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22. Portrait of Transmissible Mink Encephalopathy
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Chapters in this book
- Frontmatter I
- Table of Contents XV
- Abbreviations XXV
-
Topic I: History
- 1. Historical Introduction 3
- 2. History of Kuru Research 28
- 3. History of Prion Research 44
-
Topic II: Molecular Biology and Genetics
- 4. The Physical Nature of the Prion 59
- 5. Folding of the Recombinant Prion Protein 69
- 6. Structural Studies of Prion Proteins 79
- 7. Function of Cellular Prion Protein (PrPC) in Copper Homeostasis and Redox Signaling at the Synapse 95
- 8. The Scarpie Isoform of the Prion Protein PrPSe Compared to the Celluar Isoform PrPC 104
- 9. The Phylogeny of Mammalian and Nonmammalian Prion Proteins 119
- 10. Knockouts and Transgenic Mice in Prion Research 134
- 11. Transplantation as a Tool in Prion Research 160
- 12. Prion Strains 166
-
Topic III: Portraits of Prion Diseases
- 13. Portrait of Kuru 187
- 14. Portrait of Creutzfeldt-Jakob Disease 195
- 15. Portrait of Variant Creutzfeldt-Jakob Disease 204
- 16. Portrait of Gerstmann-Sträussler-Scheinker Disease 210
- 17. Portrait of Fatal Familial Insomnia and Sporadic Fatal Insomnia 216
- 18. Portrait of Scrapie in Sheep and Goat 222
- 19. Portrait of Bovine Spongiform Encephalopathy in Cattle and Other Ungulates 233
- 20. Portrait of Prion Diseases in Zoo Animals 250
- 21. Portrait of Chronic Wasting Disease in Deer Species 257
- 22. Portrait of Transmissible Mink Encephalopathy 265
- 23. Portrait of Transmissible Feline Spongiform Encephalopathy 271
- 24. Portrait of Experimental BSE in Pigs 275
- 25. Portrait of a Spongiform Encephalopathy in Birds and the Transmissibility of Mammalian Prior Diseases to Birds 279
-
Topic IV: Pathology
- 26. Pathology and Genetics of Human Prion Diseases 287
- 27. The Pathology of Prion Diseases in Animals 315
- 28. Pathophysiology of Prion Diseases Following Peripheral Infection 328
-
Topic V: Surveillance, Clinical Aspects and Diagnostics
- 29. Introduction of Surveillance for Human Prion Diseases 339
- 30. Clinical Findings in Human Prion Diseases 347
- 31. Methods for the Clinical Diagnosis of Human Prion Deseases 363
- 32. Introduction to Surveillance for Animal Prion Diseases 382
- 33. Clinical Findings in Bovine Spongiform Encephalopathy 389
- 34. Clinical Findings in Scrapie 398
- 35. Diagnosis of Bovine Spongiform Encephalopathy by Immunological Methods 408
-
Topic VI: Epidemiology
- 36. Epidemiology and Risk Factors of Creutzfeldt-Jakob Disease 423
- 37. Creutzfeldt-Jakob Disease in Germany 433
- 38. The Epidemiology of Kuru 440
- 39. The Course of the BSE Epidemic - Retrospective Epidemiological Considerations 449
- 40. The Causes of the BSE Epidemic 464
-
Topic VII: Transmissibility
- 41. The Experimental Transmissibility of Prions and Infectivity Distribution in the Body 473
- 42. Iatrogenic and "Natural" Transmissibility of Prion Diseases 483
-
Topic VIII: Agent Inactivation
- 43. Inactivation in Practice - Risk Assessment and Validation for Food Gelatin 499
- 44. Chemical Disinfection and Inactivation of Prions 504
- 45. Thermal Inactivation of Prions 515
-
Topic IX: Prevention
- 46. Prevention of Prion Diseases in the Production of Medicinal Products, Medical Devices, and Cosmetics 529
- 47. Prevention of the Transmission of Prion Diseases in Healthcare Settings 546
- 48. Precautionary Measures for Autopsies Performed in Cases of Suspected Prion Disease 561
- 49. Prevention of Prion Diseases in Research Laboratories 565
-
Topic X: Risk Assessment
- 50. Evidence for a Link between Variant Creutzfeldt-Jakob Disease and Bovine Spongiform Encephalopathy 573
- 51. Risk Assessment of Transmitting Prion Diseases through Blood, Cornea, and Dura Mater 579
- 52. BSE Risk Assessment and Minimization 601
- 53. BSE Control - Internationally Recommended Approaches 620
- 54. Atypical Scrapie-Nor98 630
- 55. Scrapie Control - Internationally Recommended Approaches 635
- 56. The PrP Genotype as a Marker for Scrapie Susceptibility in Sheep 640
- 57. Scrapie control at the National level: The Norwegian Example 648
- Backmatter 655
Chapters in this book
- Frontmatter I
- Table of Contents XV
- Abbreviations XXV
-
Topic I: History
- 1. Historical Introduction 3
- 2. History of Kuru Research 28
- 3. History of Prion Research 44
-
Topic II: Molecular Biology and Genetics
- 4. The Physical Nature of the Prion 59
- 5. Folding of the Recombinant Prion Protein 69
- 6. Structural Studies of Prion Proteins 79
- 7. Function of Cellular Prion Protein (PrPC) in Copper Homeostasis and Redox Signaling at the Synapse 95
- 8. The Scarpie Isoform of the Prion Protein PrPSe Compared to the Celluar Isoform PrPC 104
- 9. The Phylogeny of Mammalian and Nonmammalian Prion Proteins 119
- 10. Knockouts and Transgenic Mice in Prion Research 134
- 11. Transplantation as a Tool in Prion Research 160
- 12. Prion Strains 166
-
Topic III: Portraits of Prion Diseases
- 13. Portrait of Kuru 187
- 14. Portrait of Creutzfeldt-Jakob Disease 195
- 15. Portrait of Variant Creutzfeldt-Jakob Disease 204
- 16. Portrait of Gerstmann-Sträussler-Scheinker Disease 210
- 17. Portrait of Fatal Familial Insomnia and Sporadic Fatal Insomnia 216
- 18. Portrait of Scrapie in Sheep and Goat 222
- 19. Portrait of Bovine Spongiform Encephalopathy in Cattle and Other Ungulates 233
- 20. Portrait of Prion Diseases in Zoo Animals 250
- 21. Portrait of Chronic Wasting Disease in Deer Species 257
- 22. Portrait of Transmissible Mink Encephalopathy 265
- 23. Portrait of Transmissible Feline Spongiform Encephalopathy 271
- 24. Portrait of Experimental BSE in Pigs 275
- 25. Portrait of a Spongiform Encephalopathy in Birds and the Transmissibility of Mammalian Prior Diseases to Birds 279
-
Topic IV: Pathology
- 26. Pathology and Genetics of Human Prion Diseases 287
- 27. The Pathology of Prion Diseases in Animals 315
- 28. Pathophysiology of Prion Diseases Following Peripheral Infection 328
-
Topic V: Surveillance, Clinical Aspects and Diagnostics
- 29. Introduction of Surveillance for Human Prion Diseases 339
- 30. Clinical Findings in Human Prion Diseases 347
- 31. Methods for the Clinical Diagnosis of Human Prion Deseases 363
- 32. Introduction to Surveillance for Animal Prion Diseases 382
- 33. Clinical Findings in Bovine Spongiform Encephalopathy 389
- 34. Clinical Findings in Scrapie 398
- 35. Diagnosis of Bovine Spongiform Encephalopathy by Immunological Methods 408
-
Topic VI: Epidemiology
- 36. Epidemiology and Risk Factors of Creutzfeldt-Jakob Disease 423
- 37. Creutzfeldt-Jakob Disease in Germany 433
- 38. The Epidemiology of Kuru 440
- 39. The Course of the BSE Epidemic - Retrospective Epidemiological Considerations 449
- 40. The Causes of the BSE Epidemic 464
-
Topic VII: Transmissibility
- 41. The Experimental Transmissibility of Prions and Infectivity Distribution in the Body 473
- 42. Iatrogenic and "Natural" Transmissibility of Prion Diseases 483
-
Topic VIII: Agent Inactivation
- 43. Inactivation in Practice - Risk Assessment and Validation for Food Gelatin 499
- 44. Chemical Disinfection and Inactivation of Prions 504
- 45. Thermal Inactivation of Prions 515
-
Topic IX: Prevention
- 46. Prevention of Prion Diseases in the Production of Medicinal Products, Medical Devices, and Cosmetics 529
- 47. Prevention of the Transmission of Prion Diseases in Healthcare Settings 546
- 48. Precautionary Measures for Autopsies Performed in Cases of Suspected Prion Disease 561
- 49. Prevention of Prion Diseases in Research Laboratories 565
-
Topic X: Risk Assessment
- 50. Evidence for a Link between Variant Creutzfeldt-Jakob Disease and Bovine Spongiform Encephalopathy 573
- 51. Risk Assessment of Transmitting Prion Diseases through Blood, Cornea, and Dura Mater 579
- 52. BSE Risk Assessment and Minimization 601
- 53. BSE Control - Internationally Recommended Approaches 620
- 54. Atypical Scrapie-Nor98 630
- 55. Scrapie Control - Internationally Recommended Approaches 635
- 56. The PrP Genotype as a Marker for Scrapie Susceptibility in Sheep 640
- 57. Scrapie control at the National level: The Norwegian Example 648
- Backmatter 655