MTHFD1 R653Q polymorphism is a maternal genetic risk factor for severe abruptio placentae
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Association between MTHFD1 G1958A polymorphism and neural tube defects susceptibility: a meta-analysis.Polymorphisms in thrombophilia and renin-angiotensin system pathways, preterm delivery, and evidence of placental hemorrhage.Effects of folate and vitamin B12 deficiencies during pregnancy on fetal, infant, and child development.Mthfd1 is a modifier of chemically induced intestinal carcinogenesis.Maternal Mthfd1 disruption impairs fetal growth but does not cause neural tube defects in miceAssociations between 2 polymorphisms in the methylenetetrahydrofolate reductase gene and placental abruption.A genome-wide association study of variations in maternal cardiometabolic genes and risk of placental abruption.Polymorphisms in 1-carbon metabolism, epigenetics and folate-related pathologies.Association of methylenetetrahydrofolate dehydrogenase 1 polymorphisms with cancer: a meta-analysisMthfd1 is an essential gene in mice and alters biomarkers of impaired one-carbon metabolism.Genome-wide and candidate gene association studies of placental abruptionAnalysis of the MTHFD1 promoter and risk of neural tube defects.The search for genetic polymorphisms in the homocysteine/folate pathway that contribute to the etiology of human neural tube defects.Genetic and epigenomic footprints of folate.Lack of association between methylenetetrahydrofolate dehydrogenase 1 G1958A polymorphism and prostate cancer risk: a meta-analysis.Association of methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism with preterm delivery and placental abruption: a systematic review and meta-analysis.Maternal polymorphisms in folic acid metabolic genes are associated with nonsyndromic cleft lip and/or palate in the Brazilian population.Polymorphic variants of folate metabolism genes and the risk of laryngeal cancer.The MTHFD1 p.Arg653Gln variant alters enzyme function and increases risk for congenital heart defects.MTHFR rs2274976 polymorphism is a risk marker for nonsyndromic cleft lip with or without cleft palate in the Brazilian population.Confirmation of the R653Q polymorphism of the trifunctional C1-synthase enzyme as a maternal risk for neural tube defects in the Irish population
P2860
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P2860
MTHFD1 R653Q polymorphism is a maternal genetic risk factor for severe abruptio placentae
description
2005 nî lūn-bûn
@nan
2005 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
MTHFD1 R653Q polymorphism is a maternal genetic risk factor for severe abruptio placentae
@ast
MTHFD1 R653Q polymorphism is a maternal genetic risk factor for severe abruptio placentae
@en
MTHFD1 R653Q polymorphism is a maternal genetic risk factor for severe abruptio placentae
@nl
type
label
MTHFD1 R653Q polymorphism is a maternal genetic risk factor for severe abruptio placentae
@ast
MTHFD1 R653Q polymorphism is a maternal genetic risk factor for severe abruptio placentae
@en
MTHFD1 R653Q polymorphism is a maternal genetic risk factor for severe abruptio placentae
@nl
prefLabel
MTHFD1 R653Q polymorphism is a maternal genetic risk factor for severe abruptio placentae
@ast
MTHFD1 R653Q polymorphism is a maternal genetic risk factor for severe abruptio placentae
@en
MTHFD1 R653Q polymorphism is a maternal genetic risk factor for severe abruptio placentae
@nl
P2093
P356
P1476
MTHFD1 R653Q polymorphism is a maternal genetic risk factor for severe abruptio placentae
@en
P2093
Anne M Molloy
Anne Parle-McDermott
Caroline C Signore
Christopher Cox
Colm O'Herlihy
Faith J Pangilinan
James L Mills
John M Scott
Lawrence C Brody
Peadar N Kirke
P356
10.1002/AJMG.A.30354
P407
P577
2005-02-01T00:00:00Z