Characterization of Anchorless Human PrP With Q227X Stop Mutation Linked to Gerstmann-Sträussler-Scheinker Syndrome In Vivo and In Vitro.
Adult
Animals
Antibodies
/ metabolism
Autopsy
Brain
/ metabolism
Cell Line, Tumor
Cell Membrane
/ metabolism
Centrifugation, Density Gradient
Codon, Nonsense
/ genetics
Female
Gerstmann-Straussler-Scheinker Disease
/ genetics
Glycosylation
Humans
Mice, Transgenic
Prions
/ chemistry
Protein Aggregates
Protein Folding
Allelic origin
Gerstmann-Sträussler-Scheinker (GSS) syndrome
Glycosylphosphatidylinositol (GPI) anchor
Mutation
Prion disease
Prion protein
Prions
Protein misfolding cyclic amplification (PMCA)
Journal
Molecular neurobiology
ISSN: 1559-1182
Titre abrégé: Mol Neurobiol
Pays: United States
ID NLM: 8900963
Informations de publication
Date de publication:
Jan 2021
Jan 2021
Historique:
received:
22
04
2020
accepted:
25
08
2020
pubmed:
6
9
2020
medline:
5
8
2021
entrez:
5
9
2020
Statut:
ppublish
Résumé
Alteration in cellular prion protein (PrP
Identifiants
pubmed: 32889654
doi: 10.1007/s12035-020-02098-8
pii: 10.1007/s12035-020-02098-8
pmc: PMC7695670
doi:
Substances chimiques
Antibodies
0
Codon, Nonsense
0
Prions
0
Protein Aggregates
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
21-33Subventions
Organisme : NINDS NIH HHS
ID : R01 NS088604
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS109532
Pays : United States
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