<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/GSE278nnn/GSE278126/</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=GSE278126</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>scRNAseq of brain micrometastasis</name><description>Heterogeneity of brain micrometastasis was analyzed by terms of intracardiac injection of H2030-BrM cell (lung adenocarcinoma model with tropism to the brain) into mice. After 14 days, mice were sacrified in order to obtain metastatic cells from micrometastases performing vascular co-option and in proliferative pause to study their heterogeneity. Apart from control cells, H2030-BrM with reduced levels of MXD4 (shRNAs), a discovered driver of the prolfierative pause, were also injected and analyzed by scRNAseq to compare their differences.</description><dates><publication>2026/08/21</publication></dates><accession>GSE278126</accession><cross_references><GSM>GSM8540543</GSM><GSM>GSM8540544</GSM><GPL>34281</GPL><GSE>278126</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>