The UCSD/UCLA/Salk/Cedars-Sinai Diabetes Research Center Enrichment Program serves as the focus of interaction within and between the four institutions, organizing meetings, seminar series, and retreats to facilitate communication, learning, training, and collaboration. It plays a vital role in advancing diabetes research, catalyzing interdisciplinary, inter-institutional research programs, disseminating new research findings, fostering junior scientists, and increasing awareness of the importance of diabetes research. Directed by Dr. Maike Sander (UCSD) and Dr. Mark Goodarzi (Cedars-Sinai), this enrichment program is vital, exciting and multidisciplinary, reaching broadly across pediatric and adult diabetes, Los Angeles and San Diego, and inviting seminar and retreat speakers nationwide relevant to all five research bases, and coordinating with the P&F program to feature our junior faculty and foster training of junior faculty, clinical fellows, postdoctoral fellows, medical students, and graduate students, drawing the next generation of outstanding scientists into diabetes research. The Enrichment Program has four goals: 1). Advance communication,.integration, and interaction between the investigators in diabetes research within the four affiliated institutions. 2). Organize annual retreats including DRC Day Retreats, the P&F Symposium and our DRC Seminar Series in Los Angeles and La Jolla. 3). Promote the careers of investigators in diabetes and metabolic diseases, and 4). Promote collaborative interactions among DRC investigators. This highly successful effort is crucial to the UCSD/UCLA DRC and the scientific community it serves.
The Enrichment Program of the DRC is essential to our mission of advancing diabetes research. It is particularly important for a Diabetes Center such as ours that brings together researchers from four institutions across Southern California and reaching our five research bases in type I and type II diabetes research.
|Keaton, Jacob M; Hellwege, Jacklyn N; Ng, Maggie C Y et al. (2016) GENOME-WIDE INTERACTION WITH SELECTED TYPE 2 DIABETES LOCI REVEALS NOVEL LOCI FOR TYPE 2 DIABETES IN AFRICAN AMERICANS. Pac Symp Biocomput 22:242-253|
|Below, Jennifer E; Parra, Esteban J; Gamazon, Eric R et al. (2016) Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs. Sci Rep 6:19429|
|Chung, Heekyung; Chou, Winjet; Sears, Dorothy D et al. (2016) Time-restricted feeding improves insulin resistance and hepatic steatosis in a mouse model of postmenopausal obesity. Metabolism 65:1743-1754|
|Wang, Shuai; Zhao, Jing Hua; An, Ping et al. (2016) General Framework for Meta-Analysis of Haplotype Association Tests. Genet Epidemiol 40:244-52|
|Golden, Diana; Kolmakova, Antonina; Sura, Sunitha et al. (2016) Lymphocyte activation gene 3 and coronary artery disease. JCI Insight 1:e88628|
|Gholkar, Ankur A; Senese, Silvia; Lo, Yu-Chen et al. (2016) The X-Linked-Intellectual-Disability-Associated Ubiquitin Ligase Mid2 Interacts with Astrin and Regulates Astrin Levels to Promote Cell Division. Cell Rep 14:180-8|
|Larson, Nicholas B; Decker, Paul A; Wassel, Christina L et al. (2016) Blood group antigen loci demonstrate multivariate genetic associations with circulating cellular adhesion protein levels in the Multi-Ethnic Study of Atherosclerosis. Hum Genet 135:415-23|
|Tian, Xiao Yu; Ganeshan, Kirthana; Hong, Cynthia et al. (2016) Thermoneutral Housing Accelerates Metabolic Inflammation to Potentiate Atherosclerosis but Not Insulin Resistance. Cell Metab 23:165-78|
|(2016) A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape. Nat Commun 7:13357|
|Sajuthi, Satria P; Sharma, Neeraj K; Chou, Jeff W et al. (2016) Mapping adipose and muscle tissue expression quantitative trait loci in African Americans to identify genes for type 2 diabetes and obesity. Hum Genet 135:869-80|
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