http://purl.uniprot.org/citations/7679696 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
http://purl.uniprot.org/citations/7679696 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
http://purl.uniprot.org/citations/7679696 | http://www.w3.org/2000/01/rdf-schema#comment | "TNF-stimulated gene (TSG)-14 was originally identified as a TNF-inducible gene in a differentially screened cDNA library derived from TNF-treated normal human FS-4 fibroblasts. Analysis of the TSG-14 cDNA sequence revealed a major open reading frame encoding a protein of 381 amino acids, including a hydrophobic signal peptide sequence. The predicted protein shows 23 to 27% sequence homology to C-reactive protein and serum amyloid P-component, members of the pentaxin family of acute phase proteins. In addition, TSG-14 protein contains a sequence motif common among the pentaxin proteins. The ability of the TSG-14 cDNA to encode a protein of the correct molecular size was confirmed in a cell-free transcription/translation system. In vitro translation in the presence of microsomes confirmed that the protein has a cleavable signal peptide sequence, and that it is glycosylated. TSG-14 mRNA is rapidly elevated from almost undetectable levels in untreated FS-4 cells to high levels in cells treated with TNF or IL-1. A moderate increase in TSG-14 mRNA was observed in FS-4 cells treated with the glucocorticoid dexamethasone. Nuclear run-on analysis indicated that TNF induces the expression of the TSG-14 gene at the transcriptional level, and that de novo protein synthesis is not required for induction of TSG-14 mRNA. Expression of TSG-14 mRNA was also detected after exposure to TNF in vascular endothelial cells; however, little or not expression of TSG-14 message was observed in cell lines derived from malignant tumors. Our data strongly suggest that TSG-14 is a novel member of the pentaxin family of acute phase proteins."xsd:string |
http://purl.uniprot.org/citations/7679696 | http://purl.uniprot.org/core/author | "Lee T.H."xsd:string |
http://purl.uniprot.org/citations/7679696 | http://purl.uniprot.org/core/author | "Lee T.H."xsd:string |
http://purl.uniprot.org/citations/7679696 | http://purl.uniprot.org/core/author | "Lee G.W."xsd:string |
http://purl.uniprot.org/citations/7679696 | http://purl.uniprot.org/core/author | "Lee G.W."xsd:string |
http://purl.uniprot.org/citations/7679696 | http://purl.uniprot.org/core/author | "Vilcek J."xsd:string |
http://purl.uniprot.org/citations/7679696 | http://purl.uniprot.org/core/author | "Vilcek J."xsd:string |
http://purl.uniprot.org/citations/7679696 | http://purl.uniprot.org/core/date | "1993"xsd:gYear |
http://purl.uniprot.org/citations/7679696 | http://purl.uniprot.org/core/date | "1993"xsd:gYear |
http://purl.uniprot.org/citations/7679696 | http://purl.uniprot.org/core/name | "J. Immunol."xsd:string |
http://purl.uniprot.org/citations/7679696 | http://purl.uniprot.org/core/name | "J. Immunol."xsd:string |
http://purl.uniprot.org/citations/7679696 | http://purl.uniprot.org/core/pages | "1804-1812"xsd:string |
http://purl.uniprot.org/citations/7679696 | http://purl.uniprot.org/core/pages | "1804-1812"xsd:string |
http://purl.uniprot.org/citations/7679696 | http://purl.uniprot.org/core/title | "TSG-14, a tumor necrosis factor- and IL-1-inducible protein, is a novel member of the pentaxin family of acute phase proteins."xsd:string |
http://purl.uniprot.org/citations/7679696 | http://purl.uniprot.org/core/title | "TSG-14, a tumor necrosis factor- and IL-1-inducible protein, is a novel member of the pentaxin family of acute phase proteins."xsd:string |
http://purl.uniprot.org/citations/7679696 | http://purl.uniprot.org/core/volume | "150"xsd:string |
http://purl.uniprot.org/citations/7679696 | http://purl.uniprot.org/core/volume | "150"xsd:string |
http://purl.uniprot.org/citations/7679696 | http://www.w3.org/2004/02/skos/core#exactMatch | http://purl.uniprot.org/pubmed/7679696 |
http://purl.uniprot.org/citations/7679696 | http://www.w3.org/2004/02/skos/core#exactMatch | http://purl.uniprot.org/pubmed/7679696 |
http://purl.uniprot.org/citations/7679696 | http://xmlns.com/foaf/0.1/primaryTopicOf | https://pubmed.ncbi.nlm.nih.gov/7679696 |
http://purl.uniprot.org/citations/7679696 | http://xmlns.com/foaf/0.1/primaryTopicOf | https://pubmed.ncbi.nlm.nih.gov/7679696 |
http://purl.uniprot.org/uniprot/P26022 | http://purl.uniprot.org/core/citation | http://purl.uniprot.org/citations/7679696 |
http://purl.uniprot.org/embl-cds/AAA61234.1 | http://purl.uniprot.org/core/citation | http://purl.uniprot.org/citations/7679696 |