Zobrazeno 1 - 2
of 2
pro vyhledávání: '"MoPrP, mouse PrP"'
Autor:
Gerold Schmitt-Ulms, Mohadeseh Mehrabian, Hamza Arshad, Joel C. Watts, Zaid A.M. Al-Azzawi, Matthew E. C. Bourkas, Zeel Patel
Publikováno v:
The Journal of Biological Chemistry
The study of prions and the discovery of candidate therapeutics for prion disease have been facilitated by the ability of prions to replicate in cultured cells. Paradigms in which prion proteins from different species are expressed in cells with low
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c611fbe68ad93669b9774e2ea00b43d4
https://pubmed.ncbi.nlm.nih.gov/34390689
https://pubmed.ncbi.nlm.nih.gov/34390689
Autor:
Elena Quaglio, Vanessa Capone, Vladimiro Artuso, Fabio Fiordaliso, Ignazio Roiter, Davide Ortolan, Michele Sallese, Alessandro Corbelli, Galina V. Beznoussenko, Elena Restelli, Manuela Pozzoli, Roberto Chiesa
Publikováno v:
The Journal of Biological Chemistry
Fatal familial insomnia (FFI), genetic Creutzfeldt–Jakob disease (gCJD), and Gerstmann–Sträussler–Scheinker (GSS) syndrome are neurodegenerative disorders linked to prion protein (PrP) mutations. The pathogenic mechanisms are not known, but in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d3782460cda7c20d4fd5164939fecf2
https://doi.org/10.1016/j.jbc.2021.100490
https://doi.org/10.1016/j.jbc.2021.100490