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These results suggest that the observed interactions in our structure exhibit functional consequences when mutated and that partial compensation of single R-domain mutants by other phosphorylation sites can maintain some activity

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The proliferation rate of CYP2E1-overexpressing HepG2 cells is slower than the non-CYP2E1 expressing control HepG2 cells along with increased oxidative stress [22]

Tryptophan metabolism, regulatory T cells, and inflammatory bowel disease: a mini review

[DOI] [PubMed] [Google Scholar] 166.Wu C.W., Liu H.C., Yu Y.L., Hung Y.T., Wei C.W., Yiang G.T