Homocysteine metabolism in pregnancies complicated by neural-tube defects.
about
Bioinformatic and genetic association analysis of microRNA target sites in one-carbon metabolism genesMTHFR C677T and MTR A2756G polymorphisms and the homocysteine lowering efficacy of different doses of folic acid in hypertensive Chinese adults'Mendelian randomization': can genetic epidemiology contribute to understanding environmental determinants of disease?Maternal vitamin B12 status and risk of neural tube defects in a population with high neural tube defect prevalence and no folic Acid fortificationTeratogenic mechanisms of medical drugsGenetics of human neural tube defectsNovel associations of CPS1, MUT, NOX4, and DPEP1 with plasma homocysteine in a healthy population: a genome-wide evaluation of 13 974 participants in the Women's Genome Health StudyModulation of cystathionine beta-synthase activity by the Arg-51 and Arg-224 mutationsRegulation of human methylenetetrahydrofolate reductase by phosphorylationThe "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.Cobalamin deficiency, hyperhomocysteinemia, and dementiaFolic Acid and EpilepsyMaternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifidaA polymorphism, R653Q, in the trifunctional enzyme methylenetetrahydrofolate dehydrogenase/methenyltetrahydrofolate cyclohydrolase/formyltetrahydrofolate synthetase is a maternal genetic risk factor for neural tube defects: report of the Birth DefecThe reduced folate carrier (SLC19A1) c.80G>A polymorphism is associated with red cell folate concentrations among womenMethylenetetrahydrofolate reductase and transcobalamin genetic polymorphisms in human spontaneous abortion: biological and clinical implicationsMining literature for a comprehensive pathway analysis: a case study for retrieval of homocysteine related genes for genetic and epigenetic studiesStopped-flow kinetic analysis of the reaction catalyzed by the full-length yeast cystathionine beta-synthase.Neural tube defects in mice with reduced levels of inositol 1,3,4-trisphosphate 5/6-kinaseTargeted disruption of the methionine synthase gene in miceFolate and vitamin B12Early origins of adult disease: approaches for investigating the programmable epigenome in humans, nonhuman primates, and rodentsA genetic signature of spina bifida risk from pathway-informed comprehensive gene-variant analysisIs low iron status a risk factor for neural tube defects?The C677T mutation of the 5,10-methylenetetrahydrofolate reductase gene is a moderate risk factor for spina bifida in Italy.Neural tube defects 1974-94--down but not outHomocysteine.Pharmacogenetic screening for susceptibility to fetal malformations in women.Metabolic effects and the methylenetetrahydrofolate reductase (MTHFR) polymorphism associated with neural tube defects in southern Brazil.Neonatal and fetal methylenetetrahydrofolate reductase genetic polymorphisms: an examination of C677T and A1298C mutations.Maternal choline concentrations during pregnancy and choline-related genetic variants as risk factors for neural tube defects.Neural tube defects and maternal biomarkers of folate, homocysteine, and glutathione metabolism.A critical evaluation of the application of biomarkers in epidemiological studies on diet and health.A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?Hyperhomocysteinaemia and human reproduction.New chemodosimetric reagents as ratiometric probes for cysteine and homocysteine and possible detection in living cells and in blood plasma.Genetic and biochemical determinants of serum concentrations of monocyte chemoattractant protein-1, a potential neural tube defect risk factor.Socio-economic disparities in preterm birth: causal pathways and mechanisms.Schizophrenia and neural tube defects: comparisons from an epidemiological perspective.Effects of folate and vitamin B12 deficiencies during pregnancy on fetal, infant, and child development.
P2860
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P2860
Homocysteine metabolism in pregnancies complicated by neural-tube defects.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年学术文章
@wuu
1995年学术文章
@zh
1995年学术文章
@zh-cn
1995年学术文章
@zh-hans
1995年学术文章
@zh-my
1995年学术文章
@zh-sg
1995年學術文章
@yue
1995年學術文章
@zh-hant
name
Homocysteine metabolism in pregnancies complicated by neural-tube defects.
@en
Homocysteine metabolism in pregnancies complicated by neural-tube defects.
@nl
type
label
Homocysteine metabolism in pregnancies complicated by neural-tube defects.
@en
Homocysteine metabolism in pregnancies complicated by neural-tube defects.
@nl
prefLabel
Homocysteine metabolism in pregnancies complicated by neural-tube defects.
@en
Homocysteine metabolism in pregnancies complicated by neural-tube defects.
@nl
P2093
P1433
P1476
Homocysteine metabolism in pregnancies complicated by neural-tube defects.
@en
P2093
P304
P356
10.1016/S0140-6736(95)90165-5
P407
P577
1995-01-01T00:00:00Z