<HashMap><database>ENA</database><scores/><additional><omics_type>Genomics</omics_type><center_name>University of Washington</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA120035</full_dataset_link><scientific_name>Mus musculus</scientific_name><tag>xref:PubMed:19734230</tag><long_description>We noticed that ThPOK repression is readily abrogated upon in vitro TCR stimulation of peripheral CD8 T cells. This observation prompted us to investigate a role of ThPOK in the CD8 T cell response to an acute viral infection. We observed that clonal expansion is significantly less in both primary and secondary CD8 T cell responses in the absence of functional ThPOK. To approach this mechanism, we carried out a microarray analysis for comparison of gene expression between ThPOKhd/hd and ThPOKwt/wt P14 memory T cells. Overall design: To identify genes either directly or indirectly regulated by ThPOK in CD8 T cells, we performed a microarray analysis of ThPOKhd/hd and ThPOKwt/wt memory P14 T cells. We analyzed gene expression profiles of memory cells since they showed the highest and most uniform ThPOK expression compared to not only naïve but also effector CD8 T cells. The two memory subsets were FACS purified during the memory phase, more than 100 days after LCMV infection.</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Mus musculus</name><description>Gene expression profiling from memory P14 T cells with control or mutated ThPOK</description><dates><last_updated>2025-09-24</last_updated><first_public>2014-02-11</first_public></dates><accession>PRJNA120035</accession><cross_references><GEO>GSE17812</GEO><taxon>10090</taxon><PubMed>19734230</PubMed></cross_references></HashMap>