| scholarly article | Q13442814 |
| P50 | author | Stephane Marcand | Q42762847 |
| Benjamin Pardo | Q59824157 | ||
| P2093 | author name string | Emilie Ma | |
| P2860 | cites work | Activity of DNA ligase IV stimulated by complex formation with XRCC4 protein in mammalian cells | Q24320116 |
| Association of DNA polymerase mu (pol mu) with Ku and ligase IV: role for pol mu in end-joining double-strand break repair | Q24540101 | ||
| Saccharomyces cerevisiae Ku70 potentiates illegitimate DNA double-strand break repair and serves as a barrier to error-prone DNA repair pathways | Q24561996 | ||
| A newly identified DNA ligase of Saccharomyces cerevisiae involved in RAD52-independent repair of DNA double-strand breaks | Q24609020 | ||
| Crystal structures of a template-independent DNA polymerase: murine terminal deoxynucleotidyltransferase | Q27637560 | ||
| Implication of DNA polymerase lambda in alignment-based gap filling for nonhomologous DNA end joining in human nuclear extracts. | Q27919645 | ||
| A gradient of template dependence defines distinct biological roles for family X polymerases in nonhomologous end joining | Q27919680 | ||
| Yeast open reading frame YCR14C encodes a DNA beta-polymerase-like enzyme | Q27935195 | ||
| A physical and functional interaction between yeast Pol4 and Dnl4-Lif1 links DNA synthesis and ligation in nonhomologous end joining | Q27935436 | ||
| Rap1 prevents telomere fusions by nonhomologous end joining | Q27936253 | ||
| Efficient processing of DNA ends during yeast nonhomologous end joining. Evidence for a DNA polymerase beta (Pol4)-dependent pathway | Q27938668 | ||
| Immunoglobulin kappa light chain gene rearrangement is impaired in mice deficient for DNA polymerase mu | Q28202970 | ||
| DNA joint dependence of pol X family polymerase action in nonhomologous end joining | Q28257407 | ||
| Yeast recombination: the association between double-strand gap repair and crossing-over | Q28265497 | ||
| Telomerase-dependent repeat divergence at the 3' ends of yeast telomeres | Q33616690 | ||
| Role of yeast SIR genes and mating type in directing DNA double-strand breaks to homologous and non-homologous repair paths. | Q33869149 | ||
| The generation of proper constitutive G-tails on yeast telomeres is dependent on the MRX complex | Q34510751 | ||
| Capture of extranuclear DNA at fission yeast double-strand breaks | Q34586796 | ||
| A role for FEN-1 in nonhomologous DNA end joining: the order of strand annealing and nucleolytic processing events | Q34988376 | ||
| Non-homologous end-joining: bacteria join the chromosome breakdance | Q35063174 | ||
| Complexity of damage produced by ionizing radiation | Q35132590 | ||
| Indecent exposure: when telomeres become uncapped | Q35632849 | ||
| Genetic regulation of telomere-telomere fusions in the yeast Saccharomyces cerevisae | Q35978538 | ||
| Nonhomologous end joining in yeast | Q36312212 | ||
| A biochemically defined system for mammalian nonhomologous DNA end joining | Q38333666 | ||
| Highly frequent frameshift DNA synthesis by human DNA polymerase mu | Q39529040 | ||
| Non-homologous end joining as an important mutagenic process in cell cycle-arrested cells | Q39756406 | ||
| Microhomology-dependent end joining and repair of transposon-induced DNA hairpins by host factors in Saccharomyces cerevisiae. | Q40468984 | ||
| The Saccharomyces cerevisiae Ku autoantigen homologue affects radiosensitivity only in the absence of homologous recombination | Q41813747 | ||
| Enhancement of Saccharomyces cerevisiae end-joining efficiency by cell growth stage but not by impairment of recombination | Q42019079 | ||
| TBP-associated factors are not generally required for transcriptional activation in yeast | Q42522148 | ||
| Purification and characterization of a new DNA polymerase from budding yeast Saccharomyces cerevisiae. A probable homolog of mammalian DNA polymerase beta | Q42610613 | ||
| Taz1, Rap1 and Rif1 act both interdependently and independently to maintain telomeres | Q42957239 | ||
| The Mre11/Rad50/Xrs2 complex and non-homologous end-joining of incompatible ends in S. cerevisiae | Q46618397 | ||
| Lesion bypass by human DNA polymerase mu reveals a template-dependent, sequence-independent nucleotidyl transferase activity. | Q54516425 | ||
| Transient stability of DNA ends allows nonhomologous end joining to precede homologous recombination | Q64387672 | ||
| Biochemical properties of Saccharomyces cerevisiae DNA polymerase IV | Q64388776 | ||
| Non-homologous end joining dependency of gamma-irradiation-induced adaptive frameshift mutation formation in cell cycle-arrested yeast cells | Q64388854 | ||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Saccharomyces cerevisiae | Q719725 |
| P1104 | number of pages | 6 | |
| P304 | page(s) | 2689-2694 | |
| P577 | publication date | 2006-02-01 | |
| P1433 | published in | Genetics | Q3100575 |
| P1476 | title | Mismatch tolerance by DNA polymerase Pol4 in the course of nonhomologous end joining in Saccharomyces cerevisiae | |
| P478 | volume | 172 |
| Q42147106 | Conferring a template-dependent polymerase activity to terminal deoxynucleotidyltransferase by mutations in the Loop1 region |
| Q38848161 | Consider the workhorse: Nonhomologous end-joining in budding yeast |
| 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 |
| Q27919720 | End-bridging is required for pol mu to efficiently promote repair of noncomplementary ends by nonhomologous end joining |
| Q34559710 | End-processing during non-homologous end-joining: a role for exonuclease 1 |
| Q39022234 | Eukaryotic DNA Polymerases in Homologous Recombination |
| Q38866701 | How do telomeres and NHEJ coexist? |
| Q35911019 | Microhomology-mediated end joining in fission yeast is repressed by pku70 and relies on genes involved in homologous recombination |
| Q36585488 | Multiple pathways inhibit NHEJ at telomeres. |
| Q42913220 | Mutational effects of γ-rays and carbon ion beams on Arabidopsis seedlings |
| Q37774662 | Polymerases in nonhomologous end joining: building a bridge over broken chromosomes |
| Q36591704 | Requirement of POL3 and POL4 on non-homologous and microhomology-mediated end joining in rad50/xrs2 mutants of Saccharomyces cerevisiae. |
| 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 |
| Q36709911 | Telomere length homeostasis responds to changes in intracellular dNTP pools |
| Q24298401 | The yeast Fun30 and human SMARCAD1 chromatin remodellers promote DNA end resection |
| Q34846094 | Yeast pol4 promotes tel1-regulated chromosomal translocations |
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