<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/GSE328nnn/GSE328742/</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=GSE328742</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Smad4/SKI/SKIL-mediated chromatin accessibility changes during the CD8 T cell response</name><description>Transforming growth factor-β (TGF-β) is an immunosuppressive cytokine that regulates both innate and adaptive immune responses. Earlier studies have shown that TGF-β plays a role in promoting T cell exhaustion during the later stages of chronic viral infection. In this dataset we examined the global chromatin accessibility changes in CD8 T cells that are dependent on SMAD4. Our findings documenting the striking requirement for Smad4-SKI-SKIL mediated restraint of TGF-β-associated program during the effector phase of the CD8 T cell response have implications for developing immunotherapeutic approaches against chronic viral infections and cancer.</description><dates><publication>2026/09/03</publication></dates><accession>GSE328742</accession><cross_references><GSM>GSM9688450</GSM><GSM>GSM9688452</GSM><GSM>GSM9688451</GSM><GSM>GSM9688454</GSM><GSM>GSM9688453</GSM><GSM>GSM9688445</GSM><GSM>GSM9688456</GSM><GSM>GSM9688455</GSM><GSM>GSM9688444</GSM><GSM>GSM9688458</GSM><GSM>GSM9688447</GSM><GSM>GSM9688457</GSM><GSM>GSM9688446</GSM><GSM>GSM9688449</GSM><GSM>GSM9688448</GSM><GSM>GSM9688459</GSM><GPL>24247</GPL><GSE>328742</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>