The overall goal is to enhance diabetes research and training via a comprehensive and integrated set of activities that promote a cohesive intellectual community characterized by collaborations, free discussion of ideas, and access to current scientific developments and concepts.
The specific aims are to : 1. Sponsor the monthly Diabetes Plenary Lecture Series, and the DRC co-sponsored lectureships for speakers presenting original diabetes research in partnership with seminar series of other departments and centers. These lectures feature national and international leaders studying multiple aspects of diabetes. 2. Sponsor UAB Diabetes Day annually, and other symposia and conferences that introduce new ideas, discoveries, and technologies. 3. Conduct round-table discussions involving DRC investigators centered on various research themes, as well as workshops, conferences, and short courses, designed to develop cross-disciplinary collaborative projects, and the development of new lines of investigation and research grant applications . 3. Sponsor mini-sabbaticals and consultantships for DRC investigators for new technology acquisition. 4. Work synergistically with existing training grant programs to enhance the environment for trainees conducting diabetes-related research, and access of students/fellows wishing to study with DRC Members. 5. Sponsor diabetes journal clubs and travel grants for trainees. 6. Continue new non-research base DCR membership categories (Trainee, Clinical, Affiliate) designed to engage trainees in DRC activities and intellectual environment, and enhance capacity for collaborations. 7. Establish novel evidence-based models of multi-disciplinary health care and informatics systems in collaboration with the UAB Health System and the CCTS (i.e., the CTSA at UAB) to establish effective venues for diabetes patient care, training, and research. 8. Establish mechanisms for evaluating the effectiveness of the enrichment programs, and for monitoring and responding to the evolving needs of the DRC research members.

Public Health Relevance

The DRC Enrichment and Training Component Program is an integrated program fostering new ideas and new collaborations as well as an outstanding training environment for the next generation of diabetes investigators and clinicians. The environment will breed innovation and new discoveries necessary for a better understanding of diabetes and improved startegies for prevention and treatment.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
4P30DK079626-09
Application #
9012086
Study Section
Special Emphasis Panel (ZDK1-GRB-S)
Project Start
Project End
Budget Start
2016-03-01
Budget End
2017-02-28
Support Year
9
Fiscal Year
2016
Total Cost
$8,397
Indirect Cost
$2,665
Name
University of Alabama Birmingham
Department
Type
DUNS #
063690705
City
Birmingham
State
AL
Country
United States
Zip Code
35294
Gupta, Rajesh; Nguyen, Dan C; Schaid, Michael D et al. (2018) Complement 1q-like-3 protein inhibits insulin secretion from pancreatic ?-cells via the cell adhesion G protein-coupled receptor BAI3. J Biol Chem 293:18086-18098
And, Ay?e; Sylvester, Maria D; Turan, Bulent et al. (2018) The Turkish Palatable Eating Motives Scale (T-PEMS): utility in predicting binge-eating eating and obesity risk in university students. Eat Weight Disord 23:527-531
Ma, Elizabeth; Fu, Yuchang; Garvey, W Timothy (2018) Relationship of Circulating miRNAs with Insulin Sensitivity and Associated Metabolic Risk Factors in Humans. Metab Syndr Relat Disord 16:82-89
Gibbs, Victoria K; Schwartz, Tonia S; Johnson, Maria S et al. (2018) No Significant Effect of Maternal Perception of the Food Environment on Reproductive Success or Pup Outcomes in C57BL/6J Mice. Obesity (Silver Spring) 26:723-729
Demark-Wahnefried, Wendy; Cases, Mallory G; Cantor, Alan B et al. (2018) Pilot Randomized Controlled Trial of a Home Vegetable Gardening Intervention among Older Cancer Survivors Shows Feasibility, Satisfaction, and Promise in Improving Vegetable and Fruit Consumption, Reassurance of Worth, and the Trajectory of Central Adipos J Acad Nutr Diet 118:689-704
Dunham-Snary, Kimberly J; Sandel, Michael W; Sammy, Melissa J et al. (2018) Mitochondrial - nuclear genetic interaction modulates whole body metabolism, adiposity and gene expression in vivo. EBioMedicine 36:316-328
Snyder, Peter J; Bhasin, Shalender; Cunningham, Glenn R et al. (2018) Lessons From the Testosterone Trials. Endocr Rev 39:369-386
Patel, Mikita; Yarlagadda, Vidhush; Adedoyin, Oreoluwa et al. (2018) Oxalate induces mitochondrial dysfunction and disrupts redox homeostasis in a human monocyte derived cell line. Redox Biol 15:207-215
Kang, Minsung; Liu, Xiaobing; Fu, Yuchang et al. (2018) Improved systemic metabolism and adipocyte biology in miR-150 knockout mice. Metabolism 83:139-148
Buford, Thomas W; Carter, Christy S; VanDerPol, William J et al. (2018) Composition and richness of the serum microbiome differ by age and link to systemic inflammation. Geroscience 40:257-268

Showing the most recent 10 out of 643 publications