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論文 2022年

  1. Shinohara, M,K., Honda, N., Tanaka,T.,Tatehana, M., Kikkawa,T., Osumi, N., Shinohara,T.:Regulation of male germline transmission patterns by the Trp53-Cdkn1a pathway. Stem Cell Reports (2022).
  2. Nagai,M., Iemura,K., Kikkawa,T., Naher,S., Hattori,S., Hagihara,H., Nagata,K., Anzawa, H., Kugisaki, R., Wanibuchi, H., et al.:Deficiency of CHAMP1, a gene related to intellectual disability, causes impaired neuronal development and a mild behavioral phenotype. Brain Communications 30 August 2022.
  3. Mai, L., Inada, H., Kimura, R., Kanno, K., Matsuda,T., Tachibana, R O.,
    Tucci,V., Komaki ,F., Hiroi, N.,Osum, N.:Advanced paternal age diversifies individual trajectories of vocalization patterns in neonatal mice. iScience (2022).
  4. Corales, L G., Inada, H., Hiraoka, K., Araki, S., Yamanaka, S., Kikkawa, T., Osumi, N.:The subcommissural organ maintains features of neuroepithelial cells in the adult mouse. Journal of Anatomy.31 May 2022.
  5. Ochi, S., Manabe, S., Kikkawa, T., Osumi, N. :Thirty Years’ History since the Discovery of Pax6: From Central Nervous System Development to Neurodevelopmental Disorders. Int. J. Mol. Sci. 2022, 23(11), 6115.