シナプスオーガナイザーの機能破綻から神経発達障害の発症に至るシナプス病態の解明

Status	Finished
Effective start/end date	2013/04/01 → 2015/03/31

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IL1RAPL1欠損マウスの表現型解析
安村美里, 吉田知之 & 三品昌美, 2015, In: 日本薬理学雑誌. 145, p. 187-192
Research output: Contribution to journal › Article › peer-review
Is d-aspartate produced by glutamic-oxaloacetic transaminase-1 like 1 (Got1l1): A putative aspartate racemase?
Tanaka-Hayashi, A., Hayashi, S., Inoue, R., Ito, T., Konno, K., Yoshida, T., Watanabe, M., Yoshimura, T. & Mori, H., 2015/01/01, In: Amino Acids. 47, 1, p. 79-86 8 p.
Research output: Contribution to journal › Article › peer-review

Open Access
36 Scopus citations
A590T mutation in KCNQ1 C-terminal helix D decreases I_Ks channel trafficking and function but not Yotiao interaction
Kinoshita, K., Komatsu, T., Nishide, K., Hata, Y., Hisajima, N., Takahashi, H., Kimoto, K., Aonuma, K., Tsushima, E., Tabata, T., Yoshida, T., Mori, H., Nishida, K., Yamaguchi, Y., Ichida, F., Fukurotani, K., Inoue, H. & Nishida, N., 2014/07, In: Journal of Molecular and Cellular Cardiology. 72, p. 273-280 8 p.
Research output: Contribution to journal › Article › peer-review
8 Scopus citations