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