| scholarly article | Q13442814 |
| P2093 | author name string | J C Barrett | |
| J I Risinger | |||
| T A Kunkel | |||
| A Umar | |||
| 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 | ||
| Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction | Q25938986 | ||
| Mutation of a mutL homolog in hereditary colon cancer | Q28114939 | ||
| Cloning, characterization and chromosomal assignment of the human genes homologous to yeast PMS1, a member of mismatch repair genes | Q28119040 | ||
| 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 | ||
| Structure of the human MSH2 locus and analysis of two Muir-Torre kindreds for msh2 mutations | Q28299699 | ||
| Microsatellite instability in cancer of the proximal colon | Q29620692 | ||
| Specificity of mismatch repair following transformation of Saccharomyces cerevisiae with heteroduplex plasmid DNA. | Q33857769 | ||
| 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 | ||
| Cloning and nucleotide sequence of DNA mismatch repair gene PMS1 from Saccharomyces cerevisiae: homology of PMS1 to procaryotic MutL and HexB. | Q36182527 | ||
| An alkylation-tolerant, mutator human cell line is deficient in strand-specific mismatch repair. | Q36412005 | ||
| Dual requirement in yeast DNA mismatch repair for MLH1 and PMS1, two homologs of the bacterial mutL gene | Q36643609 | ||
| Defective mismatch binding and a mutator phenotype in cells tolerant to DNA damage | Q38320078 | ||
| Mismatch repair, genetic stability, and cancer | Q40556409 | ||
| DNA damage tolerance, mismatch repair and genome instability | Q40582064 | ||
| 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 | ||
| Mutagenesis of yeast MW104-1B strain has identified the uncharacterized PMS6 DNA mismatch repair gene locus and additional alleles of existing PMS1, PMS2 and MSH2 genes | Q45976982 | ||
| Mutations of the E-cadherin gene in human gynecologic cancers | Q48082880 | ||
| Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer | Q48084125 | ||
| A further tetranucleotide repeat polymorphism in the vWF gene | Q48168540 | ||
| Genetic mapping of a second locus predisposing to hereditary non–polyposis colon cancer | Q58862199 | ||
| P433 | issue | 31 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | DNA mismatch repair | Q2984243 |
| P304 | page(s) | 18183-18186 | |
| P577 | publication date | 1995-08-01 | |
| P1433 | published in | Journal of Biological Chemistry | Q867727 |
| P1476 | title | A hPMS2 mutant cell line is defective in strand-specific mismatch repair | |
| P478 | volume | 270 |
| Q36540457 | A personal historical view of DNA mismatch repair with an emphasis on eukaryotic DNA mismatch repair |
| Q44616192 | A single amino acid substitution in MSH5 results in DNA alkylation tolerance |
| Q28910215 | Altered spectra of hypermutation in antibodies from mice deficient for the DNA mismatch repair protein PMS2 |
| Q41617067 | Cancer cells exhibit a mutator phenotype |
| Q41005472 | Characterization of distinct human endometrial carcinoma cell lines deficient in mismatch repair that originated from a single tumor |
| Q74063639 | Chromosomal instability, reproductive cell death and apoptosis induced by O6-methylguanine in Mex-, Mex+ and methylation-tolerant mismatch repair compromised cells: facts and models |
| Q41174585 | Cisplatin and adriamycin resistance are associated with MutLalpha and mismatch repair deficiency in an ovarian tumor cell line |
| Q40893852 | Cytotoxicity and mutagenicity of frameshift-inducing agent ICR191 in mismatch repair-deficient colon cancer cells |
| Q40939179 | DNA-mismatch repair. The intricacies of eukaryotic spell-checking |
| Q53365304 | Defective mismatch repair in the pathogenesis of low-grade appendiceal mucinous neoplasms and adenocarcinomas. |
| Q33888905 | Deficiency of a novel mismatch repair activity in a bladder tumor cell line |
| Q34478988 | Functional role of DNA mismatch repair gene PMS2 in prostate cancer cells. |
| Q37522716 | Human MutSalpha recognizes damaged DNA base pairs containing O6-methylguanine, O4-methylthymine, or the cisplatin-d(GpG) adduct |
| Q58074493 | Human MutSα Specifically Binds to DNA Containing Aminofluorene and Acetylaminofluorene Adducts |
| Q36451916 | Human mismatch repair protein hMutLα is required to repair short slipped-DNAs of trinucleotide repeats |
| Q40920177 | Identification of hMutLbeta, a heterodimer of hMLH1 and hPMS1. |
| Q40022432 | Instability of CAG and CTG trinucleotide repeats in Saccharomyces cerevisiae |
| Q48065235 | MSH6, a Saccharomyces cerevisiae protein that binds to mismatches as a heterodimer with MSH2. |
| Q28510650 | Meiotic pachytene arrest in MLH1-deficient mice |
| Q41082110 | Mismatch repair defects and O6-methylguanine-DNA methyltransferase expression in acquired resistance to methylating agents in human cells |
| Q53416148 | Mismatch repair, G(2)/M cell cycle arrest and lethality after DNA damage. |
| Q41005399 | Molecular events after antisense inhibition of hMSH2 in a HeLa cell line |
| Q40601230 | Msh2 deficiency does not contribute to cisplatin resistance in mouse embryonic stem cells |
| Q28592583 | Mutation in the mismatch repair gene Msh6 causes cancer susceptibility |
| Q24318892 | Mutation of MSH3 in endometrial cancer and evidence for its functional role in heteroduplex repair |
| Q34123282 | Mutations within the hMLH1 and hPMS2 subunits of the human MutLalpha mismatch repair factor affect its ATPase activity, but not its ability to interact with hMutSalpha |
| Q33909895 | Novel PMS2 pseudogenes can conceal recessive mutations causing a distinctive childhood cancer syndrome |
| Q40751829 | Preparation of DNA substrates for in vitro mismatch repair |
| Q36565271 | Recognition and repair of compound DNA lesions (base damage and mismatch) by human mismatch repair and excision repair systems |
| Q40969083 | 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 |
| Q38336291 | Requirement for DNA mismatch repair proteins in the transcription-coupled repair of thymine glycols in Saccharomyces cerevisiae |
| Q53437948 | Reversal of methylation tolerance by transfer of human chromosome 2. |
| Q30454407 | Role of DNA mismatch repair and p53 in signaling induction of apoptosis by alkylating agents. |
| Q40878184 | Somatic mutation of hPMS2 as a possible cause of sporadic human colon cancer with microsatellite instability |
| Q40990759 | Specificity of mutations in the PMS2-deficient human tumor cell line HEC-1-A. |
| Q77413342 | Stability of microsatellites in myeloid neoplasias |
| Q41602506 | Strand-specific mismatch repair in mammalian cells |
| Q35753518 | The clinicopathological features of gastric carcinomas with microsatellite instability may be mediated by mutations of different "target genes": a study of the TGFbeta RII, IGFII R, and BAX genes |
| Q31833517 | The instability within: problems in current analyses of microsatellite instability |
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