Molecular pathology of the prions / edited by Harry F. Baker.

Contributor(s): Baker, Harry F
Material type: TextTextSeries: Methods in molecular medicine: 59.Publisher: Totowa, N.J. : Humana Press, ©2001Description: 1 online resource (xii, 279 pages) : illustrationsContent type: text Media type: computer Carrier type: online resourceISBN: 9781592591343; 0896039242; 9780896039247; 1592591345; 1280821019; 9781280821011; 9786610821013; 6610821011Subject(s): Prion diseases -- Research -- Methodology | Proteins | Neurodegenerative Diseases | Central Nervous System Infections | Central Nervous System Diseases | Nervous System Diseases | Amino Acids, Peptides, and Proteins | Disease | Chemicals and Drugs | Prion Diseases | Prions | Maladies à prions -- Recherche -- Méthodologie | HEALTH & FITNESS -- Diseases -- Alzheimer's & Dementia | MEDICAL -- Neurology | Medicine | Pathology | Prionen | Wetenschappelijke techniekenGenre/Form: Electronic books. Additional physical formats: Molecular pathology of the prionsDDC classification: 616.8/3 LOC classification: QR201.P737 | M65 2001Other classification: 44.75 Online resources: Click here to access online
Contents:
What would Thomas Henry Huxley have made of prion diseases? / R.M. Ridley -- Prion protein as copper-binding protein at the synapse / H.A. Kretzschmar [and others] -- A function for the prion protein? / D.R. Brown and I.M. Jones -- Prion protein peptide / D.R. Brown -- Characterization of bovine spongiform encephalopathy and scrapie strains/isolates by immunochemical analysis of PRPSC / M.H. Groschup [and others] -- Differential targeting of neurons by prion strains / S.J. DeArmond -- Transgenic studies of prion diseases / G.C. Telling -- Prions: From neurografts to neuroinvasion / M. Glatzel [and others] -- Cellular and transgenic models of familial prion diseases / D.A. Harris [and others] -- Central nervous system inflammation and prion disease pathogenesis / S. Betmouni and V. Hugh Perry -- The electroneuropathology of prion disease / J. Richard Greene -- Transmissible spongiform encephalopathy neurobiology and ultrastructure suggests extracellular PRPSC conversion consistent with classical amyloidosis / M. Jeffrey and J.R. Fraser -- Conformation as therapeutic target in the prionoses and other neurodegenerative conditions / T. Wisniewski [and others] -- Prions of yeast from cytoplasmic genes to heritable amyloidosis / R.B. Wickner [and others].
Action note: digitized 2010 committed to preserve In: Springer ProtocolsSummary: It is now widely agreed that the prion protein plays a key role in the molecular pathogenesis of prion diseases-diseases that involve the misfolding of proteins-in both humans and animals. In Molecular Pathology of the Prions, noted prion researcher Harry Baker has asked internationally recognized investigators to review the latest developments in, and novel approaches to, understanding the prion protein and prion diseases at the molecular level. Utilizing a variety of cutting-edge techniques, these distinguished scientists seek to define the normal function of a prion protein, to detect and measure the early immune response to prion disease, and to discover possible therapeutic targets. They also use transgenic mice and new electrophysiological investigations to elucidate the pathogenetic mechanisms involved in prion diseases. Other topics addressed include the neuronal death that occurs in prion disease, the different strains of prion disease agents, and the accumulation of protein deposits within brain parenchyma. State-of-the-art and richly insightful, Molecular Pathology of the Prions captures for basic and clinical neuropathologists the latest developments and approaches to understanding the pathogenesis of prion diseases, including research techniques now likely to enjoy broader application for the more common proteinopathies, such as Alzheimer's and Parkinson's diseases.
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Includes bibliographical references and index.

What would Thomas Henry Huxley have made of prion diseases? / R.M. Ridley -- Prion protein as copper-binding protein at the synapse / H.A. Kretzschmar [and others] -- A function for the prion protein? / D.R. Brown and I.M. Jones -- Prion protein peptide / D.R. Brown -- Characterization of bovine spongiform encephalopathy and scrapie strains/isolates by immunochemical analysis of PRPSC / M.H. Groschup [and others] -- Differential targeting of neurons by prion strains / S.J. DeArmond -- Transgenic studies of prion diseases / G.C. Telling -- Prions: From neurografts to neuroinvasion / M. Glatzel [and others] -- Cellular and transgenic models of familial prion diseases / D.A. Harris [and others] -- Central nervous system inflammation and prion disease pathogenesis / S. Betmouni and V. Hugh Perry -- The electroneuropathology of prion disease / J. Richard Greene -- Transmissible spongiform encephalopathy neurobiology and ultrastructure suggests extracellular PRPSC conversion consistent with classical amyloidosis / M. Jeffrey and J.R. Fraser -- Conformation as therapeutic target in the prionoses and other neurodegenerative conditions / T. Wisniewski [and others] -- Prions of yeast from cytoplasmic genes to heritable amyloidosis / R.B. Wickner [and others].

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It is now widely agreed that the prion protein plays a key role in the molecular pathogenesis of prion diseases-diseases that involve the misfolding of proteins-in both humans and animals. In Molecular Pathology of the Prions, noted prion researcher Harry Baker has asked internationally recognized investigators to review the latest developments in, and novel approaches to, understanding the prion protein and prion diseases at the molecular level. Utilizing a variety of cutting-edge techniques, these distinguished scientists seek to define the normal function of a prion protein, to detect and measure the early immune response to prion disease, and to discover possible therapeutic targets. They also use transgenic mice and new electrophysiological investigations to elucidate the pathogenetic mechanisms involved in prion diseases. Other topics addressed include the neuronal death that occurs in prion disease, the different strains of prion disease agents, and the accumulation of protein deposits within brain parenchyma. State-of-the-art and richly insightful, Molecular Pathology of the Prions captures for basic and clinical neuropathologists the latest developments and approaches to understanding the pathogenesis of prion diseases, including research techniques now likely to enjoy broader application for the more common proteinopathies, such as Alzheimer's and Parkinson's diseases.

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