<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/GSE327nnn/GSE327194/</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> Other</gds_type><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE327194</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Modelling B cell development with pluripotent stem cells</name><description>The ability to generate functional B cells from human pluripotent stem cells (hPSCs) would open new opportunities to develop novel B cell-based therapies to treat a range of human diseases and disorders. Towards this goal, we established a MS-5 stromal based protocol that promotes the efficient development of B lineage cells from definitive hematopoietic progenitors generated from different hPSC lines. Flow cytometric and multi-omic scRNA-seq analyses revealed that B cell development from hPSCs transitions through the well-established pro- B, pre-B and naïve B cell stages, accurately recapitulating B lymphopoiesis in the human adult bone marrow.</description><dates><publication>2026/08/21</publication></dates><accession>GSE327194</accession><cross_references><GSM>GSM9651130</GSM><GSM>GSM9651126</GSM><GSM>GSM9651129</GSM><GSM>GSM9651128</GSM><GSM>GSM9651127</GSM><GPL>24676</GPL><GSE>327194</GSE><taxon>Homo sapiens</taxon><PMID>[42146710]</PMID></cross_references></HashMap>