InhaltsangabeWhat Would Thomas Henry Huxley Have Made of Prion Diseases?

Rosalind M. Ridley



Prion Protein as Copper-Binding Protein at the Synapse

Hans A. Kretzschmar, Tobias Tings, Axel Madlung, Armin Giese, and Jochen Herms



A Function for the Prion Protein?

David R. Brown and Ian M. Jones



Prion Protein Peptide: Agents of Death for Neurons

David R. Brown



Characterization of Bovine Spongiform Encephalopathy and Scrapie Strains/Isolates by Immunochemical Analysis of PrPSc

Martin H. Groschup, Frauke Junghans, Martin Eiden, and Thorsten Kuczius



Differential Targeting of Neurons by Prion Strains

Stephen J. DeArmond



Transgenic Studies of Prion Diseases

Glenn C. Telling



Prions: From Neurografts to Neuroinvasion

Markus Glatzel, Sebastian Brandner, Michael A. Klein, and Adriano Aguzzi



Cellular and Transgenic Models of Familial Prion Diseases

David A. Harris, Roberto Chiesa, Antonio Migheli, Pedro Piccardo, and Bernardino Ghetti



Central Nervous System Inflammation and Prion Disease Pathogenesis

Samar Betmouni and V. Hugh Perry



The Electroneuropathology of Prion Disease

J. Richard Greene



Transmissible Spongiform Encephalopathy Neurobiology and Ultrastructure Suggests Extracellular PrPSc Conversion Consistent with Classical Amyloidosis

Martin Jeffrey and Jan R. Fraser



Conformation as Therapeutic Target in the Prionoses and Other Neurodegenerative Conditions

Thomas Wisniewski, Einar M. Sigurdsson, Pierre Aucouturier, and Blas Frangione



Prions of Yeast: From Cytoplasmic Genes to Heritable Amyloidosis

Reed B. Wickner, Herman K. Edskes, Kimberly L. Taylor, Marie-Lise Maddelein, Hiromitsu Moriyama, and B. Tibor Roberts