The purpose of the administrative and clinical chemistry core is to provide overall daily administrative guidance for the project and laboratory support for the myriad of biochemical analyses proposed under the umbrella of this program project grant. By performing these determinations in a core laboratory setting, we will attain cost-effective utilization of the supplies and laboratory personnel required for this proposal. More importantly, it will insure quality control over the performance of these analyses and minimize the potential variation that might occur between several laboratories performing their own testing protocols. All of the urinary analyses will be performed in the Mineral Metabolism laboratory, a CLIA-approved laboratory. The procedures are all standardized and appropriate quality control specimens are included with each run. The analyses to be performed in this laboratory will subserve each component as specified in Table A. Components I, II, IV, and V will require 24-hour urine analyses for stone-risk parameters. Similar testing will also be accomplished on 2-hour fasting specimens as part of Components I and II. Titratable acidities will be a major need for component II and a minor part of component IV. Serum assays will require the use of both ELISA and radioisotopic methods. These assays will be performed in the RIA laboratory under the direction of Dr. Zerwekh. Except for the vitamin D metabolite analyses, all of the proposed tests are performed with commercially available kits and are currently employed assays in this laboratory. Component III will require a limited electrolyte assessment on rat urine and plasma. Three of the assays specific to component II, namely serum insulin, free fatty acid, and lactate will be performed in the laboratory of Dr. Nicola Abate, co-investigator for Component II.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Program Projects (P01)
Project #
5P01DK020543-29
Application #
7210582
Study Section
Special Emphasis Panel (ZDK1)
Project Start
Project End
Budget Start
2005-12-01
Budget End
2006-11-30
Support Year
29
Fiscal Year
2006
Total Cost
$325,538
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Type
DUNS #
800771545
City
Dallas
State
TX
Country
United States
Zip Code
75390
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Sakhaee, Khashayar; Poindexter, John; Aguirre, Crystal (2016) The effects of bariatric surgery on bone and nephrolithiasis. Bone 84:1-8
Hu, Ming Chang; Shi, Mingjun; Cho, Han Jun et al. (2015) Klotho and phosphate are modulators of pathologic uremic cardiac remodeling. J Am Soc Nephrol 26:1290-302
Hajibeigi, Asghar; Dioum, Elhadji M; Guo, Jianfei et al. (2015) Identification of novel regulatory NFAT and TFII-I binding elements in the calbindin-D28k promoter in response to serum deprivation. Biochem Biophys Res Commun 465:414-420
Yoon, Vivienne; Adams-Huet, Beverley; Sakhaee, Khashayar et al. (2013) Hyperinsulinemia and urinary calcium excretion in calcium stone formers with idiopathic hypercalciuria. J Clin Endocrinol Metab 98:2589-94
Capolongo, Giovanna; Abul-Ezz, Sameh; Moe, Orson W et al. (2012) Subclinical celiac disease and crystal-induced kidney disease following kidney transplant. Am J Kidney Dis 60:662-7
Cameron, MaryAnn; Maalouf, Naim M; Poindexter, John et al. (2012) The diurnal variation in urine acidification differs between normal individuals and uric acid stone formers. Kidney Int 81:1123-30
Sakhaee, Khashayar; Capolongo, Giovanna; Maalouf, Naim M et al. (2012) Metabolic syndrome and the risk of calcium stones. Nephrol Dial Transplant 27:3201-9
Nguyen, Trang Q; Maalouf, Naim M; Sakhaee, Khashayar et al. (2011) Comparison of insulin action on glucose versus potassium uptake in humans. Clin J Am Soc Nephrol 6:1533-9

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