<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/GSE334nnn/GSE334496/</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=GSE334496</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>EIF1 coordinates transcriptomic and splicing networks associated with cell cycle dysregulation in diabetic retinopathy</name><description>EIF1, an RNA-binding protein implicated in multiple diseases, remains poorly characterized in diabetic retinopathy (DR). To investigate its role in DR, human retinal pigment epithelial cells (ARPE-19) were exposed to 50 mM glucose to model the condition. Under hyperglycemic conditions, EIF1 was knocked down using siRNA, followed by transcriptome sequencing (RNA-seq) to profile differentially expressed genes (DEGs) and alternative splicing events (ASEs).</description><dates><publication>2026/06/08</publication></dates><accession>GSE334496</accession><cross_references><GSM>GSM9789677</GSM><GSM>GSM9789675</GSM><GSM>GSM9789676</GSM><GSM>GSM9789673</GSM><GSM>GSM9789674</GSM><GSM>GSM9789672</GSM><GPL>24676</GPL><GSE>334496</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>