Biosynthesis and cellular processing of the prion protein
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Publisher
Elsevier
Reference120 articles.
1. Plasmalemmal caveolae and GPI-anchored membrane proteins
2. The abnormal isoform of the prion protein accumulates in late-endosome-like organelles in scrapie-infected mouse brain
3. Nearly ubiquitous tissue distribution of the scrapie agent precursor protein
4. Biochemical and physical properties of the prion protein from two strains of the transmissible mink encephalopathy agent
5. Rapid anterograde axonal transport of the cellular prion glycoprotein in the peripheral and central nervous systems.
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1. Ultrastructural changes in the progress of natural Scrapie regardless fixation protocol;Histochemistry and Cell Biology;2015-02-28
2. The role of rafts in the fibrillization and aggregation of prions;Chemistry and Physics of Lipids;2006-06
3. The crucial role of metal ions in neurodegeneration: the basis for a promising therapeutic strategy;British Journal of Pharmacology;2005-12
4. Checking the pH-Induced Conformational Transition of Prion Protein by Molecular Dynamics Simulations: Effect of Protonation of Histidine Residues;Biophysical Journal;2004-12
5. Propagation of a protease-resistant form of prion protein in long-term cultured human glioblastoma cell line T98G;Journal of General Virology;2004-11-01
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