<HashMap><database>ENA</database><scores/><additional><omics_type>Genomics</omics_type><center_name>Second Military Medical University</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA242798</full_dataset_link><scientific_name>Rattus norvegicus</scientific_name><long_description>To further investigate the potential molecular basis of the protective effects of MASM on irradiation (6.5Gy) damage, gene expression analysis was conducted on rats liver tissues using microarrays. Pre-treatment with MASM prevented differential expression of 53% (766 genes) of 1445 genes differentially expressed in response to radiation. Pathway enrichment analysis indicated that these genes were mainly involved in a total of 21 pathways, such as metabolic pathways, pathways in cancer, and MAPK signaling pathway. Overall design: The rats were randomly assigned to one of the three following treatment groups (10-12 animals per group): normal control, radiation and MASM dose (30 mg/kg body weight/day) + radiation. MASM dissolved in double distilled water were administered intragastrically to the male animals for 3 consecutive days before irradiation. Radiation induced gene expression in rat liver was measured at 24 hours after 6.5 Gy exposure.</long_description><tag>xref:PubMed:27196884</tag><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Rattus norvegicus</name><description>Matrine derivative 1b(MASM) offers radioprotection and modulates acute lethal total-body irradiation-induced alterations of gene expression</description><dates><last_updated>2025-09-24</last_updated><first_public>2014-03-28</first_public></dates><accession>PRJNA242798</accession><cross_references><GEO>GSE56263</GEO><taxon>10116</taxon><PubMed>27196884</PubMed></cross_references></HashMap>