| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0027-5107(97)00244-3 |
| P698 | PubMed publication ID | 9626969 |
| P2093 | author name string | Zhu W | |
| Mironov N | |||
| Yamasaki H | |||
| P2860 | cites work | Molecular analysis of mutations in mutator colorectal carcinoma cell lines | Q70972736 |
| Microsatellite alterations in human and rat esophageal tumors at selective loci | Q72276724 | ||
| hMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6 | Q24323176 | ||
| Restoration of mismatch repair to nuclear extracts of H6 colorectal tumor cells by a heterodimer of human MutL homologs | Q34554581 | ||
| Mutator phenotypes in human colorectal carcinoma cell lines | Q35568305 | ||
| A mismatch recognition defect in colon carcinoma confers DNA microsatellite instability and a mutator phenotype | Q35753566 | ||
| In vivo evidence for endogenous DNA alkylation damage as a source of spontaneous mutation in eukaryotic cells | Q36155707 | ||
| An alkylation-tolerant, mutator human cell line is deficient in strand-specific mismatch repair. | Q36412005 | ||
| Competency in mismatch repair prohibits clonal expansion of cancer cells treated with N-methyl-N'-nitro-N-nitrosoguanidine | Q37357197 | ||
| APC mutations in colorectal tumors with mismatch repair deficiency | Q37383704 | ||
| Human MutSalpha recognizes damaged DNA base pairs containing O6-methylguanine, O4-methylthymine, or the cisplatin-d(GpG) adduct | Q37522716 | ||
| Differences in the spectrum of spontaneous mutations in the hprt gene between tumor cells of the microsatellite mutator phenotype | Q38358374 | ||
| 3-aminobenzamide and/or O6-benzylguanine evaluated as an adjuvant to temozolomide or BCNU treatment in cell lines of variable mismatch repair status and O6-alkylguanine-DNA alkyltransferase activity | Q40069172 | ||
| DNA damage tolerance, mismatch repair and genome instability | Q40582064 | ||
| Microsatellite instability and DNA mismatch repair in human cancer | Q41025066 | ||
| Mutation rate at the hprt locus in human cancer cell lines with specific mismatch repair-gene defects | Q41140973 | ||
| A role for mismatch repair in production of chromosome aberrations by methylating agents in human cells | Q41353262 | ||
| Hypermutability and mismatch repair deficiency in RER+ tumor cells | Q41508298 | ||
| Clues to the pathogenesis of familial colorectal cancer | Q42622043 | ||
| Reversible inhibition of intercellular junctional communication by glycyrrhetinic acid | Q44325495 | ||
| Novel mutational spectrum induced by N-methyl-N'-nitro-N-nitrosoguanidine in the coding region of the hypoxanthine (guanine) phosphoribosyltransferase gene in diploid human fibroblasts | Q44703313 | ||
| Frequent genetic instability in small intestinal carcinomas. | Q55078049 | ||
| P433 | issue | 1-2 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 93-99 | |
| P577 | publication date | 1998-02-01 | |
| P1433 | published in | Mutation Research | Q6943732 |
| P1476 | title | Frequency of HPRT gene mutations induced by N-methyl-N'-nitro-N-nitrosoguanidine corresponds to replication error phenotypes of cell lines | |
| P478 | volume | 398 |
| Q28587976 | Acceleration of lymphomagenesis in mismatch-repair deficient mice by exposure to genotoxic agents |
| Q33444726 | Attaching and effacing Escherichia coli downregulate DNA mismatch repair protein in vitro and are associated with colorectal adenocarcinomas in humans |
| Q77106386 | Chimeraplasty validation |
| Q33864863 | Genomic instability in multistage carcinogenesis |
| Q40735855 | Methylation tolerance in mismatch repair proficient cells with low MSH2 protein level |
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