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1  Blood cultures were positive for Klebsiella oxytoca.
2 yclodextrin-specific channel from Klebsiella oxytoca.
3 either Rhodobacter sphaeroides or Klebsiella oxytoca.
4  coli, Klebsiella pneumoniae, and Klebsiella oxytoca.
5  was discovered in both K. pneumoniae and K. oxytoca.
6 d klebicin D gene cluster was detected in K. oxytoca.
7  coli, Klebsiella pneumoniae, and Klebsiella oxytoca.
8 ce of nitrogenase activity than that from K. oxytoca.
9 involved in pullulanase export in Klebsiella oxytoca.
10 g isolates of E. coli, K. pneumoniae, and K. oxytoca.
11 nd Cas12a in Escherichia coli and Klebsiella oxytoca.
12                                       The K. oxytoca 11492-1 draft genome contains multiple antibioti
13 bacter spp., 23/24 with E. coli, 2/3 with K. oxytoca, 16/17 with K. pneumoniae, and 0/1 with Proteus
14 (4.3%), Proteus mirabilis (4.0%), Klebsiella oxytoca (2.7%), and Citrobacter freundii (2.0%).
15 i (69), Klebsiella aerogenes (4), Klebsiella oxytoca (3), Klebsiella pneumoniae (29), Proteus mirabil
16 koseri, 9 Citrobacter freundii, 8 Klebsiella oxytoca, 5 Klebsiella aerogenes, 3 Providencia stuartii,
17 6%), Klebsiella pneumoniae (14%), Klebsiella oxytoca (6%), Salmonella spp. (6%), Acinetobacter bauman
18 tections exceeded 96%, except for Klebsiella oxytoca (92.2%), which achieved 98.3% sensitivity after
19 0%; Klebsiella pneumoniae, 92.9%; Klebsiella oxytoca, 95.5%; Enterobacter spp., 99.3%; Pseudomonas ae
20  naturally processed peptide from Klebsiella oxytoca acts as a superagonist for autoreactive T cells
21        In a supplemental study of Klebsiella oxytoca, an organism possessing a chromosomal beta-lacta
22 d that 72% of Klebsiella sp. were Klebsiella oxytoca and 8.7% were K. planticola.
23  for all Klebsiella pneumoniae or Klebsiella oxytoca and E. coli isolates screened and confirmed as E
24 reases in common NICU organisms including K. oxytoca and E. faecalis and increases in common adult or
25  is associated frequently with strains of K. oxytoca and rarely with strains of K. pneumoniae.
26 des ovatus , Kluyvera georgiana , Klebsiella oxytoca , and Enterococcus faecium , with lower levels o
27 lla pneumoniae, Escherichia coli, Klebsiella oxytoca, and Citrobacter freundii.
28 idermidis, Klebsiella pneumoniae, Klebsiella oxytoca, and Clostridioides difficile.
29 ella quintana, Shigella flexneri, Klebsiella oxytoca, and Cryptococcus neoformans.
30 f ESBLs in Klebsiella pneumoniae, Klebsiella oxytoca, and Escherichia coli.
31 o metabolize tryptophan (E. coli, Klebsiella oxytoca, and Haemophilus influenzae) were grouped and fo
32 or prevalent in clinical lung isolates of K. oxytoca, and leupeptin-derived pyrazinone biosynthesis.
33 chia coli, Klebsiella pneumoniae, Klebsiella oxytoca, and Proteus mirabilis isolates, including pheno
34 chia coli, Klebsiella pneumoniae, Klebsiella oxytoca, and Proteus mirabilis with an ertapenem-suscept
35 e species, Klebsiella pneumoniae, Klebsiella oxytoca, and Providencia alcalifaciens, all members of t
36  Our results show that these reactions in K. oxytoca are catalyzed by a two-component oxygenase (HpxE
37 olated and identified a toxin produced by K. oxytoca as the pyrrolobenzodiazepine tilivalline and dem
38 d the plant-associated diazotroph Klebsiella oxytoca at 23 degrees C, but not at 30 degrees C.
39 ost common, and of hyperproduction of the K. oxytoca beta-lactamase, a situation which engenders a le
40 against Klebsiella pneumoniae and Klebsiella oxytoca, both in liquid in vitro culture and an in vivo
41 nally discovered in the bacterium Klebsiella oxytoca, but it has recently been shown that mammalian A
42                                   Klebsiella oxytoca can assimilate nitrate and nitrite by using enzy
43                                   Klebsiella oxytoca can use nitrate and nitrite as sole nitrogen sou
44 chia coli, Klebsiella pneumoniae, Klebsiella oxytoca, Citrobacter koseri, Citrobacter freundii group,
45 HC) caused by intestinal resident Klebsiella oxytoca Colitogenic strains produce the nonribosomal pep
46  Hungatella hathewayi to pathogen Klebsiella oxytoca, crossing phyla simultaneously.
47 terspecies variation, with C. farmeri and K. oxytoca displaying the highest plasmid loads.
48 guingly, the OM protein CymA from Klebsiella oxytoca does not depend on TonB but nevertheless mediate
49 vel GES-5-encoding plasmid was present in K. oxytoca,E. coli and E. cloacae isolates from unlinked pa
50 urally relevant gene cluster from Klebsiella oxytoca encoding the nitrogen fixation pathway for conve
51                                In Klebsiella oxytoca, enzymes required for nitrate assimilation are e
52 d the major pseudopilin GspG from Klebsiella oxytoca: EpsH contains a large beta-sheet in the variabl
53 vel GES-5-encoding plasmid was present in K. oxytoca, Escherichia coli, and Enterobacter cloacae isol
54 cal isolates of K. pneumoniae and Klebsiella oxytoca for the presence of bla(KPC) genes.
55 anisms beyond E. coli, K. pneumoniae, and K. oxytoca Future molecular diagnostic panels would benefit
56 ts, Hcp1, is required for killing Klebsiella oxytoca in vitro and that this activity is mediated by t
57 er a GES-5 carbapenemase-positive Klebsiella oxytoca infection was identified by whole genome sequenc
58 um (GES)-5 carbapenemase-positive Klebsiella oxytoca infection was identified by whole-genome sequenc
59                                   Klebsiella oxytoca is a gram-negative bacterium found in fecal micr
60                     Finally, we show that K. oxytoca is killed in the host gut in an Hcp1-dependent m
61     The identification of the first GES-5 K. oxytoca isolate was delayed, being identified by WGS.
62     The identification of the first GES-5 K. oxytoca isolate was delayed, being identified on WGS.
63  tested an additional 43 stock strains of K. oxytoca isolated from newborns by using eight biochemica
64 linical isolates (39 K. pneumoniae and 30 K. oxytoca isolates).
65 r cloacae, Enterococcus faecalis, Klebsiella oxytoca, Klebsiella pneumoniae, and Staphylococcus aureu
66 te positive for Escherichia coli, Klebsiella oxytoca, Klebsiella pneumoniae, or Proteus mirabilis and
67 , Escherichia coli/Shigella spp., Klebsiella oxytoca, Klebsiella pneumoniae, Proteus spp., Pseudomona
68 leotide sequence of the 51,601-bp Klebsiella oxytoca linear plasmid pKO2, and we demonstrate experime
69  (3%), P. aeruginosa (2%), E. coli (<1%), K. oxytoca (&lt;1%), and S. marcescens (<1%).
70 combinants of Escherichia coli B, Klebsiella oxytoca M5A1, and Erwinia chrysanthemi EC16.
71 rformed with either panel and isolates of K. oxytoca, MICs of ceftazidime, cefotaxime, and ceftizoxim
72 ), Enterobacter cloacae (n = 23), Klebsiella oxytoca (n = 8), Serratia marcescens (n = 6), Citrobacte
73 ed the corresponding positions of Klebsiella oxytoca NasR to site-directed alanine substitutions and
74 it the modularity of a refactored Klebsiella oxytoca nitrogen fixation (nif) gene cluster (16 genes,
75 model for a T2SS pseudopilus from Klebsiella oxytoca, obtained by fitting the NMR structure of its ca
76 chia coli, Klebsiella pneumoniae, Klebsiella oxytoca, or Proteus mirabilis at >=50 000 colony-forming
77  Escherichia coli, Klebsiella pneumoniae, K. oxytoca, or Proteus mirabilis at >=50,000 CFU/mL, (2) id
78 chia coli, Klebsiella pneumoniae, Klebsiella oxytoca, or Proteus mirabilis BSI from a urinary source
79 re of the protelomerase TelK from Klebsiella oxytoca phage varphiKO2, in complex with the palindromic
80                                In Klebsiella oxytoca (pneumoniae), enzymes required for nitrate assim
81 cal in amino acid sequence to the Klebsiella oxytoca propanediol dehydratase; this is a much higher i
82 lly includes type II systems from Klebsiella oxytoca (pul), Erwinia chrysanthemi and carotovora (out)
83             Thus, several enzymes in this K. oxytoca purine utilization pathway differ from those in
84        Here, we characterized a family of K. oxytoca pyrazine and pyrazinone autoinducers and explore
85 lates of Citrobacter freundii and Klebsiella oxytoca recovered from different patients in a Michigan
86 ergrowth of the enteric bacterium Klebsiella oxytoca results in antibiotic-associated hemorrhagic col
87 marily Enterobacter roggenkampii, Klebsiella oxytoca, Serratia marcescens, and Citrobacter farmeri.
88 rains of Clostridium perfringens, Klebsiella oxytoca, Staphylococcus aureus, and Bacteroides fragilis
89                                   Klebsiella oxytoca strain 11492-1 was isolated from a perianal swab
90 ySENI and StySGI R-M systems from Klebsiella oxytoca strain M5a1, Salmonella eastbourne, Salmonella e
91                          Virulent Klebsiella oxytoca strains are associated with gut and lung patholo
92 re effective at killing K. pneumoniae and K. oxytoca strains compared with monophage treatments.
93 lineates distinct autoinducer pathways in K. oxytoca that may have differential effects on bacterial
94 omplex, Klebsiella pneumoniae, or Klebsiella oxytoca that were recovered from sterile-site or urine c
95                                In Klebsiella oxytoca, the pathway was enriched in clinical isolates a
96  coli, Klebsiella pneumoniae, and Klebsiella oxytoca, there is an ever-increasing prevalence of beta-
97  present here a case of colitis caused by K. oxytoca toxin-producing strains that evolved in chronic
98 ulE-K putative pilin genes of the Klebsiella oxytoca type II secretion system with the complete comG
99               The enterobacterium Klebsiella oxytoca uses a variety of inorganic and organic nitrogen
100 luster of 11 patients with GES-5-positive K. oxytoca was identified over 18 weeks in the same hospita
101 luster of 11 patients with GES-5-positive K. oxytoca was identified over 18 weeks in the same hospita
102 six isolates of Klebsiella pneumoniae and K. oxytoca were recovered from wild mammals in Australia.
103 milar to the pseudopilin found in Klebsiella oxytoca, while PilA2 is more similar to true pilins foun

 
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