Thermolabile methylenetetrahydrofolate reductase: an inherited risk factor for coronary artery disease.
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Hereditary thrombophiliaAmerican College of Medical Genetics consensus statement on factor V Leiden mutation testingSeven novel mutations in the methylenetetrahydrofolate reductase gene and genotype/phenotype correlations in severe methylenetetrahydrofolate reductase deficiencyResponse of serum and red blood cell folate concentrations to folic acid supplementation depends on methylenetetrahydrofolate reductase C677T genotype: Results from a crossover trialVenous thrombosis and prothrombotic factors in inflammatory bowel disease.Hyperhomocysteinemia and hypercoagulability in primary biliary cirrhosis.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.Thrombophilia in pregnancy.Is there any genetic predisposition of MMP-9 gene C1562T and MTHFR gene C677T polymorphisms with essential hypertension?Intermediate hyperhomocysteinemia resulting from compound heterozygosity of methylenetetrahydrofolate reductase mutations.Neural tube defects: from a proteomic standpointIs folic acid the ultimate functional food component for disease prevention?Genetic interactions between MTHFR (C677T), methionine synthase (A2756G, C2758G) variants with vitamin B12 and folic acid determine susceptibility to premature coronary artery disease in Indian population.Methylene tetrahydrofolate reductase genotype and the risk and extent of coronary artery disease in a population with low plasma folate.Genetic polymorphisms influence runners' responses to the dietary ingestion of antioxidant supplementation based on pequi oil (Caryocar brasiliense Camb.): a before-after study.Thermolabile 5,10-methylenetetrahydrofolate reductase as a cause of mild hyperhomocysteinemiaThermolabile methylenetetrahydrofolate reductase C677T polymorphism and homocysteine are risk factors for coronary artery disease in Moroccan population.Structural perturbations in the Ala --> Val polymorphism of methylenetetrahydrofolate reductase: how binding of folates may protect against inactivationSevere and mild mutations in cis for the methylenetetrahydrofolate reductase (MTHFR) gene, and description of five novel mutations in MTHFR.C677T Methylenetetrahydrofolate Reductase (MTHFR) Gene Polymorphism in Schizophrenia and Bipolar Disorder: An Association Study in Iranian PopulationSulfur as a signaling nutrient through hydrogen sulfide.Polygenic association with total homocysteine in the post-folic acid fortification era: the CARDIA study.Homocystinuria: what about mild hyperhomocysteinaemia?Methylenetetrahydrofolate Reductase C677T and A1298C Polymorphisms in Male Partners of Recurrent Miscarriage Couples.Therapeutical approach to plasma homocysteine and cardiovascular risk reduction.Hyperhomocysteinaemia and premature coronary artery disease in the Chinese.Mendelian randomization analysis of the effect of maternal homocysteine during pregnancy, as represented by maternal MTHFR C677T genotype, on birth weightAssociation of C677T MTHFR and G20210A FII prothrombin polymorphisms with susceptibility to myocardial infarctionLack of association of methylenetetrahydrofolate reductase 677C>T mutation with coronary artery disease in a Pakistani populationThe effect of a subnormal vitamin B-6 status on homocysteine metabolism.The search for genetic polymorphisms in the homocysteine/folate pathway that contribute to the etiology of human neural tube defects.A love affair with vitamins.Extrahepatic portal vein thrombosis in children and adolescents: Influence of genetic thrombophilic disorders.Genetic impairments in folate enzymes increase dependence on dietary choline for phosphatidylcholine production at the expense of betaine synthesis.Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease.Genes, greens, and homocysteine.Nutritional ecogenetics: homocysteine-related arteriosclerotic vascular disease, neural tube defects, and folic acid.Pulmonary thromboembolism due to severe hyperhomocysteinemia associated with a methyltetrahydrofolate reductase mutation.The (Ala-Val) mutation of methylenetetrahydrofolate reductase as a genetic risk factor for vascular disease in non-insulin-dependent diabetic patients.Methylenetetrahydrofolate reductase thermolabile variant and human longevity.
P2860
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P2860
Thermolabile methylenetetrahydrofolate reductase: an inherited risk factor for coronary artery disease.
description
1991 nî lūn-bûn
@nan
1991 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի մարտին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
Thermolabile methylenetetrahyd ...... r for coronary artery disease.
@ast
Thermolabile methylenetetrahyd ...... r for coronary artery disease.
@en
type
label
Thermolabile methylenetetrahyd ...... r for coronary artery disease.
@ast
Thermolabile methylenetetrahyd ...... r for coronary artery disease.
@en
prefLabel
Thermolabile methylenetetrahyd ...... r for coronary artery disease.
@ast
Thermolabile methylenetetrahyd ...... r for coronary artery disease.
@en
P2093
P2860
P1476
Thermolabile methylenetetrahyd ...... or for coronary artery disease
@en
P2093
P2860
P304
P407
P577
1991-03-01T00:00:00Z