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656 related items for PubMed ID: 16556865

  • 21. Mutant MiRP1 subunits modulate HERG K+ channel gating: a mechanism for pro-arrhythmia in long QT syndrome type 6.
    Lu Y, Mahaut-Smith MP, Huang CL, Vandenberg JI.
    J Physiol; 2003 Aug 15; 551(Pt 1):253-62. PubMed ID: 12923204
    [Abstract] [Full Text] [Related]

  • 22. The role of abnormal trafficking of KCNE1 in long QT syndrome 5.
    Harmer SC, Tinker A.
    Biochem Soc Trans; 2007 Nov 15; 35(Pt 5):1074-6. PubMed ID: 17956282
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  • 23. The S140G KCNQ1 atrial fibrillation mutation affects 'I(KS)' profile during both atrial and ventricular action potentials.
    El Harchi A, Zhang H, Hancox JC.
    J Physiol Pharmacol; 2010 Dec 15; 61(6):759-64. PubMed ID: 21224508
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  • 24. KCNQ1 assembly and function is blocked by long-QT syndrome mutations that disrupt interaction with calmodulin.
    Ghosh S, Nunziato DA, Pitt GS.
    Circ Res; 2006 Apr 28; 98(8):1048-54. PubMed ID: 16556866
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  • 25. KCNE1 and KCNE3 stabilize and/or slow voltage sensing S4 segment of KCNQ1 channel.
    Nakajo K, Kubo Y.
    J Gen Physiol; 2007 Sep 28; 130(3):269-81. PubMed ID: 17698596
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  • 26. The rate-dependent biophysical properties of the LQT1 H258R mutant are counteracted by a dominant negative effect on channel trafficking.
    Labro AJ, Boulet IR, Timmermans JP, Ottschytsch N, Snyders DJ.
    J Mol Cell Cardiol; 2010 Jun 28; 48(6):1096-104. PubMed ID: 19913547
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  • 27. A double-point mutation in the selectivity filter site of the KCNQ1 potassium channel results in a severe phenotype, LQT1, of long QT syndrome.
    Ikrar T, Hanawa H, Watanabe H, Okada S, Aizawa Y, Ramadan MM, Komura S, Yamashita F, Chinushi M, Aizawa Y.
    J Cardiovasc Electrophysiol; 2008 May 28; 19(5):541-9. PubMed ID: 18266681
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  • 28. External barium affects the gating of KCNQ1 potassium channels and produces a pore block via two discrete sites.
    Gibor G, Yakubovich D, Peretz A, Attali B.
    J Gen Physiol; 2004 Jul 28; 124(1):83-102. PubMed ID: 15226366
    [Abstract] [Full Text] [Related]

  • 29. Insights into Cardiac IKs (KCNQ1/KCNE1) Channels Regulation.
    Wu X, Larsson HP.
    Int J Mol Sci; 2020 Dec 11; 21(24):. PubMed ID: 33322401
    [Abstract] [Full Text] [Related]

  • 30. Allosteric mechanism for KCNE1 modulation of KCNQ1 potassium channel activation.
    Kuenze G, Vanoye CG, Desai RR, Adusumilli S, Brewer KR, Woods H, McDonald EF, Sanders CR, George AL, Meiler J.
    Elife; 2020 Oct 23; 9():. PubMed ID: 33095155
    [Abstract] [Full Text] [Related]

  • 31. The KCNE1 beta-subunit exerts a transient effect on the KCNQ1 K+ channel.
    Poulsen AN, Klaerke DA.
    Biochem Biophys Res Commun; 2007 Nov 09; 363(1):133-9. PubMed ID: 17845799
    [Abstract] [Full Text] [Related]

  • 32. Long-QT mutation p.K557E-Kv7.1: dominant-negative suppression of IKs, but preserved cAMP-dependent up-regulation.
    Spätjens RL, Bébarová M, Seyen SR, Lentink V, Jongbloed RJ, Arens YH, Heijman J, Volders PG.
    Cardiovasc Res; 2014 Oct 01; 104(1):216-25. PubMed ID: 25139741
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  • 37. A new KCNQ1 mutation at the S5 segment that impairs its association with KCNE1 is responsible for short QT syndrome.
    Moreno C, Oliveras A, de la Cruz A, Bartolucci C, Muñoz C, Salar E, Gimeno JR, Severi S, Comes N, Felipe A, González T, Lambiase P, Valenzuela C.
    Cardiovasc Res; 2015 Sep 01; 107(4):613-23. PubMed ID: 26168993
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  • 40. Mutation of colocalized residues of the pore helix and transmembrane segments S5 and S6 disrupt deactivation and modify inactivation of KCNQ1 K+ channels.
    Seebohm G, Westenskow P, Lang F, Sanguinetti MC.
    J Physiol; 2005 Mar 01; 563(Pt 2):359-68. PubMed ID: 15649981
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