Biochemical basis of genotoxicity of heterocyclic arylamine food mutagens: Human DNA polymerase eta selectively produces a two-base deletion in copying the N2-guanyl adduct of 2-amino-3-methylimidazo[4,5-f]quinoline but not the C8 adduct at the NarI

Biochemical basis of genotoxicity of heterocyclic arylamine food mutagens: Human DNA polymerase eta selectively produces a two-base deletion in copying the N2-guanyl adduct of 2-amino-3-methylimidazo[4,5-f]quinoline but not the C8 adduct at the NarI

Item

http://www.wikidata.org/entity/Q33249850

Q33249850

about

Hydrogen bonding of 7,8-dihydro-8-oxodeoxyguanosine with a charged residue in the little finger domain determines miscoding events in Sulfolobus solfataricus DNA polymerase Dpo4 Base-displaced intercalation of the 2-amino-3-methylimidazo[4,5-f]quinolone N2-dG adduct in the NarI DNA recognition sequence Mass spectrometry for the assessment of the occurrence and biological consequences of DNA adducts Metabolism and biomarkers of heterocyclic aromatic amines in molecular epidemiology studies: lessons learned from aromatic amines Conformational differences of the C8-deoxyguanosine adduct of 2-amino-3-methylimidazo[4,5-f]quinoline (IQ) within the NarI recognition sequence.The C8-2'-deoxyguanosine adduct of 2-amino-3-methylimidazo[1,2-d]naphthalene, a carbocyclic analogue of the potent mutagen 2-amino-3-methylimidazo[4,5-f]quinoline, is a block to replication in vitro.Translesion synthesis across abasic lesions by human B-family and Y-family DNA polymerases α, δ, η, ι, κ, and REV1 Synthesis of oligonucleotides containing the N2-deoxyguanosine adduct of the dietary carcinogen 2-amino-3-methylimidazo[4,5-f]quinoline.Translesion synthesis past the C8- and N2-deoxyguanosine adducts of the dietary mutagen 2-Amino-3-methylimidazo[4,5-f]quinoline in the NarI recognition sequence by prokaryotic DNA polymerases Base-Displaced Intercalated Conformation of the 2-Amino-3-methylimidazo[4,5-f]quinoline N(2)-dG DNA Adduct Positioned at the Nonreiterated G(1) in the NarI Restriction Site.DNA polymerases κ and ζ cooperatively perform mutagenic translesion synthesis of the C8-2'-deoxyguanosine adduct of the dietary mutagen IQ in human cells Effects of the N terminus of mouse DNA polymerase κ on the bypass of a guanine-benzo[a]pyrenyl adduct Replication past the N5-methyl-formamidopyrimidine lesion of deoxyguanosine by DNA polymerases and an improved procedure for sequence analysis of in vitro bypass products by mass spectrometry.Translesional DNA synthesis through a C8-guanyl adduct of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) in Vitro: REV1 inserts dC opposite the lesion, and DNA polymerase kappa potentially catalyzes extension reaction from the 3'-dC terminus 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.Kinetic analysis of translesion synthesis opposite bulky N2- and O6-alkylguanine DNA adducts by human DNA polymerase REV1.Translesion Synthesis of the N(2)-2'-Deoxyguanosine Adduct of the Dietary Mutagen IQ in Human Cells: Error-Free Replication by DNA Polymerase κ and Mutagenic Bypass by DNA Polymerases η, ζ, and Rev1.Replication bypass of N2-deoxyguanosine interstrand cross-links by human DNA polymerases η and ι.

P2860

Q27644639-5E9FA93F-2E00-4A5A-A3F1-E7D547D18F67 Q27681071-F189DC22-9C11-487C-8906-84398B5C5445 Q28082391-FD671BC8-8C63-469A-9357-17E37F6C515C Q28391158-E454FA35-EBB4-473B-9AF8-F24B6DB2B621 Q33274726-9004BCF0-5518-4F1F-BB73-018361F57C52 Q33936400-2854CCD5-3D18-48E6-BD07-66ED30733691 Q34479547-6780C72C-5CF5-45E5-9549-713F5D80956B Q35111701-C9A26FA4-D3F1-49BD-A877-2DFB2B22FD09 Q35148064-E9395DC5-F309-4406-A8C0-80E0A821440C Q35879285-1F20109E-CE42-4DAC-A84B-1883BB54DF06 Q36676696-86EF6ABC-C607-4328-B026-C692B6653462 Q36948837-A5F05EDB-658E-4210-A5A7-904824D68B9C Q37367873-48EBB0D9-E7D8-4234-8A08-61D9E7E8DF6A Q37377617-3DA83578-31BD-45F7-8BE1-6AFEF6A5E45F Q37523212-45A52699-54A1-4B70-B81E-1F4241AE22E1 Q38289676-5A12A692-8EFA-4139-AA47-90F7E0C51B9A Q41142464-F5716EC1-87A4-45C3-88F2-3FDCA5DFFA3B Q43074239-EC0872CA-32DE-44B5-9135-BCD5D7BC7CFB

P2860

Biochemical basis of genotoxicity of heterocyclic arylamine food mutagens: Human DNA polymerase eta selectively produces a two-base deletion in copying the N2-guanyl adduct of 2-amino-3-methylimidazo[4,5-f]quinoline but not the C8 adduct at the NarI

Item

http://www.wikidata.org/entity/Q33249850

description

2006 nî lūn-bûn

@nan

2006 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2006 թվականի հուլիսին հրատարակված գիտական հոդված

@hy

2006年の論文

@ja

2006年論文

@yue

2006年論文

@zh-hant

2006年論文

@zh-hk

2006年論文

@zh-mo

2006年論文

@zh-tw

2006年论文

@wuu