Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:14634647rdf:typepubmed:Citationlld:pubmed
pubmed-article:14634647lifeskim:mentionsumls-concept:C0238288lld:lifeskim
pubmed-article:14634647pubmed:issue4lld:pubmed
pubmed-article:14634647pubmed:dateCreated2003-12-3lld:pubmed
pubmed-article:14634647pubmed:databankReferencehttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:14634647pubmed:abstractTextThe autosomal dominant myopathy facioscapulohumeral muscular dystrophy (FSHD1, OMIM 158900) is caused by contraction of the D4Z4 repeat array on 4qter. We show that this contraction causes marked hypomethylation of the contracted D4Z4 allele in individuals with FSHD1. Individuals with phenotypic FSHD1, who are clinically identical to FSHD1 but have an unaltered D4Z4, also have hypomethylation of D4Z4. These results strongly suggest that hypomethylation of D4Z4 is a key event in the cascade of epigenetic events causing FSHD1.lld:pubmed
pubmed-article:14634647pubmed:languageenglld:pubmed
pubmed-article:14634647pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:14634647pubmed:citationSubsetIMlld:pubmed
pubmed-article:14634647pubmed:statusMEDLINElld:pubmed
pubmed-article:14634647pubmed:monthDeclld:pubmed
pubmed-article:14634647pubmed:issn1061-4036lld:pubmed
pubmed-article:14634647pubmed:authorpubmed-author:van der...lld:pubmed
pubmed-article:14634647pubmed:authorpubmed-author:FrantsRune...lld:pubmed
pubmed-article:14634647pubmed:authorpubmed-author:SandkuijlLode...lld:pubmed
pubmed-article:14634647pubmed:authorpubmed-author:van...lld:pubmed
pubmed-article:14634647pubmed:authorpubmed-author:PadbergGeorge...lld:pubmed
pubmed-article:14634647pubmed:authorpubmed-author:WinokurSara...lld:pubmed
pubmed-article:14634647pubmed:authorpubmed-author:van...lld:pubmed
pubmed-article:14634647pubmed:authorpubmed-author:EnthovenLeoLlld:pubmed
pubmed-article:14634647pubmed:authorpubmed-author:LemmersRichar...lld:pubmed
pubmed-article:14634647pubmed:authorpubmed-author:BakelsFloorFlld:pubmed
pubmed-article:14634647pubmed:issnTypePrintlld:pubmed
pubmed-article:14634647pubmed:volume35lld:pubmed
pubmed-article:14634647pubmed:ownerNLMlld:pubmed
pubmed-article:14634647pubmed:authorsCompleteYlld:pubmed
pubmed-article:14634647pubmed:pagination315-7lld:pubmed
pubmed-article:14634647pubmed:dateRevised2006-11-15lld:pubmed
pubmed-article:14634647pubmed:meshHeadingpubmed-meshheading:14634647...lld:pubmed
pubmed-article:14634647pubmed:meshHeadingpubmed-meshheading:14634647...lld:pubmed
pubmed-article:14634647pubmed:meshHeadingpubmed-meshheading:14634647...lld:pubmed
pubmed-article:14634647pubmed:meshHeadingpubmed-meshheading:14634647...lld:pubmed
pubmed-article:14634647pubmed:meshHeadingpubmed-meshheading:14634647...lld:pubmed
pubmed-article:14634647pubmed:meshHeadingpubmed-meshheading:14634647...lld:pubmed
pubmed-article:14634647pubmed:meshHeadingpubmed-meshheading:14634647...lld:pubmed
pubmed-article:14634647pubmed:meshHeadingpubmed-meshheading:14634647...lld:pubmed
pubmed-article:14634647pubmed:meshHeadingpubmed-meshheading:14634647...lld:pubmed
pubmed-article:14634647pubmed:meshHeadingpubmed-meshheading:14634647...lld:pubmed
pubmed-article:14634647pubmed:year2003lld:pubmed
pubmed-article:14634647pubmed:articleTitleHypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy.lld:pubmed
pubmed-article:14634647pubmed:affiliationDepartment of Human Genetics, Center for Human and Clinical Genetics, Leiden University Medical Center, P.O. Box 9502, 2300 RA Leiden, The Netherlands.lld:pubmed
pubmed-article:14634647pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:14634647pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
pubmed-article:14634647pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14634647lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14634647lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14634647lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14634647lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14634647lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14634647lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14634647lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14634647lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14634647lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14634647lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14634647lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14634647lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14634647lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14634647lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14634647lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14634647lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14634647lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14634647lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14634647lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14634647lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14634647lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14634647lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14634647lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14634647lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14634647lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14634647lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14634647lld:pubmed