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357 related items for PubMed ID: 11179391

  • 1. 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]

  • 2. 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]

  • 3. 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]

  • 4. 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]

  • 5. Thiocyanate as a probe of the cystic fibrosis transmembrane conductance regulator chloride channel pore.
    Linsdell P.
    Can J Physiol Pharmacol; 2001 Jul 01; 79(7):573-9. PubMed ID: 11478590
    [Abstract] [Full Text] [Related]

  • 6. Molecular determinants of anion selectivity in the cystic fibrosis transmembrane conductance regulator chloride channel pore.
    Linsdell P, Evagelidis A, Hanrahan JW.
    Biophys J; 2000 Jun 01; 78(6):2973-82. PubMed ID: 10827976
    [Abstract] [Full Text] [Related]

  • 7. 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 01; 110(4):341-54. PubMed ID: 9379167
    [Abstract] [Full Text] [Related]

  • 8. Anion permeation in Ca(2+)-activated Cl(-) channels.
    Qu Z, Hartzell HC.
    J Gen Physiol; 2000 Dec 01; 116(6):825-44. PubMed ID: 11099350
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. Interactions between permeant and blocking anions inside the CFTR chloride channel pore.
    Linsdell P.
    Biochim Biophys Acta; 2015 Jul 04; 1848(7):1573-90. PubMed ID: 25892339
    [Abstract] [Full Text] [Related]

  • 11. 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 04; 110(4):355-64. PubMed ID: 9379168
    [Abstract] [Full Text] [Related]

  • 12. Multi-Ion mechanism for ion permeation and block in the cystic fibrosis transmembrane conductance regulator chloride channel.
    Linsdell P, Tabcharani JA, Hanrahan JW.
    J Gen Physiol; 1997 Oct 04; 110(4):365-77. PubMed ID: 9379169
    [Abstract] [Full Text] [Related]

  • 13. Cystic fibrosis transmembrane conductance regulator. Physical basis for lyotropic anion selectivity patterns.
    Smith SS, Steinle ED, Meyerhoff ME, Dawson DC.
    J Gen Physiol; 1999 Dec 04; 114(6):799-818. PubMed ID: 10578016
    [Abstract] [Full Text] [Related]

  • 14. Mouse bestrophin-2 is a bona fide Cl(-) channel: identification of a residue important in anion binding and conduction.
    Qu Z, Fischmeister R, Hartzell C.
    J Gen Physiol; 2004 Apr 04; 123(4):327-40. PubMed ID: 15051805
    [Abstract] [Full Text] [Related]

  • 15. 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 04; 65(3):233-41. PubMed ID: 25673337
    [Abstract] [Full Text] [Related]

  • 16. Mutation-induced blocker permeability and multiion block of the CFTR chloride channel pore.
    Gong X, Linsdell P.
    J Gen Physiol; 2003 Dec 04; 122(6):673-87. PubMed ID: 14610019
    [Abstract] [Full Text] [Related]

  • 17. Anion selectivity of apical membrane conductance of Calu 3 human airway epithelium.
    Illek B, Tam AW, Fischer H, Machen TE.
    Pflugers Arch; 1999 May 04; 437(6):812-22. PubMed ID: 10370058
    [Abstract] [Full Text] [Related]

  • 18. Extent of the selectivity filter conferred by the sixth transmembrane region in the CFTR chloride channel pore.
    Gupta J, Lindsell P.
    Mol Membr Biol; 2003 May 04; 20(1):45-52. PubMed ID: 12745925
    [Abstract] [Full Text] [Related]

  • 19. Monovalent: Divalent Anion Selectivity in the CFTR Channel Pore.
    Linsdell P.
    Cell Biochem Biophys; 2021 Dec 04; 79(4):863-871. PubMed ID: 34031860
    [Abstract] [Full Text] [Related]

  • 20. Mutations in the putative pore-forming domain of CFTR do not change anion selectivity of the cAMP activated Cl- conductance.
    Hipper A, Mall M, Greger R, Kunzelmann K.
    FEBS Lett; 1995 Nov 06; 374(3):312-6. PubMed ID: 7589561
    [Abstract] [Full Text] [Related]

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