<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kobeissy FH</submitter><funding>BLRD VA</funding><funding>RRD VA</funding><funding>National Natural Science Foundation of China</funding><funding>NINDS NIH HHS</funding><funding>National Institutes of Health</funding><funding>U.S. Department of Veterans Affairs</funding><pagination>98</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5065984</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9</volume><pubmed_abstract>&lt;i>Emx1&lt;/i> has long been implicated in embryonic brain development. Previously we found that mice null of &lt;i>Emx1&lt;/i> gene had smaller dentate gyri and reduced neurogenesis, although the molecular mechanisms underlying this defect was not well understood. To decipher the role of &lt;i>Emx1&lt;/i> gene in neural regeneration and the timing of its involvement, we determine the frequency of neural stem cells (NSCs) in embryonic and adult forebrains of &lt;i>Emx1&lt;/i> wild type (WT) and knock out (KO) mice in the neurosphere assay. &lt;i>Emx1&lt;/i> gene deletion reduced the frequency and self-renewal capacity of NSCs of the embryonic brain but did not affect neuronal or glial differentiation. &lt;i>Emx1&lt;/i> KO NSCs also exhibited a reduced migratory capacity in response to serum or vascular endothelial growth </pubmed_abstract><journal>Frontiers in molecular neuroscience</journal><pubmed_title>Deciphering the Role of &lt;i>Emx1&lt;/i> in Neurogenesis: A Neuroproteomics Approach.</pubmed_title><pmcid>PMC5065984</pmcid><funding_grant_id>I01 BX003335</funding_grant_id><funding_grant_id>81403479</funding_grant_id><funding_grant_id>R21 NS051576</funding_grant_id><funding_grant_id>I01RX000655</funding_grant_id><funding_grant_id>I01 RX000655</funding_grant_id><funding_grant_id>I01BX003335</funding_grant_id><funding_grant_id>R01 NS071050</funding_grant_id><pubmed_authors>Kobeissy FH</pubmed_authors><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Fu S</pubmed_authors><pubmed_authors>Hansen K</pubmed_authors><pubmed_authors>Neumann M</pubmed_authors><pubmed_authors>Jin K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Deciphering the Role of &lt;i>Emx1&lt;/i> in Neurogenesis: A Neuroproteomics Approach.</name><description>&lt;i>Emx1&lt;/i> has long been implicated in embryonic brain development. Previously we found that mice null of &lt;i>Emx1&lt;/i> gene had smaller dentate gyri and reduced neurogenesis, although the molecular mechanisms underlying this defect was not well understood. To decipher the role of &lt;i>Emx1&lt;/i> gene in neural regeneration and the timing of its involvement, we determine the frequency of neural stem cells (NSCs) in embryonic and adult forebrains of &lt;i>Emx1&lt;/i> wild type (WT) and knock out (KO) mice in the neurosphere assay. &lt;i>Emx1&lt;/i> gene deletion reduced the frequency and self-renewal capacity of NSCs of the embryonic brain but did not affect neuronal or glial differentiation. &lt;i>Emx1&lt;/i> KO NSCs also exhibited a reduced migratory capacity in response to serum or vascular endothelial growth </description><dates><release>2016-01-01T00:00:00Z</release><publication>2016</publication><modification>2026-04-12T20:21:38.087Z</modification><creation>2019-03-27T02:26:48Z</creation></dates><accession>S-EPMC5065984</accession><cross_references><pubmed>27799894</pubmed><doi>10.3389/fnmol.2016.00098</doi></cross_references></HashMap>