<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE292nnn/GSE292837/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Mus musculus</species><gds_type>Genome binding/occupancy profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE292837</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Dlx1&amp;2 Directly Promote Expression of Cxcl14 to Control Synapse Development and Interneuron Survival [ChIP-seq]</name><description>Dlx genes have fundamental roles in the generation, differentiation and functions of virtually all forebrain GABAergic neurons. Here we focused on defining the key genes that are dysregulated in Dlx1/2 conditional mutants in mouse immature cortical GABAergic interneurons (CINs), and by identifying DLX-bound putative regulatory elements (pREs) of these Dlx-regulated genes. Within the Dlx-expressing lineage, some DLX-bound pREs were specific to CINs, others appeared to be constitutively bound; the latter class having activity in mature CINs. One such pRE and its associated gene, Cxcl14, is strongly activated by Dlx1/2 and is essential for synaptogenesis onto CINs and for CIN survival.</description><dates><publication>2026/05/01</publication></dates><accession>GSE292837</accession><cross_references><GSM>GSM8866289</GSM><GSM>GSM8866288</GSM><GSM>GSM8866287</GSM><GSM>GSM8866286</GSM><GSM>GSM8866295</GSM><GSM>GSM8866294</GSM><GSM>GSM8866293</GSM><GSM>GSM8866292</GSM><GSM>GSM8866291</GSM><GSM>GSM8866290</GSM><GPL>24247</GPL><GSE>292837</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>