<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/GSE326nnn/GSE326421/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</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=GSE326421</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Mitochondrial transfer from astrocytes to endothelial cells reinforces redox homeostasis and barrier integrity in brain arteriovenous malformation</name><description>Brain arteriovenous malformation (BAVM) is a high-flow vascular shunt that predisposes to intracranial hemorrhage and represents a leading cause of stroke in young adults. Somatic mutations in KRAS or BRAF drive endothelial dysfunction and lesion formation, yet the contribution of non-endothelial cells within the neuro-glial-vascular unit remains incompletely understood.</description><dates><publication>2026/04/27</publication></dates><accession>GSE326421</accession><cross_references><GSM>GSM9630819</GSM><GSM>GSM9630818</GSM><GSM>GSM9630817</GSM><GSM>GSM9630816</GSM><GSM>GSM9630815</GSM><GSM>GSM9630822</GSM><GSM>GSM9630821</GSM><GSM>GSM9630820</GSM><GPL>34290</GPL><GSE>326421</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>