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Anaerobic physiology of Pseudomonas aeruginosa in the cystic fibrosis lung
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/bit.20812openalex-snapshot
Competition between oxygen and nitrate respirations in continuous culture of Pseudomonas aeruginosa performing aerobic denitrification
inferredcites →https://doi.org/10.1007/s002039900127openalex-snapshot
Mechanism, regulation, and ecological role of bacterial cyanide biosynthesis
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/10.1016/0014-5793(95)00885-dopenalex-snapshot
Expression of the nir and nor genes for denitrification of Pseudomonas aeruginosa requires a novel CRP/FNR‐related transcriptional regulator, DNR, in addition to ANR
inferredcites →https://doi.org/10.1016/0378-1119(90)90493-bopenalex-snapshot
The arc operon for anaerobic arginine catabolism in Pseudomonas aeruginosa contains an additional gene, arcD, encoding a membrane protein
inferredcites →https://doi.org/10.1016/j.addr.2005.04.004openalex-snapshot
Bacterial resistance to antibiotics: Active efflux and reduced uptake
inferredcites →https://doi.org/10.1016/j.bbrc.2007.02.017openalex-snapshot
Participation of nitric oxide reductase in survival of Pseudomonas aeruginosa in LPS-activated macrophages
inferredcites →https://doi.org/10.1016/j.ijmm.2006.01.043openalex-snapshot
Impact of quorum sensing on fitness of Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1016/j.jcf.2005.05.018openalex-snapshot
Eradication of early Pseudomonas aeruginosa infection
inferredcites →https://doi.org/10.1016/j.jmb.2008.03.013openalex-snapshot
NO sensing in Pseudomonas aeruginosa: Structure of the Transcriptional Regulator DNR
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.micpath.2006.09.002openalex-snapshot
Role of the universal stress protein UspA of Salmonella in growth arrest, stress and virulence
inferredcites →https://doi.org/10.1016/j.molmed.2008.01.002openalex-snapshot
Airway epithelial control of Pseudomonas aeruginosa infection in cystic fibrosis
inferredcites →https://doi.org/10.1016/j.pupt.2007.12.001openalex-snapshot
Pseudomonas aeruginosa biofilm formation in the cystic fibrosis airway
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/s0065-2911(01)45002-8openalex-snapshot
Nitrate reduction in the periplasm of gram-negative bacteria
inferredcites →https://doi.org/10.1016/s0065-2911(06)52001-6openalex-snapshot
Oxygen, Cyanide and Energy Generation in the Cystic Fibrosis Pathogen Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1016/s0076-6879(07)37025-0openalex-snapshot
Microbial Responses to Nitric Oxide and Nitrosative Stress: Growth, “Omic,” and Physiological Methods
inferredcites →https://doi.org/10.1016/s0304-4165(98)00045-2openalex-snapshot
The nirQ gene, which is required for denitrification of Pseudomonas aeruginosa, can activate the RubisCO from Pseudomonas hydrogenothermophila
inferredcites →https://doi.org/10.1016/s0378-1097(01)00202-6openalex-snapshot
Dual control of hydrogen cyanide biosynthesis by the global activator GacA in Pseudomonas aeruginosa PAO1
inferredcites →https://doi.org/10.1016/s0923-2508(03)00081-0openalex-snapshot
Universal stress proteins and Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1016/s0966-842x(00)01918-1openalex-snapshot
Cystic fibrosis pathogenesis and the role of biofilms in persistent infection
inferredcites →https://doi.org/10.1016/s1369-5274(03)00025-0openalex-snapshot
The bacterial universal stress protein: function and regulation
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/nm1748openalex-snapshot
Ceramide accumulation mediates inflammation, cell death and infection susceptibility in cystic fibrosis
inferredcites →https://doi.org/10.1038/nrmicro1004openalex-snapshot
Antimicrobial reactive oxygen and nitrogen species: concepts and controversies
inferredcites →https://doi.org/10.1038/nrmicro1838openalex-snapshot
Physiological heterogeneity in biofilms
inferredcites →https://doi.org/10.1038/sj.emboj.7601787openalex-snapshot
Two‐pronged survival strategy for the major cystic fibrosis pathogen, Pseudomonas aeruginosa, lacking the capacity to degrade nitric oxide during anaerobic respiration
inferredcites →https://doi.org/10.1046/j.1365-2958.1997.3291701.xopenalex-snapshot
The global activator GacA of Pseudomonas aeruginosa PAO positively controls the production of the autoinducer N‐butyryl‐homoserine lactone and the formation of the virulence factors pyocyanin, cyanide, and lipase
inferredcites →https://doi.org/10.1046/j.1365-2958.1997.3561728.xopenalex-snapshot
The cioAB genes from Pseudomonas aeruginosa code for a novel cyanide‐insensitive terminal oxidase related to the cytochrome bd quinol oxidases
inferredcites →https://doi.org/10.1046/j.1365-2958.1997.5431906.xopenalex-snapshot
Cascade regulation of the two CRP/FNR‐related transcriptional regulators (ANR and DNR) and the denitrification enzymes in Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1046/j.1365-2958.2002.03046.xopenalex-snapshot
Pseudomonas aeruginosa RoxR, a response regulator related to Rhodobacter sphaeroides PrrA, activates expression of the cyanide‐insensitive terminal oxidase
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03904.xopenalex-snapshot
Differences in two Pseudomonas aeruginosa cbb3 cytochrome oxidases
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.0709804104openalex-snapshot
Molecular identification of bacteria in bronchoalveolar lavage fluid from 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/10.1086/598644openalex-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/jac/22.5.667openalex-snapshot
Antibiotic interaction and diffusion through alginate and exopolysaccharide of cystic fibrosis-derived Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1093/jac/dki171openalex-snapshot
Efflux-mediated antimicrobial resistance
inferredcites →https://doi.org/10.1099/00221287-135-9-2445openalex-snapshot
The Effect of Oxygen on Denitrification in Paracoccus denitrificans and Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1099/00221287-148-10-3195openalex-snapshot
Physiological responses of Pseudomonas aeruginosa PAO1 to oxidative stress in controlled microaerobic and aerobic cultures
inferredcites →https://doi.org/10.1099/00222615-45-2-110openalex-snapshot
The high amino-acid content of sputum from cystic fibrosis patients promotes growth of auxotrophic 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.0.028027-0openalex-snapshot
The transcription factor DNR from Pseudomonas aeruginosa specifically requires nitric oxide and haem for the activation of a target promoter in Escherichia coli
inferredcites →https://doi.org/10.1099/mic.0.2006/004077-0openalex-snapshot
Microbial ecology of the cystic fibrosis lung
inferredcites →https://doi.org/10.1099/mic.0.2008/018929-0openalex-snapshot
Nitrate-responsive NarX-NarL represses arginine-mediated induction of the Pseudomonas aeruginosa arginine fermentation arcDABC operon
inferredcites →https://doi.org/10.1099/mic.0.25936-0openalex-snapshot
Transcriptional regulation of the nos genes for nitrous oxide reductase in Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1099/mic.0.26017-0openalex-snapshot
Regulation of expression of the cyanide-insensitive terminal oxidase in Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1099/mic.0.26276-0openalex-snapshot
Iron deficiency leads to inhibition of oxygen transfer and enhanced formation of virulence factors in cultures of Pseudomonas aeruginosa PAO1
inferredcites →https://doi.org/10.1099/mic.0.26443-0openalex-snapshot
Alterations in the formation of lipopolysaccharide and membrane vesicles on the surface of Pseudomonas aeruginosa PAO1 under oxygen stress conditions
inferredcites →https://doi.org/10.1111/j.1365-2672.2008.04035.xopenalex-snapshot
Inhibition spectrum studies of microthecin and other anhydrofructose derivatives using selected strains of Gram-positive and -negative bacteria, yeasts and moulds, and investigation of the cytotoxicity of microthecin to malignant blood cell lines
inferredcites →https://doi.org/10.1111/j.1365-2796.2006.01744.xopenalex-snapshot
Evidence for airway surface dehydration as the initiating event in CF airway disease
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.1365-2958.2007.05772.xopenalex-snapshot
Responses of Pseudomonas aeruginosa to low oxygen indicate that growth in the cystic fibrosis lung is by aerobic respiration
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.1462-5822.2008.01271.xopenalex-snapshot
Cystic fibrosis and innate immunity: how chloride channel mutations provoke lung disease
inferredcites →https://doi.org/10.1111/j.1469-0691.2008.02659.xopenalex-snapshot
Antibiotic-resistant obligate anaerobes during exacerbations of cystic fibrosis patients
inferredcites →https://doi.org/10.1111/j.1574-6968.2006.00426.xopenalex-snapshot
A universal stress protein ofPorphyromonas gingivalisis involved in stress responses and biofilm formation
inferredcites →https://doi.org/10.1111/j.1574-6968.2008.01472.xopenalex-snapshot
Gene expression characteristics of a cystic fibrosis epidemic strain ofPseudomonas aeruginosaduring biofilm and planktonic growth
inferredcites →https://doi.org/10.1111/j.1574-6976.2006.00061.xopenalex-snapshot
Regulators of bacterial responses to nitric oxide
inferredcites →https://doi.org/10.1126/science.284.5418.1318openalex-snapshot
Bacterial Biofilms: A Common Cause of Persistent Infections
inferredcites →https://doi.org/10.1128/aac.32.4.518openalex-snapshot
Inhibition of tobramycin diffusion by binding to alginate
inferredcites →https://doi.org/10.1128/aac.37.4.715openalex-snapshot
Interaction of gentamicin with the A band and B band lipopolysaccharides of Pseudomonas aeruginosa and its possible lethal effect
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.50.1.382-384.2006openalex-snapshot
Arginine or Nitrate Enhances Antibiotic Susceptibility of Pseudomonas aeruginosa in Biofilms
inferredcites →https://doi.org/10.1128/aem.45.4.1247-1253.1983openalex-snapshot
Comparison of denitrification by Pseudomonas stutzeri, Pseudomonas aeruginosa, and Paracoccus denitrificans
inferredcites →https://doi.org/10.1128/aem.72.1.695-701.2006openalex-snapshot
Involvement of NarK1 and NarK2 Proteins in Transport of Nitrate and Nitrite in the Denitrifying Bacterium Pseudomonas aeruginosa PAO1
inferredcites →https://doi.org/10.1128/cmr.15.2.194-222.2002openalex-snapshot
Lung Infections Associated with Cystic Fibrosis
inferredcites →https://doi.org/10.1128/iai.00201-07openalex-snapshot
Nitrate Sensing and Metabolism Modulate Motility, Biofilm Formation, and Virulence in Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1128/iai.00755-09openalex-snapshot
Instantaneous Within-Patient Diversity of Pseudomonas aeruginosa Quorum-Sensing Populations from Cystic Fibrosis Lung Infections
inferredcites →https://doi.org/10.1128/iai.00822-09openalex-snapshot
Nitrite Reductase NirS Is Required for Type III Secretion System Expression and Virulence in the Human Monocyte Cell Line THP-1 by Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1128/iai.01807-06openalex-snapshot
In Vivo Evidence of Pseudomonas aeruginosa Nutrient Acquisition and Pathogenesis in the Lungs of Cystic Fibrosis Patients
inferredcites →https://doi.org/10.1128/iai.28.2.546-556.1980openalex-snapshot
Production of mucoid microcolonies by Pseudomonas aeruginosa within infected lungs in cystic fibrosis
inferredcites →https://doi.org/10.1128/iai.73.1.444-452.2005openalex-snapshot
Use of Phage Display To Identify Potential Pseudomonas aeruginosa Gene Products Relevant to Early Cystic Fibrosis Airway Infections
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.00162-07openalex-snapshot
Membrane-Bound Nitrate Reductase Is Required for Anaerobic Growth in Cystic Fibrosis Sputum
inferredcites →https://doi.org/10.1128/jb.00240-07openalex-snapshot
The Anaerobic Regulatory Network Required for Pseudomonas aeruginosa Nitrate Respiration
inferredcites →https://doi.org/10.1128/jb.00289-07openalex-snapshot
Quorum Sensing Regulates Denitrification in Pseudomonas aeruginosa PAO1
inferredcites →https://doi.org/10.1128/jb.00308-06openalex-snapshot
The Pseudomonas aeruginosa Universal Stress Protein PA4352 Is Essential for Surviving Anaerobic Energy Stress
inferredcites →https://doi.org/10.1128/jb.00505-07openalex-snapshot
Pyocyanin Alters Redox Homeostasis and Carbon Flux through Central Metabolic Pathways in Pseudomonas aeruginosa PA14
inferredcites →https://doi.org/10.1128/jb.00600-08openalex-snapshot
SpoT-Triggered Stringent Response Controls usp Gene Expression in Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1128/jb.00779-06openalex-snapshot
Involvement of Nitric Oxide in Biofilm Dispersal of Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1128/jb.00968-08openalex-snapshot
Influence of thePseudomonasQuinolone Signal on Denitrification inPseudomonas aeruginosa
inferredcites →https://doi.org/10.1128/jb.00975-09openalex-snapshot
Nitric Oxide Signaling in Pseudomonas aeruginosa Biofilms Mediates Phosphodiesterase Activity, Decreased Cyclic Di-GMP Levels, and Enhanced Dispersal
inferredcites →https://doi.org/10.1128/jb.01138-07openalex-snapshot
Nutritional Cues Control Pseudomonas aeruginosa Multicellular Behavior in Cystic Fibrosis Sputum
inferredcites →https://doi.org/10.1128/jb.01683-07openalex-snapshot
Proteomic, Microarray, and Signature-Tagged Mutagenesis Analyses of AnaerobicPseudomonas aeruginosaat pH 6.5, Likely Representing Chronic, Late-Stage Cystic Fibrosis Airway Conditions
inferredcites →https://doi.org/10.1128/jb.01687-06openalex-snapshot
Interrelationships between Colonies, Biofilms, and Planktonic Cells of Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1128/jb.160.3.928-934.1984openalex-snapshot
Pseudomonas aeruginosa mutants affected in anaerobic growth on arginine: evidence for a four-gene cluster encoding the arginine deiminase pathway
inferredcites →https://doi.org/10.1128/jb.173.15.4742-4750.1991openalex-snapshot
Anaerobic regulation of transcription initiation in the arcDABC operon of Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1128/jb.177.12.3606-3609.1995openalex-snapshot
Anaerobic activation of the entire denitrification pathway in Pseudomonas aeruginosa requires Anr, an analog of Fnr
inferredcites →https://doi.org/10.1128/jb.177.2.432-438.1995openalex-snapshot
Isolation and characterization of mutants defective in the cyanide-insensitive respiratory pathway of Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1128/jb.178.24.7322-7325.1996openalex-snapshot
Anaerobic production of alginate by Pseudomonas aeruginosa: alginate restricts diffusion of oxygen
inferredcites →https://doi.org/10.1128/jb.181.17.5303-5308.1999openalex-snapshot
The napF and narG Nitrate Reductase Operons in Escherichia coli Are Differentially Expressed in Response to Submicromolar Concentrations of Nitrate but Not Nitrite
inferredcites →https://doi.org/10.1128/jb.181.8.2459-2464.1999openalex-snapshot
The ArgR Regulatory Protein, a Helper to the Anaerobic Regulator ANR during Transcriptional Activation of the arcD Promoter in Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1128/jb.182.24.6940-6949.2000openalex-snapshot
Transcriptional Control of the Hydrogen Cyanide Biosynthetic Genes hcnABC by the Anaerobic Regulator ANR and the Quorum-Sensing Regulators LasR and RhlR in Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1128/jb.183.18.5395-5401.2001openalex-snapshot
Alginate Overproduction Affects Pseudomonas aeruginosa Biofilm Structure and Function
inferredcites →https://doi.org/10.1128/jb.184.5.1314-1323.2002openalex-snapshot
Periplasmic Nitrate Reductase (NapABC Enzyme) Supports Anaerobic Respiration byEscherichia coliK-12
inferredcites →https://doi.org/10.1128/jb.184.6.1693-1702.2002openalex-snapshot
Regulation ofnapGene Expression and Periplasmic Nitrate Reductase Activity in the Phototrophic BacteriumRhodobacter sphaeroidesDSM158
inferredcites →https://doi.org/10.1128/jb.186.12.3837-3847.2004openalex-snapshot
Expression Analysis of a Highly Adherent and Cytotoxic Small Colony Variant of Pseudomonas aeruginosa Isolated from a Lung of a Patient with Cystic Fibrosis
inferredcites →https://doi.org/10.1128/jb.186.14.4596-4604.2004openalex-snapshot
Long-Term Anaerobic Survival of the Opportunistic Pathogen Pseudomonas aeruginosa via Pyruvate Fermentation
inferredcites →https://doi.org/10.1128/jb.186.20.6837-6844.2004openalex-snapshot
The Transcriptional Regulator AlgR Controls Cyanide Production in Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1128/jb.187.14.4875-4883.2005openalex-snapshot
Quorum-Sensing-Negative ( lasR ) Mutants of Pseudomonas aeruginosa Avoid Cell Lysis and Death
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.187.18.6571-6576.2005openalex-snapshot
Transcriptome Analysis of Pseudomonas aeruginosa Growth: Comparison of Gene Expression in Planktonic Cultures and Developing and Mature Biofilms
inferredcites →https://doi.org/10.1128/jb.187.2.554-566.2005openalex-snapshot
Staphylococcus aureus Serves as an Iron Source for Pseudomonas aeruginosa during In Vivo Coculture
inferredcites →https://doi.org/10.1128/jb.188.2.659-668.2006openalex-snapshot
Anaerobic Survival of Pseudomonas aeruginosa by Pyruvate Fermentation Requires an Usp-Type Stress Protein
inferredcites →https://doi.org/10.1128/jcm.42.11.5176-5183.2004openalex-snapshot
Characterization of Bacterial Community Diversity in Cystic Fibrosis Lung Infections by Use of 16S Ribosomal DNA Terminal Restriction Fragment Length Polymorphism Profiling
inferredcites →https://doi.org/10.1128/jcm.43.10.5085-5090.2005openalex-snapshot
Antibiotic Susceptibilities of Pseudomonas aeruginosa Isolates Derived from Patients with Cystic Fibrosis under Aerobic, Anaerobic, and Biofilm Conditions
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/10.1128/mmbr.61.4.533-616.1997openalex-snapshot
Cell biology and molecular basis of denitrification
inferredcites →https://doi.org/10.1136/adc.78.1.49openalex-snapshot
Nitric oxide metabolites in cystic fibrosis lung disease
inferredcites →https://doi.org/10.1139/m75-088openalex-snapshot
Hydrogen cyanide, a secondary metabolite of Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1146/annurev.med.58.071905.105316openalex-snapshot
Airway Surface Dehydration in Cystic Fibrosis: Pathogenesis and Therapy
inferredcites →https://doi.org/10.1152/ajpcell.00417.2002openalex-snapshot
Role of airway surface liquid and submucosal glands in cystic fibrosis lung disease
inferredcites →https://doi.org/10.1164/rccm.200708-1151ocopenalex-snapshot
Detection of Anaerobic Bacteria in High Numbers in Sputum from Patients with Cystic Fibrosis
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/10.1172/jci24684openalex-snapshot
Anaerobic killing of mucoid Pseudomonas aeruginosa by acidified nitrite derivatives under cystic fibrosis airway conditions
inferredcites →https://doi.org/10.1177/1753425909106436openalex-snapshot
Review: Lipopolysaccharide biosynthesis in Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1183/09031936.00152407openalex-snapshot
Bacterial cyanogenesis occurs in the cystic fibrosis lung
inferredcites →https://doi.org/10.1183/09031936.00159607openalex-snapshot
Pseudomonas aeruginosa, cyanide accumulation and lung function in CF and non-CF bronchiectasis patients
inferredcites →https://doi.org/10.1371/journal.ppat.1000460openalex-snapshot
Mycobacterium tuberculosis Universal Stress Protein Rv2623 Regulates Bacillary Growth by ATP-Binding: Requirement for Establishing Chronic Persistent Infection
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1016/j.chemosphere.2022.135002openalex-snapshot
Toxicity of nZVI in the growth of bacteria present in contaminated soil
inferred← citeshttps://doi.org/10.1016/j.colsurfb.2019.110512openalex-snapshot
Enzyme-encapsulating polymeric nanoparticles: A potential adjunctive therapy in Pseudomonas aeruginosa biofilm-associated infection treatment
inferred← citeshttps://doi.org/10.1016/j.colsurfb.2020.110989openalex-snapshot
Self-defensive antimicrobial biomaterial surfaces
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2020.07.309openalex-snapshot
Biodegradability in aquatic system of thin materials based on chitosan, PBAT and HDPE polymers: Respirometric and physical-chemical analysis
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2021.121388openalex-snapshot
Developing ciprofloxacin dry powder for inhalation: A story of challenges and rational design in the treatment of cystic fibrosis lung infection
inferred← citeshttps://doi.org/10.1016/j.isci.2021.103404openalex-snapshot
Nitric-oxide-driven oxygen release in anoxic Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2012.09.015openalex-snapshot
Construction and characterization of nitrate and nitrite respiring Pseudomonas putida KT2440 strains for anoxic biotechnical applications
inferred← citeshttps://doi.org/10.1016/j.jcf.2013.12.001openalex-snapshot
Elevated metal concentrations in the CF airway correlate with cellular injury and disease severity
inferred← citeshttps://doi.org/10.1016/j.jddst.2023.104541openalex-snapshot
Investigation through the antimicrobial activity of electrospun PCL nanofiber mats with green synthesized Ag–Fe nanoparticles
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.jtbi.2014.08.043openalex-snapshot
Modelling and analysis of a gene-regulatory feed-forward loop with basal expression of the second regulator
inferred← citeshttps://doi.org/10.1016/j.micpath.2019.103702openalex-snapshot
Identification of genomic loci associated with genotypic and phenotypic variation among Pseudomonas aeruginosa clinical isolates from pneumonia
inferred← citeshttps://doi.org/10.1016/j.micres.2022.127140openalex-snapshot
Achromobacter spp. prevalence and adaptation in cystic fibrosis lung infection
inferred← citeshttps://doi.org/10.1016/j.microb.2026.100767openalex-snapshot
Global transcriptomic profiling of Pseudomonas aeruginosa PAO1 biofilm grown in flow cell system
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2021.151855openalex-snapshot
Antibacterial peptide RP557 increases the antibiotic sensitivity of Mycobacterium abscessus by inhibiting biofilm formation
inferred← citeshttps://doi.org/10.1016/j.soilbio.2024.109401openalex-snapshot
Virus decay and community composition in virus-amended sterile soil under slurry and unsaturated conditions
inferred← citeshttps://doi.org/10.1016/j.temicr.2025.100010openalex-snapshot
Pangenome analysis of Aquipseudomonas alcaligenes 67P: insights into ecological distribution, environmental adaptation, and metabolic versatility
inferred← citeshttps://doi.org/10.1016/j.tim.2019.05.003openalex-snapshot
Antimicrobial Tolerance and Metabolic Adaptations in Microbial Biofilms
inferred← citeshttps://doi.org/10.1021/acs.jproteome.7b00561openalex-snapshot
Pseudomonas aeruginosa Proteome under Hypoxic Stress Conditions Mimicking the Cystic Fibrosis Lung
inferred← citeshttps://doi.org/10.1021/acs.molpharmaceut.8b00011openalex-snapshot
PEGylation of Tobramycin Improves Mucus Penetration and Antimicrobial Activity against Pseudomonas aeruginosa Biofilms in Vitro
inferred← citeshttps://doi.org/10.1021/acsinfecdis.9b00016openalex-snapshot
Antibiofilm Efficacy of Nitric Oxide-Releasing Alginates against Cystic Fibrosis Bacterial Pathogens
inferred← citeshttps://doi.org/10.1021/acsomega.4c02343openalex-snapshot
Nanoparticle-Based Strategies for Managing Biofilm Infections in Wounds: A Comprehensive Review
inferred← citeshttps://doi.org/10.1021/acssynbio.7b00428openalex-snapshot
Modulation of Intracellular O2 Concentration in Escherichia coli Strains Using Oxygen Consuming Devices
inferred← citeshttps://doi.org/10.1021/jacs.4c14786openalex-snapshot
Nitric Oxide Inhibition of Glycyl Radical Enzymes and Their Activases
inferred← citeshttps://doi.org/10.1021/jp204644hopenalex-snapshot
Coupling of Protonation, Reduction, and Conformational Change in azurin from Pseudomonas aeruginosa Investigated with Free Energy Measures of Cooperativity
inferred← citeshttps://doi.org/10.1021/pr500491ropenalex-snapshot
Coping with Anoxia: A Comprehensive Proteomic and Transcriptomic Survey of Denitrification
inferred← citeshttps://doi.org/10.1038/ismej.2014.124openalex-snapshot
Predominant pathogen competition and core microbiota divergence in chronic airway infection
inferred← citeshttps://doi.org/10.1038/ismej.2014.234openalex-snapshot
A Winogradsky-based culture system shows an association between microbial fermentation and cystic fibrosis exacerbation
inferred← citeshttps://doi.org/10.1038/s41598-017-14051-2openalex-snapshot
A single point mutation in class III ribonucleotide reductase promoter renders Pseudomonas aeruginosa PAO1 inefficient for anaerobic growth and infection
inferred← citeshttps://doi.org/10.1038/s41598-018-35087-yopenalex-snapshot
Pseudomonas aeruginosa mutants defective in glucose uptake have pleiotropic phenotype and altered virulence in non-mammal infection models
inferred← citeshttps://doi.org/10.1038/s41598-019-42952-xopenalex-snapshot
Anaerobiosis influences virulence properties of Pseudomonas aeruginosa cystic fibrosis isolates and the interaction with Staphylococcus aureus
inferred← citeshttps://doi.org/10.1042/etls20220092openalex-snapshot
Bacterial acetate metabolism and its influence on human epithelia.
inferred← citeshttps://doi.org/10.1073/pnas.1307862110openalex-snapshot
Evolutionary genomics of epidemic and nonepidemic strains of Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1074/mcp.m114.043463openalex-snapshot
A Metaproteomics Approach to Elucidate Host and Pathogen Protein Expression during Catheter-Associated Urinary Tract Infections (CAUTIs)
inferred← citeshttps://doi.org/10.1080/1040841x.2018.1549019openalex-snapshot
Anaerobes in cystic fibrosis patients’ airways
inferred← citeshttps://doi.org/10.1080/14787210.2022.1990755openalex-snapshot
Phage therapy in pediatrics: the way forward for difficult-to-treat infections?
inferred← citeshttps://doi.org/10.1089/phage.2020.0041openalex-snapshot
The Effect of Oxygen Availability on Bacteriophage Infection: A Review
inferred← citeshttps://doi.org/10.1093/femsec/fiv006openalex-snapshot
Anaerobic naphthalene degradation by sulfate-reducing Desulfobacteraceae from various anoxic aquifers
inferred← citeshttps://doi.org/10.1093/femsle/fnad076openalex-snapshot
Pseudomonas aeruginosa is oxygen-deprived during infection in cystic fibrosis lungs, reducing the effectiveness of antibiotics
inferred← citeshttps://doi.org/10.1093/femspd/fty043openalex-snapshot
Hypoxia arising from concerted oxygen consumption by neutrophils and microorganisms in biofilms
inferred← citeshttps://doi.org/10.1093/femsre/fuac048openalex-snapshot
Origins of symbiosis: shared mechanisms underlying microbial pathogenesis, commensalism and mutualism of plants and animals
inferred← citeshttps://doi.org/10.1093/femsre/fux020openalex-snapshot
Structure, function and regulation of Pseudomonas aeruginosa porins
inferred← citeshttps://doi.org/10.1093/gbe/evx061openalex-snapshot
A Pan-Genomic Approach to Understand the Basis of Host Adaptation in Achromobacter
inferred← citeshttps://doi.org/10.1093/infdis/jix139openalex-snapshot
Hypoxia Reduces the Pathogenicity of Pseudomonas aeruginosa by Decreasing the Expression of Multiple Virulence Factors
inferred← citeshttps://doi.org/10.1093/molbev/msaa226openalex-snapshot
Evolutionary Genomics of Niche-Specific Adaptation to the Cystic Fibrosis Lung in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1096/fj.201902861ropenalex-snapshot
Gradual adaptation of facultative anaerobic pathogens to microaerobic and anaerobic conditions
inferred← citeshttps://doi.org/10.1097/md.0000000000031291openalex-snapshot
Homeostatic microbiome disruption as a cause of insulin secretion disorders. Candida albicans, a new factor in pathogenesis of diabetes: A STROBE compliant cross-sectional study
inferred← citeshttps://doi.org/10.1099/jmm.0.001116openalex-snapshot
The third quorum-sensing system of Pseudomonas aeruginosa: Pseudomonas quinolone signal and the enigmatic PqsE protein
inferred← citeshttps://doi.org/10.1099/mic.0.000093openalex-snapshot
Diversity of metabolic profiles of cystic fibrosis Pseudomonas aeruginosa during the early stages of lung infection
inferred← citeshttps://doi.org/10.1099/mic.0.001678openalex-snapshot
Pseudomonas aeruginosa gene expression changes during established biofilm infection in a cystic fibrosis lung model
inferred← citeshttps://doi.org/10.1099/mic.0.053850-0openalex-snapshot
Transcriptional regulation of nitrate assimilation in Pseudomonas aeruginosa occurs via transcriptional antitermination within the nirBD–PA1779–cobA operon
inferred← citeshttps://doi.org/10.1099/mic.0.056127-0openalex-snapshot
A novel host-responsive sensor mediates virulence and type III secretion during Pseudomonas aeruginosa–host cell interactions
inferred← citeshttps://doi.org/10.1101/2022.06.30.498312openalex-snapshot
How long does it take to cue a Pseudomonas aeruginosa chronic infection phenotype in the lab? Insights from transcriptome analysis in a cystic fibrosis lung model
inferred← citeshttps://doi.org/10.1101/2024.04.17.589660openalex-snapshot
BatR: A novel regulator of antibiotic tolerance in Pseudomonas aeruginosa biofilms
inferred← citeshttps://doi.org/10.1101/2024.07.12.603315openalex-snapshot
An energy coupling factor transporter of Streptococcus sanguinis impacts antibiotic susceptibility as well as metal and membrane homeostasis
inferred← citeshttps://doi.org/10.1107/s2059798320003101openalex-snapshot
The crystal structure of the heme d 1 biosynthesis-associated small c -type cytochrome NirC reveals mixed oligomeric states in crystallo
inferred← citeshttps://doi.org/10.1111/1751-7915.12851openalex-snapshot
Protein complex formation during denitrification by Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1111/2049-632x.12180openalex-snapshot
Mimicking the host and its microenvironmentin vitrofor studying mucosal infections byPseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1111/2049-632x.12188openalex-snapshot
Catheter-related infections caused byPseudomonas aeruginosa: virulence factors involved and their relationships
inferred← citeshttps://doi.org/10.1111/apm.12668openalex-snapshot
Microenvironmental characteristics and physiology of biofilms in chronic infections of CF patients are strongly affected by the host immune response
inferred← citeshttps://doi.org/10.1111/j.1462-2920.2012.02840.xopenalex-snapshot
Metabolic adaptations of Pseudomonas aeruginosa during cystic fibrosis chronic lung infections
inferred← citeshttps://doi.org/10.1111/mmi.12018openalex-snapshot
Microcolony formation by the opportunistic pathogen P seudomonas aeruginosa requires pyruvate and pyruvate fermentation
inferred← citeshttps://doi.org/10.1126/sciadv.aau1908openalex-snapshot
Niche partitioning of a pathogenic microbiome driven by chemical gradients
inferred← citeshttps://doi.org/10.1128/aac.01081-23openalex-snapshot
Identifying and mathematically modeling the time-course of extracellular metabolic markers associated with resistance to ceftolozane/tazobactam in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1128/aac.02556-14openalex-snapshot
The Pseudomonas aeruginosa CreBC Two-Component System Plays a Major Role in the Response to β-Lactams, Fitness, Biofilm Growth, and Global Regulation
inferred← citeshttps://doi.org/10.1128/aem.00439-22openalex-snapshot
Visualization of mRNA Expression in Pseudomonas aeruginosa Aggregates Reveals Spatial Patterns of Fermentative and Denitrifying Metabolism
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.06161-11openalex-snapshot
Vitamin B 12 -Mediated Restoration of Defective Anaerobic Growth Leads to Reduced Biofilm Formation in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1128/jb.00022-12openalex-snapshot
Heterogeneity in Pseudomonas aeruginosa Biofilms Includes Expression of Ribosome Hibernation Factors in the Antibiotic-Tolerant Subpopulation and Hypoxia-Induced Stress Response in the Metabolically Active Population
inferred← citeshttps://doi.org/10.1128/jb.00182-15openalex-snapshot
Links between Anr and Quorum Sensing in Pseudomonas aeruginosa Biofilms
inferred← citeshttps://doi.org/10.1128/jb.00307-19openalex-snapshot
Conceptual Model of Biofilm Antibiotic Tolerance That Integrates Phenomena of Diffusion, Metabolism, Gene Expression, and Physiology
inferred← citeshttps://doi.org/10.1128/jb.00385-25openalex-snapshot
The interplay between temperature and growth phase shapes the transcriptional landscape of Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1128/jb.00587-21openalex-snapshot
Biofilm Maintenance as an Active Process: Evidence that Biofilms Work Hard to Stay Put
inferred← citeshttps://doi.org/10.1128/jb.02176-14openalex-snapshot
Enzymatic Characterization and In Vivo Function of Five Terminal Oxidases in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1128/mbio.00269-18openalex-snapshot
Convergent Metabolic Specialization through Distinct Evolutionary Paths in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1128/mbio.00956-13openalex-snapshot
Biogeochemical Forces Shape the Composition and Physiology of Polymicrobial Communities in the Cystic Fibrosis Lung
inferred← citeshttps://doi.org/10.1128/mbio.00992-14openalex-snapshot
Oxygen Limitation within a Bacterial Aggregate
inferred← citeshttps://doi.org/10.1128/mbio.01319-19openalex-snapshot
Ubiquinone Biosynthesis over the Entire O 2 Range: Characterization of a Conserved O 2 -Independent Pathway
inferred← citeshttps://doi.org/10.1128/mbio.02624-22openalex-snapshot
Metabolic Mechanism and Physiological Role of Glycerol 3-Phosphate in Pseudomonas aeruginosa PAO1
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.01533-22openalex-snapshot
An Important Role of the Type VI Secretion System of Pseudomonas aeruginosa Regulated by Dnr in Response to Anaerobic Environments
inferred← citeshttps://doi.org/10.1128/spectrum.02731-23openalex-snapshot
Acidic pH modulates Burkholderia cenocepacia antimicrobial susceptibility in the cystic fibrosis nutritional environment
inferred← citeshttps://doi.org/10.1155/2014/678301openalex-snapshot
Emergent Bacteria in Cystic Fibrosis:In VitroBiofilm Formation and Resilience under Variable Oxygen Conditions
inferred← citeshttps://doi.org/10.1155/2020/6915483openalex-snapshot
Transcriptomic Response inPseudomonas aeruginosatowards Treatment with a Kaempferol Isolated fromMelastoma malabathricumLinn Leaves
inferred← citeshttps://doi.org/10.11606/d.9.2021.tde-23022022-144741openalex-snapshot
Incerteza de medição associada à contagem microbiana de produtos farmacêuticos
inferred← citeshttps://doi.org/10.1172/jci167957openalex-snapshot
Pharmacologic improvement of CFTR function rapidly decreases sputum pathogen density, but lung infections generally persist
inferred← citeshttps://doi.org/10.1177/1479972317694621openalex-snapshot
Bacterial infections in patients with primary ciliary dyskinesia: Comparison with cystic fibrosis
inferred← citeshttps://doi.org/10.1186/1471-2180-12-181openalex-snapshot
Characterization of biofilm-like structures formed by Pseudomonas aeruginosa in a synthetic mucus medium
inferred← citeshttps://doi.org/10.1186/1741-7007-10-28openalex-snapshot
Real-time determination of intracellular oxygen in bacteria using a genetically encoded FRET-based biosensor
inferred← citeshttps://doi.org/10.1186/s12934-018-0888-9openalex-snapshot
Oxygen effects on rhamnolipids production by Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1186/s12934-021-01593-4openalex-snapshot
Anaerobic biosynthesis of rhamnolipids by Pseudomonas aeruginosa: performance, mechanism and its application potential for enhanced oil recovery
inferred← citeshttps://doi.org/10.1186/s12934-021-01676-2openalex-snapshot
Glycerol or crude glycerol as substrates make Pseudomonas aeruginosa achieve anaerobic production of rhamnolipids
inferred← citeshttps://doi.org/10.1186/s13104-016-1840-xopenalex-snapshot
Molybdate transporter ModABC is important for Pseudomonas aeruginosa chronic lung infection
inferred← citeshttps://doi.org/10.1371/annotation/a1b0d6de-c6b4-4a5f-97ac-d500fbde806fopenalex-snapshot
Correction: A Quorum Sensing Regulated Small Volatile Molecule Reduces Acute Virulence and Promotes Chronic Infection Phenotypes
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1005544openalex-snapshot
BacArena: Individual-based metabolic modeling of heterogeneous microbes in complex communities
inferred← citeshttps://doi.org/10.1371/journal.pone.0024965openalex-snapshot
Universal Stress Proteins Are Important for Oxidative and Acid Stress Resistance and Growth of Listeria monocytogenes EGD-e In Vitro and In Vivo
inferred← citeshttps://doi.org/10.1371/journal.pone.0068484openalex-snapshot
Complete Genome Sequence of the Cystic Fibrosis Pathogen Achromobacter xylosoxidans NH44784-1996 Complies with Important Pathogenic Phenotypes
inferred← citeshttps://doi.org/10.1371/journal.pone.0072939openalex-snapshot
Response of Burkholderia cenocepacia H111 to Micro-Oxia
inferred← citeshttps://doi.org/10.1371/journal.pone.0091813openalex-snapshot
Catalase (KatA) Plays a Role in Protection against Anaerobic Nitric Oxide in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1371/journal.pone.0118319openalex-snapshot
Pyocycanin, a Contributory Factor in Haem Acquisition and Virulence Enhancement of Porphyromonas gingivalis in the Lung
inferred← citeshttps://doi.org/10.1371/journal.ppat.1002192openalex-snapshot
A Quorum Sensing Regulated Small Volatile Molecule Reduces Acute Virulence and Promotes Chronic Infection Phenotypes
inferred← citeshttps://doi.org/10.1371/journal.ppat.1004083openalex-snapshot
Cationic Antimicrobial Peptides Promote Microbial Mutagenesis and Pathoadaptation in Chronic Infections
inferred← citeshttps://doi.org/10.1371/journal.ppat.1005258openalex-snapshot
Cystic Fibrosis Lung Infections: Polymicrobial, Complex, and Hard to Treat
inferred← citeshttps://doi.org/10.1371/journal.ppat.1009681openalex-snapshot
Genome-wide association study of signature genetic alterations among pseudomonas aeruginosa cystic fibrosis isolates
inferred← citeshttps://doi.org/10.1517/14728222.2012.708025openalex-snapshot
AnaerobicPseudomonas aeruginosaand other obligately anaerobic bacterial biofilms growing in the thick airway mucus of chronically infected cystic fibrosis patients: an emerging paradigm or “Old Hat”?
inferred← citeshttps://doi.org/10.1586/17476348.2013.814411openalex-snapshot
The future of antimicrobial therapy in the era of antibiotic resistance in cystic fibrosis pulmonary infection
inferred← citeshttps://doi.org/10.21276/ap.2019.8.2.4openalex-snapshot
An overview on biosynthesis and applications of extracellular pyocyanin pigment and its role in Pseudomonas aeruginosa pathogenesis
inferred← citeshttps://doi.org/10.2139/ssrn.6544418openalex-snapshot
Global transcriptomic profiling of Pseudomonas aeruginosa PAO1 biofilm grown in flow cell system
inferred← citeshttps://doi.org/10.21608/ajnsa.2023.184230.1705openalex-snapshot
Study on the Production of Vitamin B12 by Newly Isolated and Identified Pseudomonas aeruginosa and Effect of Gamma Irradiation on Fermentation Substrate.
inferred← citeshttps://doi.org/10.24996/ijs.2022.63.11.9openalex-snapshot
Influence of Distance and Argon Flow rate on Pseudomonas aeruginosa Bacteria Exposed to Non thermal Plasma at Atmospheric Pressure
inferred← citeshttps://doi.org/10.25335/m5cx0sopenalex-snapshot
PSEUDOMONAS AERUGINOSA METABOLISM IN THE CYSTIC FIBROSIS LUNG
inferred← citeshttps://doi.org/10.26686/wgtn.17060858openalex-snapshot
The Role of Outer-Membrane Vesicles in Intercellular Communication in Pseudomonas Aeruginosa
inferred← citeshttps://doi.org/10.26717/bjstr.2020.30.004951openalex-snapshot
What is the Advantage for Bacteria to Use Polycyclic Aromatic Hydrocarbons as Carbon Source under Aerobic Condition?
inferred← citeshttps://doi.org/10.3389/fcimb.2022.969326openalex-snapshot
Biofilm aggregates and the host airway-microbial interface
inferred← citeshttps://doi.org/10.3389/fcimb.2023.1092317openalex-snapshot
Metabolic pathways that permit Mycobacterium avium subsp. hominissuis to transition to different environments encountered within the host during infection
inferred← citeshttps://doi.org/10.3389/fgene.2022.883199openalex-snapshot
Unveiling Co-Infection in Cystic Fibrosis Airways: Transcriptomic Analysis of Pseudomonas aeruginosa and Staphylococcus aureus Dual-Species Biofilms
inferred← citeshttps://doi.org/10.3389/fimmu.2026.1979311openalex-snapshot
Lactate dynamics at the Pseudomonas aeruginosa–host interface: bacterial metabolism, host defense, and emerging links to histone lactylation
inferred← citeshttps://doi.org/10.3389/fmicb.2011.00103openalex-snapshot
Regulation and Function of Versatile Aerobic and Anaerobic Respiratory Metabolism in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.3389/fmicb.2014.00554openalex-snapshot
Physiological levels of nitrate support anoxic growth by denitrification of Pseudomonas aeruginosa at growth rates reported in cystic fibrosis lungs and sputum
inferred← citeshttps://doi.org/10.3389/fmicb.2016.00688openalex-snapshot
Pseudomonas aeruginosa Exhibits Deficient Biofilm Formation in the Absence of Class II and III Ribonucleotide Reductases Due to Hindered Anaerobic Growth
inferred← citeshttps://doi.org/10.3389/fmicb.2016.02146openalex-snapshot
Insights into Cystic Fibrosis Polymicrobial Consortia: The Role of Species Interactions in Biofilm Development, Phenotype, and Response to In-Use Antibiotics
inferred← citeshttps://doi.org/10.3389/fmicb.2017.01353openalex-snapshot
Nitrate Sensing and Metabolism Inhibit Biofilm Formation in the Opportunistic Pathogen Burkholderia pseudomallei by Reducing the Intracellular Concentration of c-di-GMP
inferred← citeshttps://doi.org/10.3389/fmicb.2018.00986openalex-snapshot
Aerobic Vitamin B12 Biosynthesis Is Essential for Pseudomonas aeruginosa Class II Ribonucleotide Reductase Activity During Planktonic and Biofilm Growth
inferred← citeshttps://doi.org/10.3389/fmicb.2018.01277openalex-snapshot
Transcriptome Analysis of the Global Response of Pseudomonas fragi NMC25 to Modified Atmosphere Packaging Stress
inferred← citeshttps://doi.org/10.3389/fmicb.2018.03018openalex-snapshot
Contribution of the Alkylquinolone Quorum-Sensing System to the Interaction of Pseudomonas aeruginosa With Bronchial Epithelial Cells
inferred← citeshttps://doi.org/10.3389/fmicb.2021.691608openalex-snapshot
The Small RNA ErsA Impacts the Anaerobic Metabolism of Pseudomonas aeruginosa Through Post-Transcriptional Modulation of the Master Regulator Anr
inferred← citeshttps://doi.org/10.3389/fmicb.2022.903146openalex-snapshot
The Impact of Chromate on Pseudomonas aeruginosa Molybdenum Homeostasis
inferred← citeshttps://doi.org/10.3390/antibiotics10111393openalex-snapshot
Sub-Inhibitory Antibiotic Exposure and Virulence in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.3390/ijms221910878openalex-snapshot
Parasite Survival and Disease Persistence in Cystic Fibrosis, Schistosomiasis and Pathogenic Bacterial Diseases: A Role for Universal Stress Proteins?
inferred← citeshttps://doi.org/10.3390/life12121953openalex-snapshot
Temporal Hierarchy and Context-Dependence of Quorum Sensing Signal in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.3390/microorganisms8050698openalex-snapshot
Exposure of Mycobacterium abscessus to Environmental Stress and Clinically Used Antibiotics Reveals Common Proteome Response among Pathogenic Mycobacteria
inferred← citeshttps://doi.org/10.3390/pathogens3030680openalex-snapshot
Pseudomonas aeruginosa Diversification during Infection Development in Cystic Fibrosis Lungs—A Review
inferred← citeshttps://doi.org/10.3923/crc.2020.1.10openalex-snapshot
Novel Metal2+ complexes of N-(1,4-dihydro-1,4- oxonaphthalen-3-yl) pyrazine-2-carboxamide: Synthesis, structural characterization, magnetic properties and antimicrobial activities
inferred← citeshttps://doi.org/10.4315/0362-028x.jfp-19-188openalex-snapshot
Comparison of Extracellular Proteins from Virulent and Avirulent Vibrio parahaemolyticus Strains to Identify Potential Virulence Factors
inferred← citeshttps://doi.org/10.5114/ada.2020.100747openalex-snapshot
Ecthyma gangrenosum as a serious complication of Pseudomonas aeruginosa infection in departments of pediatric oncology
inferred← citeshttps://doi.org/10.5530/jam.4.1.1openalex-snapshot
Challenges and Opportunities with Pyocyanin Pigment of Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.5851/kosfa.2019.e16openalex-snapshot
Dynamics of Bacterial Communities of Lamb Meat Packaged in Air and Vacuum Pouch during Chilled Storage
inferred← citeshttps://doi.org/10.70675/6d02bc34z7b72z46c3zbdb7zde2cfad6ddb6openalex-snapshot
Achromobacter & Pandoraea : diversité et évolution adaptative de populations persistantes au cours de la mucoviscidose et dans l'environnement
inferred← citeshttps://doi.org/10.7287/peerj.1495v0.1/reviews/1openalex-snapshot
Peer Review #1 of "The role of 2,4-dihydroxyquinoline (DHQ) in Pseudomonas aeruginosa pathogenicity (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.1495v0.1/reviews/2openalex-snapshot
Peer Review #2 of "The role of 2,4-dihydroxyquinoline (DHQ) in Pseudomonas aeruginosa pathogenicity (v0.1)"
inferred← citeshttps://doi.org/10.7717/peerj.1495openalex-snapshot
The role of 2,4-dihydroxyquinoline (DHQ) in Pseudomonas aeruginosa pathogenicity
inferred← citeshttps://doi.org/10.7912/c2/2178openalex-snapshot
Role of a putative bacterial lipoprotein in Pseudomonas aeruginosa-mediated cytotoxicity toward airway cells
inferred← citeshttps://doi.org/10.7939/r3rr1ps1qopenalex-snapshot
Coupled effects on the transport and deposition of biocolloidal particles in saturated porous media
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