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Acknowledgements This work was supported in part by the 2023 AACR-AstraZeneca Breast Cancer Research Fellowship (J.H.), The Ludwig Cancer at Harvard Medical School (T.M.), and the NIH grants R35CA253027 (W.W.)
6I), indicating that STK38-mediated phosphorylation at S309 interferes with MK2 binding
Template biosynthesis of polypeptide chains on ribosomes usually does not produce a functional protein
These findings support the development of GSNO as a potential adjunct pharmacological agent or incorporated into NO releasing biomaterials to mitigate I/R injury
Redox Signal 14 (10), 20132054
