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Biochemistry|April 5, 2000

Factors determining mutagenic potential for individual cis and trans opened benzo[c]phenanthrene diol epoxide-deoxyadenosine adductsI Pontén, J M Sayer, A S Pilcher, et al.

Chemico-Biological Interactions|October 21, 1999

The proximate carcinogen trans-3,4-dihydroxy-3,4-dihydro-dibenz[c,h]acridine is oxidized stereoselectively and regioselectively by cytochrome 1A1, epoxide hydrolase and hepatic microsomes from 3-methylcholanthrene-treated ratsJ D Adams, J M Sayer, A Chadha, et al.

Chemical Research in Toxicology|September 18, 2001

Patterns of resistance to exonuclease digestion of oligonucleotides containing polycyclic aromatic hydrocarbon diol epoxide adducts at N6 of deoxyadenosineP Ilankumaran, L K Pannell, P Gebreselassie, et al.

Carcinogenesis|October 1, 1986

Disposition of the naturally occurring antimutagenic plant phenol, ellagic acid, and its synthetic derivatives, 3-O-decylellagic acid and 3,3'-di-O-methylellagic acid in miceR C Smart, M T Huang, R L Chang, et al.

The Journal of Biological Chemistry|August 25, 1985

Differential stereoselectivity of cytochromes P-450b and P-450c in the formation of naphthalene and anthracene 1,2-oxides. The role of epoxide hydrolase in determining the enantiomer composition of the 1,2-dihydrodiols formedP J van Bladeren, J M Sayer, D E Ryan, et al.

Biochemistry|June 24, 1998

Sequence context profoundly influences the mutagenic potency of trans-opened benzo[a]pyrene 7,8-diol 9,10-epoxide-purine nucleoside adducts in site-specific mutation studiesJ E Page, B Zajc, T Oh-hara, et al.

Chemical Research in Toxicology|April 1, 1995

Multiple fluorescence lifetimes for oligonucleotides containing single, site-specific modifications at guanine and adenine corresponding to trans addition of exocyclic amino groups to (+)-(7R,8S,9S,10R)- and (+)-(7S,8R,9R,10S) -7,8-dihydroxy-9,10-epoxy-7,8,9,10-tetrahydrobenzo[a]pyreneP R LeBreton, C R Huang, H Fernando, et al.

Biochemistry|January 31, 1995

NMR solution structure of a nonanucleotide duplex with a dG mismatch opposite a 10R adduct derived from trans addition of a deoxyadenosine N6-amino group to (-)-(7S,8R,9R,10S)-7,8-dihydroxy-9,10-epoxy-7,8,9,10- tetrahydrobenzo[a]pyreneE J Schurter, H J Yeh, J M Sayer, et al.

Proceedings of the National Academy of Sciences of the United States of America|September 1, 1982

Mechanism of the inhibition of mutagenicity of a benzo[a]pyrene 7,8-diol 9,10-epoxide by riboflavin 5'-phosphateA W Wood, J M Sayer, H L Newmark, et al.

Molecular Pharmacology|July 1, 1983

Regioselectivity and stereoselectivity in the metabolism of trans-1,2-dihydroxy-1,2-dihydrobenz[a]anthracene by rat liver microsomesK P Vyas, P J van Bladeren, D R Thakker, et al.

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Showing results (21-30 of 57) with videos related to

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Biochemistry|April 5, 2000

Factors determining mutagenic potential for individual cis and trans opened benzo[c]phenanthrene diol epoxide-deoxyadenosine adductsI Pontén, J M Sayer, A S Pilcher, et al.

Chemico-Biological Interactions|October 21, 1999

The proximate carcinogen trans-3,4-dihydroxy-3,4-dihydro-dibenz[c,h]acridine is oxidized stereoselectively and regioselectively by cytochrome 1A1, epoxide hydrolase and hepatic microsomes from 3-methylcholanthrene-treated ratsJ D Adams, J M Sayer, A Chadha, et al.

Chemical Research in Toxicology|September 18, 2001

Patterns of resistance to exonuclease digestion of oligonucleotides containing polycyclic aromatic hydrocarbon diol epoxide adducts at N6 of deoxyadenosineP Ilankumaran, L K Pannell, P Gebreselassie, et al.

Carcinogenesis|October 1, 1986

Disposition of the naturally occurring antimutagenic plant phenol, ellagic acid, and its synthetic derivatives, 3-O-decylellagic acid and 3,3'-di-O-methylellagic acid in miceR C Smart, M T Huang, R L Chang, et al.

The Journal of Biological Chemistry|August 25, 1985

Differential stereoselectivity of cytochromes P-450b and P-450c in the formation of naphthalene and anthracene 1,2-oxides. The role of epoxide hydrolase in determining the enantiomer composition of the 1,2-dihydrodiols formedP J van Bladeren, J M Sayer, D E Ryan, et al.

Biochemistry|June 24, 1998

Sequence context profoundly influences the mutagenic potency of trans-opened benzo[a]pyrene 7,8-diol 9,10-epoxide-purine nucleoside adducts in site-specific mutation studiesJ E Page, B Zajc, T Oh-hara, et al.

Chemical Research in Toxicology|April 1, 1995

Multiple fluorescence lifetimes for oligonucleotides containing single, site-specific modifications at guanine and adenine corresponding to trans addition of exocyclic amino groups to (+)-(7R,8S,9S,10R)- and (+)-(7S,8R,9R,10S) -7,8-dihydroxy-9,10-epoxy-7,8,9,10-tetrahydrobenzo[a]pyreneP R LeBreton, C R Huang, H Fernando, et al.

Biochemistry|January 31, 1995

NMR solution structure of a nonanucleotide duplex with a dG mismatch opposite a 10R adduct derived from trans addition of a deoxyadenosine N6-amino group to (-)-(7S,8R,9R,10S)-7,8-dihydroxy-9,10-epoxy-7,8,9,10- tetrahydrobenzo[a]pyreneE J Schurter, H J Yeh, J M Sayer, et al.

Proceedings of the National Academy of Sciences of the United States of America|September 1, 1982

Mechanism of the inhibition of mutagenicity of a benzo[a]pyrene 7,8-diol 9,10-epoxide by riboflavin 5'-phosphateA W Wood, J M Sayer, H L Newmark, et al.

Molecular Pharmacology|July 1, 1983

Regioselectivity and stereoselectivity in the metabolism of trans-1,2-dihydroxy-1,2-dihydrobenz[a]anthracene by rat liver microsomesK P Vyas, P J van Bladeren, D R Thakker, et al.

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