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論文2013年

  1. Izumi, R., Niihori, T., Aoki, Y., Suzuki, N., Kato, M., Warita, H., Takahashi, T., Tateyama, M., Nagashima, T., Funayama, R., Abe, K., Nakayama, K., Aoki, M. & Matsubara, Y.: Exome sequencing identifies a novel TTN mutation in a family with hereditary myopathy with early respiratory failure. J Hum Genet, 58(5):259-266. (2013)
  2. Sun, S., Horino, S., Itoh-Nakadai, A., Kawabe, T., Asao, A., Takahashi, T., So, T., Funayama, R., Kondo, M., Saitsu, H., Matsumoto, N., Nakayama, K., Ishii, N.: Y-Chromosome-linked B- and NK-cell deficiency in mice. J. Immunol, 190(12):6209-6220. (2013).
  3. Ishikawa, Y., Hosogane, M., Okuyama, R., Aoyama, S., Onoyama, I., Nakayama, KI., Nakayama, K.: Opposing functions of Fbxw7 in keratinocyte growth-differentiation and skin tumorigenesis mediated through negative regulation of c-Myc and Notch. Oncogene, 32, 1921-1932 (2013).
  4. Ninomiya, M., Kondo, Y., Funayama, R., Nagashima, T., Kogure, T., Kakazu, E., Kimura, O., Ueno, Y., Nakayama, K., Shimosegawa, T.: Distinct MicroRNAs Expression Profile in Primary Biliary Cirrhosis and Evaluation of miR 505-3p and miR197-3p as Novel Biomarkers. PloS one 8, e66086 (2013).
  5. Aoki, Y., Niihori, T., Banjo, T., Okamoto, N., Mizuno, S., Kurosawa, K., Ogata, T., Takada, F., Yano, M., Ando, T., Hoshika, T., Barnett, C., Ohashi, H., Kawame, H., Hasegawa, T., Okutani, T., Nagashima, T., Hasegawa, S., Funayama, R., Nagashima, T., Nakayama, K., Inoue, S. I., Watanabe, Y., Ogura, T., Matsubara, Y.: Gain-of-Function Mutations in RIT1 Cause Noonan Syndrome, a RAS/MAPK Pathway Syndrome. Am J Hum Genet, 93(1):173-180.（2013).
  6. Zhao, H., Bauzon, F., Fu, H., Lu, Z., Cui, J., Nakayama, K., Nakayama, K.I., Locker, J., Zhu, L. Skp2 Deletion Unmasks a p27 Safeguard that Blocks Tumorigenesis in the Absence of pRb and p53 Tumor Suppressors. Cancer cell 24, 645-659 (2013).
  7. Khor, E.C., Abel, T., Tickner, J., Chim, S.M., Wang, C., Cheng, T., Ng, B., Ng, P.Y., Teguh, D.A., Kenny, J., Yang, X., Chen, H., Nakayama, K.I., Nakayama, K., Pavlos, N., Zheng, M.H., Xu, J. Loss of protein kinase C-delta protects against LPS-induced osteolysis owing to an intrinsic defect in osteoclastic bone resorption. PloS one 8, e70815 (2013).
  8. Hosogane, M., Funayama, R., Nishida, Y., Nagashima, T., Nakayama, K. Ras-induced changes in H3K27me3 occur after those in transcriptional activity. PLoS genetics 9, e1003698 (2013).