Sertraline slows disease progression and increases neurogenesis in N171-82Q mouse model of Huntington's disease
Huntington's disease (HD) is an inherited progressive neurodegenerative disorder resulting from CAG repeat expansion in the gene that encodes for the protein huntingtin. To identify neuroprotective compound (s) that can slow down disease progression and can be administered long term with few si...
Main Authors: | Wenzhen Duan, Qi Peng, Naoki Masuda, Eric Ford, Erik Tryggestad, Bruce Ladenheim, Ming Zhao, Jean Lud Cadet, John Wong, Christopher A. Ross |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2008-06-01
|
Series: | Neurobiology of Disease |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S0969996108000259 |
Similar Items
-
Mood disorders in Huntington’s disease: from behavior to cellular and molecular mechanisms
by: Patrick ePla, et al.
Published: (2014-04-01) -
Tiagabine is neuroprotective in the N171-82Q and R6/2 mouse models of Huntington's disease
by: Naoki Masuda, et al.
Published: (2008-06-01) -
Dopaminergic manipulations and its effects on neurogenesis and motor function in a transgenic mouse model of Huntington's disease
by: M.L. Choi, et al.
Published: (2014-06-01) -
Altered selenium status in Huntington's disease: Neuroprotection by selenite in the N171-82Q mouse model
by: Zhen Lu, et al.
Published: (2014-11-01) -
Differential Effects of Sertraline in a Predator Exposure Animal Model of Post-Traumatic Stress Disorder
by: C. Brad eWilson, et al.
Published: (2014-07-01)