トップページ > 研究組織一覧 > 分野・独立ユニットグループ > がん進展研究分野 > 論文業績 > 2023年
2023年
- Makishima, H., Saiki, R., Nannya, Y., Korotev, S. C., Gurnari, C., Takeda, J., Momozawa, Y., Best, S., Krishnamurthy, P., Yoshizato, T., Atsuta, Y., Shiozawa, Y., Iijima-Yamashita, Y., Yoshida K., Shiraishi, Y., Nagata, Y., Kakiuchi, N., Onizuka, M., Chiba, K., Tanaka, H., Kon, A., Ochi, Y., Nakagawa, M. M., Okuda, R., Mori, T., Yoda, A., Itonaga, H., Miyazaki, Y., Sanada, M., Ishikawa, T., Chiba, S., Tsurumi, H., Kasahara, S., Muller-Tidow, C., Takaori-Kondo, A., Ohyashiki, K., Kiguchi, T., Matsuda, F., Jansen, J. H., Polprasert, C., Blombery, P., Kamatani, Y., Miyano, S., Malcovati, L., Haferlach, T., Kubo, M., Cazzola, M., Kulasekararaj, A. G., Godley, L. A., Maciejewski, J. P., Ogawa, S.: Germline DDX41 mutations define a unique subtype of myeloid neoplasms. Blood, 141: 534-549 (2023).
- Kaburagi, T., Shiba, N., Yamato, G., Yoshida K., Tabuchi, K., Ohki, K., Ishikita, E., Hara, Y., Shiraishi, Y., Kawasaki, H., Sotomatsu, M., Takizawa, T., Taki, T., Kiyokawa, N., Tomizawa, D., Horibe, K., Miyano, S., Taga, T., Adachi, S., Ogawa, S., Hayashi, Y.: UBTF-internal tandem duplication as a novel poor prognostic factor in pediatric acute myeloid leukemia. Genes Chromosomes Cancer, 62: 202-209 (2023).
- Nishimura, T., Kakiuchi, N., Yoshida, K., Sakurai, T., Kataoka, T. R., Kondoh, E., Chigusa, Y., Kawai, M., Sawada, M., Inoue, T., Takeuchi, Y., Maeda, H., Baba, S., Shiozawa, Y., Saiki, R., Nakagawa, M. M., Nannya, Y., Ochi, Y., Hirano, T., Nakagawa, T., Inagaki-Kawata, Y., Aoki, K., Hirata, M., Nanki, K., Matano, M., Saito, M., Suzuki, E., Takada, M., Kawashima, M., Kawaguchi, K., Chiba, K., Shiraishi, Y., Takita, J., Miyano, S., Mandai, M., Sato, T., Takeuchi, K., Haga, H., Toi, M., Ogawa, S.: Evolutionary histories of breast cancer and related clones. Nature, 620: 607-614 (2023)
- Briest, F., Noerenberg, D., Hennch, C., Yoshida, K., Hablesreiter, R., Nimo, J., Sasca, D., Kirchner, M., Mansouri, L., Inoue, Y., Wiegand, L., Staiger, AM., Casadei, B., Korkolopoulou, P., Weiner, J., Lopez-Guillermo, A., Warth, A., Schneider, T., Nagy, Á., Klapper, W., Hummel, M., Kanellis, G., Anagnostopoulos, I., Mertins, P., Bullinger, L., Rosenquist, R., Vassilakopoulos, TP., Ott, G., Ogawa, S., Damm, F.: Frequent ZNF217 mutations lead to transcriptional deregulation of interferon signal transduction via altered chromatin accessibility in B cell lymphoma. Leukemia, 37: 2237-2249 (2023)
