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Pseudomonas aeruginosa Diversification during Infection Development in Cystic Fibrosis Lungs—A Review
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/14651858.cd001021.pub2openalex-snapshot
Inhaled antibiotics for long-term therapy in cystic fibrosis
inferredcites →https://doi.org/10.1002/emmm.201000115openalex-snapshot
Staphylococcus aureus phenotype switching: an effective bacterial strategy to escape host immune response and establish a chronic infection
inferredcites →https://doi.org/10.1002/ppul.21011openalex-snapshot
Pseudomonas aeruginosa biofilms in the respiratory tract of cystic fibrosis patients
inferredcites →https://doi.org/10.1002/ppul.21521openalex-snapshot
Reduced mortality in cystic fibrosis patients treated with tobramycin inhalation solution
inferredcites →https://doi.org/10.1002/ppul.22543openalex-snapshot
Clearance of initial mucoid Pseudomonas aeruginosa in patients with cystic fibrosis
inferredcites →https://doi.org/10.1002/ppul.22669openalex-snapshot
Optimization of anti‐pseudomonal antibiotics for cystic fibrosis pulmonary exacerbations: II. cephalosporins and penicillins
inferredcites →https://doi.org/10.1007/bf03256204openalex-snapshot
Targeted Therapy for Cystic Fibrosis
inferredcites →https://doi.org/10.1007/s00253-010-2498-2openalex-snapshot
Rhamnolipids: diversity of structures, microbial origins and roles
inferredcites →https://doi.org/10.1007/s00253-012-4258-yopenalex-snapshot
Rhamnolipid production: effect of oxidative stress on virulence factors and proteome of Pseudomonas aeruginosa PA1
inferredcites →https://doi.org/10.1007/s10096-005-0031-9openalex-snapshot
Effect of oxygen limitation on the in vitro antimicrobial susceptibility of clinical isolates of Pseudomonas aeruginosa grown planktonically and as biofilms
inferredcites →https://doi.org/10.1007/s10096-013-1916-7openalex-snapshot
Virulence factor expression patterns in Pseudomonas aeruginosa strains from infants with cystic fibrosis
inferredcites →https://doi.org/10.1016/j.biologicals.2013.11.001openalex-snapshot
Pseudomonas aeruginosa biofilm: Potential therapeutic targets
inferredcites →https://doi.org/10.1016/j.clinbiochem.2012.05.034openalex-snapshot
Cystic fibrosis: Insight into CFTR pathophysiology and pharmacotherapy
inferredcites →https://doi.org/10.1016/j.coph.2006.12.005openalex-snapshot
Opportunistic infections in lung disease: Pseudomonas infections in cystic fibrosis
inferredcites →https://doi.org/10.1016/j.ijantimicag.2009.12.011openalex-snapshot
Antibiotic resistance of bacterial biofilms
inferredcites →https://doi.org/10.1016/j.ijmm.2010.08.003openalex-snapshot
Adaptation of Staphylococcus aureus to the cystic fibrosis lung
inferredcites →https://doi.org/10.1016/j.ijmm.2010.08.006openalex-snapshot
Multicellular signalling and growth of Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1016/j.ijmm.2010.08.007openalex-snapshot
Anaerobic physiology of Pseudomonas aeruginosa in the cystic fibrosis lung
inferredcites →https://doi.org/10.1016/j.ijmm.2010.08.008openalex-snapshot
Adaptation of Pseudomonas aeruginosa during persistence in the cystic fibrosis lung
inferredcites →https://doi.org/10.1016/j.jcf.2008.02.003openalex-snapshot
Spread of colistin resistant non-mucoid Pseudomonas aeruginosa among chronically infected Danish cystic fibrosis patients
inferredcites →https://doi.org/10.1016/j.jcf.2012.07.008openalex-snapshot
Eradication therapy for Pseudomonas aeruginosa colonization episodes in cystic fibrosis patients not chronically colonized by P. aeruginosa
inferredcites →https://doi.org/10.1016/j.jcf.2012.10.004openalex-snapshot
Treatment of lung infection in patients with cystic fibrosis: Current and future strategies
inferredcites →https://doi.org/10.1016/j.jcf.2013.01.002openalex-snapshot
Importance of bacteriology in upper airways of patients with Cystic Fibrosis
inferredcites →https://doi.org/10.1016/j.meegid.2013.05.016openalex-snapshot
Small colony variants (SCVs) of Staphylococcus aureus – A bacterial survival strategy
inferredcites →https://doi.org/10.1016/j.mib.2013.06.013openalex-snapshot
Bacterial biofilm development as a multicellular adaptation: antibiotic resistance and new therapeutic strategies
inferredcites →https://doi.org/10.1016/j.micinf.2003.08.009openalex-snapshot
Antimicrobial resistance of Pseudomonas aeruginosa biofilms
inferredcites →https://doi.org/10.1016/j.mimet.2013.09.020openalex-snapshot
Improvements on colony morphology identification towards bacterial profiling
inferredcites →https://doi.org/10.1016/j.molcel.2010.01.003openalex-snapshot
Sublethal Antibiotic Treatment Leads to Multidrug Resistance via Radical-Induced Mutagenesis
inferredcites →https://doi.org/10.1016/j.tim.2004.11.007openalex-snapshot
Sociomicrobiology: the connections between quorum sensing and biofilms
inferredcites →https://doi.org/10.1016/j.tim.2004.11.010openalex-snapshot
Survival strategies of infectious biofilms
inferredcites →https://doi.org/10.1016/j.tim.2008.11.004openalex-snapshot
Staphylococcus aureus as an intracellular pathogen: the role of small colony variants
inferredcites →https://doi.org/10.1016/j.tim.2008.12.003openalex-snapshot
Pseudomonas aeruginosa hypoxic or anaerobic biofilm infections within cystic fibrosis airways
inferredcites →https://doi.org/10.1016/s0169-409x(02)00152-7openalex-snapshot
Anaerobic metabolism and quorum sensing by Pseudomonas aeruginosa biofilms in chronically infected cystic fibrosis airways: rethinking antibiotic treatment strategies and drug targets
inferredcites →https://doi.org/10.1016/s0966-842x(00)88974-xopenalex-snapshot
Pseudomonas aeruginosa, mucoidy and the chronic infection phenotype in cystic fibrosis
inferredcites →https://doi.org/10.1016/s1534-5807(02)00295-2openalex-snapshot
Pseudomonas aeruginosa Anaerobic Respiration in Biofilms
inferredcites →https://doi.org/10.1034/j.1399-3003.2000.16d30.xopenalex-snapshot
Antibiotic therapy against Pseudomonas aeruginosa in cystic fibrosis: a European consensus
inferredcites →https://doi.org/10.1038/ismej.2011.83openalex-snapshot
Evolution and diversification of Pseudomonas aeruginosa in the paranasal sinuses of cystic fibrosis children have implications for chronic lung infection
inferredcites →https://doi.org/10.1038/ng.997openalex-snapshot
Parallel bacterial evolution within multiple patients identifies candidate pathogenicity genes
inferredcites →https://doi.org/10.1038/nrd1008openalex-snapshot
Understanding biofilm resistance to antibacterial agents
inferredcites →https://doi.org/10.1038/nrmicro1384openalex-snapshot
Small colony variants: a pathogenic form of bacteria that facilitates persistent and recurrent infections
inferredcites →https://doi.org/10.1038/nrmicro1838openalex-snapshot
Physiological heterogeneity in biofilms
inferredcites →https://doi.org/10.1038/nrmicro2907openalex-snapshot
Adaptation of Pseudomonas aeruginosa to the cystic fibrosis airway: an evolutionary perspective
inferredcites →https://doi.org/10.1046/j.1365-2958.2001.02469.xopenalex-snapshot
Pseudomonas aeruginosa GacA, a factor in multihost virulence, is also essential for biofilm formation
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03261.xopenalex-snapshot
Impact of large chromosomal inversions on the adaptation and evolution of Pseudomonas aeruginosa chronically colonizing cystic fibrosis lungs
inferredcites →https://doi.org/10.1073/pnas.0407460101openalex-snapshot
Self-generated diversity produces “insurance effects” in biofilm communities
inferredcites →https://doi.org/10.1073/pnas.0602138103openalex-snapshot
Genetic adaptation by Pseudomonas aeruginosa to the airways of cystic fibrosis patients
inferredcites →https://doi.org/10.1073/pnas.0702660104openalex-snapshot
Regulated proteolysis controls mucoid conversion in Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1073/pnas.0801499105openalex-snapshot
Endogenous oxidative stress produces diversity and adaptability in biofilm communities
inferredcites →https://doi.org/10.1073/pnas.90.18.8377openalex-snapshot
Mechanism of conversion to mucoidy in Pseudomonas aeruginosa infecting cystic fibrosis patients.
inferredcites →https://doi.org/10.1073/pnas.96.4.1463openalex-snapshot
Biodiversity and ecosystem productivity in a fluctuating environment: The insurance hypothesis
inferredcites →https://doi.org/10.1086/318075openalex-snapshot
Longitudinal Assessment ofPseudomonas aeruginosain Young Children with Cystic Fibrosis
inferredcites →https://doi.org/10.1086/431516openalex-snapshot
NonmucoidPseudomonas aeruginosaExpresses Alginate in the Lungs of Patients with Cystic Fibrosis and in a Mouse Model
inferredcites →https://doi.org/10.1086/509821openalex-snapshot
Stage‐Specific Adaptation of HypermutablePseudomonas aeruginosaIsolates during Chronic Pulmonary Infection in Patients with Cystic Fibrosis
inferredcites →https://doi.org/10.1086/598644openalex-snapshot
Small-Colony Variants of Pseudomonas aeruginosa in Cystic Fibrosis
inferredcites →https://doi.org/10.1086/599360openalex-snapshot
Dynamics of Adaptive Microevolution of HypermutablePseudomonas aeruginosaduring Chronic Pulmonary Infection in Patients with Cystic Fibrosis
inferredcites →https://doi.org/10.1093/infdis/jir690openalex-snapshot
Intrinsic and Environmental Mutagenesis Drive Diversification and Persistence of Pseudomonas aeruginosa in Chronic Lung Infections
inferredcites →https://doi.org/10.1093/jac/dkn044openalex-snapshot
Increased mutability of Pseudomonas aeruginosa in biofilms
inferredcites →https://doi.org/10.1097/01.mcp.0000245712.51514.a1openalex-snapshot
Treatment of early Pseudomonas aeruginosa infection in patients with cystic fibrosis
inferredcites →https://doi.org/10.1099/00221287-146-10-2345openalex-snapshot
The causes of Pseudomonas diversity
inferredcites →https://doi.org/10.1099/jmm.0.024083-0openalex-snapshot
Bacterial hypermutation: clinical implications
inferredcites →https://doi.org/10.1099/jmm.0.05069-0openalex-snapshot
Highly adherent small-colony variants of Pseudomonas aeruginosa in cystic fibrosis lung infection
inferredcites →https://doi.org/10.1099/jmm.0.45617-0openalex-snapshot
Analysis of quorum sensing-deficient clinical isolates of Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1099/jmm.0.45969-0openalex-snapshot
Microcolony formation: a novel biofilm model of Pseudomonas aeruginosa for the cystic fibrosis lung
inferredcites →https://doi.org/10.1099/mic.0.033993-0openalex-snapshot
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
inferredcites →https://doi.org/10.1099/mic.0.2006/003400-0openalex-snapshot
Biological cost of hypermutation in Pseudomonas aeruginosa strains from patients with cystic fibrosis
inferredcites →https://doi.org/10.1099/mic.0.2007/009092-0openalex-snapshot
Biofilm differentiation and dispersal in mucoid Pseudomonas aeruginosa isolates from patients with cystic fibrosis
inferredcites →https://doi.org/10.1099/mic.0.2008/019281-0openalex-snapshot
Role of quorum sensing by Pseudomonas aeruginosa in microbial keratitis and cystic fibrosis
inferredcites →https://doi.org/10.1099/mic.0.29175-0openalex-snapshot
Sequence diversity of the mucABD locus in Pseudomonas aeruginosa isolates from patients with cystic fibrosis
inferredcites →https://doi.org/10.1101/cshperspect.a009589openalex-snapshot
CFTR, Mucins, and Mucus Obstruction in Cystic Fibrosis
inferredcites →https://doi.org/10.1101/cshperspect.a010306openalex-snapshot
Bacterial Biofilms: Development, Dispersal, and Therapeutic Strategies in the Dawn of the Postantibiotic Era
inferredcites →https://doi.org/10.1111/j.1365-2958.2005.04552.xopenalex-snapshot
Understanding the control of Pseudomonas aeruginosa alginate synthesis and the prospects for management of chronic infections in cystic fibrosis
inferredcites →https://doi.org/10.1111/j.1365-2958.2007.05678.xopenalex-snapshot
Growth phenotypes of Pseudomonas aeruginosa lasR mutants adapted to the airways of cystic fibrosis patients
inferredcites →https://doi.org/10.1111/j.1440-1843.2010.01819.xopenalex-snapshot
Pseudomonas aeruginosa: Host defence in lung diseases
inferredcites →https://doi.org/10.1111/j.1462-2920.2004.00618.xopenalex-snapshot
Biofilm formation by the small colony variant phenotype of Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1111/j.1462-2920.2010.02211.xopenalex-snapshot
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
inferredcites →https://doi.org/10.1111/j.1462-2920.2010.02253.xopenalex-snapshot
How Pseudomonas aeruginosa adapts to various environments: a metabolomic approach
inferredcites →https://doi.org/10.1111/j.1462-2920.2011.02483.xopenalex-snapshot
Microevolution of the major common Pseudomonas aeruginosa clones C and PA14 in cystic fibrosis lungs
inferredcites →https://doi.org/10.1111/j.1469-0691.2008.02097.xopenalex-snapshot
Chromosomal mechanisms of aminoglycoside resistance in Pseudomonas aeruginosa isolates from cystic fibrosis patients
inferredcites →https://doi.org/10.1111/j.1469-0691.2010.03250.xopenalex-snapshot
Bacterial hypermutation in cystic fibrosis, not only for antibiotic resistance
inferredcites →https://doi.org/10.1111/j.1469-0691.2011.03627.xopenalex-snapshot
Initial Pseudomonas aeruginosa infection in patients with cystic fibrosis: characteristics of eradicated and persistent isolates
inferredcites →https://doi.org/10.1111/j.1574-695x.2012.00983.xopenalex-snapshot
Phenotypes selected during chronic lung infection in cystic fibrosis patients: implications for the treatment ofPseudomonas aeruginosabiofilm infections
inferredcites →https://doi.org/10.1111/j.1574-695x.2012.01006.xopenalex-snapshot
Biofilm dispersal cells of a cystic fibrosisPseudomonas aeruginosaisolate exhibit variability in functional traits likely to contribute to persistent infection
inferredcites →https://doi.org/10.1111/j.1574-6968.2007.00664.xopenalex-snapshot
An intragenic deletion inpilQleads to nonpiliation of aPseudomonas aeruginosastrain isolated from cystic fibrosis lung
inferredcites →https://doi.org/10.1111/j.1574-6976.2010.00237.xopenalex-snapshot
Differential adaptation of microbial pathogens to airways of patients with cystic fibrosis and chronic obstructive pulmonary disease
inferredcites →https://doi.org/10.1111/j.1574-6976.2011.00269.xopenalex-snapshot
Pseudomonas genomes: diverse and adaptable
inferredcites →https://doi.org/10.1126/science.280.5361.295openalex-snapshot
The Involvement of Cell-to-Cell Signals in the Development of a Bacterial Biofilm
inferredcites →https://doi.org/10.1126/science.288.5469.1251openalex-snapshot
High Frequency of Hypermutable Pseudomonas aeruginosa in Cystic Fibrosis Lung Infection
inferredcites →https://doi.org/10.1128/aac.00174-07openalex-snapshot
Influence of High Mutation Rates on the Mechanisms and Dynamics of In Vitro and In Vivo Resistance Development to Single or Combined Antipseudomonal Agents
inferredcites →https://doi.org/10.1128/aac.01393-12openalex-snapshot
High β-Lactamase Levels Change the Pharmacodynamics of β-Lactam Antibiotics in Pseudomonas aeruginosa Biofilms
inferredcites →https://doi.org/10.1128/aac.35.5.1008openalex-snapshot
Induction of beta-lactamase production in Pseudomonas aeruginosa biofilm
inferredcites →https://doi.org/10.1128/aac.36.1.71openalex-snapshot
High-level beta-lactamase activity in sputum samples from cystic fibrosis patients during antipseudomonal treatment
inferredcites →https://doi.org/10.1128/aac.44.3.710-712.2000openalex-snapshot
Molecular Mechanisms of Fluoroquinolone Resistance in Pseudomonas aeruginosa Isolates from Cystic Fibrosis Patients
inferredcites →https://doi.org/10.1128/aac.48.4.1168-1174.2004openalex-snapshot
Dynamics and Spatial Distribution of β-Lactamase Expression in Pseudomonas aeruginosa Biofilms
inferredcites →https://doi.org/10.1128/aac.48.7.2659-2664.2004openalex-snapshot
Oxygen Limitation Contributes to Antibiotic Tolerance of Pseudomonas aeruginosa in Biofilms
inferredcites →https://doi.org/10.1128/aac.49.6.2276-2282.2005openalex-snapshot
Occurrence of HypermutablePseudomonas aeruginosain Cystic Fibrosis Patients Is Associated with the Oxidative Stress Caused by Chronic Lung Inflammation
inferredcites →https://doi.org/10.1128/aac.49.8.3382-3386.2005openalex-snapshot
Hypermutation Is a Key Factor in Development of Multiple-Antimicrobial Resistance inPseudomonas aeruginosaStrains Causing Chronic Lung Infections
inferredcites →https://doi.org/10.1128/aem.71.8.4809-4821.2005openalex-snapshot
Characterization of Colony Morphology Variants Isolated from Pseudomonas aeruginosa Biofilms
inferredcites →https://doi.org/10.1128/iai.73.4.2504-2514.2005openalex-snapshot
Novel Mouse Model of Chronic Pseudomonas aeruginosa Lung Infection Mimicking Cystic Fibrosis
inferredcites →https://doi.org/10.1128/jb.00119-09openalex-snapshot
Pseudomonas aeruginosa Rugose Small-Colony Variants Have Adaptations That Likely Promote Persistence in the Cystic Fibrosis Lung
inferredcites →https://doi.org/10.1128/jb.01147-08openalex-snapshot
Genetic Adaptation of Pseudomonas aeruginosa to the Airways of Cystic Fibrosis Patients Is Catalyzed by Hypermutation
inferredcites →https://doi.org/10.1128/jb.182.2.425-431.2000openalex-snapshot
The Global Carbon Metabolism Regulator Crc Is a Component of a Signal Transduction Pathway Required for Biofilm Development by Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1128/jb.183.4.1195-1204.2001openalex-snapshot
Initiation of Biofilm Formation by Pseudomonas aeruginosa 57RP Correlates with Emergence of Hyperpiliated and Highly Adherent Phenotypic Variants Deficient in Swimming, Swarming, and Twitching Motilities
inferredcites →https://doi.org/10.1128/jb.184.16.4544-4554.2002openalex-snapshot
Phosphorylation of thePseudomonas aeruginosaResponse Regulator AlgR Is Essential for Type IV Fimbria-Mediated Twitching Motility
inferredcites →https://doi.org/10.1128/jb.184.4.1140-1154.2002openalex-snapshot
Pseudomonas aeruginosa Displays Multiple Phenotypes during Development as a Biofilm
inferredcites →https://doi.org/10.1128/jb.186.21.7312-7326.2004openalex-snapshot
Characterization of Nutrient-Induced Dispersion in Pseudomonas aeruginosa PAO1 Biofilm
inferredcites →https://doi.org/10.1128/jb.186.22.7575-7585.2004openalex-snapshot
MucA-Mediated Coordination of Type III Secretion and Alginate Synthesis in Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1128/jb.187.15.5267-5277.2005openalex-snapshot
Cystic Fibrosis Sputum Supports Growth and Cues Key Aspects of Pseudomonas aeruginosa Physiology
inferredcites →https://doi.org/10.1128/jb.187.23.8114-8126.2005openalex-snapshot
Characterization of Temporal Protein Production in Pseudomonas aeruginosa Biofilms
inferredcites →https://doi.org/10.1128/jcm.33.1.37-40.1995openalex-snapshot
Auxotrophic variants of Pseudomonas aeruginosa are selected from prototrophic wild-type strains in respiratory infections in patients with cystic fibrosis
inferredcites →https://doi.org/10.1128/mbio.00094-12openalex-snapshot
Identification of Genes in the σ22Regulon of Pseudomonas aeruginosa Required for Cell Envelope Homeostasis in Either the Planktonic or the Sessile Mode of Growth
inferredcites →https://doi.org/10.1128/mbio.00199-10openalex-snapshot
Parallel Evolution in Pseudomonas aeruginosa over 39,000 Generations In Vivo
inferredcites →https://doi.org/10.1128/mmbr.60.3.539-574.1996openalex-snapshot
Microbial pathogenesis in cystic fibrosis: mucoid Pseudomonas aeruginosa and Burkholderia cepacia
inferredcites →https://doi.org/10.1134/s0026261707020014openalex-snapshot
Biofilm—“City of microbes” or an analogue of multicellular organisms?
inferredcites →https://doi.org/10.1136/thorax.55.9.795openalex-snapshot
Increased sputum amino acid concentrations and auxotrophy of Pseudomonas aeruginosa in severe cystic fibrosis lung disease
inferredcites →https://doi.org/10.1136/thx.2009.121657openalex-snapshot
Treatment of early Pseudomonas aeruginosa infection in patients with cystic fibrosis: the ELITE trial
inferredcites →https://doi.org/10.1164/rccm.200812-1943ocopenalex-snapshot
Pseudomonas aeruginosa Microevolution during Cystic Fibrosis Lung Infection Establishes Clones with Adapted Virulence
inferredcites →https://doi.org/10.1164/rccm.201009-1430ocopenalex-snapshot
Pseudomonas aeruginosa Population Diversity and Turnover in Cystic Fibrosis Chronic Infections
inferredcites →https://doi.org/10.1165/ajrcmb.22.6.4023openalex-snapshot
Mucoid Pseudomonas aeruginosa , TNF-α, and IL-1 β, but Not IL-6, Induce Human β-Defensin-2 in Respiratory Epithelia
inferredcites →https://doi.org/10.1172/jci0213870openalex-snapshot
Effects of reduced mucus oxygen concentration in airway Pseudomonas infections of cystic fibrosis patients
inferredcites →https://doi.org/10.1172/jci13870openalex-snapshot
Effects of reduced mucus oxygen concentration in airway Pseudomonas infections of cystic fibrosis patients
inferredcites →https://doi.org/10.1177/1753465811398267openalex-snapshot
New and investigational treatments in cystic fibrosis
inferredcites →https://doi.org/10.1186/1471-2180-13-170openalex-snapshot
Sub-inhibitory concentrations of some antibiotics can drive diversification of Pseudomonas aeruginosa populations in artificial sputum medium
inferredcites →https://doi.org/10.1186/1471-2180-5-43openalex-snapshot
Characterization of Pseudomonas aeruginosa isolated from chronically infected children with cystic fibrosis in India
inferredcites →https://doi.org/10.1186/1755-7682-1-24openalex-snapshot
Pulmonary bacterial pathogens in cystic fibrosis patients and antibiotic therapy: a tool for the health workers
inferredcites →https://doi.org/10.1371/journal.pone.0002908openalex-snapshot
Molecular Detection of Multiple Emerging Pathogens in Sputa from Cystic Fibrosis Patients
inferredcites →https://doi.org/10.1371/journal.pone.0027842openalex-snapshot
Evolution and Adaptation in Pseudomonas aeruginosa Biofilms Driven by Mismatch Repair System-Deficient Mutators
inferredcites →https://doi.org/10.1371/journal.pone.0060225openalex-snapshot
Phenotypic Heterogeneity of Pseudomonas aeruginosa Populations in a Cystic Fibrosis Patient
inferredcites →https://doi.org/10.1371/journal.pone.0083124openalex-snapshot
Loss of Social Behaviours in Populations of Pseudomonas aeruginosa Infecting Lungs of Patients with Cystic Fibrosis
inferredcites →https://doi.org/10.1517/14728220903454988openalex-snapshot
Pseudomonas aeruginosa biofilm infections in cystic fibrosis: insights into pathogenic processes and treatment strategies
inferredcites →https://doi.org/10.1586/ers.12.39openalex-snapshot
Current dilemmas in antimicrobial therapy in cystic fibrosis
inferredcites →https://doi.org/10.2174/1570164043379307openalex-snapshot
Proteomics of Biofilm Bacteria
inferredcites →https://doi.org/10.2217/fmb.10.125openalex-snapshot
Pseudomonas Aeruginosa Biofilms in Cystic fibrosis
inferredcites →https://doi.org/10.2217/fmb.12.76openalex-snapshot
Biofilm-Specific Antibiotic Resistance
inferredcites →https://doi.org/10.3390/s120302519openalex-snapshot
Quorum Sensing and Bacterial Social Interactions in Biofilms
inferredcites →https://doi.org/10.4187/aarc0427openalex-snapshot
Cystic Fibrosis: Pathogenesis and Future Treatment Strategies
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.12688/openreseurope.19781.1zenodo-depositor-declared
Cell motility influences microfluidics capturing in scRNA-seq
inferred← citeshttps://doi.org/10.2139/ssrn.4792714openalex-extracted
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inferred← citeshttps://doi.org/10.1002/advs.202301357openalex-snapshot
Bacterial Membrane Vesicles: Physiological Roles, Infection Immunology, and Applications
inferred← citeshttps://doi.org/10.1002/bies.201500121openalex-snapshot
Defining heterogeneity within bacterial populations via single cell approaches
inferred← citeshttps://doi.org/10.1002/bit.26572openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cbdv.71734openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cmdc.202300544openalex-snapshot
Diagnosis and Therapeutic Strategies Based on Nucleic Acid Aptamers Selected against Pseudomonas aeruginosa: The Challenge of Cystic Fibrosis
inferred← citeshttps://doi.org/10.1002/elsc.201600108openalex-snapshot
Zero‐growth bioprocesses: A challenge for microbial production strains and bioprocess engineering
inferred← citeshttps://doi.org/10.1002/iub.2442openalex-snapshot
Cellulophaga algicola alginate lyase inhibits biofilm formation of a clinical Pseudomonas aeruginosa strain MCC 2081
inferred← citeshttps://doi.org/10.1002/jlb.3a1219-686rropenalex-snapshot
Annexin A2 regulates unfolded protein response via IRE1–XBP1 axis in macrophages duringP. aeruginosainfection
inferred← citeshttps://doi.org/10.1002/lipd.12184openalex-snapshot
Phospholipid Content of Pseudomonas aeruginosa PAO1 Is Modulated by the Growth Phase Rather Than the Immobilization State
inferred← citeshttps://doi.org/10.1002/mbo3.720openalex-snapshot
Efficacy of levofloxacin against biofilms of Pseudomonas aeruginosa isolated from patients with respiratory tract infections in vitro
inferred← citeshttps://doi.org/10.1002/ppul.24005openalex-snapshot
Interaction among variants in the SLC gene family (SLC6A14, SLC26A9, SLC11A1, and SLC9A3) and CFTR mutations with clinical markers of cystic fibrosis
inferred← citeshttps://doi.org/10.1002/ppul.25294openalex-snapshot
Pseudomonas aeruginosa colonization in cystic fibrosis: Impact on neutrophil functions and cytokine secretion capacity
inferred← citeshttps://doi.org/10.1007/978-3-319-39658-3_14openalex-snapshot
Antimicrobial Drug Efflux Pumps in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1007/978-3-319-61452-6_12openalex-snapshot
Pseudomonas aeruginosa and Bronchiectasis
inferred← citeshttps://doi.org/10.1007/978-3-319-74932-7_6openalex-snapshot
Computational Systems Biology of Metabolism in Infection
inferred← citeshttps://doi.org/10.1007/978-981-10-6141-7_16openalex-snapshot
Pseudomonas aeruginosa and Its Arsenal of Proteases: Weapons to Battle the Host
inferred← citeshttps://doi.org/10.1007/978-981-13-0848-2_17openalex-snapshot
Novel Super-Regulators of Quorum Sensing in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1007/978-981-15-1695-5_13openalex-snapshot
Pathogenesis and Drug Resistance of Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1007/s00011-019-01227-xopenalex-snapshot
Pseudomonas aeruginosa biofilm is a potent inducer of phagocyte hyperinflammation
inferred← citeshttps://doi.org/10.1007/s00203-024-03900-0openalex-snapshot
Unveiling the hidden language of bacteria: anti-quorum sensing strategies for gram-negative bacteria infection control
inferred← citeshttps://doi.org/10.1007/s00203-026-04750-8openalex-snapshot
Triad warfare against biofilms: disrupting quorum sensing, nanotechnology-driven precision, and host immunomodulation to conquer antimicrobial resistance
inferred← citeshttps://doi.org/10.1007/s00253-015-7177-xopenalex-snapshot
The cystic fibrosis microbiome in an ecological perspective and its impact in antibiotic therapy
inferred← citeshttps://doi.org/10.1007/s00253-019-09618-0openalex-snapshot
Natural quorum sensing inhibitors effectively downregulate gene expression of Pseudomonas aeruginosa virulence factors
inferred← citeshttps://doi.org/10.1007/s00253-021-11638-8openalex-snapshot
Quorum quenchers affect the virulence regulation of non-mucoid, mucoid and heavily mucoid biofilms co-cultured on cell lines
inferred← citeshttps://doi.org/10.1007/s10482-015-0642-9openalex-snapshot
Genes from pUM505 plasmid contribute to Pseudomonas aeruginosa virulence
inferred← citeshttps://doi.org/10.1007/s10753-020-01304-yopenalex-snapshot
Exploring the Therapeutic Efficacy of Zingerone Nanoparticles in Treating Biofilm-Associated Pyelonephritis Caused by Pseudomonas aeruginosa in the Murine Model
inferred← citeshttps://doi.org/10.1007/s11095-018-2350-4openalex-snapshot
Sweetening Inhaled Antibiotic Treatment for Eradication of Chronic Respiratory Biofilm Infection
inferred← citeshttps://doi.org/10.1007/s11274-025-04512-6openalex-snapshot
Updates on therapeutic targeting of diguanylate cyclase for addressing bacterial infections: A comprehensive review
inferred← citeshttps://doi.org/10.1007/s42770-019-00169-0openalex-snapshot
In vitro anti-biofilm activity of 14-deoxy-11,12-didehydroandrographolide from Andrographis paniculata against Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1016/bs.aambs.2018.01.003openalex-snapshot
Biofilm: A Hotspot for Emerging Bacterial Genotypes
inferred← citeshttps://doi.org/10.1016/bs.ampbs.2023.12.002openalex-snapshot
Antimicrobials: An update on new strategies to diversify treatment for bacterial infections
inferred← citeshttps://doi.org/10.1016/j.arcmed.2020.12.004openalex-snapshot
Pseudomonas Aeruginosa: Genetic Adaptation, A Strategy for its Persistence in Cystic Fibrosis
inferred← citeshttps://doi.org/10.1016/j.bioflm.2023.100122openalex-snapshot
Cold atmospheric pressure plasma-antibiotic synergy in Pseudomonas aeruginosa biofilms is mediated via oxidative stress response
inferred← citeshttps://doi.org/10.1016/j.bioflm.2024.100250openalex-snapshot
Aqueous extracts of Moringa oleifera and Cinnamomum cassia as promising sources of antibiofilm compounds against mucoid and small colony variants of Pseudomonas aeruginosa and Staphylococcus aureus
inferred← citeshttps://doi.org/10.1016/j.bioflm.2025.100265openalex-snapshot
Cellulophaga algicola alginate lyase and Pseudomonas aeruginosa Psl glycoside hydrolase inhibit biofilm formation by Pseudomonas aeruginosa CF2843 on three-dimensional aggregates of lung epithelial cells
inferred← citeshttps://doi.org/10.1016/j.cbi.2025.111850openalex-snapshot
Stereochemical insight for MexXY-OprM efflux system inhibition in Pseudomonas aeruginosa from a pool of dihydro and tetrahydro berberine derivatives
inferred← citeshttps://doi.org/10.1016/j.celrep.2026.118037openalex-snapshot
Processing of lysophosphatidylcholines by ExoU secreted by P. aeruginosa leads to inflammasome activation and cell death
inferred← citeshttps://doi.org/10.1016/j.chom.2019.02.007openalex-snapshot
Neutrophil Extracellular Traps Confine Pseudomonas aeruginosa Ocular Biofilms and Restrict Brain Invasion
inferred← citeshttps://doi.org/10.1016/j.diagmicrobio.2015.02.011openalex-snapshot
Genomic diversification and virulence features in SPM-1–producing Pseudomonas aeruginosa 13years later
inferred← citeshttps://doi.org/10.1016/j.ejmech.2025.118294openalex-snapshot
Design, synthesis and biological evaluation of novel coumarin derivatives as Pseudomonas aeruginosa biofilm inhibitors
inferred← citeshttps://doi.org/10.1016/j.ejpb.2025.114966openalex-snapshot
Development of spray-dried phage-aztreonam microparticles for inhalation therapy of Pseudomonas aeruginosa lung infections
inferred← citeshttps://doi.org/10.1016/j.ijantimicag.2023.106887openalex-snapshot
Ceftolozane/tazobactam plus tobramycin against free-floating and biofilm bacteria of hypermutable Pseudomonas aeruginosa epidemic strains: Resistance mechanisms and synergistic activity
inferred← citeshttps://doi.org/10.1016/j.ijmm.2017.07.004openalex-snapshot
Relevance of multidrug-resistant Pseudomonas aeruginosa infections in cystic fibrosis
inferred← citeshttps://doi.org/10.1016/j.ijmm.2018.10.003openalex-snapshot
Unveiling the early events of Pseudomonas aeruginosa adaptation in cystic fibrosis airway environment using a long-term in vitro maintenance
inferred← citeshttps://doi.org/10.1016/j.intimp.2016.04.044openalex-snapshot
Pseudomonas aeruginosa promotes autophagy to suppress macrophage-mediated bacterial eradication
inferred← citeshttps://doi.org/10.1016/j.jbiosc.2020.02.001openalex-snapshot
Characterization of Pseudomonas lytic phages and their application as a cocktail with antibiotics in controlling Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1016/j.jcf.2020.03.004openalex-snapshot
Antibiofilm and mucolytic action of nitric oxide delivered via gas or macromolecular donor using in vitro and ex vivo models
inferred← citeshttps://doi.org/10.1016/j.jgar.2015.04.002openalex-snapshot
Pseudomonas aeruginosa carrying blaCTX-M-2 in Brazil: The occurrence of ‘high-risk clones’?
inferred← citeshttps://doi.org/10.1016/j.jmb.2015.09.002openalex-snapshot
The Limitations of In Vitro Experimentation in Understanding Biofilms and Chronic Infection
inferred← citeshttps://doi.org/10.1016/j.matbio.2020.04.003openalex-snapshot
Multi-scale models of lung fibrosis
inferred← citeshttps://doi.org/10.1016/j.meegid.2020.104462openalex-snapshot
Immunoinformatics design of multivalent chimeric vaccine for modulation of the immune system in Pseudomonas aeruginosa infection
inferred← citeshttps://doi.org/10.1016/j.micpath.2017.09.060openalex-snapshot
Plasmid pUM505 encodes a Toxin–Antitoxin system conferring plasmid stability and increased Pseudomonas aeruginosa virulence
inferred← citeshttps://doi.org/10.1016/j.micpath.2017.10.017openalex-snapshot
Serine/threonine protein kinase PpkA contributes to the adaptation and virulence in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1016/j.micpath.2020.104240openalex-snapshot
Protective effects of anti-alginate monoclonal antibody against Pseudomonas aeruginosa infection of HeLa cells
inferred← citeshttps://doi.org/10.1016/j.micpath.2024.106874openalex-snapshot
Combating bacterial biofilms and related drug resistance: Role of phyto-derived adjuvant and nanomaterials
inferred← citeshttps://doi.org/10.1016/j.micpath.2024.107020openalex-snapshot
Assessment of inhaled cationic antibiotics in an in vitro model of Pseudomonas aeruginosa lung biofilm
inferred← citeshttps://doi.org/10.1016/j.micpath.2026.108312openalex-snapshot
Contribution of viable but non culturable cells and small colony variants in antibiotic insusceptibility and therapeutic failure against S. aureus and P. aeruginosa biofilm co-infections
inferred← citeshttps://doi.org/10.1016/j.micres.2016.06.005openalex-snapshot
Role of ppGpp in Pseudomonas aeruginosa acute pulmonary infection and virulence regulation
inferred← citeshttps://doi.org/10.1016/j.microb.2025.100463openalex-snapshot
Disruption of aprF result in alkaline protease secretion-deficiency in Pseudomonas aeruginosa clinical isolates that enhances host inflammatory responses via Toll-like receptor 5
inferred← citeshttps://doi.org/10.1016/j.rvsc.2026.106367openalex-snapshot
Outer membrane vesicles in Pseudomonas aeruginosa pathogenesis: a systematic review of virulence dissemination, immune modulation, and antimicrobial resistance, with perspectives for veterinary and one health practice
inferred← citeshttps://doi.org/10.1016/j.sajb.2016.01.006openalex-snapshot
Piper betle L. (betel quid) shows bacteriostatic, additive, and synergistic antimicrobial action when combined with conventional antibiotics
inferred← citeshttps://doi.org/10.1016/j.str.2022.06.002openalex-snapshot
Insights into the atypical autokinase activity of the Pseudomonas aeruginosa GacS histidine kinase and its interaction with RetS
inferred← citeshttps://doi.org/10.1021/acs.biochem.5b01229openalex-snapshot
Visualizing the Mechanism of Epoxide Hydrolysis by the Bacterial Virulence Enzyme Cif
inferred← citeshttps://doi.org/10.1021/acs.jproteome.9b00520openalex-snapshot
Characterization of the Proteomic Response of A549 Cells Following Sequential Exposure to Aspergillus fumigatus and Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1021/acsinfecdis.0c00337openalex-snapshot
Exogenous Nitric Oxide Improves Antibiotic Susceptibility in Resistant Bacteria
inferred← citeshttps://doi.org/10.1021/acsomega.0c03634openalex-snapshot
Anti-quorum Sensing and Anti-biofilm Activity of Zinc Oxide Nanospikes
inferred← citeshttps://doi.org/10.1038/nmicrobiol.2016.184openalex-snapshot
LadS is a calcium-responsive kinase that induces acute-to-chronic virulence switch in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1038/s41396-022-01221-yopenalex-snapshot
Pseudomonas aeruginosa polysaccharide Psl supports airway microbial community development
inferred← citeshttps://doi.org/10.1038/s41467-026-68622-xopenalex-snapshot
Dual-functional quorum sensing signal synthases DspII and DspI coordinate virulence switch in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1038/s41522-019-0088-3openalex-snapshot
Extracellular DNA release, quorum sensing, and PrrF1/F2 small RNAs are key players in Pseudomonas aeruginosa tobramycin-enhanced biofilm formation
inferred← citeshttps://doi.org/10.1038/s41564-024-01842-3openalex-snapshot
Pseudomonas aeruginosa faces a fitness trade-off between mucosal colonization and antibiotic tolerance during airway infection
inferred← citeshttps://doi.org/10.1038/s41598-018-30813-yopenalex-snapshot
Characterization of lasR-deficient clinical isolates of Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1038/s41598-019-49371-yopenalex-snapshot
In vitro evolution of Pseudomonas aeruginosa AA2 biofilms in the presence of cystic fibrosis lung microbiome members
inferred← citeshttps://doi.org/10.1038/s41598-021-85100-0openalex-snapshot
Pseudomonas aeruginosa PA80 is a cystic fibrosis isolate deficient in RhlRI quorum sensing
inferred← citeshttps://doi.org/10.1038/s41598-021-85956-2openalex-snapshot
Crystal structure of RahU, an aegerolysin protein from the human pathogen Pseudomonas aeruginosa, and its interaction with membrane ceramide phosphorylethanolamine
inferred← citeshttps://doi.org/10.1038/s41598-021-99467-7openalex-snapshot
Alkyl-Quinolones derivatives as potential biomarkers for Pseudomonas aeruginosa infection chronicity in Cystic Fibrosis
inferred← citeshttps://doi.org/10.1038/s41598-023-39005-9openalex-snapshot
Phenotypic and genotypic characteristics of Pseudomonas aeruginosa isolated from cystic fibrosis patients with chronic infections
inferred← citeshttps://doi.org/10.1038/s42003-023-04540-8openalex-snapshot
Genome-scale model of Pseudomonas aeruginosa metabolism unveils virulence and drug potentiation
inferred← citeshttps://doi.org/10.1038/s44259-025-00088-1openalex-snapshot
R-pyocins as targeted antimicrobials against Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1038/sigtrans.2016.32openalex-snapshot
Lyn prevents aberrant inflammatory responses to Pseudomonas infection in mammalian systems by repressing a SHIP-1-associated signaling cluster
inferred← citeshttps://doi.org/10.1039/c9bm01051copenalex-snapshot
Antimicrobial peptide HPA3NT3-A2 effectively inhibits biofilm formation in mice infected with drug-resistant bacteria
inferred← citeshttps://doi.org/10.1039/d5lp00285kopenalex-snapshot
High-throughput bioprinted 3D cultures for probing host–pathogen interactions in bioinspired microenvironments
inferred← citeshttps://doi.org/10.1073/pnas.1721270115openalex-snapshot
Rapid diversification of Pseudomonas aeruginosa in cystic fibrosis lung-like conditions
inferred← citeshttps://doi.org/10.1080/07853890.2024.2307503openalex-snapshot
Burkholderia cepacia complex in cystic fibrosis: critical gaps in diagnosis and therapy
inferred← citeshttps://doi.org/10.1080/0972060x.2018.1505555openalex-snapshot
Evaluation of Chemical Composition and Antibacterial Properties of Froriepia subpinnta Essential Oils from Guilan Region: Before and After Flowering
inferred← citeshttps://doi.org/10.1080/1040841x.2020.1735991openalex-snapshot
Role of interspecies bacterial communication in the virulence of pathogenic bacteria
inferred← citeshttps://doi.org/10.1080/1040841x.2020.1854172openalex-snapshot
Prokaryotic life finds a way: insights from evolutionary experimentation in bacteria
inferred← citeshttps://doi.org/10.1080/14787210.2020.1751610openalex-snapshot
Further understanding of Pseudomonas aeruginosa’s ability to horizontally acquire virulence: possible intervention strategies
inferred← citeshttps://doi.org/10.1080/21505594.2025.2580097openalex-snapshot
Colistin-induced transition from non-mucoid to mucoid phenotype in resistant Pseudomonas aeruginosa ST3351
inferred← citeshttps://doi.org/10.1086/726895openalex-snapshot
On the De Novo Emergence of Ecological Interactions during Evolutionary Diversification: A Conceptual Framework and Experimental Test
inferred← citeshttps://doi.org/10.1089/mdr.2016.0087openalex-snapshot
Biofilms: Microbial Shelters Against Antibiotics
inferred← citeshttps://doi.org/10.1093/femsle/fnx104openalex-snapshot
Two-component systems required for virulence in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1093/femsle/fnx128openalex-snapshot
The role of multispecies social interactions in shaping Pseudomonas aeruginosa pathogenicity in the cystic fibrosis lung
inferred← citeshttps://doi.org/10.1093/femsle/fnx151openalex-snapshot
Pseudomonas aeruginosa Trent and zinc homeostasis
inferred← citeshttps://doi.org/10.1093/femspd/ftv069openalex-snapshot
Residence in biofilms allows Burkholderia cepacia complex (Bcc) bacteria to evade the anti-microbial activities of neutrophil-like dHL60 cells
inferred← citeshttps://doi.org/10.1093/infdis/jiaf527openalex-snapshot
Culture and Adaptation of Pseudomonas aeruginosa During Early Infection in Children With Cystic Fibrosis
inferred← citeshttps://doi.org/10.1093/nar/gkab506openalex-snapshot
Acetylation of the CspA family protein CspC controls the type III secretion system through translational regulation ofexsAinPseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1093/nar/gkaf471openalex-snapshot
An antibiotic-responsive regulator orchestrates chronic-to-acute virulence switch in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1097/inf.0000000000002714openalex-snapshot
Pseudomonas aeruginosa Isolates From a Cohort of Mexican Children With Cystic Fibrosis Show Adaptation to a Chronic Phenotype
inferred← citeshttps://doi.org/10.1097/qco.0000000000000217openalex-snapshot
Managing Pseudomonas aeruginosa respiratory infections in cystic fibrosis
inferred← citeshttps://doi.org/10.1097/won.0000000000000373openalex-snapshot
Prevalence, Antimicrobial Susceptibility, and Clonal Diversity of Pseudomonas aeruginosa in Chronic Wounds
inferred← citeshttps://doi.org/10.1098/rspb.2020.2272openalex-snapshot
The evolution of virulence in Pseudomonas aeruginosa during chronic wound infection
inferred← citeshttps://doi.org/10.1098/rstb.2024.0080openalex-snapshot
Bacteria–phage infection network structure and genomic defence system content predict efficacy of a phage therapy cocktail against Pseudomonas aeruginosa from chronic lung infections
inferred← citeshttps://doi.org/10.1099/jmm.0.001085openalex-snapshot
Genomic and phenotypic comparison of environmental and patient-derived isolates of Pseudomonas aeruginosa suggest that antimicrobial resistance is rare within the environment
inferred← citeshttps://doi.org/10.1099/mgen.0.000513openalex-snapshot
From genotype to phenotype: adaptations of Pseudomonas aeruginosa to the cystic fibrosis environment
inferred← citeshttps://doi.org/10.1099/mgen.0.000681openalex-snapshot
Genome evolution drives transcriptomic and phenotypic adaptation in Pseudomonas aeruginosa during 20 years of infection
inferred← citeshttps://doi.org/10.1099/mic.0.000155openalex-snapshot
Phenotypic characterization of an international Pseudomonas aeruginosa reference panel: strains of cystic fibrosis (CF) origin show less in vivo virulence than non-CF strains
inferred← citeshttps://doi.org/10.1099/mic.0.000393openalex-snapshot
Virulence adaptations of Pseudomonas aeruginosa isolated from patients with non-cystic fibrosis bronchiectasis
inferred← citeshttps://doi.org/10.1099/mic.0.000692openalex-snapshot
Cinnamaldehyde disrupts biofilm formation and swarming motility of Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1099/mic.0.000730openalex-snapshot
Anti-Pseudomonas activity of 3-nitro-4-phenylfuroxan
inferred← citeshttps://doi.org/10.1099/mic.0.000911openalex-snapshot
ChpC controls twitching motility-mediated expansion of Pseudomonas aeruginosa biofilms in response to serum albumin, mucin and oligopeptides
inferred← citeshttps://doi.org/10.1101/2021.02.01.429126openalex-snapshot
Terpenoid components, antioxidant and antibacterial activities of essential oils from fresh immature and mature leaves of Blumea balsamifera, extracted with different hydrodistillation periods
inferred← citeshttps://doi.org/10.1101/2021.04.22.441042openalex-snapshot
A Two-Component System FleS/FleR Regulates Multiple Virulence-Related Traits in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1101/2022.06.23.497436openalex-snapshot
Pseudomonas aeruginosa mediates PqsA-dependent iron regulation of the RsmY and RsmZ sRNAs in static conditions
inferred← citeshttps://doi.org/10.1101/2022.07.20.500912openalex-snapshot
Emergence of Small Colony Variants (SCVs) is an adaptive strategy used by Pseudomonas aeruginosa to palliate O 2 limitations
inferred← citeshttps://doi.org/10.1101/2024.09.09.611974openalex-snapshot
Pseudomonas aeruginosa faces a fitness trade-off between mucosal colonization and antibiotic tolerance during airway infections
inferred← citeshttps://doi.org/10.1101/2025.02.14.638290openalex-snapshot
Proteomic characterisation of three independent series of sequential cystic fibrosis strains in an International Pseudomonas aeruginosa reference panel indicates positive selection in late infection strains
inferred← citeshttps://doi.org/10.1101/2025.09.20.677542openalex-snapshot
Pseudomonas aeruginosa biofilm-deficient mutants undergo parallel adaptation during chronic infection
inferred← citeshttps://doi.org/10.1111/1751-7915.14487openalex-snapshot
Antibiotic influx and efflux in Pseudomonas aeruginosa : Regulation and therapeutic implications
inferred← citeshttps://doi.org/10.1111/1751-7915.70239openalex-snapshot
Attenuated Strains of Pseudomonas aeruginosa : A Promising Cell Factory for Rhamnolipid Production
inferred← citeshttps://doi.org/10.1111/1758-2229.13190openalex-snapshot
Exposure to endocrine disruptors promotes biofilm formation and contributes to increased virulence of Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1126/sciadv.adz1415openalex-snapshot
A choline-sensing regulator coordinates metabolic adaptation and pathogenesis in Pseudomonas aeruginosa pulmonary infections
inferred← citeshttps://doi.org/10.1128/aac.00496-22openalex-snapshot
Whole-Genome Sequencing Reveals Diversity of Carbapenem-Resistant Pseudomonas aeruginosa Collected through CDC’s Emerging Infections Program, United States, 2016–2018
inferred← citeshttps://doi.org/10.1128/aac.00848-18openalex-snapshot
Broad-Spectrum Adaptive Antibiotic Resistance Associated with Pseudomonas aeruginosa Mucin-Dependent Surfing Motility
inferred← citeshttps://doi.org/10.1128/aac.02203-21openalex-snapshot
Simulated Intravenous versus Inhaled Tobramycin with or without Intravenous Ceftazidime Evaluated against Hypermutable Pseudomonas aeruginosa via a Dynamic Biofilm Model and Mechanism-Based Modeling
inferred← citeshttps://doi.org/10.1128/aac.03113-15openalex-snapshot
Elucidation of Mechanisms of Ceftazidime Resistance among Clinical Isolates of Pseudomonas aeruginosa by Using Genomic Data
inferred← citeshttps://doi.org/10.1128/aem.02593-19openalex-snapshot
PA0335, a Gene Encoding Histidinol Phosphate Phosphatase, Mediates Histidine Auxotrophy in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1128/aem.02701-16openalex-snapshot
Environmental Pseudomonads Inhibit Cystic Fibrosis Patient-Derived Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1128/cmr.00138-18openalex-snapshot
Cystic Fibrosis and Pseudomonas aeruginosa: the Host-Microbe Interface
inferred← citeshttps://doi.org/10.1128/iai.00136-20openalex-snapshot
Achromobacter xylosoxidans Cellular Pathology Is Correlated with Activation of a Type III Secretion System
inferred← citeshttps://doi.org/10.1128/iai.00410-25openalex-snapshot
Activation of the Pseudomonas aeruginosa glycerol regulon reduces antibiotic susceptibility and modulates virulence phenotypes
inferred← citeshttps://doi.org/10.1128/iai.00430-26openalex-snapshot
Calcium promotes Pseudomonas aeruginosa adherence to airway epithelial cells during infection
inferred← citeshttps://doi.org/10.1128/iai.00911-19openalex-snapshot
For the Greater (Bacterial) Good: Heterogeneous Expression of Energetically Costly Virulence Factors
inferred← citeshttps://doi.org/10.1128/jb.00145-21openalex-snapshot
OsaR (PA0056) Functions as a Repressor of the Gene fleQ Encoding an Important Motility Regulator in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1128/jb.00278-23openalex-snapshot
Iron starvation increases the production of the Pseudomonas aeruginosa RsmY and RsmZ sRNAs in static conditions
inferred← citeshttps://doi.org/10.1128/jb.00520-25openalex-snapshot
Pseudomonas aeruginosa biofilm-deficient mutants undergo parallel evolution during chronic infection
inferred← citeshttps://doi.org/10.1128/jcm.02938-15openalex-snapshot
The BioFilm Ring Test: a Rapid Method for Routine Analysis of Pseudomonas aeruginosa Biofilm Formation Kinetics
inferred← citeshttps://doi.org/10.1128/mbio.00140-17openalex-snapshot
New Mouse Model for Chronic Infections by Gram-Negative Bacteria Enabling the Study of Anti-Infective Efficacy and Host-Microbe Interactions
inferred← citeshttps://doi.org/10.1128/mbio.00831-25openalex-snapshot
Flagellar motility and the mucus environment influence aggregation-mediated antibiotic tolerance of Pseudomonas aeruginosa in chronic lung infection
inferred← citeshttps://doi.org/10.1128/mbio.02376-23openalex-snapshot
The end of the reign of a “master regulator’’? A defect in function of the LasR quorum sensing regulator is a common feature of Pseudomonas aeruginosa isolates
inferred← citeshttps://doi.org/10.1128/mbio.03067-22openalex-snapshot
Impact of Growth Rate on the Protein-mRNA Ratio in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1128/mbio.03968-25openalex-snapshot
Energy expenditure and cellular activity underlie antibiotic tolerance of Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1128/spectrum.00192-21openalex-snapshot
Combined Treatment of 6-Gingerol Analog and Tobramycin for Inhibiting Pseudomonas aeruginosa Infections
inferred← citeshttps://doi.org/10.1128/spectrum.00449-23openalex-snapshot
Pooling isolates to address the diversity in antimicrobial susceptibility of Pseudomonas aeruginosa in cystic fibrosis
inferred← citeshttps://doi.org/10.1128/spectrum.01354-25openalex-snapshot
Glycoside hydrolases enhance antibiotic activity against Pseudomonas aeruginosa biofilms from cystic fibrosis airways
inferred← citeshttps://doi.org/10.1128/spectrum.03299-25openalex-snapshot
Intra-strain genomic microevolution and phage resistance in Pseudomonas aeruginosa PAO1 laboratory isolates
inferred← citeshttps://doi.org/10.1134/s0026261717030109openalex-snapshot
Long-term survival and resistance of submerged pseudomonad cultures in the exopolymer mass
inferred← citeshttps://doi.org/10.1142/9789814749411_0051openalex-snapshot
COMPUTATIONAL APPROACHES TO STUDY MICROBES AND MICROBIOMES
inferred← citeshttps://doi.org/10.1146/annurev-micro-020518-120044openalex-snapshot
Small Is Mighty—Chemical Communication Systems inPseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1155/2022/7794227openalex-snapshot
Phenolics, Antioxidant and Antibacterial Activities of Immature and Mature Blumea balsamifera Leaf Extracts Eluted with Different Solvents
inferred← citeshttps://doi.org/10.11575/prism/27474openalex-snapshot
Pseudomonas aeruginosa Exopolysaccharide Biosynthesis and Immunosuppressive Role in Vivo
inferred← citeshttps://doi.org/10.11575/prism/38808openalex-snapshot
The influence of non-inhibitory concentrations of purified pyocin S2 on Pseudomonas aeruginosa isolates
inferred← citeshttps://doi.org/10.1165/rcmb.2021-0125ocopenalex-snapshot
Airway Administration of Flagellin Regulates the Inflammatory Response to Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1186/s12864-025-12282-6openalex-snapshot
A systematic longitudinal study of microbiome: integrating temporal-spatial dimensions with causal and deep learning models
inferred← citeshttps://doi.org/10.1186/s12931-023-02609-wopenalex-snapshot
Age-dependent inflammatory response is altered in an ex vivo model of bacterial pneumonia
inferred← citeshttps://doi.org/10.1186/s12934-026-03091-xopenalex-snapshot
Harnessing the endophytic Clavispora lusitaniae for the biogenic synthesis of ethylene glycol-capped cerium oxide nanoparticles: a green approach to combat respiratory Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1186/s12941-017-0193-1openalex-snapshot
Activity of AMP2041 against human and animal multidrug resistant Pseudomonas aeruginosa clinical isolates
inferred← citeshttps://doi.org/10.1186/s13104-018-3308-7openalex-snapshot
A multi-host approach to identify a transposon mutant of Pseudomonas aeruginosa LESB58 lacking full virulence
inferred← citeshttps://doi.org/10.1186/s13568-026-02083-9openalex-snapshot
Surfactant-driven quorum sensing of Pseudomonas aeruginosa in cystic fibrosis
inferred← citeshttps://doi.org/10.1186/s41043-022-00305-xopenalex-snapshot
A Middle East systematic review and meta-analysis of prevalence and antibiotic susceptibility pattern in MRSA Staphylococcus aureus isolated from patients with cystic fibrosis
inferred← citeshttps://doi.org/10.1371/journal.pone.0156690openalex-snapshot
Comparative Activity of Ciprofloxacin, Levofloxacin and Moxifloxacin against Klebsiella pneumoniae, Pseudomonas aeruginosa and Stenotrophomonas maltophilia Assessed by Minimum Inhibitory Concentrations and Time-Kill Studies
inferred← citeshttps://doi.org/10.1371/journal.pone.0160975openalex-snapshot
Understanding the Pathogenicity of Burkholderia contaminans, an Emerging Pathogen in Cystic Fibrosis
inferred← citeshttps://doi.org/10.1371/journal.pone.0168577openalex-snapshot
The Pig: A Relevant Model for Evaluating the Neutrophil Serine Protease Activities during Acute Pseudomonas aeruginosa Lung Infection
inferred← citeshttps://doi.org/10.1371/journal.pone.0172882openalex-snapshot
Identification of extensive drug resistant Pseudomonas aeruginosa strains: New clone ST1725 and high-risk clone ST233
inferred← citeshttps://doi.org/10.1371/journal.pone.0195635openalex-snapshot
Present-day monitoring underestimates the risk of exposure to pathogenic bacteria from cold water storage tanks
inferred← citeshttps://doi.org/10.1371/journal.pone.0204167openalex-snapshot
Great phenotypic and genetic variation among successive chronic Pseudomonas aeruginosa from a cystic fibrosis patient
inferred← citeshttps://doi.org/10.1371/journal.pone.0266742openalex-snapshot
Nucleotide substitutions in the mexR, nalC and nalD regulator genes of the MexAB-OprM efflux pump are maintained in Pseudomonas aeruginosa genetic lineages
inferred← citeshttps://doi.org/10.1371/journal.ppat.1005987openalex-snapshot
Swimming Motility Mediates the Formation of Neutrophil Extracellular Traps Induced by Flagellated Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1371/journal.ppat.1006300openalex-snapshot
A commensal streptococcus hijacks a Pseudomonas aeruginosa exopolysaccharide to promote biofilm formation
inferred← citeshttps://doi.org/10.1371/journal.ppat.1007511openalex-snapshot
Bacterial fitness in chronic wounds appears to be mediated by the capacity for high-density growth, not virulence or biofilm functions
inferred← citeshttps://doi.org/10.1371/journal.ppat.1011221openalex-snapshot
Current concepts on Pseudomonas aeruginosa interaction with human airway epithelium
inferred← citeshttps://doi.org/10.1371/journal.ppat.1012922openalex-snapshot
Intracellular Pseudomonas aeruginosa persist and evade antibiotic treatment in a wound infection model
inferred← citeshttps://doi.org/10.14232/phd.10228openalex-snapshot
Development of dry powder inhalation systems using ciprofloxacin hydrochloride
inferred← citeshttps://doi.org/10.14715/cmb/2023.69.5.6openalex-snapshot
Molecular detection of different virulence factors genes harbor pslA, pelA, exoS, toxA and algD among biofilm-forming clinical isolates of Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1515/rrlm-2017-0027openalex-snapshot
Comparison of virulence factors and antibiotic resistance of Pseudomonas aeruginosa strains isolated from patients with and without cystic fibrosis
inferred← citeshttps://doi.org/10.1517/21678707.2015.1064308openalex-snapshot
T100: nebulized-concentrated tobramycin formulation for treatment ofPseudomonas aeruginosainfection in cystic fibrosis patients
inferred← citeshttps://doi.org/10.18006/2024.12(2).274.283openalex-snapshot
Antibiotic-Induced Changes in Efflux Transporter Expression: A Key Factor in Pseudomonas aeruginosa Biofilm Resistance
inferred← citeshttps://doi.org/10.20381/ruor-26847openalex-snapshot
The Evolution of Ecological Interactions During Adaptive Diversification in Pseudomonas Aeruginosa
inferred← citeshttps://doi.org/10.21161/mjm.190534openalex-snapshot
Microbial quality of utility water at universities in Nigeria
inferred← citeshttps://doi.org/10.21203/rs.3.rs-33039/v1openalex-snapshot
Quercetin attenuates the production of pro-inflammatory cytokines in H292 human lung epithelial cells infected with Pseudomonas aeruginosa, by modulating ExoS production
inferred← citeshttps://doi.org/10.21203/rs.3.rs-33039/v2openalex-snapshot
Quercetin attenuates the production of pro-inflammatory cytokines in H292 human lung epithelial cells infected with Pseudomonas aeruginosa, by modulating ExoS production
inferred← citeshttps://doi.org/10.21203/rs.3.rs-56805/v1openalex-snapshot
Genetic Variations in MexAB-OprM Efflux Pump Regulators and Their Association with Antibiotic Resistance and Sequence type in Clinical and Epidemiologically High-risk Clones of Pseudomonas Aeruginosa.
inferred← citeshttps://doi.org/10.2147/idr.s168868openalex-snapshot
Peptide dendrimers as “lead compounds” for the treatment of chronic lung infections by Pseudomonas aeruginosa in cystic fibrosis patients: in vitro and in vivo studies
inferred← citeshttps://doi.org/10.2147/idr.s230178openalex-snapshot
Capsule Thickness, Not Biofilm Formation, Gives Rise to Mucoid Acinetobacter baumannii Phenotypes That are More Prevalent in Long-Term Infections: A Study of Clinical Isolates from a Hospital in China
inferred← citeshttps://doi.org/10.2147/idr.s374335openalex-snapshot
Differentially Expressed Genes of Pseudomonas aeruginosa Isolates from Eyes with Keratitis and Healthy Conjunctival Sacs
inferred← citeshttps://doi.org/10.21814/cebsam2017openalex-snapshot
BOOK OF ABSTRACTS OF CEB ANNUAL MEETING 2017
inferred← citeshttps://doi.org/10.2217/fmb-2021-0025openalex-snapshot
Long-Term Coexistence of Pseudomonas Aeruginosa and Staphylococcus Aureus Using an In Vitro Cystic Fibrosis Model
inferred← citeshttps://doi.org/10.2217/fmb-2022-0155openalex-snapshot
Bacterial Synergies and Antagonisms Affecting Pseudomonas Aeruginosa Virulence in the Human Lung, Skin and Intestine
inferred← citeshttps://doi.org/10.2217/fmb.15.117openalex-snapshot
Management of Pseudomonas Aeruginosa Infection in Cystic Fibrosis Patients using Inhaled Antibiotics with a Focus on Nebulized Liposomal Amikacin
inferred← citeshttps://doi.org/10.22207/jpam.15.4.79openalex-snapshot
Antimicrobial Resistance in Pseudomonas aeruginosa Biofilms
inferred← citeshttps://doi.org/10.22215/etd/2019-13815openalex-snapshot
Genome-wide association study of Pseudomonas aeruginosa adaptations to the cystic fibrosis lung
inferred← citeshttps://doi.org/10.22541/au.168450001.11449110/v1openalex-snapshot
Myosin 16 mimicries may explain post- COVID-19 related neurological consequences
inferred← citeshttps://doi.org/10.25148/etd.fidc001220openalex-snapshot
Elucidating The Role of MifS-MifR Two-Component System in Regulating Pseudomonas aeruginosa Pathogenicity
inferred← citeshttps://doi.org/10.30699/ijmm.12.3.189openalex-snapshot
Effect of Supernatant Extract and Cell Lysate of Probiotic Yeast of Saccharomyces Cerevisiae on Biofilm and Alginate Production in Pseudomonas Aeruginosa
inferred← citeshttps://doi.org/10.32657/10356/137289openalex-snapshot
Understanding the complications of pseudomonas aeruginosa biofilm exudates on wound healing
inferred← citeshttps://doi.org/10.32920/25417300openalex-snapshot
Outer Membrane Protease Regulation and Function in Enterobacterales
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