Identification of DAPK1 as an autophagy-related biomarker for myotonic dystrophy type 1

Myotonic dystrophy type I (DM1), a CTG repeat expansion hereditary disorder, is primarily characterized by myotonia. Several studies have reported that abnormal autophagy pathway has a close relationship with DM1. However, the underlying key regulatory molecules dictating autophagy disturbance still...

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Detalles Bibliográficos
Autores principales: Hu, Min, Ge, Meng-Ru, Li, Hong-Xia, Zhang, Bei, Li, Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9634726/
https://www.ncbi.nlm.nih.gov/pubmed/36338967
http://dx.doi.org/10.3389/fgene.2022.1022640

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9634726/
https://www.ncbi.nlm.nih.gov/pubmed/36338967
http://dx.doi.org/10.3389/fgene.2022.1022640

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