Aggregation Condition–Structure Relationship of Mouse Prion Protein Fibrils

Prion diseases are associated with conformational conversion of cellular prion protein into a misfolded pathogenic form, which resembles many properties of amyloid fibrils. The same prion protein sequence can misfold into different conformations, which are responsible for variations in prion disease...

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Detalles Bibliográficos
Autores principales: Fridmanis, Jēkabs, Toleikis, Zigmantas, Sneideris, Tomas, Ziaunys, Mantas, Bobrovs, Raitis, Smirnovas, Vytautas, Jaudzems, Kristaps
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8431800/
https://www.ncbi.nlm.nih.gov/pubmed/34502545
http://dx.doi.org/10.3390/ijms22179635

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8431800/
https://www.ncbi.nlm.nih.gov/pubmed/34502545
http://dx.doi.org/10.3390/ijms22179635

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