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1 he corresponding N-terminally acetylated and nonacetylated 15-residue synthetic peptides.
2  more mutagenic and prone to repair than the nonacetylated AF adducts.
3 evealed that AlgL operates preferentially on nonacetylated alginate or its precursor mannuronan.
4 ed that strains deficient in algIJF produced nonacetylated alginate.
5 ains missing only algJ or algI also produced nonacetylated alginates.
6 by titration of 10-80% mixture of acetylated/nonacetylated alpha-tubulin peptides in the background o
7 fies mechanisms mediating the degradation of nonacetylated alphaSyn, and illustrates potential therap
8 apo state, and in complex with GDP, GDP-Fuc, nonacetylated and acetylated trisaccharide acceptors, an
9 n their population distributions compared to nonacetylated arrays and demonstrate the above features.
10                                          For nonacetylated arrays, the end-distance data demonstrate
11 inetics were observed between acetylated and nonacetylated aS.
12 required for the transport and catabolism of nonacetylated chitin residues; and (iv) the constitutive
13                      This contrasts with the nonacetylated counterpart, which exhibits an equilibrium
14 rred to a much lesser extent than from their nonacetylated counterparts.
15           WbgU is also capable of converting nonacetylated derivatives but with much lower efficiency
16 ediate opsonic killing bind primarily to the nonacetylated epitopes of this antigen, which indicates
17 Alba, and that Alba exists in acetylated and nonacetylated forms.
18              Whereas streptococci expressing nonacetylated GspB with increased glucosylation were sig
19 We found that Yta7 binds both acetylated and nonacetylated H3 peptides but with a higher affinity for
20 utagenesis study illustrate a first-in-class nonacetylated lysine (KAc) binding site located at the h
21 erences in the mobilities were found for the nonacetylated, monoacetylated, and biacetylated compound
22 tiate the assembly of an enhancer complex on nonacetylated nucleosomes.
23 that a MAb (MAb F598) that bound the best to nonacetylated or backbone epitopes on PNAG had superior
24 tituted to various subsaturating levels with nonacetylated or hyperacetylated HeLa histones.
25 stituted to various subsaturated levels with nonacetylated or hyperacetylated HeLa histones.
26 xyeicosatetraenoic acid from AA, whereas the nonacetylated partner monomer forms mainly PGH(2) but on
27                                The remaining nonacetylated primary amino groups were utilized for con
28                                 Salsalate, a nonacetylated prodrug of salicylate, has been shown to d
29  of 21 nM and discriminates against both the nonacetylated protein and histone H4 proteins acetylated
30 l studies show that mutation of Lys-120 to a nonacetylated residue, as occurs in human cancer, inhibi
31                                   Salsalate (nonacetylated salicylate, 4500 mg/d), a compound that in
32  of the available clinical observations that nonacetylated salicylates are as efficacious as one of t
33  Anecdotal evidence has accumulated that the nonacetylated salicylates are as efficacious as the othe
34                                  Because the nonacetylated salicylates are weak prostaglandin inhibit
35                                              Nonacetylated Smc3 is required as a substrate for cohesi
36 utation of K56 to arginine, which mimics the nonacetylated state.