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Emerging Infectious Diseases|November 6, 2013
Atypical scrapie prions from sheep and lack of disease in transgenic mice overexpressing human prion proteinJonathan D F Wadsworth, Susan Joiner, Jacqueline M Linehan, et al.Journal of Neuropathology and Experimental Neurology|August 22, 2008
First report of Creutzfeldt-Jakob disease occurring in 2 siblings unexplained by PRNP mutationThomas E F Webb, Suvankar Pal, Durrenajaf Siddique, et al.Nature Communications|July 10, 2014
Prion neuropathology follows the accumulation of alternate prion protein isoforms after infective titre has peakedMalin K Sandberg, Huda Al-Doujaily, Bernadette Sharps, et al.Proceedings of the National Academy of Sciences of the United States of America|June 11, 2026
Strain-specific propagation of variant Creutzfeldt-Jakob disease prions in humanized neural cellsMelissa L D Rayner, Parineeta Arora, Jacqueline M Linehan, et al.Plos Pathogens|February 20, 2025
Isolation of a novel human prion strain from a PRNP codon 129 heterozygous vCJD patientFuquan Zhang, Susan Joiner, Jacqueline M Linehan, et al.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.The Journal of Infectious Diseases|January 27, 2021
Humanized Transgenic Mice Are Resistant to Chronic Wasting Disease Prions From Norwegian Reindeer and MooseJonathan D F Wadsworth, Susan Joiner, Jacqueline M Linehan, et al.The Journal of Biological Chemistry|July 31, 2014
N-terminal domain of prion protein directs its oligomeric associationClare R Trevitt, Laszlo L P Hosszu, Mark Batchelor, et al.Science (New York, N.Y.)|September 24, 2005
An aneuploid mouse strain carrying human chromosome 21 with Down syndrome phenotypesAideen O'Doherty, Sandra Ruf, Claire Mulligan, et al.Open Biology|December 4, 2015
A systematic investigation of production of synthetic prions from recombinant prion proteinChristian Schmidt, Jeremie Fizet, Francesca Properzi, et al.Pageof 5