Immunoreactivity of cerebral amyloidosis is enhanced by protein denaturation treatments
- 1 September 1991
- journal article
- Published by Springer Nature in Acta Neuropathologica
- Vol. 82 (4) , 260-265
- https://doi.org/10.1007/bf00308810
Abstract
No abstract availableKeywords
This publication has 32 references indexed in Scilit:
- Scrapie prion proteins accumulate in the cytoplasm of persistently infected cultured cells.The Journal of cell biology, 1990
- Creutzfeldt‐Jakob disease patients with congophilic kuru plaques have the missense variant prion protein common to Gerstmann‐Sträussler syndromeAnnals of Neurology, 1990
- 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
- Amyloid A4 Protein and Its Precursor in Down's Syndrome and Alzheimer's DiseaseNew England Journal of Medicine, 1989
- Immunohistochemical verification of senile and kuru plaques in Creutzfeldt‐Jakob disease and the allied diseaseAnnals of Neurology, 1988
- Gerstmann‐Sträussler‐Scheinker disease: Immunohistological and experimental studiesAnnals of Neurology, 1988
- Alzheimer's disease: Initial report of the purification and characterization of a novel cerebrovascular amyloid proteinBiochemical and Biophysical Research Communications, 1984
- Novel Proteinaceous Infectious Particles Cause ScrapieScience, 1982
- Properties of the transmissible agent derived from chronic spongiform encephalopathyAnnals of Neurology, 1980
- Creutzfeldt-Jakob Disease (Spongiform Encephalopathy): Transmission to the ChimpanzeeScience, 1968