ISHIKAWA Kinya 石川欽也

Researcher Number	30313240
Other IDs
External Links
Affiliation (Current)	2025: 東京科学大学, 大学院医歯学総合研究科, 教授
Affiliation (based on the past Project Information) *help	2023 – 2024: 東京医科歯科大学, 大学院医歯学総合研究科, 教授 2021 – 2023: 東京医科歯科大学, 東京医科歯科大学病院, 教授 2021: 東京医科歯科大学, 附属病院, 教授 2014 – 2020: 東京医科歯科大学, 医学部附属病院, 教授 2003 – 2013: 東京医科歯科大学, 医学部附属病院, 講師 … More 2007: Tokyo Medical and Dental University, Dept Neural, Lecturer 2004: 医科歯科大, 医学部附属病院, 講師 2002: TOKYO MEDICAL AND DENTAL UNIVERSITY, DEPARTMENT OF NEUROLOGY AND NEUROLOGICAL SCIENCE, ASSISTANT LECTURER, 医学部附属病院, 助手 2001: 東京医科歯科大学, 医学部・附属病院, 助手 2000: 東京医科歯科大学, 医学部・付属病院, 助手 2000: 東京医科歯科大学, 大学院・附属病院, 助手 Less
Review Section/Research Field	Principal Investigator Neurology / Biological Sciences / Basic Section 52020:Neurology-related / Biological Sciences / Basic Section 51030:Pathophysiologic neuroscience-related / Neurochemistry/Neuropharmacology Except Principal Investigator Neurology / Basic Section 57050:Prosthodontics-related / Neurology / Intelligent mechanics/Mechanical systems
Keywords	Principal Investigator 脊髄小脳変性症 / 遺伝子 / 小脳 / 神経疾患 / 神経変性疾患 / ＲＮＡ / RNA / 脳 / ゲノム / 神経難病 … More / 動物モデル / 神経科学 / ヒトゲノム / RNA-seq / ＲＮＡ結合蛋白 / 神経細胞 / トランスジェニックマウス / マイクロアレー / 分子標的治療 / 蛋白 / Purkinje細胞 / カルシウムチャネル / 脊髄小脳失調症6型 / 分子遺伝学 / iPS細胞 / プルキンエ細胞 / 蛋白質 / TDP-43 / タンパク / Purkinje / 抗体 / 遺伝子異常 / モデル動物 / degeneration / ataxia / neuron / genetics / cerebellum / α1A-カルシウムチャネル / トランスジェニック・マウス / 遺伝子工学 / ポリグルタミン病 / 神経遺伝学 / 脂質代謝 / 次世代シークエンサー / 病態 / 脳科学 / 遺伝子改変 / 実験動物 / 難病 / プロテオーム / 脳神経疾患 / 拡散 / 遺伝子治療 / 脊随小脳変性症 / 免疫治療 / モノクローナル抗体 / 細胞 / イオンチャネル / 遺伝 / 神経 / 神経細胞死 / 神経病理 / 遺伝子変異 / 蛋白工学 / SCA6 / DNA / 第16番染色体 / 遺伝性神経変性疾患 / 遺伝子情報 … More Except Principal Investigator SCA6 / 脊髄小脳変性症 / 動物モデル / Caチャンネル / P / αTTP / CACNA1A / 培養細胞 / 脳神経疾患 / 咳テスト / 高齢者 / 咳反射 / エクソーム / exome / Spinocerebeller ataxia / Neuroscience / Central nervous system disease / 原因遺伝子 / 16q-ADCA typeIII / 細胞骨格蛋白 / two-hybrid system法 / puratrophin-1 / 優性遺伝性小脳変性症 / 第16番染色体長腕 / 脳神経科学 / splicing / neurodegeneration / gene therapy / Q type calcium channel / polyglutamine disease / RNAi / 脊髄小脳変性症6型 / スプライス / 神経変性 / 遺伝子治療 / Q型カルシウムチャネル / 脊髓小脳変性症 / ポリグルタミン病 / ANIMAL MODEL / PURKINJE CELL / CA CHANNEL / CAG REPEAT / SPINOCEREBELLAR DEGENERATION / CACNAIA / ES細胞 / 脊髄小脳変形症 / CACN1A / ノックインマウス / CAGピート / プルキンエ細胞 / CAGリピート / 力学モデル / 小脳疾患 / 姿勢制御 / 封入体 / 脊髄小脳失調症 / 内科 / 応用動物 / 蛋白質 / 遺伝子 Less

Understanding the pathogenesis of spinocerebellar ataxia using iPS-derived Purkinje cells and long-read RNA-seq techniquePrincipal Investigator
- Principal Investigator
  
  石川欽也
- Project Period (FY)
  2024 – 2026
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52020:Neurology-related
- Research Institution
  Tokyo Medical and Dental University
クエン酸を用いた咳テストはMRIによる無症候性脳梗塞をスクリーニングできるか
- Principal Investigator
  
  中根綾子
- Project Period (FY)
  2022 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 57050:Prosthodontics-related
- Research Institution
  Tokyo Medical and Dental University
A study on Purkinje cell-specific gene expression in SCA31 model micePrincipal Investigator
- Principal Investigator
  
  Ishikawa Kinya
- Project Period (FY)
  2021 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52020:Neurology-related
- Research Institution
  Tokyo Medical and Dental University
Exploring a balancing mechanism between RNA and its binding protein partnersPrincipal Investigator
- Principal Investigator
  
  Ishikawa Kinya
- Project Period (FY)
  2018 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 51030:Pathophysiologic neuroscience-related
- Research Institution
  Tokyo Medical and Dental University
Exploring a pathogenic mechanism underlying neurodegenerative disorders caused by mutated RNA repeatPrincipal Investigator
- Principal Investigator
  
  ISHIKAWA Kinya
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Tokyo Medical and Dental University
Analysis of genetic back ground and pathomechanism of spinocerebellar degeneration
- Principal Investigator
  
  DOI Hiroshi
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Yokohama City University
Elucidation of the posture control disability in cerebellar ataxia from the model-based evaluation of patients and rodents
- Principal Investigator
  
  Funato Tetsuro
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Intelligent mechanics/Mechanical systems
- Research Institution
  The University of Electro-Communications
多系統型脊髄小脳失調症の遺伝子同定Principal Investigator
- Principal Investigator
  
  石川欽也
- Project Period (FY)
  2013 – 2014
- Research Category
  
  Grant-in-Aid for Scientific Research on Innovative Areas (Research in a proposed research area)
- Review Section
  
  Biological Sciences
- Research Institution
  Tokyo Medical and Dental University
A search for abnormal RNA metabolism in spinocerebellar ataxia type 31Principal Investigator
- Principal Investigator
  
  ISHIKAWA Kinya
- Project Period (FY)
  2012 – 2014
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Tokyo Medical and Dental University
優性遺伝型脊髄小脳変性症のハイスループット遺伝子変異探索Principal Investigator
- Principal Investigator
  
  石川欽也
- Project Period (FY)
  2011 – 2012
- Research Category
  
  Grant-in-Aid for Scientific Research on Innovative Areas (Research in a proposed research area)
- Review Section
  
  Biological Sciences
- Research Institution
  Tokyo Medical and Dental University
A basic research for identifying fundamental therapy for SCA6 and SCA31
- Principal Investigator
  
  MIZUSAWA Hidehiro
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Neurology
- Research Institution
  Tokyo Medical and Dental University
A research for dissecting molecular pathogenesis of SCA31.Principal Investigator
- Principal Investigator
  
  ISHIKAWA Kinya
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Tokyo Medical and Dental University
Investigation for developing a novel immunotherapy for a degenerative ataxia common in Japan.Principal Investigator
- Principal Investigator
  
  ISHIKAWA Kinya
- Project Period (FY)
  2007 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Tokyo Medical and Dental University
Elucidation of pathomechanism and development of treatment of spinocerebellar ataxia type 6
- Principal Investigator
  
  MIZUSAWA Hidehiro
- Project Period (FY)
  2005 – 2007
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Neurology
- Research Institution
  Tokyo Medical and Dental University
The functional analysis of !6q-linled autosomal dominant cerabeller ataxia associated gene.
- Principal Investigator
  
  TORU Shuta
- Project Period (FY)
  2005 – 2006
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Tokyo Medical and Dental University
第16番染色体連鎖型脊髄小脳変性症(16q-ADCCA)の原因と分子病態の解明Principal Investigator
- Principal Investigator
  
  石川欽也
- Project Period (FY)
  2004
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas
- Review Section
  
  Biological Sciences
- Research Institution
  Tokyo Medical and Dental University
第16番染色体連鎖型優性遺伝性脊髄小脳変性症の原因遺伝子同定と分子病態の解明Principal Investigator
- Principal Investigator
  
  石川欽也
- Project Period (FY)
  2003
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas
- Review Section
  
  Biological Sciences
- Research Institution
  Tokyo Medical and Dental University
Generation of transgenic mice expressing alphalA-calcium channel protein with highly expanded polyglutamine tract.Principal Investigator
- Principal Investigator
  
  ISHIKAWA Kinya
- Project Period (FY)
  2003 – 2004
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Tokyo Medical and Dental University
第16番染色体に連鎖する常染色体優性遺伝性脊髄小脳変性症の原因と病態の解明Principal Investigator
- Principal Investigator
  
  石川欽也
- Project Period (FY)
  2002
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas
- Review Section
  
  Biological Sciences
- Research Institution
  Tokyo Medical and Dental University
第16番染色体に連鎖する常染色体優性遺伝性脊髄小脳変性症の原因遺伝子の解明Principal Investigator
- Principal Investigator
  
  石川欽也
- Project Period (FY)
  2001
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas (C)
- Review Section
  
  Biological Sciences
- Research Institution
  Tokyo Medical and Dental University
脊髄小脳失調症6型脳内で凝集する新規蛋白分子の同定と細胞変性機序の解明Principal Investigator
- Principal Investigator
  
  石川欽也
- Project Period (FY)
  2001 – 2002
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Neurochemistry/Neuropharmacology
- Research Institution
  Tokyo Medical and Dental University
第16番染色体に連鎖する常染色体優性遺伝性脊髄小脳変性症の原因遺伝子の解明Principal Investigator
- Principal Investigator
  
  石川欽也
- Project Period (FY)
  2000
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas (C)
- Review Section
  
  Biological Sciences
- Research Institution
  Tokyo Medical and Dental University
STUDIES ON MOLECULAR AND CLINICAL PATHOMECHANISM OF SPINOCEREBELLAR DEGENERATION
- Principal Investigator
  
  MIZUSAWA Hidehiro
- Project Period (FY)
  2000 – 2002
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Neurology
- Research Institution
  Tokyo Medical and Dental University

[Book] 日本臨床　増刊号　医薬品副作用学(第3版)下2019
- Author(s)
  石川欽也
- Total Pages
  545
- Publisher
  日本臨床社
- Data Source
  KAKENHI-PROJECT-18H02715
[Book] XV.小脳の障害と運動失調．1．小脳の解剖と機能．In: 橋本信夫監修、三國信啓、深谷　親編集，「脳神経外科プラックティス. 3.脳神経外科医のための脳機能と局在診断」文光堂.　278-282，2014． 87.2014
- Author(s)
  石川欽也．
- Publisher
  文光堂
- Data Source
  KAKENHI-PROJECT-24591252
[Book] XV.小脳の障害と運動失調．1．小脳の解剖と機能．In: 橋本信夫監修、三國信啓、深谷　親編集，「脳神経外科プラックティス. 3.脳神経外科医のための脳機能と局在診断」文光堂.　278-282，2014． 87.2014
- Author(s)
  石川欽也．
- Publisher
  文光堂
- Data Source
  KAKENHI-PUBLICLY-25129703
[Book] XV.小脳の障害と運動失調．3．小脳機能障害の評価．In: 橋本信夫監修、三國信啓、深谷　親編集，「脳神経外科プラックティス. 3.脳神経外科医のための脳機能と局在診断」2014
- Author(s)
  石川欽也．
- Publisher
  文光堂
- Data Source
  KAKENHI-PUBLICLY-25129703
[Book] XV.小脳の障害と運動失調．2．小脳機能障害の分類．In: 橋本信夫監修、三國信啓、深谷　親編集，「脳神経外科プラックティス. 3.脳神経外科医のための脳機能と局在診断」2014
- Author(s)
  石川欽也．
- Publisher
  文光堂
- Data Source
  KAKENHI-PUBLICLY-25129703
[Book] XV.小脳の障害と運動失調．2．小脳機能障害の分類．In: 橋本信夫監修、三國信啓、深谷　親編集，「脳神経外科プラックティス. 3.脳神経外科医のための脳機能と局在診断」2014
- Author(s)
  石川欽也．
- Publisher
  文光堂
- Data Source
  KAKENHI-PROJECT-24591252
[Book] XV.小脳の障害と運動失調．3．小脳機能障害の評価．In: 橋本信夫監修、三國信啓、深谷　親編集，「脳神経外科プラックティス. 3.脳神経外科医のための脳機能と局在診断」2014
- Author(s)
  石川欽也．
- Publisher
  文光堂
- Data Source
  KAKENHI-PROJECT-24591252
[Book] 「神経・精神疾患診療マニュアル」2013
- Author(s)
  石川欽也，水澤英洋．
- Publisher
  日本医師会雑誌
- Data Source
  KAKENHI-PUBLICLY-25129703
[Book] 脊髄小脳変性症の治療．薬物治療を中心に．In: 辻　省次総編集、西澤正豊専門編集,「小脳と運動失調．　小脳はなにをしているのか」アクチュアル　脳・神経疾患の臨床．2013
- Author(s)
  石川欽也，水澤英洋.
- Publisher
  中山書店
- Data Source
  KAKENHI-PROJECT-24591252
[Book] 「小脳と運動失調．　小脳はなにをしているのか」アクチュアル　脳・神経疾患の臨床．2013
- Author(s)
  石川欽也，水澤英洋．
- Publisher
  中山書店
- Data Source
  KAKENHI-PROJECT-24591252
[Book] 「小脳と運動失調．　小脳はなにをしているのか」アクチュアル　脳・神経疾患の臨床．2013
- Author(s)
  石川欽也，水澤英洋．
- Publisher
  中山書店
- Data Source
  KAKENHI-PUBLICLY-25129703
[Book] 脊髄小脳変性症の治療．薬物治療を中心に．辻　省次総編集、西澤正豊専門編集,「小脳と運動失調．　小脳はなにをしているのか」アクチュアル　脳・神経疾患の臨床．2013
- Author(s)
  石川欽也, 水澤英洋
- Total Pages
  9
- Publisher
  中山書店
- Data Source
  KAKENHI-PUBLICLY-23129503
[Book] 「神経・精神疾患診療マニュアル」2013
- Author(s)
  石川欽也，水澤英洋．
- Publisher
  日本医師会雑誌.
- Data Source
  KAKENHI-PROJECT-24591252
[Book] 脊髄小脳失調症31型(SCA31)2011
- Author(s)
  石川欽也,佐藤望,網野猛志,新美祐介,融衆太,水澤英洋
- Publisher
  Annual Review神経
- Data Source
  KAKENHI-PROJECT-21249054
[Book] 脊髄小脳失調症31型(SCA31). Annual Review神経2011
- Author(s)
  石川欽也,佐藤望,網野猛志,新美祐介,融衆太,水澤英洋
- Data Source
  KAKENHI-PROJECT-21591072
[Book] 不随意運動.雑誌「内科」特集「内科疾患の診断基準病型分類・重症度」2010
- Author(s)
  石川欽也、水澤英洋
- Total Pages
  1398
- Data Source
  KAKENHI-PROJECT-21591072
[Book] 不随意運動.雑誌「内科」特集「内科疾患の診断基準病型分類・重症度」2010
- Author(s)
  石川欽也、水澤英洋
- Total Pages
  1398
- Publisher
  南江堂、東京
- Data Source
  KAKENHI-PROJECT-21249054
[Book] 脊髄小脳変性症の分類と治療.鈴木則宏・編「からだの科学」神経内科の病気のすべて2010
- Author(s)
  石川欽也、水澤英洋
- Publisher
  日本評論社
- Data Source
  KAKENHI-PROJECT-21591072
[Book] 遺伝性脊髄小脳変性症.雑誌「内科」特集「内科疾患の診断基準病型分類・重症度」2010
- Author(s)
  石川欽也、水澤英洋
- Data Source
  KAKENHI-PROJECT-21591072
[Book] 脊髄小脳変性症の分類と治療2010
- Author(s)
  石川欽也、水澤英洋
- Publisher
  日本評論社,東京
- Data Source
  KAKENHI-PROJECT-21249054
[Book] 遺伝性脊髄小脳変性症.雑誌「内科」特集「内科疾患の診断基準病型分類・重症度」2010
- Author(s)
  石川欽也、水澤英洋
- Publisher
  南江堂、東京
- Data Source
  KAKENHI-PROJECT-21249054
[Book] 多系統萎縮症. In :落合滋之監修森田明夫、吉澤利弘編集,「脳神経疾患ビジュアルブック」2009
- Author(s)
  石川欽也
- Publisher
  学研
- Data Source
  KAKENHI-PROJECT-21591072
[Book] 脊髄小脳変性症2009
- Author(s)
  石川欽也
- Publisher
  学研,東京
- Data Source
  KAKENHI-PROJECT-21249054
[Book] 多系統萎縮症2009
- Author(s)
  石川欽也
- Publisher
  学研,東京
- Data Source
  KAKENHI-PROJECT-21249054
[Book] 脊髄小脳変性症. In :落合滋之監修森田明夫、吉澤利弘編集,「脳神経疾患ビジュアルブック」2009
- Author(s)
  石川欽也
- Publisher
  学研
- Data Source
  KAKENHI-PROJECT-21591072
[Book] Research Advances in Spinocerebellar Degeneration and Spastic Paraplegia22008
- Author(s)
  Kinya Ishikawa.
- Publisher
  Research Signpost Publishers, Kerara, India.(In press)
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17209031
[Book] Research Advances in Spinocerebellar Degeneration and Spastic Paraplegia2008
- Author(s)
  Ishikawa K, Flanigan K, Mizusawa H.
- Publisher
  Research Signpost Publishers, Kerara, India.(In press)
- Data Source
  KAKENHI-PROJECT-17209031
[Book] Spineocerebellar Ataxia Type 6. Genetic Instabilities Neurological Diseases2006
- Author(s)
  H Mizusawa, Kinya Ishikawa
- Publisher
  Academic Press
- Data Source
  KAKENHI-PROJECT-17209031
[Book] Chromosome 16q22.1-linked autosomal dominant cerebellar ataxia and spinocerebellar ataxia type 4, the clinically distinct ataxias linked to the same locus. In, "Research advances in spinocerebellar degeneration and spastic paraplegia"
- Author(s)
  Ishikawa K, Flanigan K, Mizusawa H
- Publisher
  Nishizawa M & Takiyama Y, Editors Research SignPost, Kerala, India
- Data Source
  KAKENHI-PROJECT-19590981
[Journal Article] Subcellular localization and ER-mediated cytotoxic function of α1A and α1ACT in spinocerebellar ataxia type 62024
- Author(s)
  Wang Di、Honda Shinya、Shin Min Kyoung、Watase Kei、Mizusawa Hidehiro、Ishikawa Kinya、Shimizu Shigeomi
- Journal Title
  
  Biochemical and Biophysical Research Communications
  
  Volume: 695 Pages: 149481-149481
- DOI
  10.1016/j.bbrc.2024.149481
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-22K07345, KAKENHI-PROJECT-23K06960, KAKENHI-PROJECT-21K07432
[Journal Article] FUS regulates RAN translation through modulating the G-quadruplex structure of GGGGCC repeat RNA in C9orf72-linked ALS/FTD2023
- Author(s)
  Fujino Yuzo、Ueyama Morio、Ishiguro Taro、Ozawa Daisaku、Ito Hayato、Sugiki Toshihiko、Murata Asako、Ishiguro Akira et al.
- Journal Title
  
  eLife
  
  Volume: 12 Pages: 1-31
- DOI
  10.7554/elife.84338
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-22K07032, KAKENHI-PROJECT-23K06836, KAKENHI-PROJECT-20K07737, KAKENHI-PROJECT-21K07432, KAKENHI-PUBLICLY-23H04265, KAKENHI-PROJECT-21H02840
[Journal Article] Spinocerebellar ataxia type 31 (SCA31).2023
- Author(s)
  Ishikawa K.
- Journal Title
  
  J Hum Genet
  
  Volume: 68(3) Issue: 3 Pages: 153-156
- DOI
  10.1038/s10038-022-01091-4
- NAID
  40019323170
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21K07432
[Journal Article] Gait disorders induced by photothrombotic cerebellar stroke in mice.2023
- Author(s)
  Inoue K, Asaka M, Lee S, Ishikawa K, Yanagihara D.
- Journal Title
  
  Scientific Reports
  
  Volume: 13 Issue: 1 Pages: 15805-15805
- DOI
  10.1038/s41598-023-42817-4
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K07432, KAKENHI-PROJECT-21K11260, KAKENHI-PROJECT-20KK0226
[Journal Article] Spinocerebellar ataxia type 31: A clinical and radiological literature review.2023
- Author(s)
  Saucier J, Al-Qadi M, Amor MB, Ishikawa K, Chamard-Witkowski L.
- Journal Title
  
  J Neurol Sci.
  
  Volume: 444 Pages: 120527-120527
- DOI
  10.1016/j.jns.2022.120527
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K07432
[Journal Article] Thymidine kinase 2 and mitochondrial protein COX I in the cerebellum of patients with spinocerebellar ataxia type 31 caused by penta-nucleotide repeats (TTCCA) n.2022
- Author(s)
  Aoki H, Higashi M, Okita M, Ando N, Murayama S, Ishikawa K*, Yokota T.
- Journal Title
  
  Cerebellum.
  
  Volume: Jan 27 Issue: 1 Pages: 70-84
- DOI
  10.1007/s12311-021-01364-2
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02715, KAKENHI-PROJECT-21K07432, KAKENHI-PROJECT-22K07538, KAKENHI-PROJECT-22K07550, KAKENHI-PROJECT-19K07988, KAKENHI-PROJECT-22H04923
[Journal Article] Insight into spinocerebellar ataxia type 31 (SCA31) from Drosophila model.2021
- Author(s)
  Ishiguro T*, Nagai Y*, Ishikawa K*.
- Journal Title
  
  Front Neurosci.
  
  Volume: 15 Pages: 648133-648133
- DOI
  10.3389/fnins.2021.648133
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18H02715, KAKENHI-PROJECT-21K07432, KAKENHI-PLANNED-20H05927
[Journal Article] Neuropathology of SCA34 showing widespread oligodendroglial pathology with vacuolar white matter degeneration: a case study2021
- Author(s)
  Ozaki Kokoro、Irioka Takashi、Uchihara Toshiki、Yamada Akane、Nakamura Ayako、Majima Takamasa、Igarashi Susumu、Shintaku Hiroshi、Yakeishi Mayumi、Tsuura Yukio、Okazaki Yasushi、Ishikawa Kinya、Yokota Takanori
- Journal Title
  
  Acta Neuropathologica Communications
  
  Volume: 9 Issue: 1 Pages: 172-172
- DOI
  10.1186/s40478-021-01272-w
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K15441, KAKENHI-PROJECT-17H03555, KAKENHI-PROJECT-18H02715, KAKENHI-PROJECT-21K07432
[Journal Article] Comorbid argyrophilic grain disease in an 87-year-old male with spinocerebellar ataxia type 31 with dementia: a case report2020
- Author(s)
  S. Toru S. Ishida T. Uchihara K. Hirokawa M. Kitagawa and K. Ishikawa
- Journal Title
  
  BMC Neurol
  
  Volume: 20 Issue: 1 Pages: 136-136
- DOI
  10.1186/s12883-020-01723-2
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K14572, KAKENHI-PROJECT-17H03555, KAKENHI-PROJECT-18H02715
[Journal Article] Molecular mechanisms and future therapeutics for spinocerebrellar ataxia type 31 (SCA31).2019
- Author(s)
  *Ishikawa K., Nagai Y.
- Journal Title
  
  Neurotherapeutics
  
  Volume: 16 Issue: 4 Pages: 1106-1114
- DOI
  10.1007/s13311-019-00804-6
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K19658, KAKENHI-PUBLICLY-17H05699, KAKENHI-PROJECT-16H05325, KAKENHI-PROJECT-18H02715
[Journal Article] RNA結合タンパクと病態機序．2019
- Author(s)
  石川欽也、石黒太郎、佐藤望、永井義隆．
- Journal Title
  
  脳神経内科
  
  Volume: 91 Pages: 458-464
- Data Source
  KAKENHI-PROJECT-18H02715
[Journal Article] Tandem internal models execute motor learning in the cerebellum2018
- Author(s)
  Honda Takeru、Nagao Soichi、Hashimoto Yuji、Ishikawa Kinya、Yokota Takanori、Mizusawa Hidehiro、Ito Masao
- Journal Title
  
  Proceedings of the National Academy of Sciences
  
  Volume: 115 Issue: 28 Pages: 7428-7433
- DOI
  10.1073/pnas.1716489115
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K21649, KAKENHI-PROJECT-18H02715
[Journal Article] Spinocerebellar Ataxia Type 31 with Blepharospasm2018
- Author(s)
  Itaya S, Kobayashi Z, Ozaki K, Sato N, Numasawa Y, Ishikawa K, Yokota T, Matsuda H, Shintani S.
- Journal Title
  
  Intern. Med.
  
  Volume: 57 Issue: 11 Pages: 1651-1654
- DOI
  10.2169/internalmedicine.0068-17
- NAID
  130007382858
- ISSN
  0918-2918, 1349-7235
- Year and Date
  2018-06-01
- Language
  English
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18H02715
[Journal Article] A diagnostic decision tree for adult cerebellar ataxia based on pontine magnetic resonance imaging2018
- Author(s)
  Higashi Miwa、Ozaki Kokoro、Hattori Takaaki、Ishii Takashi、Soga Kazumasa、Sato Nozomu、Tomita Makoto、Mizusawa Hidehiro、Ishikawa Kinya、Yokota Takanori
- Journal Title
  
  Journal of the Neurological Sciences
  
  Volume: 387 Pages: 187-195
- DOI
  10.1016/j.jns.2018.02.022
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K11189, KAKENHI-PROJECT-18H02715
[Journal Article] A novel mutation in ELOVL4 leading to spinocerebellar ataxia (SCA) with the hot cross bun sign but lacking erythrokeratodermia: a broadened spectrum of SCA34.2015
- Author(s)
  Ozaki K, Doi H, Mitsui J, Sato N, Iikuni Y, Majima T, Yamane K, Irioka T, Ishiura H, Doi K, Morishita S, Higashi M, Sekiguchi T, Koyama K, Ueda N, Miura Y, Miyatake S, Matsumoto N, Yokota T, Tanaka F, Tsuji S, Mizusawa H, Ishikawa K.
- Journal Title
  
  JAMA Neurology
  
  Volume: 72 Issue: 7 Pages: 797-805
- DOI
  10.1001/jamaneurol.2015.0610
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09335, KAKENHI-PROJECT-15K09344, KAKENHI-PROJECT-26461549, KAKENHI-PROJECT-221S0002, KAKENHI-ORGANIZER-24118001, KAKENHI-PLANNED-24118007, KAKENHI-PROJECT-25461287
[Journal Article] Quantitative evaluation of human cerebellum-dependent motor learning through prism adaptation of hand-reaching movement.2015
- Author(s)
  Hashimoto Y, Honda T, Matsumura K, Nakao M, Soga K, Katano K, Yokota T, Mizusawa H, Nagao S, Ishikawa K
- Journal Title
  
  PLoS One.
  
  Volume: 10(3) Issue: 3 Pages: e0119376-e0119376
- DOI
  10.1371/journal.pone.0119376
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-24591252, KAKENHI-PUBLICLY-25129703, KAKENHI-PROJECT-26289063
[Journal Article] CADASIL with a novel NOTCH3 mutation (Cys478Tyr).2015
- Author(s)
  Ozaki K, Irioka T, Ishikawa K, Mizusawa H
- Journal Title
  
  J Stroke Cerebrovasc Dis.
  
  Volume: Mar;24(3) Issue: 3 Pages: e61-e62
- DOI
  10.1016/j.jstrokecerebrovasdis.2014.11.022
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591252, KAKENHI-PUBLICLY-25129703
[Journal Article] A novel mutation in ELOVL4 leading to spinocerebellar ataxia with the hot cross bun sign but lacking erythrokeratodermia: a broadened spectrum of SCA34.2015
- Author(s)
  Ozaki K, Doi H, Mitsui J, Sato N, Iikuni Y, Majima T, Yamane K, Irioka T, Ishiura H, Doi K, Morishita S, Higashi M, Sekiguchi T, Koyama K, Ueda N, Miura Y, Miyatake S, Matsumoto N, Yokota T, Tanaka F, Tsuji S, Mizusawa H, Ishikawa K.
- Journal Title
  
  JAMA Neurology
  
  Volume: 6
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PUBLICLY-25129703
[Journal Article] A novel mutation in ELOVL4 leading to spinocerebellar ataxia with the hot cross bun sign but lacking erythrokeratodermia: a broadened spectrum of SCA34.2015
- Author(s)
  Ozaki K, Doi H, Mitsui J, Sato N, Iikuni Y, Majima T, Yamane K, Irioka T, Ishiura H, Doi K, Morishita S, Higashi M, Sekiguchi T, Koyama K, Ueda N, Miura Y, Miyatake S, Matsumoto N, Yokota T, Tanaka F, Tsuji S, Mizusawa H, Ishikawa K.
- Journal Title
  
  JAMA Neurology
  
  Volume: 6
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-24591252
[Journal Article] Rare frequency of downbeat positioning nystagmus in spinocerebellar ataxia type 31.2015
- Author(s)
  Yabe I, Matsushima M, Yoshida K, Ishikawa K, Shirai S, Takahashi I, Sasaki H.
- Journal Title
  
  J Neurol Sci.
  
  Volume: Mar 15;350(1-2) Issue: 1-2 Pages: 90-92
- DOI
  10.1016/j.jns.2014.12.042
- NAID
  120005722547
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-24591252, KAKENHI-PROJECT-24591255, KAKENHI-PUBLICLY-25129703
[Journal Article] Analysis of Muscle Synergy Contribution on Human Standing-up Motion Using Human Neuro-Musculoskeletal Model2015
- Author(s)
  Qi An, Yuki Ishikawa, Shinya Aoi, Tetsuro Funato, Hiroyuki Oka, Hiroshi Yamakawa, Atsushi Yamashita, Hajime Asama
- Journal Title
  
  Proceedings of 2015 IEEE International Conference on Robotics and Automation
  
  Volume: -
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26289063
[Journal Article] Analysis of Muscle Synergy Contribution on Human Standing-up Motion Using Human Neuro-Musculoskeletal Model.2015
- Author(s)
  Qi An, Yuki Ishikawa, Shinya Aoi, Tetsuro Funato, Hiroyuki Oka, Hiroshi Yamakawa, Atsushi Yamashita, and Hajime Asama.
- Journal Title
  
  Proceeding of the IEEE International Conference on Robotics and Automation
  
  Volume: - Pages: 5885-5890
- DOI
  10.1109/icra.2015.7140023
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-15H01660, KAKENHI-PROJECT-26289063, KAKENHI-PLANNED-26120006
[Journal Article] Analysis of Human Standing-up Motion Using Forward Dynamic Simulation with Four Body Segment Model2014
- Author(s)
  Qi An, Yuki Ishikawa, Tetsuro Funato, Shinya Aoi, Hiroyuki Oka, Hiroshi Yamakawa, Atsushi Yamashita, Hajime Asama
- Journal Title
  
  Proceedings of the 12th International Symposium on Distributed Autonomous Robotic Systems
  
  Volume: - Pages: 249-261
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26289063
[Journal Article] Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion.2014
- Author(s)
  Obayashi M, Stevanin G, Synofzik M, Monin ML, Duyckaerts C, Sato N, Streichenberger N, Vighetto A, Desestret V, Tesson C, Wichmann HE, Illig T, Huttenlocher J, Kita Y, Izumi Y, Mizusawa H, Schoels L, Klopstock T, Brice A, Ishikawa K, Duerr A
- Journal Title
  
  J Neurol Neurosurg Psychiatry.
  
  Volume: Dec 4 Issue: 9 Pages: 986-995
- DOI
  10.1136/jnnp-2014-309153
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-24591252, KAKENHI-PUBLICLY-25129703
[Journal Article] Muscle Synergy Analysis of Human Standing-up Motion in Different Seat Heights and Speeds2014
- Author(s)
  Qi An，石川雄己，舩戸徹郎，青井伸也，岡敬之，山川博司，山下淳，淺間一
- Journal Title
  
  Transactions of the Society of Instrument and Control Engineers
  
  Volume: 50 Issue: 8 Pages: 560-568
- DOI
  10.9746/sicetr.50.560
- NAID
  130004679646
- ISSN
  0453-4654, 1883-8189
- Language
  Japanese
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26289063
[Journal Article] Generation of human standing-up motion with muscle synergies using forward dynamic simulation2014
- Author(s)
  Qi An, Yuki Ishikawa, Tetsuro Funato, Shinya Aoi, Hiroyuki Oka, Hiroshi Yamakawa, Atsushi Yamashita, Hajime Asama
- Journal Title
  
  Proceedings of 2014 IEEE International Conference on Robotics and Automation
  
  Volume: - Pages: 730-735
- DOI
  10.1109/icra.2014.6906935
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26289063
[Journal Article] Relocation of p25α/tubulin polymerization promoting protein from the nucleus to the perinuclear cytoplasm in the oligodendroglia of sporadic and COQ2 mutant multiple system atrophy.2014
- Author(s)
  Ota K, Obayashi M, Ozaki K, Ichinose S, Kakita A, Tada M, Takahashi H, Ando N, Eishi Y, Mizusawa H, Ishikawa K.
- Journal Title
  
  Acta Neuropathol Commun
  
  Volume: Sep 11;2 Issue: 1 Pages: 136-136
- DOI
  10.1186/s40478-014-0136-4
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-24591252, KAKENHI-PUBLICLY-25129703
[Journal Article] The evaluation of polyglutamine repeats in autosomal dominant Parkinson's disease.2014
- Author(s)
  Yamashita C, Tomiyama H, Funayama M, Inamizu S, Ando M, Li Y, Yoshino H, Araki T, Ichikawa T, Ehara Y, Ishikawa K, Mizusawa H, Hattori N.
- Journal Title
  
  Neurobiol Aging.
  
  Volume: 35 Issue: 7 Pages: 1779.e17-1779.e21
- DOI
  10.1016/j.neurobiolaging.2014.01.022
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PLANNED-23111003, KAKENHI-PROJECT-24390224, KAKENHI-PROJECT-24591252, KAKENHI-PUBLICLY-25129703, KAKENHI-PUBLICLY-25129707, KAKENHI-PROJECT-25461291, KAKENHI-PROJECT-25461292, KAKENHI-PROJECT-25860725
[Journal Article] Abnormal RNA structures (RNA foci) containing a penta-nucleotide repeat (UGGAA)n in the Purkinje cell nucleus is associated with spinocerebellar ataxia type 31 pathogenesis.2013
- Author(s)
  Niimi Y, Takahashi M, Sugawara E, Umeda S, Obayashi M, Sato N, Ishiguro T, Higashi M, Eishi Y, Mizusawa H, Ishikawa K.
- Journal Title
  
  Neuropathology
  
  Volume: 33(6) Issue: 6 Pages: 600-611
- DOI
  10.1111/neup.12032
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591252, KAKENHI-PUBLICLY-25129703, KAKENHI-PUBLICLY-23129503
[Journal Article] Cytoplasmic location of α1A voltage-gated calcium channel C-terminal fragment (Cav2.1-CTF) aggregate is sufficient to cause cell death.2013
- Author(s)
  Takahashi M, Obayashi M, Ishiguro T, Sato N, Niimi Y, Ozaki K, Mogushi K, Mahmut Y, Tanaka H, Tsuruta F, Dolmetsch R, Yamada M, Takahashi H, Kato T, Mori O, Eishi Y, Mizusawa H, Ishikawa K.
- Journal Title
  
  PLoS ONE
  
  Volume: 8(3) Issue: 3 Pages: e50121-e50121
- DOI
  10.1371/journal.pone.0050121
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591252, KAKENHI-PUBLICLY-23129503
[Journal Article] Development of Purkinje cell degeneration in a knockin mouse model reveals lysosomal involvement in the pathogenesis of SCA6.2012
- Author(s)
  Unno, T., Wakamori, M., Koike, M., Uchiyama, Y., Ishikawa, K., Kubota, H., Yoshida, T., Sasakawa, H., Peters, C., Mizusawa, H. and Watase K
- Journal Title
  
  Proc. Natl. Acad. Sci. USA
  
  Volume: 109(43) Issue: 43 Pages: 17693-17698
- DOI
  10.1073/pnas.1212786109
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590924, KAKENHI-PROJECT-22659335, KAKENHI-PROJECT-23790238, KAKENHI-PROJECT-24591252, KAKENHI-PUBLICLY-23129503
[Journal Article] Prevalence of inositol 1, 4, 5-triphosphate receptor type 1 gene(ITPR1) deletion, the mutation for spinocerebellar ataxia type 15(SCA15), in Japan screened by gene dosage2012
- Author(s)
  Obayashi M, Ishikawa K, Izumi Y, Takahashi M, Niimi Y, Sato N, Onodera O, Kaji R, Nishizawa M, Mizusawa H
- Journal Title
  
  J Hum Genet
  
  Volume: 57(3) Pages: 202-206
- Data Source
  KAKENHI-PROJECT-21249054
[Journal Article] Reduced brain-derived neurotrophic factor(BDNF) mRNA expression and presence of BDNF-immunoreactive granules in the spinocerebellar ataxia type 6(SCA6) cerebellum.2012
- Author(s)
  Takahashi M, Ishikawa K, Sato N, Obayashi M, Niimi Y, Ishiguro T, Yamada M, Toyoshima Y, Takahashi H, Kato T, Takao M, Murayama M, Mori O, Eishi Y, Mizusawa H
- Journal Title
  
  Neuropathology
  
  Volume: (in press)
- Data Source
  KAKENHI-PROJECT-21249054
[Journal Article] A commentary on confirmation and refinement of an autosomal dominant congenital motor nystagmus locus in chromosome 1q31.3-q32.1.2012
- Author(s)
  Ishikawa K.
- Journal Title
  
  Journal of Human Genetics
  
  Volume: 57(12) Issue: 12 Pages: 755-755
- DOI
  10.1038/jhg.2012.122
- NAID
  10031145880
- Data Source
  KAKENHI-PUBLICLY-23129503
[Journal Article] Reduced brain-derived neurotrophic factor (BDNF) mRNA expression and presence of BDNF-immunoreactive granules in the spinocerebellar ataxia type 6 (SCA6) cerebellum2012
- Author(s)
  Takahashi M, Ishikawa K, Sato N, Obayashi M, Niimi Y, Ishiguro T, Yamada M, Toyoshima Y, Takahashi H, Kato T, Takao M, Murayama M, Mori O, Eishi Y, Mizusawa H
- Journal Title
  
  Neuropathology
  
  Volume: (in press) Issue: 6 Pages: 593-603
- DOI
  10.1111/j.1440-1789.2012.01302.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21249054, KAKENHI-PROJECT-21591072, KAKENHI-PROJECT-22300118, KAKENHI-PUBLICLY-23129503, KAKENHI-PROJECT-23500435, KAKENHI-PROJECT-24300133, KAKENHI-PROJECT-24591252, KAKENHI-PROJECT-24659402
[Journal Article] Prevalence of inositol 1,4,5-triphosphate receptor type 1 gene (ITPR1) deletion, the mutation for spinocerebellar ataxia type 15 (SCA15), in Japan screened by gene dosage2012
- Author(s)
  Obayashi M, Ishikawa K, Izumi Y, Takahashi M, Niimi Y, Sato N, Onodera O, Kaji R, Nishizawa M, Mizusawa H
- Journal Title
  
  J Hum Genet
  
  Volume: 57(3) Issue: 3 Pages: 202-206
- DOI
  10.1038/jhg.2012.5
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21249054, KAKENHI-PROJECT-21591072, KAKENHI-PUBLICLY-23129503, KAKENHI-PROJECT-24591252
[Journal Article] Prevalence of inositol 1, 4, 5-triphosphate receptor type 1 gene(ITPR1) deletion, the mutation forspinocerebellar ataxia type 15(SCA15), in Japan screened by gene dosage2012
- Author(s)
  Obayashi M, Ishikawa K, Izumi Y, Takahashi M, Niimi Y, Sato N, Onodera O, Kaji R, Nishizawa M, Mizusawa H.
- Journal Title
  
  J Hum Genet
  
  Volume: 57(3) Pages: 202-206
- Data Source
  KAKENHI-PROJECT-21591072
[Journal Article] The chromosome 16q-linked autosomal dominant cerebellar ataxia (16q-ADCA^*) : A newly identified degenerative ataxia in Japan showing peculiar morphological changes of the Purkinje cell2012
- Author(s)
  Ishikawa K, Mizusawa H
- Journal Title
  
  Neuropathology
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591072
[Journal Article] Reduced brain-derived neurotrophic factor(BDNF) mRNA expression and presence of BDNF-immunoreactive granules in the spinocerebellar ataxia type 6(SCA6) cerebellum2012
- Author(s)
  Takahashi M, Ishikawa K, Sato N, Obayashi M, Niimi Y, Ishiguro T, Yamada M, Toyoshima Y, Takahashi H, Kato T, Takao M, Murayama M, Mori O, Eishi Y, Mizusawa H.
- Journal Title
  
  Neuropathology
  
  Volume: (in press)
- Data Source
  KAKENHI-PROJECT-21591072
[Journal Article] Pentanucleotide repeats at the spinocerebellar ataxia type 32 (SCA31) locus in Caucasians2011
- Author(s)
  Ishikawa K, Durr A, Klopstock T, Muller S, De Toffol B, Vighetto A, Marelli C, Wichmann HE, Illig T, Niimi Y, Sato N, Amino T, Stevanin G, Brice A, Mizusawa H
- Journal Title
  
  Neurology
  
  Volume: 77(20) Pages: 1853-1855
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21249054
[Journal Article] Pentanucleotide repeats at the spinocerebellar ataxia type 32(SCA31) locus in Caucasians2011
- Author(s)
  Ishikawa K, Durr A, Klopstock T, M ller S, De Toffol B, Vighetto A, Marelli C, Wichmann HE, Illig T, Niimi Y, Sato N, Amino T, Stevanin G, Brice A, Mizusawa H
- Journal Title
  
  Neurology
  
  Volume: 77(20) Pages: 1853-1855
- Data Source
  KAKENHI-PROJECT-21249054
[Journal Article] Pentanucleotide repeats at the spinocerebellar ataxia type 32 (SCA31) locus in Caucasians2011
- Author(s)
  Ishikawa K, Durr A, Klopstock T, Muller S, De Toffol B, Vighetto A, Marelli C, Wichmann HE, Illig T, Niimi Y, Sato N, Amino T, Stevanin G, Brice A, Mizusawa H
- Journal Title
  
  Neurology
  
  Volume: 77(20) Pages: 1853-1855
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591072
[Journal Article] Pentanucleotide repeats at the spinocerebellar ataxia type 32(SCA31) locus in Caucasians2011
- Author(s)
  Ishikawa K, D rr A, Klopstock T, M ller S, De Toffol B, Vighetto A, Marelli C, Wichmann HE, Illig T, Niimi Y, Sato N, Amino T, Stevanin G, Brice A, Mizusawa H.
- Journal Title
  
  Neurology
  
  Volume: 77(20) Pages: 1853-1855
- Data Source
  KAKENHI-PROJECT-21591072
[Journal Article] Pentanucleotide repeats at the spinocerebellar ataxia type 32 (SCA31) locus in Caucasians2011
- Author(s)
  Ishikawa K, Durr A, Klopstock T, Muller S, De Toffol B, Vighetto A, Marelli C, Wichmann HE, Illig T, Niimi Y, Sato N, Amino T, Stevanin G, Brice A, Mizusawa H
- Journal Title
  
  Neurology
  
  Volume: 77(20) Pages: 1853-1855
- Peer Reviewed
- Data Source
  KAKENHI-PUBLICLY-23129503
[Journal Article] The chromosome 16q-linked autosomal dominant cerebellar ataxia (16q-ADCA^*) : A newly identified degenerative ataxia in Japan showing peculiar morphological changes of the Purkinje cell.2010
- Author(s)
  Ishikawa K, Mizusawa H.
- Journal Title
  
  Neuropathology
  
  Volume: (Epub)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591072
[Journal Article] The carboxy-terminal fragment of alphalA calcium channelpreferentially aggregates in the cytoplasm of human spino-cerebellar ataxia type 6 Purkinje cells.2010
- Author(s)
  Ishiguro T, Ishikawa K, Takahashi M, Obayashi M, Amino T, Sato N, Sakamoto M, Fujigasaki H, Tsuruta F, Dolmetsch R, Arai T, Sasaki H, Nagashima K, Kato T, Yamada M, Takahashi H, Hashizume Y, Mizusawa H.
- Journal Title
  
  Acta Neuropathologica
  
  Volume: 119(4) Pages: 447-464
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21249054
[Journal Article] The chromosome 16q-linked autosomal dominant cerebellarataxia (16q-ADCA*) : A newly identified degenerative ataxiain Japan showing peculiar morphological changes of the Purkinje cell.2010
- Author(s)
  Ishikawa K, Mizusawa H
- Journal Title
  
  Neuropathology
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21249054
[Journal Article] The carboxy-terminal fragment of alphalA calcium channel preferentially aggregates in the cytoplasm of human spino-cerebellar ataxia type 6 Purkinje cells.2010
- Author(s)
  Ishiguro T, Ishikawa K, Takahashi M, Obayashi M, Amino T, Sato N, Sakamoto M, Fujigasaki H, Tsuruta F, Dolmetsch R, Arai T, Sasaki H, Nagashima K, Kato T, Yamada M, Takahashi H, Hashizume Y, Mizusawa H.
- Journal Title
  
  Acta Neuropathologica
  
  Volume: 119(4) Pages: 447-464
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591072
[Journal Article] The chromosome 16q-linked autosomal dominant cerebellar ataxia(16q-ADCA*): A newly identified degenerative ataxia in Japan showing peculiar morphological changes of the Purkinje cell2010
- Author(s)
  Ishikawa K, Mizusawa H.
- Journal Title
  
  Neuropathology
  
  Volume: 30(5) Pages: 490-494
- Data Source
  KAKENHI-PROJECT-21591072
[Journal Article] The carboxy-terminal fragment of alpha1A calcium channel preferentially aggregates in the cytoplasm of human spinocerebellar ataxia type 6 Purkinje cells2010
- Author(s)
  Ishiguro T, Ishikawa K, Takahashi M, Obayashi M, Amino T, Sato N, Sakamoto M, Fujigasaki H, Tsuruta F, Dolmetsch R, Arai T, Sasaki H, Nagashima K, Kato T, Yamada M, Takahashi H, Hashizume Y, Mizusawa H.
- Journal Title
  
  Acta Neuropathol
  
  Volume: 119(4) Pages: 447-464
- Data Source
  KAKENHI-PROJECT-21591072
[Journal Article] The chromosome 16q-linked autosomal dominant cerebellar ataxia(16q-ADCA*): A newly identified degenerative ataxia in Japan showing peculiar morphological changes of the Purkinje cell2010
- Author(s)
  Ishikawa K, Mizusawa H
- Journal Title
  
  Neuropathology
  
  Volume: 30(5) Pages: 490-494
- Data Source
  KAKENHI-PROJECT-21249054
[Journal Article] The carboxy-terminal fragment of alpha1A calcium channel preferentially aggregates in the cytoplasm of human spinocerebellar ataxia type 6 Purkinje cells2010
- Author(s)
  Ishiguro T, Ishikawa K, Takahashi M, Obayashi M, Amino T, Sato N, Sakamoto M, Fujigasaki H, Tsuruta F, Dolmetsch R, Arai T, Sasaki H, Nagashima K, Kato T, Yamada M, Takahashi H, Hashizume Y, Mizusawa H
- Journal Title
  
  Acta Neuropathol
  
  Volume: 119(4) Pages: 447-464
- Data Source
  KAKENHI-PROJECT-21249054
[Journal Article] The carboxy-terminal fragment of alpha1A calcium channel preferentially aggregates in the cytoplasm of human spino-cerebellar ataxia type 6 Purkinje cells.2010
- Author(s)
  Ishiguro T, Ishikawa K, Takahashi M, Obayashi M, Amino T, Sato N, Sakamoto M, Fujigasaki H, Tsuruta F, Dolmetsch R, Arai T, Sasaki H, Nagashima K, Kato T, Yamada M, Takahashi H, Hashizume Y, Mizusawa H.
- Journal Title
  
  Acta Neuropathologica
  
  Volume: 119(4) Pages: 447-464
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591072
[Journal Article] The chromosome 16q-linked autosomal dominant cerebellar ataxia (16q-ADCA*) : A newly identified degenerative ataxia in Japan showing peculiar morphological changes of the Purkinje cell.2010
- Author(s)
  Ishikawa K, Mizusawa H.
- Journal Title
  
  Neuropathology
  
  Volume: (Epub)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591072
[Journal Article] Spinocerebellar ataxia type 31 is associated with "inserted" penta-nucleotide repeats containing(TGGAA) n2009
- Author(s)
  Sato N, Amino T, Kobayashi K, Asakawa S, Ishiguro T, Tsunemi T, Takahashi M, Matsuura T, Flanigan KM, Iwasaki S, Ishino F, Saito Y, Murayama S, Yoshida M, Hashizume Y, Takahashi Y, Tsuji S, Shimizu N, Toda T, Ishikawa K, Mizusawa H
- Journal Title
  
  Am J Hum Genet
  
  Volume: 85(5) Pages: 544-557
- Data Source
  KAKENHI-PROJECT-21249054
[Journal Article] The carboxy-terminal fragment of alpha1A calcium channel preferentially aggregates in the cytoplasm of human spinocerebellar ataxia type 6 Purkinje cells.2009
- Author(s)
  Ishiguro T, Ishikawa K, Takahashi M, Obayashi M, Amino T, Sato N, Sakamoto M, Fujigasaki H, Tsuruta F, Dolmetsch R, Arai T, Sasaki H, Nagashima K, Kato T, Yamada M, Takahashi H, Hashizume Y, Mizusawa H.
- Journal Title
  
  Acta Neuropathol
  
  Volume: Dec 31(Epub ahead of print)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21249054
[Journal Article] Spinocerebellar ataxia type 31 is associated with "inserted" penta-nucleotide repeats containing(TGGAA) n2009
- Author(s)
  Sato N, Amino T, Kobayashi K, Asakawa S, Ishiguro T, Tsunemi T, Takahashi M, Matsuura T, Flanigan KM, Iwasaki S, Ishino F, Saito Y, Murayama S, Yoshida M, Hashizume Y, Takahashi Y, Tsuji S, Shimizu N, Toda T, Ishikawa K, Mizusawa H.
- Journal Title
  
  Am J Hum Genet
  
  Volume: 85(5) Pages: 554-557
- Data Source
  KAKENHI-PROJECT-21591072
[Journal Article] Direct and accurate measurement of CAG repeat configuration in the ataxin-1(ATXN-1)gene by "dual-fluorescence labeled PCR-restriction fragment length analysis"2008
- Author(s)
  Lin J. X, Ishikawa K(Corresponding author), Sakamoto M, Tsunemi T, Ishiguro T, Amino T, Toru S, Kondo I, Mizusawa H
- Journal Title
  
  J Hum Genet 53
  
  Pages: 287-295
- NAID
  10021248419
- Data Source
  KAKENHI-PROJECT-19590981
[Journal Article] Cell-type-specific alternative splicing in spinocerebellar ataxia type 62008
- Author(s)
  Tsunemi T, Ishikawa K, Jin H, Mizusawa H
- Journal Title
  
  Neurosci Lett 30
- Data Source
  KAKENHI-PROJECT-19590981
[Journal Article] Analyses of copy number and mRNA expression level of the [alpha]-synuclein gene in multiple system atrophy2008
- Author(s)
  Honglian Jin, Ishikawa K(Corresponding author), Tsunemi T, Ishiguro T, Mizusawa H
- Journal Title
  
  J Med Dent Sci 55
  
  Pages: 145-153
- Data Source
  KAKENHI-PROJECT-19590981
[Journal Article] Spinocerebellar ataxia type 6 knock-in mice develop a progressive neuronal dysfunction with age-dependent accumulation of mutant CaV2.1 channels2008
- Author(s)
  Watase K, Barrett CF, Miyazaki T, Ishiguro T, Ishikawa K, Hu Y, Unno T, Sun Y, Kasai S, Watanabe M, Gomez CM, Mizusawa H, Tsien RW and Zoghbi HY
- Journal Title
  
  Proc Natl Acad Sci USA 105(33)
  
  Pages: 11987-92
- Data Source
  KAKENHI-PROJECT-19590981
[Journal Article] Direct and accurate measurement of CAG repeat configuration in the ataxin-l(ATXN-I)gene by "dual-fluorescence labeled PCR-restriction fragment length analysis"2008
- Author(s)
  Lin JX, Ishikawa K, Sakamoto M, Tsunemi T, Ishiguro T, Amino T, Toru S, Kondo 1, Mizusawa H.
- Journal Title
  
  Journal of Human Genetics 53
  
  Pages: 287-295
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17209031
[Journal Article] Cell-type-specific alternative splicing in spino-cerebellar ataxia type 6.2008
- Author(s)
  Tsunemi T, Ishikawa K, Jin H, Mizusawa H.
- Journal Title
  
  Neurosci Lett. 447(1)
  
  Pages: 78-81
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19590981
[Journal Article] Spinocerebellar ataxia type 6 knockin mice devel op aprogressive neuronal dysfunction with age-dependentaccumulation of mutant Ca_v2. 1 channels.2008
- Author(s)
  Watase K, Barrett CF, Miyazaki T, Ishiguro T, Ishikawa K, Hu Y, Sun Y, Kasai S, Watanabe M, Gomez CM, Mizusawa H, Tsien RW, Zoghbi HY.
- Journal Title
  
  Proc Natl Acad Sci USA 105(33)
  
  Pages: 11987-11992
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19590981
[Journal Article] Bax-inhibiting peptide protects cells from polyglutamine toxicity caused by Ku70 acetylation2007
- Author(s)
  Li Y, Yokota T, Gama V, Yoshida T, Gomez JA, Ishikawa K, Sasaguri H, Cohen HY, Sinclair DA, Mizusawa H, Matsuyama S.
- Journal Title
  
  Cell Death & Differentiation 14
  
  Pages: 2058-2067
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17209031
[Journal Article] Bax-inhibiting peptide protects cells from polyglutamine toxicity caused by Ku70 acetylation2007
- Author(s)
  Li Y, Yokota T, Gama V, Yoshida T, Gomez JA, Ishikawa K, Sasaguri H, Cohen HY, Sinclair DA, Mizusawa H, Matsuyama S
- Journal Title
  
  Cell Death Differ 14(12)
  
  Pages: 2058-67
- Data Source
  KAKENHI-PROJECT-19590981
[Journal Article] Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia2007
- Author(s)
  Amino T, Ishikawa K(Corresponding author), Toru S, Ishiguro T, Sato N, Tsunemi T, Murata M, Kobayashi K, Inazawa J, Toda T, Mizusawa H
- Journal Title
  
  J Hum Genet 52
  
  Pages: 643-649
- NAID
  10019812756
- Data Source
  KAKENHI-PROJECT-19590981
[Journal Article] Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia.2007
- Author(s)
  Amino T, Ishikawa K, Toru S, Ishiguro T, Sato N, Tsunemi T, Murata M, Kobayashi K, Inazawa J, Toda T, Mizusawa H.
- Journal Title
  
  Journal of Human Genetics 52
  
  Pages: 643-649
- NAID
  10019812756
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17209031
[Journal Article] 16q-linked autosomal dominant cerebellar ataxia : a clinical and genetic study.2006
- Author(s)
  Ouyang Y, Sakoe K, Shimazaki H, Namekawa M, Ogawa T, Ando Y, Kawakami T, Kaneko J, Hasegawa Y, Yoshizawa K, Amino T, Ishikawa K, Mizusawa H, Nakano I, Takiyama Y.
- Journal Title
  
  J Neurol Sci. 247(2)
  
  Pages: 180-186
- Data Source
  KAKENHI-PROJECT-17590866
[Journal Article] On autosomal dominant cerebellar ataxia (ADCA) other than polyglutamine diseases with special reference to chromosome 16q22. 1-linked ADCA.2006
- Author(s)
  Ishikawa K., Mizusawa H.
- Journal Title
  
  Neuropathology 26(4)
  
  Pages: 352-360
- Data Source
  KAKENHI-PROJECT-17590866
[Journal Article] A -16C>T substitution in the 5' UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in Nagano.2006
- Author(s)
  Ohata T, Yoshida K, Sakai H, Hamanoue H, Mizuguchi T, Shimizu Y, Okano T, Takada F, Ishikawa K, Mizusawa H, Yoshiura K, Fukushima Y, Ikeda S, Matsumoto N.
- Journal Title
  
  Journal of Human Genetics 51(5)
  
  Pages: 461-466
- NAID
  10019168027
- Data Source
  KAKENHI-PROJECT-17590866
[Journal Article] On autosomal dominant cerebellar ataxia(ADCA) other than polyglutamine diseases, with special reference to chromosome 16g22.1-linked ADCA2006
- Author(s)
  Ishikawa K, Mizusawa H.
- Journal Title
  
  Neuropathology 26
  
  Pages: 352-360
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17209031
[Journal Article] On autosomal dominant cerebellar ataxia (ADCA) other than polyglutamine diseases, with special reference to chromosome 16q22.1-linked ADCA.2006
- Author(s)
  Ishikawa K, Mizusawa H.
- Journal Title
  
  Neuropathology 26(4)
  
  Pages: 352-360
- NAID
  10018059239
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17590866
[Journal Article] 16q-linked autosomal dominant cerebellar ataxia : a clinical and genetic study2006
- Author(s)
  Ouyang Y, Sakoe K, Shimazaki H, Namekawa M, Ogawa T, Ando Y, Kawakami T, Kaneko J, Hasegawa Y, Yoshizawa K, Amino T, Ishikawa K, et al.
- Journal Title
  
  J Neurol Sci 247(2)
  
  Pages: 180-186
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17590866
[Journal Article] A-16C>T substitution in the 5'UTR of the puratrophin-I gene is prevalent in autosomal dominant cerebellar ataxia in Nagano.2006
- Author(s)
  Ohata T, Yshida K, Sakai H, Hamanoue H, Mizuguchi T, Shimizu Y, Okano T, Takada F, Ishikawa K, Mizusawa H, Yoshiura K, Fukushima Y, Ikeda S, Matsumoto N
- Journal Title
  
  J Hum Gene 51
  
  Pages: 461-466
- Data Source
  KAKENHI-PROJECT-17209031
[Journal Article] On autosomal dominant cerebellar ataxia (ADCA) other than polyglutamine diseases, with special reference to chromosome 16q22.1-linked ADCA.2006
- Author(s)
  Ishikawa K, Mizusawa H
- Journal Title
  
  Neuropathology 26(4)
  
  Pages: 352-360
- NAID
  10018059239
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17590866
[Journal Article] 【脊髄小脳変性症研究の最近の進歩】常染色体優性遺伝性脊髄小脳変性症第16番染色体長腕に連鎖する優性遺伝性脊髄小脳変性症2006
- Author(s)
  石川欽也, 融衆太, 水澤英洋
- Journal Title
  
  神経研究の進歩 50巻3号
  
  Pages: 355-362
- Data Source
  KAKENHI-PROJECT-17590866
[Journal Article] A -16C>T substitution in the 5' UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in Nagano.2006
- Author(s)
  Ohata T, Yoshida K, Sakai H, Hamanoue H, Mizuguchi T, Shimizu Y, Okano T, Takada F, Ishikawa K, et al.
- Journal Title
  
  J Hum Genet 51(5)
  
  Pages: 461-466
- NAID
  10019168027
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17590866
[Journal Article] On autosomal dominant cerebellar ataxia(ADCA)other than polyglutamine diseases, with special reference to chromosome 16q22.1-linked ADCA.2006
- Author(s)
  Ishikawa K, Mizusawa H.
- Journal Title
  
  Neuropathology 26
  
  Pages: 352-360
- NAID
  10018059239
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17209031
[Journal Article] An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains.2006
- Author(s)
  Ishikawa K, Toru S, Tsunemi T, Li M, Kobayashi K, Yokota T, Amino T, et al.
- Journal Title
  
  Am J Hum Genet 77(2)
  
  Pages: 280-296
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17590866
[Journal Article] A -16C>T substitution in the 5'UTR of the puratrophin-1 gene is prevalent is autosomal dominant cerebellar ataxia in Nagano.2006
- Author(s)
  Ohata T, Yoshida K, Sakai H, Hamanoue H, Mizuguchi T, Shimizu Y, Okano T, Takada F, Ishikawa K, et al.
- Journal Title
  
  J Hum Genet 51(5)
  
  Pages: 461-466
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17590866
[Journal Article] 16q-linked autosomal dominant cerebellar ataxia : A clinical and genetic study.2006
- Author(s)
  Ouyang Y, Sakoe K, Shimazaki H, Namekawa M, Ogawa T, Ando Y, Kawakakmi T, Kaneko J, Hasegawa Y, Yoshizawa K, Amino T, Ishikawa K, Mizusawa H, Nakano I, Takiyama Y
- Journal Title
  
  Neurological Science 247(2006)
  
  Pages: 180-186
- Data Source
  KAKENHI-PROJECT-17209031
[Journal Article] New RNAi strategy for selective suppression of a mutant allele in polyglutamine disease.2005
- Author(s)
  Kubodera T, Yokota T, Ishikawa K, Mizusawa H
- Journal Title
  
  Oligonucleotides 15
  
  Pages: 298-302
- Data Source
  KAKENHI-PROJECT-17209031
[Journal Article] A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA type III2005
- Author(s)
  Owada K, Ishikawa K, Toru S, Ishida G, et al.
- Journal Title
  
  Neurology 65(4)
  
  Pages: 629-632
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17590866
[Journal Article] A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA type III.2005
- Author(s)
  Owada K, Ishikawa K, Toru S, Ishida G, Gomyoda M, Tao O, Noguchi Y, Mizusawa H et al.
- Journal Title
  
  Neurology 65
  
  Pages: 629-632
- Data Source
  KAKENHI-PROJECT-17209031
[Journal Article] A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA typeIII.2005
- Author(s)
  Owada K, Ishikawa K, Toru S, Ishida G, Gomyoda M, Tao O, Noguchi Y, Kitayama K, Kondo I, Noguchi E, Arinami T, Mizusawa H.
- Journal Title
  
  Neurology 65(4)
  
  Pages: 629-632
- Data Source
  KAKENHI-PROJECT-17590866
[Journal Article] An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5'untranslated region of the gene encoding a protein with spectrin repeat and rho guanine-nucleotide exchange-factor domains.2005
- Author(s)
  Ishikawa K, Toru S, Tsunemi T, Li M, Kobayashi K, Yokota T, Amino T, Mizusawa H et al.
- Journal Title
  
  Am.J.Hum.Genet 77
  
  Pages: 280-296
- Data Source
  KAKENHI-PROJECT-17209031
[Journal Article] An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotidesubstitution in the 5 untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains.2005
- Author(s)
  Ishikawa K, Toru S, Tsunemi T, Li M, Kobayashi K, Yokota T, Amino T, Owada K, Fujigasaki H, Sakamoto M, Tomimitsu H, Takashima M, Kumagai J, Noguchi Y, Kawashima Y, Ohkoshi N, Ishida G, Gomyoda M, Yoshida M, Hashizume Y, Saito Y, Murayama S, Yamanouchi H, Mizutani T, Kondo I, Toda T, Mizusawa H.
- Journal Title
  
  Am J Hum Genet. 77(2)
  
  Pages: 280-296
- Data Source
  KAKENHI-PROJECT-17590866
[Journal Article] An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslafed region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domain2005
- Author(s)
  Ishikawa K, et. al.
- Journal Title
  
  Am J Hum Genet 77
  
  Pages: 280-96
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17209031
[Journal Article] A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA type III.2005
- Author(s)
  Owada K, Ishikawa K, Toru S, Ishida G, et al.
- Journal Title
  
  Neurology 65(4)
  
  Pages: 629-632
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17590866
[Journal Article] An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains.2005
- Author(s)
  Ishikawa K, Toru S, Tsunemi T, Li M, Kobayashi K, Yokota T, Amino T, Owada K, et al.
- Journal Title
  
  Am J Hum Genet 77(2)
  
  Pages: 280-296
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17590866
[Journal Article] An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domain.2005
- Author(s)
  Ishikawa K, et. al.
- Journal Title
  
  American Journal of Human Genetics 77
  
  Pages: 280-296
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17209031
[Journal Article] A clinical and genetic study in a large cohort of patients with spinocerebellar ataxia type 6.2004
- Author(s)
  Takahashi H, Ishikawa K, et al.
- Journal Title
  
  Journal of Human Genetics 49
  
  Pages: 256-264
- NAID
  10013090010
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15590881
[Journal Article] A clinical and genetic study in a large cohort of patients with spinocerebellar ataxia type 6.2004
- Author(s)
  Takahashi H, Ishikawa K, et al.
- Journal Title
  
  Journal of Human Genetics 49(5)
  
  Pages: 256-264
- NAID
  10013090010
- Data Source
  KAKENHI-PROJECT-15590881
[Journal Article] A clinical and genetic study in a large cohort of patients with spinocerebellar ataxia type 6.2004
- Author(s)
  Takahashi H., Ishikawa K., et al.
- Journal Title
  
  Journal of Human Genetics 49(5)
  
  Pages: 256-264
- NAID
  10013090010
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15590881
[Journal Article] Proteolytic cleavage and cellular toxicity of the human alpha1A-calcium channel in spinocerebellar ataxia type 6.2003
- Author(s)
  Kubodera T, Ishikawa K, et al.
- Journal Title
  
  Neuroscience Letter 341
  
  Pages: 74-78
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15590881
[Journal Article] Proteolytic cleavage and cellular toxicity of the human alpha1A calcium channel in spinocerebellar ataxia type 6.2003
- Author(s)
  Kubodera T., Yokota T., Ohwada K., Ishikawa K., et al.
- Journal Title
  
  Neuroscience Letter 341(1)
  
  Pages: 74-78
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15590881
[Patent] 脊髄小脳失調症３１型（SCA31）治療剤2014
- Inventor(s)
  石川欽也、水澤英洋、永井義隆、石黒太郎、佐藤　望、和田圭司
- Industrial Property Rights Holder
  石川欽也、水澤英洋、永井義隆、石黒太郎、佐藤　望、和田圭司
- Industrial Property Rights Type
  特許
- Filing Date
  2014-12-02
- Data Source
  KAKENHI-PROJECT-24591252
[Patent] ALSの原因タンパク毒性を軽減する核酸2014
- Inventor(s)
  石川欽也、水澤英洋、永井義隆、横田隆徳、石黒太郎、他2名
- Industrial Property Rights Holder
  石川欽也、水澤英洋、永井義隆、横田隆徳、石黒太郎、他2名
- Industrial Property Rights Type
  特許
- Filing Date
  2014-12-02
- Data Source
  KAKENHI-PROJECT-24591252
[Presentation] The expression analysis using RNA-seq on human cerebellar tissues.2023
- Author(s)
  Kinya Ishikawa
- Organizer
  The American Society of Human Genetics
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K07432
[Presentation] Pathogenesis of spinocerebellar ataxia type 31 (SCA31)2019
- Author(s)
  石川欽也．
- Organizer
  第60回日本神経学会学術大会, 2019/ 5/ 23,　国内,　口頭
- Invited
- Data Source
  KAKENHI-PROJECT-18H02715
[Presentation] Role of RNA chaperone TDP-43 in the pathogenesis of spinocerebellar ataxia type 31 (SCA31)2018
- Author(s)
  Kinya Ishikawa
- Organizer
  The 9th International Conference on Unstable Microsatellite and Human Disease.
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02715
[Presentation] The clinical and pathological features of autosomal-dominant SCA with CACNA1G mutation.2016
- Author(s)
  Doi H, Koyano S, Shiina M, Ogata K, Hirashima F, Inoue Y, Hashiguchi S, Kunii M, Kishida H, Yokota T, Mizusawa H, Mitsui J, Tsuji S, Matsumoto N, Ishikawa K and Tanaka F.
- Organizer
  第57回日本神経学会学術大会
- Place of Presentation
  神戸国際会議場（兵庫）
- Data Source
  KAKENHI-PROJECT-15K09344
[Presentation] Analysis of Muscle Synergy Contribution on Human Standing-up Motion Using Human Neuro-Musculoskeletal Model.2015
- Author(s)
  Qi An, Yuki Ishikawa, Shinya Aoi, Tetsuro Funato, Hiroyuki Oka, Hiroshi Yamakawa, Atsushi Yamashita, and Hajime Asama.
- Organizer
  IEEE International Conference on Robotics and Automation
- Place of Presentation
  Washington, USA
- Year and Date
  2015-05-26
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26289063
[Presentation] 筋シナジーの時間パターンがヒト起立動作に与える影響の神経筋骨格モデルを用いた解明.2015
- Author(s)
  安琪, 石川雄己, 青井伸也, 舩戸徹郎, 岡敬之, 山川博司, 山下淳, 淺間一.
- Organizer
  計測自動制御学会システム・情報部門学術講演会
- Place of Presentation
  北海道函館市
- Year and Date
  2015-11-18
- Data Source
  KAKENHI-PROJECT-26289063
[Presentation] Establishment of a novel system to apply cerebellar motor learning in clinics2013
- Author(s)
  Kinya Ishikawa, Yuji Hashimoto, Takeru Honda, Soichi Nagao, and Hidehiro Mizusawa
- Organizer
  Gordon Research Conference, Cerebellum
- Place of Presentation
  New London, NH, USA
- Data Source
  KAKENHI-PROJECT-24591252
[Presentation] A BAC transgenic mouse model of spinocerebellar ataxia type 31 (SCA31) exhibits RNA foci in Purkinje cells.2013
- Author(s)
  Sato N, Ishikawa K, Niimi Y, Mizusawa H.
- Organizer
  The 65th Annual Meeting, The American Academy of Neurology.
- Place of Presentation
  San Diego Convention Center
- Year and Date
  2013-03-16
- Data Source
  KAKENHI-PUBLICLY-23129503
[Presentation] A BAC transgenic mouse model of spinocerebellar ataxia type 31 (SCA31) exhibits RNA foci in Purkinje cells.2013
- Author(s)
  Sato N, Ishikawa K, Niimi Y, Mizusawa H.
- Organizer
  The 65th Annual Meeting, The American Academy of Neurology.
- Place of Presentation
  San Diego Convention Center
- Data Source
  KAKENHI-PROJECT-24591252
[Presentation] Spinocerebellar ataxia type 36 (SCA36): expanding the genotype and phenotype2013
- Author(s)
  Kinya Ishikawa
- Organizer
  SPATAX
- Place of Presentation
  フランス
- Data Source
  KAKENHI-PUBLICLY-25129703
[Presentation] RNA mediated cell death is important in a cultured cell model of spinicerebellar ataxia type 31.2012
- Author(s)
  Niimi Y, Ishikawa K, Sato N, Mizusawa H.
- Organizer
  The 2nd International Conference of Neural Tissue and Cell Culture.
- Place of Presentation
  東京医科歯科大学
- Data Source
  KAKENHI-PROJECT-24591252
[Presentation] A non-coding penta-nucleotide (UGGAA)n is essential for SCA31 pathogenesis.2012
- Author(s)
  Ishikawa K.
- Organizer
  The 7th International Conference on Unstable Microsatellite and Human Disease.
- Place of Presentation
  Ste.Odile, France.
- Invited
- Data Source
  KAKENHI-PROJECT-24591252
[Presentation] A gene search for a new spinocerebellar ataxia.2012
- Author(s)
  Ishikawa K., Sato N, Ozaki K, Mitsui J, Ishiura H, Hashimoto Y, Obayashi M, Matsuo H, Tsuji S, Mizusawa H.
- Organizer
  The 62nd Annual Meeting of the American Society of Human Genetics.
- Place of Presentation
  Moscone Convention Center, San Francisco.
- Year and Date
  2012-11-06
- Data Source
  KAKENHI-PUBLICLY-23129503
[Presentation] A non-coding penta-nucleotide (UGGAA)n is essential for SCA31 pathogenesis.2012
- Author(s)
  Ishikawa K.
- Organizer
  The 7th International Conference on Unstable Microsatellite and Human Disease.
- Place of Presentation
  Ste.Odile, France.
- Year and Date
  2012-06-09
- Invited
- Data Source
  KAKENHI-PUBLICLY-23129503
[Presentation] 細胞モデルを用いた脊髄小脳失調症31型(SCA31)の病態探索2011
- Author(s)
  新美祐介,佐藤望,網野猛志,高橋真,大林正人,石黒太郎,石川欽也,水澤英洋
- Organizer
  第52回日本神経学会学術大会
- Place of Presentation
  名古屋
- Year and Date
  2011-05-18
- Data Source
  KAKENHI-PROJECT-21591072
[Presentation] 細胞モデルを用いた脊髄小脳失調症31型(SCA31)の病態探索2011
- Author(s)
  新美祐介,佐藤望,網野猛志,高橋真,大林正人,石黒太郎,石川欽也,水澤英洋
- Organizer
  第52回日本神経学会学術大会
- Place of Presentation
  名古屋
- Year and Date
  2011-05-18
- Data Source
  KAKENHI-PROJECT-21249054
[Presentation] 細胞モデルを用いた脊髄小脳失調症31型(SCA31)の病態探索2011
- Author(s)
  新美祐介, 佐藤望, 網野猛志, 高橋真, 大林正人, 石黒太郎, 石川欽也, 水澤英洋
- Organizer
  第52回日本神経学会学術大会
- Place of Presentation
  名古屋
- Year and Date
  2011-05-18
- Data Source
  KAKENHI-PUBLICLY-23129503
[Presentation] シンポジウム「神経変性疾患とRNA」演題:SCA312010
- Author(s)
  石川欽也、網野猛志、佐藤望、新美祐介、融衆太、水澤英洋
- Organizer
  第51回日本神経学会総会
- Place of Presentation
  東京
- Year and Date
  2010-05-22
- Data Source
  KAKENHI-PROJECT-21591072
[Presentation] SCA6原因の同定から治療法の開発へ2010
- Author(s)
  渡瀬啓,石川欽也,水澤英洋
- Organizer
  第51回日本神経学会総会
- Place of Presentation
  東京
- Year and Date
  2010-05-22
- Data Source
  KAKENHI-PROJECT-21249054
[Presentation] シンポジウム16.「Neurodegenerative diseases and RNA.」SCA312010
- Author(s)
  石川欽也、網野猛志、佐藤望,新美祐介,融衆太,水澤英洋
- Organizer
  第51回日本神経学会総会
- Place of Presentation
  東京
- Year and Date
  2010-05-22
- Data Source
  KAKENHI-PROJECT-21249054
[Presentation] 教育講演:「脊髄小脳変性症」2010
- Author(s)
  石川欽也, 網野猛志, 佐藤望, 新美祐介, 融衆太, 水澤英洋
- Organizer
  日本人類遺伝学会第55回大会
- Place of Presentation
  さいたま市
- Year and Date
  2010-10-28
- Data Source
  KAKENHI-PROJECT-21591072
[Presentation] SCA6原因の同定から治療法の開発へ2010
- Author(s)
  渡瀬啓,石川欽也,水澤英洋
- Organizer
  第51回日本神経学会総会
- Place of Presentation
  東京
- Year and Date
  2010-05-22
- Data Source
  KAKENHI-PROJECT-21591072
[Presentation] SCA31 : Anew SCA identified in Japan showing peculiar pathology of Purkinje cells.2010
- Author(s)
  K.Ishikawa, (途中7名), H.Mizusawa.
- Organizer
  17^<th> International Congress of Neuropathology
- Place of Presentation
  ザルツブルク市、オーストリア
- Year and Date
  2010-09-13
- Data Source
  KAKENHI-PROJECT-21249054
[Presentation] Prominent respiratory muscle involvement in adPEO with POLG1 mutation.2010
- Author(s)
  Ishikawa K., et al.
- Organizer
  The 15^<th> International Congress of the World Muscle Society.
- Place of Presentation
  熊本市
- Year and Date
  2010-10-15
- Data Source
  KAKENHI-PROJECT-21591072
[Presentation] シンポジウム16.「Neurodegenerative diseases and RNA.」SCA312010
- Author(s)
  石川欽也、網野猛志、佐藤望,新美祐介,融衆太,水澤英洋
- Organizer
  第51回日本神経学会総会
- Place of Presentation
  東京
- Year and Date
  2010-05-22
- Data Source
  KAKENHI-PROJECT-21591072
[Presentation] The carboxy-terminal fragment of alA-calcium channel behavior underlies SCA6 neurodegeneration.2010
- Author(s)
  T.Ishiguro, K.Ishikawa, (途中12名), H.Mizusawa.
- Organizer
  17^<th> International Congress of Neuropathology
- Place of Presentation
  ザルツブルク市、オーストリア
- Year and Date
  2010-09-14
- Data Source
  KAKENHI-PROJECT-21249054
[Presentation] シンポジウム「神経変性疾患とRNA」演題:SCA312010
- Author(s)
  石川欽也, 網野猛志, 佐藤望, 新美祐介, 融衆太, 水澤英洋
- Organizer
  第51回日本神経学会総会
- Place of Presentation
  東京
- Year and Date
  2010-05-22
- Data Source
  KAKENHI-PROJECT-21591072
[Presentation] シンポジウム:神経難病の克服 -単一遺伝子病からのアプローチーSCA6-原因の同定から治療法の開発へ-2010
- Author(s)
  渡瀬啓, 石川欽也, 水澤英洋
- Organizer
  第51回日本神経学会総会
- Place of Presentation
  東京
- Year and Date
  2010-05-22
- Data Source
  KAKENHI-PROJECT-21249054
[Presentation] Prominent respiratory muscle involvement in adPEO with POLG1 mutation.2010
- Author(s)
  Ishikawa K., et al.
- Organizer
  The 15th International Congress of the World Muscle Society.
- Place of Presentation
  熊本市
- Year and Date
  2010-10-15
- Data Source
  KAKENHI-PROJECT-21591072
[Presentation] Tsien RW, Zoghbi HY. SCA6ノックインマウス表現型の経時的検討2009
- Author(s)
  渡瀬啓, Barrett CF,宮崎太輔、海野敏紀、石川欽也、笠井沙由美、渡辺雅彦、水澤英洋
- Organizer
  第50回日本神経学会総会
- Place of Presentation
  仙台
- Year and Date
  2009-05-20
- Data Source
  KAKENHI-PROJECT-21591072
[Presentation] シンポジウム9-1ポリグルタミン病への分子生物学的アプローチ.「脊髄小脳変性症への分子生物学的アプローチ」2009
- Author(s)
  石川欽也,石黒太郎,高橋真,佐藤望,網野猛志,新美祐介,水澤英洋
- Organizer
  第50回日本神経学会総会
- Place of Presentation
  仙台
- Year and Date
  2009-05-22
- Data Source
  KAKENHI-PROJECT-21591072
[Presentation] 50周年記念標本提示「日本が世界に発信したあの疾患」本邦で同定された新しい脊髄小脳変性症16q-ADCA-その特異的Purkinje細胞変性-2009
- Author(s)
  石川欽也,水澤英洋
- Organizer
  第50回日本神経病理学会総会学術研究会
- Place of Presentation
  高松
- Data Source
  KAKENHI-PROJECT-21249054
[Presentation] 50周年記念標本提示「日本が世界に発信したあの疾患」本邦で同定された新しい脊髄小脳変性症16q-ADCA-その特異的Purkinje細胞変性2009
- Author(s)
  石川欽也,水澤英洋
- Organizer
  第50回日本神経病理学会総会学術研究会
- Place of Presentation
  高松
- Data Source
  KAKENHI-PROJECT-21591072
[Presentation] シンポジウム9-1ポリグルタミン病への分子生物学的アプローチ.「脊髄小脳変性症への分子生物学的アプローチ」2009
- Author(s)
  石川欽也,石黒太郎,高橋真,佐藤望,網野猛志,新美祐介,水澤英洋
- Organizer
  第50回日本神経学会総会
- Place of Presentation
  仙台
- Year and Date
  2009-05-22
- Data Source
  KAKENHI-PROJECT-21249054
[Presentation] SCA6ノックインマウス表現型の経時的検討2009
- Author(s)
  渡瀬啓, Barrett CF,宮崎太輔、海野敏紀、石川欽也、笠井沙由美、渡辺雅彦、水澤英洋、Tsien RW, Zoghbi HY
- Organizer
  第50回日本神経学会総会
- Place of Presentation
  仙台
- Year and Date
  2009-05-20
- Data Source
  KAKENHI-PROJECT-21249054
[Presentation] Spinocerebellar ataxia type 6 (SCA6) is associ ated withsmall alA-calcium channel protein aggregates containingexpanded polyglutamine in the cytoplasm and the nucleusof human Purkinje cells.2008
- Author(s)
  Ishikawa K, Ishiguro T, Takahashi M, Amino T, Mizusawa H.
- Organizer
  第58回米国人類遺伝学会年次大会
- Place of Presentation
  米国フィラデルフィア市
- Year and Date
  2008-11-13
- Data Source
  KAKENHI-PROJECT-19590981
[Presentation] Spinocerebellar ataxia type 6(SCA6)is associated withsmall α1A-calcium channel protein aggregates containing expanded polyglutamine in the cytoplasm and the nucleusof human Purkinje cells2008
- Author(s)
  Ishikawa K, Ishiguro T, Takahashi M, Amino T, Mizusawa H
- Organizer
  第58回米国人類遺伝学会年次大会
- Place of Presentation
  米国フィラデルフィア市
- Year and Date
  2008-11-13
- Data Source
  KAKENHI-PROJECT-19590981
[Presentation] 小脳のMRI・PET画像解析:脊髄小脳変性症の進行度と画像所見の関連.2007
- Author(s)
  石川欽也, 他
- Organizer
  第30回日本脳神経CI学会総会
- Place of Presentation
  大阪
- Year and Date
  2007-02-03
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17209031
[Presentation] 16q-linked autosomal dominant cerebellar ataxia(16q-ADCA)2007
- Author(s)
  Ishikawa K.
- Organizer
  3rd International Symposium of Tokyo Med Dent Univ 21st COE program "Brain Integration and Its Disorders"
- Place of Presentation
  Tokyo
- Year and Date
  2007-02-17
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17209031
[Presentation] 16q-linked autosomal dominant cerebellar ataxia (16q-ADCA).2007
- Author(s)
  Ishikawa K.
- Organizer
  Tokyo Medical and Dental University 21st Century COE Program. "Brain Integration and Its Disorders" The Third International Symposium. "The cerebellum-from Molecules to Pathogenesis"
- Place of Presentation
  東京
- Year and Date
  2007-02-17
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17209031
[Presentation] Bax-inhibiting peptide protects cells from polyglutamine toxicity caused by Ku70 acetylation.2007
- Author(s)
  Yoshida T, Yokota T, Li Y, GamaV, Gomez J, Ishikawa K, SasaguriH, Mizusawa H, Matsuyama S.
- Organizer
  37th Annual Meeting of the Society for Neuroscience.
- Place of Presentation
  San Diego, CA(米国)
- Year and Date
  2007-11-04
- Data Source
  KAKENHI-PROJECT-17209031
[Presentation] 16番染色体連鎖型脊髄小脳変性症ホモ接合体家系の臨床および分子遺伝学的研究.2007
- Author(s)
  石川欽也, 他
- Organizer
  第48回日本神経学会総会
- Place of Presentation
  名古屋
- Year and Date
  2007-05-18
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17209031
[Presentation] Effectiveness of anti-androgen therapy for spinobulbar muscular atrophy(SBMA): An open study of 4 cases for 3 years.2007
- Author(s)
  Niimi Y, Ishikawa K, Yamawaki M, Mizusawa H.
- Organizer
  59th Annual Meeting of the American Academy of Neurology
- Place of Presentation
  Boston, MA(米国)
- Year and Date
  2007-05-04
- Data Source
  KAKENHI-PROJECT-17209031
[Presentation] 第16番染色体長腕連鎖型優性遺伝性脊髄小脳変性症でのPurkinje細胞の形態的変化.2007
- Author(s)
  石川欽也, 他
- Organizer
  第48回日本神経病理学会総会学術研究会
- Place of Presentation
  東京
- Year and Date
  2007-05-30
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17209031
[Presentation] 16番染色体長腕連鎖型優性遺伝性脊髄小脳変性症の原因遺伝子座の解析.2007
- Author(s)
  網野猛志, 佐藤望, 石黒太郎, 常深泰司, 融衆太, 戸田達史, 水澤英洋, 石川欽也.
- Organizer
  第48回日本神経学会総会
- Place of Presentation
  名古屋
- Year and Date
  2007-05-17
- Data Source
  KAKENHI-PROJECT-17209031
[Presentation] The effect of 3, 4-diaminopyridine on the postural imbalance and downbeat nystagmus in patients with ataxia.2007
- Author(s)
  Tsunemi T, Ishikawa K, Mizusawa H.
- Organizer
  59th Annual Meeting of the American Academy of Neurology
- Place of Presentation
  Boston,MA(米国)
- Year and Date
  2007-05-01
- Data Source
  KAKENHI-PROJECT-17209031
[Presentation] Clinical and genetic correlations in subjects with puratrophin-1(-16C>T) genetic change2006
- Author(s)
  Ishikawa K, et. al.
- Organizer
  56th Annual Meeting of Am Soc of Human Genetics
- Place of Presentation
  New Orleans
- Year and Date
  2006-10-11
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17209031
[Presentation] Autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is acommon subtype among spinocerebellar ataxias in Japan.2006
- Author(s)
  Ishikawa K, et. al.
- Organizer
  58th Annual Meeting of Am Acad of Neurology
- Place of Presentation
  San Diego
- Year and Date
  2006-10-06
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17209031
[Presentation] 第16番染色体連鎖型優性遺伝性失調症の臨床病理像と関連遺伝子同定.2006
- Author(s)
  石川欽也, 他
- Organizer
  第47回日本神経学会総会
- Place of Presentation
  東京
- Year and Date
  2006-05-11
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17209031
[Presentation] Clinical and genetic correlations in subjects with puratrophin-1(-16C>T)genetic change.2006
- Author(s)
  Ishikawa K, et. al.
- Organizer
  Am Soc of Human Genetics 56th Ann Meeting
- Place of Presentation
  New Orleans
- Year and Date
  2006-10-11
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17209031
[Presentation] Autosomal dominant cerebellar ataxia linked to chromosome 16g22.1 is a common subtype among Spinocerebellar ataxias in Japan2006
- Author(s)
  Ishikawa K, et. al.
- Organizer
  58th Annual Meeting of the Am Acad of Neurology
- Place of Presentation
  San Diego
- Year and Date
  2006-04-09
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17209031
[Presentation] Clinical features and molecular genetic analysis of two autosomal dominant cerebellar ataxias common in Japan2006
- Author(s)
  Ishikawa K.
- Organizer
  1st Workshop on Polyglutamine Disease and Related Disorders-New Perspectives
- Place of Presentation
  Tokyo
- Year and Date
  2006-09-23
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17209031
[Presentation] 16番染色体長腕連鎖型優性遺伝性小脳皮質萎縮症(16q-ADCCA)の臨床・病理・遺伝的特徴.2005
- Author(s)
  石川欽也, 他
- Organizer
  第46回日本神経学会総会
- Place of Presentation
  鹿児島
- Year and Date
  2005-05-25
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17209031
[Presentation] 本邦に高頻度に存在し、創始者効果を認める第16番染色体長腕連鎖型常染色体優性遺伝性脊髄小脳変性症(16q-ADCA)の原因遺伝子探索.2005
- Author(s)
  石川欽也, 他
- Organizer
  日本人類遺伝学会第50回大会
- Place of Presentation
  倉敷
- Year and Date
  2005-09-22
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17209031
[Presentation] A single nucleotide substitution in the 5'-UTR in the gene encoding spectrin repeat and Rho guanine nucleotide exchange factor domains is strongly associated with autosomal dominant cerebellara atxia linked to chromosome 16q22.12005
- Author(s)
  Ishikawa K, et. al.
- Organizer
  55th Annual Meeting of Am Soc of Human Genetics
- Place of Presentation
  Salt Lake City
- Year and Date
  2005-10-25
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17209031
[Presentation] A single nucleotide substitution in the 5'-UTR in the gene encoding spectrin repeat and Rho guanine nucleotide exchange factor domains is strongly associated with autosomal dominant cerebellara atxia linked to chromosome 16q22.1.2005
- Author(s)
  Ishikawa K, et. al.
- Organizer
  Am Soc of Human Genetics 55th Ann Meeting
- Place of Presentation
  Salt Lake City, UT
- Year and Date
  2005-10-25
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17209031
[Presentation] Identification of a single nucleotide substitution in the 5'-UTR in the gene encoding spectrin repeat and Rho guanine nucleotide exchange factor domains within the founder chromosomal region for the autosomal dominant cerebellar ataxia linked to chromosome 16q22.12005
- Author(s)
  Ishikawa K.
- Organizer
  Ataxia 2005. A Satellite Meeting to the World Congress of Neurology
- Place of Presentation
  Gold Coast, Queensland
- Year and Date
  2005-11-03
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17209031
[Presentation] Clinical features and molecular genetic analysis of two autosomal dominant cerebellar ataxias common in Japan.2005
- Author(s)
  Ishikawa K.
- Organizer
  1st Workshop on Polyglutamine Disease and Related Disorders -New Perspectives
- Place of Presentation
  東京
- Year and Date
  2005-09-23
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17209031
[Presentation] ポリグルタミン病以外の優性遺伝性失調症:第16番染色体連鎖型(16q-linked ADCA type III)を中心に.2005
- Author(s)
  石川欽也、水澤英洋.
- Organizer
  第46回日本神経病理学会学術研究会.
- Place of Presentation
  宇都宮
- Year and Date
  2005-05-12
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17209031
[Presentation] Identification of a single nucleotide substitution in the 5-UTR in the gene encoding spectrin repeat and Rho guanine nucleotide exchange factor domains within the founder chromosomal region for the autosomal dominant cerebellar ataxia linked to chromosome 16q22.1.2005
- Author(s)
  Ishikawa K.
- Organizer
  Ataxia 2005. A Satellite Meeting to the World Congress of Neurology.
- Place of Presentation
  Gold Coast, Queensland
- Year and Date
  2005-11-03
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17209031
[Presentation] 異なる環境における起立動作からの筋シナジー抽出と神経筋骨格モデルを用いた起立動作生成
- Author(s)
  Qi An, 石川雄己, 青井伸也, 舩戸徹郎, 岡敬之, 山川博司, 山下淳, 浅間一
- Organizer
  第８回モーターコントロール研究会
- Place of Presentation
  筑波
- Year and Date
  2014-08-07 – 2014-08-09
- Data Source
  KAKENHI-PROJECT-26289063
[Presentation] Analysis of Muscle Synergy Contribution on Human Standing-up Motion Using Human Neuro-Musculoskeletal Model
- Author(s)
  Qi An, Yuki Ishikawa, Shinya Aoi, Tetsuro Funato, Hiroyuki Oka, Hiroshi Yamakawa, Atsushi Yamashita, Hajime Asama
- Organizer
  IEEE International Conference on Robotics and Automation 2015
- Place of Presentation
  Washington, USA
- Year and Date
  2015-05-26 – 2015-05-30
- Data Source
  KAKENHI-PROJECT-26289063
[Presentation] 「脊髄小脳変性症の分子病態」シンポジウム4-S-5-3(シンポジウム4.こころと神経:「神経変性疾患の病態と治療(脊髄小脳変性症を含む)」
- Author(s)
  石川欽也、水澤英洋
- Organizer
  第28回日本医学会総会
- Data Source
  KAKENHI-PROJECT-21591072
[Presentation] 脊髄小脳変性症の分子病態
- Author(s)
  石川欽也、水澤英洋
- Organizer
  第28回日本医学会総会
- Place of Presentation
  震災のため抄録発表のみ
- Data Source
  KAKENHI-PROJECT-21249054
[Presentation] Analysis of Human Standing-up Motion Using Forward Dynamic Simulation with Four Body Segment Model
- Author(s)
  Qi An, Yuki Ishikawa, Tetsuro Funato, Shinya Aoi, Hiroyuki Oka, Hiroshi Yamakawa, Atsushi Yamashita, Hajime Asama
- Organizer
  12th International Symposium on Distributed Autonomous Robotic Systems
- Place of Presentation
  Daejeon, Korea
- Year and Date
  2014-11-02 – 2014-11-05
- Data Source
  KAKENHI-PROJECT-26289063
[Presentation] Generation of human standing-up motion with muscle synergies using forward dynamic simulation
- Author(s)
  Qi An, Yuki Ishikawa, Tetsuro Funato, Shinya Aoi, Hiroyuki Oka, Hiroshi Yamakawa, Atsushi Yamashita, Hajime Asama
- Organizer
  2014 IEEE International Conference on Robotics and Automation
- Place of Presentation
  Hong Kong, China
- Year and Date
  2014-05-31 – 2014-06-07
- Data Source
  KAKENHI-PROJECT-26289063
[]

1. MIZUSAWA Hidehiro (30144091)

# of Collaborated Projects: 3 results

# of Collaborated Products: 43 results
2. 柳原大 (90252725)

# of Collaborated Projects: 3 results

# of Collaborated Products: 1 results
3. WATASE Kei (30376800)

# of Collaborated Projects: 2 results

# of Collaborated Products: 4 results
4. YOKOTA Takanori (90231688)

# of Collaborated Projects: 2 results

# of Collaborated Products: 4 results
5. TORU Shuta (50376711)

# of Collaborated Projects: 2 results

# of Collaborated Products: 12 results
6. Funato Tetsuro (40512869)

# of Collaborated Projects: 1 results

# of Collaborated Products: 10 results
7. KANOUCHI Tadashi (50345287)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
8. DOI Hiroshi (10326035)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
9. MATSUMOTO Naomichi (80325638)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
10. 青井伸也 (60432366)

# of Collaborated Projects: 1 results

# of Collaborated Products: 9 results
11. 大和田潔 (40313241)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
12. 常深泰司 (50401344)

# of Collaborated Projects: 1 results

# of Collaborated Products: 5 results
13. 田中章景 (30378012)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
14. 田中健一 (50722881)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
15. 國井美紗子 (80725200)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
16. 中根綾子 (30431943)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
17. 戸原玄 (00396954)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
18. 山脇正永 (30302855)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
19. 田頭いとゑ (50826683)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
20. 吉住結 (60771863)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
21. 尾崎研一郎 (60460557)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
22. MAKOTO Tomita

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
23. HONDA Shinya

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
24. 本多武尊

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
25. 永井義隆

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
26. 石黒亮

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
27. 内原俊記

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
28. 尾崎心

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
29. 服部信孝

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

ISHIKAWA Kinya 石川 欽也

Research Projects

Research Products

Co-Researchers

Understanding the pathogenesis of spinocerebellar ataxia using iPS-derived Purkinje cells and long-read RNA-seq techniquePrincipal Investigator

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クエン酸を用いた咳テストはMRIによる無症候性脳梗塞をスクリーニングできるか

Principal Investigator

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A study on Purkinje cell-specific gene expression in SCA31 model micePrincipal Investigator

Principal Investigator

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Exploring a balancing mechanism between RNA and its binding protein partnersPrincipal Investigator

Principal Investigator

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Review Section

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Exploring a pathogenic mechanism underlying neurodegenerative disorders caused by mutated RNA repeatPrincipal Investigator

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Analysis of genetic back ground and pathomechanism of spinocerebellar degeneration

Principal Investigator

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Elucidation of the posture control disability in cerebellar ataxia from the model-based evaluation of patients and rodents

Principal Investigator

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多系統型脊髄小脳失調症の遺伝子同定Principal Investigator

Principal Investigator

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Research Institution

A search for abnormal RNA metabolism in spinocerebellar ataxia type 31Principal Investigator

Principal Investigator

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優性遺伝型脊髄小脳変性症のハイスループット遺伝子変異探索Principal Investigator

Principal Investigator

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A basic research for identifying fundamental therapy for SCA6 and SCA31

Principal Investigator

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A research for dissecting molecular pathogenesis of SCA31.Principal Investigator

Principal Investigator

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Investigation for developing a novel immunotherapy for a degenerative ataxia common in Japan.Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

ISHIKAWA Kinya 石川欽也

[Book] 日本臨床　増刊号　医薬品副作用学(第3版)下2019

[Book] XV.小脳の障害と運動失調．1．小脳の解剖と機能．In: 橋本信夫監修、三國信啓、深谷　親編集，「脳神経外科プラックティス. 3.脳神経外科医のための脳機能と局在診断」文光堂.　278-282，2014． 87.2014