<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Humphries LA</submitter><funding>NICHD NIH HHS</funding><funding>NIAID NIH HHS</funding><funding>NCI NIH HHS</funding><pagination>e45276</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3445470</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7(9)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The polarized reorganization of the T cell membrane and intracellular signaling molecules in response to T cell receptor (TCR) engagement has been implicated in the modulation of T cell development and effector responses. In siRNA-based studies Dlg1, a MAGUK scaffold protein and member of the Scribble polarity complex, has been shown to play a role in T cell polarity and TCR signal specificity, however the role of Dlg1 in T cell development and function in vivo remains unclear.&lt;h4>Methodology/principal findings&lt;/h4>Here we present the combined data from three independently-derived dlg1-knockout mouse models; two germline deficient knockouts and one conditional knockout. While defects were not observed in T cell development, TCR-induced early phospho-signaling, actin-medi</pubmed_abstract><journal>PloS one</journal><pubmed_title>Characterization of in vivo Dlg1 deletion on T cell development and function.</pubmed_title><pmcid>PMC3445470</pmcid><funding_grant_id>2-T32-AI-07323</funding_grant_id><funding_grant_id>P01 CA093615</funding_grant_id><funding_grant_id>R01-AI067253-10</funding_grant_id><funding_grant_id>R01 AI067253</funding_grant_id><funding_grant_id>T32-HD07516</funding_grant_id><funding_grant_id>T32 AI007323</funding_grant_id><funding_grant_id>T32 HD007516</funding_grant_id><pubmed_authors>Round JL</pubmed_authors><pubmed_authors>Russell SM</pubmed_authors><pubmed_authors>Sacirbegovic F</pubmed_authors><pubmed_authors>Silva O</pubmed_authors><pubmed_authors>Tomassian T</pubmed_authors><pubmed_authors>Miceli MC</pubmed_authors><pubmed_authors>McMahon KA</pubmed_authors><pubmed_authors>Burkhardt JK</pubmed_authors><pubmed_authors>Takamiya K</pubmed_authors><pubmed_authors>Humphries LA</pubmed_authors><pubmed_authors>Humbert PO</pubmed_authors><pubmed_authors>Shaffer MH</pubmed_authors><pubmed_authors>Huganir RL</pubmed_authors></additional><is_claimable>false</is_claimable><name>Characterization of in vivo Dlg1 deletion on T cell development and function.</name><description>&lt;h4>Background&lt;/h4>The polarized reorganization of the T cell membrane and intracellular signaling molecules in response to T cell receptor (TCR) engagement has been implicated in the modulation of T cell development and effector responses. In siRNA-based studies Dlg1, a MAGUK scaffold protein and member of the Scribble polarity complex, has been shown to play a role in T cell polarity and TCR signal specificity, however the role of Dlg1 in T cell development and function in vivo remains unclear.&lt;h4>Methodology/principal findings&lt;/h4>Here we present the combined data from three independently-derived dlg1-knockout mouse models; two germline deficient knockouts and one conditional knockout. While defects were not observed in T cell development, TCR-induced early phospho-signaling, actin-medi</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012</publication><modification>2026-04-20T03:17:20.733Z</modification><creation>2026-04-20T03:10:17.379Z</creation></dates><accession>S-EPMC3445470</accession><cross_references><pubmed>23028902</pubmed><doi>10.1371/journal.pone.0045276</doi></cross_references></HashMap>