TGF-β signaling alters H4K20me3 status via miR-29 and contributes to cellular senescence and cardiac aging. [electronic resource]
- Nature communications 07 2018
- 2560 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
2041-1723
10.1038/s41467-018-04994-z doi
Aging--genetics Animals Cellular Senescence--genetics DNA Methylation--genetics Embryo, Mammalian Epigenesis, Genetic Female Fibroblasts HEK293 Cells Heart--physiology Heterocyclic Compounds, 4 or More Rings--pharmacology Histone-Lysine N-Methyltransferase--antagonists & inhibitors Histones--metabolism Human Umbilical Vein Endothelial Cells Humans Male Mice Mice, Inbred C57BL MicroRNAs--metabolism Myocytes, Cardiac--physiology Oxidative Stress--physiology Primary Cell Culture Signal Transduction--genetics Transforming Growth Factor beta--metabolism