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...
Tallennettuna:
| Julkaisussa: | J Virol |
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| Päätekijät: | , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
American Society for Microbiology (ASM)
2003
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| Aiheet: | |
| Linkit: | 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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