These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
374 related articles for article (PubMed ID: 8612275)
1. Cystic fibrosis airway epithelia fail to kill bacteria because of abnormal airway surface fluid. Smith JJ; Travis SM; Greenberg EP; Welsh MJ Cell; 1996 Apr; 85(2):229-36. PubMed ID: 8612275 [TBL] [Abstract][Full Text] [Related]
2. New models of the tracheal airway define the glandular contribution to airway surface fluid and electrolyte composition. Wang X; Zhang Y; Amberson A; Engelhardt JF Am J Respir Cell Mol Biol; 2001 Feb; 24(2):195-202. PubMed ID: 11159054 [TBL] [Abstract][Full Text] [Related]
3. Calcium and cAMP activate different chloride channels in the apical membrane of normal and cystic fibrosis epithelia. Anderson MP; Welsh MJ Proc Natl Acad Sci U S A; 1991 Jul; 88(14):6003-7. PubMed ID: 1712478 [TBL] [Abstract][Full Text] [Related]
4. Defective fluid transport by cystic fibrosis airway epithelia. Smith JJ; Karp PH; Welsh MJ J Clin Invest; 1994 Mar; 93(3):1307-11. PubMed ID: 8132771 [TBL] [Abstract][Full Text] [Related]
5. Loss of CFTR chloride channels alters salt absorption by cystic fibrosis airway epithelia in vitro. Zabner J; Smith JJ; Karp PH; Widdicombe JH; Welsh MJ Mol Cell; 1998 Sep; 2(3):397-403. PubMed ID: 9774978 [TBL] [Abstract][Full Text] [Related]
7. Modulation of Ca2+-activated Cl- secretion by basolateral K+ channels in human normal and cystic fibrosis airway epithelia. Mall M; Gonska T; Thomas J; Schreiber R; Seydewitz HH; Kuehr J; Brandis M; Kunzelmann K Pediatr Res; 2003 Apr; 53(4):608-18. PubMed ID: 12612194 [TBL] [Abstract][Full Text] [Related]
8. Abnormal regulation of ion channels in cystic fibrosis epithelia. Welsh MJ FASEB J; 1990 Jul; 4(10):2718-25. PubMed ID: 1695593 [TBL] [Abstract][Full Text] [Related]
9. Bioelectric properties of chloride channels in human, pig, ferret, and mouse airway epithelia. Liu X; Luo M; Zhang L; Ding W; Yan Z; Engelhardt JF Am J Respir Cell Mol Biol; 2007 Mar; 36(3):313-23. PubMed ID: 17008635 [TBL] [Abstract][Full Text] [Related]
10. Chloride channels in the apical membrane of normal and cystic fibrosis airway and intestinal epithelia. Anderson MP; Sheppard DN; Berger HA; Welsh MJ Am J Physiol; 1992 Jul; 263(1 Pt 1):L1-14. PubMed ID: 1322048 [TBL] [Abstract][Full Text] [Related]
11. Gene therapy for cystic fibrosis using E1-deleted adenovirus: a phase I trial in the nasal cavity. The University of North Carolina at Chapel Hill. Boucher RC; Knowles MR; Johnson LG; Olsen JC; Pickles R; Wilson JM; Engelhardt J; Yang Y; Grossman M Hum Gene Ther; 1994 May; 5(5):615-39. PubMed ID: 7519885 [TBL] [Abstract][Full Text] [Related]
12. A novel host defense system of airways is defective in cystic fibrosis. Moskwa P; Lorentzen D; Excoffon KJ; Zabner J; McCray PB; Nauseef WM; Dupuy C; Bánfi B Am J Respir Crit Care Med; 2007 Jan; 175(2):174-83. PubMed ID: 17082494 [TBL] [Abstract][Full Text] [Related]
13. Neutrophil extracellular trap (NET)-mediated killing of Pseudomonas aeruginosa: evidence of acquired resistance within the CF airway, independent of CFTR. Young RL; Malcolm KC; Kret JE; Caceres SM; Poch KR; Nichols DP; Taylor-Cousar JL; Saavedra MT; Randell SH; Vasil ML; Burns JL; Moskowitz SM; Nick JA PLoS One; 2011; 6(9):e23637. PubMed ID: 21909403 [TBL] [Abstract][Full Text] [Related]
14. The effect of chloride concentration on human neutrophil functions: potential relevance to cystic fibrosis. Tager AM; Wu J; Vermeulen MW Am J Respir Cell Mol Biol; 1998 Oct; 19(4):643-52. PubMed ID: 9761762 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Normalization of raised sodium absorption and raised calcium-mediated chloride secretion by adenovirus-mediated expression of cystic fibrosis transmembrane conductance regulator in primary human cystic fibrosis airway epithelial cells. Johnson LG; Boyles SE; Wilson J; Boucher RC J Clin Invest; 1995 Mar; 95(3):1377-82. PubMed ID: 7533790 [TBL] [Abstract][Full Text] [Related]
17. Adenovirus-mediated generation of cAMP-stimulated Cl- transport in cystic fibrosis airway epithelia in vitro: effect of promoter and administration method. Zabner J; Wadsworth SC; Smith AE; Welsh MJ Gene Ther; 1996 May; 3(5):458-65. PubMed ID: 9156806 [TBL] [Abstract][Full Text] [Related]