Orexin loss in Huntington's disease-Reference-Cited by-同舟云学术

Orexin loss in Huntington's disease

Published:2004-11-03 Issue:1 Volume:14 Page:39-47
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Petersén Åsa,Gil Joana,Maat-Schieman Marion L.C.,Björkqvist Maria,Tanila Heikki,Araújo Inês M.,Smith Ruben,Popovic Natalija,Wierup Nils,Norlén Per,Li Jia-Yi,Roos Raymund A.C.,Sundler Frank,Mulder Hindrik,Brundin Patrik

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/14/1/39/17241999/ddi004.pdf

Reference42 articles.

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2. The Huntington's Disease Collaborative Research Group. ( 1993 ) A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell , 72 , 971 –983.

3. Reiner, A., Dragatsis, I., Zeitlin, S. and Goldowitz, D. ( 2003 ) Wild-type huntingtin plays a role in brain development and neuronal survival. Mol. Neurobiol. , 28 , 259 –276.

4. Cattaneo, E., Rigamonti, D., Goffredo, D., Zuccato, C., Squitieri, F. and Sipione, S. ( 2001 ) Loss of normal huntingtin function: new developments in Huntington's disease research. Trends Neurosci. , 24 , 182 –188.

5. DiFiglia, M., Sapp, E., Chase, K.O., Davies, S.W., Bates, G.P., Vonsattel, J.P. and Aronin, N. ( 1997 ) Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain. Science , 277 , 1990 –1993.

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