(Q43715479)

English

Evidence for reductive activation of carcinogenic aristolochic acids by prostaglandin H synthase -- (32)P-postlabeling analysis of DNA adduct formation

scientific article published in June 2001

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

Evidence for reductive activation of carcinogenic aristolochic acids by prostaglandin H synthase -- (32)P-postlabeling analysis of DNA adduct formation (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

Marie Stiborová

1

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

author name string

E Frei

2

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

A Breuer

3

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

M Wiessler

4

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

H H Schmeiser

5

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

language of work or name

0 references

publication date

1 June 2001

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Europe PubMed Central

PubMed publication ID

26 November 2017

Mutation Research

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Europe PubMed Central

PubMed publication ID

26 November 2017

493

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

1-2

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

149-160

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

Rapidly progressive interstitial renal fibrosis in young women: association with slimming regimen including Chinese herbs

1 reference

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32P-post-labelling analysis of DNA adducts formed by aristolochic acid in tissues from patients with Chinese herbs nephropathy

1 reference

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7 January 2021

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Aristolactam I a metabolite of aristolochic acid I upon activation forms an adduct found in DNA of patients with Chinese herbs nephropathy.

1 reference

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Urothelial carcinoma associated with the use of a Chinese herb (Aristolochia fangchi)

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Misuse of herbal remedies: the case of an outbreak of terminal renal failure in Belgium (Chinese herbs nephropathy)

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Chinese herbs nephropathy or the evils of nature

1 reference

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Characterization of DNA adducts formed by aristolochic acids in the target organ (forestomach) of rats by 32P-postlabelling analysis using different chromatographic procedures

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Urothelial malignancy in nephropathy due to Chinese herbs

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Urothelial lesions in Chinese-herb nephropathy.

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Comparison of DNA adduct formation by aristolochic acids in various in vitro activation systems by 32P-post-labelling: evidence for reductive activation by peroxidases

1 reference

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Prostaglandin H synthase and xenobiotic oxidation

1 reference

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Xenobiotic metabolism by prostaglandin H synthase

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Mutagenicity of the two main components of commercially available carcinogenic aristolochic acid in Salmonella typhimurium.

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Oxidation and genotoxicity of fecapentaene-12 are potentiated by prostaglandin H synthase.

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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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Benzenediazonium ion derived from Sudan I forms an 8-(phenylazo)guanine adduct in DNA.

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Mechanism of formation and structural characterization of DNA adducts derived from peroxidative activation of benzidine

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Inactivation of prostaglandin endoperoxide synthase by acylating derivatives of indomethacin

1 reference

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7 January 2021

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Selective inhibitors of cytochromes P450.

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Reversible inhibition of NADPH-cytochrome P450 reductase by alpha-lipoic acid

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

1 reference

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7 January 2021

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32P-adduct assay: comparative recoveries of structurally diverse DNA adducts in the various enhancement procedures

1 reference

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7 January 2021

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DNA adduct formation of aristolochic acid I and II in vitro and in vivo

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Improved reversed-phase high-performance liquid chromatographic separation of 32P-labelled nucleoside 3',5'-bisphosphate adducts of polycyclic aromatic hydrocarbons

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

1 reference

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7 January 2021

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Aristolochic acid binds covalently to the exocyclic amino group of purine nucleotides in DNA.

1 reference

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7 January 2021

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N6-Adenyl arylation of DNA by aristolochic acid II and a synthetic model for the putative proximate carcinogen

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Co-oxidation of diethylstilbestrol and structural analogs by prostaglandin synthase.

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Interactions between cytochrome P450 and cytochrome b5.

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32P-postlabelling analysis of the DNA adducts formed by aristolochic acid I and II.

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Metabolism of nitro-polycyclic aromatic hydrocarbons

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Human cytochrome P450 enzymes: a status report summarizing their reactions, substrates, inducers, and inhibitors

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Heme Peroxidases: Structure, Function, Mechanism and Involvement in Activation of Carcinogens. A Review

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One-electron-transfer reactions in biochemical systems. II. The reaction of free radicals formed in the enzymic oxidation.

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Identifiers

10.1016/S1383-5718(01)00171-1

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

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