Expression of sialylated or paragloboside-like lipooligosaccharides are not required for pustule formation by Haemophilus ducreyi in human volunteers.
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Killing of dsrA mutants of Haemophilus ducreyi by normal human serum occurs via the classical complement pathway and is initiated by immunoglobulin M bindingThe lbgAB gene cluster of Haemophilus ducreyi encodes a beta-1,4-galactosyltransferase and an alpha-1,6-DD-heptosyltransferase involved in lipooligosaccharide biosynthesisIdentification of genes involved in the expression of atypical lipooligosaccharide structures from a second class of Haemophilus ducreyi.Experimental infection of human volunteers with Haemophilus ducreyi: fifteen years of clinical data and experience.Role played by CD4+FOXP3+ regulatory T Cells in suppression of host responses to Haemophilus ducreyi during experimental infection of human volunteersLocalization of Haemophilus ducreyi at the pustular stage of disease in the human model of infectionEvaluation of an isogenic major outer membrane protein-deficient mutant in the human model of Haemophilus ducreyi infection.Expression of peptidoglycan-associated lipoprotein is required for virulence in the human model of Haemophilus ducreyi infection.Transcription of candidate virulence genes of Haemophilus ducreyi during infection of human volunteersExpression of cytolethal distending toxin and hemolysin is not required for pustule formation by Haemophilus ducreyi in human volunteers.Characterization of Haemophilus ducreyi-specific T-cell lines from lesions of experimentally infected human subjectsHaemophilus ducreyi lipooligosaccharide mutant defective in expression of beta-1,4-glucosyltransferase is virulent in humans.A (p)ppGpp-null mutant of Haemophilus ducreyi is partially attenuated in humans due to multiple conflicting phenotypes.A superoxide dismutase C mutant of Haemophilus ducreyi is virulent in human volunteers.Immunopathogenesis of Haemophilus ducreyi infection (chancroid)Haemophilus ducreyi requires an intact flp gene cluster for virulence in humans.A humoral immune response confers protection against Haemophilus ducreyi infectionSialylation of lipooligosaccharides is dispensable for the virulence of Haemophilus ducreyi in humansDksA and (p)ppGpp have unique and overlapping contributions to Haemophilus ducreyi pathogenesis in humans.Differences in host susceptibility to disease progression in the human challenge model of Haemophilus ducreyi infection.Carbon storage regulator A contributes to the virulence of Haemophilus ducreyi in humans by multiple mechanisms.
P2860
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P2860
Expression of sialylated or paragloboside-like lipooligosaccharides are not required for pustule formation by Haemophilus ducreyi in human volunteers.
description
1999 nî lūn-bûn
@nan
1999 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Expression of sialylated or pa ...... s ducreyi in human volunteers.
@ast
Expression of sialylated or pa ...... s ducreyi in human volunteers.
@en
Expression of sialylated or pa ...... s ducreyi in human volunteers.
@nl
type
label
Expression of sialylated or pa ...... s ducreyi in human volunteers.
@ast
Expression of sialylated or pa ...... s ducreyi in human volunteers.
@en
Expression of sialylated or pa ...... s ducreyi in human volunteers.
@nl
prefLabel
Expression of sialylated or pa ...... s ducreyi in human volunteers.
@ast
Expression of sialylated or pa ...... s ducreyi in human volunteers.
@en
Expression of sialylated or pa ...... s ducreyi in human volunteers.
@nl
P2093
P2860
P1476
Expression of sialylated or pa ...... s ducreyi in human volunteers.
@en
P2093
A A Campagnari
R S Munson
S M Spinola
P2860
P304
P407
P577
1999-12-01T00:00:00Z