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Nature Reviews. Disease Primers|February 29, 2024
Creutzfeldt-Jakob disease and other prion diseasesInga Zerr, Anna Ladogana, Simon Mead, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 18, 2008
Single treatment with RNAi against prion protein rescues early neuronal dysfunction and prolongs survival in mice with prion diseaseMelanie D White, Michael Farmer, Ilaria Mirabile, et al.
The Journal of General Virology|November 19, 2010
A standardized comparison of commercially available prion decontamination reagents using the Standard Steel-Binding AssayJulie Ann Edgeworth, Anita Sicilia, Jackie Linehan, et al.
Neuroscience Letters|April 15, 2004
Pathogenic human prion protein rescues PrP null phenotype in transgenic miceEmmanuel A Asante, Yuan-Gen Li, Ian Gowland, et al.
ACS Nano|February 21, 2023
Direct Observation of Competing Prion Protein Fibril Populations with Distinct Structures and KineticsYuanzi Sun, Kezia Jack, Tiziana Ercolani, et al.
Acta Neuropathologica|July 3, 2013
Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementiaPietro Fratta, Mark Poulter, Tammaryn Lashley, et al.
Human Molecular Genetics|January 3, 2012
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNPSimon Mead, James Uphill, John Beck, et al.
Scientific Reports|September 5, 2020
Association of TDP-43 proteinopathy, cerebral amyloid angiopathy, and Lewy bodies with cognitive impairment in individuals with or without Alzheimer's disease neuropathologyDavid X Thomas, Sumali Bajaj, Kevin McRae-McKee, et al.
Biochemistry|January 3, 2007
Inhibition of proteinase K activity by copper(II) ionsLisa A Stone, Graham S Jackson, John Collinge, et al.
Transfusion|June 22, 2010
A highly sensitive immunoassay for the detection of prion-infected material in whole human blood without the use of proteinase KM Howard Tattum, Samantha Jones, Suvankar Pal, et al.
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