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1329 related items for PubMed ID: 9261986

  • 21. Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells.
    Rich DP, Anderson MP, Gregory RJ, Cheng SH, Paul S, Jefferson DM, McCann JD, Klinger KW, Smith AE, Welsh MJ.
    Nature; 1990 Sep 27; 347(6291):358-63. PubMed ID: 1699126
    [Abstract] [Full Text] [Related]

  • 22. Mutations in CFTR associated with mild-disease-form Cl- channels with altered pore properties.
    Sheppard DN, Rich DP, Ostedgaard LS, Gregory RJ, Smith AE, Welsh MJ.
    Nature; 1993 Mar 11; 362(6416):160-4. PubMed ID: 7680769
    [Abstract] [Full Text] [Related]

  • 23. The cystic fibrosis mutation (delta F508) does not influence the chloride channel activity of CFTR.
    Li C, Ramjeesingh M, Reyes E, Jensen T, Chang X, Rommens JM, Bear CE.
    Nat Genet; 1993 Apr 11; 3(4):311-6. PubMed ID: 7526932
    [Abstract] [Full Text] [Related]

  • 24. Defective regulation of gap junctional coupling in cystic fibrosis pancreatic duct cells.
    Chanson M, Scerri I, Suter S.
    J Clin Invest; 1999 Jun 11; 103(12):1677-84. PubMed ID: 10377174
    [Abstract] [Full Text] [Related]

  • 25. Expression of cystic fibrosis transmembrane conductance regulator in human gallbladder epithelial cells.
    Dray-Charier N, Paul A, Veissiere D, Mergey M, Scoazec JY, Capeau J, Brahimi-Horn C, Housset C.
    Lab Invest; 1995 Dec 11; 73(6):828-36. PubMed ID: 8558844
    [Abstract] [Full Text] [Related]

  • 26. Mouse cystic fibrosis transmembrane conductance regulator forms cAMP-PKA-regulated apical chloride channels in cortical collecting duct.
    Lu M, Dong K, Egan ME, Giebisch GH, Boulpaep EL, Hebert SC.
    Proc Natl Acad Sci U S A; 2010 Mar 30; 107(13):6082-7. PubMed ID: 20231442
    [Abstract] [Full Text] [Related]

  • 27. 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 30; 168(2):373-84. PubMed ID: 8707873
    [Abstract] [Full Text] [Related]

  • 28. Regulation of the cystic fibrosis transmembrane conductance regulator chloride channel by MgATP.
    Welsh MJ, Anderson MP.
    Soc Gen Physiol Ser; 1993 Aug 30; 48():119-27. PubMed ID: 7684867
    [Abstract] [Full Text] [Related]

  • 29. Chloride channels in the kidney: lessons learned from knockout animals.
    Devuyst O, Guggino WB.
    Am J Physiol Renal Physiol; 2002 Dec 30; 283(6):F1176-91. PubMed ID: 12426234
    [Abstract] [Full Text] [Related]

  • 30. CFTR null mutation altered cAMP-sensitive and swelling-activated Cl- currents in primary cultures of mouse nephron.
    Barrière H, Belfodil R, Rubera I, Tauc M, Poujeol C, Bidet M, Poujeol P.
    Am J Physiol Renal Physiol; 2003 Apr 30; 284(4):F796-811. PubMed ID: 12475744
    [Abstract] [Full Text] [Related]

  • 31. [CFTR protein and molecular mechanisms of pulmonary involvement in cystic fibrosis].
    Chinet T.
    Rev Pneumol Clin; 1995 Apr 30; 51(3):122-9. PubMed ID: 7569573
    [Abstract] [Full Text] [Related]

  • 32. [Cystic fibrosis lung disease and its management].
    Hidaka N, Hidaka Y.
    Nihon Rinsho; 1999 Sep 30; 57(9):2139-44. PubMed ID: 10497420
    [Abstract] [Full Text] [Related]

  • 33. Impact of the cystic fibrosis mutation F508del-CFTR on renal cyst formation and growth.
    Li H, Yang W, Mendes F, Amaral MD, Sheppard DN.
    Am J Physiol Renal Physiol; 2012 Oct 15; 303(8):F1176-86. PubMed ID: 22874761
    [Abstract] [Full Text] [Related]

  • 34. Early embryonic renal tubules of wild-type and polycystic kidney disease kidneys respond to cAMP stimulation with cystic fibrosis transmembrane conductance regulator/Na(+),K(+),2Cl(-) Co-transporter-dependent cystic dilation.
    Magenheimer BS, St John PL, Isom KS, Abrahamson DR, De Lisle RC, Wallace DP, Maser RL, Grantham JJ, Calvet JP.
    J Am Soc Nephrol; 2006 Dec 15; 17(12):3424-37. PubMed ID: 17108316
    [Abstract] [Full Text] [Related]

  • 35. Defective regulation of outwardly rectifying Cl- channels by protein kinase A corrected by insertion of CFTR.
    Egan M, Flotte T, Afione S, Solow R, Zeitlin PL, Carter BJ, Guggino WB.
    Nature; 1992 Aug 13; 358(6387):581-4. PubMed ID: 1380129
    [Abstract] [Full Text] [Related]

  • 36. CFTR regulation of epithelial sodium channel.
    Qadri YJ, Cormet-Boyaka E, Benos DJ, Berdiev BK.
    Methods Mol Biol; 2011 Aug 13; 742():35-50. PubMed ID: 21547725
    [Abstract] [Full Text] [Related]

  • 37. Correction of the Delta phe508 cystic fibrosis transmembrane conductance regulator trafficking defect by the bioavailable compound glafenine.
    Robert R, Carlile GW, Liao J, Balghi H, Lesimple P, Liu N, Kus B, Rotin D, Wilke M, de Jonge HR, Scholte BJ, Thomas DY, Hanrahan JW.
    Mol Pharmacol; 2010 Jun 13; 77(6):922-30. PubMed ID: 20200141
    [Abstract] [Full Text] [Related]

  • 38. [Ion transport in nasal and paranasal sinus mucosa in mucoviscidosis and chronic sinusitis].
    Rückes-Nilges C, Weber U, Popp C, Fryen A, Klimek T, Glanz H, Lindemann H, Münker G, Clauss W, Weber WM.
    HNO; 1999 Mar 13; 47(3):157-66. PubMed ID: 10231698
    [Abstract] [Full Text] [Related]

  • 39. mGluR1 interacts with cystic fibrosis transmembrane conductance regulator and modulates the secretion of IL-10 in cystic fibrosis peripheral lymphocytes.
    Shanshiashvili LV, Dabrundashvili N, Natsvlishvili N, Kvaratskhelia E, Zhuravliova E, Barbakadze T, Koriauli S, Maisuradze E, Topuria T, Mikeladze DG.
    Mol Immunol; 2012 Jul 13; 51(3-4):310-5. PubMed ID: 22520513
    [Abstract] [Full Text] [Related]

  • 40. Functional expression of cystic fibrosis transmembrane conductance regulator in mouse chondrocytes.
    Liang H, Yang L, Ma T, Zhao Y.
    Clin Exp Pharmacol Physiol; 2010 Apr 13; 37(4):506-8. PubMed ID: 19843093
    [Abstract] [Full Text] [Related]

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