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1 reports connecting quorum sensing to TTS in enterohemorrhagic and enteropathogenic Escherichia coli
2 protein required for intimate attachment of enterohemorrhagic and enteropathogenic Escherichia coli
6 hanisms for enterotoxigenic, enteroadherent, enterohemorrhagic, and enteroinvasive Escherichia coli.
9 coli (2.4%), enteroinvasive E. coli (1.2%), enterohemorrhagic E. coli (0.6%), enteroaggregative E. c
11 of enteropathogenic Escherichia coli (EPEC), enterohemorrhagic E. coli (EHEC) and Citrobacter rodenti
12 rains of enteropathogenic E. coli (EPEC) and enterohemorrhagic E. coli (EHEC) and in 6 strains origin
13 ein also functions as an adhesion factor for enterohemorrhagic E. coli (EHEC) and Shiga toxin-produci
15 Enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli (EHEC) are related intestinal
17 gene profile was similar to the profiles of enterohemorrhagic E. coli (EHEC) clones of E. coli: it i
19 enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli (EHEC) is incompletely underst
20 that an unidentified trans-acting factor in enterohemorrhagic E. coli (EHEC) is responsible for this
21 med that the related LEE-containing pathogen enterohemorrhagic E. coli (EHEC) lacks PerC-dependent ac
23 enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli (EHEC) might contribute to hos
24 Escherichia coli, Citrobacter rodentium, and enterohemorrhagic E. coli (EHEC) O157:H7 that mediate at
25 Enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli (EHEC) possess a filamentous t
28 erence of Escherichia coli O157:H7 and other enterohemorrhagic E. coli (EHEC) strains to intestinal e
29 cherichia coli (EPEC), human EPEC, and human enterohemorrhagic E. coli (EHEC) strains, identified cro
31 species of Gram-negative bacteria, including enterohemorrhagic E. coli (EHEC), and as it is essential
32 Stx)-producing Escherichia coli, also called enterohemorrhagic E. coli (EHEC), are important food-bor
34 ee datasets comprising approximately 250,000 enterohemorrhagic E. coli (EHEC), generic E. coli, and S
35 strains can be further classified as either enterohemorrhagic E. coli (EHEC), typical enteropathogen
36 infant diarrhea in the developing world, and enterohemorrhagic E. coli (EHEC), which has caused large
40 , katP, and espP, were acquired later by the enterohemorrhagic E. coli 1 complex in a stepwise manner
41 cluding enteropathogenic E. coli 2 (EPEC 2), enterohemorrhagic E. coli 2 (EHEC 2), and EHEC-O121.
42 y enzyme immunoassay (EIA) (ImmunoCard STAT! enterohemorrhagic E. coli [EHEC]; Meridian Bioscience) a
43 timin is regulated by quorum sensing in both enterohemorrhagic E. coli and enteropathogenic E. coli.
44 d effacing effect characteristic of EPEC and enterohemorrhagic E. coli and has been posited to play s
45 Enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli are extracellular pathogens th
47 ked other characteristics usually present in enterohemorrhagic E. coli constituted 8.4% of the isolat
48 A three-way genome comparison of the CFT073, enterohemorrhagic E. coli EDL933, and laboratory strain
50 enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli employ a type 3 secretion syst
52 the toxin-induced renal injury occurring in enterohemorrhagic E. coli infection remains undefined.
55 inase C-zeta by enteropathogenic E. coli and enterohemorrhagic E. coli may in part explain the less p
58 Enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli O157:H7 (EHEC) form characteri
59 ding uropathogenic E. coli CFT073 and UTI89, enterohemorrhagic E. coli O157:H7, and enterotoxigenic E
60 ) is clinically most closely associated with enterohemorrhagic E. coli O157:H7-mediated hemorrhagic c
62 E. coli K-12, EPEC serotypes H6 and H34, and enterohemorrhagic E. coli serotype H7 all induced IL-8 r
63 Shiga toxin in the highly pathogenic O157:H7 enterohemorrhagic E. coli strain, also carries a gene en
65 ll as enterotoxigenic, enteropathogenic, and enterohemorrhagic E. coli strains, behaved like avirulen
66 se virulence in several pathogens, including enterohemorrhagic E. coli The mechanisms that allow path
68 urella haemolytica leukotoxin (LktA) and the enterohemorrhagic E. coli toxin (EhxA), were also examin
70 kinase C-zeta enzyme activity stimulated by enterohemorrhagic E. coli was transient and minor, and p
71 yers infected by enteropathogenic E. coli or enterohemorrhagic E. coli were used for these studies.
72 Escherichia coli strains (enteroinvasive and enterohemorrhagic E. coli) show low survival whether inc
74 hogens enteropathogenic Escherichia coli and enterohemorrhagic E. coli, adheres to the apical membran
77 E. coli, including enteropathogenic E. coli, enterohemorrhagic E. coli, enterotoxigenic E. coli, and
78 ion of virulence genes characteristic of the enterohemorrhagic E. coli, including intimin, translocat
79 spC from enteropathogenic E. coli, EspP from enterohemorrhagic E. coli, Sat from uropathogenic E. col
87 -based PCR assay was evaluated using various enterohemorrhagic (EHEC) and Shiga-like toxin-producing
89 ion of the attaching and effacing lesions by enterohemorrhagic Escherichia coli (EHEC) and enteropath
100 s of Vibrio cholerae, Vibrio vulnificus, and enterohemorrhagic Escherichia coli (EHEC) GspG were eluc
115 ocus of enterocyte effacement (LEE) genes in enterohemorrhagic Escherichia coli (EHEC) is regulated b
116 2 Salmonella species, 39 Shigella species, 3 enterohemorrhagic Escherichia coli (EHEC) isolates, 2 Ye
117 or Shiga toxins in parallel with the Premier enterohemorrhagic Escherichia coli (EHEC) kit (Meridian
118 la, Campylobacter, and Shiga toxin-producing enterohemorrhagic Escherichia coli (EHEC) O157 in seeded
119 The StcE zinc metalloprotease is secreted by enterohemorrhagic Escherichia coli (EHEC) O157:H7 and co
124 suckling neonatal piglets are susceptible to enterohemorrhagic Escherichia coli (EHEC) O157:H7 diseas
129 pression of the long polar fimbriae (LPF) of enterohemorrhagic Escherichia coli (EHEC) O157:H7 is con
130 ing infection in the gastrointestinal tract, enterohemorrhagic Escherichia coli (EHEC) O157:H7 is exp
133 yte effacement (LEE) pathogenicity island of enterohemorrhagic Escherichia coli (EHEC) O157:H7 posses
137 important reservoir of Shiga toxin-producing enterohemorrhagic Escherichia coli (EHEC) O157:H7 strain
140 ntimin-gamma is an outer membrane protein of enterohemorrhagic Escherichia coli (EHEC) O157:H7 that i
142 operons (LEE1 through LEE4 and tir), enables enterohemorrhagic Escherichia coli (EHEC) O157:H7 to pro
143 various pathogens and specifically focus on enterohemorrhagic Escherichia coli (EHEC) O157:H7, Salmo
153 emic effects of the Shiga toxins produced by enterohemorrhagic Escherichia coli (EHEC) require toxin
163 erved among the attaching/effacing pathogens enterohemorrhagic Escherichia coli (EHEC), enteropathoge
165 airy manure containing Campylobacter jejuni, enterohemorrhagic Escherichia coli (EHEC), or Salmonella
166 n predominantly associated with infection by enterohemorrhagic Escherichia coli (EHEC), such as E. co
167 on during the course of infection, including enterohemorrhagic Escherichia coli (EHEC), which utilize
173 oded regulator (Ler) of enteropathogenic and enterohemorrhagic Escherichia coli (EPEC and EHEC) funct
174 The human pathogens enteropathogenic and enterohemorrhagic Escherichia coli (EPEC and EHEC) share
176 related human pathogens enteropathogenic and enterohemorrhagic Escherichia coli (EPEC and EHEC, respe
177 homologues of EspJ from enteropathogenic and enterohemorrhagic Escherichia coli (EPEC and EHEC, respe
178 III secretion system of enteropathogenic and enterohemorrhagic Escherichia coli (EPEC and EHEC, respe
180 for the isolation and identification of the enterohemorrhagic Escherichia coli (serotype O157:H7) in
181 tected sRNAs for three predicted toxins from enterohemorrhagic Escherichia coli and Bacillus subtilis
182 dentium is used to model the human pathogens enterohemorrhagic Escherichia coli and enteropathogenic
183 re in children, often follows infection with enterohemorrhagic Escherichia coli and is mediated by th
185 tein (RIP) related to Shiga-like toxins from enterohemorrhagic Escherichia coli and that Howardula ri
186 produced by Shigella dysenteriae type 1 and enterohemorrhagic Escherichia coli are the most common c
189 Shiga toxin 1 (Stx-1) and Stx-2 produced by enterohemorrhagic Escherichia coli cause the diarrhea-as
194 nding B subunit of verotoxin VT-1 (VTB) from enterohemorrhagic Escherichia coli in association with t
203 Intimin, the product of the eaeA gene in enterohemorrhagic Escherichia coli O157:H7 (EHEC), is re
206 briae) is one of the few adhesive factors of enterohemorrhagic Escherichia coli O157:H7 associated wi
207 ly, the effacement effector protein Tir from enterohemorrhagic Escherichia coli O157:H7 expressed in
210 y was performed to estimate the frequency of enterohemorrhagic Escherichia coli O157:H7 or O157:nonmo
211 enterocyte effacement (LEE) from EDL933, an enterohemorrhagic Escherichia coli O157:H7 serovar origi
216 ) is associated with intestinal infection by enterohemorrhagic Escherichia coli strains that produce
217 is perceived to be an important property of enterohemorrhagic Escherichia coli strains, enabling the
218 QseC is a membrane sensor kinase shown in enterohemorrhagic Escherichia coli to respond to host an
219 hesis of the AI-3 autoinducer that activates enterohemorrhagic Escherichia coli virulence genes.
220 ), one of the principal virulence factors of enterohemorrhagic Escherichia coli, is encoded by 933W,
221 However, the TTSS of enteropathogenic and enterohemorrhagic Escherichia coli, two important human
231 with a benign Escherichia coli (G58-1) or a enterohemorrhagic strain (933D) derived from O157:H7, an
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