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DNA polymerases and cancer

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/(sici)1097-0215(19990315)80:6<919::aid-ijc19>3.0.co;2-uopenalex-snapshot

Detection of mutations in the DNA polymerase ? gene of human sporadic colorectal cancers and colon cancer cell lines

inferredcites →https://doi.org/10.1002/1521-4141(200211)32:11<3152::aid-immu3152>3.0.co;2-2openalex-snapshot

DNA polymerase κ deficiency does not affect somatic hypermutation in mice

inferredcites →https://doi.org/10.1002/anie.200905724openalex-snapshot

Structures of DNA Polymerases Caught Processing Size‐Augmented Nucleotide Probes

inferredcites →https://doi.org/10.1002/ijc.11666openalex-snapshot

DNA polymerase θ is preferentially expressed in lymphoid tissues and upregulated in human cancers

inferredcites →https://doi.org/10.1002/ijc.22099openalex-snapshot

Mutations in DNA polymerase η are not detected in squamous cell carcinoma of the skin

inferredcites →https://doi.org/10.1002/mc.20509openalex-snapshot

Role of TLS DNA polymerases eta and kappa in processing naturally occurring structured DNA in human cells

inferredcites →https://doi.org/10.1007/978-90-481-3471-7_11openalex-snapshot

The Mitochondrial DNA Polymerase in Health and Disease

inferredcites →https://doi.org/10.1016/j.bbrc.2006.11.021openalex-snapshot

Anti-tumor effects of dehydroaltenusin, a specific inhibitor of mammalian DNA polymerase α

inferredcites →https://doi.org/10.1016/j.biochi.2009.06.007openalex-snapshot

High fidelity and lesion bypass capability of human DNA polymerase δ

inferredcites →https://doi.org/10.1016/j.bmc.2008.02.071openalex-snapshot

Inhibitors of DNA polymerase β: Activity and mechanism

inferredcites →https://doi.org/10.1016/j.bmc.2009.08.051openalex-snapshot

Synthesis and structure–activity relationships of dehydroaltenusin derivatives as selective DNA polymerase α inhibitors

inferredcites →https://doi.org/10.1016/j.canlet.2004.07.021openalex-snapshot

Down-regulation of DNA polymerases κ, η, ι, and ζ in human lung, stomach, and colorectal cancers

inferredcites →https://doi.org/10.1016/j.canlet.2004.07.049openalex-snapshot

Frequent mutation related with overexpression of DNA polymerase beta in primary tumors and precancerous lesions of human stomach

inferredcites →https://doi.org/10.1016/j.cell.2010.02.028openalex-snapshot

The RAD6 DNA Damage Tolerance Pathway Operates Uncoupled from the Replication Fork and Is Functional Beyond S Phase

inferredcites →https://doi.org/10.1016/j.cub.2006.01.063openalex-snapshot

ATR Homolog Mec1 Controls Association of DNA Polymerase ζ-Rev1 Complex with Regions near a Double-Strand Break

inferredcites →https://doi.org/10.1016/j.dnarep.2005.01.005openalex-snapshot

The overexpression of specialized DNA polymerases in cancer

inferredcites →https://doi.org/10.1016/j.dnarep.2005.04.002openalex-snapshot

Overproduction of DNA polymerase eta does not raise the spontaneous mutation rate in diploid human fibroblasts

inferredcites →https://doi.org/10.1016/j.dnarep.2005.09.009openalex-snapshot

Database of mouse strains carrying targeted mutations in genes affecting biological responses to DNA damage Version 7

inferredcites →https://doi.org/10.1016/j.dnarep.2006.09.012openalex-snapshot

A unique error signature for human DNA polymerase ν

inferredcites →https://doi.org/10.1016/j.dnarep.2007.01.009openalex-snapshot

A unified view of base excision repair: Lesion-dependent protein complexes regulated by post-translational modification

inferredcites →https://doi.org/10.1016/j.dnarep.2007.02.003openalex-snapshot

Translesion synthesis: Y-family polymerases and the polymerase switch

inferredcites →https://doi.org/10.1016/j.dnarep.2007.06.002openalex-snapshot

Double-strand breaks induce homologous recombinational repair of interstrand cross-links via cooperation of MSH2, ERCC1-XPF, REV3, and the Fanconi anemia pathway

inferredcites →https://doi.org/10.1016/j.dnarep.2008.04.002openalex-snapshot

Reevaluation of the role of DNA polymerase θ in somatic hypermutation of immunoglobulin genes

inferredcites →https://doi.org/10.1016/j.dnarep.2008.05.012openalex-snapshot

Role of DNA polymerases η, ι and ζ in UV resistance and UV-induced mutagenesis in a human cell line

inferredcites →https://doi.org/10.1016/j.dnarep.2009.09.003openalex-snapshot

Polk mutant mice have a spontaneous mutator phenotype

inferredcites →https://doi.org/10.1016/j.dnarep.2009.09.006openalex-snapshot

Mammalian polymerase ζ is essential for post-replication repair of UV-induced DNA lesions

inferredcites →https://doi.org/10.1016/j.dnarep.2009.10.004openalex-snapshot

Near-full-length REV3L appears to be a scarce maternal factor in Xenopus laevis eggs that changes qualitatively in early embryonic development

inferredcites →https://doi.org/10.1016/j.dnarep.2010.03.004openalex-snapshot

Oxygen as a friend and enemy: How to combat the mutational potential of 8-oxo-guanine

inferredcites →https://doi.org/10.1016/j.dnarep.2010.03.013openalex-snapshot

Requirement for functional DNA polymerase eta in genome-wide repair of UV-induced DNA damage during S phase

inferredcites →https://doi.org/10.1016/j.dnarep.2010.09.001openalex-snapshot

Lack of DNA polymerase μ affects the kinetics of DNA double-strand break repair and impacts on cellular senescence

inferredcites →https://doi.org/10.1016/j.immuni.2006.04.013openalex-snapshot

Nonoverlapping Functions of DNA Polymerases Mu, Lambda, and Terminal Deoxynucleotidyltransferase during Immunoglobulin V(D)J Recombination In Vivo

inferredcites →https://doi.org/10.1016/j.jmb.2009.05.026openalex-snapshot

Structure of the Human Rev1–DNA–dNTP Ternary Complex

inferredcites →https://doi.org/10.1016/j.molcel.2004.11.017openalex-snapshot

A Biochemically Defined System for Mammalian Nonhomologous DNA End Joining

inferredcites →https://doi.org/10.1016/j.molcel.2005.10.016openalex-snapshot

Dual Roles for DNA Polymerase η in Homologous DNA Recombination and Translesion DNA Synthesis

inferredcites →https://doi.org/10.1016/j.molcel.2005.11.015openalex-snapshot

Multiple Mechanisms Control Chromosome Integrity after Replication Fork Uncoupling and Restart at Irreparable UV Lesions

inferredcites →https://doi.org/10.1016/j.molcel.2006.05.038openalex-snapshot

REV1 Protein Interacts with PCNA: Significance of the REV1 BRCT Domain In Vitro and In Vivo

inferredcites →https://doi.org/10.1016/j.molcel.2006.07.032openalex-snapshot

Vertebrate POLQ and POLβ Cooperate in Base Excision Repair of Oxidative DNA Damage

inferredcites →https://doi.org/10.1016/j.molcel.2007.11.037openalex-snapshot

DNA Repair Synthesis Facilitates RAD52-Mediated Second-End Capture during DSB Repair

inferredcites →https://doi.org/10.1016/j.molcel.2008.03.024openalex-snapshot

PCNA Ubiquitination and REV1 Define Temporally Distinct Mechanisms for Controlling Translesion Synthesis in the Avian Cell Line DT40

inferredcites →https://doi.org/10.1016/j.molcel.2009.12.018openalex-snapshot

CRL4Cdt2 E3 Ubiquitin Ligase Monoubiquitinates PCNA to Promote Translesion DNA Synthesis

inferredcites →https://doi.org/10.1016/j.molcel.2009.12.039openalex-snapshot

Regulation of Translesion Synthesis DNA Polymerase η by Monoubiquitination

inferredcites →https://doi.org/10.1016/j.molcel.2010.02.009openalex-snapshot

Three DNA Polymerases, Recruited by Different Mechanisms, Carry Out NER Repair Synthesis in Human Cells

inferredcites →https://doi.org/10.1016/j.molimm.2005.09.017openalex-snapshot

The catalytic activity of REV1 is employed during immunoglobulin gene diversification in DT40

inferredcites →https://doi.org/10.1016/j.mrfmmm.2008.02.006openalex-snapshot

Translesion synthesis of 7,8-dihydro-8-oxo-2′-deoxyguanosine by DNA polymerase eta in vivo

inferredcites →https://doi.org/10.1016/s0006-291x(02)00341-8openalex-snapshot

An essential role for REV3 in mammalian cell survival: absence of REV3 induces p53-independent embryonic death

inferredcites →https://doi.org/10.1016/s0027-5107(02)00253-1openalex-snapshot

hREV3 is essential for error-prone translesion synthesis past UV or benzo[a]pyrene diol epoxide-induced DNA lesions in human fibroblasts

inferredcites →https://doi.org/10.1016/s0960-9822(00)00724-7openalex-snapshot

Disruption of mouse polymerase ζ (Rev3) leads to embryonic lethality and impairs blastocyst development in vitro

inferredcites →https://doi.org/10.1016/s0960-9822(00)00725-9openalex-snapshot

Disruption of the developmentally regulated Rev3l gene causes embryonic lethality

inferredcites →https://doi.org/10.1016/s0960-9822(00)00726-0openalex-snapshot

Disruption of the Rev3l-encoded catalytic subunit of polymerase ζ in mice results in early embryonic lethality

inferredcites →https://doi.org/10.1016/s1074-7613(03)00203-6openalex-snapshot

Immunoglobulin κ Light Chain Gene Rearrangement Is Impaired in Mice Deficient for DNA Polymerase Mu

inferredcites →https://doi.org/10.1016/s1568-7864(03)00094-6openalex-snapshot

Sequence context-dependent replication of DNA templates containing UV-induced lesions by human DNA polymerase ι

inferredcites →https://doi.org/10.1016/s1876-1623(08)78004-0openalex-snapshot

Separate Roles of Structured and Unstructured Regions of Y-Family DNA Polymerases

inferredcites →https://doi.org/10.1021/bi00015a012openalex-snapshot

Nucleotide Excision Repair DNA Synthesis by DNA Polymerase .epsilon. in the Presence of PCNA, RFC, and RPA

inferredcites →https://doi.org/10.1021/bi025549kopenalex-snapshot

Translesion Synthesis by Human DNA Polymerase η across Thymine Glycol Lesions

inferredcites →https://doi.org/10.1021/bi800529fopenalex-snapshot

Mutational Specificity of γ-Radiation-Induced Guanine−Thymine and Thymine−Guanine Intrastrand Cross-Links in Mammalian Cells and Translesion Synthesis Past the Guanine−Thymine Lesion by Human DNA Polymerase η

inferredcites →https://doi.org/10.1021/bi801179fopenalex-snapshot

DNA Polymerases as Therapeutic Targets

inferredcites →https://doi.org/10.1021/bi9015346openalex-snapshot

Evidence for the Involvement of Human DNA Polymerase N in the Repair of DNA Interstrand Cross-Links

inferredcites →https://doi.org/10.1021/bi902169qopenalex-snapshot

Cross-Link Structure Affects Replication-Independent DNA Interstrand Cross-Link Repair in Mammalian Cells

inferredcites →https://doi.org/10.1021/tx800174aopenalex-snapshot

Replication Bypass of the Acrolein-Mediated Deoxyguanine DNA-Peptide Cross-Links by DNA Polymerases of the DinB Family

inferredcites →https://doi.org/10.1021/tx900449uopenalex-snapshot

Novel Enzymatic Function of DNA Polymerase ν in Translesion DNA Synthesis Past Major Groove DNA−Peptide and DNA−DNA Cross-Links

inferredcites →https://doi.org/10.1038/311752a0openalex-snapshot

Insertion of N regions into heavy-chain genes is correlated with expression of terminal deoxytransferase in B cells

inferredcites →https://doi.org/10.1038/35023030openalex-snapshot

Eukaryotic polymerases ι and ζ act sequentially to bypass DNA lesions

inferredcites →https://doi.org/10.1038/88740openalex-snapshot

DNA polymerase η is an A-T mutator in somatic hypermutation of immunoglobulin variable genes

inferredcites →https://doi.org/10.1038/cr.2007.114openalex-snapshot

Eukaryotic DNA damage tolerance and translesion synthesis through covalent modifications of PCNA

inferredcites →https://doi.org/10.1038/cr.2008.4openalex-snapshot

The fidelity of DNA synthesis by eukaryotic replicative and translesion synthesis polymerases

inferredcites →https://doi.org/10.1038/emboj.2008.210openalex-snapshot

Human DNA polymerase iota protects cells against oxidative stress

inferredcites →https://doi.org/10.1038/emboj.2008.281openalex-snapshot

Two‐polymerase mechanisms dictate error‐free and error‐prone translesion DNA synthesis in mammals

inferredcites →https://doi.org/10.1038/emboj.2008.303openalex-snapshot

Bypass specialists operate together

inferredcites →https://doi.org/10.1038/emboj.2009.357openalex-snapshot

DNA polymerase β is critical for mouse meiotic synapsis

inferredcites →https://doi.org/10.1038/emboj.2010.64openalex-snapshot

Replication through an abasic DNA lesion: structural basis for adenine selectivity

inferredcites →https://doi.org/10.1038/jid.2008.48openalex-snapshot

Xeroderma Pigmentosum-Variant Patients from America, Europe, and Asia

inferredcites →https://doi.org/10.1038/nature02692openalex-snapshot

Replication by human DNA polymerase-ι occurs by Hoogsteen base-pairing

inferredcites →https://doi.org/10.1038/nature04318openalex-snapshot

A single amino acid governs enhanced activity of DinB DNA polymerases on damaged templates

inferredcites →https://doi.org/10.1038/nature09097openalex-snapshot

Ubiquitin-dependent DNA damage bypass is separable from genome replication

inferredcites →https://doi.org/10.1038/nature09104openalex-snapshot

Structural basis for the suppression of skin cancers by DNA polymerase η

inferredcites →https://doi.org/10.1038/nature09196openalex-snapshot

Structure and mechanism of human DNA polymerase η

inferredcites →https://doi.org/10.1038/nchembio.139openalex-snapshot

DNA damage tolerance: when it's OK to make mistakes

inferredcites →https://doi.org/10.1038/nrg2345openalex-snapshot

DNA polymerases and human disease

inferredcites →https://doi.org/10.1038/onc.2008.212openalex-snapshot

Novel evidences for a tumor suppressor role of Rev3, the catalytic subunit of Pol ζ

inferredcites →https://doi.org/10.1038/onc.2009.327openalex-snapshot

Cells deficient in the base excision repair protein, DNA polymerase beta, are hypersensitive to oxaliplatin chemotherapy

inferredcites →https://doi.org/10.1038/onc.2009.378openalex-snapshot

A ‘DNA replication’ signature of progression and negative outcome in colorectal cancer

inferredcites →https://doi.org/10.1038/sj.emboj.7600424openalex-snapshot

High‐efficiency bypass of DNA damage by human DNA polymerase Q

inferredcites →https://doi.org/10.1038/sj.onc.1205573openalex-snapshot

Cloning and characterization of the common fragile site FRA6F harboring a replicative senescence gene and frequently deleted in human tumors

inferredcites →https://doi.org/10.1046/j.1365-2443.2001.00478.xopenalex-snapshot

Expression of human and mouse genes encoding polκ: testis‐specific developmental regulation and AhR‐dependent inducible transcription

inferredcites →https://doi.org/10.1056/nejmoa043331openalex-snapshot

MGMT Gene Silencing and Benefit from Temozolomide in Glioblastoma

inferredcites →https://doi.org/10.1073/pnas.0505166102openalex-snapshot

Expression of DNA polymerase β cancer-associated variants in mouse cells results in cellular transformation

inferredcites →https://doi.org/10.1073/pnas.0510167103openalex-snapshot

The critical mutagenic translesion DNA polymerase Rev1 is highly expressed during G 2 /M phase rather than S phase

inferredcites →https://doi.org/10.1073/pnas.0605247103openalex-snapshot

Participation of mouse DNA polymerase ι in strand-biased mutagenic bypass of UV photoproducts and suppression of skin cancer

inferredcites →https://doi.org/10.1073/pnas.0607057103openalex-snapshot

Human cancers express a mutator phenotype

inferredcites →https://doi.org/10.1073/pnas.062038699openalex-snapshot

Quantitative measurement of translesion replication in human cells: Evidence for bypass of abasic sites by a replicative DNA polymerase

inferredcites →https://doi.org/10.1073/pnas.0907147106openalex-snapshot

DNA polymerase ε and δ proofreading suppress discrete mutator and cancer phenotypes in mice

inferredcites →https://doi.org/10.1073/pnas.0907526106openalex-snapshot

A cancer-associated DNA polymerase δ variant modeled in yeast causes a catastrophic increase in genomic instability

inferredcites →https://doi.org/10.1073/pnas.0908492106openalex-snapshot

Limited terminal transferase in human DNA polymerase μ defines the required balance between accuracy and efficiency in NHEJ

inferredcites →https://doi.org/10.1073/pnas.0909507106openalex-snapshot

Error-prone translesion replication of damaged DNA suppresses skin carcinogenesis by controlling inflammatory hyperplasia

inferredcites →https://doi.org/10.1073/pnas.0910759107openalex-snapshot

DNA polymerase θ up-regulation is associated with poor survival in breast cancer, perturbs DNA replication, and promotes genetic instability

inferredcites →https://doi.org/10.1073/pnas.1007795107openalex-snapshot

Error-free replicative bypass of thymine glycol by the combined action of DNA polymerases κ and ζ in human cells

inferredcites →https://doi.org/10.1073/pnas.1011409107openalex-snapshot

Suppression of Rev3, the catalytic subunit of Polζ, sensitizes drug-resistant lung tumors to chemotherapy

inferredcites →https://doi.org/10.1073/pnas.1011412107openalex-snapshot

Error-prone translesion synthesis mediates acquired chemoresistance

inferredcites →https://doi.org/10.1073/pnas.222377899openalex-snapshot

Polκ protects mammalian cells against the lethal and mutagenic effects of benzo[ a ]pyrene

inferredcites →https://doi.org/10.1073/pnas.231611798openalex-snapshot

UV-induced replication arrest in the xeroderma pigmentosum variant leads to DNA double-strand breaks, γ-H2AX formation, and Mre11 relocalization

inferredcites →https://doi.org/10.1073/pnas.232340999openalex-snapshot

High incidence of epithelial cancers in mice deficient for DNA polymerase δ proofreading

inferredcites →https://doi.org/10.1073/pnas.95.12.6876openalex-snapshot

A human homolog of the Saccharomyces cerevisiae REV3 gene, which encodes the catalytic subunit of DNA polymerase ζ

inferredcites →https://doi.org/10.1073/pnas.96.24.13926openalex-snapshot

Association of terminal deoxynucleotidyl transferase with Ku

inferredcites →https://doi.org/10.1074/jbc.275.11.7447openalex-snapshot

Fidelity of Human DNA Polymerase η

inferredcites →https://doi.org/10.1074/jbc.c600071200openalex-snapshot

REV3 and REV1 Play Major Roles in Recombination-independent Repair of DNA Interstrand Cross-links Mediated by Monoubiquitinated Proliferating Cell Nuclear Antigen (PCNA)

inferredcites →https://doi.org/10.1074/jbc.m102051200openalex-snapshot

Interactions in the Error-prone Postreplication Repair Proteins hREV1, hREV3, and hREV7

inferredcites →https://doi.org/10.1074/jbc.m207774200openalex-snapshot

Translesion Synthesis past Acrolein-derived DNA Adduct, γ-Hydroxypropanodeoxyguanosine, by Yeast and Human DNA Polymerase η

inferredcites →https://doi.org/10.1074/jbc.m305399200openalex-snapshot

Localization of the Deoxyribose Phosphate Lyase Active Site in Human DNA Polymerase ι by Controlled Proteolysis

inferredcites →https://doi.org/10.1074/jbc.m305646200openalex-snapshot

POLN, a Nuclear PolA Family DNA Polymerase Homologous to the DNA Cross-link Sensitivity Protein Mus308

inferredcites →https://doi.org/10.1074/jbc.m405249200openalex-snapshot

Investigating the Role of the Little Finger Domain of Y-family DNA Polymerases in Low Fidelity Synthesis and Translesion Replication

inferredcites →https://doi.org/10.1074/jbc.m411864200openalex-snapshot

DNA Polymerase λ Mediates a Back-up Base Excision Repair Activity in Extracts of Mouse Embryonic Fibroblasts

inferredcites →https://doi.org/10.1074/jbc.m604317200openalex-snapshot

Human DNA Polymerase N (POLN) Is a Low Fidelity Enzyme Capable of Error-free Bypass of 5S-Thymine Glycol

inferredcites →https://doi.org/10.1074/jbc.m801238200openalex-snapshot

Role for DNA Polymerase κ in the Processing of N2-N2-Guanine Interstrand Cross-links

inferredcites →https://doi.org/10.1083/jcb.200912012openalex-snapshot

DNA polymerases ν and θ are required for efficient immunoglobulin V gene diversification in chicken

inferredcites →https://doi.org/10.1084/jem.20030767openalex-snapshot

129-derived Strains of Mice Are Deficient in DNA Polymerase ι and Have Normal Immunoglobulin Hypermutation

inferredcites →https://doi.org/10.1084/jem.20050292openalex-snapshot

Contribution of DNA polymerase η to immunoglobulin gene hypermutation in the mouse

inferredcites →https://doi.org/10.1084/jem.20052227openalex-snapshot

Strand-biased defect in C/G transversions in hypermutating immunoglobulin genes in Rev1-deficient mice

inferredcites →https://doi.org/10.1084/jem.20062131openalex-snapshot

DNA polymerase η is the sole contributor of A/T modifications during immunoglobulin gene hypermutation in the mouse

inferredcites →https://doi.org/10.1084/jem.20080669openalex-snapshot

Polζ ablation in B cells impairs the germinal center reaction, class switch recombination, DNA break repair, and genome stability

inferredcites →https://doi.org/10.1093/emboj/18.12.3491openalex-snapshot

Xeroderma pigmentosum variant (XP‐V) correcting protein from HeLa cells has a thymine dimer bypass DNA polymerase activity

inferredcites →https://doi.org/10.1093/emboj/19.12.3100openalex-snapshot

Mechanisms of accurate translesion synthesis by human DNA polymerase η

inferredcites →https://doi.org/10.1093/emboj/19.6.1397openalex-snapshot

Neonatal lethality with abnormal neurogenesis in mice deficient in DNA polymerase β

inferredcites →https://doi.org/10.1093/emboj/cdg161openalex-snapshot

Rev1 is essential for DNA damage tolerance and non‐templated immunoglobulin gene mutation in a vertebrate cell line

inferredcites →https://doi.org/10.1093/emboj/cdg308openalex-snapshot

Multiple roles of Rev3, the catalytic subunit of polζ in maintaining genome stability in vertebrates

inferredcites →https://doi.org/10.1093/emboj/cdg626openalex-snapshot

Mouse Rev1 protein interacts with multiple DNA polymerases involved in translesion DNA synthesis

inferredcites →https://doi.org/10.1093/genetics/147.3.1017openalex-snapshot

A Role for REV3 in Mutagenesis During Double-Strand Break Repair in Saccharomyces cerevisiae

inferredcites →https://doi.org/10.1093/genetics/162.3.1063openalex-snapshot

The Roles of REV3 and RAD57 in Double-Strand-Break-Repair-Induced Mutagenesis of Saccharomyces cerevisiae

inferredcites →https://doi.org/10.1093/genetics/163.3.1031openalex-snapshot

Phenotype-Based Identification of Mouse Chromosome Instability Mutants

inferredcites →https://doi.org/10.1093/genetics/68.1.21openalex-snapshot

MUTANTS OF YEAST DEFECTIVE IN MUTATION INDUCED BY ULTRAVIOLET LIGHT

inferredcites →https://doi.org/10.1093/hmg/ddi184openalex-snapshot

Mitochondrial DNA polymerase gamma is essential for mammalian embryogenesis

inferredcites →https://doi.org/10.1093/mutage/gel070openalex-snapshot

Overexpression of DNA polymerase results in an increased rate of frameshift mutations during base excision repair

inferredcites →https://doi.org/10.1093/nar/27.22.4468openalex-snapshot

The human REV1 gene codes for a DNA template-dependent dCMP transferase

inferredcites →https://doi.org/10.1093/nar/gki189openalex-snapshot

The BRCT domain of mammalian Rev1 is involved in regulating DNA translesion synthesis

inferredcites →https://doi.org/10.1093/nar/gki279openalex-snapshot

Vertebrate DNA damage tolerance requires the C-terminus but not BRCT or transferase domains of REV1

inferredcites →https://doi.org/10.1093/nar/gkn310openalex-snapshot

Low-fidelity DNA synthesis by human DNA polymerase theta

inferredcites →https://doi.org/10.1093/nar/gkn651openalex-snapshot

REV1 restrains DNA polymerase ζ to ensure frame fidelity during translesion synthesis of UV photoproducts in vivo

inferredcites →https://doi.org/10.1093/nar/gkp035openalex-snapshot

Human DNA polymerase possesses 5'-dRP lyase activity and functions in single-nucleotide base excision repair in vitro

inferredcites →https://doi.org/10.1093/nar/gkp641openalex-snapshot

A real-time fluorescence method for enzymatic characterization of specialized human DNA polymerases

inferredcites →https://doi.org/10.1093/nar/gkq048openalex-snapshot

Evolutionary conservation of residues in vertebrate DNA polymerase N conferring low fidelity and bypass activity

inferredcites →https://doi.org/10.1093/nar/gkq239openalex-snapshot

Constitutive fusion of ubiquitin to PCNA provides DNA damage tolerance independent of translesion polymerase activities

inferredcites →https://doi.org/10.1093/nar/gkq261openalex-snapshot

Loop 1 modulates the fidelity of DNA polymerase

inferredcites →https://doi.org/10.1093/nar/gkq379openalex-snapshot

Synthesis-dependent microhomology-mediated end joining accounts for multiple types of repair junctions

inferredcites →https://doi.org/10.1093/nass/nrn171openalex-snapshot

Translesion synthesis across the (6-4) photoproduct and its Dewar valence isomer by the Y-family and engineered DNA polymerases

inferredcites →https://doi.org/10.1093/neuonc/nop074openalex-snapshot

Analysis of specialized DNA polymerases expression in human gliomas: association with prognostic significance

inferredcites →https://doi.org/10.1097/01.shk.0000232588.61871.ffopenalex-snapshot

DNA REPAIR AND MUTAGENESIS, 2ND EDITION

inferredcites →https://doi.org/10.1111/j.1356-9597.2004.00747.xopenalex-snapshot

Interaction of hREV1 with three human Y‐family DNA polymerases

inferredcites →https://doi.org/10.1111/j.1365-2443.2006.00974.xopenalex-snapshot

A human DNA polymerase η complex containing Rad18, Rad6 and Rev1; proteomic analysis and targeting of the complex to the chromatin‐bound fraction of cells undergoing replication fork arrest

inferredcites →https://doi.org/10.1111/j.1365-2443.2008.01255.xopenalex-snapshot

Identification of a novel REV1‐interacting motif necessary for DNA polymerase κ function

inferredcites →https://doi.org/10.1124/mol.109.058131openalex-snapshot

The Translesion Polymerase Rev3L in the Tolerance of Alkylating Anticancer Drugs

inferredcites →https://doi.org/10.1126/science.1058386openalex-snapshot

5'-Deoxyribose Phosphate Lyase Activity of Human DNA Polymerase ɩ in Vitro

inferredcites →https://doi.org/10.1126/science.1140735openalex-snapshot

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inferredcites →https://doi.org/10.1126/science.272.5268.1646openalex-snapshot

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inferredcites →https://doi.org/10.1128/mcb.00071-09openalex-snapshot

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inferredcites →https://doi.org/10.1128/mcb.00115-09openalex-snapshot

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Gap-filling and bypass at the replication fork are both active mechanisms for tolerance of low-dose ultraviolet-induced DNA damage in the human genome

inferred← citeshttps://doi.org/10.1016/j.dnarep.2013.12.008openalex-snapshot

In vivo evidence that phenylalanine 171 acts as a molecular brake for translesion DNA synthesis across benzo[a]pyrene DNA adducts by human DNA polymerase κ

inferred← citeshttps://doi.org/10.1016/j.dnarep.2014.09.002openalex-snapshot

In vivo evidence that DNA polymerase kappa is responsible for error-free bypass across DNA cross-links induced by mitomycin C

inferred← citeshttps://doi.org/10.1016/j.dnarep.2015.02.006openalex-snapshot

UV-induced mutations in epidermal cells of mice defective in DNA polymerase η and/or ι

inferred← citeshttps://doi.org/10.1016/j.dnarep.2015.09.020openalex-snapshot

How Y-Family DNA polymerase IV is more accurate than Dpo4 at dCTP insertion opposite an N2-dG adduct of benzo[a]pyrene

inferred← citeshttps://doi.org/10.1016/j.dnarep.2016.05.003openalex-snapshot

DNA polymerase θ (POLQ), double-strand break repair, and cancer

inferred← citeshttps://doi.org/10.1016/j.dnarep.2016.06.002openalex-snapshot

Sensitivity of human cells expressing low-fidelity or weak-catalytic-activity variants of DNA polymerase ζ to genotoxic stresses

inferred← citeshttps://doi.org/10.1016/j.dnarep.2017.02.013openalex-snapshot

Genetic variants of the DNA repair genes from Exome Aggregation Consortium (EXAC) database: significance in cancer

inferred← citeshttps://doi.org/10.1016/j.dnarep.2017.06.017openalex-snapshot

Close encounters: Moving along bumps, breaks, and bubbles on expanded trinucleotide tracts

inferred← citeshttps://doi.org/10.1016/j.dnarep.2017.09.007openalex-snapshot

Not breathing is not an option: How to deal with oxidative DNA damage

inferred← citeshttps://doi.org/10.1016/j.dnarep.2019.02.004openalex-snapshot

Cooperation between non-essential DNA polymerases contributes to genome stability in Saccharomyces cerevisiae

inferred← citeshttps://doi.org/10.1016/j.dnarep.2019.02.007openalex-snapshot

POLE proofreading defects: Contributions to mutagenesis and cancer

inferred← citeshttps://doi.org/10.1016/j.dnarep.2021.103052openalex-snapshot

Error-prone bypass patch by a low-fidelity variant of DNA polymerase zeta in human cells

inferred← citeshttps://doi.org/10.1016/j.dnarep.2021.103079openalex-snapshot

DNA repair gene polymorphisms and chromosomal aberrations in healthy, nonsmoking population

inferred← citeshttps://doi.org/10.1016/j.drudis.2012.04.008openalex-snapshot

DNA polymerase beta (pol β) inhibitors: A comprehensive overview

inferred← citeshttps://doi.org/10.1016/j.envres.2023.115771openalex-snapshot

Therapeutic potential of marine peptides in malignant melanoma

inferred← citeshttps://doi.org/10.1016/j.fct.2013.06.027openalex-snapshot

Inhibitory effects of α-mangostin on mammalian DNA polymerase, topoisomerase, and human cancer cell proliferation

inferred← citeshttps://doi.org/10.1016/j.febslet.2011.03.069openalex-snapshot

Ubiquitylation of DNA polymerase λ

inferred← citeshttps://doi.org/10.1016/j.febslet.2011.04.044openalex-snapshot

Roles of sequential ubiquitination of PCNA in DNA‐damage tolerance

inferred← citeshttps://doi.org/10.1016/j.febslet.2011.04.053openalex-snapshot

Ubiquitin family modifications and template switching

inferred← citeshttps://doi.org/10.1016/j.febslet.2012.07.021openalex-snapshot

The C‐terminal domain of human Rev1 contains independent binding sites for DNA polymerase η and Rev7 subunit of polymerase ζ

inferred← citeshttps://doi.org/10.1016/j.foodchem.2013.04.048openalex-snapshot

Cycloartenyl trans-ferulate, a component of the bran byproduct of sake-brewing rice, inhibits mammalian DNA polymerase and suppresses inflammation

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2016.11.039openalex-snapshot

Coordination of DNA single strand break repair

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2018.12.010openalex-snapshot

Defective repair capacity of variant proteins of the DNA glycosylase NTHL1 for 5-hydroxyuracil, an oxidation product of cytosine

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2018.12.012openalex-snapshot

The key role of UVA-light induced oxidative stress in human Xeroderma Pigmentosum Variant cells

inferred← citeshttps://doi.org/10.1016/j.gene.2018.01.030openalex-snapshot

Polymerase epsilon mutations and concomitant β2-microglobulin mutations in cancer

inferred← citeshttps://doi.org/10.1016/j.gpb.2020.02.001openalex-snapshot

MSIsensor-Pro: Fast, Accurate, and Matched-Normal-Sample-Free Detection of Microsatellite Instability

inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e37488openalex-snapshot

Worldwide analysis of actionable genomic alterations in lung cancer and targeted pharmacogenomic strategies

inferred← citeshttps://doi.org/10.1016/j.htct.2020.05.006openalex-snapshot

c.9253-6T > c REV3L: A novel marker of poor prognosis in Myelodysplastic syndrome

inferred← citeshttps://doi.org/10.1016/j.humgen.2026.201597openalex-snapshot

Helicobacter pylori infection alters the transcriptional expression of DNA polymerase genes involved in DNA repair in AGS gastric cancer cells

inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.131965openalex-snapshot

A conserved polar residue plays a critical role in mismatch detection in A-family DNA polymerases

inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.133924openalex-snapshot

Exploring the molecular aspect and updating evolutionary approaches to the DNA polymerase enzymes for biotechnological needs: A comprehensive review

inferred← citeshttps://doi.org/10.1016/j.isci.2023.108653openalex-snapshot

Adipose-specific overexpression of human AGPAT2 in mice causes increased adiposity and mild hepatic dysfunction

inferred← citeshttps://doi.org/10.1016/j.jbc.2024.107361openalex-snapshot

Sugar ring alignment and dynamics underline cytarabine and gemcitabine inhibition on Pol η catalyzed DNA synthesis

inferred← citeshttps://doi.org/10.1016/j.jmoldx.2017.04.005openalex-snapshot

Improving Mutation Screening in Patients with Colorectal Cancer Predisposition Using Next-Generation Sequencing

inferred← citeshttps://doi.org/10.1016/j.jri.2021.103307openalex-snapshot

Eutopic endometrium from women with endometriosis and chlamydial endometritis share immunological cell types and DNA repair imbalance: A transcriptome meta-analytical perspective

inferred← citeshttps://doi.org/10.1016/j.lungcan.2020.05.021openalex-snapshot

Clinical and Molecular Correlates of Tumor Mutation Burden in Non-Small Cell Lung Cancer

inferred← citeshttps://doi.org/10.1016/j.mce.2015.05.022openalex-snapshot

Lack of Rev7 function results in development of tubulostromal adenomas in mouse ovary

inferred← citeshttps://doi.org/10.1016/j.molcel.2012.10.012openalex-snapshot

The Auto-Generated Fragment of the Usp1 Deubiquitylase Is a Physiological Substrate of the N-End Rule Pathway

inferred← citeshttps://doi.org/10.1016/j.molcel.2016.05.003openalex-snapshot

DNA Replication—A Matter of Fidelity

inferred← citeshttps://doi.org/10.1016/j.molcel.2019.07.012openalex-snapshot

REV1-POL ζ Inhibition and Cancer Therapy

inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2012.06.002openalex-snapshot

Defect of Dpb2p, a noncatalytic subunit of DNA polymerase ε, promotes error prone replication of undamaged chromosomal DNA in Saccharomyces cerevisiae

inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2012.11.003openalex-snapshot

Tumor-specific microsatellite instability: Do distinct mechanisms underlie the MSI-L and EMAST phenotypes?

inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2014.01.003openalex-snapshot

Frequent POLE1 p.S297F mutation in Chinese patients with ovarian endometrioid carcinoma

inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2016.08.004openalex-snapshot

The role of DNA polymerase ζ in translesion synthesis across bulky DNA adducts and cross-links in human cells

inferred← citeshttps://doi.org/10.1016/j.mrgentox.2018.02.001openalex-snapshot

Impact of DNA polymerase ζ mutations on genotoxic thresholds of oxidative mutagens

inferred← citeshttps://doi.org/10.1016/j.mrgentox.2018.02.004openalex-snapshot

Filling gaps in translesion DNA synthesis in human cells

inferred← citeshttps://doi.org/10.1016/j.mrrev.2012.06.002openalex-snapshot

Recognition, signaling, and repair of DNA double-strand breaks produced by ionizing radiation in mammalian cells: The molecular choreography

inferred← citeshttps://doi.org/10.1016/j.mrrev.2017.10.002openalex-snapshot

Nucleosomes regulate base excision repair in chromatin

inferred← citeshttps://doi.org/10.1016/j.pharmthera.2016.02.007openalex-snapshot

Cancer TARGETases: DSB repair as a pharmacological target

inferred← citeshttps://doi.org/10.1016/j.phyplu.2022.100299openalex-snapshot

Chemosensitizing effect of neferine on cisplatin-resistant colorectal cancer: Identification of potential candidate genes and pathways through whole transcriptome profiling

inferred← citeshttps://doi.org/10.1016/j.prp.2017.11.012openalex-snapshot

Prognostic impact of changes in base excision repair machinery in sporadic colorectal cancer

inferred← citeshttps://doi.org/10.1016/j.taap.2012.06.010openalex-snapshot

2,6-Dithiopurine, a nucleophilic scavenger, protects against mutagenesis in mouse skin treated in vivo with 2-(chloroethyl) ethyl sulfide, a mustard gas analog

inferred← citeshttps://doi.org/10.1016/j.toxlet.2015.12.006openalex-snapshot

Crosstalk-eliminated quantitative determination of aflatoxin B1-induced hepatocellular cancer stem cells based on concurrent monitoring of CD133, CD44, and aldehyde dehydrogenase1

inferred← citeshttps://doi.org/10.1016/j.trecan.2017.10.005openalex-snapshot

Fanconi Anemia Signaling and Cancer

inferred← citeshttps://doi.org/10.1016/j.trecan.2024.09.010openalex-snapshot

Mitochondrial DNA damage, repair, and replacement in cancer

inferred← citeshttps://doi.org/10.1016/j.xcrp.2025.102777openalex-snapshot

Reaction pathways and technologies of in vitro DNA synthesis

inferred← citeshttps://doi.org/10.1016/j.xjon.2022.09.001openalex-snapshot

Germline mutations in high penetrance genes are associated with worse clinical outcomes in patients with non–small cell lung cancer

inferred← citeshttps://doi.org/10.1016/j.xjon.2022.09.002openalex-snapshot

Discussion

inferred← citeshttps://doi.org/10.1016/j.yexcr.2014.07.009openalex-snapshot

Tolerating DNA damage during eukaryotic chromosome replication

inferred← citeshttps://doi.org/10.1021/acs.accounts.5b00437openalex-snapshot

Mass Spectrometry-Based Quantitative Strategies for Assessing the Biological Consequences and Repair of DNA Adducts

inferred← citeshttps://doi.org/10.1021/acs.accounts.6c00391openalex-snapshot

Atomistic Simulations Decode the Mechanisms of DNA and RNA Processing Enzymes: Function through Motion

inferred← citeshttps://doi.org/10.1021/acs.accounts.9b00054openalex-snapshot

DNA Adduct-Directed Synthetic Nucleosides

inferred← citeshttps://doi.org/10.1021/acs.analchem.2c01764openalex-snapshot

Next-Generation Sequencing-Based Analysis of the Effects of N1- and N6-Methyldeoxyadenosine Adducts on DNA Transcription

inferred← citeshttps://doi.org/10.1021/acs.biochem.3c00670openalex-snapshot

Melanoma-Derived DNA Polymerase Theta Variants Exhibit Altered DNA Polymerase Activity

inferred← citeshttps://doi.org/10.1021/acs.biochem.6b01213openalex-snapshot

Replication Protein A Prohibits Diffusion of the PCNA Sliding Clamp along Single-Stranded DNA

inferred← citeshttps://doi.org/10.1021/acs.chemrestox.3c00233openalex-snapshot

Biochemical Activity of 17 Cancer-Associated Variants of DNA Polymerase Kappa Predicted by Electrostatic Properties

inferred← citeshttps://doi.org/10.1021/acs.chemrestox.5b00233openalex-snapshot

Enhancing Bulge Stabilization through Linear Extension of C8-Aryl-Guanine Adducts to Promote Polymerase Blockage or Strand Realignment to Produce a C:C Mismatch

inferred← citeshttps://doi.org/10.1021/acs.chemrestox.5b00468openalex-snapshot

DNA Polymerases η and ζ Combine to Bypass O2-[4-(3-Pyridyl)-4-oxobutyl]thymine, a DNA Adduct Formed from Tobacco Carcinogens

inferred← citeshttps://doi.org/10.1021/acs.chemrestox.6b00244openalex-snapshot

Six Germline Genetic Variations Impair the Translesion Synthesis Activity of Human DNA Polymerase κ

inferred← citeshttps://doi.org/10.1021/acs.chemrestox.6b00451openalex-snapshot

Honokiol Inhibits DNA Polymerases β and λ and Increases Bleomycin Sensitivity of Human Cancer Cells

inferred← citeshttps://doi.org/10.1021/acs.chemrestox.6b00466openalex-snapshot

Mutagenic Replication of N2-Deoxyguanosine Benzo[a]pyrene Adducts by Escherichia coli DNA Polymerase I and Sulfolobus solfataricus DNA Polymerase IV

inferred← citeshttps://doi.org/10.1021/acs.chemrestox.7b00157openalex-snapshot

Translesion DNA Synthesis in Cancer: Molecular Mechanisms and Therapeutic Opportunities

inferred← citeshttps://doi.org/10.1021/acs.chemrestox.7b00161openalex-snapshot

Computational Simulations of DNA Polymerases: Detailed Insights on Structure/Function/Mechanism from Native Proteins to Cancer Variants

inferred← citeshttps://doi.org/10.1021/acs.chemrestox.7b00227openalex-snapshot

Mechanism of Error-Free DNA Replication Past Lucidin-Derived DNA Damage by Human DNA Polymerase κ

inferred← citeshttps://doi.org/10.1021/acs.chemrev.7b00046openalex-snapshot

Eukaryotic Translesion DNA Synthesis on the Leading and Lagging Strands: Unique Detours around the Same Obstacle

inferred← citeshttps://doi.org/10.1021/acs.jctc.6c00345openalex-snapshot

Decoding Cancer-Associated Mutations in DNA Polymerase η through Atomistic Simulations

inferred← citeshttps://doi.org/10.1021/acs.jmedchem.6b00596openalex-snapshot

Targeting the Translesion Synthesis Pathway for the Development of Anti-Cancer Chemotherapeutics

inferred← citeshttps://doi.org/10.1021/acs.joc.0c01204openalex-snapshot

Completing the β,γ-CXY-dNTP Stereochemical Probe Toolkit: Synthetic Access to the dCTP Diastereomers and 31P and 19F NMR Correlations with Absolute Configurations

inferred← citeshttps://doi.org/10.1021/acs.jpcb.5b10381openalex-snapshot

DNA Distortion Caused by Uracil-Containing Intrastrand Cross-Links

inferred← citeshttps://doi.org/10.1021/acs.jpcb.6b08581openalex-snapshot

Uniform Free-Energy Profiles of the P–O Bond Formation and Cleavage Reactions Catalyzed by DNA Polymerases β and λ

inferred← citeshttps://doi.org/10.1021/acs.jpcb.6b09973openalex-snapshot

Effects of Active Site Mutations on Specificity of Nucleobase Binding in Human DNA Polymerase η

inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00799openalex-snapshot

Two Scaffolds from Two Flips: (α,β)/(β,γ) CH2/NH “Met-Im” Analogues of dTTP

inferred← citeshttps://doi.org/10.1021/acscatal.8b03363openalex-snapshot

The Catalytic Mechanism of DNA and RNA Polymerases

inferred← citeshttps://doi.org/10.1021/acscatal.8b04889openalex-snapshot

Exploring the Identity of the General Base for a DNA Polymerase Catalyzed Reaction Using QM/MM: The Case Study of Human Translesion Synthesis Polymerase η

inferred← citeshttps://doi.org/10.1021/acschembio.6b00085openalex-snapshot

Roles of Aag, Alkbh2, and Alkbh3 in the Repair of Carboxymethylated and Ethylated Thymidine Lesions

inferred← citeshttps://doi.org/10.1021/acschembio.8b00072openalex-snapshot

DNA Polymerase θ Increases Mutational Rates in Mitochondrial DNA

inferred← citeshttps://doi.org/10.1021/acsnano.4c11259openalex-snapshot

Bioengineered Nanomaterials for siRNA Therapy of Chemoresistant Cancers

inferred← citeshttps://doi.org/10.1021/bi300566zopenalex-snapshot

NMR Structure and Dynamics of the C-Terminal Domain from Human Rev1 and Its Complex with Rev1 Interacting Region of DNA Polymerase η

inferred← citeshttps://doi.org/10.1021/bi300956topenalex-snapshot

Differential Temperature-Dependent Multimeric Assemblies of Replication and Repair Polymerases on DNA Increase Processivity

inferred← citeshttps://doi.org/10.1021/bi4014215openalex-snapshot

RB69 DNA Polymerase Structure, Kinetics, and Fidelity

inferred← citeshttps://doi.org/10.1021/cb4007562openalex-snapshot

Expanding the Scope of Human DNA Polymerase λ and β Inhibitors

inferred← citeshttps://doi.org/10.1021/ja403842jopenalex-snapshot

Amino Acid Substitution in the Active Site of DNA Polymerase β Explains the Energy Barrier of the Nucleotidyl Transfer Reaction

inferred← citeshttps://doi.org/10.1021/ja512547gopenalex-snapshot

Nucleotides with Altered Hydrogen Bonding Capacities Impede Human DNA Polymerase η by Reducing Synthesis in the Presence of the Major Cisplatin DNA Adduct

inferred← citeshttps://doi.org/10.1021/jacs.5b08451openalex-snapshot

Relative Binding Free Energies of Adenine and Guanine to Damaged and Undamaged DNA in Human DNA Polymerase η: Clues for Fidelity and Overall Efficiency

inferred← citeshttps://doi.org/10.1021/jacs.6b05475openalex-snapshot

A Self-Activated Mechanism for Nucleic Acid Polymerization Catalyzed by DNA/RNA Polymerases

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