scholarly article | Q13442814 |
P2093 | author name string | H Ogawa | |
H Tsubouchi | |||
P2860 | cites work | Crossover interference is abolished in the absence of a synaptonemal complex protein | Q72790781 |
The many interfaces of Mre11 | Q77654630 | ||
Human exonuclease 1 functionally complements its yeast homologues in DNA recombination, RNA primer removal, and mutation avoidance | Q22009967 | ||
The 3' to 5' exonuclease activity of Mre 11 facilitates repair of DNA double-strand breaks | Q24311761 | ||
Identification and characterization of Saccharomyces cerevisiae EXO1, a gene encoding an exonuclease that interacts with MSH2 | Q24314329 | ||
Nuclease activities in a complex of human recombination and DNA repair factors Rad50, Mre11, and p95 | Q24323459 | ||
Components of the Ku-dependent non-homologous end-joining pathway are involved in telomeric length maintenance and telomeric silencing | Q24533190 | ||
Saccharomyces cerevisiae Ku70 potentiates illegitimate DNA double-strand break repair and serves as a barrier to error-prone DNA repair pathways | Q24561996 | ||
Meiotic chromosomes: it takes two to tango | Q27930023 | ||
A pathway for generation and processing of double-strand breaks during meiotic recombination in S. cerevisiae | Q27930541 | ||
Distinct roles of two separable in vitro activities of yeast Mre11 in mitotic and meiotic recombination | Q27930776 | ||
Mutations in Saccharomyces cerevisiae That Block Meiotic Prophase Chromosome Metabolism and Confer Cell Cycle Arrest at Pachytene Identify Two New Meiosis-Specific Genes SAE1 and SAE3 | Q27931736 | ||
Mutations in two Ku homologs define a DNA end-joining repair pathway in Saccharomyces cerevisiae | Q27932896 | ||
DMC1: a meiosis-specific yeast homolog of E. coli recA required for recombination, synaptonemal complex formation, and cell cycle progression | Q27933115 | ||
The product of the DNA damage-inducible gene of Saccharomyces cerevisiae, DIN7, specifically functions in mitochondria | Q27933751 | ||
Rad51 protein involved in repair and recombination in S. cerevisiae is a RecA-like protein | Q27933995 | ||
Zip2, a meiosis-specific protein required for the initiation of chromosome synapsis | Q27934770 | ||
Characterization of a novel DNA damage-inducible gene of Saccharomyces cerevisiae, DIN7, which is a structural homolog of the RAD2 and RAD27 DNA repair genes. | Q27935693 | ||
Complex formation and functional versatility of Mre11 of budding yeast in recombination | Q27935743 | ||
The nuclease activity of Mre11 is required for meiosis but not for mating type switching, end joining, or telomere maintenance | Q27937328 | ||
Interaction of Mre11 and Rad50: two proteins required for DNA repair and meiosis-specific double-strand break formation in Saccharomyces cerevisiae. | Q27937499 | ||
The transcriptional program of sporulation in budding yeast | Q27938344 | ||
Identification of new genes required for meiotic recombination in Saccharomyces cerevisiae | Q27938429 | ||
Functional specificity of MutL homologs in yeast: evidence for three Mlh1-based heterocomplexes with distinct roles during meiosis in recombination and mismatch correction | Q27939611 | ||
New yeast-Escherichia coli shuttle vectors constructed with in vitro mutagenized yeast genes lacking six-base pair restriction sites | Q28131597 | ||
One-step gene disruption in yeast | Q28131598 | ||
A method for gene disruption that allows repeated use of URA3 selection in the construction of multiply disrupted yeast strains | Q28131619 | ||
The two-hybrid system: a method to identify and clone genes for proteins that interact with a protein of interest | Q28131694 | ||
Identification of a human gene encoding a homologue of Saccharomyces cerevisiae EXO1, an exonuclease implicated in mismatch repair and recombination | Q28289308 | ||
Multiple functions of MutS- and MutL-related heterocomplexes | Q28776215 | ||
The DNA-binding protein Hdf1p (a putative Ku homologue) is required for maintaining normal telomere length in Saccharomyces cerevisiae | Q29465403 | ||
Saccharomyces Ku70, mre11/rad50 and RPA proteins regulate adaptation to G2/M arrest after DNA damage | Q29614221 | ||
Analysis of wild-type and rad50 mutants of yeast suggests an intimate relationship between meiotic chromosome synapsis and recombination | Q29615272 | ||
Sterile host yeasts (SHY): A eukaryotic system of biological containment for recombinant DNA experiments | Q29620758 | ||
[12] One-step gene disruption in yeast | Q29642800 | ||
Sporulation Synchrony of Saccharomyces cerevisiae Grown in Various Carbon Sources | Q33789395 | ||
The yeast RAD50 gene encodes a predicted 153-kD protein containing a purine nucleotide-binding domain and two large heptad-repeat regions | Q33955345 | ||
XRS2, a DNA repair gene of Saccharomyces cerevisiae, is needed for meiotic recombination | Q33960085 | ||
Evidence for two types of allelic recombination in yeast | Q33980168 | ||
Identification of a Saccharomyces cerevisiae Ku80 homologue: roles in DNA double strand break rejoining and in telomeric maintenance | Q34411525 | ||
Alteration of N-terminal phosphoesterase signature motifs inactivates Saccharomyces cerevisiae Mre11. | Q34605521 | ||
Exonuclease I of Saccharomyces cerevisiae functions in mitotic recombination in vivo and in vitro | Q36568265 | ||
Genetic recombination and commitment to meiosis in Saccharomyces | Q37456227 | ||
Mutations in XRS2 and RAD50 delay but do not prevent mating-type switching in Saccharomyces cerevisiae | Q38308503 | ||
The Saccharomyces cerevisiae MER3 gene, encoding a novel helicase-like protein, is required for crossover control in meiosis | Q38319411 | ||
Mlh1 is unique among mismatch repair proteins in its ability to promote crossing-over during meiosis | Q38344945 | ||
A novel mre11 mutation impairs processing of double-strand breaks of DNA during both mitosis and meiosis | Q39631261 | ||
Cloning and characterisation of the Schizosaccharomyces pombe rad32 gene: a gene required for repair of double strand breaks and recombination | Q40392825 | ||
In vivo biochemistry: physical monitoring of recombination induced by site-specific endonucleases. | Q40465998 | ||
Molecular cloning of the actin gene from yeast Saccharomyces cerevisiae | Q40480837 | ||
Characterization of double-strand break-induced recombination: homology requirements and single-stranded DNA formation | Q40653881 | ||
Intermediates of recombination during mating type switching in Saccharomyces cerevisiae | Q41203841 | ||
Meiotic recombination in yeast: coronation of the double-strand-break repair model | Q41285976 | ||
A super new twist on the initiation of meiotic recombination | Q41434983 | ||
Tosca: a Drosophila gene encoding a nuclease specifically expressed in the female germline. | Q47070291 | ||
Telomere maintenance is dependent on activities required for end repair of double-strand breaks | Q47946099 | ||
Mutation of a meiosis-specific MutS homolog decreases crossing over but not mismatch correction | Q48076989 | ||
A role for exonuclease I from S. pombe in mutation avoidance and mismatch correction. | Q53963518 | ||
RecA-like recombination proteins in eukaryotes: functions and structures of RAD51 genes | Q56937930 | ||
Double-strand breaks at an initiation site for meiotic gene conversion | Q59068287 | ||
Alteration of telomeric sequences and senescence caused by mutations in RAD50 of Saccharomyces cerevisiae | Q64389209 | ||
Extensive 3'-overhanging, single-stranded DNA associated with the meiosis-specific double-strand breaks at the ARG4 recombination initiation site | Q64389995 | ||
A genetic study of x-ray sensitive mutants in yeast | Q69356688 | ||
MSH5, a novel MutS homolog, facilitates meiotic reciprocal recombination between homologs in Saccharomyces cerevisiae but not mismatch repair | Q71919357 | ||
DNA structure-dependent requirements for yeast RAD genes in gene conversion | Q72356626 | ||
P433 | issue | 7 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Saccharomyces cerevisiae | Q719725 |
P304 | page(s) | 2221-33 | |
P577 | publication date | 2000-07-01 | |
P1433 | published in | Molecular Biology of the Cell | Q2338259 |
P1476 | title | Exo1 roles for repair of DNA double-strand breaks and meiotic crossing over in Saccharomyces cerevisiae | |
P478 | volume | 11 |
Q33886547 | 14-3-3 Proteins regulate exonuclease 1-dependent processing of stalled replication forks |
Q24299584 | A critical role for the ubiquitin-conjugating enzyme Ubc13 in initiating homologous recombination |
Q27931208 | A role for the MutL homologue MLH2 in controlling heteroduplex formation and in regulating between two different crossover pathways in budding yeast. |
Q34266467 | A target based approach identifies genomic predictors of breast cancer patient response to chemotherapy |
Q36457060 | ATR-dependent pathways control hEXO1 stability in response to stalled forks. |
Q33855288 | Alteration of gene conversion tract length and associated crossing over during plasmid gap repair in nuclease-deficient strains of Saccharomyces cerevisiae |
Q28513971 | Altered somatic hypermutation and reduced class-switch recombination in exonuclease 1-mutant mice |
Q34614513 | Analysis of conditional mutations in the Saccharomyces cerevisiae MLH1 gene in mismatch repair and in meiotic crossing over. |
Q27934521 | Analysis of the proteins involved in the in vivo repair of base-base mismatches and four-base loops formed during meiotic recombination in the yeast Saccharomyces cerevisiae |
Q51782566 | Arabidopsis SPO11-2 functions with SPO11-1 in meiotic recombination. |
Q44267791 | AtATM is essential for meiosis and the somatic response to DNA damage in plants |
Q33726437 | Bi-directional routing of DNA mismatch repair protein human exonuclease 1 to replication foci and DNA double strand breaks |
Q27930407 | Bidirectional resection of DNA double-strand breaks by Mre11 and Exo1 |
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 |
Q38206208 | Biology of telomeres: lessons from budding yeast |
Q35757748 | Brc1-mediated rescue of Smc5/6 deficiency: requirement for multiple nucleases and a novel Rad18 function |
Q48829348 | Caenorhabditis elegans Ce-rdh-1/rad-51 functions after double-strand break formation of meiotic recombination |
Q39859714 | Cdc2-cyclin B kinase activity links Crb2 and Rqh1-topoisomerase III |
Q24302011 | Characterization of human exonuclease 1 in complex with mismatch repair proteins, subcellular localization and association with PCNA |
Q27934255 | Characterization of nuclease-dependent functions of Exo1p in Saccharomyces cerevisiae |
Q34816808 | Checkpoint-dependent phosphorylation of Exo1 modulates the DNA damage response |
Q34569381 | Competing crossover pathways act during meiosis in Saccharomyces cerevisiae |
Q35161764 | Competition between the Rad50 complex and the Ku heterodimer reveals a role for Exo1 in processing double-strand breaks but not telomeres |
Q38351980 | Complementary functions of the Saccharomyces cerevisiae Rad2 family nucleases in Okazaki fragment maturation, mutation avoidance, and chromosome stability |
Q37224128 | Ctp1 and Exonuclease 1, alternative nucleases regulated by the MRN complex, are required for efficient meiotic recombination |
Q37361939 | DNA double-strand break processing: the beginning of the end. |
Q34612802 | DNA end resection--unraveling the tail |
Q24654725 | DNA end resection: many nucleases make light work |
Q42280794 | DNA interstrand cross-link repair in the Saccharomyces cerevisiae cell cycle: overlapping roles for PSO2 (SNM1) with MutS factors and EXO1 during S phase |
Q36429457 | DNA repair protein: endo-exonuclease as a new frontier in cancer therapy |
Q34611088 | Decreased meiotic intergenic recombination and increased meiosis I nondisjunction in exo1 mutants of Saccharomyces cerevisiae |
Q33945750 | Delineation of WRN helicase function with EXO1 in the replicational stress response |
Q34614221 | Differential suppression of DNA repair deficiencies of Yeast rad50, mre11 and xrs2 mutants by EXO1 and TLC1 (the RNA component of telomerase). |
Q27931609 | Din7 and Mhr1 expression levels regulate double-strand-break-induced replication and recombination of mtDNA at ori5 in yeast |
Q37226108 | Dna2 is involved in CA strand resection and nascent lagging strand completion at native yeast telomeres |
Q27931988 | Dual role for Saccharomyces cerevisiae Tel1 in the checkpoint response to double-strand breaks |
Q36002464 | EXO1 is critical for embryogenesis and the DNA damage response in mice with a hypomorphic Nbs1 allele |
Q42426732 | EXO1 plays a role in generating type I and type II survivors in budding yeast |
Q39860143 | EXO1-dependent single-stranded DNA at telomeres activates subsets of DNA damage and spindle checkpoint pathways in budding yeast yku70Delta mutants |
Q37062471 | End Resection Initiates Genomic Instability in the Absence of Telomerase |
Q33938581 | End resection at double-strand breaks: mechanism and regulation |
Q34559710 | End-processing during non-homologous end-joining: a role for exonuclease 1 |
Q33222159 | Evidence of meiotic crossover control in Saccharomyces cerevisiae through Mec1-mediated phosphorylation of replication protein A. |
Q38335994 | Exo1 and Rad24 differentially regulate generation of ssDNA at telomeres of Saccharomyces cerevisiae cdc13-1 mutants |
Q89533185 | Exo1 phosphorylation inhibits exonuclease activity and prevents fork collapse in rad53 mutants independently of the 14-3-3 proteins |
Q90292067 | Exonuclease 1 (Exo1) Participates in Mammalian Non-Homologous End Joining and Contributes to Drug Resistance in Ovarian Cancer |
Q38919536 | Exonuclease 1 and its versatile roles in DNA repair |
Q28261787 | Exonuclease 1-dependent and independent mismatch repair |
Q42268671 | Failed gene conversion leads to extensive end processing and chromosomal rearrangements in fission yeast |
Q42043478 | Fen-1 facilitates homologous recombination by removing divergent sequences at DNA break ends |
Q27935172 | Functional and genetic analysis of the Saccharomyces cerevisiae RNC1/TRM2: evidences for its involvement in DNA double-strand break repair |
Q47246612 | Genetic Evidence for Roles of Yeast Mitotic Cyclins at Single-Stranded Gaps Created by DNA Replication |
Q33404063 | Genetic evidence for single-strand lesions initiating Nbs1-dependent homologous recombination in diversification of Ig v in chicken B lymphocytes |
Q40975957 | Genome-wide analysis to identify pathways affecting telomere-initiated senescence in budding yeast. |
Q28185113 | Germline deletions of EXO1 do not cause colorectal tumors and lesions which are null for EXO1 do not have microsatellite instability |
Q24291378 | HNPCC mutations in the human DNA mismatch repair gene hMLH1 influence assembly of hMutLalpha and hMLH1-hEXO1 complexes |
Q38358603 | Identification of the human HEX1/hExo1 gene promoter and characterization of elements responsible for promoter activity |
Q28182219 | Inactivation of Exonuclease 1 in mice results in DNA mismatch repair defects, increased cancer susceptibility, and male and female sterility |
Q43993843 | Inactivation of Mre11 does not affect VSG gene duplication mediated by homologous recombination in Trypanosoma brucei. |
Q37215365 | Involvement of Exo1b in DNA damage-induced apoptosis |
Q34211299 | Ku prevents Exo1 and Sgs1-dependent resection of DNA ends in the absence of a functional MRX complex or Sae2 |
Q40380499 | Laboratory variability does not preclude identification of biological functions impacted by hydroxyurea |
Q37622790 | MRN and the race to the break |
Q36991032 | Mammalian Exo1 encodes both structural and catalytic functions that play distinct roles in essential biological processes |
Q35954448 | Mec1p associates with functionally compromised telomeres |
Q29618789 | Mechanism and control of meiotic recombination initiation |
Q37118849 | Mechanism and regulation of DNA end resection in eukaryotes |
Q37774547 | Mechanisms and regulation of DNA end resection |
Q26864428 | Mechanisms and regulation of mitotic recombination in Saccharomyces cerevisiae |
Q38618828 | Meiotic Recombination: The Essence of Heredity |
Q35910256 | Meiotic recombination intermediates and mismatch repair proteins |
Q24292290 | Molecular interactions of human Exo1 with DNA |
Q40078013 | Mrc1 protects uncapped budding yeast telomeres from exonuclease EXO1. |
Q36916670 | Mre11-Rad50-Nbs1 is a keystone complex connecting DNA repair machinery, double-strand break signaling, and the chromatin template. |
Q27012760 | Multiple cellular mechanisms prevent chromosomal rearrangements involving repetitive DNA |
Q64065581 | Noncanonical Contributions of MutLγ to VDE-Initiated Crossovers During Meiosis |
Q58128099 | Novel Sensitive Fluorometric Determination of Exonuclease I Using Polydopamine Nanospheres |
Q35661319 | Nuclease-deficient FEN-1 blocks Rad51/BRCA1-mediated repair and causes trinucleotide repeat instability |
Q37011985 | Nucleosome dynamics regulates DNA processing |
Q34613942 | Overlapping functions of the Saccharomyces cerevisiae Mre11, Exo1 and Rad27 nucleases in DNA metabolism |
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. |
Q37058652 | Positive regulation of meiotic DNA double-strand break formation by activation of the DNA damage checkpoint kinase Mec1(ATR). |
Q36779483 | Processing of DNA double-stranded breaks and intermediates of recombination and repair by Saccharomyces cerevisiae Mre11 and its stimulation by Rad50, Xrs2, and Sae2 proteins |
Q27939123 | Processing of meiotic DNA double strand breaks requires cyclin-dependent kinase and multiple nucleases |
Q38214443 | Quality control of homologous recombination |
Q24301788 | RECQ1 helicase interacts with human mismatch repair factors that regulate genetic recombination |
Q36542150 | Rad50S alleles of the Mre11 complex: questions answered and questions raised |
Q34661452 | RecQ helicase and RecJ nuclease provide complementary functions to resect DNA for homologous recombination |
Q34108141 | Recombination at double-strand breaks and DNA ends: conserved mechanisms from phage to humans. |
Q48015207 | Recombination at subtelomeres is regulated by physical distance, double-strand break resection and chromatin status. |
Q60920607 | Replication stress-induced Exo1 phosphorylation is mediated by Rad53/Pph3 and Exo1 nuclear localization is controlled by 14-3-3 proteins |
Q40292461 | Requirement of the Mre11 complex and exonuclease 1 for activation of the Mec1 signaling pathway. |
Q33317311 | Rice exonuclease-1 homologue, OsEXO1, that interacts with DNA polymerase lambda and RPA subunit proteins, is involved in cell proliferation |
Q29618204 | Role of RAD52 epistasis group genes in homologous recombination and double-strand break repair |
Q34643127 | Role of replication protein A in double holliday junction dissolution mediated by the BLM-Topo IIIα-RMI1-RMI2 protein complex |
Q60927678 | Role of the Mre11 Complex in Preserving Genome Integrity |
Q34644404 | Role of the nuclease activity of Saccharomyces cerevisiae Mre11 in repair of DNA double-strand breaks in mitotic cells. |
Q36540776 | Roles for mismatch repair family proteins in promoting meiotic crossing over |
Q46127945 | Saccharomyces cerevisiae Mer3 helicase stimulates 3'-5' heteroduplex extension by Rad51; implications for crossover control in meiotic recombination |
Q42408271 | Saccharomyces cerevisiae Mre11/Rad50/Xrs2 and Ku proteins regulate association of Exo1 and Dna2 with DNA breaks |
Q35945630 | Saccharomyces cerevisiae Sae2- and Tel1-dependent single-strand DNA formation at DNA break promotes microhomology-mediated end joining |
Q33667306 | Schizosaccharomyces pombe MutSα and MutLα Maintain Stability of Tetra-Nucleotide Repeats and Msh3 of Hepta-Nucleotide Repeats |
Q27931367 | Separate roles for the DNA damage checkpoint protein kinases in stabilizing DNA replication forks. |
Q29615269 | Sgs1 helicase and two nucleases Dna2 and Exo1 resect DNA double-strand break ends |
Q37058602 | Sharpening the ends for repair: mechanisms and regulation of DNA resection |
Q37971853 | Similarities and differences between "uncapped" telomeres and DNA double-strand breaks. |
Q29618612 | Srs2 and Sgs1-Top3 suppress crossovers during double-strand break repair in yeast |
Q27631960 | Structural biochemistry and interaction architecture of the DNA double-strand break repair Mre11 nuclease and Rad50-ATPase |
Q38235791 | Structural studies of DNA end detection and resection in homologous recombination |
Q36189334 | Sumoylation regulates EXO1 stability and processing of DNA damage |
Q27933098 | Supercomplex formation between Mlh1-Mlh3 and Sgs1-Top3 heterocomplexes in meiotic yeast cells |
Q27936152 | Synergistic effect of TRM2/RNC1 and EXO1 in DNA double-strand break repair in Saccharomyces cerevisiae |
Q34463536 | Systematic mutagenesis of the Saccharomyces cerevisiae MLH1 gene reveals distinct roles for Mlh1p in meiotic crossing over and in vegetative and meiotic mismatch repair |
Q28550291 | Tel1 and Rif2 Regulate MRX Functions in End-Tethering and Repair of DNA Double-Strand Breaks |
Q40294605 | Telomerase- and recombination-independent immortalization of budding yeast |
Q28301386 | Temporally and biochemically distinct activities of Exo1 during meiosis: double-strand break resection and resolution of double Holliday junctions |
Q27932618 | The MER3 DNA helicase catalyzes the unwinding of holliday junctions |
Q30990610 | The MER3 helicase involved in meiotic crossing over is stimulated by single-stranded DNA-binding proteins and unwinds DNA in the 3' to 5' direction. |
Q27937197 | The Mnd1 protein forms a complex with hop2 to promote homologous chromosome pairing and meiotic double-strand break repair |
Q37574070 | The Mre11 nuclease is not required for 5' to 3' resection at multiple HO-induced double-strand breaks |
Q40950715 | The RNA binding protein Npl3 promotes resection of DNA double-strand breaks by regulating the levels of Exo1. |
Q27931846 | The budding yeast Msh4 protein functions in chromosome synapsis and the regulation of crossover distribution |
Q28155868 | 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 |
Q33822400 | The extent of error-prone replication restart by homologous recombination is controlled by Exo1 and checkpoint proteins. |
Q36900911 | The multiple roles of the Mre11 complex for meiotic recombination |
Q36483126 | The role of DNA exonucleases in protecting genome stability and their impact on ageing. |
Q34016542 | The role of Exo1p exonuclease in DNA end resection to generate gene conversion tracts in Saccharomyces cerevisiae |
Q41893760 | To trim or not to trim: progression and control of DSB end resection |
Q36740600 | Unique and important consequences of RECQ1 deficiency in mammalian cells |
Q36595565 | Unique and overlapping functions of the Exo1, Mre11 and Pso2 nucleases in DNA repair |
Q42162427 | VDE-initiated intein homing in Saccharomyces cerevisiae proceeds in a meiotic recombination-like manner. |
Q78025737 | Wild-type levels of Spo11-induced DSBs are required for normal single-strand resection during meiosis |
Q27935389 | exo1-Dependent mutator mutations: model system for studying functional interactions in mismatch repair |
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