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2021年

  1. Fujii, Y., Sato, Y., Suzuki, H., Kakiuchi, N., Yoshizato, T., Lenis, A. T., Maekawa, S., Yokoyama, A., Takeuchi, Y., Inoue, Y., Ochi, Y., Shiozawa, Y., Aoki, K., Yoshida K., Kataoka, K., Nakagawa, M. M., Nannya, Y., Makishima, H., Miyakawa, J., Kawai, T., Morikawa, T., Shiraishi, Y., Chiba, K., Tanaka, H., Nagae, G., Sanada, M., Sugihara, E., Sato, T. A., Nakagawa, T., Fukayama, M., Ushiku, T., Aburatani, H., Miyano, S., Coleman, J. A., Homma, Y., Solit, D. B., Kume, H., Ogawa, S.: Molecular classification and diagnostics of upper urinary tract urothelial carcinoma. Cancer Cell, 39: 793-809 e798 (2021).
  2. Honda, T., Yamaoka, M., Terao, Y. M., Hasegawa, D., Kumamoto, T., Takagi, M., Yoshida K., Ogawa, S., Goto, H., Akiyama, M.: Successful treatment of hepatosplenic T-cell lymphoma with fludarabine, high-dose cytarabine and subsequent unrelated umbilical cord blood transplantation. Int J Hematol,   (2021).
  3. Hoyer, K., Hablesreiter, R., Inoue, Y., Yoshida K., Briest, F., Christen, F., Kakiuchi, N., Yoshizato, T., Shiozawa, Y., Shiraishi, Y., Striefler, J. K., Bischoff, S., Lohneis, P., Putter, H., Blau, O., Keilholz, U., Bullinger, L., Pelzer, U., Hummel, M., Riess, H., Ogawa, S., Sinn, M., Damm, F.: A genetically defined signature of responsiveness to erlotinib in early-stage pancreatic cancer patients: Results from the CONKO-005 trial. EBioMedicine, 66: 103327 (2021).
  4. Ishida, Y., Kakiuchi, N., Yoshida K., Inoue, Y., Irie, H., Kataoka, T. R., Hirata, M., Funakoshi, T., Matsushita, S., Hata, H., Uchi, H., Yamamoto, Y., Fujisawa, Y., Fujimura, T., Saiki, R., Takeuchi, K., Shiraishi, Y., Chiba, K., Tanaka, H., Otsuka, A., Miyano, S., Kabashima, K., Ogawa, S.: Unbiased Detection of Driver Mutations in Extramammary Paget Disease. Clin Cancer Res, 27: 1756-1765 (2021).
  5. Kaburagi, T., Yamato, G., Shiba, N., Yoshida K., Hara, Y., Tabuchi, K., Shiraishi, Y., Ohki, K., Sotomatsu, M., Arakawa, H., Matsuo, H., Shimada, A., Taki, T., Kiyokawa, N., Tomizawa, D., Horibe, K., Miyano, S., Taga, T., Adachi, S., Ogawa, S., Hayashi, Y.: Clinical significance of RAS pathway alterations in pediatric acute myeloid leukemia. Haematologica,   (2021).
  6. Kimura, S., Sekiguchi, M., Watanabe, K., Hiwatarai, M., Seki, M., Yoshida K., Isobe, T., Shiozawa, Y., Suzuki, H., Hoshino, N., Hayashi, Y., Oka, A., Miyano, S., Ogawa, S., Takita, J.: Association of high-risk neuroblastoma classification based on expression profiles with differentiation and metabolism. PLoS One, 16: e0245526 (2021).
  7. Koyamaishi, S., Kamio, T., Kobayashi, A., Sato, T., Kudo, K., Sasaki, S., Kanezaki, R., Hasegawa, D., Muramatsu, H., Takahashi, Y., Sasahara, Y., Hiramatsu, H., Kakuda, H., Tanaka, M., Ishimura, M., Nishi, M., Ishiguro, A., Yabe, H., Sarashina, T., Yamamoto, M., Yuza, Y., Hyakuna, N., Yoshida K., Kanno, H., Ohga, S., Ohara, A., Kojima, S., Miyano, S., Ogawa, S., Toki, T., Terui, K., Ito, E.: Reduced-intensity conditioning is effective for hematopoietic stem cell transplantation in young pediatric patients with Diamond-Blackfan anemia. Bone Marrow Transplant, 56: 1013-1020 (2021).
  8. Mu A, H. A., Niwa A, Osawa M, Yoshida K, Mori M, Okamoto Y, Inoue K, Kondo K, Kanemaki MT, Matsuda T, Ito E, Kojima S, Nakahata T, Ogawa S, Tanaka K, Matsuo K, Saito MK, Takata M.: Analysis of disease model iPSCs derived from patients with a novel Fanconi anemia–like IBMFS ADH5/ALDH2 deficiency. Blood, 137: 2021-2032 (2021).
  9. Nishimura, A., Hirabayashi, S., Hasegawa, D., Yoshida K., Shiraishi, Y., Ashiarai, M., Hosoya, Y., Fujiwara, T., Harigae, H., Miyano, S., Ogawa, S., Manabe, A.: Acquisition of monosomy 7 and a RUNX1 mutation in Pearson syndrome. Pediatr Blood Cancer, 68: e28799 (2021).
  10. Ochi, Y., Yoshida K., Huang, Y. J., Kuo, M. C., Nannya, Y., Sasaki, K., Mitani, K., Hosoya, N., Hiramoto, N., Ishikawa, T., Branford, S., Shanmuganathan, N., Ohyashiki, K., Takahashi, N., Takaku, T., Tsuchiya, S., Kanemura, N., Nakamura, N., Ueda, Y., Yoshihara, S., Bera, R., Shiozawa, Y., Zhao, L., Takeda, J., Watatani, Y., Okuda, R., Makishima, H., Shiraishi, Y., Chiba, K., Tanaka, H., Sanada, M., Takaori-Kondo, A., Miyano, S., Ogawa, S., Shih, L. Y.: Clonal evolution and clinical implications of genetic abnormalities in blastic transformation of chronic myeloid leukaemia. Nat Commun, 12: 2833 (2021).
  11. Ono, R., Ueno, H., Yoshida K., Takahashi, S., Yoshihara, H., Nozaki, T., Suzuki, K., Nakazawa, A., Saiki, R., Seki, M., Takita, J., Ogawa, S., Manabe, A., Hasegawa, D.: Clonal evidence for the development of neuroblastoma with extensive copy-neutral loss of heterozygosity arising in a mature teratoma. Cancer Sci, 112: 2921-2927 (2021).
  12. Polprasert, C., Takeuchi, Y., Makishima, H., Wudhikarn, K., Kakiuchi, N., Tangnuntachai, N., Assanasen, T., Sitthi, W., Muhamad, H., Lawasut, P., Kongkiatkamon, S., Bunworasate, U., Izutsu, K., Shiraishi, Y., Chiba, K., Tanaka, H., Miyano, S., Ogawa, S., Yoshida K., Rojnuckarin, P.: Frequent mutations in HLA and related genes in extranodal NK/T cell lymphomas. Leuk Lymphoma, 62: 95-103 (2021).
  13. Sasaki, K., Tsujimoto, S., Miyake, M., Uchiyama, Y., Ikeda, J., Yoshitomi, M., Shimosato, Y., Tokumasu, M., Matsuo, H., Yoshida K., Ohki, K., Kaburagi, T., Yamato, G., Hara, Y., Takeuchi, M., Kinoshita, A., Tomizawa, D., Taga, T., Adachi, S., Tawa, A., Horibe, K., Hayashi, Y., Matsumoto, N., Ito, S., Shiba, N.: Droplet digital polymerase chain reaction assay for the detection of the minor clone of KIT D816V in paediatric acute myeloid leukaemia especially showing RUNX1-RUNX1T1 transcripts. Br J Haematol, 194: 414-422 (2021).
  14. Senda, N., Kawaguchi-Sakita, N., Kawashima, M., Inagaki-Kawata, Y., Yoshida K., Takada, M., Kataoka, M., Torii, M., Nishimura, T., Kawaguchi, K., Suzuki, E., Kataoka, Y., Matsumoto, Y., Yoshibayashi, H., Yamagami, K., Tsuyuki, S., Takahara, S., Yamauchi, A., Shinkura, N., Kato, H., Moriguchi, Y., Okamura, R., Kan, N., Suwa, H., Sakata, S., Mashima, S., Yotsumoto, F., Tachibana, T., Tanaka, M., Togashi, K., Haga, H., Yamada, T., Kosugi, S., Inamoto, T., Sugimoto, M., Ogawa, S., Toi, M.: Optimization of prediction methods for risk assessment of pathogenic germline variants in the Japanese population. Cancer Sci, 112: 3338-3348 (2021).
  15. Shimada, K., Yoshida K., Suzuki, Y., Iriyama, C., Inoue, Y., Sanada, M., Kataoka, K., Yuge, M., Takagi, Y., Kusumoto, S., Masaki, Y., Ito, T., Inagaki, Y., Okamoto, A., Kuwatsuka, Y., Nakatochi, M., Shimada, S., Miyoshi, H., Shiraishi, Y., Chiba, K., Tanaka, H., Miyano, S., Shiozawa, Y., Nannya, Y., Okabe, A., Kohno, K., Atsuta, Y., Ohshima, K., Nakamura, S., Ogawa, S., Tomita, A., Kiyoi, H.: Frequent genetic alterations in immune checkpoint-related genes in intravascular large B-cell lymphoma. Blood, 137: 1491-1502 (2021).
  16. Spencer Chapman, M., Ranzoni, A. M., Myers, B., Williams, N., Coorens, T. H. H., Mitchell, E., Butler, T., Dawson, K. J., Hooks, Y., Moore, L., Nangalia, J., Robinson, P. S., Yoshida K., Hook, E., Campbell, P. J., Cvejic, A.: Lineage tracing of human development through somatic mutations. Nature, 595: 85-90 (2021).
  17. Yasudo, H., Ando, T., Maehara, A., Ando, T., Izawa, K., Tanabe, A., Kaitani, A., Nomura, S., Seki, M., Yoshida K., Oda, H., Okamoto, Y., Wang, H., Kamei, A., Kojima, M., Kimura, M., Uchida, K., Nakano, N., Kaneko, J., Ebihara, N., Hasegawa, K., Shimizu, T., Takita, J., Ogawa, H., Okumura, K., Ogawa, S., Tamura, N., Kitaura, J.: A Possible Association Between a Nucleotide-Binding Domain LRR-Containing Protein Family PYD-Containing Protein 1 Mutation and an Autoinflammatory Disease Involving Liver Cirrhosis. Hepatology, 74: 2296-2299 (2021).
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