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1  (5-CHO-THF) is formed by a side reaction of serine hydroxymethyltransferase.
2 rotein, two tRNA synthetases, and a putative serine hydroxymethyltransferase.
3 f several folate-dependent enzymes including serine hydroxymethyltransferase.
4          The 5'-untranslated region (UTR) of serine hydroxymethyltransferase 1 (SHMT1) contains an in
5                                              Serine hydroxymethyltransferase 1 (SHMT1) expression lim
6                                              Serine hydroxymethyltransferase 1 (SHMT1) is an essentia
7 d their de novo biosynthesis is regulated by serine hydroxymethyltransferase 1 (SHMT1).
8 ation and repair and consists of the enzymes serine hydroxymethyltransferase 1 and 2alpha (SHMT1 and
9 atase (PSPH)) and de novo glycine synthesis (serine hydroxymethyltransferase 2 (SHMT2)).
10 ded a 30 kDa chloroplast membrane protein, a serine hydroxymethyltransferase, a nuclease, and two pro
11 and PLP-stimulated (35%; P=0.004) lymphocyte serine hydroxymethyltransferase activities in vitro.
12  show that this assay can be used to measure serine hydroxymethyltransferase activity at 10(-8) to 10
13 ggest that 5-formyltetrahydrofolate inhibits serine hydroxymethyltransferase activity in vivo and tha
14 s assay, the 5,10-CH(2)-H(4)PteGlu formed by serine hydroxymethyltransferase activity is reduced to 5
15 ed a novel HPLC-based fluorometric assay for serine hydroxymethyltransferase activity.
16 ric quaternary structure of liganded E. coli serine hydroxymethyltransferase also differs in symmetry
17                           The gene encodes a serine hydroxymethyltransferase, an enzyme that is ubiqu
18 red to the other two enzymes in the cytosol, serine hydroxymethyltransferase and C1-tetrahydrofolate
19 o thymidylate synthesis, and suggesting that serine hydroxymethyltransferase and FTHFS compete for a
20 h define the folate cofactor binding site in serine hydroxymethyltransferase and the differences in o
21 of genes encoding a glycine cleavage system, serine hydroxymethyltransferase, and serine dehydratase.
22                                   The active serine hydroxymethyltransferase, and two other enzymes t
23 ing the in vitro folding of Escherichia coli serine hydroxymethyltransferase at 4 degrees C, both mon
24                            The maturation of serine hydroxymethyltransferase by ICP55 is unusual, as
25 orted to be the viable in vivo substrate for serine hydroxymethyltransferase-catalyzed formation of 5
26                                  Cytoplasmic serine hydroxymethyltransferase (cSHMT) enzyme levels ar
27 ism is associated with decreased cytoplasmic serine hydroxymethyltransferase (cSHMT) expression in MC
28                        The human cytoplasmic serine hydroxymethyltransferase (CSHMT) gene was isolate
29                                  Cytoplasmic serine hydroxymethyltransferase (cSHMT) is a tetrameric,
30 slated region (UTR) of the human cytoplasmic serine hydroxymethyltransferase (cSHMT) message is alter
31                 The influence of cytoplasmic serine hydroxymethyltransferase (cSHMT) on this competit
32 the preferential partitioning of cytoplasmic serine hydroxymethyltransferase (cSHMT)-derived methylen
33 n of the folate-dependent enzyme cytoplasmic serine hydroxymethyltransferase (cSHMT).
34 ate reductase [MTHFR] and C1420T cytoplasmic serine hydroxymethyltransferase [cSHMT]).
35                                              Serine hydroxymethyltransferase (EC 2.1.2.1), a member o
36 ase and the transcription of the cytoplasmic serine hydroxymethyltransferase gene (SHMT1).
37  it was an indirect consequence of damage to serine hydroxymethyltransferase (GlyA; E.C. 2.1.2.1).
38  the Rhg4 gene encodes a predicted cytosolic serine hydroxymethyltransferase (GmSHMT08); however, the
39 in vitro folding pathway of Escherichia coli serine hydroxymethyltransferase has both monomer and dim
40 ture at 2.4 A resolution of Escherichia coli serine hydroxymethyltransferase in ternary complex with
41                      The human mitochondrial serine hydroxymethyltransferase (mSHMT) gene was isolate
42               A cDNA clone for mitochondrial serine hydroxymethyltransferase (mSHMT) that was capable
43 similar to sequences in rabbit mitochondrial serine hydroxymethyltransferase (mSHMT).
44                  However, addition of either serine hydroxymethyltransferase or C1-tetrahydrofolate s
45 ehydrogenase reaction to an excess of either serine hydroxymethyltransferase or C1-tetrahydrofolate s
46 n 16 days were viable and lacked cytoplasmic serine hydroxymethyltransferase protein, confirming that
47 coding a protein with sequence similarity to serine hydroxymethyltransferases, resulting in the propo
48 ay, we characterized a family of Arabidopsis serine hydroxymethyltransferase (SHM) genes.
49     Unexpectedly, mutation of both cytosolic serine hydroxymethyltransferase (SHM2) and one-carbon te
50 PLC)-based fluorometric method for measuring serine hydroxymethyltransferase (SHMT) activity toward f
51 luding several with defects in mitochondrial serine hydroxymethyltransferase (SHMT) activity.
52 is formed via a second catalytic activity of serine hydroxymethyltransferase (SHMT) and strongly inhi
53                                              Serine hydroxymethyltransferase (SHMT) catalyzes the rev
54                                              Serine hydroxymethyltransferase (SHMT) catalyzes the rev
55                                              Serine hydroxymethyltransferase (SHMT) catalyzes the rev
56                                              Serine hydroxymethyltransferase (SHMT) catalyzes the rev
57                                              Serine hydroxymethyltransferase (SHMT) from all sources
58                                              Serine hydroxymethyltransferase (SHMT) from plant mitoch
59 etrahydrofolate dehydrogenase 1 (MTHFD1) and serine hydroxymethyltransferase (SHMT) generate 5,10-met
60                                              Serine hydroxymethyltransferase (SHMT) is a pyridoxal 5'
61                                              Serine hydroxymethyltransferase (SHMT) is a pyridoxal ph
62                                    Mammalian serine hydroxymethyltransferase (SHMT) is a tetrameric,
63                                              Serine hydroxymethyltransferase (SHMT) is the major prov
64 on the folding mechanism of Escherichia coli serine hydroxymethyltransferase (SHMT) showed that the f
65 olyglutamate forms to rabbit liver cytosolic serine hydroxymethyltransferase (SHMT) were determined b
66 methylenetetrahydrofolate reductase (MTHFR), serine hydroxymethyltransferase (SHMT), and cystathionin
67                                Mitochondrial serine hydroxymethyltransferase (SHMT), combined with gl
68 opyran-based inhibitors targeting the enzyme serine hydroxymethyltransferase (SHMT), designed to impr
69                             Nevertheless for serine hydroxymethyltransferase (SHMT), one of the key e
70 synthesis, a pathway composed of the enzymes serine hydroxymethyltransferase (SHMT), thymidylate synt
71 ormylTHF, a slow, tight-binding inhibitor of serine hydroxymethyltransferase (SHMT), was enriched in
72 tability observed for reactions catalyzed by serine hydroxymethyltransferase (SHMT).
73                                              Serine hydroxymethyltransferase (SHMT; EC 2.1.2.1) catal
74 structures of the human and rabbit cytosolic serine hydroxymethyltransferases (SHMT) confirmed their
75  disrupted at the genes encoding one or both serine hydroxymethyltransferases (SHMT) or at the genes
76 reductase-thymidylate synthase, dhfr-ts, and serine hydroxymethyltransferase, shmt) gave the most abu
77 n methionine synthase (MS A2756G), cytosolic serine hydroxymethyltransferase (SHMT1 C1420T), and a do
78 folate reductase (MTHFR 677C>T and 1298A>C); serine hydroxymethyltransferase (SHMT1 C1420T); reduced
79 onucleotide transformylase (ATIC) 347GG, and serine hydroxymethyltransferase (SHMT1) 1420CC were meas
80                                              Serine hydroxymethyltransferase (SHMT1) partitions folat
81                                  Cytoplasmic serine hydroxymethyltransferase (SHMT1) regulates the pa
82 human glioblastoma multiforme, mitochondrial serine hydroxymethyltransferase (SHMT2) and glycine deca
83 ine, through the activities of mitochondrial serine hydroxymethyltransferase (SHMT2), thymidylate syn
84 parison with the unliganded rabbit cytosolic serine hydroxymethyltransferase structure identifies cha
85  in vivo of specific proteins indicated that serine hydroxymethyltransferase was affected in icp55.

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