scholarly article | Q13442814 |
P2093 | author name string | R. Curtiss | |
H. A. Lockman | |||
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The Role of Pili and Capsule in the Pathogenesis of Neonatal Infection with Escherichia coli Kl | Q44592160 | ||
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Distribution and properties of the mannose-resistant hemagglutinin produced by Salmonella species | Q50200092 | ||
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The Attachment to, and Invasion of HeLa Cells by Salmonella typhimurium: The Contribution of Mannose-sensitive and Mannoseresistant Haemagglutinating Activities | Q50215674 | ||
Fimbriae and infectivity in Salmonella typhimurium | Q50226858 | ||
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Fimbriae and adhesive properties in Salmonellae | Q95788728 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Salmonella Typhimurium | Q166491 |
P304 | page(s) | 491-496 | |
P577 | publication date | 1992-02-01 | |
P1433 | published in | Infection and Immunity | Q6029193 |
P1476 | title | Virulence of non-type 1-fimbriated and nonfimbriated nonflagellated Salmonella typhimurium mutants in murine typhoid fever | |
P478 | volume | 60 |
Q50141418 | Antimicrobial activity of chicken and turkey heterophil peptides CHP1, CHP2, THP1, and THP3. |
Q36951109 | Bacterial motility is a colonization factor in experimental urinary tract infection |
Q36971527 | Characterization and protective properties of attenuated mutants of Salmonella choleraesuis |
Q33995341 | Characterization of grvA, an antivirulence gene on the gifsy-2 phage in Salmonella enterica serovar typhimurium |
Q37667983 | Comparative analysis of Salmonella genomes identifies a metabolic network for escalating growth in the inflamed gut. |
Q35532558 | Construction of a flagellum-negative mutant of Proteus mirabilis: effect on internalization by human renal epithelial cells and virulence in a mouse model of ascending urinary tract infection |
Q35493173 | Contribution of fimbrial operons to attachment to and invasion of epithelial cell lines by Salmonella typhimurium. |
Q36814156 | Distribution, gene sequence and expression in vivo of the plasmid encoded fimbrial antigen of Salmonella serotype Enteritidis |
Q64268775 | Everything You Always Wanted to Know About Type 1 Fimbriae, but Were Afraid to Ask |
Q21558786 | Evolution of Salmonella enterica virulence via point mutations in the fimbrial adhesin |
Q33764112 | Evolution of host adaptation in Salmonella enterica |
Q39930412 | FimH family of type 1 fimbrial adhesins: functional heterogeneity due to minor sequence variations among fimH genes |
Q33995282 | FimW is a negative regulator affecting type 1 fimbrial expression in Salmonella enterica serovar typhimurium |
Q38324920 | Functional heterogeneity of type 1 fimbriae of Escherichia coli |
Q36669927 | Genetic map of Salmonella typhimurium, edition VIII |
Q37845999 | How to become a top model: impact of animal experimentation on human Salmonella disease research. |
Q39836359 | Identification and sequence analysis of lpfABCDE, a putative fimbrial operon of Salmonella typhimurium |
Q35510490 | Induction of cytokine granulocyte-macrophage colony-stimulating factor and chemokine macrophage inflammatory protein 2 mRNAs in macrophages by Legionella pneumophila or Salmonella typhimurium attachment requires different ligand-receptor systems |
Q36127265 | Lesions in two Escherichia coli type 1 pilus genes alter pilus number and length without affecting receptor binding |
Q39654238 | Lipopolysaccharide-specific but not anti-flagellar immunoglobulin A monoclonal antibodies prevent Salmonella enterica serotype enteritidis invasion and replication within HEp-2 cell monolayers |
Q33558343 | Molecular basis of the interaction of Salmonella with the intestinal mucosa. |
Q33754964 | Multiple fimbrial adhesins are required for full virulence of Salmonella typhimurium in mice |
Q39826417 | Mutants of Streptococcus suis types 1 and 2 impaired in expression of muramidase-released protein and extracellular protein induce disease in newborn germfree pigs |
Q64448664 | Pili Assembled by the Chaperone/Usher Pathway in and |
Q35662912 | RtsA and RtsB coordinately regulate expression of the invasion and flagellar genes in Salmonella enterica serovar Typhimurium. |
Q40277304 | Salmonella enterica serovar Typhimurium requires the Lpf, Pef, and Tafi fimbriae for biofilm formation on HEp-2 tissue culture cells and chicken intestinal epithelium. |
Q35955975 | The Non-Fimbriate Phenotype Is Predominant among Salmonella enterica Serovar Choleraesuis from Swine and Those Non-Fimbriate Strains Possess Distinct Amino Acid Variations in FimH |
Q33788226 | The Salmonella enterica serotype Typhimurium lpf, bcf, stb, stc, std, and sth fimbrial operons are required for intestinal persistence in mice |
Q34709533 | The leucine-responsive regulatory protein, Lrp, activates transcription of the fim operon in Salmonella enterica serovar typhimurium via the fimZ regulatory gene. |
Q35461269 | The pef fimbrial operon of Salmonella typhimurium mediates adhesion to murine small intestine and is necessary for fluid accumulation in the infant mouse. |
Q34636651 | The role of flagella and chemotaxis genes in host pathogen interaction of the host adapted Salmonella enterica serovar Dublin compared to the broad host range serovar S. Typhimurium. |
Q35338623 | Type 1 fimbriae are important factors limiting the dissemination and colonization of mice by Salmonella Enteritidis and contribute to the induction of intestinal inflammation during Salmonella invasion. |
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