<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/GSE324nnn/GSE324584/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</species><gds_type> Other</gds_type><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE324584</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Effect of TAPIR on mNSCs in self-renewing conditions</name><description>Cellular translation rates are hypothesized to impact various cellular processes. Changes in rRNA expression levels are often implicated in diseases. This study reports a novel approach using a CRISPR activation (referred to as TAPIR) to manipulate rRNA levels. Induction of rRNA stimulates protein synthesis and cell proliferation, amongst others</description><dates><publication>2026/07/01</publication></dates><accession>GSE324584</accession><cross_references><GSM>GSM9579838</GSM><GSM>GSM9707082</GSM><GSM>GSM9579839</GSM><GSM>GSM9707083</GSM><GSM>GSM9579836</GSM><GSM>GSM9707084</GSM><GSM>GSM9579837</GSM><GSM>GSM9579834</GSM><GSM>GSM9579835</GSM><GSM>GSM9579832</GSM><GSM>GSM9579833</GSM><GSM>GSM9707081</GSM><GSM>GSM9579841</GSM><GSM>GSM9579830</GSM><GSM>GSM9579831</GSM><GSM>GSM9579840</GSM><GPL>24247</GPL><GPL>34290</GPL><GSE>324584</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>