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1 ation to human infections, e.g. Fic and VbhA toxin-antitoxin system.
2 Rts1 plasmid is ensured in part by the HigBA toxin-antitoxin system.
3  the repression complex in contrast to other toxin-antitoxin systems.
4 etween persister frequency and the number of toxin-antitoxin systems.
5  including acting as antitoxic components in toxin-antitoxin systems.
6 s and regulatory sequences-encode functional toxin-antitoxin systems.
7 is genome harbors a striking number (>40) of toxin-antitoxin systems.
8 n, genetic phase variation and activation of toxin/antitoxin systems.
9                                    In type I toxin-antitoxin systems, a small RNA acts as an antitoxi
10 romotes the expansion and diversification of toxin-antitoxin systems and other paralogous protein fam
11  to population dynamics for a large class of toxin-antitoxin systems and suggests answers to several
12 systems, such as restriction-modification or toxin-antitoxin systems, and qualitative, including the
13    Three homologues of the plasmid RK2 ParDE toxin-antitoxin system are present in the Vibrio cholera
14        This study shows that active Type III toxin-antitoxin systems are far more diverse than previo
15                          In prokaryotes, the toxin-antitoxin systems are thought to play important ro
16                                              Toxin-antitoxin systems are ubiquitous and have been imp
17                                              Toxin-antitoxin systems are ubiquitous in nature and pre
18                                              Toxin-antitoxin systems are ubiquitous in prokaryotic an
19                                              Toxin-antitoxin systems are widespread in bacteria and a
20                                     Multiple toxin-antitoxin systems can be cooperatively marshaled f
21                   Loss of GmvAT and a second toxin-antitoxin system, CcdAB, from pINV reduces S. sonn
22                                The bacterial toxin-antitoxin system CcdB-CcdA provides a mechanism fo
23 thetical, but thousands were associated with toxin-antitoxin systems, DNA repair, cell membrane funct
24                  As is characteristic of all toxin-antitoxin systems, each of the mazF-mt toxin genes
25                                          The toxin-antitoxin system eliminates plasmid-free cells tha
26             The recently discovered Type III toxin-antitoxin systems encode protein toxins that are i
27   The P1 plasmid addiction operon (a classic toxin-antitoxin system) encodes Phd, an unstable 73-amin
28 s a bacterial toxin encoded by the yefM-yoeB toxin-antitoxin system found in various bacterial genome
29 oxin component of the Escherichia coli RelBE toxin-antitoxin system has been extensively studied in v
30  toxin from bacteriophage P1 (of the phd-doc toxin-antitoxin system) has served as a model for the fa
31                                              Toxin-antitoxin systems have been divided into three typ
32 he role and regulation of this operon, since toxin-antitoxin systems have been suggested to play a pa
33 om a co-residing plasmid encoding a putative toxin-antitoxin system; iii) a mutation in the host's gl
34 e of Molecular Cell, Aarke et al. identify a toxin-antitoxin system in Caulobacter crescentus that ac
35 ce-specific endoribonucleases encoded by the toxin-antitoxin systems in the bacterial genomes.
36  P1 plasmid addiction operon, a prototypical toxin-antitoxin system, is negatively autoregulated by t
37                                     GmvAT, a toxin-antitoxin system, is responsible for the differenc
38 n is distinct from the majority derived from toxin-antitoxin systems: it does not cleave RNA; in fact
39                     BsrE/SR5 is a new type I toxin/antitoxin system located on the prophage-like regi
40                           MazEF is a type II toxin-antitoxin system present on the chromosome of Esch
41                  The generic architecture of toxin-antitoxin systems provides the potential for bista
42                                  In type III toxin-antitoxin systems, small processed RNAs directly a
43                                              Toxin-antitoxin systems (TAS) are abundant, diverse, hor
44              Lastly, we describe the role of toxin-antitoxin systems (TAS) in the induction of the VB
45                            Additionally, the toxin/antitoxin systems that we investigated (MqsR, MazF
46 an operon that also has characteristics of a toxin-antitoxin system, thus joining several enigmatic f
47 e-Txe is one of the first functional proteic toxin-antitoxin systems to be accurately described for G
48                              Using bacterial toxin-antitoxin systems, we demonstrate the plausibility
49                     To discover novel type I toxin-antitoxin systems, we developed a set of search pa
50                                      Plasmid toxin-antitoxin systems, which kill daughter cells that

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