<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/GSE285nnn/GSE285969/</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=GSE285969</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>T, NK, NKT cells in the brain from WT or 15q dup mice [brain]</name><description>Autism Spectrum Disorder (ASD) is a neurodevelopmental disorder with no effective treatment, caused by genetic factors such as copy number variations (CNVs) and immunological factors such as maternal infection. The role of immunity in genetic ASD remains unclear. Here, we investigated the immun cells in the brains of a mouse model of ASD (15q11-13 duplication), a common CNV associated with ASD.</description><dates><publication>2026/04/01</publication></dates><accession>GSE285969</accession><cross_references><GSM>GSM8714185</GSM><GSM>GSM8714196</GSM><GSM>GSM8714195</GSM><GSM>GSM8714194</GSM><GSM>GSM8714193</GSM><GSM>GSM8714189</GSM><GSM>GSM8714200</GSM><GSM>GSM8714199</GSM><GSM>GSM8714188</GSM><GSM>GSM8714187</GSM><GSM>GSM8714198</GSM><GSM>GSM8714197</GSM><GSM>GSM8714186</GSM><GSM>GSM8714192</GSM><GSM>GSM8714191</GSM><GSM>GSM8714190</GSM><GPL>24247</GPL><GSE>285969</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>