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Prion Diseases: A Unique Transmissible Agent or a Model for Neurodegenerative Diseases?

The accumulation and propagation in the brain of misfolded proteins is a pathological hallmark shared by many neurodegenerative diseases such as Alzheimer’s disease (Aβ and tau), Parkinson’s disease (α-synuclein), and prion disease (prion protein). Currently, there is no epidemiological evidence to...

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Foilsithe in:Biomolecules
Main Authors: Ritchie, Diane L., Barria, Marcelo A.
Formáid: Artigo
Teanga:Inglês
Foilsithe: MDPI 2021
Ábhair:
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC7912988/
https://ncbi.nlm.nih.gov/pubmed/33540845
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/biom11020207
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