Delay of EGF-Stimulated EGFR Degradation in Myotonic Dystrophy Type 1 (DM1)

Myotonic dystrophy type 1 (DM1) is an autosomal dominant disease caused by a CTG repeat expansion in the 3′ untranslated region of the dystrophia myotonica protein kinase gene. AKT dephosphorylation and autophagy are associated with DM1. Autophagy has been widely studied in DM1, although the endocyt...

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Detalles Bibliográficos
Autores principales: Alegre-Cortés, Eva, Giménez-Bejarano, Alberto, Uribe-Carretero, Elisabet, Paredes-Barquero, Marta, Marques, André R. A., Lopes-da-Silva, Mafalda, Vieira, Otília V., Canales-Cortés, Saray, Camello, Pedro J., Martínez-Chacón, Guadalupe, Aiastui, Ana, Fernández-Torrón, Roberto, López de Munain, Adolfo, Gomez-Suaga, Patricia, Niso-Santano, Mireia, González-Polo, Rosa A., Fuentes, José M., Yakhine-Diop, Sokhna M. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9562898/
https://www.ncbi.nlm.nih.gov/pubmed/36230978
http://dx.doi.org/10.3390/cells11193018

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9562898/
https://www.ncbi.nlm.nih.gov/pubmed/36230978
http://dx.doi.org/10.3390/cells11193018

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