<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/GSE318nnn/GSE318190/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Drosophila melanogaster</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=GSE318190</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>The E-cadherin-Wnt-mir-994 Axis Repurposes a Cadherin Switch for Niche Robustness and Germline Stem Cell Maintenance</name><description>E-cadherin is encoded by the shg gene and is also expressed in Drosophila ovarian IGS cells. Its knockdown leads to a reduction in GSCs. To investigate the downstream molecular mechanisms and changes in gene expression, we labeled IGS cells with GFP, sorted GFP-positive cells one week after shg knockdown, and performed RNA sequencing. Finally, differential gene expression analysis along with GO and KEGG analyses were conducted.</description><dates><publication>2026/07/08</publication></dates><accession>GSE318190</accession><cross_references><GSM>GSM9489033</GSM><GSM>GSM9489032</GSM><GSM>GSM9489031</GSM><GSM>GSM9489030</GSM><GSM>GSM9489029</GSM><GSM>GSM9489028</GSM><GPL>13304</GPL><GSE>318190</GSE><taxon>Drosophila melanogaster</taxon><PMID>[42359497]</PMID></cross_references></HashMap>