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Drosophila models of prionopathies: insight into prion protein function, transmission, and neurotoxicity
Prion diseases (PrD) are unique neurodegenerative conditions that can present with sporadic, genetic, and infectious etiologies. The agent responsible for these pathologies in humans and mammals is a misfolded conformation of the prion protein (PrP), a membrane-anchored protein highly expressed in t...
Tallennettuna:
| Julkaisussa: | Curr Opin Genet Dev |
|---|---|
| Päätekijät: | , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2017
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5474952/ https://ncbi.nlm.nih.gov/pubmed/28415023 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.gde.2017.03.013 |
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