<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/GSE313nnn/GSE313725/</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=GSE313725</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Hepatic multilineage organoids derived from hypoimmunogenic iPSCs for liver regenerative medicine</name><description>Hypoimmunogenic multicellular hepatic organoids were characterised by single-cell RNA sequencing to understand their cellular composition. Lineage cell identity was confirmed by gene and protein expression combined with ultrastructural analysis of cells by electron microscopy. Hepatic functional maturation was demonstrated by the production of liver-specific proteins, as shown by immunoassays. Together with the presence of a highly functional endothelial network, these properties confer therapeutic potential for inherited hepatic plasma protein deficiencies, end-stage liver disease and metabolic disorders.</description><dates><publication>2026/03/26</publication></dates><accession>GSE313725</accession><cross_references><GSM>GSM9373070</GSM><GSM>GSM9373071</GSM><GSM>GSM9373068</GSM><GSM>GSM9373069</GSM><GPL>30173</GPL><GSE>313725</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>