<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/GSE316nnn/GSE316338/</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=GSE316338</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Human spinal cord organoids recapitulate developmental and disease-associated oligodendrocyte lineage signatures [scRNA-Seq]</name><description>Human spinal organoids (hSpO), assembloids (human cortical organoid assembled to hSpO and 3D human muscle), and assembloids treated with cytokine cocktail TNF-α, IL-1α, and C1q (TIC) were dissociated. All dissociations were enriched for either astrocytes or oligodendrocytes through immunopanning, then sequenced.</description><dates><publication>2026/06/01</publication></dates><accession>GSE316338</accession><cross_references><GSM>GSM9450495</GSM><GSM>GSM9450494</GSM><GSM>GSM9450497</GSM><GSM>GSM9450496</GSM><GSM>GSM9450499</GSM><GSM>GSM9450498</GSM><GSM>GSM9450501</GSM><GSM>GSM9450500</GSM><GSM>GSM9450493</GSM><GSM>GSM9450492</GSM><GPL>34284</GPL><GSE>316338</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>