Citations for
1MTR, MTRR
Association between MTR A2756G and MTRR A66G polymorphisms and maternal risk for neural tube defects: a meta-analysis.
Ouyang S, Li Y, Liu Z, Chang H, Wu J.
Gene 515(2):308-12. doi: 10.1016/j.gene.2012.11.070. Epub 2012 Dec 22. 2013
2MTR, MTRR
Haplotype analysis of the folate-related genes MTHFR, MTRR, and MTR and migraine with aura.
Roecklein KA, Scher AI, Smith A, Harris T, Eiriksdottir G, Garcia M, Gudnason V, Launer LJ.
Cephalalgia 33(7):469-82. doi: 10.1177/0333102413477738. Epub 2013 Feb 19. 2013
3MTR, MTRR
Folate gene polymorphisms MTR A2756G, MTRR A66G, and BHMT G742A and risk for coronary artery disease: a meta-analysis.
Singh PR, Lele SS.
Genet Test Mol Biomarkers 16(6):471-5. doi: 10.1089/gtmb.2011.0237. Epub 2012 Feb 17. 2012
4MTR, MTRR
Association of MTHFR, MTR, and MTRR polymorphisms with Parkinson's disease among ethnic Chinese in Taiwan.
Fong CS, Shyu HY, Shieh JC, Fu YP, Chin TY, Wang HW, Cheng CW.
Clin Chim Acta 412(3-4):332-8. doi: 10.1016/j.cca.2010.11.004. Epub 2010 Nov 8. 2011
5CBS, MTHFR, MTRR
Polymorphisms in the CBS gene and homocysteine, folate and vitamin B12 levels: association with polymorphisms in the MTHFR and MTRR genes in Brazilian children.
Aléssio AC, Siqueira LH, Bydlowski SP, Höehr NF, Annichino-Bizzacchi JM.
Am J Med Genet A 146A(20):2598-602. 2008
6HMAG, MMAA, MMAB, MMACHC, MTR, MTRR, MUT
Mitochondrial vitamin B12-binding proteins in patients with inborn errors of cobalamin metabolism.
Moras E, Hosack A, Watkins D, Rosenblatt DS.
Mol Genet Metab 90(2):140-7. Epub 2006 Sep 29. 2007
7MTR, MTRR
Human methionine synthase reductase is a molecular chaperone for human methionine synthase.
Yamada K, Gravel RA, Toraya T, Matthews RG.
Proc Natl Acad Sci U S A 103(25):9476-81. Epub 2006 Jun 12. 2006
8MTHFR, MTRR, SHMT2, SLC19A1
Gene-gene interaction in folate-related genes and risk of neural tube defects in a UK population.
Relton CL, Wilding CS, Pearce MS, Laffling AJ, Jonas PA, Lynch SA, Tawn EJ, Burn J.
J Med Genet 41(4):256-60. 2004
9MTR, MTRR
Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida.
Doolin MT, Barbaux S, McDonnell M, Hoess K, Whitehead AS, Mitchell LE.
Am J Hum Genet 71(5):1222-6. 2002
10MTRR, NTDS1
Altered folate metabolism and disposition in mothers affected by a spina bifida pregnancy: influence of 677c --> t methylenetetrahydrofolate reductase and 2756a --> g methionine synthase genotypes.
Lucock M, Daskalakis I, Briggs D, Yates Z, Levene M.
Mol Genet Metab 70(1):27-44. 2000
11MTRR, NTDS1
Investigation of folate pathway gene polymorphisms and the incidence of neural tube defects in a Texas hispanic population.
Barber R, Shalat S, Hendricks K, Joggerst B, Larsen R, Suarez L, Finnell R.
Mol Genet Metab 70(1):45-52. 2000
12MTRR
A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida.
Wilson A, et al.
Mol Genet Metab 67(4):317-23 1999
13MTRR, MTRRD
Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folate/cobalamin metabolism.
Wilson A, et al.
Hum Mol Genet 8(11):2009-16 1999
14MTRR
Molecular cloning, expression and physical mapping of the human methionine synthase reductase gene.
Leclerc D, Odievre M, Wu Q, Wilson A, Huizenga JJ, Rozen R, Scherer SW, Gravel RA.
Gene 240(1):75-88. 1999
15MTRR
Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria.
Leclerc D, et al.
Proc Natl Acad Sci U S A 95 : 3059-3064. 1998
16MTR, MTRR, MTRRD
Defects in auxiliary redox proteins lead to functional methionine synthase deficiency.
Gulati S, et al.
J Biol Chem 272 : 19171-19175. 1997