| pubmed-article:18556568 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:18556568 | lifeskim:mentions | umls-concept:C0017296 | lld:lifeskim |
| pubmed-article:18556568 | lifeskim:mentions | umls-concept:C0032105 | lld:lifeskim |
| pubmed-article:18556568 | lifeskim:mentions | umls-concept:C0042974 | lld:lifeskim |
| pubmed-article:18556568 | lifeskim:mentions | umls-concept:C0205082 | lld:lifeskim |
| pubmed-article:18556568 | lifeskim:mentions | umls-concept:C1336938 | lld:lifeskim |
| pubmed-article:18556568 | lifeskim:mentions | umls-concept:C0087086 | lld:lifeskim |
| pubmed-article:18556568 | lifeskim:mentions | umls-concept:C1522492 | lld:lifeskim |
| pubmed-article:18556568 | lifeskim:mentions | umls-concept:C2349182 | lld:lifeskim |
| pubmed-article:18556568 | lifeskim:mentions | umls-concept:C0205410 | lld:lifeskim |
| pubmed-article:18556568 | lifeskim:mentions | umls-concept:C0719517 | lld:lifeskim |
| pubmed-article:18556568 | pubmed:issue | 9 | lld:pubmed |
| pubmed-article:18556568 | pubmed:dateCreated | 2008-8-21 | lld:pubmed |
| pubmed-article:18556568 | pubmed:abstractText | Gene therapy for severe von Willebrand disease (vWD) seems an interesting treatment alternative with long-term therapeutic potential. We investigated the feasibility of targeting the liver for ectopic expression of physiologically active von Willebrand factor (vWF). | lld:pubmed |
| pubmed-article:18556568 | pubmed:language | eng | lld:pubmed |
| pubmed-article:18556568 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18556568 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:18556568 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:18556568 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:18556568 | pubmed:issn | 1524-4636 | lld:pubmed |
| pubmed-article:18556568 | pubmed:author | pubmed-author:LentingPeter... | lld:pubmed |
| pubmed-article:18556568 | pubmed:author | pubmed-author:DeckmynHansH | lld:pubmed |
| pubmed-article:18556568 | pubmed:author | pubmed-author:VandenDriessc... | lld:pubmed |
| pubmed-article:18556568 | pubmed:author | pubmed-author:ChuahMarinee... | lld:pubmed |
| pubmed-article:18556568 | pubmed:author | pubmed-author:Vanhoorelbeke... | lld:pubmed |
| pubmed-article:18556568 | pubmed:author | pubmed-author:PareynIngeI | lld:pubmed |
| pubmed-article:18556568 | pubmed:author | pubmed-author:De... | lld:pubmed |
| pubmed-article:18556568 | pubmed:author | pubmed-author:VandeputteNel... | lld:pubmed |
| pubmed-article:18556568 | pubmed:author | pubmed-author:PetrusIngeI | lld:pubmed |
| pubmed-article:18556568 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:18556568 | pubmed:volume | 28 | lld:pubmed |
| pubmed-article:18556568 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:18556568 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:18556568 | pubmed:pagination | 1621-6 | lld:pubmed |
| pubmed-article:18556568 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
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| pubmed-article:18556568 | pubmed:year | 2008 | lld:pubmed |
| pubmed-article:18556568 | pubmed:articleTitle | Restoration of plasma von Willebrand factor deficiency is sufficient to correct thrombus formation after gene therapy for severe von Willebrand disease. | lld:pubmed |
| pubmed-article:18556568 | pubmed:affiliation | Laboratory for Thrombosis Research, K.U. Leuven Campus Kortrijk, Belgium. | lld:pubmed |
| pubmed-article:18556568 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:18556568 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:22371 | entrezgene:pubmed | pubmed-article:18556568 | lld:entrezgene |
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| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:18556568 | lld:pubmed |
