<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/GSE346nnn/GSE346108/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></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=GSE346108</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>CPEB1 Overexpression Rewires Alternative Splicing in T98G Cells: A Resource for Alzheimer's Disease Research</name><description>Alzheimer's disease is a multifactorial neurodegenerative disorder with incompletely understood molecular mechanisms. Cytoplasmic polyadenylation element-binding protein 1 (CPEB1) is an RNA-binding protein implicated in post-transcriptional regulation and synaptic function, but its regulatory network in human neural cells remains underexplored. In this study, bulk RNA sequencing was performed on T98G human glioblastoma cells transfected with a CPEB1 overexpression construct or the corresponding empty-vector control. Differential gene expression and alternative splicing analyses were performed using DESeq2 and the ABLas pipeline, respectively. Functional enrichment analysis and comparison with Alzheimer's disease-associated gene sets were used to identify candidate CPEB1-regulated genes and splicing events relevant to Alzheimer's disease research.</description><dates><publication>2026/09/06</publication></dates><accession>GSE346108</accession><cross_references><GSM>GSM10024692</GSM><GSM>GSM10024694</GSM><GSM>GSM10024693</GSM><GSM>GSM10024696</GSM><GSM>GSM10024695</GSM><GSM>GSM10024697</GSM><GPL>24676</GPL><GSE>346108</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>