Altered signaling surrounding the C-lobe of cardiac troponin C in myofilaments containing an -tropomyosin mutation linked to familial hypertrophic cardiomyopathy

By Burkart E.M.   Arteaga G.M.   Sumandea M.P.   Prabhakar R.   Wieczorek D.F.   Solaro R.J.  

Journal of Molecular and Cellular Cardiology, Vol. 35, Iss. 10, 2003-10 ,pp. : 1285-1293

Elsevier

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Functional Consequences of the Mutations in Human Cardiac Troponin I Gene Found in Familial Hypertrophic Cardiomyopathy

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Mutations in the cardiac troponin T gene show various prognoses in Japanese patients with hypertrophic cardiomyopathy

By Fujita Etsuko   Nakanishi Toshio   Nishizawa Tsutomu   Hagiwara Nobuhisa   Matsuoka Rumiko  

Heart and Vessels, Vol. 28, Iss. 6, 2013-11 ,pp. : 785-794

Springer Publishing Company

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Mechanisms of the Pathogenesis of Troponin T-Based Familial Hypertrophic Cardiomyopathy

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Trends in Cardiovascular Medicine, Vol. 13, Iss. 6, 2003-08 ,pp. : 232-237

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Effect of Hypertrophic Cardiomyopathy Mutations in Human Cardiac Muscle  -tropomyosin (Asp175Asn and Glu180Gly) on the Regulatory Properties of Human Cardiac Troponin Determined by in vitro Motility Assay

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