<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/GSE303nnn/GSE303148/</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>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE303148</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>A critical role of necroptosis in the oil cyst formation associated with autologous fat transplantation</name><description>Autologous fat grafting is limited by unpredictable long-term outcomes, with oil cyst formation being a major complication whose molecular mechanisms remain elusive. We established a novel surgically-induced mouse model demonstrating that ischemia duration time as the primary driver of oil cyst pathogenesis. Through RNA-sequencing of viable grafts (n=5) versus oil cysts (n=5), we identified the activation of RIPK3-MLKL signaling axis, revealing necroptosis-related pathways as critical molecular divergences.</description><dates><publication>2026/04/21</publication></dates><accession>GSE303148</accession><cross_references><GSM>GSM9118831</GSM><GSM>GSM9118832</GSM><GSM>GSM9118830</GSM><GSM>GSM9118828</GSM><GSM>GSM9118839</GSM><GSM>GSM9118829</GSM><GSM>GSM9118837</GSM><GSM>GSM9118838</GSM><GSM>GSM9118835</GSM><GSM>GSM9118836</GSM><GSM>GSM9118833</GSM><GSM>GSM9118834</GSM><GPL>23479</GPL><GSE>303148</GSE><taxon>Mus musculus</taxon><PMID>[41857749]</PMID></cross_references></HashMap>