Allele frequencies for candidate genes in atherosclerosis and diabetes among trinidadian neonates

Human Biology

Volumn 73, Issue 4, 2001, Pages 525-531

  Hegele, R A ^a   Ban, M R ^a   Carrington, C V ^a   Ramdath, D D ^a  

^a ROBARTS RESEARCH INSTITUTE   (Canada)

Author keywords

Hypertension; Lipids; Polygenic disease

Indexed keywords

EID: 0034882136     PISSN: 00187143     EISSN: None     Source Type: Journal    
DOI: 10.1353/hub.2001.0052     Document Type: Article

References (25)

1. Association of PON2 variation with birth weight in Trinidadian neonates of South Asian ancestry
2. Hepatic lipase: New insights from genetic and metabolic studies
3. Apolipoprotein E and atherosclerosis: Insight from animal and human studies
4. Coronary heart disease risks in Asian Indians
5. Candidate genes, small effects, and the prediction of atherosclerosis
6. A review of intestinal fatty acid binding protein gene variation and the plasma lipoprotein response to dietary components
7. Paraoxonase-genes and disease
8. A polymorphism of the angiotensinogen gene associatedwith variation in blood pressure in a genetic isolate
9. Genetic variation of intestinal fatty acid-binding protein associated with variation in body mass in aboriginal Canadians
10. Common genomic variants associated with variation in plasma lipoproteins in young aboriginal Canadians
11. Paraoxonase-2 gene (PON2) G148 variant associated with elevated fasting plasma glucose in noninsulin-dependent diabetes mellitus
12. Factor V Leiden (F5 Q506) and vascular disease in Canadian Oji-Cree
13. Methylenetetrahydrofolate reductase gene, dietaryfolate, NIDDM, and atherosclerosis in Canadian Oji-Cree
14. Variation in the AU(AT)-rich element within the 3′-untranslated region of PPP1R3 is associated with variation in plasma glucose in aboriginal Canadians
15. Absence of association between genetic variation of the beta 3-adrenergic receptor and metabolic phenotypes in Oji-Cree
16. Absence of association between genetic variation in the LIPC gene promoter and plasma lipoproteins in three Canadian populations
17. Molecular basis of human hypertension: Role of angiotensinogen
18. Common genetic variation in the promoter of the human APO CIII gene abolishes regulation by insulin and may contribute to hypertriglyceridemia
19. Phenotypic characterization of the Trp64Arg polymorphism in the beta-3-adrenergic receptor gene in normal weight and obese subjects
20. Atherosclerosis
21. Ethnicity and other characteristics predictive of coronary heart disease in a developing community: Principal results of the St. James Survey, Trinidad
22. Nutritional ecogenetics: Homocysteine-related arteriosclerotic vascular disease, neural tube defects and folic acid
23. Hepatic lipase gene polymorphisms influence plasma HDL levels
24. Factor V Leiden mutation and the risks for thromboembolic disease: A clinical perspective