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1 ages to the dynamics of lateral transfer and plasmid integration.
2 e possible to obtain the insertion strain by plasmid integration.
3 hat the efficacy can be enhanced by targeted plasmid integration.
4 hat were genetically uniform for single-copy plasmid integration.
5 ity, significantly reduced etoposide-induced plasmid integration.
6 ite the large size of the DNA fragment, both plasmid integration and duplication reduction can be acc
7  the cross-link- and DSB-induced patterns of plasmid integration and gene conversion were similar in
8                               In addition, a plasmid integration assay showed that integrative recomb
9  be delivered to the host chromosome through plasmid integration events, thus stabilizing important a
10 ere constructed in Myxococcus xanthus with a plasmid integration-excision strategy facilitated by sac
11                                              Plasmid integration experiments indicated that all 22 ge
12                Etoposide strongly stimulated plasmid integration in CAD cDNA-complemented mouse embry
13 hs of gene conversion tracts associated with plasmid integration into TRAP suggests that an ends-in s
14 hat may be important in biofilm formation, a plasmid integration library of S. gordonii V288 was used
15                               By screening a plasmid integration library of S. gordonii, genes were i
16 le-strand break (DSB) were often lost during plasmid integration, mutations located 600 bp and farthe
17 f BenR and BenS transformants suggested that plasmid integration occurred most frequently at the chro
18                                 We show that plasmid integration occurs via a double-strand gap repai
19 he DNA sequences immediately surrounding the plasmid integrations revealed no known coding sequences
20 recombinant protein expression) flanking the plasmid integration site from a recombinant Chinese hams
21 verted duplication of the genomic DNA at the plasmid integration site.
22 xpression by itself and in the presence of a plasmid integration substrate was able to mediate this d
23  KpnI increased the efficiency of linearized plasmid integration up to 5-fold in CHO cells.
24 diseases, we studied the effects of targeted plasmid integration using a phage integrase (phiC31) tha
25                                              Plasmid integration was dependent on recombinase activit
26 rating PAI movement by a mechanism involving plasmid integration, we observed transfer of a selectabl

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