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1 of sarcosine is coupled to the formation of 5,10-methylenetetrahydrofolate.
2 one-carbon group to tetrahydrofolate to form 5,10-methylenetetrahydrofolate.
3 ernary complex formation with [32P]FdUMP and 5,10-methylenetetrahydrofolate.
5 e ALL relapse risk by potentially increasing 5,10-methylenetetrahydrofolate and dTMP, enhancing DNA s
6 n units for dTMP biosynthesis in the form of 5,10-methylenetetrahydrofolate, are direct targets of As
7 Escherichia coli catalyzes the reduction of 5,10-methylenetetrahydrofolate (CH(2)-H(4)folate) by NAD
8 catalyze the NAD(P)H-dependent reduction of 5,10-methylenetetrahydrofolate (CH(2)-H(4)folate) to 5-m
9 THFR) catalyzes the NADH-linked reduction of 5,10-methylenetetrahydrofolate (CH(2)-H(4)folate) to 5-m
10 Escherichia coli catalyzes the reduction of 5,10-methylenetetrahydrofolate (CH(2)-H(4)folate) to 5-m
11 reductase (MTHFR) catalyzes the reduction of 5,10-methylenetetrahydrofolate (CH(2)-H(4)folate) to 5-m
12 ere 5-90 times higher, while K(m) values for 5,10-methylenetetrahydrofolate (CH(2)H(4)folate) were 1.
14 haromyces cerevisiae possesses two cytosolic 5,10-methylenetetrahydrofolate (CH2-THF) dehydrogenases
15 s the enzyme that catalyzes the oxidation of 5,10-methylenetetrahydrofolate (CH2-THF) in adult mammal
17 e contains a monofunctional NAD(+)-dependent 5,10-methylenetetrahydrofolate dehydrogenase (yMTD).
18 arboxamide ribonucleotide formyltransferase, 5,10-methylenetetrahydrofolate dehydrogenase, and 10-for
19 ng association in premenopausal women of the 5,10-methylenetetrahydrofolate dehydrogenase-1958A gene
20 viduals who were carriers of the very common 5,10-methylenetetrahydrofolate dehydrogenase-1958A gene
21 ine hydroxymethyltransferase (SHMT) generate 5,10-methylenetetrahydrofolate for de novo dTMP biosynth
26 or previous metabolic studies that indicated 5,10-methylenetetrahydrofolate is preferentially directe
27 ces colon cancer risk, perhaps by increasing 5,10-methylenetetrahydrofolate levels for DNA synthesis,
28 tal cancer probably because higher levels of 5,10-methylenetetrahydrofolate may prevent imbalances of
31 494del6, IVS6 -68C>T, 1122A>G, and 1053C>T); 5,10-methylenetetrahydrofolate reductase (MTHFR 677C>T a
32 s of genes coding for folate pathway enzymes 5,10-methylenetetrahydrofolate reductase (MTHFR) 677C-->
37 y investigated whether a polymorphism in the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene (C
38 r a variant form (the C677T genotype) of the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene an
39 viously reported that 2 polymorphisms in the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene at
41 the association between polymorphisms in the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene, i
45 r V gene (Factor V Leiden), a variant in the 5,10-methylenetetrahydrofolate reductase gene (MTHFR), a
46 se, cystathionine-gamma-lyase, paraxonase 1, 5,10-methylenetetrahydrofolate reductase, betaine:homocy
47 eductase (MTHFR) catalyzes the conversion of 5,10-methylenetetrahydrofolate, required for purine and
48 hydrofolate; (2) chemical reduction of liver 5,10-methylenetetrahydrofolate (stabilized at pH 10) to
50 (MTD) catalyzes the reversible oxidation of 5,10-methylenetetrahydrofolate to 5,10-methenyltetrahydr
51 NA replication by blocking the conversion of 5,10-methylenetetrahydrofolate to 5-methyltetrahydrofola
52 reductase (MTHFR) catalyzes the reduction of 5,10-methylenetetrahydrofolate to 5-methyltetrahydrofola
53 HFR, EC 1.5.1.20) catalyzes the reduction of 5,10-methylenetetrahydrofolate to 5-methyltetrahydrofola
54 reductase (MTHFR) catalyzes the reduction of 5,10-methylenetetrahydrofolate to 5-methyltetrahydrofola
55 netetrahydrofolate reductase (MTHFR) directs 5,10-methylenetetrahydrofolate toward methionine synthes
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