<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/GSE320nnn/GSE320191/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Homo sapiens</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=GSE320191</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>High-Dose Vitamin D3 Supplementation Associates with Innate Immune Chromatin Remodeling and Context-Dependent Transcriptomic Responses in Multiple Sclerosis [ATAC-seq]</name><description>We performed longitudinal RNA-seq and ATAC-seq profiling of PBMCs from multiple sclerosis patients receiving vitamin D₃ supplementation for day 0 and day 84. MS samples remained molecularly distinct from controls, with supplementation modulating discrete, context-dependent immune pathways rather than inducing global transcriptomic shifts. Integrated analysis identified candidate vitamin D–responsive regulatory mechanisms with potential relevance to MS pathophysiology.</description><dates><publication>2026/08/24</publication></dates><accession>GSE320191</accession><cross_references><GSM>GSM9537080</GSM><GSM>GSM9537091</GSM><GSM>GSM9537090</GSM><GSM>GSM9537086</GSM><GSM>GSM9537085</GSM><GSM>GSM9537077</GSM><GSM>GSM9537088</GSM><GSM>GSM9537087</GSM><GSM>GSM9537076</GSM><GSM>GSM9537093</GSM><GSM>GSM9537082</GSM><GSM>GSM9537092</GSM><GSM>GSM9537081</GSM><GSM>GSM9537095</GSM><GSM>GSM9537084</GSM><GSM>GSM9537083</GSM><GSM>GSM9537094</GSM><GSM>GSM9537079</GSM><GSM>GSM9537078</GSM><GSM>GSM9537089</GSM><GPL>18573</GPL><GSE>320191</GSE><taxon>Homo sapiens</taxon><PMID>[42601952]</PMID></cross_references></HashMap>