Rchr
J-GLOBAL ID：201501075037024126
Update date: Jun. 02, 2020
Date Hidetoshi
ダテ ヒデトシ | Date Hidetoshi
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Homepage URL (1)：
https://kaken.nii.ac.jp/d/r/30401037.ja.html
Research field (1)：
Neuroanatomy and physiology
Research keywords (10)：
包括脳ネットワーク
, iPS細胞
, 分子・神経細胞科学
, 連鎖解析
, 分子・細胞神経科学
, 天然変性タンパク質
, 遺伝子同定
, ポリグルタミン病
, エピジェネティクス
, 神経疾患
Research theme for competitive and other funds (2)：
2000 - 2004 中枢神経系のDNA修復機構におけるAprataxinの機能解析
2000 - 2004 Analysis for Aprataxin in Central Nervos System
Papers (10)：
Jun Mitsui, Takashi Matsukawa, Hidenao Sasaki, Ichiro Yabe, Masaaki Matsushima, Alexandra Duerr, Alexis Brice, Hiroshi Takashima, Akio Kikuchi, Masashi Aoki, et al. Variants associated with Gaucher disease in multiple system atrophy. ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY. 2015. 2. 4. 417-426
Yuji Takahashi, Yoko Fukuda, Jun Yoshimura, Atsushi Toyoda, Kari Kurppa, Hiroyoko Moritoyo, Veronique V. Belzil, Patrick A. Dion, Koichiro Higasa, Koichiro Doi, et al. ERBB4 Mutations that Disrupt the Neuregulin-ErbB4 Pathway Cause Amyotrophic Lateral Sclerosis Type 19. AMERICAN JOURNAL OF HUMAN GENETICS. 2013. 93. 5. 900-905
Hiroyuki Ishiura, Yuji Takahashi, Jun Mitsui, Sohei Yoshida, Tameko Kihira, Yasumasa Kokubo, Shigeki Kuzuhara, Laura P. W. Ranum, Tomoko Tamaoki, Yaeko Ichikawa, et al. C9ORF72 Repeat Expansion in Amyotrophic Lateral Sclerosis in the Kii Peninsula of Japan. ARCHIVES OF NEUROLOGY. 2012. 69. 9. 1154-1158
Hiroyuki Ishiura, Wataru Sako, Mari Yoshida, Toshitaka Kawarai, Osamu Tanabe, Jun Goto, Yuji Takahashi, Hidetoshi Date, Jun Mitsui, Budrul Ahsan, et al. The TRK-Fused Gene Is Mutated in Hereditary Motor and Sensory Neuropathy with Proximal Dominant Involvement. AMERICAN JOURNAL OF HUMAN GENETICS. 2012. 91. 2. 320-329
Akio Yokoseki, Tomohiko Ishihara, Akihide Koyama, Atsushi Shiga, Mitsunori Yamada, Chieko Suzuki, Yoshiki Sekijima, Kyoko Maruta, Miyuki Tsuchiya, Hidetoshi Date, et al. Genotype-phenotype correlations in early onset ataxia with ocular motor apraxia and hypoalbuminaemia. BRAIN. 2011. 134. Pt 5. 1387-1399
ｍore...
MISC (2)：
Early-onset Ataxia with Ocular Motor Apraxia and Hypoalbuminemia is Caused by Mutations in a New HIT Superfamily Gene. Nature Genetics. 2001. 29(2), 184-188
Early-onset Ataxia with Ocular Motor Apraxia and Hypoalbuminemia is Caused by Mutations in a New HIT Superfamily Gene. Nature Genetics. 2001. 29(2), 184-188
Professional career (1)：
Master (Science) (Japan Advanced Institute of Science and Technology)
Work history (1)：
2008 - 2010 The University of Tokyo Faculty of Medicine University Hospital
Awards (2)：
2001 - 米国人類遺伝学会 学生賞
American Society of Human Genetics Student Award (Predoctoral Clinical)
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