Altered Ca(2+) homeostasis induces Calpain-Cathepsin axis activation in sporadic Creutzfeldt-Jakob disease

Sporadic Creutzfeldt-Jakob disease (sCJD) is the most prevalent form of human prion disease and it is characterized by the presence of neuronal loss, spongiform degeneration, chronic inflammation and the accumulation of misfolded and pathogenic prion protein (PrP(Sc)). The molecular mechanisms under...

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Detalles Bibliográficos
Autores principales: Llorens, Franc, Thüne, Katrin, Sikorska, Beata, Schmitz, Matthias, Tahir, Waqas, Fernández-Borges, Natalia, Cramm, Maria, Gotzmann, Nadine, Carmona, Margarita, Streichenberger, Nathalie, Michel, Uwe, Zafar, Saima, Schuetz, Anna-Lena, Rajput, Ashish, Andréoletti, Olivier, Bonn, Stefan, Fischer, Andre, Liberski, Pawel P., Torres, Juan Maria, Ferrer, Isidre, Zerr, Inga
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5408381/
https://www.ncbi.nlm.nih.gov/pubmed/28449707
http://dx.doi.org/10.1186/s40478-017-0431-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5408381/
https://www.ncbi.nlm.nih.gov/pubmed/28449707
http://dx.doi.org/10.1186/s40478-017-0431-y

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