Thermolabile 5,10-methylenetetrahydrofolate reductase as a cause of mild hyperhomocysteinemia
about
The "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother.Neural tube defects and folate: case far from closedPolymorphisms in the methylenetetrahydrofolate reductase gene are associated with susceptibility to acute leukemia in adultsHyperhomocyst(e)inaemia, but not MTHFR C677T mutation, as a risk factor for non-arteritic ischaemic optic neuropathyLow enzymatic activity haplotypes of the human catechol-O-methyltransferase gene: enrichment for marker SNPs.Hyperhomocysteinaemia in young patients with non-arteritic anterior ischaemic optic neuropathy.A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?The screening power of methylenetetrahydrofolate reductase C677T polymorphism versus plasma homocysteine concentration in patients with stenosis of the internal carotid arteryInsights into metabolic mechanisms underlying folate-responsive neural tube defects: a minireview.Thermolabile 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 inactivationDiet, genetics, and disease: a focus on the middle East and north Africa region.High prevalence of a mutation in the cystathionine beta-synthase gene.Sulfur as a signaling nutrient through hydrogen sulfide.Blood Concentrations of Homocysteine and Methylmalonic Acid among Demented and Non-Demented Swedish Elderly with and without Home Care Services and Vitamin B(12) Prescriptions.Physical activity is inversely associated with total homocysteine levels, independent of C677T MTHFR genotype and plasma B vitamins.Homocystinuria: what about mild hyperhomocysteinaemia?Dietary methionine effects on plasma homocysteine and HDL metabolism in mice.Homocysteine metabolism in ZDF (type 2) diabetic rats.CT genotype of 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism is protector factor of major depressive disorder in the Tunisian population: a case control study.A Meta-Analysis of Association between Methylenetetrahydrofolate Reductase Gene (MTHFR) 677C/T Polymorphism and Diabetic Retinopathy.Polymorphisms of the methylenetetrahydrofolate reductase, vascular endothelial growth factor, endothelial nitric oxide synthase, monocyte chemoattractant protein-1 and apolipoprotein E genes are not associated with carotid intima-media thicknessDefective cystathionine beta-synthase regulation by S-adenosylmethionine in a partially pyridoxine responsive homocystinuria patient.Determinants and vitamin responsiveness of intermediate hyperhomocysteinemia (> or = 40 micromol/liter). The Hordaland Homocysteine Study.The association and significance of H3K27me3 and a folate metabolic gene ACat2 in neural tube defects.Methylenetetrahydrofolate reductase (MTHFR) 677C>T gene polymorphism as a possible factor for reducing clinical severity of psoriasis.Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease.Elevated total plasma homocysteine and 677C-->T mutation of the 5,10-methylenetetrahydrofolate reductase gene in thrombotic vascular disease.Nutritional ecogenetics: homocysteine-related arteriosclerotic vascular disease, neural tube defects, and folic acid.Red cell N5-methyltetrahydrofolate concentrations and C677T methylenetetrahydrofolate reductase genotype in patients with stroke.The frequency of the methylenetetrahydrofolate reductase-gene mutation varies with age in the normal population.Methylenetetrahydrofolate reductase thermolabile variant and human longevity.Heart attacks and homocysteine.No evidence for association of MTHFR 677C>T and 1298A>C variants with placental DNA methylation.Methylenetetrahydrofolate reductase and psychiatric diseases
P2860
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P2860
Thermolabile 5,10-methylenetetrahydrofolate reductase as a cause of mild hyperhomocysteinemia
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
1995年论文
@zh
1995年论文
@zh-cn
name
Thermolabile 5,10-methylenetet ...... e of mild hyperhomocysteinemia
@ast
Thermolabile 5,10-methylenetet ...... e of mild hyperhomocysteinemia
@en
type
label
Thermolabile 5,10-methylenetet ...... e of mild hyperhomocysteinemia
@ast
Thermolabile 5,10-methylenetet ...... e of mild hyperhomocysteinemia
@en
prefLabel
Thermolabile 5,10-methylenetet ...... e of mild hyperhomocysteinemia
@ast
Thermolabile 5,10-methylenetet ...... e of mild hyperhomocysteinemia
@en
P2093
P2860
P1476
Thermolabile 5,10-methylenetet ...... e of mild hyperhomocysteinemia
@en
P2093
P2860
P304
P407
P577
1995-01-01T00:00:00Z