| scholarly article | Q13442814 |
| P50 | author | Nadine Kolas | Q30303526 |
| P2093 | author name string | Thomas A Kunkel | |
| Richard D Kolodner | |||
| Tchaiko Parris | |||
| Winfried Edelmann | |||
| Edmund Wong | |||
| Michael F Kane | |||
| Alan B Clark | |||
| Robert Russell | |||
| Paula E Cohen | |||
| Burkhard Kneitz | |||
| Harry Hou | |||
| Dan J Mazur | |||
| Kaichun Wei | |||
| Guohze Yang | |||
| P2860 | cites work | Human exonuclease I interacts with the mismatch repair protein hMSH2 | Q22004013 |
| The RAD2 domain of human exonuclease 1 exhibits 5' to 3' exonuclease and flap structure-specific endonuclease activities | Q22010967 | ||
| The interaction of DNA mismatch repair proteins with human exonuclease I | Q24291370 | ||
| Human exonuclease I is required for 5' and 3' mismatch repair | Q24292224 | ||
| Molecular interactions of human Exo1 with DNA | Q24292290 | ||
| Identification and characterization of Saccharomyces cerevisiae EXO1, a gene encoding an exonuclease that interacts with MSH2 | Q24314329 | ||
| MutS homolog 4 localization to meiotic chromosomes is required for chromosome pairing during meiosis in male and female mice | Q24606421 | ||
| The Saccharomyces cerevisiae MLH3 gene functions in MSH3-dependent suppression of frameshift mutations | Q27935158 | ||
| exo1-Dependent mutator mutations: model system for studying functional interactions in mismatch repair | Q27935389 | ||
| Functional specificity of MutL homologs in yeast: evidence for three Mlh1-based heterocomplexes with distinct roles during meiosis in recombination and mismatch correction | Q27939611 | ||
| Exo1 roles for repair of DNA double-strand breaks and meiotic crossing over in Saccharomyces cerevisiae | Q28140402 | ||
| Germline mutations of EXO1 gene in patients with hereditary nonpolyposis colorectal cancer (HNPCC) and atypical HNPCC forms | Q28190757 | ||
| EXO1 variants occur commonly in normal population: evidence against a role in hereditary nonpolyposis colorectal cancer | Q28202143 | ||
| Biochemistry and genetics of eukaryotic mismatch repair | Q28282377 | ||
| Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over | Q28282791 | ||
| Identification of a human gene encoding a homologue of Saccharomyces cerevisiae EXO1, an exonuclease implicated in mismatch repair and recombination | Q28289308 | ||
| Mammalian MutS homologue 5 is required for chromosome pairing in meiosis | Q28295022 | ||
| Somatic Apc mutations are selected upon their capacity to inactivate the beta-catenin downregulating activity | Q28507875 | ||
| Tumour susceptibility and spontaneous mutation in mice deficient in Mlh1, Pms1 and Pms2 DNA mismatch repair | Q28508905 | ||
| Meiotic pachytene arrest in MLH1-deficient mice | Q28510650 | ||
| The DNA mismatch repair genes Msh3 and Msh6 cooperate in intestinal tumor suppression | Q28513250 | ||
| Expression specificity of the mouse exonuclease 1 (mExo1) gene | Q28585040 | ||
| Mouse models for hereditary nonpolyposis colorectal cancer | Q28585761 | ||
| Meiotic prophase abnormalities and metaphase cell death in MLH1-deficient mouse spermatocytes: insights into regulation of spermatogenic progress | Q28586542 | ||
| Tumorigenesis in Mlh1 and Mlh1/Apc1638N mutant mice | Q28589732 | ||
| Spontaneous intestinal carcinomas and skin neoplasms in Msh2-deficient mice | Q28593189 | ||
| Meiotic arrest and aneuploidy in MLH3-deficient mice | Q28593875 | ||
| Isolation of MutSbeta from human cells and comparison of the mismatch repair specificities of MutSbeta and MutSalpha | Q28610863 | ||
| Redundancy of Saccharomyces cerevisiae MSH3 and MSH6 in MSH2-dependent mismatch repair | Q29615027 | ||
| Mismatch repair in replication fidelity, genetic recombination, and cancer biology | Q29616483 | ||
| Meiotic prophase arrest with failure of chromosome synapsis in mice deficient for Dmc1, a germline-specific RecA homolog | Q29618405 | ||
| Interactions of Exo1p with components of MutLalpha in Saccharomyces cerevisiae | Q33933718 | ||
| 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 | ||
| Genetic analysis of mouse embryonic stem cells bearing Msh3 and Msh2 single and compound mutations | Q33961252 | ||
| Destabilization of simple repetitive DNA sequences by transcription in yeast. | Q33967667 | ||
| Mbd4 inactivation increases Cright-arrowT transition mutations and promotes gastrointestinal tumor formation | Q34157868 | ||
| Deficient DNA mismatch repair: a common etiologic factor for colon cancer | Q34189020 | ||
| Restoration of mismatch repair to nuclear extracts of H6 colorectal tumor cells by a heterodimer of human MutL homologs | Q34554581 | ||
| Functional overlap in mismatch repair by human MSH3 and MSH6. | Q34603929 | ||
| EXO1 and MSH6 are high-copy suppressors of conditional mutations in the MSH2 mismatch repair gene of Saccharomyces cerevisiae | Q34609730 | ||
| A DNA polymerase epsilon mutant that specifically causes +1 frameshift mutations within homonucleotide runs in yeast | Q34610131 | ||
| Decreased meiotic intergenic recombination and increased meiosis I nondisjunction in exo1 mutants of Saccharomyces cerevisiae | Q34611088 | ||
| Differential suppression of DNA repair deficiencies of Yeast rad50, mre11 and xrs2 mutants by EXO1 and TLC1 (the RNA component of telomerase). | Q34614221 | ||
| In vivo requirement for RecJ, ExoVII, ExoI, and ExoX in methyl-directed mismatch repair | Q36235057 | ||
| Exonuclease I of Saccharomyces cerevisiae functions in mitotic recombination in vivo and in vitro | Q36568265 | ||
| Mechanisms and biological effects of mismatch repair | Q37041860 | ||
| Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis | Q38293261 | ||
| Bidirectional excision in methyl-directed mismatch repair | Q38318540 | ||
| Methyl-directed mismatch repair is bidirectional | Q38318556 | ||
| Mismatch-, MutS-, MutL-, and helicase II-dependent unwinding from the single-strand break of an incised heteroduplex | Q38337751 | ||
| MutS and MutL activate DNA helicase II in a mismatch-dependent manner | Q38337755 | ||
| Saccharomyces cerevisiae exonuclease-1 plays a role in UV resistance that is distinct from nucleotide excision repair | Q39724404 | ||
| EXO1-dependent single-stranded DNA at telomeres activates subsets of DNA damage and spindle checkpoint pathways in budding yeast yku70Delta mutants | Q39860143 | ||
| The FEN-1 family of structure-specific nucleases in eukaryotic DNA replication, recombination and repair | Q41396267 | ||
| A 5'-3' exonuclease from Saccharomyces cerevisiae is required for in vitro recombination between linear DNA molecules with overlapping homology | Q42151362 | ||
| MLH1, PMS1, and MSH2 interactions during the initiation of DNA mismatch repair in yeast | Q42427955 | ||
| The mouse RecA-like gene Dmc1 is required for homologous chromosome synapsis during meiosis | Q47858327 | ||
| A DNA exonuclease induced during meiosis of Schizosaccharomyces pombe. | Q53926783 | ||
| A role for exonuclease I from S. pombe in mutation avoidance and mismatch correction. | Q53963518 | ||
| Mutations predisposing to hereditary nonpolyposis colorectal cancer: Database and results of a collaborative study. The International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer | Q61946741 | ||
| EXO1 and MSH4 differentially affect crossing-over and segregation | Q73899517 | ||
| Redundant exonuclease involvement in Escherichia coli methyl-directed mismatch repair | Q74064844 | ||
| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | DNA mismatch repair | Q2984243 |
| P304 | page(s) | 603-14 | |
| P577 | publication date | 2003-03-01 | |
| P1433 | published in | Genes & Development | Q1524533 |
| P1476 | title | Inactivation of Exonuclease 1 in mice results in DNA mismatch repair defects, increased cancer susceptibility, and male and female sterility | |
| P478 | volume | 17 |
| Q35583181 | 14-3-3 proteins restrain the Exo1 nuclease to prevent overresection. |
| Q51769143 | A Reassessment of Genes Modulating Aging in Mice Using Demographic Measurements of the Rate of Aging. |
| Q24298110 | A defined human system that supports bidirectional mismatch-provoked excision |
| Q36749550 | A mutation in EXO1 defines separable roles in DNA mismatch repair and post-replication repair. |
| Q36540457 | A personal historical view of DNA mismatch repair with an emphasis on eukaryotic DNA mismatch repair |
| Q37181822 | A possible mechanism for exonuclease 1-independent eukaryotic mismatch repair |
| Q36457060 | ATR-dependent pathways control hEXO1 stability in response to stalled forks. |
| Q35690218 | Activation of Saccharomyces cerevisiae Mlh1-Pms1 Endonuclease in a Reconstituted Mismatch Repair System |
| Q36954874 | Activities of human exonuclease 1 that promote cleavage of transcribed immunoglobulin switch regions |
| Q50671986 | Age-associated alteration of gene expression patterns in mouse oocytes. |
| Q28513971 | Altered somatic hypermutation and reduced class-switch recombination in exonuclease 1-mutant mice |
| Q33822488 | An Msh2 conditional knockout mouse for studying intestinal cancer and testing anticancer agents |
| Q47445150 | Analysis of factors decreasing testis weight in MRL mice |
| Q33247666 | Analysis of the excision step in human DNA mismatch repair |
| Q37699397 | Associations between single-nucleotide polymorphisms of human exonuclease 1 and the risk of hepatocellular carcinoma |
| Q33791321 | Biochemical characterization of a cancer-associated E109K missense variant of human exonuclease 1. |
| Q33604620 | Biochemistry of Meiotic Recombination: Formation, Processing, and Resolution of Recombination Intermediates |
| Q46726051 | Bound nucleotide controls the endonuclease activity of mismatch repair enzyme MutL. |
| Q28534478 | Breast tumors with elevated expression of 1q candidate genes confer poor clinical outcome and sensitivity to Ras/PI3K inhibition |
| Q28115810 | CSB-PGBD3 Mutations Cause Premature Ovarian Failure |
| Q45129820 | Cadmium inhibits the functions of eukaryotic MutS complexes. |
| Q27026386 | Causal link between microsatellite instability and hMRE11 dysfunction in human cancers |
| Q85228405 | Characterization of C- and N-terminal domains of Aquifex aeolicus MutL endonuclease: N-terminal domain stimulates the endonuclease activity of C-terminal domain in a zinc-dependent manner |
| Q37072156 | Characterization of a highly conserved binding site of Mlh1 required for exonuclease I-dependent mismatch repair |
| Q34411080 | Checkpoint genes and Exo1 regulate nearby inverted repeat fusions that form dicentric chromosomes in Saccharomyces cerevisiae |
| Q57784307 | Coordinating Multi-Protein Mismatch Repair by Managing Diffusion Mechanics on the DNA |
| Q33703015 | CtIP-mediated resection is essential for viability and can operate independently of BRCA1. |
| Q36884849 | DNA Mismatch Repair Interacts with CAF-1- and ASF1A-H3-H4-dependent Histone (H3-H4)2 Tetramer Deposition |
| Q38036830 | DNA damage checkpoints in stem cells, ageing and cancer. |
| Q34814254 | DNA mismatch repair and infertility |
| Q28291067 | DNA mismatch repair in eukaryotes and bacteria |
| Q24647002 | DNA mismatch repair: molecular mechanism, cancer, and ageing |
| Q52605096 | DNA repair and cell cycle checkpoint defects in a mouse model of 'BRCAness' are partially rescued by 53BP1 deletion. |
| Q35020482 | DNA repair gene polymorphisms and tobacco smoking in the risk for colorectal adenomas |
| Q36487307 | DNA-damage repair; the good, the bad, and the ugly |
| Q52720061 | Deoxyribonucleic Acid Damage and Repair: Capitalizing on Our Understanding of the Mechanisms of Maintaining Genomic Integrity for Therapeutic Purposes. |
| Q51039462 | Detection of coding microsatellite frameshift mutations in DNA mismatch repair-deficient mouse intestinal tumors. |
| Q50666210 | Developmental regulation and in vitro culture effects on expression of DNA repair and cell cycle checkpoint control genes in rhesus monkey oocytes and embryos. |
| Q44761854 | Differential requirement for proliferating cell nuclear antigen in 5' and 3' nick-directed excision in human mismatch repair |
| Q33529100 | Distinct activities of exonuclease 1 and flap endonuclease 1 at telomeric g4 DNA |
| Q36670109 | Distinct effects of the recurrent Mlh1G67R mutation on MMR functions, cancer, and meiosis |
| Q47070570 | DmGEN shows a flap endonuclease activity, cleaving the blocked-flap structure and model replication fork |
| Q28534756 | Dominant mutations in S. cerevisiae PMS1 identify the Mlh1-Pms1 endonuclease active site and an exonuclease 1-independent mismatch repair pathway |
| Q97073533 | EXO1 Plays a Carcinogenic Role in Hepatocellular Carcinoma and is related to the regulation of FOXP3 |
| Q36002464 | EXO1 is critical for embryogenesis and the DNA damage response in mice with a hypomorphic Nbs1 allele |
| Q48587042 | EXO1 suppresses double-strand break induced homologous recombination between diverged sequences in mammalian cells |
| Q37964747 | Emerging evidence for the role of genomic instability in male factor infertility |
| Q36764079 | Endonuclease activities of MutLα and its homologs in DNA mismatch repair |
| Q33711830 | Eukaryotic Mismatch Repair in Relation to DNA Replication |
| Q28551519 | Evidence of a Mild Mutator Phenotype in Cambodian Plasmodium falciparum Malaria Parasites |
| Q36115776 | Evidence that the DNA mismatch repair system removes 1-nucleotide Okazaki fragment flaps |
| Q38974172 | Exo1 independent DNA mismatch repair involves multiple compensatory nucleases |
| Q35564759 | Exo1 phosphorylation status controls the hydroxyurea sensitivity of cells lacking the Pol32 subunit of DNA polymerases delta and zeta |
| Q36421123 | Exonuclease 1 (Exo1) is required for activating response to S(N)1 DNA methylating agents |
| Q38919536 | Exonuclease 1 and its versatile roles in DNA repair |
| Q33573646 | Exonuclease 1 is a critical mediator of survival during DNA double strand break repair in nonquiescent hematopoietic stem and progenitor cells |
| Q28261787 | Exonuclease 1-dependent and independent mismatch repair |
| Q33297433 | Exonuclease-1 deletion impairs DNA damage signaling and prolongs lifespan of telomere-dysfunctional mice |
| Q42043478 | Fen-1 facilitates homologous recombination by removing divergent sequences at DNA break ends |
| Q35663520 | Gene-targeted mice lacking the Trex1 (DNase III) 3'-->5' DNA exonuclease develop inflammatory myocarditis |
| Q36046488 | Genetic risk of lung cancer associated with a single nucleotide polymorphism from EXO1: a meta analysis. |
| Q33631793 | Genome-wide identification of CBX2 targets: insights in the human sex development network |
| Q47766916 | Human DNA polymerase delta double-mutant D316A;E318A interferes with DNA mismatch repair in vitro |
| Q35170755 | Human exonuclease 1 connects nucleotide excision repair (NER) processing with checkpoint activation in response to UV irradiation |
| Q33224078 | Human mismatch repair: reconstitution of a nick-directed bidirectional reaction |
| Q33791326 | Hydrolytic function of Exo1 in mammalian mismatch repair. |
| Q90647988 | Identification of Exo1-Msh2 interaction motifs in DNA mismatch repair and new Msh2-binding partners |
| Q64376748 | Identification of a panel of MYC and Tip60 co-regulated genes functioning primarily in cell cycle and DNA replication |
| Q36741556 | Identification of regulatory factor X as a novel mismatch repair stimulatory factor |
| Q28074585 | Impact of DNA mismatch repair system alterations on human fertility and related treatments |
| Q39991083 | Inhibition of the 5' to 3' exonuclease activity of hEXO1 by 8-oxoguanine |
| Q52769433 | Interplay of catalysis, fidelity, threading, and processivity in the exo- and endonucleolytic reactions of human exonuclease I. |
| Q47135454 | Involvement of DNA mismatch repair in the maintenance of heterochromatic DNA stability in Saccharomyces cerevisiae. |
| Q37215365 | Involvement of Exo1b in DNA damage-induced apoptosis |
| Q35792957 | Known components of the immunoglobulin A:T mutational machinery are intact in Burkitt lymphoma cell lines with G:C bias |
| Q33369076 | MUS81 generates a subset of MLH1-MLH3-independent crossovers in mammalian meiosis |
| Q48256770 | Main steps in DNA double-strand break repair: an introduction to homologous recombination and related processes. |
| Q37590653 | Male infertility: a risk factor for testicular cancer |
| Q35585478 | Male reproductive cancers and infertility: a mutual relationship |
| Q35875365 | Male reproductive health and prostate cancer risk |
| Q36991032 | Mammalian Exo1 encodes both structural and catalytic functions that play distinct roles in essential biological processes |
| Q26740310 | Manipulation of DNA Repair Proficiency in Mouse Models of Colorectal Cancer |
| Q51793302 | Measuring strand discontinuity-directed mismatch repair in yeast Saccharomyces cerevisiae by cell-free nuclear extracts. |
| Q24300483 | Mechanism of 5'-directed excision in human mismatch repair |
| Q36547669 | Mechanism of DNA resection during intrachromosomal recombination and immunoglobulin class switching |
| Q28262719 | Mechanisms and functions of DNA mismatch repair |
| Q36564560 | Mechanisms in eukaryotic mismatch repair |
| Q38618828 | Meiotic Recombination: The Essence of Heredity |
| Q38153644 | Meiotic recombination in mammals: localization and regulation |
| Q35910256 | Meiotic recombination intermediates and mismatch repair proteins |
| Q34248904 | Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways |
| Q44447213 | Mismatch repair in human nuclear extracts: effects of internal DNA-hairpin structures between mismatches and excision-initiation nicks on mismatch correction and mismatch-provoked excision |
| Q34773522 | Mismatch repair proteins MSH2, MLH1, and EXO1 are important for class-switch recombination events occurring in B cells that lack nonhomologous end joining |
| Q57058967 | Mlh1 deficiency increases the risk of hematopoietic malignancy after simulated space radiation exposure |
| Q24630140 | Molecular mechanisms of the whole DNA repair system: a comparison of bacterial and eukaryotic systems |
| Q37084734 | Mouse models in male fertility research |
| Q57472222 | MutLγ promotes repeat expansion in a Fragile X mouse model while EXO1 is protective |
| Q28084645 | New insights into the mechanism of DNA mismatch repair |
| Q35829272 | Nuclear localization of human DNA mismatch repair protein exonuclease 1 (hEXO1) |
| Q26822478 | Nucleases in homologous recombination as targets for cancer therapy |
| Q37011985 | Nucleosome dynamics regulates DNA processing |
| Q37037194 | O6-methylguanine-induced cell death involves exonuclease 1 as well as DNA mismatch recognition in vivo |
| Q35893147 | Okazaki fragment maturation involves α-segment error editing by the mammalian FEN1/MutSα functional complex |
| Q24632622 | Okazaki fragment maturation: nucleases take centre stage |
| Q33961620 | PCNA and Msh2-Msh6 activate an Mlh1-Pms1 endonuclease pathway required for Exo1-independent mismatch repair. |
| Q24606670 | PCNA function in the activation and strand direction of MutLα endonuclease in mismatch repair |
| Q36258155 | PHF11 promotes DSB resection, ATR signaling, and HR. |
| Q34068165 | PMS2 endonuclease activity has distinct biological functions and is essential for genome maintenance |
| Q33519468 | Phosphorylation of Exo1 modulates homologous recombination repair of DNA double-strand breaks |
| Q34488378 | Pif1- and Exo1-dependent nucleases coordinate checkpoint activation following telomere uncapping. |
| Q21133598 | Predicting the proteins of Angomonas deanei, Strigomonas culicis and their respective endosymbionts reveals new aspects of the trypanosomatidae family |
| Q64132285 | Quantitative trait loci analysis of heat stress resistance of spermatocytes in the MRL/MpJ mouse |
| Q36972154 | Rad9 plays an important role in DNA mismatch repair through physical interaction with MLH1 |
| Q33556873 | Reconstitution of Saccharomyces cerevisiae DNA polymerase ε-dependent mismatch repair with purified proteins |
| Q37319600 | Reconstitution of long and short patch mismatch repair reactions using Saccharomyces cerevisiae proteins |
| Q34016965 | Repair of endogenous DNA base lesions modulate lifespan in mice |
| Q33317311 | Rice exonuclease-1 homologue, OsEXO1, that interacts with DNA polymerase lambda and RPA subunit proteins, is involved in cell proliferation |
| Q37058602 | Sharpening the ends for repair: mechanisms and regulation of DNA resection |
| Q42373192 | Significant association of the EXO1 rs851797 polymorphism with clinical outcome of ovarian cancer. |
| Q35027619 | Single molecule studies of DNA mismatch repair |
| Q35925569 | Single-molecule imaging reveals the mechanism of Exo1 regulation by single-stranded DNA binding proteins |
| Q26999680 | Single-molecule views of MutS on mismatched DNA. |
| Q54430309 | Somatic mutation of EXO1 gene in gastric and colorectal cancers with microsatellite instability. |
| Q36521428 | Structure and function of the components of the human DNA mismatch repair system |
| Q27667527 | Structures of Human Exonuclease 1 DNA Complexes Suggest a Unified Mechanism for Nuclease Family |
| Q36895121 | Targeted next-generation sequencing of 22 mismatch repair genes identifies Lynch syndrome families |
| Q28301386 | Temporally and biochemically distinct activities of Exo1 during meiosis: double-strand break resection and resolution of double Holliday junctions |
| Q51312086 | The Major Replicative Histone Chaperone CAF-1 Suppresses the Activity of the DNA Mismatch Repair System in the Cytotoxic Response to a DNA-methylating Agent. |
| Q52671466 | The Role of Oncogenic Tyrosine Kinase NPM-ALK in Genomic Instability. |
| Q37334051 | The concerted action of Msh2 and UNG stimulates somatic hypermutation at A . T base pairs |
| Q36744624 | The interplay between hMLH1 and hMRE11: role in MMR and the effect of hMLH1 mutations |
| Q36448284 | The multifaceted mismatch-repair system |
| Q34551905 | The oxidized deoxynucleoside triphosphate pool is a significant contributor to genetic instability in mismatch repair-deficient cells |
| Q53195871 | The significance of Exonuclease 1 K589E polymorphism on hepatocellular carcinoma susceptibility in the Turkish population: a case-control study. |
| Q58789945 | Timing of Expansion of Fragile X Premutation Alleles During Intergenerational Transmission in a Mouse Model of the Fragile X-Related Disorders |
| Q90211035 | Tocotrienol Rich Fraction Supplementation Modulate Brain Hippocampal Gene Expression in APPswe/PS1dE9 Alzheimer's Disease Mouse Model |
| Q54442651 | Tumor progression in Apc(1638N) mice with Exo1 and Fen1 deficiencies. |
| Q27005670 | Unpairing and gating: sequence-independent substrate recognition by FEN superfamily nucleases |
| Q55283304 | Validating the concept of mutational signatures with isogenic cell models. |
| Q47439130 | Variation in DNA-Damage Responses to an Inhalational Carcinogen (1,3-Butadiene) in Relation to Strain-Specific Differences in Chromatin Accessibility and Gene Transcription Profiles in C57BL/6J and CAST/EiJ Mice |
| Q37776339 | Wot the ‘L—Does MutL do? |
| Q92458719 | XPG-related nucleases are hierarchically recruited for double-stranded rDNA break resection |
| Q34166799 | hMRE11 deficiency leads to microsatellite instability and defective DNA mismatch repair |
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