| scholarly article | Q13442814 |
| P50 | author | Carmen Buchrieser | Q21256225 |
| P2093 | author name string | Carniel E | |
| Brosch R | |||
| Guiyoule A | |||
| Bach S | |||
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| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Yersinia pseudotuberculosis | Q139928 |
| P304 | page(s) | 965-978 | |
| P577 | publication date | 1998-12-01 | |
| P1433 | published in | Molecular Microbiology | Q6895967 |
| P1476 | title | The high-pathogenicity island of Yersinia pseudotuberculosis can be inserted into any of the three chromosomal asn tRNA genes | |
| P478 | volume | 30 |
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| Q35777668 | Enteroaggregative Escherichia coli isolated from Chinese diarrhea patients with high-pathogenicity island of Yersinia is involved in synthesis of siderophore yersiniabactin |
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| Q33759099 | Excision dynamics of Vibrio pathogenicity island-2 from Vibrio cholerae: role of a recombination directionality factor VefA |
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| Q37410263 | Genetic structure and distribution of the colibactin genomic island among members of the family Enterobacteriaceae. |
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| Q28189059 | Geographical heterogeneity between Far Eastern and Western countries in prevalence of the virulence plasmid, the superantigen Yersinia pseudotuberculosis-derived mitogen, and the high-pathogenicity island among Yersinia pseudotuberculosis strains |
| Q33992694 | High-frequency RecA-dependent and -independent mechanisms of Congo red binding mutations in Yersinia pestis |
| Q33970729 | High-pathogenicity island of Yersinia spp. in Escherichia coli strains isolated from diarrhea patients in China |
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| Q34660429 | How the structural gene products of Yersinia pestis relate to virulence |
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| Q33551386 | Instability of pathogenicity islands in uropathogenic Escherichia coli 536. |
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| Q41477303 | Integrative module of the high-pathogenicity island of Yersinia |
| Q41961184 | Iron acquisition in the marine actinomycete genus Salinispora is controlled by the desferrioxamine family of siderophores |
| Q39887013 | Irp9, encoded by the high-pathogenicity island of Yersinia enterocolitica, is able to convert chorismate into salicylate, the precursor of the siderophore yersiniabactin |
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| Q34028938 | Mobilisation and remobilisation of a large archetypal pathogenicity island of uropathogenic Escherichia coli in vitro support the role of conjugation for horizontal transfer of genomic islands. |
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| Q34853267 | Novel virulence-associated type II secretion system unique to high-pathogenicity Yersinia enterocolitica |
| Q41465446 | Occurrence of the Yersinia high-pathogenicity island and iron uptake systems in clinical isolates of Klebsiella pneumoniae. |
| Q35910491 | Pathogenesis of Y. enterocolitica and Y. pseudotuberculosis in Human Yersiniosis |
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| Q38882963 | Pectobacterium atrosepticum and Pectobacterium carotovorum Harbor Distinct, Independently Acquired Integrative and Conjugative Elements Encoding Coronafacic Acid that Enhance Virulence on Potato Stems |
| Q40559072 | Precise excision of the large pathogenicity island, SPI7, in Salmonella enterica serovar Typhi |
| Q37263470 | Revised nomenclature for transposable genetic elements |
| Q41447490 | Ribotyping and virulence markers of Yersinia pseudotuberculosis strains isolated from animals in Brazil |
| Q33398511 | Role of intraspecies recombination in the spread of pathogenicity islands within the Escherichia coli species |
| Q27976508 | Role of pathogenicity island-associated integrases in the genome plasticity of uropathogenic Escherichia coli strain 536 |
| Q33551329 | Salmonella enterica serovar Typhi strains from which SPI7, a 134-kilobase island with genes for Vi exopolysaccharide and other functions, has been deleted |
| Q34232631 | Shiga toxin 2e-producing Escherichia coli isolates from humans and pigs differ in their virulence profiles and interactions with intestinal epithelial cells |
| Q34005545 | Silencing and reactivation of urease in Yersinia pestis is determined by one G residue at a specific position in the ureD gene |
| Q30756935 | The 102-kilobase pgm locus of Yersinia pestis: sequence analysis and comparison of selected regions among different Yersinia pestis and Yersinia pseudotuberculosis strains |
| Q33996488 | The SHI-3 iron transport island of Shigella boydii 0-1392 carries the genes for aerobactin synthesis and transport |
| Q41465644 | The Yersinia HPI is present in Serratia liquefaciens isolated from meat |
| Q33952323 | The Yersinia high-pathogenicity island: an iron-uptake island |
| Q34513312 | The high-pathogenicity island is absent in human pathogens of Salmonella enterica subspecies I but present in isolates of subspecies III and VI. |
| Q34002012 | The high-pathogenicity island of Yersinia enterocolitica Ye8081 undergoes low-frequency deletion but not precise excision, suggesting recent stabilization in the genome. |
| Q34045712 | The importance of the small RNA chaperone Hfq for growth of epidemic Yersinia pestis, but not Yersinia pseudotuberculosis, with implications for plague biology |
| Q35706094 | The recent emergence of plague: a process of felonious evolution |
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