<HashMap><database>ENA</database><scores/><additional><omics_type>Genomics</omics_type><center_name>Duke University</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA255417</full_dataset_link><scientific_name>Homo sapiens</scientific_name><long_description>MiR-33a is involved in the maintenance of Glioma Initiating Cells (GIC) and tumor progression. MicroRNA-33a could promote GIC growth and self-renewal by regulating two pathways including cAMP/PKA pathway and Notch pathway. We used microarrays to identify the direct target genes of miR-33a in a glioblastoma cell line D456MG. We used microarrays to detail the global change of gene expression after miR-33a over-expression and identified target genes during this process. Overall design: Cells were infected with lenti-virus expressing a control vector (pWPXLD) or human primary miR-33a. Then RNA was extracted and gene expression was profiled by Affymetrix microarray.</long_description><tag>xref:PubMed:25202981</tag><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Homo sapiens</name><description>Expression data for miR-33a over-expression in CD133-negative D456MG cells</description><dates><last_updated>2025-09-24</last_updated><first_public>2014-07-18</first_public></dates><accession>PRJNA255417</accession><cross_references><GEO>GSE59484</GEO><taxon>9606</taxon><PubMed>25202981</PubMed></cross_references></HashMap>