CpG Demethylation Enhances Alpha-Synuclein Expression and Affects the Pathogenesis of Parkinson's Disease

Por Matsumoto, Lumine, Takuma, Hiroshi, Tamaoka, Akira, Kurisaki, Hiroshi, Date, Hidetoshi, Tsuji, Shoji, Iwata, Atsushi
Publicado em 2010

Intranuclear Degradation of Polyglutamine Aggregates by the Ubiquitin-Proteasome System

Por Iwata, Atsushi, Nagashima, Yu, Matsumoto, Lumine, Suzuki, Takahiro, Yamanaka, Tomoyuki, Date, Hidetoshi, Deoka, Ken, Nukina, Nobuyuki, Tsuji, Shoji
Publicado em 2009

SNP HiTLink: a high-throughput linkage analysis system employing dense SNP data

Por Kuwano Ryozo, Miyashita Akinori, Goto Jun, Takahashi Yuji, Date Hidetoshi, Nakahara Yasuo, Fukuda Yoko, Adachi Hiroki, Nakamura Eiji, Tsuji Shoji
Publicado em 2009-04-01

SNP HiTLink: a high-throughput linkage analysis system employing dense SNP data

Por Fukuda, Yoko, Nakahara, Yasuo, Date, Hidetoshi, Takahashi, Yuji, Goto, Jun, Miyashita, Akinori, Kuwano, Ryozo, Adachi, Hiroki, Nakamura, Eiji, Tsuji, Shoji
Publicado em 2009

Aprataxin, causative gene product for EAOH/AOA1, repairs DNA single-strand breaks with damaged 3′-phosphate and 3′-phosphoglycolate ends

Por Takahashi, Tetsuya, Tada, Masayoshi, Igarashi, Shuichi, Koyama, Akihide, Date, Hidetoshi, Yokoseki, Akio, Shiga, Atsushi, Yoshida, Yutaka, Tsuji, Shoji, Nishizawa, Masatoyo, Onodera, Osamu
Publicado em 2007

The TRK-Fused Gene Is Mutated in Hereditary Motor and Sensory Neuropathy with Proximal Dominant Involvement

Por Ishiura, Hiroyuki, Sako, Wataru, Yoshida, Mari, Kawarai, Toshitaka, Tanabe, Osamu, Goto, Jun, Takahashi, Yuji, Date, Hidetoshi, Mitsui, Jun, Ahsan, Budrul, Ichikawa, Yaeko, Iwata, Atsushi, Yoshino, Hiide, Izumi, Yuishin, Fujita, Koji, Maeda, Kouji, Goto, Satoshi, Koizumi, Hidetaka, Morigaki, Ryoma, Ikemura, Masako, Yamauchi, Naoko, Murayama, Shigeo, Nicholson, Garth A., Ito, Hidefumi, Sobue, Gen, Nakagawa, Masanori, Kaji, Ryuji, Tsuji, Shoji
Publicado em 2012

ERBB4 Mutations that Disrupt the Neuregulin-ErbB4 Pathway Cause Amyotrophic Lateral Sclerosis Type 19

Por Takahashi, Yuji, Fukuda, Yoko, Yoshimura, Jun, Toyoda, Atsushi, Kurppa, Kari, Moritoyo, Hiroyoko, Belzil, Veronique V., Dion, Patrick A., Higasa, Koichiro, Doi, Koichiro, Ishiura, Hiroyuki, Mitsui, Jun, Date, Hidetoshi, Ahsan, Budrul, Matsukawa, Takashi, Ichikawa, Yaeko, Moritoyo, Takashi, Ikoma, Mayumi, Hashimoto, Tsukasa, Kimura, Fumiharu, Murayama, Shigeo, Onodera, Osamu, Nishizawa, Masatoyo, Yoshida, Mari, Atsuta, Naoki, Sobue, Gen, Fifita, Jennifer A., Williams, Kelly L., Blair, Ian P., Nicholson, Garth A., Gonzalez-Perez, Paloma, Brown, Robert H., Nomoto, Masahiro, Elenius, Klaus, Rouleau, Guy A., Fujiyama, Asao, Morishita, Shinichi, Goto, Jun, Tsuji, Shoji
Publicado em 2013

Variants associated with Gaucher disease in multiple system atrophy

Por Mitsui, Jun, Matsukawa, Takashi, Sasaki, Hidenao, Yabe, Ichiro, Matsushima, Masaaki, Dürr, Alexandra, Brice, Alexis, Takashima, Hiroshi, Kikuchi, Akio, Aoki, Masashi, Ishiura, Hiroyuki, Yasuda, Tsutomu, Date, Hidetoshi, Ahsan, Budrul, Iwata, Atsushi, Goto, Jun, Ichikawa, Yaeko, Nakahara, Yasuo, Momose, Yoshio, Takahashi, Yuji, Hara, Kenju, Kakita, Akiyoshi, Yamada, Mitsunori, Takahashi, Hitoshi, Onodera, Osamu, Nishizawa, Masatoyo, Watanabe, Hirohisa, Ito, Mizuki, Sobue, Gen, Ishikawa, Kinya, Mizusawa, Hidehiro, Kanai, Kazuaki, Hattori, Takamichi, Kuwabara, Satoshi, Arai, Kimihito, Koyano, Shigeru, Kuroiwa, Yoshiyuki, Hasegawa, Kazuko, Yuasa, Tatsuhiko, Yasui, Kenichi, Nakashima, Kenji, Ito, Hijiri, Izumi, Yuishin, Kaji, Ryuji, Kato, Takeo, Kusunoki, Susumu, Osaki, Yasushi, Horiuchi, Masahiro, Kondo, Tomoyoshi, Murayama, Shigeo, Hattori, Nobutaka, Yamamoto, Mitsutoshi, Murata, Miho, Satake, Wataru, Toda, Tatsushi, Filla, Alessandro, Klockgether, Thomas, Wüllner, Ullrich, Nicholson, Garth, Gilman, Sid, Tanner, Caroline M, Kukull, Walter A, Stern, Mathew B, Lee, Virginia M-Y, Trojanowski, John Q, Masliah, Eliezer, Low, Phillip A, Sandroni, Paola, Ozelius, Laurie J, Foroud, Tatiana, Tsuji, Shoji
Publicado no Ann Clin Transl Neurol (2015)