Systematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathy - Wikidata - awgldk - TriplyDB

Systematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathy

Systematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathy

http://www.wikidata.org/entity/Q28211536

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Early ketamine exposure results in cardiac enlargement and heart dysfunction in Xenopus embryos.Diastolic dysfunction in familial hypertrophic cardiomyopathy transgenic model mice In the thick of it: HCM-causing mutations in myosin binding proteins of the thick filament Acceleration of stretch activation in murine myocardium due to phosphorylation of myosin regulatory light chain Gene expression throughout a vertebrate's embryogenesis.Familial hypertrophic cardiomyopathy can be characterized by a specific pattern of orientation fluctuations of actin molecules .Cross-bridge kinetics in myofibrils containing familial hypertrophic cardiomyopathy R58Q mutation in the regulatory light chain of myosin Proteome expression and carbonylation changes during Trypanosoma cruzi infection and Chagas disease in rats.Unconventional myosins, actin dynamics and endocytosis: a ménage à trois?Effect of a myosin regulatory light chain mutation K104E on actin-myosin interactions.A Novel Method of Determining the Functional Effects of a Minor Genetic Modification of a Protein.Myofibrillar remodeling in cardiac hypertrophy, heart failure and cardiomyopathies.Myosin regulatory light chain phosphorylation enhances cardiac β-myosin in vitro motility under load.Proteomic analysis of short-term preload-induced eccentric cardiac hypertrophy.Malignant familial hypertrophic cardiomyopathy D166V mutation in the ventricular myosin regulatory light chain causes profound effects in skinned and intact papillary muscle fibers from transgenic mice.Regulatory light chain mutations associated with cardiomyopathy affect myosin mechanics and kinetics Diversity and similarity of motor function and cross-bridge kinetics in papillary muscles of transgenic mice carrying myosin regulatory light chain mutations D166V and R58Q Depletion of zebrafish essential and regulatory myosin light chains reduces cardiac function through distinct mechanisms Thick and thin filament gene mutations in striated muscle diseases.Gene expression patterns in transgenic mouse models of hypertrophic cardiomyopathy caused by mutations in myosin regulatory light chain.Heavy and light roles: myosin in the morphogenesis of the heart.Genetic biomarkers in hypertrophic cardiomyopathy.Pseudophosphorylation of cardiac myosin regulatory light chain: a promising new tool for treatment of cardiomyopathy.Male-specific genetic effect on hypertension and metabolic disorders.Kinetics of a single cross-bridge in familial hypertrophic cardiomyopathy heart muscle measured by reverse Kretschmann fluorescence.Single molecule kinetics in the familial hypertrophic cardiomyopathy D166V mutant mouse heart.A One Health Approach to Hypertrophic Cardiomyopathy.Molecular and Functional Effects of a Splice Site Mutation in the MYL2 Gene Associated with Cardioskeletal Myopathy and Early Cardiac Death in Infants.Genetic basis of end-stage hypertrophic cardiomyopathy.Single molecule detection approach to muscle study: kinetics of a single cross-bridge during contraction of muscle.Hypertrophic cardiomyopathy mutation R58Q in the myosin regulatory light chain perturbs thick filament-based regulation in cardiac muscle.

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Systematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathy

http://www.wikidata.org/entity/Q28211536

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2002 nî lūn-bûn

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2002 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

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2002 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2002年の論文

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2002年論文

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2002年論文

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name

Systematic analysis of the reg ...... in hypertrophic cardiomyopathy

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Systematic analysis of the reg ...... in hypertrophic cardiomyopathy

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Systematic analysis of the reg ...... in hypertrophic cardiomyopathy

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type

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Systematic analysis of the reg ...... in hypertrophic cardiomyopathy

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Systematic analysis of the reg ...... in hypertrophic cardiomyopathy

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Systematic analysis of the reg ...... in hypertrophic cardiomyopathy

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Systematic analysis of the reg ...... in hypertrophic cardiomyopathy

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Systematic analysis of the reg ...... in hypertrophic cardiomyopathy

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Systematic analysis of the reg ...... in hypertrophic cardiomyopathy

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SJ.EJHG.5200872

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European Journal of Human Genetics

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Systematic analysis of the reg ...... in hypertrophic cardiomyopathy

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Bastian Wolter

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Hagen D Schulte

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João Martins Correia

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Karl Josef Osterziel

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Mirsaid M Mirrakhimov

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Nuno Cardim

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Rainer Dietz

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Zhyldyz T Kabaeva

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P2860

Familial hypertrophic cardiomyopathy mutations in the regulatory light chains of myosin affect their structure, Ca2+ binding, and phosphorylation

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

Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations

Three-dimensional structure of myosin subfragment-1: a molecular motor

Tuning the human heart molecular motors by myosin light chains

Localization of the gene coding for ventricular myosin regulatory light chain (MYL2) to human chromosome 12q23-q24.3

Different expressivity of a ventricular essential myosin light chain gene Ala57Gly mutation in familial hypertrophic cardiomyopathy

Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy

Contractile protein mutations and heart disease

The Genetic Basis for Cardiomyopathy

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11

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11060153

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