Molecular Pathology of the Prions

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Harry F. Baker
Springer Science & Business Media, 2 feb 2008 - 279 pagine
Internationally recognized investigators review the latest developments in, and novel approaches to, understanding the prion protein and prion diseases at the molecular level. Utilizing a variety of cutting-edge techniques, these distinguished scientists seek to define the normal function of a prion protein, to detect and measure the early immune response to prion disease, and to discover possible therapeutic targets. They also use transgenic mice and new electrophysiological investigations to elucidate the pathogenetic mechanisms involved in prion diseases. State-of-the-art and richly insightful, Molecular Pathology of the Prions captures for basic and clinical neuropathologists the latest developments and approaches to understanding the pathogenesis of prion diseases, and by analogy suggests possible research techniques for the more common proteinopthies, such as Alzheimer's and Parkinson's diseases.

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Sommario

Prion Protein as CopperBinding Protein at the Synapse
17
A Function for the Prion Protein?
31
Agents of Death for Neurons
51
Characterization of Bovine Spongiform Encephalopathy
71
Differential Targeting of Neurons by Prion Strains
85
MARIELISE MADDELEIN Laboratory of Biochemistry and Genetics National
105
Transgenic Studies of Prion Diseases
111
From Neurografts to Neuroinvasion
129
Cellular and Transgenic Models of Familial Prion Diseases
149
Central Nervous System Inflammation and Prion
163
The Electroneuropathology of Prion Disease
181
Transmissible Spongiform Encephalopathy Neurobiology
199
Conformation as Therapeutic Target in the Prionoses and Other
223
From Cytoplasmic Genes to Heritable Amyloidosis
237
Index
269
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