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