Inducible Prion Diseases Caused by Artificial Mutation
Principal Investigator
Publications
Baskakov, I.V., Legname, G., et al. (2001) Folding of prion protein to its native alpha-helical conformation is under kinetic control. J. Biol. Chem. 276(23):19687-19690. 
Supattapone, S., Bouzamondo, E., et al. (2001) A protease-resistant 61-residue prion peptide causes neurodegeneration in transgenic mice. Mol. Cell. Biol. 21(7): 2608-2616.
Baskakov, I.V., Aagaard, C., et al. (2000) Self -assembly of recombinant prion protein of 106 residues. Biochemistry 39(10):2792-2804.
Supattapone, S., Bosque, P., et al. (1999) Prion protein of 106 residues creates an artificial transmission barrier for prion replication in transgenic mice. Cell. 96(6):869-878.
First published on: June 11, 2008
Last modified on: November 20, 2024