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Yang, Y. -P., et al. “The Mammal-Specific Pdx1 Area Ii Enhancer Has Multiple Essential Functions In Early Endocrine Cell Specification And Postnatal Β-Cell Maturation.”. Development (Cambridge, England), pp. 248-257.
Vanderbilt
Ediger, B. N., et al. “Lim Domain-Binding 1 Maintains The Terminally Differentiated State Of Pancreatic Β Cells.”. The Journal Of Clinical Investigation, pp. 215-229.
Penn
Greeley, S. A. W., et al. “Preservation Of Reduced Numbers Of Insulin-Positive Cells In Sulfonylurea-Unresponsive Kcnj11-Related Diabetes.”. The Journal Of Clinical Endocrinology And Metabolism, pp. 1-5.
Chicago
Peek, C. B., et al. “Circadian Clock Interaction With Hif1Α Mediates Oxygenic Metabolism And Anaerobic Glycolysis In Skeletal Muscle.”. Cell Metabolism, pp. 86-92.
Chicago
Sheikh, S., et al. “Reduced Β-Cell Secretory Capacity In Pancreatic-Insufficient, But Not Pancreatic-Sufficient, Cystic Fibrosis Despite Normal Glucose Tolerance.”. Diabetes, pp. 134-144.
Penn
Wu, L., et al. “An Ancient, Unified Mechanism For Metformin Growth Inhibition In C. Elegans And Cancer.”. Cell, pp. 1705-1718.e13.
Boston Area
Fitzpatrick, S. L., et al. “Effect Of Decide (Decision-Making Education For Choices In Diabetes Everyday) Program Delivery Modalities On Clinical And Behavioral Outcomes In Urban African Americans With Type 2 Diabetes: A Randomized Trial.”. Diabetes Care, pp. 2149-2157.
JHU-UMD
Mondesir, F. L., et al. “Diabetes, Diabetes Severity, And Coronary Heart Disease Risk Equivalence: Reasons For Geographic And Racial Differences In Stroke (Regards).”. American Heart Journal, pp. 43-51.
UAB
Lee, J., et al. “Rpl13A Small Nucleolar Rnas Regulate Systemic Glucose Metabolism.”. The Journal Of Clinical Investigation, pp. 4616-4625.
WUSTL
Li, P., et al. “Hematopoietic-Derived Galectin-3 Causes Cellular And Systemic Insulin Resistance.”. Cell, pp. 973-984.e12.
UCSD-UCLA
Syring, K. E., et al. “Combined Deletion Of Slc30A7 And Slc30A8 Unmasks A Critical Role For Znt8 In Glucose-Stimulated Insulin Secretion.”. Endocrinology, pp. 4534-4541.
Vanderbilt
Sas, K. M., et al. “Tissue-Specific Metabolic Reprogramming Drives Nutrient Flux In Diabetic Complications.”. Jci Insight, p. e86976.
Michigan