| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1002328755 |
| P356 | DOI | 10.1038/81708 |
| P3181 | OpenCitations bibliographic resource ID | 114695 |
| P698 | PubMed publication ID | 11062484 |
| P2093 | author name string | D Clark | |
| R D Kolodner | |||
| H Flores-Rozas | |||
| P2860 | cites work | Nucleotide-promoted release of hMutSalpha from heteroduplex DNA is consistent with an ATP-dependent translocation mechanism | Q28610864 |
| Redundancy of Saccharomyces cerevisiae MSH3 and MSH6 in MSH2-dependent mismatch repair | Q29615027 | ||
| The distribution of the numbers of mutants in bacterial populations | Q29620123 | ||
| The Escherichia coli MutL protein stimulates binding of Vsr and MutS to heteroduplex DNA. | Q34657088 | ||
| A mutational analysis of the yeast proliferating cell nuclear antigen indicates distinct roles in DNA replication and DNA repair | Q36553838 | ||
| Biochemical characterization of the interaction between the Saccharomyces cerevisiae MSH2-MSH6 complex and mispaired bases in DNA. | Q38320783 | ||
| 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 | ||
| DNA-replication fidelity, mismatch repair and genome instability in cancer cells | Q41016785 | ||
| MLH1, PMS1, and MSH2 interactions during the initiation of DNA mismatch repair in yeast | Q42427955 | ||
| The MutL ATPase is required for mismatch repair | Q73586223 | ||
| Isolation and identification of the third subunit of mammalian DNA polymerase delta by PCNA-affinity chromatography of mouse FM3A cell extracts | Q22009456 | ||
| Identification of replication factor C from Saccharomyces cerevisiae: a component of the leading-strand DNA replication complex | Q27929854 | ||
| The Saccharomyces cerevisiae Msh2 and Msh6 proteins form a complex that specifically binds to duplex oligonucleotides containing mismatched DNA base pairs | Q27930815 | ||
| Genetic and biochemical analysis of Msh2p-Msh6p: role of ATP hydrolysis and Msh2p-Msh6p subunit interactions in mismatch base pair recognition. | Q27932001 | ||
| Enhancement of MSH2-MSH3-mediated mismatch recognition by the yeast MLH1-PMS1 complex | Q27932428 | ||
| The Saccharomyces cerevisiae MLH3 gene functions in MSH3-dependent suppression of frameshift mutations | Q27935158 | ||
| Evidence for involvement of yeast proliferating cell nuclear antigen in DNA mismatch repair | Q27938608 | ||
| Eukaryotic DNA mismatch repair | Q27939116 | ||
| Requirement for PCNA in DNA mismatch repair at a step preceding DNA resynthesis | Q27939891 | ||
| The human mismatch recognition complex hMSH2-hMSH6 functions as a novel molecular switch | Q28258968 | ||
| PCNA binding through a conserved motif | Q28274063 | ||
| ATP-dependent interaction of human mismatch repair proteins and dual role of PCNA in mismatch repair | Q28610858 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 375-8 | |
| P577 | publication date | 2000-11-01 | |
| P1433 | published in | Nature Genetics | Q976454 |
| P1476 | title | Proliferating cell nuclear antigen and Msh2p-Msh6p interact to form an active mispair recognition complex | |
| P478 | volume | 26 |
| Q36677284 | A Delicate Balance Between Repair and Replication Factors Regulates Recombination Between Divergent DNA Sequences in Saccharomyces cerevisiae |
| Q35648418 | A fluorescent bimolecular complementation screen reveals MAF1, RNF7 and SETD3 as PCNA-associated proteins in human cells |
| Q36540457 | A personal historical view of DNA mismatch repair with an emphasis on eukaryotic DNA mismatch repair |
| Q50991068 | A role for Myh1 in DNA repair after treatment with strand-breaking and crosslinking chemotherapeutic agents. |
| Q33944779 | A universal protein-protein interaction motif in the eubacterial DNA replication and repair systems. |
| Q35690218 | Activation of Saccharomyces cerevisiae Mlh1-Pms1 Endonuclease in a Reconstituted Mismatch Repair System |
| Q34616364 | Alleles of the yeast Pms1 mismatch-repair gene that differentially affect recombination- and replication-related processes |
| Q34443496 | Base composition of mononucleotide runs affects DNA polymerase slippage and removal of frameshift intermediates by mismatch repair in Saccharomyces cerevisiae |
| Q33726437 | Bi-directional routing of DNA mismatch repair protein human exonuclease 1 to replication foci and DNA double strand breaks |
| Q36420091 | Cellular response to DNA damage |
| Q27934255 | Characterization of nuclease-dependent functions of Exo1p in Saccharomyces cerevisiae |
| Q35910253 | Chromosomal directionality of DNA mismatch repair in Escherichia coli |
| Q42424836 | Clamping down on mismatches |
| Q40744193 | Contribution of human mlh1 and pms2 ATPase activities to DNA mismatch repair |
| Q33855528 | Cooperative nuclear localization sequences lend a novel role to the N-terminal region of MSH6. |
| Q27640487 | Crystal structure and biochemical analysis of the MutS.ADP.beryllium fluoride complex suggests a conserved mechanism for ATP interactions in mismatch repair |
| 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 |
| Q34298096 | DNA methyltransferases, DNA damage repair, and cancer |
| Q36527421 | DNA mismatch repair and Lynch syndrome |
| Q28211143 | DNA mismatch repair and mutation avoidance pathways |
| Q34568596 | DNA mismatch repair defects: role in colorectal carcinogenesis |
| Q36453321 | DNA mismatch repair system. Classical and fresh roles |
| Q40478691 | DNA mismatch repair-dependent response to fluoropyrimidine-generated damage. |
| Q24647002 | DNA mismatch repair: molecular mechanism, cancer, and ageing |
| Q36493831 | DNA repair in antibody somatic hypermutation |
| Q28709604 | DNA repair mechanisms and the bypass of DNA damage in Saccharomyces cerevisiae |
| Q64387816 | DNA template requirements for human mismatch repair in vitro |
| Q37491462 | Deoxyribonucleic acid damage induced by doxorubicin in peripheral blood mononuclear cells: possible roles for the stress response and the deoxyribonucleic acid repair process |
| Q35034387 | Different roles of eukaryotic MutS and MutL complexes in repair of small insertion and deletion loops in yeast. |
| Q44761854 | Differential requirement for proliferating cell nuclear antigen in 5' and 3' nick-directed excision in human mismatch repair |
| Q27679146 | Distinct Structural Alterations in Proliferating Cell Nuclear Antigen Block DNA Mismatch Repair |
| Q45962906 | DnaN clamp zones provide a platform for spatiotemporal coupling of mismatch detection to DNA replication. |
| Q38289639 | Dominant Saccharomyces cerevisiae msh6 mutations cause increased mispair binding and decreased dissociation from mispairs by Msh2-Msh6 in the presence of ATP. |
| Q28534756 | Dominant mutations in S. cerevisiae PMS1 identify the Mlh1-Pms1 endonuclease active site and an exonuclease 1-independent mismatch repair pathway |
| Q92203157 | Effective mismatch repair depends on timely control of PCNA retention on DNA by the Elg1 complex |
| Q37438949 | Epigenetic Enhancement of the Post-replicative DNA Mismatch Repair of Mammalian Genomes by a Hemi-(m)CpG-Np95-Dnmt1 Axis |
| Q95267862 | Evaluation of Concordance Between Deficient Mismatch Repair and Microsatellite Instability Testing and Their Association with Clinicopathological Features in Colorectal Cancer |
| Q38355096 | Evidence for Preferential Mismatch Repair of Lagging Strand DNA Replication Errors in Yeast |
| Q24316068 | Evidence for involvement of HMGB1 protein in human DNA mismatch repair |
| Q35564759 | Exo1 phosphorylation status controls the hydroxyurea sensitivity of cells lacking the Pol32 subunit of DNA polymerases delta and zeta |
| Q28261787 | Exonuclease 1-dependent and independent mismatch repair |
| Q43862921 | Functional interaction of MutY homolog with proliferating cell nuclear antigen in fission yeast, Schizosaccharomyces pombe |
| Q34425450 | Functional interactions and signaling properties of mammalian DNA mismatch repair proteins |
| Q33836026 | Genomic and epigenetic instability in colorectal cancer pathogenesis |
| Q44068446 | HNPCC mutations in hMSH2 result in reduced hMSH2-hMSH6 molecular switch functions |
| Q36328799 | Human DNA mismatch repair: coupling of mismatch recognition to strand-specific excision |
| Q31119964 | Human MutL homolog (MLH1) function in DNA mismatch repair: a prospective screen for missense mutations in the ATPase domain |
| Q36424326 | Human MutY homolog induces apoptosis in etoposide-treated HEK293 cells |
| Q24292187 | Human MutY homolog, a DNA glycosylase involved in base excision repair, physically and functionally interacts with mismatch repair proteins human MutS homolog 2/human MutS homolog 6 |
| Q53665463 | Hypothesis: biological role for J-C intronic matrix attachment regions in the molecular mechanism of antigen-driven somatic hypermutation. |
| Q42373259 | Identification and analysis of biomarkers for mismatch repair proteins: A bioinformatic approach |
| Q40762811 | Identification and functional characterization of the promoter region of the human MSH6 gene |
| Q33812133 | Interaction between human mismatch repair recognition proteins and checkpoint sensor Rad9-Rad1-Hus1 |
| Q45144500 | Interaction of checkpoint proteins Hus1/Rad1/Rad9 with DNA base excision repair enzyme MutY homolog in fission yeast, Schizosaccharomyces pombe |
| Q34311670 | Interaction of the beta sliding clamp with MutS, ligase, and DNA polymerase I. |
| Q27939439 | Interactions among DNA ligase I, the flap endonuclease and proliferating cell nuclear antigen in the expansion and contraction of CAG repeat tracts in yeast |
| Q33933718 | Interactions of Exo1p with components of MutLalpha in Saccharomyces cerevisiae |
| Q37432125 | Involvement of the beta clamp in methyl-directed mismatch repair in vitro. |
| Q39675432 | Isolation and characterization of new proliferating cell nuclear antigen (POL30) mutator mutants that are defective in DNA mismatch repair |
| Q37215085 | Loading clamps for DNA replication and repair |
| Q95729094 | MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1 |
| Q34614229 | Maternal effect for DNA mismatch repair in the mouse. |
| Q28262719 | Mechanisms and functions of DNA mismatch repair |
| Q35910256 | Meiotic recombination intermediates and mismatch repair proteins |
| Q33305049 | Mismatch Repair proteins are recruited to replicating DNA through interaction with Proliferating Cell Nuclear Antigen (PCNA) |
| Q39656168 | Mismatch recognition-coupled stabilization of Msh2-Msh6 in an ATP-bound state at the initiation of DNA repair |
| Q34660590 | Mismatch repair causes the dynamic release of an essential DNA polymerase from the replication fork |
| Q42936455 | Mismatch repair, but not heteroduplex rejection, is temporally coupled to DNA replication |
| Q36209738 | Mismatch repair-dependent processing of methylation damage gives rise to persistent single-stranded gaps in newly replicated DNA. |
| Q34293069 | Molecular mechanisms of DNA mismatch repair |
| Q28214396 | Mouse models for human DNA mismatch-repair gene defects |
| Q44522189 | Msh2 separation of function mutations confer defects in the initiation steps of mismatch repair |
| Q38271431 | Multiple factors insulate Msh2-Msh6 mismatch repair activity from defects in Msh2 domain I. |
| Q35891592 | Multiple functions for the N-terminal region of Msh6 |
| Q33799870 | MutLalpha and proliferating cell nuclear antigen share binding sites on MutSbeta |
| Q39612088 | MutSα maintains the mismatch repair capability by inhibiting PCNA unloading. |
| Q28818262 | MutSβ promotes trinucleotide repeat expansion by recruiting DNA polymerase β to nascent (CAG)n or (CTG)n hairpins for error-prone DNA synthesis |
| Q57655214 | Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors |
| Q36107008 | Mutations at the Subunit Interface of Yeast Proliferating Cell Nuclear Antigen Reveal a Versatile Regulatory Domain |
| Q35313485 | N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) triggers MSH2 and Cdt2 protein-dependent degradation of the cell cycle and mismatch repair (MMR) inhibitor protein p21Waf1/Cip1 |
| Q27011117 | New insights and challenges in mismatch repair: getting over the chromatin hurdle |
| Q28084645 | New insights into the mechanism of DNA mismatch repair |
| Q34097342 | Novel PMS1 alleles preferentially affect the repair of primer strand loops during DNA replication |
| Q33643516 | Nuclear reorganization of DNA mismatch repair proteins in response to DNA damage |
| Q35953749 | On the molecular mechanism of somatic hypermutation of rearranged immunoglobulin genes |
| Q38022938 | Overview for the histone codes for DNA repair |
| Q33961620 | PCNA and Msh2-Msh6 activate an Mlh1-Pms1 endonuclease pathway required for Exo1-independent mismatch repair. |
| Q39028575 | PCNA dependent cellular activities tolerate dramatic perturbations in PCNA client interactions |
| Q24814841 | PCNA-MutSalpha-mediated binding of MutLalpha to replicative DNA with mismatched bases to induce apoptosis in human cells |
| Q28610670 | Partial reconstitution of human DNA mismatch repair in vitro: characterization of the role of human replication protein A |
| Q30978715 | Partial reconstitution of human interstrand cross-link repair in vitro: characterization of the roles of RPA and PCNA. |
| Q35590357 | Phosphorylation of PCNA by EGFR inhibits mismatch repair and promotes misincorporation during DNA synthesis |
| Q35634443 | Physical and functional interactions between Escherichia coli MutY glycosylase and mismatch repair protein MutS |
| Q27690911 | Postreplicative mismatch repair |
| Q40309902 | Postreplicative mismatch repair factors are recruited to Epstein-Barr virus replication compartments |
| Q45966811 | Predictive models for breast cancer susceptibility from multiple single nucleotide polymorphisms. |
| Q24299392 | Proliferating cell nuclear antigen (PCNA) may function as a double homotrimer complex in the mammalian cell |
| Q30397641 | Proliferating cell nuclear antigen (PCNA): a key factor in DNA replication and cell cycle regulation |
| Q37319600 | Reconstitution of long and short patch mismatch repair reactions using Saccharomyces cerevisiae proteins |
| Q37625834 | Regulation of interactions with sliding clamps during DNA replication and repair. |
| Q36540486 | Regulation of mismatch repair by histone code and posttranslational modifications in eukaryotic cells |
| Q35858504 | Regulation of the DNA replication fork: a way to fight genomic instability |
| Q93063783 | Replication stress triggers microsatellite destabilization and hypermutation leading to clonal expansion in vitro |
| Q30662232 | Retinoblastoma tumor suppressor protein signals through inhibition of cyclin-dependent kinase 2 activity to disrupt PCNA function in S phase |
| Q36313742 | Role of DNA mismatch repair and double-strand break repair in genome stability and antifungal drug resistance in Candida albicans |
| Q27938184 | Role of proliferating cell nuclear antigen interactions in the mismatch repair-dependent processing of mitotic and meiotic recombination intermediates in yeast |
| Q44142880 | Saccharomyces cerevisiae RRM3, a 5' to 3' DNA helicase, physically interacts with proliferating cell nuclear antigen |
| Q33667306 | Schizosaccharomyces pombe MutSα and MutLα Maintain Stability of Tetra-Nucleotide Repeats and Msh3 of Hepta-Nucleotide Repeats |
| Q49236774 | Sensing and Processing of DNA Interstrand Crosslinks by the Mismatch Repair Pathway. |
| Q26999680 | Single-molecule views of MutS on mismatched DNA. |
| Q39559227 | Spatiotemporally different DNA repair systems participate in Epstein-Barr virus genome maturation |
| Q57784305 | Stochastic Processes and Component Plasticity Governing DNA Mismatch Repair |
| Q28285134 | Structural, molecular and cellular functions of MSH2 and MSH6 during DNA mismatch repair, damage signaling and other noncanonical activities |
| Q28551589 | The Eukaryotic Mismatch Recognition Complexes Track with the Replisome during DNA Synthesis |
| Q36961147 | The Many Roles of PCNA in Eukaryotic DNA Replication |
| Q24657814 | The MutSalpha-proliferating cell nuclear antigen interaction in human DNA mismatch repair |
| Q36026779 | The N terminus of Saccharomyces cerevisiae Msh6 is an unstructured tether to PCNA |
| Q35813300 | The PCNA-RFC families of DNA clamps and clamp loaders |
| Q55024465 | The Role of HSP40 Conserved Motifs in the Response to Cytotoxic Stress. |
| Q52569390 | The beta sliding clamp binds to multiple sites within MutL and MutS. |
| Q24339204 | The histone mark H3K36me3 regulates human DNA mismatch repair through its interaction with MutSα |
| Q36162012 | The unstructured linker arms of Mlh1-Pms1 are important for interactions with DNA during mismatch repair |
| Q44219222 | Transfer of the MSH2.MSH6 complex from proliferating cell nuclear antigen to mispaired bases in DNA. |
| Q38940317 | Understanding how mismatch repair proteins participate in the repair/anti-recombination decision |
| Q36338245 | Visualization of eukaryotic DNA mismatch repair reveals distinct recognition and repair intermediates. |
| Q52956515 | Why do mammalian mitochondria possess a mismatch repair activity? |
| Q52644492 | YB-1 disrupts mismatch repair complex formation, interferes with MutSα recruitment on mismatch and inhibits mismatch repair through interacting with PCNA. |
| Q27935389 | exo1-Dependent mutator mutations: model system for studying functional interactions in mismatch repair |
| Q24292227 | hMutSalpha forms an ATP-dependent complex with hMutLalpha and hMutLbeta on DNA. |
| Q34276816 | hMutSbeta is required for the recognition and uncoupling of psoralen interstrand cross-links in vitro |
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