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{ <http://www.tkuhn.ch/bel2nanopub/RABKJRv4P8Lfg3Cxp02siF1TxFd52smPOeYpn9_3BMvqU#_3> ?p ?o ?g. }
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C2-ceramide (C2), a cell-permeable analog, inhibited GSTA2 induction by oltipraz or tert-butylhydroquinone (t-BHQ) in H4IIE cells, whereas dihydro-C2-ceramide (dihydro-C2), an inactive analog, had no effect.
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