<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/GSE337nnn/GSE337880/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></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=GSE337880</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Comparative RNA-seq profiling of human HER2+ JIMT1-BR3 and JIMT1-BR3-LM4 breast cancer cells</name><description>A human HER2-positive leptomeningeal colonization model, JIMT1-BR3-LM4, was established by intrathecal injection of the JIMT1-BR3 HER2+ cell line, which already formed parenchymal brain metastases and occasional leptomeningeal metastases. In this study, bulk RNA sequencing was performed to define transcriptomic differences between parental JIMT1-BR3 cells and the leptomeningeal-tropic derivative JIMT1-BR3-LM4. These data provide a resource for identifying gene expression changes associated with HER2-positive breast cancer leptomeningeal colonization.</description><dates><publication>2026/09/15</publication></dates><accession>GSE337880</accession><cross_references><GSM>GSM9862263</GSM><GSM>GSM9862262</GSM><GSM>GSM9862261</GSM><GSM>GSM9862260</GSM><GSM>GSM9862265</GSM><GSM>GSM9862264</GSM><GPL>30173</GPL><GSE>337880</GSE><taxon>Homo sapiens</taxon><PMID>[42637135]</PMID></cross_references></HashMap>