Del i serien Methods in Molecular Medicine

Prion Diseases

Häftad, Engelska, 2013

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Harry Baker and Rosalind Ridley have done an admirable job in assem bling this collection of articles that describe the methodology frequently used to study a group of CNS illnesses often referred to as the "prion diseases."

Produktinformation

Utgivningsdatum2013-08-11
Mått152 x 229 x undefined mm
FormatHäftad
SpråkEngelska
SerieMethods in Molecular Medicine
Antal sidor319
FörlagHumana Press Inc.
ISBN9781489940407

Tillhör följande kategorier

Cellbiologi inom Naturvetenskap och teknik

The Paradox of Prion Disease.- Human Spongiform Encephalopathy.- Neuropathological Diagnosis of Human Prion Disease.- Neuropathological Diagnosis of Human Prion Disease.- The Diagnosis of Bovine Spongiform Encephalopathy and Scrapie by the Detection of Fibrils and the Abnormal Protein lsoform.- Exposure to, and Inactivation of, the Unconventional Agents that Cause Transmissible Degenerative Encephalopathies.- Surveillance of Prion Diseases in Humans.- Environmental Causes of Human Spongiform Encephalopathy.- Bovine Spongiform Encephalopathy.- Handling the BSE Epidemic in Great Britain.- Special Problems of Genetic Counseling in Adult-Onset Diseases.- Genotyping and Susceptibility of Sheep to Scrapie.- Strain Typing Studies of Scrapie and BSE.- PrP-Deficient Mice in the Study of Transmissible Spongiform Encephalopathies.- Transgenic Approaches to Prion “Species-Barrier” Effects.- Methods for Studying Prion Protein Amyloid.- Methods for Studying Prion Protein (PrP) Metabolism and the Formation of Protease-Resistant PrP in Cell Culture and Cell-Free Systems.- Immunohistochemistry of Resinated Tissues for Light and Electron Microscopy.