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Dissecting α-synuclein inclusion pathology diversity in multiple system atrophy: implications for the prion-like transmission hypothesis

Synucleinopathies are a group of neurodegenerative diseases characterized by the accumulation of insoluble, aggregated α-synuclein (αS) pathological inclusions. Multiple system atrophy (MSA) presents with extensive oligodendroglial αS pathology and additional more limited neuronal inclusions while m...

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Bibliografske podrobnosti
izdano v:Lab Invest
Main Authors: Dhillon, Jess-Karan S., Trejo-Lopez, Jorge A., Riffe, Cara, McFarland, Nikolaus R., Hiser, Wesley M., Giasson, Benoit I., Yachnis, Anthony T.
Format: Artigo
Jezik:Inglês
Izdano: 2019
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC7209695/
https://ncbi.nlm.nih.gov/pubmed/30737468
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41374-019-0198-9
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