<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/GSE335nnn/GSE335098/</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=GSE335098</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Effect of Tyrphostin-AG4178 on ex-vivo mouse ovarian follicles in eIVFG ovulation system</name><description>Ovulation is a coordinated, multicellular process carried out in the antral follicle involving gonadotropin-stimulus, cumulos-oocyte complex expansion, follicle rupture, followed by luteinization. Ovulation can be prevented by targeted inhibition of upstream signalling molecules via tool compounds such as Tyrphostin-AG4178, which binds to EGFR and thus prevents downstream MEK/ERK, prostaglandin, and Pgr signaling. We exposed ex vivo mouse ovarian follicles grown in an encapsulated in-vitro follicle growth (eIVFG) system to Tyrphostin-AG4178 after stimulus with hCG and performed bulk-RNA sequencing on whole follicles to observe the transcriptomic response to targeted ovulation inhibition.</description><dates><publication>2026/06/23</publication></dates><accession>GSE335098</accession><cross_references><GSM>GSM9805786</GSM><GSM>GSM9805775</GSM><GSM>GSM9805776</GSM><GSM>GSM9805777</GSM><GSM>GSM9805778</GSM><GSM>GSM9805779</GSM><GSM>GSM9805780</GSM><GSM>GSM9805781</GSM><GSM>GSM9805770</GSM><GSM>GSM9805771</GSM><GSM>GSM9805782</GSM><GSM>GSM9805783</GSM><GSM>GSM9805772</GSM><GSM>GSM9805784</GSM><GSM>GSM9805773</GSM><GSM>GSM9805774</GSM><GSM>GSM9805785</GSM><GPL>30172</GPL><GSE>335098</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>