Prion Diseases Diagnosis and Pathogenesis /

Detalles Bibliográficos
Autor Corporativo: SpringerLink (Online service)
Otros Autores: Groschup, Martin H. (Editor ), Kretzschmar, Hans. (Editor )
Formato: eBook
Lenguaje:English
Publicado: Vienna : Springer Vienna : Imprint: Springer, 2000.
Edición:1st ed. 2000.
Colección:Archives of Virology. Supplementa, 16
Materias:
Acceso en línea:https://doi.org/10.1007/978-3-7091-6308-5
LEADER 03532nam a22003255i 4500
001 978-3-7091-6308-5
005 20191027191830.0
007 cr nn 008mamaa
008 121227s2000 au | s |||| 0|eng d
020 |a 9783709163085 
024 7 |a 10.1007/978-3-7091-6308-5  |2 doi 
040 |a Sistema de Bibliotecas del Tecnológico de Costa Rica 
245 1 0 |a Prion Diseases  |b Diagnosis and Pathogenesis /  |c edited by Martin H. Groschup, Hans Kretzschmar. 
250 |a 1st ed. 2000. 
260 # # |a Vienna :  |b Springer Vienna :  |b Imprint: Springer,  |c 2000. 
300 |a IX, 294 p.  |b online resource. 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
490 1 |a Archives of Virology. Supplementa,  |v 16 
505 0 |a Pathogenesis of Prion Diseases -- Prions: from neurografts to neuroinvasion -- Follicular dendritic cells in scrapie pathogenesis -- Cellular and sub-cellular localisation of PrP in the lymphoreticular system of mice and sheep -- Pharmacological manipulation of early PrPres accumulation in the spleen of scrapie-infected mice -- Pathogenesis of natural scrapie in sheep -- Animal Models for Priorn Diseases -- Detection of cattle-derived BSE prions using transgenic mice overexpressing bovine PrPC -- Analyzing the influence of PrP primary structure on prion pathogenesis in transgenic mice -- A single amino acid alteration in murine PrP dramatically alters TSE incubation time -- A transgenic model of a familial prion disease -- Transgenic models of prion disease -- Epidemiology and Diagnosis of Prion Diseases -- Surveillance of BSE -- Histopathology and immunohistochemistry of human transmissible spongiform encephalopathies (TSEs) -- Pathology of variant Creutzfeldt-Jakob disease -- Clinical and differential diagnosis of Creutzfeldt-Jakob disease -- Putting prions into focus: application of single molecule detection to the diagnosis of prion diseases -- Detection of PrPSc in subclinical BSE with the paraffin-embedded tissue (PET) blot -- Sheep and goats: natural and experimental TSEs and factors influencing incidence of disease -- Application of Prionics Western blotting procedure to screen for BSE in cattle regularly slaughtered at Swiss abattoirs -- Specific determination of the proteinase K-resistant form of the prion protein using two-site immunometric assays. Application to the post-mortem diagnosis of BSE -- Characterization of the Infectious Agent -- PrPSc typing by N-terminal sequencing and mass spectrometry -- Characterization of BSE and scrapie strains/isolates -- Quantitative traits of prion strains are enciphered in the conformation of the prion protein -- Structure and Function of PrP -- Function of PrPc as a copper-binding protein at the synapse -- The prion protein globular domain and disease-related mutants studied by molecular dynamics simulations -- Neurotoxicity but not infectivity of prion proteins can be induced reversibly in vitro -- PrP Conversion -- Inhibition of formation of protease-resistant prion protein by Trypan Blue, Sirius Red and other Congo Red analogs -- The use of monoclonal antibody epitopes for tagging PrP in conversion experiments -- Listed in Current Contents. 
650 0 |a Virology. 
650 0 |a Pathology. 
650 1 4 |a Virology. 
650 2 4 |a Pathology. 
700 1 |a Groschup, Martin H.  |e editor. 
700 1 |a Kretzschmar, Hans.  |e editor. 
710 2 |a SpringerLink (Online service) 
773 0 |t Springer eBooks 
856 4 0 |u https://doi.org/10.1007/978-3-7091-6308-5