| pubmed-article:12526739 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:12526739 | lifeskim:mentions | umls-concept:C0072475 | lld:lifeskim |
| pubmed-article:12526739 | lifeskim:mentions | umls-concept:C1160340 | lld:lifeskim |
| pubmed-article:12526739 | lifeskim:mentions | umls-concept:C1704735 | lld:lifeskim |
| pubmed-article:12526739 | lifeskim:mentions | umls-concept:C1511545 | lld:lifeskim |
| pubmed-article:12526739 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:12526739 | pubmed:dateCreated | 2003-1-15 | lld:pubmed |
| pubmed-article:12526739 | pubmed:abstractText | Disabled-1 (Dab1) is an intracellular adaptor protein that regulates migrations of various classes of neurons during mammalian brain development. Dab1 function depends on its tyrosine phosphorylation, which is stimulated by Reelin, an extracellular signaling molecule. Reelin increases the stoichiometry of Dab1 phosphorylation and downregulates Dab1 protein levels. Reelin binds to various cell surface receptors, including two members of the low-density lipoprotein receptor family that also bind to Dab1. Mutations in Dab1, its phosphorylation sites, Reelin, or the Reelin receptors cause a common phenotype. However, the molecular mechanism whereby Reelin regulates Dab1 tyrosine phosphorylation is poorly understood. | lld:pubmed |
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| pubmed-article:12526739 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:12526739 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:12526739 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:12526739 | pubmed:month | Jan | lld:pubmed |
| pubmed-article:12526739 | pubmed:issn | 0960-9822 | lld:pubmed |
| pubmed-article:12526739 | pubmed:author | pubmed-author:CooperJonatha... | lld:pubmed |
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| pubmed-article:12526739 | pubmed:author | pubmed-author:BallifBryan... | lld:pubmed |
| pubmed-article:12526739 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:12526739 | pubmed:day | 8 | lld:pubmed |
| pubmed-article:12526739 | pubmed:volume | 13 | lld:pubmed |
| pubmed-article:12526739 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:12526739 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:12526739 | pubmed:pagination | 9-17 | lld:pubmed |
| pubmed-article:12526739 | pubmed:dateRevised | 2010-3-23 | lld:pubmed |
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| pubmed-article:12526739 | pubmed:year | 2003 | lld:pubmed |
| pubmed-article:12526739 | pubmed:articleTitle | Fyn tyrosine kinase is a critical regulator of disabled-1 during brain development. | lld:pubmed |
| pubmed-article:12526739 | pubmed:affiliation | Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue North, 98109, Seattle, WA, USA. | lld:pubmed |
| pubmed-article:12526739 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:12526739 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:12526739 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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