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Journal Abstract Search

251 related items for 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
    [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 01; 309(2):296-304. PubMed ID: 16051214
    [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 01; 7(5):485-91. PubMed ID: 1384582
    [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 01; 2(4 Suppl):280-4. PubMed ID: 11875272
    [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 01; 40(4):388-97. PubMed ID: 18931328
    [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 01; 2(3):240-8. PubMed ID: 1285365
    [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 01; 580(Pt 1):301-14. PubMed ID: 17204498
    [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 01; 22(2):166-75. PubMed ID: 10657937
    [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 01; 7(11):1439-49. PubMed ID: 16001392
    [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 01; 15(1):122-31. PubMed ID: 8679216
    [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 Jul 01; 443 Suppl 1():S28-35. PubMed ID: 11845299
    [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 01; 37(6):631-9. PubMed ID: 17641299
    [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 01; 36(2):137-43. PubMed ID: 7526324
    [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 01; 20(4):684-91. PubMed ID: 10101000
    [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 01; 20(6):1107-15. PubMed ID: 10340929
    [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 01; 18(7):875-7. PubMed ID: 15001557
    [Abstract] [Full Text] [Related]

  • 17. Human tracheobronchial submucosal gland cells in culture.
    Sommerhoff CP, Finkbeiner WE.
    Am J Respir Cell Mol Biol; 1990 Jan 01; 2(1):41-50. PubMed ID: 2306368
    [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 01; 168(2):373-84. PubMed ID: 8707873
    [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 01; 10(4):355-62. PubMed ID: 7510983
    [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 05; 411(3):471-6. PubMed ID: 21723850
    [Abstract] [Full Text] [Related]

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