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Home > Organization > Divisions and Independent Research Units > Division of Cancer Evolution > Research Papers > 2023

2023

  1. 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).
  2. 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).
  3. 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)
  4. 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)