Consistent with this, both C2C12-SKO cells treated with si-Tgf-β3 and dual si-Tgf-β(1+3) siRNAs showed a trend to recovery of the MYH4 protein.
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Nuclear corepressor SMRT acts as a strong regulator of both β-oxidation and suppressor of fibrosis in the differentiation process of mouse skeletal muscle cells.
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