scholarly article | Q13442814 |
P819 | ADS bibcode | 2010PLoSO...512669F |
P356 | DOI | 10.1371/JOURNAL.PONE.0012669 |
P932 | PMC publication ID | 2937033 |
P698 | PubMed publication ID | 20844762 |
P5875 | ResearchGate publication ID | 46282121 |
P50 | author | Jose Luis Bocco | Q37838190 |
P2093 | author name string | Carlos E Argaraña | |
Patricia Montanaro | |||
Adela M Luján | |||
Alejandro J Moyano | |||
Andrea M Smania | |||
Claudia Sola | |||
Liliana Fernández Canigia | |||
Sofía Feliziani | |||
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Pathophysiology and Management of Pulmonary Infections in Cystic Fibrosis | Q35557791 | ||
Nonmotility and phagocytic resistance of Pseudomonas aeruginosa isolates from chronically colonized patients with cystic fibrosis | Q35773317 | ||
Influence of high mutation rates on the mechanisms and dynamics of in vitro and in vivo resistance development to single or combined antipseudomonal agents. | Q35879111 | ||
Resistance mechanisms of multiresistant Pseudomonas aeruginosa strains from Germany and correlation with hypermutation | Q36295397 | ||
Genetic diversity of Pseudomonas aeruginosa strains isolated from patients with cystic fibrosis revealed by restriction fragment length polymorphism of the rRNA gene region | Q36522578 | ||
Mechanism of conversion to mucoidy in Pseudomonas aeruginosa infecting cystic fibrosis patients | Q36528781 | ||
Association between hypermutator phenotype, clinical variables, mucoid phenotype, and antimicrobial resistance in Pseudomonas aeruginosa | Q36933558 | ||
Pseudomonas aeruginosa lasR mutants are associated with cystic fibrosis lung disease progression. | Q37074619 | ||
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Growth phenotypes of Pseudomonas aeruginosa lasR mutants adapted to the airways of cystic fibrosis patients | Q37342706 | ||
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Contribution of the MexXY Multidrug Transporter to Aminoglycoside Resistance in Pseudomonas aeruginosa Clinical Isolates | Q39913368 | ||
A major Pseudomonas aeruginosa clone common to patients and aquatic habitats | Q39915020 | ||
Lack of association between hypermutation and antibiotic resistance development in Pseudomonas aeruginosa isolates from intensive care unit patients | Q39955018 | ||
Auxotrophic variants of Pseudomonas aeruginosa are selected from prototrophic wild-type strains in respiratory infections in patients with cystic fibrosis. | Q40006567 | ||
Flagella and motility alterations in Pseudomonas aeruginosa strains from patients with cystic fibrosis: relationship to patient clinical condition | Q40170508 | ||
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Detection and susceptibility testing of hypermutable Pseudomonas aeruginosa strains with the Etest and disk diffusion | Q40968218 | ||
Genetic adaptation of Pseudomonas aeruginosa to the airways of cystic fibrosis patients is catalyzed by hypermutation | Q41366386 | ||
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Antibiotic resistance in Pseudomonas aeruginosa strains with increased mutation frequency due to inactivation of the DNA oxidative repair system. | Q41937031 | ||
Hypermutation is a key factor in development of multiple-antimicrobial resistance in Pseudomonas aeruginosa strains causing chronic lung infections | Q41974061 | ||
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Pseudomonas aeruginosa MutL protein functions in Escherichia coli | Q42932258 | ||
Genetic adaptation of Pseudomonas aeruginosa during chronic lung infection of patients with cystic fibrosis: strong and weak mutators with heterogeneous genetic backgrounds emerge in mucA and/or lasR mutants | Q43216787 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 9 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Pseudomonas aeruginosa | Q31856 |
DNA mismatch repair | Q2984243 | ||
cystic fibrosis | Q178194 | ||
antibiotic resistance | Q380775 | ||
quorum sensing | Q905754 | ||
P304 | page(s) | e815 | |
P577 | publication date | 2010-09-10 | |
P1433 | published in | PLOS One | Q564954 |
P1476 | title | Mucoidy, quorum sensing, mismatch repair and antibiotic resistance in Pseudomonas aeruginosa from cystic fibrosis chronic airways infections | |
P478 | volume | 5 |
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Q50282134 | Aminoglycoside resistance of Pseudomonas aeruginosa in cystic fibrosis results from convergent evolution in the mexZ gene |
Q34916610 | Analysis of changes in diversity and abundance of the microbial community in a cystic fibrosis patient over a multiyear period |
Q38686620 | Burkholderia cenocepacia phenotypic clonal variation during a 3.5-year colonization in the lungs of a cystic fibrosis patient. |
Q38207078 | Chronic pulmonary pseudomonal infection in patients with cystic fibrosis: A model for early phase symbiotic evolution |
Q34491552 | Clinical significance of microbial infection and adaptation in cystic fibrosis |
Q34948367 | Clonal dissemination, emergence of mutator lineages and antibiotic resistance evolution in Pseudomonas aeruginosa cystic fibrosis chronic lung infection. |
Q35350270 | Coexistence and within-host evolution of diversified lineages of hypermutable Pseudomonas aeruginosa in long-term cystic fibrosis infections. |
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Q29346787 | Deep sequencing analyses expands the Pseudomonas aeruginosa AmpR regulon to include small RNA-mediated regulation of iron acquisition, heat shock and oxidative stress response |
Q34680321 | Elimination of Pseudomonas aeruginosa through Efferocytosis upon Binding to Apoptotic Cells. |
Q42152337 | Emergence of a mutL mutation causing multilocus sequence typing-pulsed-field gel electrophoresis discrepancy among Pseudomonas aeruginosa isolates from a cystic fibrosis patient. |
Q40438064 | Environmental Pseudomonads Inhibit Cystic Fibrosis Patient-Derived Pseudomonas aeruginosa. |
Q34082906 | Evolution and adaptation in Pseudomonas aeruginosa biofilms driven by mismatch repair system-deficient mutators. |
Q38211644 | Evolution and impact of bacterial drug resistance in the context of cystic fibrosis disease and nosocomial settings |
Q41812492 | Fosfomycin enhances the active transport of tobramycin in Pseudomonas aeruginosa |
Q34310496 | Genetic diversity of Burkholderia contaminans isolates from cystic fibrosis patients in Argentina |
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Q89766030 | Hypermutator Pseudomonas aeruginosa exploits multiple genetic pathways to develop multidrug resistance during long-term infections in the airways of cystic fibrosis patients |
Q92676465 | ImuB and ImuC contribute to UV-induced mutagenesis as part of the SOS regulon in Pseudomonas aeruginosa |
Q36158775 | Long-term colonization of the cystic fibrosis lung by Burkholderia cepacia complex bacteria: epidemiology, clonal variation, and genome-wide expression alterations |
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Q36450695 | MexXY multidrug efflux system of Pseudomonas aeruginosa |
Q34753386 | Microbial community adaptation to quaternary ammonium biocides as revealed by metagenomics |
Q37544527 | Multiple mutations lead to MexXY-OprM-dependent aminoglycoside resistance in clinical strains of Pseudomonas aeruginosa |
Q57806910 | Mutations causing low level antibiotic resistance ensure bacterial survival in antibiotic-treated hosts |
Q34661901 | Phenotypic heterogeneity of Pseudomonas aeruginosa populations in a cystic fibrosis patient. |
Q38270707 | Proteomics of hosts and pathogens in cystic fibrosis |
Q35975439 | Pseudomonas aeruginosa AmpR: an acute-chronic switch regulator |
Q38268531 | Pseudomonas aeruginosa biofilm infections: from molecular biofilm biology to new treatment possibilities. |
Q36364034 | Pseudomonas aeruginosa syntrophy in chronically colonized airways of cystic fibrosis patients |
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Q44908378 | Quorum Sensing Down-Regulation Counteracts the Negative Impact of Pseudomonas aeruginosa on CFTR Channel Expression, Function and Rescue in Human Airway Epithelial Cells. |
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Q92864466 | Repair Process Impairment by Pseudomonas aeruginosa in Epithelial Tissues: Major Features and Potential Therapeutic Avenues |
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