| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Lynne S Cox | Q47503394 |
| P2093 | author name string | Penelope A Mason | |
| P2860 | cites work | Structure of the DNA repair and replication endonuclease and exonuclease FEN-1: coupling DNA and PCNA binding to FEN-1 activity | Q22003979 |
| Human homologs of Schizosaccharomyces pombe rad1, hus1, and rad9 form a DNA damage-responsive protein complex | Q22008596 | ||
| Human exonuclease 1 functionally complements its yeast homologues in DNA recombination, RNA primer removal, and mutation avoidance | Q22009967 | ||
| Identification and expression of the TREX1 and TREX2 cDNA sequences encoding mammalian 3'-->5' exonucleases | Q22010206 | ||
| A human DNA editing enzyme homologous to the Escherichia coli DnaQ/MutD protein | Q22010212 | ||
| The RAD2 domain of human exonuclease 1 exhibits 5' to 3' exonuclease and flap structure-specific endonuclease activities | Q22010967 | ||
| Eukaryotic DNA Polymerases | Q22065416 | ||
| Human DNA damage checkpoint protein hRAD9 is a 3' to 5' exonuclease | Q22253323 | ||
| Ku complex interacts with and stimulates the Werner protein | Q22253994 | ||
| Characterization of the human and mouse WRN 3'-->5' exonuclease | Q22254412 | ||
| Structure and expression of the TREX1 and TREX2 3' --> 5' exonuclease genes | Q24291021 | ||
| Excision of 3' termini by the Trex1 and TREX2 3'-->5' exonucleases. Characterization of the recombinant proteins | Q24291054 | ||
| p53 Modulates the exonuclease activity of Werner syndrome protein | Q24291371 | ||
| Modeling Werner Syndrome in Drosophila melanogaster: hyper-recombination in flies lacking WRN-like exonuclease | Q47070640 | ||
| Cloning of senescent cell-derived inhibitors of DNA synthesis using an expression screen | Q48084448 | ||
| A functional EXO1 promoter variant is associated with prolonged life expectancy in centenarians. | Q51618454 | ||
| Caenorhabditis elegans DNA-2 helicase/endonuclease plays a vital role in maintaining genome stability, morphogenesis, and life span. | Q51886397 | ||
| Increase in mitochondrial DNA mutations impairs retinal function and renders the retina vulnerable to injury | Q57537758 | ||
| Cdkn1a deletion improves stem cell function and lifespan of mice with dysfunctional telomeres without accelerating cancer formation | Q60284598 | ||
| Two Pathways for Base Excision Repair in Mammalian Cells | Q60702220 | ||
| p53 Protein exhibits 3'-to-5' exonuclease activity | Q71170481 | ||
| Fanconi anemia | Q72146633 | ||
| Second human protein with homology to the Escherichia coli abasic endonuclease exonuclease III | Q73384174 | ||
| A 3'-5' exonuclease in human leukemia cells: implications for resistance to 1-beta -D-arabinofuranosylcytosine and 9-beta -D-arabinofuranosyl-2-fluoroadenine 5'-monophosphate | Q73838487 | ||
| Defective DNA polymerase-delta proofreading causes cancer susceptibility in mice | Q73954766 | ||
| The fidelity of human DNA polymerase gamma with and without exonucleolytic proofreading and the p55 accessory subunit | Q74371876 | ||
| Biochemical characterization of the DNA substrate specificity of Werner syndrome helicase | Q77948758 | ||
| A nuclear 3'-5' exonuclease proofreads for the exonuclease-deficient DNA polymerase alpha | Q78804406 | ||
| Evidence that errors made by DNA polymerase alpha are corrected by DNA polymerase delta | Q82346662 | ||
| Werner syndrome protein interacts with human flap endonuclease 1 and stimulates its cleavage activity | Q24291787 | ||
| Human exonuclease I is required for 5' and 3' mismatch repair | Q24292224 | ||
| An exonucleolytic activity of human apurinic/apyrimidinic endonuclease on 3' mispaired DNA | Q24292267 | ||
| BLM-DNA2-RPA-MRN and EXO1-BLM-RPA-MRN constitute two DNA end resection machineries for human DNA break repair | Q24293244 | ||
| Premature ageing in mice expressing defective mitochondrial DNA polymerase | Q24294365 | ||
| Feedback between p21 and reactive oxygen production is necessary for cell senescence | Q24299631 | ||
| The human Rad9 checkpoint protein stimulates the carbamoyl phosphate synthetase activity of the multifunctional protein CAD | Q24301815 | ||
| Telomere-binding protein TRF2 binds to and stimulates the Werner and Bloom syndrome helicases | Q24304488 | ||
| Identification and biochemical characterization of a Werner's syndrome protein complex with Ku70/80 and poly(ADP-ribose) polymerase-1 | Q24305550 | ||
| POT1 stimulates RecQ helicases WRN and BLM to unwind telomeric DNA substrates | Q24308828 | ||
| Asymmetry of DNA replication fork progression in Werner's syndrome | Q24311409 | ||
| The 3' to 5' exonuclease activity of Mre 11 facilitates repair of DNA double-strand breaks | Q24311761 | ||
| p53 target gene AEN is a nuclear exonuclease required for p53-dependent apoptosis | Q24312817 | ||
| Human DNA2 is a mitochondrial nuclease/helicase for efficient processing of DNA replication and repair intermediates | Q24312975 | ||
| A human homologue of the Schizosaccharomyces pombe rad1+ checkpoint gene encodes an exonuclease | Q24314103 | ||
| Identification and characterization of Saccharomyces cerevisiae EXO1, a gene encoding an exonuclease that interacts with MSH2 | Q24314329 | ||
| Human SLX4 is a Holliday junction resolvase subunit that binds multiple DNA repair/recombination endonucleases | Q24314357 | ||
| Human Dna2 is a nuclear and mitochondrial DNA maintenance protein | Q24316108 | ||
| Bloom's and Werner's syndrome genes suppress hyperrecombination in yeast sgs1 mutant: implication for genomic instability in human diseases | Q24317166 | ||
| WRN exonuclease structure and molecular mechanism imply an editing role in DNA end processing | Q24318651 | ||
| XPG endonuclease makes the 3' incision in human DNA nucleotide excision repair | Q24320768 | ||
| The characterization of a mammalian DNA structure-specific endonuclease | Q24336672 | ||
| Identification of KIAA1018/FAN1, a DNA repair nuclease recruited to DNA damage by monoubiquitinated FANCD2 | Q24337575 | ||
| Deficiency of FANCD2-associated nuclease KIAA1018/FAN1 sensitizes cells to interstrand crosslinking agents | Q24337605 | ||
| A genetic screen identifies FAN1, a Fanconi anemia-associated nuclease necessary for DNA interstrand crosslink repair | Q24337655 | ||
| Circulating mitochondrial DAMPs cause inflammatory responses to injury | Q29614470 | ||
| Choreography of the DNA damage response: spatiotemporal relationships among checkpoint and repair proteins | Q29615270 | ||
| Positional cloning of the Werner's syndrome gene | Q29618393 | ||
| Endurance exercise rescues progeroid aging and induces systemic mitochondrial rejuvenation in mtDNA mutator mice | Q30498491 | ||
| DNA replication: partners in the Okazaki two-step | Q30755185 | ||
| The protein components and mechanism of eukaryotic Okazaki fragment maturation | Q31034204 | ||
| On the roles of Saccharomyces cerevisiae Dna2p and Flap endonuclease 1 in Okazaki fragment processing | Q31038690 | ||
| Length-dependent degradation of single-stranded 3' ends by the Werner syndrome protein (WRN): implications for spatial orientation and coordinated 3' to 5' movement of its ATPase/helicase and exonuclease domains | Q33234879 | ||
| Tissue specific mutagenic and carcinogenic responses in NER defective mouse models | Q33246534 | ||
| Exonuclease-1 deletion impairs DNA damage signaling and prolongs lifespan of telomere-dysfunctional mice | Q33297433 | ||
| Interplay of Mre11 nuclease with Dna2 plus Sgs1 in Rad51-dependent recombinational repair | Q33402478 | ||
| FEN1 functions in long patch base excision repair under conditions of oxidative stress in vertebrate cells | Q33670045 | ||
| The Werner syndrome gene product co-purifies with the DNA replication complex and interacts with PCNA and topoisomerase I. | Q33884556 | ||
| Accumulating mitochondrial DNA mutations drive premature hematopoietic aging phenotypes distinct from physiological stem cell aging | Q33891793 | ||
| ATM-dependent phosphorylation of human Rad9 is required for ionizing radiation-induced checkpoint activation | Q33940379 | ||
| Delineation of WRN helicase function with EXO1 in the replicational stress response | Q33945750 | ||
| The 3'-->5' exonucleases of DNA polymerases delta and epsilon and the 5'-->3' exonuclease Exo1 have major roles in postreplication mutation avoidance in Saccharomyces cerevisiae | Q33957467 | ||
| Stability of the human fragile X (CGG)(n) triplet repeat array in Saccharomyces cerevisiae deficient in aspects of DNA metabolism | Q33958980 | ||
| Novel function of Rad27 (FEN-1) in restricting short-sequence recombination | Q33967784 | ||
| DNA damage-dependent nuclear dynamics of the Mre11 complex | Q33975168 | ||
| An mre11 mutation that promotes telomere recombination and an efficient bypass of senescence | Q34007895 | ||
| Evidence for extrinsic exonucleolytic proofreading. | Q34010452 | ||
| Haploinsufficiency of Flap endonuclease (Fen1) leads to rapid tumor progression | Q34098053 | ||
| FAN1 Acts with FANCI-FANCD2 to Promote DNA Interstrand Cross-Link Repair | Q34128701 | ||
| Homologous recombination resolution defect in werner syndrome | Q34150355 | ||
| Novel function of the flap endonuclease 1 complex in processing stalled DNA replication forks | Q34166526 | ||
| Identification and characterization of the human mus81-eme1 endonuclease | Q34193657 | ||
| Deficiency in the nuclease activity of xeroderma pigmentosum G in mice leads to hypersensitivity to UV irradiation | Q34302249 | ||
| Hereditary non-polyposis colorectal cancer and the role of hPMS2 and hEXO1 mutations | Q34544905 | ||
| Somatic point mutations in the p53 gene of human tumors and cell lines: updated compilation | Q34587260 | ||
| The helix-hairpin-helix DNA-binding motif: a structural basis for non-sequence-specific recognition of DNA. | Q34602847 | ||
| A DNA polymerase epsilon mutant that specifically causes +1 frameshift mutations within homonucleotide runs in yeast | Q34610131 | ||
| Overlapping functions of the Saccharomyces cerevisiae Mre11, Exo1 and Rad27 nucleases in DNA metabolism | Q34613942 | ||
| The Mre11 complex: at the crossroads of dna repair and checkpoint signalling | Q34623788 | ||
| Drosophila and human RecQ5 exist in different isoforms generated by alternative splicing | Q24548864 | ||
| Human xeroderma pigmentosum group G gene encodes a DNA endonuclease | Q24562951 | ||
| Telomerase reactivation reverses tissue degeneration in aged telomerase-deficient mice | Q24598687 | ||
| DNA mismatch repair: molecular mechanism, cancer, and ageing | Q24647002 | ||
| Rapamycin fed late in life extends lifespan in genetically heterogeneous mice | Q24647805 | ||
| Caloric restriction delays disease onset and mortality in rhesus monkeys | Q24655994 | ||
| Biochemical and cellular characteristics of the 3' -> 5' exonuclease TREX2 | Q24677826 | ||
| A conserved and species-specific functional interaction between the Werner syndrome-like exonuclease atWEX and the Ku heterodimer in Arabidopsis | Q24810688 | ||
| trt-1 is the Caenorhabditis elegans catalytic subunit of telomerase | Q25257224 | ||
| The Werner syndrome protein operates in base excision repair and cooperates with DNA polymerase beta | Q25257806 | ||
| Structure of the replicating complex of a pol alpha family DNA polymerase | Q27632340 | ||
| Crystal structure of the rad9-rad1-hus1 DNA damage checkpoint complex--implications for clamp loading and regulation | Q27655485 | ||
| Structure and Functional Implications of the Human Rad9-Hus1-Rad1 Cell Cycle Checkpoint Complex | Q27656003 | ||
| Human Flap Endonuclease Structures, DNA Double-Base Flipping, and a Unified Understanding of the FEN1 Superfamily | Q27667524 | ||
| Structures of Human Exonuclease 1 DNA Complexes Suggest a Unified Mechanism for Nuclease Family | Q27667527 | ||
| Novel DNA binding motifs in the DNA repair enzyme endonuclease III crystal structure | Q27729885 | ||
| WAF1, a potential mediator of p53 tumor suppression | Q27861121 | ||
| Analysis of the role of the NUC1 endo/exonuclease in yeast mitochondrial DNA recombination | Q27930773 | ||
| Distinct roles of two separable in vitro activities of yeast Mre11 in mitotic and meiotic recombination | Q27930776 | ||
| Mutations in DNA replication genes reduce yeast life span | Q27934618 | ||
| Endonuclease G regulates budding yeast life and death | Q27934853 | ||
| Purification and properties of the major nuclease from mitochondria of Saccharomyces cerevisiae. | Q27936136 | ||
| The nuclease activity of Mre11 is required for meiosis but not for mating type switching, end joining, or telomere maintenance | Q27937328 | ||
| Identification of Holliday junction resolvases from humans and yeast | Q27937498 | ||
| Polymerase epsilon is required to maintain replicative senescence | Q27938473 | ||
| Evidence for a role of FEN1 in maintaining mitochondrial DNA integrity | Q27939094 | ||
| EXOG, a novel paralog of Endonuclease G in higher eukaryotes | Q28114799 | ||
| The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder | Q28115238 | ||
| The Werner syndrome helicase and exonuclease cooperate to resolve telomeric D loops in a manner regulated by TRF1 and TRF2 | Q28116237 | ||
| Retention of the human Rad9 checkpoint complex in extraction-resistant nuclear complexes after DNA damage | Q28138254 | ||
| Exo1 roles for repair of DNA double-strand breaks and meiotic crossing over in Saccharomyces cerevisiae | Q28140402 | ||
| Human homologue of S. pombe Rad9 interacts with BCL-2/BCL-xL and promotes apoptosis | Q28141886 | ||
| The exonucleolytic and endonucleolytic cleavage activities of human exonuclease 1 are stimulated by an interaction with the carboxyl-terminal region of the Werner syndrome protein | Q28155868 | ||
| Characterisation of the interaction between WRN, the helicase/exonuclease defective in progeroid Werner's syndrome, and an essential replication factor, PCNA | Q28182710 | ||
| Germline mutations of EXO1 gene in patients with hereditary nonpolyposis colorectal cancer (HNPCC) and atypical HNPCC forms | Q28190757 | ||
| S-phase-specific interaction of the Fanconi anemia protein, FANCD2, with BRCA1 and RAD51 | Q28202527 | ||
| Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway | Q28203777 | ||
| Endonuclease G is an apoptotic DNase when released from mitochondria | Q28206238 | ||
| Human Mus81-associated endonuclease cleaves Holliday junctions in vitro | Q28210371 | ||
| Mammalian mitochondrial endonuclease G. Digestion of R-loops and localization in intermembrane space | Q28215595 | ||
| Human Ape2 protein has a 3'-5' exonuclease activity that acts preferentially on mismatched base pairs | Q28239438 | ||
| Homologous regions of Fen1 and p21Cip1 compete for binding to the same site on PCNA: a potential mechanism to co-ordinate DNA replication and repair | Q28240258 | ||
| DNA repair | Q28247467 | ||
| The biologic clock: the mitochondria? | Q28249363 | ||
| The exonuclease TREX1 is in the SET complex and acts in concert with NM23-H1 to degrade DNA during granzyme A-mediated cell death | Q28250070 | ||
| Reconstitution of complete SV40 DNA replication with purified replication factors | Q28251397 | ||
| Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus | Q28252435 | ||
| The Werner syndrome protein has separable recombination and survival functions | Q28256444 | ||
| The Mre11 complex and the metabolism of chromosome breaks: the importance of communicating and holding things together | Q28274236 | ||
| Linking functional decline of telomeres, mitochondria and stem cells during ageing | Q28277689 | ||
| The Werner syndrome protein at the crossroads of DNA repair and apoptosis | Q28279631 | ||
| A new progeroid syndrome reveals that genotoxic stress suppresses the somatotroph axis | Q28280037 | ||
| Identification of a human gene encoding a homologue of Saccharomyces cerevisiae EXO1, an exonuclease implicated in mismatch repair and recombination | Q28289308 | ||
| The high fidelity and unique error signature of human DNA polymerase epsilon | Q28297227 | ||
| Sequence of human FEN-1, a structure-specific endonuclease, and chromosomal localization of the gene (FEN1) in mouse and human | Q28302765 | ||
| Mitochondrial DNA mutations induce mitochondrial dysfunction, apoptosis and sarcopenia in skeletal muscle of mitochondrial DNA mutator mice | Q28474793 | ||
| Do mtDNA deletions drive premature aging in mtDNA mutator mice? | Q28742556 | ||
| Mammalian mitochondrial endonuclease G | Q29300273 | ||
| Blinded by the Light: The Growing Complexity of p53 | Q29547590 | ||
| Displacement of DNA-PKcs from DNA ends by the Werner syndrome protein | Q39688137 | ||
| Three prime exonuclease I (TREX1) is Fos/AP-1 regulated by genotoxic stress and protects against ultraviolet light and benzo(a)pyrene-induced DNA damage | Q39698684 | ||
| Mitofusin 2 inhibits mitochondrial antiviral signaling | Q39811050 | ||
| Biochemical properties of mammalian TREX1 and its association with DNA replication and inherited inflammatory disease | Q39851605 | ||
| C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy | Q40101085 | ||
| Roles of ATM and NBS1 in chromatin structure modulation and DNA double-strand break repair | Q40135858 | ||
| Genetic association of single nucleotide polymorphisms in endonuclease G-like 1 gene with type 2 diabetes in a Japanese population. | Q40148417 | ||
| Correction of proliferation and drug sensitivity defects in the progeroid Werner's Syndrome by Holliday junction resolution. | Q40155557 | ||
| Mitochondrial role in cell aging | Q40300244 | ||
| Exogenous expression of exonuclease domain-deleted WRN interferes with the repair of radiation-induced DNA damages | Q40333594 | ||
| Tumour suppressors, kinases and clamps: how p53 regulates the cell cycle in response to DNA damage. | Q40422537 | ||
| Defective telomere lagging strand synthesis in cells lacking WRN helicase activity. | Q40481955 | ||
| Structural basis for recruitment of human flap endonuclease 1 to PCNA | Q41106952 | ||
| Fanconi's anemia and malignancies | Q41189229 | ||
| Deletion of mouse rad9 causes abnormal cellular responses to DNA damage, genomic instability, and embryonic lethality | Q41283109 | ||
| Multiple pathways control cell growth and transformation: overlapping and independent activities of p53 and p21Cip1/WAF1/Sdi1. | Q41656068 | ||
| The Fanconi anemia pathway promotes replication-dependent DNA interstrand cross-link repair | Q41914934 | ||
| Biochemical characterization of an exonuclease from Arabidopsis thaliana reveals similarities to the DNA exonuclease of the human Werner syndrome protein | Q42606844 | ||
| Hydrolysis of 3'-terminal mispairs in vitro by the 3'----5' exonuclease of DNA polymerase delta permits subsequent extension by DNA polymerase alpha | Q42632067 | ||
| Defective DSB repair correlates with abnormal nuclear morphology and is improved with FTI treatment in Hutchinson-Gilford progeria syndrome fibroblasts | Q42989281 | ||
| The RecQ helicase WRN is required for normal replication fork progression after DNA damage or replication fork arrest | Q43189875 | ||
| Live fast, die young: new lessons in mammalian longevity. | Q43282002 | ||
| Mus81-Eme1 and Rqh1 involvement in processing stalled and collapsed replication forks | Q44041879 | ||
| Biochemical characterization of the WRN-FEN-1 functional interaction | Q44160517 | ||
| The exonuclease activity of human apurinic/apyrimidinic endonuclease (APE1). Biochemical properties and inhibition by the natural dinucleotide Gp4G. | Q44353890 | ||
| Structural and functional characterization of mitochondrial EndoG, a sugar non-specific nuclease which plays an important role during apoptosis | Q44831847 | ||
| Dna2 helicase/nuclease causes replicative fork stalling and double-strand breaks in the ribosomal DNA of Saccharomyces cerevisiae | Q46123466 | ||
| DmWRNexo is a 3'-5' exonuclease: phenotypic and biochemical characterization of mutants of the Drosophila orthologue of human WRN exonuclease | Q46290652 | ||
| Evidence that yeast SGS1, DNA2, SRS2, and FOB1 interact to maintain rDNA stability | Q46510173 | ||
| Fen1 mutations result in autoimmunity, chronic inflammation and cancers | Q46593630 | ||
| A nanomachine for making ends meet: MRN is a flexing scaffold for the repair of DNA double-strand breaks. | Q46845186 | ||
| Endonuclease G: a role for the enzyme in recombination and cellular proliferation | Q34694745 | ||
| Trex1 exonuclease degrades ssDNA to prevent chronic checkpoint activation and autoimmune disease | Q34719398 | ||
| Activation and regulation of ATM kinase activity in response to DNA double-strand breaks | Q34722727 | ||
| Identification of germ plasm-associated transcripts by microarray analysis of Xenopus vegetal cortex RNA. | Q34726011 | ||
| DNA structure dependent checkpoints as regulators of DNA repair | Q35046592 | ||
| Characterization of the endonuclease and ATP-dependent flap endo/exonuclease of Dna2. | Q35085004 | ||
| Fen1 mutations that specifically disrupt its interaction with PCNA cause aneuploidy-associated cancer | Q35085696 | ||
| The DNA repair endonuclease XPG interacts directly and functionally with the WRN helicase defective in Werner syndrome | Q35159006 | ||
| The human Rad9/Rad1/Hus1 damage sensor clamp interacts with DNA polymerase beta and increases its DNA substrate utilisation efficiency: implications for DNA repair | Q35618148 | ||
| Gene-targeted mice lacking the Trex1 (DNase III) 3'-->5' DNA exonuclease develop inflammatory myocarditis | Q35663520 | ||
| Extension of base mispairs by Taq DNA polymerase: implications for single nucleotide discrimination in PCR | Q35927120 | ||
| Deficient mismatch repair improves organismal fitness and survival of mice with dysfunctional telomeres | Q35946397 | ||
| Sequence and expression of NUC1, the gene encoding the mitochondrial nuclease in Saccharomyces cerevisiae | Q36000714 | ||
| Cockayne's syndrome: a case report. Literature review. | Q36464213 | ||
| Exonuclease I of Saccharomyces cerevisiae functions in mitotic recombination in vivo and in vitro | Q36568265 | ||
| Inflammaging and anti-inflammaging: a systemic perspective on aging and longevity emerged from studies in humans | Q36658296 | ||
| Identification and characterization of a Drosophila ortholog of WRN exonuclease that is required to maintain genome integrity | Q36691491 | ||
| Evolving views of DNA replication (in)fidelity | Q36772885 | ||
| DNA replication and transcription in mammalian mitochondria | Q36780113 | ||
| New insights into the combined Cockayne/xeroderma pigmentosum complex: human XPG protein can function in transcription factor stability | Q36805145 | ||
| Removal of oxidative DNA damage via FEN1-dependent long-patch base excision repair in human cell mitochondria | Q36845992 | ||
| The premature ageing syndrome protein, WRN, is a 3'-->5' exonuclease | Q37083237 | ||
| Mre11 nuclease activity has essential roles in DNA repair and genomic stability distinct from ATM activation | Q37104813 | ||
| Chemical-induced cancer incidence and underlying mechanisms in Fen1 mutant mice | Q37320331 | ||
| Saccharomyces cerevisiae flap endonuclease 1 uses flap equilibration to maintain triplet repeat stability | Q37424442 | ||
| Cytoplasmic functions of the tumour suppressor p53. | Q37466228 | ||
| Increasing longevity through caloric restriction or rapamycin feeding in mammals: common mechanisms for common outcomes? | Q37485742 | ||
| DNA2 resolves expanding flap in mitochondrial base excision repair | Q37668905 | ||
| The human Rad9-Rad1-Hus1 checkpoint complex stimulates flap endonuclease 1. | Q37695856 | ||
| Crystallization and preliminary crystallographic analysis of the catalytic domain of human flap endonuclease 1 in complex with a nicked DNA product: use of a DPCS kit for efficient protein-DNA complex crystallization | Q38271895 | ||
| A conserved 5' to 3' exonuclease activity in the yeast and human nucleotide excision repair proteins RAD2 and XPG. | Q38301223 | ||
| DNA-binding and strand-annealing activities of human Mre11: implications for its roles in DNA double-strand break repair pathways | Q38303463 | ||
| Fidelity of eucaryotic DNA polymerase delta holoenzyme from Schizosaccharomyces pombe | Q38313569 | ||
| Newly discovered archaebacterial flap endonucleases show a structure-specific mechanism for DNA substrate binding and catalysis resembling human flap endonuclease-1. | Q38332703 | ||
| Properties of and substrate determinants for the exonuclease activity of human apurinic endonuclease Ape1. | Q38352576 | ||
| P433 | issue | 6 | |
| P921 | main subject | genome stability | Q98655700 |
| P304 | page(s) | 1317-1340 | |
| P577 | publication date | 2011-09-23 | |
| P1433 | published in | Age | Q4691832 |
| P1476 | title | The role of DNA exonucleases in protecting genome stability and their impact on ageing | |
| P478 | volume | 34 |
| Q41877420 | A fluorescence-based exonuclease assay to characterize DmWRNexo, orthologue of human progeroid WRN exonuclease, and its application to other nucleases |
| Q96434565 | Artificial selection reveals the role of transcriptional constraints in the maintenance of life history variation |
| Q38485116 | Degradation systems in heart failure |
| Q41144456 | Differential expression profile analysis of DNA damage repair genes in CD133+/CD133- colorectal cancer cells |
| Q56637826 | Fidelity of DNA replication—a matter of proofreading |
| Q34031638 | Free radicals and antioxidants: updating a personal view |
| Q34052630 | Implications of the colonic deposition of free hemoglobin-α chain: a previously unknown tissue by-product in inflammatory bowel disease |
| Q38870074 | POLD1: Central mediator of DNA replication and repair, and implication in cancer and other pathologies |
| Q34619374 | The DNA2 nuclease/helicase is an estrogen-dependent gene mutated in breast and ovarian cancers |
| Q24618841 | The antioxidant paradox: less paradoxical now? |
| Q55322083 | The mitochondrial outer-membrane location of the EXD2 exonuclease contradicts its direct role in nuclear DNA repair. |
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