PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 22697478-2 2012 This protective effect is blunted upon mutation of residues T105, E107 and E110 in human TNF into alanine or upon pre-incubation of the cytokine with the disaccharide N,N"-diacetylchitobiose. Disaccharides 154-166 tumor necrosis factor Homo sapiens 89-92 26046354-7 2015 A disaccharide fraction of enoxaparin inhibited the release of IL-4, IL-5, IL-13 and TNF-alpha by more than 57% while a tetrasaccharide fraction was found to inhibit the release of tested cytokines by more than 68%. Disaccharides 2-14 tumor necrosis factor Homo sapiens 85-94 11159885-6 2001 RESULTS: Specific disaccharides suppressed spontaneous and TNF-alpha-induced mediator secretion in a dose-dependent manner. Disaccharides 18-31 tumor necrosis factor Homo sapiens 59-68 22187328-13 2012 Compositional analysis of labeled disaccharides showed changes in the amount of 6-O-sulfated glucosamine residues after treatment with TNF-alpha, IL-1alpha and IL-1beta. Disaccharides 34-47 tumor necrosis factor Homo sapiens 135-144 17918767-1 2007 A cyclic disulfide heptadecapeptide (TIP17ox; 2) derived from the lectin-like 17-amino acid domain of human tumor necrosis factor-alpha [TNF-alpha (100-116)] was synthesised and demonstrated to bind specifically to N,N-diacetylchitobiose, a disaccharide present in many glycan structures of glycoproteins. Disaccharides 241-253 tumor necrosis factor Homo sapiens 108-135 17918767-1 2007 A cyclic disulfide heptadecapeptide (TIP17ox; 2) derived from the lectin-like 17-amino acid domain of human tumor necrosis factor-alpha [TNF-alpha (100-116)] was synthesised and demonstrated to bind specifically to N,N-diacetylchitobiose, a disaccharide present in many glycan structures of glycoproteins. Disaccharides 241-253 tumor necrosis factor Homo sapiens 137-146 15020655-1 2004 We previously reported that disaccharides (DS), generated by enzymatic degradation of heparin or heparan sulfate, inhibit T cell-mediated immune reactions in rodents and regulate cytokine [tumor necrosis factor alpha (TNF-alpha), interleukin (IL)-8, and IL-1beta] secretion by T cells, macrophages, or intestinal epithelial cells. Disaccharides 28-41 tumor necrosis factor Homo sapiens 189-216 15020655-1 2004 We previously reported that disaccharides (DS), generated by enzymatic degradation of heparin or heparan sulfate, inhibit T cell-mediated immune reactions in rodents and regulate cytokine [tumor necrosis factor alpha (TNF-alpha), interleukin (IL)-8, and IL-1beta] secretion by T cells, macrophages, or intestinal epithelial cells. Disaccharides 28-41 tumor necrosis factor Homo sapiens 218-227 15020655-1 2004 We previously reported that disaccharides (DS), generated by enzymatic degradation of heparin or heparan sulfate, inhibit T cell-mediated immune reactions in rodents and regulate cytokine [tumor necrosis factor alpha (TNF-alpha), interleukin (IL)-8, and IL-1beta] secretion by T cells, macrophages, or intestinal epithelial cells. Disaccharides 43-45 tumor necrosis factor Homo sapiens 189-216 15020655-1 2004 We previously reported that disaccharides (DS), generated by enzymatic degradation of heparin or heparan sulfate, inhibit T cell-mediated immune reactions in rodents and regulate cytokine [tumor necrosis factor alpha (TNF-alpha), interleukin (IL)-8, and IL-1beta] secretion by T cells, macrophages, or intestinal epithelial cells. Disaccharides 43-45 tumor necrosis factor Homo sapiens 218-227 12782582-4 2003 Here, we show that treatment of cultured human adenocarcinoma cells with micromolar concentrations of the peracetylated disaccharide, (Ac)(6)GlcNAcbeta1,3Galbeta-O-naphthalenemethanol (AcGnG-NM) reduces the expression of sLe(X) and diminishes binding in vitro to selectin-coated dishes, thrombin-activated platelets, and tumor necrosis factor alpha-activated endothelial cells. Disaccharides 120-132 tumor necrosis factor Homo sapiens 321-348 10651945-1 2000 We have found previously that disaccharides (DS) enzymatically generated from heparin or heparan sulphate can modulate tumour necrosis factor-alpha (TNF-alpha) secretion from immune cells in vitro and cell-mediated immune reactions in vivo. Disaccharides 30-43 tumor necrosis factor Homo sapiens 149-158 10651945-1 2000 We have found previously that disaccharides (DS) enzymatically generated from heparin or heparan sulphate can modulate tumour necrosis factor-alpha (TNF-alpha) secretion from immune cells in vitro and cell-mediated immune reactions in vivo. Disaccharides 45-47 tumor necrosis factor Homo sapiens 149-158 9352356-3 1997 We now report that the cleavage of heparin by the enzyme heparinase I generates sulfated disaccharide (DS) molecules that can inhibit the production of TNF-alpha. Disaccharides 89-101 tumor necrosis factor Homo sapiens 152-161 9352356-3 1997 We now report that the cleavage of heparin by the enzyme heparinase I generates sulfated disaccharide (DS) molecules that can inhibit the production of TNF-alpha. Disaccharides 103-105 tumor necrosis factor Homo sapiens 152-161