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Journal Abstract Search


180 related items for PubMed ID: 8789091

  • 1. Slow conversions among subconductance states of cystic fibrosis transmembrane conductance regulator chloride channel.
    Tao T, Xie J, Drumm ML, Zhao J, Davis PB, Ma J.
    Biophys J; 1996 Feb; 70(2):743-53. PubMed ID: 8789091
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  • 2. Rectification of cystic fibrosis transmembrane conductance regulator chloride channel mediated by extracellular divalent cations.
    Zhao J, Zerhusen B, Xie J, Drumm ML, Davis PB, Ma J.
    Biophys J; 1996 Nov; 71(5):2458-66. PubMed ID: 8913585
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  • 3. Human epithelial cystic fibrosis transmembrane conductance regulator without exon 5 maintains partial chloride channel function in intracellular membranes.
    Xie J, Drumm ML, Zhao J, Ma J, Davis PB.
    Biophys J; 1996 Dec; 71(6):3148-56. PubMed ID: 8968585
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  • 9. Acute inhibition of the cystic fibrosis transmembrane conductance regulator (CFTR) Cl- channel by thyroid hormones involves multiple mechanisms.
    Cai Z, Li H, Chen JH, Sheppard DN.
    Am J Physiol Cell Physiol; 2013 Oct 15; 305(8):C817-28. PubMed ID: 23784545
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  • 11. Conformational states of CFTR associated with channel gating: the role ATP binding and hydrolysis.
    Gunderson KL, Kopito RR.
    Cell; 1995 Jul 28; 82(2):231-9. PubMed ID: 7543023
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  • 12. 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
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  • 13. Inhibition of heterologously expressed cystic fibrosis transmembrane conductance regulator Cl- channels by non-sulphonylurea hypoglycaemic agents.
    Cai Z, Lansdell KA, Sheppard DN.
    Br J Pharmacol; 1999 Sep 07; 128(1):108-18. PubMed ID: 10498841
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  • 14. Functional and pharmacological induced structural changes of the cystic fibrosis transmembrane conductance regulator in the membrane solved using SAXS.
    Baroni D, Zegarra-Moran O, Moran O.
    Cell Mol Life Sci; 2015 Apr 07; 72(7):1363-75. PubMed ID: 25274064
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  • 17. Function of the R domain in the cystic fibrosis transmembrane conductance regulator chloride channel.
    Ma J, Zhao J, Drumm ML, Xie J, Davis PB.
    J Biol Chem; 1997 Oct 31; 272(44):28133-41. PubMed ID: 9346969
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  • 18. Cl- absorption across the thick ascending limb is not altered in cystic fibrosis mice. A role for a pseudo-CFTR Cl- channel.
    Marvão P, De Jesus Ferreira MC, Bailly C, Paulais M, Bens M, Guinamard R, Moreau R, Vandewalle A, Teulon J.
    J Clin Invest; 1998 Dec 01; 102(11):1986-93. PubMed ID: 9835624
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