Excitatory neuron-prone prion propagation and excitatory neuronal loss in prion-infected mice
The accumulation of a disease-specific isoform of prion protein (PrPSc) and histopathological lesions, such as neuronal loss, are unevenly distributed in the brains of humans and animals affected with prion diseases. This distribution varies depending on the diseases and/or the combinations of prion...
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| Asıl Yazarlar: | , , , , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Frontiers Media S.A.
2024-12-01
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| Seri Bilgileri: | Frontiers in Molecular Neuroscience |
| Konular: | |
| Online Erişim: | https://www.frontiersin.org/articles/10.3389/fnmol.2024.1498142/full |
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