Molecular Mechanisms Involved in the Pathogenesis of Huntington's Disease - Brossura

Perandones, Claudia; Micheli, Federico Eduardo; Radrizzani, Martin

Brossura

ISBN 10: 161728971X ISBN 13: 9781617289712

Casa editrice: Nova Novinka, 2011

Riassunto

Huntington's disease (HD) is an autosomal-dominant, progressive neurodegenerative disorder with a distinct phenotype, including chorea, incoordination, cognitive decline, and behavioural difficulties. The underlying genetic defect responsible for the disease is the expansion of a CAG repeat in the gene coding for the HD protein, huntingtin (htt). This CAG repeat is an unstable triplet repeat DNA sequence, and its length is inversely correlated with the age at onset of the disease. Expanded CAG repeats have been found in 8 other inherited neurodegenerative diseases. Despite its widespread distribution, mutant htt causes selective neurodegeneration, which occurs preferentially and most prominently in the striatum and deeper layers of the cortex. This book focuses on HD, outlining the effects of mutant htt in the nucleus and cytoplasm as well as the role of cell-cell interactions in the HD pathology.

Dettagli dell'edizione

• Editore: Nova Novinka
• Data di pubblicazione: 2011
• Lingua: Inglese
• ISBN 10: 161728971X
• ISBN 13: 9781617289712
• Rilegatura: Copertina flessibile
• Numero edizione: 1
• Numero di pagine: 56
• Contatto del produttore: non disponibile
• Persona responsabile: non disponibile