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論文2014年

  1. Okae, H., Matoba, S., Nagashima, T., Mizutani, E., Inoue, K., Ogonuki, N., Chiba, H., Funayama, R., Tanaka, S., Yaegashi, N., Nakayama, K., Sasaki, H., Ogura, A. & Arima, T. RNA sequencing-based identification of aberrant imprinting in cloned mice. Human molecular genetics 23, 992-1001 (2014).
  2. Ogata, T., Niihori, T., Tanaka, N., Kawai, M., Nagashima, T., Funayama, R., Nakayama, K., Nakashima, S., Kato, F., Fukami, M., Aoki, Y. & Matsubara, Y. TBX1 Mutation Identified by Exome Sequencing in a Japanese Family with 22q11.2 Deletion Syndrome-Like Craniofacial Features and Hypocalcemia. PloS one 9, e91598 (2014).
  3. Kotoshiba, S., Gopinathan, L., Pfeiffenberger, E., Rahim, A., Vardy, L.A., Nakayama, K., Nakayama, K.I. & Kaldis, P. p27 is regulated independently of Skp2 in the absence of Cdk2. Biochimica et biophysica acta 1843, 436-445 (2014).
  4. Fujiwara, T., Fukuhara, N., Funayama, R., Nariai, N., Kamata, M., Nagashima, T., Kojima, K., Onishi, Y., Sasahara, Y., Ishizawa, K., Nagasaki, M., Nakayama, K. & Harigae, H. Identification of acquired mutations by whole-genome sequencing in GATA-2 deficiency evolving into myelodysplasia and acute leukemia. Ann Hematol 93, 1515-1522 (2014).
  5. Lu, Z., Bauzon, F., Fu, H., Cui, J., Zhao, H., Nakayama, K., Nakayama, K.I. & Zhu, L. Skp2 suppresses apoptosis in Rb1-deficient tumours by limiting E2F1 activity. Nature communications 5, 3463 (2014).
  6. Kondo, Y., Ninomiya, M., Kimura, O., Machida, K., Funayama, R., Nagashima, T., Kobayashi, K., Kakazu, E., Kato, T., Nakayama, K., Lai, M. M. & Shimosegawa, T. HCV infection enhances Th17 commitment, which could affect the pathogenesis of autoimmune diseases. PLoS One 9, e98521 (2014)
  7. Izumi, R., Niihori, T., Suzuki, N., Sasahara, Y., Rikiishi, T., Nishiyama, A., Nishiyama, S., Endo, K., Kato, M., Warita, H., Konno, H., Takahashi, T., Tateyama, M., Nagashima, T., Funayama, R., Nakayama, K., Kure, S., Matsubara, Y., Aoki, Y. & Aoki, M. GNE myopathy associated with congenital thrombocytopenia: A report of two siblings. Neuromuscul Disord 24, 1068-1072 (2014).