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Journal Abstract Search

336 related items for PubMed ID: 11121762

  • 1. The role of the CFTR in susceptibility to Pseudomonas aeruginosa infections in cystic fibrosis.
    Goldberg JB, Pier GB.
    Trends Microbiol; 2000 Nov; 8(11):514-20. PubMed ID: 11121762
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  • 2. The role of CFTR protein susceptibility to bacterial infections in cystic fibrosis.
    Ramphal R.
    Trends Microbiol; 2001 Feb; 9(2):63. PubMed ID: 11286194
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  • 3. How mutant CFTR may contribute to Pseudomonas aeruginosa infection in cystic fibrosis.
    Pier GB, Grout M, Zaidi TS, Goldberg JB.
    Am J Respir Crit Care Med; 1996 Oct; 154(4 Pt 2):S175-82. PubMed ID: 8876538
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  • 6. Transgenic cystic fibrosis mice exhibit reduced early clearance of Pseudomonas aeruginosa from the respiratory tract.
    Schroeder TH, Reiniger N, Meluleni G, Grout M, Coleman FT, Pier GB.
    J Immunol; 2001 Jun 15; 166(12):7410-8. PubMed ID: 11390493
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  • 9. Quorum Sensing Down-Regulation Counteracts the Negative Impact of Pseudomonas aeruginosa on CFTR Channel Expression, Function and Rescue in Human Airway Epithelial Cells.
    Maillé É, Ruffin M, Adam D, Messaoud H, Lafayette SL, McKay G, Nguyen D, Brochiero E.
    Front Cell Infect Microbiol; 2017 Jun 15; 7():470. PubMed ID: 29177135
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  • 10. Role of the cystic fibrosis transmembrane conductance regulator in innate immunity to Pseudomonas aeruginosa infections.
    Pier GB.
    Proc Natl Acad Sci U S A; 2000 Aug 01; 97(16):8822-8. PubMed ID: 10922041
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  • 11. Cystic fibrosis transmembrane conductance regulator and caveolin-1 regulate epithelial cell internalization of Pseudomonas aeruginosa.
    Bajmoczi M, Gadjeva M, Alper SL, Pier GB, Golan DE.
    Am J Physiol Cell Physiol; 2009 Aug 01; 297(2):C263-77. PubMed ID: 19386787
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  • 12. Airway epithelial control of Pseudomonas aeruginosa infection in cystic fibrosis.
    Campodónico VL, Gadjeva M, Paradis-Bleau C, Uluer A, Pier GB.
    Trends Mol Med; 2008 Mar 01; 14(3):120-33. PubMed ID: 18262467
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  • 13. Deleterious impact of Pseudomonas aeruginosa on cystic fibrosis transmembrane conductance regulator function and rescue in airway epithelial cells.
    Trinh NT, Bilodeau C, Maillé É, Ruffin M, Quintal MC, Desrosiers MY, Rousseau S, Brochiero E.
    Eur Respir J; 2015 Jun 01; 45(6):1590-602. PubMed ID: 25792634
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  • 17. Cystic fibrosis transmembrane conductance regulator dysfunction in platelets drives lung hyperinflammation.
    Ortiz-Muñoz G, Yu MA, Lefrançais E, Mallavia B, Valet C, Tian JJ, Ranucci S, Wang KM, Liu Z, Kwaan N, Dawson D, Kleinhenz ME, Khasawneh FT, Haggie PM, Verkman AS, Looney MR.
    J Clin Invest; 2020 Apr 01; 130(4):2041-2053. PubMed ID: 31961827
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  • 18. Binding of Pseudomonas aeruginosa to respiratory epithelial cells from patients with various mutations in the cystic fibrosis transmembrane regulator.
    Zar H, Saiman L, Quittell L, Prince A.
    J Pediatr; 1995 Feb 01; 126(2):230-3. PubMed ID: 7531240
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  • 20. Pseudomonas aeruginosa Homoserine lactone activates store-operated cAMP and cystic fibrosis transmembrane regulator-dependent Cl- secretion by human airway epithelia.
    Schwarzer C, Wong S, Shi J, Matthes E, Illek B, Ianowski JP, Arant RJ, Isacoff E, Vais H, Foskett JK, Maiellaro I, Hofer AM, Machen TE.
    J Biol Chem; 2010 Nov 05; 285(45):34850-63. PubMed ID: 20739289
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