<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/GSE308nnn/GSE308541/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</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=GSE308541</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Transcriptomic effects of miR-21-5p on preimplantation mouse blastocysts</name><description>Preimplantation embryos cultured in vitro exhibit increased stress and apoptosis compared with in vivo development. miR-21-5p is a conserved, highly abundant microRNA in reproductive-tract extracellular vesicles and has been implicated in cell-survival pathways. To define its transcriptomic impact on early embryos, we performed RNA-seq on mouse blastocysts generated by IVF and cultured in KSOM with either miR-21-5p agomir (50 nM) or blank control. Each biological replicate consisted of five pooled blastocysts; n=4 replicates per group. Sequencing was carried out on an Illumina NovaSeq X Plus.</description><dates><publication>2026/06/15</publication></dates><accession>GSE308541</accession><cross_references><GSM>GSM9247782</GSM><GSM>GSM9247783</GSM><GSM>GSM9247780</GSM><GSM>GSM9247781</GSM><GSM>GSM9247779</GSM><GSM>GSM9247776</GSM><GSM>GSM9247777</GSM><GSM>GSM9247778</GSM><GPL>34290</GPL><GSE>308541</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>