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1 ) has a lowered specificity for recognition (relaxed-specificity).
2 cterization of Flp variants that show either relaxed specificity (active on FRT and mFRT) or moderate
3  cleavage at the cognate restriction site or relaxed specificity allowing cleavage of degenerate 'sta
4  on lysine 16, NSL-associated MOF exhibits a relaxed specificity and also acetylates nucleosomal hist
5                      These enzymes exhibit a relaxed specificity and are able to transfer a variety o
6                               The pattern of relaxed specificity at this position roughly correlates
7                                  Despite the relaxed specificity between SK and RRs, HTCSs remained i
8 , LpxA from B. parapertussis did not display relaxed specificity but was selective for C(10)OH-ACP.
9  site than does wild-type EcoRI yet displays relaxed specificity deriving from tighter binding and fa
10 icrobial change, whereas a species with more relaxed specificity does not show such microbiome change
11                                         This relaxed specificity enabled us to rewire a HTCS successf
12 hat the ancestor of GNAT toxins was likely a relaxed specificity enzyme capable of acetylating multip
13  to respond to chi, and six that suggested a relaxed specificity for chi recognition.
14 ndence on APC, while hCDH1 shows a much more relaxed specificity for the D-box.
15  the V. cholerae CqsA/CqsS counterparts show relaxed specificity in both production and detection.
16 s CArGs for the degenerate CArGs resulted in relaxed specificity in cultured cells.
17 utant restriction endonucleases that exhibit relaxed specificity in vivo nevertheless bind more tight
18  contacts to flanking bases as important for relaxed specificity, local effects are not sufficient to
19 es structural constraints, thus allowing the relaxed specificity mutants in the acceptor binding doma
20                                          The relaxed-specificity mutants still recognize canonical ch
21                                          The relaxed specificity of the CRISPR/Cas system limits esca
22                In contrast to the relatively relaxed specificity of the loading AT domain, the methyl
23                         We conclude that the relaxed specificity of the P. gingivalis lipid A acyltra
24 n be transferred onto protein indicating the relaxed specificity of the putative oligosaccharyltransf
25 e modeling provides a rationale for the more relaxed specificity of these kinases, of which the natur
26 at, as opposed to type I and II systems, the relaxed specificity of type III CRISPR-Cas targeting pro
27 log, Esp638I cleaves GCS downward arrow SGC (relaxed specificity RCN downward arrow NGY, containing a
28 ndent cyclic NMP phosphodiesterase that uses relaxed specificity to target Pycsar cyclic pyrimidine m
29 trates revealed that WaaL possesses a highly relaxed specificity toward both the lipid moiety and the
30 lcNAc/Glc 4-epimerases indicated that it has relaxed specificity toward the four substrates, the firs
31 ulfovibrio vulgaris, exhibited significantly relaxed specificity towards the -2 position compared to