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Osamu Komure

Research Profile

Chemicals & Drugs

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Japan

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Asian Continental Ancestry Group

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Publications

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Hirofumi Maruyama; Hiroyuki Morino; Hidefumi Ito; Yuishin Izumi; Hidemasa Kato; Yasuhito Watanabe; Yoshimi Kinoshita; Masaki Kamada; Hiroyuki Nodera; Hidenori Suzuki; Osamu Komure; Shinya Matsuura; Keitaro Kobatake; Nobutoshi Morimoto; Koji Abe; Naoki Suzuki; Masashi Aoki; Akihiro Kawata; Takeshi Hirai; Takeo Kato; Kazumasa Ogasawara; Asao Hirano; Toru Takumi; Hirofumi Kusaka; Koichi Hagiwara; Ryuji Kaji; Hideshi Kawakami
Mutations of optineurin in amyotrophic lateral sclerosis.
Masaya Yanagi; Takeshi Hashimoto; Noboru Kitamura; Masaaki Fukutake; Osamu Komure; Naoki Nishiguchi; Toshio Kawamata; Kiyoshi Maeda; Osamu Shirakawa
Expression of Kruppel-like factor 5 gene in human brain and association of the gene with the susceptibility to schizophrenia.
Minoru Yasuda; Yoshitsugu Nakamura; Toshio Kawamata; Hiroshi Kaneyuki; Kiyoshi Maeda; Osamu Komure
Phenotypic heterogeneity within a new family with the MAPT p301s mutation.

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All Publications

2010: Hirofumi Maruyama; Hiroyuki Morino; Hidefumi Ito; Yuishin Izumi; Hidemasa Kato; Yasuhito Watanabe; Yoshimi Kinoshita; Masaki Kamada; Hiroyuki Nodera; Hidenori Suzuki; Osamu Komure; Shinya Matsuura; Keitaro Kobatake; Nobutoshi Morimoto; Koji Abe; Naoki Suzuki; Masashi Aoki; Akihiro Kawata; Takeshi Hirai; Takeo Kato; Kazumasa Ogasawara; Asao Hirano; Toru Takumi; Hirofumi Kusaka; Koichi Hagiwara; Ryuji Kaji; Hideshi Kawakami
Mutations of optineurin in amyotrophic lateral sclerosis.
Nature 2010;465(7295):223-6.
2008: Masaya Yanagi; Takeshi Hashimoto; Noboru Kitamura; Masaaki Fukutake; Osamu Komure; Naoki Nishiguchi; Toshio Kawamata; Kiyoshi Maeda; Osamu Shirakawa
Expression of Kruppel-like factor 5 gene in human brain and association of the gene with the susceptibility to schizophrenia.
Schizophrenia research 2008;100(1-3):291-301.
2005: Minoru Yasuda; Yoshitsugu Nakamura; Toshio Kawamata; Hiroshi Kaneyuki; Kiyoshi Maeda; Osamu Komure
Phenotypic heterogeneity within a new family with the MAPT p301s mutation.
Annals of neurology 2005;58(6):920-8.
2004: Sonoyo Yoshida; Makoto Matsui; Hui-Yun Wang; Tomoko Oeda; Tomoko Sasaki; Osamu Komure; Kyoko Ozawa; Tetsurou Konisi; Takahiko Saida; Hiroo Yoshikawa; Yukifumi Nawa
[A case of myeloradiculitis as a complication of visceral larva migrans due to Ascaris suum].
Rinshō shinkeigaku = Clinical neurology 2004;44(3):198-202.
2004: Masaya Oda; Hirofumi Maruyama; Osamu Komure; Hiroyuki Morino; Hideo Terasawa; Yuishin Izumi; Tohru Imamura; Minoru Yasuda; Keiji Ichikawa; Masafumi Ogawa; Masayasu Matsumoto; Hideshi Kawakami
Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17.
Archives of neurology 2004;61(2):209-12.
2003: Yuishin Izumi; Hirofumi Maruyama; Masaya Oda; Hiroyuki Morino; Takayuki Okada; Hidefumi Ito; Iwao Sasaki; Hiroyasu Tanaka; Osamu Komure; Fukashi Udaka; Shigenobu Nakamura; Hideshi Kawakami
SCA8 repeat expansion: large CTA/CTG repeat alleles are more common in ataxic patients, including those with SCA6.
American journal of human genetics 2003;72(3):704-9.
2002: Yoshio Tsuboi; Matt Baker; Michael Hutton; Ryan Uitti; Olivier Rascol; Marie-Bernadette Delisle; X Soulages; Jill R Murrell; Bernardino Ghetti; Minoru Yasuda; Osamu Komure; S Kuno; K Arima; N Sunohara; T Kobayashi; Yoshikuni Mizuno; Zbigniew K Wszolek
Clinical and genetic studies of families with the tau N279K mutation (FTDP-17).
Neurology 2002;59(11):1791-3.
2002: Masataka Nishimura; Hideshi Kawakami; Osamu Komure; Hirofumi Maruyama; Hiroyuki Morino; Yuishin Izumi; Shigenobu Nakamura; Ryuji Kaji; Sadako Kuno
Contribution of the interleukin-1beta gene polymorphism in multiple system atrophy.
Movement disorders : official journal of the Movement Disorder Society 2002;17(4):808-11.
2000: Hiroyuki Morino; T Kawarai; Yuishin Izumi; T Kazuta; Masaya Oda; Osamu Komure; Fukashi Udaka; M Kameyama; Shigenobu Nakamura; Hideshi Kawakami
A single nucleotide polymorphism of dopamine transporter gene is associated with Parkinson's disease.
Annals of neurology 2000;47(4):528-31.
1999: Minoru Yasuda; Toshio Kawamata; Osamu Komure; S Kuno; Ian D'Souza; Parvoneh Poorkaj-Navas; J Kawai; Satoshi Tanimukai; Y Yamamoto; Hiroshi Hasegawa; Masakiyo Sasahara; F Hazama; Gerard D Schellenberg; Chikako Tanaka
A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration.
Neurology 1999;53(4):864-8.
1999: Yumiko Kaseda; Hideshi Kawakami; Z Matsuyama; Rumi Kumagai; M Toji; Osamu Komure; M Nishimura; Yuishin Izumi; Fukashi Udaka; M Kameyama; T Nishio; N Sunohara; Y Kuroda; Shigenobu Nakamura
Spinocerebellar ataxia type 6 in relation to CAG repeat length.
Acta neurologica Scandinavica 1999;99(4):209-12.
1998: Hiromasa Toji; Hideshi Kawakami; T Kawarai; T Nakayama; Osamu Komure; S Kuno; Shigenobu Nakamura
No association between apolipoprotein E alleles and olivopontocerebellar atrophy.
Journal of the neurological sciences 1998;158(1):110-2.
1997: Z Matsuyama; Hideshi Kawakami; Hirofumi Maruyama; Yuishin Izumi; Osamu Komure; Fukashi Udaka; M Kameyama; T Nishio; Y Kuroda; M Nishimura; Shigenobu Nakamura
Molecular features of the CAG repeats of spinocerebellar ataxia 6 (SCA6).
Human molecular genetics 1997;6(8):1283-7.