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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.
4 the synthesis of thymidylate, which requires 5,10-methylenetetrahydrofolate (5,10-CH(2)-THF).
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.
13 ahydrofolate (H4folate) to yield glycine and 5,10-methylenetetrahydrofolate (CH2-H4folate).
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
16                                              5,10-Methylenetetrahydrofolate dehydrogenase (MTD) catal
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
22                              SHMT1 generates 5,10-methylenetetrahydrofolate for de novo thymidylate b
23            A method for the determination of 5,10-methylenetetrahydrofolate in liver is described.
24 n of (1) from (3) gives the concentration of 5,10-methylenetetrahydrofolate in liver.
25                          The folate coenzyme 5,10-methylenetetrahydrofolate is an important folate me
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
29                                 Reduction of 5,10-methylenetetrahydrofolate (methyleneTHF), a donor f
30 s metabolized to methionine by the action of 5,10 methylenetetrahydrofolate reductase (MTHFR).
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-->
33           Four fetal genetic variants of the 5,10-methylenetetrahydrofolate reductase (MTHFR) and dih
34                     The authors analyzed the 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T g
35                                   The enzyme 5,10-methylenetetrahydrofolate reductase (MTHFR) catalyz
36                                   The enzyme 5,10-methylenetetrahydrofolate reductase (MTHFR) catalyz
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
40                 A common polymorphism in the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene ha
41 the association between polymorphisms in the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene, i
42                                   The enzyme 5,10-methylenetetrahydrofolate reductase (MTHFR) is invo
43 or for methionine synthesis, is catalyzed by 5,10-methylenetetrahydrofolate reductase (MTHFR).
44  to thymine (T) polymorphism in the gene for 5,10-methylenetetrahydrofolate reductase (MTHFR).
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
49              The sarcosine dehydrogenase and 5,10-methylenetetrahydrofolate synthase sites are 35 A a
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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