<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/GSE325nnn/GSE325789/</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><gds_type> Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE325789</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Phosphoproteomic dysregulation drives tumor proliferation in Cushing’s disease</name><description>Cushing's disease causes severe morbidity and mortality, yet its underlying mechanisms are poorly understood. We used snMutiome (RNAseq +ATACseq) to compare the transcriptomes and epigenomes of CD adenomas to their normal adjacent pituitary glands</description><dates><publication>2026/09/15</publication></dates><accession>GSE325789</accession><cross_references><GSM>GSM9613450</GSM><GSM>GSM9613448</GSM><GSM>GSM9613449</GSM><GSM>GSM9613444</GSM><GSM>GSM9613445</GSM><GSM>GSM9613446</GSM><GSM>GSM9613447</GSM><GSM>GSM9613451</GSM><GSM>GSM9613452</GSM><GSM>GSM9613442</GSM><GSM>GSM9613453</GSM><GSM>GSM9613443</GSM><GPL>18573</GPL><GSE>325789</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>