ArrayExpress Uploaderarrayexpress_sid6788normalwild_type3-nitropropionic acidnormalwild_type3-nitropropionic acidnormalwild_type3-nitropropionic acid3-NP-induced neurodegeneration model of Huntingtons diseasewild_typenone3-NP-induced neurodegeneration model of Huntingtons diseasewild_typenone3-NP-induced neurodegeneration model of Huntingtons diseasewild_typenonemouse model of Huntingtons diseasehuntingtin mutantnonemouse model of Huntingtons diseasehuntingtin mutantnonemouse model of Huntingtons diseasehuntingtin mutantnone06Affymetrix MG430 2.0 expression levels of wild-type (STHdhQ7/Q7), 3NP-treated wild-type (STHdhQ7/Q7NP), and mutant (STHdhQ111/Q111)...17708681/profile/8773/arrayexpressuploader39diseaseDec.12, 2014FalseE-GEOD-3583_A-AFFY-45transcription-profiling-of-two-different-mouse-modhttp://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-3583Transcription profiling of two different mouse models of Huntington's disease - changes caused by Hdh CAG mutation or 3-nitropropionic acid in striatal cellsNov.12, 2014Affymetrix MG430 2.0 expression levels of wild-type (STHdhQ7/Q7), 3NP-treated wild-type (STHdhQ7/Q7NP), and mutant (STHdhQ111/Q111) striatal cells Experiment Overall Design: Investigation of HD disease mechanism by gene expression profiling of two HD model systemsE-GEOD-3583mousehttp://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-3583/samples/