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Cell|October 6, 1995
Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another proteinG C Telling, M Scott, J Mastrianni, et al.Pediatrics|March 1, 1987
Pyruvate dehydrogenase complex deficiency as a cause of subacute necrotizing encephalopathy (Leigh disease)H A Kretzschmar, S J DeArmond, T K Koch, et al.Neuroreport|August 12, 1996
Aberrant induction of neuropeptide Y mRNA in hippocampal CA3 pyramidal neurones in scrapie-infected miceM Diez, J Koistinaho, S J DeArmond, et al.Journal of Virology|January 11, 2001
Identification of two prion protein regions that modify scrapie incubation timeS Supattapone, T Muramoto, G Legname, et al.Neurosurgery|April 1, 1994
Creutzfeldt-Jakob disease in a pregnant woman with an implanted dura mater graftK L Lane, P Brown, D N Howell, et al.Microbiological Sciences|January 1, 1985
Scrapie and Creutzfeldt-Jakob disease prionsS B Prusiner, R A Barry, M P McKinley, et al.Proceedings of the National Academy of Sciences of the United States of America|February 15, 1992
Mouse model of neurodegeneration: atrophy of basal forebrain cholinergic neurons in trisomy 16 transplantsD M Holtzman, Y W Li, S J DeArmond, et al.Nature|April 16, 1992
Normal development and behaviour of mice lacking the neuronal cell-surface PrP proteinH Büeler, M Fischer, Y Lang, et al.Proceedings of the National Academy of Sciences of the United States of America|November 15, 1993
Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodiesS B Prusiner, D Groth, A Serban, et al.Archives of Neurology|May 1, 1988
Subacute structural myopathy associated with human immunodeficiency virus infectionM F Gonzales, R K Olney, Y T So, et al.Pageof 13