327 related articles for article (PubMed ID: 7680322)
1. Localization of the cystic fibrosis transmembrane conductance regulator in airway secretory glands.
Jacquot J; Puchelle E; Hinnrasky J; Fuchey C; Bettinger C; Spilmont C; Bonnet N; Dieterle A; Dreyer D; Pavirani A
Eur Respir J; 1993 Feb; 6(2):169-76. PubMed ID: 7680322
[TBL] [Abstract][Full Text] [Related]
2. Abnormal ion content, hydration and granule expansion of the secretory granules from cystic fibrosis airway glandular cells.
Baconnais S; Delavoie F; Zahm JM; Milliot M; Terryn C; Castillon N; Banchet V; Michel J; Danos O; Merten M; Chinet T; Zierold K; Bonnet N; Puchelle E; Balossier G
Exp Cell Res; 2005 Oct; 309(2):296-304. PubMed ID: 16051214
[TBL] [Abstract][Full Text] [Related]
3. Differential localization of the cystic fibrosis transmembrane conductance regulator in normal and cystic fibrosis airway epithelium.
Puchelle E; Gaillard D; Ploton D; Hinnrasky J; Fuchey C; Boutterin MC; Jacquot J; Dreyer D; Pavirani A; Dalemans W
Am J Respir Cell Mol Biol; 1992 Nov; 7(5):485-91. PubMed ID: 1384582
[TBL] [Abstract][Full Text] [Related]
4. HCO3- transport in relation to mucus secretion from submucosal glands.
Joo NS; Krouse ME; Wu JV; Saenz Y; Jayaraman S; Verkman AS; Wine JJ
JOP; 2001 Jul; 2(4 Suppl):280-4. PubMed ID: 11875272
[TBL] [Abstract][Full Text] [Related]
5. Salmeterol restores secretory functions in cystic fibrosis airway submucosal gland serous cells.
Delavoie F; Molinari M; Milliot M; Zahm JM; Coraux C; Michel J; Balossier G
Am J Respir Cell Mol Biol; 2009 Apr; 40(4):388-97. PubMed ID: 18931328
[TBL] [Abstract][Full Text] [Related]
6. Submucosal glands are the predominant site of CFTR expression in the human bronchus.
Engelhardt JF; Yankaskas JR; Ernst SA; Yang Y; Marino CR; Boucher RC; Cohn JA; Wilson JM
Nat Genet; 1992 Nov; 2(3):240-8. PubMed ID: 1285365
[TBL] [Abstract][Full Text] [Related]
7. Mucus secretion by single tracheal submucosal glands from normal and cystic fibrosis transmembrane conductance regulator knockout mice.
Ianowski JP; Choi JY; Wine JJ; Hanrahan JW
J Physiol; 2007 Apr; 580(Pt 1):301-14. PubMed ID: 17204498
[TBL] [Abstract][Full Text] [Related]
8. Efficient gene transfer into human normal and cystic fibrosis tracheal gland serous cells with synthetic vectors.
Allo JC; Midoux P; Merten M; Souil E; Lipecka J; Figarella C; Monsigny M; Briand P; Fajac I
Am J Respir Cell Mol Biol; 2000 Feb; 22(2):166-75. PubMed ID: 10657937
[TBL] [Abstract][Full Text] [Related]
9. Inhibition by TNF-alpha and IL-4 of cationic lipid mediated gene transfer in cystic fibrosis tracheal gland cells.
Bastonero S; Gargouri M; Ortiou S; Guéant JL; Merten MD
J Gene Med; 2005 Nov; 7(11):1439-49. PubMed ID: 16001392
[TBL] [Abstract][Full Text] [Related]
10. Developmental expression patterns of CFTR in ferret tracheal surface airway and submucosal gland epithelia.
Sehgal A; Presente A; Engelhardt JF
Am J Respir Cell Mol Biol; 1996 Jul; 15(1):122-31. PubMed ID: 8679216
[TBL] [Abstract][Full Text] [Related]
11. Ultrastructural changes in exocrine tissues of a DeltaF-508 CFTR mouse model.
Thomopoulos GN; Shori DK; Asking B; Kosta A; Dimopoulou A; Paterson K; Hartley R; Colledge WH
Pflugers Arch; 2001; 443 Suppl 1():S28-35. PubMed ID: 11845299
[TBL] [Abstract][Full Text] [Related]
12. Cellular localization and activity of Ad-delivered GFP-CFTR in airway epithelial and tracheal cells.
Granio O; Norez C; Ashbourne Excoffon KJ; Karp PH; Lusky M; Becq F; Boulanger P; Zabner J; Hong SS
Am J Respir Cell Mol Biol; 2007 Dec; 37(6):631-9. PubMed ID: 17641299
[TBL] [Abstract][Full Text] [Related]
13. Immunohistochemical localization of cystic fibrosis transmembrane conductance regulator in human fetal airway and digestive mucosa.
Gaillard D; Ruocco S; Lallemand A; Dalemans W; Hinnrasky J; Puchelle E
Pediatr Res; 1994 Aug; 36(2):137-43. PubMed ID: 7526324
[TBL] [Abstract][Full Text] [Related]
14. A cystic fibrosis tracheal gland cell line, CF-KM4. Correction by adenovirus-mediated CFTR gene transfer.
Kammouni W; Moreau B; Becq F; Saleh A; Pavirani A; Figarella C; Merten MD
Am J Respir Cell Mol Biol; 1999 Apr; 20(4):684-91. PubMed ID: 10101000
[TBL] [Abstract][Full Text] [Related]
15. Restoration of cyclic adenosine monophosphate-stimulated chloride channel activity in human cystic fibrosis tracheobronchial submucosal gland cells by adenovirus-mediated and cationic lipid-mediated gene transfer.
Jiang C; Finkbeiner WE; Widdicombe JH; Fang SL; Wang KX; Nietupski JB; Hehir KM; Cheng SH
Am J Respir Cell Mol Biol; 1999 Jun; 20(6):1107-15. PubMed ID: 10340929
[TBL] [Abstract][Full Text] [Related]
16. A small molecule CFTR inhibitor produces cystic fibrosis-like submucosal gland fluid secretions in normal airways.
Thiagarajah JR; Song Y; Haggie PM; Verkman AS
FASEB J; 2004 May; 18(7):875-7. PubMed ID: 15001557
[TBL] [Abstract][Full Text] [Related]
17. Human tracheobronchial submucosal gland cells in culture.
Sommerhoff CP; Finkbeiner WE
Am J Respir Cell Mol Biol; 1990 Jan; 2(1):41-50. PubMed ID: 2306368
[TBL] [Abstract][Full Text] [Related]
18. Turnover of the cystic fibrosis transmembrane conductance regulator (CFTR): slow degradation of wild-type and delta F508 CFTR in surface membrane preparations of immortalized airway epithelial cells.
Wei X; Eisman R; Xu J; Harsch AD; Mulberg AE; Bevins CL; Glick MC; Scanlin TF
J Cell Physiol; 1996 Aug; 168(2):373-84. PubMed ID: 8707873
[TBL] [Abstract][Full Text] [Related]
19. Regional expression of CFTR in developing human respiratory tissues.
Tizzano EF; O'Brodovich H; Chitayat D; Bènichou JC; Buchwald M
Am J Respir Cell Mol Biol; 1994 Apr; 10(4):355-62. PubMed ID: 7510983
[TBL] [Abstract][Full Text] [Related]
20. Reduced expression of Tis7/IFRD1 protein in murine and human cystic fibrosis airway epithelial cell models homozygous for the F508del-CFTR mutation.
Blanchard E; Marie S; Riffault L; Bonora M; Tabary O; Clement A; Jacquot J
Biochem Biophys Res Commun; 2011 Aug; 411(3):471-6. PubMed ID: 21723850
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]