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Proceedings of the National Academy of Sciences of the United States of America|July 15, 1993
Three scrapie prion isolates exhibit different accumulation patterns of the prion protein scrapie isoformS J DeArmond, S L Yang, A Lee, et al.Journal of Neuro-Oncology|January 1, 1994
Development of a non-selecting, non-perturbing method to study human brain tumor cell invasion in murine brainS J DeArmond, L Stowring, A Amar, et al.Cell|May 1, 1985
Identification of prion amyloid filaments in scrapie-infected brainS J DeArmond, M P McKinley, R A Barry, et al.Neurology|August 1, 1987
Changes in the localization of brain prion proteins during scrapie infectionS J DeArmond, W C Mobley, D L DeMott, et al.Annals of Neurology|February 1, 1989
Dominantly inherited dementia and parkinsonism, with non-Alzheimer amyloid plaques: a new neurogenetic disorderR N Rosenberg, J B Green, C L White, et al.Neurology|August 1, 1985
A microangiopathic syndrome of encephalopathy, hearing loss, and retinal arteriolar occlusionsM L Monteiro, R A Swanson, J R Coppeto, et al.Proceedings of the National Academy of Sciences of the United States of America|December 28, 1999
Compelling transgenetic evidence for transmission of bovine spongiform encephalopathy prions to humansM R Scott, R Will, J Ironside, et al.Progress in Clinical and Biological Research|January 1, 1989
Immunoaffinity purification and neutralization of scrapie prionsR Gabizon, M P McKinley, D Groth, et al.Neurology|January 5, 2002
Inherited prion disease caused by the V210I mutation: transmission to transgenic miceJ A Mastrianni, S Capellari, G C Telling, et al.Journal of Virology|November 23, 2000
Affinity-tagged miniprion derivatives spontaneously adopt protease-resistant conformationsS Supattapone, H O Nguyen, T Muramoto, et al.Pageof 13