Molecular Pathology of the Prions
| 企業作者: | |
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| 其他作者: | |
| 總結: | XII, 279 p. text |
| 語言: | 英语 |
| 出版: |
Totowa, NJ :
Humana Press : Imprint: Humana,
2001.
|
| 版: | 1st ed. 2001. |
| 叢編: | Methods in Molecular Medicine,
59 |
| 主題: | |
| 在線閱讀: | https://doi.org/10.1385/1592591345 |
| 格式: | 電子 圖書 |
書本目錄:
- 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.