Abstract

Administration Core The Administration Core of the Michigan Diabetes Research Center (MDRC) provides leadership, infrastructure, and resources to: ? Raise awareness of, interest in, and support for research in diabetes, its complications and related endocrine and metabolic disorders and create an environment that facilitates such research. ? Coordinate the activities of the MDRC and provide guidance and coordination to the support for diabetes research at the UM and its regional partners ? Recruit new investigators to diabetes research and the MDRC, and support new and established investigators in diabetes research. ? Administer Cores that provide MDRC members with expertise and services to support diabetes related research. ? Administer the MDRC Pilot and Feasibility Study (P/FS) Grants Programs. ? Provide enrichment, education, and training for investigators from diverse schools, departments, and institutes to foster interdisciplinary collaborations. ? Maintain the Center's website.

Public Health Relevance

Diabetes and its complications are enormous clinical and public health problems. The MDRC provides researchers with expertise and shared resources to enhance biomedical and clinical research to prevent, treat, and ultimately cure diabetes and its complications. The Administration Core guides and oversees the provision of resources to enhance the productivity, efficiency, and cost-effectiveness of multidisciplinary and collaborative research related to diabetes.

  Funding Agency

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
2P30DK020572-36
Application #
8441333
Study Section
Special Emphasis Panel (ZDK1-GRB-S (O2))
Project Start
Project End
Budget Start
2012-12-01
Budget End
2013-11-30
Support Year
36
Fiscal Year
2013
Total Cost
$727,799
Indirect Cost
$259,761

  Institution

Name
University of Michigan Ann Arbor
Department
Type
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109

  Publications

Miller, Alison L; Gearhardt, Ashley N; Fredericks, Emily M et al. (2018) Targeting self-regulation to promote health behaviors in children. Behav Res Ther 101:71-81
Prasad, Suchitra; Neef, Tobias; Xu, Dan et al. (2018) Tolerogenic Ag-PLG nanoparticles induce tregs to suppress activated diabetogenic CD4 and CD8 T cells. J Autoimmun 89:112-124
Mahajan, Anubha (see original citation for additional authors) (2018) Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. Nat Genet 50:559-571
Hussain, Syed Saad; Harris, Megan T; Kreutzberger, Alex J B et al. (2018) Control of insulin granule formation and function by the ABC transporters ABCG1 and ABCA1 and by oxysterol binding protein OSBP. Mol Biol Cell 29:1238-1257
Muir, Lindsey A; Kiridena, Samadhi; Griffin, Cameron et al. (2018) Frontline Science: Rapid adipose tissue expansion triggers unique proliferation and lipid accumulation profiles in adipose tissue macrophages. J Leukoc Biol 103:615-628
Rumora, Amy E; Lentz, Stephen I; Hinder, Lucy M et al. (2018) Dyslipidemia impairs mitochondrial trafficking and function in sensory neurons. FASEB J 32:195-207
Woodworth, Hillary L; Perez-Bonilla, Patricia A; Beekly, Bethany G et al. (2018) Identification of Neurotensin Receptor Expressing Cells in the Ventral Tegmental Area across the Lifespan. eNeuro 5:
Orozco, Luz D; Farrell, Colin; Hale, Christopher et al. (2018) Epigenome-wide association in adipose tissue from the METSIM cohort. Hum Mol Genet 27:1830-1846
Lee, Pearl G; Damschroder, Laura J; Holleman, Robert et al. (2018) Older Adults and Diabetes Prevention Programs in the Veterans Health Administration. Diabetes Care 41:2644-2647
Spencer, Michael S; Kieffer, Edith C; Sinco, Brandy et al. (2018) Outcomes at 18 Months From a Community Health Worker and Peer Leader Diabetes Self-Management Program for Latino Adults. Diabetes Care 41:1414-1422

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