<HashMap><database>GEO</database><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</species><gds_type>Expression profiling by array</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE314981</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Microarray analysis of quadriceps muscle of fed or 24 h-fasted wild type mice and skeletal muscle-specific FoxO1,3,4 knockout mice</name><description>Catabolic conditions, such as starvation, inactivity, and cancer cachexia, induce Forkhead box O (FoxO) transcription factor(s) expression and severe muscle atrophy via the induction of ubiquitin–proteasome system-mediated muscle proteolysis, resulting in frailty and poor quality of life. Microarray analysis of quadriceps muscle of fed or 24 h-fasted wild type mice and skeletal muscle-specific FoxO1,3,4 knockout mice identified the potential novel FoxOs-target genes in skeletal muscle including Redd1, Sestrin1, Castor2, Chac1, Depp1, Lat3, as well as Cebpd. This study comprehensively identifies novel potential FoxOs-target genes in skeletal muscle and clarifies the pathophysiological role of FoxOs, master regulators of skeletal muscle atrophy.</description><dates><publication>2026/04/20</publication></dates><accession>GSE314981</accession><cross_references><GSM>GSM9419757</GSM><GSM>GSM9419746</GSM><GSM>GSM9419745</GSM><GSM>GSM9419756</GSM><GSM>GSM9419759</GSM><GSM>GSM9419748</GSM><GSM>GSM9419747</GSM><GSM>GSM9419758</GSM><GSM>GSM9419753</GSM><GSM>GSM9419752</GSM><GSM>GSM9419744</GSM><GSM>GSM9419755</GSM><GSM>GSM9419754</GSM><GSM>GSM9419749</GSM><GSM>GSM9419751</GSM><GSM>GSM9419750</GSM><GPL>13912</GPL><GSE>314981</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>