Abstract Protein arginine methyltransferase 5 (PRMT5) catalyzes mono-methylation and symmetric di-methylation on arginine residues and has emerged as a potential antitumor target with inhibitors being tested in clinical trials. However. it remains unknown how the efficacy of PRMT5 inhibitors is regulated. Here we report that autophagy blockage enhances cellular sensitivity to PRMT5 in... https://www.diegojavierfares.com/special-deal-Elektrosatz-Anhangevorrichtung-fur-BJ-2008-2012-E-Satz-ECS-flash-find/
Autophagy dictates sensitivity to PRMT5 inhibitor in breast cancer
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