Rchr
J-GLOBAL ID:202001008728069500
Update date: Nov. 12, 2024
Tanaka Hikari
タナカ ヒカリ | Tanaka Hikari
Affiliation and department:
Research theme for competitive and other funds (6):
Papers (23):
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Yuki Yoshioka, Yong Huang, Xiaocen Jin, Kien Xuan Ngo, Tomohiro Kumaki, Meihua Jin, Saori Toyoda, Sumire Takayama, Maiko Inotsume, Kyota Fujita, et al. PQBP3 prevents senescence by suppressing PSME3-mediated proteasomal Lamin B1 degradation. The EMBO journal. 2024
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Hidenori Homma, Kien Xuan Ngo, Yuki Yoshioka, Hikari Tanaka, Maiko Inotsume, Kyota Fujita, Toshio Ando, Hitoshi Okazawa. PQBP3/NOL7 is an intrinsically disordered protein. Biochemical and biophysical research communications. 2024. 736. 150453-150453
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Hidenori Homma, Yuki Yoshioka, Kyota Fujita, Shinichi Shirai, Yuka Hama, Hajime Komano, Yuko Saito, Ichiro Yabe, Hideyuki Okano, Hidenao Sasaki, et al. Dynamic molecular network analysis of iPSC-Purkinje cells differentiation delineates roles of ISG15 in SCA1 at the earliest stage. Communications biology. 2024. 7. 1. 413-413
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Hidenori Homma, Hikari Tanaka, Kyota Fujita, Hitoshi Okazawa. Necrosis Links Neurodegeneration and Neuroinflammation in Neurodegenerative Disease. International journal of molecular sciences. 2024. 25. 7
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Yuki Yoshioka, Juliana Bosso Taniguchi, Hidenori Homma, Takuya Tamura, Kyota Fujita, Maiko Inotsume, Kazuhiko Tagawa, Kazuharu Misawa, Naomichi Matsumoto, Masanori Nakagawa, et al. AAV-mediated editing of PMP22 rescues Charcot-Marie-Tooth disease type 1A features in patient-derived iPS Schwann cells. Communications medicine. 2023. 3. 1. 170-170
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MISC (7):
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Tanaka Hikari, Kondo Kanoh, Chen Xigui, Homma Hidenori, Tagawa Kazuhiko, Saido Takaomi, Muramatsu Shin-ichi, Fujita Kyota, Okazawa Hitoshi. 超早期アルツハイマー病においてSRRM2リン酸化はシナプス病理を誘発する(Phosphorylation of SRRM2 leads to synaptic pathology at ultra-early phase of Alzheimer's disease). 臨床神経学. 2020. 60. Suppl. S345-S345
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田中 ひかり, 岡澤 均. 【神経変性疾患の治療開発の現状-新たな戦略構築の基盤をめざして】各分野の動向 ダウンストリームを治療する 神経細胞死. 医学のあゆみ. 2020. 273. 1. 93-97
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田中ひかり, 田中ひかり, 本間秀典, 藤田慶大, 近藤和, JIN Xiaocen, 田川一彦, 岡澤均. YAP依存的ネクローシスは超早期アルツハイマー病態を制御する. Dementia Japan. 2020. 34. 4
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田中ひかり, 田中ひかり, 近藤和, 陳西貴, 本間秀典, 田川一彦, 藤田慶大, 岡澤均. 発達障害原因遺伝子PQBP1はアルツハイマー病態を制御する. Dementia Japan. 2020. 34. 4
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田中ひかり, 岡澤均. よくわかる遺伝子治療-実用化の現状と展望 C.遺伝子治療各論 脊髄小脳失調症. Clinical Neuroscience. 2020. 38. 3. 365-368
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Lectures and oral presentations (2):
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発達障害原因遺伝子PQBP1はアルツハイマー病態を制御する
(日本認知症学会 2020)
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YAP依存的ネクローシスは超早期アルツハイマー病態を制御する
(2020)
Education (2):
- 2017 - 2020 Tokyo Medical and Dental University Graduate School of Medical and Dental Sciences Track of Medical and Dental Sciences
- 2015 - 2017 Tokyo Medical and Dental University Graduate School of Medical and Dental Sciences
Work history (6):
- 2022/05 - 現在 Tokyo Medical and Dental University Medical Research Institute Pathophysiology Junior Associate Professor
- 2021/06 - 2022/04 Tokyo Medical and Dental University Medical Research Institute Pathophysiology Neuropathology Assistant Professor
- 2020/04 - 2021/05 Tokyo Medical and Dental University Medical Research Institute Pathophysiology Neuropathology
- 2020/04 - 2021/05 Tokyo Medical and Dental University Medical Research Institute
- 2017/04/01 - 2020/03/31 Tokyo Medical and Dental University Graduate School of Medical and Dental Sciences Medical and Dental Sciences Cognitive and Behavioral Medicine Neuropathology Graduate Student
- 2015/04/01 - 2017/03/31 Tokyo Medical and Dental University Graduate School of Medical and Dental Sciences Medical and Dental Sciences Cognitive and Behavioral Medicine Neuropathology Graduate Student
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Awards (7):
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