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1 genes (e.g., cystathionine-beta-synthase and methionine synthase reductase).
2 ein, which is comparable with that seen with methionine synthase reductase.
3 e P450 reductase, nitric oxide synthase, and methionine synthase reductase.
4  component of the nitric-oxide synthases and methionine-synthase reductase.
5 298AC/CC), methionine synthase (2756AA), and methionine synthase reductase (66GG).
6 s, the electron is thought to be provided by methionine synthase reductase, a protein containing a do
7 cloned and expressed the cDNA encoding human methionine synthase reductase and demonstrate that it is
8 and cblG classes of patients with defects in methionine synthase reductase and methionine synthase, r
9 ptophan in related diflavin reductases (e.g. methionine synthase reductase and novel reductase 1), an
10 on methionine synthase (MS, encoded by MTR), methionine synthase reductase, and methylenetetrahydrofo
11 of mutations in the gene encoding a putative methionine synthase reductase in the cblE class of patie
12 PH is 2.6 +/- 0.5 microm, and the K(act) for methionine synthase reductase is 80.7 +/- 13.7 nm for NA
13                                              Methionine synthase reductase is a soluble, monomeric pr
14                                              Methionine synthase reductase (MSR) catalyzes the conver
15  also showed that purified recombinant human methionine synthase reductase (MSR) in combination with
16                                              Methionine synthase reductase (MSR) is a diflavin oxidor
17                                        Human methionine synthase reductase (MSR) is a protein contain
18 d A1298C), methionine synthase (MTR A2756G), methionine synthase reductase (MTRR A66G), cystathionine
19 ma cobalamin status in participants with the methionine synthase reductase (MTRR) 524CC genotype only
20 te reductase (MTHFR) 677C-->T and 1298A-->C, methionine synthase reductase (MTRR) 66A-->G, and cystat
21 thesis--methionine synthase (MTR) A2756G and methionine synthase reductase (MTRR) A66G--provided evid
22 to oxidative inactivation and is repaired by methionine synthase reductase (MTRR) in the presence of
23                                              Methionine synthase reductase (MTRR) is another enzyme e
24                                   The enzyme methionine synthase reductase (Mtrr) is necessary for ut
25 eductase (MTHFR), methionine synthase (MTR), methionine synthase reductase (MTRR), and cystathionine
26 hylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR), have generated con
27       We investigated 5 polymorphisms in the methionine synthase reductase (MTRR), methylenetetrahydr
28 ytotoxicity was observed in cells expressing methionine synthase reductase (MTRR), novel diflavin oxi
29 tathionine beta-synthase [CBS] 844ins68, and methionine synthase reductase [MTRR] 66A>G) in 452 young
30  oxidoreductase with significant homology to methionine synthase reductase, NR1, has been described r
31                                              Methionine synthase reductase reduces cytochrome c in an
32 he soluble dual flavoprotein oxidoreductase, methionine synthase reductase, serves as a redox partner
33 thionine synthase is required for NR1 versus methionine synthase reductase, suggesting that it may re