By X. William Yang M.D. Ph.D., Myriam Heiman PhD, Leslie M. Thompson Ph.D.
Huntington’s disease (HD) is one of the most common dominantly inherited neurodegenerative disorders, characterized by a clinical triad of movement disorder, cognitive deficits, and psychiatric symptoms. Huntington’s Disease: Pathogenic Mechanisms and Implications for Therapeutics reviews the most up-do-date content on HD pathogenic mechanisms and cutting-edge thinking on therapeutic strategies for HD. Chapters explore areas that include the clinical features and genetic studies of HD, the cellular and molecular biology of normal huntingtin, a range of HD models, the diverse pathogenic mechanisms linked to mutant huntingtin, new approaches to HD pathogenesis, as well as emerging preclinical therapeutic approaches and clinical programs in the field.
- Reviews the clinical course and genetics of HD
- Reviews the biology of human huntingtin and HD-relevant cell types
- Reviews the wide range of pathobiology associated with mutant huntingtin
- Reviews genetic studies of HD and how these studies are informing the development of new therapeutic approaches
- Reviews new tools and model systems for basic and translational research in HD, including new human-derived model systems, as well as systems biology and artificial intelligence–driven approaches
- Provides an overview of new therapeutic approaches and current clinical programs in HD
Product Details
- Publisher : Academic Press; 1st edition (March 7, 2024)
- Language : English
- Paperback : 618 pages
- ISBN-10 : 0323956726
- ISBN-13 : 978-0323956727




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