| pubmed-article:11772882 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:11772882 | lifeskim:mentions | umls-concept:C0086418 | lld:lifeskim |
| pubmed-article:11772882 | lifeskim:mentions | umls-concept:C0001675 | lld:lifeskim |
| pubmed-article:11772882 | lifeskim:mentions | umls-concept:C0018787 | lld:lifeskim |
| pubmed-article:11772882 | lifeskim:mentions | umls-concept:C0225828 | lld:lifeskim |
| pubmed-article:11772882 | lifeskim:mentions | umls-concept:C1257975 | lld:lifeskim |
| pubmed-article:11772882 | lifeskim:mentions | umls-concept:C0031437 | lld:lifeskim |
| pubmed-article:11772882 | lifeskim:mentions | umls-concept:C0591833 | lld:lifeskim |
| pubmed-article:11772882 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:11772882 | pubmed:dateCreated | 2002-1-4 | lld:pubmed |
| pubmed-article:11772882 | pubmed:abstractText | Cellular cardiomyoplasty has been proposed as an alternative strategy for augmenting the function of diseased myocardium. We investigated the potential of human mesenchymal stem cells (hMSCs) from adult bone marrow to undergo myogenic differentiation once transplanted into the adult murine myocardium. | lld:pubmed |
| pubmed-article:11772882 | pubmed:language | eng | lld:pubmed |
| pubmed-article:11772882 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11772882 | pubmed:citationSubset | AIM | lld:pubmed |
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| pubmed-article:11772882 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:11772882 | pubmed:month | Jan | lld:pubmed |
| pubmed-article:11772882 | pubmed:issn | 1524-4539 | lld:pubmed |
| pubmed-article:11772882 | pubmed:author | pubmed-author:TomaCatalinC | lld:pubmed |
| pubmed-article:11772882 | pubmed:author | pubmed-author:PittengerMark... | lld:pubmed |
| pubmed-article:11772882 | pubmed:author | pubmed-author:CahillKevin... | lld:pubmed |
| pubmed-article:11772882 | pubmed:author | pubmed-author:ByrneBarry... | lld:pubmed |
| pubmed-article:11772882 | pubmed:author | pubmed-author:KesslerPaul... | lld:pubmed |
| pubmed-article:11772882 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:11772882 | pubmed:day | 1 | lld:pubmed |
| pubmed-article:11772882 | pubmed:volume | 105 | lld:pubmed |
| pubmed-article:11772882 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:11772882 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:11772882 | pubmed:pagination | 93-8 | lld:pubmed |
| pubmed-article:11772882 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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| pubmed-article:11772882 | pubmed:year | 2002 | lld:pubmed |
| pubmed-article:11772882 | pubmed:articleTitle | Human mesenchymal stem cells differentiate to a cardiomyocyte phenotype in the adult murine heart. | lld:pubmed |
| pubmed-article:11772882 | pubmed:affiliation | Department of Medicine, Division of Cardiology, Johns Hopkins School of Medicine, Baltimore, Md, USA. | lld:pubmed |
| pubmed-article:11772882 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:11772882 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
| pubmed-article:11772882 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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