Dilated cardiomyopathy: the complexity of a diverse genetic architecture.
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A Review of the Giant Protein Titin in Clinical Molecular Diagnostics of CardiomyopathiesNext-Generation Sequencing in Post-mortem Genetic Testing of Young Sudden Cardiac Death CasesPhysiological and Pathophysiological Insights of Nav1.4 and Nav1.5 ComparisonHuman-induced pluripotent stem cell models of inherited cardiomyopathiesEnsemble force changes that result from human cardiac myosin mutations and a small-molecule effectorClinical and Mechanistic Insights Into theĀ Genetics of CardiomyopathyWhy Is there a Limit to the Changes in Myofilament Ca2+-Sensitivity Associated with Myopathy Causing Mutations?Molecular mechanisms of cardiomyopathy phenotypes associated with myosin light chain mutationsFBXO32, encoding a member of the SCF complex, is mutated in dilated cardiomyopathyGenetic epidemiology of titin-truncating variants in the etiology of dilated cardiomyopathy.Genetic determinants of myocardial dysfunction.Correction of human phospholamban R14del mutation associated with cardiomyopathy using targeted nucleases and combination therapy.Actin binding GFP allows 4D in vivo imaging of myofilament dynamics in the zebrafish heart and the identification of Erbb2 signaling as a remodeling factor of myofibril architecture.Titin-truncating variants affect heart function in disease cohorts and the general population.Novel nesprin-1 mutations associated with dilated cardiomyopathy cause nuclear envelope disruption and defects in myogenesis.Decoding the complex genetic causes of heart diseases using systems biologyMechano-signaling in heart failureComparison of clinical outcomes in peripartum cardiomyopathy and age-matched dilated cardiomyopathy: A 15-year nationwide population-based study in Asia.RAF1 mutations in childhood-onset dilated cardiomyopathyHereditary Dilated Cardiomyopathy: Recent Advances in Genetic Diagnostics.Obscure functions: the location-function relationship of obscurins.Genotype-specific pathogenic effects in human dilated cardiomyopathy.Missing heritability of common diseases and treatments outside the protein-coding exome.HEART DISEASE. Titin mutations in iPS cells define sarcomere insufficiency as a cause of dilated cardiomyopathy.Structural and protein interaction effects of hypertrophic and dilated cardiomyopathic mutations in alpha-tropomyosin.Effects of naturally occurring arginine 14 deletion on phospholamban conformational dynamics and membrane interactionsCaffeine exposure alters cardiac gene expression in embryonic cardiomyocytes.GENETIC CAUSES OF DILATED CARDIOMYOPATHY.Peripartum cardiomyopathy and dilated cardiomyopathy: different at heart.Arrhythmogenic cardiomyopathy in a patient with a rare loss-of-function KCNQ1 mutation.Novel familial dilated cardiomyopathy mutation in MYL2 affects the structure and function of myosin regulatory light chain.OBSCN Mutations Associated with Dilated Cardiomyopathy and Haploinsufficiency.A novel human R25C-phospholamban mutation is associated with super-inhibition of calcium cycling and ventricular arrhythmiaTargeted Next-Generation Sequencing Reveals Hot Spots and Doubly Heterozygous Mutations in Chinese Patients with Familial CardiomyopathyIntegrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and diseaseGenetics and genotype-phenotype correlations in Finnish patients with dilated cardiomyopathycAMP induces hypertrophy and alters DNA methylation in HL-1 cardiomyocytes.Genetic Variation in Cardiomyopathy and Cardiovascular Disorders.Gene-Targeted Mice with the Human Troponin T R141W Mutation Develop Dilated Cardiomyopathy with Calcium DesensitizationTitin Truncating Variants in Dilated Cardiomyopathy - Prevalence and Genotype-Phenotype Correlations.
P2860
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P2860
Dilated cardiomyopathy: the complexity of a diverse genetic architecture.
description
article cientĆfic
@ca
article scientifique
@fr
articol ČtiinČific
@ro
articolo scientifico
@it
artigo cientĆfico
@gl
artigo cientĆfico
@pt
artigo cientĆfico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artĆculo cientĆfico
@es
name
Dilated cardiomyopathy: the complexity of a diverse genetic architecture.
@en
type
label
Dilated cardiomyopathy: the complexity of a diverse genetic architecture.
@en
prefLabel
Dilated cardiomyopathy: the complexity of a diverse genetic architecture.
@en
P1476
Dilated cardiomyopathy: the complexity of a diverse genetic architecture
@en
P2093
Ana Morales
Dale J Hedges
P304
P356
10.1038/NRCARDIO.2013.105
P407
P577
2013-07-30T00:00:00Z