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- W2109708124 endingPage "1134" @default.
- W2109708124 startingPage "1128" @default.
- W2109708124 abstract "Although vascular bypass grafting remains the mainstay for revascularization for ischemic heart disease and peripheral vascular disease, many patients do not have healthy vessels suitable for harvest. Thus, prosthetic grafts made of synthetic polymers were developed, but their use is limited to high-flow/low-resistance conditions because of poor elasticity, low compliance, and thrombogenicity of their synthetic surfaces. To fill this need, several laboratories have produced in vivo or in vitro tissue-engineered blood vessels using molds or prosthetic or biodegradable scaffolds, but each artificial graft has significant problems. Recently, conduits have been grown in the peritoneal cavity of the same animals in which they will be grafted, ensuring no rejection, in the short time of 2 to 3 weeks. Remodeling occurs after grafting such that the tissue is almost indistinguishable from native vessels. This conduit is derived from cells of bone marrow origin, opening new possibilities in vascular modeling and remodeling." @default.
- W2109708124 created "2016-06-24" @default.
- W2109708124 creator A5016010497 @default.
- W2109708124 creator A5028525838 @default.
- W2109708124 creator A5033433137 @default.
- W2109708124 creator A5058819034 @default.
- W2109708124 date "2005-06-01" @default.
- W2109708124 modified "2023-10-14" @default.
- W2109708124 title "Tissue-Engineered Blood Vessels" @default.
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