Polymorphism in Apoprotein-CIII Gene and Coronary Heart Disease-Reference-Cited by-同舟云学术

Polymorphism in Apoprotein-CIII Gene and Coronary Heart Disease

Published:1999-05 Issue:3 Volume:19 Page:201-205
ISSN:0256-4947
Container-title:Annals of Saudi Medicine
language:en
Short-container-title:Ann Saudi Med

Author:

Hussain Syed S.¹,Buraiki Jehad¹,Dzimiri Nduna¹,Butt Abdul Islam¹,Vencer Leticia¹,Basco Maria C.¹,Khan Bashir¹

Affiliation:

1. From the Departments of Biological and Medical Research, Cardiovascular Diseases, and Biomedical Statistics and Scientific Computing, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia

Publisher

King Faisal Specialist Hospital and Research Centre

Subject

General Medicine

Reference25 articles.

1. Deoxyribonucleic acid polymorphism in the apolipoprotein A-l-C-III gene cluster: association with hypertriglyceridemia;Rees A;J Clin Invest,1985

2. Strong association of a single nucleotide substitution in the 3’-untranslated region of the apoliprotein-CIII gene with common hypertriglyceridemia in Arabs;Tas S;Clin Chem,1989

3. Association of a DNA polymorphism in the apolipoprotein C-III gene with diverse hyperlipidemic phenotypes;Henderson HE;Hum Genet,1987

4. Genetic polymorphisms of apolipoprotein C-III and insulin in survivors of myocardial infarction;Ferns GA;Lancet,1985

5. C-III DNA restriction fragment length polymorphism and myocardial infarction;Ferns GA;Lancet,1986

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1. Endothelial nitric oxide synthase Glu 298 Asp (G894T) and Apolipoprotein E gene polymorphism as possible risk factors for coronary heart disease among Egyptians;The Egyptian Heart Journal;2018-12

2. Association of a DNA polymorphism of the apolipoprotein AI–CIII–AIV gene cluster with myocardial infarction in a Tunisian population;European Journal of Internal Medicine;2011-08

3. Genetic Disorders in Saudi Arabia;Genetic Disorders Among Arab Populations;2010

4. Genetic studies on the APOA1-C3-A5 gene cluster in Asian Indians with premature coronary artery disease;Lipids in Health and Disease;2008