<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>16</volume><submitter>Qin C</submitter><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Spinal cord injury (SCI) often causes continuous neurological damage to clinical patients. Circular RNAs (circRNAs) are related to a lot of diseases, including SCI. We previously found five candidate circRNAs which were likely to regulate the secondary pathophysiological changes in rat model after traumatic SCI.&lt;h4>Methods&lt;/h4>In this study, we first selected and overexpressed target circRNA in rats. We then explored its functional roles using various functional assays in a rat model after SCI.&lt;h4>Results&lt;/h4>We found that rno-circRNA-013017-the selected target circRNA-reduced neuron apoptosis, preserved the survival and activity of motor neurons, and regulated apoptosis-related proteins at 3 days post-SCI using western blot, immunofluorescence and polymerase chain rea</pubmed_abstract><journal>Frontiers in neuroscience</journal><pagination>1065897</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9797719</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Inhibition by rno-circRNA-013017 of the apoptosis of motor neurons in anterior horn and descending axonal degeneration in rats after traumatic spinal cord injury.</pubmed_title><pmcid>PMC9797719</pmcid><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Talifu Z</pubmed_authors><pubmed_authors>Zhao LX</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Liu JY</pubmed_authors><pubmed_authors>Jing YL</pubmed_authors><pubmed_authors>Li JJ</pubmed_authors><pubmed_authors>Gao F</pubmed_authors><pubmed_authors>Xu PP</pubmed_authors><pubmed_authors>Qin C</pubmed_authors><pubmed_authors>Bai F</pubmed_authors><pubmed_authors>Yu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Inhibition by rno-circRNA-013017 of the apoptosis of motor neurons in anterior horn and descending axonal degeneration in rats after traumatic spinal cord injury.</name><description>&lt;h4>Introduction&lt;/h4>Spinal cord injury (SCI) often causes continuous neurological damage to clinical patients. Circular RNAs (circRNAs) are related to a lot of diseases, including SCI. We previously found five candidate circRNAs which were likely to regulate the secondary pathophysiological changes in rat model after traumatic SCI.&lt;h4>Methods&lt;/h4>In this study, we first selected and overexpressed target circRNA in rats. We then explored its functional roles using various functional assays in a rat model after SCI.&lt;h4>Results&lt;/h4>We found that rno-circRNA-013017-the selected target circRNA-reduced neuron apoptosis, preserved the survival and activity of motor neurons, and regulated apoptosis-related proteins at 3 days post-SCI using western blot, immunofluorescence and polymerase chain rea</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2026-05-29T20:13:51.921Z</modification><creation>2025-04-07T10:14:07.539Z</creation></dates><accession>S-EPMC9797719</accession><cross_references><pubmed>36590290</pubmed><doi>10.3389/fnins.2022.1065897</doi></cross_references></HashMap>