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Nature|June 11, 2015
A naturally occurring variant of the human prion protein completely prevents prion diseaseEmmanuel A Asante, Michelle Smidak, Andrew Grimshaw, et al.
Brain : a Journal of Neurology|May 28, 2011
Inherited prion disease with 4-octapeptide repeat insertion: disease requires the interaction of multiple genetic risk factorsDiego N Kaski, Catherine Pennington, Jon Beck, et al.
Plos One|December 17, 2011
Sex effects in mouse prion disease incubation timeShaheen Akhtar, Adam Wenborn, Sebastian Brandner, et al.
Neurobiology of Disease|July 22, 2008
Hippocampal bursts caused by changes in NMDA receptor-dependent excitation in a mouse model of variant CJDStéphanie Ratté, Steven A Prescott, John Collinge, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|October 14, 2008
Mortuary rites of the South Fore and kuruJerome T Whitfield, Wandagi H Pako, John Collinge, et al.
BMC Neuroscience|March 25, 2014
Microglial Cx3cr1 knockout reduces prion disease incubation time in miceJulia Grizenkova, Shaheen Akhtar, Sebastian Brandner, et al.
Cell and Tissue Research|August 26, 2022
Prion strains viewed through the lens of cryo-EMSzymon W Manka, Adam Wenborn, John Collinge, et al.
Molecular Psychiatry|March 6, 2021
Evaluation of plasma tau and neurofilament light chain biomarkers in a 12-year clinical cohort of human prion diseasesAndrew G B Thompson, Prodromos Anastasiadis, Ronald Druyeh, et al.
Archives of Neurology|April 17, 2008
Parietal lobe deficits in frontotemporal lobar degeneration caused by a mutation in the progranulin geneJonathan D Rohrer, Jason D Warren, Rohani Omar, et al.
Brain : a Journal of Neurology|February 28, 2012
Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological featuresColin J Mahoney, Jon Beck, Jonathan D Rohrer, et al.
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