scholarly article | Q13442814 |
P50 | author | Leticia Busato Migliorini | Q89457899 |
Rodrigo S Galhardo | Q42557808 | ||
Patricia Severino | Q50281335 | ||
P2093 | author name string | Holger Brüggemann | |
Andrea Vieira de Souza | |||
Marines Dalla Valle Martino | |||
Paula Célia Mariko Koga | |||
Romario Oliveira de Sales | |||
P2860 | cites work | SOS response induces persistence to fluoroquinolones in Escherichia coli | Q21144990 |
Inhibition of mutation and combating the evolution of antibiotic resistance | Q21146100 | ||
Lateral gene transfer and the nature of bacterial innovation | Q22122396 | ||
All three SOS-inducible DNA polymerases (Pol II, Pol IV and Pol V) are involved in induced mutagenesis | Q24597093 | ||
DNA gyrase, topoisomerase IV, and the 4-quinolones | Q24643546 | ||
An SOS-regulated operon involved in damage-inducible mutagenesis in Caulobacter crescentus | Q24800880 | ||
Dispersal and regulation of an adaptive mutagenesis cassette in the bacteria domain | Q25257029 | ||
Bacterial Responses and Genome Instability Induced by Subinhibitory Concentrations of Antibiotics | Q27008535 | ||
Crystal structure of Escherichia coli sigmaE with the cytoplasmic domain of its anti-sigma RseA | Q27641084 | ||
Dynamics of adaptation and diversification: a 10,000-generation experiment with bacterial populations | Q28245607 | ||
Common Virulence Factors for Bacterial Pathogenicity in Plants and Animals | Q28292772 | ||
Selection of resistant bacteria at very low antibiotic concentrations | Q28479239 | ||
Essential roles for imuA'- and imuB-encoded accessory factors in DnaE2-dependent mutagenesis in Mycobacterium tuberculosis | Q28486379 | ||
Mycobacterium tuberculosis DNA repair in response to subinhibitory concentrations of ciprofloxacin | Q28486678 | ||
The glycerol-3-phosphate permease GlpT is the only fosfomycin transporter in Pseudomonas aeruginosa | Q28492495 | ||
Regulation of pyocin genes in Pseudomonas aeruginosa by positive (prtN) and negative (prtR) regulatory genes | Q28492731 | ||
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 fibrosis | Q28493131 | ||
Widespread distribution of a lexA-regulated DNA damage-inducible multiple gene cassette in the Proteobacteria phylum. | Q29346678 | ||
Defining the Pseudomonas aeruginosa SOS response and its role in the global response to the antibiotic ciprofloxacin | Q29346807 | ||
The mutagenesis protein UmuC is a DNA polymerase activated by UmuD', RecA, and SSB and is specialized for translesion replication | Q31422789 | ||
Identification of a genomic island present in the majority of pathogenic isolates of Pseudomonas aeruginosa | Q31869621 | ||
Genome diversity of Pseudomonas aeruginosa PAO1 laboratory strains | Q33519844 | ||
Cloning, nucleotide sequence, and expression of the chromate resistance determinant of Pseudomonas aeruginosa plasmid pUM505 | Q33884667 | ||
The pyocins of Pseudomonas aeruginosa | Q33962385 | ||
Comparative Genomics of Nonoutbreak Pseudomonas aeruginosa Strains Underlines Genome Plasticity and Geographic Relatedness of the Global Clone ST235 | Q60511530 | ||
Proteins required for ultraviolet light and chemical mutagenesis. Identification of the products of the umuC locus of Escherichia coli | Q67286950 | ||
Genetic recombination in Pseudomonas aeruginosa | Q73881599 | ||
Localization of a sigma70 binding site on the N terminus of the Escherichia coli RNA polymerase beta' subunit | Q77545229 | ||
Study of involvement of ImuB and DnaE2 in stationary-phase mutagenesis in Pseudomonas putida | Q79854682 | ||
Microevolution of the major common Pseudomonas aeruginosa clones C and PA14 in cystic fibrosis lungs | Q83862019 | ||
A plasmid-encoded mobile genetic element from Pseudomonas aeruginosa that confers heavy metal resistance and virulence | Q90664592 | ||
Maintenance of chromosome structure in Pseudomonas aeruginosa | Q33991987 | ||
Biological cost of pyocin production during the SOS response in Pseudomonas aeruginosa. | Q34056908 | ||
DnaE2 polymerase contributes to in vivo survival and the emergence of drug resistance in Mycobacterium tuberculosis | Q34191816 | ||
In vitro serial passage of Staphylococcus aureus: changes in physiology, virulence factor production, and agr nucleotide sequence | Q34306089 | ||
Antibiotics and antibiotic resistance: a bitter fight against evolution. | Q34334527 | ||
Can laboratory reference strains mirror "real-world" pathogenesis? | Q34389413 | ||
In vitro biofilm formation of commensal and pathogenic Escherichia coli strains: impact of environmental and genetic factors | Q34696678 | ||
Vibrio cholerae triggers SOS and mutagenesis in response to a wide range of antibiotics: a route towards multiresistance | Q34933315 | ||
Analysis of the promoters involved in enterocin AS-48 expression. | Q35110796 | ||
Significance of antibiotics in the environment | Q35153853 | ||
Laboratory adaptation of Bordetella pertussis is associated with the loss of type three secretion system functionality | Q35191908 | ||
UmuD'(2)C is an error-prone DNA polymerase, Escherichia coli pol V. | Q35588920 | ||
Error-prone replication for better or worse | Q35785643 | ||
Quinolones in 2005: an update. | Q36067593 | ||
Cystic fibrosis lung environment and Pseudomonas aeruginosa infection. | Q36213685 | ||
Ongoing evolution of Pseudomonas aeruginosa PAO1 sublines complicates studies of DNA damage repair and tolerance | Q36322378 | ||
SERS detection of the biomarker hydrogen cyanide from Pseudomonas aeruginosa cultures isolated from cystic fibrosis patients | Q37724020 | ||
Microbiological effects of sublethal levels of antibiotics. | Q38214805 | ||
PBP3 inhibition elicits adaptive responses in Pseudomonas aeruginosa. | Q38309969 | ||
The Use and Abuse of LexA by Mobile Genetic Elements | Q38771839 | ||
Role of the recA-related gene adjacent to the recA gene in Pseudomonas aeruginosa | Q39928069 | ||
The phenotypic evolution of Pseudomonas aeruginosa populations changes in the presence of subinhibitory concentrations of ciprofloxacin. | Q40764020 | ||
Isolation and characterization of mutants of Escherichia coli deficient in induction of mutations by ultraviolet light | Q40850491 | ||
A plasmid-encoded UmuD homologue regulates expression of Pseudomonas aeruginosa SOS genes. | Q41006803 | ||
Ciprofloxacin-Mediated Mutagenesis Is Suppressed by Subinhibitory Concentrations of Amikacin in Pseudomonas aeruginosa | Q42021837 | ||
Sublethal ciprofloxacin treatment leads to rapid development of high-level ciprofloxacin resistance during long-term experimental evolution of Pseudomonas aeruginosa | Q42572942 | ||
Complete genome sequence of enterohemorrhagic Escherichia coli O157:H7 and genomic comparison with a laboratory strain K-12. | Q42645426 | ||
Pseudomonas biofilm formation and antibiotic resistance are linked to phenotypic variation | Q42674600 | ||
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 | ||
Sub-lethal concentrations of antibiotics increase mutation frequency in the cystic fibrosis pathogen Pseudomonas aeruginosa | Q43647829 | ||
A simple method for genome-wide screening for advantageous insertions of mobile DNAs in Escherichia coli | Q43996519 | ||
Sputum antibiotic concentrations: implications for treatment of cystic fibrosis lung infection. | Q44275415 | ||
Nature of the SOS mutator activity: genetic characterization of untargeted mutagenesis in Escherichia coli | Q44285208 | ||
Variable plasmid fitness effects and mobile genetic element dynamics across Pseudomonas species | Q46243806 | ||
Evolutionary loss of the rdar morphotype in Salmonella as a result of high mutation rates during laboratory passage | Q47928367 | ||
In vitro and in vivo expression of virulence genes in Vibrio isolates belonging to the Harveyi clade in relation to their virulence towards gnotobiotic brine shrimp (Artemia franciscana). | Q49087135 | ||
Growth rates made easy. | Q51147152 | ||
Discovery and Function of a General Core Hormetic Stress Response in E. coli Induced by Sublethal Concentrations of Antibiotics. | Q51452645 | ||
A hydrophobic patch on the flap-tip helix of E.coli RNA polymerase mediates sigma(70) region 4 function. | Q52560431 | ||
Purification and properties of pyocin S2. | Q53785382 | ||
The SOS response increases bacterial fitness, but not evolvability, under a sublethal dose of antibiotic. | Q53786053 | ||
Effect of recA inactivation on mutagenesis of Escherichia coli exposed to sublethal concentrations of antimicrobials. | Q54372713 | ||
Cloning and characterization of the umu operon responsible for inducible mutagenesis in Escherichia coli | Q54493691 | ||
Effect of iron concentration in the growth medium on the sensitivity of Pseudomonas aeruginosa to pyocin S2. | Q54562849 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P921 | main subject | Pseudomonas aeruginosa | Q31856 |
P304 | page(s) | 1553 | |
P577 | publication date | 2019-07-10 | |
P1433 | published in | Frontiers in Microbiology | Q27723481 |
P1476 | title | Mutagenesis Induced by Sub-Lethal Doses of Ciprofloxacin: Genotypic and Phenotypic Differences Between the Pseudomonas aeruginosa Strain PA14 and Clinical Isolates | |
P478 | volume | 10 |
Q89671585 | Predicting antimicrobial resistance in Pseudomonas aeruginosa with machine learning-enabled molecular diagnostics | cites work | P2860 |
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