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Therapeutic targeting of cellular prion protein: toward the development of dual mechanism anti-prion compounds

PrPSc, a misfolded, aggregation-prone isoform of the cellular prion protein (PrPC), is the infectious prion agent responsible for fatal neurodegenerative diseases of humans and other mammals. PrPSc can adopt different pathogenic conformations (prion strains), which can be resistant to potential drug...

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Detalles Bibliográficos
Principais autores: Antonio Masone, Chiara Zucchelli, Enrico Caruso, Giovanna Musco, Roberto Chiesa
Formato: Artigo
Idioma:Inglês
Publicado: Wolters Kluwer Medknow Publications 2025-04-01
Series:Neural Regeneration Research
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Acceso en liña:https://journals.lww.com/10.4103/NRR.NRR-D-24-00181
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