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1 ns ) and via the release of parasites (e.g., temperate phage ).
2 tic infection but tolerate lysogenization by temperate phages.
3 ol phage production have been studied in few temperate phages.
4 are known to induce the lytic cycle of many temperate phages.
5 This difference may come about because the temperate phages acquire more sequence characteristics o
6 uginosa with or without a community of three temperate phages active in cystic fibrosis (CF) lung inf
7 es the efficient induction of toxin-encoding temperate phage and the resultant conversion of Tox(-) f
9 This phage is a member of a group of related temperate phages, and we show here that not all speA-car
11 are molecular parasites that exploit certain temperate phages as helpers, using a variety of elegant
12 ndings suggest that presence of a CD119-like temperate phage can influence toxin gene regulation in t
13 ity both to lytic and lysogenic infection by temperate phages-compromising the genetic stability of t
14 temperate phages within hosts suggests that temperate phages could promote within-host evolution of
18 Streptomyces plasmid Xis proteins shows that temperate phage excisionases may use variations of a hel
20 ngs by integrating CRISPR/Cas9 system into a temperate phage genome, removing major virulence genes f
22 ry Acr characterized to date originated from temperate phages, genomic islands, or prophages (4-8) ,
29 y to repel invasions, whereas the release of temperate phage is superior as a strategy of invasion.
30 ruses, the second one includes more variable temperate phages, like GIL16 or Bam35, whose hosts are B
37 n-converting bacteriophages (Stx phages) are temperate phages of Escherichia coli, and can cause seve
39 c chromosomes often contain islands, such as temperate phages or pathogenicity islands, delivered by
41 tion of relA using an att- derivative of the temperate phage phi C31 abolished ppGpp synthesis on ami
44 omyces coelicolor, using a derivative of the temperate phage phiC31 that expresses Cre recombinase du
48 tous in eubacteria, prevalent in archaea and temperate phages, present in certain yeast strains, but
50 DNA level homologies with other lactococcal temperate phage repressors suggest that evolutionary eve
51 ys contain spacers homologous to plasmid and temperate phage sequences and, in some cases, chromosoma
54 Mycobacteriophage L5 is a well-characterized temperate phage that forms stable lysogens in Mycobacter
56 at interfere with the infection of lytic and temperate phages that are either closely related (homoty
57 urveyed, and with viromes dominated by a few temperate phages that exhibit remarkable genetic stabili
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