Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification.
about
Association of the maternal MTHFR C677T polymorphism with susceptibility to neural tube defects in offsprings: evidence from 25 case-control studiesFunctional characterization of human methylenetetrahydrofolate reductase in Saccharomyces cerevisiaeInsights into severe 5,10-methylenetetrahydrofolate reductase deficiency: molecular genetic and enzymatic characterization of 76 patientsNonsyndromic cleft lip and palate: CRISPLD genes and the folate gene pathway connectionRegulation of human methylenetetrahydrofolate reductase by phosphorylationThe "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother.Effects of common polymorphisms on the properties of recombinant human methylenetetrahydrofolate reductaseThe methylenetetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with auraMetabolic correction in the management of diabetic peripheral neuropathy: improving clinical results beyond symptom controlMethylenetetrahydrofolate reductase C677T and A1298C polymorphisms and gastric cancer susceptibilityDisruption of six novel Saccharomyces cerevisiae genes reveals that YGL129c is necessary for growth in non-fermentable carbon sources, YGL128c for growth at low or high temperatures and YGL125w is implicated in the biosynthesis of methionine.Genetics of Common Antipsychotic-Induced Adverse EffectsExogenous estrogen may exacerbate thrombophilia, impair bone healing and contribute to development of chronic facial painFolate deficiency and folic acid supplementation: the prevention of neural-tube defects and congenital heart defectsThe frequent 5,10-methylenetetrahydrofolate reductase C677T polymorphism is associated with a common haplotype in whites, Japanese, and AfricansThermolabile MTHFR genotype and retinal vascular occlusive diseaseA common mutation in the methylenetetrahydrofolate reductase gene is associated with an accumulation of formylated tetrahydrofolates in red blood cellsSeven novel mutations in the methylenetetrahydrofolate reductase gene and genotype/phenotype correlations in severe methylenetetrahydrofolate reductase deficiencyPhylogeny and evolution of aldehyde dehydrogenase-homologous folate enzymesFolate during reproduction: the Canadian experience with folic acid fortification.Mutated 5,10-methylenetetrahydrofolate reductase, hyperhomocysteinemia and risk for cardiovascular disease. Nature, nurture or nonsense?MALDI-TOF MS and TaqMan assisted SNP genotyping of DNA isolated from formalin-fixed and paraffin-embedded tissues (FFPET).Heteropolymeric triplex-based genomic assay to detect pathogens or single-nucleotide polymorphisms in human genomic samplesLiver transplantation for aHUS: still needed in the eculizumab era?Pretreatment Effect of Folic Acid on 13-Cis-RA-Induced Cellular Damage of Developing Midfacial Processes in Cultured Rat Embryos.Analysis of the MTHFR C677T variant with migraine phenotypes.Homocysteine.Total homocysteine and cardiovascular disease.Homocysteine, methylenetetrahydrofolate reductase and risk of schizophrenia: a meta-analysis.Biochemical and genetic analysis of methylenetetrahydrofolate reductase in Leishmania metabolism and virulence.A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status.Methylenetetrahydrofolate reductase: a common human polymorphism and its biochemical implications.Methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms and the risk of primary hepatocellular carcinoma (HCC) in a Chinese populationUpdate and new concepts in vitamin responsive disorders of folate transport and metabolism.Molecular characterization of folate receptor 1 mutations delineates cerebral folate transport deficiency.Molecular typing of Treponema pallidum in the Czech Republic during 2011 to 2013: increased prevalence of identified genotypes and of isolates with macrolide resistance.Understanding the interaction between environmental exposures and molecular events in colorectal carcinogenesis.Methylenetetrahydrofolate reductase polymorphisms and risk of acute lymphoblastic leukemia-evidence from an updated meta-analysis including 35 studies.Association between MTHFR gene polymorphism and NTDs in Chinese Han population.Update on selected inherited venous thrombotic disorders.
P2860
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P2860
Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification.
description
1994 nî lūn-bûn
@nan
1994 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
name
Human methylenetetrahydrofolat ...... g and mutation identification.
@ast
Human methylenetetrahydrofolat ...... g and mutation identification.
@en
Human methylenetetrahydrofolat ...... g and mutation identification.
@nl
type
label
Human methylenetetrahydrofolat ...... g and mutation identification.
@ast
Human methylenetetrahydrofolat ...... g and mutation identification.
@en
Human methylenetetrahydrofolat ...... g and mutation identification.
@nl
prefLabel
Human methylenetetrahydrofolat ...... g and mutation identification.
@ast
Human methylenetetrahydrofolat ...... g and mutation identification.
@en
Human methylenetetrahydrofolat ...... g and mutation identification.
@nl
P2093
P4510
P356
P1433
P1476
Human methylenetetrahydrofolat ...... g and mutation identification.
@en
P2093
Matthews RG
Rosenblatt DS
P2888
P304
P356
10.1038/NG0694-195
P407
P577
1994-06-01T00:00:00Z