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Journal Abstract Search

177 related items for PubMed ID: 15634668

  • 1. 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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  • 2. 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 11; 71(5):1360-8. PubMed ID: 17293558
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  • 8. 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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  • 9. Two positively charged amino acid side-chains in the inner vestibule of the CFTR channel pore play analogous roles in controlling anion binding and anion conductance.
    Linsdell P, Irving CL, Cowley EA, El Hiani Y.
    Cell Mol Life Sci; 2021 Jun 19; 78(12):5213-5223. PubMed ID: 34023918
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  • 10. 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 19; 457(2):351-60. PubMed ID: 18449561
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  • 11. Probing an open CFTR pore with organic anion blockers.
    Zhou Z, Hu S, Hwang TC.
    J Gen Physiol; 2002 Nov 19; 120(5):647-62. PubMed ID: 12407077
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  • 12. 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
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  • 16. 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 13; 78(1):15-22. PubMed ID: 31893350
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  • 17. Non-pore lining amino acid side chains influence anion selectivity of the human CFTR Cl- channel expressed in mammalian cell lines.
    Linsdell P, Zheng SX, Hanrahan JW.
    J Physiol; 1998 Oct 01; 512 ( Pt 1)(Pt 1):1-16. PubMed ID: 9729613
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  • 18. 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
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  • 19. 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 05; 78(6):2973-82. PubMed ID: 10827976
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  • 20. Substrates of multidrug resistance-associated proteins block the cystic fibrosis transmembrane conductance regulator chloride channel.
    Linsdell P, Hanrahan JW.
    Br J Pharmacol; 1999 Mar 05; 126(6):1471-7. PubMed ID: 10217542
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