Year |
Citation |
Score |
2023 |
Xu R, Pan Z, Nakagawa T. Gross Chromosomal Rearrangement at Centromeres. Biomolecules. 14. PMID 38254628 DOI: 10.3390/biom14010028 |
0.413 |
|
2023 |
Mongia P, Toyofuku N, Pan Z, Xu R, Kinoshita Y, Oki K, Takahashi H, Ogura Y, Hayashi T, Nakagawa T. Fission yeast Srr1 and Skb1 promote isochromosome formation at the centromere. Communications Biology. 6: 551. PMID 37237082 DOI: 10.1038/s42003-023-04925-9 |
0.548 |
|
2021 |
Su J, Xu R, Mongia P, Toyofuku N, Nakagawa T. Fission yeast Rad8/HLTF facilitates Rad52-dependent chromosomal rearrangements through PCNA lysine 107 ubiquitination. Plos Genetics. 17: e1009671. PMID 34292936 DOI: 10.1371/journal.pgen.1009671 |
0.467 |
|
2020 |
Onaka AT, Su J, Katahira Y, Tang C, Zafar F, Aoki K, Kagawa W, Niki H, Iwasaki H, Nakagawa T. DNA replication machinery prevents Rad52-dependent single-strand annealing that leads to gross chromosomal rearrangements at centromeres. Communications Biology. 3: 202. PMID 32355220 DOI: 10.1038/s42003-020-0934-0 |
0.613 |
|
2019 |
Okita AK, Zafar F, Su J, Weerasekara D, Kajitani T, Takahashi TS, Kimura H, Murakami Y, Masukata H, Nakagawa T. Heterochromatin suppresses gross chromosomal rearrangements at centromeres by repressing Tfs1/TFIIS-dependent transcription. Communications Biology. 2: 17. PMID 31924891 DOI: 10.1038/s42003-018-0251-z |
0.324 |
|
2019 |
Nakagawa T, Okita AK. Transcriptional silencing of centromere repeats by heterochromatin safeguards chromosome integrity. Current Genetics. PMID 30997531 DOI: 10.1007/S00294-019-00975-X |
0.425 |
|
2019 |
Okita AK, Zafar F, Su J, Weerasekara D, Kajitani T, Takahashi TS, Kimura H, Murakami Y, Masukata H, Nakagawa T. Heterochromatin suppresses gross chromosomal rearrangements at centromeres by repressing Tfs1/TFIIS-dependent transcription. Communications Biology. 2: 17. PMID 30652128 DOI: 10.1038/s42003-018-0251-z |
0.324 |
|
2018 |
Ogawa S, Kido S, Handa T, Ogawa H, Asakawa H, Takahashi TS, Nakagawa T, Hiraoka Y, Masukata H. Shelterin promotes tethering of late replication origins to telomeres for replication-timing control. The Embo Journal. PMID 29997179 DOI: 10.15252/Embj.201898997 |
0.537 |
|
2018 |
Terui R, Nagao K, Kawasoe Y, Taki K, Higashi TL, Tanaka S, Nakagawa T, Obuse C, Masukata H, Takahashi TS. Nucleosomes around a mismatched base pair are excluded via an Msh2-dependent reaction with the aid of SNF2 family ATPase Smarcad1. Genes & Development. 32: 806-821. PMID 29899141 DOI: 10.1101/Gad.310995.117 |
0.557 |
|
2018 |
Zafar F, Okita AK, Onaka AT, Su J, Katahira Y, Nakayama JI, Takahashi TS, Masukata H, Nakagawa T. Regulation of mitotic recombination between DNA repeats in centromeres. Nucleic Acids Research. PMID 29346669 DOI: 10.1093/Nar/Gkx1310 |
0.656 |
|
2017 |
Zafar F, Okita AK, Onaka AT, Su J, Katahira Y, Nakayama JI, Takahashi TS, Masukata H, Nakagawa T. Regulation of mitotic recombination between DNA repeats in centromeres. Nucleic Acids Research. PMID 28977643 DOI: 10.1093/Nar/Gkx763 |
0.6 |
|
2016 |
Onaka AT, Toyofuku N, Inoue T, Okita AK, Sagawa M, Su J, Shitanda T, Matsuyama R, Zafar F, Takahashi TS, Masukata H, Nakagawa T. Rad51 and Rad54 promote noncrossover recombination between centromere repeats on the same chromatid to prevent isochromosome formation. Nucleic Acids Research. PMID 27697832 DOI: 10.1093/Nar/Gkw874 |
0.557 |
|
2016 |
Kawasoe Y, Tsurimoto T, Nakagawa T, Masukata H, Takahashi TS. MutSα maintains the mismatch repair capability by inhibiting PCNA unloading. Elife. 5. PMID 27402201 DOI: 10.7554/Elife.15155 |
0.612 |
|
2016 |
Kawasoe Y, Tsurimoto T, Nakagawa T, Masukata H, Takahashi TS. Author response: MutSα maintains the mismatch repair capability by inhibiting PCNA unloading Elife. DOI: 10.7554/Elife.15155.032 |
0.335 |
|
2014 |
Blaikley EJ, Tinline-Purvis H, Kasparek TR, Marguerat S, Sarkar S, Hulme L, Hussey S, Wee BY, Deegan RS, Walker CA, Pai CC, Bähler J, Nakagawa T, Humphrey TC. The DNA damage checkpoint pathway promotes extensive resection and nucleotide synthesis to facilitate homologous recombination repair and genome stability in fission yeast. Nucleic Acids Research. 42: 5644-56. PMID 24623809 DOI: 10.1093/Nar/Gku190 |
0.604 |
|
2012 |
Tazumi A, Fukuura M, Nakato R, Kishimoto A, Takenaka T, Ogawa S, Song JH, Takahashi TS, Nakagawa T, Shirahige K, Masukata H. Telomere-binding protein Taz1 controls global replication timing through its localization near late replication origins in fission yeast. Genes & Development. 26: 2050-62. PMID 22987637 DOI: 10.1101/Gad.194282.112 |
0.556 |
|
2012 |
Handa T, Kanke M, Takahashi TS, Nakagawa T, Masukata H. DNA polymerization-independent functions of DNA polymerase epsilon in assembly and progression of the replisome in fission yeast. Molecular Biology of the Cell. 23: 3240-53. PMID 22718908 DOI: 10.1091/Mbc.E12-05-0339 |
0.612 |
|
2012 |
Higashi TL, Ikeda M, Tanaka H, Nakagawa T, Bando M, Shirahige K, Kubota Y, Takisawa H, Masukata H, Takahashi TS. The prereplication complex recruits XEco2 to chromatin to promote cohesin acetylation in Xenopus egg extracts. Current Biology : Cb. 22: 977-88. PMID 22560615 DOI: 10.1016/J.Cub.2012.04.013 |
0.545 |
|
2012 |
Kanke M, Kodama Y, Takahashi TS, Nakagawa T, Masukata H. Mcm10 plays an essential role in origin DNA unwinding after loading of the CMG components. The Embo Journal. 31: 2182-94. PMID 22433840 DOI: 10.1038/Emboj.2012.68 |
0.661 |
|
2011 |
Maki K, Inoue T, Onaka A, Hashizume H, Somete N, Kobayashi Y, Murakami S, Shigaki C, Takahashi TS, Masukata H, Nakagawa T. Abundance of prereplicative complexes (Pre-RCs) facilitates recombinational repair under replication stress in fission yeast. The Journal of Biological Chemistry. 286: 41701-10. PMID 21971174 DOI: 10.1074/Jbc.M111.285619 |
0.574 |
|
2011 |
Fukuura M, Nagao K, Obuse C, Takahashi TS, Nakagawa T, Masukata H. CDK promotes interactions of Sld3 and Drc1 with Cut5 for initiation of DNA replication in fission yeast. Molecular Biology of the Cell. 22: 2620-33. PMID 21593208 DOI: 10.1091/Mbc.E10-12-0995 |
0.485 |
|
2011 |
Kanke M, Nishimura K, Kanemaki M, Kakimoto T, Takahashi TS, Nakagawa T, Masukata H. Auxin-inducible protein depletion system in fission yeast. Bmc Cell Biology. 12: 8. PMID 21314938 DOI: 10.1186/1471-2121-12-8 |
0.349 |
|
2009 |
Hayashi MT, Takahashi TS, Nakagawa T, Nakayama J, Masukata H. The heterochromatin protein Swi6/HP1 activates replication origins at the pericentromeric region and silent mating-type locus. Nature Cell Biology. 11: 357-62. PMID 19182789 DOI: 10.1038/Ncb1845 |
0.507 |
|
2008 |
Nakamura K, Okamoto A, Katou Y, Yadani C, Shitanda T, Kaweeteerawat C, Takahashi TS, Itoh T, Shirahige K, Masukata H, Nakagawa T. Rad51 suppresses gross chromosomal rearrangement at centromere in Schizosaccharomyces pombe. The Embo Journal. 27: 3036-46. PMID 18923422 DOI: 10.1038/Emboj.2008.215 |
0.402 |
|
2008 |
Nitani N, Yadani C, Yabuuchi H, Masukata H, Nakagawa T. Mcm4 C-terminal domain of MCM helicase prevents excessive formation of single-stranded DNA at stalled replication forks. Proceedings of the National Academy of Sciences of the United States of America. 105: 12973-8. PMID 18753627 DOI: 10.1073/Pnas.0805307105 |
0.646 |
|
2007 |
Hayashi M, Katou Y, Itoh T, Tazumi A, Tazumi M, Yamada Y, Takahashi T, Nakagawa T, Shirahige K, Masukata H. Genome-wide localization of pre-RC sites and identification of replication origins in fission yeast. The Embo Journal. 26: 1327-39. PMID 17304213 DOI: 10.1038/Sj.Emboj.7601585 |
0.526 |
|
2007 |
Hayashi M, Katou Y, Itoh T, Tazumi A, Yamada Y, Takahashi T, Nakagawa T, Shirahige K, Masukata H. Erratum: Genome-wide localization of pre-RC sites and identification of replication origins in fission yeast (The EMBO Journal (2007) 26 (1327-1339) DOI: 10.1038/sj.emboj.7601585) The Embo Journal. 26. DOI: 10.1038/Sj.Emboj.7601708 |
0.319 |
|
2006 |
Yabuuchi H, Yamada Y, Uchida T, Sunathvanichkul T, Nakagawa T, Masukata H. Ordered assembly of Sld3, GINS and Cdc45 is distinctly regulated by DDK and CDK for activation of replication origins. The Embo Journal. 25: 4663-74. PMID 16990792 DOI: 10.1038/Sj.Emboj.7601347 |
0.582 |
|
2006 |
Nitani N, Nakamura K, Nakagawa C, Masukata H, Nakagawa T. Regulation of DNA replication machinery by Mrc1 in fission yeast. Genetics. 174: 155-65. PMID 16849602 DOI: 10.1534/Genetics.106.060053 |
0.614 |
|
2004 |
Yamada Y, Nakagawa T, Masukata H. A novel intermediate in initiation complex assembly for fission yeast DNA replication. Molecular Biology of the Cell. 15: 3740-50. PMID 15194812 DOI: 10.1091/Mbc.E04-04-0292 |
0.525 |
|
2004 |
Mazina OM, Mazin AV, Nakagawa T, Kolodner RD, Kowalczykowski SC. Saccharomyces cerevisiae Mer3 helicase stimulates 3′-5′ heteroduplex extension by Rad51: Implications for crossover control in meiotic recombination Cell. 117: 47-56. PMID 15066281 DOI: 10.1016/S0092-8674(04)00294-6 |
0.73 |
|
2003 |
Ono Y, Tomita K, Matsuura A, Nakagawa T, Masukata H, Uritani M, Ushimaru T, Ueno M. A novel allele of fission yeast rad11 that causes defects in DNA repair and telomere length regulation. Nucleic Acids Research. 31: 7141-9. PMID 14654689 DOI: 10.1093/Nar/Gkg917 |
0.641 |
|
2002 |
Nakagawa T, Kolodner RD. The MER3 DNA helicase catalyzes the unwinding of Holliday junctions Journal of Biological Chemistry. 277: 28019-28024. PMID 12039965 DOI: 10.1074/Jbc.M204165200 |
0.705 |
|
2002 |
Nakagawa T, Kolodner RD. Saccharomyces cerevisiae Mer3 is a DNA helicase involved in meiotic crossing over. Molecular and Cellular Biology. 22: 3281-91. PMID 11971962 DOI: 10.1128/Mcb.22.10.3281-3291.2002 |
0.713 |
|
2001 |
Nakagawa T, Flores-Rozas H, Kolodner RD. The MER3 helicase involved in meiotic crossing over is stimulated by single-stranded DNA-binding proteins and unwinds DNA in the 3' to 5' direction. The Journal of Biological Chemistry. 276: 31487-93. PMID 11376001 DOI: 10.1074/Jbc.M104003200 |
0.69 |
|
1999 |
Nakagawa T, Datta A, Kolodner RD. Multiple functions of MutS- and MutL-related heterocomplexes Proceedings of the National Academy of Sciences of the United States of America. 96: 14186-14188. PMID 10588673 DOI: 10.1073/Pnas.96.25.14186 |
0.648 |
|
1999 |
Nakagawa T, Ogawa H. The Saccharomyces cerevisiae MER3 gene, encoding a novel helicase-like protein, is required for crossover control in meiosis. The Embo Journal. 18: 5714-5723. PMID 10523314 DOI: 10.1093/Emboj/18.20.5714 |
0.542 |
|
1997 |
Nakagawa T, Ogawa H. Involvement of the MRE2 gene of yeast in formation of meiosis-specific double-strand breaks and crossover recombination through RNA splicing. Genes to Cells. 2: 65-79. PMID 9112441 DOI: 10.1046/J.1365-2443.1997.D01-283.X |
0.475 |
|
1995 |
Ogawa H, Johzuka K, Nakagawa T, Leem S, Hagihara AH. Functions of the yeast meiotic recombination genes, MRE11 and MRE2. Advances in Biophysics. 31: 67-76. PMID 7625279 DOI: 10.1016/0065-227X(95)99383-Z |
0.434 |
|
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