Molecular Pathology of the Prions
It is now widely agreed that the prion protein plays a key role in the molecular pathogenesis of prion diseases-diseases that involve the misfolding of proteins-in both humans and animals. In Molecular Pathology of the Prions, noted prion researcher Harry Baker has asked internationally recognized i...
Other Authors: | |
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Format: | eBook |
Language: | English |
Published: |
Totowa, NJ
Humana
2001, 2001
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Edition: | 1st ed. 2001 |
Series: | Methods in Molecular Medicine
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Online Access: | |
Collection: | Springer Book Archives -2004 - Collection details see MPG.ReNa |
Table of Contents:
- What Would Thomas Henry Huxley Have Made of Prion Diseases?
- Prion Protein as Copper-Binding Protein at the Synapse
- A Function for the Prion Protein?
- Prion Protein Peptide
- Characterization of Bovine Spongiform Encephalopathy and Scrapie Strains/Isolates by Immunochemical Analysis of PrPSc
- Differential Targeting of Neurons by Prion Strains
- Transgenic Studies of Prion Diseases
- Prions: From Neurografts to Neuroinvasion
- Cellular and Transgenic Models of Familial Prion Diseases
- Central Nervous System Inflammation and Prion Disease Pathogenesis
- The Electroneuropathology of Prion Disease
- Transmissible Spongiform Encephalopathy Neurobiology and Ultrastructure Suggests Extracellular PrPSc Conversion Consistent with Classical Amyloidosis
- Conformation as Therapeutic Target in the Prionoses and Other Neurodegenerative Conditions
- Prions of Yeast From Cytoplasmic Genes to Heritable Amyloidosis