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196 related items for PubMed ID: 9729613

  • 21. Disulphonic stilbene block of cystic fibrosis transmembrane conductance regulator Cl- channels expressed in a mammalian cell line and its regulation by a critical pore residue.
    Linsdell P, Hanrahan JW.
    J Physiol; 1996 Nov 01; 496 ( Pt 3)(Pt 3):687-93. PubMed ID: 8930836
    [Abstract] [Full Text] [Related]

  • 22. Molecular determinants of Au(CN)(2)(-) binding and permeability within the cystic fibrosis transmembrane conductance regulator Cl(-) channel pore.
    Gong X, Burbridge SM, Cowley EA, Linsdell P.
    J Physiol; 2002 Apr 01; 540(Pt 1):39-47. PubMed ID: 11927667
    [Abstract] [Full Text] [Related]

  • 23. Anion conductance selectivity mechanism of the CFTR chloride channel.
    Linsdell P.
    Biochim Biophys Acta; 2016 Apr 01; 1858(4):740-7. PubMed ID: 26779604
    [Abstract] [Full Text] [Related]

  • 24. Location of a permeant anion binding site in the cystic fibrosis transmembrane conductance regulator chloride channel pore.
    Rubaiy HN, Linsdell P.
    J Physiol Sci; 2015 May 01; 65(3):233-41. PubMed ID: 25673337
    [Abstract] [Full Text] [Related]

  • 25. The two halves of CFTR form a dual-pore ion channel.
    Yue H, Devidas S, Guggino WB.
    J Biol Chem; 2000 Apr 07; 275(14):10030-4. PubMed ID: 10744680
    [Abstract] [Full Text] [Related]

  • 26. Regulation of conductance by the number of fixed positive charges in the intracellular vestibule of the CFTR chloride channel pore.
    Zhou JJ, Li MS, Qi J, Linsdell P.
    J Gen Physiol; 2010 Mar 07; 135(3):229-45. PubMed ID: 20142516
    [Abstract] [Full Text] [Related]

  • 27. Intracellular loop between transmembrane segments IV and V of cystic fibrosis transmembrane conductance regulator is involved in regulation of chloride channel conductance state.
    Xie J, Drumm ML, Ma J, Davis PB.
    J Biol Chem; 1995 Nov 24; 270(47):28084-91. PubMed ID: 7499295
    [Abstract] [Full Text] [Related]

  • 28. Functional organization of cytoplasmic portals controlling access to the cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel pore.
    Li MS, Cowley EA, El Hiani Y, Linsdell P.
    J Biol Chem; 2018 Apr 13; 293(15):5649-5658. PubMed ID: 29475947
    [Abstract] [Full Text] [Related]

  • 29. Mutations at arginine 352 alter the pore architecture of CFTR.
    Cui G, Zhang ZR, O'Brien AR, Song B, McCarty NA.
    J Membr Biol; 2008 Mar 13; 222(2):91-106. PubMed ID: 18421494
    [Abstract] [Full Text] [Related]

  • 30. Direct comparison of the functional roles played by different transmembrane regions in the cystic fibrosis transmembrane conductance regulator chloride channel pore.
    Ge N, Muise CN, Gong X, Linsdell P.
    J Biol Chem; 2004 Dec 31; 279(53):55283-9. PubMed ID: 15504721
    [Abstract] [Full Text] [Related]

  • 31. Arg352 is a major determinant of charge selectivity in the cystic fibrosis transmembrane conductance regulator chloride channel.
    Guinamard R, Akabas MH.
    Biochemistry; 1999 Apr 27; 38(17):5528-37. PubMed ID: 10220340
    [Abstract] [Full Text] [Related]

  • 32. Functional differences in pore properties between wild-type and cysteine-less forms of the CFTR chloride channel.
    Holstead RG, Li MS, Linsdell P.
    J Membr Biol; 2011 Oct 27; 243(1-3):15-23. PubMed ID: 21796426
    [Abstract] [Full Text] [Related]

  • 33. Role of Hydrophobic Amino-Acid Side-Chains in the Narrow Selectivity Filter of the CFTR Chloride Channel Pore in Conductance and Selectivity.
    Linsdell P.
    J Membr Biol; 2023 Dec 27; 256(4-6):433-442. PubMed ID: 37823914
    [Abstract] [Full Text] [Related]

  • 34. Contribution of the eighth transmembrane segment to the function of the CFTR chloride channel pore.
    Negoda A, Hogan MS, Cowley EA, Linsdell P.
    Cell Mol Life Sci; 2019 Jun 27; 76(12):2411-2423. PubMed ID: 30758641
    [Abstract] [Full Text] [Related]

  • 35. Interaction between permeation and gating in a putative pore domain mutant in the cystic fibrosis transmembrane conductance regulator.
    Zhang ZR, McDonough SI, McCarty NA.
    Biophys J; 2000 Jul 27; 79(1):298-313. PubMed ID: 10866956
    [Abstract] [Full Text] [Related]

  • 36. The Fifth Transmembrane Segment of Cystic Fibrosis Transmembrane Conductance Regulator Contributes to Its Anion Permeation Pathway.
    Zhang J, Hwang TC.
    Biochemistry; 2015 Jun 23; 54(24):3839-50. PubMed ID: 26024338
    [Abstract] [Full Text] [Related]

  • 37. Halide permeation in wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels.
    Tabcharani JA, Linsdell P, Hanrahan JW.
    J Gen Physiol; 1997 Oct 23; 110(4):341-54. PubMed ID: 9379167
    [Abstract] [Full Text] [Related]

  • 38. Permeability of wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels to polyatomic anions.
    Linsdell P, Tabcharani JA, Rommens JM, Hou YX, Chang XB, Tsui LC, Riordan JR, Hanrahan JW.
    J Gen Physiol; 1997 Oct 23; 110(4):355-64. PubMed ID: 9379168
    [Abstract] [Full Text] [Related]

  • 39. Identification of a region of strong discrimination in the pore of CFTR.
    McCarty NA, Zhang ZR.
    Am J Physiol Lung Cell Mol Physiol; 2001 Oct 23; 281(4):L852-67. PubMed ID: 11557589
    [Abstract] [Full Text] [Related]

  • 40. Functional Architecture of the Cytoplasmic Entrance to the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel Pore.
    El Hiani Y, Linsdell P.
    J Biol Chem; 2015 Jun 19; 290(25):15855-15865. PubMed ID: 25944907
    [Abstract] [Full Text] [Related]

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