Fig. 1From: Mitochondrial-to-nuclear communications through multiple routes regulate cardiomyocyte proliferationDisruption of mitochondrial protein translation and FAO metabolism promote cardiomyocyte proliferation through two distinct intermediates, UPRmt mediated by ATF4, and H3k4me3 modifications through αKG and Kdm5, respectively. Dox: DoxycyclineBack to article page