<HashMap><database>ENA</database><scores/><additional><omics_type>Genomics</omics_type><center_name>UCSF</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA186616</full_dataset_link><scientific_name>Mus musculus</scientific_name><long_description>There was a remarkable similarity in the molecular properties of the MGE-GFP+ and ES-GFP+ cells. In particular, genes that are important for medial ganglionic eminence (MGE) and cortical interneurons development are both high in expression in both MGE-Lhx6-GFP+ and ES-Lhx6-GFP+ cells (compared to ES-Lhx6-GFP- cells). Overall design: To investigate how closely ES cells-derived Lhx6-GFP+ cells resembled authentic Lhx6+ MGE cells, and to define the molecular properties of the Lhx6-GFP+ and Lhx6-GFP- cells from differentiated ES cells, we compared their gene expression profiles. We used FACS to purify GFP+ cells from the E12.5 MGE of Lhx6-GFP transgenic mice. ES-Lhx6-GFP+ cells and ES-Lhx6-GFP- cells (both from D12 EB aggregates) were also isolated by fluorescent activated cell sorting (FACS) and all of the RNA samples were subjected to RNA expression microarray analyses.</long_description><tag>xref:PubMed:23658702</tag><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Mus musculus</name><description>Comparison of gene expression signature between nascent Lhx6-GFP+ cells from mouse embryonic brain and differentiated Lhx6-GFP+ cells from ES cells (as well as comparing those of Lhx6-GFP+ and Lhx6-GFP- cells from ES cells)</description><dates><last_updated>2025-09-24</last_updated><first_public>2014-02-11</first_public></dates><accession>PRJNA186616</accession><cross_references><GEO>GSE43508</GEO><taxon>10090</taxon><PubMed>23658702</PubMed></cross_references></HashMap>