pubmed-article:18163533 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:18163533 | lifeskim:mentions | umls-concept:C0038250 | lld:lifeskim |
pubmed-article:18163533 | lifeskim:mentions | umls-concept:C0007620 | lld:lifeskim |
pubmed-article:18163533 | lifeskim:mentions | umls-concept:C0220825 | lld:lifeskim |
pubmed-article:18163533 | lifeskim:mentions | umls-concept:C1708481 | lld:lifeskim |
pubmed-article:18163533 | pubmed:issue | 6 | lld:pubmed |
pubmed-article:18163533 | pubmed:dateCreated | 2008-2-18 | lld:pubmed |
pubmed-article:18163533 | pubmed:abstractText | Therapeutic effects from injection of stem cells are often hampered by acute donor cell death as well as migration away from damaged areas. This is likely due to the fact that injected cells do not have the physical and biochemical cues for ordered engrafment. Here we evaluate 3 common biomatrices (Matrigel, Collagen I, Purmatrix) that has the potential of providing suitable scaffolds needed to enhance stem cell survival. The longitudinal fate of transplanted stem cells was monitored by reporter imaging techniques. | lld:pubmed |
pubmed-article:18163533 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18163533 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18163533 | pubmed:language | eng | lld:pubmed |
pubmed-article:18163533 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18163533 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:18163533 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18163533 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:18163533 | pubmed:issn | 1932-6254 | lld:pubmed |
pubmed-article:18163533 | pubmed:author | pubmed-author:WuJoseph CJC | lld:pubmed |
pubmed-article:18163533 | pubmed:author | pubmed-author:CaoFengF | lld:pubmed |
pubmed-article:18163533 | pubmed:author | pubmed-author:WangHaichangH | lld:pubmed |
pubmed-article:18163533 | pubmed:author | pubmed-author:ZarinsChristo... | lld:pubmed |
pubmed-article:18163533 | pubmed:author | pubmed-author:AbilezOscar... | lld:pubmed |
pubmed-article:18163533 | pubmed:author | pubmed-author:Sadrzadeh... | lld:pubmed |
pubmed-article:18163533 | pubmed:author | pubmed-author:BlundoJennife... | lld:pubmed |
pubmed-article:18163533 | pubmed:author | pubmed-author:PruittBethB | lld:pubmed |
pubmed-article:18163533 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:18163533 | pubmed:volume | 1 | lld:pubmed |
pubmed-article:18163533 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:18163533 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:18163533 | pubmed:pagination | 465-8 | lld:pubmed |
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pubmed-article:18163533 | pubmed:articleTitle | In vivo imaging and evaluation of different biomatrices for improvement of stem cell survival. | lld:pubmed |
pubmed-article:18163533 | pubmed:affiliation | Department of Radiology and Molecular Imaging Program at Stanford (MIPS), Stanford, CA, USA. | lld:pubmed |
pubmed-article:18163533 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:18163533 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
pubmed-article:18163533 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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