<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/GSE274nnn/GSE274111/</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=GSE274111</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Effect of the depletion of YAP1 in adult spinal cord neural stem cells</name><description>Mouse spinal cord neural stem cells are know to be multipotent in vitro but mainly produce astrocytes in vivo. RNA sequencing and proteomic analysis showed that neural stem cells downregulate the Hippo/YAP1 pathway during OPC formation. To understand the implication of YAP1 in the oligodendrogliogenesis, we used transgenic cells expressing a truncated form of YAP1 and analyzed their mRNA expression in proliferation and differentiation</description><dates><publication>2026/08/06</publication></dates><accession>GSE274111</accession><cross_references><GSM>GSM8443541</GSM><GSM>GSM8443552</GSM><GSM>GSM8443542</GSM><GSM>GSM8443553</GSM><GSM>GSM8443550</GSM><GSM>GSM8443551</GSM><GSM>GSM8443560</GSM><GSM>GSM8443549</GSM><GSM>GSM8443547</GSM><GSM>GSM8443558</GSM><GSM>GSM8443559</GSM><GSM>GSM8443548</GSM><GSM>GSM8443556</GSM><GSM>GSM8443545</GSM><GSM>GSM8443557</GSM><GSM>GSM8443546</GSM><GSM>GSM8443554</GSM><GSM>GSM8443543</GSM><GSM>GSM8443544</GSM><GSM>GSM8443555</GSM><GPL>28330</GPL><GSE>274111</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>