scholarly article | Q13442814 |
P2093 | author name string | Comeau Y | |
Villemur R | |||
Déziel E | |||
P2860 | cites work | Microbial biofilms | Q22255624 |
Swarming of Pseudomonas aeruginosa is dependent on cell-to-cell signaling and requires flagella and pili | Q24548960 | ||
Inorganic polyphosphate is needed for swimming, swarming, and twitching motilities of Pseudomonas aeruginosa | Q24676026 | ||
The chemotaxis system, but not chemotaxis, is essential for swarming motility in Escherichia coli | Q24681611 | ||
Flagellar and twitching motility are necessary for Pseudomonas aeruginosa biofilm development | Q27976516 | ||
Two simple media for the demonstration of pyocyanin and fluorescin | Q28210604 | ||
Genetic identification of chemotactic transducers for amino acids in Pseudomonas aeruginosa | Q28492799 | ||
Isolation and characterization of chemotaxis mutants and genes of Pseudomonas aeruginosa | Q28492848 | ||
Characterization of a gene, pilU, required for twitching motility but not phage sensitivity in Pseudomonas aeruginosa | Q28493138 | ||
Roles of Pseudomonas aeruginosa las and rhl quorum-sensing systems in control of elastase and rhamnolipid biosynthesis genes | Q28493170 | ||
Effect of rpoS mutation on the stress response and expression of virulence factors in Pseudomonas aeruginosa | Q28493200 | ||
Genes involved in the biogenesis and function of type-4 fimbriae in Pseudomonas aeruginosa | Q28493284 | ||
Biosurfactant production by a soil pseudomonas strain growing on polycyclic aromatic hydrocarbons | Q28768347 | ||
Microbial pathogenesis in cystic fibrosis: mucoid Pseudomonas aeruginosa and Burkholderia cepacia | Q29615286 | ||
Initiation of biofilm formation in Pseudomonas fluorescens WCS365 proceeds via multiple, convergent signalling pathways: a genetic analysis | Q29616613 | ||
Type IV pili and cell motility | Q33601596 | ||
Abiotic surface sensing and biofilm-dependent regulation of gene expression in Escherichia coli. | Q33635823 | ||
Negative control of flagellum synthesis in Pseudomonas aeruginosa is modulated by the alternative sigma factor AlgT (AlgU). | Q33636917 | ||
Biofilms | Q33670989 | ||
Molecular switches--the ON and OFF of bacterial phase variation. | Q33727880 | ||
Swarming motility. | Q33801645 | ||
Biofilm, city of microbes | Q33899018 | ||
Selective Outgrowth of Fimbriate Bacteria in Static Liquid Medium | Q34222744 | ||
Pseudomonas aeruginosa sodA and sodB mutants defective in manganese- and iron-cofactored superoxide dismutase activity demonstrate the importance of the iron-cofactored form in aerobic metabolism | Q35598025 | ||
Exopolysaccharide production in biofilms: substratum activation of alginate gene expression by Pseudomonas aeruginosa | Q36064885 | ||
Studies on gonococcus infection. I. Pili and zones of adhesion: their relation to gonococcal growth patterns | Q36271009 | ||
Regulation of Pseudomonas aeruginosa chemotaxis by the nitrogen source | Q36278718 | ||
Cell-to-cell signaling and Pseudomonas aeruginosa infections | Q37092561 | ||
Antigen 43 and type 1 fimbriae determine colony morphology of Escherichia coli K-12. | Q39499098 | ||
Comparisons between colony phase variation of Neisseria gonorrhoeae FA1090 and pilus, pilin, and S-pilin expression. | Q39570993 | ||
Characterization of Shigella type 1 fimbriae: expression, FimA sequence, and phase variation. | Q39830217 | ||
The pilG gene product, required for Pseudomonas aeruginosa pilus production and twitching motility, is homologous to the enteric, single-domain response regulator CheY. | Q39936971 | ||
Flagella and motility alterations in Pseudomonas aeruginosa strains from patients with cystic fibrosis: relationship to patient clinical condition | Q40170508 | ||
The role of the sigma factor sigma S (KatF) in bacterial global regulation | Q40572983 | ||
The type-4 pilus is the major virulence-associated adhesin of Pseudomonas aeruginosa--a review | Q41532678 | ||
Molecular genetic analysis of type-4 pilus biogenesis and twitching motility using Pseudomonas aeruginosa as a model system--a review | Q41532683 | ||
Phenotypic Switching Affecting Chemotaxis, Xanthan Production, and Virulence in Xanthomonas campestris. | Q41930230 | ||
Characterisation of a Pseudomonas aeruginosa twitching motility gene and evidence for a specialised protein export system widespread in eubacteria | Q42614584 | ||
Genetic and functional evidence that Type IV pili are required for social gliding motility in Myxococcus xanthus | Q42635820 | ||
Spontaneous duplication of a 661 bp element within a two-component sensor regulator gene causes phenotypic switching in colonies of Pseudomonas tolaasii, cause of brown blotch disease of mushrooms | Q42663004 | ||
The adsorption of Pseudomonas aeruginosa pilus-dependent bacteriophages to a host mutant with nonretractile pili | Q44138973 | ||
Determining chemotactic responses by two subsurface microaerophiles using a simplified capillary assay method | Q44863906 | ||
Characterization of a Pseudomonas aeruginosa gene cluster involved in pilus biosynthesis and twitching motility: sequence similarity to the chemotaxis proteins of enterics and the gliding bacterium Myxococcus xanthus | Q48086659 | ||
A re-examination of twitching motility in Pseudomonas aeruginosa | Q57020102 | ||
Environmental gasoline-utilizing isolates and clinical isolates of Pseudomonas aeruginosa are taxonomically indistinguishable by chemotaxonomic and molecular techniques | Q61827536 | ||
The role of motility and aerotaxis in the selective increase of avirulent bacteria in still broth cultures of Pseudomonas solanacearum | Q69558836 | ||
A new modification of the carbazole analysis: Application to heteropolysaccharides | Q72223066 | ||
DNA rearrangements and phenotypic switching in prokaryotes | Q72825743 | ||
Mass spectrometry monitoring of rhamnolipids from a growing culture of Pseudomonas aeruginosa strain 57RP | Q73835667 | ||
Genetic analysis of Escherichia coli biofilm formation: roles of flagella, motility, chemotaxis and type I pili | Q77472923 | ||
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Pseudomonas aeruginosa | Q31856 |
biofilm | Q467410 | ||
twitching | Q21117302 | ||
P304 | page(s) | 1195-1204 | |
P577 | publication date | 2001-02-01 | |
P1433 | published in | Journal of Bacteriology | Q478419 |
P1476 | title | 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 | |
P478 | volume | 183 |
Q35215240 | Adaptation by phase variation in pathogenic bacteria. |
Q34933370 | Adaptation genomics of a small-colony variant in a Pseudomonas chlororaphis 30-84 biofilm. |
Q35638257 | Altered Proteome of Burkholderia pseudomallei Colony Variants Induced by Exposure to Human Lung Epithelial Cells |
Q41312052 | An early mechanical coupling of planktonic bacteria in dilute suspensions |
Q37760252 | An update on Pseudomonas aeruginosa biofilm formation, tolerance, and dispersal |
Q33185288 | Anaerobic metabolism and quorum sensing by Pseudomonas aeruginosa biofilms in chronically infected cystic fibrosis airways: rethinking antibiotic treatment strategies and drug targets. |
Q57291289 | Antibiofilm activity substances derived from coral symbiotic bacterial extract inhibit biofouling by the model strain Pseudomonas aeruginosa PAO1 |
Q44678280 | Antibiotics at subinhibitory concentrations improve the quorum sensing behavior of Chromobacterium violaceum |
Q37700072 | Arginine Is a Critical Substrate for the Pathogenesis of Pseudomonas aeruginosa in Burn Wound Infections |
Q28492790 | Autolysis and autoaggregation in Pseudomonas aeruginosa colony morphology mutants |
Q28207244 | Bacterial Biofilms: An Emerging Link to Disease Pathogenesis |
Q44842599 | Bacterial biofilms of importance to medicine and bioterrorism: proteomic techniques to identify novel vaccine components and drug targets |
Q37623383 | Bacteriophage and phenotypic variation in Pseudomonas aeruginosa biofilm development. |
Q33509952 | Bacteriophage cocktail for the prevention of biofilm formation by Pseudomonas aeruginosa on catheters in an in vitro model system. |
Q35130159 | BdlA, a chemotaxis regulator essential for biofilm dispersion in Pseudomonas aeruginosa |
Q38310578 | Bile enhances cell surface hydrophobicity and biofilm formation of bifidobacteria |
Q39739614 | Biofilm formation by hyperpiliated mutants of Pseudomonas aeruginosa |
Q35772673 | Biofilm formation by the small colony variant phenotype of Pseudomonas aeruginosa |
Q92563791 | Biofilm-Constructing Variants of Paraburkholderia phytofirmans PsJN Outcompete the Wild-Type Form in Free-Living and Static Conditions but Not In Planta |
Q43116681 | Biofilms 2003: emerging themes and challenges in studies of surface-associated microbial life |
Q36727572 | Biofilms and their relevance to veterinary medicine |
Q24676000 | Biological relevance of colony morphology and phenotypic switching by Burkholderia pseudomallei |
Q35109339 | Changes in the proteome of the cadmium-tolerant bacteria Cupriavidus taiwanensis KKU2500-3 in response to cadmium toxicity |
Q98237958 | Characterization of a SPM-1 metallo-beta-lactamase-producing Pseudomonas aeruginosa by comparative genomics and phenotypic analysis |
Q42105451 | Characterization of colony morphology variants isolated from Pseudomonas aeruginosa biofilms |
Q35759418 | Characterization of colony morphology variants isolated from Streptococcus pneumoniae biofilms |
Q37583328 | Characterization of nutrient-induced dispersion in Pseudomonas aeruginosa PAO1 biofilm |
Q41822160 | Characterization of the integrated filamentous phage Pf5 and its involvement in small-colony formation |
Q36277198 | Chemotaxis of Marinobacter adhaerens and its impact on attachment to the diatom Thalassiosira weissflogii |
Q38609243 | Clinical characteristics associated with isolation of small-colony variants of Staphylococcus aureus and Pseudomonas aeruginosa from respiratory secretions of patients with cystic fibrosis |
Q34491552 | Clinical significance of microbial infection and adaptation in cystic fibrosis |
Q45973870 | Comparative physiological study of the wild type and the small colony variant of Pseudomonas aeruginosa 20265 under controlled growth conditions. |
Q43856828 | Contribution of quorum sensing to the virulence of Pseudomonas aeruginosa in pressure ulcer infection in rats. |
Q33196154 | Cross-sectional analysis of clinical and environmental isolates of Pseudomonas aeruginosa: biofilm formation, virulence, and genome diversity |
Q35198665 | Culturable bacterial diversity from a feed water of a reverse osmosis system, evaluation of biofilm formation and biocontrol using phages |
Q38734889 | Defining motility in the Staphylococci |
Q57896750 | Detergent-induced cell aggregation in subpopulations of Pseudomonas aeruginosa as a preadaptive survival strategy |
Q41273938 | Developing genome-reduced Pseudomonas chlororaphis strains for the production of secondary metabolites. |
Q49364960 | Diguanylate cyclase activity of the Mycobacterium leprae T cell antigen ML1419c |
Q42551289 | Ecological advantages of autolysis during the development and dispersal of Pseudoalteromonas tunicata biofilms |
Q46937586 | Effect of antibiotic-induced morphological changes on surface properties, motility and adhesion of nosocomial Pseudomonas aeruginosa strains under different physiological states |
Q46298751 | Effect of bacterial components of mixed culture supernatants of planktonic and biofilm Pseudomonas aeruginosa with commensal Escherichia coli on the neutrophil response in vitro. |
Q58555995 | Effect of inactivation of luxS gene on the properties of Serratia proteamaculans 94 strain |
Q46590167 | Effect of interspecific competition on trait variation in Phaeobacter inhibens biofilms |
Q46254016 | Effect of long-term starvation in salty microcosm on biofilm formation and motility in Pseudomonas aeruginosa. |
Q51357982 | Effect of mixed culture supernatants of Pseudomonas aeruginosa and Escherichia coli on apoptosis, necrosis, and oxidative activity of neutrophils. |
Q40210441 | Effects of an autoinducer analogue on antibiotic tolerance in Pseudomonas aeruginosa. |
Q39371275 | Effects of sodium chloride on heat resistance, oxidative susceptibility, motility, biofilm and plaque formation of Burkholderia pseudomallei. |
Q34032484 | Effects of the twin-arginine translocase on secretion of virulence factors, stress response, and pathogenesis |
Q91793517 | Efficacy of Artesunate against Pseudomonas aeruginosa Biofilm Mediated by Iron |
Q37743206 | Emergence of complex behavior in pili-based motility in early stages of P. aeruginosa surface adaptation |
Q36858633 | Endogenous oxidative stress produces diversity and adaptability in biofilm communities |
Q35486124 | Endophytic colonization and biocontrol performance of Pseudomonas fluorescens PICF7 in olive (Olea europaea L.) are determined neither by pyoverdine production nor swimming motility. |
Q33788110 | Enhanced Pseudomonas aeruginosa biofilm development mediated by human neutrophils |
Q39743204 | Enhanced toxic metal accumulation in engineered bacterial cells expressing Arabidopsis thaliana phytochelatin synthase |
Q43049918 | Environmental cues and genes involved in establishment of the superinfective Pf4 phage of Pseudomonas aeruginosa |
Q28492966 | Epigenetic control of virulence gene expression in Pseudomonas aeruginosa by a LysR-type transcription regulator |
Q64448206 | Ethanol decreases flagellar motility through the regulation of flagellar stators |
Q34082906 | Evolution and adaptation in Pseudomonas aeruginosa biofilms driven by mismatch repair system-deficient mutators. |
Q28359832 | Evolutionary diversification of Pseudomonas aeruginosa in an artificial sputum model |
Q61798003 | Evolutionary highways to persistent bacterial infection |
Q26768691 | Experimental evolution in biofilm populations. |
Q35798007 | Exploiting the fungal highway: development of a novel tool for the in situ isolation of bacteria migrating along fungal mycelium. |
Q34351123 | Expression analysis of a highly adherent and cytotoxic small colony variant of Pseudomonas aeruginosa isolated from a lung of a patient with cystic fibrosis |
Q33472685 | Expression of Pseudomonas aeruginosa CupD fimbrial genes is antagonistically controlled by RcsB and the EAL-containing PvrR response regulators |
Q64449435 | Factors associated with the adherence and biofilm formation by Aeromonas caviae on glass surfaces |
Q42735109 | Flagellated but not hyperfimbriated Salmonella enterica serovar Typhimurium attaches to and forms biofilms on cholesterol-coated surfaces |
Q36933242 | Formation of Streptococcus pneumoniae non-phase-variable colony variants is due to increased mutation frequency present under biofilm growth conditions |
Q58697525 | Formation of phenotypic lineages in Salmonella enterica by a pleiotropic fimbrial switch |
Q55385962 | Genetic Determinants Associated With in Vivo Survival of Burkholderia cenocepacia in the Caenorhabditis elegans Model. |
Q37342508 | Genetic Identification of a PilT Motor in Geobacter sulfurreducens Reveals a Role for Pilus Retraction in Extracellular Electron Transfer |
Q39714129 | Genetic analysis of the AdnA regulon in Pseudomonas fluorescens: nonessential role of flagella in adhesion to sand and biofilm formation |
Q59349072 | Genomic analysis and immune response in a murine mastitis model of vB_EcoM-UFV13, a potential biocontrol agent for use in dairy cows |
Q64108075 | Genomic and transcriptomic characterization of Pseudomonas aeruginosa small colony variants derived from a chronic infection model |
Q44573552 | Ginseng aqueous extract attenuates the production of virulence factors, stimulates twitching and adhesion, and eradicates biofilms of Pseudomonas aeruginosa |
Q43112697 | In vivo growth of Pseudomonas aeruginosa strains PAO1 and PA14 and the hypervirulent strain LESB58 in a rat model of chronic lung infection |
Q48040927 | Influence of periplasmic oxidation of glucose on pyoverdine synthesis in Pseudomonas putida S11. |
Q54495544 | Influence of siderophore pyoverdine synthesis and iron-uptake on abiotic and biotic surface colonization of Pseudomonas putida S11. |
Q38647093 | Inhibition of quorum sensing-controlled virulence factor production in Pseudomonas aeruginosa by Quercus infectoria gall extracts |
Q40419746 | Initial Phases of biofilm formation in Shewanella oneidensis MR-1. |
Q33389073 | Insight into the microbial multicellular lifestyle via flow-cell technology and confocal microscopy |
Q30734993 | Inter- and intraclonal diversity of the Pseudomonas aeruginosa proteome manifests within the secretome |
Q51511489 | Interactions of Pseudomonas aeruginosa in predominant biofilm or planktonic forms of existence in mixed culture with Escherichia coli in vitro. |
Q35759797 | Inverse regulation of biofilm formation and swarming motility by Pseudomonas aeruginosa PA14 |
Q33381392 | Involvement of a phospholipase C in the hemolytic activity of a clinical strain of Pseudomonas fluorescens |
Q47097030 | Isolation and characterization of HepP: a virulence-related Pseudomonas aeruginosa heparinase |
Q64956419 | Low concentrations of local honey modulate Exotoxin A expression, and quorum sensing related virulence in drug-resistant Pseudomonas aeruginosa recovered from infected burn wounds. |
Q73507950 | Membrane filter (pore size, 0.22-0.45 micro m; thickness, 150 micro m) passing-through activity of Pseudomonas aeruginosa and other bacterial species with indigenous infiltration ability |
Q43349782 | Membrane fouling potentials and cellular properties of bacteria isolated from fouled membranes in a MBR treating municipal wastewater |
Q28477164 | MexEF-OprN efflux pump exports the Pseudomonas quinolone signal (PQS) precursor HHQ (4-hydroxy-2-heptylquinoline) |
Q37623753 | Modulation of swarming and virulence by fatty acids through the RsbA protein in Proteus mirabilis. |
Q36488561 | Molecular basis of in vivo biofilm formation by bacterial pathogens |
Q58589549 | Molecular epidemiology, antimicrobial susceptibility, and pulsed-field gel electrophoresis genotyping of isolates from mink |
Q40282450 | Morphotypic conversion in Listeria monocytogenes biofilm formation: biological significance of rough colony isolates. |
Q42206889 | Mucin inhibits Pseudomonas aeruginosa biofilm formation by significantly enhancing twitching motility |
Q35797143 | Multicellular microorganisms: laboratory versus nature |
Q36112333 | Multidrug resistant Pseudomonas aeruginosa survey in a stream receiving effluents from ineffective wastewater hospital plants. |
Q28828961 | Pea Broth Enhances the Biocontrol Efficacy of Lysobacter capsici AZ78 by Triggering Cell Motility Associated with Biogenesis of Type IV Pilus |
Q24561666 | Phase and antigenic variation in bacteria |
Q39807599 | Phase variation has a role in Burkholderia ambifaria niche adaptation. |
Q38645992 | Phenotypic and genetic heterogeneity within biofilms with particular emphasis on persistence and antimicrobial tolerance. |
Q28478449 | Phenotypic and genome-wide analysis of an antibiotic-resistant small colony variant (SCV) of Pseudomonas aeruginosa |
Q33261957 | Phenotypic diversification and adaptation of Serratia marcescens MG1 biofilm-derived morphotypes |
Q39678493 | Phenotypic selection and phase variation occur during alfalfa root colonization by Pseudomonas fluorescens F113. |
Q33319084 | Physiological heterogeneity in biofilms |
Q45327952 | Plant exudates promote PCB degradation by a rhodococcal rhizobacteria. |
Q39762313 | Predation in homogeneous and heterogeneous phage environments affects virulence determinants of Pseudomonas aeruginosa |
Q92953784 | Proteomic Analysis of the Pseudomonas aeruginosa Iron Starvation Response Reveals PrrF Small Regulatory RNA-Dependent Iron Regulation of Twitching Motility, Amino Acid Metabolism, and Zinc Homeostasis Proteins |
Q29346788 | Pseudomonas aeruginosa AlgR regulates type IV pilus biosynthesis by activating transcription of the fimU-pilVWXY1Y2E operon |
Q37321989 | Pseudomonas aeruginosa Condensins Support Opposite Differentiation States |
Q38273318 | Pseudomonas aeruginosa Diversification during Infection Development in Cystic Fibrosis Lungs-A Review. |
Q38268531 | Pseudomonas aeruginosa biofilm infections: from molecular biofilm biology to new treatment possibilities. |
Q28493110 | Pseudomonas aeruginosa cupA-encoded fimbriae expression is regulated by a GGDEF and EAL domain-dependent modulation of the intracellular level of cyclic diguanylate |
Q34099061 | Pseudomonas aeruginosa fimL regulates multiple virulence functions by intersecting with Vfr-modulated pathways |
Q35852550 | Pseudomonas aeruginosa in Dairy Goats: Genotypic and Phenotypic Comparison of Intramammary and Environmental Isolates. |
Q51569454 | Pseudomonas aeruginosa population structure revisited under environmental focus: impact of water quality and phage pressure. |
Q37191781 | Pseudomonas aeruginosa rugose small-colony variants have adaptations that likely promote persistence in the cystic fibrosis lung |
Q37358382 | Pseudomonas aeruginosa virulence and therapy: evolving translational strategies |
Q24611111 | Pseudomonas aeruginosa-plant root interactions. Pathogenicity, biofilm formation, and root exudation |
Q53025843 | Pseudomonas community structure and antagonistic potential in the rhizosphere: insights gained by combining phylogenetic and functional gene-based analyses. |
Q46348666 | Pseudomonas putida 06909 genes expressed during colonization on mycelial surfaces and phenotypic characterization of mutants |
Q91996687 | Quercus infectoria gall extracts reduce quorum sensing-controlled virulence factors production and biofilm formation in Pseudomonas aeruginosa recovered from burn wounds |
Q53606301 | Quorum sensing and phenazines are involved in biofilm formation by Pseudomonas chlororaphis (aureofaciens) strain 30-84. |
Q34314375 | Quorum sensing is not required for twitching motility in Pseudomonas aeruginosa |
Q31077054 | Reactive oxygen species in the signaling and adaptation of multicellular microbial communities |
Q33911477 | Repression of phase-variable cup gene expression by H-NS-like proteins in Pseudomonas aeruginosa |
Q39701994 | Response to Gaseous NO2 Air Pollutant of P. fluorescens Airborne Strain MFAF76a and Clinical Strain MFN1032. |
Q24536028 | Rhamnolipids modulate swarming motility patterns of Pseudomonas aeruginosa |
Q37718628 | Rhamnolipids: diversity of structures, microbial origins and roles. |
Q36727650 | Role of Multicellular Aggregates in Biofilm Formation |
Q28544815 | Second-hand cigarette smoke impairs bacterial phagocytosis in macrophages by modulating CFTR dependent lipid-rafts |
Q37621081 | Self-generated diversity produces "insurance effects" in biofilm communities |
Q34679421 | Self-produced extracellular stimuli modulate the Pseudomonas aeruginosa swarming motility behaviour. |
Q42554707 | Sensor kinase PA4398 modulates swarming motility and biofilm formation in Pseudomonas aeruginosa PA14. |
Q38358624 | Small colony variants of Pseudomonas aeruginosa in chronic bacterial infection of the lung in cystic fibrosis |
Q44549591 | Specific maltose derivatives modulate the swarming motility of nonswarming mutant and inhibit bacterial adhesion and biofilm formation by Pseudomonas aeruginosa |
Q92505582 | SprI/SprR Quorum Sensing System of Serratia proteamaculans 94 |
Q35544150 | Stationary phase mutagenesis: mechanisms that accelerate adaptation of microbial populations under environmental stress |
Q30828372 | Statistical analysis of Pseudomonas aeruginosa biofilm development: impact of mutations in genes involved in twitching motility, cell-to-cell signaling, and stationary-phase sigma factor expression. |
Q33480816 | Swarming of Pseudomonas aeruginosa is controlled by a broad spectrum of transcriptional regulators, including MetR. |
Q43794686 | Swimming, swarming, twitching, and chemotactic responses of Cupriavidus metallidurans CH34 and Pseudomonas putida mt2 in the presence of cadmium |
Q33455287 | Tangled bank of experimentally evolved Burkholderia biofilms reflects selection during chronic infections |
Q45791598 | Tannin derived materials can block swarming motility and enhance biofilm formation in Pseudomonas aeruginosa |
Q45988653 | Tetracycline and chloramphenicol efficiency against selected biofilm forming bacteria. |
Q93001868 | The N-flagella problem: elastohydrodynamic motility transition of multi-flagellated bacteria |
Q46921729 | The Pseudomonas viridiflava phylogroups in the P. syringae species complex are characterized by genetic variability and phenotypic plasticity of pathogenicity-related traits |
Q50243678 | The activity of ferulic and gallic acids in biofilm prevention and control of pathogenic bacteria |
Q36602687 | The broad host range pathogen Pseudomonas aeruginosa strain PA14 carries two pathogenicity islands harboring plant and animal virulence genes |
Q53618798 | The effect of a bacteriophage on diversification of the opportunistic bacterial pathogen, Pseudomonas aeruginosa. |
Q46299071 | The effect of interactions between a bacterial strain isolated from drinking water and a pathogen surrogate on biofilms formation diverged under static vs flow conditions. |
Q61813591 | The extracellular matrix of mycobacterial biofilms: could we shorten the treatment of mycobacterial infections? |
Q92296650 | The lytic transglycosylase, LtgG, controls cell morphology and virulence in Burkholderia pseudomallei |
Q34030980 | The multiple signaling systems regulating virulence in Pseudomonas aeruginosa |
Q28493156 | The regulatory repertoire of Pseudomonas aeruginosa AmpC ß-lactamase regulator AmpR includes virulence genes |
Q36289571 | The role of phenotypic variation in rhizosphere Pseudomonas bacteria |
Q34412347 | Themes and Variations: Regulation of RpoN-Dependent Flagellar Genes across Diverse Bacterial Species |
Q36575038 | Tobramycin-Treated Pseudomonas aeruginosa PA14 Enhances Streptococcus constellatus 7155 Biofilm Formation in a Cystic Fibrosis Model System |
Q40993746 | Two genetic loci produce distinct carbohydrate-rich structural components of the Pseudomonas aeruginosa biofilm matrix |
Q34984280 | Type II Protein Secretion in Pseudomonas aeruginosa : the Pseudopilus Is a Multifibrillar and Adhesive Structure |
Q42949086 | Type IV pili of Acidithiobacillus ferrooxidans are necessary for sliding, twitching motility, and adherence |
Q92956497 | Unusual extracellular appendages deployed by the model strain Pseudomonas fluorescens C7R12 |
Q41031369 | Use of fluorescent lectin probes for analysis of footprints from Pseudomonas aeruginosa MDC on hydrophilic and hydrophobic glass substrata |
Q39648657 | Variability in Pseudomonas aeruginosa lipopolysaccharide expression during crude oil degradation |
Q40429705 | Virulence Adaptations of Pseudomonas aeruginosa Isolated from Patients with Non-Cystic Fibrosis Bronchiectasis. |
Q24598939 | Why do microorganisms produce rhamnolipids? |
Q43322876 | Worldwide distribution of Pseudomonas aeruginosa clone C strains in the aquatic environment and cystic fibrosis patients |
Search more.