Cellular and molecular mechanisms implicated in pathogenesis of selective neurodegeneration in Huntington’s disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Ecology,Ecology, Evolution, Behavior and Systematics,Biotechnology
Link
http://link.springer.com/content/pdf/10.1007/s11515-012-1246-7.pdf
Reference184 articles.
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2. Albin R L, Reiner A, Anderson K D, Dure L S 4th, Handelin B, Balfour R, Whetsell W O Jr, Penney J B, Young A B (1992). Preferential loss of striato-external pallidal projection neurons in presymptomatic Huntington’s disease. Ann Neurol, 31(4): 425–430
3. Albin R L, Reiner A, Anderson K D, Penney J B, Young A B (1990). Striatal and nigral neuron subpopulations in rigid Huntington’s disease: implications for the functional anatomy of chorea and rigidity-akinesia. Ann Neurol, 27(4): 357–365
4. Altar C A, Cai N, Bliven T, Juhasz M, Conner J M, Acheson A L, Lindsay R M, Wiegand S J (1997). Anterograde transport of brainderived neurotrophic factor and its role in the brain. Nature, 389(6653): 856–860
5. Arning L, Saft C, Wieczorek S, Andrich J, Kraus P H, Epplen J T (2007). NR2A and NR2B receptor gene variations modify age at onset in Huntington disease in a sex-specific manner. Hum Genet, 122(2): 175–182
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