Brain-derived growth factor and nerve growth factor concentrations are decreased in the substantia nigra in Parkinson's disease
Mogi, Makio, Togari, Akifumi, Kondo, Tomoyoshi, Mizuno, Yoshikuni, Komure, Osamu, Kuno, Sadako, Ichinose, Hiroshi, Nagatsu, Toshiharu
Published in Neuroscience letters (23.07.1999)
Published in Neuroscience letters (23.07.1999)
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Caspase activities and tumor necrosis factor receptor R1 (p55) level are elevated in the substantia nigra from Parkinsonian brain
MOGI, M, TOGARI, A, KONDO, T, MIZUNO, Y, KOMURE, O, KUNO, S, ICHINOSE, H, NAGATSU, T
Published in Journal of Neural Transmission (01.01.2000)
Published in Journal of Neural Transmission (01.01.2000)
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Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p
Kurosawa, H, Murayama, N, Takeda, T, Furukawa, T, Nihei, K, Kanazawa, I, Sato, K, Yoshizawa, T, Nagafuchi, S, Shirayama, T, Yamada, M, Takahashi, M, Yanagisawa, H, Tanaka, Y, Bundo, M, Umino, K, Komure, O, Kondo, I, Ohsaki, E, Kikushima, H, Inoue, T, Tadokoro, K, Sano, A
Published in Nature genetics (01.01.1994)
Published in Nature genetics (01.01.1994)
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Clinical and genetic studies of families with the tau N279K mutation (FTDP-17)
Tsuboi, Y, Baker, M, Hutton, M L, Uitti, R J, Rascol, O, Delisle, M-B, Soulages, X, Murrell, J R, Ghetti, B, Yasuda, M, Komure, O, Kuno, S, Arima, K, Sunohara, N, Kobayashi, T, Mizuno, Y, Wszolek, Z K
Published in Neurology (10.12.2002)
Published in Neurology (10.12.2002)
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DNA analysis in hereditary dentatorubral-pallidoluysian atrophy: correlation between CAG repeat length and phenotypic variation and the molecular basis of anticipation
Komure, O, Sano, A, Nishino, N, Yamauchi, N, Ueno, S, Kondoh, K, Sano, N, Takahashi, M, Murayama, N, Kondo, I
Published in Neurology (01.01.1995)
Published in Neurology (01.01.1995)
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A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration
Yasuda, M, Kawamata, T, Komure, O, Kuno, S, D'Souza, I, Poorkaj, P, Kawai, J, Tanimukai, S, Yamamoto, Y, Hasegawa, H, Sasahara, M, Hazama, F, Schellenberg, G D, Tanaka, C
Published in Neurology (11.09.1999)
Published in Neurology (11.09.1999)
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Spinocerebellar ataxia type 6 in relation to CAG repeat length
Kaseda, Y., Kawakami, H., Matsuyama, Z., Kumagai, R., Toji, M., Komure, O., Nishimura, M., Izumi, Y., Udaka, F., Kameyama, M., Nishio, T., Sunohara, N., Kuroda, Y., Nakamura, S.
Published in Acta neurologica Scandinavica (01.04.1999)
Published in Acta neurologica Scandinavica (01.04.1999)
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Pallidonigroluysian degeneration with iron deposition: a study of three autopsy cases
Kawai, J, Sasahara, M, Hazama, F, Kuno, S, Komure, O, Nomura, S, Yamaguchi, M
Published in Acta neuropathologica (01.11.1993)
Published in Acta neuropathologica (01.11.1993)
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Phenotypic heterogeneity within a new family with the MAPT p301s mutation
Yasuda, Minoru, Nakamura, Yoshitsugu, Kawamata, Toshio, Kaneyuki, Hiroshi, Maeda, Kiyoshi, Komure, Osamu
Published in Annals of neurology (01.12.2005)
Published in Annals of neurology (01.12.2005)
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Intra-axonal polysaccharide deposits in the peripheral nerve seen in adult polysaccharide storage myopathy
Komure, O, Ichikawa, K, Tsutsumi, A, Hiyama, K, Fujioka, A
Published in Acta neuropathologica (01.01.1985)
Published in Acta neuropathologica (01.01.1985)
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SCA8 Repeat Expansion: Large CTA/CTG Repeat Alleles Are More Common in Ataxic Patients, Including Those with SCA6
Izumi, Yuishin, Maruyama, Hirofumi, Oda, Masaya, Morino, Hiroyuki, Okada, Takayuki, Ito, Hidefumi, Sasaki, Iwao, Tanaka, Hiroyasu, Komure, Osamu, Udaka, Fukashi, Nakamura, Shigenobu, Kawakami, Hideshi
Published in American journal of human genetics (01.03.2003)
Published in American journal of human genetics (01.03.2003)
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Contribution of the interleukin-1β gene polymorphism in multiple system atrophy
Nishimura, Masataka, Kawakami, Hideshi, Komure, Osamu, Maruyama, Hirofumi, Morino, Hiroyuki, Izumi, Yuishin, Nakamura, Shigenobu, Kaji, Ryuji, Kuno, Sadako
Published in Movement disorders (01.07.2002)
Published in Movement disorders (01.07.2002)
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Molecular Features of the CAG Repeats of Spinocerebellar Ataxia 6 (SCA6)
Matsuyama, Zenjiro, Kawakami, Hideshi, Maruyama, Hirofumi, Izumi, Yuishin, Komure, Osamu, Udaka, Fukashi, Kameyama, Masakuni, Nishio, Takeshi, Kuroda, Yasuo, Nishimura, Masataka, Nakamura, Shigenobu
Published in Human molecular genetics (01.08.1997)
Published in Human molecular genetics (01.08.1997)
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Transgenic Mice Harboring a Full-Length Human Mutant DRPLA Gene Exhibit Age-Dependent Intergenerational and Somatic Instabilities of CAG repeats Comparable with Those in DRPLA patients
Sato, Toshiya, Oyake, Mutsuo, Nakamura, Kenji, Nakao, Kazuki, Fukusima, Yoshimitsu, Onodera, Osamu, Igarashi, Shuichi, Takano, Hiroki, Kikugawa, Koki, Ishida, Yoshinori, Shimohata, Takayoshi, Koide, Reiji, Ikeuchi, Takeshi, Tanaka, Hajime, Futamura, Naonobu, Matsumura, Ryusuke, Takayanagi, Tetsuya, Tanaka, Fumiaki, Sobue, Gen, Komure, Osamu, Takahashi, Mie, Sano, Akira, Ichikawa, Yaeko, Goto, Jun, Kanazawa, Ichiro, Katsuki, Motoya, Tsuji, Shoji
Published in Human molecular genetics (01.01.1999)
Published in Human molecular genetics (01.01.1999)
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Adult polysaccharide storage myopathy
Ichikawa, K, Komure, O, Tsutsumi, A, Hiyama, K, Fujioka, A
Published in Rinshō shinkeigaku (01.10.1989)
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Published in Rinshō shinkeigaku (01.10.1989)
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Triplet repeat disorders: from the clinical view
Komure, O, Ueno, S, Sano, A
Published in Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme (01.08.1997)
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Published in Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme (01.08.1997)
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An autopsy case of intracranial fungal (Aspergillus) mycotic aneurysm
Ichikawa, K, Tsutsumi, A, Hiyama, K, Komure, O, Fujioka, A
Published in Rinshō shinkeigaku (01.06.1984)
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Published in Rinshō shinkeigaku (01.06.1984)
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The Effect of tau genotype on clinical features in FTDP-17
Baba, Yasuhiko, Tsuboi, Yoshio, Baker, Matthew C., Uitti, Ryan J., Hutton, Michael L., Dickson, Dennis W., Farrer, Matthew, Putzke, John D., Woodruff, Bryan K., Ghetti, Bernardino, Murrell, Jill R., Boeve, Bradley F., Petersen, Ronald C., Verpillat, Patrice, Brice, Alexis, Delisle, Marie-Bernadette, Rascol, Oliver, Arima, Kunimasa, Dysken, Maurice W., Yasuda, Minoru, Kobayashi, Tomonori, Sunohara, Nobuhiko, Komure, Osamu, Kuno, Sadako, Sperfeld, Anne D., Stoppe, Gabriela, Kohlhase, Jürgen, Pickering-Brown, Stuart, Neary, David, Bugiani, Orso, Wszolek, Zbigniew K.
Published in Parkinsonism & related disorders (01.06.2005)
Published in Parkinsonism & related disorders (01.06.2005)
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A single nucleotide polymorphism of dopamine transporter gene is associated with Parkinson's disease
Morino, Hiroyuki, Kawarai, Toshitaka, Izumi, Yuishin, Kazuta, Toshinari, Oda, Masaya, Komure, Osamu, Udaka, Fukashi, Kameyama, Masakuni, Nakamura, Shigenobu, Kawakami, Hideshi
Published in Annals of neurology (01.04.2000)
Published in Annals of neurology (01.04.2000)
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Triggering of neuronal cell death by accumulation of activated SEK1 on nuclear polyglutamine aggregations in PML bodies
Yasuda, Shingo, Inoue, Kiyoshi, Hirabayashi, Miho, Higashiyama, Hiroyuki, Yamamoto, Yukio, Fuyuhiro, Haruko, Komure, Osamu, Tanaka, Fumiaki, Sobue, Gen, Tsuchiya, Kuniaki, Hamada, Koji, Sasaki, Hidenao, Takeda, Kohsuke, Ichijo, Hidenori, Kakizuka, Akira
Published in Genes to cells : devoted to molecular & cellular mechanisms (01.12.1999)
Published in Genes to cells : devoted to molecular & cellular mechanisms (01.12.1999)
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