<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/GSE297nnn/GSE297397/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Homo sapiens</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE297397</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Leukemia risk factor ARID5B Coordinates HDAC-Mediated Transcriptional Repression [RNA-Seq]</name><description>We employed a combination of proteomics, genomics and transcriptomics to describe the molecular mechanisms of ARID5B. We identify that ARID5B interacts with MIER1, C16ORF87, HDAC1 and HDAC2 forming a repressor complex. The former localizes to active regions of the genome, tethering HDAC1 and HDAC2 to enhancers and promoters. Genes actively repressed by the ARID5B repressor complex are involved in B cell-specific signaling.</description><dates><publication>2026/05/19</publication></dates><accession>GSE297397</accession><cross_references><GSM>GSM8990109</GSM><GSM>GSM8990108</GSM><GSM>GSM8990099</GSM><GSM>GSM8990110</GSM><GSM>GSM8990103</GSM><GSM>GSM8990102</GSM><GSM>GSM8990101</GSM><GSM>GSM8990100</GSM><GSM>GSM8990107</GSM><GSM>GSM8990106</GSM><GSM>GSM8990105</GSM><GSM>GSM8990104</GSM><GPL>24676</GPL><GSE>297397</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>