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Center Publications

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Darcy, J., et al. “Integrated Metabolomics Reveals Altered Lipid Metabolism In Adipose Tissue In A Model Of Extreme Longevity.”. Geroscience, pp. 1527-1546.
Joslin
Hu, K. H., et al. “Zipseq: Barcoding For Real-Time Mapping Of Single Cell Transcriptomes.”. Nature Methods, pp. 833-843.
UCSF
Nguyen, L. D., et al. “Calpain Inhibitor And Ibudilast Rescue Β Cell Functions In A Cellular Model Of Wolfram Syndrome.”. Proceedings Of The National Academy Of Sciences Of The United States Of America, pp. 17389-17398.
WUSTL
Wu, H., et al. “A Negative Reciprocal Regulatory Axis Between Cyclin D1 And Hnf4Α Modulates Cell Cycle Progression And Metabolism In The Liver.”. Proceedings Of The National Academy Of Sciences Of The United States Of America, pp. 17177-17186.
Penn
Losiewicz, M. K., et al. “Mtorc1 And Mtorc2 Expression In Inner Retinal Neurons And Glial Cells.”. Experimental Eye Research, p. 108131.
Michigan
Callaghan, B. C., et al. “Central Obesity Is Associated With Neuropathy In The Severely Obese.”. Mayo Clinic Proceedings, pp. 1342-1353.
Michigan
Reyes, K. J. C., et al. “Bone Density, Microarchitecture And Strength Estimates In White Versus African American Youth With Obesity.”. Bone, p. 115514.
Boston Area
Wie, J., et al. “Intellectual Disability-Associated Unc80 Mutations Reveal Inter-Subunit Interaction And Dendritic Function Of The Nalcn Channel Complex.”. Nature Communications, p. 3351.
Penn
Assali, E. A., et al. “Nclx Prevents Cell Death During Adrenergic Activation Of The Brown Adipose Tissue.”. Nature Communications, p. 3347.
UCSD-UCLA
Rahman, A. H., and D. Homann. “Mass Cytometry And Type 1 Diabetes Research In The Age Of Single-Cell Data Science.”. Current Opinion In Endocrinology, Diabetes, And Obesity, pp. 231-239.
Einstein
Sims, E. K., et al. “The Role Of Beta-Cell Dysfunction In Early Type 1 Diabetes.”. Current Opinion In Endocrinology, Diabetes, And Obesity, pp. 215-224.
Indiana
Marcheva, B., et al. “A Role For Alternative Splicing In Circadian Control Of Exocytosis And Glucose Homeostasis.”. Genes & Development, pp. 1089-1105.
Chicago