Differential Accumulation of Misfolded Prion Strains in Natural Hosts of Prion Diseases.
Creutzfeldt–Jakob disease
Gerstmann–Straussler–Scheinker disease
Kuru
bovine spongiform encephalopathy
cerebellar cortex
chronic wasting disease
enteric nervous system
prion neuroinvasion
retinal ganglion cells
scrapie
Journal
Viruses
ISSN: 1999-4915
Titre abrégé: Viruses
Pays: Switzerland
ID NLM: 101509722
Informations de publication
Date de publication:
07 12 2021
07 12 2021
Historique:
received:
05
11
2021
revised:
01
12
2021
accepted:
03
12
2021
entrez:
28
12
2021
pubmed:
29
12
2021
medline:
15
2
2022
Statut:
epublish
Résumé
Prion diseases, also known as transmissible spongiform encephalopathies (TSEs), are a group of neurodegenerative protein misfolding diseases that invariably cause death. TSEs occur when the endogenous cellular prion protein (PrP
Identifiants
pubmed: 34960722
pii: v13122453
doi: 10.3390/v13122453
pmc: PMC8706046
pii:
doi:
Substances chimiques
Prion Proteins
0
Types de publication
Journal Article
Research Support, U.S. Gov't, Non-P.H.S.
Review
Langues
eng
Sous-ensembles de citation
IM
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