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Mouse Models in Arrhythmogenic Right Ventricular Cardiomyopathy

Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heart muscle disorder characterized by fibro-fatty replacement of cardiomyocytes. The cardinal manifestations are arrhythmias, sudden cardiac death, and seldom heart failure. Mutations in genes encoding desmosomal proteins and their interac...

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Detalles Bibliográficos
Autores principales: Lodder, Elisabeth M., Rizzo, Stefania
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3380338/
https://www.ncbi.nlm.nih.gov/pubmed/22737134
http://dx.doi.org/10.3389/fphys.2012.00221
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author Lodder, Elisabeth M.
Rizzo, Stefania
author_facet Lodder, Elisabeth M.
Rizzo, Stefania
author_sort Lodder, Elisabeth M.
collection PubMed
description Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heart muscle disorder characterized by fibro-fatty replacement of cardiomyocytes. The cardinal manifestations are arrhythmias, sudden cardiac death, and seldom heart failure. Mutations in genes encoding desmosomal proteins and their interaction partners have been implicated in the pathogenesis of ARVC and it is now widely accepted that ARVC is a disease caused by abnormal cell–cell adhesion. The mechanism(s) by which mutations in desmosomal proteins lead to fibro-fatty replacement remains to be fully elucidated. To this aim over the last 10 years different transgenic and targeted mouse models have been developed, these models and what they have taught us will be discussed in this review.
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spelling pubmed-33803382012-06-25 Mouse Models in Arrhythmogenic Right Ventricular Cardiomyopathy Lodder, Elisabeth M. Rizzo, Stefania Front Physiol Physiology Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heart muscle disorder characterized by fibro-fatty replacement of cardiomyocytes. The cardinal manifestations are arrhythmias, sudden cardiac death, and seldom heart failure. Mutations in genes encoding desmosomal proteins and their interaction partners have been implicated in the pathogenesis of ARVC and it is now widely accepted that ARVC is a disease caused by abnormal cell–cell adhesion. The mechanism(s) by which mutations in desmosomal proteins lead to fibro-fatty replacement remains to be fully elucidated. To this aim over the last 10 years different transgenic and targeted mouse models have been developed, these models and what they have taught us will be discussed in this review. Frontiers Research Foundation 2012-06-21 /pmc/articles/PMC3380338/ /pubmed/22737134 http://dx.doi.org/10.3389/fphys.2012.00221 Text en Copyright © 2012 Lodder and Rizzo. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
spellingShingle Physiology
Lodder, Elisabeth M.
Rizzo, Stefania
Mouse Models in Arrhythmogenic Right Ventricular Cardiomyopathy
title Mouse Models in Arrhythmogenic Right Ventricular Cardiomyopathy
title_full Mouse Models in Arrhythmogenic Right Ventricular Cardiomyopathy
title_fullStr Mouse Models in Arrhythmogenic Right Ventricular Cardiomyopathy
title_full_unstemmed Mouse Models in Arrhythmogenic Right Ventricular Cardiomyopathy
title_short Mouse Models in Arrhythmogenic Right Ventricular Cardiomyopathy
title_sort mouse models in arrhythmogenic right ventricular cardiomyopathy
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3380338/
https://www.ncbi.nlm.nih.gov/pubmed/22737134
http://dx.doi.org/10.3389/fphys.2012.00221
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