<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Verzi MP</submitter><funding>NIDDK NIH HHS</funding><funding>Crohn&amp;apos;s and Colitis Foundation</funding><funding>National Institutes of Health</funding><pagination>591-600</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2955860</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>135(2)</volume><pubmed_abstract>&lt;h4>Background &amp; aims&lt;/h4>The gastric mucosa provides a stringent epithelial barrier and produces acid and enzymes that initiate digestion. In this regenerating tissue, progenitors differentiate continually into 4 principal specialized cell types, yet underlying mechanisms of differentiation are poorly understood. We identified stomach-restricted expression of the forkhead transcription factor FOXQ1.&lt;h4>Methods&lt;/h4>We used a combination of genetic, histochemical, ultrastructural, and molecular analysis to study gastric cell lineages with respect to FOXQ1.&lt;h4>Results&lt;/h4>Within the developing and adult gastrointestinal tract, Foxq1 messenger RNA (mRNA) is restricted to the stomach and expressed predominantly in foveolar (pit) cells, the abundant mucin-producing cells that line the mucosal s</pubmed_abstract><journal>Gastroenterology</journal><pubmed_title>Transcription factor foxq1 controls mucin gene expression and granule content in mouse stomach surface mucous cells.</pubmed_title><pmcid>PMC2955860</pmcid><funding_grant_id>R01 DK061139</funding_grant_id><funding_grant_id>T32DK07477</funding_grant_id><funding_grant_id>R01DK61139</funding_grant_id><funding_grant_id>T32 DK007477</funding_grant_id><funding_grant_id>T32 DK007533</funding_grant_id><funding_grant_id>T32DK007533</funding_grant_id><pubmed_authors>Khan AH</pubmed_authors><pubmed_authors>Verzi MP</pubmed_authors><pubmed_authors>Shivdasani RA</pubmed_authors><pubmed_authors>Ito S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Transcription factor foxq1 controls mucin gene expression and granule content in mouse stomach surface mucous cells.</name><description>&lt;h4>Background &amp; aims&lt;/h4>The gastric mucosa provides a stringent epithelial barrier and produces acid and enzymes that initiate digestion. In this regenerating tissue, progenitors differentiate continually into 4 principal specialized cell types, yet underlying mechanisms of differentiation are poorly understood. We identified stomach-restricted expression of the forkhead transcription factor FOXQ1.&lt;h4>Methods&lt;/h4>We used a combination of genetic, histochemical, ultrastructural, and molecular analysis to study gastric cell lineages with respect to FOXQ1.&lt;h4>Results&lt;/h4>Within the developing and adult gastrointestinal tract, Foxq1 messenger RNA (mRNA) is restricted to the stomach and expressed predominantly in foveolar (pit) cells, the abundant mucin-producing cells that line the mucosal s</description><dates><release>2008-01-01T00:00:00Z</release><publication>2008 Aug</publication><modification>2026-05-04T04:02:29.885Z</modification><creation>2026-04-07T20:05:44.356Z</creation></dates><accession>S-EPMC2955860</accession><cross_references><pubmed>18558092</pubmed><doi>10.1053/j.gastro.2008.04.019</doi></cross_references></HashMap>