<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/GSE342nnn/GSE342343/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Other</omics_type><species>Mus musculus</species><gds_type>Other</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE342343</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>The role of Angiopoietin 1 in acute-on-chronic liver failure</name><description>Acute-on-chronic liver failure (ACLF) is an acute liver and multisystem failure in patients with pre-existing liver disease. A common precipitating factor for ACLF is sepsis. Our recent work shows that sepsis-ACLF is associated with loss of Angiopoietin 1 (ANG-1) and endothelial dysfunction that in turn promotes loss of hepatocyte differentiation and liver failure. However, the mechanism of angiopoietin-mediated endothelial to hepatocyte crosstalk in ACLF is not fully understood. We aimed to study Angiopoietin 1-induced changes in liver cells using spatial transcritomics.</description><dates><publication>2026/09/01</publication></dates><accession>GSE342343</accession><cross_references><GSM>GSM9928801</GSM><GPL>33896</GPL><GSE>342343</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>