OGT Controls Mammalian Cell Viability by Regulating the Proteasome/mTOR/ Mitochondrial Axis

Investigators performed a genome-wide CRISPR–Cas9 screen in mESCs to identify candidates whose depletion rescued the block in cell proliferation induced by O-GlcNAc transferase (OGT) deficiency.
[Proceedings Of The National Academy Of Sciences Of The United States Of America]
AbstractPress Release
spot_img

Stay up-to-date with your field!

Subscribe for free weekly science newsletters.

Related News