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1 ee datasets comprising approximately 250,000 enterohemorrhagic E. coli (EHEC), generic E. coli, and S
2 coli (2.4%), enteroinvasive E. coli (1.2%), enterohemorrhagic E. coli (0.6%), enteroaggregative E. c
7 inase C-zeta by enteropathogenic E. coli and enterohemorrhagic E. coli may in part explain the less p
8 hogens enteropathogenic Escherichia coli and enterohemorrhagic E. coli, adheres to the apical membran
11 Escherichia coli strains (enteroinvasive and enterohemorrhagic E. coli) show low survival whether inc
12 ll as enterotoxigenic, enteropathogenic, and enterohemorrhagic E. coli strains, behaved like avirulen
13 d effacing effect characteristic of EPEC and enterohemorrhagic E. coli and has been posited to play s
14 rains of enteropathogenic E. coli (EPEC) and enterohemorrhagic E. coli (EHEC) and in 6 strains origin
15 Enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli (EHEC) are related intestinal
16 enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli (EHEC) is incompletely underst
17 enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli (EHEC) might contribute to hos
18 Enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli (EHEC) possess a filamentous t
19 Enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli are extracellular pathogens th
20 enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli employ a type 3 secretion syst
21 Enteropathogenic Escherichia coli (EPEC) and enterohemorrhagic E. coli O157:H7 (EHEC) form characteri
22 E. coli K-12, EPEC serotypes H6 and H34, and enterohemorrhagic E. coli serotype H7 all induced IL-8 r
24 Escherichia coli, Citrobacter rodentium, and enterohemorrhagic E. coli (EHEC) O157:H7 that mediate at
26 infant diarrhea in the developing world, and enterohemorrhagic E. coli (EHEC), which has caused large
28 timin is regulated by quorum sensing in both enterohemorrhagic E. coli and enteropathogenic E. coli.
30 kinase C-zeta enzyme activity stimulated by enterohemorrhagic E. coli was transient and minor, and p
31 Stx)-producing Escherichia coli, also called enterohemorrhagic E. coli (EHEC), are important food-bor
32 A three-way genome comparison of the CFT073, enterohemorrhagic E. coli EDL933, and laboratory strain
34 E. coli, including enteropathogenic E. coli, enterohemorrhagic E. coli, enterotoxigenic E. coli, and
37 strains can be further classified as either enterohemorrhagic E. coli (EHEC), typical enteropathogen
38 of enteropathogenic Escherichia coli (EPEC), enterohemorrhagic E. coli (EHEC) and Citrobacter rodenti
40 ein also functions as an adhesion factor for enterohemorrhagic E. coli (EHEC) and Shiga toxin-produci
41 spC from enteropathogenic E. coli, EspP from enterohemorrhagic E. coli, Sat from uropathogenic E. col
43 Shiga toxin in the highly pathogenic O157:H7 enterohemorrhagic E. coli strain, also carries a gene en
44 cherichia coli (EPEC), human EPEC, and human enterohemorrhagic E. coli (EHEC) strains, identified cro
46 that an unidentified trans-acting factor in enterohemorrhagic E. coli (EHEC) is responsible for this
47 the toxin-induced renal injury occurring in enterohemorrhagic E. coli infection remains undefined.
48 ked other characteristics usually present in enterohemorrhagic E. coli constituted 8.4% of the isolat
49 species of Gram-negative bacteria, including enterohemorrhagic E. coli (EHEC), and as it is essential
50 se virulence in several pathogens, including enterohemorrhagic E. coli The mechanisms that allow path
54 gene profile was similar to the profiles of enterohemorrhagic E. coli (EHEC) clones of E. coli: it i
57 yers infected by enteropathogenic E. coli or enterohemorrhagic E. coli were used for these studies.
58 erence of Escherichia coli O157:H7 and other enterohemorrhagic E. coli (EHEC) strains to intestinal e
59 med that the related LEE-containing pathogen enterohemorrhagic E. coli (EHEC) lacks PerC-dependent ac
60 y enzyme immunoassay (EIA) (ImmunoCard STAT! enterohemorrhagic E. coli [EHEC]; Meridian Bioscience) a
62 urella haemolytica leukotoxin (LktA) and the enterohemorrhagic E. coli toxin (EhxA), were also examin
63 , katP, and espP, were acquired later by the enterohemorrhagic E. coli 1 complex in a stepwise manner
64 ion of virulence genes characteristic of the enterohemorrhagic E. coli, including intimin, translocat
67 ding uropathogenic E. coli CFT073 and UTI89, enterohemorrhagic E. coli O157:H7, and enterotoxigenic E
70 ) is clinically most closely associated with enterohemorrhagic E. coli O157:H7-mediated hemorrhagic c
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