| pubmed-article:21464574 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:21464574 | lifeskim:mentions | umls-concept:C0086418 | lld:lifeskim |
| pubmed-article:21464574 | lifeskim:mentions | umls-concept:C1414669 | lld:lifeskim |
| pubmed-article:21464574 | lifeskim:mentions | umls-concept:C0024236 | lld:lifeskim |
| pubmed-article:21464574 | lifeskim:mentions | umls-concept:C0423848 | lld:lifeskim |
| pubmed-article:21464574 | lifeskim:mentions | umls-concept:C1522604 | lld:lifeskim |
| pubmed-article:21464574 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:21464574 | lifeskim:mentions | umls-concept:C0277785 | lld:lifeskim |
| pubmed-article:21464574 | lifeskim:mentions | umls-concept:C0039082 | lld:lifeskim |
| pubmed-article:21464574 | lifeskim:mentions | umls-concept:C0011546 | lld:lifeskim |
| pubmed-article:21464574 | lifeskim:mentions | umls-concept:C1524003 | lld:lifeskim |
| pubmed-article:21464574 | pubmed:issue | 5 | lld:pubmed |
| pubmed-article:21464574 | pubmed:dateCreated | 2011-8-23 | lld:pubmed |
| pubmed-article:21464574 | pubmed:abstractText | Human lymphoedema distichiasis syndrome (LDS) results from germline mutations in transcription factor FOXC2. In a mouse model, lack of lymphatic and venous valves is observed plus abnormal smooth muscle cell recruitment to initial lymphatics. We investigated the mechanism of lymphoedema in humans with FOXC2 mutations, specifically the effect of gravitational forces on dermal lymphatic function. | lld:pubmed |
| pubmed-article:21464574 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21464574 | pubmed:language | eng | lld:pubmed |
| pubmed-article:21464574 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21464574 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:21464574 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21464574 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21464574 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:21464574 | pubmed:issn | 1423-0135 | lld:pubmed |
| pubmed-article:21464574 | pubmed:author | pubmed-author:MäkinenTaijaT | lld:pubmed |
| pubmed-article:21464574 | pubmed:author | pubmed-author:BurnandKevin... | lld:pubmed |
| pubmed-article:21464574 | pubmed:author | pubmed-author:SmithAlbertoA | lld:pubmed |
| pubmed-article:21464574 | pubmed:author | pubmed-author:MortimerPeter... | lld:pubmed |
| pubmed-article:21464574 | pubmed:author | pubmed-author:JefferySteveS | lld:pubmed |
| pubmed-article:21464574 | pubmed:author | pubmed-author:MellorRussell... | lld:pubmed |
| pubmed-article:21464574 | pubmed:author | pubmed-author:StantonAnthon... | lld:pubmed |
| pubmed-article:21464574 | pubmed:author | pubmed-author:LevickJ... | lld:pubmed |
| pubmed-article:21464574 | pubmed:author | pubmed-author:TateNaomiN | lld:pubmed |
| pubmed-article:21464574 | pubmed:author | pubmed-author:HubertCharlot... | lld:pubmed |
| pubmed-article:21464574 | pubmed:copyrightInfo | Copyright © 2011 S. Karger AG, Basel. | lld:pubmed |
| pubmed-article:21464574 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:21464574 | pubmed:volume | 48 | lld:pubmed |
| pubmed-article:21464574 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:21464574 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:21464574 | pubmed:pagination | 397-407 | lld:pubmed |
| pubmed-article:21464574 | pubmed:meshHeading | pubmed-meshheading:21464574... | lld:pubmed |
| pubmed-article:21464574 | pubmed:meshHeading | pubmed-meshheading:21464574... | lld:pubmed |
| pubmed-article:21464574 | pubmed:meshHeading | pubmed-meshheading:21464574... | lld:pubmed |
| pubmed-article:21464574 | pubmed:meshHeading | pubmed-meshheading:21464574... | lld:pubmed |
| pubmed-article:21464574 | pubmed:meshHeading | pubmed-meshheading:21464574... | lld:pubmed |
| pubmed-article:21464574 | pubmed:meshHeading | pubmed-meshheading:21464574... | lld:pubmed |
| pubmed-article:21464574 | pubmed:meshHeading | pubmed-meshheading:21464574... | lld:pubmed |
| pubmed-article:21464574 | pubmed:meshHeading | pubmed-meshheading:21464574... | lld:pubmed |
| pubmed-article:21464574 | pubmed:meshHeading | pubmed-meshheading:21464574... | lld:pubmed |
| pubmed-article:21464574 | pubmed:meshHeading | pubmed-meshheading:21464574... | lld:pubmed |
| pubmed-article:21464574 | pubmed:meshHeading | pubmed-meshheading:21464574... | lld:pubmed |
| pubmed-article:21464574 | pubmed:meshHeading | pubmed-meshheading:21464574... | lld:pubmed |
| pubmed-article:21464574 | pubmed:meshHeading | pubmed-meshheading:21464574... | lld:pubmed |
| pubmed-article:21464574 | pubmed:meshHeading | pubmed-meshheading:21464574... | lld:pubmed |
| pubmed-article:21464574 | pubmed:meshHeading | pubmed-meshheading:21464574... | lld:pubmed |
| pubmed-article:21464574 | pubmed:meshHeading | pubmed-meshheading:21464574... | lld:pubmed |
| pubmed-article:21464574 | pubmed:meshHeading | pubmed-meshheading:21464574... | lld:pubmed |
| pubmed-article:21464574 | pubmed:year | 2011 | lld:pubmed |
| pubmed-article:21464574 | pubmed:articleTitle | Mutations in FOXC2 in humans (lymphoedema distichiasis syndrome) cause lymphatic dysfunction on dependency. | lld:pubmed |
| pubmed-article:21464574 | pubmed:affiliation | Cardiac and Vascular Sciences (Dermatology), St. George's, University of London, London, UK. | lld:pubmed |
| pubmed-article:21464574 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:21464574 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:2303 | entrezgene:pubmed | pubmed-article:21464574 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:21464574 | lld:entrezgene |
