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Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|October 14, 2008
Central and peripheral pathology of kuru: pathological analysis of a recent case and comparison with other forms of human prion diseaseSebastian Brandner, Jerome Whitfield, Ken Boone, et al.Plos Pathogens|October 3, 2013
Inherited prion disease A117V is not simply a proteinopathy but produces prions transmissible to transgenic mice expressing homologous prion proteinEmmanuel A Asante, Jacqueline M Linehan, Michelle Smidak, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|August 28, 2014
R47H TREM2 variant increases risk of typical early-onset Alzheimer's disease but not of prion or frontotemporal dementiaCatherine F Slattery, Jonathan A Beck, Lorna Harper, et al.Brain : a Journal of Neurology|April 7, 2006
Phenotypic heterogeneity in inherited prion disease (P102L) is associated with differential propagation of protease-resistant wild-type and mutant prion proteinJonathan D F Wadsworth, Susan Joiner, Jacqueline M Linehan, et al.The Journal of General Virology|February 17, 2009
Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteinsEmmanuel A Asante, Ian Gowland, Andrew Grimshaw, et al.Journal of Molecular Biology|February 14, 2006
Elongated oligomers assemble into mammalian PrP amyloid fibrilsM Howard Tattum, Sara Cohen-Krausz, Kanjana Thumanu, et al.The Lancet. Neurology|June 24, 2017
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association studyDavina J Hensman Moss, Antonio F Pardiñas, Douglas Langbehn, et al.Annals of Neurology|January 1, 2019
Early onset cerebral amyloid angiopathy following childhood exposure to cadaveric duraGargi Banerjee, Matthew E Adams, Zane Jaunmuktane, et al.Human Molecular Genetics|April 30, 2004
Somatic and germline mosaicism in sporadic early-onset Alzheimer's diseaseJonathan A Beck, Mark Poulter, Tracy A Campbell, et al.The Journal of General Virology|July 9, 2010
Chronic wasting disease prions are not transmissible to transgenic mice overexpressing human prion proteinMalin K Sandberg, Huda Al-Doujaily, Christina J Sigurdson, et al.Pageof 36