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Journal Abstract Search

598 related items for PubMed ID: 15649981

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  • 6. Pharmacological activation of normal and arrhythmia-associated mutant KCNQ1 potassium channels.
    Seebohm G, Pusch M, Chen J, Sanguinetti MC.
    Circ Res; 2003 Nov 14; 93(10):941-7. PubMed ID: 14576198
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  • 10. KCNE1 and KCNE3 modulate KCNQ1 channels by affecting different gating transitions.
    Barro-Soria R, Ramentol R, Liin SI, Perez ME, Kass RS, Larsson HP.
    Proc Natl Acad Sci U S A; 2017 Aug 29; 114(35):E7367-E7376. PubMed ID: 28808020
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  • 11. Interaction of KCNE subunits with the KCNQ1 K+ channel pore.
    Panaghie G, Tai KK, Abbott GW.
    J Physiol; 2006 Feb 01; 570(Pt 3):455-67. PubMed ID: 16308347
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  • 12. Structural basis of slow activation gating in the cardiac I Ks channel complex.
    Strutz-Seebohm N, Pusch M, Wolf S, Stoll R, Tapken D, Gerwert K, Attali B, Seebohm G.
    Cell Physiol Biochem; 2011 Feb 01; 27(5):443-52. PubMed ID: 21691061
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  • 13. The residue I257 at S4-S5 linker in KCNQ1 determines KCNQ1/KCNE1 channel sensitivity to 1-alkanols.
    Xie C, Liu HW, Pan N, Ding JP, Yao J.
    Acta Pharmacol Sin; 2016 Jan 01; 37(1):124-33. PubMed ID: 26725740
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  • 14. KCNE3 truncation mutants reveal a bipartite modulation of KCNQ1 K+ channels.
    Gage SD, Kobertz WR.
    J Gen Physiol; 2004 Dec 01; 124(6):759-71. PubMed ID: 15572349
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  • 19. Molecular basis of slow activation of the human ether-a-go-go related gene potassium channel.
    Subbiah RN, Clarke CE, Smith DJ, Zhao J, Campbell TJ, Vandenberg JI.
    J Physiol; 2004 Jul 15; 558(Pt 2):417-31. PubMed ID: 15181157
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  • 20. Identification of specific pore residues mediating KCNQ1 inactivation. A novel mechanism for long QT syndrome.
    Seebohm G, Scherer CR, Busch AE, Lerche C.
    J Biol Chem; 2001 Apr 27; 276(17):13600-5. PubMed ID: 11278406
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