<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/GSE288nnn/GSE288017/</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=GSE288017</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Mouse embryoid body differentiation in Profilin-2 3'UTR cis-element mutants</name><description>The coordinated actions of post-transcriptional regulation are essential for stem cell differentiation. The Profilin-2 transcript can be targeted by microRNAs and RNA binding proteins, specifically Ago2 and ESCC family of miRNAs -- miR-291-3p/294-3p/295-3p/302-3p -- and the Iron Regulatory Proteins IRP1/2. Earlier studies described the role of the conserved Profilin-2 ESCC miRNA site. This study describes the role of the conserved Profilin-2 IRP/iron-response-element site by CRISPR-mediated disruption of the Profilin-2 3'UTR iron response element site. The transcriptomic data reported indicates impaired germ layer formation and distribution during embryoid body differentiation when compared to wild-type mouse embryonic stem cells.</description><dates><publication>2026/08/18</publication></dates><accession>GSE288017</accession><cross_references><GSM>GSM8457698</GSM><GSM>GSM8457699</GSM><GSM>GSM8457697</GSM><GSM>GSM8457708</GSM><GSM>GSM8457706</GSM><GSM>GSM8457707</GSM><GSM>GSM8457704</GSM><GSM>GSM8457705</GSM><GSM>GSM8457702</GSM><GSM>GSM8457703</GSM><GSM>GSM8457700</GSM><GSM>GSM8457701</GSM><GPL>21103</GPL><GSE>288017</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>