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Journal Abstract Search

224 related items for PubMed ID: 9379167

  • 1. 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; 110(4):341-54. PubMed ID: 9379167
    [Abstract] [Full Text] [Related]

  • 2. CFTR channels expressed in CHO cells do not have detectable ATP conductance.
    Grygorczyk R, Tabcharani JA, Hanrahan JW.
    J Membr Biol; 1996 May; 151(2):139-48. PubMed ID: 8661502
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. 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 15; 110(4):355-64. PubMed ID: 9379168
    [Abstract] [Full Text] [Related]

  • 5. 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 15; 110(4):365-77. PubMed ID: 9379169
    [Abstract] [Full Text] [Related]

  • 6. Clusters of Cl- channels in CFTR-expressing Sf9 cells switch spontaneously between slow and fast gating modes.
    Larsen EH, Price EM, Gabriel SE, Stutts MJ, Boucher RC.
    Pflugers Arch; 1996 Jul 15; 432(3):528-37. PubMed ID: 8766014
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  • 10. Interaction between permeation and gating in a putative pore domain mutant in the cystic fibrosis transmembrane conductance regulator.
    Zhang ZR, McDonough SI, McCarty NA.
    Biophys J; 2000 Jul 15; 79(1):298-313. PubMed ID: 10866956
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  • 11. Positive charges at the intracellular mouth of the pore regulate anion conduction in the CFTR chloride channel.
    Aubin CN, Linsdell P.
    J Gen Physiol; 2006 Nov 15; 128(5):535-45. PubMed ID: 17043152
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  • 12. CFTR channels in immortalized human airway cells.
    Haws C, Krouse ME, Xia Y, Gruenert DC, Wine JJ.
    Am J Physiol; 1992 Dec 15; 263(6 Pt 1):L692-707. PubMed ID: 1282304
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  • 14. 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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  • 15. Expression of cystic fibrosis transmembrane conductance regulator alters the responses to hypotonic cell swelling and ATP of Chinese hamster ovary cells.
    Thiele IE, Hug MJ, Hübner M, Greger R.
    Cell Physiol Biochem; 1998 Jun 05; 8(1-2):61-74. PubMed ID: 9547020
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  • 16. 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
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  • 18. Adenosine triphosphate-dependent asymmetry of anion permeation in the cystic fibrosis transmembrane conductance regulator chloride channel.
    Linsdell P, Hanrahan JW.
    J Gen Physiol; 1998 Apr 04; 111(4):601-14. PubMed ID: 9524141
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  • 19. 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
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