| pubmed-article:20506137 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:20506137 | lifeskim:mentions | umls-concept:C0019552 | lld:lifeskim |
| pubmed-article:20506137 | lifeskim:mentions | umls-concept:C0409959 | lld:lifeskim |
| pubmed-article:20506137 | lifeskim:mentions | umls-concept:C0042333 | lld:lifeskim |
| pubmed-article:20506137 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
| pubmed-article:20506137 | lifeskim:mentions | umls-concept:C0919432 | lld:lifeskim |
| pubmed-article:20506137 | pubmed:issue | 8 | lld:pubmed |
| pubmed-article:20506137 | pubmed:dateCreated | 2010-8-12 | lld:pubmed |
| pubmed-article:20506137 | pubmed:abstractText | Smad3 (or, MADH3) is a key intracellular messenger in the transforming growth factor beta signaling pathway. In mice, Smad3 deficiency accelerates growth plate chondrocyte maturation and leads to an osteoarthritis (OA)-like disease. We undertook this study to investigate the role of genetic variation in SMAD3 in the risk of large-joint OA in humans. | lld:pubmed |
| pubmed-article:20506137 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20506137 | pubmed:language | eng | lld:pubmed |
| pubmed-article:20506137 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20506137 | pubmed:citationSubset | AIM | lld:pubmed |
| pubmed-article:20506137 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20506137 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:20506137 | pubmed:month | Aug | lld:pubmed |
| pubmed-article:20506137 | pubmed:issn | 1529-0131 | lld:pubmed |
| pubmed-article:20506137 | pubmed:author | pubmed-author:HartDeborah... | lld:pubmed |
| pubmed-article:20506137 | pubmed:author | pubmed-author:SpectorTim... | lld:pubmed |
| pubmed-article:20506137 | pubmed:author | pubmed-author:CooperCyrusC | lld:pubmed |
| pubmed-article:20506137 | pubmed:author | pubmed-author:ValdesAna MAM | lld:pubmed |
| pubmed-article:20506137 | pubmed:author | pubmed-author:DohertyMichae... | lld:pubmed |
| pubmed-article:20506137 | pubmed:author | pubmed-author:ManginoMassim... | lld:pubmed |
| pubmed-article:20506137 | pubmed:author | pubmed-author:DennisonElain... | lld:pubmed |
| pubmed-article:20506137 | pubmed:author | pubmed-author:ArdenNigel... | lld:pubmed |
| pubmed-article:20506137 | pubmed:author | pubmed-author:LoriesRik JRJ | lld:pubmed |
| pubmed-article:20506137 | pubmed:author | pubmed-author:AliTaraT | lld:pubmed |
| pubmed-article:20506137 | pubmed:author | pubmed-author:TammAnnA | lld:pubmed |
| pubmed-article:20506137 | pubmed:author | pubmed-author:KisandKalleK | lld:pubmed |
| pubmed-article:20506137 | pubmed:author | pubmed-author:DohertySally... | lld:pubmed |
| pubmed-article:20506137 | pubmed:author | pubmed-author:WheelerMargar... | lld:pubmed |
| pubmed-article:20506137 | pubmed:author | pubmed-author:KernaIrinaI | lld:pubmed |
| pubmed-article:20506137 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:20506137 | pubmed:volume | 62 | lld:pubmed |
| pubmed-article:20506137 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:20506137 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:20506137 | pubmed:pagination | 2347-52 | lld:pubmed |
| pubmed-article:20506137 | pubmed:meshHeading | pubmed-meshheading:20506137... | lld:pubmed |
| pubmed-article:20506137 | pubmed:meshHeading | pubmed-meshheading:20506137... | lld:pubmed |
| pubmed-article:20506137 | pubmed:meshHeading | pubmed-meshheading:20506137... | lld:pubmed |
| pubmed-article:20506137 | pubmed:meshHeading | pubmed-meshheading:20506137... | lld:pubmed |
| pubmed-article:20506137 | pubmed:meshHeading | pubmed-meshheading:20506137... | lld:pubmed |
| pubmed-article:20506137 | pubmed:meshHeading | pubmed-meshheading:20506137... | lld:pubmed |
| pubmed-article:20506137 | pubmed:meshHeading | pubmed-meshheading:20506137... | lld:pubmed |
| pubmed-article:20506137 | pubmed:meshHeading | pubmed-meshheading:20506137... | lld:pubmed |
| pubmed-article:20506137 | pubmed:meshHeading | pubmed-meshheading:20506137... | lld:pubmed |
| pubmed-article:20506137 | pubmed:meshHeading | pubmed-meshheading:20506137... | lld:pubmed |
| pubmed-article:20506137 | pubmed:meshHeading | pubmed-meshheading:20506137... | lld:pubmed |
| pubmed-article:20506137 | pubmed:meshHeading | pubmed-meshheading:20506137... | lld:pubmed |
| pubmed-article:20506137 | pubmed:meshHeading | pubmed-meshheading:20506137... | lld:pubmed |
| pubmed-article:20506137 | pubmed:year | 2010 | lld:pubmed |
| pubmed-article:20506137 | pubmed:articleTitle | Genetic variation in the SMAD3 gene is associated with hip and knee osteoarthritis. | lld:pubmed |
| pubmed-article:20506137 | pubmed:affiliation | Department of Twin Research and Genetic Epidemiology, St. Thomas' Hospital Campus, King's College London, London SE1 7EH, UK. ana.valdes@kcl.ac.uk | lld:pubmed |
| pubmed-article:20506137 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:20506137 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:20506137 | pubmed:publicationType | Meta-Analysis | lld:pubmed |
| pubmed-article:20506137 | pubmed:publicationType | Twin Study | lld:pubmed |
| entrez-gene:4088 | entrezgene:pubmed | pubmed-article:20506137 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:20506137 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:20506137 | lld:entrezgene |
