<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/GSE300nnn/GSE300563/</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=GSE300563</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>RNA-seq analysis for the Fluo-4 abnormal myofibers in aged mice</name><description>In a rapidly aging society, the age-related decline in muscle mass and force, sarcopenia, is an urgent medical and economic issue. However, the molecular mechanisms of sarcopenia are still largely unknown. Using Ca2+ indicator Fluo-4, we identified the presence of the Fluo-4 abnormal muscle fibers only in aged mice. The Fluo-4 abnormal muscle fibers had a tubular aggregate-like structure and morphologically abnormal mitochondria. Furthermore, a cluster of mitochondria-related genes, including mitochondrially-encoded genes, were downregulated in Ca2+-abnormal muscle fibers. These results indicate that the Fluo-4 abnormal muscle fibers are accumulated in aged mice, and that age-related mitochondrial abnormalities are more prominent in these fibers.</description><dates><publication>2026/04/23</publication></dates><accession>GSE300563</accession><cross_references><GSM>GSM9064590</GSM><GSM>GSM9064591</GSM><GSM>GSM9064589</GSM><GSM>GSM9064598</GSM><GSM>GSM9064599</GSM><GSM>GSM9064588</GSM><GSM>GSM9064596</GSM><GSM>GSM9064597</GSM><GSM>GSM9064594</GSM><GSM>GSM9064595</GSM><GSM>GSM9064592</GSM><GSM>GSM9064593</GSM><GPL>24247</GPL><GSE>300563</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>