Pathogenesis of prion diseases: a progress report
Open Access
- 28 September 2000
- journal article
- review article
- Published by Springer Nature in Cell Death & Differentiation
- Vol. 7 (10) , 889-902
- https://doi.org/10.1038/sj.cdd.4400737
Abstract
No abstract availableKeywords
This publication has 96 references indexed in Scilit:
- Impaired Prion Replication in Spleens of Mice Lacking Functional Follicular Dendritic CellsScience, 2000
- Ataxia in prion protein (PrP)-deficient mice is associated with upregulation of the novel PrP-like protein doppelJournal of Molecular Biology, 1999
- Identification of Candidate Proteins Binding to Prion ProteinNeurobiology of Disease, 1997
- Evidence for the Conformation of the Pathologic Isoform of the Prion Protein Enciphering and Propagating Prion DiversityScience, 1996
- A suspicious signatureNature, 1996
- Developmental expression of the prion protein gene in glial cellsNeuron, 1995
- Mutation of the Prion Protein in Libyan Jews with Creutzfeldt–Jakob DiseaseNew England Journal of Medicine, 1991
- Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndromeExperimental Neurology, 1989
- The role of the spleen in the neuroinvasion of scrapie in miceVirus Research, 1989
- Cloning the chromosomal breakpoint of t(14;18) human lymphomas: clustering around Jh on chromosome 14 and near a transcriptional unit on 18Cell, 1985