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R E Lehr

Showing results (11-20 of 30) with videos related to

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Cancer Research|June 1, 1986
Bacterial and mammalian cell mutagenicity of four optically active bay-region 3,4-diol-1,2-epoxides and other derivatives of the nitrogen heterocycle dibenz[c,h]acridineA W Wood, R L Chang, W Levin, et al.
Cancer Research|March 1, 1981
Tumorigenicity of the diastereomeric bay-region benzo(e)pyrene 9,10-diol-11,12-epoxides in newborn miceR L Chang, W Levin, A W Wood, et al.
Cancer Research|October 1, 1983
Tumor-initiating activity of benz[c]acridine and twelve of its derivatives on mouse skinW Levin, A W Wood, R L Chang, et al.
Cancer Research|November 1, 1984
Tumorigenicity of dihydrodiols and diol-epoxides of benz[c]acridine in newborn miceR L Chang, W Levin, A W Wood, et al.
Cancer Research|January 1, 1982
Tumorigenicity of bay-region diol-epoxides and other benzo-ring derivatives of dibenzo(a,h)pyrene and dibenzo(a,i)pyrene on mouse skin and in newborn miceR L Chang, W Levin, A W Wood, et al.
Cancer Research|April 1, 1981
Species-specific enhancement by 7,8-benzoflavone of hepatic microsomal metabolism of benzo[e]pyrene 9,10-dihydrodiol to bay-region diol epoxidesD R Thakker, W Levin, M Buening, et al.
Cancer Research|November 1, 1981
Reduction of tumorigenicity and of dihydrodiol formation by fluorine substitution in the angular rings of dibenzo(a,i)pyreneS S Hecht, E J LaVoie, V Bedenko, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1977
Mutagenicity and cytotoxicity of benz[alpha]anthracene diol epoxides and tetrahydro-epoxides: exceptional activity of the bay region 1,2-epoxidesA W Wood, R L Chang, W Levin, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1977
Tumorigenicity of five dihydrodiols of benz(a)anthracene on mouse skin: exceptional activity of benz(a)anthracene 3,4-dihydrodiolA W Wood, W Levin, R L Chang, et al.
Journal of Medicinal Chemistry|September 29, 1995
In vivo and in vitro studies on the neurotoxic potential of 6-hydroxydopamine analogsS Ma, L Lin, R Raghavan, et al.
Pageof 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
Cancer Research|June 1, 1986
Bacterial and mammalian cell mutagenicity of four optically active bay-region 3,4-diol-1,2-epoxides and other derivatives of the nitrogen heterocycle dibenz[c,h]acridineA W Wood, R L Chang, W Levin, et al.
Cancer Research|March 1, 1981
Tumorigenicity of the diastereomeric bay-region benzo(e)pyrene 9,10-diol-11,12-epoxides in newborn miceR L Chang, W Levin, A W Wood, et al.
Cancer Research|October 1, 1983
Tumor-initiating activity of benz[c]acridine and twelve of its derivatives on mouse skinW Levin, A W Wood, R L Chang, et al.
Cancer Research|November 1, 1984
Tumorigenicity of dihydrodiols and diol-epoxides of benz[c]acridine in newborn miceR L Chang, W Levin, A W Wood, et al.
Cancer Research|January 1, 1982
Tumorigenicity of bay-region diol-epoxides and other benzo-ring derivatives of dibenzo(a,h)pyrene and dibenzo(a,i)pyrene on mouse skin and in newborn miceR L Chang, W Levin, A W Wood, et al.
Cancer Research|April 1, 1981
Species-specific enhancement by 7,8-benzoflavone of hepatic microsomal metabolism of benzo[e]pyrene 9,10-dihydrodiol to bay-region diol epoxidesD R Thakker, W Levin, M Buening, et al.
Cancer Research|November 1, 1981
Reduction of tumorigenicity and of dihydrodiol formation by fluorine substitution in the angular rings of dibenzo(a,i)pyreneS S Hecht, E J LaVoie, V Bedenko, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1977
Mutagenicity and cytotoxicity of benz[alpha]anthracene diol epoxides and tetrahydro-epoxides: exceptional activity of the bay region 1,2-epoxidesA W Wood, R L Chang, W Levin, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1977
Tumorigenicity of five dihydrodiols of benz(a)anthracene on mouse skin: exceptional activity of benz(a)anthracene 3,4-dihydrodiolA W Wood, W Levin, R L Chang, et al.
Journal of Medicinal Chemistry|September 29, 1995
In vivo and in vitro studies on the neurotoxic potential of 6-hydroxydopamine analogsS Ma, L Lin, R Raghavan, et al.
Pageof 3