<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/GSE296nnn/GSE296759/</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=GSE296759</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Elucidating the impact of chemotherapy on skeletal progenitors [bulk ATAC-seq]</name><description>Mice receiving cyclic doxorubicin (DOX) treatment exhibited long-term skeletal defects. Lineage tracing experiments revealed loss of osteogenesis from bone marrow mesenchymal stem and progenitor cells. We performed molecular characterization on MSPCs to understand the mechanisms underying MSPC dysfunction folloiwng DOX treatment.</description><dates><publication>2026/06/15</publication></dates><accession>GSE296759</accession><cross_references><GSM>GSM8975989</GSM><GSM>GSM8975987</GSM><GSM>GSM8975988</GSM><GSM>GSM8975990</GSM><GSM>GSM8975991</GSM><GSM>GSM8975986</GSM><GPL>34328</GPL><GSE>296759</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>