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Aggregated, Wild-Type Prion Protein Causes Neurological Dysfunction and Synaptic Abnormalities
The neurotoxic forms of the prion protein (PrP) that cause neurodegeneration in prion diseases remain to be conclusively identified. Considerable evidence points to the importance of noninfectious oligomers of PrP in the pathogenic process. In this study, we describe lines of Tg(WT) transgenic mice...
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| Hlavní autoři: | , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Society for Neuroscience
2008
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2646838/ https://ncbi.nlm.nih.gov/pubmed/19052217 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.3109-08.2008 |
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