Genetic Pathogenesis of Hypertrophic and Dilated Cardiomyopathy.

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Impact of the Myosin Modulator Mavacamten on Force Generation and Cross-Bridge Behavior in a Murine Model of Hypercontractility Too much of a good thing Prolonged cross-bridge binding triggers muscle dysfunction in a model of myosin-based hypertrophic cardiomyopathy

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P2860

Genetic Pathogenesis of Hypertrophic and Dilated Cardiomyopathy.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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name

Genetic Pathogenesis of Hypertrophic and Dilated Cardiomyopathy.

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Genetic Pathogenesis of Hypertrophic and Dilated Cardiomyopathy.

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Genetic Pathogenesis of Hypertrophic and Dilated Cardiomyopathy.

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Genetic Pathogenesis of Hypertrophic and Dilated Cardiomyopathy.

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Genetic Pathogenesis of Hypertrophic and Dilated Cardiomyopathy.

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Genetic Pathogenesis of Hypertrophic and Dilated Cardiomyopathy.

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P1476

Genetic Pathogenesis of Hypertrophic and Dilated Cardiomyopathy.

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P2093

Amanda C Garfinkel

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Christine E Seidman

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Jonathan G Seidman

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P2860

Mutation-Specific Phenotypes in hiPSC-Derived Cardiomyocytes Carrying Either Myosin-Binding Protein C Or α-Tropomyosin Mutation for Hypertrophic Cardiomyopathy.

Three-Dimensional Reconstruction of Tarantula Myosin Filaments Suggests How Phosphorylation May Regulate Myosin Activity

Clinical and Mechanistic Insights Into the Genetics of Cardiomyopathy

Cardiac myosin-binding protein C mutations and hypertrophic cardiomyopathy: haploinsufficiency, deranged phosphorylation, and cardiomyocyte dysfunction

Perturbed length-dependent activation in human hypertrophic cardiomyopathy with missense sarcomeric gene mutations

Cardiac myosin missense mutations cause dilated cardiomyopathy in mouse models and depress molecular motor function.

Titin-truncating variants affect heart function in disease cohorts and the general population.

Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults.

Truncations of titin causing dilated cardiomyopathy.

HEART DISEASE. Titin mutations in iPS cells define sarcomere insufficiency as a cause of dilated cardiomyopathy.

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139-146

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scholarly article

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10.1016/J.HFC.2017.12.004

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2018-04-01T00:00:00Z

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Genetic Pathogenesis of Hypertrophic and Dilated Cardiomyopathy.

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P2860

P2860

Genetic Pathogenesis of Hypertrophic and Dilated Cardiomyopathy.

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type

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P932