Arrhythmogenic cardiomyopathy: a disease of intercalated discs (Q38262612)

1 September 2017

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title

Arrhythmogenic cardiomyopathy: a disease of intercalated discs (English)

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1 September 2017

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Martina Calore

1

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1 September 2017

Alessandra Lorenzon

2

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1 September 2017

Marzia De Bortoli

3

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1 September 2017

Giulia Poloni

4

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1 September 2017

Alessandra Rampazzo

5

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1 September 2017

publication date

26 October 2014

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1 September 2017

published in

Cell and Tissue Research

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1 September 2017

volume

360

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1 September 2017

issue

3

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1 September 2017

page(s)

491-500

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https://scigraph.springernature.com/pub.10.1007/s00441-014-2015-5

1 September 2017

exact match

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cites work

Super-resolution fluorescence microscopy of the cardiac connexome reveals plakophilin-2 inside the connexin43 plaque

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A novel dominant mutation in plakoglobin causes arrhythmogenic right ventricular cardiomyopathy

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Identification of a new modulator of the intercalated disc in a zebrafish model of arrhythmogenic cardiomyopathy.

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Pathophysiology of arrhythmogenic cardiomyopathy

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Comparison of clinical features of arrhythmogenic right ventricular cardiomyopathy in men versus women.

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Multiple mutations in desmosomal proteins encoding genes in arrhythmogenic right ventricular cardiomyopathy/dysplasia

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Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1

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Epidermolytic palmoplantar keratoderma with woolly hair and dilated cardiomyopathy

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Modeling of arrhythmogenic right ventricular cardiomyopathy with human induced pluripotent stem cells

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The hippo pathway is activated and is a causal mechanism for adipogenesis in arrhythmogenic cardiomyopathy.

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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.

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Suppression of canonical Wnt/beta-catenin signaling by nuclear plakoglobin recapitulates phenotype of arrhythmogenic right ventricular cardiomyopathy

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Desmosome structure, composition and function

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Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy

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A unique and specific interaction between alphaT-catenin and plakophilin-2 in the area composita, the mixed-type junctional structure of cardiac intercalated discs

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Hippo pathway inhibits Wnt signaling to restrain cardiomyocyte proliferation and heart size

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Mutations in the area composita protein αT-catenin are associated with arrhythmogenic right ventricular cardiomyopathy

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Intercellular adhesion, signalling and the cytoskeleton

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PKC-dependent phosphorylation may regulate the ability of connexin43 to inhibit DNA synthesis

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Studying arrhythmogenic right ventricular dysplasia with patient-specific iPSCs

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De novo desmin-mutation N116S is associated with arrhythmogenic right ventricular cardiomyopathy

21 January 2018

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Restrictive loss of plakoglobin in cardiomyocytes leads to arrhythmogenic cardiomyopathy

21 January 2018

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Cardiac tissue-restricted deletion of plakoglobin results in progressive cardiomyopathy and activation of {beta}-catenin signaling

21 January 2018

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Identification of a PKP2 gene deletion in a family with arrhythmogenic right ventricular cardiomyopathy

21 January 2018

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Genetic fate mapping identifies second heart field progenitor cells as a source of adipocytes in arrhythmogenic right ventricular cardiomyopathy

21 January 2018

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Nuclear plakoglobin is essential for differentiation of cardiac progenitor cells to adipocytes in arrhythmogenic right ventricular cardiomyopathy

21 January 2018

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Connexin defects underlie arrhythmogenic right ventricular cardiomyopathy in a novel mouse model

21 January 2018

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Generation of patient-specific induced pluripotent stem cell-derived cardiomyocytes as a cellular model of arrhythmogenic right ventricular cardiomyopathy.

21 January 2018

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Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease).

21 January 2018

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Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene

21 January 2018

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Familial occurrence of right ventricular dysplasia: a study involving nine families

21 January 2018

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Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma

21 January 2018

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21 January 2018

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Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy

21 January 2018

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Myocyte necrosis underlies progressive myocardial dystrophy in mouse dsg2-related arrhythmogenic right ventricular cardiomyopathy

21 January 2018

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Arrhythmogenic cardiomyopathy with ectodermal dysplasia

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Mutations in the Lamin A/C gene mimic arrhythmogenic right ventricular cardiomyopathy.

21 January 2018

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Genetic bases of arrhythmogenic right ventricular Cardiomyopathy

21 January 2018

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Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy

21 January 2018

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Compound and digenic heterozygosity predicts lifetime arrhythmic outcome and sudden cardiac death in desmosomal gene-related arrhythmogenic right ventricular cardiomyopathy

21 January 2018

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Intercalated disc abnormalities, reduced Na(+) current density, and conduction slowing in desmoglein-2 mutant mice prior to cardiomyopathic changes

21 January 2018

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Detection of genomic deletions of PKP2 in arrhythmogenic right ventricular cardiomyopathy

21 January 2018

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Inhibition of adipogenesis by Wnt signaling

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00441-014-2015-5

Loss of plakophilin-2 expression leads to decreased sodium current and slower conduction velocity in cultured cardiac myocytes

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00441-014-2015-5

Arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00441-014-2015-5

Genetic variation in titin in arrhythmogenic right ventricular cardiomyopathy-overlap syndromes

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00441-014-2015-5

Right ventricular cardiomyopathy and sudden death in young people

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00441-014-2015-5

Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00441-014-2015-5

Compound and digenic heterozygosity contributes to arrhythmogenic right ventricular cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00441-014-2015-5

Phospholamban R14del mutation in patients diagnosed with dilated cardiomyopathy or arrhythmogenic right ventricular cardiomyopathy: evidence supporting the concept of arrhythmogenic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00441-014-2015-5

Mutational Heterogeneity, Modifier Genes, and Environmental Influences Contribute to Phenotypic Diversity of Arrhythmogenic Cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00441-014-2015-5

The area composita of adhering junctions connecting heart muscle cells of vertebrates. VII. The different types of lateral junctions between the special cardiomyocytes of the conduction system of ovine and bovine hearts

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00441-014-2015-5

Remodeling of myocyte gap junctions in arrhythmogenic right ventricular cardiomyopathy due to a deletion in plakoglobin (Naxos disease)

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00441-014-2015-5

10.1007/S00441-014-2015-5

21 January 2018

Identifiers

DOI

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Dimensions Publication ID

1 September 2017

1049147251

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