pubmed-article:10720694 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:10720694 | lifeskim:mentions | umls-concept:C0086418 | lld:lifeskim |
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pubmed-article:10720694 | lifeskim:mentions | umls-concept:C1335876 | lld:lifeskim |
pubmed-article:10720694 | lifeskim:mentions | umls-concept:C1367307 | lld:lifeskim |
pubmed-article:10720694 | lifeskim:mentions | umls-concept:C0005821 | lld:lifeskim |
pubmed-article:10720694 | lifeskim:mentions | umls-concept:C0022702 | lld:lifeskim |
pubmed-article:10720694 | lifeskim:mentions | umls-concept:C1704241 | lld:lifeskim |
pubmed-article:10720694 | lifeskim:mentions | umls-concept:C0205263 | lld:lifeskim |
pubmed-article:10720694 | lifeskim:mentions | umls-concept:C0079411 | lld:lifeskim |
pubmed-article:10720694 | pubmed:issue | 3 | lld:pubmed |
pubmed-article:10720694 | pubmed:dateCreated | 2000-4-24 | lld:pubmed |
pubmed-article:10720694 | pubmed:abstractText | Thrombopoietin (TPO) is the pivotal regulator of thrombocytopoiesis and megakaryocytopoiesis, and binding to its receptor c-Mpl leads to activation of at least two different signaling pathways: the Jak-Stat pathway and the Ras-MAPK pathway. Our aim was to elucidate which Stat-complexes are formed in TPO signal transduction in human blood platelets. | lld:pubmed |
pubmed-article:10720694 | pubmed:language | eng | lld:pubmed |
pubmed-article:10720694 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10720694 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:10720694 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:10720694 | pubmed:month | Mar | lld:pubmed |
pubmed-article:10720694 | pubmed:issn | 0301-472X | lld:pubmed |
pubmed-article:10720694 | pubmed:author | pubmed-author:SchulzeHH | lld:pubmed |
pubmed-article:10720694 | pubmed:author | pubmed-author:WelteKK | lld:pubmed |
pubmed-article:10720694 | pubmed:author | pubmed-author:BallmaierMM | lld:pubmed |
pubmed-article:10720694 | pubmed:author | pubmed-author:GermeshausenM... | lld:pubmed |
pubmed-article:10720694 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:10720694 | pubmed:volume | 28 | lld:pubmed |
pubmed-article:10720694 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:10720694 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:10720694 | pubmed:pagination | 294-304 | lld:pubmed |
pubmed-article:10720694 | pubmed:dateRevised | 2008-11-21 | lld:pubmed |
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pubmed-article:10720694 | pubmed:year | 2000 | lld:pubmed |
pubmed-article:10720694 | pubmed:articleTitle | Thrombopoietin induces the generation of distinct Stat1, Stat3, Stat5a and Stat5b homo- and heterodimeric complexes with different kinetics in human platelets. | lld:pubmed |
pubmed-article:10720694 | pubmed:affiliation | Department of Pediatric Hematology and Oncology, Medical School Hannover, Hannover, Germany. | lld:pubmed |
pubmed-article:10720694 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:10720694 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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