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Biofilm modifies expression of ribonucleotide reductase genes in Escherichia coliGlobal functional atlas of Escherichia coli encompassing previously uncharacterized proteinsDown regulation of virulence factors of Pseudomonas aeruginosa by salicylic acid attenuates its virulence on Arabidopsis thaliana and Caenorhabditis elegansRhamnolipids modulate swarming motility patterns of Pseudomonas aeruginosaRhamnolipid surfactant production affects biofilm architecture in Pseudomonas aeruginosa PAO1Riddle of biofilm resistanceMolecular dissection of an outbreak of carbapenem-resistant enterobacteriaceae reveals Intergenus KPC carbapenemase transmission through a promiscuous plasmidAn alternative polyamine biosynthetic pathway is widespread in bacteria and essential for biofilm formation in Vibrio choleraeBiofilm formation by nontypeable Haemophilus influenzae: strain variability, outer membrane antigen expression and role of pili.Analysis of bacterial biofilms using NMR-based metabolomicsAdhesive fiber stratification in uropathogenic Escherichia coli biofilms unveils oxygen-mediated control of type 1 piliVibriophages Differentially Influence Biofilm Formation by Vibrio anguillarum Strains.Rapid radiation in bacteria leads to a division of labourTransition state analogs of 5'-methylthioadenosine nucleosidase disrupt quorum sensing.Structure of the Cytoplasmic Region of PelD, a Degenerate Diguanylate Cyclase Receptor That Regulates Exopolysaccharide Production in Pseudomonas aeruginosaBacteriophages with the ability to degrade uropathogenic Escherichia coli biofilmsThe global carbon metabolism regulator Crc is a component of a signal transduction pathway required for biofilm development by Pseudomonas aeruginosaSadB is required for the transition from reversible to irreversible attachment during biofilm formation by Pseudomonas aeruginosa PA14PelA deacetylase activity is required for Pel polysaccharide synthesis in Pseudomonas aeruginosaSadC reciprocally influences biofilm formation and swarming motility via modulation of exopolysaccharide production and flagellar functionThe Pel and Psl polysaccharides provide Pseudomonas aeruginosa structural redundancy within the biofilm matrixA cell cycle and nutritional checkpoint controlling bacterial surface adhesionOligomeric lipoprotein PelC guides Pel polysaccharide export across the outer membrane of Pseudomonas aeruginosa.Analysis of HmsH and its role in plague biofilm formation.Interplay of physical mechanisms and biofilm processes: review of microfluidic methodsA novel two-component response regulator links rpf with biofilm formation and virulence of Xanthomonas axonopodis pv. citri.Upstream migration of Xylella fastidiosa via pilus-driven twitching motility.Pseudomonas syringae coordinates production of a motility-enabling surfactant with flagellar assembly.Bacterial flagella explore microscale hummocks and hollows to increase adhesion.Biofilm formation by the fungal pathogen Candida albicans: development, architecture, and drug resistanceBiofilm formation by Candida dubliniensis.Evidence for Escherichia coli Diguanylate Cyclase DgcZ Interlinking Surface Sensing and Adhesion via Multiple Regulatory Routes.The sporulation transcription factor Spo0A is required for biofilm development in Bacillus subtilis.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.The stringent response genes relA and spoT are important for Escherichia coil biofilms under slow-growth conditions.HecA, a member of a class of adhesins produced by diverse pathogenic bacteria, contributes to the attachment, aggregation, epidermal cell killing, and virulence phenotypes of Erwinia chrysanthemi EC16 on Nicotiana clevelandii seedlings.Biocontrol of Bacillus subtilis against infection of Arabidopsis roots by Pseudomonas syringae is facilitated by biofilm formation and surfactin production.Identification of a novel two-component system in Streptococcus gordonii V288 involved in biofilm formationStaphylococcus aureus virulence factors identified by using a high-throughput Caenorhabditis elegans-killing modelCross-sectional analysis of clinical and environmental isolates of Pseudomonas aeruginosa: biofilm formation, virulence, and genome diversity
P2860
Q21133960-7562A5A2-0314-4B48-B859-1E5B10D9A3C5Q21145830-6B034D89-FF8B-4F2E-9DF3-50A9B45893FDQ24534761-68C03C2D-A6A4-4339-BA8A-5B41F476212BQ24536028-BEF63B68-8B51-4CBD-B76D-23D8ABB9B1E1Q24542424-CFE17F13-5DEB-4708-A47A-32D2A5E9C3CAQ24550611-F614B768-1D58-4C32-90BE-C2C276599B5DQ24633808-C39F0268-746F-43FC-B07D-C22116085EDEQ24647333-9A66544F-A399-4225-B9EA-4CAC31098B3FQ24793297-CE0A9506-D56B-41A7-923C-3B92E9D7F352Q26851303-B089F3AB-3A9A-4C11-89A0-5AA3062602A0Q27321012-9248770E-EB7E-4A11-8CE7-2AFD50E5232BQ27324015-7FEE842B-53C0-4933-A034-B8E613FB0B24Q27334342-249717C9-05AD-4D9B-9688-85289F24E35DQ27654037-A964011F-A5C2-4BD1-8884-E1D3B65EF6D7Q27679157-EF7AA1B1-F185-4136-A9BF-EA88119FF6B1Q28384149-26F66DA4-C007-4575-835F-960A34167809Q28492496-9D5B5EF2-090E-433F-9680-C77863BD4F2EQ28492651-0A777D58-EE89-4AEB-9E6E-0CE1AB153647Q28492812-5982D9DE-4836-4CCE-BC9C-D6F069649D7FQ28492826-F43FA02B-54BD-40FA-9576-3DF40A6080F0Q28492919-A730ACFD-26AB-4BAA-9998-26C040A4865BQ28539050-A12F4096-4427-4E85-9BF7-C502474F429CQ30152656-4797D953-598D-43A4-B217-FEAE5C87B84FQ30156986-7417F388-94D2-4C73-A8C0-F6A27FA8AFAEQ30394297-D4DE7CA4-7C00-4375-98AB-E179C3071E55Q30419796-005206AB-082E-46DC-82D2-C656C8AD6B51Q30476104-926C072B-ED31-4332-84B5-AC340FC9E88BQ30506459-C4E9981E-9BC4-4CB3-B7CD-D75A53CF9764Q30538499-36D97BBD-64CB-4FC7-9ADC-5AF79ED2ECE5Q30701532-F75AD528-FF03-4E98-9F9D-54920A94023EQ30705127-F557D9B8-6333-42AA-855A-98BFC7B8A929Q30804252-BDE3F01B-FF56-4B67-AA74-D64776FA33E5Q30826281-D38C7E49-B110-4B36-8C1B-F02664E3F335Q30828372-91AD9106-DAC8-426B-A276-FF75EAD7A7E0Q30847312-FF64E91A-3017-4D9E-93C6-F95575DF16FCQ30852463-61F6E858-8A5A-4F10-BE4F-FAF7CB5A259CQ31033561-C2237A5E-262F-4F4C-B425-B185F86C8CDAQ31064153-EDE2D633-47B3-4AE0-AA91-85CDDDE49E6AQ31142975-39885D8C-8AD2-427C-8BB9-A493F047F5C2Q33196154-D42E7CD5-BC7C-499A-AF8A-939D5D830F94
P2860
description
1999 nî lūn-bûn
@nan
1999 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Genetic approaches to study of biofilms.
@ast
Genetic approaches to study of biofilms.
@en
type
label
Genetic approaches to study of biofilms.
@ast
Genetic approaches to study of biofilms.
@en
prefLabel
Genetic approaches to study of biofilms.
@ast
Genetic approaches to study of biofilms.
@en
P2093
P1476
Genetic approaches to study of biofilms.
@en
P2093
D K Newman
G A O'Toole
P I Watnick
V B Weaver
P304
P356
10.1016/S0076-6879(99)10008-9
P407
P577
1999-01-01T00:00:00Z