| scholarly article | Q13442814 |
| P2093 | author name string | X. Yao | |
| N. Arnheim | |||
| R. M. Liskay | |||
| A. B. Buermeyer | |||
| D. Tran | |||
| L. Narayanan | |||
| P. M. Glazer | |||
| S. M. Baker | |||
| T. A. Prolla | |||
| P2860 | cites work | Elevated levels of mutation in multiple tissues of mice deficient in the DNA mismatch repair gene Pms2 | Q22248073 |
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| DNA-mismatch repair. The intricacies of eukaryotic spell-checking | Q40939179 | ||
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| Somatic frameshift mutations in DNA mismatch repair and proapoptosis genes in hereditary nonpolyposis colorectal cancer | Q44366534 | ||
| Microsatellite instability and mutations of the transforming growth factor beta type II receptor gene in colorectal cancer | Q45345220 | ||
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| Somatic frameshift mutations in the BAX gene in colon cancers of the microsatellite mutator phenotype. | Q53445992 | ||
| Differential involvement of the human mismatch repair proteins, hMLH1 and hMSH2, in transcription-coupled repair | Q56765940 | ||
| Microsatellite instability in the insulin–like growth factor II receptor gene in gastrointestinal tumours | Q63407701 | ||
| Frequent spontaneous deletions at a shuttle vector locus in transgenic mice | Q71163209 | ||
| P433 | issue | 12 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | MutL homolog 1 | Q14911713 |
| Mismatch repair endonuclease PMS2 | Q21980091 | ||
| P304 | page(s) | 6850–6855 | |
| P577 | publication date | 1999-06-08 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Different mutator phenotypes in Mlh1- versus Pms2-deficient mice | |
| P478 | volume | 96 |
| Q41882366 | A systems approach defining constraints of the genome architecture on lineage selection and evolvability during somatic cancer evolution |
| Q40677027 | A:T --> G:C base pair substitutions occur at a higher rate than other substitution events in Pms2 deficient mouse cells |
| Q83174919 | Accelerated growth of intestinal tumours after radiation exposure in Mlh1-knockout mice: evaluation of the late effect of radiation on a mouse model of HNPCC |
| Q36614680 | An intact Pms2 ATPase domain is not essential for male fertility |
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| Q34820495 | Apoptotic function of human PMS2 compromised by the nonsynonymous single-nucleotide polymorphic variant R20Q |
| Q35694485 | Chlorinated Water Modulates the Development of Colorectal Tumors with Chromosomal Instability and Gut Microbiota in Apc-Deficient Mice |
| Q39652175 | Conservation of functional asymmetry in the mammalian MutLα ATPase |
| Q35788926 | DNA mismatch repair deficiency accelerates endometrial tumorigenesis in Pten heterozygous mice |
| Q35062449 | DNA repair defects in colon cancer |
| Q33938090 | Database of mouse strains carrying targeted mutations in genes affecting cellular responses to DNA damage. Version 4. |
| Q39745939 | Decreased Expression of the DNA Mismatch Repair Gene Mlh1 under Hypoxic Stress in Mammalian Cells |
| Q33596701 | Defective mismatch repair, microsatellite mutation bias, and variability in clinical cancer phenotypes |
| Q39549181 | Deficiency in DNA mismatch repair increases the rate of telomere shortening in normal human cells. |
| Q51039462 | Detection of coding microsatellite frameshift mutations in DNA mismatch repair-deficient mouse intestinal tumors. |
| Q22242924 | Differing patterns of genetic instability in mice deficient in the mismatch repair genes Pms2, Mlh1, Msh2, Msh3 and Msh6 |
| Q28592033 | Elevated mutant frequencies and increased C : G-->T : A transitions in Mlh1-/- versus Pms2-/- murine small intestinal epithelial cells |
| Q37357503 | Epigenetic repression of DNA mismatch repair by inflammation and hypoxia in inflammatory bowel disease-associated colorectal cancer |
| Q37053442 | Extrapolating the effect of deleterious nsSNPs in the binding adaptability of flavopiridol with CDK7 protein: a molecular dynamics approach |
| Q31464606 | Genetic predisposition and somatic diversification in tumor development and progression |
| Q24670186 | Genetic reconstruction of individual colorectal tumor histories |
| Q43869182 | Germ cells microsatellite instability. The effect of different mutagens in a mismatch repair mutant of Drosophila (spel1). |
| Q52551102 | Germline mutations at microsatellite loci in homozygous and heterozygous mutants for mismatch repair and PCNA genes in Drosophila. |
| Q37411879 | Helicobacter pylori infection and expression of DNA mismatch repair proteins |
| Q73794909 | Human DNA repair genes |
| Q39913958 | Human MutL-complexes monitor homologous recombination independently of mismatch repair |
| Q36812749 | Human postmeiotic segregation 2 exhibits biased repair at tetranucleotide microsatellite sequences |
| Q40920177 | Identification of hMutLbeta, a heterodimer of hMLH1 and hPMS1. |
| Q50919937 | Ikaros is a mutational target for lymphomagenesis in Mlh1-deficient mice. |
| Q50487055 | Involvement of the Arabidopsis thaliana AtPMS1 gene in somatic repeat instability. |
| Q37416970 | Long-lived Min mice develop advanced intestinal cancers through a genetically conservative pathway |
| Q78002492 | Loss of heterozygosity and point mutation at Aprt locus in T cells and fibroblasts of Pms2-/- mice |
| Q22010995 | MLH3: a DNA mismatch repair gene associated with mammalian microsatellite instability |
| Q34614229 | Maternal effect for DNA mismatch repair in the mouse. |
| Q73311211 | Mediating mismatch repair |
| Q24627393 | Microsatellite instability in colorectal cancer |
| Q33885063 | Mismatch repair defects in cancer |
| Q36387895 | Mismatch repair deficiency: a temozolomide resistance factor in medulloblastoma cell lines that is uncommon in primary medulloblastoma tumours |
| Q34194518 | Mismatch repair in correction of replication errors and processing of DNA damage |
| Q33984294 | Mismatch repair proteins and mitotic genome stability |
| Q73709670 | Mlh1 deficiency accelerates myeloid leukemogenesis in neurofibromatosis 1 (Nf1) heterozygous mice |
| Q28588324 | Mlh1 deficiency enhances several phenotypes of Apc(Min)/+ mice |
| Q57058967 | Mlh1 deficiency increases the risk of hematopoietic malignancy after simulated space radiation exposure |
| Q28586588 | Mlh1 mediates tissue-specific regulation of mitotic recombination |
| Q25257401 | Molecular models for the tissue specificity of DNA mismatch repair-deficient carcinogenesis |
| Q28214396 | Mouse models for human DNA mismatch-repair gene defects |
| Q34254602 | Msh6 protects mature B cells from lymphoma by preserving genomic stability |
| Q40744422 | Multiple mutations are common at mouse Aprt in genotoxin-exposed mismatch repair deficient cells |
| Q28506014 | Mutagenesis in PMS2- and MSH2-deficient mice indicates differential protection from transversions and frameshifts |
| Q35019548 | Mutation theory of aging, assessed in transgenic mice and knockout mice. |
| Q52720227 | Mutational signatures of DNA mismatch repair deficiency in C. elegans and human cancers. |
| Q57742646 | Non-Hodgkin lymphoma related to hereditary nonpolyposis colorectal cancer in a patient with a novel heterozygous complex deletion in theMSH2 gene |
| Q34068165 | PMS2 endonuclease activity has distinct biological functions and is essential for genome maintenance |
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| Q28506086 | Pms2 suppresses large expansions of the (GAA·TTC)n sequence in neuronal tissues |
| Q41471973 | Regulation of mRNA expression in macrophages after Yersinia enterocolitica infection. Role of different Yop effectors. |
| Q33896699 | Steady-state regulation of the human DNA mismatch repair system. |
| Q28507252 | Stepwise deletions of polyA sequences in mismatch repair-deficient colorectal cancers |
| Q40222264 | The E705K mutation in hPMS2 exerts recessive, not dominant, effects on mismatch repair |
| Q33656549 | The Mutyh base excision repair gene influences the inflammatory response in a mouse model of ulcerative colitis |
| Q37619794 | The mutational profile and infiltration pattern of murine MLH1-/- tumors: concurrences, disparities and cell line establishment for functional analysis |
| Q26864622 | Tumor-specific microsatellite instability: do distinct mechanisms underlie the MSI-L and EMAST phenotypes? |
| Q44100502 | Visualization of mosaicism in tissues of normal and mismatch-repair-deficient mice carrying a microsatellite-containing transgene |
| Q79361502 | [Microsatellite instability in colorectal cancer: concept, detection methods and clinical utility] |
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