IndraLab
Statements
sparser
"In particular, one of these mechanisms involves a dynamic regulation of the interaction between MEF2C and the transcriptional co-repressors class IIa histone deacetylases (HDACs) such as HDAC4 and −5: in proliferating myoblasts MEF2C interacts with HDACs and its activity is repressed, and myogenic signals disrupt this interaction, thereby alleviating the repression of MEF2C activity xref xref xref xref xref ."