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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Different Pathophysiology of Cardiac Hypertrophy in Hypertension and Hypertrophic Cardiomyopathy

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Familial Hypertrophic Cardiomyopathy Associated with a Novel Missense Mutation Affecting the ATP-binding Region of the Cardiac Beta-myosin Heavy Chain

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Journal of Molecular and Cellular Cardiology, Vol. 31, Iss. 4, 1999-04 ,pp. : 745-750

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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.  

Journal of Molecular and Cellular Cardiology, Vol. 35, Iss. 12, 2003-12 ,pp. : 1421-1427

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A Novel Missense Mutation, Leu390Val, in the Cardiac β-myosin Heavy Chain Associated with Pronounced Septal Hypertrophy in Two Families with Hypertrophic Cardiomyopathy

By Havndrup Ole   Bundgaard Henning   Andersen Paal Skytt   Larsen Lars Allan   Vuust Jens   Kjeldsen Keld   Christiansen Michael  

Scandinavian Cardiovascular Journal, Vol. 34, Iss. 6, 2000-12 ,pp. : 558-563

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