scholarly article | Q13442814 |
P2093 | author name string | R D Kolodner | |
S Oh | |||
M N Nguyen | |||
N S Amin | |||
P2860 | cites work | Isolation and identification of the third subunit of mammalian DNA polymerase delta by PCNA-affinity chromatography of mouse FM3A cell extracts | Q22009456 |
Functional interaction of proliferating cell nuclear antigen with MSH2-MSH6 and MSH2-MSH3 complexes | Q24290314 | ||
DNA polymerase delta is required for human mismatch repair in vitro | Q24313002 | ||
Identification and characterization of Saccharomyces cerevisiae EXO1, a gene encoding an exonuclease that interacts with MSH2 | Q24314329 | ||
The Saccharomyces cerevisiae protein YJR043C (Pol32) interacts with the catalytic subunit of DNA polymerase alpha and is required for cell cycle progression in G2/M | Q77937435 | ||
Mismatch repair in replication fidelity, genetic recombination, and cancer biology | Q29616483 | ||
An atypical topoisomerase II from Archaea with implications for meiotic recombination | Q29618230 | ||
The distribution of the numbers of mutants in bacterial populations | Q29620123 | ||
Methylation of the hMLH1 promoter correlates with lack of expression of hMLH1 in sporadic colon tumors and mismatch repair-defective human tumor cell lines | Q29620526 | ||
Microsatellite instability in cancer of the proximal colon | Q29620692 | ||
Mismatch repair in Escherichia coli cells lacking single-strand exonucleases ExoI, ExoVII, and RecJ | Q33724726 | ||
Mismatch repair defects in cancer | Q33885063 | ||
Functional interaction between the Werner Syndrome protein and DNA polymerase delta | Q33899465 | ||
Interactions of Exo1p with components of MutLalpha in Saccharomyces cerevisiae | Q33933718 | ||
Unlinked noncomplementation: isolation of new conditional-lethal mutations in each of the tubulin genes of Saccharomyces cerevisiae | Q33954146 | ||
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 | ||
Mutator phenotypes conferred by MLH1 overexpression and by heterozygosity for mlh1 mutations. | Q33957827 | ||
Genetic evidence for functional interactions between actin noncomplementing (Anc) gene products and actin cytoskeletal proteins in Saccharomyces cerevisiae | Q33961605 | ||
Restoration of mismatch repair to nuclear extracts of H6 colorectal tumor cells by a heterodimer of human MutL homologs | Q34554581 | ||
Characterization of the repeat-tract instability and mutator phenotypes conferred by a Tn3 insertion in RFC1, the large subunit of the yeast clamp loader | Q34606398 | ||
A mutation of the yeast gene encoding PCNA destabilizes both microsatellite and minisatellite DNA sequences | Q34606404 | ||
EXO1 and MSH6 are high-copy suppressors of conditional mutations in the MSH2 mismatch repair gene of Saccharomyces cerevisiae | Q34609730 | ||
Decreased meiotic intergenic recombination and increased meiosis I nondisjunction in exo1 mutants of Saccharomyces cerevisiae | Q34611088 | ||
A mutational analysis of the yeast proliferating cell nuclear antigen indicates distinct roles in DNA replication and DNA repair | Q36553838 | ||
Exonuclease I of Saccharomyces cerevisiae functions in mitotic recombination in vivo and in vitro | Q36568265 | ||
Hypermutability of homonucleotide runs in mismatch repair and DNA polymerase proofreading yeast mutants. | Q36568353 | ||
Functional domains of the Saccharomyces cerevisiae Mlh1p and Pms1p DNA mismatch repair proteins and their relevance to human hereditary nonpolyposis colorectal cancer-associated mutations | Q36570003 | ||
Dual requirement in yeast DNA mismatch repair for MLH1 and PMS1, two homologs of the bacterial mutL gene | Q36643609 | ||
Structure and processivity of two forms of Saccharomyces cerevisiae DNA polymerase delta | Q38335236 | ||
hMSH2 and hMSH6 play distinct roles in mismatch binding and contribute differently to the ATPase activity of hMutSalpha | Q38336441 | ||
Saccharomyces cerevisiae pol30 (proliferating cell nuclear antigen) mutations impair replication fidelity and mismatch repair | Q39449001 | ||
Microsatellite instability in yeast: dependence on repeat unit size and DNA mismatch repair genes | Q40022200 | ||
Microsatellite instability in inherited and sporadic neoplasms | Q40493550 | ||
Mismatch Repair Deficiency in Phenotypically Normal Human Cells | Q41347026 | ||
Novel dominant mutations in Saccharomyces cerevisiae MSH6. | Q41711225 | ||
Single-strand DNA-specific exonucleases in Escherichia coli. Roles in repair and mutation avoidance. | Q41777210 | ||
MLH1, PMS1, and MSH2 interactions during the initiation of DNA mismatch repair in yeast | Q42427955 | ||
Chromosomal rearrangements occur in S. cerevisiae rfa1 mutator mutants due to mutagenic lesions processed by double-strand-break repair | Q46348708 | ||
Characterization of the two small subunits of Saccharomyces cerevisiae DNA polymerase delta | Q47791987 | ||
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 | ||
A novel mutation avoidance mechanism dependent on S. cerevisiae RAD27 is distinct from DNA mismatch repair | Q64389285 | ||
Somatic mutations in the hMSH2 gene in microsatellite unstable colorectal carcinomas | Q70972741 | ||
POL32, a subunit of the Saccharomyces cerevisiae DNA polymerase delta, defines a link between DNA replication and the mutagenic bypass repair pathway | Q73319794 | ||
Methylation of the hMLH1 promoter but no hMLH1 mutations in sporadic gastric carcinomas with high-level microsatellite instability | Q73911349 | ||
Methylation of hMLH1 in a population-based series of endometrial carcinomas | Q74352335 | ||
The evolutionarily conserved zinc finger motif in the largest subunit of human replication protein A is required for DNA replication and mismatch repair but not for nucleotide excision repair | Q24321288 | ||
hMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6 | Q24323176 | ||
Transformation of MutL by ATP binding and hydrolysis: a switch in DNA mismatch repair | Q27617873 | ||
Crystal structures of mismatch repair protein MutS and its complex with a substrate DNA | Q27627633 | ||
The crystal structure of DNA mismatch repair protein MutS binding to a G x T mismatch | Q27627644 | ||
Crystal structure of the eukaryotic DNA polymerase processivity factor PCNA | Q27730804 | ||
Crystal structure and ATPase activity of MutL: implications for DNA repair and mutagenesis | Q27766073 | ||
A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae | Q27860636 | ||
Functional studies on the candidate ATPase domains of Saccharomyces cerevisiae MutLalpha. | Q27929951 | ||
Saccharomyces cerevisiae Msh2p and Msh6p ATPase activities are both required during mismatch repair | Q27932017 | ||
Enhancement of MSH2-MSH3-mediated mismatch recognition by the yeast MLH1-PMS1 complex | Q27932428 | ||
The product of the DNA damage-inducible gene of Saccharomyces cerevisiae, DIN7, specifically functions in mitochondria | Q27933751 | ||
Role of yeast Rth1 nuclease and its homologs in mutation avoidance, DNA repair, and DNA replication | Q27934260 | ||
A mutation in the MSH6 subunit of the Saccharomyces cerevisiae MSH2-MSH6 complex disrupts mismatch recognition | Q27934451 | ||
The Saccharomyces cerevisiae MLH3 gene functions in MSH3-dependent suppression of frameshift mutations | Q27935158 | ||
A requirement for recombinational repair in Saccharomyces cerevisiae is caused by DNA replication defects of mec1 mutants | Q27935496 | ||
Evidence for involvement of yeast proliferating cell nuclear antigen in DNA mismatch repair | Q27938608 | ||
Eukaryotic DNA mismatch repair | Q27939116 | ||
ATP-dependent assembly of a ternary complex consisting of a DNA mismatch and the yeast MSH2-MSH6 and MLH1-PMS1 protein complexes | Q27939412 | ||
Requirement for PCNA in DNA mismatch repair at a step preceding DNA resynthesis | Q27939891 | ||
Multifunctional yeast high-copy-number shuttle vectors | Q28131605 | ||
The interaction of the human MutL homologues in hereditary nonpolyposis colon cancer | Q28137782 | ||
Exo1 roles for repair of DNA double-strand breaks and meiotic crossing over in Saccharomyces cerevisiae | Q28140402 | ||
Proliferating cell nuclear antigen and Msh2p-Msh6p interact to form an active mispair recognition complex | Q28142999 | ||
Biochemistry and genetics of eukaryotic mismatch repair | Q28282377 | ||
Identification of a human gene encoding a homologue of Saccharomyces cerevisiae EXO1, an exonuclease implicated in mismatch repair and recombination | Q28289308 | ||
Isolation of an hMSH2-p160 Heterodimer That Restores DNA Mismatch Repair to Tumor Cells | Q28292781 | ||
hMutSbeta, a heterodimer of hMSH2 and hMSH3, binds to insertion/deletion loops in DNA | Q28610839 | ||
ATP-dependent interaction of human mismatch repair proteins and dual role of PCNA in mismatch repair | Q28610858 | ||
Isolation of MutSbeta from human cells and comparison of the mismatch repair specificities of MutSbeta and MutSalpha | Q28610863 | ||
Multiple functions of MutS- and MutL-related heterocomplexes | Q28776215 | ||
Redundancy of Saccharomyces cerevisiae MSH3 and MSH6 in MSH2-dependent mismatch repair | Q29615027 | ||
P433 | issue | 15 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | cell biology | Q7141 |
DNA mismatch repair | Q2984243 | ||
Rad2 family nuclease EXO1 YOR033C | Q27548669 | ||
P304 | page(s) | 5142-55 | |
P577 | publication date | 2001-08-01 | |
P1433 | published in | Molecular and Cellular Biology | Q3319478 |
P1476 | title | exo1-Dependent mutator mutations: model system for studying functional interactions in mismatch repair | |
P478 | volume | 21 |
Q24298110 | A defined human system that supports bidirectional mismatch-provoked excision |
Q93270681 | A genetic screen pinpoints ribonucleotide reductase residues that sustain dNTP homeostasis and specifies a highly mutagenic type of dNTP imbalance |
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 |
Q40248007 | Alterations in cellular metabolism triggered by URA7 or GLN3 inactivation cause imbalanced dNTP pools and increased mutagenesis |
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. |
Q33791321 | Biochemical characterization of a cancer-associated E109K missense variant of human exonuclease 1. |
Q37351850 | C-terminal flap endonuclease (rad27) mutations: lethal interactions with a DNA ligase I mutation (cdc9-p) and suppression by proliferating cell nuclear antigen (POL30) in Saccharomyces cerevisiae |
Q37072156 | Characterization of a highly conserved binding site of Mlh1 required for exonuclease I-dependent mismatch repair |
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 |
Q35865056 | Chimeric Saccharomyces cerevisiae Msh6 protein with an Msh3 mispair-binding domain combines properties of both proteins. |
Q35881387 | Chromosome position determines the success of double-strand break repair |
Q35782915 | Colorectal cancer as a complex disease: defining at-risk subjects in the general population - a preventive strategy |
Q38351980 | Complementary functions of the Saccharomyces cerevisiae Rad2 family nucleases in Okazaki fragment maturation, mutation avoidance, and chromosome stability |
Q34611390 | Cotransport of the heterodimeric small subunit of the Saccharomyces cerevisiae ribonucleotide reductase between the nucleus and the cytoplasm |
Q36884849 | DNA Mismatch Repair Interacts with CAF-1- and ASF1A-H3-H4-dependent Histone (H3-H4)2 Tetramer Deposition |
Q28211143 | DNA mismatch repair and mutation avoidance pathways |
Q36540658 | DNA mismatch repair and the DNA damage response |
Q34568596 | DNA mismatch repair defects: role in colorectal carcinogenesis |
Q37685729 | DNA mismatch repair gene MSH6 implicated in determining age at natural menopause |
Q24647002 | DNA mismatch repair: molecular mechanism, cancer, and ageing |
Q28709604 | DNA repair mechanisms and the bypass of DNA damage in Saccharomyces cerevisiae |
Q34297803 | DNA repair mechanisms and their biological roles in the malaria parasite Plasmodium falciparum |
Q28295863 | DNA replication fidelity and cancer |
Q33888905 | Deficiency of a novel mismatch repair activity in a bladder tumor cell line |
Q35910908 | Detection of activity centers in cellular pathways using transcript profiling |
Q35034387 | Different roles of eukaryotic MutS and MutL complexes in repair of small insertion and deletion loops in yeast. |
Q34396924 | Differential correction of lagging-strand replication errors made by DNA polymerases {alpha} and {delta} |
Q44761854 | Differential requirement for proliferating cell nuclear antigen in 5' and 3' nick-directed excision in human mismatch repair |
Q28534756 | Dominant mutations in S. cerevisiae PMS1 identify the Mlh1-Pms1 endonuclease active site and an exonuclease 1-independent mismatch repair pathway |
Q39882599 | Drug-sensitive DNA polymerase δ reveals a role for mismatch repair in checkpoint activation in yeast. |
Q48587042 | EXO1 suppresses double-strand break induced homologous recombination between diverged sequences in mammalian cells |
Q92203157 | Effective mismatch repair depends on timely control of PCNA retention on DNA by the Elg1 complex |
Q47632050 | Embryonic-endometrial interactions at implantation in humans |
Q36764079 | Endonuclease activities of MutLα and its homologs in DNA mismatch repair |
Q36436073 | Engineered disulfide-forming amino acid substitutions interfere with a conformational change in the mismatch recognition complex Msh2-Msh6 required for mismatch repair |
Q73576845 | Enhanced expression of the DNA damage-inducible gene DIN7 results in increased mutagenesis of mitochondrial DNA in Saccharomyces cerevisiae |
Q33711830 | Eukaryotic Mismatch Repair in Relation to DNA Replication |
Q24316068 | Evidence for involvement of HMGB1 protein in human DNA mismatch repair |
Q28551519 | Evidence of a Mild Mutator Phenotype in Cambodian Plasmodium falciparum Malaria Parasites |
Q35564759 | Exo1 phosphorylation status controls the hydroxyurea sensitivity of cells lacking the Pol32 subunit of DNA polymerases delta and zeta |
Q90292067 | Exonuclease 1 (Exo1) Participates in Mammalian Non-Homologous End Joining and Contributes to Drug Resistance in Ovarian Cancer |
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 |
Q36553485 | Exonuclease 1 preferentially repairs mismatches generated by DNA polymerase α |
Q28261787 | Exonuclease 1-dependent and independent mismatch repair |
Q33739955 | Functional analysis of human mismatch repair gene mutations identifies weak alleles and polymorphisms capable of polygenic interactions |
Q24619622 | Functional studies and homology modeling of Msh2-Msh3 predict that mispair recognition involves DNA bending and strand separation |
Q28185113 | Germline deletions of EXO1 do not cause colorectal tumors and lesions which are null for EXO1 do not have microsatellite instability |
Q35318165 | Heteroduplex rejection during single-strand annealing requires Sgs1 helicase and mismatch repair proteins Msh2 and Msh6 but not Pms1 |
Q47766916 | Human DNA polymerase delta double-mutant D316A;E318A interferes with DNA mismatch repair in vitro |
Q60934518 | Human Exonuclease 1 (EXO1) Regulatory Functions in DNA Replication with Putative Roles in Cancer |
Q31119964 | Human MutL homolog (MLH1) function in DNA mismatch repair: a prospective screen for missense mutations in the ATPase domain |
Q24292224 | Human exonuclease I is required for 5' and 3' mismatch repair |
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 |
Q36741556 | Identification of regulatory factor X as a novel mismatch repair stimulatory factor |
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 |
Q24629057 | Interaction between the Msh2 and Msh6 nucleotide-binding sites in the Saccharomyces cerevisiae Msh2-Msh6 complex |
Q33933718 | Interactions of Exo1p with components of MutLalpha in Saccharomyces cerevisiae |
Q47135454 | Involvement of DNA mismatch repair in the maintenance of heterochromatic DNA stability in Saccharomyces cerevisiae. |
Q39675432 | Isolation and characterization of new proliferating cell nuclear antigen (POL30) mutator mutants that are defective in DNA mismatch repair |
Q36991032 | Mammalian Exo1 encodes both structural and catalytic functions that play distinct roles in essential biological processes |
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 |
Q28262719 | Mechanisms and functions of DNA mismatch repair |
Q43990123 | Mismatch repair in human nuclear extracts. Time courses and ATP requirements for kinetically distinguishable steps leading to tightly controlled 5' to 3' and aphidicolin-sensitive 3' to 5' mispair-provoked excision |
Q42936455 | Mismatch repair, but not heteroduplex rejection, is temporally coupled to DNA replication |
Q35165645 | Mlh2 is an accessory factor for DNA mismatch repair in Saccharomyces cerevisiae |
Q91404367 | MutL sliding clamps coordinate exonuclease-independent Escherichia coli mismatch repair |
Q50989071 | MutS stimulates the endonuclease activity of MutL in an ATP-hydrolysis-dependent manner. |
Q39612088 | MutSα maintains the mismatch repair capability by inhibiting PCNA unloading. |
Q34123282 | Mutations within the hMLH1 and hPMS2 subunits of the human MutLalpha mismatch repair factor affect its ATPase activity, but not its ability to interact with hMutSalpha |
Q28084645 | New insights into the mechanism of DNA mismatch repair |
Q26822478 | Nucleases in homologous recombination as targets for cancer therapy |
Q57009219 | Nucleosomes around a mismatched base pair are excluded via an Msh2-dependent reaction with the aid of SNF2 family ATPase Smarcad1 |
Q37037194 | O6-methylguanine-induced cell death involves exonuclease 1 as well as DNA mismatch recognition in vivo |
Q33961620 | PCNA and Msh2-Msh6 activate an Mlh1-Pms1 endonuclease pathway required for Exo1-independent mismatch repair. |
Q37482417 | PCNA mono-ubiquitination and activation of translesion DNA polymerases by DNA polymerase {alpha}. |
Q37271214 | PCNA promotes processive DNA end resection by Exo1. |
Q28610670 | Partial reconstitution of human DNA mismatch repair in vitro: characterization of the role of human replication protein A |
Q27938949 | Pol32, a subunit of Saccharomyces cerevisiae DNA polymerase delta, suppresses genomic deletions and is involved in the mutagenic bypass pathway |
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 |
Q34187018 | Rapid analysis of Saccharomyces cerevisiae genome rearrangements by multiplex ligation-dependent probe amplification |
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 |
Q33317311 | Rice exonuclease-1 homologue, OsEXO1, that interacts with DNA polymerase lambda and RPA subunit proteins, is involved in cell proliferation |
Q27931230 | Saccharomyces cerevisiae Msh2-Msh3 acts in repair of base-base mispairs |
Q33667306 | Schizosaccharomyces pombe MutSα and MutLα Maintain Stability of Tetra-Nucleotide Repeats and Msh3 of Hepta-Nucleotide Repeats |
Q28242820 | Sensitivity to phosphonoacetic acid: a new phenotype to probe DNA polymerase delta in Saccharomyces cerevisiae. |
Q34243555 | Sgs1 and Exo1 suppress targeted chromosome duplication during ends-in and ends-out gene targeting. |
Q26999680 | Single-molecule views of MutS on mismatched DNA. |
Q40412801 | Somatic hypermutation and mismatch repair in non-B cells |
Q27684073 | Structure of the MutLα C-terminal domain reveals how Mlh1 contributes to Pms1 endonuclease site |
Q27667527 | Structures of Human Exonuclease 1 DNA Complexes Suggest a Unified Mechanism for Nuclease Family |
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 |
Q28301386 | Temporally and biochemically distinct activities of Exo1 during meiosis: double-strand break resection and resolution of double Holliday junctions |
Q27932484 | The multiple biological roles of the 3'-->5' exonuclease of Saccharomyces cerevisiae DNA polymerase delta require switching between the polymerase and exonuclease domains |
Q91595501 | The properties of Msh2-Msh6 ATP binding mutants suggest a signal amplification mechanism in DNA mismatch repair |
Q54442651 | Tumor progression in Apc(1638N) mice with Exo1 and Fen1 deficiencies. |
Q96022920 | Tumour predisposition and cancer syndromes as models to study gene-environment interactions |
Q36338245 | Visualization of eukaryotic DNA mismatch repair reveals distinct recognition and repair intermediates. |
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