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Journal Abstract Search

317 related items for PubMed ID: 27311317

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  • 2. Conformational changes opening and closing the CFTR chloride channel: insights from cysteine scanning mutagenesis.
    El Hiani Y, Linsdell P.
    Biochem Cell Biol; 2014 Dec; 92(6):481-8. PubMed ID: 25367045
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  • 5. Cystic fibrosis transmembrane conductance regulator (CFTR): Making an ion channel out of an active transporter structure.
    Linsdell P.
    Channels (Austin); 2018 Dec; 12(1):284-290. PubMed ID: 30152709
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  • 6. The gating of the CFTR channel.
    Moran O.
    Cell Mol Life Sci; 2017 Jan; 74(1):85-92. PubMed ID: 27696113
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  • 9. Molecular Dynamics Flexible Fitting Simulations Identify New Models of the Closed State of the Cystic Fibrosis Transmembrane Conductance Regulator Protein.
    Simhaev L, McCarty NA, Ford RC, Senderowitz H.
    J Chem Inf Model; 2017 Aug 28; 57(8):1932-1946. PubMed ID: 28657312
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  • 15. 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. The role of cystic fibrosis transmembrane conductance regulator phenylalanine 508 side chain in ion channel gating.
    Cui L, Aleksandrov L, Hou YX, Gentzsch M, Chen JH, Riordan JR, Aleksandrov AA.
    J Physiol; 2006 Apr 15; 572(Pt 2):347-58. PubMed ID: 16484308
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  • 17. Functional architecture of the CFTR chloride channel.
    Linsdell P.
    Mol Membr Biol; 2014 Feb 15; 31(1):1-16. PubMed ID: 24341413
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