<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/GSE256nnn/GSE256148/</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=GSE256148</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>IL-17 signaling pathway and NMDAR1 antibodies shape NMDAR encephalitis</name><description>Human forebrain organoids (hFOs, day 110) derived from U2F iPS cell line were exposed with or without 10 μg/mL anti-NMDAR1 antibody for 24 hours. Organoids were then randomly selected for RNA sequencing (RNA-seq). By performing RNA-seq analysis, we showed that anti-NMDAR1 antibody exposure in hFOs downregulated expression of genes enriched with multiple neuronal functions including the glutamatergic synapse.These downregulated genes were also enriched with neuropsychiatric disorder-related genes.</description><dates><publication>2026/04/08</publication></dates><accession>GSE256148</accession><cross_references><GSM>GSM8086465</GSM><GSM>GSM8086466</GSM><GSM>GSM8086467</GSM><GSM>GSM8086468</GSM><GSM>GSM8086463</GSM><GSM>GSM8086464</GSM><GSM>GSM8086469</GSM><GPL>29480</GPL><GSE>256148</GSE><taxon>Homo sapiens</taxon><PMID>[41436585]</PMID></cross_references></HashMap>