Center Publications

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Lee, S. M., et al. “Hepatocyte-Specific Loss Of Pparγ Protects Mice From Nash And Increases The Therapeutic Effects Of Rosiglitazone In The Liver.”. Cellular And Molecular Gastroenterology And Hepatology, pp. 1291-1311.
Chicago
Daemen, S., et al. “Dynamic Shifts In The Composition Of Resident And Recruited Macrophages Influence Tissue Remodeling In Nash.”. Cell Reports, p. 108626.
WUSTL
 Multicenter
Arslanian, S. A., et al. “Ogtt Glucose Response Curves, Insulin Sensitivity, And Β-Cell Function In Rise: Comparison Between Youth And Adults At Randomization And In Response To Interventions To Preserve Β-Cell Function.”. Diabetes Care, pp. 817-825.
Indiana
Chicago
Washington
Yale
 Multicenter
Chaudhari, S. N., et al. “A Microbial Metabolite Remodels The Gut-Liver Axis Following Bariatric Surgery.”. Cell Host & Microbe, pp. 408-424.e7.
Boston Area
Joslin
Zhao, Z., et al. “Hepatic Metabolic Regulation By Nuclear Factor E4Bp4.”. Journal Of Molecular Endocrinology, pp. R15-R21.
Michigan
Redondo, M. J., et al. “The Evolution Of Hemoglobin A Targets For Youth With Type 1 Diabetes: Rationale And Supporting Evidence.”. Diabetes Care, pp. 301-312.
Stanford
Harrington, K. R., et al. “Associations Of Diabetes Self-Management Characteristics, Hba1C, And Psychosocial Outcomes With Depressive Symptoms In A Contemporary Sample Of Adolescents With Type 1 Diabetes.”. Journal Of Diabetes And Its Complications, p. 107838.
Joslin
Roy, B., and S. S. Palaniyandi. “A Role For Aldehyde Dehydrogenase (Aldh) 2 In Angiotensin Ii-Mediated Decrease In Angiogenesis Of Coronary Endothelial Cells.”. Microvascular Research, p. 104133.
Michigan
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