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pubmed-article:20581169 | lifeskim:mentions | umls-concept:C0935989 | lld:lifeskim |
pubmed-article:20581169 | lifeskim:mentions | umls-concept:C2911692 | lld:lifeskim |
pubmed-article:20581169 | lifeskim:mentions | umls-concept:C1706817 | lld:lifeskim |
pubmed-article:20581169 | lifeskim:mentions | umls-concept:C0443211 | lld:lifeskim |
pubmed-article:20581169 | lifeskim:mentions | umls-concept:C0205412 | lld:lifeskim |
pubmed-article:20581169 | pubmed:issue | 9 | lld:pubmed |
pubmed-article:20581169 | pubmed:dateCreated | 2010-11-2 | lld:pubmed |
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pubmed-article:20581169 | pubmed:abstractText | Pulmonary arterial hypertension (PAH) is a progressive condition with a poor prognosis. Platelet-derived growth factor receptor (PDGFR) signaling plays an important role in its pathobiology. | lld:pubmed |
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pubmed-article:20581169 | pubmed:language | eng | lld:pubmed |
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pubmed-article:20581169 | pubmed:citationSubset | AIM | lld:pubmed |
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pubmed-article:20581169 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:20581169 | pubmed:month | Nov | lld:pubmed |
pubmed-article:20581169 | pubmed:issn | 1535-4970 | lld:pubmed |
pubmed-article:20581169 | pubmed:author | pubmed-author:GrimmingerFri... | lld:pubmed |
pubmed-article:20581169 | pubmed:author | pubmed-author:HoeperMarius... | lld:pubmed |
pubmed-article:20581169 | pubmed:author | pubmed-author:OlschewskiHor... | lld:pubmed |
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pubmed-article:20581169 | pubmed:author | pubmed-author:GolponHeikoH | lld:pubmed |
pubmed-article:20581169 | pubmed:author | pubmed-author:GhofraniHosse... | lld:pubmed |
pubmed-article:20581169 | pubmed:author | pubmed-author:PeacockAndrew... | lld:pubmed |
pubmed-article:20581169 | pubmed:author | pubmed-author:ToshnerMarkM | lld:pubmed |
pubmed-article:20581169 | pubmed:author | pubmed-author:PascoeSteveS | lld:pubmed |
pubmed-article:20581169 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:20581169 | pubmed:day | 1 | lld:pubmed |
pubmed-article:20581169 | pubmed:volume | 182 | lld:pubmed |
pubmed-article:20581169 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:20581169 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:20581169 | pubmed:pagination | 1171-7 | lld:pubmed |
pubmed-article:20581169 | pubmed:dateRevised | 2011-7-28 | lld:pubmed |
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pubmed-article:20581169 | pubmed:year | 2010 | lld:pubmed |
pubmed-article:20581169 | pubmed:articleTitle | Imatinib in pulmonary arterial hypertension patients with inadequate response to established therapy. | lld:pubmed |
pubmed-article:20581169 | pubmed:affiliation | Pulmonary Hypertension Division, Medical Clinic II/V, University Hospital Giessen und Marburg GmbH, Giessen, Germany. ardeschir.ghofrani@innere.med.uni-giessen.de | lld:pubmed |
pubmed-article:20581169 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:20581169 | pubmed:publicationType | Randomized Controlled Trial | lld:pubmed |
pubmed-article:20581169 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
pubmed-article:20581169 | pubmed:publicationType | Clinical Trial, Phase II | lld:pubmed |
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