| Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome S Kitao, A Shimamoto, M Goto, RW Miller, WA Smithson, NM Lindor, ... Nature genetics 22 (1), 82-84, 1999 | 779 | 1999 |
| miR-22 represses cancer progression by inducing cellular senescence D Xu, F Takeshita, Y Hino, S Fukunaga, Y Kudo, A Tamaki, J Matsunaga, ... Journal of Cell Biology 193 (2), 409-424, 2011 | 363 | 2011 |
| Bloom’s and Werner’s syndrome genes suppress hyperrecombination in yeast sgs1 mutant: Implication for genomic instability in human diseases K Yamagata, J Kato, A Shimamoto, M Goto, Y Furuichi, H Ikeda Proceedings of the National Academy of Sciences 95 (15), 8733-8738, 1998 | 340 | 1998 |
| Cloning of two new human helicase genes of the RecQ family: biological significance of multiple species in higher eukaryotes S Kitao, I Ohsugi, K Ichikawa, M Goto, Y Furuichi, A Shimamoto Genomics 54 (3), 443-452, 1998 | 315 | 1998 |
| DNA helicase activity in Werner's syndrome gene product synthesized in a baculovirus system N Suzuki, A Shimamoto, O Imamura, J Kuromitsu, S Kitao, M Goto, ... Nucleic acids research 25 (15), 2973-2978, 1997 | 242 | 1997 |
| Molecular mechanisms underlying prostaglandin E2-exacerbated inflammation and immune diseases K Tsuge, T Inazumi, A Shimamoto, Y Sugimoto International immunology 31 (9), 597-606, 2019 | 236 | 2019 |
| DNA damage caused by bisphenol A and estradiol through estrogenic activity T Iso, T Watanabe, T Iwamoto, A Shimamoto, Y Furuichi Biological and Pharmaceutical Bulletin 29 (2), 206-210, 2006 | 227 | 2006 |
| Impaired nuclear localization of defective DNA helicases in Werner's syndrome T Matsumoto, A Shimamoto, M Goto, Y Furuichi Nature genetics 16 (4), 335-336, 1997 | 215 | 1997 |
| Small interfering RNA delivery to the liver by intravenous administration of galactosylated cationic liposomes in mice A Sato, M Takagi, A Shimamoto, S Kawakami, M Hashida Biomaterials 28 (7), 1434-1442, 2007 | 206 | 2007 |
| Werner helicase relocates into nuclear foci in response to DNA damaging agents and co‐localizes with RPA and Rad51 S Sakamoto, K Nishikawa, SJ Heo, M Goto, Y Furuichi, A Shimamoto Genes to Cells 6 (5), 421-430, 2001 | 202 | 2001 |
| Rothmund–Thomson syndrome responsible gene, RECQL4: genomic structure and products S Kitao, NM Lindor, M Shiratori, Y Furuichi, A Shimamoto Genomics 61 (3), 268-276, 1999 | 201 | 1999 |
| Human RecQ5β, a large isomer of RecQ5 DNA helicase, localizes in the nucleoplasm and interacts with topoisomerases 3α and 3β A Shimamoto, K Nishikawa, S Kitao, Y Furuichi Nucleic acids research 28 (7), 1647-1655, 2000 | 184 | 2000 |
| Biochemical characterization of the RECQ4 protein, mutated in Rothmund-Thomson syndrome MA Macris, L Krejci, W Bussen, A Shimamoto, P Sung DNA repair 5 (2), 172-180, 2006 | 175 | 2006 |
| Accumulation of Werner protein at DNA double-strand breaks in human cells L Lan, S Nakajima, K Komatsu, A Nussenzweig, A Shimamoto, J Oshima, ... Journal of cell science 118 (18), 4153-4162, 2005 | 154 | 2005 |
| Polymer brush-stabilized polyplex for a siRNA carrier with long circulatory half-life A Sato, SW Choi, M Hirai, A Yamayoshi, R Moriyama, T Yamano, ... Journal of controlled release 122 (3), 209-216, 2007 | 147 | 2007 |
| Regulation of CDK4 activity by a novel CDK4-binding protein, p34SEI-1 M Sugimoto, T Nakamura, N Ohtani, L Hampson, IN Hampson, ... Genes & development 13 (22), 3027-3033, 1999 | 147 | 1999 |
| Differential regulation of human RecQ family helicases in cell transformation and cell cycle T Kawabe, N Tsuyama, S Kitao, K Nishikawa, A Shimamoto, M Shiratori, ... Oncogene 19 (41), 4764-4772, 2000 | 143 | 2000 |
| Mutations in the gene encoding the E2 conjugating enzyme UBE2T cause Fanconi anemia A Hira, K Yoshida, K Sato, Y Okuno, Y Shiraishi, K Chiba, H Tanaka, ... The American Journal of Human Genetics 96 (6), 1001-1007, 2015 | 141 | 2015 |
| Mutation and haplotype analyses of the Werner’s syndrome gene based on its genomic structure: genetic epidemiology in the Japanese population T Matsumoto, O Imamura, Y Yamabe, J Kuromitsu, Y Tokutake, ... Human genetics 100, 123-130, 1997 | 140 | 1997 |
| Diagnostic criteria for Werner syndrome based on Japanese nationwide epidemiological survey M Takemoto, S Mori, M Kuzuya, S Yoshimoto, A Shimamoto, M Igarashi, ... Geriatrics & gerontology international 13 (2), 475-481, 2013 | 138 | 2013 |
