<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/GSE298nnn/GSE298032/</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=GSE298032</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Host-Directed Antiviral Activity of SB2960 Through Selective Induction and Remodeling of Stress Granules</name><description>The increasing prevalence of emerging infectious diseases highlights the urgent need for broad-spectrum antiviral therapeutics. Here, we report the discovery of SB2960, a small molecule that promotes stress granule (SG) formation and exhibits potent antiviral activity across diverse viral species. Here, we applied genetically-encoded photosentisizer miniSOG induced RNA labeling technique CAP-seq to profile RNA components in SG induced by poly(I:C) and drug SB2960 to investigate how SB2960 modulates the RNAs composition of SGs.</description><dates><publication>2026/04/28</publication></dates><accession>GSE298032</accession><cross_references><GSM>GSM9005460</GSM><GSM>GSM9005462</GSM><GSM>GSM9005451</GSM><GSM>GSM9005461</GSM><GSM>GSM9005450</GSM><GSM>GSM9005442</GSM><GSM>GSM9005453</GSM><GSM>GSM9005463</GSM><GSM>GSM9005452</GSM><GSM>GSM9005455</GSM><GSM>GSM9005444</GSM><GSM>GSM9005443</GSM><GSM>GSM9005454</GSM><GSM>GSM9005457</GSM><GSM>GSM9005446</GSM><GSM>GSM9005456</GSM><GSM>GSM9005445</GSM><GSM>GSM9005459</GSM><GSM>GSM9005448</GSM><GSM>GSM9005458</GSM><GSM>GSM9005447</GSM><GSM>GSM9005449</GSM><GPL>24676</GPL><GSE>298032</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>