<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Shan X</submitter><funding>NIDDK NIH HHS</funding><funding>Michael Smith Foundation for Health Research</funding><funding>NIDDK</funding><pagination>101378</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11459652</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>18(5)</volume><pubmed_abstract>&lt;h4>Background &amp; aims&lt;/h4>Addition of sialic acids (sialylation) to glycoconjugates is a common capping step of glycosylation. Our study aims to determine the roles of the overall sialylation in intestinal mucosal homeostasis.&lt;h4>Methods&lt;/h4>Mice with constitutive deletion of intestinal epithelial sialylation (IEC Slc35a1&lt;sup>-/-&lt;/sup> mice) and mice with inducible deletion of sialylation in intestinal epithelium (TM-IEC Slc35a1&lt;sup>-/-&lt;/sup> mice) were generated, which were used to determine the roles of overall sialylation in intestinal mucosal homeostasis by ex vivo and mutiomics studies.&lt;h4>Results&lt;/h4>IEC Slc35a1&lt;sup>-/-&lt;/sup> mice developed mild spontaneous microbiota-dependent colitis. Additionally, 30% of IEC Slc35a1&lt;sup>-/-&lt;/sup> mice had spontaneous tumors in the rectum greater t</pubmed_abstract><journal>Cellular and molecular gastroenterology and hepatology</journal><pubmed_title>Ablation of Intestinal Epithelial Sialylation Predisposes to Acute and Chronic Intestinal Inflammation in Mice.</pubmed_title><pmcid>PMC11459652</pmcid><funding_grant_id>R01 DK085691</funding_grant_id><pubmed_authors>Nitin</pubmed_authors><pubmed_authors>Ghosh S</pubmed_authors><pubmed_authors>Shan X</pubmed_authors><pubmed_authors>Letef CL</pubmed_authors><pubmed_authors>Zandberg W</pubmed_authors><pubmed_authors>Kniffen D</pubmed_authors><pubmed_authors>Xia L</pubmed_authors><pubmed_authors>Bergstrom KS</pubmed_authors><pubmed_authors>Gao L</pubmed_authors><pubmed_authors>Rathore S</pubmed_authors><pubmed_authors>Shi H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ablation of Intestinal Epithelial Sialylation Predisposes to Acute and Chronic Intestinal Inflammation in Mice.</name><description>&lt;h4>Background &amp; aims&lt;/h4>Addition of sialic acids (sialylation) to glycoconjugates is a common capping step of glycosylation. Our study aims to determine the roles of the overall sialylation in intestinal mucosal homeostasis.&lt;h4>Methods&lt;/h4>Mice with constitutive deletion of intestinal epithelial sialylation (IEC Slc35a1&lt;sup>-/-&lt;/sup> mice) and mice with inducible deletion of sialylation in intestinal epithelium (TM-IEC Slc35a1&lt;sup>-/-&lt;/sup> mice) were generated, which were used to determine the roles of overall sialylation in intestinal mucosal homeostasis by ex vivo and mutiomics studies.&lt;h4>Results&lt;/h4>IEC Slc35a1&lt;sup>-/-&lt;/sup> mice developed mild spontaneous microbiota-dependent colitis. Additionally, 30% of IEC Slc35a1&lt;sup>-/-&lt;/sup> mice had spontaneous tumors in the rectum greater t</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024</publication><modification>2026-07-14T19:40:30.01Z</modification><creation>2025-04-19T19:25:51.317Z</creation></dates><accession>S-EPMC11459652</accession><cross_references><pubmed>38992465</pubmed><doi>10.1016/j.jcmgh.2024.101378</doi></cross_references></HashMap>