Successful transmission of Creutzfeldt-Jakob disease from human to mouse verified by prion protein accumulation in mouse brains
- 1 December 1992
- journal article
- research article
- Published by Elsevier in Brain Research
- Vol. 599 (2) , 309-316
- https://doi.org/10.1016/0006-8993(92)90406-y
Abstract
No abstract availableKeywords
This publication has 33 references indexed in Scilit:
- Organ Distribution of Proteinase-resistant Prion Protein in Humans and Mice with Creutzfeldt-Jakob DiseaseJournal of General Virology, 1989
- Pro→Leu change at position 102 of prinon protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndromeBiochemical and Biophysical Research Communications, 1989
- Gerstmann‐Sträussler‐Scheinker disease: Immunohistological and experimental studiesAnnals of Neurology, 1988
- Diagnosis of Creutzfeldt-Jakob Disease by Western Blot Identification of Marker Protein in Human Brain TissueNew England Journal of Medicine, 1986
- Creutzfeldt–Jakob Disease Prion Proteins in Human BrainsNew England Journal of Medicine, 1985
- Amyloid plaques in the brains of mice with Creutzfeldt–Jakob diseaseAnnals of Neurology, 1984
- Novel Proteinaceous Infectious Particles Cause ScrapieScience, 1982
- Transmission of Creutzfeldt–Jakob disease with scrapie-like syndromes to miceNature, 1978
- TRANSMISSION OF CREUTZFELDT-JAKOB DISEASE TO SYRIAN HAMSTERThe Lancet, 1977
- Creutzfeldt-Jakob Disease (Spongiform Encephalopathy): Transmission to the ChimpanzeeScience, 1968