<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/GSE339nnn/GSE339137/</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=GSE339137</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Taxus cuspidata extract attenuates allergic airway inflammation, and its constituent taxinine targets the IL-17/TNF program in mast cells</name><description>Mast cells are central effectors of IgE-mediated allergic inflammation. To define, transcriptome-wide, how the Taxus cuspidata-derived diterpenoid taxinine modulates mast-cell activation, we profiled bone-marrow-derived mast cells (BMMCs) from C57BL/6 mice in three conditions: untreated control, IgE-sensitized cells stimulated with DNP-BSA (BSA), and DNP-BSA-stimulated cells treated with taxinine. Differential expression, functional enrichment, and gene-set enrichment analysis showed that IgE/antigen stimulation induced a strong inflammatory signature that taxinine partially attenuated, with the IL-17 and TNF signaling programs enriched by stimulation and reciprocally suppressed by taxinine.</description><dates><publication>2026/07/24</publication></dates><accession>GSE339137</accession><cross_references><GSM>GSM9888978</GSM><GSM>GSM9888979</GSM><GSM>GSM9888976</GSM><GSM>GSM9888977</GSM><GSM>GSM9888971</GSM><GSM>GSM9888974</GSM><GSM>GSM9888975</GSM><GSM>GSM9888972</GSM><GSM>GSM9888973</GSM><GPL>24247</GPL><GSE>339137</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>