Molecular Pathology of the Prions Book

What 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