PITX2 induction leads to impaired cardiomyocyte function in arrhythmogenic cardiomyopathy

Arrhythmogenic cardiomyopathy (ACM) is an inherited progressive disease characterized by electrophysiological and structural remodeling of the ventricles. However, the disease-causing molecular pathways, as a consequence of desmosomal mutations, are poorly understood. Here, we identified a novel mis...

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Detalles Bibliográficos
Autores principales: van Kampen, Sebastiaan J., Han, Su Ji, van Ham, Willem B., Kyriakopoulou, Eirini, Stouthart, Elizabeth W., Goversen, Birgit, Monshouwer-Kloots, Jantine, Perini, Ilaria, de Ruiter, Hesther, van der Kraak, Petra, Vink, Aryan, van Laake, Linda W., Groeneweg, Judith A., de Boer, Teun P., Tsui, Hoyee, Boogerd, Cornelis J., van Veen, Toon A.B., van Rooij, Eva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10031305/
https://www.ncbi.nlm.nih.gov/pubmed/36868229
http://dx.doi.org/10.1016/j.stemcr.2023.01.015

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10031305/
https://www.ncbi.nlm.nih.gov/pubmed/36868229
http://dx.doi.org/10.1016/j.stemcr.2023.01.015

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