<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/GSE344nnn/GSE344232/</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>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE344232</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>HOXA3 regulates thymic epithelial cell differentiation from hESCs and supports T-cell differentiation through CXCL12</name><description>H9 human embryonic stem cells were differentiated into thymic epithelial cells (TECs) via a three-stage protocol. HOXA3 was knocked down during the 3PPE-to-TEC transition to investigate its role in TEC differentiation and function. RNA-seq was performed on HOXA3 knockdown and control TEC-like cells (3 biological replicates each). HOXA3 knockdown disrupted epithelial differentiation and reduced TEC-associated gene expression, including K8, AIRE, and CD205, along with decreased FOXN1 protein. HOXA3-deficient TECs showed impaired support for T-cell generation from CD34+ progenitors. CXCL12 was identified as a downregulated gene and confirmed at mRNA and protein levels. Exogenous CXCL12 partially rescued the impaired T-cell-supporting function. This dataset provides insights into molecular regulation of human TEC differentiation.</description><dates><publication>2026/08/24</publication></dates><accession>GSE344232</accession><cross_references><GSM>GSM9973282</GSM><GSM>GSM9973281</GSM><GSM>GSM9973280</GSM><GSM>GSM9973279</GSM><GSM>GSM9973284</GSM><GSM>GSM9973283</GSM><GPL>24676</GPL><GSE>344232</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>