pubmed-article:19460416 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:19460416 | lifeskim:mentions | umls-concept:C0040034 | lld:lifeskim |
pubmed-article:19460416 | lifeskim:mentions | umls-concept:C0031727 | lld:lifeskim |
pubmed-article:19460416 | lifeskim:mentions | umls-concept:C1274040 | lld:lifeskim |
pubmed-article:19460416 | lifeskim:mentions | umls-concept:C1425975 | lld:lifeskim |
pubmed-article:19460416 | lifeskim:mentions | umls-concept:C1515655 | lld:lifeskim |
pubmed-article:19460416 | pubmed:issue | 8 | lld:pubmed |
pubmed-article:19460416 | pubmed:dateCreated | 2009-7-17 | lld:pubmed |
pubmed-article:19460416 | pubmed:abstractText | A missense mutation in the microtubule-associated serine/threonine-like kinase gene (MASTL, FLJ14813) on human chromosome 10 was previously linked to a novel form of autosomal dominant inherited thrombocytopenia in a single pedigree. The mutation results in an amino acid change from glutamic acid at position 167 to aspartic acid and segregates perfectly with thrombocytopenic individuals within this extended family. The phenotype is characterized by mild thrombocytopenia with an average platelet count of 60,000 platelets per microliter of blood. We wanted to determine the expression and localization of MASTL, as well as its role in developing thrombocytes using an in vivo model system. | lld:pubmed |
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pubmed-article:19460416 | pubmed:language | eng | lld:pubmed |
pubmed-article:19460416 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19460416 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:19460416 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:19460416 | pubmed:month | Aug | lld:pubmed |
pubmed-article:19460416 | pubmed:issn | 1873-2399 | lld:pubmed |
pubmed-article:19460416 | pubmed:author | pubmed-author:GilliganDiana... | lld:pubmed |
pubmed-article:19460416 | pubmed:author | pubmed-author:DrachmanJonat... | lld:pubmed |
pubmed-article:19460416 | pubmed:author | pubmed-author:ShafizadehEbr... | lld:pubmed |
pubmed-article:19460416 | pubmed:author | pubmed-author:PawBarry HBH | lld:pubmed |
pubmed-article:19460416 | pubmed:author | pubmed-author:JohnsonH... | lld:pubmed |
pubmed-article:19460416 | pubmed:author | pubmed-author:GandhiManish... | lld:pubmed |
pubmed-article:19460416 | pubmed:author | pubmed-author:LangerNathani... | lld:pubmed |
pubmed-article:19460416 | pubmed:author | pubmed-author:PierceEric... | lld:pubmed |
pubmed-article:19460416 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:19460416 | pubmed:volume | 37 | lld:pubmed |
pubmed-article:19460416 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:19460416 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:19460416 | pubmed:pagination | 901-8 | lld:pubmed |
pubmed-article:19460416 | pubmed:dateRevised | 2011-9-26 | lld:pubmed |
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pubmed-article:19460416 | pubmed:year | 2009 | lld:pubmed |
pubmed-article:19460416 | pubmed:articleTitle | In vivo inactivation of MASTL kinase results in thrombocytopenia. | lld:pubmed |
pubmed-article:19460416 | pubmed:affiliation | Puget Sound Blood Center, Seattle, Wash. 98104-1256, USA. janj@psbc.org | lld:pubmed |
pubmed-article:19460416 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:19460416 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
pubmed-article:19460416 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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