| scholarly article | Q13442814 |
| review article | Q7318358 |
| P2093 | author name string | Peltomäki P | |
| 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 | ||
| ERCC2: cDNA cloning and molecular characterization of a human nucleotide excision repair gene with high homology to yeast RAD3 | Q24321908 | ||
| Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis | Q24671692 | ||
| Cloning, characterization and chromosomal assignment of the human genes homologous to yeast PMS1, a member of mismatch repair genes | Q28119040 | ||
| 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 | ||
| Genetic mapping of a locus predisposing to human colorectal cancer | Q28268634 | ||
| Isolation and characterization of cDNA clones derived from the divergently transcribed gene in the region upstream from the human dihydrofolate reductase gene | Q28275920 | ||
| Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over | Q28282791 | ||
| 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 | ||
| MSH2 deficient mice are viable and susceptible to lymphoid tumours | Q28508486 | ||
| Destabilization of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair | Q29618879 | ||
| Microsatellite instability in cancer of the proximal colon | Q29620692 | ||
| Mutations in the MSH3 gene preferentially lead to deletions within tracts of simple repetitive DNA in Saccharomyces cerevisiae | Q33842093 | ||
| Genomic organization of the human PMS2 gene family. | Q34373629 | ||
| A simple p53 functional assay for screening cell lines, blood, and tumors | Q34397902 | ||
| Cloning and expression of the Xenopus and mouse Msh2 DNA mismatch repair genes. | Q35004871 | ||
| Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction | Q35247229 | ||
| Mutator phenotypes in human colorectal carcinoma cell lines | Q35568305 | ||
| Microsatellite alterations as clonal markers for the detection of human cancer | Q35819311 | ||
| How many mutations are required for tumorigenesis? Implications from human cancer data | Q36782475 | ||
| 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 | ||
| High frequencies of short frameshifts in poly-CA/TG tandem repeats borne by bacteriophage M13 in Escherichia coli K-12. | Q40388905 | ||
| Mechanisms of DNA excision repair | Q40556396 | ||
| Mismatch repair, genetic stability, and cancer | Q40556409 | ||
| Microsatellite instability: marker of a mutator phenotype in cancer. | Q40630726 | ||
| Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: an updated review | Q40901949 | ||
| Genetics of hereditary colon cancer | Q41126304 | ||
| Monoallelic mutation analysis (MAMA) for identifying germline mutations | Q41306100 | ||
| Mismatch Repair Deficiency in Phenotypically Normal Human Cells | Q41347026 | ||
| DNA loop repair by human cell extracts | Q41429743 | ||
| Defective mismatch repair in extracts of colorectal and endometrial cancer cell lines exhibiting microsatellite instability | Q41467421 | ||
| Hypermutability and mismatch repair deficiency in RER+ tumor cells | Q41508298 | ||
| 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 | ||
| Clues to the pathogenesis of familial colorectal cancer | Q42622043 | ||
| Genomic instability in repeated sequences is an early somatic event in colorectal tumorigenesis that persists after transformation | Q46049171 | ||
| Microsatellite instability in sporadic endometrial carcinoma | Q46250416 | ||
| Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer | Q48084125 | ||
| Instability of short tandem repeats (microsatellites) in human cancers. | Q48181678 | ||
| Microsatellite instability in colorectal cancer: improved assessment using fluorescent polymerase chain reaction. | Q52870388 | ||
| Sporadic gastric carcinomas with microsatellite instability display a particular clinicopathologic profile. | Q53465959 | ||
| Genomic instability of microsatellite repeats and its association with the evolution of chronic myelogenous leukemia. | Q53471593 | ||
| Genetic instability in pancreatic cancer and poorly differentiated type of gastric cancer. | Q53477421 | ||
| DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer | Q57200636 | ||
| Loss of the wild type MLH1 gene is a feature of hereditary nonpolyposis colorectal cancer | Q57568035 | ||
| Analysis of mismatch repair genes in hereditary non–polyposis colorectal cancer patients | Q57570041 | ||
| A transforming growth factor beta receptor type II gene mutation common in colon and gastric but rare in endometrial cancers with microsatellite instability | Q59156997 | ||
| Heteroduplex repair in extracts of human HeLa cells | Q68198738 | ||
| In vitro transcription/translation assay for the screening of hMLH1 and hMSH2 mutations in familial colon cancer | Q71737275 | ||
| Mismatch repair, somatic mutations, and the origins of cancer | Q71805147 | ||
| Microsatellite instability occurs frequently and in both diploid and aneuploid cell populations of Barrett's-associated esophageal adenocarcinomas | Q72018711 | ||
| A hereditary genetic marker closely associated with microsatellite instability in lung cancer | Q72033731 | ||
| Genomic instability of microsatellite repeats and mutations of H-, K-, and N-ras, and p53 genes in renal cell carcinoma | Q72065156 | ||
| Replication error-type genetic instability at 1q42-43 in human male germ cell tumors | Q72065274 | ||
| Mismatch repair gene defects in sporadic colorectal cancers with microsatellite instability | Q72127255 | ||
| High frequency of mutator phenotype in human prostatic adenocarcinoma | Q72185095 | ||
| Microsatellite instability and loss of heterozygosity in breast cancer | Q72313887 | ||
| Replication errors in benign and malignant tumors from hereditary nonpolyposis colorectal cancer patients | Q72313890 | ||
| Microsatellite instability and other molecular abnormalities in non-small cell lung cancer | Q72368568 | ||
| Genetic instability of microsatellite sequences in many non-small cell lung carcinomas | Q72399771 | ||
| Frequent microsatellite instability in primary small cell lung cancer | Q72399781 | ||
| Chromosome 9 allelic losses and microsatellite alterations in human bladder tumors | Q72428452 | ||
| Genetic instability of microsatellites in endometrial carcinoma | Q72559451 | ||
| Accumulation of multiple mutations in tumour suppressor genes during colorectal tumorigenesis in HNPCC patients | Q72608543 | ||
| Microsatellite instability in bladder cancer | Q72613246 | ||
| Genomic instability in colorectal cancer: relationship to clinicopathological variables and family history | Q72657539 | ||
| Microsatellite instability is associated with tumors that characterize the hereditary non-polyposis colorectal carcinoma syndrome | Q72657543 | ||
| Microsatellite instability occurs frequently in human gastric carcinoma | Q72760038 | ||
| Instability of microsatellites in rat colon tumors induced by heterocyclic amines | Q72875184 | ||
| P921 | main subject | DNA repair | Q210538 |
| genetic variation | Q349856 | ||
| mutation | Q42918 | ||
| Lynch syndrome | Q783644 | ||
| DNA mismatch repair | Q2984243 | ||
| P304 | page(s) | 775-780 | |
| P577 | publication date | 1997-06-01 | |
| P1433 | published in | Environmental Health Perspectives | Q1345904 |
| P1476 | title | DNA mismatch repair gene mutations in human cancer | |
| P478 | volume | 105 Suppl 4 |
| Q34638914 | 12th meeting of the Scientific Group on Methodologies for the Safety Evaluation of Chemicals: susceptibility to environmental hazards |
| Q74462661 | A comparative analysis of allelic imbalance events in chemically induced rat mammary, colon, and bladder tumors |
| Q35836701 | Assay validation for identification of hereditary nonpolyposis colon cancer-causing mutations in mismatch repair genes MLH1, MSH2, and MSH6 |
| Q56890419 | Cytolytic Activity Score to Assess Anticancer Immunity in Colorectal Cancer |
| Q37169725 | Genetic changes of p53, K-ras, and microsatellite instability in gallbladder carcinoma in high-incidence areas of Japan and Hungary |
| Q33764029 | Genetic susceptibility to non-polyposis colorectal cancer |
| Q36622540 | Immunohistochemical analysis of expression and allelotype of mismatch repair genes (hMLH1 and hMSH2) in bladder cancer |
| Q47630690 | Lynch syndrome and sextuple primary malignancies. |
| Q35548710 | Mismatch repair and response to DNA-damaging antitumour therapies |
| Q84301243 | Missense mutations in MLH1, MSH2, KRAS, and APC genes in colorectal cancer patients in Malaysia |
| Q64389865 | Regulation of DNA repair by non-coding miRNAs |
| Q35827560 | Rheumatoid Arthritis as a Therapeutic Challenge in a Patient with Lynch Syndrome |
| Q33984337 | The Saccharomyces repair genes at the end of the century |
| Q45296256 | The influence of DNA glycosylases on spontaneous mutation |
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