Melatonin protects against behavioural dysfunctions and dendritic spine damage in 3-nitropropionic acid-induced rat model of Huntington's disease
Author:
Funder
Neurodegenerative Diseases: Causes and Corrections
CSIR
CSIR-IICB
Publisher
Elsevier BV
Subject
Behavioral Neuroscience
Reference71 articles.
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2. Rhes, a striatal specific protein, mediates mutant-huntingtin cytotoxicity;Subramaniam;Science,2009
3. Distinct conformations of in vitro and in vivo amyloids of huntingtin-exon1 show different cytotoxicity;Nekooki-Machida;Proc Natl Acad Sci USA,2009
4. Striatal dopamine level contributes to hydroxyl radical generation and subsequent neurodegeneration in the striatum in 3-nitropropionic acid-induced Huntington's disease in rats;Pandey;Neurochem Int,2009
5. Dopamine modulates the susceptibility of striatal neurons to 3-nitropropionic acid in the rat model of Huntington's disease;Reynolds;J Neurosci,1998
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