Gender related association between genetic variations of APOC-III gene and lipid and lipoprotein variables in northern France.
暂无分享,去创建一个
P. Amouyel | D. Cottel | J. Dallongeville | A. Meirhaeghe | J. Fruchart | N. Helbecque | P. Amouyel | J. Fruchart | Jean Dallongeville
[1] H. Tunstall-Pedoe,et al. Myocardial Infarction and Coronary Deaths in the World Health Organization MONICA Project: Registration Procedures, Event Rates, and Case‐Fatality Rates in 38 Populations From 21 Countries in Four Continents , 1994, Circulation.
[2] J. Rotter,et al. Apolipoprotein A-I/C-III/A-IV gene cluster in familial combined hyperlipidemia: effects on LDL-cholesterol and apolipoproteins B and C-III. , 1996, Journal of lipid research.
[3] J. Viikari,et al. DNA polymorphisms of the apolipoprotein B and A-I/C-III genes are associated with variations of serum low density lipoprotein cholesterol level in childhood. , 1991, Journal of lipid research.
[4] Hoffer,et al. Increased risk for endogenous hypertriglyceridaemia is associated with an apolipoprotein C3 haplotype specified by the SstI polymorphism , 1998, European journal of clinical investigation.
[5] R. Mahley,et al. Plasma lipoproteins: apolipoprotein structure and function. , 1984, Journal of lipid research.
[6] A. Kessling,et al. Patterns of association between genetic variability in apolipoprotein (apo) B, apo AI-CIII-AIV, and cholesterol ester transfer protein gene regions and quantitative variation in lipid and lipoprotein traits: influence of gender and exogenous hormones. , 1992, American journal of human genetics.
[7] D. C. Rao,et al. Estimation of myriad haplotype frequencies , 1985, Genetic epidemiology.
[8] T. Lehtimäki,et al. Variability gene effects of DNA polymorphisms at the apo B, apo AI/C III and apo E loci on serum lipids: the Cardiovascular Risk in Young Finns Study , 1994, Clinical genetics.
[9] Chun-Fang Xu,et al. Association between genetic variation at the APO AI‐CIII‐AIV gene cluster and familial combined hyperlipidaemia , 1994, Clinical genetics.
[10] K. Mullis,et al. Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia. , 1985, Science.
[11] D. Galton,et al. Haplotypes identified by DNA restriction-fragment-length polymorphisms in the A-1 C-III A-IV gene region and hypertriglyceridemia. , 1987, American journal of human genetics.
[12] S. Grundy,et al. Variation at the hepatic lipase and apolipoprotein AI/CIII/AIV loci is a major cause of genetically determined variation in plasma HDL cholesterol levels. , 1994, The Journal of clinical investigation.
[13] E. Wijsman,et al. Evidence against linkage of familial combined hyperlipidemia to the apolipoprotein AI-CIII-AIV gene complex. , 1998, Arteriosclerosis, thrombosis, and vascular biology.
[14] V. Gudnason,et al. Variation at the lipoprotein lipase and apolipoprotein AI‐CIII gene loci are associated with fasting lipid and lipoprotein traits in a population sample from Iceland: Interaction between genotype, gender, and smoking status , 1997, Genetic epidemiology.
[15] Jin Q. Kim,et al. Association between genetic variations of apo AI-CIII-AIV cluster gene and hypertriglyceridemic subjects. , 1997, Clinical chemistry.
[16] Chun-Fang Xu,et al. Role of genetic variation at the Apo AI‐CIII‐AIV gene cluster in determining plasma Apo AI levels in boys and girls , 1993, Genetic epidemiology.
[17] C. Sing,et al. Cladistic analysis of the apolipoprotein AI‐CIH‐AIV gene cluster using a healthy French Canadian sample. I. Haploid analysis , 1995, Annals of human genetics.
[18] D. Arveiler,et al. Lack of association between genetic variations of apo A-I-C-III-A-IV gene cluster and myocardial infarction in a sample of European male: ECTIM study. , 1999, Atherosclerosis.
[19] S. Humphries,et al. A variation in the apolipoprotein C-III gene is associated with an increased number of circulating VLDL and IDL particles in familial combined hyperlipidemia. , 1997, Journal of lipid research.
[20] Y. Ko,et al. Interaction between obesity and genetic polymorphisms in the apolipoprotein CIII gene and lipoprotein lipase gene on the risk of hypertriglyceridemia in Chinese , 1997, Human Genetics.
[21] T. Burns,et al. Restriction fragment length polymorphisms associated with abnormal lipid levels in an adolescent population. , 1989, Atherosclerosis.
[22] P. Talmud,et al. Variation at the apolipoprotein (apo) AI-CIII-AIV gene cluster and apo B gene loci is associated with lipoprotein and apolipoprotein levels in Italian children. , 1990, American journal of human genetics.
[23] N. Cox,et al. Linkage disequilibrium in the human insulin/insulin-like growth factor II region of human chromosome II. , 1988, American journal of human genetics.
[24] N. Cox,et al. Hypertriglyceridemia and the apolipoprotein CIII gene locus: lack of association with the variant insulin response element in Italian school children , 1996, Human Genetics.
[25] E. Boerwinkle,et al. Polymorphic markers in apolipoprotein C-III gene flanking regions and hypertriglyceridemia. , 1996, Arteriosclerosis, thrombosis, and vascular biology.
[26] J. Rotter,et al. Complex genetic contribution of the Apo AI-CIII-AIV gene cluster to familial combined hyperlipidemia. Identification of different susceptibility haplotypes. , 1997, The Journal of clinical investigation.
[27] P. Talmud,et al. Apolipoprotein C-III gene variation and dyslipidaemia. , 1997, Current opinion in lipidology.
[28] L. Peltonen,et al. Haplotypes of the ApoA-I/C-III/A-IV gene cluster and familial combined hyperlipidemia. , 1998, Arteriosclerosis, thrombosis, and vascular biology.
[29] B. Zinman,et al. Common genomic variants associated with variation in plasma lipoproteins in young aboriginal Canadians. , 1997, Arteriosclerosis, thrombosis, and vascular biology.
[30] Shirley A. Miller,et al. A simple salting out procedure for extracting DNA from human nucleated cells. , 1988, Nucleic acids research.
[31] B. Zinman,et al. Common genomic variation in the APOC3 promoter associated with variation in plasma lipoproteins. , 1997, Arteriosclerosis, thrombosis, and vascular biology.
[32] M. Hayden,et al. Lack of association of the apolipoprotein A-I-C-III-A-IV gene XmnI and SstI polymorphisms and of the lipoprotein lipase gene mutations in familial combined hyperlipoproteinemia in French Canadian subjects. , 1996, Journal of lipid research.
[33] J. Breslow,et al. An apolipoprotein CIII haplotype protective against hypertriglyceridemia is specified by promoter and 3' untranslated region polymorphisms. , 1993, Proceedings of the National Academy of Sciences of the United States of America.
[34] C. Shoulders,et al. Deoxyribonucleic acid polymorphism in the apolipoprotein A-1-C-III gene cluster. Association with hypertriglyceridemia. , 1985, The Journal of clinical investigation.
[35] D. Arveiler,et al. The role of a triplet repeat sequence of the very low density lipoprotein receptor gene in plasma lipid and lipoprotein level variability in humans. , 1997, Arteriosclerosis, thrombosis, and vascular biology.