Prion protein immunocytochemistry helps to establish the true incidence of prion diseases
- 23 November 1992
- journal article
- Published by Elsevier in Neuroscience Letters
- Vol. 147 (1), 67-71
- https://doi.org/10.1016/0304-3940(92)90776-4
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- INHERITED PRION DISEASE WITH 144 BASE PAIR GENE INSERTION: 2. CLINICAL AND PATHOLOGICAL FEATURESBrain, 1992
- Nearly ubiquitous tissue distribution of the scrapie agent precursor proteinNeurology, 1992
- Immunocytochemical confirmation of prion proteinThe Lancet, 1990
- Prion dementia without characteristic pathologyThe Lancet, 1990
- Precise targeting of the pathology of the sialoglycoprotein, PrP, and vacuolar degeneration in mouse scrapieNeuroscience Letters, 1989
- Post-mortem immunodiagnosis of scrapie and bovine spongiform encephalopathyJournal of Virological Methods, 1989
- Linkage of a prion protein missense variant to Gerstmann–Sträussler syndromeNature, 1989
- Changes in the localization of brain prion proteins during scrapie infectionNeurology, 1987
- Identification of a Protein That Purifies with the Scrapie PrionScience, 1982
- Encephalopathy of mink: I. Epizootiologic and clinical observationsThe Journal of Infectious Diseases, 1965