Perspectives on prion biology, prion disease pathogenesis, and pharmacologic approaches to treatment
- 1 March 2003
- journal article
- review article
- Published by Elsevier in Clinics In Laboratory Medicine
- Vol. 23 (1) , 1-41
- https://doi.org/10.1016/s0272-2712(02)00041-0
Abstract
No abstract availableKeywords
This publication has 99 references indexed in Scilit:
- Decreased MK-801 Binding in Discrete Hippocampal Regions of Prion-Infected MiceNeurobiology of Disease, 2001
- A synthetic peptide initiates Gerstmann-Sträussler-Scheinker (GSS) disease in transgenic miceJournal of Molecular Biology, 2000
- Ataxia in prion protein (PrP)-deficient mice is associated with upregulation of the novel PrP-like protein doppelJournal of Molecular Biology, 1999
- Evidence for the Conformation of the Pathologic Isoform of the Prion Protein Enciphering and Propagating Prion DiversityScience, 1996
- Prion Protein AmyloidosisBrain Pathology, 1996
- Homozygosity for prion protein alleles encoding glutamine-171 renders sheep susceptible to natural scrapie.Genes & Development, 1994
- Replication of distinct scrapie prion isolates is region specific in brains of transgenic mice and hamsters.Genes & Development, 1992
- Fatal Familial Insomnia, a Prion Disease with a Mutation at Codon 178 of the Prion Protein GeneNew England Journal of Medicine, 1992
- Evidence for a secretory form of the cellular prion proteinBiochemistry, 1987
- Neuronal spread of scrapie agent and targeting of lesions within the retino-tectal pathwayNature, 1982