<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>16</volume><submitter>Schmitt LM</submitter><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Fragile X Syndrome (FXS) is a monogenic condition that leads to intellectual disability along with behavioral and learning difficulties. Among behavioral and learning difficulties, cognitive flexibility impairments are among the most commonly reported in FXS, which significantly impacts daily living. Despite the extensive use of the &lt;i>Fmr1&lt;/i> knockout (KO) mouse to understand molecular, synaptic and behavioral alterations related to FXS, there has been limited development of translational paradigms to understand cognitive flexibility that can be employed in both animal models and individuals with FXS to facilitate treatment development.&lt;h4>Methods&lt;/h4>To begin addressing this limitation, a parallel set of studies were carried out that investigated probabilistic rever</pubmed_abstract><journal>Frontiers in behavioral neuroscience</journal><pagination>1074682</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9849779</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Parallel learning and cognitive flexibility impairments between &lt;i>Fmr1&lt;/i> knockout mice and individuals with fragile X syndrome.</pubmed_title><pmcid>PMC9849779</pmcid><pubmed_authors>Schmitt LM</pubmed_authors><pubmed_authors>Duncan J</pubmed_authors><pubmed_authors>Erickson CA</pubmed_authors><pubmed_authors>Larson JR</pubmed_authors><pubmed_authors>Arzuaga AL</pubmed_authors><pubmed_authors>Ragozzino ME</pubmed_authors><pubmed_authors>Dapore A</pubmed_authors><pubmed_authors>Patel M</pubmed_authors><pubmed_authors>Sweeney JA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Parallel learning and cognitive flexibility impairments between &lt;i>Fmr1&lt;/i> knockout mice and individuals with fragile X syndrome.</name><description>&lt;h4>Introduction&lt;/h4>Fragile X Syndrome (FXS) is a monogenic condition that leads to intellectual disability along with behavioral and learning difficulties. Among behavioral and learning difficulties, cognitive flexibility impairments are among the most commonly reported in FXS, which significantly impacts daily living. Despite the extensive use of the &lt;i>Fmr1&lt;/i> knockout (KO) mouse to understand molecular, synaptic and behavioral alterations related to FXS, there has been limited development of translational paradigms to understand cognitive flexibility that can be employed in both animal models and individuals with FXS to facilitate treatment development.&lt;h4>Methods&lt;/h4>To begin addressing this limitation, a parallel set of studies were carried out that investigated probabilistic rever</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-18T15:45:14.473Z</modification><creation>2025-04-07T02:31:33.523Z</creation></dates><accession>S-EPMC9849779</accession><cross_references><pubmed>36688132</pubmed><doi>10.3389/fnbeh.2022.1074682</doi></cross_references></HashMap>