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1 formed by N-acetoxy-2-acetylaminofluorene or benzo(a)pyrene diol epoxide.
2 porter gene damaged by exposure to 75 microM benzo(a)pyrene diol epoxide.
3 e prototype polycyclic aromatic hydrocarbon, benzo(a)pyrene diol epoxide [B(a)PDE], or B(a)PDE plus U
4 formation of Syrian hamster embryo cells and benzo(a)pyrene diol-epoxide [B(a)PDE]-induced activator
5 gene by a variety of carcinogens, including benzo(a)pyrene diol epoxide, benzo(g)chrysene diol epoxi
6 ed PCR (LMPCR) we have previously shown that benzo(a)pyrene diol epoxide (BPDE) adduct formation alon
7 ytes exposed in vitro to a model carcinogen, benzo(a)pyrene diol epoxide (BPDE) by 32P-postlabeling.
8 al aberrations induced in vitro by activated benzo(a)pyrene diol epoxide (BPDE) in lymphocyte culture
9 he levels of DNA adducts induced in vitro by benzo(a)pyrene diol epoxide (BPDE), a bioactivated form
12 lity of p53 codons 157, 248, 249, and 250 to benzo(a)pyrene-diol-epoxide (BPDE), an active metabolite
13 Higher tail moments of gamma-radiation and benzo(a)pyrene diol epoxide-induced comets were signific
16 four dose levels each of gamma-irradiation, benzo(a)pyrene diol epoxide, N-methyl-N-nitro-N-nitrosog
17 ximum tolerated concentrations of (+/-) anti-benzo(a)pyrene diol-epoxide, no induced mitochondrial mu
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