Langue: anglais
Edité par Caister Academic Press Limited, 2019
ISBN 10 : 1910190950 ISBN 13 : 9781910190951
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Langue: anglais
Edité par Caister Academic Press Limited, 2013
ISBN 10 : 190823024X ISBN 13 : 9781908230249
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Langue: anglais
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Ajouter au panierEtat : New.
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Edité par Caister Academic Press Limited, 2013
ISBN 10 : 190823024X ISBN 13 : 9781908230249
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Edité par Caister Academic Press Limited, 2019
ISBN 10 : 1910190950 ISBN 13 : 9781910190951
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Langue: anglais
Edité par Caister Academic Press Limited, 2013
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Edité par Caister Academic Press Limited, 2019
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Edité par Caister Academic Press Limited, 2013
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Langue: anglais
Edité par Caister Academic Press Limited, 2013
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Ajouter au panierKartoniert / Broschiert. Etat : New. KlappentextrnrnPrion diseases or transmissible spongiform encephalopathies (TSEs) are fatal neurological diseases that include, for example, Creutzfeldt-Jakob Disease (CJD) in humans and bovine spongiform encephalopathy (BSE) in cattle. Since th.
Langue: anglais
Edité par Caister Academic Press Limited Mär 2019, 2019
ISBN 10 : 1910190950 ISBN 13 : 9781910190951
Vendeur : AHA-BUCH GmbH, Einbeck, Allemagne
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Ajouter au panierTaschenbuch. Etat : Neu. Neuware - Prion diseases or transmissible spongiform encephalopathies (TSEs) are fatal neurological diseases that include, for example, Creutzfeldt-Jakob Disease (CJD) in humans and bovine spongiform encephalopathy (BSE) in cattle. Since the publication of the first edition of this book in 2013 significant progress has been made in advanced prion research creating a need for this timely revised and updated edition. The book opens with an introductory chapter that provides an overview. This is followed by four chapters (chapters 2-5) dealing with fundamental aspects of prion biology, including functions of the cellular isoform of prion protein (PrPC) and molecular mechanisms of prion diseases. The next two chapters (chapters 6-7) focus on clinical aspects of human prion diseases and current approaches for effective inactivation methods. The last part of the book (chapters 8-9) summarizes animal prion diseases, including BSE, scrapie and chronic wasting disease (CWD). In the final chapter, Professor Onodera discusses the likely future direction of research. This book is essential reading for everyone working with prions from the PhD student to the experienced scientist, in academia, the pharmaceutical or biotechnology industries and for those working in clinical environments.
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Ajouter au panierHRD. Etat : New. New Book. Shipped from UK. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.
Vendeur : PBShop.store UK, Fairford, GLOS, Royaume-Uni
EUR 249,79
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Ajouter au panierHRD. Etat : New. New Book. Delivered from our UK warehouse in 4 to 14 business days. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.
Langue: anglais
Edité par Caister Academic Press Limited, 2013
ISBN 10 : 190823024X ISBN 13 : 9781908230249
Vendeur : AHA-BUCH GmbH, Einbeck, Allemagne
EUR 322,46
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Ajouter au panierBuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Prions are infectious, self-propagating proteinaceous agents that cause fatal neurodegenerative diseases, including Creutzfeldt-Jakob Disease (CJD) in humans, scrapie in sheep and goats, and bovine spongiform encephalopathy (BSE) in cattle. In recent years great strides have been made in our understanding of the mechanism of prion propagation and neurotoxicity, however much remains to be discovered. A better understanding of the cell biology of the prion protein is essential for this and to allow the development of novel anti-prion strategies. In this book, renowned prion experts review the most recent advances to provide a timely and up-to-date overview of the field. Topics covered include: prion proteins (PrP) and their family members; PrP function; molecular mechanisms of prions diseases; immunological strategies for the prevention and treatment of prion disease; microglial inflammation and prion diseases; methods for prion inactivation; clinical aspects of CJD; the BSE and scrapie prions; chronic wasting disease; future strategies for the prevention and treatment of prion diseases. The book closes with a look to the future of prion research. Essential reading for everyone with an interest in prions and prion diseases. A recommended book for all biology, veterinary and medical libraries.