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

Risks at the DNA Replication Fork: Effects upon Carcinogenesis and Tumor Heterogeneity

Mertz, T. M., Harcy, V., & Roberts, S. A. (2017) · Genes · doi:10.3390/genes8010046 · Cited by 34

Reconstitution of Saccharomyces cerevisiae DNA polymerase ε-dependent mismatch repair with purified proteins

Bowen, N., & Kolodner, R. D. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1701753114 · Cited by 33

Heteroduplex DNA in Meiotic Recombination in Drosophila mei-9 Mutants

Radford, S. J., McMahan, S., Blanton, H. L., & Sekelsky, J. J. (2007) · Genetics · doi:10.1534/genetics.107.070557 · Cited by 32

Functions of Multiple Clamp and Clamp-Loader Complexes in Eukaryotic DNA Replication

Ohashi, E., & Tsurimoto, T. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-981-10-6955-0_7 · Cited by 34

Conformations of an Adenine Bulge in a DNA Octamer and Its Influence on DNA Structure from Molecular Dynamics Simulations

Feig, M., Zacharias, M., & Pettitt, B. M. (2001) · Biophysical Journal · doi:10.1016/s0006-3495(01)75705-0 · Cited by 32

Proper functioning of the GINS complex is important for the fidelity of DNA replication in yeast

Grabowska, E. A., Wronska, U., Denkiewicz-Kruk, M., Jaszczur, M. M., Respondek, A., Alabrudzińska, M., Suski, C., Makiela‐Dzbenska, K., Jonczyk, P., & Fijałkowska, I. J. (2014) · Molecular Microbiology · doi:10.1111/mmi.12580 · Cited by 31

Why do mammalian mitochondria possess a mismatch repair activity?

Mason, P. A., & Lightowlers, R. N. (2003) · FEBS Letters · doi:10.1016/s0014-5793(03)01169-4 · Cited by 31

Differential effects of the mismatch repair genes

Selva, E. M., Maderazo, A. B., & Lahue, R. S. (1997) · Molecular and General Genetics MGG · doi:10.1007/pl00008619 · Cited by 31

Cellular resistance and hypermutability in mismatch repair-deficient human cancer cell lines following treatment with methyl methanesulfonate

Glaab, W. E., Risinger, J. I., Umar, A., Barrett, J. C., Kunkel, T. A., & Tindall, K. R. (1998) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/s0027-5107(98)00004-9 · Cited by 31

Application of molecular diagnostics for the detection of Lynch syndrome

Pino, M. S., & Chung, D. C. (2010) · Expert Review of Molecular Diagnostics · doi:10.1586/erm.10.45 · Cited by 30

Biochemical basis for dominant mutations in the Saccharomyces cerevisiae MSH6 gene

Heß, M., Mendillo, M. L., Mazur, D. J., & Kolodner, R. D. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0510078103 · Cited by 30

DNA polymerase δ proofreads errors made by DNA polymerase ε

Bulock, C. R., Xing, X., & Shcherbakova, P. V. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1917624117 · Cited by 30

Overlapping contributions of Msh1p and putative recombination proteins Cce1p, Din7p, and Mhr1p in large-scale recombination and genome sorting events in the mitochondrial genome of Saccharomyces cerevisiae

Mookerjee, S. A., & Sia, E. A. (2005) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2005.10.006 · Cited by 32

Opposing roles for DNA structure‐specific proteins Rad1, Msh2, Msh3, and Sgs1 in yeast gene targeting

Langston, L. D., & Symington, L. S. (2005) · The EMBO Journal · doi:10.1038/sj.emboj.7600698 · Cited by 30

Alleles of the Yeast PMS1 Mismatch-Repair Gene That Differentially Affect Recombination- and Replication-Related Processes

Welz-Voegele, C., Stone, J. E., Tran, P. T., Kearney, H. M., Liskay, R. M., Petes, T. D., & Jinks-Robertson, S. (2002) · Genetics · doi:10.1093/genetics/162.3.1131 · Cited by 31

Mismatch repair and immunoglobulin gene hypermutation: did we learn something?

Reynaud, C., Bertocci, B., Frey, S., Delbos, F., Quint, L., & Weill, J. (1999) · Immunology Today · doi:10.1016/s0167-5699(99)01540-6 · Cited by 30

Effective mismatch repair depends on timely control of PCNA retention on DNA by the Elg1 complex

Devakumar, L. J. P. S., Gaubitz, C., Lundblad, V., Kelch, B. A., & Kubota, T. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz441 · Cited by 29

Mutational spectrum analysis of RNase H(35) deficient Saccharomyces cerevisiae using fluorescence-based directed termination PCR

Chen, J. Z. (2000) · Nucleic Acids Research · doi:10.1093/nar/28.18.3649 · Cited by 29

Efficient repair of large DNA loops in Saccharomyces cerevisiae

Corrette-Bennett, S. E. (2001) · Nucleic Acids Research · doi:10.1093/nar/29.20.4134 · Cited by 29

Pathogenesis and clinical management of hereditary non-polyposis colorectal cancer

Lawes, D., SenGupta, S. B., & Boulos, P. B. (2002) · British journal of surgery · doi:10.1046/j.1365-2168.2002.02290.x · Cited by 29

Identification of a Mutant DNA Polymerase δ in Saccharomyces cerevisiae With an Antimutator Phenotype for Frameshift Mutations

Hadjimarcou, M., Kokoska, R. J., Petes, T. D., & Reha-Krantz, L. J. (2001) · Genetics · doi:10.1093/genetics/158.1.177 · Cited by 29

Replication-dependent and selection-induced mutations in respiration-competent and respiration-deficient strains of Saccharomyces cerevisiae

Heidenreich, E., & Wintersberger, U. (1998) · Molecular and General Genetics MGG · doi:10.1007/s004380050909 · Cited by 30

Mismatch repair protein expression and microsatellite instability: a comparison of clear cell sarcoma of soft parts and metastatic melanoma

García, J. J., Kramer, M. J., O’Donnell, R. J., & Horvai, A. (2006) · Modern Pathology · doi:10.1038/modpathol.3800611 · Cited by 28

Molecular cloning and characterization of the DNA mismatch repair gene class 2 from the Trypanosoma cruzi

Augusto-Pinto, L., Bartholomeu, D. C., Teixeira, S. M. R., Pena, S. D. J., & Machado, C. R. (2001) · Gene · doi:10.1016/s0378-1119(01)00549-2 · Cited by 28

Correction of Large Mispaired DNA Loops by Extracts ofSaccharomyces cerevisiae

Corrette-Bennett, S. E., Parker, B. O., Mohlman, N. L., & Lahue, R. S. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.25.17605 · Cited by 28

Anti-recombination function of MutSα restricts telomere extension by ALT-associated homology-directed repair

González, J. B., García-Expósito, L., Galaviz, P., Lynskey, M. L., Allen, J. A. M., Hoang, S. M., Watkins, S. C., Pickett, H. A., & O’Sullivan, R. J. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.110088 · Cited by 28

Genetic predisposition and somatic diversification in tumor development and progression

Shibata, D. K., & Aaltonen, L. A. (2001) · Advances in cancer research · doi:10.1016/s0065-230x(01)80013-0 · Cited by 27

Control of GT Repeat Stability in Schizosaccharomyces pombe by Mismatch Repair Factors

Mansour, A. A., Tornier, C., Lehmann, E., Darmon, M. Y., & Fleck, O. (2001) · Genetics · doi:10.1093/genetics/158.1.77 · Cited by 27

MutSβ Stimulates Holliday Junction Resolution by the SMX Complex

Young, S. J., Sebald, M., Punatar, R. S., Larin, M., Masino, L., Rodrigo-Brenni, M. C., Liang, C., & West, S. C. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.108289 · Cited by 29

Identification and characterization of the mouse MutS homolog 5: Msh5

Her, C. (1999) · Mammalian Genome · doi:10.1007/s003359901161 · Cited by 27

MSH2 missense mutations alter cisplatin cytotoxicity and promote cisplatin-induced genome instability

Clodfelter, J. E. (2005) · Nucleic Acids Research · doi:10.1093/nar/gki646 · Cited by 27

Mutations of the 'minor' mismatch repair gene MSH6 in typical and atypical hereditary nonpolyposis colorectal cancer

Cordisco, E. L., Rovella, V., Carrara, S., Percesepe, A., Pedroni, M., Bellacosa, A., Caluseriu, O., Forasarig, M., Anti, M., Neri, G., et al. (2001) · Familial Cancer · doi:10.1023/a:1013872914474 · Cited by 27

Roles of the DNA mismatch repair and nucleotide excision repair proteins during meiosis

Kirkpatrick, D. T. (1999) · Cellular and Molecular Life Sciences · doi:10.1007/s000180050300 · Cited by 27

CYS3, a Hotspot of Meiotic Recombination in Saccharomyces cerevisiae: Effects of Heterozygosity and Mismatch Repair Functions on Gene Conversion and Recombination Intermediates

Vedel, M., & Nicolas, A. G. (1999) · Genetics · doi:10.1093/genetics/151.4.1245 · Cited by 27

The properties of Msh2–Msh6 ATP binding mutants suggest a signal amplification mechanism in DNA mismatch repair

Graham, W. J., Putnam, C. D., & Kolodner, R. D. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.005439 · Cited by 26

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

Genetic evidence for the involvement of mismatch repair proteins, PMS2 and MLH3, in a late step of homologous recombination

Rahman, M. M., Mohiuddin, M., Keka, I. S., Yamada, K., Tsuda, M., Sasanuma, H., Andréani, J., Guérois, R., Borde, V., Charbonnier, J., et al. (2020) · Journal of Biological Chemistry · doi:10.1074/jbc.ra120.013521 · Cited by 25

Saccharomyces cerevisiae Msh2-Msh6 DNA binding kinetics reveal a mechanism of targeting sites for DNA mismatch repair

Zhai, J., & Hingorani, M. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0908302107 · Cited by 25

DNA Mismatch Repair Gene Variants in Sporadic Solid Cancers

Čaja, F., Vodičková, Ľ., Král, J., Vymetalkova, V. P., Naccarati, A., & Vodička, P. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21155561 · Cited by 25

Rad27 and Exo1 function in different excision pathways for mismatch repair in Saccharomyces cerevisiae

Calil, F. A., Li, B.-Z., Torres, K. A., Nguyen, K. G., Bowen, N., Putnam, C. D., & Kolodner, R. D. (2021) · Nature Communications · doi:10.1038/s41467-021-25866-z · Cited by 25

Mouse MutS homolog 4 is predominantly expressed in testis and interacts with MutS homolog 5

Her, C., Wu, X., Bailey, S. M., & Doggett, N. A. (2001) · Mammalian Genome · doi:10.1007/s003350010231 · Cited by 25

Conditional nuclear localization of hMLH3 suggests a minor activity in mismatch repair and supports its role as a low-risk gene in HNPCC

Korhonen, M. K., Raevaara, T. E., Lohi, H., & Nyström, M. (2007) · Oncology Reports · doi:10.3892/or.17.2.351 · Cited by 25

Identification of a Distinctive Mutation Spectrum Associated with High Levels of Transcription in Yeast

Lippert, M. J., Freedman, J. A., Barber, M. A., & Jinks-Robertson, S. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.11.4801-4809.2004 · Cited by 26

MSH6 immunohistochemical heterogeneity in colorectal cancer: comparative sequencing from different tumor areas

Chen, W., Pearlman, R., Hampel, H., Pritchard, C. C., Markow, M., Arnold, C. A., Knight, D. A., & Frankel, W. L. (2019) · Human Pathology · doi:10.1016/j.humpath.2019.11.003 · Cited by 24

Detection of Heterozygous Mutations in the Genome of Mismatch Repair Defective Diploid Yeast Using a Bayesian Approach

Zanders, S. E., Ma, X., RoyChoudhury, A., Hernandez, R. D., Demogines, A., Barker, B., Gu, Z., Bustamante, C. D., & Alani, E. (2010) · Genetics · doi:10.1534/genetics.110.120105 · Cited by 24

REVIEWS IN BASIC AND CLINICAL GASTROENTEROLOGY

Lynch, J. P., Metz, D. C., Schuppan, D., Junker, Y., & Barisani, D. (2009) · Cited by 24

Antimutator variants of DNA polymerases

Herr, A. J., Williams, L. N., & Preston, B. D. (2011) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.3109/10409238.2011.620941 · Cited by 24

Functional genetic tests of DNA mismatch repair protein activity in Saccharomyces cerevisiae

Polaczek, P., Putzke, A. P., Leong, K., & Bitter, G. A. (1998) · Gene · doi:10.1016/s0378-1119(98)00150-4 · Cited by 24

Genomic Instability Induced by Mutations in Saccharomyces cerevisiae POL1

Gutiérrez, P. J. A., & Wang, T. S. ‐. (2003) · Genetics · doi:10.1093/genetics/165.1.65 · Cited by 24

Spectrum of DNA mismatch repair failures viewed through the lens of cancer genomics and implications for therapy

Mas-Ponte, D., McCullough, M., & Supek, F. (2022) · Clinical Science · doi:10.1042/cs20210682 · Cited by 24

Mismatch recognition function of Arabidopsis thaliana MutSγ

Gómez, R., & Spampinato, C. P. (2013) · DNA repair · doi:10.1016/j.dnarep.2013.01.002 · Cited by 23

Role of microsatellite instability-low as a diagnostic biomarker of Lynch syndrome in colorectal cancer

Vilar, E., Mork, M. E., Cuddy, A., Borràs, E., Bannon, S. A., Taggart, M. W., Ying, B., Broaddus, R. R., Luthra, R., Rodrı́guez-Bigas, M. A., et al. (2014) · Cancer Genetics · doi:10.1016/j.cancergen.2014.10.002 · Cited by 23

The role of mismatch repair in small-cell lung cancer cells

Hansen, L. T., Thykjær, T., Orntoft, T. F., Rasmussen, L. J., Keller, P., Spang‐Thomsen, M., Edmonston, T. B., Schmütte, C., Fishel, R. A., & Pétersen, L. N. (2003) · European Journal of Cancer · doi:10.1016/s0959-8049(03)00306-x · Cited by 23

Bacterial DNA repair genes and their eukaryotic homologues: 2. Role of bacterial mutator gene homologues in human disease. Overview of nucleotide pool sanitization and mismatch repair systems.

Arczewska, K. D., & Kuśmierek, J. T. (2007) · Acta Biochimica Polonica · doi:10.18388/abp.2007_3220 · Cited by 23

Research on Plants for the Understanding of Diseases of Nuclear and Mitochondrial Origin

Spampinato, C. P., & Gomez‐Casati, D. F. (2012) · BioMed Research International · doi:10.1155/2012/836196 · Cited by 22

A new transgene assay to study microsatellite instability in wild-type and mismatch-repair defective plant progenies

Depeiges, A., Farget, S., Degroote, F., & Picard, G. (2004) · Plant Science · doi:10.1016/j.plantsci.2004.11.006 · Cited by 22

Mutation Rates of TGFBR2 and ACVR2 Coding Microsatellites in Human Cells with Defective DNA Mismatch Repair

Chung, H., Young, D. J., López, C. G., Le, T.-A. T., Lee, J. K., Ream-Robinson, D., Huang, S. C., & Carethers, J. M. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003463 · Cited by 22

The Genetics of Colorectal Cancer

Hankey, W., & Groden, J. L. (2013) · Springer eBooks · doi:10.1007/978-1-4614-8412-7_1 · Cited by 21

Requirement for Msh6, but Not for Swi4 (Msh3), in Msh2-Dependent Repair of Base-Base Mismatches and Mononucleotide Loops in Schizosaccharomyces pombe

Tornier, C., Bessone, S., Varlet, I., Rudolph, C., Darmon, M. Y., & Fleck, O. (2001) · Genetics · doi:10.1093/genetics/158.1.65 · Cited by 21

Novel PMS1 Alleles Preferentially Affect the Repair of Primer Strand Loops during DNA Replication

Erdeniz, N., Dudley, S., Gealy, R., Jinks-Robertson, S., & Liskay, R. M. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.21.9221-9231.2005 · Cited by 21

Eukaryotic Mismatch Repair

Schär, P., & Jiricny, J. (1998) · Nucleic acids and molecular biology · doi:10.1007/978-3-642-48770-5_10 · Cited by 21

Molecular adaptations to heat stress in the thermophilic ant genus Cataglyphis

Perez, R., Araujo, N. D. S., Defrance, M., & Aron, S. (2021) · Molecular Ecology · doi:10.1111/mec.16134 · Cited by 20

Distinct Structural Alterations in Proliferating Cell Nuclear Antigen Block DNA Mismatch Repair

Dieckman, L. M., Boehm, E. M., Hingorani, M., & Washington, M. T. (2013) · Biochemistry · doi:10.1021/bi400378e · Cited by 20

Meiotic segregation of a homeologous chromosome pair

Boumil, R. M., Kemp, B., Angelichio, M. J., Nilsson‐Tillgren, T., & Dawson, D. (2003) · Molecular Genetics and Genomics · doi:10.1007/s00438-002-0796-9 · Cited by 20

The yeast MSH1 gene is not involved in DNA repair or recombination during meiosis

Sia, E. A., & Kirkpatrick, D. T. (2004) · DNA repair · doi:10.1016/j.dnarep.2004.10.002 · Cited by 20

Analysis of yeast pms1, msh2, and mlh1 mutators points to differences in mismatch correction efficiencies between prokaryotic and eukaryotic cells

Yang, Y., Karthikeyan, R., Mack, S., Vonarx, E. J., & Kunz, B. A. (1999) · Molecular and General Genetics MGG · doi:10.1007/s004380050021 · Cited by 20

A Novel, Drug Resistance-Independent, Fluorescence-Based Approach To Measure Mutation Rates in Microbial Pathogens

Shor, E., Schuyler, J., & Perlin, D. S. (2019) · mBio · doi:10.1128/mbio.00120-19 · Cited by 19

Clinical Testing for Mismatch Repair in Neoplasms Using Multiple Laboratory Methods

Yang, R. K., Chen, H., Roy‐Chowdhuri, S., Rashid, A., Álvarez, H., Routbort, M. J., Patel, K. P., Luthra, R., Medeiros, L. J., & Törüner, G. (2022) · Cancers · doi:10.3390/cancers14194550 · Cited by 19

Reciprocal regulation of nuclear import of the yeast MutSα DNA mismatch repair proteins Msh2 and Msh6

Hayes, A. P., Sevi, L. A., Feldt, M. C., Rose, M. D., & Gammie, A. E. (2009) · DNA repair · doi:10.1016/j.dnarep.2009.02.003 · Cited by 20

The absence of the catalytic domains of Saccharomyces cerevisiae DNA polymerase ϵ strongly reduces DNA replication fidelity

Garbacz, M. A., Cox, P. B., Sharma, S., Lujan, S. A., Chabes, A., & Kunkel, T. A. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz048 · Cited by 19

Frameshift Mutagenesis: The Roles of Primer–Template Misalignment and the Nonhomologous End-Joining Pathway inSaccharomyces cerevisiae

Lehner, K. R., Mudrak, S. V., Minesinger, B. K., & Jinks-Robertson, S. (2011) · Genetics · doi:10.1534/genetics.111.134890 · Cited by 19

MSH3 deficiency is not sufficient for a mutator phenotype in Chinese hamster ovary cells

Hinz, J. M. (1999) · Carcinogenesis · doi:10.1093/carcin/20.2.215 · Cited by 19

Multiple roles for MSH2 in the repair of a deletion mutation directed by modified single-stranded oligonucleotides

Maguire, K., & Kmiec, E. B. (2006) · Gene · doi:10.1016/j.gene.2006.08.014 · Cited by 19

Building Bridges in Cancer

Hussein, M. R., & Wood, G. S. (2002) · American Journal of Dermatopathology · doi:10.1097/00000372-200202000-00016 · Cited by 19

Low prevalence of germline hMSH6 mutations in colorectal cancer families from Spain

de Abajo, A. S. (2005) · World Journal of Gastroenterology · doi:10.3748/wjg.v11.i37.5770 · Cited by 18

DNA polymerase 3′→5′ exonuclease activity: Different roles of the beta hairpin structure in family-B DNA polymerases

Darmawan, H., Harrison, M., & Reha-Krantz, L. J. (2015) · DNA repair · doi:10.1016/j.dnarep.2015.02.014 · Cited by 18

A genetic screen pinpoints ribonucleotide reductase residues that sustain dNTP homeostasis and specifies a highly mutagenic type of dNTP imbalance

Schmidt, T. T., Sharma, S., Reyes, G. X., Gries, K., Gross, M., Zhao, B., Yuan, J.-H., Wade, R. C., Chabes, A., & Hombauer, H. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky1154 · Cited by 18

Defects in the GINS complex increase the instability of repetitive sequences via a recombination-dependent mechanism

Jedrychowska, M., Denkiewicz-Kruk, M., Alabrudzińska, M., Skoneczna, A., Jonczyk, P., Dmowski, M., & Fijałkowska, I. J. (2019) · PLoS Genetics · doi:10.1371/journal.pgen.1008494 · Cited by 19

The functional role of Pescadillo ribosomal biogenesis factor 1 in cancer

Li, Y., Zhang, C., Pei, J., Zhang, W., Zhang, C., & Dai, D. (2021) · Journal of Cancer · doi:10.7150/jca.58982 · Cited by 18

Evolutionary Significance of Fungal Hypermutators: Lessons Learned from Clinical Strains and Implications for Fungal Plant Pathogens

Gambhir, N., Harris, S. D., & Everhart, S. E. (2022) · mSphere · doi:10.1128/msphere.00087-22 · Cited by 18

Complementation of mismatch repair gene defects by chromosome transfer

Tindall, K. R., Glaab, W. E., Umar, A., Risinger, J. I., Koi, M., Barrett, J. C., & Kunkel, T. A. (1998) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/s0027-5107(97)00277-7 · Cited by 18

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

Zhang, S., Lloyd, R., Bowden, G. N., Glickman, B. W., & de Boer, J. G. (2001) · Oncogene · doi:10.1038/sj.onc.1204730 · Cited by 18

hMSH2 and nm23 Expression in Sporadic Colorectal Cancer and its Clinical Significance

Wu, H.-W., Gao, L., & Wei, G. (2013) · Asian Pacific Journal of Cancer Prevention · doi:10.7314/apjcp.2013.14.3.1995 · Cited by 17

The Eukaryotic Mismatch Recognition Complexes Track with the Replisome during DNA Synthesis

Haye, J. E., & Gammie, A. E. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005719 · Cited by 17

Frequency of constitutional MSH6 mutations in a consecutive series of families with clinical suspicion of HNPCC

Roncari, B., Pedroni, M., Maffei, S., Gregorio, C. D., Ponti, G., Scarselli, A., Losi, L., Benatti, P., Roncucci, L., Gaetani, C. D., et al. (2007) · Clinical Genetics · doi:10.1111/j.1399-0004.2007.00856.x · Cited by 17

Structure and expression of the Zea mays mutS-homologs Mus1 and Mus2

Horwath, M., Kramer, W., & Kunze, R. (2002) · Theoretical and Applied Genetics · doi:10.1007/s00122-002-0955-8 · Cited by 17

DNA Replication Errors are Frequent in Mucinous Cystadenocarcinoma of the Ovary

Ohwada, M., Suzuki, M., Saga, Y., & Sato, I. (2000) · Cancer Genetics and Cytogenetics · doi:10.1016/s0165-4608(99)00145-4 · Cited by 17

Expression of mismatch repair proteins, hMLH1/hMSH2, in non‐small cell lung cancer tissues and its clinical significance

Kouso, H., Yoshino, I., Miura, N., Takenaka, T., Ohba, T., Yohena, T., Osoegawa, A., Shoji, F., & Maehara, Y. (2008) · Journal of Surgical Oncology · doi:10.1002/jso.21108 · Cited by 16

Transient suppression of MLH1 allows effective single-nucleotide substitution by single-stranded DNA oligonucleotides

Dekker, M., de Vries, S., Aarts, M., Dekker, R., Brouwers, C. M., Wiebenga, O. T., de Wind, N., Cantelli, E., Tonelli, R., & Riele, H. T. (2011) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2011.07.008 · Cited by 16

Visualization of mismatch repair complexes using fluorescence microscopy

Schmidt, T. T., & Hombauer, H. (2015) · DNA repair · doi:10.1016/j.dnarep.2015.11.014 · Cited by 16

Coordination of Rad1–Rad10 interactions with Msh2–Msh3, Saw1 and RPA is essential for functional 3′ non-homologous tail removal

Eichmiller, R., Medina‐Rivera, M., DeSanto, R., Minca, E. C., Kim, C., Holland, C., Seol, J.-H., Schmit, M., Oramus, D., Smith, J., et al. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky254 · Cited by 16

Multiple Factors Insulate Msh2–Msh6 Mismatch Repair Activity from Defects in Msh2 Domain I

Kumar, C., Piacente, S. C., Sibert, J. G., Bukata, A. R., O'Connor, J., Alani, E., & Surtees, J. A. (2011) · Journal of Molecular Biology · doi:10.1016/j.jmb.2011.06.030 · Cited by 16

Extensive Microsatellite Variation in Rice Induced by Introgression from Wild Rice (Zizania latifolia Griseb.)

Dong, Z., Wang, H., Dong, Y., Wang, Y., Liu, W., Miao, G., Lin, X., Wang, D., & Liu, B. (2013) · PLoS ONE · doi:10.1371/journal.pone.0062317 · Cited by 16

HIM1, a new yeast Saccharomyces cerevisiae gene playing a role in control of spontaneous and induced mutagenesis

Kelberg, E. P., Ковальцова, С. В., Alekseev, S., Федорова, И. В., Gracheva, L. M., Evstuhina, T. A., & Королев, В. Г. (2005) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2005.03.003 · Cited by 16

Refined chromosomal localization of the mismatch repair and hereditary nonpolyposis colorectal cancer genes hMSH2 and hMSH6.

Schmütte, C., Marinescu, R. C., Copeland, N. G., Jenkins, N. A., Overhauser, J., & Fishel, R. (1998) · PubMed · Cited by 16

Role of MutSalpha in the recognition of iododeoxyuridine in DNA.

Berry, S. E., Loh, T., Yan, T., & Kinsella, T. J. (2003) · PubMed · Cited by 16

Signaling Mismatch Repair: The Mechanics of an Adenosine-Nucleotide Molecular SwitchPreprint

Fishel, R. A., ACHARYA, S., Berardini, M. D., Bocker, T., Charbonneau, N., Cranston, A. N., Gradia, S., Guerrette, S., Heinen, C. D., MAZUREK, A., et al. (2000) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2000.65.217 · Cited by 16

PES1 regulates sensitivity of colorectal cancer cells to anticancer drugs

Xie, W., Qu, L., Meng, L., Liu, C., Wu, J. L., & Shou, C. (2013) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2012.12.145 · Cited by 16

Mutagenesis and the three R's in yeast

Abdulovic, A. L., Kim, N., & Jinks-Robertson, S. (2006) · DNA repair · doi:10.1016/j.dnarep.2005.11.006 · Cited by 15

Genome Sequencing Variations in the Octodon degus, an Unconventional Natural Model of Aging and Alzheimer's Disease

Hurley, M. J., Urra, C., Garduño, B. M., Bruno, A., Kimbell, A., Wilkinson, B., Marino‐Buslje, C., Ezquer, M., Ezquer, F. E., Fernández‐Aburto, P., et al. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.894994 · Cited by 17

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