Development of an Automated Capillary Immunoassay to Detect Prion Glycotypes in Creutzfeldt-Jakob Disease.
Creutzfeldt-Jakob disease
Prion
capillary electrophoresis
Journal
Laboratory investigation; a journal of technical methods and pathology
ISSN: 1530-0307
Titre abrégé: Lab Invest
Pays: United States
ID NLM: 0376617
Informations de publication
Date de publication:
03 2023
03 2023
Historique:
received:
10
10
2021
revised:
23
09
2022
accepted:
07
11
2022
entrez:
16
3
2023
pubmed:
17
3
2023
medline:
21
3
2023
Statut:
ppublish
Résumé
Creutzfeldt-Jakob disease (CJD) comprises a group of transmissible neurodegenerative diseases with vast phenotypic diversity. Sporadic CJD heterogeneity is predominantly influenced by the genotype at codon 129 of the prion-encoding gene and the molecular weight of PrP
Identifiants
pubmed: 36925197
pii: S0023-6837(22)00620-1
doi: 10.1016/j.labinv.2022.100029
pii:
doi:
Substances chimiques
Prions
0
Prion Proteins
0
Peptide Hydrolases
EC 3.4.-
Codon
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
100029Informations de copyright
Crown Copyright © 2022. Published by Elsevier Inc. All rights reserved.