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Profoundly different prion diseases in knock-in mice carrying single PrP codon substitutions associated with human diseases

In man, mutations in different regions of the prion protein (PrP) are associated with infectious neurodegenerative diseases that have remarkably different clinical signs and neuropathological lesions. To explore the roots of this phenomenon, we created a knock-in mouse model carrying the mutation as...

Ausführliche Beschreibung

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Bibliographische Detailangaben
Hauptverfasser: Jackson, Walker S., Borkowski, Andrew W., Watson, Nicki E., King, Oliver D., Faas, Henryk, Jasanoff, Alan, Lindquist, Susan
Format: Artigo
Sprache:Inglês
Veröffentlicht: National Academy of Sciences 2013
Schlagworte:
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3767526/
https://ncbi.nlm.nih.gov/pubmed/23959875
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1312006110
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