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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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Dettagli Bibliografici
Pubblicato in:Biochem Soc Trans
Autori principali: Briston, Thomas, Hicks, Amy R.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Portland Press Ltd. 2018
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6103456/
https://ncbi.nlm.nih.gov/pubmed/29986938
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BST20180025
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