Hericenone C attenuates the second phase of formalin-induced nociceptive behavior by suppressing the accumulation of CD11c-positive cells in the paw epidermis via phosphorylated P6... von Li, Junhao, Hamamura, Kengo, Yoshida, Yuya, Kawano, Shimpei, Uchinomiya, Shohei, Xie, Jiahongyi, Scuteri, Damiana, Fukuoka, Kohei, Zaitsu, Orion, Tsurusaki, Fumiaki, Terada, Yuma, Tsukamoto, Ryotaro, Nishi, Takumi, Fukuda, Taiki, Oyama, Kosuke, Bagetta, Giacinto, Ojida, Akio, Shimizu, Kuniyoshi, Ohdo, Shigehiro, Matsunaga, Naoya

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Circadian rhythms in CYP2A5 expression underlie the time-dependent effect of tegafur on breast cancer von Yoshida, Yuya, Fukuda, Taiki, Tanihara, Tomohito, Nishikawa, Naoki, Iwasa, Serina, Adachi, Satoka, Zaitsu, Orion, Terada, Yuma, Tsukamoto, Ryotaro, Shimoshikiryo, Hideki, Fukuoka, Kohei, Tsurusaki, Fumiaki, Hamamura, Kengo, Oyama, Kosuke, Tsuruta, Akito, Koyanagi, Satoru, Matsunaga, Naoya, Ohdo, Shigehiro

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Inhibition of G protein-coupled receptor 68 using homoharringtonine attenuates chronic kidney disease-associated cardiac impairment von Yoshida, Yuya, Fukuoka, Kohei, Sakugawa, Miyu, Kurogi, Masayuki, Hamamura, Kengo, Hamasaki, Keika, Tsurusaki, Fumiaki, Sotono, Kurumi, Nishi, Takumi, Fukuda, Taiki, Kumamoto, Taisei, Oyama, Kosuke, Ogino, Takashi, Tsuruta, Akito, Mayanagi, Kouta, Yamashita, Tomohiro, Fuchino, Hiroyuki, Kawahara, Nobuo, Yoshimatsu, Kayo, Kawakami, Hitomi, Koyanagi, Satoru, Matsunaga, Naoya, Ohdo, Shigehiro

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Integrative Analyses of De Novo Mutations Provide Deeper Biological Insights into Autism Spectrum Disorder von Takata, Atsushi, Miyake, Noriko, Tsurusaki, Yoshinori, Fukai, Ryoko, Miyatake, Satoko, Koshimizu, Eriko, Kushima, Itaru, Okada, Takashi, Morikawa, Mako, Uno, Yota, Ishizuka, Kanako, Nakamura, Kazuhiko, Tsujii, Masatsugu, Yoshikawa, Takeo, Toyota, Tomoko, Okamoto, Nobuhiko, Hiraki, Yoko, Hashimoto, Ryota, Yasuda, Yuka, Saitoh, Shinji, Ohashi, Kei, Sakai, Yasunari, Ohga, Shouichi, Hara, Toshiro, Kato, Mitsuhiro, Nakamura, Kazuyuki, Ito, Aiko, Seiwa, Chizuru, Shirahata, Emi, Osaka, Hitoshi, Matsumoto, Ayumi, Takeshita, Saoko, Tohyama, Jun, Saikusa, Tomoko, Matsuishi, Toyojiro, Nakamura, Takumi, Tsuboi, Takashi, Kato, Tadafumi, Suzuki, Toshifumi, Saitsu, Hirotomo, Nakashima, Mitsuko, Mizuguchi, Takeshi, Tanaka, Fumiaki, Mori, Norio, Ozaki, Norio, Matsumoto, Naomichi

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De novo KIF1A mutations cause intellectual deficit, cerebellar atrophy, lower limb spasticity and visual disturbance von Ohba, Chihiro, Haginoya, Kazuhiro, Osaka, Hitoshi, Kubota, Kazuo, Ishiyama, Akihiko, Hiraide, Takuya, Komaki, Hirofumi, Sasaki, Masayuki, Miyatake, Satoko, Nakashima, Mitsuko, Tsurusaki, Yoshinori, Miyake, Noriko, Tanaka, Fumiaki, Saitsu, Hirotomo, Matsumoto, Naomichi

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De novo KCNT1 mutations in early‐onset epileptic encephalopathy von Ohba, Chihiro, Kato, Mitsuhiro, Takahashi, Nobuya, Osaka, Hitoshi, Shiihara, Takashi, Tohyama, Jun, Nabatame, Shin, Azuma, Junji, Fujii, Yuji, Hara, Munetsugu, Tsurusawa, Reimi, Inoue, Takahito, Ogata, Reina, Watanabe, Yoriko, Togashi, Noriko, Kodera, Hirofumi, Nakashima, Mitsuko, Tsurusaki, Yoshinori, Miyake, Noriko, Tanaka, Fumiaki, Saitsu, Hirotomo, Matsumoto, Naomichi

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Early onset epileptic encephalopathy caused by de novo SCN8A mutations von Ohba, Chihiro, Kato, Mitsuhiro, Takahashi, Satoru, Lerman‐Sagie, Tally, Lev, Dorit, Terashima, Hiroshi, Kubota, Masaya, Kawawaki, Hisashi, Matsufuji, Mayumi, Kojima, Yasuko, Tateno, Akihiko, Goldberg‐Stern, Hadassa, Straussberg, Rachel, Marom, Dafna, Leshinsky‐Silver, Esther, Nakashima, Mitsuko, Nishiyama, Kiyomi, Tsurusaki, Yoshinori, Miyake, Noriko, Tanaka, Fumiaki, Matsumoto, Naomichi, Saitsu, Hirotomo

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De novo WDR45 mutation in a patient showing clinically Rett syndrome with childhood iron deposition in brain von Ohba, Chihiro, Nabatame, Shin, Iijima, Yoshitaka, Nishiyama, Kiyomi, Tsurusaki, Yoshinori, Nakashima, Mitsuko, Miyake, Noriko, Tanaka, Fumiaki, Ozono, Keiichi, Saitsu, Hirotomo, Matsumoto, Naomichi

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A case of autism spectrum disorder arising from a de novo missense mutation in POGZ von Fukai, Ryoko, Hiraki, Yoko, Yofune, Hiroko, Tsurusaki, Yoshinori, Nakashima, Mitsuko, Saitsu, Hirotomo, Tanaka, Fumiaki, Miyake, Noriko, Matsumoto, Naomichi

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Novel VRK1 Mutations in a Patient with Childhood-onset Motor Neuron Disease von Yamaura, Genpei, Higashiyama, Yuichi, Kusama, Kaori, Kunii, Misako, Tanaka, Kenichi, Koyano, Shigeru, Nakashima, Mitsuko, Tsurusaki, Yoshinori, Miyake, Noriko, Saitsu, Hirotomo, Iwahashi, Yukiko, Joki, Hideto, Matsumoto, Naomichi, Doi, Hiroshi, Tanaka, Fumiaki

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Diagnostic utility of whole exome sequencing in patients showing cerebellar and/or vermis atrophy in childhood von Ohba, Chihiro, Osaka, Hitoshi, Iai, Mizue, Yamashita, Sumimasa, Suzuki, Yume, Aida, Noriko, Shimozawa, Nobuyuki, Takamura, Ayumi, Doi, Hiroshi, Tomita-Katsumoto, Atsuko, Nishiyama, Kiyomi, Tsurusaki, Yoshinori, Nakashima, Mitsuko, Miyake, Noriko, Eto, Yoshikatsu, Tanaka, Fumiaki, Matsumoto, Naomichi, Saitsu, Hirotomo

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De novo KCNH1 mutations in four patients with syndromic developmental delay, hypotonia and seizures von Fukai, Ryoko, Saitsu, Hirotomo, Tsurusaki, Yoshinori, Sakai, Yasunari, Haginoya, Kazuhiro, Takahashi, Kazumasa, Hubshman, Monika Weisz, Okamoto, Nobuhiko, Nakashima, Mitsuko, Tanaka, Fumiaki, Miyake, Noriko, Matsumoto, Naomichi

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GRIN1 mutations cause encephalopathy with infantile‐onset epilepsy, and hyperkinetic and stereotyped movement disorders von Ohba, Chihiro, Shiina, Masaaki, Tohyama, Jun, Haginoya, Kazuhiro, Lerman‐Sagie, Tally, Okamoto, Nobuhiko, Blumkin, Lubov, Lev, Dorit, Mukaida, Souichi, Nozaki, Fumihito, Uematsu, Mitsugu, Onuma, Akira, Kodera, Hirofumi, Nakashima, Mitsuko, Tsurusaki, Yoshinori, Miyake, Noriko, Tanaka, Fumiaki, Kato, Mitsuhiro, Ogata, Kazuhiro, Saitsu, Hirotomo, Matsumoto, Naomichi

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Cerebellar ataxia-dominant phenotype in patients with ERCC4 mutations von Doi, Hiroshi, Koyano, Shigeru, Miyatake, Satoko, Nakajima, Shinji, Nakazawa, Yuka, Kunii, Misako, Tomita-Katsumoto, Atsuko, Oda, Kayoko, Yamaguchi, Yukie, Fukai, Ryoko, Ikeda, Shingo, Kato, Rumiko, Ogata, Katsuhisa, Kubota, Shun, Hayashi, Noriko, Takahashi, Keita, Tada, Mikiko, Tanaka, Kenichi, Nakashima, Mitsuko, Tsurusaki, Yoshinori, Miyake, Noriko, Saitsu, Hirotomo, Ogi, Tomoo, Aihara, Michiko, Takeuchi, Hideyuki, Matsumoto, Naomichi, Tanaka, Fumiaki

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PIGN mutations cause congenital anomalies, developmental delay, hypotonia, epilepsy, and progressive cerebellar atrophy von Ohba, Chihiro, Okamoto, Nobuhiko, Murakami, Yoshiko, Suzuki, Yasuhiro, Tsurusaki, Yoshinori, Nakashima, Mitsuko, Miyake, Noriko, Tanaka, Fumiaki, Kinoshita, Taroh, Matsumoto, Naomichi, Saitsu, Hirotomo

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A Japanese case of cerebellar ataxia, spastic paraparesis and deep sensory impairment associated with a novel homozygous TTC19 mutation von Kunii, Misako, Doi, Hiroshi, Higashiyama, Yuichi, Kugimoto, Chiharu, Ueda, Naohisa, Hirata, Junichi, Tomita-Katsumoto, Atsuko, Kashikura-Kojima, Mari, Kubota, Shun, Taniguchi, Midori, Murayama, Kei, Nakashima, Mitsuko, Tsurusaki, Yoshinori, Miyake, Noriko, Saitsu, Hirotomo, Matsumoto, Naomichi, Tanaka, Fumiaki

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Experimental study on the pressure wave propagation in the artificial arterial tree in brain von Shimada, Shinya, Tsurusaki, Ryo, Iwase, Fumiaki, Matsukawa, Mami, Lagrée, Pierre-Yves

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Late-onset spastic ataxia phenotype in a patient with a homozygous DDHD2 mutation von Doi, Hiroshi, Ushiyama, Masao, Baba, Takashi, Tani, Katsuko, Shiina, Masaaki, Ogata, Kazuhiro, Miyatake, Satoko, Fukuda-Yuzawa, Yoko, Tsuji, Shoji, Nakashima, Mitsuko, Tsurusaki, Yoshinori, Miyake, Noriko, Saitsu, Hirotomo, Ikeda, Shu-ichi, Tanaka, Fumiaki, Matsumoto, Naomichi, Yoshida, Kunihiro

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Novel VRK1 Mutations in a Patient with Childhood-onset Motor Neuron Disease von Yamaura, Genpei, Higashiyama, Yuichi, Kusama, Kaori, Kunii, Misako, Tanaka, Kenichi, Koyano, Shigeru, Nakashima, Mitsuko, Tsurusaki, Yoshinori, Miyake, Noriko, Saitsu, Hirotomo, Iwahashi, Yukiko, Joki, Hideto, Matsumoto, Naomichi, Doi, Hiroshi, Tanaka, Fumiaki

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Identification of a Novel Homozygous SPG7 Mutation in a Japanese Patient with Spastic Ataxia: Making an Efficient Diagnosis Using Exome Sequencing for Autosomal Recessive Cerebella... von Doi, Hiroshi, Ohba, Chihiro, Tsurusaki, Yoshinori, Miyatake, Satoko, Miyake, Noriko, Saitsu, Hirotomo, Kawamoto, Yuko, Yoshida, Tamaki, Koyano, Shigeru, Suzuki, Yume, Kuroiwa, Yoshiyuki, Tanaka, Fumiaki, Matsumoto, Naomichi

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