Genetic association study of putative functional single nucleotide polymorphisms of genes in folate metabolism and spina bifida.
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Genetic studies of the cystathionine beta-synthase gene and myelomeningoceleThe cognitive phenotype of spina bifida meningomyeloceleGenetic variations in the GLUT3 gene associated with myelomeningoceleEvaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defects.Folate metabolism gene 5,10-methylenetetrahydrofolate reductase (MTHFR) is associated with ADHD in myelomeningocele patients.Association of retinoic acid receptor genes with meningomyelocele.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.Replication and exploratory analysis of 24 candidate risk polymorphisms for neural tube defects.Approaches for the identification of genetic modifiers of nutrient dependent phenotypes: examples from folate.The association between CBS 844ins68 polymorphism and head and neck squamous cell carcinoma risk - a case-control analysis.Deep sequencing study of the MTHFR gene to identify variants associated with myelomeningoceleA case-parent triad assessment of folate metabolic genes and the risk of childhood acute lymphoblastic leukemia.Association Study between Folate Pathway Gene Single Nucleotide Polymorphisms and Gastric Cancer in KoreansNovel single nucleotide polymorphisms in the superoxide dismutase 1 and 2 genes among children with myelomeningocele.Etiology of esophageal atresia and tracheoesophageal fistula: "mind the gap".Genetic studies of myelomeningocele.Heme oxygenase-1 promoter polymorphisms and risk of spina bifida.Mutations in genes encoding the glycine cleavage system predispose to neural tube defects in mice and humans.Maternal and infant gene-folate interactions and the risk of neural tube defects.Maternal gene-micronutrient interactions related to one-carbon metabolism and the risk of myelomeningocele among offspring.Mutations in folate transporter genes and risk for human myelomeningocele
P2860
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P2860
Genetic association study of putative functional single nucleotide polymorphisms of genes in folate metabolism and spina bifida.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 15 August 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
@cs
name
Genetic association study of p ...... e metabolism and spina bifida.
@en
Genetic association study of p ...... e metabolism and spina bifida.
@nl
type
label
Genetic association study of p ...... e metabolism and spina bifida.
@en
Genetic association study of p ...... e metabolism and spina bifida.
@nl
prefLabel
Genetic association study of p ...... e metabolism and spina bifida.
@en
Genetic association study of p ...... e metabolism and spina bifida.
@nl
P2093
P2860
P1476
Genetic association study of p ...... e metabolism and spina bifida.
@en
P2093
Carla A Martinez
Gayle H Tyerman
Hope Northrup
Jack M Fletcher
Jone-Ing Lin
Kit Sing Au
P2860
P304
P356
10.1016/J.AJOG.2009.06.042
P407
P577
2009-08-15T00:00:00Z