<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/GSE335nnn/GSE335248/</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=GSE335248</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>RNA-seq analysis of U251 cells following tRF-3021a knockdown at 8 and 48 hours</name><description>tRNA-derived fragments (tRFs) are relatively recently discovered small RNAs implicated in gene-regulatory processes in diverse biological contexts, but there have been few reports of clear phenotypic roles for these small RNAs in cancer progression. High expression of the 3' tRFs tRF-3009a, tRF-3021a, and tRF-3030a is associated with poor overall survival in low-grade glioma. In glioblastoma cells, these tRFs enhance invasion and migration, while tRF-3021a is uniquely required for cell proliferation, suppression of apoptosis, and maintenance of global protein synthesis. This RNA-seq study profiles transcriptomic changes following tRF-3021a knockdown in U251 cells at early and late time points (8 hours and 48 hours)</description><dates><publication>2026/09/25</publication></dates><accession>GSE335248</accession><cross_references><GSM>GSM9809003</GSM><GSM>GSM9809004</GSM><GSM>GSM9809001</GSM><GSM>GSM9809002</GSM><GSM>GSM9808996</GSM><GSM>GSM9808997</GSM><GSM>GSM9808994</GSM><GSM>GSM9809005</GSM><GSM>GSM9808995</GSM><GSM>GSM9808998</GSM><GSM>GSM9808999</GSM><GSM>GSM9809000</GSM><GPL>34284</GPL><GPL>34281</GPL><GSE>335248</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>