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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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| Hoofdauteurs: | , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Public Library of Science
2013
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| Onderwerpen: | |
| Online toegang: | 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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