<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/GSE243nnn/GSE243164/</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=GSE243164</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Analysis of the genomic regions controlled by RXRα in alveolar macrophages (RXR HT-ChIPmentation)</name><description>The goal of this study was to define the cistrome of RXR by HT-ChIPmentation followed by sequencing in alveolar macrophages of wild-type and RXRαβ-deficient mice, in order to identify genomic regions directly controlled by these transcription factors. Due to technical antibody limitations, the ChIPmentation was performed using only the antibody against RXRα</description><dates><publication>2026/05/13</publication></dates><accession>GSE243164</accession><cross_references><GSM>GSM7780097</GSM><GSM>GSM7780099</GSM><GSM>GSM7780098</GSM><GSM>GSM7780101</GSM><GSM>GSM7780100</GSM><GPL>30172</GPL><GSE>243164</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>