Self-Organization of Polarized Cerebellar Tissue in 3D Culture of Human Pluripotent Stem Cells von Muguruma, Keiko, Nishiyama, Ayaka, Kawakami, Hideshi, Hashimoto, Kouichi, Sasai, Yoshiki

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Optineurin deficiency impairs autophagy to cause interferon beta overproduction and increased survival of mice following viral infection von Fukushi, Masaya, Ohsawa, Ryosuke, Okinaka, Yasushi, Oikawa, Daisuke, Kiyono, Tohru, Moriwaki, Masaya, Irie, Takashi, Oda, Kosuke, Kamei, Yasuhiro, Tokunaga, Fuminori, Sotomaru, Yusuke, Maruyama, Hirofumi, Kawakami, Hideshi, Sakaguchi, Takemasa

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Vulnerability of Purkinje Cells Generated from Spinocerebellar Ataxia Type 6 Patient-Derived iPSCs von Ishida, Yoshihito, Kawakami, Hideshi, Kitajima, Hiroyuki, Nishiyama, Ayaka, Sasai, Yoshiki, Inoue, Haruhisa, Muguruma, Keiko

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The first Japanese case of primary familial brain calcification caused by an MYORG variant von Kume, Kodai, Takata, Tadayuki, Morino, Hiroyuki, Matsuda, Yukiko, Ohsawa, Ryosuke, Tada, Yui, Kurashige, Takashi, Kawakami, Hideshi

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Mutations of optineurin in amyotrophic lateral sclerosis von Kawakami, Hideshi, Kawata, Akihiro, Maruyama, Hirofumi, Nodera, Hiroyuki, Komure, Osamu, Abe, Koji, Ito, Hidefumi, Hirano, Asao, Kinoshita, Yoshimi, Kato, Hidemasa, Hagiwara, Koichi, Watanabe, Yasuhito, Ogasawara, Kazumasa, Hirai, Takeshi, Takumi, Toru, Kato, Takeo, Morimoto, Nobutoshi, Morino, Hiroyuki, Kamada, Masaki, Kobatake, Keitaro, Suzuki, Naoki, Aoki, Masashi, Izumi, Yuishin, Matsuura, Shinya, Kaji, Ryuji, Suzuki, Hidenori, Kusaka, Hirofumi

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Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease von Kawakami, Hideshi, Nakashima, Kenji, Takeda, Atsushi, Sakoda, Saburo, Hirota, Yushi, Yamamoto, Mitsutoshi, Kawaguchi, Takahisa, Nakabayashi, Yuko, Mizuta, Ikuko, Watanabe, Masahiko, Nakamura, Yusuke, Murata, Miho, Tomiyama, Hiroyuki, Hasegawa, Kazuko, Yoshikawa, Takeo, Ito, Chiyomi, Hattori, Nobutaka, Kubo, Michiaki, Toda, Tatsushi, Tsunoda, Tatsuhiko, Obata, Fumiya, Satake, Wataru

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Linear ubiquitination is involved in the pathogenesis of optineurin-associated amyotrophic lateral sclerosis von Nakazawa, Seshiru, Oikawa, Daisuke, Ishii, Ryohei, Ayaki, Takashi, Takahashi, Hirotaka, Takeda, Hiroyuki, Ishitani, Ryuichiro, Kamei, Kiyoko, Takeyoshi, Izumi, Kawakami, Hideshi, Iwai, Kazuhiro, Hatada, Izuho, Sawasaki, Tatsuya, Ito, Hidefumi, Nureki, Osamu, Tokunaga, Fuminori

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Genetic screening for potassium channel mutations in Japanese autosomal dominant spinocerebellar ataxia von Tada, Yui, Kume, Kodai, Matsuda, Yukiko, Kurashige, Takashi, Kanaya, Yuhei, Ohsawa, Ryosuke, Morino, Hiroyuki, Tabu, Hayato, Kaneko, Satoshi, Suenaga, Toshihiko, Kakizuka, Akira, Kawakami, Hideshi

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Second derivative of the finger photoplethysmogram and cardiovascular mortality in middle-aged and elderly Japanese women von Inoue, Noriko, Kawakami, Hideshi, Yamamoto, Hideya, Ito, Chikako, Fujiwara, Saeko, Sasaki, Hideo, Kihara, Yasuki

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Novel monoallelic variant in ERLIN2 causes spastic paraplegia converted to amyotrophic lateral sclerosis von Kume, Kodai, Kamada, Masaki, Shimatani, Yoshimitsu, Takata, Tadayuki, Izumi, Yuishin, Kawakami, Hideshi

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Prospects and status of the dosimetry system for atomic bomb survivor cohort study conducted at Research Institute for Radiation Biology and Medicine of Hiroshima University von Hirota, Seiko, Yasuda, Hiroshi, Kawakami, Hideshi, Yoshinaga, Shinji

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Analysis of genetic risk factors in Japanese patients with Parkinson's disease von Kanaya, Yuhei, Kume, Kodai, Morino, Hiroyuki, Ohsawa, Ryosuke, Kurashige, Takashi, Kamada, Masaki, Torii, Tsuyoshi, Izumi, Yuishin, Maruyama, Hirofumi, Kawakami, Hideshi

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Kv11 (ether‐à‐go‐go‐related gene) voltage‐dependent K+ channels promote resonance and oscillation of subthreshold membrane potentials von Matsuoka, Toshinori, Yamasaki, Miwako, Abe, Manabu, Matsuda, Yukiko, Morino, Hiroyuki, Kawakami, Hideshi, Sakimura, Kenji, Watanabe, Masahiko, Hashimoto, Kouichi

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FXTAS is difficult to differentiate from neuronal intranuclear inclusion disease through skin biopsy: a case report von Toko, Megumi, Ohshita, Tomohiko, Kurashige, Takashi, Morino, Hiroyuki, Kume, Kodai, Yamashita, Hiroshi, Sobue, Gen, Iwasaki, Yasushi, Sone, Jun, Kawakami, Hideshi, Maruyama, Hirofumi

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Optineurin and amyotrophic lateral sclerosis von Maruyama, Hirofumi, Kawakami, Hideshi

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Optineurin defects cause TDP43-pathology with autophagic vacuolar formation von Kurashige, Takashi, Kuramochi, Masahito, Ohsawa, Ryosuke, Yamashita, Yui, Shioi, Go, Morino, Hiroyuki, Kamada, Masaki, Ayaki, Takashi, Ito, Hidefumi, Sotomaru, Yusuke, Maruyama, Hirofumi, Kawakami, Hideshi

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PLK1-mediated phosphorylation of WDR62/MCPH2 ensures proper mitotic spindle orientation von Miyamoto, Tatsuo, Akutsu, Silvia Natsuko, Fukumitsu, Akihiro, Morino, Hiroyuki, Masatsuna, Yoshinori, Hosoba, Kosuke, Kawakami, Hideshi, Yamamoto, Takashi, Shimizu, Kenji, Ohashi, Hirofumi, Matsuura, Shinya

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Aggressive periodontitis and NOD2 variants von Mizuno, Noriyoshi, Kume, Kodai, Nagatani, Yukiko, Matsuda, Shinji, Iwata, Tomoyuki, Ouhara, Kazuhisa, Kajiya, Mikihito, Takeda, Katsuhiro, Matsuda, Yukiko, Tada, Yui, Ohsawa, Ryosuke, Morino, Hiroyuki, Mihara, Keichiro, Fujita, Tsuyoshi, Kawaguchi, Hiroyuki, Shiba, Hideki, Kawakami, Hideshi, Kurihara, Hidemi

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First report of a Japanese family with spinocerebellar ataxia type 10: The second report from Asia after a report from China von Naito, Hiroyuki, Takahashi, Tetsuya, Kamada, Masaki, Morino, Hiroyuki, Yoshino, Hiroyo, Hattori, Nobutaka, Maruyama, Hirofumi, Kawakami, Hideshi, Matsumoto, Masayasu

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A mutation in the low voltage-gated calcium channel CACNA1G alters the physiological properties of the channel, causing spinocerebellar ataxia von Morino, Hiroyuki, Matsuda, Yukiko, Muguruma, Keiko, Miyamoto, Ryosuke, Ohsawa, Ryosuke, Ohtake, Toshiyuki, Otobe, Reiko, Watanabe, Masahiko, Maruyama, Hirofumi, Hashimoto, Kouichi, Kawakami, Hideshi

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