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Dayoung Oh, Ph.D.

Dayoung Oh, Ph.D.

Assistant Professor

School
Medical School
Department
Internal Medicine
Graduate Programs
Cell and Molecular Biology
  • Biography

    Dayoung Oh, Ph.D., is an Assistant Professor in the Department of Internal Medicine at UT Southwestern Medical Center and a member of the Touchstone Diabetes Center

    Originally from South Korea, Dr. Oh holds a doctoral degree in molecular endocrinology. She completed her postdoctoral training at the University of California-San Diego in the laboratory of Jerrold Olefsky, M.D.

    Dr. Oh's research has focused on the diverse signaling pathways of G protein-coupled receptors (GPCRs) and ligand identification for orphan GPCRs using a high throughput system. As a result, she has developed a particular interest in the role of GPCRs in the fields of obesity, inflammation, and type 2 diabetes. Her group has had a sharp focus on the role of the omega-3 fatty acid receptor, GPR120 in macrophage-mediated chronic inflammation and insulin resistance. Her major focus is the molecular mechanism and signal transduction of GPCRs including GPR120 in various metabolic syndromes. She uses various biochemical and physiological approaches, including using GPCR KO animals (global and tissue-specific), molecular biology, nucleic acid/protein biochemistry, and eukaryotic cell-based studies. Her long-term goal is not only to elucidate how GPCRs work in regulating metabolism but also to identify new avenues for developing therapeutics to treat metabolic syndrome.

    At UT Southwestern, Dr. Oh teaches in the Graduate School of Biomedical Sciences, and has served on qualifying exam committees and the curriculum committee for the Molecular Metabolism and Metabolic Diseases Program.

  • Education
    Graduate School
    Chonnam National University (2005), Molecular Biology
  • Research Interest
    • Chronic Inflammation
    • Development of Novel Therapeutic Targets to Treat Metabolic Syndrome
    • G Protein-Coupled Receptors
    • Insulin Resistance
    • Metabolic syndrome
    • Type 2 Diabetes
  • Publications

    Star Featured Publications

    Featured Featured Featured Featured Featured Featured
    GPR84-mediated signal transduction effects metabolic function by promoting brown adipocyte activity.
    Sun X, An YA, Paschoal VA, De Souza CO, Wang MY, Vishvanath L, Bueno LM, Cobb AS, Nieto Carrion JA, Ibe ME, Li C, Kidd HA, Chen S, Li W, Gupta RK, Oh DY, J Clin Invest 2023 Oct
    Hepatic sialic acid synthesis modulates glucose homeostasis in both liver and skeletal muscle.
    Peng J, Yu L, Huang L, Paschoal VA, Chu H, de Souza CO, Varre JV, Oh DY, Kohler JJ, Xiao X, Xu L, Holland WL, Shaul PW, Mineo C, Mol Metab 2023 Sep 101812
    Adipose tissue macrophages exert systemic metabolic control by manipulating local iron concentrations.
    Joffin N, Gliniak CM, Funcke JB, Paschoal VA, Crewe C, Chen S, Gordillo R, Kusminski CM, Oh DY, Geldenhuys WJ, Scherer PE, Nat Metab 2022 Nov 4 11 1474-1494
    GPR92 activation in islet macrophages controls ? cell function in a diet-induced obesity model.
    de Souza CO, Paschoal VA, Sun XN, Vishvanath L, Zhang Q, Shao M, Onodera T, Chen S, Joffin N, Bueno LM, Gupta RK, Oh DY, J Clin Invest 2022 Sep
  • Honors & Awards
    • Young Investigator Award
      Women in Endocrinology (2015)
    • AHA Scientist Development Grant
      American Heart Association (2014-2018)
  • Professional Associations/Affiliations
    • American Aging Association (2024)
    • American Diabetes Association (2016)
    • American Heart Association (2014)
    • American Physiological Society (2024)
    • Endocrine Society (2010)
    • Women in Endocrinology (2014)