<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/GSE296nnn/GSE296110/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Homo sapiens</species><gds_type>Non-coding RNA profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE296110</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Small RNA Seq profiling of tissue specific MSCs derived EVs</name><description>Small extracellular vesicles (sEV) play a pivotal role in intercellular communication and hold immense therapeutic potential. In this study, we aimed to characterize sEV derived from bone marrow mesenchymal stromal cells (BM-MSCs) and Wharton’s jelly mesenchymal stromal cells (WJ-MSCs), cultured under normoxic and hypoxic conditions for elucidating their functional inclinations. Using high-throughput miRNA sequencing, we identified distinct miRNA profiles across cell types and oxygenation states, revealing unique signatures associated with hypoxia-driven cellular adaptations.</description><dates><publication>2026/05/01</publication></dates><accession>GSE296110</accession><cross_references><GSM>GSM8965367</GSM><GSM>GSM8965356</GSM><GSM>GSM8965366</GSM><GSM>GSM8965355</GSM><GSM>GSM8965365</GSM><GSM>GSM8965354</GSM><GSM>GSM8965364</GSM><GSM>GSM8965353</GSM><GSM>GSM8965359</GSM><GSM>GSM8965358</GSM><GSM>GSM8965368</GSM><GSM>GSM8965357</GSM><GSM>GSM8965363</GSM><GSM>GSM8965362</GSM><GSM>GSM8965361</GSM><GSM>GSM8965360</GSM><GPL>18573</GPL><GSE>296110</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>