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Mutagenesis (2004) 19(4):32530
These results suggest auspicious biocompatibility and safety for intravenous delivery (Figure S7)
Low levels of mesenchymal markers such as vimentin and fibroblast-specific protein (FSP1) indicate minimal EndMT and reflect stable endothelial phenotype
A randomized controlled clinical trial of topical insulin-like growth factor-1 therapy for sudden deafness refractory to systemic corticosteroid treatment
