<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/GSE259nnn/GSE259445/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Homo sapiens</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=GSE259445</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Analysis of androgen receptor signaling in human neuronal cells</name><description>Androgen signaling through the androgen receptor (AR), a ligand-dependent transcription factor within the steroid receptor superfamily, plays an important role in brain development and maintenance of neuron activity. However, a key unanswered question is the mechanism through which AR-mediated gene expression leads to these effects. To gain further insight into the mechanism of AR action in human neuronal cells, we identified AR-binding sites in human neuronal cells, SH-SY5Y (SS5) using ChIP-seq (chromatin immunoprecipitation coupled with sequencing).</description><dates><publication>2026/09/09</publication></dates><accession>GSE259445</accession><cross_references><GSM>GSM8116372</GSM><GSM>GSM8116371</GSM><GSM>GSM8116370</GSM><GSM>GSM8116369</GSM><GSM>GSM8116378</GSM><GSM>GSM8116377</GSM><GSM>GSM8116376</GSM><GSM>GSM8116375</GSM><GSM>GSM8116374</GSM><GSM>GSM8116373</GSM><GPL>23227</GPL><GSE>259445</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>