Post-translational modification and mitochondrial function in Parkinson’s disease

Parkinson’s disease (PD) is the second most common neurodegenerative disease with currently no cure. Most PD cases are sporadic, and about 5–10% of PD cases present a monogenic inheritance pattern. Mutations in more than 20 genes are associated with genetic forms of PD. Mitochondrial dysfunction is...

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Autors principals:	Shishi Luo, Danling Wang, Zhuohua Zhang
Format:	Artigo
Idioma:	Inglês
Publicat:	Frontiers Media S.A. 2024-01-01
Col·lecció:	Frontiers in Molecular Neuroscience
Matèries:	Parkinson’s disease post-translational modification (PTM) mitochondrial function ubiquitination phosphorylation acetylation
Accés en línia:	https://www.frontiersin.org/articles/10.3389/fnmol.2023.1329554/full
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