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論文2018年

  1. Wada, Y., Kikuchi, A., Arai-Ichinoi, N., Sakamoto, O., Takezawa, Y., Iwasawa, S., Niihori, T., Nyuzuki, H., Nakajima, Y., Ogawa, E., Ishige, M., Hirai, H., Sasai, H., Fujiki, R., Shirota, M., Funayama, R., Yamamoto, M., Ito, T., Ohara, O., Nakayama ,K., Aoki, Y., Koshiba., S, Fukao, T., Kure S. Biallelic GALM pathogenic variants cause a novel type of galactosemia. Genet Med　Genet Med 21,1286-1294 (2018)
  2. Abe, Y., Honsho, M., Itoh, R., Kawaguchi, R., Fujitani, M., Fujiwara, K., Hirokane, M., Matsuzaki, T., Nakayama, K., Ohgi, R., Marutani, T., Nakayama, KI., Yamashita, T., Fujiki, Y., Peroxisome biogenesis deficiency attenuates the BDNF-TrkB pathway-mediated development of the cerebellum. Life Sci Alliance1, e201800062 (2018).
  3. Morohoshi, A., Nakagawa, T., Nakano, S., Nagasawa, Y., Nakayama, K. The ubiquitin ligase subunit β-TrCP in Sertoli cells is essential for spermatogenesis in mice. Dev Biol 445, 178-188 (2018)
  4. Ashraf, S., Kudo, H., Rao, J., Kikuchi, A., Widmeier, E., Lawson, JA., Tan, W., Hermle, T., Warejko, JK., Shril, S., Airik ,M., Jobst-Schwan ,T., Lovric, S., Braun ,DA., Gee, HY., Schapiro, D., Majmundar, AJ., Sadowski, CE., Pabst, WL., Daga, A., van der Ven AT, Schmidt, JM., Low, BC., Gupta, AB., Tripathi ,BK., Wong ,J., Campbell, K., Metcalfe, K., Schanze, D., Niihori, T., Kaito, H., Nozu, K., Tsukaguchi, H., Tanaka, R., Hamahira, K., Kobayashi, Y., Takizawa, T., Funayama, R., Nakayama, K., Aoki, Y., Kumagai, N., Iijima, K., Fehrenbach, H., Kari, JA., El Desoky S, Jalalah, S., Bogdanovic, R., Stajić, N., Zappel, H., Rakhmetova, A., Wassmer, SR., Jungraithmayr, T., Strehlau, J., Kumar, AS., Bagga, A., Soliman, NA., Mane, SM., Kaufman, L., Lowy, DR., Jairajpuri, MA., Lifton, RP., Pei, Y., Zenker, M., Kure, S., Hildebrandt, F. Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment. Nat Commun 17, 1960 (2018)
  5. Takezawa, Y., Fujie, H., Kikuchi, A., Niihori, T., Funayama, R., Shirota, M., Nakayama, K., Aoki, Y., Sasaki, M., Kure, S. Novel IARS2 mutations in Japanese siblings with CAGSSS, Leigh, and West syndrome. Brain Dev 40, 934-938 (2018)
  6. Takahashi, K., Nagai, T., Chiba, S., Nakayama, K., Mizuno, K. Glucose deprivation induces primary cilium formation through mTORC1 inactivation. J Cell Sci 131, pii: jcs208769 (2018).
  7. Nakagawa, T., Hosogane, M., Nakagawa, M., Morohoshi, A., Funayama, R., Nakayama, K. Transforming Growth Factor β-Induced Proliferative Arrest Mediated by TRIM26-Dependent TAF7 Degradation and Its Antagonism by MYC. Mol Cell Biol38, pii: e00449-17 (2018).
  8. Kayaba, A., Itoh-Nakadai, A., Niibe, K., Shirota, M., Funayama, R., Sugahara-Tobinai ,A., Wong YL, Inui, M., Nakayama ,K., Takai ,T. Bone Marrow PDGFR +Sca-1+ Enriched Mesenchymal Stem Cells Support Survival of and Antibody Production by Plasma Cells in vitro through IL-6. Int Immunol 30, 241-253 (2018).
  9. Takezawa, Y., Kikuchi, A., Haginoya, K., Niihori, T., Numata-Uematsu, Y., Inui, T., Yamamura-Suzuki, S., Miyabayashi, T., Anzai, M., Suzuki-Muromoto, S., Okubo, Y., Endo, W., Togashi, N., Kobayashi, Y., Onuma, A., Funayama, R., Shirota, M., Nakayama, K., Aoki, Y., Kure S. Genomic analysis identifies masqueraders of full-term cerebral palsy. Ann Clin Transl Neurol5, 538-551 (2018).
  10. Ochiai, K., Kondo, H., Okamura, Y., Shima, H., Kurokochi, Y., Kimura, K., Funayama, R., Nagashima, T., Nakayama, K., Yui, K., Kinoshita, K., Igarashi, K. Zinc finger-IRF composite elements bound by Ikaros/IRF4 complexes function as gene repression in plasma cell. Blood Adv 2, 883-894 (2018).
  11. Miura, Y., Morooka, M., Sax N, Roychoudhuri R, Itoh-Nakadai, A., Brydun A, Funayama, R., Nakayama, K., Satomi, S., Matsumoto, M., Igarashi ,K., Muto, A. Bach2 Promotes B Cell Receptor-Induced Proliferation of B Lymphocytes and Represses Cyclin-Dependent Kinase Inhibitors. J Immunol. 200, 2882-2893 (2018).
  12. Nakamura, H., Uematsu, M., Numata-Uematsu, Y., Abe ,Y., Endo, W., Kikuchi, A., Takezawa, Y., Funayama, R., Shirota, M., Nakayama, K., Niihori, T., Aoki, Y., Haginoya, K., Kure S. Rett-like features and cortical visual impairment in a Japanese patient with HECW2 mutation. Brain Dev40, 410-414 (2018).