Prions : molecular and cellular biology /
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| Language: | English |
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Wymondham, Norfolk :
Horizon Scientific Press,
[1999], ©1999
Wymondham, Norfolk : c1999 Wymondham, Norfolk ; Portland, Or c1999. Wymondham, Norfolk ; Portland, Or. : [1999], ©1999 Wymondham, Norfolk ; Portland, Or. : c1999 Wymondham, Norfolk ; Portland, Or. : [1999] |
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Table of Contents:
- Ch. 1 Folding and three dimensional NMR structure of the recombinant cellular prion protein from the mouse / Rudi Glockshuber, Simone Hornemann and Roland Riek
- Ch. 2. Formation of protease-resistant prion protein in cell-free systems / Byron Caughey
- Ch. 3. Expression of heterogeneous PrP molecules blocks formation of protease-resistant prion protein in vitro: effect of amino acid mismatches at residue 138 / Suzette A. Priola and Bruce Chesebro
- Ch. 4. Cell biological studies of the prion protein / David A. Harris
- Ch. 5. Inherited prion disease: molecular pathology and cell models / Piero Parchi, Sabina Capellari and Gianluigi Zanusso
- Ch. 6. The use of genetically modified mice in prion research / Charles Weissmann, Alex J. Raber and Doron Shmerling
- Ch. 7. Neurotoxicity and neuroinvasiveness of prions in neuroectodermal transplants / Adriano Aguzzi, Thomas Blattler and Michael A. Klein
- Ch. 8. Prion diseases: PrP peptides, pathogenesis and treatment perspectives / F. Tagliavini, M. Salmona and G. Forloni
- Ch. 9. The human genetic prion diseases / Katherine Young, Perdo Piccardo and Stephen Dlouhy
- Ch. 10. Bovine spongiform encephalopathy and the new variant of Creutzfeldt-Jacob disease / Dominique Dormont
- Ch. 11. [URE3] and [PS1] are prions of yeast and evidence for new fungal prions / Daniel C. Masison, Herman K. Edskes and Marie-Lise Maddelein.
- Ch. 1 Folding and three dimensional NMR structure of the recombinant cellular prion protein from the mouse / Rudi Glockshuber, Simone Hornemann and Roland Riek
- Ch. 2. Formation of protease-resistant prion protein in cell-free systems / Byron Caughey
- Ch. 3. Expression of heterogeneous PrP molecules blocks formation of protease-resistant prion protein in vitro: effect of amino acid mismatches at residue 138 / Suzette A. Priola and Bruce Chesebro
- Ch. 4. Cell biological studies of the prion protein / David A. Harris
- Ch. 5. Inherited prion disease: molecular pathology and cell models / Piero Parchi, Sabina Capellari and Gianluigi Zanusso
- Ch. 6. use of genetically modified mice in prion research / Charles Weissmann, Alex J. Raber and Doron Shmerling
- Ch. 7. Neurotoxicity and neuroinvasiveness of prions in neuroectodermal transplants / Adriano Aguzzi, Thomas Blattler and Michael A. Klein
- Ch. 8. Prion diseases: PrP peptides, pathogenesis and treatment perspectives / F. Tagliavini, M. Salmona and G. Forloni
- Ch. 9. human genetic prion diseases / Katherine Young, Perdo Piccardo and Stephen Dlouhy
- Ch. 10. Bovine spongiform encephalopathy and the new variant of Creutzfeldt-Jacob disease / Dominique Dormont
- Ch. 11. [URE3] and [PS1] are prions of yeast and evidence for new fungal prions / Daniel C. Masison, Herman K. Edskes and Marie-Lise Maddelein.
- Folding and three dimensional NMR structure of the recombinant cellular prion protein from the mouse / Rudi Glockshuber ... [et al.]
- Formation of protease-resistant prion protein in cell-free systems / Byron Caughey
- Expression of heterogeneous PrP molecules blocks formation of protease-resistant prion protein in vitro : effect of amino acid mismatches at residue 138 / Suzette A. Priola and Bruce Chesebro
- Cell biological studies of the prion protein / David A. Harris
- Inherited prion disease : molecular pathology and cell models / Piero Parchi ... [et al.]
- Use of genetically modified mice in prion research / Charles Weissmann ... [et al.]
- Neurotoxicity and neuroinvasiveness of prions in neuroectodermal transplants / Adriano Aguzzi ... [et al.]
- Prion diseases : PrP peptides, pathogenesis and treatment perspectives / F. Tagliavini ... [et al.]
- Human genetic prion diseases / Katherine Young ... [et al.]
- Bovine spongiform encephalopathy and the new variant of Creutzfeldt-Jacob disease / Dominique Dormont
- [URE3] and [PSI] are prions of yeast and evidence for new fungal prions / Daniel C. Masison ... [et al.]