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Muscle & Nerve|February 1, 1982
Virological studies in amyotrophic lateral sclerosisR J Kascsak, R I Carp, J T Vilcek, et al.The Journal of Infectious Diseases|January 1, 1993
Brain regional distribution of prion protein PrP27-30 in mice stereotaxically microinjected with different strains of scrapieP Casaccia-Bonnefil, R J Kascsak, R Fersko, et al.Acta Neuropathologica|January 1, 1984
Alzheimer neurofibrillary tangles: monoclonal antibodies to inherent antigen(s)G P Wang, I Grundke-Iqbal, R J Kascsak, et al.Progress in Clinical and Biological Research|January 1, 1989
Classic genetics of scrapieR I Carp, Y S Kim, R J Kascsak, et al.Journal of Virology|January 1, 1987
Antisera to scrapie-associated fibril protein and prion protein decorate scrapie-associated fibrilsP A Merz, R J Kascsak, R Rubenstein, et al.Brain Research|April 30, 1986
Paired helical filaments associated with Alzheimer disease are readily soluble structuresR Rubenstein, R J Kascsak, P A Merz, et al.Developments in Biological Standardization|January 1, 1993
The role of antibodies to PrP in the diagnosis of transmissible spongiform encephalopathiesR J Kascsak, M Tonna-DeMasi, R Fersko, et al.The Journal of General Virology|August 1, 1985
Biochemical differences among scrapie-associated fibrils support the biological diversity of scrapie agentsR J Kascsak, R Rubenstein, P A Merz, et al.Biochemical and Biophysical Research Communications|May 18, 1999
Cell-lysate conversion of prion protein into its protease-resistant isoform suggests the participation of a cellular chaperoneG P Saborío, C Soto, R J Kascsak, et al.Alzheimer Disease and Associated Disorders|January 1, 1989
The nature of the unconventional slow infection agents remains a puzzleR I Carp, R J Kascsak, H M Wisniewski, et al.Pageof 4