Cardiac Myosin Binding Protein C
HSC70 is a chaperone for wild-type and mutant cardiac myosin binding protein C
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Cardiac Myosin Binding Protein C: At the Heart of Hypertrophic Cardiomyopathy in Humans and Domestic Cats
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Novel splice donor site mutation in the cardiac myosin binding protein C gene in familial hypertrophic cardiomyopathy Characterization Of cardiac transcript and protein
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Research Progress of Cardiac Myosin Binding Protein C in Dilated Cardiomyopathy and Other Cardiac Conditions
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Dilated cardiomyopathy in homozygous myosin binding protein C mutant mice
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Effects of hypertrophic and dilated cardiomyopathy mutations on power output by human β cardiac myosin
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Calcium, Actomyosin Kinetics, Myosin Binding Protein-C and Hypertrophic Cardiomyopathy
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A mouse model of myosin binding protein C human familial hypertrophic cardiomyopathy
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A cardiac myosin light chain kinase regulates sarcomere assembly in the vertebrate heart
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The Mechanisms of the Frank-Starling Law and Familial Cardiomyopathy are Different. The Function of Myosin Binding Protein-C is Retained on Myocyte Length Increase and Force Generated is Kinase controlled
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Genetic mutations and mechanisms in dilated cardiomyopathy
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Autoimmunity in Chagas' disease Identification of cardiac myosin B13 Trypanosoma cruzi protein crossreactive T cell clones in heart lesions of a chronic Chagas' cardiomyopathy patient
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Functional analysis of the mutations in the human cardiac beta myosin that are responsible for familial hypertrophic cardiomyopathy Implication for the clinical outcome
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Interactions of actin, myosin, and an actin binding protein of chronic myelogenous leukemia leukocytes
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Identification of cardiac myosin peptides capable of inducing autoimmune myocarditis in BALB/c mice
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Myosin heavy chain messenger RNA and protein isoform transitions during cardiac hypertrophy Interaction between hemodynamic and thyroid hormone induced signals
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The injury-induced myokine insulin-like 6 is protective in experimental autoimmune myositis
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Properties of the muscle proteins a comparative approach
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Mouse and computational models link Mlc2v dephosphorylation to altered myosin kinetics in early cardiac disease
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Mice Expressing Mutant Myosin Heavy Chains Are a Model for Familial Hypertrophic Cardiomyopathy
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