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Journal Abstract Search

287 related items for PubMed ID: 16873551

  • 21.
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  • 22. Conditional FKBP12.6 overexpression in mouse cardiac myocytes prevents triggered ventricular tachycardia through specific alterations in excitation-contraction coupling.
    Gellen B, Fernández-Velasco M, Briec F, Vinet L, LeQuang K, Rouet-Benzineb P, Bénitah JP, Pezet M, Palais G, Pellegrin N, Zhang A, Perrier R, Escoubet B, Marniquet X, Richard S, Jaisser F, Gómez AM, Charpentier F, Mercadier JJ.
    Circulation; 2008 Apr 08; 117(14):1778-86. PubMed ID: 18378612
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  • 24. Functional abnormalities in iPSC-derived cardiomyocytes generated from CPVT1 and CPVT2 patients carrying ryanodine or calsequestrin mutations.
    Novak A, Barad L, Lorber A, Gherghiceanu M, Reiter I, Eisen B, Eldor L, Itskovitz-Eldor J, Eldar M, Arad M, Binah O.
    J Cell Mol Med; 2015 Aug 08; 19(8):2006-18. PubMed ID: 26153920
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  • 25. Type 2 ryanodine receptor domain A contains a unique and dynamic α-helix that transitions to a β-strand in a mutant linked with a heritable cardiomyopathy.
    Amador FJ, Kimlicka L, Stathopulos PB, Gasmi-Seabrook GM, Maclennan DH, Van Petegem F, Ikura M.
    J Mol Biol; 2013 Nov 01; 425(21):4034-46. PubMed ID: 23978697
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  • 26.
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  • 27. Mechanisms of abnormal calcium homeostasis in mutations responsible for catecholaminergic polymorphic ventricular tachycardia.
    Iyer V, Hajjar RJ, Armoundas AA.
    Circ Res; 2007 Feb 02; 100(2):e22-31. PubMed ID: 17234962
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  • 30. Physiological consequences of the P2328S mutation in the ryanodine receptor (RyR2) gene in genetically modified murine hearts.
    Goddard CA, Ghais NS, Zhang Y, Williams AJ, Colledge WH, Grace AA, Huang CL.
    Acta Physiol (Oxf); 2008 Oct 02; 194(2):123-40. PubMed ID: 18419777
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  • 33. Ryanodine receptors and ventricular arrhythmias: emerging trends in mutations, mechanisms and therapies.
    George CH, Jundi H, Thomas NL, Fry DL, Lai FA.
    J Mol Cell Cardiol; 2007 Jan 02; 42(1):34-50. PubMed ID: 17081562
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  • 36. Functional heterogeneity of ryanodine receptor mutations associated with sudden cardiac death.
    Thomas NL, George CH, Lai FA.
    Cardiovasc Res; 2004 Oct 01; 64(1):52-60. PubMed ID: 15364613
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  • 37.
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  • 38. Calcium channel antagonism reduces exercise-induced ventricular arrhythmias in catecholaminergic polymorphic ventricular tachycardia patients with RyR2 mutations.
    Swan H, Laitinen P, Kontula K, Toivonen L.
    J Cardiovasc Electrophysiol; 2005 Feb 01; 16(2):162-6. PubMed ID: 15720454
    [Abstract] [Full Text] [Related]

  • 39. Conduction slowing contributes to spontaneous ventricular arrhythmias in intrinsically active murine RyR2-P2328S hearts.
    Zhang Y, Wu J, Jeevaratnam K, King JH, Guzadhur L, Ren X, Grace AA, Lei M, Huang CL, Fraser JA.
    J Cardiovasc Electrophysiol; 2013 Feb 01; 24(2):210-8. PubMed ID: 23131176
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  • 40.
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