(Q63253395)

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Direct evidence for the formation of deoxyribonucleotide adducts from carcinogenic N-nitroso-N-methylaniline revealed by the 32P-postlabeling technique

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9 December 2019

Direct evidence for the formation of deoxyribonucleotide adducts from carcinogenic N-nitroso-N-methylaniline revealed by the 32P-postlabeling technique (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10378774%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

Marie Stiborová

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9 December 2019

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H H Schmeiser

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9 December 2019

M Wiessler

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9 December 2019

E Frei

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9 December 2019

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1 April 1999

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9 December 2019

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9 December 2019

138

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9 December 2019

1-2

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9 December 2019

61-66

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9 December 2019

Toxicity and oncogenicity of nitrosomethylaniline and nitrosomethylcyclohexylamine

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Evidence for an unstable DNA adduct from N-nitroso-N-methylaniline.

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Metabolic denitrosation of N-nitroso-N-methylaniline: detection of amine-metabolites.

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Metabolism of carcinogenic N-nitroso-N-methylaniline by purified cytochromes P450 2B1 and P450 2B2.

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[Carcinogenic activity of 13 aryldialkyl triazenes in BD-rats (author's transl)]

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alpha-Hydroxylation pathway in the in vitro metabolism of carcinogenic nitrosamines: N-nitrosodimethylamine and N-nitroso-N-methylaniline

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Metabolism of 15N-labelled N-nitrosodimethylamine and N-nitroso-N-methylaniline by isolated rat hepatocytes

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The chemistry of diamantane. Part I. Synthesis and some functionalisation reactions

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The first identification of the benzenediazonium ion formation from a non-aminoazo dye, 1-phenylazo-2-hydroxynaphthalene (Sudan I) by microsomes of rat livers

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Nuclease P1-mediated enhancement of sensitivity of 32P-postlabeling test for structurally diverse DNA adducts.

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Comparison of 32P-postlabeling and high pressure liquid chromatographic analyses for 7,12-dimethylbenz[a]anthracene--DNA adducts

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Comparative DNA binding of 7,12-dimethylbenz[a]anthracene and some of its metabolites in mouse epidermis in vivo as revealed by the 32P-postlabeling technique

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32P-labeling test for DNA damage

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Mechanism of formation and 32P-postlabeling of DNA adducts derived from peroxidative activation of carcinogenic non-aminoazo dye 1-phenylazo-2-hydroxynaphthalene (Sudan I).

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DNA adduction by phenol, hydroquinone, or benzoquinone in vitro but not in vivo: nuclease P1-enhanced 32P-postlabeling of adducts as labeled nucleoside bisphosphates, dinucleotides and nucleoside monophosphates.

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Peroxidase oxidizes N-nitrosomethylaniline to ultimate carcinogens(s) binding to DNA and transfer RNA in vitro.

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Storage phosphor imaging technique for detection and quantitation of DNA adducts measured by the 32P-postlabeling assay

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Macromolecular adducts: biomarkers for toxicity and carcinogenesis

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A reconstituted cytochrome P450 system from tulip bulbs (Tulipa fosteriana L.) oxidizes xenobiotics

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Metabolism of diamantane by rat liver microsomal cytochromes P-450

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Identifiers

10.1016/S0304-3835(98)00369-3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10378774%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

PubMed publication ID

1 reference

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PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10378774%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

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