Dilated cardiomyopathy myosin mutants have reduced force-generating capacity.

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Do Actomyosin Single-Molecule Mechanics Data Predict Mechanics of Contracting Muscle?Hypertrophic cardiomyopathy disease results from disparate impairments of cardiac myosin function and auto-inhibition Controlling load-dependent kinetics of β-cardiac myosin at the single-molecule level

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Dilated cardiomyopathy myosin mutants have reduced force-generating capacity.

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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年學術文章

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Dilated cardiomyopathy myosin mutants have reduced force-generating capacity.

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Dilated cardiomyopathy myosin mutants have reduced force-generating capacity.

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Item

label

Dilated cardiomyopathy myosin mutants have reduced force-generating capacity.

@en

Dilated cardiomyopathy myosin mutants have reduced force-generating capacity.

@nl

prefLabel

Dilated cardiomyopathy myosin mutants have reduced force-generating capacity.

@en

Dilated cardiomyopathy myosin mutants have reduced force-generating capacity.

@nl

P1476

Dilated cardiomyopathy myosin mutants have reduced force-generating capacity.

@en

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Carlos D Vera

http://www.w3.org/2001/XMLSchema#string

Elizabeth Choe Yu

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James A Spudich

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Kathleen Ruppel

http://www.w3.org/2001/XMLSchema#string

Leslie A Leinwand

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Marina Svicevic

http://www.w3.org/2001/XMLSchema#string

Masataka Kawana

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Srbolujub M Mijailovich

http://www.w3.org/2001/XMLSchema#string

Zoltan Ujfalusi

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Ensemble force changes that result from human cardiac myosin mutations and a small-molecule effector

Three-dimensional image reconstruction of dephosphorylated smooth muscle heavy meromyosin reveals asymmetry in the interaction between myosin heads and placement of subfragment 2

Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy

Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy

The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms

Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy

Familial dilated cardiomyopathy mutations uncouple troponin I phosphorylation from changes in myofibrillar Ca²⁺ sensitivity

Chronic phospholamban-sarcoplasmic reticulum calcium ATPase interaction is the critical calcium cycling defect in dilated cardiomyopathy

A mouse model of familial hypertrophic cardiomyopathy

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

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scholarly article

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10.1074/JBC.RA118.001938

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English

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Michael A. Geeves

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2018-04-17T00:00:00Z

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29666183

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P932

5995530

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Dilated cardiomyopathy myosin mutants have reduced force-generating capacity.

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P2860

P2860

Dilated cardiomyopathy myosin mutants have reduced force-generating capacity.

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P1433

P1476

P2093

P2860

P31

P356

P407

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P31

P356

P407

P50

P577

P698

P932