In Vivo Conversion of Cellular Prion Protein to Pathogenic Isoforms, as Monitored by Conformation-specific Antibodies
Open Access
- 1 April 2001
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 276 (14), 11265-11271
- https://doi.org/10.1074/jbc.m008734200
Abstract
No abstract availableKeywords
This publication has 32 references indexed in Scilit:
- New Insight into Abnormal Prion Protein Using Monoclonal AntibodiesBiochemical and Biophysical Research Communications, 1999
- Loss of cerebellar Purkinje cells in aged mice homozygous for a disrupted PrP geneNature, 1996
- A cellular form of prion protein (PrPC) exists in many non-neuronal tissues of sheepJournal of General Virology, 1995
- Rescue of neurophysiological phenotype seen in PrP null mice by transgene encoding human prion proteinNature Genetics, 1995
- Mice devoid of the glial fibrillary acidic protein develop normally and are susceptible to scrapie prionsNeuron, 1995
- Prion protein is necessary for normal synaptic functionNature, 1994
- Characterization of pseudorabies virus neutralization antigen glycoprotein gIII produced in insect cells by a baculovirus expression vectorVirus Research, 1991
- Scrapie prion proteins accumulate in the cytoplasm of persistently infected cultured cells.The Journal of cell biology, 1990
- Cellular isoform of the scrapie agent protein participates in lymphocyte activationCell, 1990
- A cellular gene encodes scrapie PrP 27-30 proteinCell, 1985