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Home > Organization > Divisions and Independent Research Units > Division of Cancer Evolution > Research Papers > 2018

2018

  1. Arends, C. M., Galan-Sousa, J., Hoyer, K., Chan, W., Jager, M., Yoshida K., Seemann, R., Noerenberg, D., Waldhueter, N., Fleischer-Notter, H., Christen, F., Schmitt, C. A., Dorken, B., Pelzer, U., Sinn, M., Zemojtel, T., Ogawa, S., Mardian, S., Schreiber, A., Kunitz, A., Kruger, U., Bullinger, L., Mylonas, E., Frick, M., Damm, F.: Hematopoietic lineage distribution and evolutionary dynamics of clonal hematopoiesis. Leukemia, 32: 1908-1919 (2018).
  2. Berger, G., Kroeze, L. I., Koorenhof-Scheele, T. N., de Graaf, A. O., Yoshida K., Ueno, H., Shiraishi, Y., Miyano, S., van den Berg, E., Schepers, H., van der Reijden, B. A., Ogawa, S., Vellenga, E., Jansen, J. H.: Early detection and evolution of preleukemic clones in therapy-related myeloid neoplasms following autologous SCT. Blood, 131: 1846-1857 (2018).
  3. Cardinez, C., Miraghazadeh, B., Tanita, K., da Silva, E., Hoshino, A., Okada, S., Chand, R., Asano, T., Tsumura, M., Yoshida K., Ohnishi, H., Kato, Z., Yamazaki, M., Okuno, Y., Miyano, S., Kojima, S., Ogawa, S., Andrews, T. D., Field, M. A., Burgio, G., Morio, T., Vinuesa, C. G., Kanegane, H., Cook, M. C.: Gain-of-function IKBKB mutation causes human combined immune deficiency. J Exp Med, 215: 2715-2724 (2018).
  4. Fujisawa, M., Sakata-Yanagimoto, M., Nishizawa, S., Komori, D., Gershon, P., Kiryu, M., Tanzima, S., Fukumoto, K., Enami, T., Muratani, M., Yoshida K., Ogawa, S., Matsue, K., Nakamura, N., Takeuchi, K., Izutsu, K., Fujimoto, K., Teshima, T., Miyoshi, H., Gaulard, P., Ohshima, K., Chiba, S.: Activation of RHOA-VAV1 signaling in angioimmunoblastic T-cell lymphoma. Leukemia, 32: 694-702 (2018).
  5. Hamada, M., Doisaki, S., Okuno, Y., Muramatsu, H., Hama, A., Kawashima, N., Narita, A., Nishio, N., Yoshida K., Kanno, H., Manabe, A., Taga, T., Takahashi, Y., Miyano, S., Ogawa, S., Kojima, S.: Whole-exome analysis to detect congenital hemolytic anemia mimicking congenital dyserythropoietic anemia. Int J Hematol, 108: 306-311 (2018).
  6. Hiramoto, N., Takeda, J., Yoshida K., Ono, Y., Yoshioka, S., Yamauchi, N., Fujimoto, A., Maruoka, H., Shiraishi, Y., Tanaka, H., Chiba, K., Imai, Y., Miyano, S., Ogawa, S., Ishikawa, T.: Donor cell-derived transient abnormal myelopoiesis as a specific complication of umbilical cord blood transplantation. Bone Marrow Transplant, 53: 225-227 (2018).
  7. Hoshino, A., Takashima, T., Yoshida K., Morimoto, A., Kawahara, Y., Yeh, T. W., Okano, T., Yamashita, M., Mitsuiki, N., Imai, K., Sakatani, T., Nakazawa, A., Okuno, Y., Shiraishi, Y., Chiba, K., Tanaka, H., Miyano, S., Ogawa, S., Kojima, S., Morio, T., Kanegane, H.: Dysregulation of Epstein-Barr Virus Infection in Hypomorphic ZAP70 Mutation. J Infect Dis, 218: 825-834 (2018).
  8. Isobe, T., Seki, M., Yoshida K., Sekiguchi, M., Shiozawa, Y., Shiraishi, Y., Kimura, S., Yoshida, M., Inoue, Y., Yokoyama, A., Kakiuchi, N., Suzuki, H., Kataoka, K., Sato, Y., Kawai, T., Chiba, K., Tanaka, H., Shimamura, T., Kato, M., Iguchi, A., Hama, A., Taguchi, T., Akiyama, M., Fujimura, J., Inoue, A., Ito, T., Deguchi, T., Kiyotani, C., Iehara, T., Hosoi, H., Oka, A., Sanada, M., Tanaka, Y., Hata, K., Miyano, S., Ogawa, S., Takita, J.: Integrated Molecular Characterization of the Lethal Pediatric Cancer Pancreatoblastoma. Cancer Res, 78: 865-876 (2018).
  9. Katagiri, S., Umezu, T., Azuma, K., Asano, M., Akahane, D., Makishima, H., Yoshida K., Watatani, Y., Chiba, K., Miyano, S., Ogawa, S., Ohyashiki, J. H., Ohyashiki, K.: Hidden FLT3-D835Y clone in FLT3-ITD-positive acute myeloid leukemia that evolved into very late relapse with T-lymphoblastic leukemia. Leuk Lymphoma, 59: 1490-1493 (2018).
  10. Kataoka, K., Iwanaga, M., Yasunaga, J. I., Nagata, Y., Kitanaka, A., Kameda, T., Yoshimitsu, M., Shiraishi, Y., Sato-Otsubo, A., Sanada, M., Chiba, K., Tanaka, H., Ochi, Y., Aoki, K., Suzuki, H., Shiozawa, Y., Yoshizato, T., Sato, Y., Yoshida K., Nosaka, K., Hishizawa, M., Itonaga, H., Imaizumi, Y., Munakata, W., Shide, K., Kubuki, Y., Hidaka, T., Nakamaki, T., Ishiyama, K., Miyawaki, S., Ishii, R., Nureki, O., Tobinai, K., Miyazaki, Y., Takaori-Kondo, A., Shibata, T., Miyano, S., Ishitsuka, K., Utsunomiya, A., Shimoda, K., Matsuoka, M., Watanabe, T., Ogawa, S.: Prognostic relevance of integrated genetic profiling in adult T-cell leukemia/lymphoma. Blood, 131: 215-225 (2018).
  11. Kon, A., Yamazaki, S., Nannya, Y., Kataoka, K., Ota, Y., Nakagawa, M. M., Yoshida K., Shiozawa, Y., Morita, M., Yoshizato, T., Sanada, M., Nakayama, M., Koseki, H., Nakauchi, H., Ogawa, S.: Physiological Srsf2 P95H expression causes impaired hematopoietic stem cell functions and aberrant RNA splicing in mice. Blood, 131: 621-635 (2018).
  12. Kouzuki, K., Umeda, K., Saida, S., Kato, I., Hiramatsu, H., Funaki, T., Kanda, K., Muramatsu, H., Yoshida K., Ogawa, S., Adachi, S.: Sudden Intracranial Hemorrhage in a Patient With Atypical Chronic Myeloid Leukemia in Chronic Phase. J Pediatr Hematol Oncol, 40: e553-e556 (2018).
  13. Kudo, K., Ueno, H., Sato, T., Kubo, K., Kanezaki, R., Kobayashi, A., Kamio, T., Sasaki, S., Terui, K., Kurose, A., Yoshida K., Shiozawa, Y., Toki, T., Ogawa, S., Ito, E.: Two siblings with familial neuroblastoma with distinct clinical phenotypes harboring an ALK germline mutation. Genes Chromosomes Cancer, 57: 665-669 (2018).
  14. Matsuo, H., Yoshida K., Fukumura, K., Nakatani, K., Noguchi, Y., Takasaki, S., Noura, M., Shiozawa, Y., Shiraishi, Y., Chiba, K., Tanaka, H., Okada, A., Nannya, Y., Takeda, J., Ueno, H., Shiba, N., Yamato, G., Handa, H., Ono, Y., Hiramoto, N., Ishikawa, T., Usuki, K., Ishiyama, K., Miyawaki, S., Itonaga, H., Miyazaki, Y., Kawamura, M., Yamaguchi, H., Kiyokawa, N., Tomizawa, D., Taga, T., Tawa, A., Hayashi, Y., Mano, H., Miyano, S., Kamikubo, Y., Ogawa, S., Adachi, S.: Recurrent CCND3 mutations in MLL-rearranged acute myeloid leukemia. Blood Adv, 2: 2879-2889 (2018).
  15. Murakami, N., Okuno, Y., Yoshida K., Shiraishi, Y., Nagae, G., Suzuki, K., Narita, A., Sakaguchi, H., Kawashima, N., Wang, X., Xu, Y., Chiba, K., Tanaka, H., Hama, A., Sanada, M., Ito, M., Hirayama, M., Watanabe, A., Ueno, T., Kojima, S., Aburatani, H., Mano, H., Miyano, S., Ogawa, S., Takahashi, Y., Muramatsu, H.: Integrated molecular profiling of juvenile myelomonocytic leukemia. Blood, 131: 1576-1586 (2018).
  16. Nagata, Y., Narumi, S., Guan, Y., Przychodzen, B. P., Hirsch, C. M., Makishima, H., Shima, H., Aly, M., Pastor, V., Kuzmanovic, T., Radivoyevitch, T., Adema, V., Awada, H., Yoshida K., Li, S., Sole, F., Hanna, R., Jha, B. K., LaFramboise, T., Ogawa, S., Sekeres, M. A., Wlodarski, M. W., Cammenga, J., Maciejewski, J. P.: Germline loss-of-function SAMD9 and SAMD9L alterations in adult myelodysplastic syndromes. Blood, 132: 2309-2313 (2018).
  17. Ochi, Y., Hiramoto, N., Yoshizato, T., Ono, Y., Takeda, J., Shiozawa, Y., Yoshida K., Kakiuchi, N., Shiraishi, Y., Tanaka, H., Chiba, K., Kazuma, Y., Tabata, S., Yonetani, N., Uehara, K., Yamashita, D., Imai, Y., Nagafuji, K., Yamakawa, M., Miyano, S., Takaori-Kondo, A., Ogawa, S., Ishikawa, T.: Clonally related diffuse large B-cell lymphoma and interdigitating dendritic cell sarcoma sharing MYC translocation. Haematologica, 103: e553-e556 (2018).
  18. Sakai, H., Hosono, N., Nakazawa, H., Przychodzen, B., Polprasert, C., Carraway, H. E., Sekeres, M. A., Radivoyevitch, T., Yoshida K., Sanada, M., Yoshizato, T., Kataoka, K., Nakagawa, M. M., Ueno, H., Nannya, Y., Kon, A., Shiozawa, Y., Takeda, J., Shiraishi, Y., Chiba, K., Miyano, S., Singh, J., Padgett, R. A., Ogawa, S., Maciejewski, J. P., Makishima, H.: A novel genetic and morphologic phenotype of ARID2-mediated myelodysplasia. Leukemia, 32: 839-843 (2018).
  19. Shiozawa, Y., Malcovati, L., Galli, A., Sato-Otsubo, A., Kataoka, K., Sato, Y., Watatani, Y., Suzuki, H., Yoshizato, T., Yoshida K., Sanada, M., Makishima, H., Shiraishi, Y., Chiba, K., Hellstrom-Lindberg, E., Miyano, S., Ogawa, S., Cazzola, M.: Aberrant splicing and defective mRNA production induced by somatic spliceosome mutations in myelodysplasia. Nat Commun, 9: 3649 (2018).
  20. Takagi, M., Hoshino, A., Yoshida K., Ueno, H., Imai, K., Piao, J., Kanegane, H., Yamashita, M., Okano, T., Muramatsu, H., Okuno, Y., Shiraishi, Y., Chiba, K., Tanaka, H., Miyano, S., Ogawa, S., Hayashi, Y., Kojima, S., Morio, T.: Genetic heterogeneity of uncharacterized childhood autoimmune diseases with lymphoproliferation. Pediatr Blood Cancer, 65:  (2018).
  21. Toki, T., Yoshida K., Wang, R., Nakamura, S., Maekawa, T., Goi, K., Katoh, M. C., Mizuno, S., Sugiyama, F., Kanezaki, R., Uechi, T., Nakajima, Y., Sato, Y., Okuno, Y., Sato-Otsubo, A., Shiozawa, Y., Kataoka, K., Shiraishi, Y., Sanada, M., Chiba, K., Tanaka, H., Terui, K., Sato, T., Kamio, T., Sakaguchi, H., Ohga, S., Kuramitsu, M., Hamaguchi, I., Ohara, A., Kanno, H., Miyano, S., Kojima, S., Ishiguro, A., Sugita, K., Kenmochi, N., Takahashi, S., Eto, K., Ogawa, S., Ito, E.: De Novo Mutations Activating Germline TP53 in an Inherited Bone-Marrow-Failure Syndrome. Am J Hum Genet, 103: 440-447 (2018).
  22. Yamato, G., Shiba, N., Yoshida K., Hara, Y., Shiraishi, Y., Ohki, K., Okubo, J., Park, M. J., Sotomatsu, M., Arakawa, H., Kiyokawa, N., Tomizawa, D., Adachi, S., Taga, T., Horibe, K., Miyano, S., Ogawa, S., Hayashi, Y.: RUNX1 mutations in pediatric acute myeloid leukemia are associated with distinct genetic features and an inferior prognosis. Blood, 131: 2266-2270 (2018).
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