Pages that link to "Q42913659"

The following pages link to A bile salt hydrolase of Brucella abortus contributes to the establishment of a successful infection through the oral route in mice (Q42913659):

Displaying 28 items.

• Brucella abortus ure2 region contains an acid-activated urea transporter and a nickel transport system (Q33551503) (← links)
• Genomic characterization of the Yersinia genus (Q33762297) (← links)
• An oral vaccine based on U-Omp19 induces protection against B. abortus mucosal challenge by inducing an adaptive IL-17 immune response in mice (Q33802696) (← links)
• Global analysis of quorum sensing targets in the intracellular pathogen Brucella melitensis 16 M (Q33894505) (← links)
• Yersinia enterocolitica palearctica serobiotype O:3/4--a successful group of emerging zoonotic pathogens (Q33953002) (← links)
• Brucella abortus choloylglycine hydrolase affects cell envelope composition and host cell internalization (Q34103100) (← links)
• Laboratory Animal Models for Brucellosis Research (Q34595217) (← links)
• Establishment of systemic Brucella melitensis infection through the digestive tract requires urease, the type IV secretion system, and lipopolysaccharide O antigen (Q34995443) (← links)
• The BtaF trimeric autotransporter of Brucella suis is involved in attachment to various surfaces, resistance to serum and virulence (Q35043884) (← links)
• Protective Live Oral Brucellosis Vaccines Stimulate Th1 and Th17 Cell Responses (Q35273029) (← links)
• What have we learned from brucellosis in the mouse model? (Q36136716) (← links)
• Interaction of gut microbiota with bile acid metabolism and its influence on disease states (Q36204422) (← links)
• BtaE, an adhesin that belongs to the trimeric autotransporter family, is required for full virulence and defines a specific adhesive pole of Brucella suis (Q36646623) (← links)
• Functional and comparative metagenomic analysis of bile salt hydrolase activity in the human gut microbiome. (Q36869991) (← links)
• Immunization with recombinant Brucella species outer membrane protein Omp16 or Omp19 in adjuvant induces specific CD4 and CD8 T cells as well as systemic and oral protection against Brucella abortus infection (Q37033007) (← links)
• Interplay between two RND systems mediating antimicrobial resistance in Brucella suis. (Q37157099) (← links)
• Confronting the barriers to develop novel vaccines against brucellosis (Q37932521) (← links)
• Regulation of virulence in Brucella: an eclectic repertoire of transcription factors defines the complex architecture of the virB promoter (Q38135908) (← links)
• Penicillin acylases revisited: importance beyond their industrial utility (Q38272180) (← links)
• Brucellosis vaccines for livestock (Q38794720) (← links)
• A MarR-Type regulator directly activates transcription from the Brucella abortus virB promoter by sharing a redundant role with HutC. (Q41172591) (← links)
• TLR2 and TLR4 signaling pathways are required for recombinant Brucella abortus BCSP31-induced cytokine production, functional upregulation of mouse macrophages, and the Th1 immune response in vivo and in vitro (Q41810950) (← links)
• Allelic variation of bile salt hydrolase genes in Lactobacillus salivarius does not determine bile resistance levels. (Q41895545) (← links)
• Alternative strategies for vaccination to brucellosis (Q49486807) (← links)
• Bile salt hydrolases: Structure and function, substrate preference, and inhibitor development (Q57112170) (← links)
• MapB, the Brucella suis TamB homologue, is involved in cell envelope biogenesis, cell division and virulence (Q61795937) (← links)
• Omp19 Enables Brucella abortus to Evade the Antimicrobial Activity From Host's Proteolytic Defense System (Q91811489) (← links)
• Immune Response to Mucosal Brucella Infection (Q93088272) (← links)