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1 Escherichia coli, Klebsiella pneumoniae, and Klebsiella oxytoca.
2 excluded E. coli, Klebsiella pneumoniae, and Klebsiella oxytoca.
3 seudopilin involved in pullulanase export in Klebsiella oxytoca.
4 h CymA, a cyclodextrin-specific channel from Klebsiella oxytoca.
5 altophilia (4.3%), Proteus mirabilis (4.0%), Klebsiella oxytoca (2.7%), and Citrobacter freundii (2.0
6 l target detections exceeded 96%, except for Klebsiella oxytoca (92.2%), which achieved 98.3% sensiti
7 ia coli, 100%; Klebsiella pneumoniae, 92.9%; Klebsiella oxytoca, 95.5%; Enterobacter spp., 99.3%; Pse
10 le, results for all Klebsiella pneumoniae or Klebsiella oxytoca and E. coli isolates screened and con
14 of Escherichia coli, Klebsiella pneumoniae, Klebsiella oxytoca, and Proteus mirabilis isolates, incl
15 of Escherichia coli, Klebsiella pneumoniae, Klebsiella oxytoca, and Proteus mirabilis with an ertape
16 D was originally discovered in the bacterium Klebsiella oxytoca, but it has recently been shown that
19 of Escherichia coli, Klebsiella pneumoniae, Klebsiella oxytoca, Citrobacter koseri, Citrobacter freu
21 an agriculturally relevant gene cluster from Klebsiella oxytoca encoding the nitrogen fixation pathwa
23 lin EpsH and the major pseudopilin GspG from Klebsiella oxytoca: EpsH contains a large beta-sheet in
24 creen clinical isolates of K. pneumoniae and Klebsiella oxytoca for the presence of bla(KPC) genes.
25 tube subunits, Hcp1, is required for killing Klebsiella oxytoca in vitro and that this activity is me
26 Enterobacter cloacae, Enterococcus faecalis, Klebsiella oxytoca, Klebsiella pneumoniae, and Staphyloc
27 bacter spp., Escherichia coli/Shigella spp., Klebsiella oxytoca, Klebsiella pneumoniae, Proteus spp.,
28 omplete nucleotide sequence of the 51,601-bp Klebsiella oxytoca linear plasmid pKO2, and we demonstra
29 ologenic recombinants of Escherichia coli B, Klebsiella oxytoca M5A1, and Erwinia chrysanthemi EC16.
30 We exploit the modularity of a refactored Klebsiella oxytoca nitrogen fixation (nif) gene cluster
31 an atomic model for a T2SS pseudopilus from Klebsiella oxytoca, obtained by fitting the NMR structur
32 tal structure of the protelomerase TelK from Klebsiella oxytoca phage varphiKO2, in complex with the
34 98% identical in amino acid sequence to the Klebsiella oxytoca propanediol dehydratase; this is a mu
35 current tally includes type II systems from Klebsiella oxytoca (pul), Erwinia chrysanthemi and carot
36 sistant isolates of Citrobacter freundii and Klebsiella oxytoca recovered from different patients in
37 ts rapid overgrowth of the enteric bacterium Klebsiella oxytoca results in antibiotic-associated hemo
38 oxigenic strains of Clostridium perfringens, Klebsiella oxytoca, Staphylococcus aureus, and Bacteroid
40 StySEAI, StySENI and StySGI R-M systems from Klebsiella oxytoca strain M5a1, Salmonella eastbourne, S
41 r cloacae complex, Klebsiella pneumoniae, or Klebsiella oxytoca that were recovered from sterile-site
42 Escherichia coli, Klebsiella pneumoniae, and Klebsiella oxytoca, there is an ever-increasing prevalen
43 acing the pulE-K putative pilin genes of the Klebsiella oxytoca type II secretion system with the com
45 PilA1 is similar to the pseudopilin found in Klebsiella oxytoca, while PilA2 is more similar to true
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