<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/GSE329nnn/GSE329263/</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=GSE329263</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Transcriptomic Profiling of Thyroid Eye Disease Orbital Fibroblasts</name><description>This project aims to define the persistent transcriptomic alterations in orbital fibroblasts (OFs) derived from patients with thyroid eye disease (TED) compared to non-TED OF controls. Primary OFs were isolated from orbital connective tissue and expanded in vitro under standardized conditions. We performed high-depth RNA sequencing on these cells to characterize the differential expression of genes involved in extracellular matrix remodeling, inflammatory signaling, and metabolic activation. This dataset provides a comprehensive resource for identifying the molecular drivers of orbital remodeling in the context of TED.</description><dates><publication>2026/08/10</publication></dates><accession>GSE329263</accession><cross_references><GSM>GSM9700352</GSM><GSM>GSM9700351</GSM><GSM>GSM9700354</GSM><GSM>GSM9700353</GSM><GSM>GSM9700356</GSM><GSM>GSM9700355</GSM><GSM>GSM9700358</GSM><GSM>GSM9700357</GSM><GSM>GSM9700349</GSM><GSM>GSM9700359</GSM><GSM>GSM9700350</GSM><GPL>30173</GPL><GSE>329263</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>