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1471 related items for PubMed ID: 20203293

  • 1. Transient receptor potential canonical channel 6 links Ca2+ mishandling to cystic fibrosis transmembrane conductance regulator channel dysfunction in cystic fibrosis.
    Antigny F, Norez C, Dannhoffer L, Bertrand J, Raveau D, Corbi P, Jayle C, Becq F, Vandebrouck C.
    Am J Respir Cell Mol Biol; 2011 Jan; 44(1):83-90. PubMed ID: 20203293
    [Abstract] [Full Text] [Related]

  • 2. The low PLC-δ1 expression in cystic fibrosis bronchial epithelial cells induces upregulation of TRPV6 channel activity.
    Vachel L, Norez C, Jayle C, Becq F, Vandebrouck C.
    Cell Calcium; 2015 Jan; 57(1):38-48. PubMed ID: 25477137
    [Abstract] [Full Text] [Related]

  • 3. Abnormal spatial diffusion of Ca2+ in F508del-CFTR airway epithelial cells.
    Antigny F, Norez C, Cantereau A, Becq F, Vandebrouck C.
    Respir Res; 2008 Oct 30; 9(1):70. PubMed ID: 18973672
    [Abstract] [Full Text] [Related]

  • 4. Purinergic signaling underlies CFTR control of human airway epithelial cell volume.
    Braunstein GM, Zsembery A, Tucker TA, Schwiebert EM.
    J Cyst Fibros; 2004 Jun 30; 3(2):99-117. PubMed ID: 15463893
    [Abstract] [Full Text] [Related]

  • 5. Guanabenz, an alpha2-selective adrenergic agonist, activates Ca2+-dependent chloride currents in cystic fibrosis human airway epithelial cells.
    Norez C, Vandebrouck C, Antigny F, Dannhoffer L, Blondel M, Becq F.
    Eur J Pharmacol; 2008 Sep 11; 592(1-3):33-40. PubMed ID: 18640110
    [Abstract] [Full Text] [Related]

  • 6. Improvement of defective cystic fibrosis airway epithelial wound repair after CFTR rescue.
    Trinh NT, Bardou O, Privé A, Maillé E, Adam D, Lingée S, Ferraro P, Desrosiers MY, Coraux C, Brochiero E.
    Eur Respir J; 2012 Dec 11; 40(6):1390-400. PubMed ID: 22496330
    [Abstract] [Full Text] [Related]

  • 7. 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 11; 168(2):373-84. PubMed ID: 8707873
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. A cystic fibrosis respiratory epithelial cell chronically treated by miglustat acquires a non-cystic fibrosis-like phenotype.
    Norez C, Antigny F, Noel S, Vandebrouck C, Becq F.
    Am J Respir Cell Mol Biol; 2009 Aug 05; 41(2):217-25. PubMed ID: 19131642
    [Abstract] [Full Text] [Related]

  • 10. 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 05; 29(6):1624-34. PubMed ID: 10347100
    [Abstract] [Full Text] [Related]

  • 11. Proteomic and ionomic profiling reveals significant alterations of protein expression and calcium homeostasis in cystic fibrosis cells.
    Ciavardelli D, D'Orazio M, Pieroni L, Consalvo A, Rossi C, Sacchetta P, Di Ilio C, Battistoni A, Urbani A.
    Mol Biosyst; 2013 Jun 05; 9(6):1117-26. PubMed ID: 23609890
    [Abstract] [Full Text] [Related]

  • 12. The effect of ambroxol on chloride transport, CFTR and ENaC in cystic fibrosis airway epithelial cells.
    Varelogianni G, Hussain R, Strid H, Oliynyk I, Roomans GM, Johannesson M.
    Cell Biol Int; 2013 Nov 05; 37(11):1149-56. PubMed ID: 23765701
    [Abstract] [Full Text] [Related]

  • 13. A delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivo.
    French PJ, van Doorninck JH, Peters RH, Verbeek E, Ameen NA, Marino CR, de Jonge HR, Bijman J, Scholte BJ.
    J Clin Invest; 1996 Sep 15; 98(6):1304-12. PubMed ID: 8823295
    [Abstract] [Full Text] [Related]

  • 14. F508del-CFTR increases intracellular Ca(2+) signaling that causes enhanced calcium-dependent Cl(-) conductance in cystic fibrosis.
    Martins JR, Kongsuphol P, Sammels E, Dahimène S, Aldehni F, Clarke LA, Schreiber R, de Smedt H, Amaral MD, Kunzelmann K.
    Biochim Biophys Acta; 2011 Nov 15; 1812(11):1385-92. PubMed ID: 21907281
    [Abstract] [Full Text] [Related]

  • 15. Regulation of cystic fibrosis transmembrane conductance regulator by microRNA-145, -223, and -494 is altered in ΔF508 cystic fibrosis airway epithelium.
    Oglesby IK, Chotirmall SH, McElvaney NG, Greene CM.
    J Immunol; 2013 Apr 01; 190(7):3354-62. PubMed ID: 23436935
    [Abstract] [Full Text] [Related]

  • 16. Calcium-dependent regulation of NF-(kappa)B activation in cystic fibrosis airway epithelial cells.
    Tabary O, Boncoeur E, de Martin R, Pepperkok R, Clément A, Schultz C, Jacquot J.
    Cell Signal; 2006 May 01; 18(5):652-60. PubMed ID: 16084692
    [Abstract] [Full Text] [Related]

  • 17. Anoctamin 1 dysregulation alters bronchial epithelial repair in cystic fibrosis.
    Ruffin M, Voland M, Marie S, Bonora M, Blanchard E, Blouquit-Laye S, Naline E, Puyo P, Le Rouzic P, Guillot L, Corvol H, Clement A, Tabary O.
    Biochim Biophys Acta; 2013 Dec 01; 1832(12):2340-51. PubMed ID: 24080196
    [Abstract] [Full Text] [Related]

  • 18. Effect of VX-770 (ivacaftor) and OAG on Ca2+ influx and CFTR activity in G551D and F508del-CFTR expressing cells.
    Vachel L, Norez C, Becq F, Vandebrouck C.
    J Cyst Fibros; 2013 Dec 01; 12(6):584-91. PubMed ID: 23757361
    [Abstract] [Full Text] [Related]

  • 19. Cystic fibrosis transmembrane conductance regulator is expressed in mucin granules from Calu-3 and primary human airway epithelial cells.
    LeSimple P, Goepp J, Palmer ML, Fahrenkrug SC, O'Grady SM, Ferraro P, Robert R, Hanrahan JW.
    Am J Respir Cell Mol Biol; 2013 Oct 01; 49(4):511-6. PubMed ID: 23742042
    [Abstract] [Full Text] [Related]

  • 20. Expression of CFTR from a ciliated cell-specific promoter is ineffective at correcting nasal potential difference in CF mice.
    Ostrowski LE, Yin W, Diggs PS, Rogers TD, O'Neal WK, Grubb BR.
    Gene Ther; 2007 Oct 01; 14(20):1492-501. PubMed ID: 17637798
    [Abstract] [Full Text] [Related]

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