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Prion Protein Accumulation in Lipid Rafts of Mouse Aging Brain
The cellular form of the prion protein (PrP(C)) is a normal constituent of neuronal cell membranes. The protein misfolding causes rare neurodegenerative disorders known as transmissible spongiform encephalopathies or prion diseases. These maladies can be sporadic, genetic or infectious. Sporadic pri...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3769255/ https://ncbi.nlm.nih.gov/pubmed/24040215 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0074244 |
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