Astrocyte in prion disease: a double-edged sword

Prion diseases are infectious protein misfolding disorders of the central nervous system that result from misfolding of the cellular prion protein (PrP(C)) into the pathologic isoform PrP(Sc). Pathologic hallmarks of prion disease are depositions of pathological prion protein PrP(Sc), neuronal loss,...

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Detalles Bibliográficos
Autores principales: Tahir, Waqas, Thapa, Simrika, Schatzl, Hermann M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8820723/
https://www.ncbi.nlm.nih.gov/pubmed/35017412
http://dx.doi.org/10.4103/1673-5374.332202

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8820723/
https://www.ncbi.nlm.nih.gov/pubmed/35017412
http://dx.doi.org/10.4103/1673-5374.332202

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