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Uehara, K., et al. “Mtorc1 Controls Murine Postprandial Hepatic Glycogen Synthesis Via Ppp1R3B.”. The Journal Of Clinical Investigation.
Penn
Xia, W., et al. “Obesity Causes Mitochondrial Fragmentation And Dysfunction In White Adipocytes Due To Rala Activation.”. Nature Metabolism, pp. 273-289.
UCSD-UCLA
Asadi, F., et al. “An Orally Available Compound Suppresses Glucagon Hypersecretion And Normalizes Hyperglycemia In Type 1 Diabetes.”. Jci Insight.
WUSTL
Mukherjee, N., et al. “Ripk3 Promotes Islet Amyloid-Induced Β-Cell Loss And Glucose Intolerance In A Humanized Mouse Model Of Type 2 Diabetes.”. Molecular Metabolism, p. 101877.
Washington
Bevacqua, R. J., et al. “Multiplexed Crispr Gene Editing In Primary Human Islet Cells With Cas9 Ribonucleoprotein.”. Iscience, p. 108693.
Stanford
Weidemann, B. J., et al. “Repression Of Latent Nf-Κb Enhancers By Pdx1 Regulates Β Cell Functional Heterogeneity.”. Cell Metabolism, pp. 90-102.e7.
Chicago
Vanderbilt
Mar, D., et al. “A High-Throughput Pixul-Matrix-Based Toolbox To Profile Frozen And Formalin-Fixed Paraffin-Embedded Tissues Multiomes.”. Laboratory Investigation; A Journal Of Technical Methods And Pathology, p. 100282.
Washington
Mukhi, D., et al. “Acss2 Gene Variants Determine Kidney Disease Risk By Controlling De Novo Lipogenesis In Kidney Tubules.”. The Journal Of Clinical Investigation.
Penn
Cheruiyot, A., et al. “Sustained Hyperglycemia Specifically Targets Translation Of Mrnas For Insulin Secretion.”. The Journal Of Clinical Investigation.
Joslin
Ferrari, A., et al. “Aster-Dependent Nonvesicular Transport Facilitates Dietary Cholesterol Uptake.”. Science (New York, N.y.), p. eadf0966.
UCSD-UCLA
Sims, E. K., et al. “Inhibition Of Polyamine Biosynthesis Preserves Β Cell Function In Type 1 Diabetes.”. Cell Reports. Medicine, p. 101261.
Chicago