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Journal Abstract Search

162 related items for PubMed ID: 16020465

  • 1. Separation of P/C- and U-type inactivation pathways in Kv1.5 potassium channels.
    Kurata HT, Doerksen KW, Eldstrom JR, Rezazadeh S, Fedida D.
    J Physiol; 2005 Oct 01; 568(Pt 1):31-46. PubMed ID: 16020465
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  • 2. NH2-terminal inactivation peptide binding to C-type-inactivated Kv channels.
    Kurata HT, Wang Z, Fedida D.
    J Gen Physiol; 2004 May 01; 123(5):505-20. PubMed ID: 15078918
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  • 3. Accessory Kvbeta1 subunits differentially modulate the functional expression of voltage-gated K+ channels in mouse ventricular myocytes.
    Aimond F, Kwak SP, Rhodes KJ, Nerbonne JM.
    Circ Res; 2005 Mar 04; 96(4):451-8. PubMed ID: 15662035
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  • 5. Constitutive inactivation of the hKv1.5 mutant channel, H463G, in K+-free solutions at physiological pH.
    Zhang S, Eduljee C, Kwan DC, Kehl SJ, Fedida D.
    Cell Biochem Biophys; 2005 Mar 04; 43(2):221-30. PubMed ID: 16049347
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  • 6. External pore collapse as an inactivation mechanism for Kv4.3 K+ channels.
    Eghbali M, Olcese R, Zarei MM, Toro L, Stefani E.
    J Membr Biol; 2002 Jul 01; 188(1):73-86. PubMed ID: 12172648
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  • 9. Structural basis for competition between drug binding and Kvbeta 1.3 accessory subunit-induced N-type inactivation of Kv1.5 channels.
    Decher N, Kumar P, Gonzalez T, Renigunta V, Sanguinetti MC.
    Mol Pharmacol; 2005 Oct 01; 68(4):995-1005. PubMed ID: 16024663
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  • 12. Influence of permeating ions on Kv1.5 channel block by nifedipine.
    Lin S, Wang Z, Fedida D.
    Am J Physiol Heart Circ Physiol; 2001 Mar 01; 280(3):H1160-72. PubMed ID: 11179060
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  • 13. Rapid outer pore movements after opening in a KV1 potassium channel are revealed by TMRM fluorescence from the S3-S4 linker, and modulated by extracellular potassium.
    Vaid M, Horne A, Claydon T, Fedida D.
    Channels (Austin); 2009 Mar 01; 3(1):3-5. PubMed ID: 19077547
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  • 15. Effects of Kv1.1 channel glycosylation on C-type inactivation and simulated action potentials.
    Sutachan JJ, Watanabe I, Zhu J, Gottschalk A, Recio-Pinto E, Thornhill WB.
    Brain Res; 2005 Oct 05; 1058(1-2):30-43. PubMed ID: 16153617
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  • 16. Carvedilol blocks the cloned cardiac Kv1.5 channels in a β-adrenergic receptor-independent manner.
    Jeong I, Choi BH, Yoon SH, Hahn SJ.
    Biochem Pharmacol; 2012 Feb 15; 83(4):497-505. PubMed ID: 22146582
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  • 17. HMJ-53A accelerates slow inactivation gating of voltage-gated K+ channels in mouse neuroblastoma N2A cells.
    Chao CC, Shieh J, Kuo SC, Wu BT, Hour MJ, Leung YM.
    Neuropharmacology; 2008 Jun 15; 54(7):1128-35. PubMed ID: 18406431
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  • 18. Binding of kappa-conotoxin PVIIA to Shaker K+ channels reveals different K+ and Rb+ occupancies within the ion channel pore.
    Boccaccio A, Conti F, Olivera BM, Terlau H.
    J Gen Physiol; 2004 Jul 15; 124(1):71-81. PubMed ID: 15226365
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  • 19. N type rapid inactivation in human Kv1.4 channels: functional role of a putative C-terminal helix.
    Sankaranarayanan K, Varshney A, Mathew MK.
    Mol Membr Biol; 2005 Jul 15; 22(5):389-400. PubMed ID: 16308273
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  • 20. Slow inactivation in Shaker K channels is delayed by intracellular tetraethylammonium.
    González-Pérez V, Neely A, Tapia C, González-Gutiérrez G, Contreras G, Orio P, Lagos V, Rojas G, Estévez T, Stack K, Naranjo D.
    J Gen Physiol; 2008 Dec 15; 132(6):633-50. PubMed ID: 19029372
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