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References from Modeling incomplete penetrance in arrhythmogenic cardiomyopathy by human induced pluripotent stem cell derived cardiomyocytes. Local targets link to admitted publications; unresolved targets remain external evidence.
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Cell junctions in the specialized conduction system of the heart
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Multiple mutations in desmosomal proteins encoding genes in arrhythmogenic right ventricular cardiomyopathy/dysplasia
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Compound and digenic heterozygosity contributes to arrhythmogenic right ventricular cardiomyopathy
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High penetrance and similar disease progression in probands and in family members with arrhythmogenic cardiomyopathy
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Arrhythmogenic right ventricular cardiomyopathy/dysplasia on the basis of the revised diagnostic criteria in affected families with desmosomal mutations
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Arrhythmogenic right ventricular cardiomyopathy prevalence and arrhythmic outcomes in at-risk family members: a systematic review and meta-analysis
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Insights into genetics and pathophysiology of arrhythmogenic cardiomyopathy
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The linkage phase of the polymorphism KCNH2-K897T influences the electrophysiological phenotype in hipsc models of LQT2
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hiPSC-derived cardiomyocyte model of LQT2 syndrome derived from asymptomatic and symptomatic mutation carriers reproduces clinical differences in aggregates but not in single cells
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Mitochondrial transport mediates survival of retinal ganglion cells in affected LHON patients
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Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the Task Force Criteria
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Generation of induced pluripotent stem cells from frozen buffy coats using non-integrating episomal plasmids
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Unresolved reference
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Impact of detubulation on force and kinetics of cardiac muscle contraction
10.1085/jgp.201311125 · 2014 · External reference
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10.1186/s13059-014-0550-8
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Mechanotransduction and adrenergic stimulation in arrhythmogenic cardiomyopathy: an overview of in vitro and in vivo models
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Small non-coding RNA therapeutics for cardiovascular disease
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Intercalated disk nanoscale structure regulates cardiac conduction
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10.1016/j.hrthm.2012.11.018 · External reference
Modeling reduced contractility and impaired desmosome assembly due to plakophilin-2 deficiency using isogenic iPS cell-derived cardiomyocytes
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Abnormal connexin43 in arrhythmogenic right ventricular cardiomyopathy caused by plakophilin-2 mutations
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10.1161/circresaha.107.154252
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Myocardial transcriptome analysis of human arrhythmogenic right ventricular cardiomyopathy
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The role of Sfrp and DKK proteins in cardiomyocyte development
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Catecholamine-dependent β-adrenergic signaling in a pluripotent stem cell model of Takotsubo Cardiomyopathy
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RNA sequencing-based transcriptome profiling of cardiac tissue implicates novel putative disease mechanisms in FLNC-associated arrhythmogenic cardiomyopathy
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