<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/GSE309nnn/GSE309463/</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=GSE309463</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Bulk RNA-seq of CRH neuron_Ctr vs Tumor</name><description>Bulk RNA sequencing was performed on fluorescence-activated cell sorting (FACS)-isolated CRH-expressing neurons from the hypothalamus of control and EO771 tumor-bearing mice. The objective was to determine how breast tumor development influences transcriptional programs in CRH neurons, including acute stress-related signaling, immune-neuroendocrine communication, and downstream pathway alterations. These datasets are intended for differential gene expression analysis, pathway enrichment, and hypothesis generation for future functional validation.</description><dates><publication>2026/06/18</publication></dates><accession>GSE309463</accession><cross_references><GSM>GSM9267749</GSM><GSM>GSM9267748</GSM><GSM>GSM9267747</GSM><GSM>GSM9267746</GSM><GPL>30172</GPL><GSE>309463</GSE><taxon>Mus musculus</taxon><PMID>[41401811]</PMID></cross_references></HashMap>