Administrative Core. The UCSF Diabetes Research Center (DRC) provides Programs and Cores that foster research collaborations and interactions to accelerate the pace of diabetes research. The Administrative Core is charged with providing leadership that responds nimbly to the current and future needs of DRC members. The Administrative Core is responsible for evaluating and setting the goals of the Center and for allocating and coordinating Center resources to ensure that the DRC evolves in alignment with those goals. The Administrative Core realizes these tasks by providing a defined governing structure that coordinates leadership, infrastructure, administrative support, advice and oversight to all DRC activities. The Center Director (or when absent, the Associate Director) provides day-to-day leadership and interacts regularly with the Directors of the DRC Research Programs, DRC Cores, DRC members and administrative staff. The Center Director and the Directors of the four Research Programs (in Islet Biology, Obesity & Metabolism, Autoimmunity & Inflammation, and Translation) constitute the Executive Committee. The UCSF DRC interfaces with its membership, the NIDDK, other NIH Diabetes Centers, and the lay community through the Center Director and the Executive Committee and through outreach programs including the Enrichment Program, the Pilot & Feasibility grant program, DRC service/training Cores and the UCSF DRC web site The Executive Committee is the major, governing body that sets the long-range goals of the DRC and assesses how well the Programs and Cores achieve them. The Executive Committee meets quarterly and, when necessary on an ad hoc basis, to consult with and provide guidance to the Director of the Pilot & Feasibility Program, the Director of the Enrichment Program and the Core Coordinating Committee, which consists of all five DRC Core Directors and an overall Director of Cores who oversees the day-to-day coordination of Core activities. The Core Coordinating Committee discusses issues and solutions related to Core operations and the provision of Core services to the DRC membership. The Executive Committee also evaluates proposals from the Core Directors and Core Managers for the development of new Core services and triages DRC support for those service development proposals according to current and future DRC needs. The Executive Committee also evaluates the external reviews from the Pilot & Feasibility applications, ensures continuing mentorship and advice to Pilot & Feasibility grant recipients and evaluates DRC membership. The Executive Committee meets annually with an External Advisory Committee which provides valuable insights into the scientific and operational directions of the DRC. A biannual meeting of the Executive Committee with an Internal Advisory Committee, which consists of institutional leaders with interests in DRC-related research, coordinates DRC progress in relationship with developments and goals throughout UCSF. The Administrative Core thus coordinates all DRC activities to coordinate the future of diabetes research at UCSF.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
2P30DK063720-11
Application #
8874804
Study Section
Special Emphasis Panel (ZDK1-GRB-S (J4))
Project Start
Project End
Budget Start
2015-04-01
Budget End
2016-03-31
Support Year
11
Fiscal Year
2015
Total Cost
$371,959
Indirect Cost
$137,099
Name
University of California San Francisco
Department
Type
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Siljee, Jacqueline E; Wang, Yi; Bernard, Adelaide A et al. (2018) Subcellular localization of MC4R with ADCY3 at neuronal primary cilia underlies a common pathway for genetic predisposition to obesity. Nat Genet 50:180-185
Hennings, Thomas G; Chopra, Deeksha G; DeLeon, Elizabeth R et al. (2018) In Vivo Deletion of ?-Cell Drp1 Impairs Insulin Secretion Without Affecting Islet Oxygen Consumption. Endocrinology 159:3245-3256
Roth, Theodore L; Puig-Saus, Cristina; Yu, Ruby et al. (2018) Reprogramming human T cell function and specificity with non-viral genome targeting. Nature 559:405-409
Hirano, Arisa; Hsu, Pei-Ken; Zhang, Luoying et al. (2018) DEC2 modulates orexin expression and regulates sleep. Proc Natl Acad Sci U S A 115:3434-3439
Tan, Yu-Ting; Ye, Lin; Xie, Fei et al. (2018) Respecifying human iPSC-derived blood cells into highly engraftable hematopoietic stem and progenitor cells with a single factor. Proc Natl Acad Sci U S A 115:2180-2185
Young, Arabella; Quandt, Zoe; Bluestone, Jeffrey A (2018) The Balancing Act between Cancer Immunity and Autoimmunity in Response to Immunotherapy. Cancer Immunol Res 6:1445-1452
Paulo, Esther; Wu, Dongmei; Hecker, Peter A et al. (2018) Adipocyte HDAC4 activation leads to beige adipocyte expansion and reduced adiposity. J Endocrinol :
Mongraw-Chaffin, Morgana; Gujral, Unjali P; Kanaya, Alka M et al. (2018) Relation of Ectopic Fat with Atherosclerotic Cardiovascular Disease Risk Score in South Asians Living in the United States (from the Mediators of Atherosclerosis in South Asians Living in America [MASALA] Study). Am J Cardiol 121:315-321
Baeyens, Luc; Lemper, Marie; Staels, Willem et al. (2018) (Re)generating Human Beta Cells: Status, Pitfalls, and Perspectives. Physiol Rev 98:1143-1167
Lo, Wan-Lin; Shah, Neel H; Ahsan, Nagib et al. (2018) Lck promotes Zap70-dependent LAT phosphorylation by bridging Zap70 to LAT. Nat Immunol 19:733-741

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