Mechanical and energetic consequences of HCM-causing mutations. - Wikidata - awgldk - TriplyDB

Mechanical and energetic consequences of HCM-causing mutations.

Mechanical and energetic consequences of HCM-causing mutations.

http://www.wikidata.org/entity/Q37766181

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Poorly understood aspects of striated muscle contraction Targets for therapy in sarcomeric cardiomyopathies SERCA2 Haploinsufficiency in a Mouse Model of Darier Disease Causes a Selective Predisposition to Heart Failure Isolation and Mechanical Measurements of Myofibrils from Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes Focal energy deprivation underlies arrhythmia susceptibility in mice with calcium-sensitized myofilaments.Delineation of Molecular Pathways Involved in Cardiomyopathies Caused by Troponin T Mutations Muscle dysfunction in hypertrophic cardiomyopathy: what is needed to move to translation?Defining phenotypes and disease progression in sarcomeric cardiomyopathies: contemporary role of clinical investigations.Role of multimodality cardiac imaging in the management of patients with hypertrophic cardiomyopathy: an expert consensus of the European Association of Cardiovascular Imaging Endorsed by the Saudi Heart Association.Actomyosin based contraction: one mechanokinetic model from single molecules to muscle?Pathogenesis of Hypertrophic Cardiomyopathy is Mutation Rather Than Disease Specific: A Comparison of the Cardiac Troponin T E163R and R92Q Mouse Models.Hypothesis and theory: mechanical instabilities and non-uniformities in hereditary sarcomere myopathies.Ranolazine antagonizes catecholamine-induced dysfunction in isolated cardiomyocytes, but lacks long-term therapeutic effects in vivo in a mouse model of hypertrophic cardiomyopathy.Emerging pharmacologic and structural therapies for hypertrophic cardiomyopathy.Exacerbation of cardiac energetic impairment during exercise in hypertrophic cardiomyopathy: a potential mechanism for diastolic dysfunction Changes in the cardiac metabolome caused by perhexiline treatment in a mouse model of hypertrophic cardiomyopathy

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P2860

Mechanical and energetic consequences of HCM-causing mutations.

http://www.wikidata.org/entity/Q37766181

description

article científic

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article scientifique

@fr

articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 09 October 2009

@en

vedecký článok

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vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Mechanical and energetic consequences of HCM-causing mutations.

@en

Mechanical and energetic consequences of HCM-causing mutations.

@nl

type

label

Mechanical and energetic consequences of HCM-causing mutations.

@en

Mechanical and energetic consequences of HCM-causing mutations.

@nl

prefLabel

Mechanical and energetic consequences of HCM-causing mutations.

@en

Mechanical and energetic consequences of HCM-causing mutations.

@nl

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S12265-009-9131-8

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Journal of Cardiovascular Translational Research

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Mechanical and energetic consequences of HCM-causing mutations.

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Alexandra Belus

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Beatrice Scellini

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Cecilia Ferrantini

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Chiara Tesi

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Corrado Poggesi

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Nicoletta Piroddi

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P2860

Investigation of a truncated cardiac troponin T that causes familial hypertrophic cardiomyopathy: Ca(2+) regulatory properties of reconstituted thin filaments depend on the ratio of mutant to wild-type protein

Decreased energetics in murine hearts bearing the R92Q mutation in cardiac troponin T

Effect of extraction of myosin binding protein C on contractility of rat heart.

A Mutant Tropomyosin That Causes Hypertrophic Cardiomyopathy Is Expressed In Vivo and Associated With an Increased Calcium Sensitivity

The familial hypertrophic cardiomyopathy-associated myosin mutation R403Q accelerates tension generation and relaxation of human cardiac myofibrils

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s12265-009-9131-8

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441-451

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scholarly article

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10.1007/S12265-009-9131-8

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4

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2009-10-09T00:00:00Z

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20560002

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