<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/GSE304nnn/GSE304752/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</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=GSE304752</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Chromatin priming of skeletal stem progenitor cells governs cell fate during bone repair</name><description>Bone regeneration is driven by skeletal stem/progenitor cells (SSPCs), which form bone and cartilage after injury. SSPCs represent a diversity of cell populations localized in several bone compartments and adjacent skeletal muscles, with different contributions to bone healing. By generating 10X multiome datasets (i.e., combined single-nucleus RNA-seq and ATAC-seq) and CUT&amp;Tag datasets, we uncovered specificing epigenetic priming of SSPCs at steady-state in muscle and periosteum that dictates their fate decision after a bone fracture.</description><dates><publication>2026/09/23</publication></dates><accession>GSE304752</accession><cross_references><GSM>GSM9786079</GSM><GSM>GSM9156315</GSM><GSM>GSM9786078</GSM><GSM>GSM9156317</GSM><GSM>GSM9156316</GSM><GSM>GSM9786075</GSM><GSM>GSM9786074</GSM><GSM>GSM9786077</GSM><GSM>GSM9786076</GSM><GSM>GSM9786081</GSM><GSM>GSM9156318</GSM><GSM>GSM9786080</GSM><GPL>34475</GPL><GPL>24247</GPL><GSE>304752</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>