<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/GSE311nnn/GSE311603/</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=GSE311603</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Identification of a novel deeply quiescent neural stem cell population in the subventricular zone</name><description>This study shows that a novel genetic tool, the Penk-CreAi9 line, expressing Cre recombinase under the Proenkephalin promoter and combined with the Ai9-tdTomato line, labels a distinct group of stem cells in the SVZ together with previously identified subgroups of B-cells and neuroblasts. Single-cell RNA sequencing (scRNA-seq) demonstrates that these cells represent a previously unappreciated population of qNSCs with a unique transcriptional profile and a less differentiated state than the canonically accepted GLAST+ NSCs. In particular, the analysis further reveals expression of 5-hydroxytryptamine receptor 2C (5-HT2C receptor) and prolactin receptor (PRLR), which were previously functionally correlated with qNSCs but not captured or profiled in RNAseq experiments. This study also identifies novel markers, including Kcnj13, a gene that encodes the potassium channel KiR7.1, that define the identity of these cells.</description><dates><publication>2026/06/09</publication></dates><accession>GSE311603</accession><cross_references><GSM>GSM9327973</GSM><GSM>GSM9327972</GSM><GSM>GSM9327975</GSM><GSM>GSM9327974</GSM><GPL>21626</GPL><GSE>311603</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>