<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/GSE327nnn/GSE327147/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Other</omics_type><species>synthetic construct</species><species> Mus musculus</species><gds_type>Other</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE327147</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>MERFISH data on seven mouse brain with Abeta pathology</name><description>Microglia adopt various spatially resolved gene and functional profiles in amyloidosis mice, for example the relative enrichment of DAMs proximal to plaques. To spatially resolve these transcriptional changes and identify microglial populations responsive to TREM2 small molecule agonism, multiplexed error-robust fluorescence in situ hybridization (MERFISH) was conducted on sagittal brain sections from VG-3909–treated 5xFAD;hTREM2 mice, 12 hours post-oral dosing. Simultaneous immunostaining using an anti-amyloid antibody enabled spatial correlation of microglial transcriptomes with amyloid plaque localization. The custom MERFISH panel comprised 500 genes, included cell-type markers and microglia-focused genes.</description><dates><publication>2026/04/24</publication></dates><accession>GSE327147</accession><cross_references><GSM>GSM9649271</GSM><GSM>GSM9649273</GSM><GSM>GSM9649272</GSM><GSM>GSM9649275</GSM><GSM>GSM9649274</GSM><GSM>GSM9649277</GSM><GSM>GSM9649276</GSM><GPL>31217</GPL><GSE>327147</GSE><taxon>synthetic construct</taxon><taxon> Mus musculus</taxon></cross_references></HashMap>