scholarly article | Q13442814 |
P2093 | author name string | C W Lawrence | |
A Borden | |||
S K Banerjee | |||
J E LeClerc | |||
P2860 | cites work | Exonuclease III of Escherichia coli K-12, an AP endonuclease | Q28263572 |
Mutagenesis by apurinic/apyrimidinic sites | Q28300337 | ||
Bypass and termination at apurinic sites during replication of single-stranded DNA in vitro: a model for apurinic site mutagenesis | Q33631558 | ||
Frequency and spectrum of mutations produced by a single cis-syn thymine-thymine cyclobutane dimer in a single-stranded vector | Q33663733 | ||
Mutational specificity of depurination | Q36252034 | ||
Infidelity of DNA synthesis associated with bypass of apurinic sites | Q37601868 | ||
The role of DNA polymerase in base substitution mutagenesis on non-instructional templates. | Q41545962 | ||
Nucleotide insertion kinetics opposite abasic lesions in DNA. | Q52463152 | ||
Oligodeoxynucleotides containing synthetic abasic sites. Model substrates for DNA polymerases and apurinic/apyrimidinic endonucleases. | Q54763221 | ||
Possible reason for the preferential insertion of adenine opposite abasic lesions in DNA | Q68088975 | ||
Depurination-induced infidelity of deoxyribonucleic acid synthesis with purified deoxyribonucleic acid replication proteins in vitro | Q70261828 | ||
Insertion of nucleotides opposite apurinic/apyrimidinic sites in deoxyribonucleic acid during in vitro synthesis: uniqueness of adenine nucleotides | Q70288775 | ||
Uracil-DNA glycosylase from Escherichia coli | Q72133876 | ||
P433 | issue | 8 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 2153-2157 | |
P577 | publication date | 1990-04-01 | |
P1433 | published in | Nucleic Acids Research | Q135122 |
P1476 | title | Mutation frequency and spectrum resulting from a single abasic site in a single-stranded vector | |
P478 | volume | 18 |
Q34974947 | (5'S)-8,5'-cyclo-2'-deoxyguanosine is a strong block to replication, a potent pol V-dependent mutagenic lesion, and is inefficiently repaired in Escherichia coli |
Q40900588 | 2'-deoxyribonolactone lesion produces G->A transitions in Escherichia coli |
Q40395159 | 8-Hydroxyadenine (7, 8-dihydro-8-Oxoadenine) induces misincorporation inin vitroDNA synthesis and mutations in NIH 3T3 cells |
Q48031487 | A broadening view of recombinational DNA repair in bacteria |
Q37592326 | A comprehensive comparison of DNA replication past 2-deoxyribose and its tetrahydrofuran analog in Escherichia coli |
Q40535788 | A mechanism for deletion formation in DNA by human cell extracts: the involvement of short sequence repeats |
Q34978281 | A novel method for site specific introduction of single model oxidative DNA lesions into oligodeoxyribonucleotides |
Q35600177 | A phenotype for enigmatic DNA polymerase II: a pivotal role for pol II in replication restart in UV-irradiated Escherichia coli |
Q59049012 | A specific partner for abasic damage in DNA |
Q34603971 | A viral genome containing an unstable aflatoxin B1-N7-guanine DNA adduct situated at a unique site |
Q44525342 | Abasic translesion synthesis by DNA polymerase beta violates the "A-rule". Novel types of nucleotide incorporation by human DNA polymerase beta at an abasic lesion in different sequence contexts |
Q37296938 | Activity of the purified mutagenesis proteins UmuC, UmuD', and RecA in replicative bypass of an abasic DNA lesion by DNA polymerase III |
Q72072434 | Age-related studies on the removal of 7-methylguanine from DNA of mouse kidney tissue following N-methyl-N-nitrosourea treatment |
Q48120327 | Aging affects the levels of DNA damage in postmitotic cells |
Q41859576 | Alkylating agents induce UVM, a recA-independent inducible mutagenic phenomenon in Escherichia coli |
Q42590944 | Amino acid architecture that influences dNTP insertion efficiency in Y-family DNA polymerase V of E. coli |
Q40533907 | An abasic site analogue activates a c-Ha-ras gene by a point mutation at modified and adjacent positions |
Q33771455 | Analysis of damage tolerance pathways in Saccharomyces cerevisiae: a requirement for Rev3 DNA polymerase in translesion synthesis |
Q71265026 | Analysis of the mutagenic properties of the UmuDC, MucAB and RumAB proteins, using a site-specific abasic lesion |
Q24816897 | Base excision repair intermediates are mutagenic in mammalian cells |
Q40903454 | Biochemical basis of DNA replication fidelity |
Q36275662 | Biochemical basis of SOS-induced mutagenesis in Escherichia coli: reconstitution of in vitro lesion bypass dependent on the UmuD'2C mutagenic complex and RecA protein. |
Q33649960 | Biological properties of single chemical-DNA adducts: a twenty year perspective |
Q54343723 | CE analysis and molecular characterisation of depurinated DNA samples. |
Q38630779 | Characterization of Escherichia coli UmuC active-site loops identifies variants that confer UV hypersensitivity |
Q33649473 | Chemical Biology of N5-Substituted Formamidopyrimidine DNA Adducts. |
Q37933191 | Chemistry and structural biology of DNA damage and biological consequences |
Q27679295 | Contribution of Partial Charge Interactions and Base Stacking to the Efficiency of Primer Extension at and beyond Abasic Sites in DNA |
Q33885426 | Coping with replication 'train wrecks' in Escherichia coli using Pol V, Pol II and RecA proteins |
Q27654769 | DNA Synthesis across an Abasic Lesion by Human DNA Polymerase ι |
Q27666331 | DNA Synthesis across an Abasic Lesion by Yeast Rev1 DNA Polymerase |
Q41115177 | DNA damage induced by 3-chloro-4-(dichloromethyl)-5-hydroxy-2[5H]-furanone (MX) in HL-60 cells and purified DNA in vitro |
Q40957239 | DNA damage induced by the drinking water mutagen 3-chloro-4-(dichloromethyl)-5-hydroxy-2[5H]-furanone (MX) in mammalian cells in vitro and in mice |
Q33984301 | DNA damage-induced mutation: tolerance via translesion synthesis |
Q40645423 | DNA damages processed by base excision repair: biological consequences |
Q24532905 | DNA polymerase II of Escherichia coli in the bypass of abasic sites in vivo |
Q36593556 | DNA polymerase λ inactivation by oxidized abasic sites. |
Q53941431 | DNA repair: getting past a lesion - at a cost. |
Q37367743 | Depurination of N7-methylguanine by DNA glycosylase AlkD is dependent on the DNA backbone |
Q34397180 | Difference between deoxyribose- and tetrahydrofuran-type abasic sites in the in vivo mutagenic responses in yeast |
Q36421100 | Effects of abasic sites and DNA single-strand breaks on prokaryotic RNA polymerases |
Q78482138 | Error-free recombinational repair predominates over mutagenic translesion replication in E. coli |
Q34053164 | Factors that influence the mutagenic patterns of DNA adducts from chemical carcinogens |
Q34957121 | High-fidelity in vivo replication of DNA base shape mimics without Watson-Crick hydrogen bonds. |
Q24631768 | Historical overview: searching for replication help in all of the rec places |
Q34588314 | Homologous recombination prevents methylation-induced toxicity in Escherichia coli |
Q38297797 | In vivo and in vitro replication consequences of stereoisomeric benzo[a]pyrene-7,8-dihydrodiol 9,10-epoxide adducts on adenine N6 at the second position of N-ras codon 61. |
Q33786642 | In vivo repair of methylation damage in Aag 3-methyladenine DNA glycosylase null mouse cells |
Q52859883 | Influence of DNA repair defects (rad1, rad52) on nitrogen mustard mutagenesis in yeast. |
Q73293902 | Introduction, distribution, and removal of 7-methylguanine in different liver chromatin fractions of young and old mice |
Q35968216 | Isolation and characterization of novel plasmid-encoded umuC mutants |
Q44007612 | Kinetics of deoxyribonucleotide insertion and extension at abasic template lesions in different sequence contexts using HIV-1 reverse transcriptase |
Q27667194 | Learning from directed evolution: Thermus aquaticus DNA polymerase mutants with translesion synthesis activity |
Q34385155 | Lesion bypass DNA polymerases replicate across non-DNA segments |
Q34834214 | Mechanism of mutation on DNA templates containing synthetic abasic sites: study with a double strand vector |
Q54357348 | Modulating the pKa of a tyrosine in KlenTaq DNA polymerase that is crucial for abasic site bypass by in vivo incorporation of a non-canonical amino acid. |
Q77363798 | Modulation of the toxic and mutagenic effects induced by methyl methanesulfonate in Chinese hamster ovary cells by overexpression of the rat N-alkylpurine-DNA glycosylase |
Q40401348 | Molecular basis of nitrogen mustard effects on transcription processes: role of depurination |
Q34603875 | Mutagenesis and more: umuDC and the Escherichia coli SOS response |
Q33770262 | Mutagenesis in eukaryotes dependent on DNA polymerase zeta and Rev1p |
Q40486483 | Mutagenesis induced by single UV photoproducts in E. coli and yeast |
Q35044983 | Mutagenic potentials of damaged nucleic acids produced by reactive oxygen/nitrogen species: approaches using synthetic oligonucleotides and nucleotides: survey and summary |
Q34596843 | Mutagenicity of a unique thymine-thymine dimer or thymine-thymine pyrimidine pyrimidone (6-4) photoproduct in mammalian cells |
Q74000691 | Mutation spectra induced by replication of two vicinal oxidative DNA lesions in mammalian cells |
Q39716050 | Mutation spectra of TA*, the major photoproduct of thymidylyl-(3'5')-deoxyadenosine, in Escherichia coli under SOS conditions |
Q41534370 | Mutation-spectrum of a true abasic site in codon 12 of a c-Ha-ras gene in mammalian cells |
Q34733163 | Mutational properties of the primary aflatoxin B1-DNA adduct |
Q36446106 | Mutational specificity and genetic control of replicative bypass of an abasic site in yeast |
Q54562350 | Mutational specificity of glyoxal, a product of DNA oxidation, in the lacI gene of wild-type Escherichia coli W3110. |
Q33933756 | Mutational spectra for polycyclic aromatic hydrocarbons in the supF target gene |
Q43597497 | Mutations induced by 5-formyl-2'-deoxyuridine in Escherichia coli include base substitutions that can arise from mispairs of 5-formyluracil with guanine, cytosine and thymine |
Q41076125 | Mutations induced by monofunctional and bifunctional phosphoramide mustards in supF tRNA gene |
Q35013048 | New structural and mechanistic insight into the A-rule and the instructional and non-instructional behavior of DNA photoproducts and other lesions |
Q37033853 | Nucleosome core particle-catalyzed strand scission at abasic sites |
Q38299823 | On the mechanism of preferential incorporation of dAMP at abasic sites in translesional DNA synthesis. Role of proofreading activity of DNA polymerase and thermodynamic characterization of model template-primers containing an abasic site |
Q39112035 | Propylene oxide mutagenesis at template cytosine residues |
Q46467417 | Purification and characterization of Escherichia coli DNA polymerase V. |
Q38828283 | Quality control of chemically damaged RNA. |
Q34609286 | Quantifying the energetic contributions of desolvation and π-electron density during translesion DNA synthesis |
Q34020161 | Quantitative measurement of translesion replication in human cells: evidence for bypass of abasic sites by a replicative DNA polymerase |
Q29619755 | Recombinational repair of DNA damage in Escherichia coli and bacteriophage lambda |
Q40430413 | Repair of chromosomal abasic sites in vivo involves at least three different repair pathways |
Q39719038 | Replication bypass and mutagenic effect of alpha-deoxyadenosine site-specifically incorporated into single-stranded vectors |
Q42266829 | Replication of an oxidized abasic site in Escherichia coli by a dNTP-stabilized misalignment mechanism that reads upstream and downstream nucleotides |
Q40810156 | Replication of damaged DNA and the molecular mechanism of ultraviolet light mutagenesis |
Q27660600 | Replication through an abasic DNA lesion: structural basis for adenine selectivity |
Q35255862 | Replicative bypass of abasic site in Escherichia coli and human cells: similarities and differences |
Q24631035 | Roles of DNA polymerases V and II in SOS-induced error-prone and error-free repair in Escherichia coli |
Q41734679 | Roles of E. coli DNA polymerases IV and V in lesion-targeted and untargeted SOS mutagenesis |
Q39494487 | SOS and UVM pathways have lesion-specific additive and competing effects on mutation fixation at replication-blocking DNA lesions. |
Q40797739 | SOS mutagenesis |
Q28271489 | SOS-regulated proteins in translesion DNA synthesis and mutagenesis |
Q36072617 | Skiing the black diamond slope: progress on the biochemistry of translesion DNA synthesis |
Q36646366 | Strand-biased cytosine deamination at the replication fork causes cytosine to thymine mutations in Escherichia coli. |
Q35606437 | Substitution of mucAB or rumAB for umuDC alters the relative frequencies of the two classes of mutations induced by a site-specific T-T cyclobutane dimer and the efficiency of translesion DNA synthesis |
Q36713807 | Synthesis and analysis of oligonucleotides containing abasic site analogues |
Q42634477 | T-T cyclobutane dimers are misinstructive, rather than non-instructive, mutagenic lesions |
Q24531220 | The aflatoxin B(1) formamidopyrimidine adduct plays a major role in causing the types of mutations observed in human hepatocellular carcinoma |
Q36729830 | The beta subunit sliding DNA clamp is responsible for unassisted mutagenic translesion replication by DNA polymerase III holoenzyme |
Q34206346 | The chemistry and biology of aflatoxin B(1): from mutational spectrometry to carcinogenesis |
Q34186298 | The expanding polymerase universe |
Q36099447 | The frequency and accuracy of replication past a thymine-thymine cyclobutane dimer are very different in Saccharomyces cerevisiae and Escherichia coli |
Q34390593 | The major human abasic endonuclease: formation, consequences and repair of abasic lesions in DNA. |
Q31422789 | The mutagenesis protein UmuC is a DNA polymerase activated by UmuD', RecA, and SSB and is specialized for translesion replication |
Q77231587 | The mutagenesis proteins UmuD' and UmuC prevent lethal frameshifts while increasing base substitution mutations |
Q40645425 | The study of responses to 'model' DNA breaks induced by restriction endonucleases in cells and cell-free systems: achievements and difficulties |
Q37612232 | The thymine-thymine pyrimidine-pyrimidone(6-4) ultraviolet light photoproduct is highly mutagenic and specifically induces 3' thymine-to-cytosine transitions in Escherichia coli |
Q33933749 | Toward an understanding of the role of DNA adduct conformation in defining mutagenic mechanism based on studies of the major adduct (formed at N(2)-dG) of the potent environmental carcinogen, benzo[a]pyrene |
Q54646341 | Transcription by T7 RNA polymerase of DNA containing abasic sites. |
Q34509062 | Translesion DNA Synthesis |
Q54565641 | Translesional synthesis on DNA templates containing a single abasic site. A mechanistic study of the "A rule". |
Q34999025 | U-U and T-T cyclobutane dimers have different mutational properties |
Q41828200 | Unraveling the aflatoxin-FAPY conundrum: structural basis for differential replicative processing of isomeric forms of the formamidopyrimidine-type DNA adduct of aflatoxin B1. |
Search more.