PrP Polymorphisms Tightly Control Sheep Prion Replication in Cultured Cells
Prion diseases are fatal neurodegenerative disorders of animals and humans that are characterized by the conversion of the host-encoded prion protein (PrP) to an abnormal isoform. In several species, including humans, polymorphisms in the gene encoding the PrP protein tightly control susceptibility...
Αποθηκεύτηκε σε:
| Εκδόθηκε σε: | J Virol |
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| Κύριοι συγγραφείς: | , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
American Society for Microbiology (ASM)
2003
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC141085/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/12552009/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/JVI.77.4.2696-2700.2003 |
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