| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0955-0674(98)80005-7 |
| P698 | PubMed publication ID | 9640530 |
| P2093 | author name string | T A Prolla | |
| P2860 | cites work | Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis | Q22122362 |
| Mutations of two PMS homologues in hereditary nonpolyposis colon cancer | Q24318484 | ||
| Mutation of MSH3 in endometrial cancer and evidence for its functional role in heteroduplex repair | Q24318892 | ||
| Inactivation of the type II TGF-beta receptor in colon cancer cells with microsatellite instability | Q24319995 | ||
| 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 | ||
| 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 | ||
| Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over | Q28282791 | ||
| Escherichia coli mutS-encoded protein binds to mismatched DNA base pairs | Q28287503 | ||
| 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 | ||
| Tumour susceptibility and spontaneous mutation in mice deficient in Mlh1, Pms1 and Pms2 DNA mismatch repair | Q28508905 | ||
| Meiotic pachytene arrest in MLH1-deficient mice | Q28510650 | ||
| Mutation in the mismatch repair gene Msh6 causes cancer susceptibility | Q28592583 | ||
| Redundancy of Saccharomyces cerevisiae MSH3 and MSH6 in MSH2-dependent mismatch repair | Q29615027 | ||
| Destabilization of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair | Q29618879 | ||
| Mutations in the MSH3 gene preferentially lead to deletions within tracts of simple repetitive DNA in Saccharomyces cerevisiae | Q33842093 | ||
| 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 | ||
| Repair tracts in mismatched DNA heteroduplexes | Q35037122 | ||
| Error-prone replication of repeated DNA sequences by T7 DNA polymerase in the absence of its processivity subunit | Q35598571 | ||
| Cloning and nucleotide sequence of DNA mismatch repair gene PMS1 from Saccharomyces cerevisiae: homology of PMS1 to procaryotic MutL and HexB. | Q36182527 | ||
| 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 | ||
| Repair of DNA heteroduplexes containing small heterologous sequences in Escherichia coli | Q36856385 | ||
| APC mutations in colorectal tumors with mismatch repair deficiency | Q37383704 | ||
| Mechanisms of DNA-mismatch correction | Q37858946 | ||
| 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 | ||
| Pleiotropic effects of a DNA adenine methylation mutation (dam-3) in Escherichia coli K12 | Q39938870 | ||
| High frequencies of short frameshifts in poly-CA/TG tandem repeats borne by bacteriophage M13 in Escherichia coli K-12. | Q40388905 | ||
| Molecular matchmakers | Q40885529 | ||
| Microsatellite instability and DNA mismatch repair in human cancer | Q41025066 | ||
| hMLH1 expression and cellular responses of ovarian tumour cells to treatment with cytotoxic anticancer agents | Q41100219 | ||
| 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 | ||
| Clues to the pathogenesis of familial colorectal cancer | Q42622043 | ||
| Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer | Q48084125 | ||
| Somatic frameshift mutations in the BAX gene in colon cancers of the microsatellite mutator phenotype. | Q53445992 | ||
| 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 | ||
| Mismatch correction at O 6 -methylguanine residues in E. coli DNA | Q59049241 | ||
| The E. coli uvrD gene product is DNA helicase II | Q60205950 | ||
| N-Methyl-N'-nitro-N-nitrosoguanidine sensitivity of E. coli mutants deficient in DNA methylation and mismatch repair | Q70221033 | ||
| Molecular analysis of mutations in mutator colorectal carcinoma cell lines | Q70972736 | ||
| An adaptive response to the cytotoxic effects of N-methyl-N-nitrosourea is apparently absent in normal human fibroblasts | Q71627385 | ||
| P433 | issue | 3 | |
| P921 | main subject | DNA mismatch repair | Q2984243 |
| P304 | page(s) | 311-316 | |
| P577 | publication date | 1998-06-01 | |
| P1433 | published in | Current Opinion in Cell Biology | Q13505682 |
| P1476 | title | DNA mismatch repair and cancer | |
| P478 | volume | 10 |
| Q83398654 | A convenient fluorescent-labeled assay for in vitro measurement of DNA mismatch repair activity |
| Q44177099 | Association between Mismatch-repair Genetic variation and the Risk of Multiple Primary Cancers: A Meta-Analysis |
| Q34503454 | Conditional mutation of Brca1 in mammary epithelial cells results in blunted ductal morphogenesis and tumour formation. |
| Q36643467 | Contrasting molecular pathology of colorectal carcinoma in Egyptian and Western patients |
| Q34568596 | DNA mismatch repair defects: role in colorectal carcinogenesis |
| Q33537493 | DNA secondary structure: a common and causative factor for expansion in human disease |
| Q28592033 | Elevated mutant frequencies and increased C : G-->T : A transitions in Mlh1-/- versus Pms2-/- murine small intestinal epithelial cells |
| Q48731412 | Gene expression profiling defines molecular subtypes of classical Hodgkin's disease |
| Q26810051 | Genetic and epigenetic interactions in allopolyploid plants |
| Q24553992 | Interaction of mismatch repair protein PMS2 and the p53-related transcription factor p73 in apoptosis response to cisplatin |
| Q36828042 | Measurement of DNA mismatch repair activity in live cells |
| Q44280420 | Mice defective in the mismatch repair gene Msh2 show increased predisposition to UVB radiation-induced skin cancer |
| Q83835402 | Microsatellite instability in colorectal cancer: from molecular oncogenic mechanisms to clinical implications |
| Q38314351 | Midgestation lethality in mice deficient for the RecA-related gene, Rad51d/Rad51l3. |
| Q33756019 | Mismatch repair and immunoglobulin gene hypermutation: did we learn something? |
| Q28363159 | Molecular predictors of survival after adjuvant chemotherapy for colon cancer |
| Q55060101 | Mutational signatures and mutable motifs in cancer genomes. |
| Q35063954 | Mutator phenotypes of yeast strains heterozygous for mutations in the MSH2 gene. |
| Q34612512 | Requirement for Msh6, but not for Swi4 (Msh3), in Msh2-dependent repair of base-base mismatches and mononucleotide loops in Schizosaccharomyces pombe |
| Q33941481 | Suppression of gene amplification and chromosomal DNA integration by the DNA mismatch repair system |
| Q33984337 | The Saccharomyces repair genes at the end of the century |
| Q31497967 | The intrinsically unstable life of DNA triplet repeats associated with human hereditary disorders |
| Q34804028 | The role of Alu repeat clusters as mediators of recurrent chromosomal aberrations in tumors |
| Q24621737 | Unbalanced replication as a major source of genetic instability in cancer cells |
| Q83139208 | hMLH1 and MGMT inactivation as a mechanism of tumorigenesis in monoclonal gammopathies |
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