| scholarly article | Q13442814 |
| review article | Q7318358 |
| P2093 | author name string | R D Kolodner | |
| P2860 | cites work | Mutations of two PMS homologues in hereditary nonpolyposis colon cancer | Q24318484 |
| Mutation of a mutL homolog in hereditary colon cancer | Q28114939 | ||
| Binding of mismatched microsatellite DNA sequences by the human MSH2 protein | Q28241673 | ||
| The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer | Q28256988 | ||
| Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer | Q28257360 | ||
| Identification of mismatch repair genes and their role in the development of cancer | Q28288647 | ||
| Isolation of an hMSH2-p160 Heterodimer That Restores DNA Mismatch Repair to Tumor Cells | Q28292781 | ||
| GTBP, a 160-kilodalton protein essential for mismatch-binding activity in human cells | Q28292790 | ||
| Mutations of GTBP in genetically unstable cells | Q28292802 | ||
| Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer | Q28294774 | ||
| Structure of the human MSH2 locus and analysis of two Muir-Torre kindreds for msh2 mutations | Q28299699 | ||
| DNA mismatch correction in a defined system | Q34674714 | ||
| Cloning and nucleotide sequence of DNA mismatch repair gene PMS1 from Saccharomyces cerevisiae: homology of PMS1 to procaryotic MutL and HexB. | Q36182527 | ||
| Mechanisms and biological effects of mismatch repair | Q37041860 | ||
| Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis | Q38293261 | ||
| The Saccharomyces cerevisiae Msh2 protein specifically binds to duplex oligonucleotides containing mismatched DNA base pairs and insertions | Q38299752 | ||
| Mismatch repair and cancer susceptibility | Q40535755 | ||
| Mismatch repair, genetic stability, and cancer | Q40556409 | ||
| Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: an updated review | Q40901949 | ||
| Mismatch Repair Deficiency in Phenotypically Normal Human Cells | Q41347026 | ||
| The role of heteroduplex correction in gene conversion in Saccharomyces cerevisiae | Q41430030 | ||
| Hypermutability and mismatch repair deficiency in RER+ tumor cells | Q41508298 | ||
| MLH1, PMS1, and MSH2 interactions during the initiation of DNA mismatch repair in yeast | Q42427955 | ||
| A repair system for 8-oxo-7,8-dihydrodeoxyguanine | Q43687308 | ||
| Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer | Q48084125 | ||
| The barrier to recombination between Escherichia coli and Salmonella typhimurium is disrupted in mismatch-repair mutants | Q50192890 | ||
| Mismatch repair of deaminated 5-methyl-cytosine. | Q54766647 | ||
| Loss of the wild type MLH1 gene is a feature of hereditary nonpolyposis colorectal cancer | Q57568035 | ||
| The vsr gene product of E. coli K-12 is a strand- and sequence-specific DNA mismatch endonuclease | Q59087847 | ||
| Different base/base mismatches are corrected with different efficiencies by the methyl-directed DNA mismatch-repair system of E. coli | Q70387562 | ||
| Mismatch repair gene defects in sporadic colorectal cancers with microsatellite instability | Q72127255 | ||
| P433 | issue | 10 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | DNA mismatch repair | Q2984243 |
| P1104 | number of pages | 5 | |
| P304 | page(s) | 397-401 | |
| P577 | publication date | 1995-10-01 | |
| P1433 | published in | Trends in Biochemical Sciences | Q1565711 |
| P1476 | title | Mismatch repair: mechanisms and relationship to cancer susceptibility | |
| P478 | volume | 20 |
| Q39446122 | A Uve1p-mediated mismatch repair pathway in Schizosaccharomyces pombe |
| Q47736618 | A novel missense mutation and frameshift mutations in the type II receptor of transforming growth factor-beta gene in sporadic colon cancer with microsatellite instability |
| Q64389285 | A novel mutation avoidance mechanism dependent on S. cerevisiae RAD27 is distinct from DNA mismatch repair |
| Q41031881 | A novel plasmid shuttle vector for the detection and analysis of microsatellite instability in cell lines |
| Q24548238 | A phylogenomic study of the MutS family of proteins |
| Q77758189 | A polymorphism in the hMSH2 gene (gIVS12-6T>C) associated with non-Hodgkin lymphomas |
| Q36292102 | Absence of stimulation of poly(ADP-ribose) polymerase activity in patients predisposed to colon cancer |
| Q28359649 | Affinity of mismatch-binding protein MutS for heteroduplexes containing different mismatches |
| Q36366579 | Apopain/CPP32 cleaves proteins that are essential for cellular repair: a fundamental principle of apoptotic death |
| Q30981239 | Apoptosis and mutation in the murine small intestine: loss of Mlh1- and Pms2-dependent apoptosis leads to increased mutation in vivo |
| Q37387617 | Application of metal coordination chemistry to explore and manipulate cell biology |
| Q37425820 | Aspirin, salicylates, and cancer. |
| Q42073570 | Association between the hMSH2 IVS12-6 T>C polymorphism and cancer risk: A meta-analysis |
| Q37355137 | Binding of Ru(bpy)2(eilatin)2+ to matched and mismatched DNA. |
| Q33828325 | Break-induced replication is highly inaccurate |
| Q35838174 | Catalysis of DNA cleavage and nucleoside triphosphate synthesis by NM23-H2/NDP kinase share an active site that implies a DNA repair function |
| Q37511752 | Cause and consequences of genetic and epigenetic alterations in human cancer. |
| Q41650547 | Cell-cycle regulation of mammalian DNA double-strand-break repair |
| Q22009979 | Characterization of MAD2B and other mitotic spindle checkpoint genes |
| Q37386808 | Characterization of mutant MUTYH proteins associated with familial colorectal cancer. |
| Q24317398 | Cloning and characterization of hOGG1, a human homolog of the OGG1 gene of Saccharomyces cerevisiae |
| Q33652932 | Colorectal cancer: molecules and populations |
| Q28367679 | Conformations of an adenine bulge in a DNA octamer and its influence on DNA structure from molecular dynamics simulations |
| Q35620922 | Correction of the UDP-glucuronosyltransferase gene defect in the gunn rat model of crigler-najjar syndrome type I with a chimeric oligonucleotide |
| Q24315065 | Crystal structure of a G:T/U mismatch-specific DNA glycosylase: mismatch recognition by complementary-strand interactions |
| Q37369501 | DNA base mismatch detection with bulky rhodium intercalators: synthesis and applications |
| Q35612552 | DNA binding and unwinding by self-assembled supramolecular hetero-bimetallacycles. |
| Q40765943 | DNA damage invokes mismatch repair-dependent cyclin D1 attenuation and retinoblastoma signaling pathways to inhibit CDK2. |
| Q41532551 | DNA glycosylases in the base excision repair of DNA |
| Q40513970 | DNA methyltransferase Dnmt1 and mismatch repair |
| Q35132526 | DNA mismatch repair: from structure to mechanism. |
| Q33809017 | DNA repair gene status in oesophageal cancer |
| Q73070797 | DNA-repair enzymes |
| Q35665027 | Deconstructing host-pathogen interactions in Drosophila |
| Q39841075 | Depletion of the cellular amounts of the MutS and MutH methyl-directed mismatch repair proteins in stationary-phase Escherichia coli K-12 cells |
| Q33786528 | Destabilization of yeast micro- and minisatellite DNA sequences by mutations affecting a nuclease involved in Okazaki fragment processing (rad27) and DNA polymerase delta (pol3-t). |
| Q34700427 | Detection of DNA base mismatches using DNA intercalators |
| Q43690857 | Dietary intake and microsatellite instability in colon tumors |
| Q28592891 | Different mutator phenotypes in Mlh1- versus Pms2-deficient mice |
| Q78037753 | Dissociation of mismatch recognition and ATPase activity by hMSH2-hMSH3 |
| Q27679146 | Distinct Structural Alterations in Proliferating Cell Nuclear Antigen Block DNA Mismatch Repair |
| Q62473026 | Distribution and kainate-mediated induction of the DNA mismatch repair protein MSH2 in rat brain |
| Q39716760 | Dominant negative mutator mutations in the mutL gene of Escherichia coli |
| Q37323498 | Drug resistance and DNA repair in leukaemia |
| Q35246382 | Dynamical allosterism in the mechanism of action of DNA mismatch repair protein MutS. |
| Q77768555 | EMS and UV-light-induced colony sectoring and delayed mutation in Chinese hamster cells |
| Q41883353 | Early alteration of cell-cycle-regulated gene expression in colorectal neoplasia |
| Q28591510 | Efficient repair of A/C mismatches in mouse cells deficient in long-patch mismatch repair |
| Q28592033 | Elevated mutant frequencies and increased C : G-->T : A transitions in Mlh1-/- versus Pms2-/- murine small intestinal epithelial cells |
| Q37346201 | Epigenetics and dermatological disease |
| Q77753605 | Eukaryotic mismatch repair: an update |
| Q53427542 | Evidence for a role of delayed death and genomic instability in radiation-induced neoplastic transformation of human hybrid cells. |
| Q39399379 | Evolutionary dynamics and significance of multiple subclonal mutations in cancer |
| Q38974172 | Exo1 independent DNA mismatch repair involves multiple compensatory nucleases |
| Q35559704 | Folate deficiency, mismatch repair-dependent apoptosis, and human disease |
| Q46898106 | Frameshift mutations at mononucleotide repeats in RAD50 recombinational DNA repair gene in colorectal cancers with microsatellite instability |
| Q57978049 | Frequent alterations in gene expression in colon tumor cells of the microsatellite mutator phenotype |
| Q77466413 | Genetic abnormalities in non-Hodgkin's lymphomas and chronic lymphocytic leukaemia |
| Q27932001 | Genetic and biochemical analysis of Msh2p-Msh6p: role of ATP hydrolysis and Msh2p-Msh6p subunit interactions in mismatch base pair recognition. |
| Q58074449 | Genetic and epigenetic modification of mismatch repair genes hMSH2 and hMLH1 in sporadic breast cancer with microsatellite instability |
| Q53400095 | Genetic polymorphisms in DNA repair genes and risk of lung cancer. |
| Q24546080 | Genome-wide prediction of G4 DNA as regulatory motifs: role in Escherichia coli global regulation |
| Q36115550 | Genomic loci susceptible to replication errors in cancer cells |
| Q43869182 | Germ cells microsatellite instability. The effect of different mutagens in a mismatch repair mutant of Drosophila (spel1). |
| Q52551102 | Germline mutations at microsatellite loci in homozygous and heterozygous mutants for mismatch repair and PCNA genes in Drosophila. |
| Q34301290 | HDAC6 deacetylates and ubiquitinates MSH2 to maintain proper levels of MutSα. |
| Q56928447 | Hereditary breast cancer |
| Q57247926 | Heterozygosity for p53 promotes microsatellite instability and tumorigenesis on a Msh2 deficient background |
| Q40974722 | Human Cancers Express a Mutator Phenotype: Hypothesis, Origin, and Consequences |
| Q39913958 | Human MutL-complexes monitor homologous recombination independently of mismatch repair |
| Q58074493 | Human MutSα Specifically Binds to DNA Containing Aminofluorene and Acetylaminofluorene Adducts |
| Q36085322 | Human cytomagalovirus IE1 and IE2 proteins are mutagenic and mediate "hit-and-run" oncogenic transformation in cooperation with the adenovirus E1A proteins |
| Q22009967 | Human exonuclease 1 functionally complements its yeast homologues in DNA recombination, RNA primer removal, and mutation avoidance |
| Q24314329 | Identification and characterization of Saccharomyces cerevisiae EXO1, a gene encoding an exonuclease that interacts with MSH2 |
| Q36622540 | Immunohistochemical analysis of expression and allelotype of mismatch repair genes (hMLH1 and hMSH2) in bladder cancer |
| Q33866403 | Immunohistochemical expression of mismatch repair genes: a screening tool for predicting mutator phenotype in liver fluke infection-associated intrahepatic cholangiocarcinoma |
| Q40303796 | Impairment of double-strand breaks repair and aberrant splicing of ATM and MRE11 in leukemia-lymphoma cell lines with microsatellite instability |
| Q74310269 | In vivo site-directed mutagenesis of the factor IX gene by chimeric RNA/DNA oligonucleotides |
| Q33193273 | Infrequent microsatellite instability in liver fluke infection‐associated intrahepatic cholangiocarcinomas from Thailand |
| Q37797701 | Inheritance of Epigenetic Aberrations (Constitutional Epimutations) in Cancer Susceptibility |
| Q41023029 | Intracellular transcription of G-rich DNAs induces formation of G-loops, novel structures containing G4 DNA |
| Q47761945 | Kinetics of the action of thymine DNA glycosylase |
| Q36617626 | Loss of DNA mismatch repair facilitates reactivation of a reporter plasmid damaged by cisplatin |
| Q48065235 | MSH6, a Saccharomyces cerevisiae protein that binds to mismatches as a heterodimer with MSH2. |
| Q35152335 | Meiotic recombination hotspots: shaping the genome and insights into hypervariable minisatellite DNA change |
| Q46445542 | Methods for studying mutagenesis and checkpoints in Schizosaccharomyces pombe |
| Q37144872 | Microsatellite instability induced mutations in DNA repair genes CtIP and MRE11 confer hypersensitivity to poly (ADP-ribose) polymerase inhibitors in myeloid malignancies |
| Q54053592 | Microsatellite instability is associated with genetic alteration but not with low levels of expression of the human mismatch repair proteins hMSH2 and hMLH1. |
| Q39715504 | Mismatch DNA recognition protein from an extremely thermophilic bacterium, Thermus thermophilus HB8 |
| Q33305049 | Mismatch Repair proteins are recruited to replicating DNA through interaction with Proliferating Cell Nuclear Antigen (PCNA) |
| Q33970960 | Mismatch repair by efficient nick-directed, and less efficient mismatch-specific, mechanisms in homologous recombination intermediates in Chinese hamster ovary cells. |
| Q33967893 | Mismatch repair mutants in yeast are not defective in transcription-coupled DNA repair of UV-induced DNA damage. |
| Q28219035 | Mismatch repair polymorphisms and colorectal polyps: hMLH1-93G>A variant modifies risk associated with smoking |
| Q30569509 | Mismatch repair protein hMSH2-hMSH6 recognizes mismatches and forms sliding clamps within a D-loop recombination intermediate |
| Q42797147 | Modulating the Light Switch by 3MLCT-3ππ* State Interconversion |
| Q41686589 | Molecular biology of colorectal cancer |
| Q41005399 | Molecular events after antisense inhibition of hMSH2 in a HeLa cell line |
| Q36325598 | Mouse embryonic stem cells carrying one or two defective Msh2 alleles respond abnormally to oxidative stress inflicted by low-level radiation |
| Q35171602 | Multiple biochemical activities of NM23/NDP kinase in gene regulation |
| Q24320018 | Mutations of mitotic checkpoint genes in human cancers |
| Q35633546 | Negative regulation of mutS and mutH repair gene expression by the Hfq and RpoS global regulators of Escherichia coli K-12. |
| Q33888666 | Overexpression of enzymes that repair endogenous damage to DNA. |
| Q45786391 | Polymorphisms of DNA repair gene XRCC1 and hepatocellular carcinoma risk among East Asians: a meta-analysis |
| Q33959136 | Polymorphisms of the human UDP-glucuronosyltransferase (UGT) 1A7 gene in colorectal cancer |
| Q71824297 | Processing of O6-methylguanine by mismatch correction in human cell extracts |
| Q28534843 | Reassembly of nucleosomes at the MLH1 promoter initiates resilencing following decitabine exposure |
| Q34589559 | Recognition of DNA insertion/deletion mismatches by an activity in Saccharomyces cerevisiae |
| Q37354456 | Recognition of abasic sites and single base bulges in DNA by a metalloinsertor |
| Q42660015 | Replication errors: cha(lle)nging the genome |
| Q35135405 | Risk of childhood leukemia associated with diagnostic irradiation and polymorphisms in DNA repair genes |
| Q41099585 | Saccharomyces cerevisiae DNA repair processes: an update |
| Q28586442 | Separation of killing and tumorigenic effects of an alkylating agent in mice defective in two of the DNA repair genes |
| Q36148736 | Sequence-Dependent T:G Base Pair Opening in DNA Double Helix Bound by Cren7, a Chromatin Protein Conserved among Crenarchaea |
| Q48983129 | Single cell tracking reveals that Msh2 is a key component of an early-acting DNA damage-activated G2 checkpoint |
| Q53445992 | Somatic frameshift mutations in the BAX gene in colon cancers of the microsatellite mutator phenotype. |
| Q39575932 | Specific mismatch recognition in heteroduplex intermediates by p53 suggests a role in fidelity control of homologous recombination |
| Q62571320 | Specificity of platinum–DNA adduct repair |
| Q50135105 | Structural and mechanistic bases for the induction of mitotic chromosomal loss and duplication ('malsegregation') in the yeast Saccharomyces cerevisiae: relevance to human carcinogenesis and developmental toxicology |
| Q28143945 | Structure and function of mismatch repair proteins |
| Q27667527 | Structures of Human Exonuclease 1 DNA Complexes Suggest a Unified Mechanism for Nuclease Family |
| Q31136996 | Targeting DNA Mismatches with Rhodium Metalloinsertors |
| Q37711787 | The MLH1 c.-27C>A and c.85G>T variants are linked to dominantly inherited MLH1 epimutation and are borne on a European ancestral haplotype |
| Q27933376 | The Saccharomyces cerevisiae IMP2 gene encodes a transcriptional activator that mediates protection against DNA damage caused by bleomycin and other oxidants |
| Q27930815 | The Saccharomyces cerevisiae Msh2 and Msh6 proteins form a complex that specifically binds to duplex oligonucleotides containing mismatched DNA base pairs |
| Q35746647 | The hMLH1 -93G>A Polymorphism and Risk of Ovarian Cancer in the Chinese Population |
| Q24316950 | The hMre11/hRad50 protein complex and Nijmegen breakage syndrome: linkage of double-strand break repair to the cellular DNA damage response |
| Q48010364 | The high mobility group domain protein Cmb1 of Schizosaccharomyces pombe binds to cytosines in base mismatches and opposite chemically altered guanines |
| Q33594907 | The mammalian Mre11-Rad50-nbs1 protein complex: integration of functions in the cellular DNA-damage response |
| Q41064501 | The mismatch repair system contributes to meiotic sterility in an interspecific yeast hybrid. |
| Q41438677 | The natural somatic mutation frequency and human carcinogenesis. |
| Q74599515 | The promise of cancer genetics |
| Q30666045 | The role of nucleotide excision repair and loss of p53 in mutagenesis and carcinogenesis |
| Q40176435 | The structural impact of DNA mismatches |
| Q33892826 | Thymine-DNA glycosylase and G to A transition mutations at CpG sites |
| Q35795316 | Tissues of MSH2-deficient mice demonstrate hypermutability on exposure to a DNA methylating agent. |
| Q34640431 | Transcription and DNA damage: a link to a kink |
| Q35071100 | UV radiation induces delayed hyperrecombination associated with hypermutation in human cells. |
| Q36898271 | Ubiquitin-specific Peptidase 10 (USP10) Deubiquitinates and Stabilizes MutS Homolog 2 (MSH2) to Regulate Cellular Sensitivity to DNA Damage |
| Q31948126 | Use of DNA repair-deficient XPA transgenic mice in short-term carcinogenicity testing |
| Q50160917 | Variation in DNA repair is a factor in cancer susceptibility: a paradigm for the promises and perils of individual and population risk estimation? |
| Q39718210 | XRCC1 polypeptide interacts with DNA polymerase beta and possibly poly (ADP-ribose) polymerase, and DNA ligase III is a novel molecular 'nick-sensor' in vitro |
| Q24602221 | hMSH3 and hMSH6 interact with PCNA and colocalize with it to replication foci |
| Q28610839 | hMutSbeta, a heterodimer of hMSH2 and hMSH3, binds to insertion/deletion loops in DNA |
| Q40855467 | p53 and c-Jun functionally synergize in the regulation of the DNA repair gene hMSH2 in response to UV. |
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