ライフサイエンスコーパス: Campylobacter jejuni

1 virulence of the human gut mucosal pathogen Campylobacter jejuni .

2 ed sites (eg, Aeromonas, Vibrio cholerae O1, Campylobacter jejuni).

3 with the periplasmic binding protein CeuE of Campylobacter jejuni.

4 91% for C. difficile A/B toxins; and 90% for Campylobacter jejuni.

5 the human pathogens Helicobacter pylori and Campylobacter jejuni.

6 of the major human gastrointestinal pathogen Campylobacter jejuni.

7 ies in the Gram-negative intestinal pathogen Campylobacter jejuni.

8 a part of a controlled human infection with Campylobacter jejuni.

9 f the metabolic capacity and epidemiology of Campylobacter jejuni.

10 the asaccharolytic food-borne human pathogen Campylobacter jejuni.

11 variable genomic regions between strains of Campylobacter jejuni.

12 on of sigma(54)-dependent flagellar genes in Campylobacter jejuni.

13 ssion of the multidrug efflux pump CmeABC in Campylobacter jejuni.

14 ed intragastrically with increasing doses of Campylobacter jejuni.

15 involved in biosynthesis of UDP-diNAcBac in Campylobacter jejuni.

16 he phospholipidome of the bacterial pathogen Campylobacter jejuni.

17 unosensor for the detection of food pathogen Campylobacter jejuni.

18 ectious neuropathy most frequently caused by Campylobacter jejuni.

19 In Campylobacter jejuni 2,4-diacetamido-2,4,6-trideoxy-alph

20 We report isolation and characterization of Campylobacter jejuni 81-176 lgtF and galT lipooligosacch

21 Campylobacter jejuni 81-176 lipooligosaccharide (LOS) is

22 thyltransferase gene reduced the motility of Campylobacter jejuni 81-176.

23 ranscriptional regulator csrA was mutated in Campylobacter jejuni 81-176.

24 mine whether H. pylori can transfer DNA into Campylobacter jejuni, a closely related species of the C

25 Campylobacter jejuni, a Gram-negative motile bacterium,

26 Campylobacter jejuni, a gram-negative, invasive organism

27 Campylobacter jejuni, a leading bacterial cause of foodb

28 Here we show that Campylobacter jejuni, a leading bacterial cause of human

29 Campylobacter jejuni, a leading cause of bacterial gastr

30 Campylobacter jejuni, a major human enteric pathogen, ex

31 We examined the TsdAs from Campylobacter jejuni, a microaerobic human pathogen, and

32 (NrfA) reductases have been investigated in Campylobacter jejuni, a microaerophilic food-borne patho

33 Campylobacter jejuni, a spiral-shaped gram-negative bact

34 ereas previous endeavors have focused on the Campylobacter jejuni acetyltransferase (PglD) from the N

35 specific inhibitor of PFOR of H. pylori and Campylobacter jejuni, also inhibited NADP reduction in c

36 to bacteria such as Pseudomonas aeruginosa, Campylobacter jejuni and Agrobacterium tumefaciens, whic

37 s used to detect the presence of cmeC in 131 Campylobacter jejuni and C. coli strains isolated from v

38 Human campylobacteriosis, caused by Campylobacter jejuni and C. coli, remains a leading caus

39 rized two FeEnt receptors (CfrA and CfrB) in Campylobacter jejuni and C. coli, the enteric human path

40 Campylobacter jejuni and Campylobacter coli are among th

41 Campylobacter jejuni and Campylobacter coli are zoonotic

42 Campylobacter jejuni and Campylobacter coli colonize and

43 ovide routine definitive characterization of Campylobacter jejuni and Campylobacter coli for clinical

44 true but also, in fact, the clearly distinct Campylobacter jejuni and Campylobacter coli species may

45 closely related zoonotic pathogenic species, Campylobacter jejuni and Campylobacter coli, are converg

46 athogens associated with diarrhoea-including Campylobacter jejuni and Campylobacter coli, Cryptospori

47 Campylobacteriosis in humans, caused by Campylobacter jejuni and Campylobacter coli, is the most

48 t targets mapA and ceuE for the detection of Campylobacter jejuni and Campylobacter coli, leading glo

49 hough cdtB gene sequences were found in both Campylobacter jejuni and Campylobacter coli, the product

50 resistance (AMR) in the food-borne pathogens Campylobacter jejuni and Campylobacter coli.

51 Monomeric OTases, such as the PglBs from Campylobacter jejuni and Campylobacter lari, catalyze tr

52 The bacterial genomes of Campylobacter jejuni and Escherichia coli assemble optim

53 Flagellar motility of Campylobacter jejuni and Helicobacter pylori influences

54 nella entericaserovartyphi, Shigella sonnei, Campylobacter jejuni and Helicobacter pylori.

55 to the QFR enzymes from the human pathogens Campylobacter jejuni and Helicobacter pylori.

56 ynthesis and flagellin glycosylation in both Campylobacter jejuni and Helicobacter pylori.

57 genes with higher sequence diversity in the Campylobacter jejuni and Neisseria meningitidis genomes

58 Campylobacter jejuni and Salmonella, Shigella, and Yersi

59 says demonstrate that LpxJ and homologues in Campylobacter jejuni and Wolinella succinogenes can act

60 erborne illness caused almost exclusively by Campylobacter jejuni and, to a lesser extent, by Campylo

61 nd Staphylococcus spp.; a zoonotic pathogen: Campylobacter jejuni) and antimicrobial resistance (AMR)

62 detection of Salmonella spp., Shigella spp., Campylobacter jejuni, and Campylobacter coli and an EIA

63 found from patients with ulcerative colitis, Campylobacter jejuni, and Clostridium difficile.

64 classes of inhibitors of Bacillus anthracis, Campylobacter jejuni, and Clostridium perfringens IMPDHs

65 ichia coli (ETEC), enteropathogenic E. coli, Campylobacter jejuni, and Giardia lamblia document heter

66 ne contained contaminating moieties (such as Campylobacter jejuni antigens that mimic human gangliosi

67 Campylobacter jejuni AR101 (Cj-P0) was introduced to chi

68 inked protein glycosylation (Pgl) pathway of Campylobacter jejuni are evaluated for their tolerance f

69 Multiple genes of Campylobacter jejuni are subject to phase variable gene

70 Despite the importance of Campylobacter jejuni as a pathogen, little is known abou

71 arahemeolyticus, Pseudomonas aeruginosa, and Campylobacter jejuni, as well as an additional 12 bacter

72 The central enzyme in the Campylobacter jejuni asparagine-linked glycosylation pat

73 icated a moderate probability of illness for Campylobacter jejuni at the study beaches, especially wh

74 Enterovirus, adenovirus A, Salmonella spp., Campylobacter jejuni, bovine polyomavirus, and bovine ro

75 nsible for high-affinity iron acquisition in Campylobacter jejuni but also is essential for C. jejuni

76 nic Escherichia coli, Shigella flexneri, and Campylobacter jejuni, but not Neisseria gonorrhoeae, cle

77 IA (ProSpecT), and duplex PCR to distinguish Campylobacter jejuni/C. coli and non-jejuni/coli Campylo

78 According to PCR, Campylobacter jejuni/C. coli infections represented less

79 us GII, rotavirus, and sapovirus), bacteria (Campylobacter jejuni/C. coli, Clostridium difficile, Sal

80 l specimens, including pathogenic Aeromonas, Campylobacter jejuni, Campylobacter coli, Salmonella, Sh

81 ase 3, sequences from Clostridium difficile, Campylobacter jejuni, Campylobacter concisus, and Salmon

82 ure alone detected 80/89 (89.9% sensitivity) Campylobacter jejuni/Campylobacter coli-positive cases.

83 The leading foodborne pathogen, Campylobacter jejuni, can carry multiple plasmids associ

84 Another foodborne pathogen, Campylobacter jejuni, can mimic the GM1 ganglioside rece

85 Here we report the cryo-EM structure of the Campylobacter jejuni cap complex, which reveals that Fli

86 The Campylobacter jejuni capsular polysaccharide is importan

87 The Campylobacter jejuni capsule is important for colonizati

88 Here, we report the crystal structures of Campylobacter jejuni Cas9 (CjCas9), one of the smallest

89 To investigate how Campylobacter jejuni causes the clinical symptoms of dia

90 graphene quantum dot with surface protein in Campylobacter jejuni cell membrane.

91 Campylobacter jejuni CG8486, which belongs to the HS4 co

92 Campylobacter jejuni Cj-P1-DCA-Anaero was isolated from

93 uctural studies to define the role of Fur in Campylobacter jejuni (Cj).

94 ed with those of three bacterial IMPDHs from Campylobacter jejuni, Clostridium perfringens, and Vibri

95 he structures and functional dynamics of the Campylobacter jejuni CmeB multidrug efflux pump.

96 Here the authors present the structure of Campylobacter jejuni CmeB pump combined with functional

97 oli (STEC), Shigella spp. , Salmonella spp , Campylobacter jejuni/coli , and methicillin-resistant St

98 rate per 100 child-months of infections with Campylobacter jejuni/coli and Campylobacter species duri

99 pylobacter species by enzyme immunoassay and Campylobacter jejuni/coli by quantitative PCR in stool s

100 e 6 bacterial enteric pathogens tested, only Campylobacter jejuni/coli detection was significantly re

101 d unimproved sanitation were associated with Campylobacter jejuni/coli infection.

102 The cumulative burden of both Campylobacter jejuni/coli infections and Campylobacter s

103 oth all Campylobacter species infections and Campylobacter jejuni/coli infections on growth and enter

104 ruses, enterotoxigenic Escherichia coli, and Campylobacter jejuni/coli.

105 lear whether that association is specific to Campylobacter jejuni/coli.

106 udy, the effect of sustainable probiotics on Campylobacter jejuni colonization and gut microbiome com

107 Campylobacter jejuni colonization of chickens is presuma

108 of antimicrobial agents and is essential for Campylobacter jejuni colonization of the animal intestin

109 Campylobacter jejuni contains a general N-linked glycosy

110 Campylobacter jejuni contains two globins, a truncated h

111 Campylobacter jejuni contains two hemoglobins, Cgb and C

112 claimed to be responsible for inhibition of Campylobacter jejuni could not be detected either direct

113 NA (sgRNA)-guided and catalytically impaired Campylobacter jejuni CRISPR-associated protein 9-fused a

114 actinomycetemcomitans, Escherichia coli, and Campylobacter jejuni differ in their abilities to intoxi

115 Campylobacter jejuni encodes 12 of the 14 subunits that

116 One phase-variable gene of Campylobacter jejuni encodes a homologue of an unusual T

117 Campylobacter jejuni encodes all the enzymes necessary f

118 ubform acute motor axonal neuropathy (AMAN), Campylobacter jejuni enteritis triggers the production o

119 erial species (Bacteroides thetaiotaomicron, Campylobacter jejuni, Enterococcus faecalis, Escherichia

120 d to spray-irrigated dairy manure containing Campylobacter jejuni, enterohemorrhagic Escherichia coli

121 ty against Gram-negative bacteria, including Campylobacter jejuni, Escherichia coli O157:H7, and mult

122 The dispersion of pathogens (Campylobacter jejuni, Escherichia coli O157:H7, non-O157

123 of Sn in Mphi interactions with heat-killed Campylobacter jejuni expressing a GD1a-like, sialylated

124 acterial oligosaccharyltransferase, PglB, of Campylobacter jejuni favors acceptor proteins with conse

125 The Campylobacter jejuni flagellum exports both proteins tha

126 unogenicity and protective efficacy of three Campylobacter jejuni flagellum-secreted proteins, FlaC,

127 In Campylobacter jejuni, FlhF is required for sigma(54)-dep

128 We discovered that Campylobacter jejuni FlhG is at the center of a multipar

129 ublic Health England received 25 isolates of Campylobacter jejuni from an individual with combined va

130 radish peroxidase (HRP), myoglobin (Mb), and Campylobacter jejuni globin (Cgb) are compared and signi

131 ced downregulation of NEIL2 was specific, as Campylobacter jejuni had no such effect.

132 d export; examples include Escherichia coli, Campylobacter jejuni, Haemophilus influenzae, Neisseria

133 Campylobacter jejuni harbors a branched electron transpo

134 Campylobacter jejuni has a general N-linked glycosylatio

135 Campylobacter jejuni has an energy taxis system consisti

136 Campylobacter jejuni has an N-linked protein glycosylati

137 Molecular pathogenesis of Campylobacter jejuni has lagged behind that of other ent

138 A lack of relevant disease models for Campylobacter jejuni has long been an obstacle to resear

139 Campylobacter jejuni has systems for N- and O-linked pro

140 Previous studies on Campylobacter jejuni have demonstrated the role of LuxS

141 s, we show that the flagellar filaments from Campylobacter jejuni have seven protofilaments rather th

142 n pathogens, such as Helicobacter pylori and Campylobacter jejuni, have escaped TLR5 activation by mu

143 Campylobacter jejuni helical shape is important for colo

144 and Salmonella typhimurium, the flagella of Campylobacter jejuni, Helicobacter pylori and Vibrio cho

145 in (Ig) G and IgA to Haemophilus influenzae, Campylobacter jejuni, Helicobacter pylori, Streptococcus

146 oncoding RNAs in the major zoonotic pathogen Campylobacter jejuni; however, few have been functionall

147 The Campylobacter jejuni human clinical isolates NW and D260

148 Recent work in Campylobacter jejuni identified a gene encoding a novel

149 treptococcus pneumoniae in mice, and against Campylobacter jejuni in chicken.

150 osphorylase (PNPase) facilitates survival of Campylobacter jejuni in low temperatures and favors swim

151 ude an increased appreciation of the role of Campylobacter jejuni in postinfectious sequelae, a broad

152 Also, this method for monitoring Campylobacter jejuni in poultry liver was applied and re

153 he most common food-born bacterial pathogen (Campylobacter jejuni) in the most prolific agricultural

154 he simplest system is that of the bacterium, Campylobacter jejuni, in which a heptasaccharide glycan

155 ertoire of glycoconjugates that are found in Campylobacter jejuni includes lipooligosaccharides mimic

156 zation domain-containing protein 2 (NOD2) in Campylobacter jejuni-induced intestinal inflammation.

157 the contribution of PI3K-gamma signaling in Campylobacter jejuni-induced neutrophil accumulation and

158 Campylobacter jejuni infection is a leading cause of bac

159 A human Campylobacter jejuni infection model provided controlled

160 Campylobacter jejuni infection often results in bloody,

161 Guillain-Barre syndrome is often caused by Campylobacter jejuni infection that has induced antibodi

162 en described with Haemophilus influenzae and Campylobacter jejuni infection.

163 1221 identified four large genomic elements, Campylobacter jejuni-integrated elements (CJIEs), that w

164 Although it is known that Campylobacter jejuni invade the cells that line the huma

165 Campylobacter jejuni is a commensal bacterium in the int

166 Campylobacter jejuni is a common cause of diarrhea and i

167 Campylobacter jejuni is a food-borne bacterial pathogen

168 Campylobacter jejuni is a gastrointestinal pathogen of h

169 Campylobacter jejuni is a globally distributed cause of

170 Campylobacter jejuni is a Gram-negative food-borne patho

171 Campylobacter jejuni is a helix-shaped enteric bacterial

172 Campylobacter jejuni is a leading bacterial cause of hum

173 Campylobacter jejuni is a leading cause of acute gastroe

174 Campylobacter jejuni is a leading cause of bacterial foo

175 Campylobacter jejuni is a leading cause of bacterial gas

176 Campylobacter jejuni is a leading cause of bacterial gas

177 Campylobacter jejuni is a leading cause of bacterial gas

178 Campylobacter jejuni is a leading cause of diarrheal dis

179 Campylobacter jejuni is a leading cause of enteric bacte

180 Campylobacter jejuni is a leading cause of food-borne il

181 Campylobacter jejuni is a leading cause of foodborne ill

182 Campylobacter jejuni is a leading cause of gastroenterit

183 Campylobacter jejuni is a leading cause of gastrointesti

184 Campylobacter jejuni is a leading cause of human enteroc

185 Campylobacter jejuni is a leading worldwide bacterial ca

186 Campylobacter jejuni is a major cause of bacterial diarr

187 Campylobacter jejuni is a major cause of bacterial food-

188 Campylobacter jejuni is a major cause of bacterial gastr

189 Campylobacter jejuni is a major human pathogen and a lea

190 Campylobacter jejuni is a major worldwide cause of enter

191 Campylobacter jejuni is a major zoonotic pathogen, and i

192 Campylobacter jejuni is a major zoonotic pathogen.

193 Campylobacter jejuni is a microaerophilic foodborne path

194 Campylobacter jejuni is a natural commensal of the avian

195 Campylobacter jejuni is a prevalent enteric pathogen tha

196 Campylobacter jejuni is a prevalent foodborne pathogen m

197 The microaerophilic bacterium Campylobacter jejuni is a significant food-borne pathoge

198 Campylobacter jejuni is a zoonotic pathogen and is one o

199 Campylobacter jejuni is a zoonotic pathogen, and a hyper

200 Campylobacter jejuni is an important bacterial pathogen

201 Campylobacter jejuni is an important cause of human ente

202 Campylobacter jejuni is an important human pathogen that

203 Campylobacter jejuni is an important zoonotic pathogen t

204 An apparent energy taxis system in Campylobacter jejuni is composed of two proteins, CetA a

205 The food-borne pathogen Campylobacter jejuni is dependent on a functional flagel

206 acter-associated abortion in sheep; however, Campylobacter jejuni is increasingly associated with she

207 The human pathogen Campylobacter jejuni is naturally competent for transfor

208 Campylobacter jejuni is one of the leading causes of bac

209 Campylobacter jejuni is one of the leading causes of bac

210 Campylobacter jejuni is one of the leading infectious ca

211 Campylobacter jejuni is one of the most frequent bacteri

212 c acid cycle in the microaerophilic pathogen Campylobacter jejuni is potentially vulnerable, as it em

213 Campylobacter jejuni is the leading cause of acute bacte

214 Campylobacter jejuni is the leading cause of foodborne b

215 Campylobacter jejuni is the leading cause of human bacte

216 Campylobacter jejuni is the leading cause of human bacte

217 Campylobacter jejuni is the leading cause of infectious

218 The Gram-negative organism Campylobacter jejuni is the major cause of food poisonin

219 The polysaccharide capsule (CPS) of Campylobacter jejuni is the major serodeterminant of the

220 Campylobacter jejuni is the major worldwide cause of bac

221 Campylobacter jejuni is the most common bacterial cause

222 The Gram-negative pathogen Campylobacter jejuni is the most common cause of bacteri

223 Campylobacter jejuni is the most common cause of bacteri

224 Campylobacter jejuni is the most prevalent cause of food

225 Campylobacter jejuni is the worldwide leading cause of b

226 sourceR is demonstrated using Campylobacter jejuni isolate data collected in New Zeala

227 receptor CfrA is present in the majority of Campylobacter jejuni isolates and is responsible for hig

228 Campylobacter jejuni isolates are of interest because of

229 Campylobacter jejuni isolates from clinical sources had

230 Campylobacter jejuni isolates from human (n = 65), bovin

231 he genetic basis of biofilm formation in 102 Campylobacter jejuni isolates.

232 Campylobacter jejuni, known for being a major cause of b

233 d the highest antimicrobial activity against Campylobacter jejuni, L. monocytogenes, and Pseudomonas

234 O157), shiga-toxin producing E. coli (stx2), Campylobacter jejuni (mapA), Shigella spp. (ipaH), and a

235 Campylobacter jejuni-mediated pathogenesis involves gut

236 B1a protein of the gastrointestinal pathogen Campylobacter jejuni mediates interactions with epitheli

237 Flagellar motility in Campylobacter jejuni mediates optimal interactions with

238 pecific binding of graphene quantum dot with Campylobacter jejuni membrane leads to generate a distan

239 Campylobacter jejuni monitors intestinal metabolites pro

240 oss of the gne gene in the expression of the Campylobacter jejuni N-glycosylation system in E. coli i

241 The Campylobacter jejuni N-linked glycosylation pathway has

242 o-L-gluco-heptopyranose residue found in the Campylobacter jejuni NCTC11168 (HS:2) capsular polysacch

243 tified in silico from the genome sequence of Campylobacter jejuni NCTC11168.

244 toxigenic Escherichia coli, Vibrio cholerae, Campylobacter jejuni, norovirus) in cohorts from Haiti,

245 In lack of Campylobacter jejuni or in existence of other bacterial

246 s, Vibrio cholerae, Helicobacter pylori, and Campylobacter jejuni, organisms from three classes of Pr

247 In Campylobacter jejuni, PglD acetylates the C4 amino group

248 The characterized Campylobacter jejuni phages fall into two phylogenetic g

249 ein (MOMP) typing as a screen to compare the Campylobacter jejuni porA gene sequences of clinical out

250 The food-borne pathogen Campylobacter jejuni possesses a single-domain globin (C

251 The food-borne pathogen Campylobacter jejuni possesses no known tungstoenzymes,

252 The foodborne microaerophilic pathogen, Campylobacter jejuni, possesses a periplasmic formate de

253 OTase, and PglB(Cj), the N-linked OTase from Campylobacter jejuni, preferred the native N. gonorrhoea

254 mmensalism in animals and disease in humans, Campylobacter jejuni produces a flagellar organelle for

255 75-year-old man was diagnosed with probable Campylobacter jejuni prosthetic knee infection after a d

256 The flagellum of Campylobacter jejuni provides motility essential for com

257 Campylobacter jejuni remains among the leading causes of

258 ssion essential for formation of flagella in Campylobacter jejuni requires the components of the inne

259 eropathogenic E. coli (EPEC), Shigella spp., Campylobacter jejuni, Salmonella enterica, and Aeromonas

260 rrhea-causing pathogens, including bacteria (Campylobacter jejuni, Salmonella spp., Shigella spp., en

261 ml and ability of this FRET immunosensor for Campylobacter jejuni sensing in comparison with other ba

262 y of a recombinant truncated multifunctional Campylobacter jejuni sialyltransferase CstII mutant, Cst

263 a patient with fecal specimens positive for Campylobacter jejuni (ST45) intermittently during a 10-y

264 Initial steps in flagellar biosynthesis in Campylobacter jejuni stimulate phosphotransfer from the

265 he complete flagellin glycosylation locus of Campylobacter jejuni strain 81-176 revealed a less compl

266 The major flagellin of Campylobacter jejuni strain 81-176, FlaA, has been shown

267 complex L-gluco-heptose synthesis pathway of Campylobacter jejuni strain NCTC 11168.

268 Analysis of the complete genomic sequence of Campylobacter jejuni strain RM1221 identified four large

269 the rapid high-resolution identification of Campylobacter jejuni strain types.

270 PCR probing of the genome of Campylobacter jejuni strain X using conserved capsular p

271 genetically diverse Campylobacter fetus and Campylobacter jejuni strains have been implicated in suc

272 breoganii 1C-10, Bacillus cereus ATCC 10987, Campylobacter jejuni subsp. jejuni 81-176 and C. jejuni

273 n (strain VPI-5482) [PDB:3KZT], Cj0202c from Campylobacter jejuni subsp. jejuni serotype O:2 (strain

274 ber 2013, sexual transmission of 2 clades of Campylobacter jejuni subspecies jejuni isolates resulted

275 ae, Treponema pallidum, Helicobacter pylori, Campylobacter jejuni, Synechocystis sp., and Mycobacteri

276 859c, or FspA, is a small, acidic protein of Campylobacter jejuni that is expressed by a sigma(28) pr

277 llar motility is an important determinant of Campylobacter jejuni that is required for promoting inte

278 In Campylobacter jejuni the periplasmic binding protein Ceu

279 Campylobacter jejuni, the leading cause of human bacteri

280 Campylobacter jejuni, the most common cause of bacterial

281 Campylobacter jejuni, the most frequent cause of food-bo

282 previously identified in invasive strains of Campylobacter jejuni, the most prevalent cause of bacter

283 ember of the cell-shape-determining class of Campylobacter jejuni, the peptidoglycan peptidase 3 (Pgp

284 transfer of an N-glycosylation pathway from Campylobacter jejuni to Escherichia coli in 2002 can be

285 owth of the microaerophilic mucosal pathogen Campylobacter jejuni under oxygen-limited conditions was

286 The microaerophilic food-borne pathogen Campylobacter jejuni uses complex cytochrome-rich respir

287 me loci as a previously described system for Campylobacter jejuni was developed for Campylobacter col

288 n resonance (SPR) for the rapid detection of Campylobacter jejuni was developed.

289 Campylobacter jejuni was isolated from 62% of the cases.

290 The gram-negative bacterium Campylobacter jejuni was recently discovered to contain

291 A bacterial permease, ArsP, from Campylobacter jejuni, was recently shown to confer resis

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

296 the surface of the food-borne human pathogen Campylobacter jejuni, which has a major role in adherenc

297 that the periplasmic binding protein CeuE of Campylobacter jejuni, which was previously thought to bi

298 oxide and graphene quantum dot for detection Campylobacter jejuni whole cell in food samples was desi

299 omic DNA extracted from Escherichia coli and Campylobacter jejuni, with the concentration as low as 2

300 The development of vaccines against Campylobacter jejuni would be facilitated by the ability