{"product_id":"neurobiology-of-huntingtons-disease-9780849390005","title":"Neurobiology of Huntingtons Disease","description":"\u003cb\u003eBook Synopsis\u003c\/b\u003e\u003cbr\u003e\u003cp\u003eIn 1993, the genetic mutation responsible for Huntingtonâs disease (HD) was identified. Considered a milestone in human genomics, this discovery has led to nearly two decades of remarkable progress that has greatly increased our knowledge of HD, and documented an unexpectedly large and diverse range of biochemical and genetic perturbations that seem to result directly from the expression of the mutant huntingtin gene. \u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eNeurobiology of Huntingtonâs Disease: Applications to Drug Discovery\u003c\/strong\u003e presents a thorough review of the issues surrounding drug discovery and development for the treatment of this paradigmatic neurodegenerative disease. Drawing on the expertise of key researchers in the field, the book discusses the basic neurobiology of Huntingtonâs disease and how its monogenic nature confers enormous practical advantages for translational research, including the creation of robust experimental tools, models, and assays to facilitate discovery and validation of\u003cbr\u003e\u003cbr\u003e\u003cb\u003eTrade Review\u003c\/b\u003e\u003cbr\u003e\u003c\/p\u003e\u003cp\u003eThe 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.\u003cbr\u003e--Anthony J Hannan, writing in \u003cem\u003eThe Lancet Neurology\u003c\/em\u003e, March 2011\u003c\/p\u003e\u003cbr\u003e\u003cbr\u003e\u003cb\u003eTable of Contents\u003c\/b\u003e\u003cbr\u003eIntroduction. 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.","brand":"Taylor \u0026 Francis Inc","offers":[{"title":"Default Title","offer_id":49406231642455,"sku":"9780849390005","price":185.25,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0817\/1739\/5799\/files\/9780849390005.jpg?v=1730495020","url":"https:\/\/bookcurl.com\/products\/neurobiology-of-huntingtons-disease-9780849390005","provider":"Book Curl","version":"1.0","type":"link"}