Free Access
Med Sci (Paris)
Volume 19, Number 8-9, Août-Septembre 2003
Page(s) 778 - 780
Section Le Magazine : Nouvelles
Published online 15 August 2003
  1. Collinge J. Prion diseases of humans and animals: their causes and molecular basis. Annu Rev Neurosci 2001; 24: 519–50. [Google Scholar]
  2. Zerial M, McBride H. Rab proteins as membrane organizers. Nat Rev Mol Cell Biol 2001; 2: 107–17. [Google Scholar]
  3. Beranger F, Mange A, Goud B, Lehmann S. Stimulation of PrP(C) retrograde transport toward the endoplasmic reticulum increases accumulation of PrP(Sc) in prion-infected cells. J Biol Chem 2002; 277: 38972–7. [Google Scholar]
  4. Yedidia Y, Horonchik L, Tzaban S, Yanai A, Taraboulos A. Proteasomes and ubiquitin are involved in the turnover of the wildtype prion protein. EMBO J 2001; 20: 5383–91. [Google Scholar]
  5. Ma J, Lindquist S. Wild-type PrP and a mutant associated with prion disease are subject to retrograde transport and proteasome degradation. Proc Natl Acad Sci USA 2001; 98: 14955–60. [Google Scholar]
  6. Ma J, Lindquist S. Conversion of PrP to a selfperpetuating PrPSc-like conformation in the cytosol. Science 2002; 298: 1785–8. [Google Scholar]
  7. Ma J, Wollmann R, Lindquist S. Neurotoxicity and neurodegeneration when PrP accumulates in the cytosol. Science 2002; 298: 1781–5. [Google Scholar]
  8. Cohen E, Taraboulos A. Scrapie-like prion protein accumulates in aggresomes of cyclosporin A-treated cells. EMBO J 2003; 22: 404–17. [Google Scholar]

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