Neurobiology of Huntington's Disease: Applications to Drug Discovery

Author:   Donald C. Lo ,  Robert E. Hughes
Publisher:   Taylor & Francis Inc
Volume:   v. 45
ISBN:  

9780849390005


Pages:   340
Publication Date:   02 July 2010
Format:   Hardback
Availability:   In Print   Availability explained
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Neurobiology of Huntington's Disease: Applications to Drug Discovery


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Full Product Details

Author:   Donald C. Lo ,  Robert E. Hughes
Publisher:   Taylor & Francis Inc
Imprint:   CRC Press Inc
Volume:   v. 45
Dimensions:   Width: 15.60cm , Height: 2.30cm , Length: 23.40cm
Weight:   0.612kg
ISBN:  

9780849390005


ISBN 10:   0849390001
Pages:   340
Publication Date:   02 July 2010
Audience:   Professional and scholarly ,  Professional & Vocational
Format:   Hardback
Publisher's Status:   Active
Availability:   In Print   Availability explained
This item will be ordered in for you from one of our suppliers. Upon receipt, we will promptly dispatch it out to you. For in store availability, please contact us.

Table of Contents

Introduction. Clinical Overview of HD. Genetics of HD. Molecular Pathology of Hungtingtin Function. Genomic, Protemoics, and Metabonomics of HD. High-throughput Screening in HD. High-content Screening in HD. Animal Models for HD. Pharmaceutical Development for HD. HD Clinical Trials.

Reviews

The book is written lucidly by authorities in their respective fields, covering clinical features, pathogenic mechanisms, protein interactions, preclinical models, biomarkers, small molecules and other approaches (eg, recombinant antibodies), screening strategies, and drug development. Informative figures and tables are provided, and reproduction of key figures as a set of colour plates provides a useful centrepiece. One unifying message is that the polyglutamine xpansion leads to a complex cascade of diverse molecular and cellular events, the progress of which is difficult to slow or halt. Innovative approaches described, such as the target validation process of the Cure Huntington's Disease Initiative (CHDI) Foundation, will be of interest to those studying other neurological diseases. --Anthony J Hannan, writing in The Lancet Neurology, March 2011


The book is written lucidly by authorities in their respective fields, covering clinical features, pathogenic mechanisms, protein interactions, preclinical models, biomarkers, small molecules and other approaches (eg, recombinant antibodies), screening strategies, and drug development. Informative figures and tables are provided, and reproduction of key figures as a set of colour plates provides a useful centrepiece. One unifying message is that the polyglutamine xpansion leads to a complex cascade of diverse molecular and cellular events, the progress of which is difficult to slow or halt. Innovative approaches described, such as the target validation process of the Cure Huntington's Disease Initiative (CHDI) Foundation, will be of interest to those studying other neurological diseases.--Anthony J Hannan, writing in The Lancet Neurology, March 2011


Author Information

Duke University Medical Center, Durham, North Carolina, USA Buck Institute for Age Research, Novato, California, USA

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