コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 virulence of the human gut mucosal pathogen Campylobacter jejuni .
2 ed sites (eg, Aeromonas, Vibrio cholerae O1, Campylobacter jejuni).
3 involved in biosynthesis of UDP-diNAcBac in Campylobacter jejuni.
4 the human pathogens Helicobacter pylori and Campylobacter jejuni.
5 of the major human gastrointestinal pathogen Campylobacter jejuni.
6 a part of a controlled human infection with Campylobacter jejuni.
7 f the metabolic capacity and epidemiology of Campylobacter jejuni.
8 the asaccharolytic food-borne human pathogen Campylobacter jejuni.
9 variable genomic regions between strains of Campylobacter jejuni.
10 on of sigma(54)-dependent flagellar genes in Campylobacter jejuni.
11 ssion of the multidrug efflux pump CmeABC in Campylobacter jejuni.
12 ed intragastrically with increasing doses of Campylobacter jejuni.
13 promoter and coding region of the bacterium Campylobacter jejuni.
14 unosensor for the detection of food pathogen Campylobacter jejuni.
15 ectious neuropathy most frequently caused by Campylobacter jejuni.
16 with the periplasmic binding protein CeuE of Campylobacter jejuni.
17 91% for C. difficile A/B toxins; and 90% for Campylobacter jejuni.
20 We report isolation and characterization of Campylobacter jejuni 81-176 lgtF and galT lipooligosacch
23 ecent sequencing of the virulence plasmid of Campylobacter jejuni 81-176 revealed the presence of gen
27 mine whether H. pylori can transfer DNA into Campylobacter jejuni, a closely related species of the C
36 (NrfA) reductases have been investigated in Campylobacter jejuni, a microaerophilic food-borne patho
38 ereas previous endeavors have focused on the Campylobacter jejuni acetyltransferase (PglD) from the N
39 specific inhibitor of PFOR of H. pylori and Campylobacter jejuni, also inhibited NADP reduction in c
40 s used to detect the presence of cmeC in 131 Campylobacter jejuni and C. coli strains isolated from v
42 rized two FeEnt receptors (CfrA and CfrB) in Campylobacter jejuni and C. coli, the enteric human path
46 ovide routine definitive characterization of Campylobacter jejuni and Campylobacter coli for clinical
47 true but also, in fact, the clearly distinct Campylobacter jejuni and Campylobacter coli species may
48 closely related zoonotic pathogenic species, Campylobacter jejuni and Campylobacter coli, are converg
49 athogens associated with diarrhoea-including Campylobacter jejuni and Campylobacter coli, Cryptospori
51 t targets mapA and ceuE for the detection of Campylobacter jejuni and Campylobacter coli, leading glo
52 hough cdtB gene sequences were found in both Campylobacter jejuni and Campylobacter coli, the product
53 Monomeric OTases, such as the PglBs from Campylobacter jejuni and Campylobacter lari, catalyze tr
60 genes with higher sequence diversity in the Campylobacter jejuni and Neisseria meningitidis genomes
63 says demonstrate that LpxJ and homologues in Campylobacter jejuni and Wolinella succinogenes can act
64 erborne illness caused almost exclusively by Campylobacter jejuni and, to a lesser extent, by Campylo
65 of other Helicobacter species, 8 strains of Campylobacter jejuni, and 21 strains belonging to differ
66 detection of Salmonella spp., Shigella spp., Campylobacter jejuni, and Campylobacter coli and an EIA
68 classes of inhibitors of Bacillus anthracis, Campylobacter jejuni, and Clostridium perfringens IMPDHs
69 ichia coli (ETEC), enteropathogenic E. coli, Campylobacter jejuni, and Giardia lamblia document heter
70 opsy samples were stimulated with H. pylori, Campylobacter jejuni, and/or H 2 O 2 in the presence or
71 ne contained contaminating moieties (such as Campylobacter jejuni antigens that mimic human gangliosi
72 inked protein glycosylation (Pgl) pathway of Campylobacter jejuni are evaluated for their tolerance f
75 arahemeolyticus, Pseudomonas aeruginosa, and Campylobacter jejuni, as well as an additional 12 bacter
77 icated a moderate probability of illness for Campylobacter jejuni at the study beaches, especially wh
78 developed for broth microdilution testing of Campylobacter jejuni ATCC 33560 against 14 antimicrobial
79 Enterovirus, adenovirus A, Salmonella spp., Campylobacter jejuni, bovine polyomavirus, and bovine ro
80 nsible for high-affinity iron acquisition in Campylobacter jejuni but also is essential for C. jejuni
81 nic Escherichia coli, Shigella flexneri, and Campylobacter jejuni, but not Neisseria gonorrhoeae, cle
82 IA (ProSpecT), and duplex PCR to distinguish Campylobacter jejuni/C. coli and non-jejuni/coli Campylo
84 us GII, rotavirus, and sapovirus), bacteria (Campylobacter jejuni/C. coli, Clostridium difficile, Sal
85 l specimens, including pathogenic Aeromonas, Campylobacter jejuni, Campylobacter coli, Salmonella, Sh
86 ase 3, sequences from Clostridium difficile, Campylobacter jejuni, Campylobacter concisus, and Salmon
87 ure alone detected 80/89 (89.9% sensitivity) Campylobacter jejuni/Campylobacter coli-positive cases.
91 Here, we report the crystal structures of Campylobacter jejuni Cas9 (CjCas9), one of the smallest
94 as a nitric oxide (NO)-detoxifying globin in Campylobacter jejuni, Cgb (Campylobacter globin) express
96 ed with those of three bacterial IMPDHs from Campylobacter jejuni, Clostridium perfringens, and Vibri
98 Here the authors present the structure of Campylobacter jejuni CmeB pump combined with functional
99 cell lysates of five thermophilic species of Campylobacter: jejuni, coli, lari, upsaliensis, and helv
100 oli (STEC), Shigella spp. , Salmonella spp , Campylobacter jejuni/coli , and methicillin-resistant St
101 e 6 bacterial enteric pathogens tested, only Campylobacter jejuni/coli detection was significantly re
103 of antimicrobial agents and is essential for Campylobacter jejuni colonization of the animal intestin
108 s wash was 4.9 x 10(4) cfu mL(-)(1), whereas Campylobacter jejuni could be measured at concentrations
109 claimed to be responsible for inhibition of Campylobacter jejuni could not be detected either direct
110 actinomycetemcomitans, Escherichia coli, and Campylobacter jejuni differ in their abilities to intoxi
111 s from use of an open-reading frame-specific Campylobacter jejuni DNA microarray to investigate genet
115 ubform acute motor axonal neuropathy (AMAN), Campylobacter jejuni enteritis triggers the production o
116 erial species (Bacteroides thetaiotaomicron, Campylobacter jejuni, Enterococcus faecalis, Escherichia
117 d to spray-irrigated dairy manure containing Campylobacter jejuni, enterohemorrhagic Escherichia coli
118 ty against Gram-negative bacteria, including Campylobacter jejuni, Escherichia coli O157:H7, and mult
120 of Sn in Mphi interactions with heat-killed Campylobacter jejuni expressing a GD1a-like, sialylated
121 acterial oligosaccharyltransferase, PglB, of Campylobacter jejuni favors acceptor proteins with conse
123 unogenicity and protective efficacy of three Campylobacter jejuni flagellum-secreted proteins, FlaC,
126 radish peroxidase (HRP), myoglobin (Mb), and Campylobacter jejuni globin (Cgb) are compared and signi
127 d export; examples include Escherichia coli, Campylobacter jejuni, Haemophilus influenzae, Neisseria
133 dUTPase from the important gastric pathogen Campylobacter jejuni has been solved at 1.65 A spacing.
138 s, we show that the flagellar filaments from Campylobacter jejuni have seven protofilaments rather th
140 and Salmonella typhimurium, the flagella of Campylobacter jejuni, Helicobacter pylori and Vibrio cho
141 ria, including the important human pathogens Campylobacter jejuni, Helicobacter pylori, and Bartonell
142 in (Ig) G and IgA to Haemophilus influenzae, Campylobacter jejuni, Helicobacter pylori, Streptococcus
143 study of the global population structure of Campylobacter jejuni; however, its usefulness for the in
147 osphorylase (PNPase) facilitates survival of Campylobacter jejuni in low temperatures and favors swim
148 ude an increased appreciation of the role of Campylobacter jejuni in postinfectious sequelae, a broad
149 ce and its contribution to the adaptation of Campylobacter jejuni in the intestinal tract of the chic
150 he simplest system is that of the bacterium, Campylobacter jejuni, in which a heptasaccharide glycan
151 ertoire of glycoconjugates that are found in Campylobacter jejuni includes lipooligosaccharides mimic
152 zation domain-containing protein 2 (NOD2) in Campylobacter jejuni-induced intestinal inflammation.
153 the contribution of PI3K-gamma signaling in Campylobacter jejuni-induced neutrophil accumulation and
157 th Guillain-Barre syndrome have had a recent Campylobacter jejuni infection, and axonal forms of the
159 1221 identified four large genomic elements, Campylobacter jejuni-integrated elements (CJIEs), that w
198 acter-associated abortion in sheep; however, Campylobacter jejuni is increasingly associated with she
204 c acid cycle in the microaerophilic pathogen Campylobacter jejuni is potentially vulnerable, as it em
221 receptor CfrA is present in the majority of Campylobacter jejuni isolates and is responsible for hig
227 d the highest antimicrobial activity against Campylobacter jejuni, L. monocytogenes, and Pseudomonas
228 O157), shiga-toxin producing E. coli (stx2), Campylobacter jejuni (mapA), Shigella spp. (ipaH), and a
230 B1a protein of the gastrointestinal pathogen Campylobacter jejuni mediates interactions with epitheli
232 entified from the alleles within the current Campylobacter jejuni multilocus sequence typing (MLST) d
233 oss of the gne gene in the expression of the Campylobacter jejuni N-glycosylation system in E. coli i
235 e sequence of the enteric bacterial pathogen Campylobacter jejuni NCTC 11168 (11168-GS) was published
236 lication of the complete genomic sequence of Campylobacter jejuni NCTC 11168 in February 2000, eviden
237 o-L-gluco-heptopyranose residue found in the Campylobacter jejuni NCTC11168 (HS:2) capsular polysacch
238 The genome sequence of the human pathogen Campylobacter jejuni NCTC11168 has been determined recen
241 ein (MOMP) typing as a screen to compare the Campylobacter jejuni porA gene sequences of clinical out
244 The foodborne microaerophilic pathogen, Campylobacter jejuni, possesses a periplasmic formate de
245 OTase, and PglB(Cj), the N-linked OTase from Campylobacter jejuni, preferred the native N. gonorrhoea
247 mmensalism in animals and disease in humans, Campylobacter jejuni produces a flagellar organelle for
248 75-year-old man was diagnosed with probable Campylobacter jejuni prosthetic knee infection after a d
251 ssion essential for formation of flagella in Campylobacter jejuni requires the components of the inne
252 eropathogenic E. coli (EPEC), Shigella spp., Campylobacter jejuni, Salmonella enterica, and Aeromonas
253 rrhea-causing pathogens, including bacteria (Campylobacter jejuni, Salmonella spp., Shigella spp., en
254 f Campylobacter spp. (Campylobacter coli and Campylobacter jejuni), Shigella flexneri, Yersinia enter
255 y of a recombinant truncated multifunctional Campylobacter jejuni sialyltransferase CstII mutant, Cst
256 a patient with fecal specimens positive for Campylobacter jejuni (ST45) intermittently during a 10-y
257 Initial steps in flagellar biosynthesis in Campylobacter jejuni stimulate phosphotransfer from the
258 he complete flagellin glycosylation locus of Campylobacter jejuni strain 81-176 revealed a less compl
262 Analysis of the complete genomic sequence of Campylobacter jejuni strain RM1221 identified four large
266 genetically diverse Campylobacter fetus and Campylobacter jejuni strains have been implicated in suc
267 breoganii 1C-10, Bacillus cereus ATCC 10987, Campylobacter jejuni subsp. jejuni 81-176 and C. jejuni
268 n (strain VPI-5482) [PDB:3KZT], Cj0202c from Campylobacter jejuni subsp. jejuni serotype O:2 (strain
269 ber 2013, sexual transmission of 2 clades of Campylobacter jejuni subspecies jejuni isolates resulted
270 ae, Treponema pallidum, Helicobacter pylori, Campylobacter jejuni, Synechocystis sp., and Mycobacteri
271 859c, or FspA, is a small, acidic protein of Campylobacter jejuni that is expressed by a sigma(28) pr
272 llar motility is an important determinant of Campylobacter jejuni that is required for promoting inte
274 lation locus of the human bacterial pathogen Campylobacter jejuni, the first such system found in a s
278 previously identified in invasive strains of Campylobacter jejuni, the most prevalent cause of bacter
279 fflux pump, is involved in the resistance of Campylobacter jejuni to a broad spectrum of antimicrobia
280 LST) system has been reported previously for Campylobacter jejuni to both differentiate strains and i
281 transfer of an N-glycosylation pathway from Campylobacter jejuni to Escherichia coli in 2002 can be
284 owth of the microaerophilic mucosal pathogen Campylobacter jejuni under oxygen-limited conditions was
285 The microaerophilic food-borne pathogen Campylobacter jejuni uses complex cytochrome-rich respir
287 The cytolethal distending toxin (CDT) of Campylobacter jejuni was detectable, using an in vitro a
288 me loci as a previously described system for Campylobacter jejuni was developed for Campylobacter col
292 ugh frequent recombination with it, while in Campylobacter jejuni, we find a minority population we p
293 The FlhF proteins of Bacillus subtilis and Campylobacter jejuni were recently shown to have GTPase
294 y and kinetic parameters of PglC, a PGT from Campylobacter jejuni, were quickly established using thi
295 method for determination of capsule types of Campylobacter jejuni which is simpler and more affordabl
297 the surface of the food-borne human pathogen Campylobacter jejuni, which has a major role in adherenc
298 that the periplasmic binding protein CeuE of Campylobacter jejuni, which was previously thought to bi
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。