Introduction of Unique Bag Filter KP Type Pulse Jet Collector von MIYATAKE, Shigeru

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Optical second-harmonic spectroscopy of Au(887) and Au(443) surfaces von Maeda, Yojiro, Iwai, Tetsuya, Satake, Yoshihiko, Fujii, Keishi, Miyatake, Shigeru, Miyazaki, Daisuke, Mizutani, Goro

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The Inspectability and Cleanability of the Nauta Type Mixer with the Big Door von MIYATAKE, Shigeru

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ユニークな乾式集塵機KP型パルスジェットコレクタの紹介 von 宮武, 繁

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DRAFT APPARATUS von MIYATAKE SHIGERU

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ビッグドアを採用したナウタ型ミキサーの点検性，洗浄性 von 宮武, 繁

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METHOD FOR ATTACHING AND DETACHING RUBBER CRAWLER AND TOOL FOR IT von MIYATAKE SHIGERU

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23pYC-2 Excitation light wavelength dependence of the SH intensity pattern from Au(443) von Maeda, Yojiro, Miyatake, Shigeru, Fujii, Keishi, Satake, Yoshihiko, Iwai, Tetsuya, Mizutani, Goro

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METHOD FOR PRODUCING POLYMER FINE PARTICLE von OSHIMA TAKESHI, NAKA YUKIHIKO, MIYATAKE SHIGERU

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23pYC-2 Au(443)面におけるSH光強度パターンの励起光波長依存性(23pYC 表面界面電子物性,領域9(表面・界面,結晶成長)) von 前田, 洋次郎, 宮武, 繁, 藤井, 啓史, 佐竹, 祥彦, 岩井, 哲也, 水谷, 五郎

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Haploinsufficiency of A20 caused by a novel nonsense variant or entire deletion of TNFAIP3 is clinically distinct from Behçet's disease von Tsuchida, Naomi, Kirino, Yohei, Soejima, Yutaro, Onodera, Masafumi, Arai, Katsuhiro, Tamura, Eiichiro, Ishikawa, Takashi, Kawai, Toshinao, Uchiyama, Toru, Nomura, Shigeru, Kobayashi, Daisuke, Taguri, Masataka, Mitsuhashi, Satomi, Mizuguchi, Takeshi, Takata, Atsushi, Miyake, Noriko, Nakajima, Hideaki, Miyatake, Satoko, Matsumoto, Naomichi

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Repeat conformation heterogeneity in cerebellar ataxia, neuropathy, vestibular areflexia syndrome von Miyatake, Satoko, Yoshida, Kunihiro, Koshimizu, Eriko, Doi, Hiroshi, Yamada, Mitsunori, Miyaji, Yosuke, Ueda, Naohisa, Tsuyuzaki, Jun, Kodaira, Minori, Onoue, Hiroyuki, Taguri, Masataka, Imamura, Shintaro, Fukuda, Hiromi, Hamanaka, Kohei, Fujita, Atsushi, Satoh, Mai, Miyama, Takabumi, Watanabe, Nobuko, Kurita, Yusuke, Okubo, Masaki, Tanaka, Kenichi, Kishida, Hitaru, Koyano, Shigeru, Takahashi, Tatsuya, Ono, Yoya, Higashida, Kazuhiro, Yoshikura, Nobuaki, Ogata, Katsuhisa, Kato, Rumiko, Tsuchida, Naomi, Uchiyama, Yuri, Miyake, Noriko, Shimohata, Takayoshi, Tanaka, Fumiaki, Mizuguchi, Takeshi, Matsumoto, Naomichi

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Second data release of the Hyper Suprime-Cam Subaru Strategic Program von Aihara, Hiroaki, AlSayyad, Yusra, Ando, Makoto, Armstrong, Robert, Bosch, James, Egami, Eiichi, Furusawa, Hisanori, Furusawa, Junko, Goulding, Andy, Harikane, Yuichi, Hikage, Chiaki, Ho, Paul T P, Hsieh, Bau-Ching, Huang, Song, Ikeda, Hiroyuki, Imanishi, Masatoshi, Ito, Kei, Iwata, Ikuru, Jaelani, Anton T, Kakuma, Ryota, Kawana, Kojiro, Kikuta, Satoshi, Kobayashi, Umi, Koike, Michitaro, Komiyama, Yutaka, Li, Xiangchong, Liang, Yongming, Lin, Yen-Ting, Luo, Wentao, Lupton, Robert, Lust, Nate B, MacArthur, Lauren A, Matsuoka, Yoshiki, Mineo, Sogo, Miyatake, Hironao, Miyazaki, Satoshi, More, Surhud, Murata, Ryoma, Namiki, Shigeru V, Nishizawa, Atsushi J, Oguri, Masamune, Okabe, Nobuhiro, Okamoto, Sakurako, Okura, Yuki, Ono, Yoshiaki, Onodera, Masato, Onoue, Masafusa, Osato, Ken, Ouchi, Masami, Shibuya, Takatoshi, Strauss, Michael A, Sugiyama, Naoshi, Suto, Yasushi, Takada, Masahiro, Takagi, Yuhei, Takata, Tadafumi, Takita, Satoshi, Tanaka, Masayuki, Terai, Tsuyoshi, Toba, Yoshiki, Uchiyama, Hisakazu, Utsumi, Yousuke, Wang, Shiang-Yu, Wang, Wenting, Yamada, Yoshihiko

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Ataxic phenotype with altered CaV3.1 channel property in a mouse model for spinocerebellar ataxia 42 von Hashiguchi, Shunta, Doi, Hiroshi, Kunii, Misako, Nakamura, Yukihiro, Shimuta, Misa, Suzuki, Etsuko, Koyano, Shigeru, Okubo, Masaki, Kishida, Hitaru, Shiina, Masaaki, Ogata, Kazuhiro, Hirashima, Fumiko, Inoue, Yukichi, Kubota, Shun, Hayashi, Noriko, Nakamura, Haruko, Takahashi, Keita, Katsumoto, Atsuko, Tada, Mikiko, Tanaka, Kenichi, Sasaoka, Toshikuni, Miyatake, Satoko, Miyake, Noriko, Saitsu, Hirotomo, Sato, Nozomu, Ozaki, Kokoro, Ohta, Kiyobumi, Yokota, Takanori, Mizusawa, Hidehiro, Mitsui, Jun, Ishiura, Hiroyuki, Yoshimura, Jun, Morishita, Shinichi, Tsuji, Shoji, Takeuchi, Hideyuki, Ishikawa, Kinya, Matsumoto, Naomichi, Ishikawa, Taro, Tanaka, Fumiaki

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Association between obesity and polymorphisms in SEC16B, TMEM18, GNPDA2, BDNF, FAIM2 and MC4R in a Japanese population von Hotta, Kikuko, Nakamura, Michihiro, Nakamura, Takahiro, Matsuo, Tomoaki, Nakata, Yoshio, Kamohara, Seika, Miyatake, Nobuyuki, Kotani, Kazuaki, Komatsu, Ryoya, Itoh, Naoto, Mineo, Ikuo, Wada, Jun, Masuzaki, Hiroaki, Yoneda, Masato, Nakajima, Atsushi, Funahashi, Tohru, Miyazaki, Shigeru, Tokunaga, Katsuto, Kawamoto, Manabu, Ueno, Takato, Hamaguchi, Kazuyuki, Tanaka, Kiyoji, Yamada, Kentaro, Hanafusa, Toshiaki, Oikawa, Shinichi, Yoshimatsu, Hironobu, Nakao, Kazuwa, Sakata, Toshiie, Matsuzawa, Yuji, Kamatani, Naoyuki, Nakamura, Yusuke

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A Japanese Family of Spinocerebellar Ataxia Type 21: Clinical and Neuropathological Studies von Yahikozawa, Hiroyuki, Miyatake, Satoko, Sakai, Toshiaki, Uehara, Takeshi, Yamada, Mitsunori, Hanyu, Norinao, Futatsugi, Yasuhiro, Doi, Hiroshi, Koyano, Shigeru, Tanaka, Fumiaki, Suzuki, Atsushi, Matsumoto, Naomichi, Yoshida, Kunihiro

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Patients with biallelic GGC repeat expansions in NOTCH2NLC exhibiting a typical neuronal intranuclear inclusion disease phenotype von Kameyama, Shinichi, Mizuguchi, Takeshi, Doi, Hiroshi, Koyano, Shigeru, Okubo, Masaki, Tada, Mikiko, Shimizu, Hiroshi, Fukuda, Hiromi, Tsuchida, Naomi, Uchiyama, Yuri, Koshimizu, Eriko, Hamanaka, Kohei, Fujita, Atsushi, Misawa, Kazuharu, Miyatake, Satoko, Kanai, Kazuaki, Tanaka, Fumiaki, 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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Association between type 2 diabetes genetic susceptibility loci and visceral and subcutaneous fat area as determined by computed tomography von Hotta, Kikuko, Kitamoto, Aya, Kitamoto, Takuya, Mizusawa, Seiho, Teranishi, Hajime, So, Rina, Matsuo, Tomoaki, Nakata, Yoshio, Hyogo, Hideyuki, Ochi, Hidenori, Nakamura, Takahiro, Kamohara, Seika, Miyatake, Nobuyuki, Kotani, Kazuaki, Komatsu, Ryoya, Itoh, Naoto, Mineo, Ikuo, Wada, Jun, Yoneda, Masato, Nakajima, Atsushi, Funahashi, Tohru, Miyazaki, Shigeru, Tokunaga, Katsuto, Masuzaki, Hiroaki, Ueno, Takato, Chayama, Kazuaki, Hamaguchi, Kazuyuki, Yamada, Kentaro, Hanafusa, Toshiaki, Oikawa, Shinichi, Yoshimatsu, Hironobu, Sakata, Toshiie, Tanaka, Kiyoji, Matsuzawa, Yuji, Nakao, Kazuwa, Sekine, Akihiro

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Exome Sequencing Reveals a Homozygous SYT14 Mutation in Adult-Onset, Autosomal-Recessive Spinocerebellar Ataxia with Psychomotor Retardation von Doi, Hiroshi, Yoshida, Kunihiro, Yasuda, Takao, Fukuda, Mitsunori, Fukuda, Yoko, Morita, Hiroshi, Ikeda, Shu-ichi, Kato, Rumiko, Tsurusaki, Yoshinori, Miyake, Noriko, Saitsu, Hirotomo, Sakai, Haruya, Miyatake, Satoko, Shiina, Masaaki, Nukina, Nobuyuki, Koyano, Shigeru, Tsuji, Shoji, Kuroiwa, Yoshiyuki, Matsumoto, Naomichi

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