| scholarly article | Q13442814 |
| review article | Q7318358 |
| P50 | author | Garry Laverty | Q38328219 |
| P2093 | author name string | Brendan F Gilmore | |
| Sean P Gorman | |||
| P2860 | cites work | Multicellular and aggregative behaviour of Salmonella typhimurium strains is controlled by mutations in the agfD promoter | Q47986866 |
| Sequence of the alg8 and alg44 genes involved in the synthesis of alginate by Pseudomonas aeruginosa | Q48087234 | ||
| Differentiation of Pseudomonas aeruginosa into the alginate-producing form: inactivation of mucB causes conversion to mucoidy | Q48106984 | ||
| The RpoS sigma factor relieves H-NS-mediated transcriptional repression of csgA, the subunit gene of fibronectin-binding curli in Escherichia coli | Q48134029 | ||
| Phosphorylation and processing of the quorum-sensing molecule autoinducer-2 in enteric bacteria | Q50073839 | ||
| Complex regulation of csgD promoter activity by global regulatory proteins | Q50103377 | ||
| Extracellular DNA chelates cations and induces antibiotic resistance in Pseudomonas aeruginosa biofilms | Q21090518 | ||
| Extracellular DNA Required for Bacterial Biofilm Formation | Q22065541 | ||
| Isolation of an Escherichia coli K-12 mutant strain able to form biofilms on inert surfaces: involvement of a new ompR allele that increases curli expression | Q24520852 | ||
| Rhamnolipid surfactant production affects biofilm architecture in Pseudomonas aeruginosa PAO1 | Q24542424 | ||
| SdiA of Salmonella enterica is a LuxR homolog that detects mixed microbial communities | Q24548877 | ||
| Structure of the autoinducer required for expression of Pseudomonas aeruginosa virulence genes | Q24562234 | ||
| Autoinducer-mediated regulation of rhamnolipid biosurfactant synthesis in Pseudomonas aeruginosa | Q24563771 | ||
| A small RNA acts as an antisilencer of the H-NS-silenced rcsA gene of Escherichia coli | Q24563821 | ||
| Type 1 fimbrial expression enhances Escherichia coli virulence for the urinary tract | Q24631903 | ||
| Lipid A modification systems in gram-negative bacteria | Q24650951 | ||
| Cellular Control of the Synthesis and Activity of the Bacterial Luminescent System | Q24655064 | ||
| Pseudomonas aeruginosa exhibits sliding motility in the absence of type IV pili and flagella | Q24655219 | ||
| Quinolone signaling in the cell-to-cell communication system of Pseudomonas aeruginosa | Q24670942 | ||
| Bacteria-host communication: the language of hormones | Q24678649 | ||
| Structural basis of diverse substrate recognition by the enzyme PMM/PGM from P. aeruginosa | Q27642948 | ||
| Engineering of PA-IIL lectin from Pseudomonas aeruginosa – Unravelling the role of the specificity loop for sugar preference | Q27645072 | ||
| NMR structure of the Escherichia coli type 1 pilus subunit FimF and its interactions with other pilus subunits | Q27649172 | ||
| Structure of Escherichia coli tyrosine kinase Etk reveals a novel activation mechanism | Q27650660 | ||
| The Crystal Structure of the Escherichia coli Autoinducer-2 Processing Protein LsrF | Q27657209 | ||
| Flagellar and twitching motility are necessary for Pseudomonas aeruginosa biofilm development | Q27976516 | ||
| Garlic blocks quorum sensing and promotes rapid clearing of pulmonary Pseudomonas aeruginosa infections | Q28286057 | ||
| Pseudomonas aeruginosa biofilms in cystic fibrosis | Q28299966 | ||
| Biofilms: the matrix revisited | Q28301704 | ||
| Localization of a critical interface for helical rod formation of bacterial adhesion P-pili | Q28303616 | ||
| Tyrosine phosphorylation of the UDP-glucose dehydrogenase of Escherichia coli is at the crossroads of colanic acid synthesis and polymyxin resistance | Q28473483 | ||
| Genes involved in matrix formation in Pseudomonas aeruginosa PA14 biofilms | Q28492476 | ||
| Identification and characterization of AlgZ, an AlgT-dependent DNA-binding protein required for Pseudomonas aeruginosa algD transcription | Q28492593 | ||
| Control of Pseudomonas aeruginosa algZ expression by the alternative sigma factor AlgT | Q28492627 | ||
| Mutant analysis and cellular localization of the AlgI, AlgJ, and AlgF proteins required for O acetylation of alginate in Pseudomonas aeruginosa | Q28492634 | ||
| AlgX is a periplasmic protein required for alginate biosynthesis in Pseudomonas aeruginosa | Q28492657 | ||
| The AlgT-dependent transcriptional regulator AmrZ (AlgZ) inhibits flagellum biosynthesis in mucoid, nonmotile Pseudomonas aeruginosa cystic fibrosis isolates | Q28492672 | ||
| Posttranslational control of the algT (algU)-encoded sigma22 for expression of the alginate regulon in Pseudomonas aeruginosa and localization of its antagonist proteins MucA and MucB (AlgN) | Q28492759 | ||
| The NtrC family regulator AlgB, which controls alginate biosynthesis in mucoid Pseudomonas aeruginosa, binds directly to the algD promoter | Q28492867 | ||
| Pseudomonas aeruginosa lectin LecB is located in the outer membrane and is involved in biofilm formation | Q28492872 | ||
| Fimbrial biogenesis genes of Pseudomonas aeruginosa: pilW and pilX increase the similarity of type 4 fimbriae to the GSP protein-secretion systems and pilY1 encodes a gonococcal PilC homologue | Q28492930 | ||
| Identification of an Escherichia coli pepA homolog and its involvement in suppression of the algB phenotype in mucoid Pseudomonas aeruginosa. | Q28492931 | ||
| Analysis of Pseudomonas aeruginosa diguanylate cyclases and phosphodiesterases reveals a role for bis-(3'-5')-cyclic-GMP in virulence | Q28492942 | ||
| Genetic and biochemical analyses of the Pseudomonas aeruginosa Psl exopolysaccharide reveal overlapping roles for polysaccharide synthesis enzymes in Psl and LPS production | Q28493036 | ||
| Global regulation of quorum sensing and virulence by VqsR in Pseudomonas aeruginosa | Q28493065 | ||
| Purification and characterization of phosphomannose isomerase-guanosine diphospho-D-mannose pyrophosphorylase. A bifunctional enzyme in the alginate biosynthetic pathway of Pseudomonas aeruginosa | Q28493068 | ||
| Roles of type IV pili, flagellum-mediated motility and extracellular DNA in the formation of mature multicellular structures in Pseudomonas aeruginosa biofilms | Q28493090 | ||
| The quorum-sensing negative regulator RsaL of Pseudomonas aeruginosa binds to the lasI promoter | Q28493130 | ||
| Control of AlgU, a member of the sigma E-like family of stress sigma factors, by the negative regulators MucA and MucB and Pseudomonas aeruginosa conversion to mucoidy in cystic fibrosis | Q28493131 | ||
| Expression of Pseudomonas aeruginosa virulence genes requires cell-to-cell communication | Q28493152 | ||
| The Pseudomonas aeruginosa lectins PA-IL and PA-IIL are controlled by quorum sensing and by RpoS | Q29346774 | ||
| The Pseudomonas quorum-sensing regulator RsaL belongs to the tetrahelical superclass of H-T-H proteins | Q29346820 | ||
| Type IV pili and twitching motility | Q29615262 | ||
| Attenuation of Pseudomonas aeruginosa virulence by quorum sensing inhibitors | Q29615282 | ||
| Microarray analysis of Pseudomonas aeruginosa quorum-sensing regulons: effects of growth phase and environment | Q29615283 | ||
| Microbial pathogenesis in cystic fibrosis: mucoid Pseudomonas aeruginosa and Burkholderia cepacia | Q29615286 | ||
| The involvement of cell-to-cell signals in the development of a bacterial biofilm | Q29615295 | ||
| Pathogenic Escherichia coli | Q29616738 | ||
| Identification of broadly protective human antibodies to Pseudomonas aeruginosa exopolysaccharide Psl by phenotypic screening | Q30423024 | ||
| Structure and assembly of P-pili: a protruding hinge region used for assembly of a bacterial adhesion filament | Q30477600 | ||
| Initiation of assembly and association of the structural elements of a bacterial pilus depend on two specialized tip proteins | Q34044801 | ||
| Chaperone-assisted pilus assembly and bacterial attachment. | Q34066527 | ||
| The LuxS family of bacterial autoinducers: biosynthesis of a novel quorum-sensing signal molecule | Q34086014 | ||
| luxS-dependent gene regulation in Escherichia coli K-12 revealed by genomic expression profiling | Q34231017 | ||
| The global regulatory hns gene negatively affects adhesion to solid surfaces by anaerobically grown Escherichia coli by modulating expression of flagellar genes and lipopolysaccharide production | Q34306480 | ||
| The type IV pilus assembly complex: biogenic interactions among the bundle-forming pilus proteins of enteropathogenic Escherichia coli | Q34313788 | ||
| Quorum sensing is not required for twitching motility in Pseudomonas aeruginosa | Q34314375 | ||
| Cross-talk mechanisms in biofilm formation and responses to environmental and physiological stress in Escherichia coli. | Q51735372 | ||
| Global impact of mature biofilm lifestyle on Escherichia coli K-12 gene expression. | Q52004921 | ||
| RpoS-dependent stress tolerance in Pseudomonas aeruginosa. | Q52534824 | ||
| Influence of tyrosine-kinase Wzc activity on colanic acid production in Escherichia coli K12 cells. | Q54447877 | ||
| Modification of lipopolysaccharide with colanic acid (M-antigen) repeats in Escherichia coli. | Q54448386 | ||
| Pilus chaperones represent a new type of protein-folding catalyst. | Q54499607 | ||
| β-Lactam induction of colanic acid gene expression inEscherichia coli | Q54517116 | ||
| Sigma S-dependent growth-phase induction of the csgBA promoter in Escherichia coli can be achieved in vivo by sigma 70 in the absence of the nucleoid-associated protein H-NS. | Q54628054 | ||
| The OmpR protein of Escherichia coli binds to sites in the ompF promoter region in a hierarchical manner determined by its degree of phosphorylation. | Q54635162 | ||
| Survival of FimH-expressing enterobacteria in macrophages relies on glycolipid traffic | Q57962356 | ||
| Impact of Pseudomonas aeruginosa quorum sensing on biofilm persistence in an in vivo intraperitoneal foreign-body infection model | Q59139139 | ||
| SdiA, an Escherichia coli homologue of quorum-sensing regulators, controls the expression of virulence factors in enterohaemorrhagic Escherichia coli O157:H7 | Q61857106 | ||
| Regulation of the Escherichia coli csgD promoter: interplay between five transcription factors | Q64449100 | ||
| The mdoA locus of Escherichia coli consists of an operon under osmotic control | Q67904210 | ||
| Pulmonary dehydration and infection in cystic fibrosis: evidence that ethanol activates alginate gene expression and induction of mucoidy in Pseudomonas aeruginosa | Q68473536 | ||
| A hierarchical quorum-sensing cascade in Pseudomonas aeruginosa links the transcriptional activators LasR and RhIR (VsmR) to expression of the stationary-phase sigma factor RpoS | Q71739127 | ||
| The influence of A-band and B-band lipopolysaccharide on the surface characteristics and adhesion of Pseudomonas aeruginosa to surfaces | Q71810214 | ||
| A sandwich cup method for the penetration assay of antimicrobial agents through Pseudomonas exopolysaccharides | Q72356191 | ||
| Environmental regulation of curli production in Escherichia coli | Q72399111 | ||
| Pseudomonas aeruginosa in cystic fibrosis: role of mucC in the regulation of alginate production and stress sensitivity | Q73917235 | ||
| Genome-wide profiling of promoter recognition by the two-component response regulator CpxR-P in Escherichia coli | Q77939133 | ||
| Involvement of the Cpx signal transduction pathway of E. coli in biofilm formation | Q78250629 | ||
| Synthesis and immunostimulatory properties of the phosphorothioate analogues of cdiGMP | Q81981030 | ||
| Cell-to-cell signalling in Escherichia coli and Salmonella enterica. | Q34319096 | ||
| A quorum-sensing inhibitor blocks Pseudomonas aeruginosa virulence and biofilm formation | Q34379079 | ||
| Allosteric control of cyclic di-GMP signaling | Q34559308 | ||
| Pseudomonas aeruginosa lectins I and II and their interaction with human airway cilia | Q34560126 | ||
| Independent regulation of MucD, an HtrA-like protease in Pseudomonas aeruginosa, and the role of its proteolytic motif in alginate gene regulation | Q34563383 | ||
| Bacterial adhesion: seen any good biofilms lately? | Q34587156 | ||
| Bacterial cell-to-cell communication: sorry, can't talk now - gone to lunch! | Q34588902 | ||
| Quorum-sensing regulation of the biofilm matrix genes (pel) of Pseudomonas aeruginosa. | Q34627554 | ||
| Bacterial alginates: biosynthesis and applications | Q34743438 | ||
| Contamination of abiotic surfaces: what a colonizing bacterium sees and how to blur it | Q35111609 | ||
| Alginate is not a significant component of the extracellular polysaccharide matrix of PA14 and PAO1 Pseudomonas aeruginosa biofilms | Q35147263 | ||
| Epidemiology of urinary tract infections: transmission and risk factors, incidence, and costs | Q35171757 | ||
| Quorum sensing : a novel target for the treatment of biofilm infections. | Q35192239 | ||
| Putative exopolysaccharide synthesis genes influence Pseudomonas aeruginosa biofilm development | Q35278987 | ||
| Evidence that the algI/algJ gene cassette, required for O acetylation of Pseudomonas aeruginosa alginate, evolved by lateral gene transfer | Q35279906 | ||
| Molecular mechanism of P pilus termination in uropathogenic Escherichia coli | Q35630480 | ||
| Inactivation of mdoH leads to increased expression of colanic acid capsular polysaccharide in Escherichia coli | Q35632109 | ||
| Incidence and clinical implication of nosocomial infections associated with implantable biomaterials - catheters, ventilator-associated pneumonia, urinary tract infections | Q35656865 | ||
| Quorum sensing and bacterial cross-talk in biotechnology | Q35908898 | ||
| A mutation in algN permits trans activation of alginate production by algT in Pseudomonas species | Q35911968 | ||
| Quorum sensing in Escherichia coli is signaled by AI-2/LsrR: effects on small RNA and biofilm architecture. | Q35949964 | ||
| Characterization of quorum sensing and quorum quenching soil bacteria isolated from Malaysian tropical montane forest. | Q35969742 | ||
| Mucoid-to-nonmucoid conversion in alginate-producing Pseudomonas aeruginosa often results from spontaneous mutations in algT, encoding a putative alternate sigma factor, and shows evidence for autoregulation | Q35979967 | ||
| The PapC usher forms an oligomeric channel: implications for pilus biogenesis across the outer membrane | Q35980523 | ||
| Role of alginate lyase in cell detachment of Pseudomonas aeruginosa. | Q36056700 | ||
| Understanding the control of Pseudomonas aeruginosa alginate synthesis and the prospects for management of chronic infections in cystic fibrosis | Q36090700 | ||
| Making 'sense' of metabolism: autoinducer-2, LuxS and pathogenic bacteria. | Q36111883 | ||
| Alginate synthesis in Pseudomonas aeruginosa: environmental regulation of the algC promoter | Q36136377 | ||
| Products of three accessory genes, pilB, pilC, and pilD, are required for biogenesis of Pseudomonas aeruginosa pili | Q36164735 | ||
| A cyclic-di-GMP receptor required for bacterial exopolysaccharide production | Q36319174 | ||
| 4-quinolone signalling in Pseudomonas aeruginosa: old molecules, new perspectives. | Q36398951 | ||
| The Cpx system of Escherichia coli, a strategic signaling pathway for confronting adverse conditions and for settling biofilm communities? | Q36400106 | ||
| Quorum sensing in Escherichia coli and Salmonella | Q36400159 | ||
| Mucoid Pseudomonas aeruginosa in cystic fibrosis: mutations in the muc loci affect transcription of the algR and algD genes in response to environmental stimuli | Q42038470 | ||
| AI-3 synthesis is not dependent on luxS in Escherichia coli | Q42066351 | ||
| Quorum sensing inhibition by Asparagopsis taxiformis, a marine macro alga: separation of the compound that interrupts bacterial communication | Q42115970 | ||
| Seasonal humidity may influence Pseudomonas aeruginosa hospital-acquired infection rates | Q42264415 | ||
| Adaptation in bacterial flagellar and motility systems: from regulon members to 'foraging'-like behavior in E. coli | Q42430233 | ||
| Global effects of the cell-to-cell signaling molecules autoinducer-2, autoinducer-3, and epinephrine in a luxS mutant of enterohemorrhagic Escherichia coli | Q42634023 | ||
| Quorum sensing Escherichia coli regulators B and C (QseBC): a novel two-component regulatory system involved in the regulation of flagella and motility by quorum sensing in E. coli. | Q42673580 | ||
| Let LuxS speak up in AI-2 signaling. | Q42679712 | ||
| Quorum sensing and Bacterial Pathogenicity: From Molecules to Disease | Q42763564 | ||
| Identification of an Escherichia coli operon required for formation of the O-antigen capsule | Q42875394 | ||
| Oxygen tension and nutrient starvation are major signals that regulate agfD promoter activity and expression of the multicellular morphotype in Salmonella typhimurium | Q43808598 | ||
| Autoinducer 2 activity in Escherichia coli culture supernatants can be actively reduced despite maintenance of an active synthase, LuxS. | Q44360293 | ||
| Membrane-to-cytosol redistribution of ECF sigma factor AlgU and conversion to mucoidy in Pseudomonas aeruginosa isolates from cystic fibrosis patients | Q44395502 | ||
| Escherichia coli gets the message | Q44569372 | ||
| The Pseudomonas aeruginosa quinolone signal molecule overcomes the cell density-dependency of the quorum sensing hierarchy, regulates rhl-dependent genes at the onset of stationary phase and can be produced in the absence of LasR. | Q44594934 | ||
| Lsr-mediated transport and processing of AI-2 in Salmonella typhimurium | Q44658473 | ||
| The Pseudomonas aeruginosa RpoS regulon and its relationship to quorum sensing. | Q44756516 | ||
| Bacterial adhesion and biofilm formation on various double-J stents in vivo and in vitro | Q44786161 | ||
| Protective effect of exopolysaccharide colanic acid of Escherichia coli O157:H7 to osmotic and oxidative stress | Q44911006 | ||
| Functional characterization in vitro of all two-component signal transduction systems from Escherichia coli | Q45136836 | ||
| Indole induces the expression of multidrug exporter genes in Escherichia coli | Q45247978 | ||
| Screening of SdiA inhibitors from Melia dubia seeds extracts towards the hold back of uropathogenic E.coli quorum sensing-regulated factors. | Q46046791 | ||
| The MexGHI-OpmD multidrug efflux pump controls growth, antibiotic susceptibility and virulence in Pseudomonas aeruginosa via 4-quinolone-dependent cell-to-cell communication | Q46427797 | ||
| A characterization of DNA release in Pseudomonas aeruginosa cultures and biofilms | Q46906961 | ||
| Synthesis of cyclic bis(3'-5')-2'-deoxyguanylic/guanylic acid (c-dGpGp) and its biological activities to microbes. | Q46988060 | ||
| AgfD, the checkpoint of multicellular and aggregative behaviour in Salmonella typhimurium regulates at least two independent pathways | Q47870324 | ||
| Construction and expression of recombinant plasmids encoding type 1 or D-mannose-resistant pili from a urinary tract infection Escherichia coli isolate | Q36427678 | ||
| Curli biogenesis and function | Q36480477 | ||
| Self-produced exopolysaccharide is a signal that stimulates biofilm formation in Pseudomonas aeruginosa. | Q36483723 | ||
| Structural and functional insights into the assembly of type 1 pili from Escherichia coli | Q36515692 | ||
| Alginate synthesis by Pseudomonas aeruginosa: a key pathogenic factor in chronic pulmonary infections of cystic fibrosis patients | Q36637394 | ||
| Tyrosine phosphorylation: an emerging regulatory device of bacterial physiology | Q36701604 | ||
| Look who's talking: communication and quorum sensing in the bacterial world. | Q36759802 | ||
| Inhalation with fucose and galactose for treatment of Pseudomonas aeruginosa in cystic fibrosis patients | Q36982086 | ||
| The two-component system QseEF and the membrane protein QseG link adrenergic and stress sensing to bacterial pathogenesis | Q37153762 | ||
| Regulation of RpoS proteolysis in Escherichia coli: the response regulator RssB is a recognition factor that interacts with the turnover element in RpoS | Q37211276 | ||
| Expression of type 1 fimbriae may be required for persistence of Escherichia coli in the catheterized urinary tract. | Q37223130 | ||
| Quorum sensing and environmental adaptation in Pseudomonas aeruginosa: a tale of regulatory networks and multifunctional signal molecules | Q37403126 | ||
| Nitric oxide signaling in Pseudomonas aeruginosa biofilms mediates phosphodiesterase activity, decreased cyclic di-GMP levels, and enhanced dispersal | Q37451442 | ||
| Microbial quorum sensing: a tool or a target for antimicrobial therapy? | Q37548534 | ||
| Catheter-associated urinary tract infection by Pseudomonas aeruginosa is mediated by exopolysaccharide-independent biofilms. | Q37713368 | ||
| Biomolecular mechanisms of staphylococcal biofilm formation. | Q38093647 | ||
| Biofilms, flagella, and mechanosensing of surfaces by bacteria | Q38217430 | ||
| Interactions of the quorum sensing regulator QscR: interaction with itself and the other regulators of Pseudomonas aeruginosa LasR and RhlR. | Q38356354 | ||
| Regulation of rpoS gene expression in Pseudomonas: involvement of a TetR family regulator | Q39503787 | ||
| DNA microarray-based identification of genes controlled by autoinducer 2-stimulated quorum sensing in Escherichia coli | Q39504681 | ||
| The Pseudomonas quinolone signal regulates rhl quorum sensing in Pseudomonas aeruginosa | Q39539156 | ||
| Secretion of curli fibre subunits is mediated by the outer membrane-localized CsgG protein | Q39620322 | ||
| Quorum-sensing Escherichia coli regulator A: a regulator of the LysR family involved in the regulation of the locus of enterocyte effacement pathogenicity island in enterohemorrhagic E. coli. | Q39655068 | ||
| The Pseudomonas aeruginosa rhlAB operon is not expressed during the logarithmic phase of growth even in the presence of its activator RhlR and the autoinducer N-butyryl-homoserine lactone | Q39702709 | ||
| The Pseudomonas fluorescens AlgG protein, but not its mannuronan C-5-epimerase activity, is needed for alginate polymer formation. | Q39757026 | ||
| Increased antibiotic resistance of Escherichia coli in mature biofilms | Q39881658 | ||
| Identification, cloning, and characterization of rcsF, a new regulator gene for exopolysaccharide synthesis that suppresses the division mutation ftsZ84 in Escherichia coli K-12. | Q39940203 | ||
| Transmembrane modulator-dependent bacterial tyrosine kinase activates UDP-glucose dehydrogenases | Q39958743 | ||
| Dynamic restacking of Escherichia coli P-pili. | Q40205774 | ||
| Production and characterization of the slime polysaccharide of Pseudomonas aeruginosa | Q40290468 | ||
| Structure-function and biogenesis of the type IV pili | Q40619082 | ||
| Posttranslational processing of type IV prepilin and homologs by PilD of Pseudomonas aeruginosa | Q40687599 | ||
| Regulation of uptake and processing of the quorum-sensing autoinducer AI-2 in Escherichia coli | Q40731005 | ||
| Bacterial alginate biosynthesis--recent progress and future prospects | Q40856886 | ||
| Two genetic loci produce distinct carbohydrate-rich structural components of the Pseudomonas aeruginosa biofilm matrix | Q40993746 | ||
| Analysis of Pseudomonas aeruginosa conditional psl variants reveals roles for the psl polysaccharide in adhesion and maintaining biofilm structure postattachment | Q41063615 | ||
| The chain of command in Pseudomonas quorum sensing. | Q41462584 | ||
| Molecular genetic analysis of type-4 pilus biogenesis and twitching motility using Pseudomonas aeruginosa as a model system – areview | Q41532683 | ||
| Biogenesis of E. coli Pap pili: papH, a minor pilin subunit involved in cell anchoring and length modulation | Q41791368 | ||
| The chaperone-assisted membrane release and folding pathway is sensed by two signal transduction systems | Q41908538 | ||
| Complicated catheter-associated urinary tract infections due to Escherichia coli and Proteus mirabilis | Q30491878 | ||
| MlrA, a novel regulator of curli (AgF) and extracellular matrix synthesis by Escherichia coli and Salmonella enterica serovar Typhimurium | Q30698138 | ||
| A novel type of conserved DNA-binding domain in the transcriptional regulators of the AlgR/AgrA/LytR family | Q30734775 | ||
| Small-molecule inhibitors target Escherichia coli amyloid biogenesis and biofilm formation | Q30885749 | ||
| Alginate production affects Pseudomonas aeruginosa biofilm development and architecture, but is not essential for biofilm formation | Q31074516 | ||
| Expression of the psl operon in Pseudomonas aeruginosa PAO1 biofilms: PslA performs an essential function in biofilm formation | Q33221272 | ||
| Small molecule inhibitors of bacterial quorum sensing and biofilm formation | Q33223249 | ||
| N-acyl-L-homoserine lactone signal interception by Escherichia coli | Q33234275 | ||
| Spatial patterns of DNA replication, protein synthesis, and oxygen concentration within bacterial biofilms reveal diverse physiological states | Q33276824 | ||
| Pseudomonas aeruginosa Psl is a galactose- and mannose-rich exopolysaccharide | Q33290866 | ||
| Physiological heterogeneity in biofilms | Q33319084 | ||
| Multiple roles of Pseudomonas aeruginosa TBCF10839 PilY1 in motility, transport and infection. | Q33389371 | ||
| Glycopeptide dendrimers with high affinity for the fucose-binding lectin LecB from Pseudomonas aeruginosa | Q33405133 | ||
| Structure, assembly and regulation of expression of capsules in Escherichia coli | Q33592585 | ||
| Regulation of quorum sensing by RpoS in Pseudomonas aeruginosa | Q33603136 | ||
| Presence of a classical RRM-fold palm domain in Thg1-type 3'- 5'nucleic acid polymerases and the origin of the GGDEF and CRISPR polymerase domains | Q33622038 | ||
| Abiotic surface sensing and biofilm-dependent regulation of gene expression in Escherichia coli. | Q33635823 | ||
| CpxR/OmpR interplay regulates curli gene expression in response to osmolarity in Escherichia coli | Q33714541 | ||
| Accumulation of the enterobacterial common antigen lipid II biosynthetic intermediate stimulates degP transcription in Escherichia coli. | Q33741099 | ||
| Effects of bfp mutations on biogenesis of functional enteropathogenic Escherichia coli type IV pili | Q33790099 | ||
| Paradigm shift in discovering next-generation anti-infective agents: targeting quorum sensing, c-di-GMP signaling and biofilm formation in bacteria with small molecules | Q33852436 | ||
| Epimerase active domain of Pseudomonas aeruginosa AlgG, a protein that contains a right-handed beta-helix | Q33855772 | ||
| PapD-like chaperones and pilus biogenesis | Q33874589 | ||
| Exopolysaccharide production is required for development of Escherichia coli K-12 biofilm architecture | Q33905553 | ||
| Multiple N-acyl-L-homoserine lactone signal molecules regulate production of virulence determinants and secondary metabolites in Pseudomonas aeruginosa | Q33906845 | ||
| Role of exopolysaccharides in Pseudomonas aeruginosa biofilm formation and architecture | Q33930259 | ||
| Escherichia coli RcsA, a positive activator of colanic acid capsular polysaccharide synthesis, functions To activate its own expression. | Q33991039 | ||
| Cells of Escherichia coli contain a protein-tyrosine kinase, Wzc, and a phosphotyrosine-protein phosphatase, Wzb | Q33992169 | ||
| The CpxRA signal transduction system of Escherichia coli: growth-related autoactivation and control of unanticipated target operons. | Q33993123 | ||
| The mammalian neuroendocrine hormone norepinephrine supplies iron for bacterial growth in the presence of transferrin or lactoferrin | Q33994813 | ||
| Indole can act as an extracellular signal in Escherichia coli | Q33996505 | ||
| Quorum sensing is a global regulatory mechanism in enterohemorrhagic Escherichia coli O157:H7 | Q33996772 | ||
| Complex regulatory network controls initial adhesion and biofilm formation in Escherichia coli via regulation of the csgD gene. | Q33997251 | ||
| Bacterial quorum sensing in pathogenic relationships | Q34007664 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 3 | |
| P921 | main subject | biofilm | Q467410 |
| Escherichia coli | Q25419 | ||
| Pseudomonas aeruginosa | Q31856 | ||
| P304 | page(s) | 596-632 | |
| P577 | publication date | 2014-07-18 | |
| P1433 | published in | Pathogens | Q27724554 |
| P1476 | title | Biomolecular Mechanisms of Pseudomonas aeruginosa and Escherichia coli Biofilm Formation | |
| P478 | volume | 3 |
| Q37287708 | A Novel RNase 3/ECP Peptide for Pseudomonas aeruginosa Biofilm Eradication That Combines Antimicrobial, Lipopolysaccharide Binding, and Cell-Agglutinating Activities. |
| Q28646894 | A central theory of biology |
| Q41092106 | A new Pseudomonas quinolone signal (PQS) binding partner: MexG. |
| Q92128398 | Biofilms: The Microbial "Protective Clothing" in Extreme Environments |
| Q53838498 | Cells of Escherichia coli are protected against severe chemical stress by co-habiting cell aggregates formed by Pseudomonas aeruginosa. |
| Q92969898 | Challenges of intervention, treatment, and antibiotic resistance of biofilm-forming microorganisms |
| Q36137644 | Characterization of Early Enzymes Involved in TDP-Aminodideoxypentose Biosynthesis en Route to Indolocarbazole AT2433. |
| Q40508725 | Determinants for persistence of Pseudomonas aeruginosa in hospitals: interplay between resistance, virulence and biofilm formation. |
| Q59808836 | Distribution and drug resistance of pathogenic bacteria in ventilator-associated pneumonia at a local hospital of North-eastern China |
| Q39151188 | Electrospinning of Bioactive Wound-Healing Nets |
| Q92560105 | Evaluation of antimicrobial resistance, biofilm forming potential, and the presence of biofilm-related genes among clinical isolates of Pseudomonas aeruginosa |
| Q41103592 | Genome Sequence of the Urethral Isolate Pseudomonas aeruginosa RN21. |
| Q36026123 | Iron is a signal for Stenotrophomonas maltophilia biofilm formation, oxidative stress response, OMPs expression, and virulence |
| Q37077552 | Lipopolysaccharide transport and assembly at the outer membrane: the PEZ model |
| Q89620860 | Mechanism of Action of Surface Immobilized Antimicrobial Peptides Against Pseudomonas aeruginosa |
| Q26747594 | Mechanisms of Antimicrobial Resistance in ESKAPE Pathogens |
| Q47803998 | Peptide nanomaterials as future antimicrobial technologies |
| Q41139791 | Phenotypic Heterogeneity in Attachment of Marine Bacteria toward Antifouling Copolymers Unraveled by AFM |
| Q36913948 | Polyphosphate Kinase Mediates Antibiotic Tolerance in Extraintestinal Pathogenic Escherichia coli PCN033 |
| Q64227610 | Proteomic Analysis of Resistance of Gram-Negative Bacteria to Chlorhexidine and Impacts on Susceptibility to Colistin, Antimicrobial Peptides, and Ceragenins |
| Q26768365 | Pseudomonas aeruginosa ventilator-associated pneumonia management |
| Q49908061 | Recent perspectives on the molecular basis of biofilm formation by Pseudomonas aeruginosa and approaches for treatment and biofilm dispersal |
| Q38838551 | Redox-Sensitive MarR Homologue BifR from Burkholderia thailandensis Regulates Biofilm Formation |
| Q36060114 | Structural characterization of AtmS13, a putative sugar aminotransferase involved in indolocarbazole AT2433 aminopentose biosynthesis |
| Q47114450 | Systematic identification of novel regulatory interactions controlling biofilm formation in the bacterium Escherichia coli. |
| Q95840995 | The Antimicrobial Peptide Human Beta-Defensin 2 Inhibits Biofilm Production of Pseudomonas aeruginosa Without Compromising Metabolic Activity |
| Q40075208 | The Risk of Cardiac Device-Related Infection in Bacteremic Patients Is Species Specific: Results of a 12-Year Prospective Cohort |
| Q50082618 | The effect of bacterial chemotaxis on host infection and pathogenicity |
| Q36027026 | The influence of a modified lipopolysaccharide O-antigen on the biosynthesis of xanthan in Xanthomonas campestris pv. campestris B100 |
| Q27316579 | Transcriptional profiling of Klebsiella pneumoniae defines signatures for planktonic, sessile and biofilm-dispersed cells |
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