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Correlation of Cellular Factors and Differential Scrapie Prion Permissiveness in Ovine Microglia
Prion diseases are fatal neurodegenerative disorders by which the native cellular prion protein (PrP(C)) is misfolded into an accumulating, disease-associated isoform (PrP(D)). To improve the understanding of prion pathogenesis and develop effective treatments, it is essential to elucidate factors c...
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| Vydáno v: | Virus Res |
|---|---|
| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5771472/ https://ncbi.nlm.nih.gov/pubmed/28754560 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.virusres.2017.07.016 |
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