| pubmed-article:16761279 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:16761279 | lifeskim:mentions | umls-concept:C0035820 | lld:lifeskim |
| pubmed-article:16761279 | lifeskim:mentions | umls-concept:C0410189 | lld:lifeskim |
| pubmed-article:16761279 | lifeskim:mentions | umls-concept:C0295734 | lld:lifeskim |
| pubmed-article:16761279 | lifeskim:mentions | umls-concept:C0439064 | lld:lifeskim |
| pubmed-article:16761279 | pubmed:issue | 7 | lld:pubmed |
| pubmed-article:16761279 | pubmed:dateCreated | 2006-8-7 | lld:pubmed |
| pubmed-article:16761279 | pubmed:abstractText | X-linked Emery-Dreifuss muscular dystrophy (X-EDMD) is inherited through mutations in EMD, which encodes a nuclear membrane protein named emerin. Emerin is expressed in most cells, but EDMD strikes specific tissues. This review summarizes growing evidence that emerin has roles in both tissue-specific gene regulation and the mechanical integrity of the nucleus and discusses how these roles might impact EDMD. | lld:pubmed |
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| pubmed-article:16761279 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:16761279 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:16761279 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:16761279 | pubmed:month | Jul | lld:pubmed |
| pubmed-article:16761279 | pubmed:issn | 1552-4884 | lld:pubmed |
| pubmed-article:16761279 | pubmed:author | pubmed-author:WilsonKatheri... | lld:pubmed |
| pubmed-article:16761279 | pubmed:author | pubmed-author:HolaskaJames... | lld:pubmed |
| pubmed-article:16761279 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:16761279 | pubmed:volume | 288 | lld:pubmed |
| pubmed-article:16761279 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:16761279 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:16761279 | pubmed:pagination | 676-80 | lld:pubmed |
| pubmed-article:16761279 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
| pubmed-article:16761279 | pubmed:meshHeading | pubmed-meshheading:16761279... | lld:pubmed |
| pubmed-article:16761279 | pubmed:meshHeading | pubmed-meshheading:16761279... | lld:pubmed |
| pubmed-article:16761279 | pubmed:meshHeading | pubmed-meshheading:16761279... | lld:pubmed |
| pubmed-article:16761279 | pubmed:meshHeading | pubmed-meshheading:16761279... | lld:pubmed |
| pubmed-article:16761279 | pubmed:meshHeading | pubmed-meshheading:16761279... | lld:pubmed |
| pubmed-article:16761279 | pubmed:meshHeading | pubmed-meshheading:16761279... | lld:pubmed |
| pubmed-article:16761279 | pubmed:meshHeading | pubmed-meshheading:16761279... | lld:pubmed |
| pubmed-article:16761279 | pubmed:year | 2006 | lld:pubmed |
| pubmed-article:16761279 | pubmed:articleTitle | Multiple roles for emerin: implications for Emery-Dreifuss muscular dystrophy. | lld:pubmed |
| pubmed-article:16761279 | pubmed:affiliation | Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA. | lld:pubmed |
| pubmed-article:16761279 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:16761279 | pubmed:publicationType | Review | lld:pubmed |
| pubmed-article:16761279 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:16761279 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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