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TODA TATSUSHI  戸田 達史

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… Alternative Names

TODA Tatsushi  戸田 達史

戸田 逹史  トダ タツシ

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Researcher Number 30262025
Other IDs
External Links
Affiliation (Current) 2025: 国立研究開発法人国立精神・神経医療研究センター, 病院, 院長
2025: 東京大学, 医学部附属病院, 病院診療医(出向)
Affiliation (based on the past Project Information) *help 2018 – 2024: 東京大学, 医学部附属病院, 教授
2017: 神戸大学, 医学研究科, 教授
2017: 神戸大学, 大学院・医学研究科, 教授
2016 – 2017: 神戸大学, 医学研究科, 客員教授
2016: 神戸大学, 医学部, 教授 … More
2014 – 2015: 神戸大学, 医学研究科, 教授
2014: 神戸大学, 大学院医学研究科, 教授
2011 – 2013: 神戸大学, 医学(系)研究科(研究院), 教授
2009 – 2012: Kobe University, 医学研究科, 教授
2009 – 2011: Osaka University, 大学院・医学研究科, 教授
2008: Osaka University, 医学系研究科, 教授
2007: Osaka University, 医学糸研究科, 教授
2000 – 2006: 大阪大学, 医学系研究科, 教授
2000: Biomedical Research Center, Medical Genetics Professor, バイオメディカル教育研究センター, 教授
1999: 東京大学, 医科学研究所, 助教授
1996 – 1997: Institute of Medical Science University of Tokyo, Associate Professor, 医科学研究所, 助教授
1995: 東京大学, 医学部(医), 助手
1995: 東京大学, 医学部, 助手 Less
Review Section/Research Field
Principal Investigator
Biological Sciences / Neurology / Medium-sized Section 52:General internal medicine and related fields / Human genetics / Neurology / Biological Sciences / Human genetics
Except Principal Investigator
Neurology / Educational psychology / Basic Section 10020:Educational psychology-related / Neurology / Human genetics
Keywords
Principal Investigator
福山型筋ジストロフィー / SNP / パーキンソン病 / 福山型先天性筋ジストロフィー / オーダーメイド医療 / 薬剤副作用 / 疾患感受性遺伝子 / 多因子病 / アンチセンス核酸 / ジストログリカノパチー … More / マイクロサテライト / フクチン / レトロトランスポゾン / 9番染色体長腕31 / ポジショナルクローニング / 分子標的治療 / AAV遺伝子治療 / リビトールリン酸異常症 / ジストログリカン / リビトールリン酸 / アンチセンス治療 / 次世代シーケンサー / 行動解析 / 認知機能 / BDNF / 創始者変異 / 第9番染色体長腕31 / 挿入変異 / 創始者染色体 / 連鎖不平衡 / glia limitans / 神経細胞遊走障害 / 脳奇形 / 酵母人工染色体 / 連鎖不平衡マッピング / 遺伝子ネットワーク / 定量RT-PCR / 遺伝子発現解析 / 候補遺伝子 / 病態解明 / 遺伝子発現の差 / DNAメチル化 / 一般認知機能g / 創薬データーベース / 蛋白質間相互作用データーベース / Enrichment analysis / DNAメチル化 / Methylation Sequencing / エピジェネティック / 一般認知機能g / 福山型金ジストロフィー / リビトール補充療法 / microsatellite / tailormade therapy / drug effect / susceptibility gene / Multifactorial disease / Parkinson's disease / brain anomaly / prenatal dianosis / genetic diagnosis / founder-haplotype / linkage disequilibrium / chromosome 9q31 / Fukuyama-type congenital muscular dystrophy (FCMD) / 9番染色体長腕引 / コスミドコンティグ / 出生前診断 / 遺伝子診断 / 創始者ハプロタイプ / 連鎖不均衡 / LARGE / 臨床神経分子遺伝学 / ジストログリパノカチー / ポストリン酸構造 / 次世代シークエンサー / 多型 / パーソナルゲノム / Potocki-Lupski症候群 / 22q11.2欠失症候群 / Sotos症候群 / GEMCA / CNV / 精神発達遅滞 / エピゲノム / 炎症性サイトカイン / g因子 / 網羅的DNAメチル化解析 / 網羅的遺伝子発現解析 / 一卵性双生児 / IQ / 分子遺伝学 / ゲノムワイド関連解析 / 病患感受性遺伝子 / 複合ヘテロ / 胎生致死 / FCMD遺伝子 / 点変異 / FCMD原因蛋白質 / FCMD原因遺伝子 / レトロポゾン / コスミドコンディグ … More
Except Principal Investigator
認知能力 / 双生児法 / 行動遺伝学 / 脳画像 / 遺伝と環境 / パーキンソン病 / 福山型筋ジストロフィー / B10 / 脳機能 / 児童期 / 不一致一卵性 / 縦断研究 / エピジェネティック / 主観的幸福感 / ストレスフルライフイベント / 実行機能 / 利他性 / 教育動機 / うつ / パーソナリティ / 自尊心 / メンタルヘルス / 縦断コホート研究 / 双生児 / fMRI / 成人期 / 脳・神経 / 遺伝学 / 教育系心理学 / 学業達成 / 発達 / 教育 / 社会性発達 / 認知発達 / エピジェネティクス / 分子遺伝学 / 脳神経科学 / SNCS / 重複 / 変異 / duplication / Gene chip / 二倍体 / DNA / 遺伝子 / 認知症 / びまん性レビー小体病 / 遺伝子重複 / SNCA / alpha-synuclein / association study / susceptibility gene / single nucleotide polymorphism / Parkinson's disease / 関連解析 / 疾患感受性遺伝子 / 一塩基多型 / mRNA metabolism / ISH method / the untranslated region of the gene / Fukuyama-type muscular dystrophy / mRNAの動態 / ISH法 / 遺伝子非翻訳領域 / SCAN method / Endometrial Cancer / Early onset ataxia / Hereditary defness DFNB8 / Whole Sequence / Chromosome 11 / Chromosome 22 / Chromosome 21 / 改良型SSCP法 / SCA2遺伝子 / HLA遺伝子群 / 免疫グロブリン遺伝子 / ダウン症必須領域 / 11番染色体物理地図 / 高速大規模プラスミド調整機 / 変異検出法 / 福山型先天性ジストロフィー / 自己免疫疾患APECED / MHCクラスI領域 / シークエンス地図 / 11q13領域 / Transcriptional sequencing / SKY法の改良 / PLACE-SSCP / HLAクラス1遺伝子群 / シークエンス解析 / S番染色体特異的BACクローン / ヒト11q22-23領域 / SKY法 / がん抑制遺伝子 / Bardet-Biedl症候群 / TGFβ1遺伝子 / 進行性骨異形症 / ヒト21番染色体 / 11q23 / Sotos症候群 / 遺伝性聾DFNB8・B10 / ドラフトシーケンス / 染色体カラーバンディング法 / 子宮体癌 / 遺伝性脊髄小脳変性症 / 遺伝性聾DFNB8 / 全塩基配列 / 11番染色体 / 22番染色体 / 21番染色体 / DNA polymorphism / Japanese / Y-chromosome / SRY遺伝子 / ハプロタイプ / DNA多型 / 日本人 / Y染色体 / ゲノム医科学 / 人類遺伝学 / 神経内科学 / 遺伝性神経疾患 / ゲノム / エクソーム / 神経遺伝 / 細胞膜修復 / 神経分子病態学 / ジスフェルリン / 膜修復 / 筋ジストロフィー / 細胞・組織 / 言語能力 / 社会性 / 青年期 Less
  • Research Projects

    (27 results)
  • Research Products

    (422 results)
  • Co-Researchers

    (62 People)
  •  福山型筋ジス及びDG異常症のアンチセンス核酸、糖鎖補充、AAV治療、胎児治療開発Principal Investigator

    • Principal Investigator
      戸田 達史
    • Project Period (FY)
      2023 – 2025
    • Research Category
      Grant-in-Aid for Scientific Research (A)
    • Review Section
      Medium-sized Section 52:General internal medicine and related fields
    • Research Institution
      The University of Tokyo
  •  Pathogenesis and Antisense nucleic acid, glycosylation supplementation, and AAV therapy development forFukuyama muscular dystrophy and related diseasesPrincipal Investigator

    • Principal Investigator
      TODA Tatsushi
    • Project Period (FY)
      2020 – 2022
    • Research Category
      Grant-in-Aid for Scientific Research (A)
    • Review Section
      Medium-sized Section 52:General internal medicine and related fields
    • Research Institution
      The University of Tokyo
  •  Developmental behavioral genetic study of educational processes and their outcome by the twin method.

    • Principal Investigator
      Ando Juko
    • Project Period (FY)
      2018 – 2021
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Review Section
      Basic Section 10020:Educational psychology-related
    • Research Institution
      Keio University
  •  Elucidation of pathomecanism for Fukuyama muscular dystrophy and dystroglycanopathy and their drug developmenPrincipal Investigator

    • Principal Investigator
      Toda Tatsushi
    • Project Period (FY)
      2017 – 2019
    • Research Category
      Grant-in-Aid for Scientific Research (A)
    • Research Field
      Neurology
    • Research Institution
      The University of Tokyo
      Kobe University
  •  Elucidation of pathomecanism for Fukuyama muscular dystrophy and dystroglycanopathy and their drug developmenPrincipal Investigator

    • Principal Investigator
      Toda Tatsusi
    • Project Period (FY)
      2014 – 2016
    • Research Category
      Grant-in-Aid for Scientific Research (A)
    • Research Field
      Neurology
    • Research Institution
      Kobe University
  •  Integrated behavioral genetic study of educational processes.

    • Principal Investigator
      Ando Juko
    • Project Period (FY)
      2014 – 2017
    • Research Category
      Grant-in-Aid for Scientific Research (A)
    • Research Field
      Educational psychology
    • Research Institution
      Keio University
  •  Identification of causative genes and development of a new analytical method for familial neurological diseases

    • Principal Investigator
      SATAKE WATARU
    • Project Period (FY)
      2013 – 2014
    • Research Category
      Grant-in-Aid for Challenging Exploratory Research
    • Research Field
      Neurology
    • Research Institution
      Kobe University
  •  The detection of modifier gens in alpha-synuclein multiplications

    • Principal Investigator
      Nishioka Kenya
    • Project Period (FY)
      2013 – 2016
    • Research Category
      Grant-in-Aid for Young Scientists (B)
    • Research Field
      Neurology
    • Research Institution
      Juntendo University
  •  認知機能におけるエピジェネティクスの役割とその臨床応用性Principal Investigator

    • Principal Investigator
      戸田 達史
    • Project Period (FY)
      2012 – 2014
    • Research Category
      Grant-in-Aid for JSPS Fellows
    • Research Field
      Human genetics
    • Research Institution
      Kobe University
  •  Molecular targeting therapy and pathomechanism for Fukuyama muscular dystrophy and related disordersPrincipal Investigator

    • Principal Investigator
      TATSUSHI Toda
    • Project Period (FY)
      2011 – 2013
    • Research Category
      Grant-in-Aid for Scientific Research (A)
    • Research Field
      Neurology
    • Research Institution
      Kobe University
  •  Abnormal membranerepair as a new concept for muscular dystrophy and search for new disease genes

    • Principal Investigator
      KANAGAWA Motoi
    • Project Period (FY)
      2011 – 2012
    • Research Category
      Grant-in-Aid for Challenging Exploratory Research
    • Research Field
      Neurology
    • Research Institution
      Kobe University
  •  Personal genome analysis of genes for Parkinson's disease and cognitive functionPrincipal Investigator

    • Principal Investigator
      TODA Tatsushi
    • Project Period (FY)
      2010 – 2014
    • Research Category
      Grant-in-Aid for Scientific Research on Innovative Areas (Research in a proposed research area)
    • Review Section
      Biological Sciences
    • Research Institution
      Kobe University
  •  A Twin Study on Sociability and Mental Health : A Bridge between Genes and Brain Activities

    • Principal Investigator
      ANDO Juko
    • Project Period (FY)
      2009 – 2011
    • Research Category
      Grant-in-Aid for Scientific Research (S)
    • Research Field
      Educational psychology
    • Research Institution
      Keio University
  •  Identification of Genes for Cognition and Their Functional AnalysisPrincipal Investigator

    • Principal Investigator
      TODA Tatsushi
    • Project Period (FY)
      2008 – 2010
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Human genetics
    • Research Institution
      Osaka University
  •  Search for Parkinson-related genes and their functional analysisPrincipal Investigator

    • Principal Investigator
      TODA Tatsushi
    • Project Period (FY)
      2005 – 2009
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      Osaka University
  •  Identification of susceptibility genes for sporadic Parkinson's disease by genotyping multiple SNPs

    • Principal Investigator
      MIZUTA Ikuko
    • Project Period (FY)
      2005 – 2006
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      Osaka University
  •  多因子疾患パーキンソン病遺伝子の解明とオーダーメイド医療をめざした至適薬剤の選択Principal Investigator

    • Principal Investigator
      戸田 達史
    • Project Period (FY)
      2001
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas (C)
    • Review Section
      Biological Sciences
    • Research Institution
      Osaka University
  •  多因子疾患パーキンソン病遺伝子の解明とオーダーメイド医療をめざした至適薬剤の選択Principal Investigator

    • Principal Investigator
      戸田 達史
    • Project Period (FY)
      2000
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas (C)
    • Review Section
      Biological Sciences
    • Research Institution
      Osaka University
  •  Identification of a genes for Parkinson's diseasePrincipal Investigator

    • Principal Investigator
      TODA Tatsushi
    • Project Period (FY)
      2000 – 2004
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      Osaka University
  •  未知の脳機能分子としての福山型筋ジストロフィー遺伝子産物フクチンの機能解析Principal Investigator

    • Principal Investigator
      戸田 達史
    • Project Period (FY)
      1999
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas (A)
    • Research Institution
      The University of Tokyo
  •  Molecular cytogenetic study of the Fukuyama-type muscular dystrophy caused by the aberration of the untranslated region of the gene(FCMD)

    • Principal Investigator
      SAITO Fumiko
    • Project Period (FY)
      1999 – 2000
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      Tokyo Medical & Dental University
  •  未知の脳機能分子としての福山型筋ジストロフィー遺伝子産物の同定と病態解析Principal Investigator

    • Principal Investigator
      戸田 達史
    • Project Period (FY)
      1997
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      The University of Tokyo
  •  未知の脳機能分子としての福山型先天性筋ジストロフィー遺伝子産物の同定と機能解析Principal Investigator

    • Principal Investigator
      戸田 達史
    • Project Period (FY)
      1996
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      The University of Tokyo
  •  Human Genome Analysis

    • Principal Investigator
      OHKI Misao
    • Project Period (FY)
      1996 – 2000
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas (A)
    • Research Institution
      National Cancer Center Research Institute
  •  未知の脳機能分子としての福山型先天性筋ジストロフィー遺伝子産物の同定と機能解析Principal Investigator

    • Principal Investigator
      戸田 達史
    • Project Period (FY)
      1995
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      The University of Tokyo
  •  The Characteristics of Y Chromosome in Japanese

    • Principal Investigator
      NAKAHORI Yutaka
    • Project Period (FY)
      1995 – 1997
    • Research Category
      Grant-in-Aid for Scientific Research (A)
    • Research Field
      Human genetics
    • Research Institution
      The University of Tokyshima
      The University of Tokyo
  •  Isolation of a gene for Fukuyama-type congenital muscular dystrophy and genetic diagnosisPrincipal Investigator

    • Principal Investigator
      TODA Tatsushi
    • Project Period (FY)
      1995 – 1996
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      The University of Tokyo

All 2022 2021 2020 2019 2018 2017 2016 2015 2014 2013 2012 2011 2010 2009 2008 2007 2006 2005 2003 Other

All Journal Article Presentation Book Patent Other

  • [Book] ヒトの分子遺伝学 第5班2021

    • Author(s)
      戸田達史(翻訳), 井上聡 (翻訳),松本直通(翻訳)
    • Total Pages
      904
    • Publisher
      メディカルサイエンスインターナショナル
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Book] Human Pathobiochemistry From Clinical Studies to Molecular Mechanisms,2019

    • Author(s)
      Kanagawa M, Tokuoka H, Toda T
    • Total Pages
      349
    • Publisher
      Springer
    • ISBN
      9789811329777
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Book] 先天性筋ジストロフィー(福山型先天性筋ジストロフィーを含む).今日の疾患辞典デジタル版2019

    • Author(s)
      久保田暁,戸田達史
    • Total Pages
      1000
    • Publisher
      株式会社プレシジョン
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Book] Human Pathobiochemistry From Clinical Studies to Molecular Mechanisms2019

    • Author(s)
      Kanagawa M, Tokuoka H, Toda T
    • Total Pages
      349
    • Publisher
      Springer
    • ISBN
      9789811329777
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Journal Article] CDP-ribitol prodrug treatment ameliorates ISPD-deficient muscular dystrophy mouse model2022

    • Author(s)
      Tokuoka Hideki、Imae Rieko、Nakashima Hitomi、Manya Hiroshi、Masuda Chiaki、Hoshino Shunsuke、Kobayashi Kazuhiro、Lefeber Dirk J.、Matsumoto Riki、Okada Takashi、Endo Tamao、Kanagawa Motoi、Toda Tatsushi
    • Journal Title

      Nature Communications

      Volume: 13 Issue: 1 Pages: 1847-1847

    • DOI

      10.1038/s41467-022-29473-4

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-17H03987, KAKENHI-PROJECT-22K19509, KAKENHI-PROJECT-20H00526, KAKENHI-PROJECT-21H02685, KAKENHI-PROJECT-19K07058, KAKENHI-WRAPUP-22H04899, KAKENHI-PROJECT-23K20328, KAKENHI-PROJECT-19H05648, KAKENHI-PROJECT-23K24244
  • [Journal Article] Comparative whole transcriptome analysis of Parkinson’s disease focusing on the efficacy of zonisamide2022

    • Author(s)
      Naito Tatsuhiko、Satake Wataru、Cha Pei-Chieng、Kobayashi Kazuhiro、Murata Miho、Toda Tatsushi
    • Journal Title

      Journal of Neurology, Neurosurgery & Psychiatry

      Volume: NA Issue: 5 Pages: 509-512

    • DOI

      10.1136/jnnp-2021-328742

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-20J12189, KAKENHI-PROJECT-20H00526, KAKENHI-PROJECT-23K24244
  • [Journal Article] DMD exon 2 duplication due to a complex genomic rearrangement is associated with a somatic mosaicism2022

    • Author(s)
      Akatsuki Kubota, Hiroyuki Ishiura, Kristine Joyce Linay Porto, Masaki Tanaka, Jun Mitsui, Atsushi Unuma, Hisataka Maki, Issei Komuro, Shoji Tsuji, Jun Shimizu, Tatsushi Toda
    • Journal Title

      Neuromuscular Disorders

      Volume: 32(3) Issue: 3 Pages: 263-269

    • DOI

      10.1016/j.nmd.2021.12.004

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-18K15440, KAKENHI-PROJECT-20H03588, KAKENHI-PROJECT-20H00526
  • [Journal Article] TDP-43 regulates cholesterol biosynthesis by inhibiting sterol regulatory element-binding protein 22022

    • Author(s)
      Egawa Naohiro, Seki Tsuneyoshi, Kobayashi Kazuhiro, Toda Tatsushi, Inoue Haruhisa, et al
    • Journal Title

      Scientific Reports

      Volume: 12 Issue: 1 Pages: 12133-4

    • DOI

      10.1038/s41598-022-12133-4

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-21K15697, KAKENHI-PROJECT-20K22874, KAKENHI-PROJECT-20H00526, KAKENHI-PROJECT-20K07883, KAKENHI-PROJECT-23K24244
  • [Journal Article] Muscle Transcriptomics Shows Overexpression of Cadherin 1 in Inclusion Body Myositis2022

    • Author(s)
      Chiseko Ikenaga, Hidetoshi Date, Motoi Kanagawa, Jun Mitsui, Hiroyuki Ishiura, Jun Yoshimura, Iago Pinal-Fernandez, Andrew L Mammen, Thomas E Lloyd , Shoji Tsuji, Jun Shimizu, Tatsushi Toda, Jun Goto
    • Journal Title

      Ann Neurol.

      Volume: 91 Issue: 3 Pages: 317-328

    • DOI

      10.1002/ana.26304

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-19K07956, KAKENHI-PROJECT-16H06279, KAKENHI-PROJECT-20H00526
  • [Journal Article] Alanine transaminase is predominantly increased in the active phase of anti-HMGCR myopathy2022

    • Author(s)
      Akatsuki Kubota, Jun Shimizu, Atsushi Unuma, Meiko Maeda, Yuichiro Shirota, Masato Kadoya, Naohiro Uchio, Yoshio Sakiyama, Noritoshi Arai, Yasushi Shiio, Yoshikazu Uesaka, Hideji Hashida, Nobue K Iwata, Jun Goto, Ran Nakashima, Tsuneyo Mimori, Tatsushi Toda
    • Journal Title

      Neuromuscular Disorders

      Volume: 32(1) Issue: 1 Pages: 25-32

    • DOI

      10.1016/j.nmd.2021.10.007

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-18K15440, KAKENHI-PROJECT-18K07542, KAKENHI-PROJECT-20H00526
  • [Journal Article] Assessment of the upper limb muscles in patients with Fukuyama muscular dystrophy: Noninvasive assessment using visual ultrasound muscle analysis and shear wave elastography.2022

    • Author(s)
      Risa Harada, Mariko Taniguchi-Ikeda, Miwako Nagasaka, Tatsiuya Nishii, Atsuyuki Inui, Tetsushi Yamamoto, Ichiro Morioka, Ryosuke Kuroda, Kazumoto Iijima, Kandai Nozu, Yoshitada Sakai, Tatsushi Toda,
    • Journal Title

      Neuromuscular Disorders

      Volume: Inpress Issue: 9 Pages: 754-762

    • DOI

      10.1016/j.nmd.2022.05.004

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-19K20673, KAKENHI-PROJECT-21K07789, KAKENHI-PROJECT-20H00526, KAKENHI-PROJECT-23K21430
  • [Journal Article] Laminin α5_CD239_Spectrin is a candidate association that compensates the linkage between the basement membrane and cytoskeleton in skeletal muscle fibers2022

    • Author(s)
      Kikkawa Yamato、Matsunuma Masumi、Kan Ryuji、Yamada Yuji、Hamada Keisuke、Nomizu Motoyoshi、Negishi Yoichi、Nagamori Shushi、Toda Tatsushi、Tanaka Minoru、Kanagawa Motoi
    • Journal Title

      Matrix Biology Plus

      Volume: 15 Pages: 100118-100118

    • DOI

      10.1016/j.mbplus.2022.100118

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-20H00526, KAKENHI-PROJECT-21H02685, KAKENHI-PROJECT-21H03365, KAKENHI-PROJECT-20K07622
  • [Journal Article] Genetic variations and clinical spectrum of dystroglycanopathy in a large cohort of Chinese patients2021

    • Author(s)
      Song Danyu、Dai Yi、Chen Xiaoyu、Fu Xiaona、Chang Xingzhi、Wang Ning、Zhang Cheng、Yan Chuanzhu、Zheng Hong、Wu Liwen、Jiang Li、Hua Ying、Yang Haipo、Wang Zhiqiang、Dai Tingjun、Zhu Wenhua、Han Chunxi、Yuan Yun、Kobayashi Kazuhiro、Toda Tatsushi、Xiong Hui
    • Journal Title

      Clinical Genetics

      Volume: 99 Issue: 3 Pages: 384-395

    • DOI

      10.1111/cge.13886

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Journal Article] これまでの研究と今後の展望-福山型筋ジストロフィーを含めた糖鎖合成異常症の系統的な 解明・治療に関する研究2021

    • Author(s)
      戸田達史
    • Journal Title

      神戸大学医学部医学科創立七十五周年神戸病院創立百五十周年記念誌

      Volume: 1

    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Journal Article] Phenotype and Genotype Study of Chinese POMT2-Related α-Dystroglycanopathy2021

    • Author(s)
      Chen Xiao-Yu、Song Dan-Yu、Jiang Li、Tan Dan-Dan、Liu Yi-Dan、Liu Jie-Yu、Chang Xing-Zhi、Xing Guo-Gang、Toda Tatsushi、Xiong Hui
    • Journal Title

      Frontiers in Genetics

      Volume: 12 Pages: 692479-692479

    • DOI

      10.3389/fgene.2021.692479

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Journal Article] Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy2021

    • Author(s)
      1.Bonora E, Chakrabarty S, Tsutsumi M (他63名) Taniguchi-Ikeda M (Corresponding author) and Roberto De Giorgio.
    • Journal Title

      Brain

      Volume: 0 Issue: 5 Pages: 0-0

    • DOI

      10.1093/brain/awab056

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18K07790, KAKENHI-PROJECT-21K06283, KAKENHI-PROJECT-19H03362, KAKENHI-PROJECT-21K07807, KAKENHI-PROJECT-21K19457, KAKENHI-PROJECT-20H00526, KAKENHI-PROJECT-23K21430
  • [Journal Article] A deep learning method for HLA imputation and trans-ethnic MHC fine-mapping of type 1 diabetes2021

    • Author(s)
      Naito Tatsuhiko、Suzuki Ken、Hirata Jun、Kamatani Yoichiro、Matsuda Koichi、Toda Tatsushi、Okada Yukinori
    • Journal Title

      Nature Communications

      Volume: 12 Issue: 1 Pages: 1639-1639

    • DOI

      10.1038/s41467-021-21975-x

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-19H01021, KAKENHI-PROJECT-20J12189, KAKENHI-PROJECT-20K21834, KAKENHI-PROJECT-18H01085
  • [Journal Article] Trans‐Ethnic Fine‐Mapping of the Major Histocompatibility Complex Region Linked to Parkinson's Disease2021

    • Author(s)
      Naito Tatsuhiko、Satake Wataru、Ogawa Kotaro、Suzuki Ken、Hirata Jun、Foo Jia Nee、Tan Eng‐King、Toda Tatsushi、Okada Yukinori
    • Journal Title

      Movement Disorders

      Volume: 36 Issue: 8 Pages: 1805-1814

    • DOI

      10.1002/mds.28583

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20K21834, KAKENHI-PROJECT-19H01021, KAKENHI-PROJECT-18H01085
  • [Journal Article] Restoration of the defect in radial glial fiber migration and cortical plate organization in a brain organoid model of Fukuyama muscular dystrophy2021

    • Author(s)
      Taniguchi-Ikeda Mariko、Koyanagi-Aoi Michiyo、Maruyama Tatsuo、Takaori Toru、Hosoya Akiko、Tezuka Hiroyuki、Nagase Shotaro、Ishihara Takuma、Kadoshima Taisuke、Muguruma Keiko、Ishigaki Keiko、Sakurai Hidetoshi、Mizoguchi Akira、Novitch Bennett G.、Toda Tatsushi、Watanabe Momoko、Aoi Takashi
    • Journal Title

      iScience

      Volume: 24 Issue: 10 Pages: 103140-103140

    • DOI

      10.1016/j.isci.2021.103140

    • NAID

      120007170807

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-19K07614, KAKENHI-PROJECT-21H03812, KAKENHI-PROJECT-21K19457, KAKENHI-PROJECT-20H00526, KAKENHI-PROJECT-23K21430
  • [Journal Article] 福山型筋ジストロフィー2020

    • Author(s)
      戸田達史
    • Journal Title

      遺伝子医学

      Volume: 季刊32号 Pages: 62-66

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Journal Article] Novel mutations in B3GALNT2 gene causing α-dystroglycanopathy in Chinese patients2020

    • Author(s)
      Chen Xiao-Yu、Song Dan-Yu、Fan Yan-Bin、Tan Dan-Dan、Chang Xing-Zhi、Xiao Jiang-Xi、Toda Tatsushi、Xiong Hui
    • Journal Title

      Chinese Medical Journal

      Volume: Publish Ahead of Print Issue: 12 Pages: 48-48

    • DOI

      10.1097/cm9.0000000000001283

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Journal Article] 遺伝性疾患治療の最前線(巻頭言)2020

    • Author(s)
      戸田達史
    • Journal Title

      遺伝子医学

      Volume: 季刊32号 Pages: 19-19

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Journal Article] Genome-wide association study identifies zonisamide responsive gene in Parkinson’s disease patients2020

    • Author(s)
      Cha Pei-Chieng、Satake Wataru、Ando-Kanagawa Yuko、Yamamoto Ken、Murata Miho、Toda Tatsushi
    • Journal Title

      Journal of Human Genetics

      Volume: 65 Issue: 8 Pages: 693-704

    • DOI

      10.1038/s10038-020-0760-8

    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18H01085
  • [Journal Article] Progressive length‐dependent polyneuropathy in xeroderma pigmentosum group A2020

    • Author(s)
      Tsuji Yukio、Ueda Takehiro、Sekiguchi Kenji、Nishiyama Masahiro、Kanda Fumio、Nishigori Chikako、Toda Tatsushi、Matsumoto Riki
    • Journal Title

      Muscle & Nerve

      Volume: 62 Issue: 4 Pages: 534-540

    • DOI

      10.1002/mus.27028

    • NAID

      120006892090

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Journal Article] A splice site mutation c.1251G>A of ISPD gene is a common cause of congenital muscular dystrophy in Chinese patients2020

    • Author(s)
      Song Danyu、Fu Xiaona、Ge Lin、Chang Xingzhi、Wei Cuijie、Liu Jieyu、Yang Haipo、Qu Suqing、Bao Xinhua、Toda Tatsushi、Wu Xiru、Xiong Hui
    • Journal Title

      Clinical Genetics

      Volume: 97(5) Issue: 5 Pages: 789-790

    • DOI

      10.1111/cge.13695

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-17H01563, KAKENHI-PROJECT-20H00526
  • [Journal Article] A novel mutation in ABCD1 gene in a Filipino patient with adult‐onset X‐linked ALD2020

    • Author(s)
      Porto Kristine Joyce、Matsukawa Takashi、Ishiura Hiroyuki、Mitsui Jun、Matic Alexandria、Yu Justine Megan、Dominguez Jacqueline、Damian Ludwig、Toda Tatsushi、Tsuji Shoji
    • Journal Title

      Neurology and Clinical Neuroscience

      Volume: 8 Issue: 5 Pages: 329-331

    • DOI

      10.1111/ncn3.12425

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Journal Article] 神経疾患における慢性炎症2020

    • Author(s)
      戸田達史
    • Journal Title

      別冊BIO Clinica

      Volume: 9 Pages: 100-100

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Journal Article] Congenital hearing impairment associated with peripheral cochlear nerve dysmyelination in glycosylation-deficient muscular dystrophy2020

    • Author(s)
      Morioka Shigefumi、Sakaguchi Hirofumi、Mohri Hiroaki、Taniguchi-Ikeda Mariko、Kanagawa Motoi、Suzuki Toshiaki、Miyagoe-Suzuki Yuko、Toda Tatsushi、Saito Naoaki、Ueyama Takehiko
    • Journal Title

      PLOS Genetics

      Volume: 16 Issue: 5 Pages: 1-28

    • DOI

      10.1371/journal.pgen.1008826

    • NAID

      120006863578

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-19K22472, KAKENHI-PROJECT-20H00526, KAKENHI-PROJECT-18H02616, KAKENHI-PROJECT-18K07790, KAKENHI-PROJECT-18K09383, KAKENHI-PLANNED-17H06421, KAKENHI-PROJECT-19K07519
  • [Journal Article] Neuropsychiatric adverse events of chloroquine: a real-world pharmacovigilance study using the FDA Adverse Event Reporting System (FAERS) database2020

    • Author(s)
      Sato Kenichiro、Mano Tatsuo、Iwata Atsushi、Toda Tatsushi
    • Journal Title

      BioScience Trends

      Volume: 14 Issue: 2 Pages: 139-143

    • DOI

      10.5582/bst.2020.03082

    • NAID

      130007845360

    • ISSN
      1881-7815, 1881-7823
    • Year and Date
      2020-04-30
    • Language
      English
    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-19K17027, KAKENHI-PROJECT-20J11009, KAKENHI-PROJECT-18H01085
  • [Journal Article] Pembrolizumab on pre-existing inclusion body myositis: a case report2020

    • Author(s)
      Uchio Naohiro、Unuma Atsushi、Kakumoto Toshiyuki、Osaki Masao、Zenke Yoshitaka、Sakuta Kenichi、Kubota Akatsuki、Uesaka Yoshikazu、Toda Tatsushi、Shimizu Jun
    • Journal Title

      BMC Rheumatology

      Volume: 4 Issue: 1 Pages: 48-48

    • DOI

      10.1186/s41927-020-00144-5

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-19K07956, KAKENHI-PROJECT-20H00526
  • [Journal Article] Crystal structures of fukutin-related protein (FKRP), a ribitol-phosphate transferase related to muscular dystrophy.2020

    • Author(s)
      Kuwabara N, Imae R, Manya H, Tanaka T, Mizuno M, Tsumoto H, Kanagawa M, Kobayashi K, Toda T, Senda T, Endo T, Kato R.
    • Journal Title

      Nat Commun.

      Volume: 11 Issue: 1 Pages: 303-303

    • DOI

      10.1038/s41467-019-14220-z

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-19K07058, KAKENHI-PLANNED-17H06421, KAKENHI-PROJECT-19H05648, KAKENHI-PROJECT-17H01563, KAKENHI-PROJECT-16H05353, KAKENHI-PROJECT-17H03987, KAKENHI-PROJECT-18H02616, KAKENHI-PROJECT-17H06264
  • [Journal Article] Characterization of dystroglycan binding in adhesion of human induced pluripotent stem cells to laminin-511 E8 fragment2019

    • Author(s)
      Sugawara Yumika、Hamada Keisuke、Yamada Yuji、Kumai Jun、Kanagawa Motoi、Kobayashi Kazuhiro、Toda Tatsushi、Negishi Yoichi、Katagiri Fumihiko、Hozumi Kentaro、Nomizu Motoyoshi、Kikkawa Yamato
    • Journal Title

      Scientific Reports

      Volume: 9 Issue: 1 Pages: 1-12

    • DOI

      10.1038/s41598-019-49669-x

    • NAID

      120006728095

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18K06637, KAKENHI-PROJECT-18K12085, KAKENHI-PLANNED-17H06421, KAKENHI-PROJECT-19H05648, KAKENHI-PROJECT-17H01563, KAKENHI-PROJECT-16H05353, KAKENHI-PROJECT-18H02616, KAKENHI-PROJECT-18H02873, KAKENHI-PROJECT-17K01954, KAKENHI-PROJECT-17K07180
  • [Journal Article] 筋ジストロフィー近年わかってきた分子機構と治療戦略2019

    • Author(s)
      戸田達史
    • Journal Title

      SRL宝函

      Volume: 40(4) Pages: 12-21

    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Journal Article] 福山型筋ジストロフィーを含めた糖鎖合成異常症の系統的な解明・治療に関する研究2019

    • Author(s)
      戸田達史
    • Journal Title

      日本医師会雑誌

      Volume: 148(9) Pages: 1785-1789

    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Journal Article] Elimination of fukutin reveals cellular and molecular pathomechanisms in muscular dystrophy-associated heart failure2019

    • Author(s)
      Ujihara Yoshihiro、Kanagawa Motoi、Mohri Satoshi、Takatsu Satomi、Kobayashi Kazuhiro、Toda Tatsushi、Naruse Keiji、Katanosaka Yuki
    • Journal Title

      Nature Communications

      Volume: 10 Issue: 1 Pages: 5754-5754

    • DOI

      10.1038/s41467-019-13623-2

    • NAID

      120006777089

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PLANNED-17H06421, KAKENHI-PROJECT-19H05648, KAKENHI-PROJECT-17H01563, KAKENHI-PROJECT-16H05353, KAKENHI-PROJECT-17H02085, KAKENHI-PROJECT-18H02616, KAKENHI-PROJECT-17H04740
  • [Journal Article] 福山型筋ジストロフィーを含めた糖鎖合成異常症の系統的な解明と治療を目指して2019

    • Author(s)
      戸田達史
    • Journal Title

      脳と発達.

      Volume: 51(6) Pages: 367-372

    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Journal Article] 福山幸夫(1928-2014)福山型筋ジストロフィーの発見2019

    • Author(s)
      戸田 達史
    • Journal Title

      生体の科学

      Volume: 70(5) Pages: 484-485

    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Journal Article] 希少疾患・難病への治療法開発2018

    • Author(s)
      戸田達史
    • Journal Title

      医学のあゆみ

      Volume: 266 Pages: 421-426

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Journal Article] Ribitol-phosphate-a newly identified posttranslational glycosylation unit in mammals: structure, modification enzymes and relationship to human diseases2018

    • Author(s)
      Kanagawa Motoi、Toda Tatsushi
    • Journal Title

      The Journal of Biochemistry

      Volume: 163 Issue: 5 Pages: 359-369

    • DOI

      10.1093/jb/mvy020

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-15H04352, KAKENHI-PLANNED-17H06421, KAKENHI-PROJECT-17H01563, KAKENHI-PROJECT-18H02616
  • [Journal Article] CDP-glycerol inhibits the synthesis of the functionalO-mannosyl glycan of α-dystroglycan2018

    • Author(s)
      Imae Rieko、Manya Hiroshi、Tsumoto Hiroki、Osumi Kenji、Tanaka Tomohiro、Mizuno Mamoru、Kanagawa Motoi、Kobayashi Kazuhiro、Toda Tatsushi、Endo Tamao
    • Journal Title

      Journal of Biological Chemistry

      Volume: 293 Issue: 31 Pages: 12186-12198

    • DOI

      10.1074/jbc.ra118.003197

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PLANNED-17H06421, KAKENHI-PROJECT-17H01563, KAKENHI-PROJECT-16H05353, KAKENHI-PROJECT-17H03987, KAKENHI-PROJECT-18H02616, KAKENHI-PROJECT-16K08262, KAKENHI-PROJECT-16K20996
  • [Journal Article] 福山型筋ジストロフィーに対する核酸医薬研究2018

    • Author(s)
      戸田達史
    • Journal Title

      神経内科

      Volume: 89 Pages: 518-524

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Journal Article] 福山型筋ジストロフィー2018

    • Author(s)
      戸田達史
    • Journal Title

      難病と在宅ケア

      Volume: 23 Pages: 14-17

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Journal Article] Cell endogenous activities of fukutin and FKRP coexist with the ribitol xylosyltransferase, TMEM5.2018

    • Author(s)
      Nishihara, R., Kobayashi, K., Imae, R., Tsumoto, H., Manya, H., Mizuno, M., Kanagawa, M., Endo, T., and Toda, T.
    • Journal Title

      Biochemical and Biophysical Research Communications

      Volume: 497 Issue: 4 Pages: 1025-1030

    • DOI

      10.1016/j.bbrc.2018.02.162

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-16K08262, KAKENHI-PROJECT-16K20996, KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-15H04352, KAKENHI-PLANNED-17H06421, KAKENHI-PROJECT-16H05353, KAKENHI-PROJECT-17H03987
  • [Journal Article] ニューロジェネティクスの歴史と展望2018

    • Author(s)
      戸田達史
    • Journal Title

      Clinical Neuroscience

      Volume: 36 Pages: 150-155

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Journal Article] ニューロジェネティクスの歴史と展望2018

    • Author(s)
      戸田達史
    • Journal Title

      Clinical Neuroscience別冊

      Volume: 36 Pages: 150-155

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Journal Article] Temporal requirement of dystroglycan glycosylation during brain development and rescue of severe cortical dysplasia via gene delivery in the fetal stage2018

    • Author(s)
      Sudo Atsushi、Kanagawa Motoi、Kondo Mai、Ito Chiyomi、Kobayashi Kazuhiro、Endo Mitsuharu、Minami Yasuhiro、Aiba Atsu、Toda Tatsushi
    • Journal Title

      Human molecular genetics

      Volume: 27 Issue: 7 Pages: 1174-1185

    • DOI

      10.1093/hmg/ddy032

    • NAID

      120006459805

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PLANNED-25115010, KAKENHI-PROJECT-15H04352, KAKENHI-PLANNED-17H06421, KAKENHI-PROJECT-17H01563, KAKENHI-PROJECT-16H05152, KAKENHI-PROJECT-16H05353, KAKENHI-PROJECT-18H02616
  • [Journal Article] 実験医学2018

    • Author(s)
      金川基、戸田達史.
    • Journal Title

      リビトールリン酸糖鎖異常型筋ジストロフィーの病態解明と治療法開発

      Volume: 36 Pages: 182-187

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Journal Article] 希少疾患・難病への治療法開発2018

    • Author(s)
      戸田達史
    • Journal Title

      .医学のあゆみ

      Volume: 266 Pages: 421-426

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Journal Article] National registry of patients with Fukuyama congenital muscular dystrophy in Japan.2018

    • Author(s)
      Ishigaki K, Ihara C, Nakamura H, Mori-Yoshimura M, Maruo K, Taniguchi-Ikeda M, Kimura E, Murakami T, Sato T, Toda T, Kaiya H, Osawa M.
    • Journal Title

      Neuromuscul Disord.

      Volume: 10 Issue: 10 Pages: 885-893

    • DOI

      10.1016/j.nmd.2018.08.001

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Journal Article] Cell surface flip-flop of phosphatidylserine is critical for PIEZO1-mediated myotube formation2018

    • Author(s)
      Tsuchiya Masaki、Hara Yuji、Okuda Masaki、Itoh Karin、Nishioka Ryotaro、Shiomi Akifumi、Nagao Kohjiro、Mori Masayuki、Mori Yasuo、Ikenouchi Junichi、Suzuki Ryo、Tanaka Motomu、Ohwada Tomohiko、Aoki Junken、Kanagawa Motoi、Toda Tatsushi、Nagata Yosuke、Matsuda Ryoichi、Takayama Yasunori、Tominaga Makoto、Umeda Masato
    • Journal Title

      Nature Communications

      Volume: 9 Issue: 1 Pages: 2049-2049

    • DOI

      10.1038/s41467-018-04436-w

    • NAID

      120006471161

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18K11089, KAKENHI-PROJECT-17K15793, KAKENHI-PLANNED-15H05930, KAKENHI-PUBLICLY-17H06012, KAKENHI-PLANNED-17H06421, KAKENHI-PROJECT-15H02501, KAKENHI-PROJECT-17H01563, KAKENHI-PROJECT-16H04786, KAKENHI-PROJECT-17H03805, KAKENHI-PROJECT-18H02616, KAKENHI-PROJECT-16KT0070, KAKENHI-PROJECT-16K14729
  • [Journal Article] リビトールリン酸糖鎖異常型筋ジストロフィーの病態解明と治療法開発2018

    • Author(s)
      金川基、戸田達史
    • Journal Title

      実験医学

      Volume: 36 Pages: 82-187

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Journal Article] 福山型筋ジストロフィー2017

    • Author(s)
      戸田達史
    • Journal Title

      遺伝子医学MOOK(32) 難病研究up-to-date

      Volume: 32 Pages: 175-181

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Journal Article] Muscular Dystrophy with Ribitol-Phosphate Deficiency: A Novel Post-Translational Mechanism in Dystroglycanopathy2017

    • Author(s)
      Kanagawa Motoi、Toda Tatsushi
    • Journal Title

      Journal of Neuromuscular Diseases

      Volume: 4 Issue: 4 Pages: 259-267

    • DOI

      10.3233/jnd-170255

    • NAID

      120006811130

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-26253057, KAKENHI-PLANNED-17H06421, KAKENHI-PROJECT-15H04352, KAKENHI-PROJECT-17H01563
  • [Journal Article] 福山型筋ジストロフィーのアンチセンス核酸治療2017

    • Author(s)
      戸田達史
    • Journal Title

      神経疾患治療ストラテジー

      Volume: 8 Pages: 362-367

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Journal Article] Novel FKRP mutations in a Japanese MDC1C sibship clinically diagnosed with Fukuyama congenital muscular dystrophy2017

    • Author(s)
      Yoshioka Mieko、Kobayashi Kazuhiro、Toda Tatsushi
    • Journal Title

      Brain and Development

      Volume: 39 Issue: 10 Pages: 869-872

    • DOI

      10.1016/j.braindev.2017.05.013

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-16H05353, KAKENHI-PROJECT-17H01563
  • [Journal Article] Less limb muscle involvement in myositis patients with anti-mitochondrial antibodies.2017

    • Author(s)
      Uenaka T, Kowa H, Ohtsuka Y, Seki T, Sekiguchi K, Kanda F, Toda T.
    • Journal Title

      Eur Neurol

      Volume: 78 Issue: 5-6 Pages: 290-295

    • DOI

      10.1159/000481503

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Journal Article] Cardiac involvement in Fukuyama muscular dystrophy is less severe than in Duchenne muscular dystrophy.2017

    • Author(s)
      Yamamoto T, Taniguchi-Ikeda M, Awano H, Matsumoto M, Lee T, Harada R, Imanishi T, Hayashi N, Sakai Y, Morioka I, Takeshima Y, Iijima K, Saegusa J, Toda T.
    • Journal Title

      Brain and Development

      Volume: 39 Issue: 10 Pages: 861-868

    • DOI

      10.1016/j.braindev.2017.05.008

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17K10087, KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-16H05814, KAKENHI-PROJECT-15K09621, KAKENHI-PROJECT-17H01563
  • [Journal Article] The Ror1 receptor tyrosine kinase plays a critical role in regulating satellite cell proliferation during regeneration of injured muscle2017

    • Author(s)
      Kamizaki Koki、Doi Ryosuke、Hayashi Makoto、Saji Takeshi、Kanagawa Motoi、Toda Tatsushi、Fukada So-ichiro、Ho Hsin-Yi Henry、Greenberg Michael Eldon、Endo Mitsuharu、Minami Yasuhiro
    • Journal Title

      Journal of Biological Chemistry

      Volume: 292 Issue: 38 Pages: 15939-15951

    • DOI

      10.1074/jbc.m117.785709

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26253057, KAKENHI-PLANNED-17H06421, KAKENHI-PROJECT-15H04352, KAKENHI-PROJECT-16H05152, KAKENHI-PROJECT-17H01563
  • [Journal Article] Deep-intronic variant of fukutin is the most prevalent point mutation of Fukuyama congenital muscular dystrophy in Japan2017

    • Author(s)
      Kobayashi Kazuhiro、Kato Reiko、Kondo-Iida Eri、Taniguchi-Ikeda Mariko、Osawa Makiko、Saito Kayoko、Toda Tatsushi
    • Journal Title

      Journal of Human Genetics

      Volume: 62 Issue: 11 Pages: 945-948

    • DOI

      10.1038/jhg.2017.71

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-16H05353, KAKENHI-PROJECT-15K09621, KAKENHI-PROJECT-17H01563
  • [Journal Article] The muscular dystrophy gene TMEM5encodes a ribitol β1-4 Xylosyltransferase required for the functional glycosylation of dystroglycan.2016

    • Author(s)
      Manya, H., Yamaguchi, Y., Kanagawa, M., Kobayashi, K., Tajiri, M., Akasaka-Manya, K., Kawakami, H., Mizuno, M., Wada, Y., Toda, T., and Endo, T.
    • Journal Title

      J. Biol. Chem

      Volume: 291 Issue: 47 Pages: 24618-24627

    • DOI

      10.1074/jbc.m116.751917

    • Peer Reviewed / Acknowledgement Compliant / Open Access
    • Data Source
      KAKENHI-PROJECT-15H04352, KAKENHI-PROJECT-25460054, KAKENHI-PROJECT-16K08262, KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-16H04758, KAKENHI-PROJECT-16H05353
  • [Journal Article] Carbohydrate-binding domain of the POMGnT1 stem region modulates O-mannosylation sites of α-dystroglycan.2016

    • Author(s)
      Kuwabara N, Manya H, Yamada T, Tateno H, Kanagawa M, Kobayashi K, Akasaka-Manya K, Hirose Y, Mizuno M, Ikeguchi M, Toda T, Hirabayashi J, Senda T, Endo T, Kato R.
    • Journal Title

      Proc Natl Acad Sci U S A.

      Volume: 113 Issue: 33 Pages: 9280-9285

    • DOI

      10.1073/pnas.1525545113

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-15H04352, KAKENHI-PROJECT-16H05071, KAKENHI-PROJECT-16K18522, KAKENHI-PROJECT-16K07284, KAKENHI-PROJECT-16K08262, KAKENHI-PROJECT-16H05353
  • [Journal Article] Analysis of phenotype, enzyme activity, and genotype of Chinese patients with POMT1 mutation2016

    • Author(s)
      Haipo Yang, Hiroshi Manya, Kazuhiro Kobayashi, HUI JIAO, Xiaona Fu, Jiangxi Xiao, Xiaoqing Li, Jingmin wang, Yuwu Jiang, TATSUSHI TODA, Tamao Endo, Xiru Wu,Hui Xiong,
    • Journal Title

      J. Hum. Genet

      Volume: 印刷中 Issue: 8 Pages: 753-759

    • DOI

      10.1038/jhg.2016.42

    • NAID

      40020923851

    • Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PUBLICLY-26110727, KAKENHI-PROJECT-16K08262, KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-16H05353
  • [Journal Article] Identification of a post-translational modification with ribitol-phosphate and its defect in muscular dystrophy2016

    • Author(s)
      Kanagawa M, Kobayashi K, Tajiri M, Manya H, Kuga A, Yamaguchi Y, Akasaka-Manya K, Furukawa J, Mizuno M, Kawakami H, Shinohara Y, Wada Y, Endo T, Toda T.
    • Journal Title

      Cell Reports

      Volume: 14 Issue: 9 Pages: 2209-2223

    • DOI

      10.1016/j.celrep.2016.02.017

    • NAID

      120005728438

    • Peer Reviewed / Acknowledgement Compliant / Open Access
    • Data Source
      KAKENHI-PUBLICLY-26110712, KAKENHI-PUBLICLY-26110727, KAKENHI-PROJECT-15H04352, KAKENHI-PROJECT-26670499, KAKENHI-PROJECT-25293016, KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-25460054, KAKENHI-PROJECT-16H05353
  • [Journal Article] Next-generation sequencing discloses a nonsense mutation in the dystrophin gene from long preserved dried umbilical cord and low-level somatic mosaicism in the proband mother.2016

    • Author(s)
      Taniguchi-Ikeda M, Takeshima Y, Lee T, Nishiyama M, Awano H, Yagi M, Unzaki A, Nozu K, Nishio H, Matsuo M, Kurahashi H, Toda T, Morioka I, Iijima K.
    • Journal Title

      J Hum Genet.

      Volume: 61 Issue: 4 Pages: 351-355

    • DOI

      10.1038/jhg.2015.157

    • NAID

      40020802923

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-15K09621, KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-15H04710, KAKENHI-PROJECT-26461632
  • [Journal Article] Mechanistic aspects of the formation of α-dystroglycan and therapeutic research for the treatment of α-dystroglycanopathy: A review.2016

    • Author(s)
      Taniguchi-Ikeda M, Morioka I, Iijima K, Toda T.
    • Journal Title

      Mol Aspects Med.

      Volume: 51 Pages: 115-124

    • DOI

      10.1016/j.mam.2016.07.003

    • Peer Reviewed / Acknowledgement Compliant / Open Access
    • Data Source
      KAKENHI-PROJECT-15K09621, KAKENHI-PROJECT-26253057
  • [Journal Article] Fukutin is prerequisite to ameliorate muscular dystrophic phenotype by myofiber-selective LARGE expression.2015

    • Author(s)
      Ohtsuka Y, Kanagawa M, Yu CC, Ito C, Chiyo T, Kobayashi K, Okada T, Takeda S’I, Toda T.
    • Journal Title

      Sci Rep

      Volume: 5 Issue: 1 Pages: 8316-8316

    • DOI

      10.1038/srep08316

    • NAID

      120005600773

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-12F02422, KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-24500472, KAKENHI-PROJECT-24687017, KAKENHI-PUBLICLY-26110712, KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-26670499, KAKENHI-PROJECT-26293328
  • [Journal Article] CHCHD2 mutations in autosomal dominant late-onset Parkinson’s disease: a genome-wide linkage and sequencing study.2015

    • Author(s)
      Funayama M, Ohe K, Amo T, Furuya N, Yamaguchi J, Saiki S, Yuanzhe L, Ogaki K, Ando M, Yoshinon H, Tomiyama H, Nishioka K, Hasegawa K, Saiki H, Satake W, Mogushi K, Sasaki R, Kokubo Y, Kuzuhara S, Toda T, Mizuno Y, Uchiyama Y, Ohno K, Hattori N.
    • Journal Title

      Lancet Neurol

      Volume: 14 Issue: 3 Pages: 274-282

    • DOI

      10.1016/s1474-4422(14)70266-2

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-24390224, KAKENHI-PROJECT-24500868, KAKENHI-PROJECT-24790903, KAKENHI-PUBLICLY-25110720, KAKENHI-ORGANIZER-25111001, KAKENHI-PLANNED-25111007, KAKENHI-PUBLICLY-25129707, KAKENHI-PROJECT-25461291, KAKENHI-PROJECT-25461292, KAKENHI-PROJECT-25670420, KAKENHI-PROJECT-25713015, KAKENHI-PROJECT-25860725, KAKENHI-PROJECT-25860726, KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-26870175, KAKENHI-PROJECT-15K10050, KAKENHI-ORGANIZER-23111001, KAKENHI-PLANNED-23111003, KAKENHI-PLANNED-23111004, KAKENHI-PROJECT-25257507, KAKENHI-PROJECT-15H04842, KAKENHI-PROJECT-25305030
  • [Journal Article] ABCG2 variant has opposing effects on onset ages of Parkinson's disease and gout.2015

    • Author(s)
      Matsuo H, Tomiyama H, Satake W, Chiba T, Onoue H, Kawamura Y, Nakayama A, ShimizuS, Sakiyama M, Funayama M, Nishioka K, Shimizu T, Kaida K, Kamakura K, Toda T, Hattori N, ShinomiyaN.
    • Journal Title

      Ann Clin Transl Neurol

      Volume: 2 Issue: 3 Pages: 302-306

    • DOI

      10.1002/acn3.167

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PLANNED-23111003, KAKENHI-PROJECT-24390224, KAKENHI-PUBLICLY-25110720, KAKENHI-PUBLICLY-25129707, KAKENHI-PROJECT-25293145, KAKENHI-PROJECT-25461291, KAKENHI-PROJECT-25461292, KAKENHI-PROJECT-25670307, KAKENHI-PROJECT-25670420, KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-25860726, KAKENHI-PROJECT-15H04315, KAKENHI-PROJECT-25713015
  • [Journal Article] A de novo mutation of the MYH7 gene in a large Chinese family with autosomal dominant myopathy2015

    • Author(s)
      Oda T, Xiong H, Kobayashi K, Wang S, Satake W, Jiao H, Yang Y, Cha PC, Hayashi Y, Nishino I, Suzuki Y, Sugano S, Wu X, Toda T.
    • Journal Title

      Human Genome Variation

      Volume: 2 Issue: 1 Pages: 15022-15022

    • DOI

      10.1038/hgv.2015.22

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-12F02422, KAKENHI-PROJECT-26670499, KAKENHI-PROJECT-25713015, KAKENHI-PROJECT-26253057
  • [Journal Article] A novel PIGN mutation and prenatal diagnosis of inherited glycosylphosphatidylinositol deficiency.2015

    • Author(s)
      Nakagawa T, Taniguchi-Ikeda M, Murakami Y, Nakamura S, Motooka D, Emoto T, Satake W, Nishiyama M, Toyoshima D, Morisada N, Takada S, Tairaku S, Okamoto N, Morioka I, Kurahashi H, Toda T, Kinoshita T, Iijima K.
    • Journal Title

      American Journal of Medical Genetics PartA

      Volume: 170 Issue: 1 Pages: 183-188

    • DOI

      10.1002/ajmg.a.37397

    • Peer Reviewed / Acknowledgement Compliant / Open Access
    • Data Source
      KAKENHI-PROJECT-15K09621, KAKENHI-PROJECT-26461632, KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-25713015
  • [Journal Article] Japanese founder duplications/triplications involving BHLHA9 are associated with split-hand/foot malformation with or without long bone deficiency and Gollop-Wolfgang complex.2014

    • Author(s)
      Nagata E, Kano H, Kato F, Yamaguchi R, Nakashima S, Takayama S, Kosaki R, Tonoki H, Mizuno S, Watanabe S, Yoshiura KI, Kosho T, Hasegawa T, Kimizuka M, Suzuki A, Shimizu K, Ohashi H, Haga N, Numabe H, Horii E, Nagai T, Yoshihashi H, Nishimura G, Toda T, et al.
    • Journal Title

      Orphanet J Rare Dis

      Volume: 9 Issue: 1 Pages: 125-125

    • DOI

      10.1186/s13023-014-0125-5

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PLANNED-22132004, KAKENHI-PROJECT-22227002, KAKENHI-PROJECT-25253023, KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-26870255
  • [Journal Article] Contribution of dysferlin deficiency to skeletal muscle pathology in asymptomatic and severe dystroglycanopathy models: generation of a new model for fukuyama congenital muscular dystrophy.2014

    • Author(s)
      Kanagawa M, Lu Z, Ito C, Matsuda C, Miyake K, Toda T.
    • Journal Title

      Plos ONE

      Volume: 9 Issue: 9 Pages: e106721-e106721

    • DOI

      10.1371/journal.pone.0106721

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-22390374, KAKENHI-PROJECT-24687017, KAKENHI-PUBLICLY-26110712, KAKENHI-PROJECT-26253057
  • [Journal Article] Peripheral leukocyte anomaly detected with routine automated hematology analyzer sensitive to adipose triglyceride lipase deficiency manifesting neutral lipid storage disease with myopathy/triglyceride deposit cardiomyovasculopathy.2014

    • Author(s)
      Suzuki A, Nagasaka H, Ochi Y, Kobayashi K, Nakamura H, Nakatani D, S Yamaguchi, Yamaki S, Wada A, Shirata Y, Hui SP, Toda T, Kuroda H, Chiba H, Hirano K.
    • Journal Title

      Mol Genet Metab Rep

      Volume: 1 Pages: 249-253

    • DOI

      10.1016/j.ymgmr.2014.05.001

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-23617010, KAKENHI-PROJECT-26253057
  • [Journal Article] Association of the ASCO classification with the executive function subscores of the Montreal Cognitive Assessment in patients with post-ischemic stroke.2014

    • Author(s)
      Washida K, IharaM, Tachibana H, Sekiguchi K, Kowa H, Kanda F, Toda T.
    • Journal Title

      J Stroke Cerebrovasc Dis

      Volume: 23 Issue: 9 Pages: 2250-2255

    • DOI

      10.1016/j.jstrokecerebrovasdis.2014.04.009

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-26253057
  • [Journal Article] Genetic mutations in adipose triglyceride lipase and myocardial up-regulation of peroxisome proliferated activated receptor-γ in patients with triglyceride deposit cardiomyovasculopathy.2014

    • Author(s)
      Hirano K, Tanaka T, Ikeda Y, Yamaguchi S, Zaima N, Kobayashi K, Suzuki A, Sakata Y, Sakata Y, Kobayashi K, Toda T, Fukushima N, Ishibashi-Ueda H, Tavian D, Nagasaka H, Hui SP, Chiba H, Sawa Y, Hori M.
    • Journal Title

      Biochem Biophys Res Commun.

      Volume: 443 Issue: 2 Pages: 574-579

    • DOI

      10.1016/j.bbrc.2013.12.003

    • Peer Reviewed
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-23249049, KAKENHI-PROJECT-23617010
  • [Journal Article] Disease-associated marked hyperalphalipoproteinemia.2014

    • Author(s)
      Hirano K, Nagasaka H, Kobayashi K, Yamaguchi S, Suzuki A, Toda T, Doyu M.
    • Journal Title

      Mol Genet Metab Rep

      Volume: 1 Pages: 264-268

    • DOI

      10.1016/j.ymgmr.2014.06.001

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-26253057
  • [Journal Article] ゴーシェ病の多様性2014

    • Author(s)
      戸田達史
    • Journal Title

      Medical Science Digest

      Volume: 40 Pages: 562-563

    • Data Source
      KAKENHI-PLANNED-22129006
  • [Journal Article] 福山型筋ジストロフィー 仕組みの解明 治療法開発2014

    • Author(s)
      戸田達史
    • Journal Title

      関西実験動物研究会

      Volume: 会報36号 Pages: 83-83

    • Data Source
      KAKENHI-PROJECT-26253057
  • [Journal Article] TRPV2 is critical for the maintenance of cardiac structure and function in mice.2014

    • Author(s)
      Katanosaka Y, Iwasaki K, Ujihara Y, Takatsu S, Nishitsuji K, Kanagawa M, Sudo A, Toda T, Katanosaka K, Mohri S, Naruse K.
    • Journal Title

      Nat Comm

      Volume: 5 Issue: 1 Pages: 3932-3932

    • DOI

      10.1038/ncomms4932

    • NAID

      120005690060

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-24590725, KAKENHI-PROJECT-24687017, KAKENHI-PROJECT-25350544, KAKENHI-PUBLICLY-26110712, KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-26282122, KAKENHI-PROJECT-26282127, KAKENHI-PROJECT-26560211, KAKENHI-PROJECT-26220203
  • [Journal Article] Novel calmodulin mutations associated with congenital arrhythmia susceptibility.2014

    • Author(s)
      Makita N, Tsuji Y(39人中21番目)et al
    • Journal Title

      Circ Cardiovasc Genet.

      Volume: 7 Issue: 4 Pages: 466-474

    • DOI

      10.1161/circgenetics.113.000459

    • Peer Reviewed / Acknowledgement Compliant / Open Access
    • Data Source
      KAKENHI-PLANNED-22136007, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-24591038, KAKENHI-PROJECT-24591086, KAKENHI-PUBLICLY-25110720, KAKENHI-PROJECT-25293181, KAKENHI-PROJECT-25670172, KAKENHI-PROJECT-25670420, KAKENHI-PROJECT-25713015, KAKENHI-PROJECT-26860572, KAKENHI-PROJECT-221S0002
  • [Journal Article] A case of Bardet-Biedl syndrome complicated with intracranial hypertension in a Japanese child.2014

    • Author(s)
      Saida K, Inaba Y, Hirano M, Satake W, Toda T, Suzuki Y, Sudo A, Noda S, Hidaka Y, Hirabayashi K, Imai H, Kurokawa T, Koike K.
    • Journal Title

      Brain Dev

      Volume: 印刷中 Issue: 8 Pages: 721-724

    • DOI

      10.1016/j.braindev.2013.10.013

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-23249049, KAKENHI-PUBLICLY-25110720, KAKENHI-PROJECT-25670420, KAKENHI-PROJECT-25713015
  • [Journal Article] 医学と医療の最前線 筋ジストロフィー治療の新しい展開2014

    • Author(s)
      戸田達史
    • Journal Title

      日本内科学会雑誌

      Volume: 103 Pages: 2820-2828

    • Data Source
      KAKENHI-PROJECT-26253057
  • [Journal Article] The role of Pak-interacting exchange factor-β phosphorylation at serines 340 and 583 by PKCγ in dopamine release.2014

    • Author(s)
      Shirafuji T, Ueyama T, Yoshino K, Takahashi H, Adachi N, Ago Y, Koda K, Nashida T, Hiramatsu N, Matsuda T, Toda T, Sakai N, Saito N.
    • Journal Title

      J Neurosci

      Volume: 34 Issue: 28 Pages: 9268-9280

    • DOI

      10.1523/jneurosci.4278-13.2014

    • NAID

      120005619641

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PUBLICLY-25113715, KAKENHI-PROJECT-25293060, KAKENHI-PROJECT-25293061, KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-26460340, KAKENHI-PROJECT-26670124
  • [Journal Article] 福山型筋ジストロフィー 遺伝子・病態の解明、分子標的治療を目指して2013

    • Author(s)
      戸田 達史, 谷口 真理子(池田), 金川 基, 小林 千浩
    • Journal Title

      生化学

      Volume: 85 Pages: 253-260

    • NAID

      10031169565

    • Data Source
      KAKENHI-PROJECT-23249049
  • [Journal Article] YY1 binds to α-synuclein 3'-flanking region SNP and stimulates antisense noncoding RNA expression.2013

    • Author(s)
      Mizuta I, Takafuji K, Ando Y, Satake W, Kanagawa M, Kobayashi K, Nagamori S, Shinohara T, Ito C, Yamamoto M, Hattori N, Murata M, Kanai Y, Murayama S, Nakagawa M, Toda T.
    • Journal Title

      J Hum Genet

      Volume: 58 Issue: 11 Pages: 711-719

    • DOI

      10.1038/jhg.2013.90

    • Peer Reviewed
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-23249049, KAKENHI-PUBLICLY-24110508, KAKENHI-PROJECT-24591198, KAKENHI-PUBLICLY-25110720, KAKENHI-PROJECT-25670420, KAKENHI-PROJECT-25713015
  • [Journal Article] 【次世代シーケンサーによる神経変性疾患の解析と展望】 パーソナルゲノム研究と神経疾患 overview2013

    • Author(s)
      戸田 達史
    • Journal Title

      BRAIN and NERVE: 神経研究の進歩

      Volume: 65 Pages: 227-234

    • Data Source
      KAKENHI-PLANNED-22129006
  • [Journal Article] Molecular pathology of Sandhoff disease with p.Arg505Gln in HEXB: application of simulation analysis.2013

    • Author(s)
      Yasui N, Takaoka Y, Nishio H, Nurputra DK, Sekiguchi K, Hamaguchi H, Kowa H, Maeda E, Sugano A, Miura K, Sakaeda T, Kanda F, Toda T.
    • Journal Title

      J Hum Genet

      Volume: 58 Issue: 9 Pages: 611-617

    • DOI

      10.1038/jhg.2013.68

    • NAID

      10031195298

    • Peer Reviewed
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-23249049, KAKENHI-PROJECT-25461549
  • [Journal Article] A case of juvenile parkinsonism with expanded SCA8 CTA/CTG repeats2013

    • Author(s)
      宮脇 統子, 関口 兼司, 安井 直子, 上田 健博, 苅田 典生, 戸田 達史
    • Journal Title

      Rinsho Shinkeigaku

      Volume: 53 Issue: 4 Pages: 278-282

    • DOI

      10.5692/clinicalneurol.53.278

    • NAID

      130004921088

    • ISSN
      0009-918X, 1882-0654
    • Language
      Japanese
    • Peer Reviewed
    • Data Source
      KAKENHI-PLANNED-22129006
  • [Journal Article] 【サルコペニアとアンチエイジング】 筋肉研究の最前線 筋ジストロフィー2013

    • Author(s)
      戸田 達史
    • Journal Title

      アンチ・エイジング医学

      Volume: 9 Pages: 541-547

    • Data Source
      KAKENHI-PROJECT-23249049
  • [Journal Article] 【神経・精神疾患診療マニュアル】 神経・精神疾患の動向 神経疾患と遺伝子2013

    • Author(s)
      佐竹 渉, 戸田 達史
    • Journal Title

      日本医師会雑誌

      Volume: 142

    • Data Source
      KAKENHI-PLANNED-22129006
  • [Journal Article] Myositis with antimitochondrial antibodies diagnosed by musculus rectus abdominis biopsy.2013

    • Author(s)
      Uenaka K, Kowa H, Sekiguchi K, Nagata K, Ohtsuka Y, Kanda F, Toda T.
    • Journal Title

      Muscle Nerve

      Volume: 47 Issue: 5 Pages: 766-768

    • DOI

      10.1002/mus.23730

    • Peer Reviewed
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-23249049
  • [Journal Article] 【遺伝子・再生医療研究から学ぶパーキンソン病】 PARK遺伝子研究の現状 【RAB7L1(PARK16)】 ゲノムワイド関連解析からの知見とさらなる孤発性パーキンソン病遺伝子の発見へ向けて PARK16、BST1、α-synuclein、LRRK2、Tau2013

    • Author(s)
      佐竹 渉, 戸田 達史
    • Journal Title

      医学のあゆみ

      Volume: 247 Pages: 1075-1082

    • Data Source
      KAKENHI-PLANNED-22129006
  • [Journal Article] 【パーキンソン病診療の新しい展開】 パーキンソン病の臨床遺伝学2013

    • Author(s)
      戸田 達史
    • Journal Title

      Mebio

      Volume: 30 Pages: 17-22

    • Data Source
      KAKENHI-PLANNED-22129006
  • [Journal Article] 各種疾患 神経筋疾患 福山型筋ジストロフィーの分子病態と治療2013

    • Author(s)
      戸田 達史
    • Journal Title

      Annual Review神経

      Volume: 2013 Pages: 238-245

    • Data Source
      KAKENHI-PROJECT-23249049
  • [Journal Article] A drug screening platform for Alzheimer's disease with intracellular Aβ oligomers using patient-specific iPSCs2013

    • Author(s)
      Kondo, T., (他24名), Murakami, K., Irie, K., Klein, W. L., Mori, H., Asada, T., Takahashi, R., Iwata, N., Yamanaka, S., Inoue, H
    • Journal Title

      Cell Stem Cell

      Volume: 12 Issue: 4 Pages: 487-496

    • DOI

      10.1016/j.stem.2013.01.009

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-21248015, KAKENHI-PLANNED-22129006, KAKENHI-ORGANIZER-23111001, KAKENHI-PLANNED-23111002, KAKENHI-PROJECT-23249049, KAKENHI-PROJECT-23390232, KAKENHI-PROJECT-23592093, KAKENHI-PROJECT-24220009, KAKENHI-PROJECT-24500408, KAKENHI-PROJECT-24590040, KAKENHI-PROJECT-24700367, KAKENHI-PROJECT-24790260, KAKENHI-PROJECT-24790276, KAKENHI-PUBLICLY-25123709, KAKENHI-PROJECT-25290018, KAKENHI-PROJECT-25460341, KAKENHI-PUBLICLY-23110535, KAKENHI-PUBLICLY-23123510
  • [Journal Article] A novel mutation in the C2 domain of protein kinase C gamma associated with spinocerebellar ataxia type 14.2013

    • Author(s)
      Ueda T, Seki T, Katanazaka K, Sekiguchi K, Kobayashi K, Kanda F, Toda T.
    • Journal Title

      J Neurol

      Volume: 260 Issue: 6 Pages: 1664-1666

    • DOI

      10.1007/s00415-013-6916-0

    • Peer Reviewed
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-23249049
  • [Journal Article] Novel POMGnT1 mutations cause muscle-eye-brain disease in Chinese patients2013

    • Author(s)
      Jiao H, Manya H, Wang S, Zhang Y, Li X, Xiao J, Yang Y, Kobayashi K, Toda T, Endo T, Wu X, Xiong H.
    • Journal Title

      Mol Genet Genomics

      Volume: 288 Issue: 7-8 Pages: 297-308

    • DOI

      10.1007/s00438-013-0749-5

    • Peer Reviewed
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-23249049, KAKENHI-PUBLICLY-24110523, KAKENHI-PROJECT-25293016
  • [Journal Article] 福山型筋ジストロフィーの新たな病態と分子標的治療2013

    • Author(s)
      戸田 達史, 池田 真理子, 小林 千浩
    • Journal Title

      小児科診療

      Volume: 76 Pages: 671-671

    • Data Source
      KAKENHI-PROJECT-23249049
  • [Journal Article] Impaired viability of muscle precursor cells in muscular dystrophy with glycosylation defects and amelioration. of its severe phenotype by limited gene expression.2013

    • Author(s)
      Kanagawa M, et. al.
    • Journal Title

      Hum Mol Genet

      Volume: 22 Issue: 15 Pages: 3003-3015

    • DOI

      10.1093/hmg/ddt157

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-12F02422, KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-23249049, KAKENHI-PROJECT-24590497, KAKENHI-PROJECT-24659265, KAKENHI-PROJECT-24687017, KAKENHI-PROJECT-25702044
  • [Journal Article] 【検査値を読む2013】 遺伝子・染色体検査 先天性遺伝子検査 福山型筋ジストロフィー遺伝子2013

    • Author(s)
      小林 千浩, 戸田 達史
    • Journal Title

      内科

      Volume: 111 Pages: 1087-1087

    • Data Source
      KAKENHI-PROJECT-23249049
  • [Journal Article] AGO61-dependent GlcNAc modification primes the formation of functional glycans on α-dystroglycan.2013

    • Author(s)
      Yagi H, Nakagawa N, Saito T, Kiyonari H, Abe T, Toda T, Wu SW, Khoo KH, Oka S, Kato K.
    • Journal Title

      Sci Rep

      Volume: 3 Issue: 1 Pages: 3288-3288

    • DOI

      10.1038/srep03288

    • NAID

      120005353504

    • Peer Reviewed
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PLANNED-23110006, KAKENHI-PROJECT-23249049, KAKENHI-PUBLICLY-24110512, KAKENHI-PROJECT-24249002, KAKENHI-ORGANIZER-25102001, KAKENHI-PLANNED-25102008
  • [Journal Article] Inhibition of Protein Misfolding/Aggregation Using Polyglutamine Binding Peptide QBP1 as a Therapy for the Polyglutamine Diseases.2013

    • Author(s)
      H. Akiko Popiel
    • Journal Title

      Neuro therapeutics

      Volume: (印刷中) Issue: 3 Pages: 440-446

    • DOI

      10.1007/s13311-013-0184-7

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-11J08829, KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-23249049, KAKENHI-PROJECT-23390237, KAKENHI-PROJECT-24591287, KAKENHI-PROJECT-24659438, KAKENHI-PUBLICLY-25110741, KAKENHI-PROJECT-25882021, KAKENHI-PUBLICLY-23110528
  • [Journal Article] Plasmablasts as migratory IgG-producing cells in the pathogenesis of neuromyelitis optica.2013

    • Author(s)
      Chihara N, Aranami T, Oki S, Matsuoka T, Nakamura M, Kishida H, Yokoyama K, Kuroiwa Y, Hattori N, Okamoto T, Murata M, Toda T, Miyake S, Yamamura T.
    • Journal Title

      PLoS One

      Volume: 8 Issue: 12 Pages: e83036-e83036

    • DOI

      10.1371/journal.pone.0083036

    • Peer Reviewed
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-23249049, KAKENHI-PROJECT-23390261, KAKENHI-PROJECT-24590108
  • [Journal Article] 【遺伝性筋疾患の新たな治療戦略】 福山型筋ジストロフィーの新たな病態とアンチセンス療法2012

    • Author(s)
      戸田 達史, 谷口 真理子(池田), 小林 千浩
    • Journal Title

      神経内科

      Volume: 76 Pages: 361-366

    • Data Source
      KAKENHI-PROJECT-23249049
  • [Journal Article] Genome-Wide DNA methylation and gene expression analyses of monozygotic twins discordant for intelligence levels.2012

    • Author(s)
      Yu CC
    • Journal Title

      PLoS ONE

      Volume: 7 Issue: 10 Pages: e47081-e47081

    • DOI

      10.1371/journal.pone.0047081

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-12F02422, KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-23249049, KAKENHI-PROJECT-23890250, KAKENHI-ORGANIZER-24116001
  • [Journal Article] Screening of genes involved in chromosome segregation during meiosis I: in vitro gene transfer to mouse fetal oocytes.2012

    • Author(s)
      Tsutsumi M, Kowa-Sugiyama H, Bolor H, Kogo H, Inagaki H, Ohye T, Yamada K, Taniguchi-Ikeda M, Toda T, Kurahashi H.
    • Journal Title

      J Hum Genet

      Volume: 57 Issue: 8 Pages: 515-522

    • DOI

      10.1038/jhg.2012.61

    • NAID

      10031056588

    • Peer Reviewed
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PUBLICLY-23013019, KAKENHI-PROJECT-23249049, KAKENHI-PROJECT-23659182, KAKENHI-PROJECT-24390085, KAKENHI-PROJECT-24590263
  • [Journal Article] Hsp40 Gene Therapy Exerts Therapeutic Effects on Polyglutamine Disease Micevia a Non-Cell Autonomous Mechanism.2012

    • Author(s)
      H. Akiko Popiel
    • Journal Title

      PLoS One

      Volume: 7 Issue: 11 Pages: e51069-e51069

    • DOI

      10.1371/journal.pone.0051069

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-11J08829, KAKENHI-PROJECT-21200072, KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-23249049, KAKENHI-PROJECT-23390237, KAKENHI-PROJECT-23590473, KAKENHI-PROJECT-24591287, KAKENHI-PROJECT-24659438, KAKENHI-PUBLICLY-23110515, KAKENHI-PUBLICLY-23110528
  • [Journal Article] Large-scale replication and heterogeneity in Parkinson disease genetic loci.2012

    • Author(s)
      Sharma M, Ioannidis JPA, Aasly JO, Brice A, ..., Satake W, ..., Toda T,..., Kruger R.
    • Journal Title

      Neurology

      Volume: 79 Issue: 7 Pages: 659-667

    • DOI

      10.1212/wnl.0b013e318264e353

    • Peer Reviewed
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-23249049
  • [Journal Article] 【神経筋疾患の分子標的治療開発】 福山型筋ジストロフィーの分子標的治療2012

    • Author(s)
      戸田 達史, 谷口 真理子(池田), 小林 千浩
    • Journal Title

      BIO Clinica

      Volume: 27 Pages: 925-929

    • Data Source
      KAKENHI-PROJECT-23249049
  • [Journal Article] Detection of the dystroglycanopathy protein, fukutin, using a new panel of site-specific monoclonal antibodies.2012

    • Author(s)
      Lynch TA, Lam le T, Man Nt, Kobayashi K, Toda T, Morris GE.
    • Journal Title

      Biochem Biophys Res Commun

      Volume: 424 Issue: 2 Pages: 354-357

    • DOI

      10.1016/j.bbrc.2012.06.147

    • Peer Reviewed
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-23249049
  • [Journal Article] A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants.2012

    • Author(s)
      Sharma M, Ioannidis JP, Aasly JO, ..., Satake W, ..., Toda T, ..., GEOPD consortium.
    • Journal Title

      J Med Genet

      Volume: 49 Issue: 11 Pages: 721-726

    • DOI

      10.1136/jmedgenet-2012-101155

    • Peer Reviewed
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-23249049
  • [Journal Article] Anti-Hu-associated Paraneoplastic Encephalomyelitis with Esophageal Small Cell Carcinoma2012

    • Author(s)
      Shirafuji T, Kanda F, Sekiguchi K, Higuchi M, Yokosaki H, Tanaka K, Takahashi H, Toda T.
    • Journal Title

      Intern. Med.

      Volume: 51 Issue: 17 Pages: 2423-2427

    • DOI

      10.2169/internalmedicine.51.6884

    • NAID

      130002062329

    • ISSN
      0918-2918, 1349-7235
    • Language
      English
    • Peer Reviewed
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-23249049
  • [Journal Article] 【RNAバイオロジーの最先端】 福山型先天性筋ジストロフィーの発症機序と治療戦略2012

    • Author(s)
      谷口 真理子(池田), 戸田 達史
    • Journal Title

      細胞

      Volume: 44 Pages: 598-602

    • Data Source
      KAKENHI-PROJECT-23249049
  • [Journal Article] Absence of post-phosphoryl modification in dystroglycanopathy mouse models and wild-type tissues expressing a non-laminin binding form of alpha-dystroglycan2012

    • Author(s)
      Kuga A, Kanagawa M, Sudo A, Chan YM, Tajiri M, Manya H, Kikkawa Y, Nomizu M, Kobayashi K, Endo T, Lu QL, Wada Y, Toda T
    • Journal Title

      J Biol Chem

      Volume: 287 Pages: 9560-9567

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Journal Article] 福山型筋ジストロフィーの病的スプライシング異常とアンチセンス療法2012

    • Author(s)
      谷口(池田)真理子, 小林千浩, 戸田達史
    • Journal Title

      実験医学

      Volume: 30 Pages: 950-953

    • Data Source
      KAKENHI-PROJECT-23249049
  • [Journal Article] 【神経変性疾患のゲノム・遺伝学研究】 孤発性パーキンソン病のリスク遺伝子2012

    • Author(s)
      佐竹 渉, 戸田 達史
    • Journal Title

      Dementia Japan

      Volume: 26 Pages: 155-162

    • Data Source
      KAKENHI-PLANNED-22129006
  • [Journal Article] Association analysis of LRP8 SNP rs3820198 and rs5174 with Parkinson's disease in Han Chinese population.2012

    • Author(s)
      Chen K, Chen YP, Song W, Huang R, Zhao B, Cao B, Yang Y, Satake W, Toda T, Shang HF.
    • Journal Title

      Neurol Res

      Volume: 34 Issue: 7 Pages: 725-729

    • DOI

      10.1179/1743132812y.0000000075

    • Peer Reviewed
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-23249049
  • [Journal Article] MEDICAL TOPICS(第42回) 福山型筋ジストロフィーのスプライシング異常に対するアンチセンス治療2012

    • Author(s)
      谷口 真理子(池田), 小林 千浩, 戸田 達史
    • Journal Title

      THE LUNG-perspectives

      Volume: 20 Pages: 186-191

    • Data Source
      KAKENHI-PROJECT-23249049
  • [Journal Article] Human natural killer-1 sulfotransferase (HNK-1ST)-induced sulfate-transfer regulates laminin-binding glycans on α-dystroglycan.2012

    • Author(s)
      Nakagawa N, Manya H, Toda T, Endo T, Oka S.
    • Journal Title

      J Biol Chem

      Volume: 287 Issue: 36 Pages: 30823-30832

    • DOI

      10.1074/jbc.m112.363036

    • Peer Reviewed
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-23249049, KAKENHI-PROJECT-23659153, KAKENHI-ORGANIZER-23110001, KAKENHI-PLANNED-23110006
  • [Journal Article] 【パーキンソン病発症のメカニズム】パーキンソン病の分子遺伝学ゲノム関連解析研究2011

    • Author(s)
      戸田達史
    • Journal Title

      BIO Clinica

      Volume: 26巻8号 Pages: 701-705

    • Data Source
      KAKENHI-PLANNED-22129006
  • [Journal Article] Interleukin 6 signaling promotes anti-aquaporin 4 autoantibody production from plasmablasts in neuromyelitis optica.2011

    • Author(s)
      Chihara N, Aranami T, Sato W, Miyazaki Y, Miyake S, Okamoto T, Ogawa M, Toda T, Yamamura T.
    • Journal Title

      Proc Natl Acad Sci U S A 108

      Pages: 3701-3706

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] 【パーキンソン病発症のメカニズム】パーキンソン病の分子遺伝学ゲノム関連解析研究2011

    • Author(s)
      戸田達史
    • Journal Title

      BIO Clinica

      Volume: 26巻8号 Pages: 701-705

    • Data Source
      KAKENHI-PROJECT-23249049
  • [Journal Article] 【変わりゆくパーキンソン病診療早期診断から進行期患者の治療まで】孤発性パーキンソン病の分子病態機序はどこまで解明されたか2011

    • Author(s)
      戸田達史
    • Journal Title

      内科

      Volume: 107巻5号 Pages: 759-766

    • Data Source
      KAKENHI-PROJECT-23249049
  • [Journal Article] Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy2011

    • Author(s)
      Taniguchi-Ikeda M, Kobayashi K, Kanagawa M, Yu CC, Mori K, Oda T, Kuga A, Kurahashi H, Akman HO, DiMauro S, Kaji R, Yokota T, Takeda S, Toda T
    • Journal Title

      Nature

      Volume: 478 Issue: 7367 Pages: 127-131

    • DOI

      10.1038/nature10456

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21390101, KAKENHI-PROJECT-21390269, KAKENHI-PROJECT-21689030, KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-22790980, KAKENHI-PUBLICLY-23013019, KAKENHI-PROJECT-23249049, KAKENHI-PROJECT-23659182
  • [Journal Article] 【変わりゆくパーキンソン病診療早期診断から進行期患者の治療まで】孤発性パーキンソン病の分子病態機序はどこまで解明されたか2011

    • Author(s)
      戸田達史
    • Journal Title

      内科

      Volume: 107巻5号 Pages: 759-766

    • Data Source
      KAKENHI-PLANNED-22129006
  • [Journal Article] 国際共同研究におけるGenome-Wide Association Study (GWAS)2011

    • Author(s)
      戸田達史
    • Journal Title

      Medical Science Digest

      Volume: 37巻9号 Pages: 346-347

    • Data Source
      KAKENHI-PLANNED-22129006
  • [Journal Article] Genetic and clinical analysis in a Chinese parkinsonism- predominant spinocerebellar ataxia type 2 family.2011

    • Author(s)
      Sun H, Satake W, Zhang C, Nagai Y, Tian Y, Fu S, Yu J, Qian Y, Qian Y, Chu J, Toda T
    • Journal Title

      J Hum Genet 56(4)

      Pages: 330-334

    • NAID

      10030659058

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] Defective glycosylation of α-dystroglycan contributes to podocyte flattening.2011

    • Author(s)
      Kojima K, Nosaka H, Kishimoto Y, Nishiyama Y, Fukuda S, Shimada M, Kodaka K, Saito F, Matsumura K, Shimizu T, Toda T, Takeda S, Kawachi H, Uchida S.
    • Journal Title

      Kidney Int 79

      Pages: 311-316

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] 国際共同研究におけるGenome-Wide Association Study (GWAS)2011

    • Author(s)
      戸田達史
    • Journal Title

      Medical Science Digest

      Volume: 37巻9号 Pages: 346-347

    • Data Source
      KAKENHI-PROJECT-23249049
  • [Journal Article] 福山型筋ジストロフィーの治療戦略2010

    • Author(s)
      戸田達史
    • Journal Title

      難病と在宅のケア

      Volume: 16 Pages: 41-43

    • Data Source
      KAKENHI-PLANNED-22129006
  • [Journal Article] 福山型筋ジストロフィー2010

    • Author(s)
      戸田達史
    • Journal Title

      JFNMH Newsletter

      Volume: 7 Pages: 2-6

    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] Post- translational maturation of dystroglycan is necessary for pikachurin binding and ribbon synaptic localization.2010

    • Author(s)
      Kanagawa M, Omori Y, Sato S, Kobayashi K, Miyagoe-Suzuki Y, Takeda S, Endo T, Furukawa T, Toda T
    • Journal Title

      J Biol Chem 285

      Pages: 31208-31216

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] 疾患感受性遺伝子2010

    • Author(s)
      戸田達史
    • Journal Title

      Current Therapy

      Volume: 28 Pages: 859-860

    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] ゲノムワイド関連解析によるパーキンソン病リスク遺伝子の同定2010

    • Author(s)
      戸田達史
    • Journal Title

      医学のあゆみ

      Volume: 233 Pages: 640-642

    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] 疾患感受性遺伝子2010

    • Author(s)
      戸田達史
    • Journal Title

      Current Therapy

      Volume: 28 Pages: 859-860

    • Data Source
      KAKENHI-PLANNED-22129006
  • [Journal Article] パーキンソン病のGWAS2010

    • Author(s)
      戸田達史
    • Journal Title

      Bio Clinica

      Volume: 25 Pages: 477-482

    • Data Source
      KAKENHI-PLANNED-22129006
  • [Journal Article] 孤発性パーキンソン病のリスク遺伝子2010

    • Author(s)
      戸田達史
    • Journal Title

      最新医学

      Volume: 65 Pages: 806-813

    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] パーキンソン病のGWAS2010

    • Author(s)
      戸田達史
    • Journal Title

      Bio Clinica

      Volume: 25 Pages: 477-482

    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] 孤発性パーキンソン病のリスク遺伝子2010

    • Author(s)
      戸田達史
    • Journal Title

      最新医学

      Volume: 65 Pages: 806-813

    • Data Source
      KAKENHI-PLANNED-22129006
  • [Journal Article] 福山型筋ジストロフィーの治療戦略2010

    • Author(s)
      戸田達史
    • Journal Title

      難病と在宅のケア

      Volume: 16 Pages: 41-43

    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] ゲノムワイド関連解析によるパーキンソン病リスク遺伝子の同定2010

    • Author(s)
      戸田達史
    • Journal Title

      医学のあゆみ

      Volume: 233 Pages: 640-642

    • Data Source
      KAKENHI-PLANNED-22129006
  • [Journal Article] 福山型筋ジストロフィー2010

    • Author(s)
      戸田達史
    • Journal Title

      JFNMH Newsletter

      Volume: 7 Pages: 2-6

    • Data Source
      KAKENHI-PLANNED-22129006
  • [Journal Article] 福山型先天性筋ジストロフィーについて2010

    • Author(s)
      戸田達史
    • Journal Title

      厚生労働科学研究事業 こころの健康科学研究

      Pages: 9-10

    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] 福山型先天性筋ジストロフィーについて2010

    • Author(s)
      戸田達史
    • Journal Title

      厚生労働科学研究事業こころの健康科学研究

      Pages: 9-10

    • Data Source
      KAKENHI-PLANNED-22129006
  • [Journal Article] パーキンソン病のゲノムワイド関連解析2009

    • Author(s)
      戸田達史
    • Journal Title

      細胞 41

      Pages: 198-202

    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] 孤発性パーキンソン病の分子遺伝学2009

    • Author(s)
      三井純, 戸田達史
    • Journal Title

      実験医学 増刊 27

      Pages: 1854-1859

    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] パーキンソン病関連遺伝子の全ゲノム関連解析2009

    • Author(s)
      戸田達史
    • Journal Title

      最新医学 64

      Pages: 872-879

    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Mutations for Gaucher disease confer a high susceptibility to Parkinson disease.2009

    • Author(s)
      Mitsui J, Mizuta I, Toyoda A, Ashida R, Takahashi Y, Goto J, Fukuda Y, Date H, Iwata A, Yamamoto M, Hattori N, Murata M, Toda T, Tsuji S.
    • Journal Title

      Arch Neurol 66

      Pages: 571-576

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] 福山型筋ジストロフィーおよび類縁疾患の病態・治療戦略2009

    • Author(s)
      戸田達史
    • Journal Title

      臨床神経学 49

      Pages: 859-862

    • NAID

      10026290982

    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] パーキンソン病関連遺伝子の全ゲノム関連解析2009

    • Author(s)
      戸田達史
    • Journal Title

      最新医学 64

      Pages: 872-879

    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] Delivery of the aggregate inhibitor peptide QBP1 into the mouse brain using PTDs and its therapeutic effect on polyglutamine disease mice.2009

    • Author(s)
      Popiel HA, Nagai Y, Fujikake N, Toda T.
    • Journal Title

      Neurosci Lett 449

      Pages: 87-92

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease2009

    • Author(s)
      Sidransky E, Nalls MA, Aasly JO, Aharon-Peretz J, Annesi G, Barbosa ER, Bar-Shira A, Berg D, Bras J, Brice A, Chen CM, Clark LN, Condroyer C, De Marco EV, Durr A, Eblan MJ, Fahn S, Farrer MJ, Fung HC, Gan-Or Z, Gasser T, Gershoni-Baruch R, Giladi N, Griffith A, Gurevich T, Januario C, Kropp P, Lang AE, Lee-Chen GJ, Lesage S, Marder K, Mata IF, Mirelman A, Mitsui J, Mizuta I, Nicoletti G, Oliveira C, Ottman R, Orr-Urtreger A, Pereira LV, Quattrone A, Rogaeva E, Rolfs A, Rosenbaum H, Rozenberg R, Samii A, Samaddar T, Schulte C, Sharma M, Singleton A, Spitz M, Tan EK, Tayebi N, Toda T, Troiano AR, Tsuji S, Wittstock M, Wolfsberg TG, Wu YR,
    • Journal Title

      N Engl J Med 361

      Pages: 1651-1661

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Residual laminin-binding activity and enhanced dystroglycan glycosylation in novel model mice to dystroglycanopathy.2009

    • Author(s)
      Kanagawa M, Nishimoto A, Chiyonobu T, Takeda S, Miyagoe-Suzuki Y, Wang F, Fujikake N, Taniguchi M, Lu Z, Tachikawa M, Nagai Y, Tashiro F, Miyazaki J, Tajima Y, Takeda S, Endo T, Kobayashi K, Campbell KP, Toda T
    • Journal Title

      Hum Mol Genet 18

      Pages: 621-631

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.2009

    • Author(s)
      Sidransky E, Nalls MA, Aasly JO, ...Toda T, et al.
    • Journal Title

      N Engl J Med 361

      Pages: 1651-1661

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] Residual laminin-binding activity and enhanced dystroglycan glycosylation in novel model mice to dystroglycanopathy.2009

    • Author(s)
      Kanagawa M, Nishimoto A, Chiyonobu T, Takeda S, Miyagoe-Suzuki Y, Wang F, Fujikake N, Taniguchi M, Lu Z, Tachikawa M, Nagai Y, Tashiro F, Miyazaki J, Tajima Y, Takeda S, Endo T, Kobayashi K, Campbell KP, Toda T.
    • Journal Title

      Hum Mol Genet 18

      Pages: 621-631

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease2009

    • Author(s)
      Satake W, Nakabayashi Y, Mizuta I, Hirota Y, Ito C, Kubo M, Kawaguchi T, Tsunoda T, Watanabe M, Takeda A, Tomiyama H, Nakashima K, Hasegawa K, Obata F, Yoshikawa T, Kawakami H, Sakoda S, Yamamoto M, Hattori N, Murata M, Nakamura Y, Toda T.
    • Journal Title

      Nature Genet 41

      Pages: 1303-1307

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Is g an entity? A Japanese twin study using syllogisms and intelligence tests.2009

    • Author(s)
      Shikishima C, Hiraishi K, Yamagata S, Sugimoto Y, Takemura R, Ozaki K, Okada M, Toda T, Ando J.
    • Journal Title

      Intelligence 37

      Pages: 256-267

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Surface plasmon resonance characterization of specific binding of polyglutamine aggregate inhibitors to the expanded polyglutamine stretch.2009

    • Author(s)
      Okamoto Y, Nagai Y, Fujikake N, Popiel HA, Yoshioka T, Toda T, Inui T.
    • Journal Title

      Biochem Biophys Res Commun 378

      Pages: 634-639

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] パーキンソン病のゲノミックス2009

    • Author(s)
      戸田達史
    • Journal Title

      老年精神医学雑誌 20

      Pages: 973-979

    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease.2009

    • Author(s)
      Satake W, Nakabayashi Y, Mizuta I, Hirota Y, Ito C, Kubo M, Kawaguchi T, Tsunoda T, Watanabe M, Takeda A, Tomiyama H, Nakashima K, Hasegawa K, Obata F, Yoshikawa T, Kawakami H, Sakoda S, Yamamoto M, Hattori N, Murata M, Nakamura Y, Toda T
    • Journal Title

      Nature Genet 41

      Pages: 1303-1307

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] Fukutin gene retrotransposal insertion in a non-Japanese Fukuyama congenital muscular dystrophy (FCMD) patient.2009

    • Author(s)
      Xiong H, Wang S, Kobayashi K, Jiang Y, Wang J, Chang X, Yuan Y, Liu J, Toda T, Fukuyama Y, Wu X.
    • Journal Title

      Am J Med Genet 149A

      Pages: 2403-2408

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] Mutation analysis for DJ-1 in sporadic and familial parkinsonism : screening strategy in parkinsonism.2009

    • Author(s)
      Tomiyama H, Li Y, Yoshino H, Mizuno Y, Kubo S, Toda T, Hattori N.
    • Journal Title

      Neurosci Lett 455

      Pages: 159-161

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] パーキンソン病のゲノムワイド関連解析2009

    • Author(s)
      戸田達史
    • Journal Title

      細胞 41

      Pages: 198-202

    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] Mutations for Gaucher disease confer a high susceptibility to Parkinson disease.2009

    • Author(s)
      Mitsui J, Mizuta I, Toyoda A, Ashida R, Takahashi Y, Goto J, Fukuda Y, Date H, Iwata A, Yamamoto M, Hattori N, Murata M, Toda T, Tsuji S.
    • Journal Title

      Arch Neurol 66

      Pages: 571-576

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] パーキンソン病のゲノミックス2009

    • Author(s)
      戸田達史
    • Journal Title

      老年精神医学雑誌 20

      Pages: 973-979

    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Delivery of the aggregate inhibitor peptide QBP1 into the mouse brain using PTDs and its therapeutic effect on polyglutamine disease mice.2009

    • Author(s)
      Popiel HA, Nagai Y, Fujikake N, Toda T
    • Journal Title

      Neurosci Lett 449

      Pages: 87-92

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] Is g an entity? A Japanese twin study using syllogisms and intelligence tests.2009

    • Author(s)
      Shikishima C, Hiraishi K, Yamagata S, Sugimoto Y, Takemura R, Ozaki K, Okada M, Toda T, Ando J.
    • Journal Title

      Intelligence 37

      Pages: 256-267

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] 福山型筋ジストロフィーおよび類縁疾患の病態・治療戦略2009

    • Author(s)
      戸田達史
    • Journal Title

      臨床神経学 49

      Pages: 859-862

    • NAID

      10026290982

    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] 孤発性パーキンソン病の分子遺伝学2009

    • Author(s)
      三井純, 戸田達史
    • Journal Title

      実験医学 増刊 27

      Pages: 1854-1859

    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] 福山型先天性筋ジストロフィー2009

    • Author(s)
      戸田達史
    • Journal Title

      小児科 50

      Pages: 899-906

    • NAID

      10008311277

    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] 福山型先天性筋ジストロフィー2009

    • Author(s)
      戸田達史
    • Journal Title

      小児科 50

      Pages: 899-906

    • NAID

      10008311277

    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] 孤発性パーキンソン病のゲノムワイドスクリーニング2008

    • Author(s)
      戸田達史
    • Journal Title

      ゲノム医学 8

      Pages: 21-26

    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Alzheimer病と遺伝2008

    • Author(s)
      戸田達史
    • Journal Title

      成人病と生活習慣病 38

      Pages: 1205-1210

    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] Heat shock transcription factor 1 (HSF1)-activating compounds suppress polyglutamine-induced neurodegeneration through induction of multiple molecular chaperones.2008

    • Author(s)
      Fujikake N, Nagai Y, Popiel HA, Okamoto Y, Yamaguchi M, Toda T.
    • Journal Title

      J Biol Chem 283

      Pages: 26188-26197

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] 孤発性パーキンソン病のゲノムワイドスクリーニング2008

    • Author(s)
      戸田達史
    • Journal Title

      ゲノム医学 8

      Pages: 21-26

    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] Reduced expression of sarcospan in muscles of Fukuyama congenital muscular dystrophy.2008

    • Author(s)
      Wakayama Y, Inoue M, Kojima H, Yamashita S, Shibuya S, Jimi T, Hara H, Matsuzaki Y, Oniki H, Kanagawa M, Kobayashi K, Toda T.
    • Journal Title

      Histol Histopathol 23

      Pages: 1425-1438

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] LRRK2 P755L variant in sporadic Parkinson's disease.2008

    • Author(s)
      Tomiyama H, Mizuta I, Li Y, Funayama M, Yoshino H, Li L, Murata M, Yamamoto M, Kubo SI, Mizuno Y, Toda T, Hattori N.
    • Journal Title

      J Hum Genet 53

      Pages: 1012-1015

    • NAID

      10025584966

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Alzheimer病と遺伝2008

    • Author(s)
      戸田達史
    • Journal Title

      成人病と生活習慣病 38

      Pages: 1205-1210

    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] 認知と遺伝子2008

    • Author(s)
      小林千浩, 戸田達史
    • Journal Title

      Cognition and Dementia 7

      Pages: 35-43

    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] 福山型筋ジストロフィーの発見とその類縁疾患における病態2008

    • Author(s)
      戸田達史
    • Journal Title

      蛋白質核酸酵素 53

      Pages: 1771-1780

    • NAID

      40016244595

    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Seizure-genotype relationship in Fukuyama-type congenital muscular dystrophy.2008

    • Author(s)
      Yoshioka M, Higuchi Y, Fujii T, Aiba H, Toda T.
    • Journal Title

      Brain Dev 30

      Pages: 59-67

    • NAID

      10024137147

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Calbindin 1, fibroblast growth factor 20, and ?-synuclein in Parkinson's disease.2008

    • Author(s)
      Mizuta I, Tsunoda T, Satake W, Nakabayashi Y, Watanabe M, Takeda A, Hasegawa K, Nakashima K, Yamamoto M, Hattori N, Murata M, Toda T
    • Journal Title

      Hum Genet 124

      Pages: 89-94

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] Pikachurin, a dystroglycan ligand, is essential for photoreceptor ribbon synapse formation2008

    • Author(s)
      Sato S, Omori Y, Katoh K, Kondo M, Kanagawa M, Miyata K, Funabiki K, Koyasu T, Kajimura N, Miyoshi T, Sawai H, Kobayashi K Tani A, Toda T, Usukura J, Tano Y, Fujikado T, Furukawa T.
    • Journal Title

      Nature Neurosci 11

      Pages: 923-931

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Calbindin 1, fibroblast growth factor 20, and・-synuclein in Parkinson's disease.2008

    • Author(s)
      Mizuta I, Tsunoda T, Satake W, Nakabayashi Y, Watanabe M, Takeda A, Hasegawa K, Nakashima K, Yamamoto M, Hattori N, Murata M, Toda T.
    • Journal Title

      Hum Genet 124

      Pages: 89-94

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] 福山型筋ジストロフィーの発見とその類縁疾患における病態2008

    • Author(s)
      戸田達史
    • Journal Title

      蛋白質 核酸 酵素 53

      Pages: 1771-1780

    • NAID

      40016244595

    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] Heat shock transcription factor 1 (HSF1)-activating compounds suppress polyglutamine-induced neurodegeneration through induction of multiple molecular chaperones.2008

    • Author(s)
      Fujikake N, Nagai Y, Popiel HA, Okamoto Y, Yamaguchi M, Toda T
    • Journal Title

      J Biol Chem 283

      Pages: 26188-26197

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] 福山型筋ジストロフィー2008

    • Author(s)
      戸田達史
    • Journal Title

      ビジュアル疾患解説 眼で見る遺伝病とターナ-症候群 2

      Pages: 6-7

    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] 福山型筋ジストロフィー2008

    • Author(s)
      戸田達史
    • Journal Title

      ビジュアル疾患解説眼で見る遺伝病とターナー症候群 2

      Pages: 6-7

    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Mutation analysis of the PINK1 gene in 391 patients with Parkinson's disease2008

    • Author(s)
      Kumazawa R, Tomiyama H, Li Y, Imamichi Y, Funayama M, Yoshino H, Yokochi F, Fukusako T, Takehisa Y, Kashihara K, Kondo T, Elibol B, Bostantjopoulou S, Toda T, Takahashi H, Yoshii F, Mizuno Y, Hattori N.
    • Journal Title

      Arch Neurol 65

      Pages: 802-808

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Pikachurin, a dystroglycan ligand, is essential for photoreceptor ribbon synapse formation.2008

    • Author(s)
      Sato S, Omori Y, Katoh K, Kondo M, Kanagawa M, Miyata K, Funabiki K, Koyasu T, Kajimura N, Miyoshi T, Sawai H, Kobayashi K Tani A, Toda T, Usukura J, Tano Y, Fujikado T, Furukawa T.
    • Journal Title

      Nature Neurosci 11

      Pages: 923-931

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390099
  • [Journal Article] Partial tandem duplication of GRIA3 in a male with mental retardation.2007

    • Author(s)
      Chiyonobu T, Hayashi S, Kobayashi K, Morimoto M, Miyanomae Y, Nishimura A, Nishimoto A, Ito C, Imoto I, Sugimoto T, Jia Z, Inazawa J, Toda T.
    • Journal Title

      Am J Med Genet 143

      Pages: 1448-1455

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] A toxic monomeric conformer of the polyglutamine protein.2007

    • Author(s)
      Nagai Y, Inui T, Popiel HA, Fujikake N, Hasegawa K, Urade Y, Goto Y, Naiki H, Toda T.
    • Journal Title

      Nature Struct Mol Biol 14

      Pages: 332-340

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] 神経疾患とゲノム2007

    • Author(s)
      戸田達史
    • Journal Title

      最新医学 62S

      Pages: 2153-2163

    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] 福山型遺伝子フクチン同定のヒント,幸運とそれから2007

    • Author(s)
      戸田達史
    • Journal Title

      臨床神経学 47

      Pages: 743-748

    • NAID

      10020102471

    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] 班会議に行こう?贈る言葉あれこれ2007

    • Author(s)
      戸田達史
    • Journal Title

      分子細胞治療リレー放談 6

      Pages: 494-494

    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] LRRK2 G2385R variant is a risk factor for parkinson disease in Asian population.2007

    • Author(s)
      Funayama M, Li Y, Tomiyama H, Yoshino H, Imamichi Y, Yamamoto M, Murata M, Toda T, Mizuno Y, Hattori N.
    • Journal Title

      Neuroreport 18

      Pages: 273-275

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Fibroblast growth factor 20 gene and Parkinson's disease in the Japanese population2007

    • Author(s)
      Satake W, Mizuta I, Suzuki S, Nakabayashi Y, Ito C, Watanabe M, Takeda A, Hasegawa K, Sakoda S, Yamamoto M, Hattori N, Murata M, Toda T.
    • Journal Title

      Neuroreport 18

      Pages: 937-940

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] ポストゲノム時代の神経疾患の分子遺伝学2007

    • Author(s)
      戸田達史
    • Journal Title

      神経治療学 24

      Pages: 641-645

    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] 福山型先天性筋ジストロフィー2007

    • Author(s)
      戸田達史
    • Journal Title

      Clin Neurosci 26

      Pages: 163-167

    • NAID

      10008311277

    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Defective peripheral nerve myelination and neuromuscular junction formation in fukutin-deficient chimeric mouse.2007

    • Author(s)
      Saito F, Masaki T, Saito Y, Nakamura A, Takeda S, Shimizu T, Toda T, Matsumura K.
    • Journal Title

      J Neurochem 101

      Pages: 1712-1722

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Genetically regulated epigenetic transcriptional activation of retrotransposon insertion confers mouse dactylaplasia phenotype.2007

    • Author(s)
      Kano H, Kurahashi H, Toda T.
    • Journal Title

      Proc Natl Acad Sci USA 104

      Pages: 19034-19039

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Detection of polyglutamine protein oligomers in cells by fluorescence correlation spectroscopy.2007

    • Author(s)
      Takahashi Y, Okamoto Y, Popiel HA, Fujikake N, Toda T, Kinjo M, Nagai Y.
    • Journal Title

      J Biol Chem 282

      Pages: 24039-24048

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [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

      J Hum Genet 52

      Pages: 643-649

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] PARK1, PARK4 (α-synuclein)2007

    • Author(s)
      水田 依久子, 戸田 達史
    • Journal Title

      Clinical Neuroscience 25巻1号

      Pages: 72-73

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-17590874
  • [Journal Article] パーキンソン病の分子遺伝学2007

    • Author(s)
      戸田達史
    • Journal Title

      BRAIN NERVE 59

      Pages: 815-523

    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Protein transduction domain-mediated delivery of QBP1 suppresses polyglutamine- induced neurodegeneration in vivo.2007

    • Author(s)
      Popiel HA, Nagai Y, Fujikake N, Toda T.
    • Journal Title

      Mol Ther 15

      Pages: 303-309

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Expression profiling of muscles from Fukuyama-type congenital muscular dystrophy and laminin-・2 deficient congenital muscular dystrophy; is congenital muscular dystrophy a primary fibrotic disease?2006

    • Author(s)
      Taniguchi M, Kurahashi H, Noguchi S, Sese J, Okinaga T, Tsukahara T, Guicheney P, Ozono K, Nishino I, Morishita S, Toda T.
    • Journal Title

      Biochem Biophys Res Commun 342

      Pages: 489-502

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] 121個の候補遺伝子関連解析の結果、α-synucleinが孤発性パーキンソン病の疾患感受性遺伝子であることが確実となった2006

    • Author(s)
      水田 依久子, 戸田 達史
    • Journal Title

      PD Today 15巻8号

      Pages: 17-17

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-17590874
  • [Journal Article] The genetic and molecular basis of muscular dystrophy: roles of cell-matrix linkage in the pathogenesis.2006

    • Author(s)
      Kanagawa M, Toda T.
    • Journal Title

      J Hum Genet 51

      Pages: 915-927

    • NAID

      10019380269

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries.2006

    • Author(s)
      Tomiyama H, Li Y, Funayama M, Hasegawa K, Yoshino H, Kubo S, Sato K, Hattori T, Lu CS, Inzelberg R, Djaldetti R, Melamed E, Amouri R, Gouider-Khouja N, Hentati F, Hatano Y, Wang M, Imamichi Y, Mizoguchi K, Miyajima H, Obata F, Toda T, Farrer MJ, Mizuno Y, Hattori N.
    • Journal Title

      Mov Disord 21

      Pages: 1102-1108

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Molecular interaction between fukutin and POMGnT1 in the glycosylation pathway of a-dystroglycan.2006

    • Author(s)
      Xiong H, Kobayashi K, Tachikawa M, Manya H, Takeda S, Chiyonobu T, Fujikake N, Wang F, Nishimoto A, Morris GE, Nagai Y, Kanagawa M, Endo T, Toda T.
    • Journal Title

      Biochem Biophys Res Commun 350

      Pages: 935-941

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] 福山型筋ジストロフィー2006

    • Author(s)
      戸田達史
    • Journal Title

      小児科診療 (小児科診療)

      Pages: 517-525

    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] 21個の候補遺伝子関連解析の結果、α-synucleinが孤発性パーキンソン病の疾患感受性遺伝子であることが確実となった2006

    • Author(s)
      水田 依久子, 戸田 達史
    • Journal Title

      PD Today 15巻8号

      Pages: 17-17

    • Data Source
      KAKENHI-PROJECT-17590874
  • [Journal Article] Cytoprotective effect of novel histone deacetylase inhibitors against polyglutamine toxicity.2006

    • Author(s)
      Kariya S, Hirano M, Uesato S, Nagai Y, Nagaoka Y, Furiya Y, Asai H, Fujikake N, Toda T, Ueno S.
    • Journal Title

      Neurosci Lett 392

      Pages: 213-215

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Clinical heterogeneity of a-synuclein gene duplication in Parkinson's disease.2006

    • Author(s)
      Nishioka K, Hayashi S, Farrer MJ, Singleton AB, Yoshino H, Imai H, Kitami T, Sato K, Kuroda R, Tomiyama H, Mizoguchi K, Murata M, Toda T, Imoto I, Inazawa J, Mizuno Y, Hattori N.
    • Journal Title

      Ann Neurol 59

      Pages: 298-309

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Registry of adolescent and young adult twins in the Tokyo area.2006

    • Author(s)
      Shikishima C, Ando J, Ono Y, Toda T, Yoshimura K.
    • Journal Title

      Twin Res Hum Genet 9

      Pages: 811-816

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Candidate genes for male factor infertility- validation.2006

    • Author(s)
      Mori T, Kurahashi H, Shinka T, Nakahori Y, Taniguchi M, Toda T, Iwamoto T.
    • Journal Title

      Fertil Steril 86

      Pages: 1553-1554

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Multiple candidate gene analysis identifies a-synuclein as a susceptibility gene for sporadic Parkinson's disease.2006

    • Author(s)
      Mizuta I, Satake W, Nakabayashi Y, Ito C, Suzuki S, Momose Y, Nagai Y, Oka A, Inoko H, Fukae J, Saito Y, Sawabe M, Murayama S, Yamamoto M, Hattori N, Murata M, Toda T.
    • Journal Title

      Hum Mol Genet 15

      Pages: 1151-1158

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Aberrant neuromuscular junctions and delayed terminal muscle fiber maturation in・-dystroglycanopathies2006

    • Author(s)
      Taniguchi M, Kurahashi H, Noguchi S, Fukudome T, Okinaga T, Tsukahara T, Tajima Y, Ozono K, Nishino I, Nonaka I, Toda T.
    • Journal Title

      Hum Mol Genet 15

      Pages: 1279-1289

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] A case of Fukuyama-type congenital muscular dystrophy with a very mild mental deficit.2006

    • Author(s)
      Hino-Fukuyo N, Haginoya K, Hayashi YK, Nishino I, Murakami T, Nonaka I, Togashi K, Tanaka S, Takayanagi M, Yokoyama H, Sakamoto O, Abe T, Toda T, Iinuma K.
    • Journal Title

      Neuromuscul Disord 16

      Pages: 274-276

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Unique tauopathy in Fukuyama-type congenital muscular dystrophy.2005

    • Author(s)
      Saito Y, Motoyoshi Y, Kashima K, Izumiyama-Shimomura N, Toda T, Nakano I, Hasegawa M, Murayama S.
    • Journal Title

      J Neuropath Exp Neurol 64

      Pages: 1118-1126

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Fukutin and a-dystroglycanopahties2005

    • Author(s)
      Toda T, Chiyonobu T, Xiong H, Tachikawa M, Kobayashi K, Manya H, Takeda S, Taniguchi M, Kurahashi H, EndoT.
    • Journal Title

      Acta Myologica 24

      Pages: 60-63

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] An autosomal dominant cerebellar ataxia linked to chomosome 16q22.1 is associated with a single-nucleotide substitution in the 5ォ untranslated region of the gene encoding a novel 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

      Pages: 280-296

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] b4GalT-II is a key regulator of glycosylation of the proteins involved in neuronal development.2005

    • Author(s)
      Sasaki N, Manya H, Okubo R, Kobayashi K, Ishida H, Toda T, Endo T, Nishihara S.
    • Journal Title

      Biochem Biophys Res Commun 333

      Pages: 131-137

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Basement membrane fragility underlies embryonic lethality in fukutin-null mice.2005

    • Author(s)
      Kurahashi H, Taniguchi M, Meno C, Taniguchi Y, Takeda S, Horie M, Otani H, Toda T.
    • Journal Title

      Neurobiol Dis 19

      Pages: 208-217

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Clinicogenetic study of PINK1 mutations in autosomal recessive early-onset parkinsonism2005

    • Author(s)
      Li Y, Tomiyama H, Sato K, Hatano Y, Yoshino H, Atsumi M, Kitaguchi M, Sasaki S, Kawaguchi S, Miyajima H, Toda T, Mizuno Y, Hattori N.
    • Journal Title

      Neurology 64

      Pages: 1955-1957

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Effects of fukutin deficiency in the developing mouse brain.2005

    • Author(s)
      Chiyonobu T, Sasaki J, Nagai Y, Takeda S, Funakoshi H, Nakamura T, Sugimoto T, Toda T.
    • Journal Title

      Neuromuscul Disord 15

      Pages: 416-426

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Founder SVA retrotransposal insertion in Fukuyama-type congenital muscular dystrophy and its origin in Japanese and Northeast Asian populations.2005

    • Author(s)
      Watanabe M, Kobayashi K, Jin F, Park KS, Yamada T, Tokunaga K, Toda T.
    • Journal Title

      Am J Med Genet 138

      Pages: 344-348

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Alternative splicing regulates the transcriptional activity of Drosophila heat shock transcription factor in response to heat/cold stress.2005

    • Author(s)
      Fujikake N, Nagai Y, Popiel HA, Kano H, Yamaguchi M, Toda T.
    • Journal Title

      FEBS lett 579

      Pages: 3842-3848

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Humanin attenuates apoptosis induced by DRPLA proteins with expanded polyglutamine stretches.2005

    • Author(s)
      Kariya S, Hirano M, Nagai Y, Furiya Y, Fujikake N, Toda T, Ueno S.
    • Journal Title

      J Mol Neurosci 25

      Pages: 165-169

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Genomic rearrangement at 10q24 in non-syndromic split-hand/split-foot malformation.2005

    • Author(s)
      Kano H, Kurosawa K, Horii E, Ikegawa S, Yoshikawa H, Kurahashi H, Toda T.
    • Journal Title

      Hum Genet 118

      Pages: 477-483

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Fukutin and a-dystroglycanopahties.2005

    • Author(s)
      Toda T
    • Journal Title

      Acta Myologica 24

      Pages: 60-30

    • Data Source
      KAKENHI-PROJECT-17019044
  • [Journal Article] Toward identification of susceptibility genes for sporadic Parkinson' s disease.2003

    • Author(s)
      Toda T
    • Journal Title

      J Neurol 250

      Pages: 40-43

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-14013037
  • [Journal Article] Toward identification of susceptibility genes for sporadic Parkinson' s disease.2003

    • Author(s)
      Toda T, et al.
    • Journal Title

      J Neurol 250

      Pages: 40-43

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-14013037
  • [Patent] ジストログリカン糖鎖修飾異常に伴う疾患の治療剤及び関連酵素測定法2022

    • Inventor(s)
      戸田達史,小林千浩,金川基,遠藤玉夫,萬谷博,和田芳直,田尻道子
    • Industrial Property Rights Holder
      戸田達史,小林千浩,金川基,遠藤玉夫,萬谷博,和田芳直,田尻道子
    • Industrial Property Rights Type
      特許
    • Filing Date
      2022
    • Acquisition Date
      2022
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Patent] 腎毒性軽減剤2022

    • Inventor(s)
      園家暁,藤原佳絵,戸田達史,池田真理子,小林千浩、他
    • Industrial Property Rights Holder
      園家暁,藤原佳絵,戸田達史,池田真理子,小林千浩、他
    • Industrial Property Rights Type
      特許
    • Industrial Property Number
      2021-113495
    • Filing Date
      2022
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Patent] 腎毒性軽減剤2022

    • Inventor(s)
      園家暁,藤原佳絵,戸田達史,池田真理子,小林千浩、他
    • Industrial Property Rights Holder
      園家暁,藤原佳絵,戸田達史,池田真理子,小林千浩、他
    • Industrial Property Rights Type
      特許
    • Filing Date
      2022
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Patent] 腎毒性軽減剤2022

    • Inventor(s)
      園家暁,藤原佳絵,戸田達史,池田真理子,小林千浩、他
    • Industrial Property Rights Holder
      園家暁,藤原佳絵,戸田達史,池田真理子,小林千浩、他
    • Industrial Property Rights Type
      特許
    • Filing Date
      2022
    • Overseas
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Patent] 新規CDP-リビトール誘導体2020

    • Inventor(s)
      金川基、徳岡秀紀、戸田達史
    • Industrial Property Rights Holder
      金川基、徳岡秀紀、戸田達史
    • Industrial Property Rights Type
      特許
    • Filing Date
      2020
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Patent] 福山型筋ジストロフィー治療用アンチセンス核酸2019

    • Inventor(s)
      戸田達史他
    • Industrial Property Rights Holder
      戸田達史他
    • Industrial Property Rights Type
      特許
    • Filing Date
      2019
    • Acquisition Date
      2019
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Patent] 筋ジストロフィー関連心筋症の治療又は予防剤2018

    • Inventor(s)
      片野坂 友紀、成瀬 恵治、氏原 嘉洋、戸田 達史、金川 基
    • Industrial Property Rights Holder
      片野坂 友紀、成瀬 恵治、氏原 嘉洋、戸田 達史、金川 基
    • Industrial Property Rights Type
      特許
    • Filing Date
      2018
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Patent] ジストログリカン糖鎖修飾異常に伴う疾患の治療剤及び関連酵素測定法2016

    • Inventor(s)
      戸田達史、小林千浩、金川基、遠藤玉夫、萬谷博、和田芳直、田尻道子
    • Industrial Property Rights Holder
      戸田達史、小林千浩、金川基、遠藤玉夫、萬谷博、和田芳直、田尻道子
    • Industrial Property Rights Type
      特許
    • Filing Date
      2016
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Patent] ジストログリカン糖鎖修飾異常に伴う疾患の治療剤2016

    • Inventor(s)
      戸田 達史、小林 千浩、金川 基、他
    • Industrial Property Rights Holder
      国立大学法人神戸大学、他
    • Industrial Property Rights Type
      特許
    • Industrial Property Number
      2016-160390
    • Filing Date
      2016-08-18
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Patent] 福山型筋ジストロフィー治療用医薬組成物2012

    • Inventor(s)
      戸田 達史、 小林 千浩、 池田 真理子
    • Industrial Property Rights Holder
      戸田 達史、 小林 千浩、 池田 真理子
    • Industrial Property Rights Type
      特許
    • Industrial Property Number
      2012-086891
    • Filing Date
      2012-04-05
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Patent] 福山型筋ジストロフィー治療用医薬組成物2012

    • Inventor(s)
      戸田達史, 小林千浩, 池田真理子
    • Industrial Property Rights Holder
      国立大学法人神戸大学
    • Industrial Property Rights Type
      特許
    • Filing Date
      2012-04-05
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Patent] 福山型筋ジストロフィー治療用医薬組成物2012

    • Inventor(s)
      戸田 達史、 小林 千浩、 池田 真理子
    • Industrial Property Rights Holder
      戸田 達史、 小林 千浩、 池田 真理子
    • Industrial Property Rights Type
      特許
    • Industrial Property Number
      2012-086891
    • Filing Date
      2012-04-05
    • Data Source
      KAKENHI-PLANNED-22129006
  • [Patent] パーキンソン病発症リスクマーカー2010

    • Inventor(s)
      戸田達史
    • Industrial Property Rights Holder
      エーザイ・アール・アンド・デイーマネジメント株式会社
    • Filing Date
      2010-05-14
    • Data Source
      KAKENHI-PROJECT-20390099
  • [Patent] パーキンソン病発症リスクマーカー2010

    • Inventor(s)
      戸田達史
    • Industrial Property Rights Holder
      エーザイ・アール・アンド・ディーマネジメント株式会社
    • Filing Date
      2010-05-14
    • Data Source
      KAKENHI-PLANNED-22129006
  • [Presentation] Recent advance in Fukuyma Muscular Dystrophy and dystroglycanopathies2022

    • Author(s)
      戸田 達史
    • Organizer
      12th Japanese-French Workshop
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Presentation] 福山型筋ジストロフィーの原因究明と治療開発2022

    • Author(s)
      戸田 達史
    • Organizer
      第64回小児神経学会学術集会
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Presentation] Recent advances in Alpha-dystroglycanopathy.2022

    • Author(s)
      戸田 達史
    • Organizer
      Beijing Pediatric Neurology International Forum
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Presentation] 遺伝医学の観点から見た着床前遺伝学的検査2022

    • Author(s)
      戸田 達史
    • Organizer
      日本学術会議 学術フォーラム ヒトゲノム編集と着床前遺伝学的検査について考えるー新しい医療技術の利用のあり方
    • Invited
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Presentation] 「なおらない」から「なおる」脳神経内科へ パーキンソン病と福山型筋ジストロフィーの解明と分子標的治療2022

    • Author(s)
      戸田達史
    • Organizer
      むさし神経Forum
    • Invited
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Presentation] Advance in Fukuyama muscular dystrophy & dystroglycanopathy,2022

    • Author(s)
      戸田 達史
    • Organizer
      第13回International Myotonic Dystrophy Consortium Meeting
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Presentation] Neurologists' Recommendations for Basic Research2022

    • Author(s)
      戸田 達史
    • Organizer
      NEURO2022
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Presentation] 薬事承認申請をめざした福山型筋ジストロフィーにおけるアンチセンス核酸NS-035の第1/2相試験(ステップ2)2021

    • Author(s)
      戸田達史
    • Organizer
      AMED 2020年度成果報告会
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Presentation] Antisense Oligonucleotide therapy for Fukuyama muscular dystrophy and recent advance in dystroglycanopathies2021

    • Author(s)
      戸田達史
    • Organizer
      PACTALS2021NAGOYAPan-Asia Consortium for Treatment and Research I n ALS
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Presentation] 福山型筋ジストロフィーの病態解明と治療法の開発2021

    • Author(s)
      戸田達史
    • Organizer
      みずほ総研 水曜メディカルカンファレンス
    • Invited
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Presentation] 「なおる」脳神経内科へ パーキンソン病の解明と核酸医薬による分子標的治療2021

    • Author(s)
      戸田達史
    • Organizer
      第34回山梨神経先端セミナー
    • Invited
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Presentation] 「なおらない」から「なおる」へ核酸医薬による分子標的治療2021

    • Author(s)
      戸田達史
    • Organizer
      日本腎臓研究会
    • Invited
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Presentation] 「なおらない」から「なおる」へ 脳神経内科疾患の解明と分子標的治療2021

    • Author(s)
      戸田達史
    • Organizer
      第16回第17回共催 日本神経摂食嚥下・栄養学会学術集会
    • Invited
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Presentation] Recent Advances in Alpha-dystroglycanopath2021

    • Author(s)
      戸田達史
    • Organizer
      eijing International Pediatric Neurology Forum2021
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Presentation] Genome-wide Analysis and Molecular Targeting Therapy for Neuro-Muscular Disease,2020

    • Author(s)
      戸田達史
    • Organizer
      The 11th Xiangya International Congress of the Clinical and Basic Research on Neurodegenerative Disorders and Human Neuroscience Academic Annual Conference
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Presentation] 福山型筋ジストロフィー症の核酸医薬2020

    • Author(s)
      戸田達史
    • Organizer
      第38回日本神経治療学会
    • Invited
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Presentation] 「なおらない」から「なおる」へ ゲノム科学にもとづく疾患の解明と分子標的治療~遺伝性疾患と孤発性疾患の場合2020

    • Author(s)
      戸田達史
    • Organizer
      第8回Academy of Aging and Cardiovascular-Diabetes Research
    • Invited
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] 福山型筋ジストロフィーのモデルマウスを用いた病態解明と治療戦略の開発2020

    • Author(s)
      金川基,戸田達史
    • Organizer
      第38回日本神経治療学会学術集会
    • Invited
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Presentation] 福山型筋ジストロフィーのメカニズムの解明と治療法の開発2020

    • Author(s)
      戸田達史
    • Organizer
      Kyoto Neurology Forum
    • Invited
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Presentation] 「なおらない」から「なおる」へ 脳神経内科疾患の解明と分子標的治療2020

    • Author(s)
      戸田達史
    • Organizer
      北東北神経疾患講演会2020
    • Invited
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] 福山型筋ジストロフィー~解明から克服にむけて2020

    • Author(s)
      戸田達史
    • Organizer
      第6回日本筋学会
    • Invited
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Presentation] Genome-wide Analysis and Molecular Targeting Therapy for Neuro-Muscular Disease2020

    • Author(s)
      戸田達史
    • Organizer
      JSHG-APSHG Joint Symposium
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20H00526
  • [Presentation] パーキンソン病・筋疾患の解明と分子標的治療2019

    • Author(s)
      戸田達史
    • Organizer
      第2回奈良脳神経内科フォーラム
    • Invited
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] Antisense Therapy for Fukuyama Type Congenital Muscular Dystrophy and Our Recent Advance in Parkinson’s Disease2019

    • Author(s)
      戸田達史
    • Organizer
      中国医学科学院医学生物学研究所主催セミナー
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] 福山型筋ジストロフィー遺伝子の発見から診断と治療、最新の知見2019

    • Author(s)
      戸田達史
    • Organizer
      第17回東北・北海道代謝異常症研究会
    • Invited
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] 福山型筋ジストロフィー―解明から克服に向けて―2019

    • Author(s)
      戸田達史
    • Organizer
      第6回筋ジストロフィー医療研究会
    • Invited
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] 福山型筋ジストロフィーのすべて2019

    • Author(s)
      戸田達史
    • Organizer
      第97回NeuroMuscular Conference
    • Invited
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] 福山型筋ジストロフィーを含めた糖鎖合成異常症の系統的な解明・治療に関する研究2019

    • Author(s)
      戸田達史
    • Organizer
      日本医師会設立72周年記念式典並びに医学大会
    • Invited
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] 「なおらない」から「なおる」へ パーキンソン病・筋疾患の解明と分子標的治療,2019

    • Author(s)
      戸田達史
    • Organizer
      第10回鹿児島神経内科先端セミナー
    • Invited
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] 福山型筋ジストロフィー ―解明から克服にむけて 下志津病院から始まった私の研究―2019

    • Author(s)
      戸田達史
    • Organizer
      第11回国立病院機構関東信越グループ神経筋ネットワーク研究会
    • Invited
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] 私が学んだ神経学、遺伝学2019

    • Author(s)
      戸田達史
    • Organizer
      第6回Neurology Forum
    • Invited
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] 福山型筋ジストロフィーを含む糖鎖合成異常症とパーキンソン病の統合的理解と治療をめざして2019

    • Author(s)
      戸田達史
    • Organizer
      神経化学会理事会企画シンポジウム
    • Invited
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] Recent advance and molecular targeting therapy in congenital muscular dystrophy2019

    • Author(s)
      戸田達史
    • Organizer
      Peking University Pediatric Neurology Forum
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] 福山型筋ジストロフィー フクチンの発見と根本的治療への挑戦2018

    • Author(s)
      戸田達史
    • Organizer
      平成30年度 独立行政法人国立病院機構 良質な医師を育てる研修「神経・筋(神経難病)診療中級研修」
    • Invited
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] Antisense Therapy for Fukuyama congenital muscular dystrophy (FCMD) and recent advance in dystroglycanopathies, FCMD, ISPD , and LGMD2l2018

    • Author(s)
      戸田達史
    • Organizer
      第19回国際神経病理学会
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] パーキンソン病・筋疾患の解明と分子標的治療2018

    • Author(s)
      戸田達史
    • Organizer
      Niigata Neurology Forum
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] パーキンソン病・筋疾患の解明と分子標的治療2018

    • Author(s)
      戸田達史
    • Organizer
      第17回岐阜脳神経外科研究会
    • Invited
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] 動きと神経筋疾患2018

    • Author(s)
      戸田達史
    • Organizer
      第91回日本生化学会大会
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] 福山型筋ジストロフィーをふくめた糖鎖合成異常症の系統的な解明と治療をめざして2018

    • Author(s)
      戸田達史
    • Organizer
      第4回宮城 神経・筋疾患学術講演会
    • Invited
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] 遺伝性神経難病(ALS,SCDほか)の進歩と我々の活動に関して2018

    • Author(s)
      戸田達史
    • Organizer
      第19回山梨神経難病セミナー
    • Invited
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] 筋ジストロフィーと最新治療研究開発2018

    • Author(s)
      戸田達史
    • Organizer
      平成30年度筋ジストロフィー研修会
    • Invited
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] 認知症、神経難病の解明と分子標的治療2018

    • Author(s)
      戸田達史
    • Organizer
      秋田臨床神経懇話会
    • Invited
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] Fukuyama type congenital muscular dystrophy2018

    • Author(s)
      戸田達史
    • Organizer
      IJCGM International Joint Conference on Genetics&Medicine
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] Fukutin is ribito 5-phosphate transferase: recent advance in Fukuyma muscular dystropy, ISPD, and LGMD2I2018

    • Author(s)
      戸田達史
    • Organizer
      11th Japanese-French Workshop
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] 福山型筋ジストロフィーを含めた糖鎖合成異常症の系統的な解明と治療をめざして2018

    • Author(s)
      戸田達史
    • Organizer
      第60回日本小児神経学会学術集会
    • Invited
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] 筋ジストロフィーと最新治療研究開発2018

    • Author(s)
      戸田達史
    • Organizer
      第10回生きていくこと、呼吸すること
    • Invited
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] 認知症、神経難病の解明と分子標的治療2018

    • Author(s)
      戸田達史
    • Organizer
      秋田臨床神経懇話会 特別講演会
    • Invited
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] 福山型筋ジストロフィーを含めた糖鎖合成異常症の系統的な解明と新しい糖鎖の発見2017

    • Author(s)
      戸田達史
    • Organizer
      日本筋学会第3回学術集会
    • Invited
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] 疾患遺伝子の発見から新しい治療法の開発2017

    • Author(s)
      戸田達史
    • Organizer
      生命科学系合同年次大会シンポジウム
    • Invited
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] 疾患遺伝子の発見から新しい治療法の開発2017

    • Author(s)
      戸田達史
    • Organizer
      生命科学系合同年次大会シンポジウム
    • Invited
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] Identification of a new glycosylation with ribitol-phosphate and its defect in ISPD, FCMD and LGMD2I2017

    • Author(s)
      Tatsushi Toda
    • Organizer
      5th International Workshop for Glycosylation Defects in Muscular Dystrophies
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] Fukutin is Ribitol 5-Phosphate Transferase: Recent Advance in Fukuyama Muscular Dystrophy2017

    • Author(s)
      戸田達史
    • Organizer
      14th Asian and Oceanian Congress of Child Neurology
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] Identification of a posttranslational modification with ribitol-phosphate and its defect in muscular dystrophy2017

    • Author(s)
      Tatsushi Toda
    • Organizer
      East Asian Unit of Himan Genetics Society
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] Identification of a posttranslational modification with ribitol-phosphate and its defect in muscular dystrophy2017

    • Author(s)
      戸田達史
    • Organizer
      East Asian Unit of Himan Genetics Society
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] 福山型筋ジストロフィーを含めた糖鎖合成異常症の系統的な解明と新しい糖鎖の発見2017

    • Author(s)
      戸田達史
    • Organizer
      日本筋学会第3回学術集会
    • Invited
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] Genomewide Analysis and Molecular Targeting for Neurological Diseases2017

    • Author(s)
      Tatsushi Toda
    • Organizer
      International Symposium on Smart Brain Medical Informatics and Engineering
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] Genetics and nucleic acid therapeutics of Fukuyama muscular dystrophy2017

    • Author(s)
      戸田達史
    • Organizer
      第一回国際がんプレシジョン医療カンファレンス
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] Fukutin is Ribitol 5-Phosphate Transferase: Recent Advance in Fukuyama Muscular Dystrophy2017

    • Author(s)
      Tatsushi Toda
    • Organizer
      14th Asian and Oceanian Congress of Child Neurology
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] Identification of a new glycosylation with ribitol-phosphate and its defect in ISPD, FCMD and LGMD2I2017

    • Author(s)
      戸田達史
    • Organizer
      5th International Workshop for Glycosylation Defects in Muscular Dystrophies
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-17H01563
  • [Presentation] Genetics and nucleic acid therapeutics of Fukuyama muscular dystrophy2017

    • Author(s)
      Tatsushi Toda
    • Organizer
      第一回国際がんプレシジョン医療カンファレンス
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] 福山型先天性筋ジストロフィーの治療法開発2016

    • Author(s)
      戸田 達史
    • Organizer
      第57回日本神経学会学術大会
    • Place of Presentation
      神戸国際会議場・神戸国際展示場・神戸ポートピアホテル(神戸)
    • Year and Date
      2016-05-19
    • Invited
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] Identification of a Post-translational Modification with Ribitol-Phosphate and Its Defect in Muscular Dystrophy.2016

    • Author(s)
      Tatsushi Toda
    • Organizer
      21st WMS congress 2016
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] 筋ジストロフィーの分子機構と治療戦略2016

    • Author(s)
      戸田 達史
    • Organizer
      第113回日本内科学会
    • Place of Presentation
      東京国際フォーラム(東京)
    • Year and Date
      2016-04-15
    • Invited
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] 福山型先天性筋ジストロフィーの治療法開発2016

    • Author(s)
      戸田 達史
    • Organizer
      第57回日本神経学会学術大会
    • Invited
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] 筋ジストロフィーの分子機構と治療戦略2016

    • Author(s)
      戸田 達史
    • Organizer
      第113回日本内科学会
    • Invited
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] Genome-wide Analysis and Molecular Targeting Therapy for Neuro-Muscular deisease.2016

    • Author(s)
      Tatsushi Toda
    • Organizer
      2016 Taiwan-Japan Joint Conference on Genomic Studies and Annual Retreat of Taiwan Genomics and Genetics Society.
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] Identification of a post-translational modification with ribitol-phosphate and its defect in muscular dystrophy.2016

    • Author(s)
      Tatsushi Toda
    • Organizer
      Warren Workshop VI 2016
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] 福山型筋ジストロフィーをはじめとするジストログリカン異常症の分子病態と治療2016

    • Author(s)
      戸田 達史
    • Organizer
      第2回日本筋学会学術集会
    • Invited
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] Gene Therapy for Transposon Disease2016

    • Author(s)
      Tatsushi Toda
    • Organizer
      第57回日本神経学会学術大会
    • Invited
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] Gene Therapy for Transposon Disease2016

    • Author(s)
      戸田 達史
    • Organizer
      第57回日本神経学会学術大会
    • Place of Presentation
      神戸国際会議場・神戸国際展示場・神戸ポートピアホテル(神戸)
    • Year and Date
      2016-05-19
    • Invited
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] 福山型筋ジストロフィーをはじめとするジストログリカン異常症の分子病態と治療2016

    • Author(s)
      戸田 達史
    • Organizer
      第2回日本筋学会学術集会
    • Place of Presentation
      国立精神・神経医療研究センター(東京)
    • Year and Date
      2016-08-06
    • Invited
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] Recent Advances in Muscular Dystrophy2015

    • Author(s)
      Tatsushi Toda
    • Organizer
      UNIVERSITY OF WASHINGTON-KOBE UNIVERSITY SYMPOSIUM ON CELL SIGNALING
    • Place of Presentation
      seattle, the U.S.A.
    • Year and Date
      2015-09-10
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] Genomewide analysis and molecular targeting therapy for neurological diseases2015

    • Author(s)
      Tatsushi Toda
    • Organizer
      nature conference - Genomic Variations in Precision Medicine 2015
    • Place of Presentation
      Changsha, China
    • Year and Date
      2015-05-17
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] 福山型筋ジストロフィー及び類縁疾患の糖鎖病態と分子標的治療2015

    • Author(s)
      戸田 達史
    • Organizer
      第38回日本分子生物学会年会、第88回日本生化学会大会 合同大会
    • Place of Presentation
      神戸ポートアイランド(神戸)
    • Year and Date
      2015-12-02
    • Invited
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] Use of antisense oligonucleotides in FCMD mouse models.2015

    • Author(s)
      Tatsushi Toda
    • Organizer
      212th ENMC International Workshop Animal models of Congenital Muscular Dystrophies
    • Place of Presentation
      Naarden, Netherlands
    • Year and Date
      2015-05-19
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] α-dystroglycanopathy and molecular targeting therapy.2015

    • Author(s)
      Tatsushi Toda
    • Organizer
      Fourth International Workshop for Glycosylation Defects in Muscular Dystrophies.
    • Place of Presentation
      NC, U.S.A.
    • Year and Date
      2015-04-16
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] Recent Advances in Genetics of α-Dystroglycanopathy.2015

    • Author(s)
      Tatsushi Toda
    • Organizer
      the 13th Asian & Oceanian Congress of Child Neurology (AOCCN)
    • Place of Presentation
      Taipei, Taiwan
    • Year and Date
      2015-05-14
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] Molecular pathogenesis & molecular targeting therapy for a- dystroglycanopathy.2015

    • Author(s)
      Tatsushi Toda
    • Organizer
      The 10th Japanese-French Workshop “New advances in treatments of neuromuscular diseases: From Basic to Applied Myology.”
    • Place of Presentation
      Paris, France
    • Year and Date
      2015-07-03
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] Genomewide Analysis and Molecular Targeting Therapy for Parkinson’s Disease and Muscular Dystrophy.2014

    • Author(s)
      Tatsushi Toda
    • Organizer
      SYMPOSIUM ON MEMBRANE BIOLOGY.
    • Place of Presentation
      University of Washington, Seattle U.S.A.
    • Invited
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Presentation] Risk genes and genome research of sporadic Parkinson’s disease2014

    • Author(s)
      Satake W, Toda T
    • Organizer
      The 20th International Congress of Personalized Medicine
    • Place of Presentation
      Tokyo
    • Year and Date
      2014-11-15
    • Invited
    • Data Source
      KAKENHI-PROJECT-25670420
  • [Presentation] Genomewide Analysis and Molecular Targeting Therapy for Parkinson’s Disease and Muscular Dystrophy2014

    • Author(s)
      Toda T.
    • Organizer
      SYMPOSIUM ON MEMBRANE BIOLOGY
    • Place of Presentation
      University of Washington, Seattle, U.S.A.
    • Invited
    • Data Source
      KAKENHI-PLANNED-22129006
  • [Presentation] Search for rare-variant risks of Parkinson’s disease by sequencing of candidate genes and exome sequencing.2013

    • Author(s)
      Satake W, Ando Y, Tomiyama H, Takeda A, Hasegawa K, Yamamoto M, Murata M, Hattori N, Toda T.
    • Organizer
      The MDS 17th International Congress of Parkinson's Disease and Movement Disorders.
    • Place of Presentation
      Sydney Convention and Exhibition Centre, Sydney, Australia
    • Data Source
      KAKENHI-PLANNED-22129006
  • [Presentation] Search for rare-variant risks of Parkinson’s disease by sequencing of candidate genes and exome sequencing2013

    • Author(s)
      Satake W, Ando Y, Tomiyama H, Takeda A, Hasegawa K, Yamamoto M, Murata M, Hattori N, Toda T
    • Organizer
      The MDS 17th International Congress of Parkinson's Disease and Movement Disorders
    • Place of Presentation
      Sydney Convention and Exhibition Centre, Sydney, Australia
    • Data Source
      KAKENHI-PLANNED-22129006
  • [Presentation] Alpha-dystroglycanopathy and molecular targeting therapy.2013

    • Author(s)
      Tatsushi Toda
    • Organizer
      Third International Workshop for Glycosylation Defects in Muscular Dystrophies.
    • Place of Presentation
      Omni Charlotte Hotel,Charlotte NC, U.S.A.
    • Invited
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Presentation] 福山型など糖鎖異常による筋ジストロフィーの病態と分子標的治療. 脳・神経・筋疾患と糖.2013

    • Author(s)
      戸田 達史
    • Organizer
      第32回日本糖質学会年会
    • Place of Presentation
      大阪国際交流センター
    • Invited
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Presentation] Alpha-dystroglycanopathy and molecular targeting therapy2013

    • Author(s)
      Tatsushi Toda
    • Organizer
      Third International Workshop for Glycosylation Defects in Muscular Dystrophies
    • Place of Presentation
      Omni Charlotte Hotel, Charlotte NC. U.S.A.
    • Year and Date
      2013-04-18
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Presentation] 福山型筋ジストロフィーの分子標的治療2013

    • Author(s)
      戸田 達史
    • Organizer
      第20回日本遺伝子診療学会大会
    • Place of Presentation
      アクトシティ浜松コングレスセンター 静岡
    • Invited
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Presentation] GWAS and pathology: How are they connected?2013

    • Author(s)
      Toda T.
    • Organizer
      The MDS 17th International Congress of Parkinson's Disease and Movement Disorders.
    • Place of Presentation
      Sydney Convention and Exhibition
    • Invited
    • Data Source
      KAKENHI-PLANNED-22129006
  • [Presentation] 糖鎖異常筋ジストロフィーの分子病態とAAV治療2013

    • Author(s)
      戸田 達史
    • Organizer
      日本人類遺伝学会第58回大会
    • Place of Presentation
      江陽グランドホテル
    • Invited
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Presentation] Exome sequencing of Parkinson's disease in order to identify genetic variants with high disease-risk.2013

    • Author(s)
      Satake W, Suzuki Y, Ando Y, Tomiyama H, Yamamoto M, Murata M, Hattori N, Tsuji S, Sugano S, Toda T.
    • Organizer
      American Society of Human Genetics Annual meeting 2013.
    • Place of Presentation
      Boston Convention & Exhibition Center (BCEC), Boston, U.S.A.
    • Data Source
      KAKENHI-PLANNED-22129006
  • [Presentation] Genomics and molecular targeting therapy of neurological diseases.2013

    • Author(s)
      Tatsushi Toda
    • Organizer
      The 13th Annual Meeting of East Asian Union of Human Genetics Societies in conjunction with the 9th National Congress of Genetics Society of China.
    • Place of Presentation
      Harbin, China
    • Invited
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Presentation] 福山型筋ジストロフィー―Fukutinの発見・病態から,治療をめざして2013

    • Author(s)
      戸田 達史
    • Organizer
      第55回日本小児神経学会学術集会
    • Place of Presentation
      iichiko総合文化センター 大分
    • Invited
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Presentation] Japanese 2nd GWAS Identifies Strong Association at a Novel Risk Locus and MCCC1 for Parkinson's Disease.2013

    • Author(s)
      Toda T, Satake W, Yamamoto M, Hattori N, Murata M, Japanese PD Gene Consortium.
    • Organizer
      he 11th international conference on alzheimer’s and parkinson’s diseases
    • Place of Presentation
      Firenze Fiera, Florence, Italy,
    • Data Source
      KAKENHI-PLANNED-22129006
  • [Presentation] αジストログリカノパチー 筋疾患研究最前線2013

    • Author(s)
      戸田 達史
    • Organizer
      第54回日本神経学会学術大会
    • Place of Presentation
      東京国際フォーラム
    • Invited
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Presentation] GWAS and pathology: How are they connected?2013

    • Author(s)
      Toda T.
    • Organizer
      The MDS 17th International Congress of Parkinson's Disease and Movement Disorders
    • Place of Presentation
      Sydney Convention and Exhibition Centre, Sydney, Australia
    • Invited
    • Data Source
      KAKENHI-PLANNED-22129006
  • [Presentation] 福山型筋ジストロフィーの分子標的治療2012

    • Author(s)
      戸田達史
    • Organizer
      第53回日本神経学会学術大会
    • Place of Presentation
      東京国際フォーラム
    • Invited
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Presentation] RNA-based mechanism and therapy for muscular dystrophy.2012

    • Author(s)
      戸田達史, 池田真理子, 小林千浩
    • Organizer
      第35回日本分子生物学会年会
    • Place of Presentation
      福岡国際会議場・マリンメッセ福岡
    • Invited
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Presentation] 神経筋疾患のゲノミクスと分子標的治療2012

    • Author(s)
      戸田達史
    • Organizer
      第14回日本RNA学会年会
    • Place of Presentation
      東北大学百周年記念会館
    • Invited
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Presentation] Molecular targeting therapy for muscular dystrophies.2012

    • Author(s)
      戸田達史
    • Organizer
      第18回日本遺伝子治療学会学術集会
    • Place of Presentation
      ホテル熊本テルサ
    • Invited
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Presentation] Molecular Targeting Therapy for Muscular Dystrophy.2012

    • Author(s)
      Tatsushi Toda
    • Organizer
      The 12th Annual Meeting of East Asian Union of Human Genetics Societies in conjunction with the 45th Scientific Meeting of Korean Society of Medical Genetics
    • Place of Presentation
      ソウル大学病院 こども病院 韓国
    • Invited
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Presentation] 筋ジストロフィーのモデル動物と分子標的治療2012

    • Author(s)
      戸田達史
    • Organizer
      日本人類遺伝学会第57回大会
    • Place of Presentation
      京王プラザホテル
    • Invited
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Presentation] 福山型筋ジストロフィー、パーキンソン病をはじめとする神経疾患の遺伝学的解析・ 病態治療解析2012

    • Author(s)
      戸田達史
    • Organizer
      第35回日本神経科学大会
    • Place of Presentation
      名古屋国際会議場
    • Invited
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Presentation] Pathogenic Exon-trapping by SVA Retrotransposon and Therapeutic Rescue with Antisense Oligonucleotide in Fukuyama Muscular Dystrophy.2012

    • Author(s)
      Tatsushi Toda
    • Organizer
      The 22nd CDB Meeting
    • Place of Presentation
      理化学研究所 発生・再生科学総合研究センター
    • Invited
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Presentation] Novel pathomechanism and molecular targeting therapy for Fukuyama CMD.2012

    • Author(s)
      Tatsushi Toda
    • Organizer
      9th Japanese-French Symposium for Muscular Dystrophy
    • Place of Presentation
      JA共済ビルカンファレンス・ホール. 東京
    • Invited
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Presentation] Fukuyama congenital muscular dystrophy - update.2012

    • Author(s)
      Tatsushi Toda
    • Organizer
      The 11th Annual Scientiafic Meeting of the Asian Oceanian Myology Center
    • Place of Presentation
      京都大学
    • Invited
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Presentation] ゲノム解析によるパーキンソン病及び認知機能関連遺伝子の同定2012

    • Author(s)
      戸田達史
    • Organizer
      第35回日本神経科学大会
    • Place of Presentation
      名古屋国際会議場
    • Invited
    • Data Source
      KAKENHI-PLANNED-22129006
  • [Presentation] AN A-SYNUCLEIN 3'-FLANKING REGION SNP INTERACTS WITH PARKINSON'S DISEASE SUSCEPTIBILITY VIA ALLELE-SPECIFIC BINDING OF A TRANSCRIPTION FACTOR2011

    • Author(s)
      Toda T
    • Organizer
      XXth World Congress of Neurology
    • Place of Presentation
      Mansour Eddhabi Congress Center(モロッコ)
    • Year and Date
      2011-11-13
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Presentation] Genome-Wide DNA Methylation and Gene Expression Analyses of Monozygotic Twins Discordant for Intelligence Levels2011

    • Author(s)
      Yu, CC., Furukawa, M., Kobayashi, K., Shikishima, C. Cha, PC., Sese, J., Sugawara, H., Iwamoto, K., Kato, T., Ando, J & Toda, T
    • Organizer
      日本人類遺伝学会第56回大会
    • Place of Presentation
      千葉(幕張メッセ)
    • Year and Date
      2011-11-12
    • Data Source
      KAKENHI-PROJECT-21223002
  • [Presentation] Dysferlin-mediated membrane repair system contributes to maintenance of skeletal muscle cell viability in mouse models for muscular dystrophy2011

    • Author(s)
      Toda T
    • Organizer
      16^<th> International Congress of the World Muscle Society
    • Place of Presentation
      Ria Park Hotels Almancil Algarve(ポルトガル)
    • Year and Date
      2011-10-19
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Presentation] Genome-Wide DNA Methylation and Gene Expression Analyses of Monozygotic Twins Discordant for Intelligence Levels2011

    • Author(s)
      CC Yu, M Furukawa, K Kobayashi, C Shikishima, PC Cha, J Sese, H Sugawara, K Iwamoto, T Kato, J Ando, T Toda
    • Organizer
      日本人類遺伝学会第56回大会
    • Place of Presentation
      幕張メッセ(千葉)
    • Year and Date
      2011-11-12
    • Data Source
      KAKENHI-PROJECT-21223002
  • [Presentation] The dysferlin-mediated membrane repair system contributes to maintenance of skeletal muscle cell viability in mouse models of muscular dystrophy2011

    • Author(s)
      戸田 達史
    • Organizer
      世界筋学会
    • Place of Presentation
      アルマンシル、ポルトガル
    • Data Source
      KAKENHI-PROJECT-23659454
  • [Presentation] 機能性糖鎖:基礎から疾患まで2011

    • Author(s)
      戸田達史
    • Organizer
      第84回日本生化学会大会
    • Place of Presentation
      京都国際会館(京都)(招待講演)
    • Year and Date
      2011-09-22
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Presentation] パーソナルゲノム研究のオーバービュー2011

    • Author(s)
      戸田達史
    • Organizer
      第52回日本神経学会学術大会
    • Place of Presentation
      名古屋国際会議場(名古屋)(招待講演)
    • Year and Date
      2011-05-19
    • Data Source
      KAKENHI-PLANNED-22129006
  • [Presentation] Genome-Wide DNA Methylation and Gene Expression Analyses of Monozygotic Twins Discordant for Intelligence Levels2011

    • Author(s)
      Chihchieh Yu・古川真理・小林千浩・敷鳥千鶴・Pei-Chieng Cha・瀬々潤・菅原裕子・岩本和也・加藤忠史・安藤寿康・戸田達史
    • Organizer
      第34回日本分子生物学会年会
    • Place of Presentation
      パシフィコ横浜(横浜)
    • Year and Date
      2011-12-13
    • Data Source
      KAKENHI-PROJECT-21223002
  • [Presentation] Genome-wide studies and molecular targeting therapy for neurological diseases2011

    • Author(s)
      Toda T
    • Organizer
      JAPANESE-FINNISH JOINT SYMPOSIUM
    • Place of Presentation
      Hilton Helsinki Strand(フィンランド)(招待講演)
    • Year and Date
      2011-12-14
    • Data Source
      KAKENHI-PLANNED-22129006
  • [Presentation] The dysferlin-mediated membrane repair system contributes to maintenance of skeletal muscle cell viability in mouse models of muscular dystrophy2011

    • Author(s)
      戸田 達史
    • Organizer
      World Muscle Society
    • Place of Presentation
      アルマンシル、ポルトガル
    • Data Source
      KAKENHI-PROJECT-23659454
  • [Presentation] 福山型筋ジストロフィーの新たな病態・治療戦略2011

    • Author(s)
      戸田達史
    • Organizer
      第52回日本神経学会学術大会
    • Place of Presentation
      名古屋国際会議場(名古屋)(招待講演)
    • Year and Date
      2011-05-19
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Presentation] 機能性糖鎖:基礎から疾患まで2011

    • Author(s)
      戸田達史
    • Organizer
      第84回日本生化学会大会
    • Place of Presentation
      京都国際会館(京都)(招待講演)
    • Year and Date
      2011-09-22
    • Data Source
      KAKENHI-PLANNED-22129006
  • [Presentation] 神経筋疾患のゲノムクスと分子標的治療2011

    • Author(s)
      戸田達史
    • Organizer
      日本人類遺伝学会第66回大会
    • Place of Presentation
      幕張メッセ(千葉)(招待講演)
    • Year and Date
      2011-11-12
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Presentation] パーソナルゲノム研究のオーバービュー2011

    • Author(s)
      戸田達史
    • Organizer
      第52回日本神経学会学術大会
    • Place of Presentation
      名古屋国際会議場(名古屋)(招待講演)
    • Year and Date
      2011-05-19
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Presentation] Genome-wide studies and molecular targeting therapy for-neurological diseases2011

    • Author(s)
      Toda T
    • Organizer
      JAPANESE-FINNISH JOINT SYMPOSIUM
    • Place of Presentation
      Hilton Helsinki Strand(フィンランド)(招待講演)
    • Year and Date
      2011-12-14
    • Data Source
      KAKENHI-PROJECT-23249049
  • [Presentation] Genome-wide gene expression and DNA methylation analyses of significantly discordant monozygotic twins for cognitive ability.2010

    • Author(s)
      Kobayashi, K., Furukawa, M., Yu, C.-c., Shikishima, C., Sese, J., Sugawara, H., Iwamoto, K., Kato, Y., Ando, J., Toda, T.
    • Organizer
      American Society of Human Genetics 60th Annual Meeting
    • Place of Presentation
      Washington DC, USA
    • Data Source
      KAKENHI-PROJECT-21223002
  • [Presentation] 認知能力の差が顕著な-卵性双生児の分子遺伝学的解析2010

    • Author(s)
      小林千浩、古川真理、游智傑、敷島千鶴、瀬々潤、菅原裕子、岩本和也、加藤忠史、安藤寿康、戸田達史
    • Organizer
      日本人類遺伝学会第55回大会
    • Place of Presentation
      大宮ソニックシティ
    • Data Source
      KAKENHI-PROJECT-20390099
  • [Presentation] PDの危険因子としての遺伝子異常2010

    • Author(s)
      戸田達史
    • Organizer
      第4回パーキンソン病・運動障害疾患コングレス
    • Place of Presentation
      京都ホテルオークラ(京都府)(招待講演)
    • Year and Date
      2010-10-07
    • Data Source
      KAKENHI-PLANNED-22129006
  • [Presentation] 認知能力の差が顕著な一卵性双生児のDNAメチル化解析2010

    • Author(s)
      小林千浩・古川真理・游智傑・敷島千鶴・瀬々潤・菅原裕子・岩本和也・加藤忠史・安藤寿康・戸田達史
    • Organizer
      第33回日本分子生物学会年会第83回日本生化学会大会合同大会
    • Place of Presentation
      神戸国際展示場
    • Year and Date
      2010-12-07
    • Data Source
      KAKENHI-PROJECT-21223002
  • [Presentation] パーキンソン病:genetic variantsと病態2010

    • Author(s)
      戸田達史
    • Organizer
      日本人類遺伝学会第55回大会
    • Place of Presentation
      大宮ソニックシティ(埼玉県)(招待講演)
    • Year and Date
      2010-10-29
    • Data Source
      KAKENHI-PLANNED-22129006
  • [Presentation] パーキンソン病の分子病態機序のブレークスルー2010

    • Author(s)
      戸田達史
    • Organizer
      第51回日本神経学会総会
    • Place of Presentation
      東京国際フォーラム(東京都)(招待講演)
    • Year and Date
      2010-05-21
    • Data Source
      KAKENHI-PLANNED-22129006
  • [Presentation] 認知能力の差が顕著な一卵性双生児の分子遺伝学的解析2010

    • Author(s)
      小林千浩・古川真理・游智傑・敷島千鶴・瀬々潤・菅原裕子・岩本和也・加藤忠史・安藤寿康・戸田達史
    • Organizer
      日本人類遺伝学会第55回大会
    • Place of Presentation
      大宮ソニックシティ
    • Data Source
      KAKENHI-PROJECT-21223002
  • [Presentation] 認知能力の差が顕著な-卵性双生児のDNAメチル化解析2010

    • Author(s)
      小林千浩、古川真理、游智傑、敷島千鶴、瀬々潤、菅原裕子、岩本和也、加藤忠史、安藤寿康、戸田達史
    • Organizer
      第33回日本分子生物学会年会第83回日本生化学会大会合同大会
    • Place of Presentation
      神戸ポートアイランド
    • Data Source
      KAKENHI-PROJECT-20390099
  • [Presentation] Genome-wide gene expression and DNA methylation analyses of significantly discordant monozygotic twins for cognitive ability.2010

    • Author(s)
      小林千浩、古川真理、游智傑、敷島千鶴、瀬々潤、菅原裕子、岩本和也、加藤忠史、安藤寿康、戸田達史
    • Organizer
      American Society of Human Genetics 60th Annual Meeting.
    • Place of Presentation
      Washington D.C., 米国
    • Data Source
      KAKENHI-PROJECT-20390099
  • [Presentation] Genome-wide association study for sporadic Parkinson's disease.2009

    • Author(s)
      Tatsushi Toda
    • Organizer
      Movement Disorder Society
    • Place of Presentation
      Paris, France
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Presentation] Expression analysis of monozygotic twins discordant for cognitive ability.2009

    • Author(s)
      古川真理、小林千浩、游智傑、瀬々潤、敷島千鶴、安藤寿康、戸田達史
    • Organizer
      第32回日本分子生物学会年会
    • Place of Presentation
      パシフィコ横浜
    • Data Source
      KAKENHI-PROJECT-20390099
  • [Presentation] Genomic analysis of monozygotic twins discordant for cognitive ability2009

    • Author(s)
      小林千浩、古川真理、游智傑、敷島千鶴、安藤寿康、戸田達史
    • Organizer
      第32回日本分子生物学会年会
    • Place of Presentation
      パシフィコ横浜
    • Data Source
      KAKENHI-PROJECT-20390099
  • [Presentation] パーキンソン病のゲノム解析2009

    • Author(s)
      戸田達史
    • Organizer
      第11回骨粗鬆症学会シンポジウム
    • Place of Presentation
      名古屋国際会議場(愛知県)
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Presentation] Genetic Analysis of Monozygotic Twins Discordant for Cognitive Abilities.2009

    • Author(s)
      小林千浩、古川真理、游智傑、敷島千鶴、安藤寿康、戸田達史
    • Organizer
      第59回米国人類遺伝学会年会
    • Place of Presentation
      Hawaii, 米国
    • Data Source
      KAKENHI-PROJECT-20390099
  • [Presentation] Genetic analysis of monozygotic twins discordant for cognitive abilities2009

    • Author(s)
      Kobayashi, K., Furukawa, M., Yu, C.-C., Shikishima, C., Ando, J., & Toda, T
    • Organizer
      American Society of Human Genetics 59th Annual Meeting
    • Place of Presentation
      Honolulu, USA
    • Year and Date
      2009-10-22
    • Data Source
      KAKENHI-PROJECT-21223002
  • [Presentation] Association study for Parkinson's, disease2008

    • Author(s)
      Toda T.
    • Organizer
      ETH-JSTWorkshop on Medical Research
    • Place of Presentation
      Zurich, Switzerland
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Presentation] 福山型筋ジストロフィー、パーキンソン病の分子遺伝学、病態、治療展望2008

    • Author(s)
      戸田達史
    • Organizer
      人類遺伝学会教育講演
    • Place of Presentation
      横浜
    • Year and Date
      2008-09-29
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Presentation] 精神発達遅滞児(者)における500KSNPチップを用いたコピー数変化領域のスクリーニングと原因遺伝子の同定2008

    • Author(s)
      牟禮岳男、小林千浩、金城薫、千代延友裕、西村陽、平井清、森本昌史、松尾雅文、稲澤譲治、戸田達史
    • Organizer
      日本人類遺伝学会第53回大会
    • Place of Presentation
      パシフィコ横浜
    • Data Source
      KAKENHI-PROJECT-20390099
  • [Presentation] Copy number variation screening with the 500k SNP array in patients with mental retardation.2008

    • Author(s)
      小林千浩、牟禮岳男、金城薫、千代延友裕、西村陽、平井清、森本昌史、松尾雅文、稲澤譲治、戸田達史
    • Organizer
      The American Society of Human Genetics. 58th Annual Meeting.
    • Place of Presentation
      Philadelphia, 米国
    • Data Source
      KAKENHI-PROJECT-20390099
  • [Presentation] 精神発達遅滞における500K SNPチップを用いたコピー数変化領域のスクリーニングと原因遺伝子の同定2008

    • Author(s)
      小林千浩、牟禮岳男、金城薫、千代延友裕、西村陽、平井清、森本昌史、松尾雅文、稲澤譲治、戸田達史
    • Organizer
      第31回日本分子生物学会年会第81回日本生化学会大会合同大会
    • Place of Presentation
      神戸ポートアイランド
    • Data Source
      KAKENHI-PROJECT-20390099
  • [Presentation] Recent advances in congenital muscular dystrophies.2007

    • Author(s)
      Toda, T
    • Organizer
      12nd Annual Meeting, The Chinese Society of Child Neurology
    • Place of Presentation
      WuYiShan, China
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Presentation] Recent advance in Fukuyama CMD.2007

    • Author(s)
      Toda, T
    • Organizer
      The 7th French-Japanese Workshop
    • Place of Presentation
      Hayama, Japan
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Presentation] Fibroblast growth factor 20 gene and Parkinson's disease in the Japanese population.2007

    • Author(s)
      Toda, T
    • Organizer
      11th International Congress of Parkinson's Disease and Movement Disorders
    • Place of Presentation
      Istanbul, Turkey
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Presentation] 日本発、臨床から遺伝子へ福山型筋ジストロフィ-福山型遺伝子フクチン同定のヒント、幸運とそれから2007

    • Author(s)
      戸田達史
    • Organizer
      日本神経学会総会 企画講演
    • Place of Presentation
      名古屋
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Presentation] Functional analyses of sugar chains, proteins, and genome in neurological diseases.2007

    • Author(s)
      Toda, T
    • Organizer
      COE International Symposium
    • Place of Presentation
      Osaka, Japan
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Presentation] ポストゲノム時代の神経疾患の分子遺伝学と治療戦略2007

    • Author(s)
      戸田達史
    • Organizer
      日本神経治療学会総会 教育講演
    • Place of Presentation
      仙台
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Presentation] Parkinson's disease and muscular dystrophy.2007

    • Author(s)
      Toda, T
    • Organizer
      Yunyang Medical College seminar
    • Place of Presentation
      Shiyan, China
    • Year and Date
      2007-07-24
    • Data Source
      KAKENHI-PROJECT-17019044
  • [Presentation] Exome sequencing of Parkinson's disease in order to identify genetic variants with high disease-risk

    • Author(s)
      Satake W, Ando Y, Tomiyama H, Kashihara K, Mochizuki H, Murayama S, Takeda A, Hasegawa K, Tsuji S, Yamamoto M, Murata M, Hattori N, Toda T.
    • Organizer
      The MDS 18th International Congress of Parkinson's Disease and Movement Disorders
    • Place of Presentation
      Stockholm
    • Year and Date
      2014-06-08 – 2014-06-12
    • Data Source
      KAKENHI-PROJECT-25670420
  • [Presentation] 福山型筋ジストロフィー症の遺伝子治療研究

    • Author(s)
      戸田達史
    • Organizer
      第32回全国筋ジストロフィー大阪大会
    • Place of Presentation
      大阪
    • Year and Date
      2014-10-17 – 2014-10-18
    • Invited
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] A de novo mutation of the MYH7 gene in a large Chinese family with autosomal dominant myopathy.

    • Author(s)
      Toda T, Xiong H, Oda T, Kobayashi K, Wang S, Satake W, Jiao H, Yang Y, Suzuki Y, Sugano S, Wu X.
    • Organizer
      The 19th International Congress of the World Muscle Society.
    • Place of Presentation
      Berlin, Germany.
    • Year and Date
      2014-10-07 – 2014-10-11
    • Data Source
      KAKENHI-PROJECT-12F02422
  • [Presentation] パーキンソン病のリスク遺伝子

    • Author(s)
      戸田 達史
    • Organizer
      第55回日本神経学会学術大会
    • Place of Presentation
      福岡
    • Year and Date
      2014-05-21 – 2014-05-24
    • Invited
    • Data Source
      KAKENHI-PLANNED-22129006
  • [Presentation] Genes regulated by epigenetic mechanisms in determining general intelligence (g) are over-represented in disorders that affect cognition.

    • Author(s)
      Cha PC, Kobayashi K, Yuko A, Takao K, Miyakawa T, Toda T.
    • Organizer
      The 37th Annual Meeting of the Molecular Biology Society of Japan.
    • Place of Presentation
      Yokohama, Japan.
    • Year and Date
      2014-11-25 – 2014-11-27
    • Data Source
      KAKENHI-PROJECT-12F02422
  • [Presentation] EXOME SEQUENCING AND 2ND SNP-GWAS OF PD.

    • Author(s)
      Toda T, Satake W, Hattori N, Murata M.
    • Organizer
      The 12th International Conference on Alzheimer's and Parkinson's Diseases and Related Neurological Disorders.
    • Place of Presentation
      Nice, France
    • Year and Date
      2015-03-18 – 2015-03-22
    • Data Source
      KAKENHI-PLANNED-22129006
  • [Presentation] Exome Association Study and 2nd SNP-GWAS of Japanese Parkinson’s disease.

    • Author(s)
      Satake W, Shigemizu D, Suzuki Y, Yamamoto K,Tomiyama H, Yamamoto M, Murata M, Hattori N, Tsunoda T, Kubo M, Tsuji S, Nakamura Y, Sugano S, Toda T.
    • Organizer
      American Society of Human Genetics Annual meeting 2014.
    • Place of Presentation
      San Diego U.S.A.
    • Year and Date
      2014-10-18 – 2014-10-22
    • Data Source
      KAKENHI-PLANNED-22129006
  • [Presentation] Impaired viability of muscle precursor cells in muscular dystrophy with glycosylation defects and amelioration of its severe phenotype by limited gene expression.

    • Author(s)
      Motoi Kanagawa, Chih-Chieh Yu, Chiyomi Ito, So-ichiro Fukada, Tomoko Chiyo, Kazuhiro Kobayashi, Takashi Okada, Shin’ichi Takeda, Tatsushi Toda.
    • Organizer
      The 13th International Congress on Neuromuscular Diseases (ICNMD)
    • Place of Presentation
      Nice, France
    • Year and Date
      2014-07-05 – 2014-07-10
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] Exome Association Study and 2nd SNP-GWAS of Japanese Parkinson’s disease

    • Author(s)
      Satake W, Shigemizu D, Suzuki Y, Yamamoto K, Tomiyama H, Yamamoto M, Murata M, Hattori N, Tsunoda T, Kubo M, Tsuji S, Nakamura Y, Sugano S, Toda T.
    • Organizer
      American Society of Human Genetics Annual meeting
    • Place of Presentation
      San Diego
    • Year and Date
      2014-10-18 – 2014-10-22
    • Data Source
      KAKENHI-PROJECT-25670420
  • [Presentation] 孤発性パーキンソン病のエクソーム関連解析と第2期SNP-GWAS

    • Author(s)
      佐竹渉、重水大智、鈴木穣 、山本健、富山弘幸、高橋篤、村田美穂、服部信孝、田中敏博 、角田達彦 、久保充明、辻省次、松本直通 、菅野純夫、戸田 達史
    • Organizer
      日本人類伝学会第59回大会
    • Place of Presentation
      東京
    • Year and Date
      2014-11-20 – 2014-11-22
    • Data Source
      KAKENHI-PROJECT-25670420
  • [Presentation] パーキンソン病感受性遺伝子α-synuiclein SNPとnoncoding RNA

    • Author(s)
      水田依久子、佐竹渉、村山繁雄、金川基、小林千浩、高藤和輝、永森収志、山本光利、服部信孝、村田美穂、金井好克、水野敏樹、中川正法、戸田達史
    • Organizer
      第55回日本神経学会学術大会
    • Place of Presentation
      福岡
    • Year and Date
      2014-05-21 – 2014-05-24
    • Data Source
      KAKENHI-PROJECT-25670420
  • [Presentation] 神経・筋疾患の分子メカニズム、遺伝子治療、分子標的治療 / Molecular pathogenesis, genetic counseling, and molecular targeting therapy for neurological and muscular diseases.

    • Author(s)
      戸田達史
    • Organizer
      日本人類遺伝学会第59回大会
    • Place of Presentation
      東京
    • Year and Date
      2014-11-19 – 2014-11-22
    • Invited
    • Data Source
      KAKENHI-PLANNED-22129006
  • [Presentation] 神経難病の治療と研究の現状と展望

    • Author(s)
      戸田 達史
    • Organizer
      第38回日本遺伝カウンセリング学会学術集会
    • Place of Presentation
      大阪
    • Year and Date
      2014-06-26 – 2014-06-29
    • Invited
    • Data Source
      KAKENHI-PLANNED-22129006
  • [Presentation] Exome Association Study and 2nd SNP-GWAS of Japanese Parkinson’s disease

    • Author(s)
      Satake W, Hasegawa K, Murata M, Hattori N, Toda T.
    • Organizer
      Genetic Epidemiology of Parkinson's disease Annual meeting
    • Place of Presentation
      Vancouver
    • Year and Date
      2014-09-10 – 2014-09-12
    • Data Source
      KAKENHI-PROJECT-25670420
  • [Presentation] Genes regulated by epigenetic mechanisms in determining general intelligence (g) are over-represented in disorders that affect cognition.

    • Author(s)
      Cha PC, Kobayashi K, Yuko A, Takao K, Miyakawa T, Toda T.
    • Organizer
      The 59th Annual Meeting of The Japanese Society of Human Genetics.
    • Place of Presentation
      Tokyo, Japan.
    • Year and Date
      2014-11-19 – 2014-11-22
    • Data Source
      KAKENHI-PROJECT-12F02422
  • [Presentation] Exome sequencing and 2nd SNP-GWAS of Japanese Parkinson’s disease.

    • Author(s)
      Toda T, Satake W, Yamamoto M, Murata M, Hattori N, Sugano S.
    • Organizer
      4th Asian and Oceanian Parkinson’s Disease and Movement Disorders Congress.
    • Place of Presentation
      Pattaya, Thailand
    • Year and Date
      2014-11-28 – 2014-11-30
    • Data Source
      KAKENHI-PLANNED-22129006
  • [Presentation] 福山型筋ジストロフィーの病態基盤と新たな治療法の開発

    • Author(s)
      戸田 達史
    • Organizer
      第56回日本小児神経学会学術大会
    • Place of Presentation
      浜松
    • Year and Date
      2014-05-28 – 2014-05-31
    • Invited
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] 神経・筋疾患の分子メカニズム、遺伝子治療、分子標的治療 / Molecular pathogenesis, genetic counseling, and molecular targeting therapy for neurological and muscular diseases.

    • Author(s)
      戸田達史
    • Organizer
      日本人類遺伝学会第59回大会
    • Place of Presentation
      東京
    • Year and Date
      2014-11-19 – 2014-11-22
    • Invited
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] A de novo mutation of the MYH7 gene in a large Chinese family with autosomal dominant myopathy.

    • Author(s)
      Tatsushi Toda, Hui Xiong, Tetsuya Oda, Kazuhiro Kobayashi, Shuo Wang, Wataru Satake, Hui Jiao, Yanling Yang, Yutaka Suzuki, Sumio Sugano, Xiru Wu.
    • Organizer
      19th international congress of the world muscle society
    • Place of Presentation
      Berlin, Germany
    • Year and Date
      2014-10-07 – 2014-10-11
    • Data Source
      KAKENHI-PROJECT-26253057
  • [Presentation] Genes regulated by epigenetic mechanisms in determining general intelligence (g) are over-represented in disorders that affect cognition.

    • Author(s)
      Cha PC, Kobayashi K, Yuko A, Takao K, Miyakawa T, Toda T.
    • Organizer
      The 64th Annual Meeting of The American Society of Human Genetics.
    • Place of Presentation
      San Diego, California, USA.
    • Year and Date
      2014-10-18 – 2014-10-22
    • Data Source
      KAKENHI-PROJECT-12F02422
  • [Presentation] 神経難病の治療と研究の現状と展望

    • Author(s)
      戸田 達史
    • Organizer
      第38回日本遺伝カウンセリング学会学術集会
    • Place of Presentation
      近畿大学ノーベンバーホール
    • Year and Date
      2014-06-26 – 2014-06-29
    • Invited
    • Data Source
      KAKENHI-PROJECT-26253057
  • []

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  • 1.  KOBAYASHI Kazuhiro (90324780)
    # of Collaborated Projects: 7 results
    # of Collaborated Products: 17 results
  • 2.  MURATA Miho (30282643)
    # of Collaborated Projects: 4 results
    # of Collaborated Products: 9 results
  • 3.  KANAGAWA Motoi (00448044)
    # of Collaborated Projects: 4 results
    # of Collaborated Products: 9 results
  • 4.  ANDO Juko (30193105)
    # of Collaborated Projects: 3 results
    # of Collaborated Products: 8 results
  • 5.  HATTORI Nobutaka (80218510)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 11 results
  • 6.  FUJISAWA Keiko (00453530)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 0 results
  • 7.  SATAKE Wataru (50467594)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 23 results
  • 8.  坂上 雅道 (10225782)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 0 results
  • 9.  CHA Pei Chieng
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 8 results
  • 10.  KAWAI Yasuyo (90521732)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 11.  ONO Yutaka (70138098)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 12.  HIRAISHI Kai (50343108)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 13.  IKEDA Mariko (00410738)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 14.  NAGAMORI Shushi (90467572)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 15.  MIYAKE Katsuya (30219745)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 16.  NAKAHORI Yutaka (10172389)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 17.  OHKI Misao (00158792)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 18.  INOKO Hidetoshi (10101932)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 19.  SHIMIZU Nobuyoshi (50162706)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 20.  SAKAKI Yoshiyuki (10112327)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 21.  NIIKAWA Norio (00111170)
    # of Collaborated Projects: 1 results
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  • 22.  ABE Tatsuo (60079746)
    # of Collaborated Projects: 1 results
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  • 23.  SAITO Fumiko (10158917)
    # of Collaborated Projects: 1 results
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  • 24.  MIZUTA Ikuko (80397760)
    # of Collaborated Projects: 1 results
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  • 25.  Nishioka Kenya (40348933)
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  • 26.  MANABU Funayama (70468578)
    # of Collaborated Projects: 1 results
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  • 27.  LI Yuanzhe (40549292)
    # of Collaborated Projects: 1 results
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  • 28.  YAMAGATA Shinji (60625193)
    # of Collaborated Projects: 1 results
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  • 29.  TOYODA Atsushi (10267495)
    # of Collaborated Projects: 1 results
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  • 30.  SOMEYA Yoshiaki (20392714)
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  • 31.  辻 省次 (70150612)
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  • 32.  林 健志 (00019671)
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  • 33.  Farrer Matthew J
    # of Collaborated Projects: 1 results
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  • 34.  Ross Owen A.
    # of Collaborated Projects: 1 results
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  • 35.  Kruger Rejko Kruger
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  • 36.  CHA PeiChieng
    # of Collaborated Projects: 1 results
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  • 37.  TANIGUCHI Mariko
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  • 38.  ISHIURA Hiroyuki
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  • 39.  MURAKAMI Kazuma
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    # of Collaborated Products: 1 results
  • 40.  SAKAGUCHI Hirofumi
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    # of Collaborated Products: 1 results
  • 41.  NAGATA Yosuke
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  • 42.  IMAE Rieko
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  • 43.  野水 基義
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  • 44.  萬谷 博
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 2 results
  • 45.  山口 芳樹
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 46.  久保田 暁
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 3 results
  • 47.  遠藤 玉夫
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 48.  関 恒慶
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 49.  清水 潤
    # of Collaborated Projects: 0 results
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  • 50.  倉橋 浩樹
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    # of Collaborated Products: 1 results
  • 51.  李 知子
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  • 52.  竹島 泰弘
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  • 53.  野津 寛大
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  • 54.  飯島 一誠
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    # of Collaborated Products: 1 results
  • 55.  饗場 篤
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  • 56.  入江 一浩
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 57.  岡田 随象
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 2 results
  • 58.  上山 健彦
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 59.  山本 哲志
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 60.  蒔田 直昌
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 61.  辻 幸臣
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 62.  手塚 裕之
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results

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