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MTRR gene

Known as: MSR, cblE, MTRR 
This gene plays a role in the metabolism of vitamins and amino acids.
National Institutes of Health

Related topics

Related topics

3 relations
Amino Acid BiosynthesisMTRR protein, humanOxidation-Reduction

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Association of Three Single Nucleotide Polymorphisms in MTR and MTRR Genes with Lung Cancer in a Turkish Population.
AIMS Folate metabolism plays a critical role in DNA methylation and synthesis. Polymorphisms in folate metabolism may affect… 
2014
2014
Association of seven functional polymorphisms of one-carbon metabolic pathway with total plasma homocysteine levels and susceptibility to Parkinson's disease among South Indians
2013
2013
Analysis of methionine synthase reductase polymorphism (A66G) in Indian Muslim population
BACKGROUND AND OBJECTIVES: Methionine synthase reductase (MTRR) is a vital enzyme of homocysteine/methionine metabolic pathway… 
2011
2011
Association of MTHFR, MTR, and MTRR polymorphisms with Parkinson's disease among ethnic Chinese in Taiwan.
2009
2009
Methionine synthase reductase (MTRR) A66G polymorphism is not related to plasma homocysteine concentration and the risk for vascular disease.
2008
2008
Association of MTRR 66A>G Polymorphism With Superoxide Dismutase and Disease Activity in Patients With Crohn's Disease
OBJECTIVESThe aim of this study was to evaluate the association of nutritional (folate, vitamin B12) and genetic (MTHFR, MTR… 
2007
2007
2756GG genotype of methionine synthase reductase gene is more prevalent in rheumatoid arthritis patients treated with methotrexate and is associated with methotrexate-induced nodulosis.
OBJECTIVE To investigate the distribution of the A2756G polymorphism of the methionine synthase reductase (MTR) gene in patients… 
2003
2003
CblE type of homocystinuria: Mild clinical phenotype in two patients homozygous for a novel mutation in the MTRR gene
Patients with the cblE type of homocystinuria usually present with megaloblastic anaemia, feeding difficulties, developmental… 
Highly Cited
1999
Highly Cited
1999
Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folate/cobalamin metabolism.
Methionine synthase reductase (MSR) deficiency is an autosomal recessive disorder of folate/cobalamin metabolism leading to… 
1992
1992
Heterogeneity in cblG: differential retention of cobalamin on methionine synthase.
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