A Familial Hypertrophic Cardiomyopathy  -Tropomyosin Mutation Causes Severe Cardiac Hypertrophy and Death in Mice

By Prabhakar R.   Boivin G.P.   Grupp I.L.   Hoit B.   Arteaga G.   Solaro J.R.   Wieczorek D.F.  

Journal of Molecular and Cellular Cardiology, Vol. 33, Iss. 10, 2001-10 ,pp. : 1815-1828

Academic Press

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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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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.  

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Cardiac Myosin-Binding Protein C and Hypertrophic Cardiomyopathy

By Carrier L.   Bonne G.   Schwartz K.  

Trends in Cardiovascular Medicine, Vol. 8, Iss. 4, 1998-05 ,pp. : 151-157

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Cardiac troponin T mutation R141W found in dilated cardiomyopathy stabilizes the troponin T-tropomyosin interaction and causes a Ca 2+ desensitization

By Lu Q.-W.   Morimoto S.   Harada K.   Du C.-K.   Takahashi-Yanaga F.   Miwa Y.   Sasaguri T.   Ohtsuki I.  

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