| pubmed-article:21151598 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:21151598 | lifeskim:mentions | umls-concept:C0079259 | lld:lifeskim |
| pubmed-article:21151598 | lifeskim:mentions | umls-concept:C0040711 | lld:lifeskim |
| pubmed-article:21151598 | lifeskim:mentions | umls-concept:C0021920 | lld:lifeskim |
| pubmed-article:21151598 | lifeskim:mentions | umls-concept:C0035331 | lld:lifeskim |
| pubmed-article:21151598 | lifeskim:mentions | umls-concept:C0441655 | lld:lifeskim |
| pubmed-article:21151598 | lifeskim:mentions | umls-concept:C1521991 | lld:lifeskim |
| pubmed-article:21151598 | lifeskim:mentions | umls-concept:C0851285 | lld:lifeskim |
| pubmed-article:21151598 | lifeskim:mentions | umls-concept:C1880022 | lld:lifeskim |
| pubmed-article:21151598 | pubmed:dateCreated | 2010-12-14 | lld:pubmed |
| pubmed-article:21151598 | pubmed:abstractText | Mutations in the dystrophin (DMD) gene cause Duchenne or Becker muscular dystrophy (DMD/BMD). DMD contains a retina-specific promoter in intron 29. The short R-dystrophin transcript from this promoter has a retina-specific exon 1 (R1) joined to exon 30 of the DMD gene. It has been claimed that this is responsible for the ophthalmological problems observed in DMD/BMD. This research characterizes the structure of the 5'-untranslated region (5'-UTR) of human R-dystrophin. | lld:pubmed |
| pubmed-article:21151598 | pubmed:language | eng | lld:pubmed |
| pubmed-article:21151598 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21151598 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:21151598 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21151598 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21151598 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21151598 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:21151598 | pubmed:issn | 1090-0535 | lld:pubmed |
| pubmed-article:21151598 | pubmed:author | pubmed-author:MatsuoMasafum... | lld:pubmed |
| pubmed-article:21151598 | pubmed:author | pubmed-author:MoriTakeshiT | lld:pubmed |
| pubmed-article:21151598 | pubmed:author | pubmed-author:TakeshimaYasu... | lld:pubmed |
| pubmed-article:21151598 | pubmed:author | pubmed-author:NishimuraNori... | lld:pubmed |
| pubmed-article:21151598 | pubmed:author | pubmed-author:OtaMitsunoriM | lld:pubmed |
| pubmed-article:21151598 | pubmed:author | pubmed-author:YagiMarikoM | lld:pubmed |
| pubmed-article:21151598 | pubmed:author | pubmed-author:EnomotoMasahi... | lld:pubmed |
| pubmed-article:21151598 | pubmed:author | pubmed-author:OkizukaYoY | lld:pubmed |
| pubmed-article:21151598 | pubmed:author | pubmed-author:AwanoHiroyuki... | lld:pubmed |
| pubmed-article:21151598 | pubmed:author | pubmed-author:KubokawaIkuko... | lld:pubmed |
| pubmed-article:21151598 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:21151598 | pubmed:volume | 16 | lld:pubmed |
| pubmed-article:21151598 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:21151598 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:21151598 | pubmed:pagination | 2590-7 | lld:pubmed |
| pubmed-article:21151598 | pubmed:meshHeading | pubmed-meshheading:21151598... | lld:pubmed |
| pubmed-article:21151598 | pubmed:meshHeading | pubmed-meshheading:21151598... | lld:pubmed |
| pubmed-article:21151598 | pubmed:meshHeading | pubmed-meshheading:21151598... | lld:pubmed |
| pubmed-article:21151598 | pubmed:meshHeading | pubmed-meshheading:21151598... | lld:pubmed |
| pubmed-article:21151598 | pubmed:meshHeading | pubmed-meshheading:21151598... | lld:pubmed |
| pubmed-article:21151598 | pubmed:meshHeading | pubmed-meshheading:21151598... | lld:pubmed |
| pubmed-article:21151598 | pubmed:meshHeading | pubmed-meshheading:21151598... | lld:pubmed |
| pubmed-article:21151598 | pubmed:meshHeading | pubmed-meshheading:21151598... | lld:pubmed |
| pubmed-article:21151598 | pubmed:meshHeading | pubmed-meshheading:21151598... | lld:pubmed |
| pubmed-article:21151598 | pubmed:meshHeading | pubmed-meshheading:21151598... | lld:pubmed |
| pubmed-article:21151598 | pubmed:meshHeading | pubmed-meshheading:21151598... | lld:pubmed |
| pubmed-article:21151598 | pubmed:meshHeading | pubmed-meshheading:21151598... | lld:pubmed |
| pubmed-article:21151598 | pubmed:meshHeading | pubmed-meshheading:21151598... | lld:pubmed |
| pubmed-article:21151598 | pubmed:meshHeading | pubmed-meshheading:21151598... | lld:pubmed |
| pubmed-article:21151598 | pubmed:meshHeading | pubmed-meshheading:21151598... | lld:pubmed |
| pubmed-article:21151598 | pubmed:year | 2010 | lld:pubmed |
| pubmed-article:21151598 | pubmed:articleTitle | Molecular characterization of the 5'-UTR of retinal dystrophin reveals a cryptic intron that regulates translational activity. | lld:pubmed |
| pubmed-article:21151598 | pubmed:affiliation | Department of Pediatrics, Graduate School of Medicine, Kobe University, Kobe, Japan. | lld:pubmed |
| pubmed-article:21151598 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:21151598 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:1756 | entrezgene:pubmed | pubmed-article:21151598 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:21151598 | lld:entrezgene |
