167 related articles for article (PubMed ID: 7531240)
1. 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; 126(2):230-3. PubMed ID: 7531240
[TBL] [Abstract][Full Text] [Related]
2. CFTR gene transfer reduces the binding of Pseudomonas aeruginosa to cystic fibrosis respiratory epithelium.
Davies JC; Stern M; Dewar A; Caplen NJ; Munkonge FM; Pitt T; Sorgi F; Huang L; Bush A; Geddes DM; Alton EW
Am J Respir Cell Mol Biol; 1997 Jun; 16(6):657-63. PubMed ID: 9191467
[TBL] [Abstract][Full Text] [Related]
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
[TBL] [Abstract][Full Text] [Related]
4. Genetic determinants of airways' colonisation with Pseudomonas aeruginosa in cystic fibrosis.
Kubesch P; Dörk T; Wulbrand U; Kälin N; Neumann T; Wulf B; Geerlings H; Weissbrodt H; von der Hardt H; Tümmler B
Lancet; 1993 Jan; 341(8839):189-93. PubMed ID: 7678316
[TBL] [Abstract][Full Text] [Related]
5. Asialo GM1 is a receptor for Pseudomonas aeruginosa adherence to regenerating respiratory epithelial cells.
de Bentzmann S; Roger P; Dupuit F; Bajolet-Laudinat O; Fuchey C; Plotkowski MC; Puchelle E
Infect Immun; 1996 May; 64(5):1582-8. PubMed ID: 8613364
[TBL] [Abstract][Full Text] [Related]
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; 166(12):7410-8. PubMed ID: 11390493
[TBL] [Abstract][Full Text] [Related]
7. 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
[TBL] [Abstract][Full Text] [Related]
8. Inflammation in cystic fibrosis airways: relationship to increased bacterial adherence.
Scheid P; Kempster L; Griesenbach U; Davies JC; Dewar A; Weber PP; Colledge WH; Evans MJ; Geddes DM; Alton EW
Eur Respir J; 2001 Jan; 17(1):27-35. PubMed ID: 11307750
[TBL] [Abstract][Full Text] [Related]
9. Severe deficiency of cystic fibrosis transmembrane conductance regulator messenger RNA carrying nonsense mutations R553X and W1316X in respiratory epithelial cells of patients with cystic fibrosis.
Hamosh A; Trapnell BC; Zeitlin PL; Montrose-Rafizadeh C; Rosenstein BJ; Crystal RG; Cutting GR
J Clin Invest; 1991 Dec; 88(6):1880-5. PubMed ID: 1721624
[TBL] [Abstract][Full Text] [Related]
10. Role of mutant CFTR in hypersusceptibility of cystic fibrosis patients to lung infections.
Pier GB; Grout M; Zaidi TS; Olsen JC; Johnson LG; Yankaskas JR; Goldberg JB
Science; 1996 Jan; 271(5245):64-7. PubMed ID: 8539601
[TBL] [Abstract][Full Text] [Related]
11. Cystic fibrosis transmembrane conductance regulator channel dysfunction in non-cystic fibrosis bronchiectasis.
Bienvenu T; Sermet-Gaudelus I; Burgel PR; Hubert D; Crestani B; Bassinet L; Dusser D; Fajac I
Am J Respir Crit Care Med; 2010 May; 181(10):1078-84. PubMed ID: 20167849
[TBL] [Abstract][Full Text] [Related]
12. Role of the cystic fibrosis transmembrane conductance regulator in internalization of Pseudomonas aeruginosa by polarized respiratory epithelial cells.
Darling KE; Dewar A; Evans TJ
Cell Microbiol; 2004 Jun; 6(6):521-33. PubMed ID: 15104594
[TBL] [Abstract][Full Text] [Related]
13. Pseudomonas aeruginosa-induced bleb-niche formation in epithelial cells is independent of actinomyosin contraction and enhanced by loss of cystic fibrosis transmembrane-conductance regulator osmoregulatory function.
Jolly AL; Takawira D; Oke OO; Whiteside SA; Chang SW; Wen ER; Quach K; Evans DJ; Fleiszig SM
mBio; 2015 Feb; 6(2):e02533. PubMed ID: 25714715
[TBL] [Abstract][Full Text] [Related]
14. CFTR genotype and clinical outcomes of adult patients carried as cystic fibrosis disease.
Bonadia LC; de Lima Marson FA; Ribeiro JD; Paschoal IA; Pereira MC; Ribeiro AF; Bertuzzo CS
Gene; 2014 May; 540(2):183-90. PubMed ID: 24583165
[TBL] [Abstract][Full Text] [Related]
15. Pseudomonas aeruginosa-induced apoptosis is defective in respiratory epithelial cells expressing mutant cystic fibrosis transmembrane conductance regulator.
Cannon CL; Kowalski MP; Stopak KS; Pier GB
Am J Respir Cell Mol Biol; 2003 Aug; 29(2):188-97. PubMed ID: 12878584
[TBL] [Abstract][Full Text] [Related]
16. Cysteamine re-establishes the clearance of Pseudomonas aeruginosa by macrophages bearing the cystic fibrosis-relevant F508del-CFTR mutation.
Ferrari E; Monzani R; Villella VR; Esposito S; Saluzzo F; Rossin F; D'Eletto M; Tosco A; De Gregorio F; Izzo V; Maiuri MC; Kroemer G; Raia V; Maiuri L
Cell Death Dis; 2017 Jan; 8(1):e2544. PubMed ID: 28079883
[TBL] [Abstract][Full Text] [Related]
17. Expression of delta F508 cystic fibrosis transmembrane conductance regulator protein and related chloride transport properties in the gallbladder epithelium from cystic fibrosis patients.
Dray-Charier N; Paul A; Scoazec JY; Veissière D; Mergey M; Capeau J; Soubrane O; Housset C
Hepatology; 1999 Jun; 29(6):1624-34. PubMed ID: 10347100
[TBL] [Abstract][Full Text] [Related]
18. Serum zinc concentration in cystic fibrosis patients with CFTR I1234V mutation associated with pancreatic sufficiency.
AbdulWahab A; Abushahin A; Allangawi M; Chandra P; Abdel Rahman MO; Soliman A
Clin Respir J; 2017 May; 11(3):305-310. PubMed ID: 26096753
[TBL] [Abstract][Full Text] [Related]
19. DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis.
Viel M; Hubert D; Burgel PR; Génin E; Honoré I; Martinez B; Gaitch N; Chapron J; Kanaan R; Dusser D; Girodon E; Bienvenu T
Clin Respir J; 2016 Nov; 10(6):777-783. PubMed ID: 25763772
[TBL] [Abstract][Full Text] [Related]
20. Induction of type I interferon signaling by Pseudomonas aeruginosa is diminished in cystic fibrosis epithelial cells.
Parker D; Cohen TS; Alhede M; Harfenist BS; Martin FJ; Prince A
Am J Respir Cell Mol Biol; 2012 Jan; 46(1):6-13. PubMed ID: 21778412
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
