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Journal Abstract Search

347 related items for PubMed ID: 29449639

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  • 2. A trafficking-deficient KCNQ1 mutation, T587M, causes a severe phenotype of long QT syndrome by interfering with intracellular hERG transport.
    Wu J, Sakaguchi T, Takenaka K, Toyoda F, Tsuji K, Matsuura H, Horie M.
    J Cardiol; 2019 May; 73(5):343-350. PubMed ID: 30591322
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  • 3. Differential effects of the β-adrenoceptor blockers carvedilol and metoprolol on SQT1- and SQT2-mutant channels.
    Bodi I, Franke G, Pantulu ND, Wu K, Perez-Feliz S, Bode C, Zehender M, zur Hausen A, Brunner M, Odening KE.
    J Cardiovasc Electrophysiol; 2013 Oct; 24(10):1163-71. PubMed ID: 23718892
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  • 6. The prevalence of mutations in KCNQ1, KCNH2, and SCN5A in an unselected national cohort of young sudden unexplained death cases.
    Winkel BG, Larsen MK, Berge KE, Leren TP, Nissen PH, Olesen MS, Hollegaard MV, Jespersen T, Yuan L, Nielsen N, Haunsø S, Svendsen JH, Wang Y, Kristensen IB, Jensen HK, Tfelt-Hansen J, Banner J.
    J Cardiovasc Electrophysiol; 2012 Oct; 23(10):1092-8. PubMed ID: 22882672
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  • 7. 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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  • 10. Overlapping LQT1 and LQT2 phenotype in a patient with long QT syndrome associated with loss-of-function variations in KCNQ1 and KCNH2.
    Cordeiro JM, Perez GJ, Schmitt N, Pfeiffer R, Nesterenko VV, Burashnikov E, Veltmann C, Borggrefe M, Wolpert C, Schimpf R, Antzelevitch C.
    Can J Physiol Pharmacol; 2010 Dec 04; 88(12):1181-90. PubMed ID: 21164565
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  • 12. Trafficking-deficient long QT syndrome mutation KCNQ1-T587M confers severe clinical phenotype by impairment of KCNH2 membrane localization: evidence for clinically significant IKr-IKs alpha-subunit interaction.
    Biliczki P, Girmatsion Z, Brandes RP, Harenkamp S, Pitard B, Charpentier F, Hébert TE, Hohnloser SH, Baró I, Nattel S, Ehrlich JR.
    Heart Rhythm; 2009 Dec 04; 6(12):1792-801. PubMed ID: 19959132
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  • 15. Mutation Analysis of KCNQ1, KCNH2 and SCN5A Genes in Taiwanese Long QT Syndrome Patients.
    Chang YS, Yang YW, Lin YN, Lin KH, Chang KC, Chang JG.
    Int Heart J; 2015 Dec 04; 56(4):450-3. PubMed ID: 26118593
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  • 18. Expression of genes KCNQ1 and HERG encoding potassium ion channels Ikr, Iks in long QT syndrome.
    Moric-Janiszewska E, Głogowska-Ligus J, Paul-Samojedny M, Smolik S, Woźniak M, Markiewicz-Łoskot G, Mazurek U, Węglarz L, Szydłowski L.
    Kardiol Pol; 2011 Dec 04; 69(5):423-9. PubMed ID: 21594822
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  • 19. In utero onset of long QT syndrome with atrioventricular block and spontaneous or lidocaine-induced ventricular tachycardia: compound effects of hERG pore region mutation and SCN5A N-terminus variant.
    Lin MT, Wu MH, Chang CC, Chiu SN, Thériault O, Huang H, Christé G, Ficker E, Chahine M.
    Heart Rhythm; 2008 Nov 04; 5(11):1567-74. PubMed ID: 18848812
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  • 20. 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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