Primary Myopathy and Accumulation of PrPSc-Like Molecules in Peripheral Tissues of Transgenic Mice Expressing a Prion Protein Insertional Mutation
- 30 April 2001
- journal article
- Published by Elsevier in Neurobiology of Disease
- Vol. 8 (2) , 279-288
- https://doi.org/10.1006/nbdi.2001.0400
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- RGS4 causes increased mortality and reduced cardiac hypertrophy in response to pressure overloadJournal of Clinical Investigation, 1999
- Prion Proteins Carrying Pathogenic Mutations Are Resistant to Phospholipase Cleavage of Their Glycolipid AnchorsBiochemistry, 1999
- Ultrastructural localization of cellular prion protein (PrPc) at the neuromuscular junctionJournal of Neuroscience Research, 1999
- A vector for expressing foreign genes in the brains and hearts of transgenic miceGenetic Analysis: Biomolecular Engineering, 1996
- Mutant and Infectious Prion Proteins Display Common Biochemical Properties in Cultured CellsJournal of Biological Chemistry, 1996
- Developmental expression of the prion protein gene in glial cellsNeuron, 1995
- Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteinsCell, 1994
- A new inherited prion disease (PrP‐P105L mutation) showing spastic paraparesisAnnals of Neurology, 1993
- Prion protein is abnormally accumulated in inclusion-body myositisNeuroReport, 1993
- Detection of Prion Protein mRNA in Normal and Scrapie-infected Tissues and Cell LinesJournal of General Virology, 1988