Arylamine-DNA adducts in vitro and in vivo: their role in bacterial mutagenesis and urinary bladder carcinogenesis. - Wikidata - wikimedia - TriplyDB

Arylamine-DNA adducts in vitro and in vivo: their role in bacterial mutagenesis and urinary bladder carcinogenesis.

Arylamine-DNA adducts in vitro and in vivo: their role in bacterial mutagenesis and urinary bladder carcinogenesis.

http://www.wikidata.org/entity/Q35037159

about

DNA adduct formation and mutation induction by nitropyrenes in Salmonella and Chinese hamster ovary cells: relationships with nitroreduction and acetylation Formation and persistence of arylamine DNA adducts in vivo Metabolism and biomarkers of heterocyclic aromatic amines in molecular epidemiology studies: lessons learned from aromatic amines Epigenetic alterations induced by genotoxic occupational and environmental human chemical carcinogens: A systematic literature review Biomonitoring Human Albumin Adducts: The Past, the Present, and the Future Genotoxic effect of N-hydroxy-4-acetylaminobiphenyl on human DNA: implications in bladder cancer Complex frameshift mutations mediated by plasmid pKM101: mutational mechanisms deduced from 4-aminobiphenyl-induced mutation spectra in Salmonella.Sulforaphane inhibits 4-aminobiphenyl-induced DNA damage in bladder cells and tissues.Circular dichroism of poly(dG-dC) modified by the carcinogens N-methyl-4-aminoazobenzene or 4-aminobiphenyl.Evaluation of electrochemiluminescent metabolic toxicity screening arrays using a multiple compound set.Identification of an unintended consequence of Nrf2-directed cytoprotection against a key tobacco carcinogen plus a counteracting chemopreventive intervention.Analysis of 4-aminobiphenyl-DNA adducts in human urinary bladder and lung by alkaline hydrolysis and negative ion gas chromatography-mass spectrometry.Metabolic activation routes of arylamines and their genotoxic effects Modification of plasmid and bacteriophage DNA by aromatic amines: effects on survival, template activity, and mutagenicity Summary of the National Toxicology Program benzidine dye initiative.Free-radical-mediated DNA binding Metabolism of aromatic amines by prostaglandin H synthase.The inverse relationship between bladder and liver in 4-aminobiphenyl-induced DNA damage.Knockout of phospholipase Cε attenuates N-butyl-N-(4-hydroxybutyl) nitrosamine-induced bladder tumorigenesis.Capturing labile sulfenamide and sulfinamide serum albumin adducts of carcinogenic arylamines by chemical oxidation.Multiclass Carcinogenic DNA Adduct Quantification in Formalin-Fixed Paraffin-Embedded Tissues by Ultraperformance Liquid Chromatography-Tandem Mass Spectrometry.Understanding the gender disparity in bladder cancer risk: the impact of sex hormones and liver on bladder susceptibility to carcinogens.DNA adducts of the tobacco carcinogens 2-amino-9H-pyrido[2,3-b]indole and 4-aminobiphenyl are formed at environmental exposure levels and persist in human hepatocytes.Determination of bulky DNA adducts in biomonitoring of carcinogenic chemical exposures: features and comparison of current techniques.Activation of 3,3'-dichlorobenzidine: enzymic basis and toxicological consequences.Biomonitoring DNA Adducts of Cooked Meat Carcinogens in Human Prostate by Nano Liquid Chromatography-High Resolution Tandem Mass Spectrometry: Identification of 2-Amino-1-methyl-6-phenylimidazo[4,5-b]pyridine DNA Adduct.Effects of butylated hydroxyanisole and butylated hydroxytoluene on DNA adduct formation and arylamine N-acetyltransferase activity in human bladder tumour cells.Effects of aspirin on arylamine N -acetyltransferase activity and DNA adducts in human bladder tumour cells.Human Biomonitoring of DNA Adducts by Ion Trap Multistage Mass Spectrometry Identification of N-(deoxyguanosin-8-yl)-4-azobiphenyl by (32)P-postlabeling analyses of DNA in human uroepithelial cells exposed to proximate metabolites of the environmental carcinogen 4-aminobiphenyl.Modeling human interindividual variability in metabolism and risk: the example of 4-aminobiphenyl.Glucuronidation of benzidine and its metabolites by cDNA-expressed human UDP-glucuronosyltransferases and pH stability of glucuronides.Synthesis of C8-N-Arylamine-Modified 2'-Deoxyguanosine-5'-Triphosphates and Their Effects on Primer Extension by DNA Polymerases.

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P2860

Arylamine-DNA adducts in vitro and in vivo: their role in bacterial mutagenesis and urinary bladder carcinogenesis.

http://www.wikidata.org/entity/Q35037159

description

1983 nî lūn-bûn

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1983 թուականի Մարտին հրատարակուած գիտական յօդուած

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1983 թվականի մարտին հրատարակված գիտական հոդված

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1983年の論文

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1983年学术文章

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1983年学术文章

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1983年学术文章

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1983年学术文章

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1983年学术文章

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1983年學術文章

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Arylamine-DNA adducts in vitro ...... rinary bladder carcinogenesis.

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Arylamine-DNA adducts in vitro ...... rinary bladder carcinogenesis.

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Arylamine-DNA adducts in vitro ...... rinary bladder carcinogenesis.

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Arylamine-DNA adducts in vitro ...... rinary bladder carcinogenesis.

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Arylamine-DNA adducts in vitro ...... rinary bladder carcinogenesis.

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Arylamine-DNA adducts in vitro ...... rinary bladder carcinogenesis.

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Environmental Health Perspectives

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Arylamine-DNA adducts in vitro ...... rinary bladder carcinogenesis.

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Beland FA

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Beranek DT

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Dooley KL

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P2860

Detection of carcinogens as mutagens in the Salmonella/microsome test: assay of 300 chemicals

Hepatic microsomal N-glucuronidation and nucleic acid binding of N-hydroxy arylamines in relation to urinary bladder carcinogenesis

N-acetyltransferase phenotype and risk in urinary bladder cancer: approaches in molecular epidemiology. Preliminary results in Sweden and Denmark.

Lifetime carcinogenicity study of 1- and 2-naphthylamine in dogs.

Aminofluorene-DNA adduct formation in Salmonella typhimurium exposed to the carcinogen N-hydroxy-2-acetylaminofluorene.

Covalent binding of benzidine and N-acetylbenzidine to DNA at the C-8 atom of deoxyguanosine in vivo and in vitro.

Enzymic deacetylation of carcinogenic arylacetamides by tissue microsomes of the dog and other species.

Application of the change in partition coefficient with pH to the structure determination of alkyl substituted guanosines.

Guanyl O6-arylamination and O6-arylation of DNA by the carcinogen N-hydroxy-1-naphthylamine.

The primary aromatic amines: their biological properties and structure-activity relationships.

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125-134

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10.1289/EHP.8349125

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49

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1983-03-01T00:00:00Z

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6339219

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