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Results: 1 to 20 of 123

Related Citations for PubMed (Select 24655293)

1.

Elevated levels of the second messenger c-di-GMP contribute to antimicrobial resistance of Pseudomonas aeruginosa.

Gupta K, Liao J, Petrova OE, Cherny KE, Sauer K.

Mol Microbiol. 2014 May;92(3):488-506. doi: 10.1111/mmi.12587. Epub 2014 Apr 9.

PMID:
24655293
2.

Antimicrobial tolerance of Pseudomonas aeruginosa biofilms is activated during an early developmental stage and requires the two-component hybrid SagS.

Gupta K, Marques CN, Petrova OE, Sauer K.

J Bacteriol. 2013 Nov;195(21):4975-87. doi: 10.1128/JB.00732-13. Epub 2013 Aug 30.

3.

BrlR from Pseudomonas aeruginosa is a c-di-GMP-responsive transcription factor.

Chambers JR, Liao J, Schurr MJ, Sauer K.

Mol Microbiol. 2014 May;92(3):471-87. doi: 10.1111/mmi.12562. Epub 2014 Mar 6.

PMID:
24612375
4.

The MerR-like regulator BrlR confers biofilm tolerance by activating multidrug efflux pumps in Pseudomonas aeruginosa biofilms.

Liao J, Schurr MJ, Sauer K.

J Bacteriol. 2013 Aug;195(15):3352-63. doi: 10.1128/JB.00318-13. Epub 2013 May 17.

5.

The MerR-like regulator BrlR impairs Pseudomonas aeruginosa biofilm tolerance to colistin by repressing PhoPQ.

Chambers JR, Sauer K.

J Bacteriol. 2013 Oct;195(20):4678-88. doi: 10.1128/JB.00834-13. Epub 2013 Aug 9.

6.

The MerR-like transcriptional regulator BrlR contributes to Pseudomonas aeruginosa biofilm tolerance.

Liao J, Sauer K.

J Bacteriol. 2012 Sep;194(18):4823-36. doi: 10.1128/JB.00765-12. Epub 2012 Jun 22.

7.

Bis-(3'-5')-cyclic dimeric GMP regulates antimicrobial peptide resistance in Pseudomonas aeruginosa.

Chua SL, Tan SY, Rybtke MT, Chen Y, Rice SA, Kjelleberg S, Tolker-Nielsen T, Yang L, Givskov M.

Antimicrob Agents Chemother. 2013 May;57(5):2066-75. doi: 10.1128/AAC.02499-12. Epub 2013 Feb 12.

8.
9.

Cyclic-di-GMP levels affect Pseudomonas aeruginosa fitness in the presence of imipenem.

Nicastro GG, Kaihami GH, Pereira TO, Meireles DA, Groleau MC, Déziel E, Baldini RL.

Environ Microbiol. 2014 May;16(5):1321-33. doi: 10.1111/1462-2920.12422. Epub 2014 Mar 14.

PMID:
24975931
10.

Connecting quorum sensing, c-di-GMP, pel polysaccharide, and biofilm formation in Pseudomonas aeruginosa through tyrosine phosphatase TpbA (PA3885).

Ueda A, Wood TK.

PLoS Pathog. 2009 Jun;5(6):e1000483. doi: 10.1371/journal.ppat.1000483. Epub 2009 Jun 19.

11.

The Pseudomonas aeruginosa sensor RetS switches type III and type VI secretion via c-di-GMP signalling.

Moscoso JA, Mikkelsen H, Heeb S, Williams P, Filloux A.

Environ Microbiol. 2011 Dec;13(12):3128-38. doi: 10.1111/j.1462-2920.2011.02595.x. Epub 2011 Sep 29. Erratum in: Environ Microbiol. 2012 Apr;14(4):1088-9.

PMID:
21955777
12.

Aminoglycoside antibiotics induce bacterial biofilm formation.

Hoffman LR, D'Argenio DA, MacCoss MJ, Zhang Z, Jones RA, Miller SI.

Nature. 2005 Aug 25;436(7054):1171-5.

PMID:
16121184
13.

Cyclic-di-GMP levels affect Pseudomonas aeruginosa fitness in the presence of imipenem.

Nicastro GG, Kaihami GH, Pereira TO, Meireles DA, Groleau MC, Déziel E, Baldini RL.

Environ Microbiol. 2014 May;16(5):1321-33.

PMID:
25118352
14.

Cyclic di-GMP-mediated repression of swarming motility by Pseudomonas aeruginosa PA14 requires the MotAB stator.

Kuchma SL, Delalez NJ, Filkins LM, Snavely EA, Armitage JP, O'Toole GA.

J Bacteriol. 2015 Feb;197(3):420-30. doi: 10.1128/JB.02130-14. Epub 2014 Oct 27.

PMID:
25349157
15.

The second messenger bis-(3'-5')-cyclic-GMP and its PilZ domain-containing receptor Alg44 are required for alginate biosynthesis in Pseudomonas aeruginosa.

Merighi M, Lee VT, Hyodo M, Hayakawa Y, Lory S.

Mol Microbiol. 2007 Aug;65(4):876-95. Epub 2007 Jul 21.

PMID:
17645452
16.

Nitric oxide signaling in Pseudomonas aeruginosa biofilms mediates phosphodiesterase activity, decreased cyclic di-GMP levels, and enhanced dispersal.

Barraud N, Schleheck D, Klebensberger J, Webb JS, Hassett DJ, Rice SA, Kjelleberg S.

J Bacteriol. 2009 Dec;191(23):7333-42. doi: 10.1128/JB.00975-09. Epub 2009 Oct 2.

17.

Pseudomonas aeruginosa, under DNA replication inhibition, tends to form biofilms via Arr.

Gotoh H, Zhang Y, Dallo SF, Hong S, Kasaraneni N, Weitao T.

Res Microbiol. 2008 May;159(4):294-302. doi: 10.1016/j.resmic.2008.02.002. Epub 2008 Mar 7.

PMID:
18434096
18.

The FleQ protein from Pseudomonas aeruginosa functions as both a repressor and an activator to control gene expression from the pel operon promoter in response to c-di-GMP.

Baraquet C, Murakami K, Parsek MR, Harwood CS.

Nucleic Acids Res. 2012 Aug;40(15):7207-18. doi: 10.1093/nar/gks384. Epub 2012 May 11.

19.

Multiple activities of c-di-GMP in Pseudomonas aeruginosa.

Lory S, Merighi M, Hyodo M.

Nucleic Acids Symp Ser (Oxf). 2009;(53):51-2. doi: 10.1093/nass/nrp026.

20.

Specific control of Pseudomonas aeruginosa surface-associated behaviors by two c-di-GMP diguanylate cyclases.

Merritt JH, Ha DG, Cowles KN, Lu W, Morales DK, Rabinowitz J, Gitai Z, O'Toole GA.

MBio. 2010 Oct 19;1(4). pii: e00183-10. doi: 10.1128/mBio.00183-10.

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