| scholarly article | Q13442814 |
| review article | Q7318358 |
| P356 | DOI | 10.1016/S0889-8553(05)70273-9 |
| P698 | PubMed publication ID | 8960891 |
| P2093 | author name string | Marra G | |
| Boland CR | |||
| 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 | ||
| Inactivation of the type II TGF-beta receptor in colon cancer cells with microsatellite instability | Q24319995 | ||
| A genetic model for colorectal tumorigenesis | Q27860582 | ||
| Large-scale analysis of gene expression, protein localization, and gene disruption in Saccharomyces cerevisiae | Q27937244 | ||
| The yeast gene MSH3 defines a new class of eukaryotic MutS homologues. | Q27937756 | ||
| Mutation of a mutL homolog in hereditary colon cancer | Q28114939 | ||
| Binding of mismatched microsatellite DNA sequences by the human MSH2 protein | Q28241673 | ||
| Colon cancer and DNA repair: have mismatches met their match? | Q28245366 | ||
| 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 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 | ||
| 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 | ||
| In vitro transcription/translation assay for the screening of hMLH1 and hMSH2 mutations in familial colon cancer | Q71737275 | ||
| MSH5, a novel MutS homolog, facilitates meiotic reciprocal recombination between homologs in Saccharomyces cerevisiae but not mismatch repair | Q71919357 | ||
| Mismatch repair gene defects in sporadic colorectal cancers with microsatellite instability | Q72127255 | ||
| Accumulation of multiple mutations in tumour suppressor genes during colorectal tumorigenesis in HNPCC patients | Q72608543 | ||
| Microsatellite instability in cancer of the proximal colon | Q29620692 | ||
| Detection of new mutations in six out of 10 Swiss HNPCC families by genomic sequencing of the hMSH2 and hMLH1 genes | Q33682850 | ||
| Strand-specific mismatch correction in nuclear extracts of human and Drosophila melanogaster cell lines | Q33720790 | ||
| Mutations in the MSH3 gene preferentially lead to deletions within tracts of simple repetitive DNA in Saccharomyces cerevisiae | Q33842093 | ||
| Founding mutations and Alu-mediated recombination in hereditary colon cancer | Q34297390 | ||
| Allelotype of colorectal carcinomas | Q34461209 | ||
| Restoration of mismatch repair to nuclear extracts of H6 colorectal tumor cells by a heterodimer of human MutL homologs | Q34554581 | ||
| The molecular basis of Turcot's syndrome | Q34662365 | ||
| DNA mismatch correction in a defined system | Q34674714 | ||
| Beta 2-microglobulin gene mutations: a study of established colorectal cell lines and fresh tumors | Q35282280 | ||
| Cloning and nucleotide sequence of DNA mismatch repair gene PMS1 from Saccharomyces cerevisiae: homology of PMS1 to procaryotic MutL and HexB. | Q36182527 | ||
| Self-destruction and tolerance in resistance of mammalian cells to alkylation damage | Q36277253 | ||
| An alkylation-tolerant, mutator human cell line is deficient in strand-specific mismatch repair. | Q36412005 | ||
| Mitotic crossovers between diverged sequences are regulated by mismatch repair proteins in Saccaromyces cerevisiae | Q36557503 | ||
| Misalignment-mediated DNA synthesis errors | Q36613826 | ||
| Dual requirement in yeast DNA mismatch repair for MLH1 and PMS1, two homologs of the bacterial mutL gene | Q36643609 | ||
| Isolation and characterization of allelic losses and gains in colorectal tumors by arbitrarily primed polymerase chain reaction | Q37265131 | ||
| One role for DNA methylation in vertebrate cells is strand discrimination in mismatch repair | Q37553690 | ||
| Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis | Q38293261 | ||
| Genetic instability occurs in the majority of young patients with colorectal cancer | Q38297232 | ||
| The Saccharomyces cerevisiae Msh2 protein specifically binds to duplex oligonucleotides containing mismatched DNA base pairs and insertions | Q38299752 | ||
| Defective mismatch binding and a mutator phenotype in cells tolerant to DNA damage | Q38320078 | ||
| High frequencies of short frameshifts in poly-CA/TG tandem repeats borne by bacteriophage M13 in Escherichia coli K-12. | Q40388905 | ||
| Hereditary Nonpolyposis Colorectal Cancer: the Syndrome, the Genes, and Historical Perspectives | Q40482404 | ||
| Mismatch repair, genetic stability and tumour avoidance | Q40522939 | ||
| 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 | ||
| The role of heteroduplex correction in gene conversion in Saccharomyces cerevisiae | Q41430030 | ||
| 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 | ||
| Genomic structure of human mismatch repair gene, hMLH1, and its mutation analysis in patients with hereditary non-polyposis colorectal cancer (HNPCC) | Q48075190 | ||
| 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 | ||
| CpG dinucleotides in the hMSH2 and hMLH1 genes are hotspots for HNPCC mutations. | Q55066383 | ||
| A frequent hMSH2 mutation in hereditary non-polyposis colon cancer syndrome | Q57266935 | ||
| Better survival rates in patients with MLH1-associated hereditary colorectal cancer | Q57567998 | ||
| Analysis of mismatch repair genes in hereditary non–polyposis colorectal cancer patients | Q57570041 | ||
| Genetic mapping of a second locus predisposing to hereditary non–polyposis colon cancer | Q58862199 | ||
| Mismatch correction at O 6 -methylguanine residues in E. coli DNA | Q59049241 | ||
| The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC) | Q62978412 | ||
| Somatic mutations in the hMSH2 gene in microsatellite unstable colorectal carcinomas | Q70972741 | ||
| P433 | issue | 4 | |
| P921 | main subject | colorectal cancer | Q188874 |
| P304 | page(s) | 755-772 | |
| P577 | publication date | 1996-12-01 | |
| P1433 | published in | Gastroenterology Clinics of North America | Q15756082 |
| P1476 | title | DNA repair and colorectal cancer | |
| P478 | volume | 25 |
| Q35753544 | Accumulated clonal genetic alterations in familial and sporadic colorectal carcinomas with widespread instability in microsatellite sequences |
| Q41005472 | Characterization of distinct human endometrial carcinoma cell lines deficient in mismatch repair that originated from a single tumor |
| Q40071695 | Curcumin enhances the effects of 5-fluorouracil and oxaliplatin in mediating growth inhibition of colon cancer cells by modulating EGFR and IGF-1R. |
| Q42633204 | Data sharing: Empty archives |
| Q53431346 | Genetic instability and chromosomal aberrations in colorectal cancer: a review of the current models. |
| Q41653205 | Genetic pathways to colorectal cancer |
| Q33836026 | Genomic and epigenetic instability in colorectal cancer pathogenesis |
| Q24685680 | Loss of CDX2 expression and microsatellite instability are prominent features of large cell minimally differentiated carcinomas of the colon |
| Q35129256 | Mismatch repair proficiency and in vitro response to 5-fluorouracil |
| Q43761456 | Msh2 DNA mismatch repair gene deficiency and the food-borne mutagen 2-amino-1-methy1-6-phenolimidazo [4,5-b] pyridine (PhIP) synergistically affect mutagenesis in mouse colon |
| Q33378445 | Mutation rates of TGFBR2 and ACVR2 coding microsatellites in human cells with defective DNA mismatch repair |
| Q42660015 | Replication errors: cha(lle)nging the genome |
| Q34989790 | The genetic pathogenesis of colorectal cancer |
| Q53428207 | Transient appearance of the mutator phenotype during carcinogenesis as a possible explanation for the lack of mini/microsatellite instability in many late stage tumors. |
| Q38336441 | hMSH2 and hMSH6 play distinct roles in mismatch binding and contribute differently to the ATPase activity of hMutSalpha |
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