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Prion diseases /

Prion diseases / edited by Harry F. Baker and Rosalind M. Ridley ; with a foreword by Stanley B. Prusiner. - Totowa, N.J. : Humana Press, c1996. - xv, 317 p. : ill.. , map ; 24 cm. - Methods in molecular medicine . - Methods in molecular medicine .

Includes bibliographical references and index.

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 Byron Caughey...[et. al.] -- Martin Jeffrey and Caroline M. Goodsir Paradox of prion disease / Human spongiform encephalopathy : clinical presentation and diagnostic tests Neuropathological diagnosis of human prion disease : morphological studies Neuropathological diagnosis of human prion disease : PrP immunocytochemical techniques Diagnosis of bovine spongiform encephalopathy and scrapie by the detection of fibrils and the abnormal protein isoform Rosalind M. Ridley and Harry F. Baker -- Rajith de Silva -- James W. Ironside -- Jeanne E. Bell -- Michael J. Stack, Paula Keyes, and Anthony C. Scott -- Paradox of prion disease / Human spongiform encephalopathy : clinical presentation and diagnostic tests Neuropathological diagnosis of human prion disease : morphological studies Neuropathological diagnosis of human prion disease : PrP immunocytochemical techniques Diagnosis of bovine spongiform encephalopathy and scrapie by the detection of fibrils and the abnormal protein isoform Rosalind M. Ridley and Harry F. Baker -- Rajith de Silva -- James W. Ironside -- Jeanne E. Bell -- Michael J. Stack, Paula Keyes, and Anthony C. Scott -- Paradox of prion disease / Human spongiform encephalopathy : clinical presentation and diagnostic tests Neuropathological diagnosis of human prion disease : morphological studies Neuropathological diagnosis of human prion disease : PrP immunocytochemical techniques Diagnosis of bovine spongiform encephalopathy and scrapie by the detection of fibrils and the abnormal protein isoform Rosalind M. Ridley and Harry F. Baker -- Rajith de Silva -- James W. Ironside -- Jeanne E. Bell -- Michael J. Stack, Paula Keyes, and Anthony C. Scott -- Paradox of prion disease / Human spongiform encephalopathy : clinical presentation and diagnostic tests Neuropathological diagnosis of human prion disease : morphological studies Neuropathological diagnosis of human prion disease : PrP immunocytochemical techniques Diagnosis of bovine spongiform encephalopathy and scrapie by the detection of fibrils and the abnormal protein isoform Rosalind M. Ridley and Harry F. Baker -- Rajith de Silva -- James W. Ironside -- Jeanne E. Bell -- Michael J. Stack, Paula Keyes, and Anthony C. Scott -- Paradox of prion disease / Human spongiform encephalopathy : clinical presentation and diagnostic tests Neuropathological diagnosis of human prion disease : morphological studies Neuropathological diagnosis of human prion disease : PrP immunocytochemical techniques Diagnosis of bovine spongiform encephalopathy and scrapie by the detection of fibrils and the abnormal protein isoform Rosalind M. Ridley and Harry F. Baker -- Rajith de Silva -- James W. Ironside -- Jeanne E. Bell -- Michael J. Stack, Paula Keyes, and Anthony C. Scott -- Paradox of prion disease / Human spongiform encephalopathy : clinical presentation and diagnostic tests Neuropathological diagnosis of human prion disease : morphological studies Neuropathological diagnosis of human prion disease : PrP immunocytochemical techniques Diagnosis of bovine spongiform encephalopathy and scrapie by the detection of fibrils and the abnormal protein isoform Rosalind M. Ridley and Harry F. Baker -- Rajith de Silva -- James W. Ironside -- Jeanne E. Bell -- Michael J. Stack, Paula Keyes, and Anthony C. Scott -- Paradox of prion disease / Human spongiform encephalopathy : clinical presentation and diagnostic tests Neuropathological diagnosis of human prion disease : morphological studies Neuropathological diagnosis of human prion disease : PrP immunocytochemical techniques Diagnosis of bovine spongiform encephalopathy and scrapie by the detection of fibrils and the abnormal protein isoform Rosalind M. Ridley and Harry F. Baker -- Rajith de Silva -- James W. Ironside -- Jeanne E. Bell -- Michael J. Stack, Paula Keyes, and Anthony C. Scott -- Paradox of prion disease / Human spongiform encephalopathy : clinical presentation and diagnostic tests Neuropathological diagnosis of human prion disease : morphological studies Neuropathological diagnosis of human prion disease : PrP immunocytochemical techniques Diagnosis of bovine spongiform encephalopathy and scrapie by the detection of fibrils and the abnormal protein isoform Rosalind M. Ridley and Harry F. Baker -- Rajith de Silva -- James W. Ironside -- Jeanne E. Bell -- Michael J. Stack, Paula Keyes, and Anthony C. Scott -- Paradox of prion disease / Human spongiform encephalopathy : clinical presentation and diagnostic tests Neuropathological diagnosis of human prion disease : morphological studies Neuropathological diagnosis of human prion disease : PrP immunocytochemical techniques Diagnosis of bovine spongiform encephalopathy and scrapie by the detection of fibrils and the abnormal protein isoform Rosalind M. Ridley and Harry F. Baker -- Rajith de Silva -- James W. Ironside -- Jeanne E. Bell -- Michael J. Stack, Paula Keyes, and Anthony C. Scott -- Paradox of prion disease / Human spongiform encephalopathy : clinical presentation and diagnostic tests Neuropathological diagnosis of human prion disease : morphological studies Neuropathological diagnosis of human prion disease : PrP immunocytochemical techniques Diagnosis of bovine spongiform encephalopathy and scrapie by the detection of fibrils and the abnormal protein isoform Rosalind M. Ridley and Harry F. Baker -- Rajith de Silva -- James W. Ironside -- Jeanne E. Bell -- Michael J. Stack, Paula Keyes, and Anthony C. Scott -- Exposure to, and inactivation of, the unconventional agents that cause transmissible degenerative encephalopathies / Surveillance of prion disease in humans Environmental causes of human spongiform encephalopathy Bovine spongiform encephalopathy : methods of analyzing the epidemic in the United Kingdom Handling the BSE epidemic in Great Britain David M. Taylor -- Robert G. Will -- Paul Brown -- John W. Wilesmith -- David A. J. Tyrrell and Kevin C. Taylor -- Exposure to, and inactivation of, the unconventional agents that cause transmissible degenerative encephalopathies / Surveillance of prion disease in humans Environmental causes of human spongiform encephalopathy Bovine spongiform encephalopathy : methods of analyzing the epidemic in the United Kingdom Handling the BSE epidemic in Great Britain David M. Taylor -- Robert G. Will -- Paul Brown -- John W. Wilesmith -- David A. J. Tyrrell and Kevin C. Taylor -- Exposure to, and inactivation of, the unconventional agents that cause transmissible degenerative encephalopathies / Surveillance of prion disease in humans Environmental causes of human spongiform encephalopathy Bovine spongiform encephalopathy : methods of analyzing the epidemic in the United Kingdom Handling the BSE epidemic in Great Britain David M. Taylor -- Robert G. Will -- Paul Brown -- John W. Wilesmith -- David A. J. Tyrrell and Kevin C. Taylor -- Exposure to, and inactivation of, the unconventional agents that cause transmissible degenerative encephalopathies / Surveillance of prion disease in humans Environmental causes of human spongiform encephalopathy Bovine spongiform encephalopathy : methods of analyzing the epidemic in the United Kingdom Handling the BSE epidemic in Great Britain David M. Taylor -- Robert G. Will -- Paul Brown -- John W. Wilesmith -- David A. J. Tyrrell and Kevin C. Taylor -- Exposure to, and inactivation of, the unconventional agents that cause transmissible degenerative encephalopathies / Surveillance of prion disease in humans Environmental causes of human spongiform encephalopathy Bovine spongiform encephalopathy : methods of analyzing the epidemic in the United Kingdom Handling the BSE epidemic in Great Britain David M. Taylor -- Robert G. Will -- Paul Brown -- John W. Wilesmith -- David A. J. Tyrrell and Kevin C. Taylor -- Exposure to, and inactivation of, the unconventional agents that cause transmissible degenerative encephalopathies / Surveillance of prion disease in humans Environmental causes of human spongiform encephalopathy Bovine spongiform encephalopathy : methods of analyzing the epidemic in the United Kingdom Handling the BSE epidemic in Great Britain David M. Taylor -- Robert G. Will -- Paul Brown -- John W. Wilesmith -- David A. J. Tyrrell and Kevin C. Taylor -- Exposure to, and inactivation of, the unconventional agents that cause transmissible degenerative encephalopathies / Surveillance of prion disease in humans Environmental causes of human spongiform encephalopathy Bovine spongiform encephalopathy : methods of analyzing the epidemic in the United Kingdom Handling the BSE epidemic in Great Britain David M. Taylor -- Robert G. Will -- Paul Brown -- John W. Wilesmith -- David A. J. Tyrrell and Kevin C. Taylor -- Exposure to, and inactivation of, the unconventional agents that cause transmissible degenerative encephalopathies / Surveillance of prion disease in humans Environmental causes of human spongiform encephalopathy Bovine spongiform encephalopathy : methods of analyzing the epidemic in the United Kingdom Handling the BSE epidemic in Great Britain David M. Taylor -- Robert G. Will -- Paul Brown -- John W. Wilesmith -- David A. J. Tyrrell and Kevin C. Taylor -- Exposure to, and inactivation of, the unconventional agents that cause transmissible degenerative encephalopathies / Surveillance of prion disease in humans Environmental causes of human spongiform encephalopathy Bovine spongiform encephalopathy : methods of analyzing the epidemic in the United Kingdom Handling the BSE epidemic in Great Britain David M. Taylor -- Robert G. Will -- Paul Brown -- John W. Wilesmith -- David A. J. Tyrrell and Kevin C. Taylor -- Exposure to, and inactivation of, the unconventional agents that cause transmissible degenerative encephalopathies / Surveillance of prion disease in humans Environmental causes of human spongiform encephalopathy Bovine spongiform encephalopathy : methods of analyzing the epidemic in the United Kingdom Handling the BSE epidemic in Great Britain David M. Taylor -- Robert G. Will -- Paul Brown -- John W. Wilesmith -- David A. J. Tyrrell and Kevin C. Taylor -- Special problems of genetic counseling in adult-onset diseases : huntington's disease as a model / 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 Jonathan R. Gray, Jo R. Soldan, and Peter S. Harper -- Nora Hunter -- Moira E. Bruce -- Jean C. Manson -- David Westaway -- Fabrizio Tagliavini...[et. al.] -- Special problems of genetic counseling in adult-onset diseases : huntington's disease as a model / 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 Jonathan R. Gray, Jo R. Soldan, and Peter S. Harper -- Nora Hunter -- Moira E. Bruce -- Jean C. Manson -- David Westaway -- Fabrizio Tagliavini...[et. al.] -- Special problems of genetic counseling in adult-onset diseases : huntington's disease as a model / 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 Jonathan R. Gray, Jo R. Soldan, and Peter S. Harper -- Nora Hunter -- Moira E. Bruce -- Jean C. Manson -- David Westaway -- Fabrizio Tagliavini...[et. al.] -- Special problems of genetic counseling in adult-onset diseases : huntington's disease as a model / 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 Jonathan R. Gray, Jo R. Soldan, and Peter S. Harper -- Nora Hunter -- Moira E. Bruce -- Jean C. Manson -- David Westaway -- Fabrizio Tagliavini...[et. al.] -- Special problems of genetic counseling in adult-onset diseases : huntington's disease as a model / 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 Jonathan R. Gray, Jo R. Soldan, and Peter S. Harper -- Nora Hunter -- Moira E. Bruce -- Jean C. Manson -- David Westaway -- Fabrizio Tagliavini...[et. al.] -- Special problems of genetic counseling in adult-onset diseases : huntington's disease as a model / 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 Jonathan R. Gray, Jo R. Soldan, and Peter S. Harper -- Nora Hunter -- Moira E. Bruce -- Jean C. Manson -- David Westaway -- Fabrizio Tagliavini...[et. al.] -- Special problems of genetic counseling in adult-onset diseases : huntington's disease as a model / 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 Jonathan R. Gray, Jo R. Soldan, and Peter S. Harper -- Nora Hunter -- Moira E. Bruce -- Jean C. Manson -- David Westaway -- Fabrizio Tagliavini...[et. al.] -- Special problems of genetic counseling in adult-onset diseases : huntington's disease as a model / 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 Jonathan R. Gray, Jo R. Soldan, and Peter S. Harper -- Nora Hunter -- Moira E. Bruce -- Jean C. Manson -- David Westaway -- Fabrizio Tagliavini...[et. al.] -- Special problems of genetic counseling in adult-onset diseases : huntington's disease as a model / 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 Jonathan R. Gray, Jo R. Soldan, and Peter S. Harper -- Nora Hunter -- Moira E. Bruce -- Jean C. Manson -- David Westaway -- Fabrizio Tagliavini...[et. al.] -- Special problems of genetic counseling in adult-onset diseases : huntington's disease as a model / 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 Jonathan R. Gray, Jo R. Soldan, and Peter S. Harper -- Nora Hunter -- Moira E. Bruce -- Jean C. Manson -- David Westaway -- Fabrizio Tagliavini...[et. al.] -- Special problems of genetic counseling in adult-onset diseases : huntington's disease as a model / 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 Jonathan R. Gray, Jo R. Soldan, and Peter S. Harper -- Nora Hunter -- Moira E. Bruce -- Jean C. Manson -- David Westaway -- Fabrizio Tagliavini...[et. al.] -- Special problems of genetic counseling in adult-onset diseases : huntington's disease as a model / 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 Jonathan R. Gray, Jo R. Soldan, and Peter S. Harper -- Nora Hunter -- Moira E. Bruce -- Jean C. Manson -- David Westaway -- Fabrizio Tagliavini...[et. al.] -- 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 Byron Caughey...[et. al.] -- Martin Jeffrey and Caroline M. Goodsir

9780896033429 (alk. paper) 0896033422 (alk. paper)

96003408


Prion diseases.
Human biology
Molecular biology
Neurology & clinical neurophysiology
Pre-clinical medicine: basic sciences
Cellular biology (cytology)
Prion Diseases.

QR201.P737 / P74 1996

616.8 BAK 616.8

QR201.P737P74 / 1996

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