<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Qian Q</submitter><funding>Scientific Research Projects of Medical and Health Institutions of Longhua District, Shenzhen</funding><funding>Shenzhen Science and Technology Program</funding><pagination>64</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11909235</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>25(1)</volume><pubmed_abstract>Ischemic stroke (IS), a leading cause of global disability and mortality, is characterized by white matter damage and demyelination. Despite advances, the molecular mechanisms driving post-IS myelin pathology remain poorly understood, limiting therapeutic development. This study investigates key myelin-related genes (MRGs) and their regulatory networks to identify novel therapeutic targets. A transient middle cerebral artery occlusion (MCAO) model was established in C57BL/6 mice, with brain tissues collected at four timepoints (Sham0D, MCAO0D, MCAO7D, MCAO14D). Transcriptomic and proteomic sequencing were performed, followed by soft clustering (Mfuzz), functional enrichment (GO/KEGG), and ROC analysis to identify key MRGs. Competing endogenous RNA (ceRNA) networks were constructed, and dru</pubmed_abstract><journal>Functional &amp; integrative genomics</journal><pubmed_title>Combined transcriptomic and proteomic analyses reveal relevant myelin features in mice with ischemic stroke.</pubmed_title><pmcid>PMC11909235</pmcid><funding_grant_id>2022073</funding_grant_id><funding_grant_id>RCBS20210609104401012</funding_grant_id><funding_grant_id>JCYJ20220530165207017</funding_grant_id><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Shen M</pubmed_authors><pubmed_authors>Wang Q</pubmed_authors><pubmed_authors>He Y</pubmed_authors><pubmed_authors>Li D</pubmed_authors><pubmed_authors>Lyu H</pubmed_authors><pubmed_authors>Wang W</pubmed_authors><pubmed_authors>Qian Q</pubmed_authors></additional><is_claimable>false</is_claimable><name>Combined transcriptomic and proteomic analyses reveal relevant myelin features in mice with ischemic stroke.</name><description>Ischemic stroke (IS), a leading cause of global disability and mortality, is characterized by white matter damage and demyelination. Despite advances, the molecular mechanisms driving post-IS myelin pathology remain poorly understood, limiting therapeutic development. This study investigates key myelin-related genes (MRGs) and their regulatory networks to identify novel therapeutic targets. A transient middle cerebral artery occlusion (MCAO) model was established in C57BL/6 mice, with brain tissues collected at four timepoints (Sham0D, MCAO0D, MCAO7D, MCAO14D). Transcriptomic and proteomic sequencing were performed, followed by soft clustering (Mfuzz), functional enrichment (GO/KEGG), and ROC analysis to identify key MRGs. Competing endogenous RNA (ceRNA) networks were constructed, and dru</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2026-06-14T03:09:50.818Z</modification><creation>2025-04-20T00:09:53.536Z</creation></dates><accession>S-EPMC11909235</accession><cross_references><pubmed>40085348</pubmed><doi>10.1007/s10142-025-01573-6</doi></cross_references></HashMap>