Jump to Main Contents
研究所ロゴ

Home > Organization > Divisions and Independent Research Units > Division of Cancer Evolution > Research Papers > 2014

2014

  1. Becker, H., Yoshida K., Blagitko-Dorfs, N., Claus, R., Pantic, M., Abdelkarim, M., Niemoller, C., Greil, C., Hackanson, B., Shiraishi, Y., Chiba, K., Tanaka, H., Miyano, S., Dohner, K., Schnittger, S., Henneke, P., Niemeyer, C. M., Flotho, C., Pfeifer, D., Ogawa, S., Lubbert, M.: Tracing the development of acute myeloid leukemia in CBL syndrome. Blood, 123: 1883-1886 (2014).
  2. Damm, F., Mylonas, E., Cosson, A., Yoshida K., Della Valle, V., Mouly, E., Diop, M., Scourzic, L., Shiraishi, Y., Chiba, K., Tanaka, H., Miyano, S., Kikushige, Y., Davi, F., Lambert, J., Gautheret, D., Merle-Beral, H., Sutton, L., Dessen, P., Solary, E., Akashi, K., Vainchenker, W., Mercher, T., Droin, N., Ogawa, S., Nguyen-Khac, F., Bernard, O. A.: Acquired initiating mutations in early hematopoietic cells of CLL patients. Cancer Discov, 4: 1088-1101 (2014).
  3. Haferlach, T., Nagata, Y., Grossmann, V., Okuno, Y., Bacher, U., Nagae, G., Schnittger, S., Sanada, M., Kon, A., Alpermann, T., Yoshida K., Roller, A., Nadarajah, N., Shiraishi, Y., Shiozawa, Y., Chiba, K., Tanaka, H., Koeffler, H. P., Klein, H. U., Dugas, M., Aburatani, H., Kohlmann, A., Miyano, S., Haferlach, C., Kern, W., Ogawa, S.: Landscape of genetic lesions in 944 patients with myelodysplastic syndromes. Leukemia, 28: 241-247 (2014).
  4. Hasegawa, S., Imai, K., Yoshida K., Okuno, Y., Muramatsu, H., Shiraishi, Y., Chiba, K., Tanaka, H., Miyano, S., Kojima, S., Ogawa, S., Morio, T., Mizutani, S., Takagi, M.: Whole-exome sequence analysis of ataxia telangiectasia-like phenotype. J Neurol Sci, 340: 86-90 (2014).
  5. Hosono, N., Makishima, H., Jerez, A., Yoshida K., Przychodzen, B., McMahon, S., Shiraishi, Y., Chiba, K., Tanaka, H., Miyano, S., Sanada, M., Gomez-Segui, I., Verma, A. K., McDevitt, M. A., Sekeres, M. A., Ogawa, S., Maciejewski, J. P.: Recurrent genetic defects on chromosome 7q in myeloid neoplasms. Leukemia, 28: 1348-1351 (2014).
  6. Matsunawa, M., Yamamoto, R., Sanada, M., Sato-Otsubo, A., Shiozawa, Y., Yoshida K., Otsu, M., Shiraishi, Y., Miyano, S., Isono, K., Koseki, H., Nakauchi, H., Ogawa, S.: Haploinsufficiency of Sf3b1 leads to compromised stem cell function but not to myelodysplasia. Leukemia, 28: 1844-1850 (2014).
  7. Muto, H., Sakata-Yanagimoto, M., Nagae, G., Shiozawa, Y., Miyake, Y., Yoshida K., Enami, T., Kamada, Y., Kato, T., Uchida, K., Nanmoku, T., Obara, N., Suzukawa, K., Sanada, M., Nakamura, N., Aburatani, H., Ogawa, S., Chiba, S.: Reduced TET2 function leads to T-cell lymphoma with follicular helper T-cell-like features in mice. Blood Cancer J, 4: e264 (2014).
  8. Nakamoto-Matsubara, R., Sakata-Yanagimoto, M., Enami, T., Yoshida K., Yanagimoto, S., Shiozawa, Y., Nanmoku, T., Satomi, K., Muto, H., Obara, N., Kato, T., Kurita, N., Yokoyama, Y., Izutsu, K., Ota, Y., Sanada, M., Shimizu, S., Komeno, T., Sato, Y., Ito, T., Kitabayashi, I., Takeuchi, K., Nakamura, N., Ogawa, S., Chiba, S.: Detection of the G17V RHOA mutation in angioimmunoblastic T-cell lymphoma and related lymphomas using quantitative allele-specific PCR. PLoS One, 9: e109714 (2014).
  9. Sakata-Yanagimoto, M., Enami, T., Yoshida K., Shiraishi, Y., Ishii, R., Miyake, Y., Muto, H., Tsuyama, N., Sato-Otsubo, A., Okuno, Y., Sakata, S., Kamada, Y., Nakamoto-Matsubara, R., Tran, N. B., Izutsu, K., Sato, Y., Ohta, Y., Furuta, J., Shimizu, S., Komeno, T., Sato, Y., Ito, T., Noguchi, M., Noguchi, E., Sanada, M., Chiba, K., Tanaka, H., Suzukawa, K., Nanmoku, T., Hasegawa, Y., Nureki, O., Miyano, S., Nakamura, N., Takeuchi, K., Ogawa, S., Chiba, S.: Somatic RHOA mutation in angioimmunoblastic T cell lymphoma. Nat Genet, 46: 171-175 (2014).
  10. Sato, Y., Maekawa, S., Ishii, R., Sanada, M., Morikawa, T., Shiraishi, Y., Yoshida K., Nagata, Y., Sato-Otsubo, A., Yoshizato, T., Suzuki, H., Shiozawa, Y., Kataoka, K., Kon, A., Aoki, K., Chiba, K., Tanaka, H., Kume, H., Miyano, S., Fukayama, M., Nureki, O., Homma, Y., Ogawa, S.: Recurrent somatic mutations underlie corticotropin-independent Cushing's syndrome. Science, 344: 917-920 (2014).
  11. Seki, M., Yoshida K., Shiraishi, Y., Shimamura, T., Sato, Y., Nishimura, R., Okuno, Y., Chiba, K., Tanaka, H., Kato, K., Kato, M., Hanada, R., Nomura, Y., Park, M. J., Ishida, T., Oka, A., Igarashi, T., Miyano, S., Hayashi, Y., Ogawa, S., Takita, J.: Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma. Cancer Res, 74: 2742-2749 (2014).
  12. Shen, W., Clemente, M. J., Hosono, N., Yoshida K., Przychodzen, B., Yoshizato, T., Shiraishi, Y., Miyano, S., Ogawa, S., Maciejewski, J. P., Makishima, H.: Deep sequencing reveals stepwise mutation acquisition in paroxysmal nocturnal hemoglobinuria. J Clin Invest, 124: 4529-4538 (2014).
  13. Yoshida K., Ogawa, S.: Splicing factor mutations and cancer. Wiley Interdiscip Rev RNA, 5: 445-459 (2014).
  • Our Research Focus