MTRR 66A>G polymorphism in relation to congenital heart defects.
about
Polymorphisms in mitochondrial genes and prostate cancer riskDevelopments in our understanding of the genetic basis of birth defects118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defectsMTRR rs326119 polymorphism is associated with plasma concentrations of homocysteine and cobalamin, but not with congenital heart disease or coronary atherosclerosis in Brazilian patients.Periconceptional nutrient intakes and risks of conotruncal heart defectsVariants of folate metabolism genes and risk of left-sided cardiac defects.One-carbon metabolite levels in mid-pregnancy and risks of conotruncal heart defects.Genetic polymorphisms of the TYMS gene are not associated with congenital cardiac septal defects in a Han Chinese populationVariants of folate metabolism genes and the risk of conotruncal cardiac defects.Methionine synthase reductase deficiency results in adverse reproductive outcomes and congenital heart defects in mice.Genetic variant in MTRR, but not MTR, is associated with risk of congenital heart disease: an integrated meta-analysisLack of maternal folic acid supplementation is associated with heart defects in Down syndrome: a report from the National Down Syndrome Project.Vitamin B(12) metabolism during pregnancy and in embryonic mouse models.Association between methionine synthase reductase A66G polymorphism and the risk of congenital heart defects: evidence from eight case-control studies.Second trimester serum predictors of congenital heart defects in pregnancies without chromosomal or neural tube defects.Are polymorphisms in MTRR A66G and MTHFR C677T genes associated with congenital heart diseases in Iranian population?Parental Genetic Variants, MTHFR 677C>T and MTRR 66A>G, Associated Differently with Fetal Congenital Heart DefectAnalysis of MTHFR and MTRR Gene Polymorphisms in Iranian Ventricular Septal Defect Subjects.Risk of congenital heart defects is influenced by genetic variation in folate metabolism.Mouse model for deficiency of methionine synthase reductase exhibits short-term memory impairment and disturbances in brain choline metabolism.
P2860
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P2860
MTRR 66A>G polymorphism in relation to congenital heart defects.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh-hant
name
MTRR 66A>G polymorphism in relation to congenital heart defects.
@en
MTRR 66A>G polymorphism in relation to congenital heart defects.
@nl
type
label
MTRR 66A>G polymorphism in relation to congenital heart defects.
@en
MTRR 66A>G polymorphism in relation to congenital heart defects.
@nl
prefLabel
MTRR 66A>G polymorphism in relation to congenital heart defects.
@en
MTRR 66A>G polymorphism in relation to congenital heart defects.
@nl
P2093
P2860
P356
P1476
MTRR 66A>G polymorphism in relation to congenital heart defects.
@en
P2093
Ingrid M van Beynum
Ivon J M van der Linden
Livia Kapusta
Margreet Kouwenberg
Martin den Heijer
Otto Daniels
P2860
P304
P356
10.1515/CCLM.2006.254
P50
P577
2006-01-01T00:00:00Z