Biological properties of single chemical-DNA adducts: a twenty year perspective - Test2 - elhamkhani - TriplyDB

Biological properties of single chemical-DNA adducts: a twenty year perspective

Biological properties of single chemical-DNA adducts: a twenty year perspective

http://www.wikidata.org/entity/Q33649960

about

DNA adductomics Metabolism and biomarkers of heterocyclic aromatic amines in molecular epidemiology studies: lessons learned from aromatic amines Serial analysis of mutation spectra (SAMS): a new approach for the determination of mutation spectra of site-specific DNA damage and their sequence dependence Creating 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 strategies Systems analysis of protein modification and cellular responses induced by electrophile stress.The biological and metabolic fates of endogenous DNA damage products Pyrosequencing: 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 nanoparticles Sequence-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 DNA Comparative 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 networks Mass 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 lesion Synthesis 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 consequences C8-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-5052A0C63F61 Q28391158-7F50C8B2-9EAB-4399-B6EF-3DD87616C5BE Q33371451-F55B4DA6-C1A7-4ABB-8917-51A1A00DF727 Q33501831-DB693776-EBB8-4EF7-B627-E4509F20AF8F Q33580793-A3610F0C-3061-42EB-921A-198D323DB136 Q33815796-BBBAA5C9-4B88-4857-ADAF-50832581FAF5 Q33865889-E37AC1B3-5CA0-4F2D-8918-D1F3612A892F Q34157752-35F67AF3-C5A6-4A97-9D83-A25C56CF3E07 Q34339017-A84C2D33-2341-48B6-9687-92E1772A4E70 Q34586229-457387CC-CB7E-4483-962A-CDC9FB6D2D91 Q35139079-F94DF755-A8FF-43AD-8EA5-B226D9452692 Q35214341-5DD0E787-ACFB-4BAA-B52C-F3B17182C6C2 Q35591266-EEBFCFDC-63B5-4EC0-AEBA-A972089C9089 Q36296884-F012157F-29CC-4C91-A131-03F92AB6E211 Q36444967-19FCE8C6-AD7B-4283-9605-123CC070CBE5 Q36578156-91ABBE23-623F-4171-A8E9-07188357E072 Q37202770-107AA541-6A84-4FDA-8B27-D2ED7E6DECCB Q37304675-52B7F5AD-2A21-4879-AB1F-5A7B5EE1718C Q37310062-1C8BCDF8-CCCF-4141-88E6-3F13D987F97F Q37327779-2D2D393E-A1C3-4E74-934F-AC415BDB236B Q37396568-63DB18EA-842D-4ABC-A0B6-174B827113C2 Q37593447-1981B1CD-A622-4DCA-924C-5851F61D7247 Q37827361-FE42FA8E-F6EF-446B-AD48-A26021F1779A Q37933191-10D2231C-B405-4424-BBAF-274F37F3F454 Q38054138-7E512166-5F77-42AA-B76F-85B65DC51188 Q38331712-14CFDC50-7BDB-47D9-A09F-69D9DD5401D2 Q38434331-30FF725A-AABE-411E-8BEE-6F317EEB1F6A Q38933100-92729F60-CC69-4BEE-935B-0217012C38EC Q38982647-2EFC9E14-4D8E-414F-8C0E-59984A9C5F50 Q39191797-D1448C30-3054-49EB-A119-8D7FDA4490E2 Q40994808-A10B58CF-DEAB-41CB-B5E6-E00C3A94325D Q41932407-EEE6CD9D-5C5C-4691-9AEF-0C301574BEC4 Q41952021-5B680D32-B8A5-4CBC-B645-97E1EDBF4283 Q41983538-9908BD58-C8F7-4C5E-8DB7-9C3F6C16DF77 Q42822461-0FCD3E36-F4EF-4F04-8907-130AF6DD04CE Q45961755-3B31F069-5E38-499E-8C73-106A4223F776 Q47160383-4B6C4AE3-340A-4DC8-B007-5C595AB87AE9 Q47661718-47CD1CD4-14F9-48B2-9C59-6A3F591DF61C Q53211826-0408E80D-7A3D-471C-BFDA-899C3BE3218B

P2860

Biological properties of single chemical-DNA adducts: a twenty year perspective

http://www.wikidata.org/entity/Q33649960

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

P1433

Q33649960-725EE42E-7262-417A-85BF-EA732089035D

P1476

Q33649960-244E3D07-1814-4FD3-A85D-2D845B47710D

P2093

Q33649960-212C0D8B-FF6B-4E23-A5E0-7F8753930F98

Q33649960-993F8379-1AD6-4FFC-821C-8B54BBB3B4C6

P2860

Q33649960-008080A5-F7E5-4F6F-8048-F95D2E2F9129

Q33649960-0116E1A4-260C-4616-9378-22C02317ED49

Q33649960-013392B3-B454-4073-BEB1-8A87AB4FF162

Q33649960-014A0EA3-8C4D-49D3-9650-C0F35E7044EC

Q33649960-024B5BC4-2A7C-4FF1-985C-211320621CAC

Q33649960-02AFDAFC-63B6-4530-9184-12CF8A9ED3F4

Q33649960-037B2EA7-0580-4130-9154-1BA05A1B95BA

Q33649960-03873714-A5D4-4B0C-A3F9-0CF2EA4D1904

Q33649960-041070D8-B18E-48E9-B7AE-2E0D1A4FFF40

Q33649960-04B9AC4E-A5CB-4A71-AFB4-EF9831B41B50

P304

Q33649960-D48283B6-2731-4635-A8FF-0DAE1563853E

P31

Q33649960-C0C480D1-141B-49E8-A63A-4CE6F8D6368F

P356

Q33649960-E725B423-73FC-46DD-ABFE-583F16A3FC9F

P433

Q33649960-97E30933-0580-4E90-A3B7-295B163296DD

P478

Q33649960-CD99FA38-426A-4B02-AB2C-692FA43211A4

P577

Q33649960-37C3BCA4-6EF3-40ED-B947-755C6F401AF3

P5875

Q33649960-2703627C-24C2-4A6B-92EC-0F6A430C7B2F

P698

Q33649960-D61E058D-4DBD-49E5-98AA-E65621C79FF6

P932

Q33649960-82A7CB47-31A4-4736-A544-A3BCA7D5B506

P356

P1433

Chemical Research in Toxicology

P1476

Biological properties of single chemical-DNA adducts: a twenty year perspective

@en

P2093

James C Delaney

http://www.w3.org/2001/XMLSchema#string

John M Essigmann

http://www.w3.org/2001/XMLSchema#string

P2860

The aflatoxin B(1) formamidopyrimidine adduct plays a major role in causing the types of mutations observed in human hepatocellular carcinoma

Mutagenesis, genotoxicity, and repair of 1-methyladenine, 3-alkylcytosines, 1-methylguanine, and 3-methylthymine in alkB Escherichia coli

Generating a synthetic genome by whole genome assembly: phiX174 bacteriophage from synthetic oligonucleotides

The use of native T7 DNA polymerase for site-directed mutagenesis

Molecular basis for discriminating between normal and damaged bases by the human alkyladenine glycosylase, AAG

Alleviation of 1,N6-ethanoadenine genotoxicity by the Escherichia coli adaptive response protein AlkB

Mutagenic effects of abasic and oxidized abasic lesions in Saccharomyces cerevisiae.

Preferential formation of (5S,6R)-thymine glycol for oligodeoxyribonucleotide synthesis and analysis of drug binding to thymine glycol-containing DNA.

Structure of the DNA repair enzyme endonuclease IV and its DNA complex: double-nucleotide flipping at abasic sites and three-metal-ion catalysis

DNA-bound structures and mutants reveal abasic DNA binding by APE1 and DNA repair coordination [corrected]

P304

232-252

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1021/TX700292A

http://www.w3.org/2001/XMLSchema#string

P433

1

http://www.w3.org/2001/XMLSchema#string

P478

21

http://www.w3.org/2001/XMLSchema#string

P577

2007-12-12T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

5775201

http://www.w3.org/2001/XMLSchema#string

P698

18072751

http://www.w3.org/2001/XMLSchema#string

P932

2821157

http://www.w3.org/2001/XMLSchema#string