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1 em, which is restricted to EI Tor biotype of Vibrio cholerae O1.
2 ed two novel non-toxigenic (ctxA/B-negative) Vibrio cholerae O1.
3 spected cases who tested positive to PCR for Vibrio cholerae O1.
4 ubunit of cholera toxin from classical Inaba Vibrio cholerae O1 569B; the strain also contains a merc
5 s of such infamous Gram-negative bacteria as Vibrio cholerae O1 and Escherichia coli O157:H7.
6 eal infection with certain pathogens such as Vibrio cholerae O1 and norovirus.
7  all cases of laboratory-confirmed toxigenic Vibrio cholerae O1 and O139 infection reported to the Ce
8 lus that is expressed by epidemic strains of Vibrio cholerae O1 and O139, is required for colonizatio
9                           From 2000 to 2012, Vibrio cholerae O1 and Shigella species isolates from ur
10 ulted in lower vibriocidal responses against Vibrio cholerae O1, and there was a positive relationshi
11 oled, adsorbed against in vitro-grown El Tor Vibrio cholerae O1, and used to probe a genomic expressi
12                          Epidemic strains of Vibrio cholerae O1 are divided into two biotypes, classi
13                                              Vibrio cholerae O1, biotype El Tor, accumulates inorgani
14                 The rugose colony variant of Vibrio cholerae O1, biotype El Tor, is shown to produce
15 cid sequence encoded by the VC1216 gene from Vibrio cholerae O1 biovar El Tor str.
16  important in selected sites (eg, Aeromonas, Vibrio cholerae O1, Campylobacter jejuni).
17 r advance.PXVX0200, based on live attenuated Vibrio cholerae O1 classical Inaba vaccine strain CVD 10
18 annose-sensitive hemagglutinin (MSHA) of the Vibrio cholerae O1 El Tor biotype is a member of the fam
19 utinin (MSHA) to the colonization ability of Vibrio cholerae O1 El Tor biotype strains and O139 Benga
20  phage VP5, one of the typing phages for the Vibrio cholerae O1 El Tor biotype.
21  live attenuated oral vaccine derived from a Vibrio cholerae O1 El Tor Inaba strain by a series of de
22 e it by examining the virulence phenotype of Vibrio cholerae O1 El Tor N16961.
23               The rugose colonial variant of Vibrio cholerae O1 El Tor produces an exopolysaccharide
24  investigated the transcriptional profile of Vibrio cholerae O1 El Tor strain C6706 under virulence g
25                                              Vibrio cholerae O1 El Tor strains have been responsible
26                    Volunteer challenges with Vibrio cholerae O1, enterotoxigenic Escherichia coli (ET
27                                              Vibrio cholerae O1 expresses a variety of cell surface f
28 e production of several virulence factors in Vibrio cholerae O1, including cholera toxin and the pilu
29 ing in an area in which at least one case of Vibrio cholerae O1 infection had been confirmed by cultu
30  symptomatic cholera, we estimated an annual Vibrio cholerae O1 infection incidence rate of 535 per 1
31                                              Vibrio cholerae O1 is a major cause of acute watery diar
32                                 Isolation of Vibrio cholerae O1 is necessary for cholera outbreak con
33                       Systematic testing for Vibrio cholerae O1 is rare, which means that the world's
34               We used genomic data from 1070 Vibrio cholerae O1 isolates, across 45 African countries
35 s, 73 (30%) Campylobacter isolates, 45 (18%) Vibrio cholerae O1 isolates, and 33 (14%) Salmonella iso
36  antibodies to the surface polysaccharide of Vibrio cholerae O1 (lipopolysaccharide) and of Vibrio ch
37                               The genomes of Vibrio cholerae O1 Matlab variant MJ-1236, Mozambique O1
38      This study evaluates the concordance of Vibrio cholerae O1/O139 detection from presumptive colon
39 odulates biofilm development and motility in Vibrio cholerae O1 of the classical biotype.
40                    It is caused by toxigenic Vibrio cholerae O1 or O139 bacteria.
41 ess of humans caused by toxigenic strains of Vibrio cholerae O1 or O139.
42 ss, and ecological interactions of toxigenic Vibrio cholerae O1 populations in two distinctive habita
43   From these isolates, we generated 44 whole Vibrio cholerae O1 sequences and analyzed them in the co
44 red between 1817 and 1923 and were caused by Vibrio cholerae O1 serogroup strains of the classical bi
45 ine-treated lipopolysaccharide (DeALPS) from Vibrio cholerae O1, serotype Inaba, to cholera toxin (CT
46                                              Vibrio cholerae O1, serotype Inaba, was the predominant
47  epitope of the O-specific polysaccharide of Vibrio cholerae O1, serotype Ogawa, were conjugated to b
48  pandemic that started in 1961 was caused by Vibrio cholerae O1 strains of the El Tor biotype.
49                               A total of 720 Vibrio cholerae O1 strains were recovered for investigat
50 igens of some Gram-negative bacteria such as Vibrio cholerae O1 (the causative agent of cholera) or E
51 a toxin and the toxin coregulated pilus, the Vibrio cholerae O1 virulence determinants having the lar
52 ntibodies and vibriocidal antibodies against Vibrio cholerae O1 were assessed using microneutralizati
53 between the classical and El Tor biotypes of Vibrio cholerae O1 were determined under conditions that
54  rapid, sensitive and selective detection of Vibrio cholerae O1 which converts the antibody-antigen b
55 g frame with significant homology to rfbE of Vibrio cholerae O1, which is postulated to encode perosa
56 dministration of the cholera vaccine (killed Vibrio cholerae O1 whole cells and recombinant cholera t