<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Baker JA</submitter><funding>NIAAA NIH HHS</funding><funding>National Institutes of Health</funding><pagination>139-151</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5270764</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>58</volume><pubmed_abstract>Alcohol abuse is a complex disorder, which is confounded by other factors, including stress. In the present study, we examined gene expression in the hippocampus of BXD recombinant inbred mice after exposure to ethanol (NOE), stress (RSS), and the combination of both (RSE). Mice were given an intraperitoneal (i.p.) injection of 1.8 g/kg ethanol or saline, and subsets of both groups were exposed to acute restraint stress for 15 min or controls. Gene expression in the hippocampus was examined using microarray analysis. Genes that were significantly (p &lt; 0.05, q &lt; 0.1) differentially expressed were further evaluated. Bioinformatic analyses were predominantly performed using tools available at GeneNetwork.org, and included gene ontology, presence of cis-regulation or polymorphisms, phenotype c</pubmed_abstract><journal>Alcohol (Fayetteville, N.Y.)</journal><pubmed_title>Analyses of differentially expressed genes after exposure to acute stress, acute ethanol, or a combination of both in mice.</pubmed_title><pmcid>PMC5270764</pmcid><funding_grant_id>U01 AA014425</funding_grant_id><funding_grant_id>R01 AA021951</funding_grant_id><funding_grant_id>R01AA021951</funding_grant_id><pubmed_authors>Cook MN</pubmed_authors><pubmed_authors>Lu L</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Yang M</pubmed_authors><pubmed_authors>Mulligan MK</pubmed_authors><pubmed_authors>Zhou D</pubmed_authors><pubmed_authors>Jones BC</pubmed_authors><pubmed_authors>Baker JA</pubmed_authors><pubmed_authors>Hamre KM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Analyses of differentially expressed genes after exposure to acute stress, acute ethanol, or a combination of both in mice.</name><description>Alcohol abuse is a complex disorder, which is confounded by other factors, including stress. In the present study, we examined gene expression in the hippocampus of BXD recombinant inbred mice after exposure to ethanol (NOE), stress (RSS), and the combination of both (RSE). Mice were given an intraperitoneal (i.p.) injection of 1.8 g/kg ethanol or saline, and subsets of both groups were exposed to acute restraint stress for 15 min or controls. Gene expression in the hippocampus was examined using microarray analysis. Genes that were significantly (p &lt; 0.05, q &lt; 0.1) differentially expressed were further evaluated. Bioinformatic analyses were predominantly performed using tools available at GeneNetwork.org, and included gene ontology, presence of cis-regulation or polymorphisms, phenotype c</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Feb</publication><modification>2026-04-14T19:08:07.916Z</modification><creation>2019-03-26T22:59:15Z</creation></dates><accession>S-EPMC5270764</accession><cross_references><pubmed>28027852</pubmed><doi>10.1016/j.alcohol.2016.08.008</doi></cross_references></HashMap>