Lipoprotein lipase gene polymorphisms: associations with myocardial infarction and lipoprotein levels, the ECTIM study. Etude Cas Témoin sur l'Infarctus du Myocarde.
暂无分享,去创建一个
D. Arveiler | G. Luc | L. Tiret | J. Fruchart | O. Poirier | J. Bard | A. Evans | J. Cambou | F. Fumeron | R. Jemaa | L. Lecerf | tt | Apfelbaum | Fdderic Fumeron | Odette Pokier | Dominique Ameiler | tt Jean-Pierre Cambou | Franqois Cambien
[1] A. Kessling,et al. Prevalence of alleles encoding defective lipoprotein lipase in hypertriglyceridemic patients of French Canadian descent. , 1995, Journal of lipid research.
[2] P. Elwood,et al. DNA variants at the LPL gene locus associate with angiographically defined severity of atherosclerosis and serum lipoprotein levels in a Welsh population. , 1994, Arteriosclerosis and thrombosis : a journal of vascular biology.
[3] R. Hamman,et al. Two DNA polymorphisms in the lipoprotein lipase gene and their associations with factors related to cardiovascular disease. , 1993, Journal of lipid research.
[4] B. Paulweber,et al. Heterozygous lipoprotein lipase deficiency due to a missense mutation as the cause of impaired triglyceride tolerance with multiple lipoprotein abnormalities. , 1993, The Journal of clinical investigation.
[5] S. Humphries,et al. Associations between lipoprotein lipase gene polymorphisms and plasma correlations of lipids, lipoproteins and lipase activities in young myocardial infarction survivors and age-matched healthy individuals from Sweden. , 1992, Atherosclerosis.
[6] J. K. Dunn,et al. Relation of triglyceride metabolism and coronary artery disease. Studies in the postprandial state. , 1992, Arteriosclerosis and thrombosis : a journal of vascular biology.
[7] D. Galton,et al. Lipoprotein lipase genotypes for a common premature termination codon mutation detected by PCR-mediated site-directed mutagenesis and restriction digestion. , 1992, Journal of lipid research.
[8] A. Evans,et al. A case-control study of lipoprotein particles in two populations at contrasting risk for coronary heart disease. The ECTIM Study. , 1992, Arteriosclerosis and thrombosis : a journal of vascular biology.
[9] M. Bond,et al. Postprandial Triglyceridemia and Carotid Atherosclerosis in Middle‐Aged Subjects , 1992, Stroke.
[10] K. Shirai,et al. A heterozygous mutation (the codon for Ser447----a stop codon) in lipoprotein lipase contributes to a defect in lipid interface recognition in a case with type I hyperlipidemia. , 1992, Biochemical and biophysical research communications.
[11] L. Smith,et al. Catalytic triad residue mutation (Asp156----Gly) causing familial lipoprotein lipase deficiency. Co-inheritance with a nonsense mutation (Ser447----Ter) in a Turkish family. , 1991, The Journal of biological chemistry.
[12] L. Tiret,et al. Testing for association between disease and linked marker loci: a log-linear-model analysis. , 1991, American journal of human genetics.
[13] D. Galton,et al. Lipoprotein and hepatic lipase gene variants in coronary atherosclerosis. , 1990, Atherosclerosis.
[14] M. King,et al. Atherogenic lipoprotein phenotype. A proposed genetic marker for coronary heart disease risk. , 1990, Circulation.
[15] K. Ishimura-Oka,et al. Structure and polymorphic map of human lipoprotein lipase gene. , 1990, Biochimica et biophysica acta.
[16] D. Galton,et al. DNA polymorphisms at the lipoprotein lipase gene: associations in normal and hypertriglyceridaemic subjects. , 1989, Atherosclerosis.
[17] R. Eckel,et al. Lipoprotein lipase. A multifunctional enzyme relevant to common metabolic diseases. , 1989, The New England journal of medicine.
[18] J. Brunzell. Familial lipoprotein lipase deficiency and other causes of the chylomicronemia syndrome , 1989 .
[19] E. Thompson,et al. The detection of linkage disequilibrium between closely linked markers: RFLPs at the AI-CIII apolipoprotein genes. , 1988, American journal of human genetics.
[20] N. Miller. Associations of high-density lipoprotein subclasses and apolipoproteins with ischemic heart disease and coronary atherosclerosis. , 1987, American heart journal.
[21] Henry A. Erlich,et al. Analysis of enzymatically amplified β-globin and HLA-DQα DNA with allele-specific oligonucleotide probes , 1986, Nature.