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論文2015年

  1. Vulto-van Silfhout, A. T., Nakagawa, T., Bahi-Buisson, N., Haas, S. A., Hu, H., Bienek, M., Vissers, L. E., Gilissen, C., Tzschach, A., Busche, A., Musebeck, J., Rump, P., Mathijssen, I. B., Avela, K., Somer, M., Doagu, F., Philips, A. K., Rauch, A., Baumer, A., Voesenek, K., Poirier, K., Vigneron, J., Amram, D., Odent, S., Nawara, M., Obersztyn, E., Lenart, J., Charzewska, A., Lebrun, N., Fischer, U., Nillesen, W. M., Yntema, H. G., Jarvela, I., Ropers, H. H., de Vries, B. B., Brunner, H. G., van Bokhoven, H., Raymond, F. L., Willemsen, M. A., Chelly, J., Xiong, Y., Barkovich, A. J., Kalscheuer, V. M., Kleefstra, T. & de Brouwer, A. P. Variants in CUL4B are Associated with Cerebral Malformations. Hum Mutat 36, 106-117 (2015).
  2. Nakagawa, T., Lv, L., Nakagawa, M., Yu, Y., Yu, C., D'Alessio, A. C., Nakayama, K., Fan, H. Y., Chen, X. & Xiong, Y. CRL4(VprBP) E3 Ligase Promotes Monoubiquitylation and Chromatin Binding of TET Dioxygenases. Mol Cell 57, 247-260 (2015).
  3. Hino-Fukuyo, N., Kikuchi, A., Arai-Ichinoi, N., Niihori, T., Sato, R., Suzuki, T., Kudo, H., Sato, Y., Nakayama, T., Kakisaka, Y., Kubota, Y., Kobayashi, T., Funayama, R., Nakayama, K., Uematsu, M., Aoki, Y., Haginoya, K. & Kure, S. Genomic analysis identifies candidate pathogenic variants in 9 of 18 patients with unexplained West syndrome. Hum Genet 134, 649-658 (2015).
  4. Fujiwara, I., Murakami, Y., Niihori, T., Kanno, J., Hakoda, A., Sakamoto, O., Okamoto, N., Funayama, R., Nagashima, T., Nakayama, K., Kinoshita, T., Kure, S., Matsubara, Y. & Aoki, Y. Mutations in PIGL in a patient with Mabry syndrome. Am J Med Genet A. 167A: 777-785, (2015).　
  5. Nakagawa, T. & Nakayama, K. Protein monoubiquitylation: targets and diverse functions. Genes cells 20、543-562 (2015).
  6. Kojima, T., Yamada, T., Akaishi, R., Furuta, I., Saitoh, T., Nakabayashi, K., Nakayama, K.I., Nakayama, K., Akira, S. & Minakami, H. Role of the Atg9a gene in intrauterine growth and survival of fetal mice. Reprod Biol 15, 131-138 (2015).
  7. Wong, W.F., Kohu, K., Nagashima, T., Funayama, R., Matsumoto, M., Movahed, E., Tan, G.M., Yeow, T.C., Looi, C.Y., Kurokawa, M., Osato, M., Igarashi, K., Nakayama, K. & Satake, M. The artificial loss of Runx1 reduces the expression of quiescence-associated transcription factors in CD4 T lymphocytes. Mol Immunol (2015)　
  8. Ellawindy, A., Satoh, K., Sunamura, S., Kikuchi, N., Suzuki, K., Minami, T., Ikeda, S., Tanaka, S., Shimizu, T., Enkhjargal, B., Miyata, S., Taguchi, Y., Handoh, T., Kobayashi, K., Kobayashi, K., Nakayama, K., Miura, M. & Shimokawa, H. Rho-Kinase Inhibition During Early Cardiac Development Causes Arrhythmogenic Right Ventricular Cardiomyopathy in Mice. Arterioscler Thromb Vasc Biol 35, 2172-2184（2015).
  9. Nakagawa, T., Araki, T., Nakagawa, M., Hirao, A., Unno, M. & Nakayama, K. S6 Kinase- and beta-TrCP2-Dependent Degradation of p19Arf Is Required for Cell Proliferation. Mol Cell Biol 35, 3517-3527（2015).
  10. Izumi, R., Warita, H., Niihori, T., Takahashi, T., Tateyama, M., Suzuki, N., Nishiyama, A., Shirota, M., Funayama, R., Nakayama, K., Mitsuhashi, S., Nishino, I., Aoki, Y. & Aoki, M. Isolated inclusion body myopathy caused by a multisystem proteinopathy-linked hnRNPA1 mutation. Neurol Genet 1, e23 (2015).
  11. Niihori, T., Ouchi-Uchiyama, M., Sasahara, Y., Kaneko, T., Hashii, Y., Irie, M., Sato, A., Saito-Nanjo, Y., Funayama, R., Nagashima, T., Inoue, S., Nakayama, K., Ozono, K., Kure, S., Matsubara, Y., Imaizumi, M. & Aoki, Y. Mutations in MECOM, Encoding Oncoprotein EVI1, Cause Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia. Am J Hum Genet 97, 848-854 (2015)