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Humana Press, Inc

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

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Diminished myofibril organization in mutant axolotl hearts transfected with site-directed mutants of sarcomeric tropomyosins

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

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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

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