Huntington's disease: Gene expression changes caused by Hdh CAG mutation or 3-nitropropionic acid in striatal cells . Mus musculus

Affymetrix MG430 2.0 expression levels of wild-type (STHdhQ7/Q7), 3NP-treated wild-type (STHdhQ7/Q7+3-NP), and mutant (STHdhQ111/Q111) striatal cells Keywords: Pharmacological and genetic HD cell culture models Overall design: Investigation of HD disease mechanism by gene expression profiling of two HD model systems