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Discussion Here, we identify STK38 as a novel kinase that phosphorylates RIPK1 at S309, thereby promoting RIPK1 activation, complex assembly, and cell death

3), and a comparable decrease was observed in the reciprocal binding of wild type ASXL1 EBM to the E653K mutant of BRD4 ET or the E651K mutant impaired in the contact with Q575 of ASXL1 EBM (Supplementary Fig

Dang DT, Chen F, Kohli M, Rago C, Cummins JM, Dang LH

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NDMA metabolism generates highly reactive methylating metabolites (e.g., O6-methylguanine, m6G), which bind to DNA, resulting in base mutations and an increased risk of bladder cancer (Wiench et al., 1992