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▌ Volume 154, Issue 3            【字体：小 大】

Volume 154, Issue 3 作者：佚名    期刊来源：Atherosclerosis    点击数：    更新时间：2007-6-25 A new DNA polymorphism in the 5′ untranslated region of the human SREBP-1a is related to development of atherosclerosis in high cardiovascular risk population.pdf A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.pdf A prospective evaluation of the CD14 C(-260)T gene polymorphism and the risk of myocardial infarction.pdf A prospective study of coronary heart disease and the hemochromatosis gene (HFE) C282Y mutation the Atherosclerosis Risk in Communities (ARIC) study.pdf A prospective study of paraoxonase gene QR192 polymorphism and severity, progression and regression of coronary atherosclerosis, plasma lipid levels,clinical events and response to fluvastatin.pdf Angiotensin-converting enzyme gene polymorphism in a cohort of coronary angiography patients.pdf Announcement.pdf Apolipoprotein E genotype and cardiovascular disease in the Framingham Heart Study.pdf Apoprotein E genotype and the response of serum cholesterol to dietary fat, cholesterol and cafestol.pdf Association of plasma bilirubin with coronary heart disease and segregation of bilirubin as a major gene trait the NHLBI family heart study.pdf Author index.pdf Chromosomal alterations in atherosclerotic plaques.pdf Common variants in the gene encoding ATP-binding cassette transporter 1 in men with low HDL cholesterol levels and coronary heart disease.pdf Effect of apolipoprotein E34 phenotype on postprandial triglycerides and retinyl palmitate metabolism in plasma from hyperlipidemic subjects in Japan.pdf Enhanced fractional catabolic rate of apo A-I and apo A-II in heterozygous subjects for apo A-IZaragoza (L144R).pdf Familial and genetic determinants of systemic markers of inflammation the NHLBI family heart study.pdf Fh-Souassi a founder frameshift mutation in exon 10 of the LDL-receptor gene, associated with a mild phenotype in Tunisian families.pdf Functional mutation in the promoter region of thrombomodulin gene in relation to carotid atherosclerosis.pdf Genetics and Atherosclerosis Broadening the Horizon.pdf Hepatic lipase promoter activity is reduced by the C-480T and G-216A substitutions present in the common LIPC gene variant, and is increased by Upstre.pdf Identification of six methylenetetrahydrofolate reductase (MTHFR) genotypes resulting from common polymorphisms impact on plasma homocysteine levels and development of coronary artery disease.pdf Influence of a methionine synthase (D919G) polymorphism on plasma homocysteine and folate levels and relation to risk of myocardial infarction.pdf Interaction of the glutathione S-transferase genes and cigarette smoking on risk of lower extremity arterial disease the Atherosclerosis Risk in Communities (ARIC) study.pdf Polymorphisms in endothelial nitric oxide synthase and atherogenesis John French Lecture 2000.pdf Polymorphisms in the thrombopoietin gene are associated with risk of myocardial infarction at a young age.pdf Polymorphisms within the tumor necrosis factor locus and prevalence of coronary artery disease in middle-aged men.pdf PON2 gene variants are associated with clinical manifestations of cardiovascular disease in familial hypercholesterolemia patients.pdf Sequencing of the coding exons of the LRP1 and LDLR genes on individual DNA samples reveals novel mutations in both genes.pdf Subject index.pdf The effect of the C677T and A1298C polymorphisms in the methylenetetrahydrofolate reductase gene on homocysteine levels in elderly men and women from the British regional heart study.pdf The GPIIIa (β3 integrin) PlA polymorphism in the early development of coronary atherosclerosis.pdf Variable association between genetic variation in the CYP7 gene promoter and plasma lipoproteins in three Canadian populations.pdf

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