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180 related items for PubMed ID: 7509074

  • 1. Identification of an ion channel-forming motif in the primary structure of CFTR, the cystic fibrosis chloride channel.
    Oblatt-Montal M, Reddy GL, Iwamoto T, Tomich JM, Montal M.
    Proc Natl Acad Sci U S A; 1994 Feb 15; 91(4):1495-9. PubMed ID: 7509074
    [Abstract] [Full Text] [Related]

  • 2. Design of a functional calcium channel protein: inferences about an ion channel-forming motif derived from the primary structure of voltage-gated calcium channels.
    Grove A, Tomich JM, Iwamoto T, Montal M.
    Protein Sci; 1993 Nov 15; 2(11):1918-30. PubMed ID: 7505682
    [Abstract] [Full Text] [Related]

  • 3. Anion conductance selectivity mechanism of the CFTR chloride channel.
    Linsdell P.
    Biochim Biophys Acta; 2016 Apr 15; 1858(4):740-7. PubMed ID: 26779604
    [Abstract] [Full Text] [Related]

  • 4. Rectification of cystic fibrosis transmembrane conductance regulator chloride channel mediated by extracellular divalent cations.
    Zhao J, Zerhusen B, Xie J, Drumm ML, Davis PB, Ma J.
    Biophys J; 1996 Nov 15; 71(5):2458-66. PubMed ID: 8913585
    [Abstract] [Full Text] [Related]

  • 5. Relationship between anion binding and anion permeability revealed by mutagenesis within the cystic fibrosis transmembrane conductance regulator chloride channel pore.
    Linsdell P.
    J Physiol; 2001 Feb 15; 531(Pt 1):51-66. PubMed ID: 11179391
    [Abstract] [Full Text] [Related]

  • 6. Multi-ion pore behaviour in the CFTR chloride channel.
    Tabcharani JA, Rommens JM, Hou YX, Chang XB, Tsui LC, Riordan JR, Hanrahan JW.
    Nature; 1993 Nov 04; 366(6450):79-82. PubMed ID: 7694154
    [Abstract] [Full Text] [Related]

  • 7. Effect of deletion mutations on the function of CFTR chloride channels.
    Rich DP, Gregory RJ, Cheng SH, Smith AE, Welsh MJ.
    Recept Channels; 1993 Nov 04; 1(3):221-32. PubMed ID: 7522901
    [Abstract] [Full Text] [Related]

  • 8. Synthetic peptides and four-helix bundle proteins as model systems for the pore-forming structure of channel proteins. II. Transmembrane segment M2 of the brain glycine receptor is a plausible candidate for the pore-lining structure.
    Reddy GL, Iwamoto T, Tomich JM, Montal M.
    J Biol Chem; 1993 Jul 15; 268(20):14608-15. PubMed ID: 7686901
    [Abstract] [Full Text] [Related]

  • 9. Asymmetric structure of the cystic fibrosis transmembrane conductance regulator chloride channel pore suggested by mutagenesis of the twelfth transmembrane region.
    Gupta J, Evagelidis A, Hanrahan JW, Linsdell P.
    Biochemistry; 2001 Jun 05; 40(22):6620-7. PubMed ID: 11380256
    [Abstract] [Full Text] [Related]

  • 10. A single conductance pore for chloride ions formed by two cystic fibrosis transmembrane conductance regulator molecules.
    Zerhusen B, Zhao J, Xie J, Davis PB, Ma J.
    J Biol Chem; 1999 Mar 19; 274(12):7627-30. PubMed ID: 10075649
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. Alternate translation initiation codons can create functional forms of cystic fibrosis transmembrane conductance regulator.
    Carroll TP, Morales MM, Fulmer SB, Allen SS, Flotte TR, Cutting GR, Guggino WB.
    J Biol Chem; 1995 May 19; 270(20):11941-6. PubMed ID: 7538127
    [Abstract] [Full Text] [Related]

  • 13. Slow conversions among subconductance states of cystic fibrosis transmembrane conductance regulator chloride channel.
    Tao T, Xie J, Drumm ML, Zhao J, Davis PB, Ma J.
    Biophys J; 1996 Feb 19; 70(2):743-53. PubMed ID: 8789091
    [Abstract] [Full Text] [Related]

  • 14. Identification and regulation of the cystic fibrosis transmembrane conductance regulator-generated chloride channel.
    Berger HA, Anderson MP, Gregory RJ, Thompson S, Howard PW, Maurer RA, Mulligan R, Smith AE, Welsh MJ.
    J Clin Invest; 1991 Oct 19; 88(4):1422-31. PubMed ID: 1717515
    [Abstract] [Full Text] [Related]

  • 15. Biochemical and biophysical identification of cystic fibrosis transmembrane conductance regulator chloride channels as components of endocytic clathrin-coated vesicles.
    Bradbury NA, Cohn JA, Venglarik CJ, Bridges RJ.
    J Biol Chem; 1994 Mar 18; 269(11):8296-302. PubMed ID: 7510684
    [Abstract] [Full Text] [Related]

  • 16. CFTR channels in immortalized human airway cells.
    Haws C, Krouse ME, Xia Y, Gruenert DC, Wine JJ.
    Am J Physiol; 1992 Dec 18; 263(6 Pt 1):L692-707. PubMed ID: 1282304
    [Abstract] [Full Text] [Related]

  • 17. Mechanism of chloride permeation in the cystic fibrosis transmembrane conductance regulator chloride channel.
    Linsdell P.
    Exp Physiol; 2006 Jan 18; 91(1):123-9. PubMed ID: 16157656
    [Abstract] [Full Text] [Related]

  • 18. Structural Changes Fundamental to Gating of the Cystic Fibrosis Transmembrane Conductance Regulator Anion Channel Pore.
    Linsdell P.
    Adv Exp Med Biol; 2017 Jan 18; 925():13-32. PubMed ID: 27311317
    [Abstract] [Full Text] [Related]

  • 19. Intrinsic anion channel activity of the recombinant first nucleotide binding fold domain of the cystic fibrosis transmembrane regulator protein.
    Arispe N, Rojas E, Hartman J, Sorscher EJ, Pollard HB.
    Proc Natl Acad Sci U S A; 1992 Mar 01; 89(5):1539-43. PubMed ID: 1371876
    [Abstract] [Full Text] [Related]

  • 20. 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]

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