The overall objective of the Administrative Component is to provide smooth operation of the DERC to alloweasy interaction of the DERC membership with the DERC Cores and Committees in order to enhanceDiabetes/ Endocrinology research. The responsibilities of the Administrative Component include:communications, academic enrichment, fund management, planning and organizing the annual DERC Day,preparing NIH renewals, coordinating committee business, and providing general administrative assistance.The Administrative Component consists of an Executive Committee that oversees other DERC committeesincluding the Biomedical Research Base Committee (BRBC), the Core Committee, the Advisory Committeeand the P&F Committee. It also includes administrative support services with an Information Manager andUCLA and UCSD Administrative Managers. The Executive Committee, chaired by Dr. Hsueh is composedof the Director, Co-Directors and committee chairs of the DERC. This group is familiar with all aspects of theDERC, since these members participate and have key leadership roles in DERC activities. This committeemakes the ultimate decisions regarding DERC operations. Its goal is to meet DERC objectives and to ensureoverall cost-effectiveness and maximum utilization of DERC support and resources. The Core Committee,chaired by Dr. Mellon sets priorities with regard to Core usage, and interactions, and oversees theadministration, organization, and dissemination of DERC resources to the Cores. The Biomedical ResearchBase Committee, chaired by Dr. Olefsky, is composed of all Research Base leaders and is responsible foridentifying new members and new ideas within each of the research bases and for generating an annualwritten update of the Research Base and a short state-of-the-art review for the DERC Newsletter. The Pilotand Feasibility Committee, chaired by Dr. Cohen is also responsible for soliciting and reviewing P&F grantapplications, organizing presentations of P&F recipients at DERC Day, and tracking P&F grantees.Communication is a critical objective of the Administrative Component due to geographical separation ofDERC participants and facilities. Newsletters are now published every two months and emphasize CoreServices and contacts. The DERC website is being redesigned to allow greater interaction in order to speedup communications between the investigators and the Cores. The website's new design will contain a link tospecial DERC announcements, a searchable faculty directory with direct email address links, and an optionto order DERC services by completing a form linked from a Core's main page. The Administrativecomponent will also monitor collaborative efforts among the investigators both within and betweeninstitutions by tracking publications, following Core service requests, and surveying the membership. TheAdministrative Component ultimately functions as a central service and coordinating unit for the DERC andits members.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
2P30DK063491-06
Application #
7425746
Study Section
Special Emphasis Panel (ZDK1-GRB-S (O1))
Project Start
2008-05-01
Project End
2013-04-30
Budget Start
2008-05-01
Budget End
2009-04-30
Support Year
6
Fiscal Year
2008
Total Cost
$1,468,519
Indirect Cost
Name
University of California San Diego
Department
Type
DUNS #
804355790
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Eriguchi, Masahiro; Bernstein, Ellen A; Veiras, Luciana C et al. (2018) The Absence of the ACE N-Domain Decreases Renal Inflammation and Facilitates Sodium Excretion during Diabetic Kidney Disease. J Am Soc Nephrol 29:2546-2561
Turcot, Valérie (see original citation for additional authors) (2018) Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nat Genet 50:26-41
Zhou, Zhenqi; Ribas, Vicent; Rajbhandari, Prashant et al. (2018) Estrogen receptor ? protects pancreatic ?-cells from apoptosis by preserving mitochondrial function and suppressing endoplasmic reticulum stress. J Biol Chem 293:4735-4751
Prins, Bram P; Mead, Timothy J; Brody, Jennifer A et al. (2018) Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6. Genome Biol 19:87
Xu, Jiayi; Bartz, Traci M; Chittoor, Geetha et al. (2018) Meta-analysis across Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium provides evidence for an association of serum vitamin D with pulmonary function. Br J Nutr 120:1159-1170
Keaton, Jacob M; Gao, Chuan; Guan, Meijian et al. (2018) Genome-wide interaction with the insulin secretion locus MTNR1B reveals CMIP as a novel type 2 diabetes susceptibility gene in African Americans. Genet Epidemiol 42:559-570
Skorobogatko, Yuliya; Dragan, Morgan; Cordon, Claudia et al. (2018) RalA controls glucose homeostasis by regulating glucose uptake in brown fat. Proc Natl Acad Sci U S A 115:7819-7824
Savji, Nazir; Meijers, Wouter C; Bartz, Traci M et al. (2018) The Association of Obesity and Cardiometabolic Traits With Incident HFpEF and HFrEF. JACC Heart Fail 6:701-709
Jiang, Xia; O'Reilly, Paul F; Aschard, Hugues et al. (2018) Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels. Nat Commun 9:260
Balakrishnan, Poojitha; Jones, Miranda R; Vaidya, Dhananjay et al. (2018) Ethnic, Geographic, and Genetic Differences in Arsenic Metabolism at Low Arsenic Exposure: A Preliminary Analysis in the Multi-Ethnic Study of Atherosclerosis (MESA). Int J Environ Res Public Health 15:

Showing the most recent 10 out of 926 publications