Prions and Brain Diseases in Animals and Humans: NATO Science Series A:, cartea 295
Editat de Douglas R.O. Morrisonen Limba Engleză Paperback – 6 iun 2013
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Specificații
ISBN-13: 9781489918987
ISBN-10: 1489918981
Pagini: 372
Ilustrații: XIV, 357 p.
Dimensiuni: 178 x 254 x 20 mm
Greutate: 0.64 kg
Ediția:Softcover reprint of the original 1st ed. 1998
Editura: Springer Us
Colecția Springer
Seria NATO Science Series A:
Locul publicării:New York, NY, United States
ISBN-10: 1489918981
Pagini: 372
Ilustrații: XIV, 357 p.
Dimensiuni: 178 x 254 x 20 mm
Greutate: 0.64 kg
Ediția:Softcover reprint of the original 1st ed. 1998
Editura: Springer Us
Colecția Springer
Seria NATO Science Series A:
Locul publicării:New York, NY, United States
Public țintă
ResearchCuprins
— Guide to the Talks.- Polymorphic Genotype Matching in Acquired Creutzfeldt-Jakob Disease: An Analysis of Donor/Recipient Case Pairs.- Human Prion Protein Gene Mutation at Codon 183 Associated with an Atypical Form of Prion Disease.- Fatal Familial Insomnia: A Human Model of Prion Disease.- Mechanisms of Phenotypic Heterogeneity in Human Prion Diseases.- Transgenic Mice with Neuron-Specific Expression of a Hamster Prion Protein Minigene Are Susceptible to Hamster Scrapie Agent.- The Use of Transgenic Mice in the Investigation of Transmissible Spongiform Encephalopathies.- Large-Scale Sequencing of Human, Mouse, and Sheep Prion Protein Genes.- Electron Microscopy in Prion Research: Tubulovesicular Structures Are Not Composed of Prion Protein (PrP) but They May Be Intimately Associated with PrP Amyloid Fibrils.- Familial Prion Diseases Modeled in Cell Culture.- Yeast Approach to Protein “Prionization”: SUP35-[PSI] System.- Prions of Yeast: Genetic Evidence that the Non-Mendelian Elements, [PSI] and [URE3] Are Altered Self-Replicating Forms of Sup35p and Ure2p, Respectively.- Early Clinical Detection of Brain Diseases in Animals.- Prion Biology and Diseases — Fatal Conformations of Proteins during a Journey from Heresy to Orthodoxy.- New Variant Creutzfeldt-Jakob Disease.- The Molecular Basis of Cellular Dysfunction in Prion Diseases.- Presenilin Proteins and the Pathogenesis of Early-Onset Familial Alzheimer’s Disease: ?-Amyloid Production and Parallels to Prion Diseases.- Polyene Antibiotics in Experimental Transmissible Subacute Spongiform Encephalopathies.- Scrapie Pathogenesis in Brain Grafts.- Structural Properties of Recombinant Human Prion Protein.- Autonomous Folding and Three-Dimensional Structure of the Carboxy-Terminal Domain of the Mouse PrionProtein, PrP (121–231).- Protease-Resistant Prion Protein Formation.- Biophysical Studies on Structure Structural Transitions and Infectivity of the Prion Protein.- Amyloidogenesis in Transmissible Spongiform Encephalopathies.- Neuronal Degeneration and Cell Death in Prion Disease.- Clinical, Pathological, and Molecular Characterization of Gerstmann-Sträussler-Scheinker Disease in the Indiana Kindred (PRNP F198S).- Studies on the Pathogenesis of Scrapie and the Purification of Scrapie Agent in the Hamster Model.- PrP Peptides as a Tool to Investigate the Pathogenesis of Prion Protein Amyloidoses.- Properties of the Prion Proteins in Creutzfeldt Jakob Disease Patients Heterozygous for the E200K Mutation.- Strain Variation in Scrapie and BSE.- Transmission Studies of Fatal Familial Insomnia.- Molecular, Genetic, and Transgenetic Studies of Human Prion Disease.- Molecular Biology of Prion Propagation.- Ultrastructural and Immunocytochemical Studies on Prion Pathogenesis.- Overview of the BSE Epidemic.- Assessing Risks of BSE Transmission to Humans.- Human Activities Are Causing Selection of Pathogenic Agents.- Pathogenic Similarity of Slow Infections, Induced by Prions and Virions.- Protein Folding and Misfolding.- CJD Risk Factors: Analysis of 104 Patients.- Concluding Talk: Prions from a Physicist’s Viewpoint — Is the ‘Protein Only’ Hypothesis Correct?.- List of Speakers.- Names and Addresses of Participants.