<HashMap><database>biostudies-arrayexpress</database><scores/><additional><omics_type>Metabolomics</omics_type><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><submitter>Owen Robert Dando</submitter><instrument_platform>Illumina HiSeq 2500</instrument_platform><study_type>RNA-seq of coding RNA</study_type><organism>Mus musculus</organism><species>Mus musculus</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-5688</full_dataset_link><description>The effect of the Nrf2 activator tBHQ on mouse neurons was studied both when the neurons were cultured alone, and when they were co-cultured with mouse astrocytes.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Growth Protocol - Neurons and astrocytes were cultured as described in Bell et al., Neuronal development is promoted by weakened intrinsic antioxidant defences due to epigenetic repression of Nrf2, Nature Communications 6: 7066 (2015).</sample_protocol><sample_protocol>Library Construction - RNA-seq libraries were prepared by Edinburgh Genomics using the Illumina TruSeq stranded mRNA-seq kit, according to the manufacturers protocol (Illumina).</sample_protocol><sample_protocol>Sample Treatment - Pure neuronal cultures or mixed astrocyte/neuronal cultures were treated  tBHQ (10 M) for 8h. At this point RNA was extracted and subject to RNA-seq analysis.</sample_protocol><sample_protocol>Sequencing - Libraries were sequenced paired-end on an Illumina HiSeq 2500.</sample_protocol><figure_sub>Organization</figure_sub><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><pubmed_authors>Owen Robert Dando</pubmed_authors></additional><is_claimable>false</is_claimable><name>RNA-seq of mouse neurons in mono-culture and in co-culture with astrocytes, with application of Nrf2 activator tBHQ.</name><description>The effect of the Nrf2 activator tBHQ on mouse neurons was studied both when the neurons were cultured alone, and when they were co-cultured with mouse astrocytes.</description><dates><release>2026-04-22T00:00:00Z</release><modification>2026-04-22T12:12:42.335Z</modification><creation>2022-02-03T07:43:59.383Z</creation></dates><accession>E-MTAB-5688</accession><cross_references><ENA>ERP022762</ENA><EFO>EFO_0004170</EFO><EFO>EFO_0003789</EFO><EFO>EFO_0003738</EFO><EFO>EFO_0003969</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>