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UVA-Induced DNA Single-Strand Cleavage by 1-Hydroxypyrene and Formation of Covalent Adducts between DNA and 1-Hydroxypyrene
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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MECHANISTIC QUANTITATIVE STRUCTURE–ACTIVITY RELATIONSHIP MODEL FOR THE PHOTOINDUCED TOXICITY OF POLYCYCLIC AROMATIC HYDROCARBONS: I. PHYSICAL MODEL BASED ON CHEMICAL KINETICS IN A TWO-COMPARTMENT SYSTEM
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Mechanistic quantitative structure–activity relationship model for the photoinduced toxicity of polycyclic aromatic hydrocarbons: II. An empirical model for the toxicity of 16 polycyclic aromatic hydrocarbons to the duckweed Lemna gibba L. G-3
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USE OF QUANTITATIVE SHAPE–ACTIVITY RELATIONSHIPS TO MODEL THE PHOTOINDUCED TOXICITY OF POLYCYCLIC AROMATIC HYDROCARBONS: ELECTRON DENSITY SHAPE FEATURES ACCURATELY PREDICT TOXICITY
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Polycyclic aromatic hydrocarbons; chemistry and carcinogenicity
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Biological monitoring of environmental exposure to polycyclic aromatic hydrocarbons; 1-hydroxypyrene in urine of people
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Biochemical and Clinical Aspects of Oxygen
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Base Specific and Regioselective Chemical Cross-Linking of Daunorubicin to DNA
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Identification and quantitation of benzo[a]pyrene-DNA adducts formed in mouse skin
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Dihydrodiol Dehydrogenases and Polycyclic Aromatic Hydrocarbon Activation: Generation of Reactive and Redox Active o-Quinones
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inferredcites →https://doi.org/10.1897/1551-5028(1997)016<2296:mqsarm>2.3.co;2openalex-snapshot
MECHANISTIC QUANTITATIVE STRUCTURE–ACTIVITY RELATIONSHIP MODEL FOR THE PHOTOINDUCED TOXICITY OF POLYCYCLIC AROMATIC HYDROCARBONS: II. AN EMPIRICAL MODEL FOR THE TOXICITY OF 16 POLYCYCLIC AROMATIC HYDROCARBONS TO THE DUCKWEED LEMNA GIBBA L. G-3
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