横浜薬科大学 · 健康薬学科

研究关键词●モワット・ウィルソン症候群の原因遺伝子Sip1の神経系における機能解析・●腎臓形成におけるSip1の発現と機能

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• 2. Nishizaki Y , Yoshida L, Isuzugawa T, Asai M, Sakai-Ushikubo H, Hayamizu K, Kuroiwa M, Kawashima Y, Kaneko M. Report on integrated virtual and cadaveric dissection training in anatomy education. Japanese Journal of Pharmaceutical Education. 7, 197-203 (2023)2023
• 3. Shukunami, C., Takimoto, A., Nishizaki, Y ., Yoshimoto, Y., Tanaka, S., Miura, S., Watanabe, H., Sakuma, T., Yamamoto, T., Kondoh, G., Hiraki, Y. Scleraxis is a transcriptional activator that regulates the expression of Tenomodulin, a marker of mature tenocytes and ligamentocytes. Sci Rep. 8 (1): 3155 (2018)2018
• 4. Rasouly HM, Kumar S, Chan S, Pisarek-Horowitz A, Sharma R, Xi QJ, Nishizaki Y , Higashi Y, Salant DJ, Maas RL, Lu W. Loss of Zeb2 in mesenchyme-derived nephrons causes primary glomerulocystic disease. Kidney Int. Dec; 90 (6):1262-1273 (2016)2016
• 5. Takagi T, Nishizaki Y , Matsui F, Wakamatsu N, Higashi Y. De novo inbred heterozygous Zeb2/Sip1 mutant mice uniquely generated by germ-line conditional knockout exhibit craniofacial, callosal and behavioral defects associated with Mowat-Wilson syndrome. Hum Mol Genet. 24 (22): 6390-6402 (2015)2015

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