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360 related items for PubMed ID: 9508803

  • 1. Comparison of the gating behaviour of human and murine cystic fibrosis transmembrane conductance regulator Cl- channels expressed in mammalian cells.
    Lansdell KA, Delaney SJ, Lunn DP, Thomson SA, Sheppard DN, Wainwright BJ.
    J Physiol; 1998 Apr 15; 508 ( Pt 2)(Pt 2):379-92. PubMed ID: 9508803
    [Abstract] [Full Text] [Related]

  • 2. Regulation of murine cystic fibrosis transmembrane conductance regulator Cl- channels expressed in Chinese hamster ovary cells.
    Lansdell KA, Kidd JF, Delaney SJ, Wainwright BJ, Sheppard DN.
    J Physiol; 1998 Nov 01; 512 ( Pt 3)(Pt 3):751-64. PubMed ID: 9769419
    [Abstract] [Full Text] [Related]

  • 3. Clusters of Cl- channels in CFTR-expressing Sf9 cells switch spontaneously between slow and fast gating modes.
    Larsen EH, Price EM, Gabriel SE, Stutts MJ, Boucher RC.
    Pflugers Arch; 1996 Jul 01; 432(3):528-37. PubMed ID: 8766014
    [Abstract] [Full Text] [Related]

  • 4. Two mechanisms of genistein inhibition of cystic fibrosis transmembrane conductance regulator Cl- channels expressed in murine cell line.
    Lansdell KA, Cai Z, Kidd JF, Sheppard DN.
    J Physiol; 2000 Apr 15; 524 Pt 2(Pt 2):317-30. PubMed ID: 10766914
    [Abstract] [Full Text] [Related]

  • 5. G551D and G1349D, two CF-associated mutations in the signature sequences of CFTR, exhibit distinct gating defects.
    Bompadre SG, Sohma Y, Li M, Hwang TC.
    J Gen Physiol; 2007 Apr 15; 129(4):285-98. PubMed ID: 17353351
    [Abstract] [Full Text] [Related]

  • 6. Inhibition of heterologously expressed cystic fibrosis transmembrane conductance regulator Cl- channels by non-sulphonylurea hypoglycaemic agents.
    Cai Z, Lansdell KA, Sheppard DN.
    Br J Pharmacol; 1999 Sep 15; 128(1):108-18. PubMed ID: 10498841
    [Abstract] [Full Text] [Related]

  • 7. A cluster of negative charges at the amino terminal tail of CFTR regulates ATP-dependent channel gating.
    Fu J, Ji HL, Naren AP, Kirk KL.
    J Physiol; 2001 Oct 15; 536(Pt 2):459-70. PubMed ID: 11600681
    [Abstract] [Full Text] [Related]

  • 8. Dibasic protein kinase A sites regulate bursting rate and nucleotide sensitivity of the cystic fibrosis transmembrane conductance regulator chloride channel.
    Mathews CJ, Tabcharani JA, Chang XB, Jensen TJ, Riordan JR, Hanrahan JW.
    J Physiol; 1998 Apr 15; 508 ( Pt 2)(Pt 2):365-77. PubMed ID: 9508802
    [Abstract] [Full Text] [Related]

  • 9. Mechanism of glibenclamide inhibition of cystic fibrosis transmembrane conductance regulator Cl- channels expressed in a murine cell line.
    Sheppard DN, Robinson KA.
    J Physiol; 1997 Sep 01; 503 ( Pt 2)(Pt 2):333-46. PubMed ID: 9306276
    [Abstract] [Full Text] [Related]

  • 10. Regulation of the gating of cystic fibrosis transmembrane conductance regulator C1 channels by phosphorylation and ATP hydrolysis.
    Hwang TC, Nagel G, Nairn AC, Gadsby DC.
    Proc Natl Acad Sci U S A; 1994 May 24; 91(11):4698-702. PubMed ID: 7515176
    [Abstract] [Full Text] [Related]

  • 11. Deletion of phenylalanine 508 causes attenuated phosphorylation-dependent activation of CFTR chloride channels.
    Wang F, Zeltwanger S, Hu S, Hwang TC.
    J Physiol; 2000 May 01; 524 Pt 3(Pt 3):637-48. PubMed ID: 10790148
    [Abstract] [Full Text] [Related]

  • 12. Positioning of extracellular loop 1 affects pore gating of the cystic fibrosis transmembrane conductance regulator.
    Infield DT, Cui G, Kuang C, McCarty NA.
    Am J Physiol Lung Cell Mol Physiol; 2016 Mar 01; 310(5):L403-14. PubMed ID: 26684250
    [Abstract] [Full Text] [Related]

  • 13. CFTR gating I: Characterization of the ATP-dependent gating of a phosphorylation-independent CFTR channel (DeltaR-CFTR).
    Bompadre SG, Ai T, Cho JH, Wang X, Sohma Y, Li M, Hwang TC.
    J Gen Physiol; 2005 Apr 01; 125(4):361-75. PubMed ID: 15767295
    [Abstract] [Full Text] [Related]

  • 14. Disease-associated mutations in cytoplasmic loops 1 and 2 of cystic fibrosis transmembrane conductance regulator impede processing or opening of the channel.
    Seibert FS, Jia Y, Mathews CJ, Hanrahan JW, Riordan JR, Loo TW, Clarke DM.
    Biochemistry; 1997 Sep 30; 36(39):11966-74. PubMed ID: 9305991
    [Abstract] [Full Text] [Related]

  • 15. Prolonged nonhydrolytic interaction of nucleotide with CFTR's NH2-terminal nucleotide binding domain and its role in channel gating.
    Basso C, Vergani P, Nairn AC, Gadsby DC.
    J Gen Physiol; 2003 Sep 30; 122(3):333-48. PubMed ID: 12939393
    [Abstract] [Full Text] [Related]

  • 16. Altering intracellular pH reveals the kinetic basis of intraburst gating in the CFTR Cl- channel.
    Chen JH, Xu W, Sheppard DN.
    J Physiol; 2017 Feb 15; 595(4):1059-1076. PubMed ID: 27779763
    [Abstract] [Full Text] [Related]

  • 17. Effect of ATP concentration on CFTR Cl- channels: a kinetic analysis of channel regulation.
    Winter MC, Sheppard DN, Carson MR, Welsh MJ.
    Biophys J; 1994 May 15; 66(5):1398-403. PubMed ID: 7520292
    [Abstract] [Full Text] [Related]

  • 18. Gating of cystic fibrosis transmembrane conductance regulator chloride channels by adenosine triphosphate hydrolysis. Quantitative analysis of a cyclic gating scheme.
    Zeltwanger S, Wang F, Wang GT, Gillis KD, Hwang TC.
    J Gen Physiol; 1999 Apr 15; 113(4):541-54. PubMed ID: 10102935
    [Abstract] [Full Text] [Related]

  • 19. Expression of cystic fibrosis transmembrane conductance regulator alters the responses to hypotonic cell swelling and ATP of Chinese hamster ovary cells.
    Thiele IE, Hug MJ, Hübner M, Greger R.
    Cell Physiol Biochem; 1998 Apr 15; 8(1-2):61-74. PubMed ID: 9547020
    [Abstract] [Full Text] [Related]

  • 20. 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]

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