pubmed-article:8827718 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:8827718 | lifeskim:mentions | umls-concept:C1333198 | lld:lifeskim |
pubmed-article:8827718 | lifeskim:mentions | umls-concept:C0035696 | lld:lifeskim |
pubmed-article:8827718 | lifeskim:mentions | umls-concept:C1456820 | lld:lifeskim |
pubmed-article:8827718 | lifeskim:mentions | umls-concept:C0425152 | lld:lifeskim |
pubmed-article:8827718 | pubmed:issue | 4 | lld:pubmed |
pubmed-article:8827718 | pubmed:dateCreated | 1997-1-2 | lld:pubmed |
pubmed-article:8827718 | pubmed:abstractText | Tumor necrosis factor (TNF) production by macrophages plays an important role in the host response to infection. TNF-alpha gene expression in RAW 264.7 macrophages is predominantly regulated at the translational level. A key element in this regulation is an AU-rich (AUR) sequence located in the 3' untranslated region (UTR) of TNF mRNA. In unstimulated macrophages, the translation of TNF mRNA is inhibited via this AUR sequence. Upon stimulation with LPS, this repression is overcome and translation occurs. In this study, we attempted to identify cellular proteins that interact with the AUR sequence and thereby regulate TNF mRNA translation. | lld:pubmed |
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pubmed-article:8827718 | pubmed:language | eng | lld:pubmed |
pubmed-article:8827718 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8827718 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:8827718 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:8827718 | pubmed:month | Jul | lld:pubmed |
pubmed-article:8827718 | pubmed:issn | 1076-1551 | lld:pubmed |
pubmed-article:8827718 | pubmed:author | pubmed-author:SelsAA | lld:pubmed |
pubmed-article:8827718 | pubmed:author | pubmed-author:HueyDD | lld:pubmed |
pubmed-article:8827718 | pubmed:author | pubmed-author:HouzelDD | lld:pubmed |
pubmed-article:8827718 | pubmed:author | pubmed-author:MarchantAA | lld:pubmed |
pubmed-article:8827718 | pubmed:author | pubmed-author:KruytWW | lld:pubmed |
pubmed-article:8827718 | pubmed:author | pubmed-author:GueydanCC | lld:pubmed |
pubmed-article:8827718 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:8827718 | pubmed:volume | 2 | lld:pubmed |
pubmed-article:8827718 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:8827718 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:8827718 | pubmed:pagination | 479-88 | lld:pubmed |
pubmed-article:8827718 | pubmed:dateRevised | 2009-11-19 | lld:pubmed |
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pubmed-article:8827718 | pubmed:year | 1996 | lld:pubmed |
pubmed-article:8827718 | pubmed:articleTitle | Engagement of tumor necrosis factor mRNA by an endotoxin-inducible cytoplasmic protein. | lld:pubmed |
pubmed-article:8827718 | pubmed:affiliation | Département de Biologie Moléculaire, Université Libre de Bruxelles, Belgium. | lld:pubmed |
pubmed-article:8827718 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:8827718 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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