Nonmucoid Pseudomonas aeruginosa expresses alginate in the lungs of patients with cystic fibrosis and in a mouse model.

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Nonmucoid Pseudomonas aeruginosa expresses alginate in the lungs of patients with cystic fibrosis and in a mouse model. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1086/431516
P932PMC publication ID1317300
P698PubMed publication ID15995954
P5875ResearchGate publication ID7748223

P50authorMichael GivskovQ30329016
Gerald PierQ38326393
Massimo ConeseQ40235787
Jens Bo AndersenQ40705929
Alessandra BragonziQ43269735
P2093author name stringMorten Hentzer
Martina Ulrich
Dieter Worlitzsch
Gerd Doring
Petra Timpert
P2860cites workComplete genome sequence of Pseudomonas aeruginosa PAO1, an opportunistic pathogenQ22122393
Effects of reduced mucus oxygen concentration in airway Pseudomonas infections of cystic fibrosis patientsQ24551181
Cystic fibrosisQ28212180
High mutation frequencies among Escherichia coli and Salmonella pathogensQ48057867
Differentiation of Pseudomonas aeruginosa into the alginate-producing form: inactivation of mucB causes conversion to mucoidyQ48106984
Role of mutator alleles in adaptive evolution.Q54564129
Bacterial transcription factors involved in global regulationQ56902186
Prevalence of mucoid strains of Pseudomonas aeruginosa in bacteriological specimens from patients with cystic fibrosis and patients with other diseasesQ67515117
A mouse model of chronic pulmonary infection with Pseudomonas aeruginosa and Pseudomonas cepaciaQ68544977
Pseudomonas aeruginosa in cystic fibrosis: role of mucC in the regulation of alginate production and stress sensitivityQ73917235
The mismatch repair system (mutS, mutL and uvrD genes) in Pseudomonas aeruginosa: molecular characterization of naturally occurring mutantsQ28492576
Two distinct loci affecting conversion to mucoidy in Pseudomonas aeruginosa in cystic fibrosis encode homologs of the serine protease HtrAQ28492750
Control of AlgU, a member of the sigma E-like family of stress sigma factors, by the negative regulators MucA and MucB and Pseudomonas aeruginosa conversion to mucoidy in cystic fibrosisQ28493131
Production of mucoid microcolonies by Pseudomonas aeruginosa within infected lungs in cystic fibrosisQ33903005
Genetic analysis of Pseudomonas aeruginosa isolates from the sputa of Australian adult cystic fibrosis patientsQ33963695
Gender differences in cystic fibrosis: Pseudomonas aeruginosa infectionQ34058988
High frequency of hypermutable Pseudomonas aeruginosa in cystic fibrosis lung infection.Q34508854
Hypersusceptibility of cystic fibrosis mice to chronic Pseudomonas aeruginosa oropharyngeal colonization and lung infectionQ34531184
Construction and characterization of a Pseudomonas aeruginosa mucoid exopolysaccharide-alginate conjugate vaccine.Q35106317
Endobronchial inflammation following Pseudomonas aeruginosa infection in resistant and susceptible strains of miceQ35408151
Mucoid Pseudomonas aeruginosa in cystic fibrosis: characterization of muc mutations in clinical isolates and analysis of clearance in a mouse model of respiratory infectionQ35555504
Mechanism of conversion to mucoidy in Pseudomonas aeruginosa infecting cystic fibrosis patientsQ36528781
Polysaccharide surface antigens expressed by nonmucoid isolates of Pseudomonas aeruginosa from cystic fibrosis patientsQ37208228
A rat model of chronic respiratory infection with Pseudomonas aeruginosaQ39663990
Alginate production by clinical nonmucoid Pseudomonas aeruginosa strains.Q40190281
Immunoglobulin A and immunoglobulin G antibody responses to alginates from Pseudomonas aeruginosa in patients with cystic fibrosisQ40200920
Relevance of animal models for chronic bacterial airway infections in humansQ40537117
Isolation and assay of Pseudomonas aeruginosa alginateQ40687452
Role of alginate in infection with mucoid Pseudomonas aeruginosa in cystic fibrosisQ41144869
Human monoclonal antibodies to Pseudomonas aeruginosa alginate that protect against infection by both mucoid and nonmucoid strains.Q45115153
Effect of Pseudomonas infection on weight loss, lung mechanics, and cytokines in miceQ45252511
Longitudinal development of mucoid Pseudomonas aeruginosa infection and lung disease progression in children with cystic fibrosis.Q47855663
Mucoid conversion of Pseudomonas aeruginosa by hydrogen peroxide: a mechanism for virulence activation in the cystic fibrosis lung.Q47946251
P433issue3
P407language of work or nameEnglishQ1860
P921main subjectPseudomonas aeruginosaQ31856
cystic fibrosisQ178194
patientQ181600
P304page(s)410-419
P577publication date2005-06-24
P1433published inJournal of Infectious DiseasesQ4051141
P1476titleNonmucoid Pseudomonas aeruginosa expresses alginate in the lungs of patients with cystic fibrosis and in a mouse model
P478volume192

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