Transcriptional analysis of genes involved in Pseudomonas aeruginosa biofilms

[1] Andersen JB, 1998, APPL ENVIRON MICROB, V64, P2240

[2] EXOPOLYSACCHARIDE PRODUCTION IN BIOFILMS - SUBSTRATUM ACTIVATION OF ALGINATE GENE-EXPRESSION BY PSEUDOMONAS-AERUGINOSA [J]. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1993, 59 (04) : 1181 - 1186

[3] REPLICATION OF AN ORIGIN-CONTAINING DERIVATIVE OF PLASMID RK2 DEPENDENT ON A PLASMID FUNCTION PROVIDED IN TRANS [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (04) : 1648 - 1652

[4] Negative control of flagellum synthesis in Pseudomonas aeruginosa is modulated by the alternative sigma factor AlgT (AlgU) [J]. JOURNAL OF BACTERIOLOGY, 1999, 181 (23) : 7401 - 7404

[5] Integration-proficient plasmids for Pseudomonas aeruginosa:: Site-specific integration and use for engineering of reporter and expression strains [J]. PLASMID, 2000, 43 (01) : 59 - 72

[6] A broad-host-range Flp-FRT recombination system for site-specific excision of chromosomally-located DNA sequences:: application for isolation of unmarked Pseudomonas aeruginosa mutants [J]. GENE, 1998, 212 (01) : 77 - 86

[7] PRODUCTION OF MUCOID EXOPOLYSACCHARIDE DURING DEVELOPMENT OF PSEUDOMONAS-AERUGINOSA BIOFILMS [J]. INFECTION AND IMMUNITY, 1993, 61 (02) : 777 - 780

[8] UTILIZATION OF A MINI-DLAC TRANSPOSABLE ELEMENT TO CREATE AN ALPHA-COMPLEMENTATION AND REGULATED EXPRESSION SYSTEM FOR CLONING IN PSEUDOMONAS-AERUGINOSA [J]. GENE, 1994, 140 (01) : 7 - 15

[9] Flagellar and twitching motility are necessary for Pseudomonas aeruginosa biofilm development [J]. MOLECULAR MICROBIOLOGY, 1998, 30 (02) : 295 - 304

[10] Initiation of biofilm formation in Pseudomonas fluorescens WCS365 proceeds via multiple, convergent signalling pathways:: a genetic analysis [J]. MOLECULAR MICROBIOLOGY, 1998, 28 (03) : 449 - 461

[1] Andersen JB, 1998, APPL ENVIRON MICROB, V64, P2240

[2] EXOPOLYSACCHARIDE PRODUCTION IN BIOFILMS - SUBSTRATUM ACTIVATION OF ALGINATE GENE-EXPRESSION BY PSEUDOMONAS-AERUGINOSA [J]. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1993, 59 (04) : 1181 - 1186

[3] REPLICATION OF AN ORIGIN-CONTAINING DERIVATIVE OF PLASMID RK2 DEPENDENT ON A PLASMID FUNCTION PROVIDED IN TRANS [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (04) : 1648 - 1652

[4] Negative control of flagellum synthesis in Pseudomonas aeruginosa is modulated by the alternative sigma factor AlgT (AlgU) [J]. JOURNAL OF BACTERIOLOGY, 1999, 181 (23) : 7401 - 7404

[5] Integration-proficient plasmids for Pseudomonas aeruginosa:: Site-specific integration and use for engineering of reporter and expression strains [J]. PLASMID, 2000, 43 (01) : 59 - 72

[6] A broad-host-range Flp-FRT recombination system for site-specific excision of chromosomally-located DNA sequences:: application for isolation of unmarked Pseudomonas aeruginosa mutants [J]. GENE, 1998, 212 (01) : 77 - 86

[7] PRODUCTION OF MUCOID EXOPOLYSACCHARIDE DURING DEVELOPMENT OF PSEUDOMONAS-AERUGINOSA BIOFILMS [J]. INFECTION AND IMMUNITY, 1993, 61 (02) : 777 - 780

[8] UTILIZATION OF A MINI-DLAC TRANSPOSABLE ELEMENT TO CREATE AN ALPHA-COMPLEMENTATION AND REGULATED EXPRESSION SYSTEM FOR CLONING IN PSEUDOMONAS-AERUGINOSA [J]. GENE, 1994, 140 (01) : 7 - 15

[9] Flagellar and twitching motility are necessary for Pseudomonas aeruginosa biofilm development [J]. MOLECULAR MICROBIOLOGY, 1998, 30 (02) : 295 - 304

[10] Initiation of biofilm formation in Pseudomonas fluorescens WCS365 proceeds via multiple, convergent signalling pathways:: a genetic analysis [J]. MOLECULAR MICROBIOLOGY, 1998, 28 (03) : 449 - 461