| scholarly article | Q13442814 |
| P50 | author | Carmen Buchrieser | Q21256225 |
| Michael B. Prentice | Q41463896 | ||
| P2093 | author name string | E Carniel | |
| P2860 | cites work | A rapid alkaline extraction procedure for screening recombinant plasmid DNA | Q24614998 |
| Plague pandemics investigated by ribotyping of Yersinia pestis strains | Q24645312 | ||
| Nucleotide sequence of the Yersinia enterocolitica ail gene and characterization of the Ail protein product | Q24673497 | ||
| Pathogenicity islands of virulent bacteria: structure, function and impact on microbial evolution | Q28307679 | ||
| Yersinia pestis--etiologic agent of plague | Q29619320 | ||
| Recent emergence of new variants of Yersinia pestis in Madagascar | Q30428755 | ||
| Relationship between loss of pigmentation and deletion of the chromosomal iron-regulated irp2 gene in Yersinia pestis: evidence for separate but related events | Q33601487 | ||
| Prevalence of the "high-pathogenicity island" of Yersinia species among Escherichia coli strains that are pathogenic to humans. | Q33750049 | ||
| Role of the Yersinia pestis hemin storage (hms) locus in the transmission of plague by fleas | Q34384192 | ||
| A genetic locus of enterocyte effacement conserved among diverse enterobacterial pathogens | Q34642972 | ||
| The gene coding for the 190,000-dalton iron-regulated protein of Yersinia species is present only in the highly pathogenic strains | Q35131521 | ||
| Invasin production by Yersinia pestis is abolished by insertion of an IS200-like element within the inv gene. | Q35465426 | ||
| Genetic organization of the yersiniabactin biosynthetic region and construction of avirulent mutants in Yersinia pestis | Q35546294 | ||
| Pathogenicity island sequences of pyelonephritogenic Escherichia coli CFT073 are associated with virulent uropathogenic strains. | Q35551150 | ||
| Analysis of the pesticin receptor from Yersinia pestis: role in iron-deficient growth and possible regulation by its siderophore | Q35582156 | ||
| Characterization of a large chromosomal "high-pathogenicity island" in biotype 1B Yersinia enterocolitica. | Q35617313 | ||
| Determination of genome size, macrorestriction pattern polymorphism, and nonpigmentation-specific deletion in Yersinia pestis by pulsed-field gel electrophoresis | Q36110398 | ||
| High-molecular-weight protein 2 of Yersinia enterocolitica is homologous to AngR of Vibrio anguillarum and belongs to a family of proteins involved in nonribosomal peptide synthesis | Q36121385 | ||
| A 40 kb chromosomal fragment encoding Salmonella typhimurium invasion genes is absent from the corresponding region of the Escherichia coli K-12 chromosome | Q36707901 | ||
| The pesticin receptor of Yersinia enterocolitica: a novel virulence factor with dual function | Q36729262 | ||
| cag, a pathogenicity island of Helicobacter pylori, encodes type I-specific and disease-associated virulence factors | Q37047617 | ||
| Identification and cloning of a hemin storage locus involved in the pigmentation phenotype of Yersinia pestis | Q37608986 | ||
| Identification of a virulence locus encoding a second type III secretion system in Salmonella typhimurium | Q37698755 | ||
| Two pathogenicity islands in uropathogenic Escherichia coli J96: cosmid cloning and sample sequencing. | Q39825974 | ||
| Excision of large DNA regions termed pathogenicity islands from tRNA-specific loci in the chromosome of an Escherichia coli wild-type pathogen. | Q39859232 | ||
| Genetic analysis of the yopE region of Yersinia spp.: identification of a novel conserved locus, yerA, regulating yopE expression | Q39944282 | ||
| Congo Red-Agar Plating Medium for Detecting Pigmentation in Pasteurella pestis | Q40719844 | ||
| A role for bacteriophages in the evolution and transfer of bacterial virulence determinants | Q41034498 | ||
| Sequence and genetic analysis of the hemin storage (hms) system of Yersinia pestis | Q41488040 | ||
| YbtA, an AraC-type regulator of the Yersinia pestis pesticin/yersiniabactin receptor | Q41490382 | ||
| The established Yersinia pestis biovars are characterized by typical patterns of I-CeuI restriction fragment length polymorphism | Q41494348 | ||
| Virulence-associatedfyuA/irp2gene cluster ofYersinia enterocoliticabiotype 1B carries a novel insertion sequence IS1328 | Q41494387 | ||
| Sequencing of two Yersinia pestis IS elements, IS285 and IS100. | Q41495720 | ||
| Clamped homogenous electric fields (CHEF) gel-electrophoresis of DNA restriction fragments for comparing genomic variations among strains of yersinia enterocolitica and Yersinia spp. | Q41497823 | ||
| Nucleotide sequence and structural organization of Yersinia pestis insertion sequence IS100. | Q41498440 | ||
| The pigmentation locus of Yersinia pestis KIM6+ is flanked by an insertion sequence and includes the structural genes for pesticin sensitivity and HMWP2. | Q41498763 | ||
| Survey of the irp2 gene among Yersinia pestis strains isolated during several plague outbreaks in northeast Brazil | Q41500881 | ||
| Proteins essential for expression of the Hms+ phenotype of Yersinia pestis | Q41503317 | ||
| Chromosomal irp2 gene in Yersinia: distribution, expression, deletion and impact on virulence | Q41504325 | ||
| Loss of the pigmentation phenotype in Yersinia pestis is due to the spontaneous deletion of 102 kb of chromosomal DNA which is flanked by a repetitive element | Q41505380 | ||
| Analysis of Yersinia pestis chromosomal determinants Pgm+ and Psts associated with virulence. | Q41506457 | ||
| Molecular cloning, iron-regulation and mutagenesis of the irp2 gene encoding HMWP2, a protein specific for the highly pathogenic Yersinia | Q41506793 | ||
| Intervening sequences (IVSs) in the 23S ribosomal RNA genes of pathogenic Yersinia enterocolitica strains. The IVSs in Y enterocolitica and Salmonella typhimurium have a common origin | Q41509293 | ||
| Chromosomal marker for the 'high pathogenicity' phenotype in Yersinia | Q41509851 | ||
| Varieties of Pasteurella pestis; new hypothesis | Q41574559 | ||
| Deletions of chromosomal regions coding for fimbriae and hemolysins occur in vitro and in vivo in various extraintestinal Escherichia coli isolates | Q42018719 | ||
| A putative integrase gene defines the distal end of a large cluster of ToxR-regulated colonization genes in Vibrio cholerae | Q48061736 | ||
| The purified SoxABCD quinol oxidase complex of Sulfolobus acidocaldarius contains a novel haem. | Q54026689 | ||
| P433 | issue | 9 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Yersinia pestis | Q153875 |
| P304 | page(s) | 2321-2329 | |
| P577 | publication date | 1998-05-01 | |
| P1433 | published in | Journal of Bacteriology | Q478419 |
| P1476 | title | The 102-kilobase unstable region of Yersinia pestis comprises a high-pathogenicity island linked to a pigmentation segment which undergoes internal rearrangement | |
| P478 | volume | 180 |
| Q30846631 | A 90-kilobase conjugative chromosomal element coding for biphenyl and salicylate catabolism in Pseudomonas putida KF715 |
| Q33557963 | Absence of inflammation and pneumonia during infection with nonpigmented Yersinia pestis reveals a new role for the pgm locus in pathogenesis |
| Q34334283 | Accurate, rapid and high-throughput detection of strain-specific polymorphisms in Bacillus anthracis and Yersinia pestis by next-generation sequencing |
| Q33184831 | An ABC transporter from Bacillus thuringiensis is essential for beta-exotoxin I production |
| Q33678428 | Application of DNA microarrays to study the evolutionary genomics of Yersinia pestis and Yersinia pseudotuberculosis |
| Q34381263 | Applying molecular biological techniques to detecting biological agents. |
| Q36422212 | Characterization of integrative and conjugative element ICEKp1-associated genomic heterogeneity in a Klebsiella pneumoniae strain isolated from a primary liver abscess |
| Q34007128 | Characterization of the Yersinia pestis Yfu ABC inorganic iron transport system |
| Q39512306 | Common and specific characteristics of the high-pathogenicity island of Yersinia enterocolitica |
| Q60958176 | Comparative Analysis of Genomic Island Prediction Tools |
| Q40430057 | Cultivar-specific avirulence and virulence functions assigned to avrPphF in Pseudomonas syringae pv. phaseolicola, the cause of bean halo-blight disease. |
| Q35759768 | Defining genomic islands and uropathogen-specific genes in uropathogenic Escherichia coli |
| Q41461622 | Defining the genome content of live plague vaccines by use of whole-genome DNA microarray |
| Q34119439 | Delineation and analysis of chromosomal regions specifying Yersinia pestis |
| Q34128266 | Determination of the virulence of the pigmentation-deficient and pigmentation-/plasminogen activator-deficient strains of Yersinia pestis in non-human primate and mouse models of pneumonic plague. |
| Q34466495 | Diarrhoeagenic Escherichia coli--an emerging problem? |
| Q35814177 | Dissociation of Tissue Destruction and Bacterial Expansion during Bubonic Plague. |
| Q33942640 | Efficacy of primate humoral passive transfer in a murine model of pneumonic plague is mouse strain-dependent. |
| Q36257725 | Evaluation of the effect of host immune status on short-term Yersinia pestis infection in fleas with implications for the enzootic host model for maintenance of Y. pestis during interepizootic periods |
| Q30962327 | Evolutionary diversification of an ancient gene family (rhs) through C-terminal displacement |
| Q33759099 | Excision dynamics of Vibrio pathogenicity island-2 from Vibrio cholerae: role of a recombination directionality factor VefA |
| Q34009180 | Ferric dicitrate transport system (Fec) of Shigella flexneri 2a YSH6000 is encoded on a novel pathogenicity island carrying multiple antibiotic resistance genes |
| Q33992182 | Genetic analysis of a chromosomal region containing vanA and vanB, genes required for conversion of either ferulate or vanillate to protocatechuate in Acinetobacter |
| Q37743251 | Genome dynamics and its impact on evolution of Escherichia coli. |
| Q37248338 | Genomic islands: tools of bacterial horizontal gene transfer and evolution |
| Q34002026 | Genomic subtractive hybridization and selective capture of transcribed sequences identify a novel Salmonella typhimurium fimbrial operon and putative transcriptional regulator that are absent from the Salmonella typhi genome |
| 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 |
| Q41457584 | Influence of Na(+), dicarboxylic amino acids, and pH in modulating the low-calcium response of Yersinia pestis |
| Q33551386 | Instability of pathogenicity islands in uropathogenic Escherichia coli 536. |
| Q31974757 | Iron acquisition in plague: modular logic in enzymatic biogenesis of yersiniabactin by Yersinia pestis. |
| Q41432193 | Mus spretus SEG/Pas mice resist virulent Yersinia pestis, under multigenic control. |
| Q37503760 | New Insights into Autoinducer-2 Signaling as a Virulence Regulator in a Mouse Model of Pneumonic Plague |
| 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. |
| Q27343051 | Opposing roles for interferon regulatory factor-3 (IRF-3) and type I interferon signaling during plague |
| Q34095514 | Pathogenicity islands and phage conversion: evolutionary aspects of bacterial pathogenesis |
| Q36513899 | Prevention of pneumonic plague in mice, rats, guinea pigs and non-human primates with clinical grade rV10, rV10-2 or F1-V vaccines |
| Q37688618 | Rational considerations about development of live attenuated Yersinia pestis vaccines |
| Q36361830 | RcsB contributes to the distinct stress fitness among Escherichia coli O157:H7 curli variants of the 1993 hamburger-associated outbreak strains |
| Q33943840 | Replication of Yersinia pestis in interferon gamma-activated macrophages requires ripA, a gene encoded in the pigmentation locus |
| Q30847813 | Representational difference analysis between Afa/Dr diffusely adhering Escherichia coli and nonpathogenic E. coli K-12. |
| Q33398511 | Role of intraspecies recombination in the spread of pathogenicity islands within the Escherichia coli species |
| Q21136041 | Role of the Yersinia pestis yersiniabactin iron acquisition system in the incidence of flea-borne plague |
| Q33836563 | Short palindromic repetitive DNA elements in enterobacteria: a survey |
| Q37020714 | Stochasticity and bistability in horizontal transfer control of a genomic island in Pseudomonas |
| Q36574864 | Temperature regulation of the hemin storage (Hms+) phenotype of Yersinia pestis is posttranscriptional |
| 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 |
| Q33952323 | The Yersinia high-pathogenicity island: an iron-uptake island |
| Q38859993 | The hidden life of integrative and conjugative elements |
| Q34002012 | The high-pathogenicity island of Yersinia enterocolitica Ye8081 undergoes low-frequency deletion but not precise excision, suggesting recent stabilization in the genome. |
| Q35706094 | The recent emergence of plague: a process of felonious evolution |
| Q64253637 | Whole genome sequencing based typing and characterisation of Shiga-toxin producing strains belonging to O157 and O26 serotypes and isolated in dairy farms |
| Q34007591 | Yersinia pestis YbtU and YbtT are involved in synthesis of the siderophore yersiniabactin but have different effects on regulation |
| Q89449096 | Yersinia pseudotuberculosis Prevalence and Diversity in Wild Boars in Northeast Germany |
| Q41464025 | Yersiniabactin and other siderophores produced by clinical isolates of Enterobacter spp. and Citrobacter spp. |
| Q37879258 | Yersiniabactin iron uptake: mechanisms and role in Yersinia pestis pathogenesis |
| Q34127942 | Yersiniabactin production requires the thioesterase domain of HMWP2 and YbtD, a putative phosphopantetheinylate transferase |
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