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TranscriptomicsMyocardial transcriptome analysis of human arrhythmogenic right ventricular cardiomyopathy (ARVC)
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiomyopathy primarily of the right ventricle characterized through fibrofatty replacement of cardiomyocytes. The genetic etiology in ARVC patients is most commonly caused by dominant inheritance and high genetic heterogeneity....
ORGANISM(S): Homo sapiens 
2011-11-30 | E-GEOD-29819 | biostudies-arrayexpress
ProteomicsProteomic analysis of ARVC rat with PKP2 mutation heart
To investigate the changes in sodium channel proteins in ARVC rats with PKP2 gene mutations, we performed proteomic analysis on the hearts of WT and PKP2 rats.
ORGANISM(S): Rattus norvegicus (Rat) 
2025-08-25 | PXD066271 | Pride
Heart Proteome Pkp2 Rat Arvc 
Proteomicsarrythmogenic right ventricular acrdiomayopathy (PKP2-cko in mice and Human biopsies)
Summary: Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiac disorder. It is classified as the second most common cause of unexpected sudden death by cardiac arrest in the young. ARVC has devastating psychosocial consequences, especially as many patients are young adults, ...
ORGANISM(S): Homo sapiens (Human) Mus musculus (Mouse) 
2022-11-04 | PXD025523 | Pride
Cardiovascular protemics Tmt Heart failure Arvc 
TranscriptomicsMyocardial transcriptome analysis of human arrhythmogenic right ventricular cardiomyopathy (ARVC)
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiomyopathy primarily of the right ventricle characterized through fibrofatty replacement of cardiomyocytes. The genetic etiology in ARVC patients is most commonly caused by dominant inheritance and high genetic heterogeneity....
ORGANISM(S): Homo sapiens 
2011-11-30 | GSE29819 | GEO
GenomicsElectrophysiological defects in a novel patient-derived stem cell model of desmoglein-2 mutant ARVC
Electrophysiological defects in a novel patient-derived stem cell model of desmoglein-2 mutant ARVC
PRJNA735383 | ENA
TranscriptomicsElectrophysiological defects in a novel patient-derived stem cell model of desmoglein-2 mutant ARVC
Here we developed a novel human induced pluripotent stem cell (hiPSC) model of ARVC to gain insight into the electrical and biomolecular effects of desmoglein-2 (DSG2) mutation in cardiomyocytes. hiPSC-derived cardiomyocytes (hiPSC-CMs) were generated from peripheral blood mononuclear cells donated ...
ORGANISM(S): Homo sapiens 
2021-06-06 | GSE176209 | GEO
UnknownVentricular structure in ARVC: going beyond volumes as a measure of risk.
Not available
S-EPMC5069945 | biostudies-literature
UnknownHow ARVC-Related Mutations Destabilize Desmoplakin: An MD Study.
Not available
S-EPMC6403075 | biostudies-literature
GenomicsTNYA0042: TN-401 dose-dependent efficacy study at about 10 weeks in Pkp2-cKO ARVC mouse model
TNYA0042: TN-401 dose-dependent efficacy study at about 10 weeks in Pkp2-cKO ARVC mouse model
PRJNA1064600 | ENA
UnknownAdipogenic Signaling Promotes Arrhythmia Substrates before Structural Abnormalities in TMEM43 ARVC.
Not available
S-EPMC9604824 | biostudies-literature
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