| pubmed-article:9733513 | rdf:type | pubmed:Citation | lld:pubmed |
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| pubmed-article:9733513 | lifeskim:mentions | umls-concept:C0752312 | lld:lifeskim |
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| pubmed-article:9733513 | lifeskim:mentions | umls-concept:C0086597 | lld:lifeskim |
| pubmed-article:9733513 | lifeskim:mentions | umls-concept:C1879547 | lld:lifeskim |
| pubmed-article:9733513 | pubmed:issue | 5383 | lld:pubmed |
| pubmed-article:9733513 | pubmed:dateCreated | 1998-10-7 | lld:pubmed |
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| pubmed-article:9733513 | pubmed:databankReference | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9733513 | pubmed:abstractText | The c-Jun NH2-terminal kinase (JNK) group of mitogen-activated protein (MAP) kinases is activated by the exposure of cells to multiple forms of stress. A putative scaffold protein was identified that interacts with multiple components of the JNK signaling pathway, including the mixed-lineage group of MAP kinase kinase kinases (MLK), the MAP kinase kinase MKK7, and the MAP kinase JNK. This scaffold protein selectively enhanced JNK activation by the MLK signaling pathway. These data establish that a mammalian scaffold protein can mediate activation of a MAP kinase signaling pathway. | lld:pubmed |
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| pubmed-article:9733513 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:9733513 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:9733513 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9733513 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:9733513 | pubmed:issn | 0036-8075 | lld:pubmed |
| pubmed-article:9733513 | pubmed:author | pubmed-author:YasudaJJ | lld:pubmed |
| pubmed-article:9733513 | pubmed:author | pubmed-author:TournierCC | lld:pubmed |
| pubmed-article:9733513 | pubmed:author | pubmed-author:CavanaghJJ | lld:pubmed |
| pubmed-article:9733513 | pubmed:author | pubmed-author:DavisR JRJ | lld:pubmed |
| pubmed-article:9733513 | pubmed:author | pubmed-author:WhitmarshA... | lld:pubmed |
| pubmed-article:9733513 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9733513 | pubmed:day | 11 | lld:pubmed |
| pubmed-article:9733513 | pubmed:volume | 281 | lld:pubmed |
| pubmed-article:9733513 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9733513 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9733513 | pubmed:pagination | 1671-4 | lld:pubmed |
| pubmed-article:9733513 | pubmed:dateRevised | 2011-11-2 | lld:pubmed |
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| pubmed-article:9733513 | pubmed:year | 1998 | lld:pubmed |
| pubmed-article:9733513 | pubmed:articleTitle | A mammalian scaffold complex that selectively mediates MAP kinase activation. | lld:pubmed |
| pubmed-article:9733513 | pubmed:affiliation | Program in Molecular Medicine, Department of Biochemistry and Molecular Biology, University of Massachusetts Medical School and Howard Hughes Medical Institute, Worcester, MA 01605, USA. | lld:pubmed |
| pubmed-article:9733513 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:9733513 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:9733513 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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