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1 ity to increased oxidative stress induced by tert-butylhydroperoxide.
2 ell killing, but in the presence of low-dose tert-butylhydroperoxide (25 microM), bafilomycin enhance
3 oroperoxybenzoic acid, peroxyacetic acid, or tert-butylhydroperoxide (apparent second-order rate cons
4 hese films were investigated with the aid of tert-butylhydroperoxide as a model reactant, and its red
5 easurement was performed in decane and using tert-butylhydroperoxide as substrate of the enzymatic re
8 lino oligonucleotides were more sensitive to tert-butylhydroperoxide but not tert-butylhydroquinone,
9 was unaffected by various concentrations of tert-butylhydroperoxide, but amounted to only approximat
14 iously, we showed that the oxidant chemical, tert-butylhydroperoxide (t-BuOOH), induces a mitochondri
15 We studied protective effects of NO against tert-butylhydroperoxide (t-BuOOH)-induced oxidations in
17 signed to examine the effects of the oxidant tert-butylhydroperoxide (TBH) on PPARgamma activation an
18 ng of hRPE cells, the effects of the oxidant tert-butylhydroperoxide (tBH) on the expression of FasL
20 Apoptosis was triggered with the oxidant tert-butylhydroperoxide (tBH), recombinant soluble Fas l
23 tubular cells (RPTCs) with the model oxidant tert-butylhydroperoxide (TBHP) causes mitochondrial inju
26 NB with TAML/peroxide (hydrogen peroxide and tert-butylhydroperoxide, TBHP) gave complete pollutant r
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