PMCA Applications for Prion Detection in Peripheral Tissues of Patients with Variant Creutzfeldt-Jakob Disease.
Creutzfeldt-Jakob disease
PMCA
disease biomarker
neurodegeneration
prion
Journal
Biomolecules
ISSN: 2218-273X
Titre abrégé: Biomolecules
Pays: Switzerland
ID NLM: 101596414
Informations de publication
Date de publication:
05 03 2020
05 03 2020
Historique:
received:
13
02
2020
revised:
02
03
2020
accepted:
05
03
2020
entrez:
11
3
2020
pubmed:
11
3
2020
medline:
19
3
2021
Statut:
epublish
Résumé
Prion diseases are neurodegenerative and invariably fatal conditions that affect humans and animals. In particular, Creutzfeldt-Jakob disease (CJD) and bovine spongiform encephalopathy (BSE) are paradigmatic forms of human and animal prion diseases, respectively. Human exposure to BSE through contaminated food caused the appearance of the new variant form of CJD (vCJD). These diseases are caused by an abnormal prion protein named PrP
Identifiants
pubmed: 32151109
pii: biom10030405
doi: 10.3390/biom10030405
pmc: PMC7175161
pii:
doi:
Substances chimiques
Biomarkers
0
PrPSc Proteins
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Déclaration de conflit d'intérêts
The authors declare no conflict of interest
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