| scholarly article | Q13442814 |
| P2093 | author name string | T E Wilson | |
| M R Lieber | |||
| P2860 | cites work | DNA ligase IV is essential for V(D)J recombination and DNA double-strand break repair in human precursor lymphocytes | Q22007974 |
| The 3' to 5' exonuclease activity of Mre 11 facilitates repair of DNA double-strand breaks | Q24311761 | ||
| Activity of DNA ligase IV stimulated by complex formation with XRCC4 protein in mammalian cells | Q24320116 | ||
| Mammalian DNA double-strand break repair protein XRCC4 interacts with DNA ligase IV | Q24323238 | ||
| A newly identified DNA ligase of Saccharomyces cerevisiae involved in RAD52-independent repair of DNA double-strand breaks | Q24609020 | ||
| Cell cycle and genetic requirements of two pathways of nonhomologous end-joining repair of double-strand breaks in Saccharomyces cerevisiae | Q24649768 | ||
| Crystal structures of human DNA polymerase beta complexed with gapped and nicked DNA: evidence for an induced fit mechanism | Q27742804 | ||
| Distinct roles of two separable in vitro activities of yeast Mre11 in mitotic and meiotic recombination | Q27930776 | ||
| Yeast DNA ligase IV mediates non-homologous DNA end joining | Q27931843 | ||
| Mutations in two Ku homologs define a DNA end-joining repair pathway in Saccharomyces cerevisiae | Q27932896 | ||
| Eukaryotic DNA polymerases in DNA replication and DNA repair | Q27933940 | ||
| Yeast open reading frame YCR14C encodes a DNA beta-polymerase-like enzyme | Q27935195 | ||
| Efficient bypass of a thymine-thymine dimer by yeast DNA polymerase, Poleta | Q27935465 | ||
| The nuclease activity of Mre11 is required for meiosis but not for mating type switching, end joining, or telomere maintenance | Q27937328 | ||
| Saccharomyces cerevisiae LIF1: a function involved in DNA double-strand break repair related to mammalian XRCC4. | Q27938296 | ||
| A simple and efficient method for direct gene deletion in Saccharomyces cerevisiae | Q28131603 | ||
| Late embryonic lethality and impaired V(D)J recombination in mice lacking DNA ligase IV | Q28504490 | ||
| Expression and V(D)J recombination activity of mutated RAG-1 proteins | Q28506727 | ||
| Sequences That Regulate the Divergent GAL1-GAL10 Promoter in Saccharomyces cerevisiae | Q29547797 | ||
| Saccharomyces Ku70, mre11/rad50 and RPA proteins regulate adaptation to G2/M arrest after DNA damage | Q29614221 | ||
| ProMod and Swiss-Model: Internet-based tools for automated comparative protein modelling | Q29617090 | ||
| Which DNA polymerases are used for DNA-repair in eukaryotes? | Q34422388 | ||
| Double strand break repair | Q34743014 | ||
| Noncomplementary DNA double-strand-break rejoining in bacterial and human cells | Q34974786 | ||
| A role for FEN-1 in nonhomologous DNA end joining: the order of strand annealing and nucleolytic processing events | Q34988376 | ||
| The yeast Saccharomyces cerevisiae DNA polymerase IV: possible involvement in double strand break DNA repair | Q35009312 | ||
| Life without DNA repair | Q36158486 | ||
| Exonuclease I of Saccharomyces cerevisiae functions in mitotic recombination in vivo and in vitro | Q36568265 | ||
| Mechanisms of overlap formation in nonhomologous DNA end joining | Q36645093 | ||
| Two different types of double-strand breaks in Saccharomyces cerevisiae are repaired by similar RAD52-independent, nonhomologous recombination events | Q36646569 | ||
| Nonhomologous recombination in mammalian cells: role for short sequence homologies in the joining reaction | Q36901365 | ||
| Identification of Saccharomyces cerevisiae DNA ligase IV: involvement in DNA double-strand break repair | Q38343656 | ||
| Two pathways for removal of nonhomologous DNA ends during double-strand break repair in Saccharomyces cerevisiae | Q40023936 | ||
| Cellular role of yeast Apn1 apurinic endonuclease/3'-diesterase: repair of oxidative and alkylation DNA damage and control of spontaneous mutation | Q40640344 | ||
| Structure of the Saccharomyces cerevisiae HO gene and analysis of its upstream regulatory region | Q40667868 | ||
| Requirement of mammalian DNA polymerase-beta in base-excision repair. | Q41239890 | ||
| Tying loose ends: roles of Ku and DNA-dependent protein kinase in the repair of double-strand breaks | Q41345394 | ||
| The RAD52 epistasis group in mammalian double strand break repair | Q41512966 | ||
| DNA repair: RAD alert | Q41565006 | ||
| The roles of the eukaryotic DNA polymerases in DNA repair synthesis | Q41612088 | ||
| DNA-dependent protein kinase | Q41647385 | ||
| End-joining of free radical-mediated DNA double-strand breaks in vitro is blocked by the kinase inhibitor wortmannin at a step preceding removal of damaged 3' termini | Q45097854 | ||
| Construction of a vector containing a site-specific DNA double-strand break with 3'-phosphoglycolate termini and analysis of the products of end-joining in CV-1 cells | Q45102181 | ||
| Purification and enzymatic and functional characterization of DNA polymerase beta-like enzyme, POL4. expressed during yeast meiosis | Q46412438 | ||
| Deoxyribose phosphate excision by the N-terminal domain of the polymerase beta: the mechanism revisited | Q47870418 | ||
| Involvement of the Saccharomyces cerevisiae HDF1 gene in DNA double-strand break repair and recombination. | Q52519451 | ||
| Genetic analysis of the yeast NUD1 endo-exonuclease: a role in the repair of DNA double-strand breaks. | Q54110786 | ||
| Genetic interaction between PARP and DNA-PK in V(D)J recombination and tumorigenesis | Q58326911 | ||
| Silencing factors participate in DNA repair and recombination in Saccharomyces cerevisiae | Q59052272 | ||
| P433 | issue | 33 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | DNA-directed DNA polymerase IV YCR014C | Q27550152 |
| P304 | page(s) | 23599-609 | |
| P577 | publication date | 1999-08-13 | |
| P1433 | published in | Journal of Biological Chemistry | Q867727 |
| P1476 | title | Efficient processing of DNA ends during yeast nonhomologous end joining. Evidence for a DNA polymerase beta (Pol4)-dependent pathway | |
| P478 | volume | 274 |
| Q27938387 | A genomics-based screen for yeast mutants with an altered recombination/end-joining repair ratio. |
| Q27935436 | A physical and functional interaction between yeast Pol4 and Dnl4-Lif1 links DNA synthesis and ligation in nonhomologous end joining |
| Q28492870 | A primer-dependent polymerase function of pseudomonas aeruginosa ATP-dependent DNA ligase (LigD) |
| Q28247648 | A structural solution for the DNA polymerase lambda-dependent repair of DNA gaps with minimal homology |
| Q35082618 | Accessibility control and machinery of immunoglobulin class switch recombination |
| Q27938785 | Accessibility of DNA polymerases to repair synthesis during nucleotide excision repair in yeast cell-free extracts |
| Q27935926 | Acetylation of histone H4 by Esa1 is required for DNA double-strand break repair. |
| Q34661313 | Adaptive mutation in Saccharomyces cerevisiae |
| Q24540101 | Association of DNA polymerase mu (pol mu) with Ku and ligase IV: role for pol mu in end-joining double-strand break repair |
| Q34478631 | Atomic structure and nonhomologous end-joining function of the polymerase component of bacterial DNA ligase D |
| Q98208982 | Cdc13 is predominant over Stn1 and Ten1 in preventing chromosome end fusions |
| Q24816438 | Characterization of SpPol4, a unique X-family DNA polymerase in Schizosaccharomyces pombe. |
| Q73420352 | Characterization of mutations that are synthetic lethal with pol3-13, a mutated allele of DNA polymerase delta in Saccharomyces cerevisiae |
| Q37638191 | Collaboration and competition between DNA double‐strand break repair pathways |
| Q38848161 | Consider the workhorse: Nonhomologous end-joining in budding yeast |
| Q91714735 | DNA Damage Response Pathways in Dinoflagellates |
| Q54356059 | DNA binding proteins: outline of functional classification. |
| Q39543261 | DNA double-strand break repair in cell-free extracts from Ku80-deficient cells: implications for Ku serving as an alignment factor in non-homologous DNA end joining |
| Q28257407 | DNA joint dependence of pol X family polymerase action in nonhomologous end joining |
| Q34587534 | DNA polymerase 4 of Saccharomyces cerevisiae is important for accurate repair of methyl-methanesulfonate-induced DNA damage |
| Q47378572 | DNA polymerase beta participates in DNA End-joining. |
| Q34537672 | DNA polymerase beta. |
| Q28238256 | DNA polymerase lambda mediates a back-up base excision repair activity in extracts of mouse embryonic fibroblasts |
| Q40400659 | DNA polymerase lambda protects mouse fibroblasts against oxidative DNA damage and is recruited to sites of DNA damage/repair |
| Q33770300 | DNA polymerase mu, a candidate hypermutase? |
| Q37109944 | DNA polymerases in adaptive immunity |
| Q38044298 | DNA polymerases in nonhomologous end joining: are there any benefits to standing out from the crowd? |
| Q36394254 | DNA polymerases δ and λ cooperate in repairing double-strand breaks by microhomology-mediated end-joining in Saccharomyces cerevisiae |
| Q39675323 | DNA substrate dependence of p53-mediated regulation of double-strand break repair |
| Q41980831 | DNA-binding determinants promoting NHEJ by human Polμ. |
| Q64387470 | Different genome maintenance strategies in human and tobacco cells |
| Q34569414 | End-joining repair of double-strand breaks in Drosophila melanogaster is largely DNA ligase IV independent |
| Q34559710 | End-processing during non-homologous end-joining: a role for exonuclease 1 |
| Q42019079 | Enhancement of Saccharomyces cerevisiae end-joining efficiency by cell growth stage but not by impairment of recombination |
| Q35205714 | Enhancement of silencing DNA polymerase β on the radiotherapeutic sensitivity of human esophageal carcinoma cell lines |
| Q35582961 | Error-Prone DNA Polymerases: When Making a Mistake is the Only Way to Get Ahead |
| Q33850056 | Eukaryotic DNA polymerases, a growing family |
| Q46078838 | Evaluation of the roles of Pol zeta and NHEJ in starvation-associated spontaneous mutagenesis in the yeast Saccharomyces cerevisiae |
| Q36353993 | Evidence for abasic site sugar phosphate-mediated cytotoxicity in alkylating agent treated Saccharomyces cerevisiae |
| Q42248409 | Evidence that base stacking potential in annealed 3' overhangs determines polymerase utilization in yeast nonhomologous end joining |
| Q28261381 | Flexibility in the order of action and in the enzymology of the nuclease, polymerases, and ligase of vertebrate non-homologous DNA end joining: relevance to cancer, aging, and the immune system |
| Q64387168 | Frequency of DNA end joining is not determined by the predamage spatial proximity of double-strand breaks in yeast |
| Q28297537 | Functions of DNA polymerases |
| Q41428773 | G648C variant of DNA polymerase β sensitizes esophageal cancer to chemotherapy |
| Q27933147 | Genetic interactions between HNT3/Aprataxin and RAD27/FEN1 suggest parallel pathways for 5' end processing during base excision repair |
| Q25255793 | Genome wide distribution of illegitimate recombination events in Kluyveromyces lactis |
| Q41812715 | Genomic analysis of cancer tissue reveals that somatic mutations commonly occur in a specific motif. |
| Q39529040 | Highly frequent frameshift DNA synthesis by human DNA polymerase mu |
| Q38866701 | How do telomeres and NHEJ coexist? |
| Q73234169 | Human DNA polymerase lambda possesses terminal deoxyribonucleotidyl transferase activity and can elongate RNA primers: implications for novel functions |
| Q39600750 | Human DNA polymerase mu (Pol mu) exhibits an unusual replication slippage ability at AAF lesion |
| Q28354217 | In vivo consequences of putative active site mutations in yeast DNA polymerases alpha, epsilon, delta, and zeta |
| Q35661472 | Interplay between Ku and Replication Protein A in the Restriction of Exo1-mediated DNA Break End Resection |
| Q74321385 | Introduction of point mutations into cloned genes |
| Q38181069 | Is non-homologous end-joining really an inherently error-prone process? |
| Q52676508 | Ku DNA End-Binding Activity Promotes Repair Fidelity and Influences End-Processing During Nonhomologous End-Joining in Saccharomyces cerevisiae. |
| Q39870596 | MLH1 deficiency enhances tumor cell sensitivity to ganciclovir |
| Q24631110 | Managing DNA polymerases: coordinating DNA replication, DNA repair, and DNA recombination |
| Q35542018 | Mechanism and regulation of human non-homologous DNA end-joining |
| Q33979569 | Mechanisms of chromosome number evolution in yeast |
| Q35543795 | Mending the Break: Two DNA Double-Strand Break Repair Machines in Eukaryotes |
| Q38854866 | MiR-499 Enhances the Cisplatin Sensitivity of Esophageal Carcinoma Cell Lines by Targeting DNA Polymerase β. |
| Q28592782 | Mice reconstituted with DNA polymerase beta-deficient fetal liver cells are able to mount a T cell-dependent immune response and mutate their Ig genes normally |
| Q40468984 | Microhomology-dependent end joining and repair of transposon-induced DNA hairpins by host factors in Saccharomyces cerevisiae. |
| Q35911019 | Microhomology-mediated end joining in fission yeast is repressed by pku70 and relies on genes involved in homologous recombination |
| Q48015614 | Microhomology-mediated end joining: Good, bad and ugly. |
| Q38316253 | Mismatch tolerance by DNA polymerase Pol4 in the course of nonhomologous end joining in Saccharomyces cerevisiae. |
| Q24682173 | Modes of interaction among yeast Nej1, Lif1 and Dnl4 proteins and comparison to human XLF, XRCC4 and Lig4 |
| Q34175308 | Modularly assembled designer TAL effector nucleases for targeted gene knockout and gene replacement in eukaryotes |
| Q28261218 | Modulation of DNA end joining by nuclear proteins |
| Q40701385 | Mutations of the Yku80 C terminus and Xrs2 FHA domain specifically block yeast nonhomologous end joining |
| Q38194755 | Non-homologous end joining often uses microhomology: implications for alternative end joining |
| Q35063174 | Non-homologous end-joining: bacteria join the chromosome breakdance |
| Q34813549 | Nonhomologous DNA end joining (NHEJ) and chromosomal translocations in humans |
| Q40428371 | Nonhomologous end-joining in a cell-free extract from the cultured silkworm cell line BmN4. |
| Q37406025 | Overexpression of A613T and G462T variants of DNA polymerase β weakens chemotherapy sensitivity in esophageal cancer cell lines |
| Q37774662 | Polymerases in nonhomologous end joining: building a bridge over broken chromosomes |
| Q42113628 | Polμ tumor variants decrease the efficiency and accuracy of NHEJ. |
| Q27939628 | Processing and joining of DNA ends coordinated by interactions among Dnl4/Lif1, Pol4, and FEN-1. |
| Q35864915 | Promiscuous mismatch extension by human DNA polymerase lambda |
| Q21145041 | Proofreading activity of DNA polymerase Pol2 mediates 3'-end processing during nonhomologous end joining in yeast |
| Q37802636 | RAD18 lives a double life: Its implication in DNA double-strand break repair |
| Q34643637 | Reciprocal translocations in Saccharomyces cerevisiae formed by nonhomologous end joining |
| Q38331775 | Rejoining of DNA double-strand breaks as a function of overhang length |
| Q38103528 | Repair of double-strand breaks by end joining |
| Q36277189 | Repeat instability: mechanisms of dynamic mutations |
| Q36591704 | Requirement of POL3 and POL4 on non-homologous and microhomology-mediated end joining in rad50/xrs2 mutants of Saccharomyces cerevisiae. |
| Q64387913 | Role of Dnl4-Lif1 in nonhomologous end-joining repair complex assembly and suppression of homologous recombination |
| Q43193261 | Role of budding yeast Rad18 in repair of HO-induced double-strand breaks. |
| Q37289660 | Role of the yeast DNA repair protein Nej1 in end processing during the repair of DNA double strand breaks by non-homologous end joining |
| Q36687824 | Roles of DNA polymerases in replication, repair, and recombination in eukaryotes. |
| Q35945630 | Saccharomyces cerevisiae Sae2- and Tel1-dependent single-strand DNA formation at DNA break promotes microhomology-mediated end joining |
| Q28270934 | Sibling rivalry: competition between Pol X family members in V(D)J recombination and general double strand break repair |
| Q42700256 | Systematic biochemical analysis of somatic missense mutations in DNA polymerase β found in prostate cancer reveal alteration of enzymatic function |
| Q42061406 | The DNA polymerase lambda is required for the repair of non-compatible DNA double strand breaks by NHEJ in mammalian cells |
| Q35968498 | The DNA-polymerase-X family: controllers of DNA quality? |
| Q42744119 | The fidelity of the ligation step determines how ends are resolved during nonhomologous end joining. |
| Q53653976 | The frameshift infidelity of human DNA polymerase lambda. Implications for function. |
| Q22065419 | The mechanism of double-strand DNA break repair by the nonhomologous DNA end-joining pathway |
| Q28257187 | The mechanism of human nonhomologous DNA end joining |
| Q24291484 | The role of DNA polymerase activity in human non-homologous end joining |
| Q44463888 | The role of yeast DNA 3'-phosphatase Tpp1 and rad1/Rad10 endonuclease in processing spontaneous and induced base lesions |
| Q27934796 | The yeast chromatin remodeler RSC complex facilitates end joining repair of DNA double-strand breaks |
| Q64387672 | Transient stability of DNA ends allows nonhomologous end joining to precede homologous recombination |
| Q38086224 | Translesion DNA synthesis and mutagenesis in eukaryotes |
| Q33984271 | Tying up loose ends: nonhomologous end-joining in Saccharomyces cerevisiae |
| Q27929780 | Uncoupling of 3'-phosphatase and 5'-kinase functions in budding yeast. Characterization of Saccharomyces cerevisiae DNA 3'-phosphatase (TPP1). |
| Q37693925 | Understanding the loss-of-function in a triple missense mutant of DNA polymerase β found in prostate cancer. |
| Q27919707 | XRCC4:DNA ligase IV can ligate incompatible DNA ends and can ligate across gaps |
| Q35007981 | Yeast DNA ligase IV mutations reveal a nonhomologous end joining function of BRCT1 distinct from XRCC4/Lif1 binding |
| Q40173836 | Yeast Mre11 and Rad1 proteins define a Ku-independent mechanism to repair double-strand breaks lacking overlapping end sequences |
| Q33732769 | Yeast Tdp1 regulates the fidelity of nonhomologous end joining |
| Q34846094 | Yeast pol4 promotes tel1-regulated chromosomal translocations |
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