<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/GSE294nnn/GSE294722/</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=GSE294722</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Transcriptomic profiling of a human iPSC-derived blood-brain barrier-on-chip model of ischemic stroke</name><description>Ischemic stroke is a leading cause of death and disability worldwide, characterized by reduced cerebral perfusion and blood-brain barrier (BBB) disruption. To model the human-specific pathophysiology of ischemic stroke, we developed a fully iPSC-derived blood-brain barrier-on-chip (iBBB-on-chip) comprising brain microvascular endothelial cells (iBMECs), pericytes (iPericytes), and astrocytes (iAstrocytes). After establishing a functional BBB structure, we induced ischemic injury by exposing the chip to oxygen-glucose deprivation (OGD) under static conditions. Transcriptome profiling of brain side ande endothelial side was performed to investigate molecular responses to ischemic stress.</description><dates><publication>2026/04/15</publication></dates><accession>GSE294722</accession><cross_references><GSM>GSM8917780</GSM><GSM>GSM8917778</GSM><GSM>GSM8917789</GSM><GSM>GSM8917779</GSM><GSM>GSM8917787</GSM><GSM>GSM8917788</GSM><GSM>GSM8917785</GSM><GSM>GSM8917786</GSM><GSM>GSM8917783</GSM><GSM>GSM8917784</GSM><GSM>GSM8917781</GSM><GSM>GSM8917782</GSM><GPL>29480</GPL><GSE>294722</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>