Neurodegeneration and Prion Disease
| Autor Corporativo: | |
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| Otros Autores: | |
| Formato: | eBook |
| Lenguaje: | English |
| Publicado: |
New York, NY :
Springer US : Imprint: Springer,
2005.
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| Edición: | 1st ed. 2005. |
| Materias: | |
| Acceso en línea: | https://doi.org/10.1007/b103635 |
Tabla de Contenidos:
- Neuropathology of Transmissible Spongiform Encephalopathies (Prion Diseases)
- Central Pathogenesis of Prion Diseases
- Hereditary Prion Protein Amyloidoses
- Mouse Behavioural Studies and What They Can Teach Us about Prion Diseases
- Electrophysiological Approaches to the Study of Prion Diseases
- Prion Protein, Prion Protein-Like Protein, and Neurodegeneration
- Oxidative Stress and Mitochondrial Dysfunction in Neurodegeneration of Transmissible Spongiform Encephalopathies (TSEs)
- Mechanisms of Prion Toxicity and Their Relationship to Prion Infectivity
- A Stone Guest on the Brain: Death as a Prion
- Molecular Mechanisms Mediating Neuronal Cell Death in Experimental Models of Prion Diseases, in vitro
- Processing and Mis-Processing of the Prion Protein: Insights into the Pathogenesis of Familial Prion Disorders
- Signaling Pathways Controling Prion Neurotoxicity: Role of Endoplasmic Reticulum Stress-Mediated Apoptosis
- Cell Culture Models to Unravel Prion Protein Function and Aberrancies in TSE
- Insights into the Cellular Trafficking of Prion Proteins
- The Molecular Basis of Prion Protein-Mediated Neuronal Damage
- Conclusion: Intervention, the Final Frontier.