Rchr
J-GLOBAL ID:200901066999967077   Update date: Feb. 01, 2024

Inoue Ken

イノウエ ケン | Inoue Ken
Affiliation and department:
Job title: Head
Research field  (4): Fetal medicine/Pediatrics ,  Psychiatry ,  Genetics ,  Neuroscience - general
Research keywords  (7): hypomyelinating leukodystrophy ,  神経遺伝学 ,  ミエリン ,  ヒトゲノム ,  neurogenetics ,  myelin ,  human genome
Research theme for competitive and other funds  (23):
  • 2021 - 2024 A new AAV delivery method for gene therapy of hypomyelinaitng leukodystrophy
  • 2019 - 2021 Gene therapy for CMT1A using AAV harboring artificial microRNAs
  • 2016 - 2019 Impaired ER-Golgi trafficking as a novel cellular pathology for Pelizaeus-Merzbacher disease
  • 2016 - 2019 The study of neurodegeneration as a prognostic factor in congenital dysplasia of cortical white matter
  • 2015 - 2019 Drug screening for childhood genetic disease by visualizing proteins.
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Papers (103):
  • Keiko Akahoshi, Eiji Nakagawa, Yu-Ichi Goto, Ken Inoue. Duplication within two regions distal to MECP2: clinical similarity with MECP2 duplication syndrome. BMC medical genomics. 2023. 16. 1. 43-43
  • Kazuhiko Hashimoto, Shimpei Baba, Eiji Nakagawa, Noriko Sumitomo, Eri Takeshita, Yuko Shimizu-Motohashi, Akihiko Ishiyama, Takashi Saito, Chihiro Abe-Hatano, Ken Inoue, et al. Long-term changes in electroencephalogram findings in a girl with a nonsense SMC1A variant: A case report. Brain & development. 2022. 44. 8. 551-557
  • 浅倉 佑太, 池田 尚広, 小松 和幸, 中島 光子, 才津 浩智, 井上 健, 小坂 仁, 山形 崇倫. 進行性の発達退行とMRIで広範な白質病変を呈したUBTF遺伝子異常の9歳女児. 脳と発達. 2022. 54. Suppl. S339-S339
  • Yurika Numata-Uematsu, Mitsugu Uematsu, Toshiyuki Yamamoto, Hirotomo Saitsu, Yu Katata, Yoshitsugu Oikawa, Naoya Saijyo, Takehiko Inui, Kei Murayama, Akira Ohtake, et al. Leigh syndrome-like MRI changes in a patient with biallelic HPDL variants treated with ketogenic diet. Molecular genetics and metabolism reports. 2021. 29. 100800-100800
  • 井上 健, 植松 有里佳, 黒澤 健司, 才津 浩智, 高梨 潤一, 山本 俊至, 小坂 仁. 先天性大脳白質形成不全症の診断サポート コンサルテーションを通じた疾患遺伝子変異の同定. 脳と発達. 2021. 53. Suppl. S239-S239
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MISC (67):
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Patents (2):
  • オリゴデンドロサイト特異的プロモータ、PLP1遺伝子に特異的なmiRNA、該プロモータ及び/又は該miRNAを含むベクター並びに該ベクターを含む医薬組成物
  • オリゴデンドロサイト特異的プロモータ及びベクター並びに該ベクターを含む医薬組成物
Books (8):
  • Pelizaeus-Merzbacher Disease: Molecular and Cellular Pathologies and Associated Phenotypes.
    2019
  • 集団遺伝
    2018
  • 遺伝率
    2018
  • メンデルの法則
    2018
  • 髄鞘低形成(Pelizaeus-Merzbacher病)
    2014
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Lectures and oral presentations  (63):
  • Gene suppressing therapy for Pelizaeus-Merzbacher disease using artificial miRNA
    (第64回人類遺伝学会)
  • De novoスプライスサイト変異が同定されたSLC35A2-CDGの1症例
    (第64回人類遺伝学会)
  • PLP1 gene suppression therapy for Pelizaeus-Merzbacher disease using artificial miRNA
    (The American Society of Human Genetics Annual Meeting 2019)
  • Pelizaeus-Merzbacher病に対する遺伝子治療
    (第61回日本小児神経学会)
  • To understand and fix the problems of hypomyelinating leukodystrophy.
    (Glial Section Annual Meeting of the Korean Society for Brain and Neural Sciences)
more...
Works (4):
  • SOX10遺伝子変異とヒト遺伝疾患
    2004 - 2010
  • ペリツェウス・メルツバッハ病の分子遺伝学的研究
    2004 - 2010
  • Human Inherited diseases caused by SOX10 mutations
    2004 - 2010
  • Molecular Genetics of Pelizaeus-Merzbacher disease
    2004 - 2010
Education (4):
  • 1990 - 1994 Yokohama City University Graduate Graduate School of Medicine
  • - 1994 Yokohama City University Graduate School, Division of Medicine psychiatry
  • 1982 - 1988 Yokohama City University
  • Yokohama City University School of Medicine Medicine
Professional career (2):
  • Ph.D. (Yokohama City University(Japan))
  • M.D. (Yokohama City University(Japan))
Work history (12):
  • 2004 - 現在 国立精神神経センター神経研究所 室長
  • 2004 - 現在 Division chief. National Institute of Neuroscience,
  • 2002 - 2004 ベイラー医科大学分子人類遺伝学部 アシスタントプロフェッサー
  • 2002 - 2004 Assistant Professor. Baylor College of Medicine,
  • 1997 - 2002 ベイラ医科大学分子人類遺伝学部 ポスドク
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Association Membership(s) (7):
日本精神神経学会 ,  米国人類遺伝学会 ,  日本神経学会 ,  日本人類遺伝学会 ,  American Society of Human Genetics ,  Japan Society of Human Genetics ,  The Japanese Society of Child Neurology
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