Hidden Bibliographic Details
| Other authors / contributors: | Nguyen, Hoa Huu Phuc, editor.
Cenci, M. Angela, editor.
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| ISBN: | 9783662463444
366246344X
3662463431
9783662463437
9783662463437
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| Notes: | Includes bibliographical references and index.
Online resource; title from PDF title page (Ebsco, viewed May 29, 2015).
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| Summary: | Motor dysfunction and cognitive impairment are major symptoms in both Huntington?s Disease (HD) and Parkinson?s Disease (PD). A breakthrough in HD research occurred in 1993, with the identification of the gene causing this devastating monogenetic illness. Since 1996, several genes were reported to cause familial forms of PD. Following these genetic discoveries, a variety of genetic disease models were generated, providing completely novel opportunities to explore the neurobiological basis of HD and PD. Genetic models allow us to study the earliest manifestations of the diseases both behaviorally and neuropathologically, and provide tools to probe molecular pathways of neurodegeneration. Additionally, neurotoxic animal models allow us to reproduce neurochemical and cellular events of great pathophysiological importance. In the PD field, neurotoxic animal models remain the preferred option to reproduce symptomatic features of the human disease that are responsive to dopaminergic pharmacotherapies. In addition, neurotoxic PD models are often used to investigate pathways of mitochondrial dysfunction, oxidative stress, and neuroinflammation. This book provides up-to-date reviews on current animal models of both HD and PD. These animal models are essential to investigate links between the pathobiology and the behavioral abnormalities associated with these disorders.
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| Other form: | Printed edition: 9783662463437
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| Standard no.: | 10.1007/978-3-662-46344-4
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