Redundancy of Saccharomyces cerevisiae MSH3 and MSH6 in MSH2-dependent mismatch repair

The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer

Fishel, R. A., Lescoe, M. K., Rao, M. R. S., Copeland, N. G., Jenkins, N. A., Garber, J. E., Kane, M., & Kolodner, R. D. (1993) · Cell · doi:10.1016/0092-8674(93)90546-3 · Cited by 2,884

Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis

Ionov, Y., Peinado, M. A., Malkhosyan, S. R., Shibata, D. K., & Perucho, M. (1993) · Nature · doi:10.1038/363558a0 · Cited by 2,691

Clues to the Pathogenesis of Familial Colorectal Cancer

Aaltonen, L. A., Peltomäki, P., Leach, F. S., Sistonen, P., Pylkkänen, L., Mecklin, J., Järvinen, H., Powell, S. M., Jen, J., Hamilton, S. R., et al. (1993) · Science · doi:10.1126/science.8484121 · Cited by 2,683

Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

Leach, F. S., Nicolaides, N. C., Papadopoulos, N., Liu, B., Jen, J., Parsons, R. E., Peltomäki, P., Sistonen, P., Aaltonen, L. A., Nyström, M., et al. (1993) · Cell · doi:10.1016/0092-8674(93)90330-s · Cited by 2,271

Mutation in the DNA mismatch repair gene homologue hMLH 1 is associated with hereditary non-polyposis colon cancer

Bronner, C. E., Baker, S. M., Morrison, P. T., Warren, G., Smith, L. G., Lescoe, M. K., Kane, M., Earabino, C., Lipford, J. R., Lindblom, A., et al. (1994) · Nature · doi:10.1038/368258a0 · Cited by 2,050

Mutation of a mutL Homolog in Hereditary Colon Cancer

Papadopoulos, N., Nicolaides, N. C., Wei, Y.-F., Ruben, S. M., Carter, K. C., Rosen, C. A., Haseltine, W. A., Fleischmann, R. D., Fraser, C. M., Adams, M. D., et al. (1994) · Science · doi:10.1126/science.8128251 · Cited by 1,822

Mutations of two P/WS homologues in hereditary nonpolyposis colon cancer

Nicolaides, N. C., Papadopoulos, N., Liu, B., Weit, Y.-F., Carter, K. C., Ruben, S. M., Rosen, C. A., Haseltine, W. A., Fleischmann, R. D., Fraser, C. M., et al. (1994) · Nature · doi:10.1038/371075a0 · Cited by 1,543

The distribution of the numbers of mutants in bacterial populations

Lea, D. E., & Coulson, C. A. (1949) · Journal of Genetics · doi:10.1007/bf02986080 · Cited by 1,450

Destabilization of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair

Strand, M. K., Prolla, T. A., Liskay, R. M., & Petes, T. D. (1993) · Nature · doi:10.1038/365274a0 · Cited by 1,090

Hypermutability and mismatch repair deficiency in RER+ tumor cells

Parsons, R. E., Li, G., Longley, M. J., Fang, W.-H., Papadopoulos, N., Jen, J., de la Chapelle, A., Kinzler, K. W., Vogelstein, B., & Modrich, P. L. (1993) · Cell · doi:10.1016/0092-8674(93)90331-j · Cited by 1,054

Microsatellite Instability Detection: The Current Standards, Limitations, and Misinterpretations

Yakushina, V. D., Kavun, A., Михайлович, В. Е., Grigoreva, T. V., Belova, E., Lebedeva, A., Mileyko, V., & Ivanov, M. V. (2023) · JCO Precision Oncology · doi:10.1200/po.23.00010 · Cited by 14

Mutation Rate Evolution in Partially Selfing and Partially Asexual Organisms

Gervais, C., & Roze, D. (2017) · Genetics · doi:10.1534/genetics.117.300346 · Cited by 14

Identification of MLH2/hPMS1 dominant mutations that prevent DNA mismatch repair function

Reyes, G. X., Zhao, B., Schmidt, T. T., Gries, K., Kloor, M., & Hombauer, H. (2020) · Communications Biology · doi:10.1038/s42003-020-01481-4 · Cited by 14

Evolutionarily conserved genetic interactions with budding and fission yeast MutS identify orthologous relationships in mismatch repair-deficient cancer cells

Tosti, E., Katakowski, J. A., Schaetzlein, S., Kim, H. S., Ryan, C. J., Shales, M., Roguev, A., Krogan, N. J., Palliser, D., Keogh, M., et al. (2014) · Genome Medicine · doi:10.1186/preaccept-1168696978117141 · Cited by 14

The hyper unequal sister chromatid recombination in an sgs1 mutant of budding yeast requires MSH2

Onoda, F., Seki, M., Wang, W., & Enomoto, T. (2004) · DNA repair · doi:10.1016/j.dnarep.2004.05.008 · Cited by 14

Characterization of Pathogenic Human MSH2 Missense Mutations Using Yeast as a Model System: A Laboratory Course in Molecular Biology

Gammie, A. E., & Erdeniz, N. (2004) · Cell Biology Education · doi:10.1187/cbe.03-08-0006 · Cited by 14

Correction: Mutator Suppression and Escape from Replication Error–Induced Extinction in Yeast

Herr, A. J., Ogawa, M., Lawrence, N. A., Williams, L. N., Eggington, J. M., Singh, M., Smith, R. A., & Preston, B. D. (2011) · PLoS Genetics · doi:10.1371/annotation/db1d9553-4ebd-4015-a1cd-c483dbc0d7e5 · Cited by 14

Engineered Disulfide-forming Amino Acid Substitutions Interfere with a Conformational Change in the Mismatch Recognition Complex Msh2-Msh6 Required for Mismatch Repair

Hargreaves, V. V., Putnam, C. D., & Kolodner, R. D. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.402495 · Cited by 13

Evidence That the DNA Mismatch Repair System Removes 1-Nucleotide Okazaki Fragment Flaps

Kadyrova, L. Y., Dahal, B. K., & Kadyrov, F. A. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.660357 · Cited by 13

Functional Roles of Homologous Recombination and Non-Homologous End Joining in DNA Damage Response and Microevolution in Cryptococcus neoformans

Jung, K., Jung, J., & Park, H. Y. (2021) · Journal of Fungi · doi:10.3390/jof7070566 · Cited by 14

Mlh1 interacts with both Msh2 and Msh6 for recruitment during mismatch repair

DuPrie, M. L., Palacio, T., Calil, F. A., Kolodner, R. D., & Putnam, C. D. (2022) · DNA repair · doi:10.1016/j.dnarep.2022.103405 · Cited by 13

The unstructured linker of Mlh1 contains a motif required for endonuclease function which is mutated in cancers

Torres, K. A., Calil, F. A., Zhou, A. L., DuPrie, M. L., Putnam, C. D., & Kolodner, R. D. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2212870119 · Cited by 13

Human AP endonuclease suppresses DNA mismatch repair activity leading to microsatellite instability

Chang, I. Y. (2005) · Nucleic Acids Research · doi:10.1093/nar/gki829 · Cited by 13

Mutagenesis Assays in Yeast

Crouse, G. F. (2000) · Methods · doi:10.1006/meth.2000.1051 · Cited by 13

MutSα mismatch repair protein stability is governed by subunit interaction, acetylation, and ubiquitination

Arlow, T., Kim, J., Haye, J. E., Balbás-Martínez, C., Fay, C., Zorensky, E., Rose, M. D., & Gammie, A. E. (2021) · G3 Genes Genomes Genetics · doi:10.1093/g3journal/jkaa065 · Cited by 12

Role of mismatch repair in aging

Wen, J., Wang, Y., Yuan, M., Huang, Z., Zou, Q., Pu, Y., Zhao, B., & Cai, Z. (2021) · International Journal of Biological Sciences · doi:10.7150/ijbs.64953 · Cited by 14

Aberrant DNA Methylation and Epigenetic Inactivation of hMSH2 Decrease Overall Survival of Acute Lymphoblastic Leukemia Patients via Modulating Cell Cycle and Apoptosis

Wang, C., Wang, X., Liu, H.-B., & Zhou, Z. (2014) · Asian Pacific Journal of Cancer Prevention · doi:10.7314/apjcp.2014.15.1.355 · Cited by 12

Specialized mismatch repair function of Glu339 in the Phe-X-Glu motif of yeast Msh6

Holmes, S. F., Scarpinato, K. D., McCulloch, S. D., Schaaper, R. M., & Kunkel, T. A. (2006) · DNA repair · doi:10.1016/j.dnarep.2006.10.023 · Cited by 12

Functional consequences of DNA mismatch repair missense mutations in murine models and their impact on cancer predisposition

Scherer, S. J., Avdievich, E., & Edelmann, W. (2005) · Biochemical Society Transactions · doi:10.1042/bst0330689 · Cited by 12

Humanizing mismatch repair in yeast: towards effective identification of hereditary non-polyposis colorectal cancer alleles

Aldred, P. M. R., & Borts, R. H. (2007) · Biochemical Society Transactions · doi:10.1042/bst0351525 · Cited by 12

Mutagenic specificity of the base analog 6-N-hydroxylaminopurine in the LYS2 gene of yeast Saccharomyces cerevisiae

Kulikov, V. V., Derkatch, I. L., Noskov, V. N., Tarunina, O. V., Chernoff, Y. O., Rogozin, I. B., & Pavlov, Y. I. (2001) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/s0027-5107(00)00142-1 · Cited by 12

Human mismatch-repair protein MutL homologue 1 (MLH1) interacts with Escherichia coli MutL and MutS in vivo and in vitro: a simple genetic system to assay MLH1 function

Quaresima, B., Alifano, P., Tassone, P., Avvedimento, E. V., Costanzo, F. S., & Venuta, S. (2003) · Biochemical Journal · doi:10.1042/bj20021205 · Cited by 12

Mutational Load and the Transition between Diploidy and Haploidy in Experimental Populations of the Yeast Saccharomyces cerevisiae

Śliwa, P., Kluz, J., & Korona, R. (2004) · Genetica · doi:10.1023/b:gene.0000039846.12313.98 · Cited by 12

Infrequent frameshift mutations of polynucleotide repeats in multiple primary cancers affecting the esophagus and other organs

Iwaya, T., Maesawa, C., Nishizuka, S., Suzuki, Y., Sakata, K., Sato, N., Ikeda, K., Koeda, K., Ogasawara, S., Otsuka, K., et al. (1998) · Genes Chromosomes and Cancer · doi:10.1002/(sici)1098-2264(199812)23:4 · Cited by 12

Biochemistry of Mammalian DNA Mismatch Repair

Lu, A.-L. (1998) · Humana Press eBooks · doi:10.1007/978-1-59259-455-9_7 · Cited by 12

Rad5 and Its Human Homologs, HLTF and SHPRH, Are Novel Interactors of Mismatch Repair

Miller, A. K., Mao, G., Knicely, B. G., Daniels, H. G., Rahal, C. M., Putnam, C. D., Kolodner, R. D., & Goellner, E. M. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.843121 · Cited by 11

De novo assembly, gene annotation, and marker development using Illumina paired-end transcriptome sequencing in the Crassadoma gigantea

Shanmao, C., Zhu, L., Nie, H., Yin, M., Liu, G., & Yan, X. (2018) · Gene · doi:10.1016/j.gene.2018.03.019 · Cited by 11

Heterogeneous Mutation Rates and Spectra in Yeast Hybrids

Fijarczyk, A., Hénault, M., Marsit, S., Charron, G., & Landry, C. R. (2021) · Genome Biology and Evolution · doi:10.1093/gbe/evab282 · Cited by 11

Conflicting Roles of Mismatch and Nucleotide Excision Repair in Cellular Susceptibility to Anticancer Drugs

Mello, J. A., Trimmer, E. E., Kartalou, M., & Essigmann, J. M. (1998) · Nucleic acids and molecular biology · doi:10.1007/978-3-642-48770-5_11 · Cited by 11

Saccharomyces cerevisiae pms2 Mutations Are Alleles of MLH1 , and pms2-2 Corresponds to a Hereditary Nonpolyposis Colorectal Carcinoma-Causing Missense Mutation

Jeyaprakash, A., Gupta, R. D., & Kolodner, R. D. (1996) · Molecular and Cellular Biology · doi:10.1128/mcb.16.6.3008 · Cited by 11

A conserved motif in the disordered linker of human MLH1 is vital for DNA mismatch repair and its function is diminished by a cancer family mutation

Wolf, K., Kosiński, J., Gibson, T. J., Wesch, N., Dötsch, V., Genuardi, M., Cordisco, E. L., Zeuzem, S., Brieger, A., & Plotz, G. (2023) · Nucleic Acids Research · doi:10.1093/nar/gkad418 · Cited by 10

Elevated MSH2 MSH3 expression interferes with DNA metabolism in vivo

Medina‐Rivera, M., Phelps, S. E., Sridharan, M., Becker, J. T., Lamb, N. A., Kumar, C., Sutton, M. D., Bielinsky, A., Balakrishnan, L., & Surtees, J. A. (2023) · Nucleic Acids Research · doi:10.1093/nar/gkad934 · Cited by 10

Genome-wide contributions of the MutSα- and MutSβ-dependent DNA mismatch repair pathways to the maintenance of genetic stability in Saccharomyces cerevisiae

Kadyrova, L. Y., Mieczkowski, P. A., & Kadyrov, F. A. (2023) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2023.104705 · Cited by 11

Multiplexed Guide RNA Expression Leads to Increased Mutation Frequency in Targeted Window Using a CRISPR-Guided Error-Prone DNA Polymerase in Saccharomyces cerevisiae

Gossing, M., Limeta, A., Skrekas, C., Wigglesworth, M. J., Davis, A., Siewers, V., & David, F. (2023) · ACS Synthetic Biology · doi:10.1021/acssynbio.2c00689 · Cited by 10

Mismatch Repair

Fishel, R. A., & Lee, J. (2016) · Springer eBooks · doi:10.1007/978-4-431-55873-6_12 · Cited by 10

Different frameshift mutation spectra in non-repetitive DNA of MutSα- and MutLα-deficient fission yeast cells

Marti, T. M. (2003) · DNA repair · doi:10.1016/s1568-7864(03)00023-5 · Cited by 10

Deficiency of MSH2 expression is associated with clear cell renal cell carcinoma

Yoo, K. H., Won, K. Y., Lim, S., Park, Y.-K., & Chang, S. (2014) · Oncology Letters · doi:10.3892/ol.2014.2482 · Cited by 10

C-Terminal Flap Endonuclease (rad27) Mutations: Lethal Interactions With a DNA Ligase I Mutation (cdc9-p) and Suppression by Proliferating Cell Nuclear Antigen (POL30) in Saccharomyces cerevisiae

Karanja, K. K., & Livingston, D. M. (2009) · Genetics · doi:10.1534/genetics.109.103937 · Cited by 10

Complex mutation profiles in mismatch repair and ribonucleotide reductase mutants reveal novel repair substrate specificity of MutS homolog (MSH) complexes

Lamb, N. A., Bard, J., Loll‐Krippleber, R., Brown, G. W., & Surtees, J. A. (2022) · Genetics · doi:10.1093/genetics/iyac092 · Cited by 9

Inactivation of folylpolyglutamate synthetase Met7 results in genome instability driven by an increased dUTP/dTTP ratio

Schmidt, T. T., Sharma, S., Reyes, G. X., Kolodziejczak, A. S., Wagner, T., Luke, B., Hofer, A., Chabes, A., & Hombauer, H. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz1006 · Cited by 9

Antisense inhibition of hMLH1 is not sufficient for loss of DNA mismatch repair function in the HCT116+chromosome 3 cell line.

Chauhan, D. P., Yang, Q., Carethers, J. M., Marra, G., Chang, C. L., Chamberlain, S. M., & Boland, C. R. (2000) · PubMed · Cited by 9

The Effects of Mismatch Repair and RAD1 Genes on Interchromosomal Crossover Recombination in Saccharomyces cerevisiae

Nicholson, A. C., Fabbri, R. M., Reeves, J., & Crouse, G. F. (2006) · Genetics · doi:10.1534/genetics.105.055244 · Cited by 9

Cloning of the cDNA encoding rat homologue of the mismatch repair gene MSH2 and its expression during spermatogenesis

Vani, R. G., & Rao, M. R. S. (1997) · Gene · doi:10.1016/s0378-1119(96)00622-1 · Cited by 9

Nanostructured Hybrid Organic/Inorganic Materials, Silsesquioxane Modified Plastics

Haddad, T. S., Stapleton, R. L., Jeon, H. G., Mather, P. T., & Lichtenhan, J. D. (1996) · doi:10.21236/ada386916 · Cited by 9

Fibroblast growth factor-1 stimulation of quiescent NIH 3T3 cells increases G/T mismatch-binding protein expression

Donohue, P. J., Feng, S.-L. Y., Alberts, G. F., Guo, Y. H., Peifley, K. A., Hsu, D. K. W., & Winkles, J. A. (1996) · Biochemical Journal · doi:10.1042/bj3190009 · Cited by 9

Emerging role of PES1 in disease: A promising therapeutic target?

Yuan, S., Xu, N., Yang, J., & Yuan, B. (2024) · Gene · doi:10.1016/j.gene.2024.148896 · Cited by 8

Mutagenic and Recombinagenic Responses to Defective DNA Polymerase δ Are Facilitated by the Rev1 Protein in pol3-t Mutants of Saccharomyces cerevisiae

Mito, E., Mokhnatkin, J. V., Steele, M. C., Buettner, V. L., Sommer, S. S., Manthey, G. M., & Bailis, A. M. (2008) · Genetics · doi:10.1534/genetics.108.089821 · Cited by 8

DNA Rereplication Is Susceptible to Nucleotide-Level Mutagenesis

Bui, D. T., & Li, J. J. (2019) · Genetics · doi:10.1534/genetics.119.302194 · Cited by 8

The Corynebacterium pseudotuberculosis genome contains two formamidopyrimidine-DNA glycosylase enzymes, only one of which recognizes and excises 8-oxoguanine lesion

Arantes, L. S., Nova, L. G. V., Resende, B. C., Bitar, M., Coelho, I. E. V., Miyoshi, A., Azevedo, V., dos Santos, L. L., Machado, C. R., & Lopes, D. D. O. (2015) · Gene · doi:10.1016/j.gene.2015.08.065 · Cited by 8

Msh2 Blocks an Alternative Mechanism for Non-Homologous Tail Removal during Single-Strand Annealing in Saccharomyces cerevisiae

Manthey, G. M., Naik, N., & Bailis, A. M. (2009) · PLoS ONE · doi:10.1371/journal.pone.0007488 · Cited by 8

Genomic amplification of the human DHFR/MSH3 locus remodels mismatch recognition and repair activities

Drummond, J. T. (1999) · Advances in Enzyme Regulation · doi:10.1016/s0065-2571(98)00013-2 · Cited by 8

Analysis of microsatellite instability in cervical cancer

Ou, Chang, Tseng, Wei, Su, Hsu, Chang, & Lee (1999) · International Journal of Gynecological Cancer · doi:10.1046/j.1525-1438.1999.09800.x · Cited by 8

Inadequate "Caretaker" Gene Function and Human Cancer Development

DeWeese, T. L., & Nelson, W. G. (2003) · Humana Press eBooks · doi:10.1385/1-59259-328-3:249 · Cited by 8

Review

(1996) · Biological Chemistry Hoppe-Seyler · doi:10.1515/bchm3.1996.377.11.675 · Cited by 8

Computational Analysis of Deleterious Single Nucleotide Polymorphisms (SNPs) in Human MutS Homolog6 (MSH6) Gene

Abdelraheem, N. E., Osman, M. M., Elgemaabi, O. M., FadlAlla, A. A., Alla, F., Ismail, M. M., Osman, S. A., Ibrahim, A. I., Babekir, N. E., Mekki, S. O., et al. (2016) · American Journal of Bioinformatics Research · Cited by 7

Interpreting Sequence Variation in PDAC-Predisposing Genes Using a Multi-Tier Annotation Approach Performed at the Gene, Patient, and Cohort Level

Zimmermann, M. T., Mathison, A., Stodola, T. J., Evans, D. B., Abrudan, J., Demos, W., Tschannen, M., Aldakkak, M., Geurts, J. L., Lomberk, G. A., et al. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.606820 · Cited by 7

Resolution of sequence divergence for repeat-mediated deletions shows a polarity that is mediated by MLH1

Trost, H., Merkell, A., Lopezcolorado, F. W., & Stark, J. M. (2023) · Nucleic Acids Research · doi:10.1093/nar/gkac1240 · Cited by 7

Defects in Base Excision Repair Sensitize Cells to Manganese inS. cerevisiae

Stephenson, A. P., Mazu, T. K., Miles, J. S., Freeman, M. D., Reams, R., & Flores‐Rozas, H. (2013) · BioMed Research International · doi:10.1155/2013/295635 · Cited by 7

A role for synaptonemal complex in meiotic mismatch repair

Voelkel‐Meiman, K., Oke, A., Feil, A., Shames, A. I., Fung, J. C., & MacQueen, A. J. (2021) · Genetics · doi:10.1093/genetics/iyab230 · Cited by 7

Cloning of Rat MLH1 and Expression Analysis of MSH2, MSH3, MSH6, and MLH1 during Spermatogenesis

Vani, R. G., Varghese, C. M., & Rao, M. R. S. (1999) · Genomics · doi:10.1006/geno.1999.6038 · Cited by 7

The DNA mismatch repair pathway

Martin, S. A. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-803582-5.00006-1 · Cited by 7

Molecular events after antisense inhibition of hMSH2 in a HeLa cell line

Qian, Y., Yu, Y., Cheng, X., Luo, J., Xie, H., & Shen, B. (1998) · Mutation Research/Genetic Toxicology and Environmental Mutagenesis · doi:10.1016/s1383-5718(98)00108-9 · Cited by 7

Viral characteristics of human papillomavirus infection and antioxidant levels as risk factors for cervical dysplasia

Ho, G., Palan, P. R., Basu, J., Romney, S. L., Kadish, A. S., Mikhail, M. S., Wassertheil‐Smoller, S., Runowicz, C. D., & Burk, R. D. (1998) · International Journal of Cancer · doi:10.1002/(sici)1097-0215(19981123)78:5 · Cited by 84

Microsatellite instability in colitis associated colorectal cancer

Itzkowitz, S. H. (2000) · Gut · doi:10.1136/gut.46.3.304 · Cited by 6

Involvement of DNA mismatch repair in the maintenance of heterochromatic DNA stability in Saccharomyces cerevisiae

Dahal, B. K., Kadyrova, L. Y., Delfino, K. R., Rogozin, I. B., Gujar, V. V., Lobachev, K. S., & Kadyrov, F. A. (2017) · PLoS Genetics · doi:10.1371/journal.pgen.1007074 · Cited by 6

Molecular Analysis of Carbon Ion-Induced Mutations in DNA Repair-Deficient Strains of Saccharomyces cerevisiae

Matuo, Y., Izumi, Y., Sakamoto, A. N., Hase, Y., Satoh, K., & Shimizu, K. (2019) · Quantum Beam Science · doi:10.3390/qubs3030014 · Cited by 6

Mutation spectrum of MSH3-deficient HHUA/chr.2 cells reflects in vivo activity of the MSH3 gene product in mismatch repair

Tauchi, H., Komatsu, K., Ishizaki, K., Yatagai, F., & Kato, T. (2000) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/s0027-5107(99)00199-2 · Cited by 6

OXIDATIVE DAMAGE AND COUNTERACTING MECHANISMS IN BREAST CARCINOMA

Karihtala, P., & Karihtala (2005) · Cited by 6

Genetically engineered mouse models for hereditary cancer syndromes

Biswas, K., Mohammed, A., Sharan, S. K., & Shoemaker, R. H. (2023) · Cancer Science · doi:10.1111/cas.15737 · Cited by 5

Normally lethal amino acid substitutions suppress an ultramutator DNA Polymerase δ variant

Dennis, D. G., McKay-Fleisch, J., Eitzen, K., Dowsett, I. T., Kennedy, S. R., & Herr, A. J. (2017) · Scientific Reports · doi:10.1038/srep46535 · Cited by 5

Genetic requirements for repair of lesions caused by single genomic ribonucleotides in S phase

Schindler, N., Tonn, M., Kellner, V., Fung, J. J., Lockhart, A., Vydzhak, O., Juretschke, T., Möckel, S., Beli, P., Khmelinskii, A., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-36866-6 · Cited by 5

High-Level Production of MSH2 from Arabidopsis thaliana: A DNA Mismatch Repair System Key Subunit

Gómez, R., Galles, C., & Spampinato, C. P. (2010) · Molecular Biotechnology · doi:10.1007/s12033-010-9319-9 · Cited by 5

Cloning of the PpMSH-2 cDNA of Physcomitrella patens, a moss in which gene targeting by homologous recombination occurs at high frequency

Brun, F., Gonneau, M., Doutriaux, M.-P., Laloue, M., & Nogué, F. (2001) · Biochimie · doi:10.1016/s0300-9084(01)01350-5 · Cited by 5

Detection of Mismatch Repair Deficiency in Endometrial Cancer: Assessment of IHC, Fragment Length Analysis, and Amplicon Sequencing Based MSI Testing

Sowter, P., Gallon, R., Hayes, C. M., Phelps, R., Borthwick, G. M., Prior, S., Combe, J., Buist, H., Pearlman, R., Hampel, H., et al. (2024) · Cancers · doi:10.3390/cancers16233970 · Cited by 4

Miniplatforms for Screening Biological Samples for KRAS and Four Mismatch Repair Proteins as New Tools for Fast Screening for Gastric and Colon Cancers

Staden, R. S., Bratei, A. A., Ilie‐Mihai, R., Gheorghe, D., Tuchiu-Stanca, B.-M., & Gurzu, S. (2023) · Journal of The Electrochemical Society · doi:10.1149/1945-7111/acd358 · Cited by 4

Effects of CDC45 mutations on DNA replication and genome stability

Denkiewicz-Kruk, M., Chaudhry, D., Krasilia, A., Jedrychowska, M., Fijałkowska, I. J., & Dmowski, M. (2025) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2025.119936 · Cited by 4

Somatic hypermutation and mismatch repair in non-B cells

Klasen, M., Spillmann, F. J. X., Marra, G., Ćejka, P., & Wabl, M. R. (2005) · European Journal of Immunology · doi:10.1002/eji.200526221 · Cited by 4

Molecular Basis of Diseases of the Gastrointestinal Tract

Sepulveda, A. R., & Aisner, D. L. (2009) · Elsevier eBooks · doi:10.1016/b978-0-12-374419-7.00019-6 · Cited by 4

Tumor Suppressor Genes

Plank, T. L., & Henske, E. P. (2000) · doi:10.1007/978-1-4684-8437-3_3 · Cited by 4

Diversity of mechanisms and functions of enzyme systems of DNA repair in Drosophila melanogaster

Chmuzh, E. V., Шестакова, Л. А., Volkova, V. S., & Захаров, И. К. (2006) · Russian Journal of Genetics · doi:10.1134/s1022795406040028 · Cited by 4

A Whole Genome Screen for Minisatellite Stability Genes in Stationary-Phase Yeast Cells

Alver, B., Jauert, P. A., Brosnan, L., O’Hehir, M., VanderSluis, B., Myers, C. L., & Kirkpatrick, D. T. (2013) · G3 Genes Genomes Genetics · doi:10.1534/g3.112.005397 · Cited by 4

(CA/TG) Microsatellite Sequences Escape the Inhibition of Recombination by Mismatch Repair in Saccharomyces cerevisiae

Gendrel, C.-G., & Dutreix, M. (2001) · Genetics · doi:10.1093/genetics/159.4.1539 · Cited by 4

Genetic Engineering in Potato Improvement

Rákosy-Tican, E. (2013) · CRC Press eBooks · doi:10.1201/b16352-6 · Cited by 4

Schizosaccharomyces pombeMutSα and MutLα Maintain Stability of Tetra-Nucleotide Repeats and Msh3 of Hepta-Nucleotide Repeats

Villahermosa, D., Christensen, O., Knapp, K., & Fleck, O. (2017) · G3 Genes Genomes Genetics · doi:10.1534/g3.117.040816 · Cited by 4

Investigation of G2-phase chromosomal radiosensitivity in hereditary non-polyposis colorectal cancer cells

Franchitto, A., Pichierri, P., Genuardi, M., Santis, A. D., & Palitti, F. (2001) · International Journal of Radiation Biology · doi:10.1080/09553000110050056 · Cited by 4

The Yeast HSM3 Gene Is Not Involved in DNA Mismatch Repair in Rapidly Dividing Cells

Merker, J. D., Datta, A., Kolodner, R. D., & Petes, T. D. (2000) · Genetics · doi:10.1093/genetics/154.1.491 · Cited by 4

DNA mismatch repair mediated by Mlh1–Pms1 endonuclease-catalyzed mispair excision

Palacio, T., Calil, F. A., Bowen, N., Griffith, J. D., Putnam, C. D., & Kolodner, R. D. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2528670122 · Cited by 3

Hereditary non-polyposis colorectal cancer syndrome: combined risk of gastrointestinal and gynaecological cancer

Sharma, A. K., James, M., Donaldson, A., & Fox, R. (2001) · BJOG An International Journal of Obstetrics & Gynaecology · doi:10.1016/s0306-5456(00)00174-1 · Cited by 3

Msh2-Msh3 DNA-binding is not sufficient to promote trinucleotide repeat expansions in Saccharomyces cerevisiae

Casazza, K., Williams, G. M., Johengen, L., Twoey, G., & Surtees, J. A. (2025) · Genetics · doi:10.1093/genetics/iyae222 · Cited by 2

Omics Approaches in Tropical Fruit Crops

Ravishankar, K. V., Kanupriya, P., Rekha, P. D., Upadhyay, P., Vasugi, P., Vijayakumari, P., Kishnani, P., & Dinesh, M. R. (2013) · CRC Press eBooks · doi:10.1201/b16352-10 · Cited by 2

Evidence that DNA polymerase δ proofreads errors made by DNA polymerase α across the Saccharomyces cerevisiae nuclear genome

Marks, S. A., Zhou, Z.-X., Lujan, S. A., Burkholder, A., & Kunkel, T. A. (2024) · DNA repair · doi:10.1016/j.dnarep.2024.103768 · Cited by 2

Exploiting the distinctive properties of the bacterial and human MutS homolog sliding clamps on mismatched DNA

Britton, B. M., London, J. A., Martín-López, J., Jones, N. D., Liu, J., Lee, J., & Fishel, R. A. (2022) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2022.102505 · Cited by 2

Fast Revelation of the Motif Mode for a Yeast Protein Interaction Network Through Intelligent Agent-Based Distributed Computing

Lee, W.-P., & Tzou, W. (2010) · Protein and Peptide Letters · doi:10.2174/092986610791760441 · Cited by 2

Mechanism of DNA Mismatch Repair from Bacteria to Human

Acharya, S., & Fishel, R. A. (2005) · CRC Press eBooks · doi:10.1201/9780849352683.pt4 · Cited by 2

Lynch syndrome diagnostics: decision-making process for germ-line testing

Lastra, E., García-González, M. A., Llorente, B., Bernuy, C., Barrio, M. J., Pérez‐Cabornero, L., Durán, M., & Girón, C. G. (2012) · Clinical & Translational Oncology · doi:10.1007/s12094-012-0793-3 · Cited by 2

Genetics of DNA Mismatch Repair, Microsatellite Instability, and Cancer

Prolla, T. A., Baker, S. M., & Liskay, R. M. (1998) · Humana Press eBooks · doi:10.1007/978-1-59259-455-9_20 · Cited by 2

Ploidy and the Sexual Yeast Genome in Theory, Nature, and Experiment

Zeyl, C. (2014) · ASM Press eBooks · doi:10.1128/9781555815837.ch31 · Cited by 2

The role of DNA polymerases, in particular DNA polymerase ε in DNA repair and replication

Pospiech, H. (2002) · Cited by 2

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Pan, F. (2014) · FIU - Digital Commons (Florida International University) · doi:10.25148/etd.fi15032103 · Cited by 2

Single-molecule FRET Studies on DNA Mismatch Repair

Hanne, J., Liu, J., Lee, J., & Fishel, R. A. (2013) · Open Access System for Information Sharing (Pohang University of Science and Technology) · doi:10.5923/s.biophysics.201311.03 · Cited by 1

Novel dominant mutations in Saccharomyces cerevisiae MSH6

Gupta, R. D., & Kolodner, R. D. (2000) · Nature Genetics · doi:10.1038/71684 · Cited by 66

A Mutation in the MSH6 Subunit of the Saccharomyces cerevisiae MSH2-MSH6 Complex Disrupts Mismatch Recognition

Bowers, J., Sokolsky, T. D., Quach, T., & Alani, E. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.23.16115 · Cited by 95

MSH6, a Saccharomyces cerevisiae protein that binds to mismatches as a heterodimer with MSH2

Iaccarino, I., Palombo, F., Drummond, J. T., Totty, N. F., Hsuan, J. J., Modrich, P. L., & Jiricny, J. (1996) · Current Biology · doi:10.1016/s0960-9822(02)00516-x · Cited by 100

Analysis of in vivo correction of defined mismatches in the DNA mismatch repair mutants msh2, msh3 and msh6 of Saccharomyces cerevisiae

Lühr, B., Scheller, J., Meyer, P. T., & Kramer, W. (1998) · Molecular and General Genetics MGG · doi:10.1007/s004380050658 · Cited by 26

MutS homologs in mammalian cells

Fishel, R. A., & Wilson, T. (1997) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(97)80117-7 · Cited by 161