The SIS/LXW7-DS-SILY/EPCs group showed a trend toward more rapid re-epithelialization as compared to the SIS/EPCs group, as determined by shorter residual wound length ( Fig. 8 C–D panel b).
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Bioactive extracellular matrix scaffolds engineered with proangiogenic proteoglycan mimetics and loaded with endothelial progenitor cells promote neovascularization and diabetic wound healing.
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