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Journal Abstract Search

564 related items for PubMed ID: 25344363

  • 1. LQT1 mutations in KCNQ1 C-terminus assembly domain suppress IKs using different mechanisms.
    Aromolaran AS, Subramanyam P, Chang DD, Kobertz WR, Colecraft HM.
    Cardiovasc Res; 2014 Dec 01; 104(3):501-11. PubMed ID: 25344363
    [Abstract] [Full Text] [Related]

  • 2. Calmodulin is essential for cardiac IKS channel gating and assembly: impaired function in long-QT mutations.
    Shamgar L, Ma L, Schmitt N, Haitin Y, Peretz A, Wiener R, Hirsch J, Pongs O, Attali B.
    Circ Res; 2006 Apr 28; 98(8):1055-63. PubMed ID: 16556865
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  • 3. Dominant-negative control of cAMP-dependent IKs upregulation in human long-QT syndrome type 1.
    Heijman J, Spätjens RL, Seyen SR, Lentink V, Kuijpers HJ, Boulet IR, de Windt LJ, David M, Volders PG.
    Circ Res; 2012 Jan 20; 110(2):211-9. PubMed ID: 22095730
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  • 4. A molecular mechanism for adrenergic-induced long QT syndrome.
    Wu J, Naiki N, Ding WG, Ohno S, Kato K, Zang WJ, Delisle BP, Matsuura H, Horie M.
    J Am Coll Cardiol; 2014 Mar 04; 63(8):819-27. PubMed ID: 24184248
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  • 5. Dysfunctional potassium channel subunit interaction as a novel mechanism of long QT syndrome.
    Hoosien M, Ahearn ME, Myerburg RJ, Pham TV, Miller TE, Smets MJ, Baumbach-Reardon L, Young ML, Farooq A, Bishopric NH.
    Heart Rhythm; 2013 May 04; 10(5):728-37. PubMed ID: 23291057
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  • 7. A novel mutation in KCNQ1 associated with a potent dominant negative effect as the basis for the LQT1 form of the long QT syndrome.
    Aizawa Y, Ueda K, Scornik F, Cordeiro JM, Wu Y, Desai M, Guerchicoff A, Nagata Y, Iesaka Y, Kimura A, Hiraoka M, Antzelevitch C.
    J Cardiovasc Electrophysiol; 2007 Sep 04; 18(9):972-7. PubMed ID: 17655673
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  • 8. Dynamic subunit stoichiometry confers a progressive continuum of pharmacological sensitivity by KCNQ potassium channels.
    Yu H, Lin Z, Mattmann ME, Zou B, Terrenoire C, Zhang H, Wu M, McManus OB, Kass RS, Lindsley CW, Hopkins CR, Li M.
    Proc Natl Acad Sci U S A; 2013 May 21; 110(21):8732-7. PubMed ID: 23650380
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  • 9. BACE1 modulates gating of KCNQ1 (Kv7.1) and cardiac delayed rectifier KCNQ1/KCNE1 (IKs).
    Agsten M, Hessler S, Lehnert S, Volk T, Rittger A, Hartmann S, Raab C, Kim DY, Groemer TW, Schwake M, Alzheimer C, Huth T.
    J Mol Cell Cardiol; 2015 Dec 21; 89(Pt B):335-48. PubMed ID: 26454161
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  • 11. A590T mutation in KCNQ1 C-terminal helix D decreases IKs channel trafficking and function but not Yotiao interaction.
    Kinoshita K, Komatsu T, Nishide K, Hata Y, Hisajima N, Takahashi H, Kimoto K, Aonuma K, Tsushima E, Tabata T, Yoshida T, Mori H, Nishida K, Yamaguchi Y, Ichida F, Fukurotani K, Inoue H, Nishida N.
    J Mol Cell Cardiol; 2014 Jul 21; 72():273-80. PubMed ID: 24713462
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  • 14. The N-terminal juxtamembranous domain of KCNQ1 is critical for channel surface expression: implications in the Romano-Ward LQT1 syndrome.
    Dahimène S, Alcoléa S, Naud P, Jourdon P, Escande D, Brasseur R, Thomas A, Baró I, Mérot J.
    Circ Res; 2006 Nov 10; 99(10):1076-83. PubMed ID: 17053194
    [Abstract] [Full Text] [Related]

  • 15. Chronic probucol treatment decreases the slow component of the delayed-rectifier potassium current in CHO cells transfected with KCNQ1 and KCNE1: a novel mechanism of QT prolongation.
    Taniguchi T, Uesugi M, Arai T, Yoshinaga T, Miyamoto N, Sawada K.
    J Cardiovasc Pharmacol; 2012 Apr 10; 59(4):377-86. PubMed ID: 22189896
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  • 17. Transcripts of Kv7.1 and MinK channels and slow delayed rectifier K+ current (IKs) are expressed in zebrafish (Danio rerio) heart.
    Abramochkin DV, Hassinen M, Vornanen M.
    Pflugers Arch; 2018 Dec 10; 470(12):1753-1764. PubMed ID: 30116893
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  • 18. A hERG mutation E1039X produced a synergistic lesion on IKs together with KCNQ1-R174C mutation in a LQTS family with three compound mutations.
    Wu J, Mizusawa Y, Ohno S, Ding WG, Higaki T, Wang Q, Kohjitani H, Makiyama T, Itoh H, Toyoda F, James AF, Hancox JC, Matsuura H, Horie M.
    Sci Rep; 2018 Feb 15; 8(1):3129. PubMed ID: 29449639
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  • 19. Mechanisms of disease pathogenesis in long QT syndrome type 5.
    Harmer SC, Wilson AJ, Aldridge R, Tinker A.
    Am J Physiol Cell Physiol; 2010 Feb 15; 298(2):C263-73. PubMed ID: 19907016
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