1. Lyer, R. R., Pluciennik, A., Burdett, V., and Modrich, P. L. (2006) DNA mismatch repair: Functions and mechanisms. Chemical Reviews. 106, 302–323
2. Jiricny, J. (2006) The multifaceted mismatch-repair system. Nature reviews. Molecular cell biology. 7, 335–46
3. Hoffmann, E. R., and Borts, R. H. (2004) Meiotic recombination intermediates and mismatch repair proteins. Cytogenetic and Genome Research. 107, 232–248
4. Modrich, P., and Lahue, R. (1996) Mismatch repair in replication fidelity, genetic recombination, and cancer biology. Annual review of biochemistry. 65, 101–33
5. Kunkel, T. A., and Erie, D. A. (2015) Eukaryotic Mismatch Repair in Relation to DNA Replication. Annual Review of Genetics. 49, 291–313
6. Harfe, B. D., and Jinks-Robertson, S. (2000) DNA mismatch repair and genetic instability. Annual review of genetics. 34, 359–399
7. Kolodner, R. D., and Marsischky, G. T. (1999) Eukaryotic DNA mismatch repair. Current opinion in genetics & development. 9, 89–96
8. Marsischky, G. T., Filosi, N., Kane, M. F., and Kolodner, R. (1996) Redundancy of Saccharomyces cerevisiae MSH3 and MSH6 in MSH2-dependent mismatch repair. Genes and Development. 10, 407–420
9. Sia, E. A., Kokoska, R. J., Dominska, M., Greenwell, P., and Petes, T. D. (1997) Microsatellite instability in yeast: dependence on repeat unit size and DNA mismatch repair genes. Molecular and cellular biology. 17, 2851–8
10. Srivatsan, A., Bowen, N., and Kolodner, R. D. (2014) Mispair-specific recruitment of the Mlh1-Pms1 complex identifies repair substrates of the Saccharomyces cerevisiae Msh2- Msh3 complex. Journal of Biological Chemistry. 289, 9352–9364
11. Goellner, E. M., Putnam, C. D., and Kolodner, R. D. (2015) Exonuclease 1-dependent and independent mismatch repair. DNA repair. 32, 24–32
12. Flores-Rozas, H., and Kolodner, R. D. (1998) The Saccharomyces cerevisiae MLH3 gene functions in MSH3-dependent suppression of frameshift mutations. Proceedings of the National Academy of Sciences of the United States of America. 95, 12404–9
13. N Matton 1, J Simonetti, K. W. (2000) Identification of mismatch repair protein complexes in HeLa nuclear extracts and their interaction with heteroduplex DNA. Journal of Biological Chemistry, 275, 17808-17813.
14. Gueneau, E., Dherin, C., Legrand, P., Tellier-Lebegue, C., Gilquin, B., Bonnesoeur, P., Londino, F., Quemener, C., Le Du, M.-H., Márquez, J. a, Moutiez, M., Gondry, M., Boiteux, S., and Charbonnier, J.-B. (2013) Structure of the MutLα C-terminal domain reveals how Mlh1 contributes to Pms1 endonuclease site. Nature structural & molecular biology. 10.1038/nsmb.2511
15. Kadyrov, F. A., Dzantiev, L., Constantin, N., and Modrich, P. (2006) Endonucleolytic function of MutLalpha in human mismatch repair. Cell. 126, 297–308
16. de Wind, N., Dekker, M., Berns, A., Radman, M., and te Riele, H. (1995) Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer. Cell. 82, 321–330
17. Elliott, B., and Jasin, M. (2001) Repair of Double-Strand Breaks by Homologous Recombination in Mismatch Repair-Defective Mammalian Cells. 21, 2671–2682
18. Sharma, S., Doherty, K. M., and Brosh, R. M. (2006) Mechanisms of RecQ helicases in pathways of DNA metabolism and maintenance of genomic stability. Biochemical Journal. 398, 319–337
19. Bannister, L. A., Waldman, B. C., and Waldman, A. S. (2004) Modulation of error-prone double-strand break repair in mammalian chromosomes by DNA mismatch repair protein Mlh1. DNA Repair. 10.1016/j.dnarep.2004.01.001
20. Shibata, A., Conrad, S., Birraux, J., Geuting, V., Barton, O., Ismail, A., Kakarougkas, A., Meek, K., Taucher-Scholz, G., Löbrich, M., and Jeggo, P. a (2011) Factors determining DNA double-strand break repair pathway choice in G2 phase. The EMBO journal. 30, 1079–92
21. Zakharyevich, K., Tang, S., Ma, Y., and Hunter, N. (2012) Delineation of joint molecule resolution pathways in meiosis identifies a crossover-specific resolvase. Cell. 149, 334–347
22. Toledo, M., Sun, X., Brieño-Enríquez, M. A., Raghavan, V., Gray, S., Pea, J., Milano, C. R., Venkatesh, A., Patel, L., Borst, P. L., Alani, E., and Cohen, P. E. (2019) A mutation in the endonuclease domain of mouse MLH3 reveals novel roles for mutlγ during crossover formation in meiotic prophase I. PLoS Genetics. 10.1371/journal.pgen.1008177
23. Baker, S. M., Bronner, C. E., Zhang, L., Plug, A. W., Robatzek, M., Warren, G., Elliott, E. A., Yu, J., Ashley, T., Arnheim, N., Flavell, R. A., and Liskay, R. M. (1995) Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis. Cell. 82, 309–319
24. Baker, S. M., Plug, a W., Prolla, T. a, Bronner, C. E., Harris, a C., Yao, X., Christie, D. M., Monell, C., Arnheim, N., Bradley, a, Ashley, T., and Liskay, R. M. (1996) Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over. Nature genetics. 13, 336–342
25. Edelmann, W., Cohen, P. E., Kane, M., Lau, K., Morrow, B., Bennett, S., Umar, A., Kunkel, T., Cattoretti, G., Chaganti, R., Pollard, J. W., Kolodner, R. D., and Kucherlapati, R. (1996) Meiotic pachytene arrest in MLH1-deficient mice. Cell. 85, 1125–1134
26. Lipkin, S. M., Moens, P. B., Wang, V., Lenzi, M., Shanmugarajah, D., Gilgeous, A., Thomas, J., Cheng, J., Touchman, J. W., Green, E. D., Schwartzberg, P., Collins, F. S., and Cohen, P. E. (2002) Meiotic arrest and aneuploidy in MLH3-deficient mice. Nature genetics. 31, 385–390
27. Svetlanov, A., Baudat, F., Cohen, P. E., and De Massy, B. (2008) Distinct functions of MLH3 at recombination hot spots in the mouse. Genetics. 178, 1937–1945
28. Fischer, J. M., Dudley, S., Miller, A. J., and Liskay, R. M. (2016) An intact Pms2 ATPase domain is not essential for male fertility. DNA Repair. 39, 46–51
29. Elda Cannavo, Aurore Sanchez, Roopesh Anand, Lepakshi Ranjha, Jannik Hugener, Céline Adam, Ananya Acharya, Nicolas Weyland, Xavier Aran-Guiu, Jean-Baptiste Charbonnier, Eva R. Hoffmann, Valérie Borde, J. M. & P. C. (2020) Regulation of the MLH1–MLH3 endonuclease in meiosis
30. Kulkarni, D., Owens, S., Honda, M., Ito, M., Yang, Y., Corrigan, M., Chen, L., Quan, A. and Hunter, N. (2020) PCNA activates the MutLγ endonuclease to promote meiotic crossing over. Nature. https://doi.org/10.1038/s41586-020-2645-6
31. Takeda, S., Nakamura, K., Taniguchi, Y., and Paull, T. T. (2007) Ctp1/CtIP and the MRN Complex Collaborate in the Initial Steps of Homologous Recombination. Molecular Cell. 28, 351–352
32. Bernstein, K. A., and Rothstein, R. (2009) At Loose Ends: Resecting a Double-Strand Break. Cell. 137, 807–810
33. Mehta, A., and Haber, J. E. (2014) Sources of DNA double-strand breaks and models of recombinational DNA repair. Cold Spring Harbor Perspectives in Biology. 6, a016428.
34. Sugawara, N., Wang, X., and Haber, J. E. (2003) In vivo roles of Rad52, Rad54, and Rad55 proteins in Rad51-mediated recombination. Molecular Cell. 12, 209–219
35. Dion, V., Kalck, V., Horigome, C., Towbin, B. D., and Gasser, S. M. (2012) Increased mobility of double-strand breaks requires Mec1, Rad9 and the homologous recombination machinery. Nature Cell Biology. 14, 502–509
36. Schwartz, E. K., and Heyer, W. D. (2011) Processing of joint molecule intermediates by structure-selective endonucleases during homologous recombination in eukaryotes. Chromosoma. 120, 109–127
37. West, S. C., Blanco, M. G., Chan, Y. W., Matos, J., Sarbajna, S., and Wyatt, H. D. M. (2015) Resolution of Recombination Intermediates: Mechanisms and Regulation. Cold Spring Harbor Symposia on Quantitative Biology. 80, 103-109
38. Wyatt, H. D. M., Laister, R. C., Martin, S. R., Arrowsmith, C. H., and West, S. C. (2017) The SMX DNA Repair Tri-nuclease. Molecular Cell. 65, 848-860.e11
39. Kikuchi, K., Narita, T., Pham, V. T., Iijima, J., Hirota, K., Keka, I. S., Mohiuddin, Okawa, K., Hori, T., Fukagawa, T., Essers, J., Kanaar, R., Whitby, M. C., Sugasawa, K., Taniguchi, Y., Kitagawa, K., and Takeda, S. (2013) Structure-specific endonucleases Xpf and Mus81 play overlapping but essential roles in DNA repair by homologous recombination. Cancer Research. 73, 4362–4371
40. Abraham, J., Lemmers, B., Hande, M. P., Moynahan, M. E., Chahwan, C., Ciccia, A., Essers, J., Hanada, K., Chahwan, R., Khaw, A. K., McPherson, P., Shehabeldin, A., Laister, R., Arrowsmith, C., Kanaar, R., West, S. C., Jasin, M., and Hakem, R. (2003) Eme1 is involved in DNA damage processing and maintenance of genomic stability in mammalian cells. EMBO Journal. 22, 6137–6147
41. McPherson, J. P., Lemmers, B., Chahwan, R., Pamidi, A., Migon, E., Matysiak-Zablocki, E., Moynahan, M. E., Essers, J., Hanada, K., Poonepalli, A., Sanchez-Sweatman, O., Khokha, R., Kanaar, R., Jasin, M., Hande, M. P., and Hakem, R. (2004) Involvement of mammalian Mus81 in genome integrity and tumor suppression. Science. 304, 1822–1826
42. Castor, D., Nair, N., Déclais, A. C., Lachaud, C., Toth, R., Macartney, T. J., Lilley, D. M. J., Arthur, J. S. C., and Rouse, J. (2013) Cooperative control of holliday junction resolution and DNA Repair by the SLX1 and MUS81-EME1 nucleases. Molecular Cell. 52, 221–233
43. Wang Xiaowen, Wang Herui, Guo Bin, Zhang Ya, Gong Yinv, Zhang Chi, Xu Hong, and W. X. (2016) Gen1 and Eme1 Play Redundant Roles in DNA Repair and Meiotic Recombination in Mice. DNA and Cell Biology. 35, 585-590
44. Kaur, H., DeMuyt, A., and Lichten, M. (2015) Top3-Rmi1 DNA single-strand decatenase is integral to the formation and resolution of meiotic recombination intermediates. Molecular Cell. 57, 583–594
45. Tang, S., Wu, M. K. Y., Zhang, R., and Hunter, N. (2015) Pervasive and essential roles of the top3-rmi1 decatenase orchestrate recombination and facilitate chromosome segregation in meiosis. Molecular Cell. 57, 607–621
46. Takata, M., Sasaki, M. S., Sonoda, E., Morrison, C., Hashimoto, M., Utsumi, H., Yamaguchi-Iwai, Y., Shinohara, A., and Takeda, S. (1998) Homologous recombination and non-homologous end-joining pathways of DNA double-strand break repair have overlapping roles in the maintenance of chromosomal integrity in vertebrate cells. EMBO Journal. 17, 5497–5508
47. Keka, I. S., Mohiuddin, Maede, Y., Rahman, M. M., Sakuma, T., Honma, M., Yamamoto, T., Takeda, S., and Sasanuma, H. (2015) Smarcal1 promotes double-strand-break repair by nonhomologous end-joining. Nucleic Acids Research. 10.1093/nar/gkv621
48. Murai, J., Huang, S. Y. N., Das, B. B., Renaud, A., Zhang, Y., Doroshow, J. H., Ji, J., Takeda, S., and Pommier, Y. (2012) Trapping of PARP1 and PARP2 by clinical PARP inhibitors. Cancer Research. 72, 5588–5599
49. Fowler, P., Whitwell, J., Jeffrey, L., Young, J., Smith, K., and Kirkland, D. (2010) Cadmium chloride, benzo[a]pyrene and cyclophosphamide tested in the in vitro mammalian cell micronucleus test (MNvit) in the human lymphoblastoid cell line TK6 at Covance laboratories, Harrogate UK in support of OECD draft Test Guideline 487. Mutation Research. 702, 171–174
50. Honma, M., Izumi, M., Sakuraba, M., Tadokoro, S., Sakamoto, H., Wang, W., Yatagai, F., and Hayashi, M. (2003) Deletion, Rearrangement, and Gene Conversion; Genetic Consequences of Chromosomal Double-Strand Breaks in Human Cells. Environmental and Molecular Mutagenesis. 42, 288–298
51. Neuwirth, E. a H., Honma, M., and Grosovsky, A. J. (2007) Interchromosomal crossover in human cells is associated with long gene conversion tracts. Molecular and cellular biology. 27, 5261–5274
52. Yoshimoto, K., Mizoguchi, M., Hata, N., Murata, H., Hatae, R., Amano, T., Nakamizo, A., and Sasaki, T. (2012) Complex DNA repair pathways as possible therapeutic targets to overcome temozolomide resistance in glioblastoma. Frontiers in oncology. 2, 186
53. Cejka, P., Stojic, L., Mojas, N., Russell, A. M., Heinimann, K., Cannavó, E., Di Pietro, M., Marra, G., and Jiricny, J. (2003) Methylation-induced G2/M arrest requires a full complement of the mismatch repair protein hMLH1. EMBO Journal. 22, 2245–2254
54. Kadyrov, F. A., Holmes, S. F., Arana, M. E., Lukianova, O. A., O’Donnell, M., Kunkel, T. A., and Modrich, P. (2007) Saccharomyces cerevisiae MutLalpha is a mismatch repair endonuclease. The Journal of biological chemistry. 282, 37181–90
55. Desch??nes, S. M., Tomer, G., Nguyen, M., Erdeniz, N., Juba, N. C., Sep??lveda, N., Pisani, J. E., and Michael Liskay, R. (2007) The E705K mutation in hPMS2 exerts recessive, not dominant, effects on mismatch repair. Cancer Letters. 249, 148–156
56. Nishant, K. T., Plys, A. J., and Alani, E. (2008) A mutation in the putative MLH3 endonuclease domain confers a defect in both mismatch repair and meiosis in Saccharomyces cerevisiae. Genetics. 179, 747–755
57. Kadyrova, L. Y., Gujar, V., Burdett, V., Modrich, P. L., and Kadyrov, F. A. (2020) Human MutLγ, the MLH1–MLH3 heterodimer, is an endonuclease that promotes DNA expansion. Proceedings of the National Academy of Sciences of the United States of America. 117, 3535–3542
58. Al-Sweel, N., Raghavan, V., Dutta, A., Ajith, V. P., Di Vietro, L., Khondakar, N., Manhart, C. M., Surtees, J. A., Nishant, K. T., and Alani, E. (2017) Mlh3 Mutations in Baker’S Yeast Alter Meiotic Recombination Outcomes By Increasing Noncrossover Events Genome- Wide, PLoS genetics, 13, e1007067
59. Shimizu, N., Akagawa, R., Takeda, S., and Sasanuma, H. (2020) The MRE11 nuclease promotes homologous recombination not only in DNA double-strand break resection but also in post-resection in human TK6 cells. Genome Instability & Disease. 1, 184–196
60. Hoa, N. N., Akagawa, R., Yamasaki, T., Hirota, K., Sasa, K., Natsume, T., Kobayashi, J., Sakuma, T., Yamamoto, T., Komatsu, K., Kanemaki, M. T., Pommier, Y., Takeda, S., and Sasanuma, H. (2015) Relative contribution of four nucleases, CtIP, Dna2, Exo1 and Mre11, to the initial step of DNA double-strand break repair by homologous recombination in both the chicken DT40 and human TK6 cell lines. Genes to Cells. 10.1111/gtc.12310
61. Fujita, M., Sasanuma, H., Yamamoto, K. N., Harada, H., Kurosawa, A., Adachi, N., Omura, M., Hiraoka, M., Takeda, S., and Hirota, K. (2013) Interference in DNA Replication Can Cause Mitotic Chromosomal Breakage Unassociated with Double-Strand Breaks. PLoS ONE
62. Wechsler, T., Newman, S., and West, S. C. (2011) Aberrant chromosome morphology in human cells defective for Holliday junction resolution. Nature. 471, 642–646
63. Suzuki, T., Yasui, M., and Honma, M. (2016) Mutator Phenotype and DNA Double-Strand Break Repair in BLM Helicase-Deficient Human Cells. Molecular and Cellular Biology. 36, 2877–2889
64. Sonoda, E., Sasaki, M. S., Morrison, C., Yamaguchi-Iwai, Y., Takata, M., and Takeda, S. (1999) Sister chromatid exchanges are mediated by homologous recombination in vertebrate cells. Molecular and cellular biology. 19, 5166–9
65. Wyatt, H. D. M., Sarbajna, S., Matos, J., and West, S. C. (2013) Coordinated actions of SLX1-SLX4 and MUS81-EME1 for holliday junction resolution in human cells. Molecular Cell. 52, 234–247
66. Jiricny, J. (2013) Postreplicative mismatch repair. Cold Spring Harbor Perspectives in Biology. 5, 1–23
67. Söding, J., Biegert, A., and Lupas, A. N. (2005) The HHpred interactive server for protein homology detection and structure prediction. Nucleic Acids Research. 33, 244–248
68. Zimmermann, L., Stephens, A., Nam, S. Z., Rau, D., Kübler, J., Lozajic, M., Gabler, F., Söding, J., Lupas, A. N., and Alva, V. (2018) A Completely Reimplemented MPI Bioinformatics Toolkit with a New HHpred Server at its Core. Journal of Molecular Biology. 430, 2237–2243
69. Song, Y., Dimaio, F., Wang, R. Y. R., Kim, D., Miles, C., Brunette, T., Thompson, J., and Baker, D. (2013) High-resolution comparative modeling with RosettaCM. Structure. 21, 1735–1742
70. Lorenz, A., West, S. C., and Whitby, M. C. (2010) The human Holliday junction resolvase GEN1 rescues the meiotic phenotype of a Schizosaccharomyces pombe mus81 mutant. Nucleic acids research. 38, 1866–73
71. Chan, Y. W., and West, S. C. (2014) Spatial control of the GEN1 Holliday junction resolvase ensures genome stability. Nature communications. 5, 4844
72. Mohiuddin, Keka, I. S., Evans, T. J., Hirota, K., Shimizu, H., Kono, K., Takeda, S., and Hirano, S. (2014) A novel genotoxicity assay of carbon nanotubes using functional macrophage receptor with collagenous structure (MARCO)-expressing chicken B lymphocytes. Archives of Toxicology. 88, 145–160
73. Zeng, M., Narayanan, L., Xu, X. S., Prolla, T. A., Liskay, R. M., and Glazer, P. M. (2000) Ionizing radiation-induced apoptosis via separate Pms2- and p53-dependent pathways. Cancer Research. 60, 4889–4893
74. Shcherbakova, P. V, Hall, M. C., Lewis, M. S., Bennett, S. E., Martin, K. J., Bushel, P. R., Afshari, C. A., and Kunkel, T. A. (2001) Inactivation of DNA mismatch repair by increased expression of yeast MLH1. Molecular and cellular biology. 10.1128/MCB.21.3.940- 951.2001
75. Sanchez, A., Adam, C., Rauh, F., Duroc, Y., Ranjha, L., Lombard, B., Mu, X., Loew, D., Keeney, S., Cejka, P., Guérois, R., Klein, F., Charbonnier, J.-B., and Borde, V. (2020) Mechanism of in vivo activation of the MutLγ-Exo1 complex for meiotic crossover formation. bioRxiv. 10.1101/2019.12.16.876623
76. Chen, P. C., Dudley, S., Hagen, W., Dizon, D., Paxton, L., Reichow, D., Yoon, S. R., Yang, K., Arnheim, N., Liskay, R. M., and Lipkin, S. M. (2005) Contributions by MutL homologues Mlh3 and Pms2 to DNA mismatch repair and tumor suppression in the mouse. Cancer Research. 65, 8662–8670
77. Sarbajna, S., Davies, D., and West, S. C. (2014) Roles of SLX1-SLX4, MUS81-EME1, and GEN1 in avoiding genome instability and mitotic catastrophe. Genes and Development. 28, 1124–1136
78. Garner, E., Kim, Y., Lach, F. P., Kottemann, M. C., and Smogorzewska, A. (2013) Human GEN1 and the SLX4-Associated Nucleases MUS81 and SLX1 Are Essential for the Resolution of Replication-Induced Holliday Junctions. Cell Reports. 5, 207–215
79. West, S. C., and Chan, Y. W. (2017) Genome Instability as a Consequence of Defects in the Resolution of Recombination Intermediates. Cold Spring Harbor symposia on quantitative biology. 82, 207–212
80. Hodskinson, M. R. G., Silhan, J., Crossan, G. P., Garaycoechea, J. I., Mukherjee, S., Johnson, C. M., Sch??rer, O. D., and Patel, K. J. (2014) Mouse SLX4 Is a Tumor Suppressor that Stimulates the Activity of the Nuclease XPF-ERCC1 in DNA Crosslink Repair. Molecular Cell. 54, 472–484
81. Pamidi, A., Cardoso, R., Hakem, A., Matysiak-Zablocki, E., Poonepalli, A., Tamblyn, L., Perez-Ordonez, B., Hande, M. P., Sanchez, O., and Hakem, R. (2007) Functional interplay of p53 and Mus81 in DNA damage responses and cancer. Cancer Research. 67, 8527–8535
82. Wang, T. F., Kleckner, N., and Hunter, N. (1999) Functional specificity of MutL homologs in yeast: Evidence for three Mlh1-based heterocomplexes with distinct roles during meiosis in recombination and mismatch correction. Proceedings of the National Academy of Sciences of the United States of America. 96, 13914–13919
83. Mohiuddin, M., Evans, T. J., Rahman, M. M., Keka, I. S., Tsuda, M., Sasanuma, H., and Takeda, S. (2018) SUMOylation of PCNA by PIAS1 and PIAS4 promotes template switch in the chicken and human B cell lines. Proceedings of the National Academy of Sciences of the United States of America. 10.1073/pnas.1716349115
84. Cermak, T., Doyle, E., and Christian, M. (2011) Efficient design and assembly of custom TALEN and other TAL effector-based constructs for DNA targeting. Nucleic acids …. 39, e82
85. Sakuma, T., Ochiai, H., Kaneko, T., Mashimo, T., Tokumasu, D., Sakane, Y., Suzuki, K., Miyamoto, T., Sakamoto, N., Matsuura, S., and Yamamoto, T. (2013) Repeating pattern of non-RVD variations in DNA-binding modules enhances TALEN activity. Scientific reports. 3, 3379
86. Ran, F. A., Hsu, P. D., Lin, C. Y., Gootenberg, J. S., Konermann, S., Trevino, A. E., Scott, D. A., Inoue, A., Matoba, S., Zhang, Y., and Zhang, F. (2013) Double nicking by RNA- guided CRISPR cas9 for enhanced genome editing specificity. Cell. 154, 1380–1389
87. Mohiuddin, M., Rahman, M. M., Sale, J. E., and Pearson, C. E. (2019) CtIP-BRCA1 complex and MRE11 maintain replication forks in the presence of chain terminating nucleoside analogs. Nucleic acids research. 10.1093/nar/gkz009
88. Mohiuddin, Kobayashi S, Keka IS, Guilbaud G, Sale J, Narita T, Abdel-Aziz HI, Wang X, Ogawa S, Sasanuma H, Chiu R,Oestergaard VH, Lisby M, T. S. (2016) The role of HERC2 and RNF8 ubiquitin E3 ligases in the promotion of translesion DNA synthesis in the chicken DT40 cell line. DNA Repair (Amst). . 40, 67-76.
論文の公開元へ
