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Genetic variation in genes of folate metabolism and neural-tube defect risk.

Genetic variation in genes of folate metabolism and neural-tube defect risk.

http://www.wikidata.org/entity/Q36467477

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Neural tube defects and folate: case far from closed Prenatal nutritional deficiency and risk of adult schizophrenia Folate and one-carbon metabolism gene polymorphisms and their associations with oral facial clefts Genome-wide association mapping in dogs enables identification of the homeobox gene, NKX2-8, as a genetic component of neural tube defects in humans The environment and susceptibility to schizophrenia.A classification of sociomedical health indicators: perspectives for health administrators and health planners.118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects The use of orthologous sequences to predict the impact of amino acid substitutions on protein function.A functional polymorphism in the reduced folate carrier gene and DNA hypomethylation in mothers of children with autism Identification and characterization of an inborn error of metabolism caused by dihydrofolate reductase deficiency Folate metabolism gene 5,10-methylenetetrahydrofolate reductase (MTHFR) is associated with ADHD in myelomeningocele patients.Genetic variants in the folate pathway and the risk of neural tube defects: a meta-analysis of the published literature.Association of SMO polymorphisms and neural tube defects in the Chinese population from Shanxi Province An epidemiologic study of mitochondrial membrane transporter protein gene polymorphism and risk factors for neural tube defects in Shanxi, China.Identifying women who might benefit from higher doses of folic acid in pregnancy.Clinical utility of folate-containing oral contraceptives.Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome.Polymorphisms in maternal folate pathway genes interact with arsenic in drinking water to influence risk of myelomeningocele The MTHFR C677T Variant is Associated with Responsiveness to Disulfiram Treatment for Cocaine Dependency.The prevalence of folate-remedial MTHFR enzyme variants in humans.Folate and neural tube defects: The role of supplements and food fortification A network biology model of micronutrient related health.PCMT1 gene polymorphisms, maternal folate metabolism, and neural tube defects: a case-control study in a population with relatively low folate intake.Analysis of the MTHFD1 promoter and risk of neural tube defects.Not all cases of neural-tube defect can be prevented by increasing the intake of folic acid.Mouse as a model for multifactorial inheritance of neural tube defects.The role of folic acid fortification in neural tube defects: a review.Genetic evidence in planar cell polarity signaling pathway in human neural tube defects.Classification, clinical features, and genetics of neural tube defects.Genetic polymorphisms and folate status.Claudins are essential for cell shape changes and convergent extension movements during neural tube closure High-resolution 1H NMR spectroscopic investigation of a chick embryo model of neural tube development.Folate deficiency impairs decidualization and alters methylation patterns of the genome in mice.The effect of multiple single nucleotide polymorphisms in the folic acid pathway genes on homocysteine metabolism.Analysis of methionine synthase reductase polymorphism (A66G) in Indian Muslim population Nutrigenetic impact of daily folate intake on plasma homocysteine and folate levels in patients with different methylenetetrahydrofolate reductase genotypes.Le folate et les anomalies du tube neural : le rôle des suppléments et des aliments enrichis.Altered GNAS imprinting due to folic acid deficiency contributes to poor embryo development and may lead to neural tube defects.Scribble1 plays an important role in the pathogenesis of neural tube defects through its mediating effect of Par-3 and Vangl1/2 localization.Impact of genetic variants of RFC1, DHFR and MTHFR in osteosarcoma patients treated with high-dose methotrexate.

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P2860

Genetic variation in genes of folate metabolism and neural-tube defect risk.

http://www.wikidata.org/entity/Q36467477

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2006年学术文章

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2006年学术文章

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2006年学术文章

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2006年学术文章

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2006年學術文章

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2006年學術文章

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2006年學術文章

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name

Genetic variation in genes of folate metabolism and neural-tube defect risk.

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Genetic variation in genes of folate metabolism and neural-tube defect risk.

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Genetic variation in genes of folate metabolism and neural-tube defect risk.

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Genetic variation in genes of folate metabolism and neural-tube defect risk.

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Genetic variation in genes of folate metabolism and neural-tube defect risk.

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Genetic variation in genes of folate metabolism and neural-tube defect risk.

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Proceedings of the Nutrition Society

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Genetic variation in genes of folate metabolism and neural-tube defect risk.

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Henk J Blom

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Ivon J M van der Linden

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Lydia A Afman

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Sandra G Heil

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P2860

Interaction between dietary methionine and methyl donor intake on rat liver betaine-homocysteine methyltransferase gene expression and organization of the human gene

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

Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida

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

A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida

Influence of a methionine synthase (D919G) polymorphism on plasma homocysteine and folate levels and relation to risk of myocardial infarction

Homocysteine remethylation enzyme polymorphisms and increased risks for neural tube defects

Differences in the efficiency of reductive activation of methionine synthase and exogenous electron acceptors between the common polymorphic variants of human methionine synthase reductase

Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population

Kinetic and thermodynamic characterization of the common polymorphic variants of human methionine synthase reductase

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204-215

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10.1079/PNS2006495

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2

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65

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16672082

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