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Huntingtons Disease
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4614887Huntingtons Diseasehttps://www.gandhi.com.mx/huntingtons-disease-9780323956734/phttps://gandhi.vtexassets.com/arquivos/ids/4308681/image.jpg?v=63879266894273000017951994MXNAcademic PressInStock/Ebooks/<p>Huntingtons disease (HD) is one of the most common dominantly inherited neurodegenerative disorders, characterized by a clinical trial of movement disorder, cognitive deficits, and psychiatric symptoms. Huntingtons Disease: Pathogenic Mechanisms and Implications for Therapeutics, reviews the most up-do-date content on HD pathogenic mechanisms and cutting-edge testing of therapeutic strategies for HD. Chapters explore areas such as, normal huntingtin biology in brain development and function, genetic modifiers of HD in patients, molecular pathogenic mechanism in HD, and mechanisms underlying selective neuronal vulnerability - 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 intelligencedriven approaches - Provides an overview of new therapeutic approaches and current clinical programs in HD</p>...4404146Huntingtons Disease17951994https://www.gandhi.com.mx/huntingtons-disease-9780323956734/phttps://gandhi.vtexassets.com/arquivos/ids/4308681/image.jpg?v=638792668942730000InStockMXN99999DIEbook20249780323956734_W3siaWQiOiI0Y2QyYWE4Ny0wNTgxLTRmZjItYjIxMC1iZTkzZDFmMDY4ZDQiLCJsaXN0UHJpY2UiOjE5OTQsImRpc2NvdW50IjoxOTksInNlbGxpbmdQcmljZSI6MTc5NSwiaW5jbHVkZXNUYXgiOnRydWUsInByaWNlVHlwZSI6Ildob2xlc2FsZSIsImN1cnJlbmN5IjoiTVhOIiwiZnJvbSI6IjIwMjUtMDEtMDhUMTg6MDA6MDBaIiwicmVnaW9uIjoiTVgiLCJpc1ByZW9yZGVyIjpmYWxzZX1d9780323956734_<p>Huntingtons disease (HD) is one of the most common dominantly inherited neurodegenerative disorders, characterized by a clinical trial of movement disorder, cognitive deficits, and psychiatric symptoms. <em>Huntingtons Disease: Pathogenic Mechanisms and Implications for Therapeutics</em>, reviews the most up-do-date content on HD pathogenic mechanisms and cutting-edge testing of therapeutic strategies for HD. Chapters explore areas such as, normal huntingtin biology in brain development and function, genetic modifiers of HD in patients, molecular pathogenic mechanism in HD, and mechanisms underlying selective neuronal vulnerability</p><ul><li>Reviews the clinical course and genetics of HD</li><li>Reviews the biology of human huntingtin and HD-relevant cell types</li><li>Reviews the wide range of pathobiology associated with mutant huntingtin</li><li>Reviews genetic studies of HD and how these studies are informing the development of new therapeutic approaches</li><li>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 intelligencedriven approaches</li><li>Provides an overview of new therapeutic approaches and current clinical programs in HD</li></ul>...(*_*)9780323956734_<p>Huntingtons disease (HD) is one of the most common dominantly inherited neurodegenerative disorders, characterized by a clinical trial of movement disorder, cognitive deficits, and psychiatric symptoms. Huntingtons Disease: Pathogenic Mechanisms and Implications for Therapeutics, reviews the most up-do-date content on HD pathogenic mechanisms and cutting-edge testing of therapeutic strategies for HD. Chapters explore areas such as, normal huntingtin biology in brain development and function, genetic modifiers of HD in patients, molecular pathogenic mechanism in HD, and mechanisms underlying selective neuronal vulnerability - 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 intelligencedriven approaches - Provides an overview of new therapeutic approaches and current clinical programs in HD</p>...9780323956734_Elsevier Science(*_*)9780323956734_Academic Presslibro_electonico_9780323956734_9780323956734InglésMéxico2024-02-07T00:00:00+00:00https://getbook.kobo.com/koboid-prod-public/elsevierrefmonographs-epub-4ab04de8-5e89-4c2a-956a-fa13e36ad852.epub2024-02-07T00:00:00+00:00Academic Press