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Misfolding leads the way to unraveling signaling pathways in the pathophysiology of prion diseases
A misfolded version of the prion protein represents an essential component in the pathophysiology of fatal neurodegenerative prion diseases, which affect humans and animals alike. They may be of sporadic origin, acquired through exogenous introduction of infectious misfolded prion protein, or caused...
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| Gepubliceerd in: | Prion |
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| Hoofdauteurs: | , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Taylor & Francis
2016
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5161300/ https://ncbi.nlm.nih.gov/pubmed/27870599 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/19336896.2016.1244593 |
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