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280 related items for PubMed ID: 15466629

  • 1. Hypertrophy, fibrosis, and sudden cardiac death in response to pathological stimuli in mice with mutations in cardiac troponin T.
    Maass AH, Ikeda K, Oberdorf-Maass S, Maier SK, Leinwand LA.
    Circulation; 2004 Oct 12; 110(15):2102-9. PubMed ID: 15466629
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  • 2. Severe heart failure and early mortality in a double-mutation mouse model of familial hypertrophic cardiomyopathy.
    Tsoutsman T, Kelly M, Ng DC, Tan JE, Tu E, Lam L, Bogoyevitch MA, Seidman CE, Seidman JG, Semsarian C.
    Circulation; 2008 Apr 08; 117(14):1820-31. PubMed ID: 18362229
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  • 3. Familial hypertrophic cardiomyopathy-linked mutant troponin T causes stress-induced ventricular tachycardia and Ca2+-dependent action potential remodeling.
    Knollmann BC, Kirchhof P, Sirenko SG, Degen H, Greene AE, Schober T, Mackow JC, Fabritz L, Potter JD, Morad M.
    Circ Res; 2003 Mar 07; 92(4):428-36. PubMed ID: 12600890
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  • 4. Molecular insights from a novel cardiac troponin I mouse model of familial hypertrophic cardiomyopathy.
    Tsoutsman T, Chung J, Doolan A, Nguyen L, Williams IA, Tu E, Lam L, Bailey CG, Rasko JE, Allen DG, Semsarian C.
    J Mol Cell Cardiol; 2006 Oct 07; 41(4):623-32. PubMed ID: 16950368
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  • 5. Morphological and functional alterations in ventricular myocytes from male transgenic mice with hypertrophic cardiomyopathy.
    Olsson MC, Palmer BM, Stauffer BL, Leinwand LA, Moore RL.
    Circ Res; 2004 Feb 06; 94(2):201-7. PubMed ID: 14670849
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  • 6. The role of Akt/GSK-3beta signaling in familial hypertrophic cardiomyopathy.
    Luckey SW, Walker LA, Smyth T, Mansoori J, Messmer-Kratzsch A, Rosenzweig A, Olson EN, Leinwand LA.
    J Mol Cell Cardiol; 2009 May 06; 46(5):739-47. PubMed ID: 19233194
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  • 7. Novel troponin T mutation in familial dilated cardiomyopathy with gender-dependant severity.
    Stefanelli CB, Rosenthal A, Borisov AB, Ensing GJ, Russell MW.
    Mol Genet Metab; 2004 May 06; 83(1-2):188-96. PubMed ID: 15464434
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  • 12. Dilated cardiomyopathy mutant tropomyosin mice develop cardiac dysfunction with significantly decreased fractional shortening and myofilament calcium sensitivity.
    Rajan S, Ahmed RP, Jagatheesan G, Petrashevskaya N, Boivin GP, Urboniene D, Arteaga GM, Wolska BM, Solaro RJ, Liggett SB, Wieczorek DF.
    Circ Res; 2007 Jul 20; 101(2):205-14. PubMed ID: 17556658
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  • 13. Cardiac troponin T mutations result in allele-specific phenotypes in a mouse model for hypertrophic cardiomyopathy.
    Tardiff JC, Hewett TE, Palmer BM, Olsson C, Factor SM, Moore RL, Robbins J, Leinwand LA.
    J Clin Invest; 1999 Aug 20; 104(4):469-81. PubMed ID: 10449439
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  • 14. Severe familial left ventricular non-compaction cardiomyopathy due to a novel troponin T (TNNT2) mutation.
    Luedde M, Ehlermann P, Weichenhan D, Will R, Zeller R, Rupp S, Müller A, Steen H, Ivandic BT, Ulmer HE, Kern M, Katus HA, Frey N.
    Cardiovasc Res; 2010 Jun 01; 86(3):452-60. PubMed ID: 20083571
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  • 15. Phenotypic deficits in mice expressing a myosin binding protein C lacking the titin and myosin binding domains.
    Yang Q, Osinska H, Klevitsky R, Robbins J.
    J Mol Cell Cardiol; 2001 Sep 01; 33(9):1649-58. PubMed ID: 11549344
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  • 17. IMAGE CARDIO MED: Inducible malignant ventricular tachyarrhythmia in a patient with genotyped hypertrophic cardiomyopathy in absence of left ventricular hypertrophy or enlargement.
    Ariyarajah V, Tam JW, Khadem A.
    Circulation; 2009 Jun 02; 119(21):e543-4. PubMed ID: 19487599
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