<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/GSE328010/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></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=GSE328010</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>RNA sequencing of naïve, activated and HIV-1 infected CD4+ T cells</name><description>CD4+ T cells play a major role in immune function regulation. Naive CD4+ T cells undergo major transcriptional changes upon activation through simultaneous engagement of the T-cell receptor and co-stimulatory molecules (anti-CD3/anti-CD28). Activated CD4+ T cells are the preferential target of HIV-1. Both T cell activation and HIV-1 infection modulate the expression and splicing of multiple genes. This study characterizes the transcriptome of naive, activated, and activated-HIV-1 infected CD4+ T cells from 3 healthy donors using bulk RNA-Seq, with validation of gene expression and alternative splicing by RT-qPCR and RT-PCR respectively.</description><dates><publication>2026/04/14</publication></dates><accession>GSE328010</accession><cross_references><GSM>GSM9670313</GSM><GSM>GSM9670312</GSM><GSM>GSM9670311</GSM><GSM>GSM9670310</GSM><GSM>GSM9670309</GSM><GSM>GSM9670308</GSM><GSM>GSM9670307</GSM><GSM>GSM9670306</GSM><GSM>GSM9670305</GSM><GPL>16791</GPL><GSE>328010</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>