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Arrhythmogenic right ventricular cardiomyopathy/dysplasiaCardiomyopathy classification: ongoing debate in the genomics eraA new perspective on intercalated disc organization: implications for heart diseaseSuppression of canonical Wnt/beta-catenin signaling by nuclear plakoglobin recapitulates phenotype of arrhythmogenic right ventricular cardiomyopathyArrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 geneCardiac disease and Rett syndromeMutations with pathogenic potential in proteins located in or at the composite junctions of the intercalated disk connecting mammalian cardiomyocytes: a reference thesaurus for arrhythmogenic cardiomyopathies and for Naxos and Carvajal diseasesAlterations in adhesion junction precede gap junction remodelling during the development of heart failure in cardiomyopathic hamstersArrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathyEvaluation of right and left ventricular function using speckle tracking echocardiography in patients with arrhythmogenic right ventricular cardiomyopathy and their first degree relatives.A pediatric case report on arrhythmogenic right ventricular dysplasia.Natural history of arrhythmogenic right ventricular cardiomyopathy in the boxer dog: a prospective studyNoncompaction of the ventricular myocardium is associated with a de novo mutation in the beta-myosin heavy chain geneDiagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the Task Force CriteriaDesmosomal molecules in and out of adhering junctions: normal and diseased States of epidermal, cardiac and mesenchymally derived cells.Genetics of sudden cardiac death.Novel missense mutations in exon 15 of desmoglein-2: role of the intracellular cadherin segment in arrhythmogenic right ventricular cardiomyopathy?In vitro functional analyses of arrhythmogenic right ventricular cardiomyopathy-associated desmoglein-2-missense variationsCircadian rhythms, Wnt/beta-catenin pathway and PPAR alpha/gamma profiles in diseases with primary or secondary cardiac dysfunction.DSG2 mutations contribute to arrhythmogenic right ventricular dysplasia/cardiomyopathyCardiac-specific NRAP overexpression causes right ventricular dysfunction in miceShared desmosome gene findings in early and late onset arrhythmogenic right ventricular dysplasia/cardiomyopathy.Ultrastructural changes in cardiac myocytes from Boxer dogs with arrhythmogenic right ventricular cardiomyopathyA pedigree-based genetic appraisal of Boxer ARVC and the role of the Striatin mutationGenetics of inherited cardiomyopathy.Identification of Medically Actionable Secondary Findings in the 1000 Genomes.Abnormal connexin43 in arrhythmogenic right ventricular cardiomyopathy caused by plakophilin-2 mutations.Plasma BIN1 correlates with heart failure and predicts arrhythmia in patients with arrhythmogenic right ventricular cardiomyopathy.Molecular composition of the intercalated disc in a spontaneous canine animal model of arrhythmogenic right ventricular dysplasia/cardiomyopathy.Role of cardiovascular magnetic resonance imaging in arrhythmogenic right ventricular dysplasiaChange in β-catenin localization suggests involvement of the canonical Wnt pathway in Boxer dogs with arrhythmogenic right ventricular cardiomyopathyEvolving molecular diagnostics for familial cardiomyopathies: at the heart of it allThe junctions that don't fit the scheme: special symmetrical cell-cell junctions of their own kind.Progress with genetic cardiomyopathies: screening, counseling, and testing in dilated, hypertrophic, and arrhythmogenic right ventricular dysplasia/cardiomyopathy.Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C): a review of molecular and clinical literature.Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D).Arrhythmogenic Cardiomyopathy - New Insights into Disease Mechanisms and Drug Discovery.Wnt Signaling in Cardiac Disease.Cell models of arrhythmogenic cardiomyopathy: advances and opportunities.
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
@zh
2005年论文
@zh-cn
name
Genetics of right ventricular cardiomyopathy.
@ast
Genetics of right ventricular cardiomyopathy.
@en
type
label
Genetics of right ventricular cardiomyopathy.
@ast
Genetics of right ventricular cardiomyopathy.
@en
prefLabel
Genetics of right ventricular cardiomyopathy.
@ast
Genetics of right ventricular cardiomyopathy.
@en
P2093
P1476
Genetics of right ventricular cardiomyopathy.
@en
P2093
Petros Syrris
Srijita Sen-Chowdhry
William J McKenna
P304
P356
10.1111/J.1540-8167.2005.40842.X
P577
2005-08-01T00:00:00Z