Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Diogenes Herreno-saenz"'
Publikováno v:
Polycyclic Aromatic Compounds. 16:151-159
N-(Deoxyguanosin-8-yl)-2-aminopyrene and N-(deoxyadenosin-8-yl)-2-aminopyrene were formed from metabolism of 2-nitropyrene (2-NP) in vitro and in vivo. The effects of dietary restriction (DR) and age on the formation of these DNA adducts were studied
Autor:
Peter P. Fu, Diogenes Herreno-saenz
Publikováno v:
Journal of Environmental Science and Health, Part C. 17:1-43
(1999). Halogenated‐polycyclic aromatic hydrocarbons: A class of Genotoxic environmental pollutants. Journal of Environmental Science and Health, Part C: Vol. 17, No. 2, pp. 71-109.
Autor:
Feng Yun Qui, Diogenes Herreno-Saenz, Linda S. Von Tungeln, Ping Yi, Joellen Lewtas, Peter P. Fu, De-Jin Zhan
Publikováno v:
Polycyclic Aromatic Compounds. 10:187-194
We have characterized the DNA adducts of a series of nitro-polycyclic aromatic hydrocarbons (nitro-PAHs) formed under anaerobic conditions in vitro. Although the DNA adducts of nitro-PAHs formed through enzymatic nitroreduction are generally the C8-d
Autor:
Linda S. Von Tungeln, Joellen Lewtas, De-Jin Zhan, Peter P. Fu, Yu-Sun Wu, Diogenes Herreno-Saenz, Li-Hsueh Chiu
Publikováno v:
Journal of Chromatography A. 710:149-157
32 P-Postlabeling-HPLC is a highly sensitive analytical method for identification of chemical-modified DNA adducts isolated from samples obtained from experimental animals or humans exposed to carcinogenic chemicals. To determine optimal 32 P-postlab
Publikováno v:
Chemical Research in Toxicology. 8:269-277
1-Nitropyrene, the most abundant nitro-polycyclic aromatic hydrocarbon in the environment, is a known mammalian and bacterial mutagen and a tumorigen in animals. Early studies on DNA adduct characterization for 1-nitropyrene identified N-(deoxyguanos
Publikováno v:
Chemical Research in Toxicology. 7:806-814
We recently reported that the reaction of N-hydroxy-3-aminobenzo[a] pyrene with calf thymus DNA produced 6-(deoxyguanosin-N2-yl)-3-aminobenzo[a]pyrene as the predominant adduct. The deoxyguanosinyl group of this adduct resides at the C6 position, whi
Autor:
Peter P. Fu, Diogenes Herreno-saenz, L. S. Von Tungeln, Jackson O. Lay, Frederick E. Evans, J.-S. Lai, Yu-Sen Wu
Publikováno v:
Environmental Health Perspectives
We have been interested in the structure-activity relationships of nitro-polycyclic aromatic hydrocarbons (nitro-PAHs), and have focused on the correlation of structural and electronic features with biological activities, including mutagenicity and t
Autor:
Robert H. Heflicht, Joellen Lewtas, Diogenes Herreno-Saenz, Peter P. Fu, Linda S. Von Tungeln
Publikováno v:
Polycyclic Aromatic Compounds. 6:79-85
In vivo studies of the metabolic activation of 2-nitrofluoranthene (2-NFA) were conducted by incubating Salmonella typhimurium TA98 suspension cultures with 2-NFA (10 or 20μM) for 4 hr. The DNA was isolated and the resulting DNA adducts were analyze
Autor:
Danita G. Ewing, Linda S. Von Tungeln, Robin Weitkamp, Elly Cheng, Peter P. Fu, Diogenes Herreno-Saenz, Fred E. Evans
Publikováno v:
Polycyclic Aromatic Compounds. 7:91-98
2-Nitrobenzo[a]pyrene (2-nitro-BaP) induced 100% liver tumor incidence in the neonatal mouse tumorigenicity assay and exhibited the highest mutagenicity among the 1-, 2-, 3-, and 6-nitro-BaP when tested in Salmonella typhimurium TA98 and TA100. To de
Publikováno v:
Polycyclic Aromatic Compounds. 6:71-78
We have studied in vitro metabolism, DNA adduct formation, mutagenicity, and tumorigenicity of a series of nitro−polycyclic aromatic hydrocarbons. The emphasis has been focused on the isomeric nitrobenzo−[a]pyrenes and related compounds. We have