<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/GSE324nnn/GSE324318/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></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=GSE324318</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Identification of a set of transcriptional regulators involved in the temporal regulation of neuron subtype differentiation [RNA-Seq 2]</name><description>The sequential generation of various types of neurons and glia from neural stem /progenitor cells (NSPCs) during development is a major part to build complex central nervous system. Here, we identify PHF21b, ZFP7 and ZFP57 as crucial factors that regulate the transition from early-born neuron to late-born neuron generation by NSPCs in the developing mouse cortex. Simultaneous knockdown of these genes suppressed generation of early-born neurons.</description><dates><publication>2026/06/14</publication></dates><accession>GSE324318</accession><cross_references><GSM>GSM9573558</GSM><GSM>GSM9573557</GSM><GSM>GSM9573559</GSM><GSM>GSM9573560</GSM><GPL>28330</GPL><GSE>324318</GSE><taxon>Mus musculus</taxon><PMID>[42000103]</PMID></cross_references></HashMap>