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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.
Neurophotonics|April 6, 2023
Using functional near-infrared spectroscopy to study the early developing brain: future directions and new challengesJudit Gervain, Yasuyo Minagawa, Lauren Emberson, 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.
The Biochemical Journal|January 31, 2006
Removal of the glycosylphosphatidylinositol anchor from PrP(Sc) by cathepsin D does not reduce prion infectivityPatrick A Lewis, Francesca Properzi, Kanella Prodromidou, et al.
Neurogenetics|December 17, 2002
Identification of genetic loci affecting mouse-adapted bovine spongiform encephalopathy incubation time in miceSarah E Lloyd, James B Uphill, Paul V Targonski, et al.
JAMA Neurology|February 24, 2016
Clinical Trial Simulations Based on Genetic Stratification and the Natural History of a Functional Outcome Measure in Creutzfeldt-Jakob DiseaseSimon Mead, Matthew Burnell, Jessica Lowe, et al.
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