Thermolabile defect of methylenetetrahydrofolate reductase in coronary artery disease.
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Effects of common polymorphisms on the properties of recombinant human methylenetetrahydrofolate reductaseElevated plasma homocysteine is positively associated with age independent of C677T mutation of the methylenetetrahydrofolate reductase gene in selected Egyptian subjectsMutated 5,10-methylenetetrahydrofolate reductase, hyperhomocysteinemia and risk for cardiovascular disease. Nature, nurture or nonsense?Future for folates in cardiovascular disease.Preventive health care, 2000 update: screening and management of hyperhomocysteinemia for the prevention of coronary artery disease events. The Canadian Task Force on Preventive Health Care.Diagnosis and treatment of hyperhomocysteinemia.Update on selected inherited venous thrombotic disorders.Genetic analysis of vascular factors in Alzheimer's disease.Relationship of MTHFR gene polymorphisms with renal and cardiac diseaseGenetic evaluation for coronary artery disease.Estrogens, homocysteine, vasodilatation and menopause: basic mechanisms, interactions and clinical implications.Homocysteine and cardiovascular disease in renal disease.Thermolabile methylenetetrahydrofolate reductase C677T polymorphism and homocysteine are risk factors for coronary artery disease in Moroccan population.Diet, genes and disease: implications for nutrition policy.C677T (RS1801133 ) MTHFR gene polymorphism frequency in a colombian population.The 5, 10 methylenetetrahydrofolate reductase C677T mutation and risk of fetal loss: a case series and review of the literature.Homocysteine: role and implications in atherosclerosis.Hyperhomocysteinaemia and premature coronary artery disease in the Chinese.Influence of genetic and environmental factors in peripheral arterial disease natural history: Analysis from six years follow up.Apolipoprotein gene polymorphisms and plasma levels in healthy Tunisians and patients with coronary artery disease.The effect of a subnormal vitamin B-6 status on homocysteine metabolism.Determinants and vitamin responsiveness of intermediate hyperhomocysteinemia (> or = 40 micromol/liter). The Hordaland Homocysteine Study.Influence of nitrous oxide anesthesia, B-vitamins, and MTHFR gene polymorphisms on perioperative cardiac events: the vitamins in nitrous oxide (VINO) randomized trial.Recurrent pregnancy loss: a disease of inflammation and coagulation.Association between MTHFR C677T polymorphism and osteonecrosis of the femoral head: a meta-analysis.Higher incidence of C677T polymorphism of the MTHFR gene in North Indian patients with vascular disease.Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease.Nutritional ecogenetics: homocysteine-related arteriosclerotic vascular disease, neural tube defects, and folic acid.Association of the C677T MTHFR polymorphism with homocysteine, ox-LDL levels, and thiolactonase activities in the severity of coronary syndrome.The frequency of the methylenetetrahydrofolate reductase-gene mutation varies with age in the normal population.APOC3, CETP, fibrinogen, and MTHFR are genetic determinants of carotid intima-media thickness in healthy men (the Stanislas cohort).The effect of polymorphisms of MTHER gene and vitamin B on hyperhomocysteinemia.The relation between plasma homocysteine concentration and methylenetetrahydrofolate reductase gene polymorphism in pregnant women.Serum homocysteine concentration is related to diabetes mellitus, but not to coronary heart disease, in Saudi Arabians.Association of serum total homocysteine with the extent of ischemic heart disease in a Mediterranean cohort.Plasma total homocysteine level and methylenetetrahydrofolate reductase 677C>T genetic polymorphism in Japanese patients with rheumatoid arthritis.Homocysteine reduces endothelial progenitor cells in stroke patients through apoptosis.Thermolabile methylenetetrahydrofolate reductase enzyme genotype is frequent in type 2 diabetic patients with normal fasting homocysteine levels.677TT polymorphism of methylenetetrahydrofolate reductase in combination with low serum vitamin B12 is associated with coronary in-stent restenosis.Molecular analysis of factor V Leiden, factor V Hong Kong, factor II G20210A, methylenetetrahydrofolate reductase C677T, and A1298C mutations related to Turkish thrombosis patients.
P2860
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P2860
Thermolabile defect of methylenetetrahydrofolate reductase in coronary artery disease.
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
1993年论文
@zh
1993年论文
@zh-cn
name
Thermolabile defect of methylenetetrahydrofolate reductase in coronary artery disease.
@en
type
label
Thermolabile defect of methylenetetrahydrofolate reductase in coronary artery disease.
@en
prefLabel
Thermolabile defect of methylenetetrahydrofolate reductase in coronary artery disease.
@en
P2093
P356
P1433
P1476
Thermolabile defect of methylenetetrahydrofolate reductase in coronary artery disease.
@en
P2093
P304
P356
10.1161/01.CIR.88.4.1463
P407
P433
P577
1993-10-01T00:00:00Z