<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/GSE196nnn/GSE196382/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Homo sapiens</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=GSE196382</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Defining transcripts regulated by RBBP4/p300 complex in glioblastoma [RNA-seq]</name><description>Purpose: Next-generation sequencing (NGS) has revolutionized the ability to conduct genome wide transcriptional regulation. The goals of this study was to identify potential genes regulated by RBBP4/p300 complex by comparing transcriptome profiling (RNA-seq) generated in GBM43 expressing control non-targeting shRNA with cells expressing shRNA targeting RBBP4 or p300. Commonly downregulated and upregulated genes by both shRBBP4 and shp300 were considered to potentially be regulated by RBBP4/p300 complex.</description><dates><publication>2026/06/18</publication></dates><accession>GSE196382</accession><cross_references><GSM>GSM5879882</GSM><GSM>GSM5879883</GSM><GSM>GSM5879884</GSM><GPL>20301</GPL><GSE>196382</GSE><taxon>Homo sapiens</taxon><PMID>[42291750]</PMID></cross_references></HashMap>