Molecular morphology and toxicity of cytoplasmic prion protein aggregates in neuronal and non-neuronal cells
Author:
Publisher
Wiley
Subject
Cellular and Molecular Neuroscience,Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1471-4159.2006.03837.x/fullpdf
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1. Prion Protein Protects Human Neurons against Bax-mediated Apoptosis
2. Normal host prion protein necessary for scrapie-induced neurotoxicity
3. Scrapie-like prion protein accumulates in aggresomes of cyclosporin A-treated cells
4. Intracellular clusterin causes juxtanuclear aggregate formation and mitochondrial alteration
5. Mutant PrP Is Delayed in Its Exit from the Endoplasmic Reticulum, but Neither Wild-type nor Mutant PrP Undergoes Retrotranslocation Prior to Proteasomal Degradation
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