Failure of DNA double-strand break repair by tau mediates Alzheimer’s disease pathology in vitro von Asada-Utsugi, Megumi, Uemura, Kengo, Ayaki, Takashi, T. Uemura, Maiko, Minamiyama, Sumio, Hikiami, Ryota, Morimura, Toshifumi, Shodai, Akemi, Ueki, Takatoshi, Takahashi, Ryosuke, Kinoshita, Ayae, Urushitani, Makoto

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In vivo analysis of aggregation propensity of low levels of mislocalized TDP-43 on cytopathological and behavioral phenotype of ALS/FTLD von Wada, Hideki, Hikiami, Ryota, Kusui, Makiko, Minamiyama, Sumio, Asada-Utsugi, Megumi, Shodai, Akemi, Muramatsu, Shin-ichi, Morimura, Toshifumi, Urushitani, Makoto

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Conformational change of RNA-helicase DHX30 by ALS/FTD-linked FUS induces mitochondrial dysfunction and cytosolic aggregates von Hikiami, Ryota, Morimura, Toshifumi, Ayaki, Takashi, Tsukiyama, Tomoyuki, Morimura, Naoko, Kusui, Makiko, Wada, Hideki, Minamiyama, Sumio, Shodai, Akemi, Asada-Utsugi, Megumi, Muramatsu, Shin-ichi, Ueki, Takatoshi, Takahashi, Ryosuke, Urushitani, Makoto

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Amyotrophic Lateral Sclerosis after Receiving the Human Papilloma Virus Vaccine: A Case Report of a 15-year-old Girl von Hikiami, Ryota, Yamakado, Hodaka, Tatsumi, Shinsui, Ayaki, Takashi, Hashi, Yuichiro, Yamashita, Hirofumi, Sawamoto, Nobukatsu, Tsuji, Teruyuki, Urushitani, Makoto, Takahashi, Ryosuke

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Serial EEG findings in anti‐NMDA receptor encephalitis: correlation between clinical course and EEG von Ueda, Jun, Kawamoto, Michi, Hikiami, Ryota, Ishii, Junko, Yoshimura, Hajime, Matsumoto, Riki, Kohara, Nobuo

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Charcot-Marie-Tooth disease type 2A with an autosomal-recessive inheritance: the first report of an adult-onset disease von Hikiami, Ryota, Yamashita, Hirofumi, Koita, Natsuko, Jingami, Naoto, Sawamoto, Nobukatsu, Furukawa, Kaoru, Kawai, Hiromichi, Terashima, Tomoya, Oka, Nobuyuki, Hashiguchi, Akihiro, Takashima, Hiroshi, Urushitani, Makoto, Takahashi, Ryosuke

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Efficacy of oligodendrocyte precursor cells as delivery vehicles for single-chain variable fragment to misfolded SOD1 in ALS rat model von Minamiyama, Sumio, Sakai, Madoka, Yamaguchi, Yuko, Kusui, Makiko, Wada, Hideki, Hikiami, Ryota, Tamaki, Yoshitaka, Asada-Utsugi, Megumi, Shodai, Akemi, Makino, Akiko, Fujiwara, Noriko, Ayaki, Takashi, Maki, Takakuni, Warita, Hitoshi, Aoki, Masashi, Tomonaga, Keizo, Takahashi, Ryosuke, Urushitani, Makoto

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A novel A792D mutation in the CSF1R gene causes hereditary diffuse leukoencephalopathy with axonal spheroids characterized by slow progression von Ueda, Sakiho, Yamashita, Hirofumi, Hikiami, Ryota, Sawamoto, Nobukatsu, Yoshida, Kunihiro, Takahashi, Ryosuke

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Elimination of TDP-43 inclusions linked to amyotrophic lateral sclerosis by a misfolding-specific intrabody with dual proteolytic signals von Tamaki, Yoshitaka, Shodai, Akemi, Morimura, Toshifumi, Hikiami, Ryota, Minamiyama, Sumio, Ayaki, Takashi, Tooyama, Ikuo, Furukawa, Yoshiaki, Takahashi, Ryosuke, Urushitani, Makoto

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A novel A792D mutation in the CSF1R gene causes hereditary diffuse leukoencephalopathy with axonal spheroids characterized by slow progression von Ueda, Sakiho, Yamashita, Hirofumi, Hikiami, Ryota, Sawamoto, Nobukatsu, Yoshida, Kunihiro, Takahashi, Ryosuke

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