pubmed-article:18371418 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:18371418 | lifeskim:mentions | umls-concept:C0599856 | lld:lifeskim |
pubmed-article:18371418 | lifeskim:mentions | umls-concept:C0007589 | lld:lifeskim |
pubmed-article:18371418 | lifeskim:mentions | umls-concept:C2265845 | lld:lifeskim |
pubmed-article:18371418 | lifeskim:mentions | umls-concept:C0851285 | lld:lifeskim |
pubmed-article:18371418 | lifeskim:mentions | umls-concept:C1511938 | lld:lifeskim |
pubmed-article:18371418 | pubmed:issue | 1 | lld:pubmed |
pubmed-article:18371418 | pubmed:dateCreated | 2008-3-28 | lld:pubmed |
pubmed-article:18371418 | pubmed:abstractText | Muscle satellite cells have been shown to be a heterogeneous population of committed myogenic progenitors and noncommitted stem cells. This hierarchical composition of differentiating progenitors and self-renewable stem cells assures the extraordinary regenerative capacity of skeletal muscles. Recent studies have revealed a role for asymmetric division in satellite cell maintenance and offer novel insights into the regulation of satellite cell function by the niche. A thorough understanding of the molecular regulation and cell fate determination of satellite cells and other potential stem cells resident in muscle is essential for successful stem cell-based therapies to treat muscular diseases. | lld:pubmed |
pubmed-article:18371418 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18371418 | pubmed:language | eng | lld:pubmed |
pubmed-article:18371418 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18371418 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:18371418 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:18371418 | pubmed:month | Jan | lld:pubmed |
pubmed-article:18371418 | pubmed:issn | 1875-9777 | lld:pubmed |
pubmed-article:18371418 | pubmed:author | pubmed-author:RudnickiMicha... | lld:pubmed |
pubmed-article:18371418 | pubmed:author | pubmed-author:KuangShihuanS | lld:pubmed |
pubmed-article:18371418 | pubmed:author | pubmed-author:GillespieMark... | lld:pubmed |
pubmed-article:18371418 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:18371418 | pubmed:day | 10 | lld:pubmed |
pubmed-article:18371418 | pubmed:volume | 2 | lld:pubmed |
pubmed-article:18371418 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:18371418 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:18371418 | pubmed:pagination | 22-31 | lld:pubmed |
pubmed-article:18371418 | pubmed:dateRevised | 2009-5-20 | lld:pubmed |
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pubmed-article:18371418 | pubmed:year | 2008 | lld:pubmed |
pubmed-article:18371418 | pubmed:articleTitle | Niche regulation of muscle satellite cell self-renewal and differentiation. | lld:pubmed |
pubmed-article:18371418 | pubmed:affiliation | The Sprott Center for Stem Cell Research, Regenerative Medicine Program, Ottawa Health Research Institute, 501 Smyth Road, Ottawa, ON K1H 8L6, Canada. | lld:pubmed |
pubmed-article:18371418 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:18371418 | pubmed:publicationType | Review | lld:pubmed |
pubmed-article:18371418 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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