Genetic Markers for Niddm & Pathogenic Metabolic Traits

Garvey, W Timothy

Abstract

Funding Agency

• Agency: National Institute of Health (NIH)
• Institute: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
• Type: Research Project (R01)
• Project #: 5R01DK047461-05
• Application #: 2147087
• Study Section: Diabetes, Endocrinology and Metabolic Diseases B Subcommittee (DDK)
• Program Officer: Yanovski, Susan Z
• Project Start: 1993-09-30
• Project End: 1998-08-31
• Budget Start: 1996-09-01
• Budget End: 1997-08-31
• Support Year: 5
• Fiscal Year: 1996

Institution

• Name: Medical University of South Carolina
• Department: Internal Medicine/Medicine
• Type: Schools of Medicine
• DUNS #: 183710748
• City: Charleston
• State: SC
• Country: United States
• Zip Code: 29425

Publications

Sadler, Lois S; Newlin, Kelley H; Johnson-Spruill, Ida et al. (2011) Beyond the medical model: interdisciplinary programs of community-engaged health research. Clin Transl Sci 4:285-97

Divers, Jasmin; Sale, Michèle M; Lu, Lingyi et al. (2010) The genetic architecture of lipoprotein subclasses in Gullah-speaking African American families enriched for type 2 diabetes: the Sea Islands Genetic African American Registry (Project SuGAR). J Lipid Res 51:586-97

Sale, Michèle M; Lu, Lingyi; Spruill, Ida J et al. (2009) Genome-wide linkage scan in Gullah-speaking African American families with type 2 diabetes: the Sea Islands Genetic African American Registry (Project SuGAR). Diabetes 58:260-7

McLean Jr, David C; Spruill, Ida; Argyropoulos, George et al. (2005) Mitochondrial DNA (mtDNA) haplotypes reveal maternal population genetic affinities of Sea Island Gullah-speaking African Americans. Am J Phys Anthropol 127:427-38

Nagy, Tim R; Blaylock, Matthew L; Garvey, W Timothy (2004) Role of UCP2 and UCP3 in nutrition and obesity. Nutrition 20:139-44

McLean Jr, David C; Spruill, Ida; Gevao, Sahr et al. (2003) Three novel mtDNA restriction site polymorphisms allow exploration of population affinities of African Americans. Hum Biol 75:147-61

Brown, A M; Dolan, J W; Willi, S M et al. (1999) Endogenous mutations in human uncoupling protein 3 alter its functional properties. FEBS Lett 464:189-93

Argyropoulos, G; Brown, A M; Garvey, W T (1999) Aberrant DNA sequence pattern caused by a heterozygosity. Biotechniques 26:604-6

Hanson, R L; Ehm, M G; Pettitt, D J et al. (1998) An autosomal genomic scan for loci linked to type II diabetes mellitus and body-mass index in Pima Indians. Am J Hum Genet 63:1130-8

Argyropoulos, G; Jenkins, A; Klein, R L et al. (1998) Transmission of two novel mutations in a pedigree with familial lecithin:cholesterol acyltransferase deficiency: structure-function relationships and studies in a compound heterozygous proband. J Lipid Res 39:1870-6