Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
7R01DK047461-03
Application #
2147085
Study Section
Diabetes, Endocrinology and Metabolic Diseases B Subcommittee (DDK)
Project Start
1993-09-30
Project End
1998-08-31
Budget Start
1995-08-10
Budget End
1995-08-31
Support Year
3
Fiscal Year
1994
Total Cost
Indirect Cost
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
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
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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
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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

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