Disease-Associated Prion Protein in Vessel Walls

Human prion diseases like Creutzfeldt-Jakob disease are infectious, inherited, or sporadic neurodegenerative disorders, characterized by the accumulationof an abnormal isoform of the host-encoded prion protein. This affects nervous tissue in sporadic Creutzfeldt-Jakob disease and, additionally, in l...

Full description

Saved in:
Bibliographic Details
Main Authors: Koperek, Oskar, Kovács, Gábor G., Ritchie, Diane, Ironside, James W., Budka, Herbert, Wick, Georg
Format: Artigo
Language:Inglês
Published: American Society for Investigative Pathology 2002
Subjects:
Short Communications
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC1850927/
https://ncbi.nlm.nih.gov/pubmed/12466112
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items