<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yang J</submitter><funding>NIGMS NIH HHS</funding><pagination>12</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC1533857</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Leukocyte recruitment across blood vessels is fundamental to immune surveillance and inflammation. Lymphocyte homing to peripheral lymph nodes is mediated by the adhesion molecule, L-selectin, which binds to sulfated carbohydrate ligands on high endothelial venules (HEV). These glycoprotein ligands are collectively known as peripheral node addressin (PNAd), as defined by the function-blocking monoclonal antibody known as MECA-79. The sulfation of these ligands depends on the action of two HEV-expressed N-acetylglucosamine 6-O-sulfotransferases: GlcNAc6ST-2 and to a lesser degree GlcNAc6ST-1. Induction of PNAd has also been shown to occur in a number of human inflammatory diseases including rheumatoid arthritis (RA).&lt;h4>Results&lt;/h4>In order to identify an animal model sui</pubmed_abstract><journal>BMC immunology</journal><pubmed_title>Induction of PNAd and N-acetylglucosamine 6-O-sulfotransferases 1 and 2 in mouse collagen-induced arthritis.</pubmed_title><pmcid>PMC1533857</pmcid><funding_grant_id>R01 GM057411</funding_grant_id><funding_grant_id>R37 GM023547</funding_grant_id><funding_grant_id>R37-GM23547</funding_grant_id><funding_grant_id>R01-GM57411</funding_grant_id><pubmed_authors>Rosen SD</pubmed_authors><pubmed_authors>Yang J</pubmed_authors><pubmed_authors>Hemmerich S</pubmed_authors><pubmed_authors>Bendele P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Induction of PNAd and N-acetylglucosamine 6-O-sulfotransferases 1 and 2 in mouse collagen-induced arthritis.</name><description>&lt;h4>Background&lt;/h4>Leukocyte recruitment across blood vessels is fundamental to immune surveillance and inflammation. Lymphocyte homing to peripheral lymph nodes is mediated by the adhesion molecule, L-selectin, which binds to sulfated carbohydrate ligands on high endothelial venules (HEV). These glycoprotein ligands are collectively known as peripheral node addressin (PNAd), as defined by the function-blocking monoclonal antibody known as MECA-79. The sulfation of these ligands depends on the action of two HEV-expressed N-acetylglucosamine 6-O-sulfotransferases: GlcNAc6ST-2 and to a lesser degree GlcNAc6ST-1. Induction of PNAd has also been shown to occur in a number of human inflammatory diseases including rheumatoid arthritis (RA).&lt;h4>Results&lt;/h4>In order to identify an animal model sui</description><dates><release>2006-01-01T00:00:00Z</release><publication>2006 Jun</publication><modification>2025-06-01T02:49:06.888Z</modification><creation>2019-06-05T18:49:07Z</creation></dates><accession>S-EPMC1533857</accession><cross_references><pubmed>16772045</pubmed><doi>10.1186/1471-2172-7-12</doi></cross_references></HashMap>