Author:
Thakur Ashwani K,Jayaraman Murali,Mishra Rakesh,Thakur Monika,Chellgren Veronique M,L Byeon In-Ja,Anjum Dalaver H,Kodali Ravindra,Creamer Trevor P,Conway James F,M Gronenborn Angela,Wetzel Ronald
Publisher
Springer Science and Business Media LLC
Subject
Molecular Biology,Structural Biology
Reference60 articles.
1. Bates, G.P. & Benn, C. The polyglutamine diseases. in Huntington's Disease (eds. Bates, G.P., Harper, P.S. & Jones, L.) 429–472 (Oxford University Press, Oxford, 2002).
2. Andreson, J.M. et al. The relationship between CAG repeat length and age of onset differs for Huntington's disease patients with juvenile onset or adult onset. Ann. Hum. Genet. 71, 295–301 (2007).
3. Wetzel, R. Misfolding and aggregation in Huntington's disease and other expanded polyglutamine repeat diseases. in Protein Misfolding Diseases: Current and Emerging Principles and Therapies (eds. Dobson, C.M., Kelly, J.W. & Ramirez-Alvarado, M.) (Wiley, New York, in the press).
4. Arrasate, M., Mitra, S., Schweitzer, E.S., Segal, M.R. & Finkbeiner, S. Inclusion body formation reduces levels of mutant huntingtin and the risk of neuronal death. Nature 431, 805–810 (2004).
5. Chen, S., Ferrone, F. & Wetzel, R. Huntington's disease age-of-onset linked to polyglutamine aggregation nucleation. Proc. Natl. Acad. Sci. USA 99, 11884–11889 (2002).
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