<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/GSE317nnn/GSE317464/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Danio rerio</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=GSE317464</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Diverging routes of oligodendrocyte recruitment in adaptive and regenerative myelination</name><description>Myelination by oligodendrocytes is dynamically regulated throughout life, supporting axon and circuit function during development, activity-dependent plasticity and repair after injury. How new oligodendrocytes are recruited from their lifelong pool of oligodendrocyte precursor cells (OPCs) in these distinct contexts remains unclear. We directly compared activity-induced and demyelination-induced oligodendrogenesis under otherwise matched conditions and found that OPCs activated different transcriptional programmes in these different circumstances.</description><dates><publication>2026/02/02</publication></dates><accession>GSE317464</accession><cross_references><GSM>GSM9472669</GSM><GSM>GSM9472658</GSM><GSM>GSM9472659</GSM><GSM>GSM9472656</GSM><GSM>GSM9472667</GSM><GSM>GSM9472668</GSM><GSM>GSM9472657</GSM><GSM>GSM9472665</GSM><GSM>GSM9472666</GSM><GSM>GSM9472655</GSM><GSM>GSM9472663</GSM><GSM>GSM9472674</GSM><GSM>GSM9472664</GSM><GSM>GSM9472672</GSM><GSM>GSM9472661</GSM><GSM>GSM9472673</GSM><GSM>GSM9472662</GSM><GSM>GSM9472670</GSM><GSM>GSM9472671</GSM><GSM>GSM9472660</GSM><GPL>25922</GPL><GSE>317464</GSE><taxon>Danio rerio</taxon></cross_references></HashMap>