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1 asmid R485, which originates from Morganella morganii.
2 ve high-risk clones of M morganii subspecies morganii.
3 ced by the CRC-associated species Morganella morganii.
4 ded spectrum beta-lactamases) and Morganella morganii.
5 abilis, Providencia stuartii, and Morganella morganii.
8 resent the first reported case of Morganella morganii and Enterococcus faecalis endophthalmitis after
9 endophthalmitis due to concurrent Morganella morganii and Enterococcus faecalis infections can have v
10 olitica, Serratia marcescens, and Morganella morganii) and two nonenteric members of the gamma subdiv
11 ubspecies sibonii, and M morganii subspecies morganii, and a core genome maximum likelihood phylogene
12 chrotolerans, Morganella sibonii, Morganella morganii, and a new species represented by a unique envi
14 read plates of Escherichia coli, Morganella morganii, and Pseudomonas aeruginosa containing 12 antib
16 am-negative (Escherichia coli and Morganella morganii) bacteria, as assessed by survival, body weight
20 is rare, and no previous case of Morganella morganii endophthalmitis after intravitreal injection ha
22 nection between the prevalence of Morganella morganii in the gut microbiome and the incidence of majo
24 es, 3 Providencia stuartii, and 2 Morganella morganii) included 25% extended-spectrum beta-lactamase
25 kelihood phylogenetic tree showed that the M morganii isolates can be separated into four subpopulati
27 netically modified to express the Morganella morganii (M morganii)-derived HDC gene (E coli BL21_HTW)
29 a coli, Providencia stuartii, and Morganella morganii P. mirabilis infections are particularly challe
30 up designations for 73 strains of Morganella morganii principally recovered from routine clinical spe
31 lines, but four of seven M. morganii subsp. morganii strains were cytotoxic on sheets of both cells.
33 on, 90% of all strains were identified as M. morganii subsp. morganii (trehalose negative), while the
34 p-2 or Vero cell lines, but four of seven M. morganii subsp. morganii strains were cytotoxic on sheet
36 negative [LDC-]) predominating (78%); all M. morganii subsp. sibonii strains were found to belong to
38 se that M morganii include two subspecies: M morganii subspecies morganii (the most prevalent) and M
39 organella morganii subspecies sibonii, and M morganii subspecies morganii, and a core genome maximum
41 oups: Morganella psychrotolerans, Morganella morganii subspecies sibonii, and M morganii subspecies m
42 3.0 for Y. enterocolitica and pH 5.5 for M. morganii, suggesting that in vivo activation occurs as a
43 -negative bacteria indicated that Morganella morganii survives in acidic conditions but Escherichia c
45 nclude two subspecies: M morganii subspecies morganii (the most prevalent) and M morganii subspecies
46 r colonization with SFB on the ability of M. morganii to translocate to the spleen and mesenteric lym
47 d with a gram-negative commensal, Morganella morganii, to determine if the mucosal immune system was
48 trains were identified as M. morganii subsp. morganii (trehalose negative), while the remaining 10% w
49 DNA sequence analysis of portions of the M. morganii ure locus showed that the predicted primary str
50 e properties of the Y. enterocolitica and M. morganii ureases since the L. fermentum urease also has
51 e demonstrated that Y. enterocolitica and M. morganii ureases were activated in vitro by low pH with
52 orm of a thiophene motif, whereas Morganella morganii used a cascade reaction to incorporate amino-ac
54 e report the first synthesis of a Morganella morganii ZPS repeating unit as an enabling tool in the s