| scholarly article | Q13442814 |
| P50 | author | Andreas J. Bäumler | Q4755471 |
| Sean-Paul Nuccio | Q30349068 | ||
| Valerie A Gerriets | Q55283732 | ||
| Parameth Thiennimitr | Q57039644 | ||
| Holger Rüssmann | Q130218540 | ||
| P2093 | author name string | Sebastian E Winter | |
| Maria G Winter | |||
| P2860 | cites work | Complete genome sequence of Salmonella enterica serovar Typhimurium LT2 | Q22122369 |
| Complete genome sequence of a multiple drug resistant Salmonella enterica serovar Typhi CT18 | Q22122370 | ||
| Comparative genomics of Salmonella enterica serovar Typhi strains Ty2 and CT18 | Q24554266 | ||
| Within the fold: assessing differential expression measures and reproducibility in microarray assays. | Q24793654 | ||
| Structural Analysis of the DNA-binding Domain of theErwinia amylovora RcsB Protein and Its Interaction with the RcsAB Box | Q27641203 | ||
| The Salmonella SPI1 type three secretion system responds to periplasmic disulfide bond status via the flagellar apparatus and the RcsCDB system | Q28492915 | ||
| TM4: a free, open-source system for microarray data management and analysis | Q29547339 | ||
| Construction of versatile low-copy-number vectors for cloning, sequencing and gene expression in Escherichia coli | Q29615309 | ||
| Microarray data normalization and transformation | Q29617789 | ||
| Vi polysaccharide of Salmonella typhi targets the prohibitin family of molecules in intestinal epithelial cells and suppresses early inflammatory responses | Q30448411 | ||
| A two-genome microarray for the rice pathogens Xanthomonas oryzae pv. oryzae and X. oryzae pv. oryzicola and its use in the discovery of a difference in their regulation of hrp genes | Q30482750 | ||
| Salmonella enterica serovar Typhi strains from which SPI7, a 134-kilobase island with genes for Vi exopolysaccharide and other functions, has been deleted | Q33551329 | ||
| Osmolarity and growth phase overlap in regulation of Salmonella typhi adherence to and invasion of human intestinal cells | Q33603552 | ||
| Clustering gene expression patterns | Q33882299 | ||
| The Rcs phosphorelay system is specific to enteric pathogens/commensals and activates ydeI, a gene important for persistent Salmonella infection of mice | Q33954565 | ||
| Coupling of flagellar gene expression to flagellar assembly in Salmonella enterica serovar typhimurium and Escherichia coli | Q34010272 | ||
| Cloning and molecular characterization of genes whose products allow Salmonella typhimurium to penetrate tissue culture cells | Q34298444 | ||
| Type III flagellar protein export and flagellar assembly | Q34368259 | ||
| Identification of new flagellar genes of Salmonella enterica serovar Typhimurium | Q34513676 | ||
| HilE interacts with HilD and negatively regulates hilA transcription and expression of the Salmonella enterica serovar Typhimurium invasive phenotype. | Q34714166 | ||
| MudSacI, a transposon with strong selectable and counterselectable markers: use for rapid mapping of chromosomal mutations in Salmonella typhimurium | Q35580672 | ||
| Characterization of the rcsA and rcsB genes from Salmonella typhi: rcsB through tviA is involved in regulation of Vi antigen synthesis | Q35604057 | ||
| The Rcs phosphorelay: a complex signal transduction system | Q36253588 | ||
| Expression of Salmonella typhimurium genes required for invasion is regulated by changes in DNA supercoiling | Q36984314 | ||
| Interaction of Salmonella enterica serovar Typhi with cultured epithelial cells: roles of surface structures in adhesion and invasion | Q37119291 | ||
| Contribution of flagellin pattern recognition to intestinal inflammation during Salmonella enterica serotype typhimurium infection | Q37191428 | ||
| The capsule-encoding viaB locus reduces intestinal inflammation by a Salmonella pathogenicity island 1-independent mechanism | Q37256566 | ||
| From bench to bedside: stealth of enteroinvasive pathogens | Q37310216 | ||
| Salmonella enterica serovar Enteritidis colonization of the chicken caecum requires the HilA regulatory protein | Q38444330 | ||
| Multiple factors independently regulate hilA and invasion gene expression in Salmonella enterica serovar typhimurium | Q39538569 | ||
| Transcription of the Salmonella invasion gene activator, hilA, requires HilD activation in the absence of negative regulators. | Q39714214 | ||
| Positive autoregulation of vipR expression in ViaB region-encoded Vi antigen of Salmonella typhi | Q39840503 | ||
| Coordinated regulation of expression of Salmonella pathogenicity island 1 and flagellar type III secretion systems by ATP-dependent ClpXP protease | Q40017377 | ||
| The Vi-capsule prevents Toll-like receptor 4 recognition of Salmonella. | Q40045738 | ||
| The Salmonella enterica serotype Typhi regulator TviA reduces interleukin-8 production in intestinal epithelial cells by repressing flagellin secretion | Q40088417 | ||
| Genetic Transfer of the Vi Antigen from Salmonella typhosa to Escherichia coli | Q40111973 | ||
| Characterization of defined ompR mutants of Salmonella typhi: ompR is involved in the regulation of Vi polysaccharide expression | Q40375337 | ||
| HilD, HilC and RtsA constitute a feed forward loop that controls expression of the SPI1 type three secretion system regulator hilA in Salmonella enterica serovar Typhimurium. | Q40402350 | ||
| The Vi capsular antigen of Salmonella enterica serotype Typhi reduces Toll-like receptor-dependent interleukin-8 expression in the intestinal mucosa. | Q40419113 | ||
| Activation of the RcsC/YojN/RcsB phosphorelay system attenuates Salmonella virulence | Q40507106 | ||
| Precise excision of the large pathogenicity island, SPI7, in Salmonella enterica serovar Typhi | Q40559072 | ||
| Survival of Vi-capsulated and Vi-deleted Salmonella typhi strains in cultured macrophage expressing different levels of CD14 antigen | Q40655294 | ||
| Role of the viaB locus in synthesis, transport and expression of Salmonella typhi Vi antigen. | Q40677377 | ||
| The capsule encoding the viaB locus reduces interleukin-17 expression and mucosal innate responses in the bovine intestinal mucosa during infection with Salmonella enterica serotype Typhi. | Q41985502 | ||
| Regulation of capsule synthesis and cell motility in Salmonella enterica by the essential gene igaA. | Q41990307 | ||
| Sensing structural intermediates in bacterial flagellar assembly by export of a negative regulator. | Q42502618 | ||
| hilA is a novel ompR/toxR family member that activates the expression of Salmonella typhimurium invasion genes | Q42638991 | ||
| Identification of a new iron regulated locus of Salmonella typhi | Q42648125 | ||
| The RcsCDB signaling system and swarming motility in Salmonella enterica serovar typhimurium: dual regulation of flagellar and SPI-2 virulence genes | Q42910457 | ||
| Null mutations in the essential gene yrfF (mucM) are not lethal in rcsB, yojN or rcsC strains of Salmonella enterica serovar Typhimurium | Q44448259 | ||
| Optimization of virulence functions through glucosylation of Shigella LPS. | Q45282739 | ||
| CAST: an iterative algorithm for the complexity analysis of sequence tracts. Complexity analysis of sequence tracts. | Q48693964 | ||
| Signal-dependent Requirement for the Co-activator Protein RcsA in Transcription of the RcsB-regulated ugd Gene | Q50102611 | ||
| Vi-Suppressed wild strain Salmonella typhi cultured in high osmolarity is hyperinvasive toward epithelial cells and destructive of Peyer's patches | Q50115994 | ||
| The RcsAB box. Characterization of a new operator essential for the regulation of exopolysaccharide biosynthesis in enteric bacteria | Q50122219 | ||
| The RcsB-RcsC regulatory system of Salmonella typhi differentially modulates the expression of invasion proteins, flagellin and Vi antigen in response to osmolarity | Q50129536 | ||
| Comparison of Salmonella typhi and Salmonella typhimurium invasion, intracellular growth and localization in cultured human epithelial cells | Q50146506 | ||
| Role of the Vi antigen of Salmonella typhi in resistance to host defense in vitro | Q50202630 | ||
| The invasion of HeLa cells by Salmonella typhimurium: reversible and irreversible bacterial attachment and the role of bacterial motility | Q50215677 | ||
| RcsCDB His-Asp phosphorelay system negatively regulates the flhDC operon in Escherichia coli. | Q54521795 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Salmonella enterica | Q2264864 |
| P304 | page(s) | 175-193 | |
| P577 | publication date | 2009-08-24 | |
| P1433 | published in | Molecular Microbiology | Q6895967 |
| P1476 | title | The TviA auxiliary protein renders the Salmonella enterica serotype Typhi RcsB regulon responsive to changes in osmolarity | |
| P478 | volume | 74 |
| Q41448074 | A genomewide mutagenesis screen identifies multiple genes contributing to Vi capsular expression in Salmonella enterica serovar Typhi. |
| Q33680498 | A rapid change in virulence gene expression during the transition from the intestinal lumen into tissue promotes systemic dissemination of Salmonella |
| Q39278386 | BglJ-RcsB heterodimers relieve repression of the Escherichia coli bgl operon by H-NS. |
| Q48529701 | Bi-valent polysaccharides of Vi capsular and O9 O-antigen in attenuated Salmonella Typhimurium induce strong immune responses against these two antigens |
| Q38844750 | Chronic Bacterial Pathogens: Mechanisms of Persistence |
| Q37667983 | Comparative analysis of Salmonella genomes identifies a metabolic network for escalating growth in the inflamed gut. |
| Q33654036 | Contrasting persistence strategies in Salmonella and Mycobacterium |
| Q36728030 | Differences in Host Cell Invasion and Salmonella Pathogenicity Island 1 Expression between Salmonella enterica Serovar Paratyphi A and Nontyphoidal S. Typhimurium |
| Q34075421 | Dynamic modularity of host protein interaction networks in Salmonella Typhi infection |
| Q92615136 | Endogenous Enterobacteriaceae underlie variation in susceptibility to Salmonella infection |
| Q59798201 | Evolution of Salmonella within Hosts |
| Q35947410 | Flagellin Is Required for Host Cell Invasion and Normal Salmonella Pathogenicity Island 1 Expression by Salmonella enterica Serovar Paratyphi A |
| Q38654112 | Genetic, Biochemical, and Structural Analyses of Bacterial Surface Polysaccharides |
| Q26997068 | Helicobacter and salmonella persistent infection strategies |
| Q37340368 | Host specificity of bacterial pathogens |
| Q35075822 | In vivo regulation of the Vi antigen in Salmonella and induction of immune responses with an in vivo-inducible promoter |
| Q35190035 | Integrated stress responses in Salmonella |
| Q28482256 | Intraspecies variation in the emergence of hyperinfectious bacterial strains in nature |
| Q37429384 | Live Attenuated Human Salmonella Vaccine Candidates: Tracking the Pathogen in Natural Infection and Stimulation of Host Immunity |
| Q33921859 | Live recombinant Salmonella Typhi vaccines constructed to investigate the role of rpoS in eliciting immunity to a heterologous antigen |
| Q37074488 | Loss of very-long O-antigen chains optimizes capsule-mediated immune evasion by Salmonella enterica serovar Typhi. |
| Q49923802 | Mechanisms to Evade the Phagocyte Respiratory Burst Arose by Convergent Evolution in Typhoidal Salmonella Serovars |
| Q89537685 | Molecular Mechanisms of Salmonella Effector Proteins: A Comprehensive Review |
| Q46271225 | New Insights into the Non-orthodox Two Component Rcs Phosphorelay System |
| Q35443593 | Non-typhoidal Salmonella Typhimurium ST313 isolates that cause bacteremia in humans stimulate less inflammasome activation than ST19 isolates associated with gastroenteritis |
| Q38370050 | Now you see me, now you don't: the interaction of Salmonella with innate immune receptors |
| Q50033978 | OmpR may regulate the putative YehU/YehT two-component system in Salmonella enterica serovar Typhi under hypotonic growth condition |
| Q93379629 | Persistent Infection and Long-Term Carriage of Typhoidal and Nontyphoidal Salmonellae |
| Q39144745 | Potassium transport of Salmonella is important for type III secretion and pathogenesis |
| Q38438706 | RcsB is required for inducible acid resistance in Escherichia coli and acts at gadE-dependent and -independent promoters |
| Q38974017 | RcsB positively regulates the Yersinia Ysc-Yop type III secretion system by activating expression of the master transcriptional regulator LcrF. |
| Q35836653 | Regulation of virulence: the rise and fall of gastrointestinal pathogens. |
| Q31172548 | Salmonella enterica Serovar Typhi conceals the invasion-associated type three secretion system from the innate immune system by gene regulation |
| Q33603033 | Salmonella enterica serovar Typhi impairs CD4 T cell responses by reducing antigen availability |
| Q33877264 | Taming the elephant: Salmonella biology, pathogenesis, and prevention |
| Q41845880 | The Periplasmic Nitrate Reductase NapABC Supports Luminal Growth of Salmonella enterica Serovar Typhimurium during Colitis |
| Q37781060 | The Rcs phosphorelay: more than just a two-component pathway |
| Q27324387 | The Vi capsular polysaccharide enables Salmonella enterica serovar typhi to evade microbe-guided neutrophil chemotaxis |
| Q35187597 | The flagellar regulator TviA reduces pyroptosis by Salmonella enterica serovar Typhi |
| Q34222261 | The flagellar regulator fliT represses Salmonella pathogenicity island 1 through flhDC and fliZ. |
| Q36211779 | The response regulator RcsB activates expression of Mat fimbriae in meningitic Escherichia coli |
| Q40136074 | The transcriptional regulator SsrB is involved in a molecular switch controlling virulence lifestyles of Salmonella. |
| Q26860755 | Typhoid fever: "you can't hit what you can't see" |
| Q30248288 | Typhoidal and non-typhoidal Salmonella infections in Africa. |
| Q40079316 | Vi capsular polysaccharide: Synthesis, virulence, and application. |
| Q57946303 | Why Is Eradicating Typhoid Fever So Challenging: Implications for Vaccine and Therapeutic Design |
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