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An astrocyte cell line that differentially propagates murine prions

Prion diseases are fatal infectious neurodegenerative disorders in human and animals caused by misfolding of the cellular prion protein (PrP(C)) into the pathological isoform PrP(Sc). Elucidating the molecular and cellular mechanisms underlying prion propagation may help to develop disease intervent...

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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:J Biol Chem
Egile Nagusiak: Tahir, Waqas, Abdulrahman, Basant, Abdelaziz, Dalia H., Thapa, Simrika, Walia, Rupali, Schätzl, Hermann M.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: American Society for Biochemistry and Molecular Biology 2020
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC7450132/
https://ncbi.nlm.nih.gov/pubmed/32561641
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.RA120.012596
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