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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...
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| Hoofdauteurs: | , , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
American Society for Microbiology
2003
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC141085/ https://ncbi.nlm.nih.gov/pubmed/12552009 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/JVI.77.4.2696-2700.2003 |
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