Prion Diseases: Diagnosis and Pathogenesis

Pathogenesis of Prion Diseases: Prions: from neurografts to neuroinvasion (M. Glatzel, M. A. Klein, S. Brandner, A. Aguzzi); Follicular dendritic cells in scrapie pathogenesis (K. L. Brown, K. Stewart, D. Ritchie, H. Fraser, W. I. Morrison, M. E. Bruce); Cellular and sub-cellular localisation of PrP in the lymphoreticular system of mice and sheep (M. Jeffrey, G. McGovern, S. Martin, C. M. Goodsir, K. L. Brown); Pharmacological manipulation of early PrP//res// accumulation in the spleen of scrapie-infected mice (V. Beringue, F. Lamoury, K. T. Adjou, T. Maignien, M. Demoy, P. Couvreur, D. Dormont); Pathogenesis of natural scrapie in sheep (L. J. M. van Keulen, B. E. C. Schreuder, M. E. W. Vromans, J. P. M. Langeveld, M. A. Smits).- Animal Models for Prion Diseases: Detection of cattle-derived BSE prions using transgenic mice overexpressing bovine PrP//C// (A. Buschmann, E. Pfaff, K. Reifenberg, H. M. Müller, M. H. Groschup); Analyzing the influence of PrP primary structure on prion pathogenesis in transgenic mice (S. Campbell, U. Dennchy, G. Telling); A single amino acid alteration in murine PrP dramatically alters TSE incubation time (J. C. Manson, R. Barron, E. Jamieson, H. Baybutt, N. Tuzi, I. McConnell, D. Melton, J. Hope, C. Bostock); A transgenic model of a familial prion disease (D. A. Harris, R. Chiesa, B. Drisaldi, E. Quaglio, A. Migheli, P. Picardo, B. Ghetti); Transgenic models of prion disease (M. R. Scott, S. Supattapone, H.-O. B. Nguyen, S. J. DeArmond, S. B. Prusiner).- Epidemiology and Diagnosis of Prion Diseases: Surveillance of BSE (D. Heim, J. W. Wilesmith); Histopathology and immunohistochemistry of human transmissible spongiform encephalopathies (TSEs) (H. Budka); Pathology of variant Creutzfeldt-Jakob disease (J. W. Ironside); Clinical and differential diagnosis of Creutzfeldt-Jakob disease (S. Poser, I. Zerr, A. Schroeter, M. Otto, A. Giese, B. J. Steinhoff, H. A. Kretzschmar); Putting prions into focus: application of single moleculedetection to the diagnosis of prion diseases (A. Giese, J. Bieschke, M. Eigen, H. A. Kretzschmar); Detection of PrP//Sc// in subclinical BSE with the paraffin-embedded tissue (PET) blot (W. J. Schulz-Schaeffer, R. Fatzer, M. Vandevelde, H. A. Kretzschmar); Sheep and goats: natural and experimental TSEs and factors influencing incidence of disease (N. Hunter, W. Goldmann, E. Marshall, G. O'Neill); Application of Prionics Western blotting procedure to screen for BSE in cattle regularly slaughtered at Swiss abattoirs (B. Oesch, M. Doherr, D. Heim, K. Fischer, S. Egli, S. Bolliger, K. Biffiger, O. Schaller, M. Vandevelde, M. Moser); Specific determination of the proteinase K-resistant form of the prion protein using two-site immunometric assays. Application to the post-mortem diagnosis of BSE (J. Grassi, C. Créminon, Y. Frobert, P. Frétier, I. Turbica, H. Rezaei, G. Hunsmann, E. Comoy, J.-P. Deslys).- Characterization of the Infectious Agent: PrP//Sc// typing by N-terminal sequencing and mass spectrometry (S. G. Chen, W. Zou, P. Parchi, P. Gambetti); Characterization of BSE and scrapie strains/isolates (M. Groschup, T. Kuczius, F. Junghans, T. Sweeney, W. Bodemer, A. Buschmann); Quantitative traits of prion strains are enciphered in the conformation of the prion protein (J. Safar, F. E. Cohen, S. B. Prusiner).- Structure and Function of PrP: Function of PrP//c// as a copper-binding protein at the synapse (H. A. Kretzschmar, T. Tings, A. Madlung, A. Giese, J. Herms); The prion protein globular domain and disease-related mutants studied by molecular dynamics simulations (M. Billeter, K. Wüthrich); Neurotoxicity but not infectivity of prion proteins can be induced reversibly in vitro (K. Post, D. R. Brown, M. H. Groschup, H. A. Kretzschmar, D. Riesner).- PrP Conversion: Inhibition of formation of protease-resistant prion protein by Trypan Blue, Sirius Red, and other Congo Red analogs (R. Demaimay, B. Chesebro, B. Caughey); The use of monoclonal antibody epitopes for