaodong Wu
Professor and Faculty Fellow
Office:
217A Cater-Mattil
Email:
Phone:
979-458-1521
Resume/CV
http://nfscfaculty.tamu.edu/wu
Undergraduate Education
Hubei University of Chinese Medicine (Wuhan), China. MD, Medicine, 1992
Graduate Education
Tongji Medical University (Wuhan), China. Master of Medical Science, 1995
Beijing Medical University, China. PhD in Medical Science, 1998
Awards
Junior Faculty Award, American Diabetes Association, 2010
Research Award, Minnesota Medical Foundation, 2004
Travel Award, Dept. of BMBB, the University of Minnesota, 2001
Pilot & Feasibility Research Award, Minnesota Obesity Center, 2002, 2005
Travel Award, The Center for Diabetes Research, University of Minnesota, 2001
Courses Taught
NUTR 470: Nutrition and Physiological Chemistry
NUTR 681: Nutrition Seminar

Research Interest

The long-term goal of Dr. Wu’s research program is to elucidate the mechanisms underlying the pathogenesis of obesity and overnutrition-associated metabolic diseases including insulin resistance, diabetes, and fatty liver disease so that novel dietary and/or pharmacological approaches can be developed for preventing and/or treating metabolic diseases. Using molecular, cellular, and integrative approaches, the Wu lab is focused on investigating the interaction between metabolism and inflammation.

 

Research Area

Obesity, insulin resistance, diabetes, and fatty liver disease

Publications

  1. Ding, Y, Zhu, S, Wu, C, Qian, L, Li, D, Wang, L et al.. Relationship between porcine miR-20a and its putative target LDLR based on dual luciferase reporter gene assays. Asian-australas. J. Anim. Sci. 2019; :. doi: 10.5713/ajas.18.0510. PubMed PMID:30744358 .
  2. McDaniel, K, Wu, N, Zhou, T, Huang, L, Sato, K, Venter, J et al.. Amelioration of Ductular Reaction by Stem Cell Derived Extracellular Vesicles in MDR2 knockout mice via let-7 microRNA. Hepatology. 2019; :. doi: 10.1002/hep.30542. PubMed PMID:30723922 .
  3. Wan, Y, Ceci, L, Wu, N, Zhou, T, Chen, L, Venter, J et al.. Knockout of α-calcitonin gene-related peptide attenuates cholestatic liver injury by differentially regulating cellular senescence of hepatic stellate cells and cholangiocytes. Lab. Invest. 2019; :. doi: 10.1038/s41374-018-0178-5. PubMed PMID:30700848 .
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