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Domestication of Campylobacter jejuni NCTC 11168
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/archpedi.1973.02110190134004openalex-snapshot
Enteritis Due to "Related Vibrio" in Children
inferredcites →https://doi.org/10.1016/0378-1097(96)00272-8openalex-snapshot
Expanded genomic map of Campylobacter jejuni UA580 and localization of 23S ribosomal rRNA genes by I-CeuI restriction endonuclease digestion
inferredcites →https://doi.org/10.1016/0890-8508(87)90038-7openalex-snapshot
Immunoblot and enzyme-linked immunosorbent assays of Campylobacter major outer-membrane protein and application to the differentiation of Campylobacter species
inferredcites →https://doi.org/10.1016/j.meegid.2013.03.009openalex-snapshot
Genetic heterogeneity of Campylobacter jejuni NCTC 11168 upon human infection
inferredcites →https://doi.org/10.1016/j.mimet.2013.06.031openalex-snapshot
Molecular methods to investigate adhesion, transmigration, invasion and intracellular survival of the foodborne pathogen Campylobacter jejuni
inferredcites →https://doi.org/10.1016/j.resmic.2012.10.002openalex-snapshot
Re-sequencing of a virulent strain of Campylobacter jejuni NCTC11168 reveals potential virulence factors
inferredcites →https://doi.org/10.1016/j.tim.2007.09.006openalex-snapshot
Campylobacter flagella: not just for motility
inferredcites →https://doi.org/10.1016/s0022-2836(05)80360-2openalex-snapshot
Basic Local Alignment Search Tool
inferredcites →https://doi.org/10.1016/s0022-3476(73)80131-3openalex-snapshot
Related vibrio in stools
inferredcites →https://doi.org/10.1016/s0966-842x(03)00079-9openalex-snapshot
Campylobacter – a tale of two protein glycosylation systems
inferredcites →https://doi.org/10.1016/s1369-5274(00)00161-2openalex-snapshot
Deciphering Campylobacter jejuni cell surface interactions from the genome sequence
inferredcites →https://doi.org/10.1016/s1473-3099(16)30066-4openalex-snapshot
From Escherich to the Escherichia coli genome
inferredcites →https://doi.org/10.1017/s0022172400063506openalex-snapshot
‘1001’ Campylobacters: cultural characteristics of intestinal campylobacters from man and animals
inferredcites →https://doi.org/10.1038/35001088openalex-snapshot
The genome sequence of the food-borne pathogen Campylobacter jejuni reveals hypervariable sequences
inferredcites →https://doi.org/10.1038/ismej.2015.149openalex-snapshot
Rapid host switching in generalist Campylobacter strains erodes the signal for tracing human infections
inferredcites →https://doi.org/10.1038/ismej.2016.115openalex-snapshot
Evolution by flight and fight: diverse mechanisms of adaptation by actively motile microbes
inferredcites →https://doi.org/10.1038/ng.3219openalex-snapshot
A single natural nucleotide mutation alters bacterial pathogen host tropism
inferredcites →https://doi.org/10.1038/nrmicro2405openalex-snapshot
A field guide to bacterial swarming motility
inferredcites →https://doi.org/10.1038/s41576-018-0032-zopenalex-snapshot
Population genomics of bacterial host adaptation
inferredcites →https://doi.org/10.1038/s41592-018-0046-7openalex-snapshot
Bioconda: sustainable and comprehensive software distribution for the life sciences
inferredcites →https://doi.org/10.1038/s41598-017-01133-4openalex-snapshot
Genome-wide fitness analyses of the foodborne pathogen Campylobacter jejuni in in vitro and in vivo models
inferredcites →https://doi.org/10.1038/s41598-017-09483-9openalex-snapshot
Genomic plasticity and rapid host switching can promote the evolution of generalism: a case study in the zoonotic pathogen Campylobacter
inferredcites →https://doi.org/10.1046/j.1365-2958.1996.369895.xopenalex-snapshot
Identification and characterization of genes required for post‐translational modification of Campylobacter coli VC167 flagellin
inferredcites →https://doi.org/10.1046/j.1365-2958.2000.01717.xopenalex-snapshot
Genetic and biochemical evidence of a Campylobacter jejuni capsular polysaccharide that accounts for Penner serotype specificity
inferredcites →https://doi.org/10.1046/j.1365-2958.2000.01780.xopenalex-snapshot
Multiple N‐acetyl neuraminic acid synthetase (neuB) genes in Campylobacter jejuni: identification and characterization of the gene involved in sialylation of lipo‐oligosaccharide
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03731.xopenalex-snapshot
Transcription of σ54‐dependent but not σ28‐dependent flagellar genes in Campylobacter jejuni is associated with formation of the flagellar secretory apparatus
inferredcites →https://doi.org/10.1073/pnas.0503252102openalex-snapshot
Comparative phylogenomics of the food-borne pathogen Campylobacter jejuni reveals genetic markers predictive of infection source
inferredcites →https://doi.org/10.1073/pnas.1305559110openalex-snapshot
Genome-wide association study identifies vitamin B 5 biosynthesis as a host specificity factor in Campylobacter
inferredcites →https://doi.org/10.1073/pnas.1605869113openalex-snapshot
Point mutations in the major outer membrane protein drive hypervirulence of a rapidly expanding clone of Campylobacter jejuni
inferredcites →https://doi.org/10.1074/jbc.m104529200openalex-snapshot
Identification of the Carbohydrate Moieties and Glycosylation Motifs in Campylobacter jejuni Flagellin
inferredcites →https://doi.org/10.1074/jbc.m401134200openalex-snapshot
Genome-wide Expression Analyses of Campylobacter jejuni NCTC11168 Reveals Coordinate Regulation of Motility and Virulence by flhA
inferredcites →https://doi.org/10.1084/jem.30.4.299openalex-snapshot
SOME MORPHOLOGICAL AND BIOLOGICAL CHARACTERS OF THE SPIRILLA (VIBRIO FETUS, N. SP.) ASSOCIATED WITH DISEASE OF THE FETAL MEMBRANES IN CATTLE
inferredcites →https://doi.org/10.1084/jem.53.6.853openalex-snapshot
VIBRIOS (VIBRIO JEJUNI, N.SP.) ASSOCIATED WITH INTESTINAL DISORDERS OF COWS AND CALVES
inferredcites →https://doi.org/10.1086/521946openalex-snapshot
Theodor Escherich: The First Pediatric Infectious Diseases Physician?
inferredcites →https://doi.org/10.1093/bioinformatics/btu153openalex-snapshot
Prokka: rapid prokaryotic genome annotation
inferredcites →https://doi.org/10.1093/biomet/38.3-4.330openalex-snapshot
ON THE COMPARISON OF SEVERAL MEAN VALUES: AN ALTERNATIVE APPROACH
inferredcites →https://doi.org/10.1093/gbe/evy026openalex-snapshot
Convergent Amino Acid Signatures in Polyphyletic Campylobacter jejuni Subpopulations Suggest Human Niche Tropism
inferredcites →https://doi.org/10.1093/infdis/125.4.390openalex-snapshot
Acute Enteritis Due to Related Vibrio: First Positive Stool Cultures
inferredcites →https://doi.org/10.1093/molbev/mst010openalex-snapshot
MAFFT Multiple Sequence Alignment Software Version 7: Improvements in Performance and Usability
inferredcites →https://doi.org/10.1093/nar/gku1196openalex-snapshot
Rapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins
inferredcites →https://doi.org/10.1099/00207713-23-2-122openalex-snapshot
Taxonomic Study of the Genus Campylobacter Sebald and Veron and Designation of the Neotype Strain for the Type Species, Campylobacter fetus (Smith and Taylor) Sebald and Veron
inferredcites →https://doi.org/10.1099/00221287-144-2-503openalex-snapshot
An improved physical and genetic map of Campylobacter jejuni NCTC 11168 (UA580)
inferredcites →https://doi.org/10.1099/00221287-148-2-473openalex-snapshot
A novel paralogous gene family involved in phase-variable flagella-mediated motility in Campylobacter jejuni
inferredcites →https://doi.org/10.1099/00221287-46-2-175openalex-snapshot
The Effect of Environmental Conditions on the Motility of Escherichia coli
inferredcites →https://doi.org/10.1099/mgen.0.000086openalex-snapshot
CLIMB (the Cloud Infrastructure for Microbial Bioinformatics): an online resource for the medical microbiology community
inferredcites →https://doi.org/10.1099/mgen.0.000106openalex-snapshot
Sequencing a piece of history: complete genome sequence of the original Escherichia coli strain
inferredcites →https://doi.org/10.1099/mgen.0.000198openalex-snapshot
Trends in fluoroquinolone resistance in Campylobacter
inferredcites →https://doi.org/10.1099/mgen.0.000228openalex-snapshot
PhasomeIt: an ‘omics’ approach to cataloguing the potential breadth of phase variation in the genus Campylobacter
inferredcites →https://doi.org/10.1099/mic.0.021790-0openalex-snapshot
Metabolite and transcriptome analysis of Campylobacter jejuni in vitro growth reveals a stationary-phase physiological switch
inferredcites →https://doi.org/10.1099/mic.0.038091-0openalex-snapshot
Modification of the Campylobacter jejuni flagellin glycan by the product of the Cj1295 homopolymeric-tract-containing gene
inferredcites →https://doi.org/10.1099/mic.0.045153-0openalex-snapshot
Introgression in the genus Campylobacter: generation and spread of mosaic alleles
inferredcites →https://doi.org/10.1099/mic.0.27412-0openalex-snapshot
Campylobacter jejuni gene expression in response to iron limitation and the role of Fur
inferredcites →https://doi.org/10.1101/gr.185801openalex-snapshot
Whole Genome Comparison of Campylobacter jejuni Human Isolates Using a Low-Cost Microarray Reveals Extensive Genetic Diversity
inferredcites →https://doi.org/10.1111/1462-2920.12341openalex-snapshot
Hemerythrins in the microaerophilic bacterium C ampylobacter jejuni help protect key iron–sulphur cluster enzymes from oxidative damage
inferredcites →https://doi.org/10.1111/1462-2920.13051openalex-snapshot
Enhanced biofilm formation and multi‐host transmission evolve from divergent genetic backgrounds in C ampylobacter jejuni
inferredcites →https://doi.org/10.1111/1462-2920.13628openalex-snapshot
Genome‐wide association of functional traits linked with C ampylobacter jejuni survival from farm to fork
inferredcites →https://doi.org/10.1111/1462-2920.13930openalex-snapshot
Transcriptome and proteome dynamics in chemostat culture reveal how Campylobacter jejuni modulates metabolism, stress responses and virulence factors upon changes in oxygen availability
inferredcites →https://doi.org/10.1111/j.1365-294x.2011.05179.xopenalex-snapshot
Niche segregation and genetic structure of Campylobacter jejuni populations from wild and agricultural host species
inferredcites →https://doi.org/10.1111/j.1365-2958.2006.05100.xopenalex-snapshot
Changes in flagellin glycosylation affect Campylobacter autoagglutination and virulence
inferredcites →https://doi.org/10.1111/j.1469-0691.2004.00983.xopenalex-snapshot
Campylobacter, from obscurity to celebrity
inferredcites →https://doi.org/10.1111/j.1574-695x.2007.00225.xopenalex-snapshot
Molecular mimicry inCampylobacter jejuni: role of the lipo-oligosaccharide core oligosaccharide in inducing anti-ganglioside antibodies
inferredcites →https://doi.org/10.1111/j.1574-6976.2010.00213.xopenalex-snapshot
Stationary phase in gram-negative bacteria
inferredcites →https://doi.org/10.1111/mec.12162openalex-snapshot
Progressive genome‐wide introgression in agricultural Campylobacter coli
inferredcites →https://doi.org/10.1111/mec.12742openalex-snapshot
Cryptic ecology among host generalist Campylobacter jejuni in domestic animals
inferredcites →https://doi.org/10.1111/mec.13001openalex-snapshot
Evidence of land‐sea transfer of the zoonotic pathogen Campylobacter to a wildlife marine sentinel species
inferredcites →https://doi.org/10.1111/mec.14176openalex-snapshot
Local genes for local bacteria: Evidence of allopatry in the genomes of transatlantic Campylobacter populations
inferredcites →https://doi.org/10.1126/science.1155532openalex-snapshot
Convergence of Campylobacter Species: Implications for Bacterial Evolution
inferredcites →https://doi.org/10.1128/aem.01507-07openalex-snapshot
Identification of Campylobacter jejuni Genes Involved in the Response to Acidic pH and Stomach Transit
inferredcites →https://doi.org/10.1128/aem.01878-09openalex-snapshot
Biofilm Formation by Campylobacter jejuni Is Increased under Aerobic Conditions
inferredcites →https://doi.org/10.1128/aem.03085-16openalex-snapshot
Genome-Wide Identification of Host-Segregating Epidemiological Markers for Source Attribution in Campylobacter jejuni
inferredcites →https://doi.org/10.1128/cvi.05161-11openalex-snapshot
Identification of Immunogenic and Virulence-Associated Campylobacter jejuni Proteins
inferredcites →https://doi.org/10.1128/iai.00109-10openalex-snapshot
Identification of Campylobacter jejuni Genes Involved in Its Interaction with Epithelial Cells
inferredcites →https://doi.org/10.1128/iai.01425-08openalex-snapshot
Campylobacter jejuni Glycosylation Island Important in Cell Charge, Legionaminic Acid Biosynthesis, and Colonization of Chickens
inferredcites →https://doi.org/10.1128/iai.68.12.6656-6662.2000openalex-snapshot
Sialylation of Lipooligosaccharide Cores Affects Immunogenicity and Serum Resistance of Campylobacter jejuni
inferredcites →https://doi.org/10.1128/iai.70.4.1761-1771.2002openalex-snapshot
Identification of Motility and Autoagglutination Campylobacter jejuni Mutants by Random Transposon Mutagenesis
inferredcites →https://doi.org/10.1128/iai.72.7.3769-3776.2004openalex-snapshot
Adaptation of Campylobacter jejuni NCTC11168 to High-Level Colonization of the Avian Gastrointestinal Tract
inferredcites →https://doi.org/10.1128/jb.00254-08openalex-snapshot
Characterization of Lipooligosaccharide-Biosynthetic Loci ofCampylobacter jejuniReveals New Lipooligosaccharide Classes: Evidence of Mosaic Organizations
inferredcites →https://doi.org/10.1128/jb.00347-16openalex-snapshot
Large Sequence Diversity within the Biosynthesis Locus and Common Biochemical Features of Campylobacter coli Lipooligosaccharides
inferredcites →https://doi.org/10.1128/jb.00478-10openalex-snapshot
Identification and Characterization of a New Ferric Enterobactin Receptor, CfrB, in Campylobacter
inferredcites →https://doi.org/10.1128/jb.01385-12openalex-snapshot
Complete Genome Sequence of a Variant of Campylobacter jejuni NCTC 11168
inferredcites →https://doi.org/10.1128/jb.01975-05openalex-snapshot
Proteomic Analysis ofCampylobacter jejuni11168 Biofilms Reveals a Role for the Motility Complex in Biofilm Formation
inferredcites →https://doi.org/10.1128/jb.174.7.2332-2337.1992openalex-snapshot
Genome maps of Campylobacter jejuni and Campylobacter coli
inferredcites →https://doi.org/10.1128/jb.186.11.3296-3303.2004openalex-snapshot
Secretion of Virulence Proteins from Campylobacter jejuni Is Dependent on a Functional Flagellar Export Apparatus
inferredcites →https://doi.org/10.1128/jb.186.14.4714-4729.2004openalex-snapshot
Iron Acquisition and Regulation in Campylobacter jejuni
inferredcites →https://doi.org/10.1128/jb.186.2.503-517.2004openalex-snapshot
The Genome-Sequenced Variant of Campylobacter jejuni NCTC 11168 and the Original Clonal Clinical Isolate Differ Markedly in Colonization, Gene Expression, and Virulence-Associated Phenotypes
inferredcites →https://doi.org/10.1128/jcm.20.4.636-640.1984openalex-snapshot
New, extended biotyping scheme for Campylobacter jejuni, Campylobacter coli, and "Campylobacter laridis"
inferredcites →https://doi.org/10.1128/jcm.40.3.741-745.2002openalex-snapshot
Identification of Campylobacter Heat-Stable and Heat-Labile Antigens by Combining the Penner and Lior Serotyping Schemes
inferredcites →https://doi.org/10.1128/mbio.02311-16openalex-snapshot
Nonselective Bottlenecks Control the Divergence and Diversification of Phase-Variable Bacterial Populations
inferredcites →https://doi.org/10.1128/mbio.02321-16openalex-snapshot
Fallacy of the Unique Genome: Sequence Diversity within Single Helicobacter pylori Strains
inferredcites →https://doi.org/10.1136/bmj.2.6078.9openalex-snapshot
Campylobacter enteritis: a "new" disease.
inferredcites →https://doi.org/10.1136/jcp.33.11.1122openalex-snapshot
Differentiation of enteropathogenic Campylobacter.
inferredcites →https://doi.org/10.1186/1471-2105-11-595openalex-snapshot
BIGSdb: Scalable analysis of bacterial genome variation at the population level
inferredcites →https://doi.org/10.1186/1471-2164-8-162openalex-snapshot
Re-annotation and re-analysis of the Campylobacter jejuni NCTC11168 genome sequence
inferredcites →https://doi.org/10.1186/s12864-017-4032-8openalex-snapshot
Essential genome of Campylobacter jejuni
inferredcites →https://doi.org/10.1371/journal.pcbi.1004041openalex-snapshot
ClonalFrameML: Efficient Inference of Recombination in Whole Bacterial Genomes
inferredcites →https://doi.org/10.1371/journal.pone.0009490openalex-snapshot
FastTree 2 – Approximately Maximum-Likelihood Trees for Large Alignments
inferredcites →https://doi.org/10.1371/journal.pone.0015708openalex-snapshot
Evolution of an Agriculture-Associated Disease Causing Campylobacter coli Clade: Evidence from National Surveillance Data in Scotland
inferredcites →https://doi.org/10.1371/journal.pone.0088229openalex-snapshot
Comparative Variation within the Genome of Campylobacter jejuni NCTC 11168 in Human and Murine Hosts
inferredcites →https://doi.org/10.1371/journal.pone.0092798openalex-snapshot
A Reference Pan-Genome Approach to Comparative Bacterial Genomics: Identification of Novel Epidemiological Markers in Pathogenic Campylobacter
inferredcites →https://doi.org/10.1534/genetics.108.091330openalex-snapshot
Genetic Basis of Evolutionary Adaptation by Escherichia coli to Stressful Cycles of Freezing, Thawing and Growth
inferredcites →https://doi.org/10.2217/fmb.09.44openalex-snapshot
Oxidative stress in Campylobacter jejuni : responses, resistance and regulation
inferredcites →https://doi.org/10.3389/fmicb.2015.00699openalex-snapshot
Campylobacter jejuni biofilms contain extracellular DNA and are sensitive to DNase I treatment
inferredcites →https://doi.org/10.3389/fmicb.2018.01204openalex-snapshot
Enhanced Biofilm Formation by Ferrous and Ferric Iron Through Oxidative Stress in Campylobacter jejuni
inferredcites →https://doi.org/10.3390/genes3020261openalex-snapshot
A Gene-By-Gene Approach to Bacterial Population Genomics: Whole Genome MLST of Campylobacter
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