Where and how alpha‐synuclein pathology spreads in Parkinson’s disease von Wakabayashi, Koichi

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Neuropathology of Lewy body disease: Clinicopathological crosstalk between typical and atypical cases von Kon, Tomoya, Tomiyama, Masahiko, Wakabayashi, Koichi

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Role of the Keap1/Nrf2 pathway in neurodegenerative diseases von Yamazaki, Hiromi, Tanji, Kunikazu, Wakabayashi, Koichi, Matsuura, Shin, Itoh, Ken

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Neuropathology of Multiple System Atrophy, a Glioneuronal Degenerative Disease von Wakabayashi, Koichi, Miki, Yasuo, Tanji, Kunikazu, Mori, Fumiaki

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Sigma-1 receptor is involved in degradation of intranuclear inclusions in a cellular model of Huntington's disease von Miki, Yasuo, Tanji, Kunikazu, Mori, Fumiaki, Wakabayashi, Koichi

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The Lewy body in Parkinson's disease: Molecules implicated in the formation and degradation of α-synuclein aggregates von Wakabayashi, Koichi, Tanji, Kunikazu, Mori, Fumiaki, Takahashi, Hitoshi

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Trehalose intake and exercise upregulate a glucose transporter, GLUT8, in the brain von Narita, Hidemi, Tanji, Kunikazu, Miki, Yasuo, Mori, Fumiaki, Wakabayashi, Koichi

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Cabergoline, a long-acting dopamine agonist, attenuates L-dopa-induced dyskinesia without L-dopa sparing in a rat model of Parkinson’s disease von Nishijima, Haruo, Mori, Fumiaki, Kimura, Tamaki, Miki, Yasuo, Kinoshita, Iku, Nakamura, Takashi, Kon, Tomoya, Suzuki, Chieko, Wakabayashi, Koichi, Tomiyama, Masahiko

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Alteration of autophagosomal proteins (LC3, GABARAP and GATE-16) in Lewy body disease von Tanji, Kunikazu, Mori, Fumiaki, Kakita, Akiyoshi, Takahashi, Hitoshi, Wakabayashi, Koichi

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Praja1 RING‐finger E3 ubiquitin ligase is a common suppressor of neurodegenerative disease‐associated protein aggregation von Watabe, Kazuhiko, Niida‐Kawaguchi, Motoko, Tada, Mari, Kato, Yoichiro, Murata, Makiko, Tanji, Kunikazu, Wakabayashi, Koichi, Yamada, Mitsunori, Kakita, Akiyoshi, Shibata, Noriyuki

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Autophagy Is a Common Degradation Pathway for Bunina Bodies and TDP-43 Inclusions in Amyotrophic Lateral Sclerosis von Mori, Fumiaki, Miki, Yasuo, Kon, Tomoya, Tanji, Kunikazu, Wakabayashi, Koichi

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Is amyotrophic lateral sclerosis a prion-like disorder? A case report von Miki, Yasuo, Shibuya, Eri, Yoshizawa, Tadashi, Tomiyama, Masahiko, Wakabayashi, Koichi

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Immunoreactivity of myelin‐associated oligodendrocytic basic protein in Lewy bodies von Kon, Tomoya, Tanji, Kunikazu, Mori, Fumiaki, Kimura, Akari, Kakita, Akiyoshi, Wakabayashi, Koichi

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A mouse model of adult-onset multiple system atrophy von Tanji, Kunikazu, Miki, Yasuo, Mori, Fumiaki, Nikaido, Yoshikazu, Narita, Hidemi, Kakita, Akiyoshi, Takahashi, Hitoshi, Wakabayashi, Koichi

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Alteration of mitochondrial protein PDHA1 in Lewy body disease and PARK14 von Miki, Yasuo, Tanji, Kunikazu, Mori, Fumiaki, Kakita, Akiyoshi, Takahashi, Hitoshi, Wakabayashi, Koichi

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Cellular pathology in multiple system atrophy von Wakabayashi, Koichi, Takahashi, Hitoshi

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Degeneration of Cardiac Sympathetic Nerve Begins in the Early Disease Process of Parkinson's Disease von Orimo, Satoshi, Takahashi, Atsushi, Uchihara, Toshiki, Mori, Fumiaki, Kakita, Akiyoshi, Wakabayashi, Koichi, Takahashi, Hitoshi

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Accumulation of Nonfibrillar TDP-43 in the Rough Endoplasmic Reticulum Is the Early-Stage Pathology in Amyotrophic Lateral Sclerosis von Kon, Tomoya, Mori, Fumiaki, Tanji, Kunikazu, Miki, Yasuo, Nishijima, Haruo, Nakamura, Takashi, Kinoshita, Iku, Suzuki, Chieko, Kurotaki, Hidekachi, Tomiyama, Masahiko, Wakabayashi, Koichi

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Ribosome binding protein GCN1 regulates the cell cycle and cell proliferation and is essential for the embryonic development of mice von Yamazaki, Hiromi, Kasai, Shuya, Mimura, Junsei, Ye, Peng, Inose-Maruyama, Atsushi, Tanji, Kunikazu, Wakabayashi, Koichi, Mizuno, Seiya, Sugiyama, Fumihiro, Takahashi, Satoru, Sato, Tsubasa, Ozaki, Taku, Cavener, Douglas R, Yamamoto, Masayuki, Itoh, Ken

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YOD1 attenuates neurogenic proteotoxicity through its deubiquitinating activity von Tanji, Kunikazu, Mori, Fumiaki, Miki, Yasuo, Utsumi, Jun, Sasaki, Hidenao, Kakita, Akiyoshi, Takahashi, Hitoshi, Wakabayashi, Koichi

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