review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1007/S00248-003-1022-Y |
P698 | PubMed publication ID | 15037962 |
P2093 | author name string | Brubaker RR | |
P2860 | cites work | Genome sequence of Yersinia pestis KIM | Q22065462 |
Genome sequence of Yersinia pestis, the causative agent of plague | Q22122371 | ||
Yersinia pestis, the cause of plague, is a recently emerged clone of Yersinia pseudotuberculosis | Q24642708 | ||
Common themes in microbial pathogenicity revisited | Q24643808 | ||
Reevaluation of the virulence phenotype of the inv yadA double mutants of Yersinia pseudotuberculosis | Q28300037 | ||
Yersinia pestis--etiologic agent of plague | Q29619320 | ||
The 102-kilobase pgm locus of Yersinia pestis: sequence analysis and comparison of selected regions among different Yersinia pestis and Yersinia pseudotuberculosis strains | Q30756935 | ||
The 102-kilobase unstable region of Yersinia pestis comprises a high-pathogenicity island linked to a pigmentation segment which undergoes internal rearrangement | Q33729765 | ||
Structural organization of virulence-associated plasmids of Yersinia pestis. | Q33737468 | ||
High-frequency RecA-dependent and -independent mechanisms of Congo red binding mutations in Yersinia pestis | Q33992694 | ||
Silencing and reactivation of urease in Yersinia pestis is determined by one G residue at a specific position in the ureD gene | Q34005545 | ||
Role of Yersinia murine toxin in survival of Yersinia pestis in the midgut of the flea vector | Q34125533 | ||
Mutations Influencing the Assimilation of Nitrogen by Yersinia pestis | Q34169759 | ||
Role of the Yersinia pestis hemin storage (hms) locus in the transmission of plague by fleas | Q34384192 | ||
Association between virulence of Yersinia pestis and suppression of gamma interferon and tumor necrosis factor alpha. | Q34520336 | ||
Passive immunity to yersiniae mediated by anti-recombinant V antigen and protein A-V antigen fusion peptide | Q34539663 | ||
Yersinia type III secretion: send in the effectors | Q34774578 | ||
The Yersinia Ysc-Yop 'type III' weaponry | Q34931776 | ||
Mutation rate to nonpigmentation in Pasteurella pestis | Q35156343 | ||
Interleukin-10 and inhibition of innate immunity to Yersiniae: roles of Yops and LcrV (V antigen) | Q35159314 | ||
Suppression of cytokines in mice by protein A-V antigen fusion peptide and restoration of synthesis by active immunization. | Q35429159 | ||
Invasin production by Yersinia pestis is abolished by insertion of an IS200-like element within the inv gene. | Q35465426 | ||
VIRULENCE OF PASTEURELLA PESTIS AND IMMUNITY TO PLAGUE. | Q35522212 | ||
Resistance to lipopolysaccharide mediated by the Yersinia pestis V antigen-polyhistidine fusion peptide: amplification of interleukin-10. | Q35545012 | ||
Analysis of the pesticin receptor from Yersinia pestis: role in iron-deficient growth and possible regulation by its siderophore | Q35582156 | ||
Determination of genome size, macrorestriction pattern polymorphism, and nonpigmentation-specific deletion in Yersinia pestis by pulsed-field gel electrophoresis | Q36110398 | ||
Consequences of aspartase deficiency in Yersinia pestis | Q36344235 | ||
Yersinia V-antigen exploits toll-like receptor 2 and CD14 for interleukin 10-mediated immunosuppression | Q36371199 | ||
Plasmids in Yersinia pestis. | Q36443764 | ||
Factors promoting acute and chronic diseases caused by yersiniae | Q36637747 | ||
Pathology of experimental pneumonic plague produced by fraction 1-positive and fraction 1-negative Yersinia pestis in African green monkeys (Cercopithecus aethiops). | Q36808454 | ||
In vivo comparison of avirulent Vwa- and Pgm- or Pstr phenotypes of yersiniae | Q37097219 | ||
MEIOTROPHIC MUTANTS OF Pasteurella Pestis AND THEIR USE IN THE ELUCIDATION OF NUTRITIONAL REQUIREMENTS. | Q37617124 | ||
Expression of plasminogen activator pla of Yersinia pestis enhances bacterial attachment to the mammalian extracellular matrix. | Q39573935 | ||
The Genus Yersinia: Biochemistry and Genetics of Virulence With 3 Figures | Q39914791 | ||
Vwa+ phenotype of Yersinia enterocolitica. | Q40184154 | ||
Gluconate metabolism of Pasteurellapestis | Q40251867 | ||
V and W antigens in strains of Pasteurella pseudotuberculosis. | Q40252798 | ||
GLUCOSE-6-PHOSPHATE DEHYDROGENASE AND 6-PHOSPHOGLUCONATE DEHYDROGENASE ACTIVITIES OF PASTEURELLA PESTIS AND PASTEURELLA PSEUDOTUBERCULOSIS. | Q40253207 | ||
The pigmentation of Pasteurella pestis on a defined medium containing haemin | Q40294323 | ||
Mutation to rhamnose utilization in Pasteurella pestis | Q40312862 | ||
Effect of Yersinia pestis infection on temperature preference and movement of the Oriental rat flea (Xenopsylla cheopis) (Siphonaptera: Pulicidae). | Q40723239 | ||
Yersinia enterocolitica evasion of the host innate immune response by V antigen-induced IL-10 production of macrophages is abrogated in IL-10-deficient mice | Q40756138 | ||
Relationship between virulence and immunity as revealed in recent studies of the F1 capsule of Yersinia pestis. | Q41142448 | ||
A liquid-based method for the assessment of bacterial pathogenicity using the nematode Caenorhabditis elegans | Q41471775 | ||
Caenorhabditis elegans: plague bacteria biofilm blocks food intake | Q41471909 | ||
Murine toxin of Yersinia pestis shows phospholipase D activity but is not required for virulence in mice | Q41477524 | ||
Characterization of the O-antigen gene clusters of Yersinia pseudotuberculosis and the cryptic O-antigen gene cluster of Yersinia pestis shows that the plague bacillus is most closely related to and has evolved from Y. pseudotuberculosis serotype O: | Q41478664 | ||
HmsT, a protein essential for expression of the haemin storage (Hms+) phenotype of Yersinia pestis | Q41481960 | ||
The Yfe system of Yersinia pestis transports iron and manganese and is required for full virulence of plague | Q41482999 | ||
The high-pathogenicity island of Yersinia pseudotuberculosis can be inserted into any of the three chromosomal asn tRNA genes | Q41483783 | ||
Independent acquisition and insertion into different chromosomal locations of the same pathogenicity island in Yersinia pestis and Yersinia pseudotuberculosis | Q41483794 | ||
Bubonic plague: a molecular genetic case history of the emergence of an infectious disease | Q41487506 | ||
The pigmentation locus of Yersinia pestis KIM6+ is flanked by an insertion sequence and includes the structural genes for pesticin sensitivity and HMWP2. | Q41498763 | ||
The phylogeny of the genus Yersinia based on 16S rDNA sequences | Q41501426 | ||
A surface protease and the invasive character of plague | Q41504890 | ||
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 | ||
Integration of the plasmid encoding the synthesis of capsular antigen and murine toxin into Yersinia pestis chromosome | Q41508357 | ||
Increased virulence of Yersinia pseudotuberculosis by two independent mutations | Q41516551 | ||
Plasmids of the pathogenicity of Yersinia pestis | Q41522322 | ||
Detection and characterization of the plasmids of the plague microbe which determine the synthesis of pesticin I, fraction I antigen and "mouse" toxin exotoxin | Q41530777 | ||
Essential virulence determinants of different Yersinia species are carried on a common plasmid | Q41536518 | ||
The nutritional requirements of some Pasteurella species | Q41561793 | ||
Pasteurella pestis: Role of Pesticin I and Iron in Experimental Plague | Q41562748 | ||
Dideoxysugars of Pasteurella pseudotuberculosis-specific polysaccharides, and the occurrence of ascarylose | Q41566112 | ||
Virulence of Pasteurella pestis | Q41570734 | ||
P433 | issue | 3 | |
P304 | page(s) | 293-299 | |
P577 | publication date | 2004-03-25 | |
P1433 | published in | Microbial Ecology | Q15766091 |
P1476 | title | The recent emergence of plague: a process of felonious evolution | |
P478 | volume | 47 |
Q36136727 | A surface-focused biotinylation procedure identifies the Yersinia pestis catalase KatY as a membrane-associated but non-surface-located protein |
Q37224061 | Adaptive strategies of Yersinia pestis to persist during inter-epizootic and epizootic periods |
Q36079775 | Backbone structure of Yersinia pestis Ail determined in micelles by NMR-restrained simulated annealing with implicit membrane solvation |
Q35816626 | Early emergence of Yersinia pestis as a severe respiratory pathogen |
Q41186247 | Expression, refolding, and initial structural characterization of the Y. pestis Ail outer membrane protein in lipids |
Q41440126 | Inactivation of Yersinia pseudotuberculosis 197 and Francisella tularensis LVS in beverages by high pressure processing |
Q30153291 | Influence of the lipid membrane environment on structure and activity of the outer membrane protein Ail from Yersinia pestis |
Q35892066 | Invertebrates as a source of emerging human pathogens |
Q36003056 | Molecular genetic methods for the diagnosis of fastidious microorganisms |
Q56706594 | Plague |
Q34805666 | Plague in Guinea pigs and its prevention by subunit vaccines |
Q34156441 | Recent findings regarding maintenance of enzootic variants of Yersinia pestis in sylvatic reservoirs and their significance in the evolution of epidemic plague |
Q38670813 | Structural Insights into the Yersinia pestis Outer Membrane Protein Ail in Lipid Bilayers |
Q36508686 | The co-evolution of host cationic antimicrobial peptides and microbial resistance |
Q39887644 | Yersinia pestis and host macrophages: immunodeficiency of mouse macrophages induced by YscW. |
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