Molecular Pathology of the Prions

Inbunden, Engelska, 2001

Del i serien Methods in Molecular Medicine

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Beskrivning

Internationally recognized investigators review the latest developments in, and novel approaches to, understanding the prion protein and prion diseases at the molecular level.

Produktinformation

Utgivningsdatum:2001-07-13
Mått:155 x 235 x 23 mm
Vikt:659 g
Format:Inbunden
Språk:Engelska
Serie:Methods in Molecular Medicine
Antal sidor:279
Förlag:Humana Press Inc.
ISBN:9780896039247

Utforska kategorier

Patologi inom Medicin
Neurologi och klinisk neurofysiologi inom Medicin

Innehållsförteckning

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.