Center Publications

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Sharma, A., et al. “Identification Of Non-Hla Genes Associated With Development Of Islet Autoimmunity And Type 1 Diabetes In The Prospective Teddy Cohort.”. Journal Of Autoimmunity, pp. 90-100.
Washington
White, K., et al. “Motivations For Participation In An Online Social Media Community For Diabetes.”. Journal Of Diabetes Science And Technology, pp. 712-718.
Michigan
 Featured
Williams, I. M., et al. “Insulin Exits Skeletal Muscle Capillaries By Fluid-Phase Transport.”. The Journal Of Clinical Investigation, pp. 699-714.
Vanderbilt
Letourneau, L. R., et al. “Early Intensive Insulin Use May Preserve -Cell Function In Neonatal Diabetes Due To Mutations In The Proinsulin Gene.”. Journal Of The Endocrine Society, pp. 1-8.
Chicago
 Featured
Perry, R. J., et al. “Leptin Mediates A Glucose-Fatty Acid Cycle To Maintain Glucose Homeostasis In Starvation.”. Cell, pp. 234-248.e17.
Yale
Bolus, R., et al. “Elevating Adipose Eosinophils In Obese Mice To Physiologically Normal Levels Does Not Rescue Metabolic Impairments.”. Molecular Metabolism, pp. 86-95.
Vanderbilt
Malin, S. K., et al. “A Whole-Grain Diet Reduces Peripheral Insulin Resistance And Improves Glucose Kinetics In Obese Adults: A Randomized-Controlled Trial.”. Metabolism: Clinical And Experimental, pp. 111-117.
Michigan
de Brachène, A. C., et al. “Ifn-Α Induces A Preferential Long-Lasting Expression Of Mhc Class I In Human Pancreatic Beta Cells.”. Diabetologia, pp. 636-640.
Indiana
Xiao, X., et al. “Endogenous Reprogramming Of Alpha Cells Into Beta Cells, Induced By Viral Gene Therapy, Reverses Autoimmune Diabetes.”. Cell Stem Cell, pp. 78-90.e4.
Chicago
Amengual, J., et al. “Autophagy Is Required For Sortilin-Mediated Degradation Of Apolipoprotein B100.”. Circulation Research, pp. 568-582.
Einstein
Group, W. G. for the T. R. I. G. R. S., et al. “Effect Of Hydrolyzed Infant Formula Vs Conventional Formula On Risk Of Type 1 Diabetes: The Trigr Randomized Clinical Trial.”. Jama, pp. 38-48.
Washington
Yamaguchi, S., et al. “Diurnal Variation In Pdk4 Expression Is Associated With Plasma Free Fatty Acid Availability In People.”. The Journal Of Clinical Endocrinology And Metabolism, pp. 1068-1076.
WUSTL
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