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1 ded spectrum beta-lactamases) and Morganella morganii.
2 abilis, Providencia stuartii, and Morganella morganii.
3 asmid R485, which originates from Morganella morganii.
4 olitica, Serratia marcescens, and Morganella morganii) and two nonenteric members of the gamma subdiv
6 read plates of Escherichia coli, Morganella morganii, and Pseudomonas aeruginosa containing 12 antib
7 am-negative (Escherichia coli and Morganella morganii) bacteria, as assessed by survival, body weight
12 up designations for 73 strains of Morganella morganii principally recovered from routine clinical spe
13 lines, but four of seven M. morganii subsp. morganii strains were cytotoxic on sheets of both cells.
14 on, 90% of all strains were identified as M. morganii subsp. morganii (trehalose negative), while the
15 p-2 or Vero cell lines, but four of seven M. morganii subsp. morganii strains were cytotoxic on sheet
17 negative [LDC-]) predominating (78%); all M. morganii subsp. sibonii strains were found to belong to
18 3.0 for Y. enterocolitica and pH 5.5 for M. morganii, suggesting that in vivo activation occurs as a
19 -negative bacteria indicated that Morganella morganii survives in acidic conditions but Escherichia c
20 r colonization with SFB on the ability of M. morganii to translocate to the spleen and mesenteric lym
21 d with a gram-negative commensal, Morganella morganii, to determine if the mucosal immune system was
22 trains were identified as M. morganii subsp. morganii (trehalose negative), while the remaining 10% w
23 DNA sequence analysis of portions of the M. morganii ure locus showed that the predicted primary str
24 e properties of the Y. enterocolitica and M. morganii ureases since the L. fermentum urease also has
25 e demonstrated that Y. enterocolitica and M. morganii ureases were activated in vitro by low pH with
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