Insights into metabolic mechanisms underlying folate-responsive neural tube defects: a minireview. - Wikidata - awgldk - TriplyDB

Insights into metabolic mechanisms underlying folate-responsive neural tube defects: a minireview.

Insights into metabolic mechanisms underlying folate-responsive neural tube defects: a minireview.

http://www.wikidata.org/entity/Q35619839

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Mthfs is an Essential Gene in Mice and a Component of the Purinosome Genetics of human neural tube defects Biomarkers of Nutrition for Development-Folate Review Modeling cellular compartmentation in one-carbon metabolism Genomic DNA hypomethylation is associated with neural tube defects induced by methotrexate inhibition of folate metabolism Zebrafish larvae exposed to ginkgotoxin exhibit seizure-like behavior that is relieved by pyridoxal-5'-phosphate, GABA and anti-epileptic drugs Folate deficiency facilitates recruitment of upstream binding factor to hot spots of DNA double-strand breaks of rRNA genes and promotes its transcription A hybrid stochastic model of folate-mediated one-carbon metabolism: Effect of the common C677T MTHFR variant on de novo thymidylate biosynthesis Neural tube defects, folate, and immune modulation.Safety and benefits of interventions to increase folate status in malaria-endemic areas.A functional polymorphism in the reduced folate carrier gene and DNA hypomethylation in mothers of children with autism Gene-environment interactions, folate metabolism and the embryonic nervous system.Nuclear enrichment of folate cofactors and methylenetetrahydrofolate dehydrogenase 1 (MTHFD1) protect de novo thymidylate biosynthesis during folate deficiency Polymorphisms in serine hydroxymethyltransferase 1 and methylenetetrahydrofolate reductase interact to increase cardiovascular disease risk in humans.Association of folate receptor (FOLR1, FOLR2, FOLR3) and reduced folate carrier (SLC19A1) genes with meningomyelocele.Epidemiologic and genetic aspects of spina bifida and other neural tube defects.Quantifying exploratory low dose compounds in humans with AMS.The genetic background of the curly tail strain confers susceptibility to folate-deficiency-induced exencephaly.The mandatory fortification of staple foods with folic acid: a current controversy in Germany.Maternal dietary uridine causes, and deoxyuridine prevents, neural tube closure defects in a mouse model of folate-responsive neural tube defects.Folic acid and human reproduction-ten important issues for clinicians Association between MTHFR C677T polymorphism and neural tube defect risks: A comprehensive evaluation in three groups of NTD patients, mothers, and fathers.Incrimination of heterogeneous nuclear ribonucleoprotein E1 (hnRNP-E1) as a candidate sensor of physiological folate deficiency.Folic acid supplementation in early pregnancy and asthma in children aged 6 years.The role of folate metabolism in orofacial development and clefting.Use of folic acid supplements and risk of cleft lip and palate in infants: a population-based cohort study.Folate and neural tube defects: The role of supplements and food fortification Risk factors for neural tube defects in Riyadh City, Saudi Arabia: Case-control study Neural tube defects, folic acid and methylation One-carbon metabolism-genome interactions in folate-associated pathologies.Recommendations for folate intake in women: implications for public health strategies.Has folate a role in the developing nervous system after birth and not just during embryogenesis and gestation?The role of folic acid fortification in neural tube defects: a review.Genetic studies of myelomeningocele.Genetic evidence in planar cell polarity signaling pathway in human neural tube defects.Classification, clinical features, and genetics of neural tube defects.One-Carbon Metabolism in Health and Disease.Prevalence and predictors of periconceptional folic acid uptake--prospective cohort study in an Irish urban obstetric population.Maternal folic acid supplementation trends 2009-2013.Arsenic trioxide targets MTHFD1 and SUMO-dependent nuclear de novo thymidylate biosynthesis.

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Insights into metabolic mechanisms underlying folate-responsive neural tube defects: a minireview.

http://www.wikidata.org/entity/Q35619839

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Birth Defects Research Part A: Clinical and Molecular Teratology

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Anna E Beaudin

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Patrick J Stover

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P2860

Metabolic derangement of methionine and folate metabolism in mice deficient in methionine synthase reductase

Methenyltetrahydrofolate synthetase regulates folate turnover and accumulation

Identification of an intestinal folate transporter and the molecular basis for hereditary folate malabsorption

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

Lack of association between mutations in the folate receptor-alpha gene and spina bifida

Neural tube defects and folate: case far from closed

A 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 Defec

Prevention of neural tube defects: results of the Medical Research Council Vitamin Study. MRC Vitamin Study Research Group

Betaine-homocysteine methyltransferase expression in porcine and human tissues and chromosomal localization of the human gene

The role of cystathionine beta-synthase in homocysteine metabolism

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10.1002/BDRA.20553

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