Biochemical characterisation of Troponin C mutations causing hypertrophic and dilated cardiomyopathies.

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article científic

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article scientifique

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Biochemical characterisation o ...... and dilated cardiomyopathies.

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Biochemical characterisation o ...... and dilated cardiomyopathies.

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Biochemical characterisation o ...... and dilated cardiomyopathies.

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P1476

Biochemical characterisation o ...... and dilated cardiomyopathies.

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P2093

Athanasia Kalyva

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Fragiskos I Parthenakis

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Joanna E Kontaraki

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Maria E Marketou

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Panos E Vardas

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P2860

Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy

Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotype

Alterations in thin filament regulation induced by a human cardiac troponin T mutant that causes dilated cardiomyopathy are distinct from those induced by troponin T mutants that cause hypertrophic cardiomyopathy

Structure of the core domain of human cardiac troponin in the Ca(2+)-saturated form

Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy

The dilated cardiomyopathy G159D mutation in cardiac troponin C weakens the anchoring interaction with troponin I

First mutation in cardiac troponin C, L29Q, in a patient with hypertrophic cardiomyopathy

Disease-causing mutations in cardiac troponin T: identification of a critical tropomyosin-binding region

Ca(2+)-regulated structural changes in troponin

Mapping of a second actin-tropomyosin and a second troponin C binding site within the C terminus of troponin I, and their importance in the Ca2+-dependent regulation of muscle contraction

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s10974-014-9382-0

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161-178

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scholarly article

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10.1007/S10974-014-9382-0

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2014-04-18T00:00:00Z

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1010706773

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24744096

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