Accumulation of prion protein in muscle fibers of experimental chloroquine myopathy: in vivo model for deposition of prion protein in non-neuronal tissues
- 1 July 2004
- journal article
- research article
- Published by Elsevier in Laboratory Investigation
- Vol. 84 (7) , 828-835
- https://doi.org/10.1038/labinvest.3700111
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Extraneural Pathologic Prion Protein in Sporadic Creutzfeldt–Jakob DiseaseNew England Journal of Medicine, 2003
- Prions in skeletal muscleProceedings of the National Academy of Sciences, 2002
- Increased Expression of the Normal Cellular Isoform of Prion Protein in Inclusion‐Body Myositis, Inflammatory Myopathies and Denervation AtrophyBrain Pathology, 2001
- Prion protein expression in mammalian lensesCurrent Eye Research, 2000
- Blockade of Glycosylation Promotes Acquistion of Scrapie-like Properties by the Prion Protein in Cultured CellsPublished by Elsevier ,1997
- Diagnosis of new variant Creutzfeldt-Jakob disease by tonsil biopsyThe Lancet, 1997
- Co-localization of amyloid-associated proteins with amyloid β in rat soleus muscle in chloroquine-induced myopathy: a possible model for amyloid β formation in Alzheimer's diseaseBrain Research, 1995
- Prion protein is abnormally accumulated in inclusion-body myositisNeuroReport, 1993
- Molecular Biology of Prion DiseasesScience, 1991
- EXPERIMENTAL CHLOROQUINE MYOPATHYJournal of Neuropathology and Experimental Neurology, 1970