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1 s (PARPs), is an important posttranslational modification reaction.
2 st cells was found to be unperturbed by this modification reaction.
3  replaced by a copper-sulfur bond during the modification reaction.
4 alyses reveal the molecular mechanism of the modification reaction.
5 onfiguration to fine-tune subsequent histone modification reactions.
6 as amines, keto groups, and alkynes for post modification reactions.
7 ic labeling takes advantage of two different modification reactions.
8  as for the optimization of protein chemical modification reactions.
9 re required for both the restriction and the modification reactions.
10 successfully submitted to postpolymerization modification reactions.
11  polyketide chain extension and B-keto group modification reactions.
12 roviding accessible sites for post-synthetic modification reactions.
13 can be reused for multiple cycles of protein modification reactions.
14    The pH dependence of methylation and DTNB modification reactions, and spectroscopic properties, is
15 l understood, and the enzymes performing the modification reactions are unknown.
16  quantitation of yields in COF postsynthetic modification reactions, as well as of amine defect sites
17      Although the enzyme responsible for the modification reaction at arginine 66 has been identified
18 nd antibody gene conversion are distinct DNA modification reactions, but all are initiated by activat
19 ct forms, which provide snapshots of the RNA modification reaction catalyzed by DMATase.
20 quential functional group selective chemical modification reactions coupled with high-resolution/accu
21      NADP, which will not replace NAD in the modification reaction, does support cross-linking betwee
22 oth allows for facile monitoring of chemical modification reactions during the synthesis of the PEGyl
23 oP-constitutive strain showed that the known modification reactions explain a major part of the PhoPQ
24 of sodium channels, completely prevented the modification reaction from occurring from either directi
25                                A new protein modification reaction has been developed based on a pall
26  reactive, efficient and orthogonal chemical modification reactions have enabled the engineering of m
27  yeast cells defines a novel type of protein modification reaction in eukaryotes.
28 anistic insights into nucleosomal histone H3 modification reactions in cis and in trans, that is, wit
29                                         This modification reaction is dependent on a family of relate
30  redox stimulation of the exchanger, and the modification reaction is unknown.
31                                   One of the modification reactions is the epimerization of D-glucuro
32 gly binding ligands in postsynthetic surface modification reactions, its quantification on NM surface
33 ct compensatory reductions of rates for both modification reactions, mitigation of effects of slower
34                     Three new post-synthetic modification reactions, namely amidation, esterification
35          These results suggest that mycolate modification reactions occur parallel with the synthesis
36 ith tRNA first and DMAPP second, and the RNA modification reaction occurs in the middle of the channe
37                       The post-translational modification reactions of lanthipeptides include dehydra
38 oxyl derivatives of PHB were obtained by the modification reactions of PHB with di-ethanol amine.
39 - or alpha- and beta-protomers, along with a modification reaction on an un-cross-linked beta-chain.
40 model featuring all three post-translational modification reactions: phosphorylation, elimination, an
41 metry, CD spectroscopy, and protein chemical modification reactions (protein footprinting).
42                        The polynucleotide 5' modification reaction requires the His(309) nucleophile,
43 equired for all immunoglobulin gene-specific modification reactions (somatic hypermutation, class swi
44 ndent fluorophores and pH-dependent chemical modification reactions suggest that cell walls of respir
45 f proteins is an essential, highly conserved modification reaction that occurs in all eukaryotes and
46  glycosylation is a highly conserved protein modification reaction that occurs in all eukaryotes.
47  glycosylation is a highly conserved protein modification reaction that occurs in all eukaryotic orga
48 ation and class switch recombination are DNA modification reactions that alter the genes encoding ant
49  was the last of the lymphocyte-specific DNA modification reactions to appear in the evolution of the
50                                              Modification reactions were discussed by results of FT-I
51 e the molecular details underlying the Nedd8 modification reaction, which results in covalent conjuga
52 functionalities was demonstrated in one post-modification reaction with N-Boc-ethylenediamine via red
53 lar approach that involves selective polymer modification reactions with organometallic reagents.