Methionine Synthase Reductase

[1]  S. Scherer,et al.  Molecular cloning, expression and physical mapping of the human methionine synthase reductase gene. , 1999, Gene.

[2]  D. Leclerc,et al.  Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folate/cobalamin metabolism. , 1999, Human molecular genetics.

[3]  R. Rozen,et al.  A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida. , 1999, Molecular genetics and metabolism.

[4]  T. Eskes,et al.  Open or closed? A world of difference: a history of homocysteine research. , 2009, Nutrition reviews.

[5]  R. Banerjee,et al.  Purification of Soluble Cytochrome b 5 as a Component of the Reductive Activation of Porcine Methionine Synthase* , 1998, The Journal of Biological Chemistry.

[6]  R. Matthews,et al.  The mechanism of adenosylmethionine-dependent activation of methionine synthase: a rapid kinetic analysis of intermediates in reductive methylation of Cob(II)alamin enzyme. , 1998, Biochemistry.

[7]  B. Fowler Genetic defects of folate and cobalamin metabolism , 1998, European Journal of Pediatrics.

[8]  Aaron D. Wilson,et al.  Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[9]  R. Banerjee,et al.  Defects in Auxiliary Redox Proteins Lead to Functional Methionine Synthase Deficiency* , 1997, The Journal of Biological Chemistry.

[10]  R. Banerjee,et al.  The Yin-Yang of cobalamin biochemistry. , 1997, Chemistry & biology.

[11]  H. Blom,et al.  Is the common 677C-->T mutation in the methylenetetrahydrofolate reductase gene a risk factor for neural tube defects? A meta-analysis. , 1997, QJM : monthly journal of the Association of Physicians.

[12]  R. Matthews,et al.  Structure-based perspectives on B12-dependent enzymes. , 1997, Annual review of biochemistry.

[13]  C. Wolf,et al.  Dissection of NADPH-cytochrome P450 oxidoreductase into distinct functional domains. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[14]  S. Snyder,et al.  Cloned and expressed nitric oxide synthase structurally resembles cytochrome P-450 reductase , 1991, Nature.

[15]  D. Rosenblatt,et al.  Altered vitamin B12 metabolism in fibroblasts from a patient with megaloblastic anemia and homocystinuria due to a new defect in methionine biosynthesis. , 1984, The Journal of clinical investigation.

[16]  F. Ruddle,et al.  Genetic control of cobalamin binding in normal and mutant cells: assignment of the gene for 5-methyltetrahydrofolate:L-homocysteine S-methyltransferase to human chromosome 1. , 1979, Proceedings of the National Academy of Sciences of the United States of America.