Physiological significance of WDR45, a responsible gene for β-propeller protein associated neurodegeneration (BPAN), in brain development von Noda, Mariko, Ito, Hidenori, Nagata, Koh-ichi

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Role of Per3, a circadian clock gene, in embryonic development of mouse cerebral cortex von Noda, Mariko, Iwamoto, Ikuko, Tabata, Hidenori, Yamagata, Takanori, Ito, Hidenori, Nagata, Koh-ichi

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5-Aminolevulinic acid hydrochloride enhances bupivacaine-induced hypotension in spontaneously hypertensive rats von Fukuda, Noboru, Katakawa, Mayumi, Ito, Hidenori, Hara, Takeshi, Otsuka, Noboru, Ishizuka, Masahiro, Abe, Masanori

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Erratic and blood vessel-guided migration of astrocyte progenitors in the cerebral cortex von Tabata, Hidenori, Sasaki, Megumi, Agetsuma, Masakazu, Sano, Hitomi, Hirota, Yuki, Miyajima, Michio, Hayashi, Kanehiro, Honda, Takao, Nishikawa, Masashi, Inaguma, Yutaka, Ito, Hidenori, Takebayashi, Hirohide, Ema, Masatsugu, Ikenaka, Kazuhiro, Nabekura, Junichi, Nagata, Koh-ichi, Nakajima, Kazunori

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Essential role of the nuclear isoform of RBFOX1, a candidate gene for autism spectrum disorders, in the brain development von Hamada, Nanako, Ito, Hidenori, Nishijo, Takuma, Iwamoto, Ikuko, Morishita, Rika, Tabata, Hidenori, Momiyama, Toshihiko, Nagata, Koh-Ichi

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Expression analyses of PLEKHG2, a Rho family-specific guanine nucleotide exchange factor, during mouse brain development von Nishikawa, Masashi, Ito, Hidenori, Noda, Mariko, Hamada, Nanako, Tabata, Hidenori, Nagata, Koh-ichi

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Rho family GTPases, Rac and Cdc42, control the localization of neonatal dentate granule cells during brain development von Ito, Hidenori, Morishita, Rika, Mizuno, Makoto, Tabata, Hidenori, Nagata, Koh‐ichi

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Oral administration of E-type prostanoid (EP) 1 receptor antagonist suppresses carcinogenesis and development of prostate cancer via upregulation of apoptosis in an animal model von Masato, Masahito, Miyata, Yasuyoshi, Kurata, Hiroki, Ito, Hidenori, Mitsunari, Kensuke, Asai, Akihiro, Nakamura, Yuichiro, Araki, Kyohei, Mukae, Yuta, Matsuda, Tsuyoshi, Harada, Junki, Matsuo, Tomohiro, Ohba, Kojiro, Sakai, Hideki

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Biochemical and morphological characterization of SEPT1 in mouse brain von Ito, Hidenori, Morishita, Rika, Noda, Mariko, Iwamoto, Ikuko, Nagata, Koh-ichi

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Evaluation of mRNA Localization Using Double Barrel Scanning Ion Conductance Microscopy von Nashimoto, Yuji, Takahashi, Yasufumi, Zhou, Yuanshu, Ito, Hidenori, Ida, Hiroki, Ino, Kosuke, Matsue, Tomokazu, Shiku, Hitoshi

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Functions of Rhotekin, an Effector of Rho GTPase, and Its Binding Partners in Mammals von Ito, Hidenori, Morishita, Rika, Nagata, Koh-Ichi

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The p.R66W Variant in RAC3 Causes Severe Fetopathy Through Variant-Specific Mechanisms von Sugawara, Ryota, Ito, Hidenori, Tabata, Hidenori, Ueda, Hiroshi, Scala, Marcello, Nagata, Koh-Ichi

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Complete suspension culture of human induced pluripotent stem cells supplemented with suppressors of spontaneous differentiation von Matsuo-Takasaki, Mami, Kambayashi, Sho, Hemmi, Yasuko, Wakabayashi, Tamami, Shimizu, Tomoya, An, Yuri, Ito, Hidenori, Takeuchi, Kazuhiro, Ibuki, Masato, Kawashima, Terasu, Masayasu, Rio, Suzuki, Manami, Kawai, Yoshikazu, Umekage, Masafumi, Kato, Tomoaki M, Noguchi, Michiya, Nakade, Koji, Nakamura, Yukio, Nakaishi, Tomoyuki, Nishishita, Naoki, Tsukahara, Masayoshi, Hayashi, Yohei

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Neuropathophysiological significance of the c.1449T>C/p.(Tyr64Cys) mutation in the CDC42 gene responsible for Takenouchi-Kosaki syndrome von Hamada, Nanako, Ito, Hidenori, Shibukawa, Yukinao, Morishita, Rika, Iwamoto, Ikuko, Okamoto, Nobuhiko, Nagata, Koh-ichi

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Biochemical and Morphological Characterization of a Neurodevelopmental Disorder-Related Mono-ADP-Ribosylhydrolase, MACRO Domain Containing 2 von Ito, Hidenori, Morishita, Rika, Mizuno, Makoto, Kawamura, Noriko, Tabata, Hidenori, Nagata, Koh-ichi

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Functions of CNKSR2 and Its Association with Neurodevelopmental Disorders von Ito, Hidenori, Nagata, Koh-Ichi

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The Relationship between the Presence of an Earlobe Crease and Overactive Bladder: A Cross-Sectional Case-Controlled Study von Ueda, Yasufumi, Matsuo, Tomohiro, Kawada, Ken, Ito, Hidenori, Mitsunari, Kensuke, Ohba, Kojiro, Imamura, Ryoichi

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Impaired Function of PLEKHG2, a Rho-Guanine Nucleotide-Exchange Factor, Disrupts Corticogenesis in Neurodevelopmental Phenotypes von Nishikawa, Masashi, Ito, Hidenori, Tabata, Hidenori, Ueda, Hiroshi, Nagata, Koh-Ichi

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Expression analyses of WAC, a responsible gene for neurodevelopmental disorders, during mouse brain development von Nishikawa, Masashi, Matsuki, Tohru, Hamada, Nanako, Nakayama, Atsuo, Ito, Hidenori, Nagata, Koh-ichi

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Generation of human induced pluripotent stem cell lines derived from two glucose transporter 1 deficiency syndrome patients von Li, Rui, Tsuboi, Hazuki, Ito, Hidenori, Takagi, Daigo, Chang, Yun-Hsuan, Shimizu, Tomoya, Arai, Yutaka, Matsuo-Takasaki, Mami, Noguchi, Michiya, Nakamura, Yukio, Ohnuma, Kiyoshi, Takahashi, Satoru, Hayashi, Yohei

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