Biological properties of single chemical-DNA adducts: a twenty year perspective
about
DNA adductomicsMetabolism and biomarkers of heterocyclic aromatic amines in molecular epidemiology studies: lessons learned from aromatic aminesSerial analysis of mutation spectra (SAMS): a new approach for the determination of mutation spectra of site-specific DNA damage and their sequence dependenceCreating context for the use of DNA adduct data in cancer risk assessment: I. Data organization.Nucleotide excision repair of a DNA interstrand cross-link produces single- and double-strand breaks.The mutator phenotype in cancer: molecular mechanisms and targeting strategiesSystems analysis of protein modification and cellular responses induced by electrophile stress.The biological and metabolic fates of endogenous DNA damage productsPyrosequencing: applicability for studying DNA damage-induced mutagenesis.Carcinogenicity and DNA adduct formation of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone and enantiomers of its metabolite 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol in F-344 rats.Comprehensive DNA adduct analysis reveals pulmonary inflammatory response contributes to genotoxic action of magnetite nanoparticlesSequence-specific single-molecule analysis of 8-oxo-7,8-dihydroguanine lesions in DNA based on unzipping kinetics of complementary probes in ion channel recordings.Detection of 7-(2'-carboxyethyl)guanine but not 7-carboxymethylguanine in human liver DNA.Roles of translesion synthesis DNA polymerases in the potent mutagenicity of tobacco-specific nitrosamine-derived O2-alkylthymidines in human cells.Chemical structure and properties of interstrand cross-links formed by reaction of guanine residues with abasic sites in duplex DNAComparative DNA adduct formation and induction of colonic aberrant crypt foci in mice exposed to 2-amino-9H-pyrido[2,3-b]indole, 2-amino-3,4-dimethylimidazo[4,5-f]quinoline, and azoxymethane.Comparative Toxicogenomics Database: a knowledgebase and discovery tool for chemical-gene-disease networksMass Spectrometry-Based Quantitative Strategies for Assessing the Biological Consequences and Repair of DNA Adducts.The mutagenicity of thymidine glycol in Escherichia coli is increased when it is part of a tandem lesionSynthesis of oxygen-linked 8-phenoxyl-deoxyguanosine nucleoside analogues.Biologically relevant oxidants and terminology, classification and nomenclature of oxidatively generated damage to nucleobases and 2-deoxyribose in nucleic acids.Endonuclease and Exonuclease Activities on Oligodeoxynucleotides Containing Spiroiminodihydantoin Depend on the Sequence Context and the Lesion Stereochemistry.Purine 5',8-cyclonucleoside lesions: chemistry and biology.Chemistry and structural biology of DNA damage and biological consequencesC8-linked bulky guanosine DNA adducts: experimental and computational insights into adduct conformational preferences and resulting mutagenicity.Development of single-chain variable fragment (scFv) antibodies against hapten benzo[a]pyrene: a binding study.Occurrence, Biological Consequences, and Human Health Relevance of Oxidative Stress-Induced DNA Damage.Design of a hydrogen peroxide-activatable agent that specifically targets cancer cells.Mutagenic and carcinogenic structural alerts and their mechanisms of action.Combination of pentafluorophenylhydrazine derivatization and isotope dilution LC-MS/MS techniques for the quantification of apurinic/apyrimidinic sites in cellular DNA.Biologically relevant oxidants cause bound proteins to readily oxidatively cross-link at Guanine.DNA sequence context as a determinant of the quantity and chemistry of guanine oxidation produced by hydroxyl radicals and one-electron oxidants.Nanopore detection of 8-oxo-7,8-dihydro-2'-deoxyguanosine in immobilized single-stranded DNA via adduct formation to the DNA damage site.Synthesis of DNA Oligodeoxynucleotides Containing Site-Specific 1,3-Butadiene-Deoxyadenosine Lesions.The formamidopyrimidine derivative of 7-(2-oxoethyl)-2'-deoxyguanosine.Chemical Analysis of DNA Damage.Characterization of Byproducts from Chemical Syntheses of Oligonucleotides Containing 1-Methyladenine and 3-Methylcytosine.Data-Independent Mass Spectrometry Approach for Screening and Identification of DNA Adducts.Synthesis of Oligodeoxynucleotides Containing a C8-2'-Deoxyguanosine Adduct Formed by the Carcinogen 3-Nitrobenzanthrone.
P2860
Q28384534-857FBF0B-5ADC-4DCD-8D8B-5052A0C63F61Q28391158-7F50C8B2-9EAB-4399-B6EF-3DD87616C5BEQ33371451-F55B4DA6-C1A7-4ABB-8917-51A1A00DF727Q33501831-DB693776-EBB8-4EF7-B627-E4509F20AF8FQ33580793-A3610F0C-3061-42EB-921A-198D323DB136Q33815796-BBBAA5C9-4B88-4857-ADAF-50832581FAF5Q33865889-E37AC1B3-5CA0-4F2D-8918-D1F3612A892FQ34157752-35F67AF3-C5A6-4A97-9D83-A25C56CF3E07Q34339017-A84C2D33-2341-48B6-9687-92E1772A4E70Q34586229-457387CC-CB7E-4483-962A-CDC9FB6D2D91Q35139079-F94DF755-A8FF-43AD-8EA5-B226D9452692Q35214341-5DD0E787-ACFB-4BAA-B52C-F3B17182C6C2Q35591266-EEBFCFDC-63B5-4EC0-AEBA-A972089C9089Q36296884-F012157F-29CC-4C91-A131-03F92AB6E211Q36444967-19FCE8C6-AD7B-4283-9605-123CC070CBE5Q36578156-91ABBE23-623F-4171-A8E9-07188357E072Q37202770-107AA541-6A84-4FDA-8B27-D2ED7E6DECCBQ37304675-52B7F5AD-2A21-4879-AB1F-5A7B5EE1718CQ37310062-1C8BCDF8-CCCF-4141-88E6-3F13D987F97FQ37327779-2D2D393E-A1C3-4E74-934F-AC415BDB236BQ37396568-63DB18EA-842D-4ABC-A0B6-174B827113C2Q37593447-1981B1CD-A622-4DCA-924C-5851F61D7247Q37827361-FE42FA8E-F6EF-446B-AD48-A26021F1779AQ37933191-10D2231C-B405-4424-BBAF-274F37F3F454Q38054138-7E512166-5F77-42AA-B76F-85B65DC51188Q38331712-14CFDC50-7BDB-47D9-A09F-69D9DD5401D2Q38434331-30FF725A-AABE-411E-8BEE-6F317EEB1F6AQ38933100-92729F60-CC69-4BEE-935B-0217012C38ECQ38982647-2EFC9E14-4D8E-414F-8C0E-59984A9C5F50Q39191797-D1448C30-3054-49EB-A119-8D7FDA4490E2Q40994808-A10B58CF-DEAB-41CB-B5E6-E00C3A94325DQ41932407-EEE6CD9D-5C5C-4691-9AEF-0C301574BEC4Q41952021-5B680D32-B8A5-4CBC-B645-97E1EDBF4283Q41983538-9908BD58-C8F7-4C5E-8DB7-9C3F6C16DF77Q42822461-0FCD3E36-F4EF-4F04-8907-130AF6DD04CEQ45961755-3B31F069-5E38-499E-8C73-106A4223F776Q47160383-4B6C4AE3-340A-4DC8-B007-5C595AB87AE9Q47661718-47CD1CD4-14F9-48B2-9C59-6A3F591DF61CQ53211826-0408E80D-7A3D-471C-BFDA-899C3BE3218B
P2860
Biological properties of single chemical-DNA adducts: a twenty year perspective
description
2007 nî lūn-bûn
@nan
2007 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Biological properties of single chemical-DNA adducts: a twenty year perspective
@ast
Biological properties of single chemical-DNA adducts: a twenty year perspective
@en
type
label
Biological properties of single chemical-DNA adducts: a twenty year perspective
@ast
Biological properties of single chemical-DNA adducts: a twenty year perspective
@en
prefLabel
Biological properties of single chemical-DNA adducts: a twenty year perspective
@ast
Biological properties of single chemical-DNA adducts: a twenty year perspective
@en
P2860
P356
P1476
Biological properties of single chemical-DNA adducts: a twenty year perspective
@en
P2093
James C Delaney
John M Essigmann
P2860
P304
P356
10.1021/TX700292A
P577
2007-12-12T00:00:00Z