Tumorigenicity of the optical enantiomers of the diastereomeric benzo[a]pyrene 7,8-diol-9,10-epoxides in newborn mice: exceptional activity of (+)-7beta,8alpha-dihydroxy-9alpha,10alpha-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene.
about
Noncovalent interactions of a benzo[a]pyrene diol epoxide with DNA base pairs: insight into the formation of adducts of (+)-BaP DE-2 with DNAThe N-clasp of human DNA polymerase kappa promotes blockage or error-free bypass of adenine- or guanine-benzo[a]pyrenyl lesionsDetection of phosphodiester adducts formed by the reaction of benzo[a]pyrene diol epoxide with 2'-deoxynucleotides using collision-induced dissociation electrospray ionization tandem mass spectrometryThe human DNA repair factor XPC-HR23B distinguishes stereoisomeric benzo[a]pyrenyl-DNA lesionsInfluence of local sequence context on damaged base conformation in human DNA polymerase iota: molecular dynamics studies of nucleotide incorporation opposite a benzo[a]pyrene-derived adenine lesionCrystal structure of a benzo[a]pyrene diol epoxide adduct in a ternary complex with a DNA polymeraseNucleosome Histone Tail Conformation and Dynamics: Impacts of Lysine Acetylation and a Nearby Minor Groove Benzo[a]pyrene-Derived LesionCell cycle control, checkpoint mechanisms, and genotoxic stress.Differences in mutagenicity and cytotoxicity of (+)- and (-)-benzo[a]pyrene 4,5-oxide: a synergistic interaction of enantiomers.Oral benzo[a]pyrene-induced cancer: two distinct types in different target organs depend on the mouse Cyp1 genotype.Visualizing sequence-governed nucleotide selectivities and mutagenic consequences through a replicative cycle: processing of a bulky carcinogen N2-dG lesion in a Y-family DNA polymerase.Base sequence context effects on nucleotide excision repair.Impact of cellular metabolism on the biological effects of benzo[a]pyrene and related hydrocarbons.Crystal and molecular structure of a benzo[a]pyrene 7,8-diol 9,10-epoxide N2-deoxyguanosine adduct: absolute configuration and conformationRole of diaxial versus diequatorial hydroxyl groups in the tumorigenic activity of a benzo[a]pyrene bay-region diol epoxide.Error-prone translesion synthesis by human DNA polymerase eta on DNA-containing deoxyadenosine adducts of 7,8-dihydroxy-9,10-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene.Synergistic mechanisms in carcinogenesis by polycyclic aromatic hydrocarbons and by tobacco smoke: a bio-historical perspective with updates.Formation and repair of tobacco carcinogen-derived bulky DNA adductsStereochemistry-dependent bending in oligonucleotide duplexes induced by site-specific covalent benzo[a]pyrene diol epoxide-guanine lesions.Selective clonal expansion and microenvironmental permissiveness in tobacco carcinogenesis.Formation and persistence of benzo(a)pyrene metabolite-DNA adducts.Chloride ions catalyze the formation of cis adducts in the binding of anti-benzo[a]pyrene diol epoxide to nucleic acids.Benzo[a]pyrene diol epoxide adducts in DNA are potent suppressors of a normal topoisomerase I cleavage site and powerful inducers of other topoisomerase I cleavages.Structure of DNA polymerase beta with a benzo[c]phenanthrene diol epoxide-adducted template exhibits mutagenic featuresSpecificity of chemiluminescence in the metabolism of benzo[a]pyrene to its carcinogenic diol epoxide.Exocyclic amino groups of flanking guanines govern sequence-dependent adduct conformations and local structural distortions for minor groove-aligned benzo[a]pyrenyl-guanine lesions in a GG mutation hotspot context.Differences in unwinding of supercoiled DNA induced by the two enantiomers of anti-benzo[a]pyrene diol epoxide.Benzo[a]pyrene diol epoxide-DNA cis adduct formation through a trans chlorohydrin intermediate.Effect of carcinogenic adducts on transcription by T7 RNA polymerase.Dynamic conformational heterogeneities of carcinogen-DNA adducts and their mutagenic relevance.Epoxidation reactions catalyzed by rat liver cytochromes P-450 and P-448 occur at different faces of the 8,9-double bond of 8-methylbenz[a]anthracene.Position-specific trapping of topoisomerase II by benzo[a]pyrene diol epoxide adducts: implications for interactions with intercalating anticancer agents.Fungal oxidation of (+/-)-9,10-dihydroxy-9,10-dihydrobenzo[a]pyrene: formation of diastereomeric benzo[a]pyrene 9,10-diol 7,8-epoxides.Methylation of cytosine at C5 in a CpG sequence context causes a conformational switch of a benzo[a]pyrene diol epoxide-N2-guanine adduct in DNA from a minor groove alignment to intercalation with base displacement.Site-specific carcinogen binding to DNA.Solution conformation of the major adduct between the carcinogen (+)-anti-benzo[a]pyrene diol epoxide and DNANucleotide incorporation by human DNA polymerase gamma opposite benzo[a]pyrene and benzo[c]phenanthrene diol epoxide adducts of deoxyguanosine and deoxyadenosine.Mutagenicity and tumorigenicity of the four enantiopure bay-region 3,4-diol-1,2-epoxide isomers of dibenz[a,h]anthraceneInteraction of benzo[a]pyrene diol epoxide isomers with human serum albumin: Site specific characterisation of adducts and associated kinetics.Dose-dependent differences in the profile of mutations induced by an ultimate carcinogen from benzo[a]pyrene.
P2860
Q28748797-B751DF8D-1C0B-4AD6-94CC-7886BDC6CA55Q28756561-A0FC1014-D81A-4DDA-A32A-9095C4B552C7Q28757050-56E7536B-768B-4217-A19B-ACEFB60F1263Q28757533-84D60DFB-CAD7-4D73-A47E-E79E9C8ABC4EQ30492256-34539DD6-F484-4D76-A51C-E7789116A6FAQ30535279-5E01CA05-2675-4B1F-85B0-9C0188A271D0Q30855026-F33C6A25-0E2C-40A2-A8CC-085F4C038EAAQ33608768-E66D0763-C5CA-43A0-8049-C87147E93BA9Q33972171-3F526855-7EAB-4F9F-B8DF-6B1E0C294D56Q34050632-C43B725B-0612-443B-B372-C2F70AD83858Q34087170-61615FA8-5B03-48D3-824A-FB4581ECC0B0Q34143686-DA1FCF90-2713-4C48-87EE-B8818C9F9CDBQ34196447-74AAFB38-2602-4D7E-836E-49C5CE33A17BQ34294319-AC5F75DE-1BDF-47C2-8B67-9952C1F7D70DQ34373549-625B2EB5-A3C1-44D1-BFF0-61C29D585363Q34454503-A2DCDEF0-EF59-4D15-9166-F2395CB6D195Q34467367-95ACE2F2-7230-46D6-A013-FFA9E9C9A5F1Q34475702-F17CCD2A-F9B6-4EDC-874C-BFE2A7AA4012Q34758339-C4915B16-8D8B-49F5-9394-3668010A5A34Q34963548-856873EA-A1AC-4A35-A150-A25A15235D48Q35035718-86F2F88A-C38D-4B60-BA9D-EF5304D81630Q35045383-50C03FB9-3DCD-4C54-BD82-D8353448C8A4Q35047219-B79AC356-39C3-4370-9216-9EDDD237094DQ35121667-3EE19812-EC59-43E2-8CCC-01C8FEB1F794Q35419793-03542348-90F4-476E-9EA7-4CAF537D882FQ35781834-F477ECE1-C2BC-4E93-BEF3-44CE5DFB00ADQ35935765-7FB321EE-D8C7-41F3-BF35-B21FB308E8B1Q36021210-5C78663D-106E-4A47-966E-C505E07F5E79Q36128060-E45377E7-02A9-496D-A1F5-D79FDC97C7B1Q36314384-14542BF6-A651-4451-9E59-CB3F274B2CC6Q36320140-DCFC6EA8-2837-4DA0-9D87-087736EE5727Q36350970-5CC3892C-C5B4-4F22-97BF-20BAA7D34320Q36401135-627EF308-FE1E-4A2B-847B-67B4F34DC457Q36412573-CAB7E2F9-D466-4290-B750-B6DCE145F5A2Q36605316-3F35343D-3A4B-4737-A6A9-1E79F680A096Q36868866-1A9FF28F-B2A0-4AE3-BBA4-6C265E00CC1AQ37068704-914F2E67-9942-4CBA-AD6F-E41E22BE56F9Q37151648-24C6AE0B-AA76-456E-9B5E-F99C92B1D881Q37386205-FFDCF1ED-7FA3-4F6C-B539-1CE35B89FCD1Q37643551-C0B76703-7AFA-497A-9C24-42F80E41AF3F
P2860
Tumorigenicity of the optical enantiomers of the diastereomeric benzo[a]pyrene 7,8-diol-9,10-epoxides in newborn mice: exceptional activity of (+)-7beta,8alpha-dihydroxy-9alpha,10alpha-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene.
description
1978 nî lūn-bûn
@nan
1978年の論文
@ja
1978年学术文章
@wuu
1978年学术文章
@zh-cn
1978年学术文章
@zh-hans
1978年学术文章
@zh-my
1978年学术文章
@zh-sg
1978年學術文章
@yue
1978年學術文章
@zh
1978年學術文章
@zh-hant
name
Tumorigenicity of the optical ...... 9,10-tetrahydrobenzo[a]pyrene.
@en
Tumorigenicity of the optical ...... 9,10-tetrahydrobenzo[a]pyrene.
@nl
type
label
Tumorigenicity of the optical ...... 9,10-tetrahydrobenzo[a]pyrene.
@en
Tumorigenicity of the optical ...... 9,10-tetrahydrobenzo[a]pyrene.
@nl
prefLabel
Tumorigenicity of the optical ...... 9,10-tetrahydrobenzo[a]pyrene.
@en
Tumorigenicity of the optical ...... 9,10-tetrahydrobenzo[a]pyrene.
@nl
P2093
P2860
P356
P1476
Tumorigenicity of the optical ...... 9,10-tetrahydrobenzo[a]pyrene.
@en
P2093
Buening MK
Thakker DR
Wislocki PG
P2860
P304
P356
10.1073/PNAS.75.11.5358
P407
P577
1978-11-01T00:00:00Z