Mitochondrial dysfunction and neurodegenerative proteinopathies: mechanisms and prospects for therapeutic intervention

Neurodegenerative proteinopathies are a group of pathologically similar, progressive disorders of the nervous system, characterised by structural alterations within and toxic misfolding of susceptible proteins. Oligomerisation of Aβ, tau, α-synuclein and TDP-43 leads to a toxin gain- or loss-of-func...

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Detalles Bibliográficos
Autores principales: Briston, Thomas, Hicks, Amy R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2018
Materias:
Review Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6103456/
https://www.ncbi.nlm.nih.gov/pubmed/29986938
http://dx.doi.org/10.1042/BST20180025

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6103456/
https://www.ncbi.nlm.nih.gov/pubmed/29986938
http://dx.doi.org/10.1042/BST20180025

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