<HashMap><database>iProX</database><scores/><additional><omics_type>Proteomics</omics_type><submitter>Jiajia Lu</submitter><species>Mus Musculus</species><full_dataset_link>http://www.iprox.org/page/project.html?id=IPX0016521000</full_dataset_link><submitter_email>lujiajia@smmu.edu.cn</submitter_email><submitter_affiliation>Shanghai Changzheng Hospital</submitter_affiliation><sample_protocol></sample_protocol><repository>iProX</repository><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>Based on multi-omics, revealing the key role of MOESIN lactic acidification-driven TGF-β signaling axis in improving diabetic osteoporosis through gut microbiota</name><description>Diabetic osteoporosis (DOP), as a typical representative of metabolic-immune cross-talk imbalance, has an unclear pathogenesis and lacks effective targeted intervention methods. This study aims to systematically analyze the molecular mechanism by which fecal microbiota transplantation (FMT) activates the TGF-β signaling axis through MOESIN lactic acid modification, reshapes the Treg/Th17 immune balance, and improves the pathological process of DOP based on multi-omics integrated analysis</description><dates><publication>Fri Apr 03 00:00:00 BST 2026</publication></dates><accession>PXD076650</accession><cross_references><TAXONOMY>10090</TAXONOMY></cross_references></HashMap>