review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1038/NRM1781 |
P698 | PubMed publication ID | 16341080 |
P2093 | author name string | Errol C Friedberg | |
P2860 | cites work | hRAD30 mutations in the variant form of xeroderma pigmentosum | Q22010237 |
Eukaryotic DNA Polymerases | Q22065416 | ||
Human DINB1-encoded DNA polymerase kappa is a promiscuous extender of mispaired primer termini | Q24534772 | ||
Localization of DNA polymerases eta and iota to the replication machinery is tightly co-ordinated in human cells. | Q24537708 | ||
Role of human DNA polymerase kappa as an extender in translesion synthesis | Q24541478 | ||
The products of the yeast MMS2 and two human homologs (hMMS2 and CROC-1) define a structurally and functionally conserved Ubc-like protein family | Q24548218 | ||
Rad18 guides poleta to replication stalling sites through physical interaction and PCNA monoubiquitination | Q24563236 | ||
Normal immunoglobulin gene somatic hypermutation in Pol kappa-Pol iota double-deficient mice | Q40429467 | ||
Quantitative analysis of translesion DNA synthesis across a benzo[a]pyrene-guanine adduct in mammalian cells: the role of DNA polymerase kappa | Q40505709 | ||
The Saccharomyces cerevisiae RAD18 gene encodes a protein that contains potential zinc finger domains for nucleic acid binding and a putative nucleotide binding sequence | Q40554098 | ||
Extensive chromosomal breaks are induced by tamoxifen and estrogen in DNA repair-deficient cells | Q40559170 | ||
The RAD6 DNA repair pathway in Saccharomyces cerevisiae: what does it do, and how does it do it? | Q40671595 | ||
The RAD6 gene and protein of Saccharomyces cerevisiae | Q40707410 | ||
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 | ||
Preferential cis-syn thymine dimer bypass by DNA polymerase eta occurs with biased fidelity. | Q44785638 | ||
The biochemical requirements of DNA polymerase V-mediated translesion synthesis revisited | Q44995077 | ||
DNA polymerase V and RecA protein, a minimal mutasome. | Q45274275 | ||
Positive torsional strain causes the formation of a four-way junction at replication forks | Q46674361 | ||
Constitutive and regulated expression of the mouse Dinb (Polkappa) gene encoding DNA polymerase kappa. | Q47614597 | ||
Deletion of the Saccharomyces cerevisiae gene RAD30 encoding an Escherichia coli DinB homolog confers UV radiation sensitivity and altered mutability. | Q48033074 | ||
Proliferating cell nuclear antigen-dependent coordination of the biological functions of human DNA polymerase iota. | Q53736324 | ||
Repair of radiation-induced damage in Escherichia coli. I. Effect of rec mutations on post-replication repair of damage due to ultraviolet radiation. | Q53740414 | ||
DNA damage-induced replication fork regression and processing in Escherichia coli. | Q54531654 | ||
Pivotal role of the beta-clamp in translesion DNA synthesis and mutagenesis in E. coli cells. | Q54532729 | ||
The absence of DNA polymerase kappa does not affect somatic hypermutation of the mouse immunoglobulin heavy chain gene. | Q54777328 | ||
Error-Prone DNA Polymerases | Q60998760 | ||
Gross Chromosomal Rearrangements and Elevated Recombination at an Inducible Site-Specific Replication Fork Barrier | Q63383718 | ||
A model for replication repair in mammalian cells | Q67440139 | ||
Discontinuities in the DNA synthesized in an Excision-defective strain of Escherichia coli following ultraviolet irradiation | Q69833258 | ||
Usefulness of benzoylated naphthoylated DEAE-cellulose to distinguish and fractionate double-stranded DNA bearing different extents of single-stranded regions | Q69928475 | ||
The dinB gene encodes a novel E. coli DNA polymerase, DNA pol IV, involved in mutagenesis | Q72994394 | ||
UBC13, a DNA-damage-inducible gene, is a member of the error-free postreplication repair pathway in Saccharomyces cerevisiae | Q73741858 | ||
Cutting edge: DNA polymerases mu and lambda are dispensable for Ig gene hypermutation | Q77892518 | ||
Error-free recombinational repair predominates over mutagenic translesion replication in E. coli | Q78482138 | ||
Mouse Rev1 protein interacts with multiple DNA polymerases involved in translesion DNA synthesis | Q24594244 | ||
All three SOS-inducible DNA polymerases (Pol II, Pol IV and Pol V) are involved in induced mutagenesis | Q24597093 | ||
Historical overview: searching for replication help in all of the rec places | Q24631768 | ||
The BRCT domain of mammalian Rev1 is involved in regulating DNA translesion synthesis | Q24794355 | ||
The yeast DNA repair gene RAD6 encodes a ubiquitin-conjugating enzyme | Q27933609 | ||
Two RING finger proteins mediate cooperation between ubiquitin-conjugating enzymes in DNA repair. | Q27935427 | ||
RAD6-dependent DNA repair is linked to modification of PCNA by ubiquitin and SUMO. | Q27937465 | ||
Yeast DNA repair proteins Rad6 and Rad18 form a heterodimer that has ubiquitin conjugating, DNA binding, and ATP hydrolytic activities | Q27938794 | ||
The XPV (xeroderma pigmentosum variant) gene encodes human DNA polymerase eta | Q28115711 | ||
RING finger proteins: mediators of ubiquitin ligase activity | Q28139717 | ||
Initiation of genetic recombination and recombination-dependent replication | Q28141289 | ||
Immunoglobulin kappa light chain gene rearrangement is impaired in mice deficient for DNA polymerase mu | Q28202970 | ||
RecFOR proteins load RecA protein onto gapped DNA to accelerate DNA strand exchange: a universal step of recombinational repair | Q28207059 | ||
Fork reversal and ssDNA accumulation at stalled replication forks owing to checkpoint defects | Q28216078 | ||
Interaction of hREV1 with three human Y-family DNA polymerases | Q28266239 | ||
Replication protein A phosphorylation and the cellular response to DNA damage | Q28274289 | ||
Co-localization in replication foci and interaction of human Y-family members, DNA polymerase pol eta and REVl protein | Q28283240 | ||
Polymerase mu is up-regulated during the T cell-dependent immune response and its deficiency alters developmental dynamics of spleen centroblasts | Q28586777 | ||
129-derived strains of mice are deficient in DNA polymerase iota and have normal immunoglobulin hypermutation | Q28587504 | ||
Interaction of human DNA polymerase eta with monoubiquitinated PCNA: a possible mechanism for the polymerase switch in response to DNA damage | Q28646728 | ||
Replication of UV-damaged DNA: new insights into links between DNA polymerases, mutagenesis and human disease | Q28678572 | ||
The importance of repairing stalled replication forks | Q29614220 | ||
The Y-family of DNA polymerases | Q29615308 | ||
Cell cycle checkpoint signaling through the ATM and ATR kinases | Q29617837 | ||
Control of spontaneous and damage-induced mutagenesis by SUMO and ubiquitin conjugation | Q29619155 | ||
Eukaryotic polymerases iota and zeta act sequentially to bypass DNA lesions | Q29619958 | ||
The beta clamp targets DNA polymerase IV to DNA and strongly increases its processivity | Q30641251 | ||
Replication of damaged DNA in mammalian cells: new solutions to an old problem | Q30746296 | ||
Targeting of human DNA polymerase iota to the replication machinery via interaction with PCNA. | Q30769976 | ||
A requirement for replication in activation of the ATR-dependent DNA damage checkpoint | Q30848079 | ||
The mutagenesis protein UmuC is a DNA polymerase activated by UmuD', RecA, and SSB and is specialized for translesion replication | Q31422789 | ||
DNA recombination: the replication connection. | Q33677006 | ||
Novel DNA polymerases offer clues to the molecular basis of mutagenesis | Q33730736 | ||
Role of PriA in replication fork reactivation in Escherichia coli | Q33805205 | ||
Different mutation signatures in DNA polymerase eta- and MSH6-deficient mice suggest separate roles in antibody diversification | Q33853914 | ||
Multiple pathways process stalled replication forks | Q35870700 | ||
Cellular functions of DNA polymerase zeta and Rev1 protein | Q35978838 | ||
Filling the gaps in replication restart pathways. | Q36076269 | ||
An update on the role of translesion synthesis DNA polymerases in Ig hypermutation | Q36083527 | ||
Error-prone DNA repair and translesion synthesis: focus on the replication fork | Q36089826 | ||
Discontinuous or semi-discontinuous DNA replication in Escherichia coli? | Q36126246 | ||
Trading places: how do DNA polymerases switch during translesion DNA synthesis? | Q36139683 | ||
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. | Q36275662 | ||
Contribution of DNA polymerase eta to immunoglobulin gene hypermutation in the mouse | Q36403507 | ||
Fidelity mechanisms in DNA replication | Q37285267 | ||
Activity of the purified mutagenesis proteins UmuC, UmuD', and RecA in replicative bypass of an abasic DNA lesion by DNA polymerase III | Q37296938 | ||
Enzymatic switching for efficient and accurate translesion DNA replication. | Q37509255 | ||
Mutation of cysteine-88 in the Saccharomyces cerevisiae RAD6 protein abolishes its ubiquitin-conjugating activity and its various biological functions | Q37732412 | ||
Mutation induced by DNA damage: a many protein affair | Q37892175 | ||
Identification of specific amino acid residues in the E. coli beta processivity clamp involved in interactions with DNA polymerase III, UmuD and UmuD'. | Q38340491 | ||
Uvm mutants of Escherichia coli K12 deficient in UV mutagenesis. II. Further evidence for a novel function in error-prone repair | Q39902883 | ||
Inactivation of the Escherichia coli priA DNA replication protein induces the SOS response | Q39945614 | ||
Defining the position of the switches between replicative and bypass DNA polymerases | Q40253650 | ||
Replication and recombination intersect | Q33885019 | ||
Purification and characterization of pol kappa, a DNA polymerase encoded by the human DINB1 gene | Q33920689 | ||
Recombinational repair and restart of damaged replication forks. | Q33962242 | ||
Quantitative measurement of translesion replication in human cells: evidence for bypass of abasic sites by a replicative DNA polymerase | Q34020161 | ||
Preferential binding of ATR protein to UV-damaged DNA. | Q34067234 | ||
Error-prone repair DNA polymerases in prokaryotes and eukaryotes | Q34131455 | ||
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 | ||
Damage repair DNA polymerases Y. | Q34176729 | ||
Uncoupling of leading- and lagging-strand DNA replication during lesion bypass in vivo | Q34199558 | ||
Therefore, what are recombination proteins there for? | Q34243612 | ||
Evolution of the two-step model for UV-mutagenesis | Q34244261 | ||
Hydrocephalus, situs inversus, chronic sinusitis, and male infertility in DNA polymerase lambda-deficient mice: possible implication for the pathogenesis of immotile cilia syndrome | Q34277881 | ||
Polkappa protects mammalian cells against the lethal and mutagenic effects of benzo[a]pyrene | Q34387678 | ||
Recombinational DNA repair of damaged replication forks in Escherichia coli: questions | Q34432200 | ||
Specialized DNA polymerases, cellular survival, and the genesis of mutations | Q34662609 | ||
The bacterial RecA protein and the recombinational DNA repair of stalled replication forks | Q34667410 | ||
Genome stability and the processing of damaged replication forks by RecG. | Q34762160 | ||
Translesion DNA synthesis in eukaryotes: a one- or two-polymerase affair | Q34770150 | ||
Toward maintaining the genome: DNA damage and replication checkpoints | Q34995489 | ||
Checking on the fork: the DNA-replication stress-response pathway | Q35006441 | ||
The nonmutagenic repair of broken replication forks via recombination | Q35013053 | ||
How DNA lesions are turned into mutations within cells? | Q35026386 | ||
DNA structure dependent checkpoints as regulators of DNA repair | Q35046592 | ||
Functions of human DNA polymerases eta, kappa and iota suggested by their properties, including fidelity with undamaged DNA templates. | Q35047056 | ||
Association of phiX174 DNA-dependent ATPase activity with an Escherichia coli protein, replication factor Y, required for in vitro synthesis of phiX174 DNA | Q35087454 | ||
Xeroderma pigmentosum variant: from a human genetic disorder to a novel DNA polymerase. | Q35132468 | ||
Biological functions of translesion synthesis proteins in vertebrates | Q35296361 | ||
Error-Prone DNA Polymerases: When Making a Mistake is the Only Way to Get Ahead | Q35582961 | ||
UmuD'(2)C is an error-prone DNA polymerase, Escherichia coli pol V. | Q35588920 | ||
The DNA replication priming protein, PriA, is required for homologous recombination and double-strand break repair | Q35603171 | ||
Xeroderma pigmentosum variant and error-prone DNA polymerases | Q35630346 | ||
Post-replication repair in DT40 cells: translesion polymerases versus recombinases | Q35639954 | ||
Error-prone replication for better or worse | Q35785643 | ||
Translesion DNA synthesis: little fingers teach tolerance | Q35798500 | ||
Switching from high-fidelity replicases to low-fidelity lesion-bypass polymerases | Q35804585 | ||
P433 | issue | 12 | |
P921 | main subject | DNA damage | Q5205747 |
P304 | page(s) | 943-953 | |
P577 | publication date | 2005-12-01 | |
P1433 | published in | Nature Reviews Molecular Cell Biology | Q1573120 |
P1476 | title | Suffering in silence: the tolerance of DNA damage | |
P478 | volume | 6 |
Q35219664 | A RecA protein surface required for activation of DNA polymerase V. |
Q39383082 | A UVR-induced G2-phase checkpoint response to ssDNA gaps produced by replication fork bypass of unrepaired lesions is defective in melanoma. |
Q41117294 | A defect in homologous recombination leads to increased translesion synthesis in E. coli. |
Q38313552 | A novel DNA damage recognition protein in Schizosaccharomyces pombe |
Q28652503 | A novel variant of DNA polymerase ζ, Rev3ΔC, highlights differential regulation of Pol32 as a subunit of polymerase δ versus ζ in Saccharomyces cerevisiae |
Q33283998 | ATM-mediated transcriptional and developmental responses to gamma-rays in Arabidopsis |
Q34159485 | ATR-mediated phosphorylation of DNA polymerase η is needed for efficient recovery from UV damage |
Q33963920 | Abasic sites in the transcribed strand of yeast DNA are removed by transcription-coupled nucleotide excision repair |
Q41861523 | Accessory proteins assist exonuclease-deficient bacteriophage T4 DNA polymerase in replicating past an abasic site |
Q34572161 | Alteration of the carbohydrate for deoxyguanosine analogs markedly changes DNA replication fidelity, cell cycle progression and cytotoxicity |
Q34323727 | Analysis of strand transfer and template switching mechanisms of DNA gap repair by homologous recombination in Escherichia coli: predominance of strand transfer |
Q43369571 | Application of a molecular biology concept for the detection of DNA damage and repair during UV disinfection |
Q35434721 | BRCA1 is required for postreplication repair after UV-induced DNA damage |
Q37948054 | Base excision repair targets for cancer therapy |
Q38026112 | Biological and therapeutic relevance of nonreplicative DNA polymerases to cancer |
Q35757748 | Brc1-mediated rescue of Smc5/6 deficiency: requirement for multiple nucleases and a novel Rad18 function |
Q36086302 | Bub1 in Complex with LANA Recruits PCNA To Regulate Kaposi's Sarcoma-Associated Herpesvirus Latent Replication and DNA Translesion Synthesis |
Q47190104 | Bulky Lesion Bypass Requires Dpo4 Binding in Distinct Conformations. |
Q42733330 | Bypass of DNA-Protein Cross-links Conjugated to the 7-Deazaguanine Position of DNA by Translesion Synthesis Polymerases |
Q43734888 | Cell-cycle restriction limits DNA damage and maintains self-renewal of leukaemia stem cells |
Q37276862 | Checkpoint kinase phosphorylation in response to endogenous oxidative DNA damage in repair-deficient stationary-phase Saccharomyces cerevisiae |
Q83064386 | Common polymorphisms in CYP1A1, GSTM1, GSTT1, GSTP1 and XPD genes and endogenous DNA damage |
Q27939188 | Comparative analysis of in vivo interactions between Rev1 protein and other Y-family DNA polymerases in animals and yeasts |
Q33799163 | Continued primer synthesis at stalled replication forks contributes to checkpoint activation. |
Q27933423 | DNA bending facilitates the error-free DNA damage tolerance pathway and upholds genome integrity. |
Q93103734 | DNA damage tolerance in stem cells, ageing, mutagenesis, disease and cancer therapy |
Q41860261 | DNA damage tolerance: when it's OK to make mistakes |
Q35088992 | DNA lesion identity drives choice of damage tolerance pathway in murine cell chromosomes |
Q26991961 | DNA polymerase delta in DNA replication and genome maintenance |
Q45832606 | DNA polymerase ζ as a potential biomarker of chemoradiation resistance and poor prognosis for cervical cancer. |
Q37061484 | DNA polymerase κ-dependent DNA synthesis at stalled replication forks is important for CHK1 activation. |
Q37109944 | DNA polymerases in adaptive immunity |
Q37800526 | DNA repair in organelles: Pathways, organization, regulation, relevance in disease and aging |
Q36912141 | DNA sequence context greatly affects the accuracy of bypass across an ultraviolet light 6-4 photoproduct in mammalian cells |
Q24300382 | DVC1 (C1orf124) is a DNA damage-targeting p97 adaptor that promotes ubiquitin-dependent responses to replication blocks |
Q35002361 | Damage-induced localized hypermutability. |
Q89971038 | Deciphering UV-induced DNA Damage Responses to Prevent and Treat Skin Cancer |
Q40775865 | Decision Making by p53: Life versus Death |
Q35759995 | Dysregulation of DNA polymerase κ recruitment to replication forks results in genomic instability |
Q54372713 | Effect of recA inactivation on mutagenesis of Escherichia coli exposed to sublethal concentrations of antimicrobials. |
Q42577782 | Effect of subinhibitory concentrations of antibiotics on intrachromosomal homologous recombination in Escherichia coli |
Q37424345 | Effects of Twelve Germline Missense Variations on DNA Lesion and G-Quadruplex Bypass Activities of Human DNA Polymerase REV1. |
Q38321122 | Effects of non-catalytic, distal amino acid residues on activity of E. coli DinB (DNA polymerase IV). |
Q39301938 | Eukaryotic Translesion DNA Synthesis on the Leading and Lagging Strands: Unique Detours around the Same Obstacle |
Q53553344 | Fission yeast Rnf4 homologs are required for DNA repair. |
Q39814080 | Flow cytometry analysis of single-strand DNA damage in neuroblastoma cell lines using the F7-26 monoclonal antibody. |
Q43573965 | Genetic variation in genes encoding for polymerase ζ subunits associates with breast cancer risk, tumour characteristics and survival |
Q36781920 | Genomic assay reveals tolerance of DNA damage by both translesion DNA synthesis and homology-dependent repair in mammalian cells. |
Q36054241 | HLTF and SHPRH are not essential for PCNA polyubiquitination, survival and somatic hypermutation: existence of an alternative E3 ligase |
Q38866681 | Homologous recombination maintenance of genome integrity during DNA damage tolerance |
Q21263027 | Human single-stranded DNA binding proteins are essential for maintaining genomic stability |
Q33385991 | Hypermutability of damaged single-strand DNA formed at double-strand breaks and uncapped telomeres in yeast Saccharomyces cerevisiae. |
Q34679192 | Identification of novel DNA-damage tolerance genes reveals regulation of translesion DNA synthesis by nucleophosmin. |
Q88815763 | Impact of UVA pre-radiation on UVC disinfection performance: Inactivation, repair and mechanism study |
Q92756188 | Insights into the Link between the Organization of DNA Replication and the Mutational Landscape |
Q35748440 | Inviting instability: Transposable elements, double-strand breaks, and the maintenance of genome integrity. |
Q61813569 | Mechanisms of DNA Damage Tolerance: Post-Translational Regulation of PCNA |
Q37420604 | Microenvironmental Niches and Sanctuaries: A Route to Acquired Resistance |
Q37528812 | Mismatch repair protein MSH2 regulates translesion DNA synthesis following exposure of cells to UV radiation |
Q36142135 | Molecular mechanisms of xeroderma pigmentosum (XP) proteins |
Q50645182 | Monoubiquitination of proliferating cell nuclear antigen induced by stalled replication requires uncoupling of DNA polymerase and mini-chromosome maintenance helicase activities. |
Q37711586 | Monoubiquitylation of histone H2B contributes to the bypass of DNA damage during and after DNA replication |
Q34633078 | Mouse DNA polymerase kappa has a functional role in the repair of DNA strand breaks |
Q35842713 | Multiple solutions to inefficient lesion bypass by T7 DNA polymerase. |
Q64102292 | Mutating for Good: DNA Damage Responses During Somatic Hypermutation |
Q47781755 | Nuclear insulin-like growth factor 1 receptor phosphorylates proliferating cell nuclear antigen and rescues stalled replication forks after DNA damage. |
Q34023036 | PCNA ubiquitination is important, but not essential for translesion DNA synthesis in mammalian cells. |
Q39574364 | PIDD orchestrates translesion DNA synthesis in response to UV irradiation |
Q28509424 | PTIP/Swift is required for efficient PCNA ubiquitination in response to DNA damage |
Q38476459 | Participation of translesion synthesis DNA polymerases in the maintenance of chromosome integrity in yeast Saccharomyces cerevisiae. |
Q42731981 | Pol κ in replication checkpoint |
Q37455758 | Polk mutant mice have a spontaneous mutator phenotype |
Q33929592 | Postreplication gaps at UV lesions are signals for checkpoint activation |
Q53826516 | Precision cancer therapy: profiting from tumor specific defects in the DNA damage tolerance system. |
Q36959012 | PrimPol prevents APOBEC/AID family mediated DNA mutagenesis |
Q35856709 | RAD18 and poly(ADP-ribose) polymerase independently suppress the access of nonhomologous end joining to double-strand breaks and facilitate homologous recombination-mediated repair. |
Q37802636 | RAD18 lives a double life: Its implication in DNA double-strand break repair |
Q52339242 | RNA-splicing factor SART3 regulates translesion DNA synthesis. |
Q39385329 | Rad18 is a transcriptional target of E2F3. |
Q40337884 | Rad51 replication fork recruitment is required for DNA damage tolerance. |
Q47766816 | Receptor heterogeneity in optical biosensors |
Q39127506 | Recruitment of the nucleotide excision repair endonuclease XPG to sites of UV-induced dna damage depends on functional TFIIH. |
Q35586061 | Reduced level of ribonucleotide reductase R2 subunits increases dependence on homologous recombination repair of cisplatin-induced DNA damage |
Q28289142 | Regulation of PCNA-protein interactions for genome stability |
Q38534219 | Regulation of Rad6/Rad18 Activity During DNA Damage Tolerance. |
Q53527372 | Regulation of Saccharomyces cerevisiae DNA polymerase eta transcript and protein. |
Q33750098 | Replication and recombination factors contributing to recombination-dependent bypass of DNA lesions by template switch |
Q56897943 | Requirements for the interaction of mouse Polkappa with ubiquitin and its biological significance |
Q34550677 | Rescue from replication stress during mitosis |
Q27934499 | Reversal of PCNA ubiquitylation by Ubp10 in Saccharomyces cerevisiae. |
Q36804013 | Role of p97/VCP (Cdc48) in genome stability |
Q36687824 | Roles of DNA polymerases in replication, repair, and recombination in eukaryotes. |
Q33716551 | Rosa26-GFP direct repeat (RaDR-GFP) mice reveal tissue- and age-dependence of homologous recombination in mammals in vivo. |
Q37172085 | SBF transcription factor complex positively regulates UV mutagenesis in Saccharomyces cerevisiae |
Q29871514 | SHPRH and HLTF act in a damage-specific manner to coordinate different forms of postreplication repair and prevent mutagenesis |
Q33796994 | SIVA1 directs the E3 ubiquitin ligase RAD18 for PCNA monoubiquitination |
Q33415261 | Screening a genome-wide S. pombe deletion library identifies novel genes and pathways involved in genome stability maintenance |
Q37192014 | Separate domains of Rev1 mediate two modes of DNA damage bypass in mammalian cells |
Q34336638 | Shared genetic pathways contribute to the tolerance of endogenous and low-dose exogenous DNA damage in yeast. |
Q42592723 | Simulating the temporal modulation of inducible DNA damage response in Escherichia coli |
Q42365650 | Six Germline Genetic Variations Impair the Translesion Synthesis Activity of Human DNA Polymerase κ. |
Q42102982 | Somatic hypermutation of immunoglobulin genes: lessons from proliferating cell nuclear antigenK164R mutant mice. |
Q55371894 | Spatial separation between replisome- and template-induced replication stress signaling. |
Q88737039 | Structural Basis for the Interaction of Mutasome Assembly Factor REV1 with Ubiquitin |
Q27665594 | Structural Basis of Ubiquitin Recognition by Translesion Synthesis DNA Polymerase ι |
Q40123082 | Sub-Minimum Inhibitory Concentrations of Rhubarb Water Extracts Inhibit Streptococcus suis Biofilm Formation |
Q24299250 | Systems-wide analysis of ubiquitylation dynamics reveals a key role for PAF15 ubiquitylation in DNA-damage bypass |
Q54463698 | The Bloom's syndrome helicase can promote the regression of a model replication fork. |
Q35445785 | The DNA damage checkpoint allows recombination between divergent DNA sequences in budding yeast |
Q38022544 | The Fanconi anemia pathway in replication stress and DNA crosslink repair. |
Q57753896 | The HIRAN domain of helicase-like transcription factor positions the DNA translocase motor to drive efficient DNA fork regression |
Q24616365 | The Role of PCNA Posttranslational Modifications in Translesion Synthesis |
Q57752921 | The helicase Pif1 functions in the template switching pathway of DNA damage bypass |
Q37153771 | The mismatch repair system promotes DNA polymerase zeta-dependent translesion synthesis in yeast. |
Q38301109 | The noncatalytic C-terminus of AtPOLK Y-family DNA polymerase affects synthesis fidelity, mismatch extension and translesion replication |
Q38063711 | The roles of DNA polymerase ζ and the Y family DNA polymerases in promoting or preventing genome instability |
Q38231173 | Tolerating DNA damage during eukaryotic chromosome replication. |
Q47742619 | Transport Effects on Multiple-Component Reactions in Optical Biosensors |
Q35094532 | UV irradiation induces a postreplication DNA damage checkpoint |
Q37871655 | Ubiquitin family modifications and template switching |
Q24309639 | Werner syndrome protein interacts functionally with translesion DNA polymerases |
Q89862470 | Working on Genomic Stability: From the S-Phase to Mitosis |
Q34428866 | XPC silencing in normal human keratinocytes triggers metabolic alterations that drive the formation of squamous cell carcinomas. |
Q37444742 | Y-family DNA polymerases in mammalian cells |
Q24339475 | ZRANB3 is a structure-specific ATP-dependent endonuclease involved in replication stress response |
Q92653634 | iDamage: a method to integrate modified DNA into the yeast genome |
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