<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/GSE288nnn/GSE288621/</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=GSE288621</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Comparative Single Cell RNA Sequencing of Notch2 and RBPJ-deficient mononuclear phagocyte cells from the spleen</name><description>Splenic mononuclear phagocytes are critical in various homeostatic processes as well as immune responses. We employed single-cell RNA sequencing to investigate mononuclear phagocytic cell subsets, including splenic red pulp macrophages, monocytes, and dendritic cells in the spleen, with a focus on how Notch2 and its nuclear mediator Rbpj regulate these subsets. Our study offers a comparative analysis of splenic mononuclear phagocytes and specifically red pulp macrophages examining phagocytes isolated from myeloid Notch2 (N2ΔCx3cr1)-, and Rbpj (RbpjΔCx3cr1)-deficient mice or control animals. Our findings may provide further insights into the heterogeneity and development of the splenic mononuclear phagocytic system including splenic macrophages and monocytes.</description><dates><publication>2026/08/18</publication></dates><accession>GSE288621</accession><cross_references><GSM>GSM8771408</GSM><GSM>GSM8771407</GSM><GPL>19057</GPL><GSE>288621</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>