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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 > 2016年

2016年

  1. Arashiki, N., Takakuwa, Y., Mohandas, N., Hale, J., Yoshida K., Ogura, H., Utsugisawa, T., Ohga, S., Miyano, S., Ogawa, S., Kojima, S., Kanno, H.: ATP11C is a major flippase in human erythrocytes and its defect causes congenital hemolytic anemia. Haematologica, 101: 559-565 (2016).
  2. Ikeda, F., Toki, T., Kanezaki, R., Terui, K., Yoshida K., Kanno, H., Ohga, S., Ohara, A., Kojima, S., Ogawa, S., Ito, E.: ALDH2 polymorphism in patients with Diamond-Blackfan anemia in Japan. Int J Hematol, 103: 112-114 (2016).
  3. Imashuku, S., Muramatsu, H., Sugihara, T., Okuno, Y., Wang, X., Yoshida K., Kato, A., Kato, K., Tatsumi, Y., Hattori, A., Kita, S., Oe, K., Sueyoshi, A., Usui, T., Shiraishi, Y., Chiba, K., Tanaka, H., Miyano, S., Ogawa, S., Kojima, S., Kanno, H.: PIEZO1 gene mutation in a Japanese family with hereditary high phosphatidylcholine hemolytic anemia and hemochromatosis-induced diabetes mellitus. Int J Hematol, 104: 125-129 (2016).
  4. Kataoka, K., Shiraishi, Y., Takeda, Y., Sakata, S., Matsumoto, M., Nagano, S., Maeda, T., Nagata, Y., Kitanaka, A., Mizuno, S., Tanaka, H., Chiba, K., Ito, S., Watatani, Y., Kakiuchi, N., Suzuki, H., Yoshizato, T., Yoshida K., Sanada, M., Itonaga, H., Imaizumi, Y., Totoki, Y., Munakata, W., Nakamura, H., Hama, N., Shide, K., Kubuki, Y., Hidaka, T., Kameda, T., Masuda, K., Minato, N., Kashiwase, K., Izutsu, K., Takaori-Kondo, A., Miyazaki, Y., Takahashi, S., Shibata, T., Kawamoto, H., Akatsuka, Y., Shimoda, K., Takeuchi, K., Seya, T., Miyano, S., Ogawa, S.: Aberrant PD-L1 expression through 3'-UTR disruption in multiple cancers. Nature, 534: 402-406 (2016).
  5. Kato, M., Seki, M., Yoshida K., Sato, Y., Oyama, R., Arakawa, Y., Kishimoto, H., Taki, T., Akiyama, M., Shiraishi, Y., Chiba, K., Tanaka, H., Mitsuiki, N., Kajiwara, M., Mizutani, S., Sanada, M., Miyano, S., Ogawa, S., Koh, K., Takita, J.: Genomic analysis of clonal origin of Langerhans cell histiocytosis following acute lymphoblastic leukaemia. Br J Haematol, 175: 169-172 (2016).
  6. Ki Kim, S., Ueda, Y., Hatano, E., Kakiuchi, N., Takeda, H., Goto, T., Shimizu, T., Yoshida K., Ikura, Y., Shiraishi, Y., Chiba, K., Tanaka, H., Miyano, S., Uemoto, S., Chiba, T., Ogawa, S., Marusawa, H.: TERT promoter mutations and chromosome 8p loss are characteristic of nonalcoholic fatty liver disease-related hepatocellular carcinoma. Int J Cancer, 139: 2512-2518 (2016).
  7. Kim, T., Yoshida K., Kim, Y. K., Tyndel, M. S., Park, H. J., Choi, S. H., Ahn, J. S., Jung, S. H., Yang, D. H., Lee, J. J., Kim, H. J., Kong, G., Ogawa, S., Zhang, Z., Kim, H. J., Kim, D. D.: Clonal dynamics in a single AML case tracked for 9 years reveals the complexity of leukemia progression. Leukemia, 30: 295-302 (2016).
  8. Kitamura, K., Okuno, Y., Yoshida K., Sanada, M., Shiraishi, Y., Muramatsu, H., Kobayashi, R., Furukawa, K., Miyano, S., Kojima, S., Ogawa, S., Kunishima, S.: Functional characterization of a novel GFI1B mutation causing congenital macrothrombocytopenia. J Thromb Haemost, 14: 1462-1469 (2016).
  9. Madan, V., Shyamsunder, P., Han, L., Mayakonda, A., Nagata, Y., Sundaresan, J., Kanojia, D., Yoshida K., Ganesan, S., Hattori, N., Fulton, N., Tan, K. T., Alpermann, T., Kuo, M. C., Rostami, S., Matthews, J., Sanada, M., Liu, L. Z., Shiraishi, Y., Miyano, S., Chendamarai, E., Hou, H. A., Malnassy, G., Ma, T., Garg, M., Ding, L. W., Sun, Q. Y., Chien, W., Ikezoe, T., Lill, M., Biondi, A., Larson, R. A., Powell, B. L., Lubbert, M., Chng, W. J., Tien, H. F., Heuser, M., Ganser, A., Koren-Michowitz, M., Kornblau, S. M., Kantarjian, H. M., Nowak, D., Hofmann, W. K., Yang, H., Stock, W., Ghavamzadeh, A., Alimoghaddam, K., Haferlach, T., Ogawa, S., Shih, L. Y., Mathews, V., Koeffler, H. P.: Comprehensive mutational analysis of primary and relapse acute promyelocytic leukemia. Leukemia, 30: 2430 (2016).
  10. Mansouri, L., Noerenberg, D., Young, E., Mylonas, E., Abdulla, M., Frick, M., Asmar, F., Ljungstrom, V., Schneider, M., Yoshida K., Skaftason, A., Pandzic, T., Gonzalez, B., Tasidou, A., Waldhueter, N., Rivas-Delgado, A., Angelopoulou, M., Ziepert, M., Arends, C. M., Couronne, L., Lenze, D., Baldus, C. D., Bastard, C., Okosun, J., Fitzgibbon, J., Dorken, B., Drexler, H. G., Roos-Weil, D., Schmitt, C. A., Munch-Petersen, H. D., Zenz, T., Hansmann, M. L., Strefford, J. C., Enblad, G., Bernard, O. A., Ralfkiaer, E., Erlanson, M., Korkolopoulou, P., Hultdin, M., Papadaki, T., Gronbaek, K., Lopez-Guillermo, A., Ogawa, S., Kuppers, R., Stamatopoulos, K., Stavroyianni, N., Kanellis, G., Rosenwald, A., Campo, E., Amini, R. M., Ott, G., Vassilakopoulos, T. P., Hummel, M., Rosenquist, R., Damm, F.: Frequent NFKBIE deletions are associated with poor outcome in primary mediastinal B-cell lymphoma. Blood, 128: 2666-2670 (2016).
  11. Merlevede, J., Droin, N., Qin, T., Meldi, K., Yoshida K., Morabito, M., Chautard, E., Auboeuf, D., Fenaux, P., Braun, T., Itzykson, R., de Botton, S., Quesnel, B., Commes, T., Jourdan, E., Vainchenker, W., Bernard, O., Pata-Merci, N., Solier, S., Gayevskiy, V., Dinger, M. E., Cowley, M. J., Selimoglu-Buet, D., Meyer, V., Artiguenave, F., Deleuze, J. F., Preudhomme, C., Stratton, M. R., Alexandrov, L. B., Padron, E., Ogawa, S., Koscielny, S., Figueroa, M., Solary, E.: Mutation allele burden remains unchanged in chronic myelomonocytic leukaemia responding to hypomethylating agents. Nat Commun, 7: 10767 (2016).
  12. Mitani, K., Nagata, Y., Sasaki, K., Yoshida K., Chiba, K., Tanaka, H., Shiraishi, Y., Miyano, S., Makishima, H., Nakamura, Y., Nakamura, Y., Ichikawa, M., Ogawa, S.: Somatic mosaicism in chronic myeloid leukemia in remission. Blood, 128: 2863-2866 (2016).
  13. Mori, T., Nagata, Y., Makishima, H., Sanada, M., Shiozawa, Y., Kon, A., Yoshizato, T., Sato-Otsubo, A., Kataoka, K., Shiraishi, Y., Chiba, K., Tanaka, H., Ishiyama, K., Miyawaki, S., Mori, H., Nakamaki, T., Kihara, R., Kiyoi, H., Koeffler, H. P., Shih, L. Y., Miyano, S., Naoe, T., Haferlach, C., Kern, W., Haferlach, T., Ogawa, S., Yoshida K.: Somatic PHF6 mutations in 1760 cases with various myeloid neoplasms. Leukemia, 30: 2270-2273 (2016).
  14. Nagata, Y., Kontani, K., Enami, T., Kataoka, K., Ishii, R., Totoki, Y., Kataoka, T. R., Hirata, M., Aoki, K., Nakano, K., Kitanaka, A., Sakata-Yanagimoto, M., Egami, S., Shiraishi, Y., Chiba, K., Tanaka, H., Shiozawa, Y., Yoshizato, T., Suzuki, H., Kon, A., Yoshida K., Sato, Y., Sato-Otsubo, A., Sanada, M., Munakata, W., Nakamura, H., Hama, N., Miyano, S., Nureki, O., Shibata, T., Haga, H., Shimoda, K., Katada, T., Chiba, S., Watanabe, T., Ogawa, S.: Variegated RHOA mutations in adult T-cell leukemia/lymphoma. Blood, 127: 596-604 (2016).
  15. Niemoller, C., Renz, N., Bleul, S., Blagitko-Dorfs, N., Greil, C., Yoshida K., Pfeifer, D., Follo, M., Duyster, J., Claus, R., Ogawa, S., Lubbert, M., Becker, H.: Single cell genotyping of exome sequencing-identified mutations to characterize the clonal composition and evolution of inv(16) AML in a CBL mutated clonal hematopoiesis. Leuk Res, 47: 41-46 (2016).
  16. Sakurai, M., Kasahara, H., Yoshida K., Yoshimi, A., Kunimoto, H., Watanabe, N., Shiraishi, Y., Chiba, K., Tanaka, H., Harada, Y., Harada, H., Kawakita, T., Kurokawa, M., Miyano, S., Takahashi, S., Ogawa, S., Okamoto, S., Nakajima, H.: Genetic basis of myeloid transformation in familial platelet disorder/acute myeloid leukemia patients with haploinsufficient RUNX1 allele. Blood Cancer J, 6: e392 (2016).
  17. Shiba, N., Yoshida K., Shiraishi, Y., Okuno, Y., Yamato, G., Hara, Y., Nagata, Y., Chiba, K., Tanaka, H., Terui, K., Kato, M., Park, M. J., Ohki, K., Shimada, A., Takita, J., Tomizawa, D., Kudo, K., Arakawa, H., Adachi, S., Taga, T., Tawa, A., Ito, E., Horibe, K., Sanada, M., Miyano, S., Ogawa, S., Hayashi, Y.: Whole-exome sequencing reveals the spectrum of gene mutations and the clonal evolution patterns in paediatric acute myeloid leukaemia. Br J Haematol, 175: 476-489 (2016).
  18. Tsujita, Y., Mitsui-Sekinaka, K., Imai, K., Yeh, T. W., Mitsuiki, N., Asano, T., Ohnishi, H., Kato, Z., Sekinaka, Y., Zaha, K., Kato, T., Okano, T., Takashima, T., Kobayashi, K., Kimura, M., Kunitsu, T., Maruo, Y., Kanegane, H., Takagi, M., Yoshida K., Okuno, Y., Muramatsu, H., Shiraishi, Y., Chiba, K., Tanaka, H., Miyano, S., Kojima, S., Ogawa, S., Ohara, O., Okada, S., Kobayashi, M., Morio, T., Nonoyama, S.: Phosphatase and tensin homolog (PTEN) mutation can cause activated phosphatidylinositol 3-kinase delta syndrome-like immunodeficiency. J Allergy Clin Immunol, 138: 1672-1680 e1610 (2016).
  19. Uchi, R., Takahashi, Y., Niida, A., Shimamura, T., Hirata, H., Sugimachi, K., Sawada, G., Iwaya, T., Kurashige, J., Shinden, Y., Iguchi, T., Eguchi, H., Chiba, K., Shiraishi, Y., Nagae, G., Yoshida K., Nagata, Y., Haeno, H., Yamamoto, H., Ishii, H., Doki, Y., Iinuma, H., Sasaki, S., Nagayama, S., Yamada, K., Yachida, S., Kato, M., Shibata, T., Oki, E., Saeki, H., Shirabe, K., Oda, Y., Maehara, Y., Komune, S., Mori, M., Suzuki, Y., Yamamoto, K., Aburatani, H., Ogawa, S., Miyano, S., Mimori, K.: Integrated Multiregional Analysis Proposing a New Model of Colorectal Cancer Evolution. PLoS Genet, 12: e1005778 (2016).
  20. Volkert, S., Haferlach, T., Holzwarth, J., Zenger, M., Kern, W., Staller, M., Nagata, Y., Yoshida K., Ogawa, S., Schnittger, S., Haferlach, C.: Array CGH identifies copy number changes in 11% of 520 MDS patients with normal karyotype and uncovers prognostically relevant deletions. Leukemia, 30: 257-260 (2016).
  21. Yabe, M., Yabe, H., Morimoto, T., Fukumura, A., Ohtsubo, K., Koike, T., Yoshida K., Ogawa, S., Ito, E., Okuno, Y., Muramatsu, H., Kojima, S., Matsuo, K., Hira, A., Takata, M.: The phenotype and clinical course of Japanese Fanconi Anaemia infants is influenced by patient, but not maternal ALDH2 genotype. Br J Haematol, 175: 457-461 (2016).
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