Anti-prion drugs do not improve survival in novel knock-in models of inherited prion disease.
Prion diseases uniquely manifest in three distinct forms: inherited, sporadic, and infectious. Wild-type prions are responsible for the sporadic and infectious versions, while mutant prions cause inherited variants like fatal familial insomnia (FFI) and familial Creutzfeldt-Jakob disease (fCJD). Alt...
Saved in:
| Main Authors: | Daniel J Walsh, Judy R Rees, Surabhi Mehra, Matthew E C Bourkas, Lech Kaczmarczyk, Erica Stuart, Walker S Jackson, Joel C Watts, Surachai Supattapone |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Public Library of Science (PLoS)
2024-04-01
|
| Series: | PLoS Pathogens |
| Online Access: | https://journals.plos.org/plospathogens/article/file?id=10.1371/journal.ppat.1012087&type=printable |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Epigenetic dominance of prion conformers.
by: Eri Saijo, et al.
Published: (2013-10-01) -
A systems approach to prion disease
by: Daehee Hwang, et al.
Published: (2009-03-01) -
Pathogenic prion structures at high resolution.
by: Byron Caughey, et al.
Published: (2022-06-01) -
Retraction Note: Neurotropic influenza A virus infection causes prion protein misfolding into infectious prions in neuroblastoma cells
by: Hideyuki Hara, et al.
Published: (2025-05-01) -
Prion protein-specific antibodies that detect multiple TSE agents with high sensitivity.
by: Sandra McCutcheon, et al.
Published: (2014-01-01)