pubmed-article:18947384 | rdf:type | pubmed:Citation | lld:pubmed |
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pubmed-article:18947384 | lifeskim:mentions | umls-concept:C0025914 | lld:lifeskim |
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pubmed-article:18947384 | lifeskim:mentions | umls-concept:C0262950 | lld:lifeskim |
pubmed-article:18947384 | lifeskim:mentions | umls-concept:C0162597 | lld:lifeskim |
pubmed-article:18947384 | lifeskim:mentions | umls-concept:C1171362 | lld:lifeskim |
pubmed-article:18947384 | lifeskim:mentions | umls-concept:C0017262 | lld:lifeskim |
pubmed-article:18947384 | lifeskim:mentions | umls-concept:C1515670 | lld:lifeskim |
pubmed-article:18947384 | lifeskim:mentions | umls-concept:C0281318 | lld:lifeskim |
pubmed-article:18947384 | lifeskim:mentions | umls-concept:C1710493 | lld:lifeskim |
pubmed-article:18947384 | lifeskim:mentions | umls-concept:C1705938 | lld:lifeskim |
pubmed-article:18947384 | lifeskim:mentions | umls-concept:C1527178 | lld:lifeskim |
pubmed-article:18947384 | pubmed:dateCreated | 2008-11-7 | lld:pubmed |
pubmed-article:18947384 | pubmed:abstractText | Bone marrow-derived stromal cells (BMSCs) are important for development, tissue cell replenishment, and wound healing in physiological and pathological conditions. BMSCs were found to preferably reach sites undergoing the process of cell proliferation, such as wound and tumor, suggesting that BMSCs may be used as a vehicle for gene therapy of tumor. | lld:pubmed |
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pubmed-article:18947384 | pubmed:language | eng | lld:pubmed |
pubmed-article:18947384 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18947384 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:18947384 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18947384 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18947384 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:18947384 | pubmed:issn | 1471-2407 | lld:pubmed |
pubmed-article:18947384 | pubmed:author | pubmed-author:WuYY | lld:pubmed |
pubmed-article:18947384 | pubmed:author | pubmed-author:ZhangRR | lld:pubmed |
pubmed-article:18947384 | pubmed:author | pubmed-author:WangRR | lld:pubmed |
pubmed-article:18947384 | pubmed:author | pubmed-author:ElyJ HJH | lld:pubmed |
pubmed-article:18947384 | pubmed:author | pubmed-author:LuoYY | lld:pubmed |
pubmed-article:18947384 | pubmed:author | pubmed-author:TianLL | lld:pubmed |
pubmed-article:18947384 | pubmed:author | pubmed-author:ZhaoXX | lld:pubmed |
pubmed-article:18947384 | pubmed:author | pubmed-author:SennB NBN | lld:pubmed |
pubmed-article:18947384 | pubmed:author | pubmed-author:GuiJ SJS | lld:pubmed |
pubmed-article:18947384 | pubmed:author | pubmed-author:RoyP SPS | lld:pubmed |
pubmed-article:18947384 | pubmed:author | pubmed-author:ZhangX-WXW | lld:pubmed |
pubmed-article:18947384 | pubmed:author | pubmed-author:YangJ-LJL | lld:pubmed |
pubmed-article:18947384 | pubmed:author | pubmed-author:ChenX-CXC | lld:pubmed |
pubmed-article:18947384 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:18947384 | pubmed:volume | 8 | lld:pubmed |
pubmed-article:18947384 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:18947384 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:18947384 | pubmed:pagination | 306 | lld:pubmed |
pubmed-article:18947384 | pubmed:dateRevised | 2009-11-19 | lld:pubmed |
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pubmed-article:18947384 | pubmed:year | 2008 | lld:pubmed |
pubmed-article:18947384 | pubmed:articleTitle | Anti-angiogenesis therapy based on the bone marrow-derived stromal cells genetically engineered to express sFlt-1 in mouse tumor model. | lld:pubmed |
pubmed-article:18947384 | pubmed:affiliation | State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu 610041 Sichuan, PR China. jlygym_w@163.com | lld:pubmed |
pubmed-article:18947384 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:18947384 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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