Gene-gene interaction in folate-related genes and risk of neural tube defects in a UK population
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Association of the maternal MTHFR C677T polymorphism with susceptibility to neural tube defects in offsprings: evidence from 25 case-control studiesGenetics of human neural tube defectsMetabolic derangement of methionine and folate metabolism in mice deficient in methionine synthase reductaseAn approach to predict the risk of glaucoma development by integrating different attribute data.The merits of testing Hardy-Weinberg equilibrium in the analysis of unmatched case-control data: a cautionary note.Identifying hypothetical genetic influences on complex disease phenotypes.Genetic selection? A study of individual variation in the enzymes of folate metabolism.Detecting maternal-fetal genotype interactions associated with conotruncal heart defects: a haplotype-based analysis with penalized logistic regression.Knockout of the folate transporter folt-1 causes germline and somatic defects in C. elegans.HFE gene variants modify the association between maternal lead burden and infant birthweight: a prospective birth cohort study in Mexico City, Mexico.Genetic association analyses of nitric oxide synthase genes and neural tube defects vary by phenotypeGenetic and non-genetic influences during pregnancy on infant global and site specific DNA methylation: role for folate gene variants and vitamin B12Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defects.Genetic variants in the folate pathway and the risk of neural tube defects: a meta-analysis of the published literature.Combined impact of polymorphism of folate metabolism genes; glutamate carboxypeptidase, methylene tetrahydrofolate reductase and methionine synthase reductase on breast cancer susceptibility in kashmiri women.A genetic association study detects haplotypes associated with obstructive heart defectsFolic acid and human reproduction-ten important issues for cliniciansReplication and exploratory analysis of 24 candidate risk polymorphisms for neural tube defects.Association between MTHFR C677T polymorphism and neural tube defect risks: A comprehensive evaluation in three groups of NTD patients, mothers, and fathers.Insights into metabolic mechanisms underlying folate-responsive neural tube defects: a minireview.Neural tube defects between folate metabolism and genetics.Polymorphisms of Genes Involved in the Folate Metabolic Pathway Impact the Occurrence of Unexplained Recurrent Pregnancy Loss.Genetic variation in genes of folate metabolism and neural-tube defect risk.Etiology, pathogenesis and prevention of neural tube defects.Association of folate metabolism genes MTHFR and MTRR with multiple complex congenital malformation risk in Chinese population of Shanxi.Acquired and inherited disorders of cobalamin and folate in children.Ancillary risk information and pharmacogenetic tests: social and policy implications.Reduced folate carrier 80A-->G polymorphism, plasma folate, and risk of placental abruption.Possible selection of host folate pathway gene polymorphisms in patients with malaria from a malaria endemic region in North East India.Metabolic endophenotype and related genotypes are associated with oxidative stress in children with autism.Sample size requirements to detect the effect of a group of genetic variants in case-control studiesFolic acid supplements in pregnancy and severe language delay in children.Vitamin B(12) metabolism during pregnancy and in embryonic mouse models.Neural tube defects, folic acid and methylationGene-nutrient interactions: importance of folic acid and vitamin B12 during early embryogenesis.The search for genetic polymorphisms in the homocysteine/folate pathway that contribute to the etiology of human neural tube defects.Genetic association study of putative functional single nucleotide polymorphisms of genes in folate metabolism and spina bifida.Pharmacogenetics in reproductive and perinatal medicine.Associations between homocysteine metabolism related SNPs and carotid intima-media thickness: a Chinese sib pair study.Vitamin D, folate, and potential early lifecycle environmental origin of significant adult phenotypes.
P2860
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P2860
Gene-gene interaction in folate-related genes and risk of neural tube defects in a UK population
description
2004 nî lūn-bûn
@nan
2004 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Gene-gene interaction in folat ...... ube defects in a UK population
@ast
Gene-gene interaction in folat ...... ube defects in a UK population
@en
type
label
Gene-gene interaction in folat ...... ube defects in a UK population
@ast
Gene-gene interaction in folat ...... ube defects in a UK population
@en
prefLabel
Gene-gene interaction in folat ...... ube defects in a UK population
@ast
Gene-gene interaction in folat ...... ube defects in a UK population
@en
P2093
P2860
P50
P356
P1476
Gene-gene interaction in folat ...... ube defects in a UK population
@en
P2093
P2860
P304
P356
10.1136/JMG.2003.010694
P407
P577
2004-04-01T00:00:00Z