<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/GSE333nnn/GSE333395/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Mus musculus</species><gds_type>Genome binding/occupancy profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE333395</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Depletion of endothelial KLF4 drives age-related neurovascular dysfunction and neuropsychiatric impairment [ATAC-seq]</name><description>Omni-ATAC sequencing was performed on purified brain endothelial nuclei from young and aged endothelial-specific Klf4 knockout (EC-K4KO) and WT Cre mice to investigate chromatin accessibility changes associated with endothelial aging and neurovascular dysfunction. Endothelial KLF4 loss induced chromatin remodeling enriched for inflammatory, stress-response, and senescence-associated pathways.</description><dates><publication>2026/05/28</publication></dates><accession>GSE333395</accession><cross_references><GSM>GSM9762046</GSM><GSM>GSM9762045</GSM><GSM>GSM9762055</GSM><GSM>GSM9762053</GSM><GSM>GSM9762051</GSM><GSM>GSM9762050</GSM><GSM>GSM9762049</GSM><GSM>GSM9762048</GSM><GSM>GSM9762047</GSM><GPL>24247</GPL><GSE>333395</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>