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1  of NiO, and the binding is resistant to the hydrolytic cleavage.
2 and produces only a slight inhibition of its hydrolytic cleavage.
3 e clearance of beta amyloid peptides through hydrolytic cleavage.
4 st to be resolved by a transposase-catalyzed hydrolytic cleavage.
5 ases the susceptibility of the adduct toward hydrolytic cleavage.
6 nd breaks are detected that are generated by hydrolytic cleavage and correspond closely to the observ
7 methylation, it is subject to degradation by hydrolytic cleavage and deamination by cytidine deaminas
8 btained using a combination of Pb2+ and Tb3+ hydrolytic cleavage assays on wild type and mutant riboz
9  with BLM A(5), the relative efficiencies of hydrolytic cleavage at individual sites were altered.
10 ms in the outer segment membrane may undergo hydrolytic cleavage before internalization by the retina
11 ses the reactivity of the silyl ether toward hydrolytic cleavage but also stabilizes the phenolate in
12                     Neither complex promoted hydrolytic cleavage, but efficient oxidative cleavage wa
13 ngation complex strongly promotes transcript hydrolytic cleavage by establishing a network of interac
14 modifications were also shown to be prone to hydrolytic cleavage by SIRT1-3 and SIRT6, supporting rec
15  unfolding of pro-MMP-9 near the site of the hydrolytic cleavage by stromelysin 1.
16 and analyzed for (1) their ability to resist hydrolytic cleavage by trypsin; (2) their antimicrobial
17 e the non-nucleotide-linker) is sensitive to hydrolytic cleavage catalyzed by ethylenediamine hydroch
18                                   Subsequent hydrolytic cleavage is likely assisted by the neighborin
19       After product formation, E-P undergoes hydrolytic cleavage, k = 6.3 s-1, and products NAMN, PPi
20  III proofreading domain, providing a common hydrolytic cleavage mechanism for RNA degradation and DN
21 ve kynureninases preferentially catalyze the hydrolytic cleavage of 3-hydroxy-l-kynurenine to produce
22 hosphate dependent enzyme that catalyzes the hydrolytic cleavage of 3-hydroxykynurenine to yield 3-hy
23 ylacetoacetate hydrolase (FAH) catalyzes the hydrolytic cleavage of a carbon-carbon bond in fumarylac
24  In a formal sense, this transformation is a hydrolytic cleavage of a carbon-phosphorus (C-P) bond, b
25 of the cytoplasmic membrane and catalyze the hydrolytic cleavage of a specific peptide bond of membra
26 mocysteine nucleosidase (MTAN) catalyzes the hydrolytic cleavage of adenine from methylthioadenosine
27 amidohydrolase superfamily and catalyzes the hydrolytic cleavage of beta-aspartyl dipeptides.
28 dimeric Pd complexes that mediate the facile hydrolytic cleavage of both CS2 carbon-sulfur bonds at 2
29 ct as a general base, provide a platform for hydrolytic cleavage of bound RNA in the 3' --> 5' direct
30 we propose a two-metal ion mechanism for the hydrolytic cleavage of DNA junctions.
31 protein display by reducing the unproductive hydrolytic cleavage of enzyme-protein covalent intermedi
32 te (PLP)-dependent enzyme that catalyzes the hydrolytic cleavage of l-kynurenine to anthranilic acid
33 hosphate-dependent enzyme that catalyzes the hydrolytic cleavage of l-kynurenine to give l-alanine an
34 oxal-P)-dependent enzyme which catalyzes the hydrolytic cleavage of L-tryptophan to indole and ammoni
35        Tryptophan indole-lyase catalyzes the hydrolytic cleavage of L-tryptophan to indole and ammoni
36 pendent enzyme that catalyzes the reversible hydrolytic cleavage of l-Tyr to give phenol and ammonium
37 oxaloacetate acetylhydrolase (OAH)-catalyzed hydrolytic cleavage of oxaloacetate appears to be an esp
38 er and B. cinerea is solely dependent on the hydrolytic cleavage of oxaloacetate catalyzed by OAH.
39 le analogue of deglycoBLM A(5) effected both hydrolytic cleavage of RNA in the absence of added metal
40 dogenesis in Alzheimer's disease, catalyzing hydrolytic cleavage of substrate in a pH-sensitive manne
41  by adenine DNA glycosylase, which catalyzes hydrolytic cleavage of the aberrant A nucleobase from th
42 of IAA glucose to the enzyme with subsequent hydrolytic cleavage of the acyl moiety by the hydroxyl o
43                         LTs catalyze the non-hydrolytic cleavage of the bacterial peptidoglycan cell-
44 e (MhpC) from Escherichia coli catalyses the hydrolytic cleavage of the extradiol ring fission produc
45 d dinuclear metalloenzyme that catalyzes the hydrolytic cleavage of the five-member ring of allantoin
46 folate and CO(2), consists of two steps: (i) hydrolytic cleavage of the formyl group in the N-termina
47 the uracil base excision repair pathway, the hydrolytic cleavage of the N-glycosidic bond of deoxyuri
48 nzyme uracil DNA glycosylase (UDG) catalyzes hydrolytic cleavage of the N-glycosidic bond of premutag
49 ut of double-stranded DNA and catalyzing the hydrolytic cleavage of the N-glycosidic bond to release
50 hionine aminopeptidase (MetAP) catalyzes the hydrolytic cleavage of the N-terminal methionine from ne
51 e I signal peptidase (SPase I) catalyzes the hydrolytic cleavage of the N-terminal signal peptide fro
52                                              Hydrolytic cleavage of the oxidized product at this site
53 RPSs) that release their peptide products by hydrolytic cleavage of the peptide carrier protein (PCP)
54 nol-keto tautomerization and enzyme-mediated hydrolytic cleavage of the thioester produces a reactive
55  DNA template, and RNA transcript) to induce hydrolytic cleavage of the transcript and release of the
56 ion suggests that the reaction starts with a hydrolytic cleavage of the triazole ring followed by oxi
57  and EC 3.3.2.5) is an enzyme that catalyzes hydrolytic cleavage of the vinyl ether bond of lysoplasm
58 quenched-flow measurements were used for the hydrolytic cleavage step, and the fluorescent phosphate
59 ow measurements provided the kinetics of the hydrolytic cleavage step.
60 all copper dependence of phosphorylation and hydrolytic cleavage suggests long range conformational e
61 hose that release acidic moieties only after hydrolytic cleavage, the rate of which could be potentia
62 le covalent adduct, which can undergo O-acyl hydrolytic cleavage to form the observed product.
63 e non-edited strand become hypersensitive to hydrolytic cleavage upon binding of ADAR2 RBD.
64 hoenzyme formation, as well the rates of its hydrolytic cleavage, were reduced in proportion to the A
65 -P bond that defines these compounds resists hydrolytic cleavage, while the phosphonyl group is a ver

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