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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
2
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pubmed:dateCreated |
2004-4-16
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pubmed:abstractText |
Organ cultures maintain cells within their native microstructural environment, and thus offer greater potential for studying tissue disease and remodeling than do monolayer cell cultures or pathological examinations of diseased tissue. To validate an in-vitro heart valve organ culture model, cell viability was examined within valve tissues over sustained culture periods.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0966-8519
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
13
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
290-6
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15086269-Animals,
pubmed-meshheading:15086269-Aortic Valve,
pubmed-meshheading:15086269-Cattle,
pubmed-meshheading:15086269-Cell Count,
pubmed-meshheading:15086269-Cell Survival,
pubmed-meshheading:15086269-Cells, Cultured,
pubmed-meshheading:15086269-Coloring Agents,
pubmed-meshheading:15086269-Dogs,
pubmed-meshheading:15086269-Endothelial Cells,
pubmed-meshheading:15086269-Eosine Yellowish-(YS),
pubmed-meshheading:15086269-Hematoxylin,
pubmed-meshheading:15086269-Humans,
pubmed-meshheading:15086269-Microscopy, Electron, Scanning,
pubmed-meshheading:15086269-Mitral Valve,
pubmed-meshheading:15086269-Models, Cardiovascular,
pubmed-meshheading:15086269-Organ Culture Techniques,
pubmed-meshheading:15086269-Swine,
pubmed-meshheading:15086269-Time,
pubmed-meshheading:15086269-Tricuspid Valve
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pubmed:year |
2004
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pubmed:articleTitle |
Cell viability mapping within long-term heart valve organ cultures.
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pubmed:affiliation |
Department of Biomedical Engineering, The University of Iowa, Iowa City, USA.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, U.S. Gov't, Non-P.H.S.,
Validation Studies
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