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Journal Abstract Search

156 related items for PubMed ID: 17293558

  • 1. Identification of a second blocker binding site at the cytoplasmic mouth of the cystic fibrosis transmembrane conductance regulator chloride channel pore.
    St Aubin CN, Zhou JJ, Linsdell P.
    Mol Pharmacol; 2007 May; 71(5):1360-8. PubMed ID: 17293558
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  • 2. Mechanism of chloride permeation in the cystic fibrosis transmembrane conductance regulator chloride channel.
    Linsdell P.
    Exp Physiol; 2006 Jan; 91(1):123-9. PubMed ID: 16157656
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  • 3. Location of a common inhibitor binding site in the cytoplasmic vestibule of the cystic fibrosis transmembrane conductance regulator chloride channel pore.
    Linsdell P.
    J Biol Chem; 2005 Mar 11; 280(10):8945-50. PubMed ID: 15634668
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  • 4. Evidence that extracellular anions interact with a site outside the CFTR chloride channel pore to modify channel properties.
    Zhou JJ, Linsdell P.
    Can J Physiol Pharmacol; 2009 May 11; 87(5):387-95. PubMed ID: 19448737
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  • 14. 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
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  • 15. Molecular determinants and role of an anion binding site in the external mouth of the CFTR chloride channel pore.
    Gong X, Linsdell P.
    J Physiol; 2003 Jun 01; 549(Pt 2):387-97. PubMed ID: 12679372
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  • 16. Identification of positive charges situated at the outer mouth of the CFTR chloride channel pore.
    Zhou JJ, Fatehi M, Linsdell P.
    Pflugers Arch; 2008 Nov 01; 457(2):351-60. PubMed ID: 18449561
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  • 17. Maximization of the rate of chloride conduction in the CFTR channel pore by ion-ion interactions.
    Gong X, Linsdell P.
    Arch Biochem Biophys; 2004 Jun 01; 426(1):78-82. PubMed ID: 15130785
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  • 19. Electrostatic Tuning of Anion Attraction from the Cytoplasm to the Pore of the CFTR Chloride Channel.
    Linsdell P, Negoda A, Cowley EA, El Hiani Y.
    Cell Biochem Biophys; 2020 Mar 01; 78(1):15-22. PubMed ID: 31893350
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  • 20. 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
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