The prion protein constitutively controls neuronal store-operated Ca(2+) entry through Fyn kinase

The prion protein (PrP(C)) is a cell surface glycoprotein mainly expressed in neurons, whose misfolded isoforms generate the prion responsible for incurable neurodegenerative disorders. Whereas PrP(C) involvement in prion propagation is well established, PrP(C) physiological function is still enigma...

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Detalles Bibliográficos
Autores principales: De Mario, Agnese, Castellani, Angela, Peggion, Caterina, Massimino, Maria Lina, Lim, Dmitry, Hill, Andrew F., Sorgato, M. Catia, Bertoli, Alessandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4623396/
https://www.ncbi.nlm.nih.gov/pubmed/26578881
http://dx.doi.org/10.3389/fncel.2015.00416

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4623396/
https://www.ncbi.nlm.nih.gov/pubmed/26578881
http://dx.doi.org/10.3389/fncel.2015.00416

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