Učitavanje...
Non-amyloid and amyloid prion protein deposits in prion-infected mice differ in blockage of interstitial brain fluid
AIMS: Prion diseases are characterized by brain deposits of misfolded aggregated protease-resistant prion protein (PrP), termed PrPres. In humans and animals, PrPres is found as either disorganized non-amyloid aggregates or organized amyloid fibrils. Both PrPres forms are found in extracellular spac...
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| Glavni autori: | , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2013
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3567241/ https://ncbi.nlm.nih.gov/pubmed/22998478 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1365-2990.2012.01303.x |
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