Electrophysiological abnormalities precede overt structural changes in arrhythmogenic right ventricular cardiomyopathy due to mutations in desmoplakin-A combined murine and human study.
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Disease mutations in desmoplakin inhibit Cx43 membrane targeting mediated by desmoplakin-EB1 interactions.Desmosome regulation and signaling in diseaseArrhythmogenic ventricular cardiomyopathy: A paradigm shift from right to biventricular diseaseMutations 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 diseasesDesmosomes and the sodium channel complex: implications for arrhythmogenic cardiomyopathy and Brugada syndromeSodium current deficit and arrhythmogenesis in a murine model of plakophilin-2 haploinsufficiency.Missense mutations in plakophilin-2 cause sodium current deficit and associate with a Brugada syndrome phenotypeSCN5A mutation in Chinese patients with arrhythmogenic right ventricular dysplasia.Phenotypic expression is a prerequisite for malignant arrhythmic events and sudden cardiac death in arrhythmogenic right ventricular cardiomyopathy.Microdomain-specific localization of functional ion channels in cardiomyocytes: an emerging concept of local regulation and remodelling.Modeling Inherited Arrhythmia Disorders Using Induced Pluripotent Stem Cell-Derived Cardiomyocytes.Dynamic conduction and repolarisation changes in early arrhythmogenic right ventricular cardiomyopathy versus benign outflow tract ectopy demonstrated by high density mapping & paced surface ECG analysis.Protein LUMA is a cytoplasmic plaque constituent of various epithelial adherens junctions and composite junctions of myocardial intercalated disks: a unifying finding for cell biology and cardiology.Arrhythmogenic right ventricular cardiomyopathy (ARVC): cardiovascular magnetic resonance update.Striatins as plaque molecules of zonulae adhaerentes in simple epithelia, of tessellate junctions in stratified epithelia, of cardiac composite junctions and of various size classes of lateral adherens junctions in cultures of epithelia- and carcinoPhysical developmental cues for the maturation of human pluripotent stem cell-derived cardiomyocytes.Diagnostic dilemmas: overlapping features of brugada syndrome and arrhythmogenic right ventricular cardiomyopathyArrhythmogenic right ventricular cardiomyopathy coincided with the cardiac fibrosis in the inner muscle layer of the left ventricular wall in a boxer dogTransgenic mice overexpressing desmocollin-2 (DSC2) develop cardiomyopathy associated with myocardial inflammation and fibrotic remodeling.Relationship Between Arrhythmogenic Right Ventricular Cardiomyopathy and Brugada Syndrome: New Insights From Molecular Biology and Clinical Implications.Connexin diversity in the heart: insights from transgenic mouse models.Regulation of cardiovascular connexins by mechanical forces and junctions.Identification of rare variants of DSP gene in sudden unexplained nocturnal death syndrome in the southern Chinese Han populationConnexin defects underlie arrhythmogenic right ventricular cardiomyopathy in a novel mouse model.Mouse models in arrhythmogenic right ventricular cardiomyopathy.Arrhythmogenic cardiomyopathy and Brugada syndrome: diseases of the connexome.Almanac 2014: cardiomyopathies.The usual suspects in sudden cardiac death of the young: a focus on inherited arrhythmogenic diseases.Desmosomes in the heart: a review of clinical and mechanistic analyses.Connexins in the heart.Electrical and Structural Substrate of Arrhythmogenic Right Ventricular Cardiomyopathy Determined Using Noninvasive Electrocardiographic Imaging and Late Gadolinium Magnetic Resonance Imaging.Pharmacotherapy and other therapeutic modalities for managing Arrhythmogenic Right Ventricular Cardiomyopathy.Risk stratification for sudden death in arrhythmogenic right ventricular cardiomyopathy.Cell models of arrhythmogenic cardiomyopathy: advances and opportunities.Arrhythmogenic Right Ventricular Cardiomyopathy: Risk Stratification and Indications for Defibrillator Therapy.Cardiac mesenchymal stromal cells are a source of adipocytes in arrhythmogenic cardiomyopathy.Murine Electrophysiological Models of Cardiac Arrhythmogenesis.Animal models of arrhythmogenic right ventricular cardiomyopathy: what have we learned and where do we go? Insight for therapeutics.Unmasking the molecular link between arrhythmogenic cardiomyopathy and Brugada syndrome.Pre-participation cardiovascular evaluation for athletic participants to prevent sudden death: Position paper from the EHRA and the EACPR, branches of the ESC. Endorsed by APHRS, HRS, and SOLAECE.
P2860
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P2860
Electrophysiological abnormalities precede overt structural changes in arrhythmogenic right ventricular cardiomyopathy due to mutations in desmoplakin-A combined murine and human study.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Electrophysiological abnormali ...... mbined murine and human study.
@ast
Electrophysiological abnormali ...... mbined murine and human study.
@en
type
label
Electrophysiological abnormali ...... mbined murine and human study.
@ast
Electrophysiological abnormali ...... mbined murine and human study.
@en
prefLabel
Electrophysiological abnormali ...... mbined murine and human study.
@ast
Electrophysiological abnormali ...... mbined murine and human study.
@en
P2093
P2860
P50
P356
P1476
Electrophysiological abnormali ...... ombined murine and human study
@en
P2093
Akbar K Ahmed
Andrew Tinker
Edward J Ciaccio
Giovanni Quarta
Jeffrey E Saffitz
John Gomes
Muriel Nobles
Sanjay Chaubey
P2860
P304
P356
10.1093/EURHEARTJ/EHR472
P577
2012-01-11T00:00:00Z