| scholarly article | Q13442814 |
| review article | Q7318358 |
| P2093 | author name string | R Kolodner | |
| P433 | issue | 12 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | DNA mismatch repair | Q2984243 |
| P304 | page(s) | 1433-42 | |
| P577 | publication date | 1996-06-15 | |
| P1433 | published in | Genes & Development | Q1524533 |
| P1476 | title | Biochemistry and genetics of eukaryotic mismatch repair | |
| P478 | volume | 10 |
| Q27934895 | 'Saccharomyces cerevisiae MSH2/6 complex interacts with Holliday junctions and facilitates their cleavage by phage resolution enzymes |
| Q34613824 | (CA/TG) microsatellite sequences escape the inhibition of recombination by mismatch repair in Saccharomyces cerevisiae. |
| Q34329434 | 1H NMR determination of base-pair lifetimes in oligonucleotides containing single base mismatches |
| Q42280286 | A 140-bp-Long Palindromic Sequence Induces Double-Strand Breaks During Meiosis in the Yeast Saccharomyces cerevisiae |
| Q33337019 | A DNA mismatch repair gene links to the Ph2 locus in wheat |
| Q34610131 | A DNA polymerase epsilon mutant that specifically causes +1 frameshift mutations within homonucleotide runs in yeast |
| Q39506181 | A Novel GT-Mismatch Binding Protein That Recognizes Strict DNA Sequences with High Affinity |
| Q24298110 | A defined human system that supports bidirectional mismatch-provoked excision |
| Q34162595 | A genomewide screen for suppressors of Alu-mediated rearrangements reveals a role for PIF1 |
| Q38346714 | A human PMS2 homologue from Aquifex aeolicus stimulates an ATP-dependent DNA helicase |
| Q27934451 | A mutation in the MSH6 subunit of the Saccharomyces cerevisiae MSH2-MSH6 complex disrupts mismatch recognition |
| Q34606404 | A mutation of the yeast gene encoding PCNA destabilizes both microsatellite and minisatellite DNA sequences |
| Q64389285 | A novel mutation avoidance mechanism dependent on S. cerevisiae RAD27 is distinct from DNA mismatch repair |
| Q33884321 | A phylogenomic study of DNA repair genes, proteins, and processes |
| Q24548238 | A phylogenomic study of the MutS family of proteins |
| Q36690009 | A subset of familial colorectal neoplasia kindreds linked to chromosome 9q22.2-31.2 |
| Q34770418 | AID and mismatch repair in antibody diversification |
| Q28610858 | ATP-dependent interaction of human mismatch repair proteins and dual role of PCNA in mismatch repair |
| Q38316177 | ATP-hydrolysis-dependent conformational switch modulates the stability of MutS-mismatch complexes |
| Q28587976 | Acceleration of lymphomagenesis in mismatch-repair deficient mice by exposure to genotoxic agents |
| Q34133568 | Ageing and the mismatch repair system |
| Q28513971 | Altered somatic hypermutation and reduced class-switch recombination in exonuclease 1-mutant mice |
| Q28910215 | Altered spectra of hypermutation in antibodies from mice deficient for the DNA mismatch repair protein PMS2 |
| Q33996324 | Amplification of mutator cells in a population as a result of horizontal transfer |
| Q27305562 | An Efficient Site-Specific Method for Irreversible Covalent Labeling of Proteins with a Fluorophore |
| Q41822528 | An MSH4 homolog, stpp1, from Pleurotus pulmonarius is a "silver bullet" for resolving problems caused by spores in cultivated mushrooms |
| Q35036658 | An inducible, isogenic cancer cell line system for targeting the state of mismatch repair deficiency |
| Q36287727 | An unusually low microsatellite mutation rate in Dictyostelium discoideum, an organism with unusually abundant microsatellites |
| Q37149138 | Analysis of microsatellite mutations in the mitochondrial DNA of Saccharomyces cerevisiae |
| Q38328409 | Analysis of the interaction between the Saccharomyces cerevisiae MSH2-MSH6 and MLH1-PMS1 complexes with DNA using a reversible DNA end-blocking system. |
| Q36309767 | Aspirin suppresses the mutator phenotype associated with hereditary nonpolyposis colorectal cancer by genetic selection |
| Q28302118 | Association of BRCA1 with Rad51 in mitotic and meiotic cells |
| Q40177980 | Bcl2 impedes DNA mismatch repair by directly regulating the hMSH2-hMSH6 heterodimeric complex |
| Q36213486 | Biallelic inactivation of hMLH1 by epigenetic gene silencing, a novel mechanism causing human MSI cancers. |
| Q37355137 | Binding of Ru(bpy)2(eilatin)2+ to matched and mismatched DNA. |
| Q34270970 | Biochemical basis for dominant mutations in the Saccharomyces cerevisiae MSH6 gene |
| Q38320783 | Biochemical characterization of the interaction between the Saccharomyces cerevisiae MSH2-MSH6 complex and mispaired bases in DNA. |
| Q41005472 | Characterization of distinct human endometrial carcinoma cell lines deficient in mismatch repair that originated from a single tumor |
| Q46691965 | Checkpoint-dependent activation of mutagenic repair in Saccharomyces cerevisiae pol3-01 mutants |
| Q28506066 | Chromosomal influence on meiotic spindle assembly: abnormal meiosis I in female Mlh1 mutant mice |
| Q46348708 | Chromosomal rearrangements occur in S. cerevisiae rfa1 mutator mutants due to mutagenic lesions processed by double-strand-break repair |
| Q41702067 | Cisplatin resistance and DNA repair |
| Q24312177 | Cloning and expression analysis of a meiosis-specific MutS homolog: the human MSH4 gene |
| Q77731191 | Cloning of the PpMSH-2 cDNA of Physcomitrella patens, a moss in which gene targeting by homologous recombination occurs at high frequency |
| Q58377015 | Comparative Genomics of Hemiascomycete Yeasts: Genes Involved in DNA Replication, Repair, and Recombination |
| Q24650948 | Comparative genomics and molecular dynamics of DNA repeats in eukaryotes |
| Q74801797 | Complementation of mismatch repair gene defects by chromosome transfer |
| Q27629464 | Composite active site of an ABC ATPase: MutS uses ATP to verify mismatch recognition and authorize DNA repair |
| Q28367679 | Conformations of an adenine bulge in a DNA octamer and its influence on DNA structure from molecular dynamics simulations |
| Q57451645 | Correction of large mispaired DNA loops by extracts of Saccharomyces cerevisiae |
| Q27766073 | Crystal structure and ATPase activity of MutL: implications for DNA repair and mutagenesis |
| Q40893852 | Cytotoxicity and mutagenicity of frameshift-inducing agent ICR191 in mismatch repair-deficient colon cancer cells |
| Q37369501 | DNA base mismatch detection with bulky rhodium intercalators: synthesis and applications |
| Q73054412 | DNA binding and protein-protein interaction sites in MutS, a mismatched DNA recognition protein from Thermus thermophilus HB8 |
| Q43664681 | DNA chain length dependence of formation and dynamics of hMutSalpha.hMutLalpha.heteroduplex complexes |
| Q37256043 | DNA conformations in mismatch repair probed in solution by X-ray scattering from gold nanocrystals. |
| Q54527053 | DNA loop repair by Escherichia coli cell extracts. |
| Q33772428 | DNA mismatch repair catalyzed by extracts of mitotic, postmitotic, and senescent Drosophila tissues and involvement of mei-9 gene function for full activity |
| Q34568596 | DNA mismatch repair defects: role in colorectal carcinogenesis |
| Q33947053 | DNA mismatch repair genes and colorectal cancer |
| Q89558876 | DNA mismatch repair in the context of chromatin |
| Q24313002 | DNA polymerase delta is required for human mismatch repair in vitro |
| Q43608425 | DNA repair excision nuclease attacks undamaged DNA. A potential source of spontaneous mutations |
| Q46002898 | DNA replication and postreplication mismatch repair in cell-free extracts from cultured human neuroblastoma and fibroblast cells. |
| Q38331192 | DNA-dependent activation of the hMutSalpha ATPase |
| Q39745939 | Decreased Expression of the DNA Mismatch Repair Gene Mlh1 under Hypoxic Stress in Mammalian Cells |
| Q33888905 | Deficiency of a novel mismatch repair activity in a bladder tumor cell line |
| Q74456713 | Deletion mutation analysis of the mutS gene in Escherichia coli |
| Q28513002 | Deletion of genes implicated in protecting the integrity of male germ cells has differential effects on the incidence of DNA breaks and germ cell loss |
| Q54108643 | Dependence on RAD52 and RAD1 for anticancer drug resistance mediated by inactivation of mismatch repair genes. |
| Q34700427 | Detection of DNA base mismatches using DNA intercalators |
| Q28592891 | Different mutator phenotypes in Mlh1- versus Pms2-deficient mice |
| Q31039347 | Differential expression of the mismatch repair gene hMSH2 in malignant prostate tissue is associated with cancer recurrence |
| Q24337694 | Differential specificities and simultaneous occupancy of human MutSalpha nucleotide binding sites |
| Q28362113 | Direct estimate of the mutation rate and the distribution of fitness effects in the yeast Saccharomyces cerevisiae |
| Q78037753 | Dissociation of mismatch recognition and ATPase activity by hMSH2-hMSH3 |
| Q43675423 | Distinct MutS DNA-binding modes that are differentially modulated by ATP binding and hydrolysis |
| Q40895728 | Distinct regulation of Mlh1p heterodimers in meiosis and mitosis in Saccharomyces cerevisiae. |
| Q38289639 | Dominant Saccharomyces cerevisiae msh6 mutations cause increased mispair binding and decreased dissociation from mispairs by Msh2-Msh6 in the presence of ATP. |
| Q27938305 | Dpb2p, a noncatalytic subunit of DNA polymerase epsilon, contributes to the fidelity of DNA replication in Saccharomyces cerevisiae |
| Q36574453 | Dual roles for DNA sequence identity and the mismatch repair system in the regulation of mitotic crossing-over in yeast |
| Q45855513 | Effective oligonucleotide-mediated gene disruption in ES cells lacking the mismatch repair protein MSH3. |
| Q33948391 | Efficient repair of large DNA loops in Saccharomyces cerevisiae |
| Q22248073 | Elevated levels of mutation in multiple tissues of mice deficient in the DNA mismatch repair gene Pms2 |
| Q28592464 | Elevated mutant frequencies and predominance of G:C to A:T transition mutations in Msh6(-/-) small intestinal epithelium |
| Q34615970 | Escherichia coli strains (ndk) lacking nucleoside diphosphate kinase are powerful mutators for base substitutions and frameshifts in mismatch-repair-deficient strains |
| Q27939116 | Eukaryotic DNA mismatch repair |
| Q77753605 | Eukaryotic mismatch repair: an update |
| Q32108861 | Evidence for a physical interaction between the Escherichia coli methyl-directed mismatch repair proteins MutL and UvrD. |
| Q35115265 | Evidence for short-patch mismatch repair in Saccharomyces cerevisiae |
| Q34609122 | Evidence that stationary-phase hypermutation in the Escherichia coli chromosome is promoted by recombination |
| Q39542069 | Evolutionary origin, diversification and specialization of eukaryotic MutS homolog mismatch repair proteins |
| Q28589828 | Examination of Msh6- and Msh3-deficient mice in class switching reveals overlapping and distinct roles of MutS homologues in antibody diversification |
| Q74610856 | Excision repair invades the territory of mismatch repair |
| Q38974172 | Exo1 independent DNA mismatch repair involves multiple compensatory nucleases |
| Q53448187 | Expression of hMLH1 and hMSH2 proteins in ameloblastomas and tooth germs. |
| Q47740312 | Expression of hMLH1 and hMSH2 proteins in pleomorphic adenoma of minor salivary glands: relationship with clinical and histologic findings. |
| Q74332220 | Expression of hMSH2 and hMLH1 proteins of the human DNA mismatch repair system in salivary gland tumors |
| Q24791214 | Expression of hMSH2 protein of the human DNA mismatch repair system in oral lichen planus |
| Q54559294 | Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC. |
| Q42808615 | Fibroblast growth factor-1 stimulation of quiescent NIH 3T3 cells increases G/T mismatch-binding protein expression |
| Q34710578 | Focus on colon cancer |
| Q36568343 | Frameshift intermediates in homopolymer runs are removed efficiently by yeast mismatch repair proteins |
| Q34615262 | Frequent germline mutations and somatic repeat instability in DNA mismatch-repair-deficient Caenorhabditis elegans |
| Q47713981 | Functional analysis of human MLH1 mutations in Saccharomyces cerevisiae |
| Q34693488 | Functional analysis of human MutSalpha and MutSbeta complexes in yeast |
| Q36570003 | Functional domains of the Saccharomyces cerevisiae Mlh1p and Pms1p DNA mismatch repair proteins and their relevance to human hereditary nonpolyposis colorectal cancer-associated mutations |
| Q34603929 | Functional overlap in mismatch repair by human MSH3 and MSH6. |
| Q33952944 | Functional significance of concomitant inactivation of hMLH1 and hMSH6 in tumor cells of the microsatellite mutator phenotype. |
| Q54070830 | GENETIC LOAD OF THE YEAST SACCHAROMYCES CEREVISIAE UNDER DIVERSE ENVIRONMENTAL CONDITIONS. |
| Q23919603 | Gene expression profile in BALB/c-3T3 cells transformed with beryllium sulfate |
| Q38307105 | Generation of a mouse mutant by oligonucleotide-mediated gene modification in ES cells. |
| Q33961252 | Genetic analysis of mouse embryonic stem cells bearing Msh3 and Msh2 single and compound mutations |
| Q41355776 | Genetic control of microsatellite stability |
| Q28131826 | Genetic instabilities in human cancers |
| Q22066214 | Genome sequence of the hyperthermophilic crenarchaeon Pyrobaculum aerophilum |
| Q33724516 | Genomic amplification of the human DHFR/MSH3 locus remodels mismatch recognition and repair activities |
| Q57978009 | Germline and somatic mutations in hMSH6 and hMSH3 in gastrointestinal cancers of the microsatellite mutator phenotype |
| Q40848863 | Growth control mechanisms in normal and transformed intestinal cells |
| Q52690553 | H3K36me3-mediated mismatch repair preferentially protects actively transcribed genes from mutation. |
| Q44068446 | HNPCC mutations in hMSH2 result in reduced hMSH2-hMSH6 molecular switch functions |
| Q28589491 | HNPCC-like cancer predisposition in mice through simultaneous loss of Msh3 and Msh6 mismatch-repair protein functions |
| Q34603478 | Heterogeneity of microsatellite mutations within and between loci, and implications for human demographic histories |
| Q33384939 | Heterozygosity increases microsatellite mutation rate, linking it to demographic history |
| Q74116757 | High frequency of microsatellite instability and loss of mismatch-repair protein expression in patients with double primary tumors of the endometrium and colorectum |
| Q39551436 | Homology search and choice of homologous partner during mitotic recombination |
| Q73270787 | Homozygous deletions and point mutations of the Ikaros gene in gamma-ray-induced mouse thymic lymphomas |
| Q24812717 | Human AP endonuclease suppresses DNA mismatch repair activity leading to microsatellite instability. |
| Q47766916 | Human DNA polymerase delta double-mutant D316A;E318A interferes with DNA mismatch repair in vitro |
| 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 |
| Q24292224 | Human exonuclease I is required for 5' and 3' mismatch repair |
| Q34506555 | Human genome comparison of paretic and nonparetic vastus lateralis muscle in patients with hemiparetic stroke |
| Q33770256 | Hypermutation in bacteria and other cellular systems |
| Q24314329 | Identification and characterization of Saccharomyces cerevisiae EXO1, a gene encoding an exonuclease that interacts with MSH2 |
| Q40762811 | Identification and functional characterization of the promoter region of the human MSH6 gene |
| Q33484232 | Identification of genes differentially expressed by calorie restriction in the rotifer (Brachionus plicatilis). |
| Q39895156 | Identification of genes that protect the C. elegans genome against mutations by genome-wide RNAi |
| Q35842477 | Identification of the meiotic toolkit in diatoms and exploration of meiosis-specific SPO11 and RAD51 homologs in the sexual species Pseudo-nitzschia multistriata and Seminavis robusta. |
| Q38322903 | Identification of the protein components of mismatch binding complexes in human cells using a gel-shift assay |
| Q33967139 | Inactivation of DNA mismatch repair by increased expression of yeast MLH1. |
| Q28182219 | Inactivation of Exonuclease 1 in mice results in DNA mismatch repair defects, increased cancer susceptibility, and male and female sterility |
| Q73186740 | Increased mRNA levels of xeroderma pigmentosum complementation group B (XPB) and Cockayne's syndrome complementation group B (CSB) without increased mRNA levels of multidrug-resistance gene (MDR1) or metallothionein-II (MT-II) in platinum-resistant |
| Q39455847 | Increased rates of genomic deletions generated by mutations in the yeast gene encoding DNA polymerase delta or by decreases in the cellular levels of DNA polymerase delta |
| Q43181792 | Induction and inhibition of ciprofloxacin resistance-conferring mutations in hypermutator bacteria |
| Q36617515 | Induction of JNK and c-Abl signalling by cisplatin and oxaliplatin in mismatch repair-proficient and -deficient cells |
| Q39093868 | Initiation of strand incision at G:T and O(6)-methylguanine:T base mismatches in DNA by human cell extracts |
| Q54565774 | Interaction of MutS protein with the major and minor grooves of a heteroduplex DNA. |
| Q22003969 | Interactions of human hMSH2 with hMSH3 and hMSH2 with hMSH6: examination of mutations found in hereditary nonpolyposis colorectal cancer |
| Q58074454 | Involvement of DNA mismatch repair in folate deficiency-induced apoptosis☆ |
| Q39675432 | Isolation and characterization of new proliferating cell nuclear antigen (POL30) mutator mutants that are defective in DNA mismatch repair |
| Q28610863 | Isolation of MutSbeta from human cells and comparison of the mismatch repair specificities of MutSbeta and MutSalpha |
| Q28505426 | Localization of MMR proteins on meiotic chromosomes in mice indicates distinct functions during prophase I |
| Q39452796 | Long palindromic sequences induce double-strand breaks during meiosis in yeast. |
| Q24535964 | MSH2 is essential for the preservation of genome integrity and prevents homeologous recombination in the moss Physcomitrella patens |
| Q28295022 | Mammalian MutS homologue 5 is required for chromosome pairing in meiosis |
| Q33775234 | Mapping the polarity of changes that occur in interrupted CAG repeat tracts in yeast |
| Q34157868 | Mbd4 inactivation increases Cright-arrowT transition mutations and promotes gastrointestinal tumor formation |
| Q36692800 | Measuring the rate of gross chromosomal rearrangements in Saccharomyces cerevisiae: A practical approach to study genomic rearrangements observed in cancer |
| Q24300483 | Mechanism of 5'-directed excision in human mismatch repair |
| Q28510650 | Meiotic pachytene arrest in MLH1-deficient mice |
| Q36996160 | Metallo-intercalators and metallo-insertors |
| Q44646174 | Microsatellite DNA assays reveal an allelic imbalance in p16(Ink4), GALT, p53, and APOA2 loci in patients with endometriosis. |
| Q73757902 | Microsatellite Instability and hMLH1 and hMSH2 expression analysis in familial and sporadic colorectal cancer |
| Q44201536 | Microsatellite instability and loss of heterozygosity of tumor suppressor genes in Bosnian patients with sporadic colorectal cancer |
| Q42112990 | Microsatellite instability and mismatch repair gene inactivation in sporadic pancreatic and colon tumours |
| Q40022200 | Microsatellite instability in yeast: dependence on repeat unit size and DNA mismatch repair genes |
| Q34057384 | Microsatellites: consensus and controversy |
| Q33885063 | Mismatch repair defects in cancer |
| Q36779731 | Mismatch repair deficiencies transforming stem cells into cancer stem cells and therapeutic implications |
| Q40711388 | Mismatch repair deficiency in hematological malignancies with microsatellite instability |
| Q53881837 | Mismatch repair ensures fidelity of replication and recombination in the radioresistant organism Deinococcus radiodurans. |
| Q35010942 | Mismatch repair genes (hMLH1, hPMS1, hPMS2, GTBP/hMSH6, hMSH2) in the pathogenesis of hepatocellular carcinoma |
| Q33724726 | Mismatch repair in Escherichia coli cells lacking single-strand exonucleases ExoI, ExoVII, and RecJ |
| Q33960642 | Mismatch repair processing of carcinogen-DNA adducts triggers apoptosis |
| Q35190848 | Mismatch repair protein MutL becomes limiting during stationary-phase mutation |
| Q38337751 | Mismatch-, MutS-, MutL-, and helicase II-dependent unwinding from the single-strand break of an incised heteroduplex |
| Q28588324 | Mlh1 deficiency enhances several phenotypes of Apc(Min)/+ mice |
| Q42797147 | Modulating the Light Switch by 3MLCT-3ππ* State Interconversion |
| Q33670210 | Molecular diagnostics of cancer predisposition: hereditary non-polyposis colorectal carcinoma and mismatch repair defects |
| Q41005399 | Molecular events after antisense inhibition of hMSH2 in a HeLa cell line |
| Q36192733 | Molecular testing for microsatellite instability and its value in tumor characterization |
| Q35433209 | Mononucleotide microsatellite instability and germline MSH6 mutation analysis in early onset colorectal cancer |
| Q35190411 | Mouse MutS-like protein Msh5 is required for proper chromosome synapsis in male and female meiosis |
| Q33739279 | Mouse models for colorectal cancer |
| Q28214396 | Mouse models for human DNA mismatch-repair gene defects |
| Q39844167 | Mph1 requires mismatch repair-independent and -dependent functions of MutSalpha to regulate crossover formation during homologous recombination repair |
| Q37413511 | Msh2-dependent DNA repair mitigates a unique susceptibility of B cell progenitors to c-Myc-induced lymphomas |
| Q28776215 | Multiple functions of MutS- and MutL-related heterocomplexes |
| Q24606421 | MutS homolog 4 localization to meiotic chromosomes is required for chromosome pairing during meiosis in male and female mice |
| Q38292725 | MutS recognition: multiple mismatches and sequence context effects |
| Q93357415 | MutSγ-Induced DNA Conformational Changes Provide Insights into Its Role in Meiotic Recombination |
| Q33758490 | Mutants with temperature-sensitive defects in the Escherichia coli mismatch repair system: sensitivity to mispairs generated in vivo |
| Q28592583 | Mutation in the mismatch repair gene Msh6 causes cancer susceptibility |
| Q24318892 | Mutation of MSH3 in endometrial cancer and evidence for its functional role in heteroduplex repair |
| Q40832127 | Mutation spectrum of MSH3-deficient HHUA/chr.2 cells reflects in vivo activity of the MSH3 gene product in mismatch repair |
| Q33885709 | Mutator effects in Escherichia coli caused by the expression of specific foreign genes |
| Q34833900 | Mutator genes for suppression of gross chromosomal rearrangements identified by a genome-wide screening in Saccharomyces cerevisiae |
| Q39610863 | Mutator phenotype induced by aberrant replication |
| Q33957827 | Mutator phenotypes conferred by MLH1 overexpression and by heterozygosity for mlh1 mutations. |
| Q77891937 | Notes from some crypt watchers: regulation of renewal in the mouse intestinal epithelium |
| Q28144364 | Nuclear translocation of mismatch repair proteins MSH2 and MSH6 as a response of cells to alkylating agents |
| Q36226849 | Nucleotide excision repair |
| Q30751633 | Oligomerization of a MutS mismatch repair protein from Thermus aquaticus |
| Q36139867 | Perspective on mutagenesis and repair: the standard model and alternate modes of mutagenesis |
| Q35590357 | Phosphorylation of PCNA by EGFR inhibits mismatch repair and promotes misincorporation during DNA synthesis |
| Q54558924 | Photocross-linking of the NH2-terminal region of Taq MutS protein to the major groove of a heteroduplex DNA. |
| Q36733353 | Physical interaction between components of DNA mismatch repair and nucleotide excision repair |
| Q36159638 | Positionally cloned human disease genes: patterns of evolutionary conservation and functional motifs |
| Q41736499 | Predicting functions from protein sequences--where are the bottlenecks? |
| Q38293314 | Proficient mismatch repair protein expression in Hodgkin and Reed Sternberg cells |
| Q42911480 | Proteomic Analysis Reveals a Novel Mutator S (MutS) Partner Involved in Mismatch Repair Pathway. |
| Q42932258 | Pseudomonas aeruginosa MutL protein functions in Escherichia coli |
| Q28506888 | RAB22 and RAB163/mouse BRCA2: proteins that specifically interact with the RAD51 protein |
| Q73404201 | REV3 is required for spontaneous but not methylation damage-induced mutagenesis of Saccharomyces cerevisiae cells lacking O6-methylguanine DNA methyltransferase |
| Q42243402 | Rad52 function prevents chromosome loss and truncation in Candida albicans. |
| Q34646656 | Recent advances in cancer research: mouse models of tumorigenesis |
| Q36565271 | Recognition and repair of compound DNA lesions (base damage and mismatch) by human mismatch repair and excision repair systems |
| Q41886077 | Recognition of DNA alterations by the mismatch repair system |
| Q38005951 | Recognition of damaged DNA: structure and dynamic markers |
| Q48018607 | Recombination at work for meiosis |
| Q33886585 | Recombinational repair in yeast: functional interactions between Rad51 and Rad54 proteins. |
| Q36540486 | Regulation of mismatch repair by histone code and posttranslational modifications in eukaryotic cells |
| Q34608647 | Regulation of mitotic homeologous recombination in yeast. Functions of mismatch repair and nucleotide excision repair genes |
| Q33865368 | Removal of frameshift intermediates by mismatch repair proteins in Saccharomyces cerevisiae |
| Q52929756 | Repair bias of large loop mismatches during recombination in mammalian cells depends on loop length and structure. |
| Q40969083 | Repair of large insertion/deletion heterologies in human nuclear extracts is directed by a 5' single-strand break and is independent of the mismatch repair system |
| Q34397387 | Replication error deficient and proficient colorectal cancer gene expression differences caused by 3'UTR polyT sequence deletions |
| Q42660015 | Replication errors: cha(lle)nging the genome |
| Q27939891 | Requirement for PCNA in DNA mismatch repair at a step preceding DNA resynthesis |
| Q45962588 | Rhodium metalloinsertor binding generates a lesion with selective cytotoxicity for mismatch repair-deficient cells. |
| Q46657284 | S-phase checkpoint controls mitosis via an APC-independent Cdc20p function |
| Q27932017 | Saccharomyces cerevisiae Msh2p and Msh6p ATPase activities are both required during mismatch repair |
| Q35143822 | Saccharomyces cerevisiae chromatin-assembly factors that act during DNA replication function in the maintenance of genome stability. |
| Q39449001 | Saccharomyces cerevisiae pol30 (proliferating cell nuclear antigen) mutations impair replication fidelity and mismatch repair |
| Q41627210 | Selective tumor cell death induced by irradiated riboflavin through recognizing DNA G-T mismatch |
| Q27938377 | Separation-of-function mutations in Saccharomyces cerevisiae MSH2 that confer mismatch repair defects but do not affect nonhomologous-tail removal during recombination |
| Q37132714 | Sequence context effect for hMSH2-hMSH6 mismatch-dependent activation |
| Q28585021 | Severe attenuation of the B cell immune response in Msh2-deficient mice |
| Q33754438 | Short-patch correction of C/C mismatches in human cells |
| Q40412801 | Somatic hypermutation and mismatch repair in non-B cells |
| Q33545735 | Somatic hypermutation and the three R's: repair, replication and recombination |
| Q28510640 | Somatic hypermutation in MutS homologue (MSH)3-, MSH6-, and MSH3/MSH6-deficient mice reveals a role for the MSH2-MSH6 heterodimer in modulating the base substitution pattern |
| Q34516540 | Somatic hypermutation in human B cell subsets |
| Q34619789 | Somatic hypermutation of immunoglobulin genes: merging mechanisms for genetic diversity |
| Q77198198 | Somatic hypermutation, transcription, and DNA mismatch repair |
| Q40878184 | Somatic mutation of hPMS2 as a possible cause of sporadic human colon cancer with microsatellite instability |
| Q33735536 | Specific-Locus Amplified Fragment Sequencing Reveals Spontaneous Single-Nucleotide Mutations in Rice OsMsh6 Mutants |
| Q77413342 | Stability of microsatellites in myeloid neoplasias |
| Q33958980 | Stability of the human fragile X (CGG)(n) triplet repeat array in Saccharomyces cerevisiae deficient in aspects of DNA metabolism |
| Q24681264 | Statistical significance for genomewide studies |
| Q57784305 | Stochastic Processes and Component Plasticity Governing DNA Mismatch Repair |
| Q41602506 | Strand-specific mismatch repair in mammalian cells |
| Q33888460 | Structural basis for MutH activation in E.coli mismatch repair and relationship of MutH to restriction endonucleases |
| Q28285134 | Structural, molecular and cellular functions of MSH2 and MSH6 during DNA mismatch repair, damage signaling and other noncanonical activities |
| Q28143945 | Structure and function of mismatch repair proteins |
| Q27635053 | Structure and function of the N-terminal 40 kDa fragment of human PMS2: a monomeric GHL ATPase |
| Q34048739 | Suppression of genome instability by redundant S-phase checkpoint pathways in Saccharomyces cerevisiae |
| Q36082840 | Suppression of gross chromosomal rearrangements by a new alternative replication factor C complex |
| Q46200700 | Suppression of spontaneous chromosomal rearrangements by S phase checkpoint functions in Saccharomyces cerevisiae |
| Q53049781 | The Arabidopsis DNA mismatch repair gene PMS1 restricts somatic recombination between homeologous sequences. |
| Q44607202 | The Arabidopsis MutS homolog AtMSH5 is required for normal meiosis |
| Q35732828 | The CREB Coactivator CRTC2 Is a Lymphoma Tumor Suppressor that Preserves Genome Integrity through Transcription of DNA Mismatch Repair Genes |
| Q36889776 | The DNA damage-recognition problem in human and other eukaryotic cells: the XPA damage binding protein |
| Q36026779 | The N terminus of Saccharomyces cerevisiae Msh6 is an unstructured tether to PCNA |
| Q27935158 | The Saccharomyces cerevisiae MLH3 gene functions in MSH3-dependent suppression of frameshift mutations |
| Q37355959 | The Saccharomyces cerevisiae Rad6 postreplication repair and Siz1/Srs2 homologous recombination-inhibiting pathways process DNA damage that arises in asf1 mutants |
| Q35100583 | The UvrD helicase and its modulation by the mismatch repair protein MutL. |
| Q52569390 | The beta sliding clamp binds to multiple sites within MutL and MutS. |
| Q44530427 | The coordinated functions of the E. coli MutS and MutL proteins in mismatch repair |
| Q42858522 | The effect of different chemotherapeutic agents on the enrichment of DNA mismatch repair-deficient tumour cells |
| Q24321288 | 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 |
| Q48010364 | The high mobility group domain protein Cmb1 of Schizosaccharomyces pombe binds to cytosines in base mismatches and opposite chemically altered guanines |
| Q24339204 | The histone mark H3K36me3 regulates human DNA mismatch repair through its interaction with MutSα |
| Q24596494 | The interacting domains of three MutL heterodimers in man: hMLH1 interacts with 36 homologous amino acid residues within hMLH3, hPMS1 and hPMS2 |
| Q28137782 | The interaction of the human MutL homologues in hereditary nonpolyposis colon cancer |
| Q28512554 | The mammalian mismatch repair protein MSH2 is required for correct MRE11 and RAD51 relocalization and for efficient cell cycle arrest induced by ionizing radiation in G2 phase |
| Q33984289 | The many faces of mismatch repair in meiosis |
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