<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/GSE344nnn/GSE344322/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Homo sapiens</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=GSE344322</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Effect of glutamine deprivation on naïve CD4+ T cells differentiation</name><description>Glutamine availability is a major determinant of T-cell metabolism and function. To define the transcriptional consequences of glutamine deprivation during human T-cell activation, we performed bulk RNA sequencing of naïve CD4+ T cells stimulated through the T-cell receptor under glutamine-free or physiological-range glutamine conditions. This dataset enables analysis of glutamine-dependent transcriptional programs in activated CD4+ T cells, including pathways related to cellular stress, redox regulation and inflammatory signalling.</description><dates><publication>2026/08/23</publication></dates><accession>GSE344322</accession><cross_references><GSM>GSM9975100</GSM><GSM>GSM9975101</GSM><GSM>GSM9975102</GSM><GSM>GSM9975103</GSM><GSM>GSM9975104</GSM><GSM>GSM9975105</GSM><GSM>GSM9975106</GSM><GSM>GSM9975107</GSM><GPL>34295</GPL><GSE>344322</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>