<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/GSE295nnn/GSE295204/</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=GSE295204</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Transcriptomic profiling of iPSC-derived microglia(iMGL) reveals FGL2-mediated Aβ uptake impairment and argatroban rescue associated with rs73375428 genotype.</name><description>To elucidate how the rs73375428 major allele impairs Aβ uptake and how argatroban rescues this impairment independently of thrombin inhibition, we performed RNA sequencing and bioinformatic analyses in iPSC-derived microglia(iMGL). These datasets provide insight into transcriptomic changes associated with FGL2 modulation and Alzheimer’s disease risk.</description><dates><publication>2026/04/21</publication></dates><accession>GSE295204</accession><cross_references><GSM>GSM8943560</GSM><GSM>GSM8943559</GSM><GSM>GSM8943557</GSM><GSM>GSM8943558</GSM><GSM>GSM8943555</GSM><GSM>GSM8943556</GSM><GSM>GSM8943553</GSM><GSM>GSM8943554</GSM><GSM>GSM8943552</GSM><GPL>24676</GPL><GSE>295204</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>