(Translation Core) The Translation Core will serve the needs of IDRC affiliated investigators whose research programs require measurements in human subjects or tissues. The Director and Associate Directors of this Core bring specific expertise in the design and performance of in vivo measurements for physiologic, translational and proof-of- principle studies in humans. The Translation Core is not only essential for the work of a number of established clinical investigators at Indiana University School of Medicine (IUSM) and Purdue University, but is also an important conduit facilitating entry into the field of diabetes research for investigators not traditionally working with human subjects or human subjects materials.
The Specific Aims of the Core include: (1) To enable pre-clinical and clinical IDRC investigators to test in humans, their molecular and physiologic advances made in model systems, using an innovative and formalized stepped approach, through access to banked human tissues and in vivo human studies. (2) To maintain and augment readily accessible tissue sample banks from human subjects participating in metabolic studies for use by all IDRC investigators. (3) To assist in the design, performance, and interpretation of human subjects studies requiring detailed measurements of metabolic physiology. (4) To provide IDRC core laboratory functions that support high-throughput, minimal-cost measurements of circulating hormones, cytokines, and standard chemical analytes of interest to multiple IDRC investigators, measuring samples from human, animal and cultured cell studies. (5) To provide training to IDRC investigators, fellows and students in design and conduct of human translational experimentation. (6) To actively collaborate with IDRC investigators in making available novel measurements and novel methodologies as they apply to human translation studies, including systematically assessing their relevance to human biology and disease using the Translation Core stepped approach. It is anticipated that the Translation Core will augment substantially the research capacity of the investigators in the IDRC by providing a conduit for the translation of key findings to humans.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK097512-03
Application #
9282429
Study Section
Special Emphasis Panel (ZDK1-GRB-S)
Project Start
Project End
Budget Start
2017-06-01
Budget End
2018-05-31
Support Year
3
Fiscal Year
2017
Total Cost
$117,000
Indirect Cost
$42,000
Name
Indiana University-Purdue University at Indianapolis
Department
Type
Domestic Higher Education
DUNS #
603007902
City
Indianapolis
State
IN
Country
United States
Zip Code
46202
Chen, Melinda E; Chandramouli, Aaditya G; Considine, Robert V et al. (2018) Comparison of ?-Cell Function Between Overweight/Obese Adults and Adolescents Across the Spectrum of Glycemia. Diabetes Care 41:318-325
Aslamy, Arianne; Oh, Eunjin; Ahn, Miwon et al. (2018) Exocytosis Protein DOC2B as a Biomarker of Type 1 Diabetes. J Clin Endocrinol Metab 103:1966-1976
Dong, X Charlie (2018) SCP4: A Small Nuclear Phosphatase Having a Big Effect on FoxOs in Gluconeogenesis. Diabetes 67:23-25
Anjanappa, M; Hao, Y; Simpson, E R et al. (2018) A system for detecting high impact-low frequency mutations in primary tumors and metastases. Oncogene 37:185-196
Sims, Emily K; Evans-Molina, Carmella; Tersey, Sarah A et al. (2018) Biomarkers of islet beta cell stress and death in type 1 diabetes. Diabetologia 61:2259-2265
RISE Consortium (2018) Impact of Insulin and Metformin Versus Metformin Alone on ?-Cell Function in Youth With Impaired Glucose Tolerance or Recently Diagnosed Type 2 Diabetes. Diabetes Care 41:1717-1725
Lakshmikanthan, Sribalaji; Sobczak, Magdalena; Li Calzi, Sergio et al. (2018) Rap1B promotes VEGF-induced endothelial permeability and is required for dynamic regulation of the endothelial barrier. J Cell Sci 131:
Simons, Zachary B; Morgan, Rachel C; Rose, Laurel et al. (2018) Hypoglycemia in a Patient With a Polyhormonal Pancreatic Neuroendocrine Tumor With Evidence of Endocrine Progenitors. J Endocr Soc 2:172-177
Badin, Jill K; Kole, Ayeeshik; Stivers, Benjamin et al. (2018) Alloxan-induced diabetes exacerbates coronary atherosclerosis and calcification in Ossabaw miniature swine with metabolic syndrome. J Transl Med 16:58
Tersey, Sarah A; Levasseur, Esther M; Syed, Farooq et al. (2018) Episodic ?-cell death and dedifferentiation during diet-induced obesity and dysglycemia in male mice. FASEB J :fj201800150RR

Showing the most recent 10 out of 117 publications