Phosphorylation of human cardiac troponin I G203S and K206Q linked to familial hypertrophic cardiomyopathy affects actomyosin interaction in different ways

By Deng Y.   Schmidtmann A.   Kruse S.   Filatov V.   Heilmeyer L.M.G.   Jaquet K.   Thieleczek R.  

Journal of Molecular and Cellular Cardiology, Vol. 35, Iss. 11, 2003-11 ,pp. : 1365-1374

Elsevier

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Altered Regulation of Cardiac Muscle Contraction by Troponin T Mutations that Cause Familial Hypertrophic Cardiomyopathy

By Knollmann B.C.   Potter J.D.  

Trends in Cardiovascular Medicine, Vol. 11, Iss. 5, 2001-07 ,pp. : 206-212

Elsevier

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Novel Missense Mutation in Cardiac Troponin T Gene Found in Japanese Patient with Hypertrophic Cardiomyopathy

By Nakajima-Taniguchi C.   Matsui H.   Fujio Y.   Nagata S.   Kishimoto T.   Yamauchi-Takihara K.  

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Academic Press

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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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Functional Consequences of Mutations in the Myosin Heavy Chain at Sites Implicated in Familial Hypertrophic Cardiomyopathy

By Lowey S.  

Trends in Cardiovascular Medicine, Vol. 12, Iss. 8, 2002-11 ,pp. : 348-354

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