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1 ine and (6S)-tetrahydrofolate to glycine and 5,10-methylenetetrahydrofolate.
2 of sarcosine is coupled to the formation of 5,10-methylenetetrahydrofolate.
3 one-carbon group to tetrahydrofolate to form 5,10-methylenetetrahydrofolate.
4 ernary complex formation with [32P]FdUMP and 5,10-methylenetetrahydrofolate.
6 e ALL relapse risk by potentially increasing 5,10-methylenetetrahydrofolate and dTMP, enhancing DNA s
7 n units for dTMP biosynthesis in the form of 5,10-methylenetetrahydrofolate, are direct targets of As
8 d by enabling xanthommatin biosynthesis in a 5,10-methylenetetrahydrofolate auxotroph of the platform
9 Escherichia coli catalyzes the reduction of 5,10-methylenetetrahydrofolate (CH(2)-H(4)folate) by NAD
10 catalyze the NAD(P)H-dependent reduction of 5,10-methylenetetrahydrofolate (CH(2)-H(4)folate) to 5-m
11 THFR) catalyzes the NADH-linked reduction of 5,10-methylenetetrahydrofolate (CH(2)-H(4)folate) to 5-m
12 Escherichia coli catalyzes the reduction of 5,10-methylenetetrahydrofolate (CH(2)-H(4)folate) to 5-m
13 reductase (MTHFR) catalyzes the reduction of 5,10-methylenetetrahydrofolate (CH(2)-H(4)folate) to 5-m
14 ere 5-90 times higher, while K(m) values for 5,10-methylenetetrahydrofolate (CH(2)H(4)folate) were 1.
16 haromyces cerevisiae possesses two cytosolic 5,10-methylenetetrahydrofolate (CH2-THF) dehydrogenases
17 s the enzyme that catalyzes the oxidation of 5,10-methylenetetrahydrofolate (CH2-THF) in adult mammal
19 e contains a monofunctional NAD(+)-dependent 5,10-methylenetetrahydrofolate dehydrogenase (yMTD).
20 arboxamide ribonucleotide formyltransferase, 5,10-methylenetetrahydrofolate dehydrogenase, and 10-for
21 ng association in premenopausal women of the 5,10-methylenetetrahydrofolate dehydrogenase-1958A gene
22 viduals who were carriers of the very common 5,10-methylenetetrahydrofolate dehydrogenase-1958A gene
23 ine hydroxymethyltransferase (SHMT) generate 5,10-methylenetetrahydrofolate for de novo dTMP biosynth
28 or previous metabolic studies that indicated 5,10-methylenetetrahydrofolate is preferentially directe
29 ces colon cancer risk, perhaps by increasing 5,10-methylenetetrahydrofolate levels for DNA synthesis,
30 tal cancer probably because higher levels of 5,10-methylenetetrahydrofolate may prevent imbalances of
33 494del6, IVS6 -68C>T, 1122A>G, and 1053C>T); 5,10-methylenetetrahydrofolate reductase (MTHFR 677C>T a
34 s of genes coding for folate pathway enzymes 5,10-methylenetetrahydrofolate reductase (MTHFR) 677C-->
40 y investigated whether a polymorphism in the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene (C
41 r a variant form (the C677T genotype) of the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene an
42 viously reported that 2 polymorphisms in the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene at
44 the association between polymorphisms in the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene, i
49 r V gene (Factor V Leiden), a variant in the 5,10-methylenetetrahydrofolate reductase gene (MTHFR), a
50 se, cystathionine-gamma-lyase, paraxonase 1, 5,10-methylenetetrahydrofolate reductase, betaine:homocy
51 eductase (MTHFR) catalyzes the conversion of 5,10-methylenetetrahydrofolate, required for purine and
52 hydrofolate; (2) chemical reduction of liver 5,10-methylenetetrahydrofolate (stabilized at pH 10) to
54 (MTD) catalyzes the reversible oxidation of 5,10-methylenetetrahydrofolate to 5,10-methenyltetrahydr
55 NA replication by blocking the conversion of 5,10-methylenetetrahydrofolate to 5-methyltetrahydrofola
56 reductase (MTHFR) catalyzes the reduction of 5,10-methylenetetrahydrofolate to 5-methyltetrahydrofola
57 HFR, EC 1.5.1.20) catalyzes the reduction of 5,10-methylenetetrahydrofolate to 5-methyltetrahydrofola
58 reductase (MTHFR) catalyzes the reduction of 5,10-methylenetetrahydrofolate to 5-methyltetrahydrofola
59 netetrahydrofolate reductase (MTHFR) directs 5,10-methylenetetrahydrofolate toward methionine synthes