<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/GSE337nnn/GSE337539/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE337539</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>scRNAseq of LCMV-specific P14 cells: WT, P2RX7-KO and NKG7-KO</name><description>We have used Parse Biosciences to generate single-cell RNAseq libraries from P14 CD8+ T cells (wild-type - WT, P2RX7-KO and NKG7-KO) collected from mice infected with either LCMV-Armstrong or LCMV-Clone 13 (days 0, 7 or 30 post-infection). The goal of this study was to determine the transcriptional alterations in memory or exhausted CD8+ T cells driven by the absence of either P2RX7 (a purinergic receptor that senses extracellular ATP) or NKG7 (a metabolic regulator that can downregulate mTORC1 and simultaneously induce cytotoxicity).</description><dates><publication>2026/07/08</publication></dates><accession>GSE337539</accession><cross_references><GSM>GSM9857601</GSM><GSM>GSM9857602</GSM><GSM>GSM9857603</GSM><GSM>GSM9857604</GSM><GSM>GSM9857605</GSM><GSM>GSM9857606</GSM><GSM>GSM9857607</GSM><GSM>GSM9857608</GSM><GPL>34290</GPL><GSE>337539</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>