Scrapie-like prion protein accumulates in aggresomes of cyclosporin A-treated cells
Prion diseases are infectious, sporadic and inherited fatal neurodegenerations that are propagated by an abnormal refolding of the cellular prion protein PrP(C). Which chaperones assist the normal folding of PrP(C) is unknown. The linkage of familial Gerstmann– Sträussler–Scheinker (GSS) syndrome wi...
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| Pubblicato in: | EMBO J |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Nature Publishing Group
2003
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC140730/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/12554642/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/emboj/cdg045 |
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