The Hormone Assay Core assists investigators in the measurement of hormones in biologic fluids as relatedto diabetes, endocrine and metabolic research. The core provides space, equipment, and personnel forsample analysis and method development. User charge backs support the cost of reagents, supplies andpro-rated service contracts. The analysis available include 1) insulin, 2) free insulin, 3) glucagon, 4)cortisol, 5) catecholamines, 6) growth hormone, 7) c-peptides (human, canine, porcine), 8) pancreaticpolypeptides, 9) leptin, 10) ratcorticosterone, and 11) GLP-1 (active). Several of these assays are availablein 'micro' methods for the analysis of hormone levels in very small volumes of plasma or blood.Furthermore, some assays are designed to measure hormones in a particular species. The core has thepotential to develop new tests and technologies to expand the scope of its current testing. An annual surveyis conducted to determine the needs of users for new assays. Over the past grant period, there has been anincreased demand for at least half of the services offered and a constant demand for the remainder. The corewill be expanded to meet an expected growth in demand that is anticipated as a result of funding of a MurineMetabolic and Physiology Center. An advisory Committees will deal with issues of coordination betweenthe DRTC and MMPC, as well as user fees and new service implementation.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Comprehensive Center (P60)
Project #
2P60DK020593-29
Application #
7284643
Study Section
Special Emphasis Panel (ZDK1-GRB-N (J1))
Project Start
2007-04-01
Project End
2012-03-31
Budget Start
2007-06-01
Budget End
2008-03-31
Support Year
29
Fiscal Year
2007
Total Cost
$268,273
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Type
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37212
Funkhouser-Jones, Lisa J; van Opstal, Edward J; Sharma, Ananya et al. (2018) The Maternal Effect Gene Wds Controls Wolbachia Titer in Nasonia. Curr Biol 28:1692-1702.e6
Hart, Nathaniel J; Aramandla, Radhika; Poffenberger, Gregory et al. (2018) Cystic fibrosis-related diabetes is caused by islet loss and inflammation. JCI Insight 3:
Warren Andersen, Shaneda; Blot, William J; Shu, Xiao-Ou et al. (2018) Associations Between Neighborhood Environment, Health Behaviors, and Mortality. Am J Prev Med 54:87-95
Sui, Lina; Danzl, Nichole; Campbell, Sean R et al. (2018) ?-Cell Replacement in Mice Using Human Type 1 Diabetes Nuclear Transfer Embryonic Stem Cells. Diabetes 67:26-35
Dutter, Brendan F; Ender, Anna; Sulikowski, Gary A et al. (2018) Rhodol-based thallium sensors for cellular imaging of potassium channel activity. Org Biomol Chem 16:5575-5579
Herrick, Mary K; Favela, Kristin M; Simerly, Richard B et al. (2018) Attenuation of diet-induced hypothalamic inflammation following bariatric surgery in female mice. Mol Med 24:56
Perez, Katia M; Curley, Kathleen L; Slaughter, James C et al. (2018) Glucose Homeostasis and Energy Balance in Children With Pseudohypoparathyroidism. J Clin Endocrinol Metab 103:4265-4274
Marre, Meghan L; McGinty, John W; Chow, I-Ting et al. (2018) Modifying Enzymes Are Elicited by ER Stress, Generating Epitopes That Are Selectively Recognized by CD4+ T Cells in Patients With Type 1 Diabetes. Diabetes 67:1356-1368
Creecy, Amy; Uppuganti, Sasidhar; Unal, Mustafa et al. (2018) Low bone toughness in the TallyHO model of juvenile type 2 diabetes does not worsen with age. Bone 110:204-214
Russart, Kathryn L G; Huk, Danielle; Nelson, Randy J et al. (2018) Elevated aggressive behavior in male mice with thyroid-specific Prkar1a and global Epac1 gene deletion. Horm Behav 98:121-129

Showing the most recent 10 out of 1487 publications