scholarly article | Q13442814 |
P50 | author | Adela M Luján | Q79447992 |
Alejandro J Moyano | Q79447994 | ||
Andrea M Smania | Q85058682 | ||
Søren Molin | Q26883279 | ||
Helle Krogh Johansen | Q30004123 | ||
Rasmus L Marvig | Q57162412 | ||
P2093 | author name string | Julio A Di Rienzo | |
Sofía Feliziani | |||
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Phenotypic heterogeneity of Pseudomonas aeruginosa populations in a cystic fibrosis patient. | Q34661901 | ||
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Normal mutation rate variants arise in a Mutator (Mut S) Escherichia coli population. | Q34998550 | ||
Simple sequence repeats together with mismatch repair deficiency can bias mutagenic pathways in Pseudomonas aeruginosa during chronic lung infection | Q35053587 | ||
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Mutation in Elongation Factor G Confers Resistance to the Antibiotic Argyrin in the Opportunistic PathogenPseudomonas aeruginosa | Q57542530 | ||
The GacS sensor kinase controls phenotypic reversion of small colony variants isolated from biofilms of Pseudomonas aeruginosa PA14 | Q59354522 | ||
Deletion and acquisition of genomic content during early stage adaptation of Pseudomonas aeruginosa to a human host environment | Q60451766 | ||
Biological cost of hypermutation in Pseudomonas aeruginosa strains from patients with cystic fibrosis | Q61477562 | ||
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Genomic variation among contemporary Pseudomonas aeruginosa isolates from chronically infected cystic fibrosis patients | Q36197443 | ||
Resistance mechanisms of multiresistant Pseudomonas aeruginosa strains from Germany and correlation with hypermutation | Q36295397 | ||
Respiratory tract mucin genes and mucin glycoproteins in health and disease | Q36350071 | ||
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 | ||
Random amplified polymorphic DNA typing of Pseudomonas aeruginosa isolates recovered from patients with cystic fibrosis | Q36532113 | ||
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Association between hypermutator phenotype, clinical variables, mucoid phenotype, and antimicrobial resistance in Pseudomonas aeruginosa | Q36933558 | ||
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Efflux unbalance in Pseudomonas aeruginosa isolates from cystic fibrosis patients. | Q37190771 | ||
Growth phenotypes of Pseudomonas aeruginosa lasR mutants adapted to the airways of cystic fibrosis patients | Q37342706 | ||
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Hypermutation and the preexistence of antibiotic-resistant Pseudomonas aeruginosa mutants: implications for susceptibility testing and treatment of chronic infections | Q37598703 | ||
Bacterial hypermutation in cystic fibrosis, not only for antibiotic resistance | Q37794342 | ||
Parallel evolution and local differentiation in quinolone resistance in Pseudomonas aeruginosa | Q37835568 | ||
The role of MutS oligomers on Pseudomonas aeruginosa mismatch repair system activity | Q38288456 | ||
Achieving 100% typeability of Pseudomonas aeruginosa by pulsed-field gel electrophoresis | Q39468249 | ||
Involvement of a novel efflux system in biofilm-specific resistance to antibiotics | Q39759278 | ||
A major Pseudomonas aeruginosa clone common to patients and aquatic habitats | Q39915020 | ||
Infections caused by Pseudomonas aeruginosa | Q40207100 | ||
Epidemiology of infections due to Pseudomonas aeruginosa | Q40216484 | ||
Emergence of phenotypic variants upon mismatch repair disruption in Pseudomonas aeruginosa | Q40557981 | ||
Genetic adaptation of Pseudomonas aeruginosa to the airways of cystic fibrosis patients is catalyzed by hypermutation | Q41366386 | ||
Occurrence of hypermutable Pseudomonas aeruginosa in cystic fibrosis patients is associated with the oxidative stress caused by chronic lung inflammation | Q41825397 | ||
Hypermutation is a key factor in development of multiple-antimicrobial resistance in Pseudomonas aeruginosa strains causing chronic lung infections | Q41974061 | ||
Emergence of a mutL mutation causing multilocus sequence typing-pulsed-field gel electrophoresis discrepancy among Pseudomonas aeruginosa isolates from a cystic fibrosis patient. | Q42152337 | ||
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Early adaptive developments of Pseudomonas aeruginosa after the transition from life in the environment to persistent colonization in the airways of human cystic fibrosis hosts | Q43091972 | ||
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 | ||
Pseudomonas aeruginosa population diversity and turnover in cystic fibrosis chronic infections | Q43593080 | ||
Pseudomonas aeruginosa from cystic fibrosis patients: study using whole cell RAPD and antibiotic susceptibility | Q44051014 | ||
The high amino-acid content of sputum from cystic fibrosis patients promotes growth of auxotrophic Pseudomonas aeruginosa | Q45166367 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 10 | |
P921 | main subject | cystic fibrosis | Q178194 |
Pseudomonas aeruginosa | Q31856 | ||
P304 | page(s) | e1004651 | |
P577 | publication date | 2014-10-16 | |
P1433 | published in | PLOS Genetics | Q1893441 |
P1476 | title | Coexistence and within-host evolution of diversified lineages of hypermutable Pseudomonas aeruginosa in long-term cystic fibrosis infections | |
P478 | volume | 10 |
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Q36213685 | Cystic fibrosis lung environment and Pseudomonas aeruginosa infection. |
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