| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1146/ANNUREV.GENET.37.042203.132748 |
| P953 | full work available at URL | https://www.annualreviews.org/doi/pdf/10.1146/annurev.genet.37.042203.132748 |
| P698 | PubMed publication ID | 14616055 |
| P5875 | ResearchGate publication ID | 9010475 |
| P2093 | author name string | Jeffrey N. Strathern | |
| Alison J. Rattray | |||
| P2860 | cites work | Cancer Research | Q326097 |
| The yeast Saccharomyces cerevisiae DNA polymerase IV: possible involvement in double strand break DNA repair | Q35009312 | ||
| poliota-dependent lesion bypass in vitro | Q35013038 | ||
| Functions of human DNA polymerases eta, kappa and iota suggested by their properties, including fidelity with undamaged DNA templates. | Q35047056 | ||
| UmuD'(2)C is an error-prone DNA polymerase, Escherichia coli pol V. | Q35588920 | ||
| A phenotype for enigmatic DNA polymerase II: a pivotal role for pol II in replication restart in UV-irradiated Escherichia coli | Q35600177 | ||
| The topoisomerase-related function gene TRF4 affects cellular sensitivity to the antitumor agent camptothecin | Q22009054 | ||
| Cloning and chromosomal mapping of the human DNA polymerase theta (POLQ), the eighth human DNA polymerase | Q22010228 | ||
| hRAD30 mutations in the variant form of xeroderma pigmentosum | Q22010237 | ||
| The human REV1 gene codes for a DNA template-dependent dCMP transferase | Q22010721 | ||
| Mutation enhancement by DINB1, a mammalian homologue of the Escherichia coli mutagenesis protein dinB | Q22011012 | ||
| Eukaryotic DNA Polymerases | Q22065416 | ||
| Two novel human and mouse DNA polymerases of the polX family | Q24290234 | ||
| Complementation of defective translesion synthesis and UV light sensitivity in xeroderma pigmentosum variant cells by human and mouse DNA polymerase eta | Q24515346 | ||
| The processivity factor beta controls DNA polymerase IV traffic during spontaneous mutagenesis and translesion synthesis in vivo | Q24522537 | ||
| Second pathway for completion of human DNA base excision-repair: reconstitution with purified proteins and requirement for DNase IV (FEN1). | Q24532243 | ||
| DNA polymerase II of Escherichia coli in the bypass of abasic sites in vivo | Q24532905 | ||
| Human DINB1-encoded DNA polymerase kappa is a promiscuous extender of mispaired primer termini | Q24534772 | ||
| Altered nucleotide misinsertion fidelity associated with poliota-dependent replication at the end of a DNA template. | Q24535441 | ||
| Unique misinsertion specificity of poliota may decrease the mutagenic potential of deaminated cytosines | Q24535948 | ||
| Stimulation of DNA synthesis activity of human DNA polymerase kappa by PCNA. | Q24537135 | ||
| Association of DNA polymerase mu (pol mu) with Ku and ligase IV: role for pol mu in end-joining double-strand break repair | Q24540101 | ||
| Role of human DNA polymerase kappa as an extender in translesion synthesis | Q24541478 | ||
| Physical and functional interactions of human DNA polymerase eta with PCNA | Q24548300 | ||
| Adaptive mutation: implications for evolution | Q24623723 | ||
| Multiple pathways for SOS-induced mutagenesis in Escherichia coli: an overexpression of dinB/dinP results in strongly enhancing mutagenesis in the absence of any exogenous treatment to damage DNA | Q24628966 | ||
| Association of terminal deoxynucleotidyl transferase with Ku | Q24642971 | ||
| Overexpression of DNA polymerase beta in cell results in a mutator phenotype and a decreased sensitivity to anticancer drugs | Q24644933 | ||
| The function of the human homolog of Saccharomyces cerevisiae REV1 is required for mutagenesis induced by UV light | Q24681973 | ||
| Activation-induced cytidine deaminase deaminates deoxycytidine on single-stranded DNA but requires the action of RNase | Q24683335 | ||
| The human DINB1 gene encodes the DNA polymerase Poltheta | Q24683573 | ||
| Structure of the catalytic core of S. cerevisiae DNA polymerase eta: implications for translesion DNA synthesis | Q27634744 | ||
| Deoxycytidyl transferase activity of yeast REV1 protein | Q27931173 | ||
| Specificity of DNA lesion bypass by the yeast DNA polymerase eta. | Q27933149 | ||
| Efficient and accurate replication in the presence of 7,8-dihydro-8-oxoguanine by DNA polymerase eta. | Q27934276 | ||
| Yeast DNA polymerase zeta (zeta) is essential for error-free replication past thymine glycol | Q27934657 | ||
| A physical and functional interaction between yeast Pol4 and Dnl4-Lif1 links DNA synthesis and ligation in nonhomologous end joining | Q27935436 | ||
| Efficient bypass of a thymine-thymine dimer by yeast DNA polymerase, Poleta | Q27935465 | ||
| Interaction with PCNA is essential for yeast DNA polymerase eta function | Q27935721 | ||
| UV mutagenesis in radiation-sensitive strains of yeast | Q27936517 | ||
| Distinct roles for Rev1p and Rev7p during translesion synthesis in Saccharomyces cerevisiae | Q27936722 | ||
| RAD6-dependent DNA repair is linked to modification of PCNA by ubiquitin and SUMO. | Q27937465 | ||
| Removal of nonhomologous DNA ends in double-strand break recombination: the role of the yeast ultraviolet repair gene RAD1 | Q27937863 | ||
| Thymine-thymine dimer bypass by yeast DNA polymerase zeta | Q27938043 | ||
| Role of RecA protein in untargeted UV mutagenesis of bacteriophage lambda: evidence for the requirement for the dinB gene | Q35608675 | ||
| The Ig mutator is dependent on the presence, position, and orientation of the large intron enhancer | Q35917705 | ||
| Checkpoint activation regulates mutagenic translesion synthesis | Q35963618 | ||
| The translesion DNA polymerase zeta plays a major role in Ig and bcl-6 somatic hypermutation. | Q36248087 | ||
| The role of transient hypermutators in adaptive mutation in Escherichia coli | Q36384221 | ||
| Expression of error-prone polymerases in BL2 cells activated for Ig somatic hypermutation | Q36533627 | ||
| Cloning of terminal transferase cDNA by antibody screening | Q36586899 | ||
| Mutagenesis by third-strand-directed psoralen adducts in repair-deficient human cells: high frequency and altered spectrum in a xeroderma pigmentosum variant | Q36796836 | ||
| Stationary-phase mutation in the bacterial chromosome: recombination protein and DNA polymerase IV dependence | Q37096423 | ||
| Accuracy of lesion bypass by yeast and human DNA polymerase eta. | Q37097247 | ||
| The thymine-thymine pyrimidine-pyrimidone(6-4) ultraviolet light photoproduct is highly mutagenic and specifically induces 3' thymine-to-cytosine transitions in Escherichia coli | Q37612232 | ||
| Yeast Rev1 protein is a G template-specific DNA polymerase | Q38291977 | ||
| Differential gene expression in human cancer cells resistant to cisplatin | Q38777017 | ||
| Translesion synthesis by yeast DNA polymerase zeta from templates containing lesions of ultraviolet radiation and acetylaminofluorene | Q39095697 | ||
| Preferential incorporation of G opposite template T by the low-fidelity human DNA polymerase iota | Q39455619 | ||
| Highly frequent frameshift DNA synthesis by human DNA polymerase mu | Q39529040 | ||
| Terminal deoxynucleotidyl transferase catalyzes the reaction of DNA phosphorylation | Q39542477 | ||
| Formation of an F' plasmid by recombination between imperfectly repeated chromosomal Rep sequences: a closer look at an old friend (F'(128) pro lac). | Q39714248 | ||
| Depletion of the cellular amounts of the MutS and MutH methyl-directed mismatch repair proteins in stationary-phase Escherichia coli K-12 cells | Q39841075 | ||
| Ultraviolet-induced reversion of cyc1 alleles in radiation-sensitive strains of yeast. I. rev1 Mutant strains | Q40160734 | ||
| DNA polymerase mu (Pol mu), homologous to TdT, could act as a DNA mutator in eukaryotic cells | Q40410915 | ||
| AID is essential for immunoglobulin V gene conversion in a cultured B cell line | Q40746479 | ||
| Ablation of XRCC2/3 transforms immunoglobulin V gene conversion into somatic hypermutation | Q40782991 | ||
| Increased transcription levels induce higher mutation rates in a hypermutating cell line | Q40814374 | ||
| Cell-cycle-regulated DNA double-stranded breaks in somatic hypermutation of immunoglobulin genes | Q40840741 | ||
| Isolation and characterization of mutants of Escherichia coli deficient in induction of mutations by ultraviolet light | Q40850491 | ||
| Identification and characterization of human DNA polymerase beta 2, a DNA polymerase beta -related enzyme | Q40869398 | ||
| The lyase activity of the DNA repair protein beta-polymerase protects from DNA-damage-induced cytotoxicity | Q40871857 | ||
| Role of DNA polymerase beta in the excision step of long patch mammalian base excision repair | Q40955413 | ||
| Uvm mutants of Escherichia coli K12 deficient in UV mutagenesis. I. Isolation of uvm mutants and their phenotypical characterization in DNA repair and mutagenesis | Q40958827 | ||
| Mice lacking terminal deoxynucleotidyl transferase: adult mice with a fetal antigen receptor repertoire | Q41126132 | ||
| A sensitive genetic assay for the detection of cytosine deamination: determination of rate constants and the activation energy | Q41203605 | ||
| The mechanism of untargeted mutagenesis in UV-irradiated yeast | Q41618996 | ||
| Roles of E. coli DNA polymerases IV and V in lesion-targeted and untargeted SOS mutagenesis | Q41734679 | ||
| Xeroderma pigmentosum variant (XP-V) correcting protein from HeLa cells has a thymine dimer bypass DNA polymerase activity | Q41869549 | ||
| The Escherichia coli polB locus is identical to dinA, the structural gene for DNA polymerase II. Characterization of Pol II purified from a polB mutant | Q42652215 | ||
| The activation-induced deaminase functions in a postcleavage step of the somatic hypermutation process | Q42944711 | ||
| DNA double-strand breaks: prior to but not sufficient in targeting hypermutation | Q42944715 | ||
| Levels of chromosomally encoded Umu proteins and requirements for in vivo UmuD cleavage | Q43432570 | ||
| Terminal deoxynucleotidyl transferase indiscriminately incorporates ribonucleotides and deoxyribonucleotides | Q43640424 | ||
| Roles of chromosomal and episomal dinB genes encoding DNA pol IV in targeted and untargeted mutagenesis in Escherichia coli. | Q43781879 | ||
| Expression of human and mouse genes encoding polkappa: testis-specific developmental regulation and AhR-dependent inducible transcription | Q43815506 | ||
| Efficiency and accuracy of SOS-induced DNA polymerases replicating benzo[a]pyrene-7,8-diol 9,10-epoxide A and G adducts | Q43816434 | ||
| Mistranslation induced by streptomycin provokes a RecABC/RuvABC-dependent mutator phenotype in Escherichia coli cells | Q43866930 | ||
| Repair of cyclobutyl pyrimidine dimers in human skin: variability among normal humans in nucleotide excision and in photorepair | Q44122773 | ||
| Lesion bypass activities of human DNA polymerase mu. | Q44135115 | ||
| DNA polymerase III from Escherichia coli cells expressing mutA mistranslator tRNA is error-prone | Q44153069 | ||
| Benzo[a]pyrene diol epoxide-deoxyguanosine adducts are accurately bypassed by yeast DNA polymerase zeta in vitro | Q44179104 | ||
| Immunoglobulin isotype switching is inhibited and somatic hypermutation perturbed in UNG-deficient mice | Q44194766 | ||
| 5'-Deoxyribose phosphate lyase activity of human DNA polymerase iota in vitro | Q33938237 | ||
| The "tale" of UmuD and its role in SOS mutagenesis | Q33957289 | ||
| Two enzymes, both of which process recombination intermediates, have opposite effects on adaptive mutation in Escherichia coli. | Q33966542 | ||
| The SOS response: recent insights into umuDC-dependent mutagenesis and DNA damage tolerance | Q34090796 | ||
| Eukaryotic DNA polymerases: proposal for a revised nomenclature. | Q34093113 | ||
| Correlation of somatic hypermutation specificity and A-T base pair substitution errors by DNA polymerase eta during copying of a mouse immunoglobulin kappa light chain transgene. | Q34098247 | ||
| Error-prone repair DNA polymerases in prokaryotes and eukaryotes | Q34131455 | ||
| DNA polymerase theta purified from human cells is a high-fidelity enzyme | Q34132140 | ||
| Human DNA polymerase kappa bypasses and extends beyond thymine glycols during translesion synthesis in vitro, preferentially incorporating correct nucleotides | Q34141563 | ||
| Induction of somatic hypermutation in immunoglobulin genes is dependent on DNA polymerase iota. | Q34157224 | ||
| Localisation of human DNA polymerase kappa to replication foci | Q34157610 | ||
| hREV3 is essential for error-prone translesion synthesis past UV or benzo[a]pyrene diol epoxide-induced DNA lesions in human fibroblasts | Q34161894 | ||
| Damage repair DNA polymerases Y. | Q34176729 | ||
| DNA damage control by novel DNA polymerases: translesion replication and mutagenesis | Q34260300 | ||
| Hydrocephalus, situs inversus, chronic sinusitis, and male infertility in DNA polymerase lambda-deficient mice: possible implication for the pathogenesis of immotile cilia syndrome | Q34277881 | ||
| Lack of N regions in antigen receptor variable region genes of TdT-deficient lymphocytes | Q34353297 | ||
| Mice lacking TdT: mature animals with an immature lymphocyte repertoire | Q34353306 | ||
| Polkappa protects mammalian cells against the lethal and mutagenic effects of benzo[a]pyrene | Q34387678 | ||
| Adaptive mutations, mutator DNA polymerases and genetic change strategies of pathogens | Q34392595 | ||
| Clamp loader structure predicts the architecture of DNA polymerase III holoenzyme and RFC. | Q34446488 | ||
| Neonatal lethality with abnormal neurogenesis in mice deficient in DNA polymerase beta | Q34668670 | ||
| Translesion DNA synthesis in eukaryotes: a one- or two-polymerase affair | Q34770150 | ||
| Polymerase mu is a DNA-directed DNA/RNA polymerase | Q34784888 | ||
| Efficient processing of DNA ends during yeast nonhomologous end joining. Evidence for a DNA polymerase beta (Pol4)-dependent pathway | Q27938668 | ||
| The Saccharomyces cerevisiae RAD30 gene, a homologue of Escherichia coli dinB and umuC, is DNA damage inducible and functions in a novel error-free postreplication repair mechanism | Q27938714 | ||
| Role of DNA polymerase eta in the bypass of a (6-4) TT photoproduct | Q27939380 | ||
| The fifth essential DNA polymerase phi in Saccharomyces cerevisiae is localized to the nucleolus and plays an important role in synthesis of rRNA | Q27939424 | ||
| The XPV (xeroderma pigmentosum variant) gene encodes human DNA polymerase eta | Q28115711 | ||
| Novel human and mouse homologs of Saccharomyces cerevisiae DNA polymerase eta | Q28116380 | ||
| Transcription-targeted DNA deamination by the AID antibody diversification enzyme | Q28190732 | ||
| DNA polymerase beta expression differences in selected human tumors and cell lines | Q28198269 | ||
| The role of polymerase eta in somatic hypermutation determined by analysis of mutations in a patient with xeroderma pigmentosum variant | Q28203111 | ||
| Human DNA polymerase lambda functionally and physically interacts with proliferating cell nuclear antigen in normal and translesion DNA synthesis | Q28205678 | ||
| Mechanism of DNA polymerase II-mediated frameshift mutagenesis | Q28205789 | ||
| Identification of an intrinsic 5'-deoxyribose-5-phosphate lyase activity in human DNA polymerase lambda: a possible role in base excision repair | Q28207004 | ||
| Error rate and specificity of human and murine DNA polymerase eta | Q28216092 | ||
| Rate of depurination of native deoxyribonucleic acid | Q28243811 | ||
| Human DNA polymerase beta initiates DNA synthesis during long-patch repair of reduced AP sites in DNA | Q28360244 | ||
| AID is required to initiate Nbs1/gamma-H2AX focus formation and mutations at sites of class switching | Q28366125 | ||
| Specific expression of activation-induced cytidine deaminase (AID), a novel member of the RNA-editing deaminase family in germinal center B cells | Q28509339 | ||
| DNA polymerase lambda (Pol lambda), a novel eukaryotic DNA polymerase with a potential role in meiosis | Q28586606 | ||
| Distinct and opposite diversifying activities of terminal transferase splice variants | Q28587746 | ||
| Specific interaction of DNA polymerase beta and DNA ligase I in a multiprotein base excision repair complex from bovine testis | Q28645719 | ||
| Error-free and error-prone lesion bypass by human DNA polymerase kappa in vitro | Q28646677 | ||
| Hypermutation in derepressed operons of Escherichia coli K12 | Q28776505 | ||
| The Y-family of DNA polymerases | Q29615308 | ||
| Eukaryotic polymerases iota and zeta act sequentially to bypass DNA lesions | Q29619958 | ||
| Pol kappa: A DNA polymerase required for sister chromatid cohesion. | Q30305921 | ||
| Evidence that replication fork components catalyze establishment of cohesion between sister chromatids | Q30454198 | ||
| DNA polymerase beta-like nucleotidyltransferase superfamily: identification of three new families, classification and evolutionary history | Q30559537 | ||
| Targeting of human DNA polymerase iota to the replication machinery via interaction with PCNA. | Q30769976 | ||
| The mutagenesis protein UmuC is a DNA polymerase activated by UmuD', RecA, and SSB and is specialized for translesion replication | Q31422789 | ||
| A model for SOS-lesion-targeted mutations in Escherichia coli | Q32001102 | ||
| Somatic hypermutation and the three R's: repair, replication and recombination | Q33545735 | ||
| Hypermutation in bacteria and other cellular systems | Q33770256 | ||
| Analysis of damage tolerance pathways in Saccharomyces cerevisiae: a requirement for Rev3 DNA polymerase in translesion synthesis | Q33771455 | ||
| Common pathways for ultraviolet skin carcinogenesis in the repair and replication defective groups of xeroderma pigmentosum | Q33853150 | ||
| Genome-wide hypermutation in a subpopulation of stationary-phase cells underlies recombination-dependent adaptive mutation | Q33886793 | ||
| Genetics of mutagenesis in E. coli: various combinations of translesion polymerases (Pol II, IV and V) deal with lesion/sequence context diversity | Q44267628 | ||
| Translesion synthesis past platinum DNA adducts by human DNA polymerase mu. | Q44309847 | ||
| Fidelity and processivity of DNA synthesis by DNA polymerase kappa, the product of the human DINB1 gene | Q45345090 | ||
| Diploid yeast cells yield homozygous spontaneous mutations. | Q46053570 | ||
| Purification and enzymatic and functional characterization of DNA polymerase beta-like enzyme, POL4. expressed during yeast meiosis | Q46412438 | ||
| Purification and properties of wild-type and exonuclease-deficient DNA polymerase II from Escherichia coli | Q46595699 | ||
| Somatic hypermutation in the heavy chain locus correlates with transcription | Q47713194 | ||
| Molecular cloning, expression and chromosomal localisation of the mouse Rev3l gene, encoding the catalytic subunit of polymerase zeta | Q47975722 | ||
| Deletion of the Saccharomyces cerevisiae gene RAD30 encoding an Escherichia coli DinB homolog confers UV radiation sensitivity and altered mutability. | Q48033074 | ||
| Disruption of the developmentally regulated Rev3l gene causes embryonic lethality. | Q52163744 | ||
| Disruption of the Rev3l-encoded catalytic subunit of polymerase zeta in mice results in early embryonic lethality. | Q52541355 | ||
| New mutations affecting induced mutagenesis in yeast. | Q52871941 | ||
| Insertion of N regions into heavy-chain genes is correlated with expression of terminal deoxytransferase in B cells | Q53549666 | ||
| Efficient translesion replication past oxaliplatin and cisplatin GpG adducts by human DNA polymerase eta. | Q54055057 | ||
| Damage-repair error-prone polymerases of eubacteria: association with mobile genome elements. | Q54541302 | ||
| Recombination in adaptive mutation. | Q54635736 | ||
| DNA repair. The bases for Cockayne syndrome. | Q55033948 | ||
| DNA Double-Strand Breaks in Immunoglobulin Genes Undergoing Somatic Hypermutation | Q57198273 | ||
| Position-specific codon conservation in hypervariable gene families | Q57338763 | ||
| Decreased Frequency of Somatic Hypermutation and Impaired Affinity Maturation but Intact Germinal Center Formation in Mice Expressing Antisense RNA to DNA Polymerase | Q58424602 | ||
| Elements regulating somatic hypermutation of an immunoglobulin κ gene: Critical role for the intron enhancer/matrix attachment region | Q60370477 | ||
| Pathways of ultraviolet mutability in Saccharomyces cerevisiae. II. The effect of rev genes on recombination | Q69965515 | ||
| Terminal transferase: past to present | Q70259839 | ||
| Somatic hypermutation of immunoglobulin genes is linked to transcription initiation | Q70934062 | ||
| Association of increased spontaneous mutation rates with high levels of transcription in yeast | Q72304795 | ||
| Excision repair and gene orientation modulate the strand specificity of UV mutagenesis in a plasmid-borne yeast tRNA gene | Q72589153 | ||
| Effect of umuC mutations on targeted and untargeted ultraviolet mutagenesis in bacteriophage λ | Q72820392 | ||
| The dinB gene encodes a novel E. coli DNA polymerase, DNA pol IV, involved in mutagenesis | Q72994394 | ||
| Alteration of ultraviolet-induced mutagenesis in yeast through molecular modulation of the REV3 and REV7 gene expression | Q73039820 | ||
| Mismatch extension ability of yeast and human DNA polymerase eta | Q73130869 | ||
| Lesion bypass by the Escherichia coli DNA polymerase V requires assembly of a RecA nucleoprotein filament | Q73204355 | ||
| Transcription-induced cleavage of immunoglobulin switch regions by nucleotide excision repair nucleases in vitro | Q73794379 | ||
| Evidence for a second function for Saccharomyces cerevisiae Rev1p | Q74130085 | ||
| An essential role for REV3 in mammalian cell survival: absence of REV3 induces p53-independent embryonic death | Q74250699 | ||
| Multiple sequences from downstream of the J kappa cluster can combine to recruit somatic hypermutation to a heterologous, upstream mutation domain | Q74251724 | ||
| Saccharomyces cerevisiae lacking Snm1, Rev3 or Rad51 have a normal S-phase but arrest permanently in G2 after cisplatin treatment | Q74297494 | ||
| Mammalian base excision repair and DNA polymerase beta | Q74754533 | ||
| DNA polymerase lambda from calf thymus preferentially replicates damaged DNA | Q77749013 | ||
| Cutting edge: DNA polymerases mu and lambda are dispensable for Ig gene hypermutation | Q77892518 | ||
| EXO1 of Saccharomyces cerevisiae functions in mutagenesis during double-strand break repair | Q78026677 | ||
| Mammalian sperm proteins are rapidly evolving: evidence of positive selection in functionally diverse genes | Q78461393 | ||
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | genetics | Q7162 |
| P304 | page(s) | 31-66 | |
| P577 | publication date | 2003-01-01 | |
| P1433 | published in | Annual Review of Genetics | Q567358 |
| P1476 | title | Error-prone DNA polymerases: when making a mistake is the only way to get ahead | |
| Error-Prone DNA Polymerases: When Making a Mistake is the Only Way to Get Ahead | |||
| P478 | volume | 37 |
| Q39839649 | A genomic island integrated into recA of Vibrio cholerae contains a divergent recA and provides multi-pathway protection from DNA damage |
| Q34059478 | A time-invariant principle of genome evolution |
| Q31109744 | Adaptive evolution by recombination is not associated with increased mutation rates in Maize streak virus |
| Q28478172 | An active site aromatic triad in Escherichia coli DNA Pol IV coordinates cell survival and mutagenesis in different DNA damaging agents |
| Q22122015 | An integrated view of protein evolution |
| Q35049451 | Analysis of the tolerance to DNA alkylating damage in MEC1 and RAD53 checkpoint mutants of Saccharomyces cerevisiae |
| Q36397932 | BapE DNA endonuclease induces an apoptotic-like response to DNA damage in Caulobacter |
| Q33604620 | Biochemistry of Meiotic Recombination: Formation, Processing, and Resolution of Recombination Intermediates |
| Q34925302 | Biochemistry of eukaryotic homologous recombination |
| Q26827700 | Breaking bad: The mutagenic effect of DNA repair |
| Q59128454 | Constitutional mismatch repair-deficiency: current problems and emerging therapeutic strategies |
| Q28757270 | CpG dinucleotides and the mutation rate of non-CpG DNA |
| Q36193082 | DNA lesions and repair in immunoglobulin class switch recombination and somatic hypermutation |
| Q36493831 | DNA repair in antibody somatic hypermutation |
| Q36751819 | DNA replication to aid somatic hypermutation |
| Q47293650 | DNA-repair potential of Halomonas spp. from the Salt Plains Microbial Observatory of Oklahoma |
| Q35002361 | Damage-induced localized hypermutability. |
| Q54429900 | Ectopic gene conversions in bacterial genomes. |
| Q39673476 | Effect of human cell malignancy on activity of DNA polymerase ι |
| Q39294162 | Emerging roles for histone modifications in DNA excision repair |
| Q46964025 | Enzymatic synthesis of fluorescent oligomers assembled on a DNA backbone |
| Q35017866 | Escherichia coli YafP protein modulates DNA damaging property of the nitroaromatic compounds |
| Q36391958 | Estimating the per-base-pair mutation rate in the yeast Saccharomyces cerevisiae |
| Q24796773 | Evidence for interplay among yeast replicative DNA polymerases alpha, delta and epsilon from studies of exonuclease and polymerase active site mutations |
| Q64234772 | Evolutionary Origins of Pseudogenes and Their Association with Regulatory Sequences in Plants |
| Q33334428 | Highly conserved regimes of neighbor-base-dependent mutation generated the background primary-structural heterogeneities along vertebrate chromosomes |
| Q33273825 | Highly tolerated amino acid substitutions increase the fidelity of Escherichia coli DNA polymerase I. |
| Q42126464 | Involvement of Escherichia coli DNA polymerase IV in tolerance of cytotoxic alkylating DNA lesions in vivo. |
| Q37052306 | Long-term effects of inducible mutagenic DNA repair on relative fitness and phenotypic diversification in Pseudomonas cichorii 302959. |
| Q36369839 | Long-term survival during stationary phase: evolution and the GASP phenotype |
| Q36753339 | Mechanisms of disease: DNA repair defects and neurological disease |
| Q34629238 | Microhomology-mediated mechanisms underlie non-recurrent disease-causing microdeletions of the FOXL2 gene or its regulatory domain |
| Q90004212 | Mimivirus encodes a multifunctional primase with DNA/RNA polymerase, terminal transferase and translesion synthesis activities |
| Q35842713 | Multiple solutions to inefficient lesion bypass by T7 DNA polymerase. |
| Q34504886 | Mutagenesis dependent upon the combination of activation-induced deaminase expression and a double-strand break |
| Q36836977 | Mutagenic and recombinagenic responses to defective DNA polymerase delta are facilitated by the Rev1 protein in pol3-t mutants of Saccharomyces cerevisiae |
| Q103806007 | Mutation-selection balance and compensatory mechanisms in tumour evolution |
| Q47747085 | NGS-based analysis of base-substitution signatures created by yeast DNA polymerase eta and zeta on undamaged and abasic DNA templates in vitro. |
| Q44246963 | Novel evidences for a tumor suppressor role of Rev3, the catalytic subunit of Pol zeta |
| Q36687820 | Plant responses to UV radiation and links to pathogen resistance. |
| Q36960224 | Potential role of meiosis proteins in melanoma chromosomal instability |
| Q46751740 | Pre-steady-state kinetic characterization of the DinB homologue DNA polymerase of Sulfolobus solfataricus |
| Q43726885 | Protein insertions and deletions enabled by neutral roaming in sequence space |
| Q36685881 | Recombination: an underappreciated factor in the evolution of plant genomes |
| Q42407123 | Reduced levels of DNA polymerase delta induce chromosome fragile site instability in yeast |
| Q37294797 | Somatic microindels in human cancer: the insertions are highly error-prone and derive from nearby but not adjacent sense and antisense templates |
| Q46287722 | Structure-function analysis of the barley genome: the gene-rich region of chromosome 2HL. |
| Q36337954 | Suffering in silence: the tolerance of DNA damage |
| Q44577322 | Suppression of SOS repair in E. coli: possible mechanism of antimutagenicity and protective effects of common vegetables |
| Q55073069 | Synthesis and biochemical characterization of tricyclothymidine triphosphate (tc-TTP). |
| Q51215555 | Targeted nucleotide editing using hybrid prokaryotic and vertebrate adaptive immune systems. |
| Q27931291 | The 9-1-1 checkpoint clamp physically interacts with polzeta and is partially required for spontaneous polzeta-dependent mutagenesis in Saccharomyces cerevisiae |
| Q56926775 | The UV responses of bacterioneuston and bacterioplankton isolates depend on the physiological condition and involve a metabolic shift |
| Q33526473 | The contribution of recombination to heterozygosity differs among plant evolutionary lineages and life-forms. |
| Q27934540 | The in vivo characterization of translesion synthesis across UV-induced lesions in Saccharomyces cerevisiae: insights into Pol zeta- and Pol eta-dependent frameshift mutagenesis |
| Q37153771 | The mismatch repair system promotes DNA polymerase zeta-dependent translesion synthesis in yeast. |
| Q28586941 | The mouse genomic instability mutation chaos1 is an allele of Polq that exhibits genetic interaction with Atm |
| Q35062343 | The pattern of DNA cleavage intensity around indels |
| Q39642875 | Trans-Lesion DNA Polymerases May Be Involved in Yeast Meiosis |
| Q33282474 | Transcription-related mutations and GC content drive variation in nucleotide substitution rates across the genomes of Arabidopsis thaliana and Arabidopsis lyrata |
| Q46087063 | Understanding the interaction between an obligate hyperparasitic bacterium, Pasteuria penetrans and its obligate plant-parasitic nematode host, Meloidogyne spp. |
| Q41496563 | Variants of sequence family B Thermococcus kodakaraensis DNA polymerase with increased mismatch extension selectivity |
| Q37444742 | Y-family DNA polymerases in mammalian cells |
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