Neonatal and fetal methylenetetrahydrofolate reductase genetic polymorphisms: an examination of C677T and A1298C mutations.
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Methylenetetrahydrofolate reductase and transcobalamin genetic polymorphisms in human spontaneous abortion: biological and clinical implicationsThe frequent 5,10-methylenetetrahydrofolate reductase C677T polymorphism is associated with a common haplotype in whites, Japanese, and AfricansExaminations of methylenetetrahydrofolate reductase C677T and A1298C mutations--and in utero viability.Association of blood lead levels with methylenetetrahydrofolate reductase polymorphisms among Chinese pregnant women in Wuhan cityGenetic and epigenetic contributions to human nutrition and health: managing genome-diet interactions.Association of methylenetetrahydrofolate reductase (MTHFR 677C>T and 1298A>C) polymorphisms and haplotypes with silent brain infarction and homocysteine levels in a Korean population.Usefulness of Mendelian randomization in observational epidemiology.Maternal MTHFR polymorphisms and risk of spontaneous abortion.A functional polymorphism in the reduced folate carrier gene and DNA hypomethylation in mothers of children with autismRole of the MTHFR polymorphisms in cancer risk modification and treatment.Pharmacogenetics and folate metabolism -- a promising direction.Individualization of thiopurine therapy: thiopurine S-methyltransferase and beyond.MTHFR (C677T) polymorphism and PR (PROGINS) mutation as genetic factors for preterm delivery, fetal death and low birth weight: A Northeast Indian population based studyEffect of Platelet Glycoprotein IIb/IIIa PLA2 Polymorphism on Severity of Pulmonary Thromboembolism.Genetic interactions between MTHFR (C677T), methionine synthase (A2756G, C2758G) variants with vitamin B12 and folic acid determine susceptibility to premature coronary artery disease in Indian population.Genetic determinants of folate and vitamin B12 metabolism: a common pathway in neural tube defect and Down syndrome?Correlation between the type of bcr-abl transcripts and blood cell counts in chronic myeloid leukemia - a possible influence of mdr1 gene expression.Association between maternal, fetal and paternal MTHFR gene C677T and A1298C polymorphisms and risk of recurrent pregnancy loss: a comprehensive evaluation.Incidence Assessment of MTHFR C677T and A1298C Polymorphisms in Iranian Non-syndromic Cleft Lip and/or Palate Patients.Gene-environment interactions: a review of effects on reproduction and development.Folic acid - vitamin and panacea or genetic time bomb?Atherosclerotic and thrombotic genetic and environmental determinants in Egyptian coronary artery disease patients: a pilot study.MTHFR (Ala 222 Val) polymorphism and AMI in patients with type II diabetes mellitus.Effect of Vitamin B(12) and Folate on Homocysteine levels in colorectal cancerMethylenetetrahydrofolate reductase (MTHFR) gene polymorphisms resulting in suboptimal oocyte maturation: a discussion of folate status, neural tube defects, schizophrenia, and vasculopathy.The Pediatric Methionine Requirement Should Incorporate Remethylation Potential and Transmethylation Demands.Effects of maternal 5,10-methylenetetrahydrofolate reductase C677T and A1298C Polymorphisms and tobacco smoking on infant birth weight in a Japanese population.MTHFR C677T and A1298C Genotypes and Haplotypes in Slovenian Couples with Unexplained Infertility Problems and in Embryonic Tissues from Spontaneous Abortions.Combined genotype and haplotype distributions of MTHFR C677T and A1298C polymorphisms: A cross-sectional descriptive study of 13,473 Chinese adult women.Inherited thrombophilia and IVF failure: the impact of coagulation disorders on implantation process.Geographical and ethnic distribution of MTHFR gene polymorphisms and their associations with diseases among Chinese population.Low frequency of mutated methylenetetrahydrofolate reductase 677C-->T and 1298A-->C genetics single nucleotide polymorphisms (SNPs) in Sub-Saharan populations.Polymorphisms in the MTHFR gene influence embryo viability and the incidence of aneuploidy.The impact of C677T and A1298C MTHFR polymorphisms on methotrexate therapeutic response in East Bohemian region rheumatoid arthritis patients.Methylenetetrahydrofolate reductase mutations, a genetic cause for familial recurrent neural tube defects.Severe purpura fulminans due to coexistence of homozygous protein C deficiency and homozygous methylenetetrahydrofolate reductase mutation.Neonatal sinovenous thrombosis associated with homozygous thermolabile methylenetetrahydrofolate reductase in both mother and infant.Increased frequency of combined methylenetetrahydrofolate reductase C677T and A1298C mutated alleles in spontaneously aborted embryos.Response to "genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) in ethnic populations in Texas; a report of a novel MTHFR polymorphic site, G1793A".Comment on 'increased frequency of combined methylenetetrahydrofolate reductase C677T and A1298C mutated alleles in spontaneously aborted embryos'.
P2860
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P2860
Neonatal and fetal methylenetetrahydrofolate reductase genetic polymorphisms: an examination of C677T and A1298C mutations.
description
2000 nî lūn-bûn
@nan
2000 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Neonatal and fetal methylenete ...... of C677T and A1298C mutations.
@ast
Neonatal and fetal methylenete ...... of C677T and A1298C mutations.
@en
Neonatal and fetal methylenete ...... of C677T and A1298C mutations.
@nl
type
label
Neonatal and fetal methylenete ...... of C677T and A1298C mutations.
@ast
Neonatal and fetal methylenete ...... of C677T and A1298C mutations.
@en
Neonatal and fetal methylenete ...... of C677T and A1298C mutations.
@nl
prefLabel
Neonatal and fetal methylenete ...... of C677T and A1298C mutations.
@ast
Neonatal and fetal methylenete ...... of C677T and A1298C mutations.
@en
Neonatal and fetal methylenete ...... of C677T and A1298C mutations.
@nl
P2093
P2860
P356
P1476
Neonatal and fetal methylenete ...... of C677T and A1298C mutations.
@en
P2093
P2860
P304
P356
10.1086/303082
P407
P577
2000-08-24T00:00:00Z