| scholarly article | Q13442814 |
| review article | Q7318358 |
| P356 | DOI | 10.1002/JCP.1067 |
| P8608 | Fatcat ID | release_tdwu6i2jv5emxejuvtoct2o2ku |
| P698 | PubMed publication ID | 11267994 |
| P5875 | ResearchGate publication ID | 12065069 |
| P2093 | author name string | Aquilina G | |
| Bignami M | |||
| P2860 | cites work | The tyrosine kinase c-Abl regulates p73 in apoptotic response to cisplatin-induced DNA damage | Q22010200 |
| MLH3: a DNA mismatch repair gene associated with mammalian microsatellite instability | Q22010995 | ||
| Multiple mutations and frameshifts are the hallmark of defective hPMS2 in pZ189-transfected human tumor cells | Q22254326 | ||
| 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 | ||
| Mutation of MSH3 in endometrial cancer and evidence for its functional role in heteroduplex repair | Q24318892 | ||
| Mismatch repair deficiency associated with overexpression of the MSH3 gene | Q24681589 | ||
| Transformation of MutL by ATP binding and hydrolysis: a switch in DNA mismatch repair | Q27617873 | ||
| Functional studies on the candidate ATPase domains of Saccharomyces cerevisiae MutLalpha. | Q27929951 | ||
| Enhancement of MSH2-MSH3-mediated mismatch recognition by the yeast MLH1-PMS1 complex | Q27932428 | ||
| Discrete in vivo roles for the MutL homologs Mlh2p and Mlh3p in the removal of frameshift intermediates in budding yeast | Q27934236 | ||
| Efficient and accurate replication in the presence of 7,8-dihydro-8-oxoguanine by DNA polymerase eta. | Q27934276 | ||
| Binding of insertion/deletion DNA mismatches by the heterodimer of yeast mismatch repair proteins MSH2 and MSH3. | Q27934985 | ||
| The Saccharomyces cerevisiae MLH3 gene functions in MSH3-dependent suppression of frameshift mutations | Q27935158 | ||
| Eukaryotic DNA mismatch repair | Q27939116 | ||
| Functional specificity of MutL homologs in yeast: evidence for three Mlh1-based heterocomplexes with distinct roles during meiosis in recombination and mismatch correction | Q27939611 | ||
| Requirement for PCNA in DNA mismatch repair at a step preceding DNA resynthesis | Q27939891 | ||
| hMSH2-hMSH6 forms a hydrolysis-independent sliding clamp on mismatched DNA | Q28138775 | ||
| Nuclear translocation of mismatch repair proteins MSH2 and MSH6 as a response of cells to alkylating agents | Q28144364 | ||
| The human mismatch recognition complex hMSH2-hMSH6 functions as a novel molecular switch | Q28258968 | ||
| Transcription-coupled repair deficiency and mutations in human mismatch repair genes | Q28276963 | ||
| MLH1 promoter hypermethylation is associated with the microsatellite instability phenotype in sporadic endometrial carcinomas | Q28288475 | ||
| 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 | ||
| Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer | Q28294774 | ||
| Base transitions dominate the mutational spectrum of a transgenic reporter gene in MSH2 deficient mice | Q28509599 | ||
| Msh2 status modulates both apoptosis and mutation frequency in the murine small intestine | Q28585239 | ||
| HNPCC-like cancer predisposition in mice through simultaneous loss of Msh3 and Msh6 mismatch-repair protein functions | Q28589491 | ||
| Different mutator phenotypes in Mlh1- versus Pms2-deficient mice | Q28592891 | ||
| 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 | ||
| Nucleotide-promoted release of hMutSalpha from heteroduplex DNA is consistent with an ATP-dependent translocation mechanism | Q28610864 | ||
| Role of DNA mismatch repair and p53 in signaling induction of apoptosis by alkylating agents. | Q30454407 | ||
| Products of DNA mismatch repair genes mutS and mutL are required for transcription-coupled nucleotide-excision repair of the lactose operon in Escherichia coli | Q33555494 | ||
| The role of mismatch repair in the prevention of base pair mutations in Saccharomyces cerevisiae | Q33592366 | ||
| Mammalian DNA mismatch repair | Q33847720 | ||
| Mismatch repair processing of carcinogen-DNA adducts triggers apoptosis | Q33960642 | ||
| Restoration of mismatch repair to nuclear extracts of H6 colorectal tumor cells by a heterodimer of human MutL homologs | Q34554581 | ||
| Selective recognition of a cisplatin-DNA adduct by human mismatch repair proteins. | Q34625095 | ||
| The Escherichia coli MutL protein stimulates binding of Vsr and MutS to heteroduplex DNA. | Q34657088 | ||
| Mutator phenotypes in human colorectal carcinoma cell lines | Q35568305 | ||
| The many faces of DNA polymerases: strategies for mutagenesis and for mutational avoidance | Q36099918 | ||
| Biallelic inactivation of hMLH1 by epigenetic gene silencing, a novel mechanism causing human MSI cancers. | Q36213486 | ||
| Tumors of DNA mismatch repair-deficient hosts exhibit dramatic increases in genomic instability | Q36216663 | ||
| Mouse embryonic stem cells carrying one or two defective Msh2 alleles respond abnormally to oxidative stress inflicted by low-level radiation | Q36325598 | ||
| An alkylation-tolerant, mutator human cell line is deficient in strand-specific mismatch repair. | Q36412005 | ||
| hMutSalpha- and hMutLalpha-dependent phosphorylation of p53 in response to DNA methylator damage | Q36538872 | ||
| Recognition and repair of compound DNA lesions (base damage and mismatch) by human mismatch repair and excision repair systems | Q36565271 | ||
| Mismatch repair deficiency is associated with resistance to DNA minor groove alkylating agents | Q36617973 | ||
| Competency in mismatch repair prohibits clonal expansion of cancer cells treated with N-methyl-N'-nitro-N-nitrosoguanidine | Q37357197 | ||
| Human MutSalpha recognizes damaged DNA base pairs containing O6-methylguanine, O4-methylthymine, or the cisplatin-d(GpG) adduct | Q37522716 | ||
| Defective mismatch binding and a mutator phenotype in cells tolerant to DNA damage | Q38320078 | ||
| Specific binding of human MSH2.MSH6 mismatch-repair protein heterodimers to DNA incorporating thymine- or uracil-containing UV light photoproducts opposite mismatched bases. | Q38324036 | ||
| Effect of hMSH6 cDNA expression on the phenotype of mismatch repair-deficient colon cancer cell line HCT15. | Q38326361 | ||
| Requirement for DNA mismatch repair proteins in the transcription-coupled repair of thymine glycols in Saccharomyces cerevisiae | Q38336291 | ||
| hMSH2 and hMSH6 play distinct roles in mismatch binding and contribute differently to the ATPase activity of hMutSalpha | Q38336441 | ||
| DNA damage tolerance, mismatch repair and genome instability | Q40582064 | ||
| Mismatch repair is required for O(6)-methylguanine-induced homologous recombination in human fibroblasts | Q40858308 | ||
| Spontaneous development of drug resistance: mismatch repair and p53 defects in resistance to cisplatin in human tumor cells | Q40865504 | ||
| Cytotoxicity and mutagenicity of frameshift-inducing agent ICR191 in mismatch repair-deficient colon cancer cells | Q40893852 | ||
| Identification of hMutLbeta, a heterodimer of hMLH1 and hPMS1. | Q40920177 | ||
| Combined mismatch and nucleotide excision repair defects in a human cell line: mismatch repair processes methylation but not UV- or ionizing radiation-induced DNA damage. | Q40953374 | ||
| Mismatch repair and differential sensitivity of mouse and human cells to methylating agents. | Q40968675 | ||
| 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 | Q40969083 | ||
| Characterization of distinct human endometrial carcinoma cell lines deficient in mismatch repair that originated from a single tumor | Q41005472 | ||
| Cellular resistance and hypermutability in mismatch repair-deficient human cancer cell lines following treatment with methyl methanesulfonate. | Q41034113 | ||
| Mismatch repair defects in human carcinogenesis | Q41170340 | ||
| Cisplatin and adriamycin resistance are associated with MutLalpha and mismatch repair deficiency in an ovarian tumor cell line | Q41174585 | ||
| Sister chromatid exchanges in cells defective in mismatch, post-replication and excision repair | Q41299936 | ||
| A role for mismatch repair in production of chromosome aberrations by methylating agents in human cells | Q41353262 | ||
| Genetic consequences of tolerance to methylation DNA damage in mammalian cells | Q41524494 | ||
| MLH1, PMS1, and MSH2 interactions during the initiation of DNA mismatch repair in yeast | Q42427955 | ||
| Properties of N-methyl-N-nitrosourea-resistant, Mex- derivatives of an SV40-immortalized human fibroblast cell line | Q44076028 | ||
| MSH6, a Saccharomyces cerevisiae protein that binds to mismatches as a heterodimer with MSH2. | Q48065235 | ||
| Mismatch repair, G(2)/M cell cycle arrest and lethality after DNA damage. | Q53416148 | ||
| Mice defective in the DNA mismatch gene PMS2 are hypersensitive to MNU induced thymic lymphoma and are partially protected by transgenic expression of human MGMT. | Q53420486 | ||
| Spectra of spontaneous mutations at the hprt locus in colorectal carcinoma cell lines defective in mismatch repair | Q53442791 | ||
| DNA replication arrest and tolerance to DNA methylation damage. | Q53469560 | ||
| Dependence on RAD52 and RAD1 for anticancer drug resistance mediated by inactivation of mismatch repair genes. | Q54108643 | ||
| Role of postreplicative DNA mismatch repair in the cytotoxic action of thioguanine. | Q55066538 | ||
| Analysis of mismatch repair genes in hereditary non–polyposis colorectal cancer patients | Q57570041 | ||
| Frameshift mutator mutations | Q57978058 | ||
| Human MutSα Specifically Binds to DNA Containing Aminofluorene and Acetylaminofluorene Adducts | Q58074493 | ||
| Mismatch correction at O 6 -methylguanine residues in E. coli DNA | Q59049241 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | DNA mismatch repair | Q2984243 |
| DNA damage | Q5205747 | ||
| P304 | page(s) | 145-154 | |
| P577 | publication date | 2001-05-01 | |
| P1433 | published in | Journal of Cellular Physiology | Q1524270 |
| P1476 | title | Mismatch repair in correction of replication errors and processing of DNA damage | |
| P478 | volume | 187 |
| Q47368387 | A meta-analysis on XRCC1 R399Q and R194W polymorphisms, smoking and bladder cancer risk |
| Q34573320 | A role for DNA mismatch repair protein Msh2 in error-prone double-strand-break repair in mammalian chromosomes |
| Q36315875 | Accurate homologous recombination is a prominent double-strand break repair pathway in mammalian chromosomes and is modulated by mismatch repair protein Msh2. |
| Q31130184 | Association between XRCC1 and XRCC3 polymorphisms with lung cancer risk: a meta-analysis from case-control studies |
| Q50742549 | Associations between three XRCC1 polymorphisms and glioma risk: a meta-analysis. |
| Q24302011 | Characterization of human exonuclease 1 in complex with mismatch repair proteins, subcellular localization and association with PCNA |
| Q35469387 | Characterization of pathogenic human MSH2 missense mutations using yeast as a model system: a laboratory course in molecular biology. |
| Q38564597 | Chronic inflammation in urothelial bladder cancer |
| Q64387724 | Cooperation between non-essential DNA polymerases contributes to genome stability in Saccharomyces cerevisiae |
| Q35062449 | DNA repair defects in colon cancer |
| Q38349552 | Dissimilar mispair-recognition spectra of Arabidopsis DNA-mismatch-repair proteins MSH2{middle dot}MSH6 (MutS ) and MSH2{middle dot}MSH7 (MutS ) |
| Q28592464 | Elevated mutant frequencies and predominance of G:C to A:T transition mutations in Msh6(-/-) small intestinal epithelium |
| Q42520946 | Evidence that dysregulated DNA mismatch repair characterizes human nonmelanoma skin cancer. |
| Q38382440 | Genomic instability: Crossing pathways at the origin of structural and numerical chromosome changes |
| Q38363713 | Human cells bearing homozygous mutations in the DNA mismatch repair genes hMLH1 or hMSH2 are fully proficient in transcription-coupled nucleotide excision repair |
| Q33401963 | Large-scale inference of the point mutational spectrum in human segmental duplications |
| Q37689834 | Mechanisms of base substitution mutagenesis in cancer genomes |
| Q43829355 | Mechanisms of tolerance to DNA damaging therapeutic drugs |
| Q78434019 | Microsatellite instability in thorotrast-induced human intrahepatic cholangiocarcinoma |
| Q34160987 | Microsatellites: genomic distribution, putative functions and mutational mechanisms: a review |
| Q35548710 | Mismatch repair and response to DNA-damaging antitumour therapies |
| Q52031623 | Molecular dynamics and mechanics calculations on a DNA duplex with A(+)-C, G-T and T-C mispairs. |
| Q35047565 | Mutation rate, spectrum, topology, and context-dependency in the DNA mismatch repair-deficient Pseudomonas fluorescens ATCC948. |
| Q37128670 | Mutation rates, spectra, and genome-wide distribution of spontaneous mutations in mismatch repair deficient yeast |
| Q35676307 | Novel aspects of macromolecular repair and relationship to human disease |
| Q42509532 | Polymorphisms in the DNA repair gene XRCC1 associated with basal cell carcinoma and squamous cell carcinoma of the skin in a Korean population |
| Q60305880 | Prevalence of elevated microsatellite alterations at selected tetranucleotide repeats in pancreatic ductal adenocarcinoma |
| Q35910747 | Role of DNA mismatch repair in apoptotic responses to therapeutic agents |
| Q34194512 | Role of MED1 (MBD4) Gene in DNA repair and human cancer |
| Q38315591 | Testing excision models for responses of mismatch-repair systems to UV photoproducts in DNA. |
| Q27640375 | The alternating ATPase domains of MutS control DNA mismatch repair |
| Q51891134 | Uropathogenic E. coli infection provokes epigenetic downregulation of CDKN2A (p16INK4A) in uroepithelial cells. |
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