<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/GSE311nnn/GSE311100/</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> Other</gds_type><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE311100</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Decoding the Cell-Type and Spatial Roles of H19 in Cholestatic Liver Injury Through Single-Nucleus and Spatial Transcriptomics</name><description>Despite recent advances, Primary Sclerosing Cholangitis (PSC)-a chronic obstructive biliary disease-still lacks effective therapies to prevent disease progression or the need for liver transplantation. Long non-coding RNA H19 (H19) has been implicated in promoting PSC disease progression. However, the underlying cell-specific and molecular mechanisms by which H19 contributes to PSC pathogenesis remain incompletely understood. Here we used single nucleus RNA sequencing (snRNAseq) and spatial transcriptomics to elucidate the cell- and spatial-specific expression alterations associated with H19 in the Mdr2KO PSC mouse model.</description><dates><publication>2026/04/30</publication></dates><accession>GSE311100</accession><cross_references><GSM>GSM9316939</GSM><GSM>GSM9316928</GSM><GSM>GSM9316938</GSM><GSM>GSM9316937</GSM><GSM>GSM9316936</GSM><GSM>GSM9316935</GSM><GSM>GSM9316934</GSM><GSM>GSM9316933</GSM><GSM>GSM9316932</GSM><GSM>GSM9316931</GSM><GSM>GSM9316930</GSM><GSM>GSM9316940</GSM><GSM>GSM9316929</GSM><GPL>30172</GPL><GPL>24247</GPL><GSE>311100</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>