<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Dalton GD</submitter><funding>Eunice Kennedy Shriver National Institute of Child Health and Human Development of the National Institutes of Health</funding><funding>Autism Speaks</funding><pagination>14</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11188533</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Autism Spectrum Disorder (ASD) is a group of neurodevelopmental disorders with higher incidence in males and is characterized by atypical verbal/nonverbal communication, restricted interests that can be accompanied by repetitive behavior, and disturbances in social behavior. This study investigated brain mechanisms that contribute to sociability deficits and sex differences in an ASD animal model.&lt;h4>Methods&lt;/h4>Sociability was measured in C58/J and C57BL/6J mice using the 3-chamber social choice test. Bulk RNA-Seq and snRNA-Seq identified transcriptional changes in C58/J and C57BL/6J amygdala within which DMRseq was used to measure differentially methylated regions in amygdala.&lt;h4>Results&lt;/h4>C58/J mice displayed divergent social strata in the 3-chamber test. Transcript</pubmed_abstract><journal>Behavioral and brain functions : BBF</journal><pubmed_title>Transcriptome analysis identifies an ASD-Like phenotype in oligodendrocytes and microglia from C58/J amygdala that is dependent on sex and sociability.</pubmed_title><pmcid>PMC11188533</pmcid><funding_grant_id>R01-HD-08800</funding_grant_id><funding_grant_id>10136</funding_grant_id><pubmed_authors>Siecinski SK</pubmed_authors><pubmed_authors>Nikolova VD</pubmed_authors><pubmed_authors>Hornburg KJ</pubmed_authors><pubmed_authors>Moy SS</pubmed_authors><pubmed_authors>Gregory SG</pubmed_authors><pubmed_authors>Cofer GP</pubmed_authors><pubmed_authors>Qi Y</pubmed_authors><pubmed_authors>Dalton GD</pubmed_authors><pubmed_authors>Johnson GA</pubmed_authors><pubmed_authors>Jiang YH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Transcriptome analysis identifies an ASD-Like phenotype in oligodendrocytes and microglia from C58/J amygdala that is dependent on sex and sociability.</name><description>&lt;h4>Background&lt;/h4>Autism Spectrum Disorder (ASD) is a group of neurodevelopmental disorders with higher incidence in males and is characterized by atypical verbal/nonverbal communication, restricted interests that can be accompanied by repetitive behavior, and disturbances in social behavior. This study investigated brain mechanisms that contribute to sociability deficits and sex differences in an ASD animal model.&lt;h4>Methods&lt;/h4>Sociability was measured in C58/J and C57BL/6J mice using the 3-chamber social choice test. Bulk RNA-Seq and snRNA-Seq identified transcriptional changes in C58/J and C57BL/6J amygdala within which DMRseq was used to measure differentially methylated regions in amygdala.&lt;h4>Results&lt;/h4>C58/J mice displayed divergent social strata in the 3-chamber test. Transcript</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jun</publication><modification>2025-04-04T12:48:21.232Z</modification><creation>2025-04-04T12:48:21.232Z</creation></dates><accession>S-EPMC11188533</accession><cross_references><pubmed>38898502</pubmed><doi>10.1186/s12993-024-00240-3</doi></cross_references></HashMap>