Author: Alisha Chitrakar; Sneha Rath; Jesse Donovan; Kaitlin Demarest; Yize Li; Raghavendra Rao Sridhar; Susan R. Weiss; Sergei V. Kotenko; Ned S. Wingreen; Alexei Korennykh
Title: Realtime 2-5A kinetics suggests interferons ß and ? evade global arrest of translation by RNase L Document date: 2018_11_26
ID: mxdvdw9u_18
Snippet: A number of clinically important translation inhibitors, such as rapalogs and a new generation of anticancer drugs based on INK128, work by reprogramming protein synthesis through inhibition of mTOR 48 . Our work for the first time describes RNase L not as a general RNA decay machine, but as a translation-reprogramming receptor......
Document: A number of clinically important translation inhibitors, such as rapalogs and a new generation of anticancer drugs based on INK128, work by reprogramming protein synthesis through inhibition of mTOR 48 . Our work for the first time describes RNase L not as a general RNA decay machine, but as a translation-reprogramming receptor.
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