<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/GSE298nnn/GSE298899/</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=GSE298899</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Spatial transcriptomic profiling of ischemia-reperfusion injured mouse kidneys reveals niche-specific metabolic dysfunction</name><description>This study presents spatial transcriptomic data from mouse kidneys subjected to ischemia-reperfusion injury to investigate the molecular underpinnings of localized tissue responses. Using high-resolution Stereo-seq spatial transcriptomics, we profiled gene expression across healthy and injured renal microenvironments, focusing on areas surrounding failed repair proximal tubule (FR-PT) cells. Transcriptomic analysis revealed distinct niches characterized by downregulation of oxidative phosphorylation and fatty acid β-oxidation pathways, even in proximal tubule cells considered heatlhy.</description><dates><publication>2026/08/27</publication></dates><accession>GSE298899</accession><cross_references><GSM>GSM9025645</GSM><GSM>GSM9025646</GSM><GSM>GSM9025643</GSM><GSM>GSM9025644</GSM><GSM>GSM9025641</GSM><GSM>GSM9025642</GSM><GSM>GSM9025640</GSM><GSM>GSM9025639</GSM><GPL>23479</GPL><GSE>298899</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>