<HashMap><database>GEO</database><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=GSE324988</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Effect of BHLHE40 silencing using short-hair pin RNA on CD34+ cells isolated from human cord blood, during TGF-B1 depedent Langerhans cell differentiation</name><description>Langerhans cells (LCs) are resident antigen presenting cells of the epidermis whose differentiation, immature state and tissue residency critically depend on transforming growth factor–β1 (TGF-β1) signaling. Although several downstream transcriptional regulators of TGF-β1 have been identified, how LC epithelial identity and homeostasis are transcriptionally stabilized remains incompletely understood.Human CD34⁺ hematopoietic progenitors were differentiated into LCs or monocyte-derived cells in vitro using cytokine-defined conditions, combined with lentiviral knockdown or ectopic expression of BHLHE40. Bulk-RNA seq of shBHLHE40 cells reveals blunted induction of TGF-β1 responsive genes.</description><dates><publication>2026/05/01</publication></dates><accession>GSE324988</accession><cross_references><GSM>GSM9590039</GSM><GSM>GSM9590029</GSM><GSM>GSM9590037</GSM><GSM>GSM9590038</GSM><GSM>GSM9590035</GSM><GSM>GSM9590036</GSM><GSM>GSM9590033</GSM><GSM>GSM9590034</GSM><GSM>GSM9590031</GSM><GSM>GSM9590032</GSM><GSM>GSM9590040</GSM><GSM>GSM9590030</GSM><GPL>34284</GPL><GSE>324988</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>