Detection of Type 1 Prion Protein in Variant Creutzfeldt-Jakob Disease
- 31 January 2006
- journal article
- research article
- Published by Elsevier BV in The American Journal of Pathology
- Vol. 168 (1), 151-157
- https://doi.org/10.2353/ajpath.2006.050766
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Human Prion Protein with Valine 129 Prevents Expression of Variant CJD PhenotypeScience, 2004
- Striking PrPsc heterogeneity in inherited prion diseases with the D178N mutationAnnals of Neurology, 2004
- Characterization of two distinct prion strains derived from bovine spongiform encephalopathy transmissions to inbred miceJournal of General Virology, 2004
- Standards for the assay of Creutzfeldt–Jakob disease specimensJournal of General Virology, 2004
- Effects of Different Experimental Conditions on the PrPSc Core Generated by Protease DigestionJournal of Biological Chemistry, 2004
- Discrimination between Scrapie and Bovine Spongiform Encephalopathy in Sheep by Molecular Size, Immunoreactivity, and Glycoprofile of Prion ProteinJournal of Clinical Microbiology, 2004
- Peripheral Tissue Involvement in Sporadic, Iatrogenic, and Variant Creutzfeldt-Jakob DiseaseThe American Journal of Pathology, 2004
- Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjectsAnnals of Neurology, 1999
- Molecular analysis of prion strain variation and the aetiology of 'new variant' CJDNature, 1996
- Immumohistochemical Detection and Localization of Prion Protein in Brain Tissue of Sheep With Natural ScrapieVeterinary Pathology, 1995