Human methionine synthase reductase is a molecular chaperone for human methionine synthase
about
Bioinformatic and genetic association analysis of microRNA target sites in one-carbon metabolism genesMetabolic derangement of methionine and folate metabolism in mice deficient in methionine synthase reductaseNavigating the B(12) road: assimilation, delivery, and disorders of cobalaminThe human flavoproteomeCrystal structure and solution characterization of the activation domain of human methionine synthaseTah18 transfers electrons to Dre2 in cytosolic iron-sulfur protein biogenesis.Vitamin B12 deficiency results in the abnormal regulation of serine dehydratase and tyrosine aminotransferase activities correlated with impairment of the adenylyl cyclase system in rat liverMutation in folate metabolism causes epigenetic instability and transgenerational effects on developmentGenetic disorders of vitamin B12 metabolism: eight complementation groups – eight genesGlutathione-dependent one-electron transfer reactions catalyzed by a B₁₂ trafficking protein.Haplotype analysis of the folate-related genes MTHFR, MTRR, and MTR and migraine with auraRiboflavin status modifies the effects of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) polymorphisms on homocysteine.Cobalamin- and corrinoid-dependent enzymesGenetic variant in MTRR, but not MTR, is associated with risk of congenital heart disease: an integrated meta-analysisGeographical and Ethnic Distributions of the MTHFR C677T, A1298C and MTRR A66G Gene Polymorphisms in Chinese Populations: A Meta-AnalysisRedox regulation of the epigenetic landscape in cancer: a role for metabolic reprogramming in remodeling the epigenomeImpeded electron transfer from a pathogenic FMN domain mutant of methionine synthase reductase and its responsiveness to flavin supplementationRestricted role for methionine synthase reductase defined by subcellular localization.Mechanistic Studies on the Reaction of Nitrocobalamin with Glutathione: Kinetic evidence for formation of an aquacobalamin intermediate.Population-level diversity in the association of genetic polymorphisms of one-carbon metabolism with breast cancer risk.Guidelines for diagnosis and management of the cobalamin-related remethylation disorders cblC, cblD, cblE, cblF, cblG, cblJ and MTHFR deficiency.The tinker, tailor, soldier in intracellular B12 trafficking.Vitamin B12 protects against superoxide-induced cell injury in human aortic endothelial cells.Lamarck rises from his grave: parental environment-induced epigenetic inheritance in model organisms and humans.Importance of the maintenance pathway in the regulation of the activity of Escherichia coli ribonucleotide reductase.Reactivation of methionine synthase from Thermotoga maritima (TM0268) requires the downstream gene product TM0269.Relationship between methionine synthase, methionine synthase reductase genetic polymorphisms and deep vein thrombosis among South Indians.Risk of congenital heart defects is influenced by genetic variation in folate metabolism.A80G polymorphism of reduced folate carrier 1 (RFC1) and C776G polymorphism of transcobalamin 2 (TC2) genes in Down's syndrome etiology.Neuro-fuzzy model of homocysteine metabolism.Using logic programming for modeling the one-carbon metabolism network to study the impact of folate deficiency on methylation processes.Cobalamin uptake and reactivation occurs through specific protein interactions in the methionine synthase-methionine synthase reductase complex.Multigenerational analysis of sex-specific phenotypic differences at midgestation caused by abnormal folate metabolism.Insights into the evolution of vitamin B12 auxotrophy from sequenced algal genomes.An Inframe Trinucleotide Deletion in MTRR Exon 1 is Associated with the Risk of Spina Bifida.Bcl-2/adenovirus E1B 19 kDa-interacting protein 3 (BNIP3) expression is epigenetically regulated by one-carbon metabolism in invasive duct cell carcinoma of breast.Abnormal folate metabolism causes age-, sex- and parent-of-origin-specific haematological defects in mice
P2860
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P2860
Human methionine synthase reductase is a molecular chaperone for human methionine synthase
description
2006 nî lūn-bûn
@nan
2006 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Human methionine synthase redu ...... for human methionine synthase
@ast
Human methionine synthase redu ...... for human methionine synthase
@en
Human methionine synthase redu ...... for human methionine synthase
@en-gb
Human methionine synthase redu ...... for human methionine synthase
@nl
type
label
Human methionine synthase redu ...... for human methionine synthase
@ast
Human methionine synthase redu ...... for human methionine synthase
@en
Human methionine synthase redu ...... for human methionine synthase
@en-gb
Human methionine synthase redu ...... for human methionine synthase
@nl
prefLabel
Human methionine synthase redu ...... for human methionine synthase
@ast
Human methionine synthase redu ...... for human methionine synthase
@en
Human methionine synthase redu ...... for human methionine synthase
@en-gb
Human methionine synthase redu ...... for human methionine synthase
@nl
P2093
P2860
P921
P356
P1476
Human methionine synthase redu ...... for human methionine synthase
@en
P2093
Kazuhiro Yamada
Rowena G Matthews
Roy A Gravel
Tetsuo Toraya
P2860
P304
P356
10.1073/PNAS.0603694103
P407
P577
2006-06-20T00:00:00Z