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kw.\*:("methionine synthase")

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Occurrence of Pseudovitamin B12 and Its Possible Function as the Cofactor of Cobalamin-Dependent Methionine Synthase in a Cyanobacterium Synechocystis sp. PCC6803TANIOKA, Yuri; YABUTA, Yukinori; YAMAJI, Ryoichi et al.Journal of nutritional science and vitaminology. 2009, Vol 55, Num 6, pp 518-521, issn 0301-4800, 4 p.Article

Mechanism-based design, synthesis and biological studies of N5-substituted tetrahydrofolate analogs as inhibitors of cobalamin-dependent methionine synthase and potential anticancer agentsZHILI ZHANG; CHAO TIAN; GRIFF, Roger J et al.European journal of medicinal chemistry. 2012, Vol 58, pp 228-236, issn 0223-5234, 9 p.Article

MTRR 66A>G polymorphism in relation to congenital heart defectsVAN BEYNUM, Ingrid M; KOUWENBERG, Margreet; KAPUSTA, Livia et al.Clinical chemistry and laboratory medicine. 2006, Vol 44, Num 11, pp 1317-1323, issn 1434-6621, 7 p.Article

Association between folate-metabolizing pathway polymorphism and non-Hodgkin lymphomaHEE NAM KIM; LEE, Il-Kwon; KIM, Hyeoung-Joon et al.British journal of haematology. 2008, Vol 140, Num 3, pp 287-294, issn 0007-1048, 8 p.Article

MTRR A66G polymorphism and breast cancer risk: a meta-analysisJIA HU; ZHOU, Guo-Wu; NING WANG et al.Breast cancer research and treatment. 2010, Vol 124, Num 3, pp 779-784, issn 0167-6806, 6 p.Article

Methylenetetrahydrofolate reductase (MTHFR) 677C > T and methionine synthase reductase (MTRR) 66A > G polymorphisms: association with serum homocysteine and angiographic coronary artery disease in the era of flour products fortified with folic acidBRILAKIS, Emmanouil S; BERGER, Peter B; BALLMAN, Karla V et al.Atherosclerosis. 2003, Vol 168, Num 2, pp 315-322, issn 0021-9150, 8 p.Article

A common gene variant in methionine synthase reductase is not associated with peak homocysteine concentrations after nitrous oxide anesthesiaNAGELE, Peter; ZEUGSWETTER, Barbara; EBERLE, Corinna et al.Pharmacogenetics and genomics (Print). 2009, Vol 19, Num 5, pp 325-329, issn 1744-6872, 5 p.Article

Sex-specific association of sequence variants in CBS and MTRR with risk for promoter hypermethylation in the lung epithelium of smokersFLORES, Kristina G; STIDLEY, Christine A; MACKEY, Amanda J et al.Carcinogenesis (New York. Print). 2012, Vol 33, Num 8, pp 1542-1547, issn 0143-3334, 6 p.Article

Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folate/cobalamin metabolismWILSON, A; LECLERC, D; ROSENBLATT, D. S et al.Human molecular genetics (Print). 1999, Vol 8, Num 11, pp 2009-2016, issn 0964-6906Article

Effects of polymorphisms of methionine synthase and methionine synthase reductase on total plasma homocysteine in the NHLBI Family Heart StudyJACQUES, Paul F; BOSTOM, Andrew G; SELHUB, Jacob et al.Atherosclerosis. 2003, Vol 166, Num 1, pp 49-55, issn 0021-9150, 7 p.Article

Relationship between methionine synthase, methionine synthase reductase genetic polymorphisms and deep vein thrombosis among South IndiansSHAIK MOHAMMAD NAUSHAD; MOHAMED NURUL JAIN JAMAL; CHINTAKINDI KRISHNA PRASAD et al.Clinical chemistry and laboratory medicine. 2008, Vol 46, Num 1, pp 73-79, issn 1434-6621, 7 p.Article

Methionine synthase (MTR) 2756 (A→G) polymorphism, double heterozygosity methionine synthase 2756 AG/methionine synthase reductase (MTRR) 66 AG, and elevated homocysteinemia are three risk factors for having a child with down syndromeBOSCO, Paolo; GUEANT-RODRIGUEZ, Rosa-Maria; ANELLO, Guido et al.American journal of medical genetics. 2003, Vol 121A, Num 3, pp 219-224, issn 0148-7299, 6 p.Article

Association of polymorphisms in DNMT1, DNMT3A, DNMT3B, MTHFR and MTRR genes with global DNA methylation levels and prognosis of autoimmune thyroid diseaseARAKAWA, Y; WATANABE, M; INOUE, N et al.Clinical and experimental immunology (Print). 2012, Vol 170, Num 2, pp 194-201, issn 0009-9104, 8 p.Article

Neisseria gonorrhoeae isolates with reduced susceptibility to cefixime and ceftriaxone: Association with genetic polymorphisms in penA, mtrR, porB1b, and ponALINDBERG, Robert; FREDLUND, Hans; NICHOLAS, Robert et al.Antimicrobial agents and chemotherapy. 2007, Vol 51, Num 6, pp 2117-2122, issn 0066-4804, 6 p.Article

Role of parental folate pathway single nucleotide polymorphisms in altering the susceptibility to neural tube defects in South IndiaSHAIK MOHAMMAD NAUSHAD; AKELLA RADHA RAMA DEVI.Journal of perinatal medicine. 2010, Vol 38, Num 1, pp 63-69, issn 0300-5577, 7 p.Article

Transcobalamin and methionine synthase reductase mutated polymorphisms aggravate the risk of neural tube defects in humansGUEANT-RODRIGUEZ, R. M; RENDELI, C; SALVAGGIO, E et al.Neuroscience letters. 2003, Vol 344, Num 3, pp 189-192, issn 0304-3940, 4 p.Article

Association of homocysteine (but not of MTHFE 677 C>T, MTR 2756A>G, MTRR 66 A>G and TCN2 776 C>G) with ischaemic cerebrovascular disease in SicilyBOSCO, Paolo; GUEANT-RODRIGUEZ, Rosa-Maria; ANELLO, Guido et al.Thrombosis and haemostasis. 2006, Vol 96, Num 2, pp 154-159, issn 0340-6245, 6 p.Article

Effect of folic acid intervention on the change of serum folate level in hypertensive Chinese adults: do methylenetetrahydrofolate reductase and methionine synthase gene polymorphisms affect therapeutic responses?XIANHUI QIN; JIANPING LI; XIN XU et al.Pharmacogenetics and genomics (Print). 2012, Vol 22, Num 6, pp 421-428, issn 1744-6872, 8 p.Article

Methionine Synthase Reductase (MTRR) A66G polymorphism is not related to plasma homocysteine concentration and the risk for vascular diseaseSCAZZONE, C; ACUTO, S; GUGLIELMINI, E et al.Experimental and molecular pathology. 2009, Vol 86, Num 2, pp 131-133, issn 0014-4800, 3 p.Article

Defects in homocysteine metabolism : diversity among hyperhomocyst(e)inemiasMATTHEWS, Rowena G; LEE ELMORE, C.Clinical chemistry and laboratory medicine. 2007, Vol 45, Num 12, pp 1700-1703, issn 1434-6621, 4 p.Conference Paper

INACTIVATION OF METHIONINE SYNTHASE BY NITROUS OXIDEDEACON R; LUMB M; PERRY J et al.1980; EUROP. J. BIOCHEM.; DEU; DA. 1980; VOL. 104; NO 2; PP. 419-422; BIBL. 20 REF.Article

O-ACETYLSERINE AND O-ACETYLHOMOSERINE SULFHYDRYLASE OF YEAST FURTHER PURIFICATION AND CHARACTERIZATION AS A PYRIDOXAL ENZYME.YAMAGATA S; TAKESHIMA K.1976; J. BIOCHEM.; JAP.; DA. 1976; VOL. 80; NO 4; PP. 777-785; BIBL. 23 REF.Article

A candidate gene approach to genetic contributors to the development of IgA nephropathyYAMAMOTO, Ryohei; NAGASAWA, Yasuyuki; RAKUGI, Hiromi et al.Nephrology, dialysis, transplantation (Print). 2012, Vol 27, Num 3, pp 1020-1030, issn 0931-0509, 11 p.Article

O-ACETYLSERINE AND O-ACETYLHOMOSERINE SULFHYDRYLASE OF YEAST. SUBUNIT STRUCTURE.YAMAGATA S.1976; J. BIOCHEM.; JAP.; DA. 1976; VOL. 80; NO 4; PP. 787-797; BIBL. 25 REF.Article

Lack of methionine biosynthesis de nova in Butyrivibrio fibrisolvens strain E14NILI, N; BROOKER, J. D.Letters in applied microbiology. 1997, Vol 25, Num 2, pp 85-90, issn 0266-8254Article

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