Beyond the cardiac myofilament: hypertrophic cardiomyopathy- associated mutations in genes that encode calcium-handling proteins. - sprookjes - yvandenbroek - TriplyDB

Beyond the cardiac myofilament: hypertrophic cardiomyopathy- associated mutations in genes that encode calcium-handling proteins.

Beyond the cardiac myofilament: hypertrophic cardiomyopathy- associated mutations in genes that encode calcium-handling proteins.

http://www.wikidata.org/entity/Q41991342

about

The junctophilin family of proteins: from bench to bedside Genetics and disease of ventricular muscle.Deregulated Ca2+ cycling underlies the development of arrhythmia and heart disease due to mutant obscurin Hypertrophic Cardiomyopathy Cardiac Troponin C Mutations Differentially Affect Slow Skeletal and Cardiac Muscle Regulation.Novel junctophilin-2 mutation A405S is associated with basal septal hypertrophy and diastolic dysfunction.Genetic testing for inherited cardiac disease.Emerging roles of junctophilin-2 in the heart and implications for cardiac diseases.The genetic basis of hypertrophic cardiomyopathy in cats and humans.Raf kinase inhibitor protein: lessons of a better way for β-adrenergic receptor activation in the heart.Calcium Signaling and Cardiac Arrhythmias.Just sinus bradycardia or something more serious?A proteolytic cleavage to separate the sarcolemma/T-tubule from the sarcoplasmic reticulum.The genetics of hypertrophic cardiomyopathy

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P2860

Beyond the cardiac myofilament: hypertrophic cardiomyopathy- associated mutations in genes that encode calcium-handling proteins.

http://www.wikidata.org/entity/Q41991342

description

2012 nî lūn-bûn

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2012年の論文

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2012年論文

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2012年论文

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Beyond the cardiac myofilament ...... ode calcium-handling proteins.

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Beyond the cardiac myofilament ...... ode calcium-handling proteins.

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Current Molecular Medicine

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Beyond the cardiac myofilament ...... ode calcium-handling proteins.

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A P Landstrom

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M J Ackerman

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P2860

PKA phosphorylation dissociates FKBP12.6 from the calcium release channel (ryanodine receptor): defective regulation in failing hearts

Characterization of human junctophilin subtype genes

Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

S165F mutation of junctophilin 2 affects Ca2+ signalling in skeletal muscle

Clinical phenotype and functional characterization of CASQ2 mutations associated with catecholaminergic polymorphic ventricular tachycardia

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

Sorcin associates with the pore-forming subunit of voltage-dependent L-type Ca2+ channels

Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere

Expression of a sorcin missense mutation in the heart modulates excitation-contraction coupling

Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle

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