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Combining autophagy stimulators and cellulose ethers for therapy against prion disease
Prion diseases are fatal transmissible neurodegenerative disorders that affect animals and humans. Prions are proteinaceous infectious particles consisting of a misfolded isoform of the cellular prion protein PrP(C), termed PrP(Sc). PrP(Sc) accumulates in infected neurons due to partial resistance t...
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| Publicado no: | Prion |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Taylor & Francis
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6779372/ https://ncbi.nlm.nih.gov/pubmed/31578923 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/19336896.2019.1670928 |
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