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Genetic adaptation by Pseudomonas aeruginosa to the airways of cystic fibrosis patients

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1016/s1534-5807(02)00295-2openalex-snapshot

Pseudomonas aeruginosa Anaerobic Respiration in Biofilms

inferredcites →https://doi.org/10.1038/35037627openalex-snapshot

Quorum-sensing signals indicate that cystic fibrosis lungs are infected with bacterial biofilms

inferredcites →https://doi.org/10.1038/nature03912openalex-snapshot

Aminoglycoside antibiotics induce bacterial biofilm formation

inferredcites →https://doi.org/10.1073/pnas.0507170102openalex-snapshot

A chemosensory system that regulates biofilm formation through modulation of cyclic diguanylate levels

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.91.1.197openalex-snapshot

Structure of the autoinducer required for expression of Pseudomonas aeruginosa virulence genes.

inferredcites →https://doi.org/10.1084/jem.20020005openalex-snapshot

Multidrug Efflux Systems Play an Important Role in the Invasiveness of Pseudomonas aeruginosa

inferredcites →https://doi.org/10.1086/318075openalex-snapshot

Longitudinal Assessment ofPseudomonas aeruginosain Young Children with Cystic Fibrosis

inferredcites →https://doi.org/10.1093/nar/26.4.1107openalex-snapshot

GeneMark.hmm: new solutions for gene finding

inferredcites →https://doi.org/10.1099/00221287-143-1-35openalex-snapshot

Use of Siderophores to Type Pseudomonads: The Three Pseudomonas Aeruginosa Pyoverdine Systems

inferredcites →https://doi.org/10.1099/00221287-145-10-2863openalex-snapshot

A re-examination of twitching motility in Pseudomonas aeruginosa

inferredcites →https://doi.org/10.1099/00221287-146-10-2543openalex-snapshot

Role of Pseudomonas aeruginosa PhoP-PhoQ in resistance to antimicrobial cationic peptides and aminoglycosides

inferredcites →https://doi.org/10.1101/gr.176601openalex-snapshot

Predicting Deleterious Amino Acid Substitutions

inferredcites →https://doi.org/10.1111/j.1348-0421.1988.tb01372.xopenalex-snapshot

Role of Pili in the Pathogenesis of Pseudomonas aeruginosa Burn Infection

inferredcites →https://doi.org/10.1126/science.284.5418.1322openalex-snapshot

Type III Secretion Machines: Bacterial Devices for Protein Delivery into Host Cells

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.43.11.2624openalex-snapshot

Involvement of an Active Efflux System in the Natural Resistance of Pseudomonas aeruginosa to Aminoglycosides

inferredcites →https://doi.org/10.1128/aac.43.12.2975openalex-snapshot

Characterization of a Pseudomonas aeruginosa Efflux Pump Contributing to Aminoglycoside Impermeability

inferredcites →https://doi.org/10.1128/aac.46.11.3406-3411.2002openalex-snapshot

Constitutive High Expression of Chromosomal β-Lactamase in Pseudomonas aeruginosa Caused by a New Insertion Sequence (IS 1669 ) Located in ampD

inferredcites →https://doi.org/10.1128/aac.47.10.3202-3207.2003openalex-snapshot

Contribution of the MexXY Multidrug Transporter to Aminoglycoside Resistance in Pseudomonas aeruginosa Clinical Isolates

inferredcites →https://doi.org/10.1128/aac.49.5.1782-1786.2005openalex-snapshot

Mutations in PA3574 ( nalD ) Lead to Increased MexAB-OprM Expression and Multidrug Resistance in Laboratory and Clinical Isolates of Pseudomonas aeruginosa

inferredcites →https://doi.org/10.1128/aem.60.6.1734-1738.1994openalex-snapshot

A major Pseudomonas aeruginosa clone common to patients and aquatic habitats

inferredcites →https://doi.org/10.1128/iai.42.1.170-177.1983openalex-snapshot

Pseudomonas aeruginosa isolates from patients with cystic fibrosis: a class of serum-sensitive, nontypable strains deficient in lipopolysaccharide O side chains

inferredcites →https://doi.org/10.1128/iai.50.2.572-576.1985openalex-snapshot

Avirulence and altered physiological properties of cystic fibrosis strains of Pseudomonas aeruginosa

inferredcites →https://doi.org/10.1128/iai.62.2.596-605.1994openalex-snapshot

Nonmotility and phagocytic resistance of Pseudomonas aeruginosa isolates from chronically colonized patients with cystic fibrosis

inferredcites →https://doi.org/10.1128/iai.64.1.37-43.1996openalex-snapshot

Contribution of specific Pseudomonas aeruginosa virulence factors to pathogenesis of pneumonia in a neonatal mouse model of infection

inferredcites →https://doi.org/10.1128/iai.64.2.518-523.1996openalex-snapshot

Pyoverdin is essential for virulence of Pseudomonas aeruginosa

inferredcites →https://doi.org/10.1128/iai.72.3.1677-1684.2004openalex-snapshot

An Adenylate Cyclase-Controlled Signaling Network Regulates Pseudomonas aeruginosa Virulence in a Mouse Model of Acute Pneumonia

inferredcites →https://doi.org/10.1128/jb.00790-06openalex-snapshot

FlhF Is Required for Swimming and Swarming in Pseudomonas aeruginosa

inferredcites →https://doi.org/10.1128/jb.179.2.417-422.1997openalex-snapshot

Proliferation of mutators in A cell population

inferredcites →https://doi.org/10.1128/jb.184.13.3614-3622.2002openalex-snapshot

Genetic Variation at the O-Antigen Biosynthetic Locus in Pseudomonas aeruginosa

inferredcites →https://doi.org/10.1128/jb.185.4.1316-1325.2003openalex-snapshot

Whole-Genome Sequence Variation among Multiple Isolates of Pseudomonas aeruginosa

inferredcites →https://doi.org/10.1128/jb.185.7.2066-2079.2003openalex-snapshot

Identification, Timing, and Signal Specificity of Pseudomonas aeruginosa Quorum-Controlled Genes: a Transcriptome Analysis

inferredcites →https://doi.org/10.1128/jb.186.17.5692-5698.2004openalex-snapshot

The Bvg Virulence Control System Regulates Biofilm Formation in Bordetella bronchiseptica

inferredcites →https://doi.org/10.1128/jcm.25.10.1868-1874.1987openalex-snapshot

Prospective study of serum antibodies to Pseudomonas aeruginosa exoproteins in cystic fibrosis

inferredcites →https://doi.org/10.1128/jcm.31.9.2320-2326.1993openalex-snapshot

Genome macrorestriction analysis of diversity and variability of Pseudomonas aeruginosa strains infecting cystic fibrosis patients

inferredcites →https://doi.org/10.1128/jcm.37.9.2987-2991.1999openalex-snapshot

Evaluation of Reference Dilution Test Methods for Antimicrobial Susceptibility Testing of Pseudomonas aeruginosa Strains Isolated from Patients with Cystic Fibrosis

inferredcites →https://doi.org/10.1128/jcm.9.4.538-540.1979openalex-snapshot

A More Sensitive Plate Assay for Detection of Protease Production by Pseudomonas aeruginosa

inferredcites →https://doi.org/10.1128/mmbr.60.3.539-574.1996openalex-snapshot

Microbial pathogenesis in cystic fibrosis: mucoid Pseudomonas aeruginosa and Burkholderia cepacia

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.3155764openalex-extracted

Three Dimensional Cartography of Microbiome and Metabolome Data onto Radiological Images of the Human Lung

inferred← citeshttps://doi.org/10.1002/1873-3468.12454openalex-snapshot

Insights into host–pathogen interactions from state‐of‐the‐art animal models of respiratory Pseudomonas aeruginosa infections

inferred← citeshttps://doi.org/10.1002/9780470975152.ch2openalex-snapshot

Microbes and Metabolism

inferred← citeshttps://doi.org/10.1002/9781118156247.ch5openalex-snapshot

Importance of Adaptive and Stepwise Changes in the Rise and Spread of Antimicrobial Resistance

inferred← citeshttps://doi.org/10.1002/9781118960226.ch17openalex-snapshot

Proteogenomics ofPseudomonas aeruginosain Cystic Fibrosis Infections

inferred← citeshttps://doi.org/10.1002/9781119004813.ch10openalex-snapshot

Bacterial Stress Responses as Determinants of Antimicrobial Resistance

inferred← citeshttps://doi.org/10.1002/9783527622009.ch1openalex-snapshot

Comparative Genomics of Pseudomonas

inferred← citeshttps://doi.org/10.1002/9783527622009.ch9openalex-snapshot

Pseudomonas aeruginosa: A Model for Biofilm Formation

inferred← citeshttps://doi.org/10.1002/bies.201500180openalex-snapshot

Antibiotic resistance and virulence: Understanding the link and its consequences for prophylaxis and therapy

inferred← citeshttps://doi.org/10.1002/ijch.201400128openalex-snapshot

The Pseudomonas Quinolone Signal (PQS)

inferred← citeshttps://doi.org/10.1002/jmv.21623openalex-snapshot

Respiratory syncytial virus infection facilitates acute colonization of Pseudomonas aeruginosa in mice

inferred← citeshttps://doi.org/10.1002/mbo3.141openalex-snapshot

Developing an international Pseudomonas aeruginosa reference panel

inferred← citeshttps://doi.org/10.1002/mbo3.305openalex-snapshot

The OpdQ porin of Pseudomonas aeruginosa is regulated by environmental signals associated with cystic fibrosis including nitrate‐induced regulation involving the NarXL two‐component system

inferred← citeshttps://doi.org/10.1002/mbo3.70168openalex-snapshot

Genetic Determinants Associated With the Biofilm Formation Impairment in Pseudomonas aeruginosa Clinical Isolates

inferred← citeshttps://doi.org/10.1002/path.4118openalex-snapshot

The microbiome in wound repair and tissue fibrosis

inferred← citeshttps://doi.org/10.1002/pmic.201000457openalex-snapshot

Quantitative proteomics (2‐D DIGE) reveals molecular strategies employed by Burkholderia cenocepacia to adapt to the airways of cystic fibrosis patients under antimicrobial therapy

inferred← citeshttps://doi.org/10.1002/ppul.21076openalex-snapshot

Effect of mutator P. aeruginosa on antibiotic resistance acquisition and respiratory function in cystic fibrosis

inferred← citeshttps://doi.org/10.1002/ppul.25840openalex-snapshot

Measuring the impact of an empiric antibiotic algorithm for pulmonary exacerbation in children and young adults with cystic fibrosis

inferred← citeshttps://doi.org/10.1002/wrna.1454openalex-snapshot

Cyclic‐di‐GMP regulation of virulence in bacterial pathogens

inferred← citeshttps://doi.org/10.1007/82_2011_199openalex-snapshot

Microevolution of Pseudomonas aeruginosa to a Chronic Pathogen of the Cystic Fibrosis Lung

inferred← citeshttps://doi.org/10.1007/978-1-4419-6084-9_10openalex-snapshot

Pseudomonas aeruginosa Biofilms in the Lungs of Cystic Fibrosis Patients

inferred← citeshttps://doi.org/10.1007/978-1-4614-1400-1_10openalex-snapshot

Efflux-Mediated Antimicrobial Resistance

inferred← citeshttps://doi.org/10.1007/978-1-4614-5326-0_11openalex-snapshot

Pseudomonas aeruginosa and Mucosal Defenses in the Lung

inferred← citeshttps://doi.org/10.1007/978-1-4939-0473-0_39openalex-snapshot

Transposon Mutagenesis

inferred← citeshttps://doi.org/10.1007/978-1-4939-3277-1_12openalex-snapshot

Response of Pseudomonas aeruginosa to Spaceflight and Spaceflight Analogue Culture: Implications for Astronaut Health and the Clinic

inferred← citeshttps://doi.org/10.1007/978-1-61779-089-8_1openalex-snapshot

Helicos Single-Molecule Sequencing of Bacterial Genomes

inferred← citeshttps://doi.org/10.1007/978-3-030-42382-7_6openalex-snapshot

Fungal Infections and ABPA

inferred← citeshttps://doi.org/10.1007/978-3-030-45885-0_20openalex-snapshot

Phage Therapy in Cystic Fibrosis. Challenges and Perspectives

inferred← citeshttps://doi.org/10.1007/978-3-031-08491-1_11openalex-snapshot

Transcriptional Profiling of Pseudomonas aeruginosa Infections

inferred← citeshttps://doi.org/10.1007/978-3-031-08491-1_15openalex-snapshot

Mixed Populations and Co-Infection: Pseudomonas aeruginosa and Staphylococcus aureus

inferred← citeshttps://doi.org/10.1007/978-3-031-08491-1_4openalex-snapshot

Pseudomonas aeruginosa Quorum Sensing

inferred← citeshttps://doi.org/10.1007/978-3-031-08491-1_5openalex-snapshot

Antibiotic Resistance in Pseudomonas

inferred← citeshttps://doi.org/10.1007/978-3-031-08491-1_7openalex-snapshot

Flagella, Chemotaxis and Surface Sensing

inferred← citeshttps://doi.org/10.1007/978-3-031-10992-8_3openalex-snapshot

Antibiotic Resistance Development in Bacterial Biofilms

inferred← citeshttps://doi.org/10.1007/978-3-031-10992-8_7openalex-snapshot

Chemical Regulation of Pseudomonas aeruginosa Biofilm Formation as a Potential Treatment for Persistent Infections

inferred← citeshttps://doi.org/10.1007/978-3-031-15349-5_7openalex-snapshot

Polymicrobial Biofilms in Cystic Fibrosis Lung Infections: Effects on Antimicrobial Susceptibility

inferred← citeshttps://doi.org/10.1007/978-3-031-39474-4_4openalex-snapshot

Gram-Negative Infection

inferred← citeshttps://doi.org/10.1007/978-3-031-44630-6_87openalex-snapshot

Effects of Ceftazidime Exposure on Phenotypic Characteristics of Pseudomonas Aeruginosa ATCC 9027

inferred← citeshttps://doi.org/10.1007/978-3-031-70476-5_11openalex-snapshot

Biofilm Dispersion and the Matrix

inferred← citeshttps://doi.org/10.1007/978-3-319-39658-3_14openalex-snapshot

Antimicrobial Drug Efflux Pumps in Pseudomonas aeruginosa

inferred← citeshttps://doi.org/10.1007/978-3-319-39658-3_26openalex-snapshot

Antimicrobial Drug Efflux Systems as Components of Bacterial Stress Responses

inferred← citeshttps://doi.org/10.1007/978-3-319-47266-9_9openalex-snapshot

Pseudomonas

inferred← citeshttps://doi.org/10.1007/978-3-319-61452-6_12openalex-snapshot

Pseudomonas aeruginosa and Bronchiectasis

inferred← citeshttps://doi.org/10.1007/978-3-319-67651-7_25openalex-snapshot

Pseudomonas spp.

inferred← citeshttps://doi.org/10.1007/978-3-319-78538-7_14openalex-snapshot

Staphylococcus aureus Adaptation During Infection

inferred← citeshttps://doi.org/10.1007/978-3-540-75418-3_4openalex-snapshot

Quorum Sensing and Microbial Biofilms

inferred← citeshttps://doi.org/10.1007/978-3-642-28951-4_8openalex-snapshot

Persister Cells: Molecular Mechanisms Related to Antibiotic Tolerance

inferred← citeshttps://doi.org/10.1007/978-90-481-3909-5_5openalex-snapshot

Emergence of Pseudomonas aeruginosa in Cystic Fibrosis Lung Infections

inferred← citeshttps://doi.org/10.1007/978-94-017-9555-5_1openalex-snapshot

Pseudomonas aeruginosa Host Immune Evasion

inferred← citeshttps://doi.org/10.1007/978-981-15-3028-9_12openalex-snapshot

Bacterial Metabolic Fitness During Pathogenesis

inferred← citeshttps://doi.org/10.1007/s00011-018-1132-0openalex-snapshot

NOD-like receptor(s) and host immune responses with Pseudomonas aeruginosa infection

inferred← citeshttps://doi.org/10.1007/s00203-016-1303-8openalex-snapshot

Characterization of in vitro phenotypes of Burkholderia pseudomallei and Burkholderia mallei strains potentially associated with persistent infection in mice

inferred← citeshttps://doi.org/10.1007/s00203-020-01937-5openalex-snapshot

Nutrient factor-dependent performance of bacterial quorum sensing system during population evolution

inferred← citeshttps://doi.org/10.1007/s00203-026-04839-0openalex-snapshot

Pseudomonas aeruginosa: associated pathogenesis, epidemiology, resistance mechanisms, host response and emerging treatment strategies

inferred← citeshttps://doi.org/10.1007/s00216-020-02696-4openalex-snapshot

Phenazines as potential biomarkers of Pseudomonas aeruginosa infections: synthesis regulation, pathogenesis and analytical methods for their detection

inferred← citeshttps://doi.org/10.1007/s00248-013-0297-xopenalex-snapshot

Pseudomonas aeruginosa Biofilms in Disease

inferred← citeshttps://doi.org/10.1007/s00248-017-0982-2openalex-snapshot

Contributions of Composition and Interactions to Bacterial Respiration Are Reliant on the Phylogenetic Similarity of the Measured Community

inferred← citeshttps://doi.org/10.1007/s00253-012-4466-5openalex-snapshot

Comparative analysis of temperature-dependent transcriptome of Pseudomonas aeruginosa strains from rhizosphere and human habitats

inferred← citeshttps://doi.org/10.1007/s00253-014-5904-3openalex-snapshot

A new assay for rhamnolipid detection—important virulence factors of Pseudomonas aeruginosa

inferred← citeshttps://doi.org/10.1007/s00253-015-6865-xopenalex-snapshot

Characterization of self-generated variants in Pseudoalteromonas lipolytica biofilm with increased antifouling activities

inferred← citeshttps://doi.org/10.1007/s00284-021-02729-wopenalex-snapshot

Repurposing Sitafloxacin, Prulifloxacin, Tosufloxacin, and Sisomicin as Antimicrobials Against Biofilm and Persister Cells of Pseudomonas aeruginosa

inferred← citeshttps://doi.org/10.1007/s00284-024-03769-8openalex-snapshot

Genomic Comparative of Pseudomonas aeruginosa Small Colony Variant, Mucoid and Non-mucoid Phenotypes Obtained from a Patient with Cystic Fibrosis During Respiratory Exacerbations

inferred← citeshttps://doi.org/10.1007/s00438-026-02393-4openalex-snapshot

Genomic characterization of Pseudomonas aeruginosa infecting Abidjanvirus Lucjan

inferred← citeshttps://doi.org/10.1007/s00442-015-3327-1openalex-snapshot

Gut microbes may facilitate insect herbivory of chemically defended plants

inferred← citeshttps://doi.org/10.1007/s10096-013-1916-7openalex-snapshot

Virulence factor expression patterns in Pseudomonas aeruginosa strains from infants with cystic fibrosis

inferred← citeshttps://doi.org/10.1007/s10096-025-05132-6openalex-snapshot

Differences in antimicrobial resistance between exoU and exoS isolates of Pseudomonas aeruginosa

inferred← citeshttps://doi.org/10.1007/s10123-019-00091-3openalex-snapshot

Anti-quorum sensing activity of Forsythia suspense extract against Chromobacterium violaceum by targeting CviR receptor

inferred← citeshttps://doi.org/10.1007/s10529-007-9620-2openalex-snapshot

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inferred← citeshttps://doi.org/10.1007/s10534-008-9197-9openalex-snapshot

Iron acquisition by Pseudomonas aeruginosa in the lungs of patients with cystic fibrosis

inferred← citeshttps://doi.org/10.1007/s10534-011-9464-zopenalex-snapshot

Pseudomonas siderophores in the sputum of patients with cystic fibrosis

inferred← citeshttps://doi.org/10.1007/s11274-009-0052-0openalex-snapshot

Alfalfa infection model: is it a potential alternative for mouse pneumonia model to study pathogenesis of Stenotrophomonas maltophilia?

inferred← citeshttps://doi.org/10.1007/s11274-024-04042-7openalex-snapshot

Role of bacterial multidrug efflux pumps during infection

inferred← citeshttps://doi.org/10.1007/s11515-013-1267-xopenalex-snapshot

Universal soldier: Pseudomonas aeruginosa — an opportunistic generalist

inferred← citeshttps://doi.org/10.1007/s11814-017-0132-zopenalex-snapshot

New hybrid agarose/Cu-Bioglass® biomaterials for antibacterial coatings

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inferred← citeshttps://doi.org/10.1007/s12041-011-0086-6openalex-snapshot

Hypermutation and stress adaptation in bacteria

inferred← citeshttps://doi.org/10.1007/s12052-011-0381-yopenalex-snapshot

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inferred← citeshttps://doi.org/10.1007/s12088-015-0514-zopenalex-snapshot

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inferred← citeshttps://doi.org/10.1007/s12275-021-0478-0openalex-snapshot

Extracellular products-mediated interspecific interaction between Pseudomonas aeruginosa and Escherichia coli

inferred← citeshttps://doi.org/10.1007/s13213-011-0273-yopenalex-snapshot

Contribution of an arsenal of virulence factors to pathogenesis of Pseudomonas aeruginosa infections

inferred← citeshttps://doi.org/10.1007/s13238-014-0100-xopenalex-snapshot

The hierarchy quorum sensing network in Pseudomonas aeruginosa

inferred← citeshttps://doi.org/10.1007/s13238-016-0264-7openalex-snapshot

Structural insights into the regulatory mechanism of the Pseudomonas aeruginosa YfiBNR system

inferred← citeshttps://doi.org/10.1007/s15010-011-0096-6openalex-snapshot

Fatal Pseudomonas aeruginosa pneumonia in a previously healthy woman was most likely associated with a contaminated hot tub

inferred← citeshttps://doi.org/10.1007/s40121-013-0015-5openalex-snapshot

The Role of Human Beta-Defensin-2 in Pseudomonas aeruginosa Pulmonary Infection in Cystic Fibrosis Patients

inferred← citeshttps://doi.org/10.1016/b978-0-12-369420-1.00049-4openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/b978-0-12-404634-4.00019-xopenalex-snapshot

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inferred← citeshttps://doi.org/10.1016/b978-0-12-800262-9.00001-9openalex-snapshot

Pseudomonas aeruginosa Biofilms

inferred← citeshttps://doi.org/10.1016/b978-0-12-803309-8.00005-7openalex-snapshot

Genome Instability in Bacteria

inferred← citeshttps://doi.org/10.1016/b978-0-12-809633-8.90263-2openalex-snapshot

Microbiology of the Cystic Fibrosis Airway

inferred← citeshttps://doi.org/10.1016/b978-0-12-820084-1.00014-4openalex-snapshot

Natural molecules against QS-associated biofilm formation of pathogens

inferred← citeshttps://doi.org/10.1016/b978-0-323-40181-4.00155-9openalex-snapshot

Pseudomonas aeruginosa

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Pseudomonas aeruginosa

inferred← citeshttps://doi.org/10.1016/b978-0-323-82763-8.00125-4openalex-snapshot

Pseudomonas and Related Genera

inferred← citeshttps://doi.org/10.1016/b978-0-323-85679-9.00005-2openalex-snapshot

Genome instability in bacteria: Causes and consequences

inferred← citeshttps://doi.org/10.1016/b978-0-323-88480-8.00016-9openalex-snapshot

Role of biofilm in host–pathogen interaction

inferred← citeshttps://doi.org/10.1016/b978-0-323-90590-9.00011-0openalex-snapshot

Survival and thriving behavior of bacteria in microbial jungle

inferred← citeshttps://doi.org/10.1016/b978-0-323-99886-4.00003-xopenalex-snapshot

Virulence evolution of bacterial species

inferred← citeshttps://doi.org/10.1016/b978-0-443-06839-3.00219-8openalex-snapshot

Pseudomonas aeruginosa

inferred← citeshttps://doi.org/10.1016/b978-1-4160-4044-6.50140-0openalex-snapshot

PSEUDOMONAS AND RELATED GENERA

inferred← citeshttps://doi.org/10.1016/b978-1-4557-4801-3.00073-4openalex-snapshot

Cystic Fibrosis

inferred← citeshttps://doi.org/10.1016/j.actbio.2017.07.004openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.bbamem.2019.05.008openalex-snapshot

Synergistic and antibiofilm activity of the antimicrobial peptide P5 against carbapenem-resistant Pseudomonas aeruginosa

inferred← citeshttps://doi.org/10.1016/j.bbrc.2014.05.090openalex-snapshot

Bacterial multidrug efflux pumps: Mechanisms, physiology and pharmacological exploitations

inferred← citeshttps://doi.org/10.1016/j.bbrc.2017.08.139openalex-snapshot

Structural insights into the functional role of GMP in modulating the YfiBNR system

inferred← citeshttps://doi.org/10.1016/j.bbrc.2018.07.071openalex-snapshot

Autophagy induced by type III secretion system toxins enhances clearance of Pseudomonas aeruginosa from human corneal epithelial cells

inferred← citeshttps://doi.org/10.1016/j.bej.2009.12.021openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.bioflm.2023.100129openalex-snapshot

Mechanisms of antibiotic resistance in Pseudomonas aeruginosa biofilms

inferred← citeshttps://doi.org/10.1016/j.bioflm.2026.100358openalex-snapshot

Mapping the global landscape of biofilm-associated antimicrobial resistance (1992–2025)

inferred← citeshttps://doi.org/10.1016/j.bioorg.2014.04.005openalex-snapshot

The art of antibacterial warfare: Deception through interference with quorum sensing–mediated communication

inferred← citeshttps://doi.org/10.1016/j.biotechadv.2021.107862openalex-snapshot

Rugose small colony variant and its hyper-biofilm in Pseudomonas aeruginosa: Adaption, evolution, and biotechnological potential

inferred← citeshttps://doi.org/10.1016/j.bmcl.2018.12.068openalex-snapshot

Novel 2, 8-bit derivatives of quinolines attenuate Pseudomonas aeruginosa virulence and biofilm formation

inferred← citeshttps://doi.org/10.1016/j.carres.2014.04.018openalex-snapshot

Synthesis of the tetrasaccharide outer core fragment of Burkholderia multivorans lipooligosaccharide

inferred← citeshttps://doi.org/10.1016/j.celrep.2013.07.026openalex-snapshot

Convergent Evolution of Hyperswarming Leads to Impaired Biofilm Formation in Pathogenic Bacteria

inferred← citeshttps://doi.org/10.1016/j.celrep.2013.12.019openalex-snapshot

Rapid Evolution of Culture-Impaired Bacteria during Adaptation to Biofilm Growth

inferred← citeshttps://doi.org/10.1016/j.celrep.2021.109829openalex-snapshot

Adaptation and genomic erosion in fragmented Pseudomonas aeruginosa populations in the sinuses of people with cystic fibrosis

inferred← citeshttps://doi.org/10.1016/j.celrep.2023.112540openalex-snapshot

Pyochelin biotransformation by Staphylococcus aureus shapes bacterial competition with Pseudomonas aeruginosa in polymicrobial infections

inferred← citeshttps://doi.org/10.1016/j.chest.2021.04.015openalex-snapshot

Elastase Activity From Pseudomonas aeruginosa Respiratory Isolates and ICU Mortality

inferred← citeshttps://doi.org/10.1016/j.chom.2015.07.006openalex-snapshot

Regional Isolation Drives Bacterial Diversification within Cystic Fibrosis Lungs

inferred← citeshttps://doi.org/10.1016/j.chom.2015.08.013openalex-snapshot

Bacteria in the CF Lung: Isolation Drives Diversity

inferred← citeshttps://doi.org/10.1016/j.chom.2017.04.003openalex-snapshot

Quorum Sensing Attenuates Virulence in Sodalis praecaptivus

inferred← citeshttps://doi.org/10.1016/j.chom.2017.10.001openalex-snapshot

Three-Dimensional Microbiome and Metabolome Cartography of a Diseased Human Lung

inferred← citeshttps://doi.org/10.1016/j.chom.2019.03.007openalex-snapshot

Adaptive Evolution within Gut Microbiomes of Healthy People

inferred← citeshttps://doi.org/10.1016/j.chom.2025.01.001openalex-snapshot

Competitive behaviors in Serratia marcescens are coordinately regulated by a lifestyle switch frequently inactivated in the clinical environment

inferred← citeshttps://doi.org/10.1016/j.cmi.2022.01.017openalex-snapshot

Persistence and genetic adaptation of Pseudomonas aeruginosa in patients with chronic obstructive pulmonary disease

inferred← citeshttps://doi.org/10.1016/j.coph.2006.12.005openalex-snapshot

Opportunistic infections in lung disease: Pseudomonas infections in cystic fibrosis

inferred← citeshttps://doi.org/10.1016/j.coph.2008.04.006openalex-snapshot

Front-runners for pharmacotherapeutic correction of the airway ion transport defect in cystic fibrosis

inferred← citeshttps://doi.org/10.1016/j.crmicr.2025.100348openalex-snapshot

Chronic wounds and adaptive Pseudomonas aeruginosa: A phenotypic and genotypic characterization

inferred← citeshttps://doi.org/10.1016/j.cub.2009.01.050openalex-snapshot

Quorum Sensing and the Social Evolution of Bacterial Virulence

inferred← citeshttps://doi.org/10.1016/j.cub.2018.04.093openalex-snapshot

Cheating on Cheaters Stabilizes Cooperation in Pseudomonas aeruginosa

inferred← citeshttps://doi.org/10.1016/j.cub.2018.05.034openalex-snapshot

Social Evolution: Selection on Multiple Cooperative Traits Optimizes Cost–Benefit Relationships

inferred← citeshttps://doi.org/10.1016/j.cyto.2023.156135openalex-snapshot

Immune escape strategies of Pseudomonas aeruginosa to establish chronic infection

inferred← citeshttps://doi.org/10.1016/j.ddmod.2007.11.008openalex-snapshot

Animal models of chronic Pseudomonas aeruginosa lung infection in cystic fibrosis

inferred← citeshttps://doi.org/10.1016/j.dnarep.2016.09.001openalex-snapshot

Transcription-associated mutation of lasR in Pseudomonas aeruginosa

inferred← citeshttps://doi.org/10.1016/j.drudis.2006.12.007openalex-snapshot

Disease induction by human microbial pathogens in plant-model systems: potential, problems and prospects

inferred← citeshttps://doi.org/10.1016/j.eimc.2008.05.004openalex-snapshot

Diagnóstico microbiológico de la colonización-infección broncopulmonar en el paciente con fibrosis quística

inferred← citeshttps://doi.org/10.1016/j.eimc.2010.05.006openalex-snapshot

Polimorfismo de los genes mucA y fpvA en Pseudomonas aeruginosa de pacientes con fibrosis quística: coexistencia de variantes genéticas en el mismo paciente

inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.12.076openalex-snapshot

Anti-biofilm effect of novel thiazole acid analogs against Pseudomonas aeruginosa through IQS pathways

inferred← citeshttps://doi.org/10.1016/j.ejmech.2020.112132openalex-snapshot

The cell division protein FtsZ as a cellular target to hit cystic fibrosis pathogens

inferred← citeshttps://doi.org/10.1016/j.ejps.2021.106103openalex-snapshot

Antimicrobial resistance: Prevalence, economic burden, mechanisms of resistance and strategies to overcome

inferred← citeshttps://doi.org/10.1016/j.enzmictec.2011.06.001openalex-snapshot

Developing next generation antimicrobials by intercepting AI-2 mediated quorum sensing

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2014.08.011openalex-snapshot

Nitrite modulates bacterial antibiotic susceptibility and biofilm formation in association with airway epithelial cells

inferred← citeshttps://doi.org/10.1016/j.gendis.2022.09.009openalex-snapshot

The transcriptional regulators of virulence for Pseudomonas aeruginosa: Therapeutic opportunity and preventive potential of its clinical infections

inferred← citeshttps://doi.org/10.1016/j.genrep.2020.100666openalex-snapshot

Efflux pumps of Gram-negative bacteria in brief

inferred← citeshttps://doi.org/10.1016/j.genrep.2020.101009openalex-snapshot

Prototheca spp. co-infections and their virulence factors in human protothecosis in Hillah city, Iraq

inferred← citeshttps://doi.org/10.1016/j.heliyon.2021.e07002openalex-snapshot

Quorum quenching activity of Andrographis paniculata (Burm f.) Nees andrographolide compounds on metallo-β-lactamase-producing clinical isolates of Pseudomonas aeruginosa PA22 and PA247 and their effect on lasR gene expression

inferred← citeshttps://doi.org/10.1016/j.heliyon.2022.e11566openalex-snapshot

Genome sequence of Pseudomonas aeruginosa PA1-Petro—A role model of environmental adaptation and a potential biotechnological tool

inferred← citeshttps://doi.org/10.1016/j.idc.2007.06.006openalex-snapshot

Infections in Chronic Lung Diseases

inferred← citeshttps://doi.org/10.1016/j.idc.2013.02.006openalex-snapshot

Impact of Multidrug-Resistant Organisms on Patients Considered for Lung Transplantation

inferred← citeshttps://doi.org/10.1016/j.ijmm.2010.04.010openalex-snapshot

Bacterial genome plasticity and its impact on adaptation during persistent infection

inferred← citeshttps://doi.org/10.1016/j.ijmm.2010.05.002openalex-snapshot

Listeria monocytogenes lineages: Genomics, evolution, ecology, and phenotypic characteristics

inferred← citeshttps://doi.org/10.1016/j.ijmm.2010.08.004openalex-snapshot

Clonal epidemiology of Pseudomonas aeruginosa in cystic fibrosis

inferred← citeshttps://doi.org/10.1016/j.ijmm.2010.08.007openalex-snapshot

Anaerobic physiology of Pseudomonas aeruginosa in the cystic fibrosis lung

inferred← citeshttps://doi.org/10.1016/j.ijmm.2010.08.008openalex-snapshot

Adaptation of Pseudomonas aeruginosa during persistence in the cystic fibrosis lung

inferred← citeshttps://doi.org/10.1016/j.ijmm.2010.08.009openalex-snapshot

Mutators in cystic fibrosis chronic lung infection: Prevalence, mechanisms, and consequences for antimicrobial therapy

inferred← citeshttps://doi.org/10.1016/j.ijmm.2010.10.005openalex-snapshot

Genotypic and phenotypic characterization of Pseudomonas aeruginosa isolates from urinary tract infections

inferred← citeshttps://doi.org/10.1016/j.ijmm.2013.09.012openalex-snapshot

Extended Staphylococcus aureus persistence in cystic fibrosis is associated with bacterial adaptation

inferred← citeshttps://doi.org/10.1016/j.ijmm.2014.02.008openalex-snapshot

Prevalence and persistence of Escherichia coli in the airways of cystic fibrosis patients—An unrecognized CF pathogen?

inferred← citeshttps://doi.org/10.1016/j.isci.2023.106475openalex-snapshot

Competitive survival of clonal serial Pseudomonas aeruginosa isolates from cystic fibrosis airways in human neutrophils

inferred← citeshttps://doi.org/10.1016/j.jare.2024.08.038openalex-snapshot

Dual-species proteomics and targeted intervention of animal-pathogen interactions

inferred← citeshttps://doi.org/10.1016/j.jbc.2021.101461openalex-snapshot

Isolates of Salmonella typhimurium circumvent NLRP3 inflammasome recognition in macrophages during the chronic phase of infection

inferred← citeshttps://doi.org/10.1016/j.jcf.2008.09.006openalex-snapshot

Pseudomonas aeruginosa lasR mutants are associated with cystic fibrosis lung disease progression

inferred← citeshttps://doi.org/10.1016/j.jcf.2011.03.004openalex-snapshot

Pseudomonas aeruginosa in cystic fibrosis: Pyocyanin negative strains are associated with BPI-ANCA and progressive lung disease

inferred← citeshttps://doi.org/10.1016/j.jcf.2012.10.004openalex-snapshot

Treatment of lung infection in patients with cystic fibrosis: Current and future strategies

inferred← citeshttps://doi.org/10.1016/j.jcf.2013.02.004openalex-snapshot

P. aeruginosa in the paranasal sinuses and transplanted lungs have similar adaptive mutations as isolates from chronically infected CF lungs

inferred← citeshttps://doi.org/10.1016/j.jcf.2013.04.003openalex-snapshot

Extensive diversification is a common feature of Pseudomonas aeruginosa populations during respiratory infections in cystic fibrosis

inferred← citeshttps://doi.org/10.1016/j.jcf.2014.06.009openalex-snapshot

Impact of alginate-producing Pseudomonas aeruginosa on alveolar macrophage apoptotic cell clearance

inferred← citeshttps://doi.org/10.1016/j.jcf.2016.10.013openalex-snapshot

Multilocus amplicon sequencing of Pseudomonas aeruginosa cystic fibrosis airways isolates collected prior to and after early antipseudomonal chemotherapy

inferred← citeshttps://doi.org/10.1016/j.jcf.2019.04.013openalex-snapshot

The role of geographical location and climate on recurrent Pseudomonas infection in young children with Cystic Fibrosis

inferred← citeshttps://doi.org/10.1016/j.jcf.2019.07.008openalex-snapshot

The impact of CFTR modulator therapies on CF airway microbiology

inferred← citeshttps://doi.org/10.1016/j.jcf.2021.03.007openalex-snapshot

Emergence and impact of oprD mutations in Pseudomonas aeruginosa strains in cystic fibrosis

inferred← citeshttps://doi.org/10.1016/j.jcf.2021.09.017openalex-snapshot

Risk factors for Pseudomonas aeruginosa airway infection and lung function decline in children with cystic fibrosis

inferred← citeshttps://doi.org/10.1016/j.jmb.2018.05.004openalex-snapshot

Ecology and Biogenesis of Functional Amyloids in Pseudomonas

inferred← citeshttps://doi.org/10.1016/j.jprot.2021.104192openalex-snapshot

A wide-ranging Pseudomonas aeruginosa PeptideAtlas build: A useful proteomic resource for a versatile pathogen

inferred← citeshttps://doi.org/10.1016/j.jsb.2010.07.012openalex-snapshot

Crystal structure of MexZ, a key repressor responsible for antibiotic resistance in Pseudomonas aeruginosa

inferred← citeshttps://doi.org/10.1016/j.jse.2024.02.039openalex-snapshot

2023 Neer Award for Basic Science: Genetics of Cutibacterium acnes in revision shoulder arthroplasty: a large-scale bacterial whole-genome sequencing study

inferred← citeshttps://doi.org/10.1016/j.mam.2020.100882openalex-snapshot

Structural and functional diversity of neutrophil glycosylation in innate immunity and related disorders

inferred← citeshttps://doi.org/10.1016/j.meegid.2006.12.002openalex-snapshot

VNTR analysis of selected outbreaks of Burkholderia pseudomallei in Australia

inferred← citeshttps://doi.org/10.1016/j.meegid.2009.05.014openalex-snapshot

Phylogenetic understanding of clonal populations in an era of whole genome sequencing

inferred← citeshttps://doi.org/10.1016/j.mib.2007.03.009openalex-snapshot

The role of small RNAs in quorum sensing

inferred← citeshttps://doi.org/10.1016/j.mib.2008.08.002openalex-snapshot

Has nature already identified all useful antibacterial targets?

inferred← citeshttps://doi.org/10.1016/j.mib.2008.09.015openalex-snapshot

Pattern formation in Pseudomonas aeruginosa biofilms

inferred← citeshttps://doi.org/10.1016/j.mib.2009.01.005openalex-snapshot

Quorum sensing and environmental adaptation in Pseudomonas aeruginosa: a tale of regulatory networks and multifunctional signal molecules

inferred← citeshttps://doi.org/10.1016/j.mib.2011.11.001openalex-snapshot

Bacterial host interactions in cystic fibrosis

inferred← citeshttps://doi.org/10.1016/j.mib.2020.02.003openalex-snapshot

The social life of microbes in chronic infection

inferred← citeshttps://doi.org/10.1016/j.micinf.2007.07.004openalex-snapshot

The bacterial metabolite 2,3-butanediol ameliorates endotoxin-induced acute lung injury in rats

inferred← citeshttps://doi.org/10.1016/j.micinf.2011.07.011openalex-snapshot

Innate immune responses to Pseudomonas aeruginosa infection

inferred← citeshttps://doi.org/10.1016/j.micpath.2012.03.011openalex-snapshot

Pseudomonas aeruginosa strains from the chronically infected cystic fibrosis lung display increased invasiveness of A549 epithelial cells over time

inferred← citeshttps://doi.org/10.1016/j.micpath.2014.10.011openalex-snapshot

Sputum containing zinc enhances carbapenem resistance, biofilm formation and virulence of Pseudomonas aeruginosa

inferred← citeshttps://doi.org/10.1016/j.micpath.2017.08.007openalex-snapshot

Prevention of OprD regulated antibiotic resistance in Pseudomonas aeruginosa biofilm

inferred← citeshttps://doi.org/10.1016/j.micpath.2026.108298openalex-snapshot

YXL-13 attenuates virulence in Pseudomonas aeruginosa mutants and clinical isolates by inhibiting quorum sensing regulators LasR and RhlR

inferred← citeshttps://doi.org/10.1016/j.micres.2019.05.002openalex-snapshot

Codon-usage frequency mediated SNPs selection in lasR gene of cystic fibrosis Pseudomonas aeruginosa isolates

inferred← citeshttps://doi.org/10.1016/j.mimet.2007.12.006openalex-snapshot

Application and evaluation of double digest selective label (DDSL) typing technique for Pseudomonas aeruginosa hospital isolates

inferred← citeshttps://doi.org/10.1016/j.mimet.2015.02.006openalex-snapshot

Evaluation of phenotypic screening tests for carbapenemase production in Pseudomonas aeruginosa from patients with cystic fibrosis

inferred← citeshttps://doi.org/10.1016/j.molimm.2014.04.004openalex-snapshot

Persistent cystic fibrosis isolate Pseudomonas aeruginosa strain RP73 exhibits an under-acylated LPS structure responsible of its low inflammatory activity

inferred← citeshttps://doi.org/10.1016/j.molmed.2007.05.001openalex-snapshot

Cystic fibrosis: a disease of vulnerability to airway surface dehydration

inferred← citeshttps://doi.org/10.1016/j.molmed.2008.01.002openalex-snapshot

Airway epithelial control of Pseudomonas aeruginosa infection in cystic fibrosis

inferred← citeshttps://doi.org/10.1016/j.pharmthera.2018.05.003openalex-snapshot

Therapeutic antibodies: A new era in the treatment of respiratory diseases?

inferred← citeshttps://doi.org/10.1016/j.prrv.2010.07.003openalex-snapshot

Challenging and emerging pathogens in cystic fibrosis

inferred← citeshttps://doi.org/10.1016/j.ram.2015.11.002openalex-snapshot

Cystic Fibrosis Cloud database: Un sistema informático para el almacenamiento y manejo de datos clínicos y microbiológicos del paciente con fibrosis quística

inferred← citeshttps://doi.org/10.1016/j.semcdb.2010.11.006openalex-snapshot

What can Dictyostelium bring to the study of Pseudomonas infections?

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