ライフサイエンスコーパス: modification reaction

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1 s (PARPs), is an important posttranslational modification reaction.

2 replaced by a copper-sulfur bond during the modification reaction.

3 as for the optimization of protein chemical modification reactions.

4 as amines, keto groups, and alkynes for post modification reactions.

5 roviding accessible sites for post-synthetic modification reactions.

6 ic labeling takes advantage of two different modification reactions.

7 re required for both the restriction and the modification reactions.

8 can be reused for multiple cycles of protein modification reactions.

9 onfiguration to fine-tune subsequent histone modification reactions.

10 The pH dependence of methylation and DTNB modification reactions, and spectroscopic properties, is

11 l understood, and the enzymes performing the modification reactions are unknown.

12 Although the enzyme responsible for the modification reaction at arginine 66 has been identified

13 nd antibody gene conversion are distinct DNA modification reactions, but all are initiated by activat

14 ct forms, which provide snapshots of the RNA modification reaction catalyzed by DMATase.

15 quential functional group selective chemical modification reactions coupled with high-resolution/accu

16 NADP, which will not replace NAD in the modification reaction, does support cross-linking betwee

17 oP-constitutive strain showed that the known modification reactions explain a major part of the PhoPQ

18 of sodium channels, completely prevented the modification reaction from occurring from either directi

19 A new protein modification reaction has been developed based on a pall

20 reactive, efficient and orthogonal chemical modification reactions have enabled the engineering of m

21 yeast cells defines a novel type of protein modification reaction in eukaryotes.

22 anistic insights into nucleosomal histone H3 modification reactions in cis and in trans, that is, wit

23 This modification reaction is dependent on a family of relate

24 redox stimulation of the exchanger, and the modification reaction is unknown.

25 One of the modification reactions is the epimerization of D-glucuro

26 ct compensatory reductions of rates for both modification reactions, mitigation of effects of slower

27 These results suggest that mycolate modification reactions occur parallel with the synthesis

28 ith tRNA first and DMAPP second, and the RNA modification reaction occurs in the middle of the channe

29 The post-translational modification reactions of lanthipeptides include dehydra

30 - or alpha- and beta-protomers, along with a modification reaction on an un-cross-linked beta-chain.

31 model featuring all three post-translational modification reactions: phosphorylation, elimination, an

32 metry, CD spectroscopy, and protein chemical modification reactions (protein footprinting).

33 The polynucleotide 5' modification reaction requires the His(309) nucleophile,

34 equired for all immunoglobulin gene-specific modification reactions (somatic hypermutation, class swi

35 ndent fluorophores and pH-dependent chemical modification reactions suggest that cell walls of respir

36 f proteins is an essential, highly conserved modification reaction that occurs in all eukaryotes and

37 glycosylation is a highly conserved protein modification reaction that occurs in all eukaryotes.

38 glycosylation is a highly conserved protein modification reaction that occurs in all eukaryotic orga

39 ation and class switch recombination are DNA modification reactions that alter the genes encoding ant

40 was the last of the lymphocyte-specific DNA modification reactions to appear in the evolution of the

41 e the molecular details underlying the Nedd8 modification reaction, which results in covalent conjuga

42 functionalities was demonstrated in one post-modification reaction with N-Boc-ethylenediamine via red

43 lar approach that involves selective polymer modification reactions with organometallic reagents.

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