Regulating Fibrinolysis to Engineer Skeletal Muscle from the C2C12 Cell Line
Author:
Affiliation:
1. Functional Molecular Biology Lab, Division of Molecular Physiology, University of Dundee, Dundee, United Kingdom.
Publisher
Mary Ann Liebert Inc
Subject
Biomedical Engineering,Medicine (miscellaneous),Bioengineering
Link
https://www.liebertpub.com/doi/pdf/10.1089/ten.tec.2008.0286
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1. Cultured slow vs. fast skeletal muscle cells differ in physiology and responsiveness to stimulation
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4. Regulating Myoblast Phenotype Through Controlled Gel Stiffness and Degradation
5. C2C12 Co-culture on a fibroblast substratum enables sustained survival of contractile, highly differentiated myotubes with peripheral nuclei and adult fast myosin expression
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