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Molecular genetic and functional characterization implicate muscle-restricted coiled-coil gene (MURC) as a causal gene for familial dilated cardiomyopathyHydrophobic imbalance in the cytoplasmic domain of phospholamban is a determinant for lethal dilated cardiomyopathyGenetic Variations Leading to Familial Dilated CardiomyopathyRecent advances in animal and human pluripotent stem cell modeling of cardiac laminopathyMolecular mechanisms of cardiomyopathy phenotypes associated with myosin light chain mutationsCorrection of human phospholamban R14del mutation associated with cardiomyopathy using targeted nucleases and combination therapy.Novel nesprin-1 mutations associated with dilated cardiomyopathy cause nuclear envelope disruption and defects in myogenesis.Linker of nucleoskeleton and cytoskeleton complex proteins in cardiac structure, function, and disease.Role of cardiac magnetic resonance in the evaluation of dilated cardiomyopathy: diagnostic contribution and prognostic significance.RAF1 mutations in childhood-onset dilated cardiomyopathyCardiac troponin T (TNNT2) mutations in chinese dilated cardiomyopathy patientsTruncations of titin causing dilated cardiomyopathy.The promise of whole-exome sequencing in medical genetics.Lethal Arg9Cys phospholamban mutation hinders Ca2+-ATPase regulation and phosphorylation by protein kinase A.Effects of naturally occurring arginine 14 deletion on phospholamban conformational dynamics and membrane interactionsLMNA mutations in Polish patients with dilated cardiomyopathy: prevalence, clinical characteristics, and in vitro studiesUpdate 2011: clinical and genetic issues in familial dilated cardiomyopathy.Prioritizing disease candidate proteins in cardiomyopathy-specific protein-protein interaction networks based on "guilt by association" analysis.Strategic approaches to unraveling genetic causes of cardiovascular diseases.Effects of troponin T cardiomyopathy mutations on the calcium sensitivity of the regulated thin filament and the actomyosin cross-bridge kinetics of human β-cardiac myosin.Polymorphism in the alpha cardiac muscle actin 1 gene is associated to susceptibility to chronic inflammatory cardiomyopathy.Targeted ablation of nesprin 1 and nesprin 2 from murine myocardium results in cardiomyopathy, altered nuclear morphology and inhibition of the biomechanical gene response.Acute inotropic and lusitropic effects of cardiomyopathic R9C mutation of phospholamban.Dysfunctional conformational dynamics of protein kinase A induced by a lethal mutant of phospholamban hinder phosphorylation.Novel familial dilated cardiomyopathy mutation in MYL2 affects the structure and function of myosin regulatory light chain.Genetics and genotype-phenotype correlations in Finnish patients with dilated cardiomyopathyCardiac-specific deletion of the microtubule-binding protein CENP-F causes dilated cardiomyopathyTNNT2 Gene Polymorphisms are Associated with Susceptibility to Idiopathic Dilated Cardiomyopathy in Kazak and Han ChineseModeling of lamin A/C mutation premature cardiac aging using patient‐specific induced pluripotent stem cells.Subtle abnormalities in contractile function are an early manifestation of sarcomere mutations in dilated cardiomyopathy.Recurrent and founder mutations in the Netherlands-Phospholamban p.Arg14del mutation causes arrhythmogenic cardiomyopathy.Genetic testing for dilated cardiomyopathy in clinical practice.Heart failure in sub-Saharan Africa.A rising titan: TTN review and mutation update.Deception in simplicity: hereditary phospholamban mutations in dilated cardiomyopathy.Evolving Approaches to Genetic Evaluation of Specific Cardiomyopathies.Congenital dilated cardiomyopathy caused by biallelic mutations in Filamin C.Next generation sequencing in cardiovascular diseases.Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart Failure.Population-based variation in cardiomyopathy genes
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on May 2010
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
The genetics of dilated cardiomyopathy.
@en
The genetics of dilated cardiomyopathy.
@nl
type
label
The genetics of dilated cardiomyopathy.
@en
The genetics of dilated cardiomyopathy.
@nl
prefLabel
The genetics of dilated cardiomyopathy.
@en
The genetics of dilated cardiomyopathy.
@nl
P2860
P1476
The genetics of dilated cardiomyopathy.
@en
P2093
Elizabeth M McNally
Lisa Dellefave
P2860
P304
P356
10.1097/HCO.0B013E328337BA52
P577
2010-05-01T00:00:00Z