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Takeshima Yasuhiro  竹島 泰弘

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TAKESHIMA Yasuhiro  竹島 泰弘

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Researcher Number 40281141
Other IDs
External Links
Affiliation (Current) 2022: 兵庫医科大学, 医学部, 教授
Affiliation (based on the past Project Information) *help 2014 – 2021: 兵庫医科大学, 医学部, 教授
2016: 神戸大学, 医学研究科, 客員教授
2015: 神戸大学, 医学(系)研究科(研究院), 教授
2014: 神戸大学, 医学(系)研究科(研究院), 客員教授
2013: 神戸大学, 医学(系)研究科(研究院), 特命教授 … More
2013: 神戸大学, 大学院医学研究科, 教授
2012 – 2013: 神戸大学, 医学(系)研究科(研究院), 教授
2012: 神戸大学, 医学研究科, 教授
2011: 神戸大学, 医学(系)研究科(研究院), 特命教授
2010 – 2011: 神戸大学, 医学研究科, 特命教授
2010 – 2011: Kobe University, 大学院・医学研究科, 特命教授
2008 – 2009: Kobe University, 医学研究科, 准教授
2008: 神戸大学, 大学院医学研究科, 准教授
2007: Kobe University, Graduate School of Medicine, Associate Professor
2007: Kobe University, Graduate School of Medicine, Assistant professor
2006: kobe University, Graduate School of Medicine, Associate professor, 大学院医学系研究科, 助教授
2004 – 2006: 神戸大学, 医学系研究科, 助教授
2003 – 2005: Kobe University, Graduate School of Medicine, Associate Professor, 大学院・医学系研究科, 助教授
2002: Kobe University Hospital, Asistant Professor, 医学部附属病院, 助手
2002: Kobe University Graduate School of medicine Assistant, 大学院・医学系研究科, 講師
1996 – 2001: 神戸大学, 医学部・附属病院, 助手
1998: 神戸大学, 医学部附属病院, 助手
1997: 神戸大学, 医学部・付属病院, 助手 Less
Review Section/Research Field
Principal Investigator
Pediatrics / Pediatrics / Embryonic/Neonatal medicine / Human genetics / Basic Section 52050:Embryonic medicine and pediatrics-related
Except Principal Investigator
Pediatrics / Pediatrics / Embryonic/Neonatal medicine / Basic Section 52050:Embryonic medicine and pediatrics-related / Experimental psychology … More / Metabolomics / 応用薬理学・医療系薬学 / Embryonic/Neonatal medicine / Medical pharmacy Less
Keywords
Principal Investigator
筋ジストロフィー / アンチセンスオリゴヌクレオチド / スプライシング / エクソンスキッピング / 分子治療 / 遺伝子治療 / splicing / 小児神経学 / ジストロフィン / MSUD … More / mRNA / IUGR / Insulin-like growth factor / IGF-1 / MBP / PLP / RNAi / muscular dystrophy / molecular therapy / exon skipping / シグナル伝達因子 / 筋ジストロフー / NF-κB / 線維化因子 / アンチセンスオリゴ / 炎症性物質 / プロスタグランジン / Duchenne型筋ジストロフィー / エクソンスキッピング誘導治療 / ナンセンス変異リードスルー誘導治療 / スプラシング / スプライシング促進配列 / dystrophin / splicing enhancer sequence / gene therapy / 遺伝子異常 / 新生児スクリーニング / フィリピン / メープルシロップ尿症 / E2遺伝子 / 遺伝子欠失 / gene mutation / neonatal screeing / Philippines / 胎内発育遅延 / 髄鞘化 / 子宮内発育遅延 / IU GR / insulin-like growth factor / myelin basic protein / proteolipid protein / 小児白血病 / キメラ遺伝子 / childhood leukemia / chimeric gene / エクソン・スキッピング / antisense oligonucleotide / 遺伝子診断 / 東アジア / 分子疫学 / 遺伝学 / データベース / 次世代シークエンサー / 血管作動性因子 / 血管内皮増殖因子 … More
Except Principal Investigator
ジストロフィン / スプライシング / クローニング / 筋ジストロフィー / エクソンスキッピング / 治療 / dystrophin / Duchenne型 / 遺伝子異常 / Duchenne型筋ジストロフィー / SMN1遺伝子 / SMN2遺伝子 / 脊髄性筋萎縮症 / エクソン / exon skipping / アンチセンス / Duchenne / 点突然変異 / マイクロサテライト / アイソフォーム / 小児神経学 / 分子種 / ジストロフィン遺伝子 / スプライシング促進配列 / スキッピング / splicing / splicing enhancer sequence / フィリピン / デュシェンヌ型筋ジストロフィー / muscular dystrophy / SNPs / HPLC / antisense / hnRNP C1 / C2 / ペプチド核酸 / spinal muscular atrophy / the SMN1 gene / the SMN2 gene / Glutathione S-transferase / Reduced folate carrier / アンチセンスオリゴヌクレオチド / In vitro翻訳 / 転写 / がん遺伝子 / がん / PCR / 不安定性 / RNA結合蛋白 / 核タンパク / 核抽出液 / mRNA前駆体 / タンパク / Duchenne型筋ジストロフィー児 / 知能 / 言語能力 / 筋ジストロフィー児 / 樹木画 / 人物画 / dp140 / リボゾーム / 精神発達遅滞 / プロモーター / c.-318 GCC 挿入・欠失多型 / CREB / cAMP / 転写活性 / ルシフェラーゼ / ルシフェラーゼ・アッセイ / 国際情報研究 / 国際情報交流 / 内在遺伝子 / ウェスターンブット / mRNA / 転写産物 / 次世代シークエンサー / メタゲノミック診断法 / 新生児感染症 / 小児感染症 / 周産期・新生児感染症 / 胎盤 / 臍帯 / イントロン / 拡張型心筋症 / 心筋 / isoform / exon intron / dilated cardiomyopathy / アンチセンスオリゴオヌクレオチド / treatment / G6PD欠損症 / G6PD deficienc / mutation / Philippines / Duchenne muscular dystrophy / antisense oligonucleotide / 分子治療 / キメラRNA / DNA / 点変異 / 筋細胞 / molecular therapy / 前頭骨部篩骨部脳瘤 / 神経管欠損 / メチレンテトラヒドロ葉酸還元酵素 / ホメオボックス遺伝子 / 頭部形成 / 前頭骨部〓骨部脳瘤 / 疾患責任遺伝子 / 疾患感受性遺伝子 / 頭部形成ホメオボックス遺伝子 / Neural tube defect / Frontoethmoidal encephalocele / Neural tube defects / 5, 10-methylenetetrahydrofolate reductase / Homeobox genes / craniofacial formation / 遺伝子治療 / 血中濃度 / リアルタイムPCR / gene therapy / blood concentration / real time quantitative PCR / アポトーシス / トロンビン受容体 / PAR-1 / PDGF-α受容体 / オリゴデンドロサイト / 低酸素性虚血性脳症 / 空間学習能力 / モリス水迷路 / カスペース阻害剤 / BAF / 低酸素虚血障害 / hypoxic-ischemic encephalonathy / PDGF-α receptor / oligodendrocyte / apoptosis / differentiation / 新生児黄疸 / Gilbert症候群 / UGT1A1遺伝子 / G71R変異 / G493R変異 / TATA box / マレーシア人 / UGT1 A1遺伝子 / ジャワ・インドネシア人 / マレー・マレーシア人 / DHPLCスクリーニング / neonatal jaundice / Gilbert syndrome / the UGT1A1 gene / G71R mutation / G493R mutation / TATA-box / Malaysian / in vitroスプライシング / in vitro splicing assay / peptide nucleic acid / 小児白血病 / キメラ遺伝子 / childhood leukemia / chimera mRNA / cloning / DMD / メープルシロップ尿症 / E2遺伝子 / 新生児 / Philippine / maple syrup urine disease / E2 gene / neonate / メトトレキサート / 急性リンパ性白血病 / 悪性リンパ腫 / 遺伝子型 / 急性膵炎 / アスパラギナーゼ / 遺伝子多型 / glutathione S-transferase / reduced folate carrier / Methotrexate / Acute lymphoblastic leukemia / Malignant lymphoma / Genetic polymorphism / エクソン特異的スプライシング促進化合物 / バルプロ酸 / ヒストン脱アセチル化酵素阻害剤 / 転写効率 / スプライシング効率 / エクソン7 / 遺伝子変異 / Tudorドメイン / thetic exon-specific splicing activator / valproic acid / 尿中exRNA / エクソンスキッピング治療 / イントロン内スプライシング制御配列 Less
  • Research Projects

    (43 results)
  • Research Products

    (160 results)
  • Co-Researchers

    (46 People)
  •  エクソンスキッピング誘導治療の有効性を予測する残存イントロン解析システムの検証

    • Principal Investigator
      李 知子
    • Project Period (FY)
      2021 – 2023
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 52050:Embryonic medicine and pediatrics-related
    • Research Institution
      Hyogo Medical University
  •  尿中スプライシング産物をバイオマーカーとした筋ジストロフィー治療評価系の検証

    • Principal Investigator
      田中 靖彦
    • Project Period (FY)
      2020 – 2022
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 52050:Embryonic medicine and pediatrics-related
    • Research Institution
      Hyogo Medical University
  •  筋ジストロフィーにおける血管作動性因子のスプライシング動態の解明と治療応用Principal Investigator

    • Principal Investigator
      竹島 泰弘
    • Project Period (FY)
      2020 – 2022
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 52050:Embryonic medicine and pediatrics-related
    • Research Institution
      Hyogo Medical University
  •  Non-invasive system for predicting effectiveness of the exon skipping therapy for muscular dystrophyPrincipal Investigator

    • Principal Investigator
      Yasuhiro Takeshima
    • Project Period (FY)
      2017 – 2019
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Hyogo Medical University
  •  東アジアにおける筋ジストロフィーオーダーメイド治療開発のための分子疫学的調査Principal Investigator

    • Principal Investigator
      竹島 泰弘
    • Project Period (FY)
      2016 – 2018
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Human genetics
    • Research Institution
      Hyogo Medical University
  •  Investigation of inflammatory factors affecting the efficacy of the molecular therapies for muscular dystrophyPrincipal Investigator

    • Principal Investigator
      Yasuhiro Takeshima
    • Project Period (FY)
      2014 – 2016
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Hyogo Medical University
  •  Pathogenic microorganism identification in neonatal infectious diseases by a meta-genomic analysis using the next generation sequencer

    • Principal Investigator
      MORIOKA Ichiro
    • Project Period (FY)
      2014 – 2016
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Embryonic/Neonatal medicine
    • Research Institution
      Kobe University
  •  Cloning of non-dystrophin transcript from the dystrophin gene

    • Principal Investigator
      MATSUO Masafumi
    • Project Period (FY)
      2013 – 2014
    • Research Category
      Grant-in-Aid for Challenging Exploratory Research
    • Research Field
      Pediatrics
    • Research Institution
      Kobe Gakuin University
  •  Investigation of fibrotic factors during the exon-skipping therapy using antisense oligonucleotide for muscular dystrophyPrincipal Investigator

    • Principal Investigator
      TAKESHIMA Yasuhiro
    • Project Period (FY)
      2011 – 2013
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  Correlation between cis-acing elements and effects on inducing exon skipping

    • Principal Investigator
      YAGI Mariko
    • Project Period (FY)
      2011 – 2013
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  Establishment of treatment strategy for spinal muscular atrophybased on the SMN2gene transcription control

    • Principal Investigator
      NISHIO Hisahide
    • Project Period (FY)
      2010 – 2012
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  Genes responsible for mental retardation complicating to Duchenne muscular dystrophy

    • Principal Investigator
      MATSUO Masafumi
    • Project Period (FY)
      2009 – 2011
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe Gakuin University
      Kobe University
  •  Research of signal transduction system in antisense therapy for muscular dystrophyPrincipal Investigator

    • Principal Investigator
      TAKESHIMA Yasuhiro
    • Project Period (FY)
      2008 – 2010
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  Study on treatment of Duchenne muscular dystrophy by inducing exon skipping

    • Principal Investigator
      MATSUO Masafumi
    • Project Period (FY)
      2007 – 2008
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  Development of Therapy for Spinal Muscular Atrophy Based on the Spliring Modulation Technology

    • Principal Investigator
      NISHIO Hisahide
    • Project Period (FY)
      2006 – 2007
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  Research of antisense oligonucleotide therapy for muscular dystrophy using knockout mouse as a modelPrincipal Investigator

    • Principal Investigator
      TAKESHIMA Yasuhiro
    • Project Period (FY)
      2006 – 2007
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  Elucidation of adverse events of methotrexate based on genomic and proteomic analysis in childhood leukemia patients

    • Principal Investigator
      SAKAEDA Toshiyuki
    • Project Period (FY)
      2005 – 2006
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Medical pharmacy
    • Research Institution
      Kobe University
  •  筋ジストロフィー児の認知・言語と遺伝子異常

    • Principal Investigator
      小椋 たみ子
    • Project Period (FY)
      2004 – 2006
    • Research Category
      Grant-in-Aid for Exploratory Research
    • Research Field
      Experimental psychology
    • Research Institution
      Kobe University
  •  Cellular biological study on the treatment of Duchenne muscular dystrophy with nucleic acids

    • Principal Investigator
      MATSUO Masafumi
    • Project Period (FY)
      2004 – 2005
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  Molecular epidemiolojial study on maple syrup urine disease in Philippine.

    • Principal Investigator
      MATSUO Masafumi
    • Project Period (FY)
      2004 – 2006
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  Research of novel treatment for childhood leukemia by disrupting the chimeric gene function using RNAiPrincipal Investigator

    • Principal Investigator
      TAKESHIMA Yasuhiro
    • Project Period (FY)
      2004 – 2005
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  Molecular epidemiology of neonatal Gilbert's syndrome in Malaysia

    • Principal Investigator
      NISHIO Hisahide
    • Project Period (FY)
      2003 – 2004
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Embryonic/Neonatal medicine
    • Research Institution
      Kobe University
  •  Development of a new treatment with splicing modulators for spinal muscular atrophy

    • Principal Investigator
      NSIHIO Hisahide
    • Project Period (FY)
      2003 – 2004
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  Cloning of chimera mRNA from acute myelomegakaryocytic leukemia cell with t(1;9)

    • Principal Investigator
      KAWASAKI Keiichiro
    • Project Period (FY)
      2003 – 2004
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  Protection of neonatal brain against hypoxic-ischemic injury through regulating apoptosis.

    • Principal Investigator
      YOKOYAMA Naoki, 中村 肇
    • Project Period (FY)
      2002 – 2003
    • Research Category
      Grant-in-Aid for Scientific Research (A)
    • Research Field
      Embryonic/Neonatal medicine
    • Research Institution
      Kobe University
  •  Molecular genetic study on maple syrup urine disease in PhilippinesPrincipal Investigator

    • Principal Investigator
      TAKESHIMA Yasuhiro, 中村 肇
    • Project Period (FY)
      2002 – 2003
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  Prevention of developmental disorders of intra-uterine growth retarded infants with growth factors.Principal Investigator

    • Principal Investigator
      TAKESHIMA Yasuhiro, 上谷 良行
    • Project Period (FY)
      2002 – 2003
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Embryonic/Neonatal medicine
    • Research Institution
      Kobe University
  •  ジストロフィンmRNA前駆体に結合する新規核タンパクに関する分子生物学的研究

    • Principal Investigator
      松尾 雅文
    • Project Period (FY)
      2001
    • Research Category
      Grant-in-Aid for Exploratory Research
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  Study on the treatment of Duchenne musclar dystrophy with chimera RNA/DNA

    • Principal Investigator
      MATSUO Masafumi
    • Project Period (FY)
      2001 – 2003
    • Research Category
      Grant-in-Aid for Scientific Research (A)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  Molecular genetic study of frontoethmoidal encephalocele in Indonesia

    • Principal Investigator
      MATSUO Masafumi
    • Project Period (FY)
      2001 – 2002
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University Graduate School of medicine
  •  Research for the exonic splicing enhancer sequences in dysttrophin genePrincipal Investigator

    • Principal Investigator
      TAKESHIMA Yasuhiro
    • Project Period (FY)
      2001 – 2002
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University School of Medicine
  •  Evaluation of the analytical methods of antisense oligonueleotide applicable to the antisense therapy

    • Principal Investigator
      OKUMURA Katsuhiko
    • Project Period (FY)
      2001 – 2002
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      応用薬理学・医療系薬学
    • Research Institution
      KOBE UNIVERSITY
  •  ジストロフィンmRNA前駆体のスプライシングに関与する新規タンパクのクローニング

    • Principal Investigator
      松尾 雅文
    • Project Period (FY)
      2000
    • Research Category
      Grant-in-Aid for Exploratory Research
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  Establishment of treatment of Duchenne muscular dystrophy

    • Principal Investigator
      MATSUO Masafumi
    • Project Period (FY)
      2000 – 2001
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  エクソンスキッピング誘導による筋ジストロフィー遺伝子治療に関する研究Principal Investigator

    • Principal Investigator
      竹島 泰弘
    • Project Period (FY)
      1999 – 2000
    • Research Category
      Grant-in-Aid for Encouragement of Young Scientists (A)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  Molecular genetic study on G6PD deficiency in Philippines

    • Principal Investigator
      NAKAMURA Hajime
    • Project Period (FY)
      1999 – 2000
    • Research Category
      Grant-in-Aid for Scientific Research (B).
    • Research Field
      Metabolomics
    • Research Institution
      Kobe University
  •  ジストロフィン遺伝子からの新規転写産物のクローニング

    • Principal Investigator
      松尾 雅文
    • Project Period (FY)
      1998
    • Research Category
      Grant-in-Aid for Exploratory Research
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  Establishment of treatment of Duchenne muscular dystrophy

    • Principal Investigator
      MATSUO Masafumi
    • Project Period (FY)
      1998 – 1999
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  血清中DNAのマイクロサテライトを解析するがんの早期診断法の確立

    • Principal Investigator
      松尾 雅文
    • Project Period (FY)
      1997
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      Kobe University
  •  アンチセンスオリゴDNA筋肉内投与による筋ジストロフィー遺伝子治療に関する研究Principal Investigator

    • Principal Investigator
      竹島 泰弘
    • Project Period (FY)
      1997 – 1998
    • Research Category
      Grant-in-Aid for Encouragement of Young Scientists (A)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  Study on dystrophin isoform expressed in heart

    • Principal Investigator
      MATSUO Masafumi
    • Project Period (FY)
      1997 – 1999
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  神経線維腫症1型遺伝子異常の蛋白発現ベクターを応用した診断法の確立

    • Principal Investigator
      MATSUO Masafumi
    • Project Period (FY)
      1996
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      Kobe University
  •  アンチセンスオリゴヌクレオチドを用いた筋ジストロフィー遺伝子治療に関する研究Principal Investigator

    • Principal Investigator
      竹島 泰弘
    • Project Period (FY)
      1996
    • Research Category
      Grant-in-Aid for Encouragement of Young Scientists (A)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University

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All Journal Article Presentation

  • [Journal Article] Two Closely Spaced Mutations in cis Result in Ullrich Congenital Muscular Dystrophy2019

    • Author(s)
      Shimomura Hideki、Lee Tomoko、Tanaka Yasuhiko、Awano Hiroyuki、Itoh Kyoko、Nishino Ichizo、Takeshima Yasuhiro
    • Journal Title

      Human genome variation.

      Volume: 6 Pages: 21-21

    • DOI

      10.1038/s41439-019-0052-z

    • NAID

      120006644105

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17K10087, KAKENHI-PROJECT-16K21524
  • [Journal Article] RNA sequencing reveals abnormal LDB3 splicing in sudden cardiac death2019

    • Author(s)
      Yamamoto Takuma、Miura Aya、Itoh Kyoko、Takeshima Yasuhiro、Nishio Hajime
    • Journal Title

      Forensic Science International

      Volume: 302 Pages: 109906-109906

    • DOI

      10.1016/j.forsciint.2019.109906

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17K10087
  • [Journal Article] Ambulatory capacity in Japanese patients with Duchenne muscular dystrophy Brain and Development2018

    • Author(s)
      Awano H, Itoh C, Takeshima Y, Lee T, Matsumoto M, Kida A, Kaise T, Suzuki T, Matsuo M.
    • Journal Title

      Brain Dev.

      Volume: 40 Pages: 465-472

    • DOI

      10.1016/j.braindev.2018.02.011

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17K10087, KAKENHI-PROJECT-16H05814
  • [Journal Article] Cardiac involvement in Fukuyama muscular dystrophy is less severe than in Duchenne muscular dystrophy2017

    • 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 Dev

      Volume: 39 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] 2'-O-Methyl RNA/Ethylene-Bridged Nucleic Acid Chimera Antisense Oligonucleotides to Induce Dystrophin Exon 45 Skipping.2017

    • Author(s)
      Tomoko Lee, Hiroyuki Awano, Mariko Yagi, Masaaki Matsumoto, Nobuaki Watanabe, Ryoya Goda, Makoto Koizumi, Yasuhiro Takeshima and Masafumi Matsuo
    • Journal Title

      Genes

      Volume: 8 Pages: 67-67

    • DOI

      10.3390/genes8020067

    • NAID

      120006373782

    • Peer Reviewed / Acknowledgement Compliant / Open Access
    • Data Source
      KAKENHI-PROJECT-26461545, KAKENHI-PROJECT-15K19641
  • [Journal Article] Patients with Duchenne muscular dystrophy are significantly shorter than those with Becker muscular dystrophy, with the higher incidence of short stature in Dp71 mutated subgroup2017

    • Author(s)
      Matsumoto M, Awano H, Lee T, Takeshima Y, Matsuo M, Iijima K.
    • Journal Title

      Neuromuscular disorders

      Volume: 27 Pages: 1023-1028

    • DOI

      10.1016/j.nmd.2017.06.007

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17K10087, KAKENHI-PROJECT-16H05814
  • [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 Pages: 351-355

    • DOI

      10.1038/jhg.2015.157

    • NAID

      40020802923

    • Peer Reviewed / Acknowledgement Compliant / Open Access
    • Data Source
      KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-15K09621, KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-15H04710, KAKENHI-PROJECT-26461632
  • [Journal Article] A novel splicing silencer generated by DMD exon 45 deletion junction could explain upstream exon 44 skipping that modifies dystrophinopathy2014

    • Author(s)
      Dwianingsih EK, Malueka R, Nishida A, Lee T, Yagi M, Iijima K, Takeshima Y, Ito K, Matsuo M
    • Journal Title

      J Hum Genet

      Volume: (in press)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591496
  • [Journal Article] Differences in carrier frequency between mothers of Duchenne and Becker muscular dystrophy patients2014

    • Author(s)
      Lee T, Takeshima Y, Kusunoki N, Awano H, Yagi M, Matsuo M, Iijima K.
    • Journal Title

      J Hum Genet

      Volume: 59 Pages: 46-50

    • DOI

      10.1038/jhg.2013.119

    • NAID

      40019946811

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591496
  • [Journal Article] Differences in carrier frequency between mothers of Duchenne and Becker muscular dystrophy patients2014

    • Author(s)
      Lee T, Takeshima Y, Kusunoki N, Awano H, Yagi M, Matsuo M, and Iijima K
    • Journal Title

      J Hum Genet

      Volume: 59 Pages: 46-50

    • NAID

      40019946811

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Journal Article] A novel splicing silencer generated by DMD exon 45 deletion junction could explain upstream exon 44 skipping that modifies dystrophinopathy.2014

    • Author(s)
      Ery Kus Dwianingsih, Rusdy Malueka, Atsuhiro Nishida, Tomoko Lee, Mariko Yagi, Kazumoto Iijima, Yasuhiro Takeshima, Kyoko Ito, Masafumi Matsuo.
    • Journal Title

      J Hum Genet.

      Volume: in press

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591496
  • [Journal Article] Differences in carrier frequency between mothers of Duchenne and Becker muscular dystrophy patients.2014

    • Author(s)
      Lee T, Takeshima Y, Kusunoki N, Awano H, Yagi M, Matsuo M, Iijima K.
    • Journal Title

      J Hum Genet.

      Volume: 59 Pages: 46-50

    • NAID

      40019946811

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Journal Article] Utility of transmural myocardial strain profile for prediction of early left ventricular dysfunction in patients with Duchenne muscular dystrophy2013

    • Author(s)
      Yamamoto T, Tanaka H, Matsumoto K, Lee T, Awano H, Yagi M, Imanishi T, Hayashi N, Takeshima Y, Kawai H, Kawano S, and Hirata K
    • Journal Title

      Am J Cardiol

      Volume: 111 Pages: 902-7

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Journal Article] Molecular characterization of an X(p21.2;q28) chromosomal inversion in a Duchenne muscular dystrophy patient with mental retardation reveals a novel long non-coding gene on Xq28.2013

    • Author(s)
      Tran TH, Zhang Z, Yagi M, Lee T, Awano H, Nishida A, Okinaga T, Takeshima Y, Matsuo M.
    • Journal Title

      J Hum Genet.

      Volume: 58 Pages: 33-9

    • NAID

      10031145898

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Journal Article] A prostaglandin D2 metabolite is elevated in the urine of Duchenne muscular dystrophy patients and increases further from 8 years old2013

    • Author(s)
      Nakagawa T, Takeuchi A, Kakiuchi R, Lee T, Yagi M, Awano H, Iijima K, Takeshima Y, Urade Y, Matsuo M.
    • Journal Title

      Clin Chim Acta

      Volume: 423 Pages: 10-14

    • DOI

      10.1016/j.cca.2013.03.031

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591496, KAKENHI-PROJECT-24791060
  • [Journal Article] Spinal Muscular Atrophy: From Gene Discovery to Clinical Trials2013

    • Author(s)
      Nurputra DK, Lai PS, Harahap NI, Morikawa S, Yamamoto T, Nishimura N, Kubo Y, Takeuchi A, Saito T, Takeshima Y, Tohyama Y, Tay SK, Low PS, Saito K, Nishio H
    • Journal Title

      Annals of Human Genetics

      Volume: (in press)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22591127
  • [Journal Article] A prostaglandin D2 metabolite is elevated in the urine of Duchenne muscular dystrophy patients and increases further from 8 years old2013

    • Author(s)
      Taku Nakagawa, Atsuko Takeuchi, Ryohei Kakiuchi, Tomoko Lee, Mariko Yagi, Hiroyuki Awano, Kazumoto Iijima, Yasuhiro Takeshima, Yoshihiro Urade , Masafumi Matsuo
    • Journal Title

      Clinica Chimica Acta

      Volume: in press

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Journal Article] Utility of transmural myocardial strain profile for prediction of early left ventricular dysfunction in patients with Duchenne muscular dystrophy.2013

    • Author(s)
      Yamamoto T, Tanaka H, Matsumoto K, Lee T, Awano H, Yagi M, Imanishi T, Hayashi N, Takeshima Y, Kawai H, Kawano S, Hirata K.
    • Journal Title

      Am J Cardiol.

      Volume: 111 Pages: 902-7

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Journal Article] A prostaglandin D2 metabolite is elevated in the urine of Duchenne muscular dystrophy patients and increases further from 8 years old.2013

    • Author(s)
      Nakagawa T, Takeuchi A, Kakiuchi R, Lee T, Yagi M, Awano H, Iijima K, Takeshima Y, Urade Y, Matsuo M.
    • Journal Title

      Clin Chim Acta.

      Volume: 423 Pages: 10-4

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Journal Article] A prostaglandin D2 metabolite is elevated in the urine of Duchenne muscular dystrophy patients and increases further from 8 years old2013

    • Author(s)
      Nakagawa T, Takeuchi A, Kakiuchi R, Lee T, Yagi M, Awano H, Iijima K, Takeshima Y, Urade Y, and Matsuo M
    • Journal Title

      Clin Chim Acta

      Volume: 423 Pages: 10-4

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Journal Article] Molecular characterization of an X(p21.2;q28) chromosomal inversion in a Duchenne muscular dystrophy patient with mental retardation reveals a novel long non-coding gene on Xq28.2013

    • Author(s)
      Thu Tran TH, Zhang Z, Yagi M, Lee T, Awano H, Nishida A, Okinaga T, Takeshima Y, Matsuo M.
    • Journal Title

      J Hum Genet.

      Volume: 58 Pages: 33-39

    • DOI

      10.1038/jhg.2012.131

    • NAID

      10031145898

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591496
  • [Journal Article] Molecular characterization of an X(p21.2;q28) chromosomal inversion in a Duchenne muscular dystrophy patient with mental retardation reveals a novel long non-coding gene on Xq282013

    • Author(s)
      Tran TH, Zhang Z, Yagi M, Lee T, Awano H, Nishida A, Okinaga T, Takeshima Y, and Matsuo M
    • Journal Title

      J Hum Genet

      Volume: 58 Pages: 33-9

    • NAID

      10031145898

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Journal Article] A G-to-T transversion at the splice acceptor site of dystrophin exon 14 shows multiple splicing outcomes that are not exemplified by transition mutations2012

    • Author(s)
      Ota M, Takeshima Y, Nishida A, Awano H, Lee T, Yagi M, and Matsuo M
    • Journal Title

      Genet Test Mol Biomarkers

      Volume: 16 Pages: 3-8

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Journal Article] Pathogenic orphan transduction created by a non-reference LINE-1retrotransposon2012

    • Author(s)
      Solyom S, Ewing AD, Hancks DC, Takeshima Y, Awano H, Matsuo M, Kazazian H Jr
    • Journal Title

      Hum. Mutat

      Volume: 33 Pages: 369-371

    • Data Source
      KAKENHI-PROJECT-21390311
  • [Journal Article] Valproic acid increases SMN2 expression and modulates SF2/ASF and hnRNPA1 expression in SMA fibroblast cell lines.2012

    • Author(s)
      Harahap IS, Saito T, San LP, Sasaki N, Gunadi, Nurputra DK, Yusoff S, Yamamoto T, Morikawa S, Nishimura N, Lee MJ, Takeshima Y, Matsuo M, Nishio H
    • Journal Title

      Brain Dev.

      Volume: 34 Pages: 213-222

    • DOI

      10.1016/j.braindev.2011.04.010

    • NAID

      10031050154

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22591127, KAKENHI-PROJECT-23791175
  • [Journal Article] Optimizing RNA/ENA Chimeric Antisense Oligonucleotides Using In Vitro Splicing.2012

    • Author(s)
      Takeshima Y, Yagi M, Matsuo M.
    • Journal Title

      Methods Mol Biol.

      Volume: 867 Pages: 131-41

    • Data Source
      KAKENHI-PROJECT-23591495
  • [Journal Article] Categorization of 77 dystrophin exons into 5 groups by a decision tree using indexes of plicing regulatory factors as decision markers.2012

    • Author(s)
      Rusdy Ghazali Malueka, Yutaka Takaoka, Mariko Yagi, Hiroyuki Awano, Tomoko Lee, Ery Kus Dwianingsih, Atsushi Nishida, Yasuhiro Takeshima, Masafumi Matsuo
    • Journal Title

      BMC Genet

      Volume: 13(23) Pages: 23-23

    • DOI

      10.1186/1471-2156-13-23

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22590653, KAKENHI-PROJECT-23591495, KAKENHI-PROJECT-23591496
  • [Journal Article] Optimizing RNA/ENA chimeric antisense oligonucleotides using in vitro splicing2012

    • Author(s)
      Takeshima Y, Yagi M, and Matsuo M
    • Journal Title

      Methods Mol Biol

      Volume: 867 Pages: 131-41

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Journal Article] Pathogenic orphan transduction created by a nonreference LINE-1 retrotransposon.2012

    • Author(s)
      Solyom S, Ewing AD, Hancks DC, Takeshima Y, Awano H, Matsuo M, Kazazian H H, Jr.
    • Journal Title

      Hum Mutat.

      Volume: 33(2) Pages: 369-71

    • DOI

      10.1002/humu.21663

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Journal Article] A G-to-T Transversion at the splice acceptor site of dystrophin exon 14 shows multiple splicing outcomes that are note exemplified by transition mutations.2012

    • Author(s)
      Ota M, Takeshima Y, Nishida A, Awano H, Lee T, Yagi M, Matsuo M.
    • Journal Title

      Genet Test Mol Biomarkers

      Volume: 16 Pages: 3-8

    • DOI

      10.1089/gtmb.2010.0276

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591495, KAKENHI-PROJECT-23591496
  • [Journal Article] Optimizing RNA/ENA chimeric antisense oligonucleotides using in vitro splicing2012

    • Author(s)
      Takeshima Y, Yagi M, Matsuo M.
    • Journal Title

      Methods Mol Biol

      Volume: 867 Pages: 131-141

    • DOI

      10.1007/978-1-61779-767-5_9

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591496
  • [Journal Article] athogenic orphan transduction created by a non-reference LINE-1 retrot ransposon2012

    • Author(s)
      Solyom S, Ewing AD, Hancks DC, Takeshima Y, Awano H, Matsuo M, Kazazian HH Jr
    • Journal Title

      Hum.Mutat

      Volume: 33 Pages: 369-371

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21390311
  • [Journal Article] Categorization of 77 dystrophin exons into 5 groups by a decision tree using indexes of splicing regulatory factors as decision markers.2012

    • Author(s)
      Malueka RG, Takaoka Y, Yagi M, Awano H, Lee T, Dwianingsih EK, Nishida A, Takeshima Y, Matsuo M.
    • Journal Title

      BMC Genet.

      Volume: 13 Pages: 23-23

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Journal Article] A Japanese child with geleophysic dysplasia caused by a novel mutation of FBN1.2012

    • Author(s)
      Lee T, Takeshima Y, Okizuka Y, Hamahira K, Kusunoki N, Awano H, Yagi M, Sakai N, Matsuo M, Iijima K
    • Journal Title

      Gene

      Volume: 512 Pages: 456-459

    • DOI

      10.1016/j.gene.2012.10.060

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591496
  • [Journal Article] Categorization of 77 dystrophin exons into 5 groups by a decision tree using indexes of splicing regulatory factors as decision markers2012

    • Author(s)
      Malueka RG, Takaoka Y, Yagi M, Awano H, Lee T, Dwianingsih EK, Nishida A, Takeshima Y, and Matsuo M
    • Journal Title

      BMC Genet

      Volume: 13 Pages: 23-23

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Journal Article] 小児医学最近の進歩 脊髄性筋萎縮症と SMN 蛋白と低分子量リボ核蛋白合成2011

    • Author(s)
      西尾久英, 斉藤利雄, 森川悟, 山本友人, Dian Kesumapramudya Nurputra, 寶田徹, 竹内敦子, 西村範行, 竹島泰弘, 松尾雅文
    • Journal Title

      小児科

      Volume: 52 Pages: 1535-1542

    • NAID

      40019029323

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22591127
  • [Journal Article] Chemical treatment enhances skipping of amutated exon in the dystrophin gene2011

    • Author(s)
      Nishida A, Kataoka N, Takeshima Y,Yagi M, Awano, H, Ota, M, Itoh K, Hagiwara M, and Matsuo M
    • Journal Title

      Nature Communications

      Volume: 2 Pages: 308-308

    • DOI

      10.1038/ncomms1306

    • NAID

      120003001398

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22500288, KAKENHI-PROJECT-22603002, KAKENHI-PUBLICLY-23112706, KAKENHI-PROJECT-23591496
  • [Journal Article] 非侵襲的陽圧換気療法と器械による咳介助を活用し気管内挿管から離脱した脊髄性筋萎縮症I型2011

    • Author(s)
      粟野宏之, 李知子, 八木麻理子, 竹島泰弘, 西尾久英, 松尾雅文
    • Journal Title

      日本小児科学会雑誌

      Volume: 115 Pages: 1451-1455

    • NAID

      10029704933

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22591127
  • [Journal Article] 小児医学最近の進歩脊髄性筋萎縮症とSMN蛋白と低分子量リボ核蛋白合成2011

    • Author(s)
      西尾久英, 斉藤利雄, 森川悟, 山本友人, Dian Kesumapramudya Nurputra, 實田徹, 竹内敦子, 西村範行, 竹島泰弘, 松尾雅文
    • Journal Title

      小児科

      Volume: 52 Pages: 1535-1542

    • NAID

      40019029323

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22591127
  • [Journal Article] Antisense oligonucleotide induced dystrophin exon 45 skipping at a low half-maximal effective concentration in a cell-free splicing system2011

    • Author(s)
      Malueka RG, Yagi M, Awano H, Lee T, Dwianingsih EK, Nishida A, Takeshima Y, and Matsuo M
    • Journal Title

      Nucleic Acid Ther

      Volume: 21 Pages: 347-53

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Journal Article] 非侵襲的陽圧換気療法と器械による咳介助を活用し気管内挿管から離脱した脊髄性筋萎縮症 I型.2011

    • Author(s)
      粟野宏之, 李知子, 八木麻理子, 竹島泰弘,西尾久英, 松尾雅文
    • Journal Title

      日本小児科学会雑誌

      Volume: 115 Pages: 1451-1455

    • NAID

      10029704933

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22591127
  • [Journal Article] Antisense oligonucleotide induced dystrophin exon 45 skipping at a low half-maximal effective concentration in a cell-free splicing system2011

    • Author(s)
      Malueka RG, Yagi M, Awano H, Lee T, Dwianingsih EK, Nishida A, Takeshima Y, Matsuo M
    • Journal Title

      Nucleic Acid Ther

      Volume: 21(5) Pages: 347-53

    • DOI

      10.1089/nat.2011.0310

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591496
  • [Journal Article] Moleculaar chaaracterizatioon of the 5'-UUTR of retinnal dysstrophin reveals a cryptiic intron thaat reggulates transslational acttivity2010

    • Author(s)
      Kubokawa, I., Takeshima, Y., Ota, M., Enomoto, M., Okizuka, Y., Mori, T., Nishimura, N., Awano, H., Yagi, M., Matsuo, M
    • Journal Title

      Mol Vis

      Volume: 16 Pages: 2590-2597

    • Data Source
      KAKENHI-PROJECT-21390311
  • [Journal Article] Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center.2010

    • Author(s)
      Takeshima Y, Yagi M, Okizuka Y, Awano H, Zhang Z, Yamauchi Y, Nishio H, Matsuo M.
    • Journal Title

      J Hum Genet. 55

      Pages: 379-388

    • NAID

      10030735518

    • Data Source
      KAKENHI-PROJECT-20591223
  • [Journal Article] 小児医学最近の進歩 脊髄性筋萎縮症 up to date 治療戦略2010

    • Author(s)
      西尾久英, HarahapIndra Sari Kusuma, 斉藤利雄, 西村範行, 森川悟, 山本友人, 中川卓, 竹島泰弘, 松尾雅文
    • Journal Title

      小児科

      Volume: 51 Pages: 1535-1542

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22591127
  • [Journal Article] Molecular characterization of the 5'-UTR of retinal dystrophin reveals a cryptic intron that regulates translational activity.2010

    • Author(s)
      Kubokawa I, Takeshima Y, Ota M, Enomoto M, Okizuka Y, Mori T, Nishimura N, Awano H, Yagi M, Matsuo M.
    • Journal Title

      Mol Vis. 16

      Pages: 2590-2597

    • Data Source
      KAKENHI-PROJECT-20591223
  • [Journal Article] 小児医学最近の進歩 脊髄性筋萎縮症 up to date 医学的管理2010

    • Author(s)
      西尾久英, 斉藤利雄, 西村範行, 森川悟, 山本友人, 三宅理, 粟野宏之, 竹島泰弘, 松尾雅文
    • Journal Title

      小児科

      Volume: 51 Pages: 1797-1806

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22591127
  • [Journal Article] Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center.2010

    • Author(s)
      Takeshima Y
    • Journal Title

      Journal of Human Genetics.

      Volume: 55 Pages: 379-388

    • NAID

      10030735518

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591223
  • [Journal Article] Low incidence of limb-girdle muscular dystrophy type 2C revealed by a mutation study in Japanese patients clinically diagnosed with DMD.2010

    • Author(s)
      Okizuka Y, Takeshima Y, Itoh K, Zhang Z, Awano H, MarMarrar, Mar, Marma K, Kumagai T, Yagi M, Matsuo M.
    • Journal Title

      BMC Med Genet. 30

    • Data Source
      KAKENHI-PROJECT-20591223
  • [Journal Article] Molecular characterization of the 5'-UTR of retinal dystrophin reveals a cryptic intron that regulates translational activity2010

    • Author(s)
      Kubokawa, I., Takeshima, Y., Ota, M., Enomoto, M., Okizuka, Y., Mori, T., Nishimura, N., Awano, H., Yagi, M., Matsuo, M.
    • Journal Title

      Molecular vision

      Volume: 16 Pages: 2590-2597

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21390311
  • [Journal Article] Contemporary retrotransposition of a novel non-coding gene induces exon-skipping in dystrophin mRNA.2010

    • Author(s)
      Awano H, Malueka RG, Yagi M, Okizuka Y, Takeshima Y, Matsuo M.
    • Journal Title

      J Hum Genet. 55

      Pages: 785-790

    • NAID

      10030737817

    • Data Source
      KAKENHI-PROJECT-20591223
  • [Journal Article] Insertion of the IL1RAPL1 gene into the duplication junction of the dystrophin gene.2009

    • Author(s)
      Zhang Z, Yagi M, Okizuka Y, Awano H, Takeshima Y, Matsuo M.
    • Journal Title

      J Hum Genet. 54

      Pages: 466-473

    • NAID

      10030731391

    • Data Source
      KAKENHI-PROJECT-20591223
  • [Journal Article] In vitro splicing analysis showed that availability of a cryptic splice site is not a determinant for alternative splicing patterns caused by +1G-->A mutations in introns of the dystrophin gene.2009

    • Author(s)
      Habara Y, Takeshima Y, Awano H, Okizuka Y, Zhang Z, Saiki K, Yagi M, Matsuo M.
    • Journal Title

      J Med Genet. 46

      Pages: 542-547

    • Data Source
      KAKENHI-PROJECT-20591223
  • [Journal Article] Small mutations detected by multiplex ligation-dependent probe amplification of the dystrophin gene.2009

    • Author(s)
      Okizuka Y, Takeshima Y, Awano H, Zhang Z, Yagi M, Matsuo M.
    • Journal Title

      Genet Test Mol Biomarkers. 13

      Pages: 427-431

    • Data Source
      KAKENHI-PROJECT-20591223
  • [Journal Article] A 2-bp deletion in exon 74 of the dystrophin gene does not clearly induce muscle weakness.2008

    • Author(s)
      Kimura, S. Ito, K. Ueno, H. Ikezawa, M. Takeshima,Y. Yoshioka, K.Ozasa, S. Nakamuara, K. Nomura, K. Matsukura, M. Mitsui, K. Matsuo, M. Miike, T.
    • Journal Title

      Brain & Development. 18

      Pages: 672-677

    • NAID

      10025578962

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19390284
  • [Journal Article] A strong exonic splicing enhancer in dystrophin exon 19 achieve proper splicing without an upstream polypyrimidine tract.2008

    • Author(s)
      Habara Y, Doshita M, Hirozawa S, Yokono Y, Yagi M, Takeshima Y, Matsuo M.
    • Journal Title

      J Biochem. 143

      Pages: 303-310

    • NAID

      10024908594

    • Data Source
      KAKENHI-PROJECT-20591223
  • [Journal Article] High incidence of electrocardiogram abnormalities in young patients with duchenne muscular dystrophy.2008

    • Author(s)
      Takami Y, Takeshima Y, Awano H, Okizuka Y, Yagi M, Matsuo M.
    • Journal Title

      Pediatr Neurol. 39

      Pages: 399-403

    • Data Source
      KAKENHI-PROJECT-20591223
  • [Journal Article] Dystrophin nonsense mutations can generate alternative rescue transcripts in lymphocytes.2008

    • Author(s)
      Nishiyama A, Takeshima Y, Zhang Z, Habara Y, Tran TH, Yagi M, Matsuo M.
    • Journal Title

      Ann Hum Genet. 72

      Pages: 717-724

    • Data Source
      KAKENHI-PROJECT-20591223
  • [Journal Article] Tandem duplications of two separate fragments of the dystrophin gene in a patient with Duchenne muscular dystrophy.2008

    • Author(s)
      Zhang Z, Takeshima Y, Awano H, Nishiyama A, Okizuka Y, Yagi M, Matsuo M.
    • Journal Title

      J Hum Genet. 53

      Pages: 215-219

    • NAID

      10021248166

    • Data Source
      KAKENHI-PROJECT-20591223
  • [Journal Article] In vitro splicing analysis reveals that availability of a cryptic splice site is not a determinant for alternative splicing patterns caused by +1G>A mutations in introns of the dystrophin gene.2008

    • Author(s)
      Habara, Y.,Takeshima, Y., Awano, H., Okizuka, Y., Zhang, Z., Saiki, K., Yagi, M., Matsuo, M.
    • Journal Title

      J Med Genet. in press.

      Pages: 0-0

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19390284
  • [Journal Article] A Strong Exonic Splicing Enhancer in Dystrophin Exon 19 achieve proper splicing without an upstream polypyrimidine tract.2008

    • Author(s)
      Habara,Y.Doshita,M.Hirozawa,S. Yokono,Y.Yagi,M.Takeshima,Y. Matsuo,M.
    • Journal Title

      J Biochem.143

      Pages: 303-310

    • NAID

      10024908594

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19390284
  • [Journal Article] Dystrophin nonsense mutations can generate alternative rescue transcrips in lymphocytes.2008

    • Author(s)
      Nisiyama, A., Takeshima, Y., Zhang, Z., Habara, Y., Tran, TH., Yagi, M., Matsuo, M.
    • Journal Title

      Ann Hum Genet. 72

      Pages: 717-724

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19390284
  • [Journal Article] High incidence of electrocardiogram abnormalities in young patients with duchenne muscular dystrophy.2008

    • Author(s)
      Takami, Y., Takeshima, Y., Awano, H., Okizuka, Y., Yagi, M. and Masuo, M.
    • Journal Title

      Pediatr. Neurol. 39

      Pages: 399-403

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19390284
  • [Journal Article] Wide ranges of serum myostatin concentrations in Duchenne muscular dystrophy patients.2008

    • Author(s)
      Awano, H., Takeshima, Y., Okizuka, Y., Saiki, K., Yagi, M., Matsuo, M.
    • Journal Title

      Clin Chim Acta. 391

      Pages: 115-117

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19390284
  • [Journal Article] SMN2 and NAP gene dosages in Vietnamese patients with spinal muscular atrophy2008

    • Author(s)
      Van, Khanh, TV, Teguh, Haryo, Sasongko, Dang, Diem Hong , Nguyen, Thi, Hoan, Vu, Chi, Dung, Myeongn Jin Lee , Gunadi, Indra, Sari, Kusuma, Harahap, Yasuhiro, Takeshima, Masafumi, Matsuo, Hisahide, Nishio
    • Journal Title

      Pediatr Int (in press)

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18591151
  • [Journal Article] Tandem duplications of two separate fragments of the dystrophin gene in a patient with Duchenne muscular dystrophy.2008

    • Author(s)
      Zhang,Z. Takeshima,Y. Awano,H. Nishiyama,A. Okizuka,Y. Yagi,M. Matsuo,M.
    • Journal Title

      J Hum Genet. 53

      Pages: 215-219

    • NAID

      10021248166

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19390284
  • [Journal Article] SMN2 and NAIP gene dosages in Vietnamese patients with spinal muscular atrophy.2008

    • Author(s)
      Van Khanh TV, Teguh Haryo Sasongko, Dang Diem Hong, Nguyen Thi Hoan, Vu Chi Dung, Myeong Jin Lee, Gunadi, Indra Sari Kusumma Harahap, Yasuhiro Takeshima, Masafumi Matsuo and Hisahide Nishio.
    • Journal Title

      Pediatrics International (in press)

    • NAID

      10025343726

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18591151
  • [Journal Article] A nonsense mutation-created intraexonic splice site is active in the lymphocytes, but not in the skeletal muscle of a DMD patient.2007

    • Author(s)
      Tran VK. Takeshima Y, Zhang Z, Habara Y, Haginoya K, Nishiyama A, Yagi M, Matsuo M.
    • Journal Title

      Hum Genet. 120

      Pages: 737-742

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19390284
  • [Journal Article] Two novel missense mutations in the myostation gene identified in Japanese patients with Duchenne muscular dystrophy.2007

    • Author(s)
      Nishiyama A, Takeshima Y, Saiki K, Narukage A, Ouazato Y, Yagi M, Matsuo M.
    • Journal Title

      BMC Medical Genetics.

      Pages: 624-630

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19390284
  • [Journal Article] In vitro and silico analysis reveals an efficient algorithm to predict the splicing consequences of mutations at the 5' splice sites.2007

    • Author(s)
      Sahashi K, Masuda A, Matsuure T, Shinmi J, Zhang Z, Takeshima Y, Matsuo M, Sobue G, Ohno K.
    • Journal Title

      Nucleic Acids Res.

      Pages: 1-9

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19390284
  • [Journal Article] Intravenous infusion of an antisense oligonucleotide results in exon skipping in muscle dystrophin mRNA of Duchenne muscular dystrophy.2006

    • Author(s)
      Takeshima Y
    • Journal Title

      Pediatric Research 59(5)

      Pages: 690-694

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18591152
  • [Journal Article] Intravenous infusion of an antisense oligonucleotide results in exon skipping in muscle dystrophin mRNA of Duchenne muscular dystrophy.2006

    • Author(s)
      Takeshima Y
    • Journal Title

      Pediatr Res. 59(5)

      Pages: 690-694

    • Data Source
      KAKENHI-PROJECT-18591152
  • [Journal Article] Intravenous infusion of an antisense oligonucleotide results in exon skipping in muscle dystrophin mRNA of Duchenne muscular dystrophy2006

    • Author(s)
      Takeshima, Y
    • Journal Title

      Pediatr Res 59-5

      Pages: 690-694

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18591152
  • [Journal Article] Intravenous infusion of an antisense oligonucleotide results in exon skipping in muscle dystrophin mRNA of duchenne muscular dystrophy.2006

    • Author(s)
      Takeshima Y
    • Journal Title

      Pediatr Res. 59・5

      Pages: 690-694

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-16591027
  • [Journal Article] Intravenous infusion of an antisense oligonucleotide results in exon skipping in muscle dystrophin mRNA of duchenne muscular dystrophy.2006

    • Author(s)
      Yasuhiro, Takeshima
    • Journal Title

      Pediatr Res. 59-5

      Pages: 690-694

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-16591027
  • [Journal Article] Intraperitoneal administration of phosphorothioate antisense oligodeoxynucleotide against splicing enhancer sequence induced exon skipping in dystrophin mRNA expressed in mdx skeletal muscle2005

    • Author(s)
      Takeshima, Y
    • Journal Title

      Brain Dev

      Pages: 488-493

    • NAID

      10017132332

    • Data Source
      KAKENHI-PROJECT-16653066
  • [Journal Article] Duchenne型筋ジストロフィーの分子治療2005

    • Author(s)
      竹島泰弘
    • Journal Title

      日本臨床 65・12

      Pages: 626-631

    • NAID

      40007435942

    • Data Source
      KAKENHI-PROJECT-16591027
  • [Journal Article] Intraperitoneal administration of phosphorothioate antisense oligodeoxynucleotide against splicing enhancer sequence induced exon skipping in dystrophin mRNA expressed in mdx skeletal muscle2005

    • Author(s)
      Takeshima Y
    • Journal Title

      Brain Dev 27・7

      Pages: 488-493

    • NAID

      10017132332

    • Data Source
      KAKENHI-PROJECT-16591027
  • [Journal Article] Intraperitoneal administration of phosphorothioate antisense oligodeoxynucleotide against splicing enhancer sequence induced exon skipping in dystrophin mRNA expressed in mdx skeletal muscle.2005

    • Author(s)
      Takeshima, Y., et al.
    • Journal Title

      Brain Dev 27

      Pages: 488-493

    • NAID

      10017132332

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-16390301
  • [Journal Article] Discontinuation of Methotrexate after Related Bone Marrow Transplantation ntensify the Graft-versus-Leukemia Effect in a Case of Juvenile Myelomonocytic Leukemia without Obvious Graft-versus-Host Disease2005

    • Author(s)
      Keiichiro Kawasaki, Takeshi Mori, Hironobu Takahashi, Wakako Ogino, Akira Hayakawa, Yoshiyuki Kosaka, Yasuhiro Takeshima, Masafumi Matsuo
    • Journal Title

      The Japanese Journal of Pediatric Hematology Vol.19, No.3(in press)

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15591107
  • [Journal Article] Intraperitoneal administration of phosphorothioate antisense oligodeoxynucleotide against splicing enhancer sequence induced exon skipping in dystrophin mRNA expressed in mdx skeletal musclc.2005

    • Author(s)
      Takeshima Y
    • Journal Title

      Brain Dev. 27・7

      Pages: 488-493

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-16591027
  • [Journal Article] Intraperitoneal administration of phosphorothioate antisense oligodeoxynucleotide against splicing enhancer sequence induced exon skipping in dystrophin mRNA expressed in mdx skeletal muscle.2005

    • Author(s)
      Takeshima, Y.
    • Journal Title

      Brain Dev 27

      Pages: 488-493

    • NAID

      10017132332

    • Data Source
      KAKENHI-PROJECT-16390301
  • [Journal Article] Intraperitoneal administration of phosphorothioate antisense oligodeoxynucleotide against splicing enhancer sequence induced exon skipping in dystrophin mRNA expressed in mdx skeletal muscle.2005

    • Author(s)
      Yasuhiro, Takeshima
    • Journal Title

      Brain Dev. 27-7

      Pages: 488-493

    • NAID

      10017132332

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-16591027
  • [Journal Article] C-terminal Truncated Dystrophin Identified in Skeletal Muscle of an Asymptomatic Boy with a Novel Nonsense Mutation of the Dystrophin Gene2004

    • Author(s)
      Suminaga R, Takeshima Y, Wada H, Yagi M, Matsuo M
    • Journal Title

      Pediatric Research 56

      Pages: 739-743

    • Data Source
      KAKENHI-PROJECT-16653066
  • [Journal Article] Cloning of cDNA Encoding Regeneration-associated Muscle Protease Whose Expression is Attenuated in Cell Lines Derived from Duchenne Muscular Dystrophy Patients2004

    • Author(s)
      Nakayama Y, Nara N, Kawakita Y, Takeshima Y, Arakawa M, Katoh M, Morita S, Iwatsuki K, Tanaka K, Okamoto S, Kitamura T, Seki N, Matsuda R, Matsuo M, Saito K, Hara T.
    • Journal Title

      American Journal of Pathology 164

      Pages: 1773-1782

    • Data Source
      KAKENHI-PROJECT-16653066
  • [Journal Article] Successful treatment of two cases of juvenile myelomonocytic leukemia with Neurofibromatosis type followed by unrelated allogeneic bone marrow transplantation2004

    • Author(s)
      Keiichiro Kawasaki, Takeshi Mori, Hironobu Takahashi, Wakako Ogino, Kazuko Uchide, Akira Hayakawa, Yoshiyuki Kosaka, Yasuhiro Takeshima, Masafumi Matsuo
    • Journal Title

      The Japanese Journal of Pediatric Hematology Vol.18, No.5

      Pages: 554-560

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15591107
  • [Journal Article] Chimeric RNA and 2'-O, 4'-C-ethylene-bridged nucleic acids have stronger activity than phosphorothioate oligodeoxynucleotides in induction of exon-19 skipping in dystrophin mRNA2004

    • Author(s)
      Yagi M, Takeshima Y, Surono A, Takagi M, Koizumi M, Matsuo M.
    • Journal Title

      Oligonucleotides 14

      Pages: 33-40

    • Data Source
      KAKENHI-PROJECT-16653066
  • [Journal Article] Chimeric RNA/ethylene bridged nucleic acids promote dystrophin expression in myocytes of Duchenne muscular dystrophy by inducing skipping of the nonsense-mutation-encoding exon2004

    • Author(s)
      Surono A, Khanh TV, Takeshima Y, Wada H, Yagi M, Takagi M, Koizumi M, Matsuo M
    • Journal Title

      Hum Gene Ther 15

      Pages: 749-757

    • Data Source
      KAKENHI-PROJECT-16653066
  • [Journal Article] Intravenous infusion of an antisense oligonucleotide results in exon skipping in muscle dystrophin mRNA of Duchenne muscular dystrophy.

    • Author(s)
      Takeshima, Y
    • Journal Title

      Pediatric Research in press

    • Data Source
      KAKENHI-PROJECT-16653066
  • [Presentation] ビルトラルセン治療中のDuchennne型筋ジストロフィー(DMD)患者6例の経過2022

    • Author(s)
      谷口 直子, 田中 めぐみ, 堀部 拓哉, 佐浦 龍太郎, 角田 朋大, 徳永 沙知, 李 知子, 下村 英毅, 竹島 泰弘
    • Organizer
      第35回近畿小児科学会
    • Data Source
      KAKENHI-PROJECT-21K07831
  • [Presentation] 家族歴のない高CK血症女児の臨床背景の検討2019

    • Author(s)
      李 知子, 徳永 沙知, 牟禮 慎子, 三﨑 真生子, 下村 英毅, 西野 一三, 伊東 恭子, 竹島 泰弘
    • Organizer
      第61回日本小児神経学会学術集会
    • Data Source
      KAKENHI-PROJECT-17K10087
  • [Presentation] A manifesting carrier of Duchenne Muscular Dystrophy with a balanced X-autosome translocation with a breakpoint in the dystrophin gene2019

    • Author(s)
      Lee T., Sokoda T., Misaki M., Shimomura H., Takeshima Y.
    • Organizer
      24th International Annual Congress of the World Muscle Society
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-17K10087
  • [Presentation] ジストロフェン遺伝子内に切断点を有するX染色体-常染色体均衡型転座によるデュシェンヌ型筋ジストロフィー女児2019

    • Author(s)
      李 知子, 底田 辰之, 三﨑 真生子, 下村 英毅, 奥野 美佐子, 竹島 泰弘
    • Organizer
      第60回日本人類遺伝学会
    • Data Source
      KAKENHI-PROJECT-17K10087
  • [Presentation] Clinical background of hyper-creatine-kinase-emia girls without a family history of genetic muscular diseases2019

    • Author(s)
      Tamoko L., Tokunaga S.,, Mure C., Misaki M., Shimomura H., Nishino I., Itoh K., Takeshima Y.
    • Organizer
      EUROPEAN HUMAN GENETICS CONFERENCE 2019
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-17K10087
  • [Presentation] 筋疾患の家族歴のない無症候性高CK血症女児の検討2018

    • Author(s)
      李知子, 三崎真生子, 下村英毅, 伊東恭子, 竹島泰弘
    • Organizer
      日本小児科学会
    • Data Source
      KAKENHI-PROJECT-16H05814
  • [Presentation] 新規変異を同定した重症型LMNA-related congenital muscular dystrophyの一例2018

    • Author(s)
      李 知子、下村英毅、牟禮慎子、三崎真生子、香田 翼、柴田暁男、川本久美、岡田陽子、小泉真琴、伊東恭子、竹島泰弘
    • Organizer
      日本小児神経学会
    • Data Source
      KAKENHI-PROJECT-17K10087
  • [Presentation] 次世代シークエンサーを用いた遺伝子解析によりCalpain-3遺伝子変異を同定した筋症状のない高CK血症女児2018

    • Author(s)
      李知子、西岡 隆文、三崎真生子、下村英毅、竹島泰弘
    • Organizer
      日本人類遺伝学会第63回大会
    • Data Source
      KAKENHI-PROJECT-17K10087
  • [Presentation] 家族歴のない無症候性高CK血症女児の検討2018

    • Author(s)
      李知子、三崎真生子、下村英毅、伊東恭子、竹島泰弘
    • Organizer
      第121回日本小児科学会学術集会
    • Data Source
      KAKENHI-PROJECT-17K10087
  • [Presentation] 新規変異を同定した重症型LMNA-related congenital muscular dystrophyの一例2018

    • Author(s)
      李知子、下村英毅、牟禮慎子、三崎真生子、香田翼、柴田暁男、川本久美、岡田陽子、小泉真琴、伊東恭子、竹島泰弘
    • Organizer
      日本小児神経学会
    • Data Source
      KAKENHI-PROJECT-16H05814
  • [Presentation] Duchenne型筋ジストロフィーに対するENAアンチセンスオリゴヌクレオチド(AO85)投与の効果2017

    • Author(s)
      李知子, 下村英毅, 粟野宏之, 飯島一誠, 荻寛志, 伊東恭子, 松尾雅文, 竹島泰弘
    • Organizer
      日本小児神経学会
    • Data Source
      KAKENHI-PROJECT-16H05814
  • [Presentation] 片側アレルに近接した2つの遺伝子異常を認めたUllrich型先天性筋ジストロフィーの1例2017

    • Author(s)
      下村英毅, 李知子, 松本真明, 粟野宏之, 伊東恭子, 西 一三, 竹島泰弘
    • Organizer
      日本小児神経学会
    • Data Source
      KAKENHI-PROJECT-16H05814
  • [Presentation] Advantage of next generation sequencing in molecular diagnosis in DMD -mutation screening with long preserved dried umbilical cord and detection of mosaicism-.2016

    • Author(s)
      Taniguchi-Ikeda M, Unzaki A, Takeshima Y, Lee T, Awano H, Yagi M, Kurahashi H, Morioka I, Toda T, Matsuo M, Iijima K
    • Organizer
      13th International Congress of Human Genetics
    • Place of Presentation
      Kyoto, Japan
    • Year and Date
      2016-04-03
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26461632
  • [Presentation] A new antisense oligonucleotide composed of RNA/ENA chimera (AO85) against dystrophin exon 45 significantly increased six-minute walk distance in Duchenne muscular dystrophy2016

    • Author(s)
      Yasuhiro Takeshima, Tomoko Lee, Hideki shimomura, Yasuhiko Tanaka, Hiroyuki Awano, Atsushi Nishida, Isao Ojima, Satoshi Minami, Akio Nakagawa, Kazumoto Iijima, Masafumi Matsuo
    • Organizer
      5th International Congress of Myology
    • Place of Presentation
      Lyon, France
    • Year and Date
      2016-03-14
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26461545
  • [Presentation] Advantage of next generation sequencing in molecular diagnosis in DMD - mutation screening with long preserved dried umbilical cord and detection of mosaicism-2016

    • Author(s)
      Unzaki A, Taniguchi-Ikeda M, Takeshima Y, Lee T, Awano H, Yagi M, Kurahashi H, Morioka I, Toda T, Matsuo M, Iijima K
    • Organizer
      the 13th International Congress of Human Genetics
    • Place of Presentation
      Kyoto, Japan
    • Year and Date
      2016-04-03
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26461632
  • [Presentation] RNA/ENA chimera antisense oligonucleotide (AO85) was safely administered and shown to induce dystrophin exon 45 skipping in Duchenne muscular dystrophy patient: the first clinical study2016

    • Author(s)
      Yasuhiro Takeshima, Tomoko Lee, Hideki Shimomura, Yasuhiko Tanaka, Hiroyuki Awano, Atsushi Nishida, Isao Ojima, Satoshi Minami, Akio Nakagawa, Kazumoto Iijima, Masafumi Matsuo
    • Organizer
      The 13th International Congress of Human Genetics
    • Place of Presentation
      Kyoto International Conference Center(京都府京都市)
    • Year and Date
      2016-04-04
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26461545
  • [Presentation] The carrier frequency in the mothers of 158 Japanese cases with Duchenne/Becker muscular dystrophy2013

    • Author(s)
      Lee T, Kusunoki N, Yagi M, Takeshima Y, Matsuo M. and Iijima K
    • Organizer
      European Human Genetics Conference 2013
    • Place of Presentation
      Paris, France
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Presentation] ジストロフィン遺伝子スプライシングコンセンサス配列内変異によるスプライシング型の変化 に関わる因子の検討2013

    • Author(s)
      李知子、楠典子、八木麻理子、竹島泰弘、松尾雅文、飯島一誠、
    • Organizer
      日本人類遺伝学会第58回大会
    • Place of Presentation
      宮城県仙台市
    • Data Source
      KAKENHI-PROJECT-23591496
  • [Presentation] Three-dimensional gait analysis of Duchenne muscular dystrophy; a trial to evaluate the therapeutic effect of RNA/ENA chimera antisense oligonucleotide that induces dystrophin exon 45 skipping2013

    • Author(s)
      Takeshima Y, Yagi M, Lee T, Kusunoki N, Ojima I, Minami S, Asai T, Nakagawa A, Iijima K, and Matsuo M
    • Organizer
      18th International Congress of the World Muscle Society
    • Place of Presentation
      California, USA
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Presentation] A novel splicing silencer generated by dystrophin exon 45 deletion could explain exon 44 skipping that modifies dystrophinopathy2013

    • Author(s)
      Matsuo M, Dwianingsih EM, Malueka RG, Nishida A, Lee T, Yagi M, Iijima K, and Takeshima Y
    • Organizer
      American Society of Human Genetics, the 63^<rd> Annual Meeting
    • Place of Presentation
      Boston, USA
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Presentation] The carrier frequency in the mothers of 158 Japanese cases with Duchenne/Becker muscular dystrophy.2013

    • Author(s)
      Lee T, Kusunoki N, Yagi M, Takeshima Y, Matsuo M, Iijima K.
    • Organizer
      European Human Genetics Conference 2013
    • Place of Presentation
      Paris
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Presentation] A prostaglandin D2 metabolite is elevated in the urine samples of patients with Duchenne muscular dystrophy2013

    • Author(s)
      Nakagawa T, Takeuchi A, Kakiuchi R, Lee T, Yagi M, Awano H, Iijima K, Takeshima Y, Urade Y, and Matsuo M
    • Organizer
      18th International Congress of the World Muscle Society
    • Place of Presentation
      California, USA
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Presentation] ジストロフィン遺伝子スプライシングコンセンサス配列内変異によるスプライシング型の変化に関わる因子の検討2013

    • Author(s)
      李知子、楠典子、八木麻理子、竹島泰弘、松尾雅文、飯島一誠
    • Organizer
      日本人類遺伝学会第58回大会
    • Place of Presentation
      宮城県仙台市
    • Data Source
      KAKENHI-PROJECT-23591496
  • [Presentation] A prostaglandin D2 metabolite is elevated in the urine samples of patients with Duchenne muscular dystrophy.2013

    • Author(s)
      Nakagawa T, Takeuchi A, Kakiuchi R, Lee T, Yagi M, Awano H, Iijima K, Takeshima Y, Urade Y, Matsuo M.
    • Organizer
      18th International Congress of the World Muscle Society
    • Place of Presentation
      California
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Presentation] Three-dimensional gait analysis of Duchenne muscular dystrophy; a trial to evaluate the therapeutic effect of RNA/ENA chimera antisense oligonucleotide that induces dystrophin exon 45 skipping.2013

    • Author(s)
      Takeshima Y, Yagi M, Lee T, Kusunoki N, Ojima I, Minami S, Asai T, Nakagawa A, Iijima K, Matsuo M.
    • Organizer
      18th International Congress of the World Muscle Society
    • Place of Presentation
      California
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Presentation] A novel splicing silencer generated by dystrophin exon 45 deletion could explain exon 44 skipping that modifies dystrophinopathy.2013

    • Author(s)
      Matsuo M, Dwianingsih EM, Maliueka RG, Nishida A, Lee T, Yagi M, Iijima K, Takeshima Y.
    • Organizer
      American Society of Human Genetics
    • Place of Presentation
      Boston
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Presentation] 臨床的に脊髄性筋萎縮症と診断された患者の SMN 遺伝子解析2012

    • Author(s)
      西尾久英, 西村範行, 森川悟, 山本友人, ディアン・ヌルプトラ, 中川卓, 竹島泰弘, 飯島一誠, 松尾雅文, 齊藤利雄
    • Organizer
      第82回日本衛生学会総会
    • Place of Presentation
      京都
    • Year and Date
      2012-03-25
    • Data Source
      KAKENHI-PROJECT-22591127
  • [Presentation] A small chemical, TG003, enhances skipping of mutated dystrophin exons : the third example revealing a decrease of exonic splicing enhancer density in common2012

    • Author(s)
      Nishida A, Takeshima Y, Kataoka N, Yagi M, Awano H, Lee T, Iijima K, Hagiwara M, Matsuo M
    • Organizer
      The American Society of Human Genetics, the 62th Annual Meeting
    • Place of Presentation
      San Francisco
    • Data Source
      KAKENHI-PROJECT-23591496
  • [Presentation] Dystrophin gene mutations in three dystrophinopathy patients with severe cardiomyopathy2012

    • Author(s)
      Awano H, Lee T, Yagi M, Takeshima Y, Matsuo M, Iijima K
    • Organizer
      Pediatric Academic Societies Annual Meeting
    • Place of Presentation
      Boston
    • Data Source
      KAKENHI-PROJECT-23591496
  • [Presentation] SMN2 遺伝子量解析による予測よりも軽症の経過をとった脊髄性筋萎縮症患者に対するプロモーター解析.2012

    • Author(s)
      森川悟, 中川卓, 富永康仁, 沖永剛志, 西村範行, 竹島泰弘, 松尾雅文, 西尾久英
    • Organizer
      第54回日本小児神経学会総会
    • Place of Presentation
      札幌
    • Year and Date
      2012-05-17
    • Data Source
      KAKENHI-PROJECT-22591127
  • [Presentation] A small chemical, TG003, enhances skipping of mutated dystrophin exons: the third example revealing a decrease of exonic splicing enhancer density in common.2012

    • Author(s)
      Nishida A, Takeshima Y, Kataoka N, Yagi M, Awano H, Lee T, Iijima K, Hagiwara M, Matsuo M.
    • Organizer
      The American Society of Human Genetics, the 62th Annual Meeting
    • Place of Presentation
      San Francisco
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Presentation] Duchenne型筋ジストロフィーにおける尿プロスタグランディンD2代謝産物の排泄の増加2012

    • Author(s)
      中川卓、李知子、粟野宏之、八木麻理子、松尾雅文、竹島泰弘
    • Organizer
      第54回日本小児神経学会総会
    • Place of Presentation
      札幌
    • Data Source
      KAKENHI-PROJECT-23591496
  • [Presentation] 臨床的に脊髄性筋萎縮症と診断された患者のSMN遺伝子解析2012

    • Author(s)
      西尾久英, 西村範行, 森川悟, 山本友人, ディアン ヌルプトラ, 中川卓, 竹島泰弘, 飯島一誠, 松尾雅文, 齊藤利雄
    • Organizer
      第82回日本衛生学会総会
    • Place of Presentation
      京都大学吉田キャンパス(京都)
    • Year and Date
      2012-03-25
    • Data Source
      KAKENHI-PROJECT-22591127
  • [Presentation] Duchenne/Becker型筋ジストロフィーにおけるジストロフィン遺伝子の微小変異の割合は増加傾向にある2012

    • Author(s)
      李知子、楠典子、粟野宏之、八木麻理子、竹島泰弘、松尾雅文、飯島一誠
    • Organizer
      日本人類遺伝学会57回大会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-23591496
  • [Presentation] A small chemical, TG003, enhances skipping of mutated dystrophin exons: the third example revealing a decrease of exonic splicing enhancer density in common.2012

    • Author(s)
      Nishida A, Takeshima Y, Kataoka N, Yagi M, Awano H, Lee T, Iijima K, Hagiwara M, Matsuo M.
    • Organizer
      The American Society of Human Genetics, the 62th Annual Meeting
    • Place of Presentation
      San Francisco
    • Data Source
      KAKENHI-PROJECT-23591496
  • [Presentation] Dystrophin Gene Mutations in Three Dystrophynopathy Patients with Severe Cardiomyopathy.2012

    • Author(s)
      Awano H, Lee T, Yagi M, Takeshima Y, Matsuo M, Iijima K.
    • Organizer
      Pediatric Academic Societies Annual Meeting
    • Place of Presentation
      Boston
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Presentation] Duchenne/Becker型筋ジストロフィーにおけるジストロフィン遺伝子の微小変異の割合は増加傾向にある2012

    • Author(s)
      李知子、楠典子、粟野宏之、八木麻理子、竹島泰弘、松尾雅文、飯島一誠
    • Organizer
      日本人類遺伝学会第57回大会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-23591496
  • [Presentation] Duchenne/Becker型筋ジストロフィー兄弟例における心機能障害の検討2012

    • Author(s)
      李知子、粟野宏之、八木麻理子、竹島泰弘、松尾雅文、飯島一誠
    • Organizer
      第115回日本小児科学会学術集会
    • Place of Presentation
      福岡
    • Data Source
      KAKENHI-PROJECT-23591496
  • [Presentation] A small chemical, TG003, enhances skipping of mutated dystrophin exons : the third example revealing a decrease of exonic splicing enhancer density in common2012

    • Author(s)
      Nishida A, Takeshima Y, Kataoka N, Yagi M, Awano H, Lee T, Iijima K, Hagiwara M, and Matsuo M
    • Organizer
      The American Society of Human Genetics, the 62^<nd> Annual Meeting
    • Place of Presentation
      San Francisco, USA
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Presentation] ベサフィブラートにより骨格筋症状が改善した極長鎖アシルCoA脱水素酵素欠損症の1例2012

    • Author(s)
      八木麻理子、楠典子、李知子、粟野宏之、但馬剛、小林弘典、長谷川有紀、山口清次、竹島泰弘、飯島一誠
    • Organizer
      第54回日本先天代謝異常学会
    • Place of Presentation
      岐阜
    • Data Source
      KAKENHI-PROJECT-23591496
  • [Presentation] Antisense RNA/Ethylene-bridged nucleic acid chimera induces exon 45 skipping in cultured myocytes from DMD patients with 6 different deletion mutations2011

    • Author(s)
      Yagi M, Lee T, Awano H, Takeshima Y, Matsuo M
    • Organizer
      The American Society of Human Genetics 61st Annual Meeting
    • Place of Presentation
      Montreal
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Presentation] Antisense RNA/Ethylene-bridged nucleic acid chimera induces exon 45 skipping in cultured myocytes from DMD patients with 6 different deletion mutaions2011

    • Author(s)
      Yagi M, Lee T, Awano H, Takeshima Y, Matsuo M
    • Organizer
      The American Society of Human Genetics 61th Annual Meeting
    • Place of Presentation
      Montreal
    • Data Source
      KAKENHI-PROJECT-23591496
  • [Presentation] Antisense RNA/ ethylene-bridged nucleic acid chimera induces exon skipping in cultured myocytes from DMD patients with 6 different deletion mutations2011

    • Author(s)
      Yagi M, Lee T, Awano H, Takeshima Y, and Matsuo M
    • Organizer
      The American Society of Human Genetics 61st Annual Meeting
    • Place of Presentation
      Montral, Canada
    • Data Source
      KAKENHI-PROJECT-23591495
  • [Presentation] ジストロフィン遺伝子エクソンスキッピングを誘導する低分子化合物の同定と治療への応用2011

    • Author(s)
      八木麻理子、李知子、粟野宏之、伊東恭子、竹島泰弘、松尾雅文
    • Organizer
      第53回日本小児神経学会総会
    • Place of Presentation
      横浜
    • Data Source
      KAKENHI-PROJECT-23591496
  • [Presentation] 非侵襲的陽圧換気療法と器械による咳介助で呼吸ケアをおこなっている脊髄性筋萎縮症1 型の1例2010

    • Author(s)
      粟野宏之, 李知子, 八木麻理子, 竹島泰弘, 西尾久英, 松尾雅文
    • Organizer
      第43回日本小児呼吸器疾患学会
    • Place of Presentation
      福岡
    • Year and Date
      2010-10-29
    • Data Source
      KAKENHI-PROJECT-22591127
  • [Presentation] Long-term administration of antisense oligonucleotide against dystrophin exon 19 for the treatment of Duchenne muscular dystrophy with exon 20 deletion.2010

    • Author(s)
      Matsuo M, Takeshima Y, Yagi M, Awano H.
    • Organizer
      XII International Congress on Neuromusular Diseases.
    • Place of Presentation
      Naples.
    • Data Source
      KAKENHI-PROJECT-20591223
  • [Presentation] Genotype-phenotype correlation of the dystrophinopathy cases with small mutations in the dystrophin gene.2010

    • Author(s)
      Awano H, Takeshima Y, Yagi M, Yamauchi Y, Malueka RG, Dwianingsih EK, Matsuo M.
    • Organizer
      Pediatric Academic Societies' 2010 Annual Meeting.
    • Place of Presentation
      Vancouver.
    • Data Source
      KAKENHI-PROJECT-20591223
  • [Presentation] Antisense RNA/ENA chimera against dystrophin exon 45 leads exon 45 skipping followed by dystrophin expression in cells from duchenne muscular dystrophy.2010

    • Author(s)
      Yagi M, Takeshima Y, Awano H, Ota M, Malueka RG, Dwianingsih EK, Nishida A, Lee T, Matsuo M.
    • Organizer
      6th Annual Meeting of the Oligonucleotide Therapeutics Society.
    • Place of Presentation
      Southern California
    • Data Source
      KAKENHI-PROJECT-20591223
  • [Presentation] Antisense RNA/ethylene-bridged nucleic acids chimera induces exon 45 skipping and restores dystrophin expression in myocytes of Duchenne muscular dystrophy.2010

    • Author(s)
      Yagi M, Ota M, Awano H, Takeshima Y, Matsuo M.
    • Organizer
      15th International Congress of The World Muscle Society.
    • Place of Presentation
      Kumamoto
    • Data Source
      KAKENHI-PROJECT-20591223
  • [Presentation] Antisense RNA/ethylene- bridged nucleic acid chimera induces exon 45 skipping and restores dystrophin expression in DMD muscle cells.2010

    • Author(s)
      Yagi M, Ota M, Awano H, Takeshima Y, Matsuo M.
    • Organizer
      XII International Congress on Neuromusular Diseases.
    • Place of Presentation
      Naples.
    • Data Source
      KAKENHI-PROJECT-20591223
  • [Presentation] SMN1 遺伝子の片側アレルの欠失を認め、もう一方のアレルに点突然変異を認めた脊髄性筋萎縮症の1 例2010

    • Author(s)
      森川悟, 山本友人,西村範行, 西尾久英, 竹島泰弘, 松尾雅文
    • Organizer
      第250回日本小児科学会兵庫県地方会総会
    • Place of Presentation
      神戸
    • Year and Date
      2010-05-29
    • Data Source
      KAKENHI-PROJECT-22591127
  • [Presentation] Mutation spectrum of the dystrophin gene in 456 Duchienne/Becker muscular dystrophy cases from one Japanese referral center.2010

    • Author(s)
      Takeshima Y, Yagi M, Ota M, Awano H, Yamauchi Y, Malueka RG, Dwianingsih EK, Nishio H, Matsuo M.
    • Organizer
      15th International Congress of The World Muscle Society.
    • Place of Presentation
      Kumamoto.
    • Data Source
      KAKENHI-PROJECT-20591223
  • [Presentation] Chemical treatment of muscular dystrophy that enhances skipping of the mutated exon in the dystrophin gene.2010

    • Author(s)
      Nishida A, Kataoka N, Takeshima Y, Yagi M, Awano H, Ota M, Itoh K, Hagiwara M, Matsuo M.
    • Organizer
      The American Society of Human Genetics 60th Annual Meeting.
    • Place of Presentation
      Washigton, DC.
    • Data Source
      KAKENHI-PROJECT-20591223
  • [Presentation] 非侵襲的陽圧換気療法でよりよい QOL を維持できている脊髄性筋萎縮症 1 型の 1 例.2010

    • Author(s)
      粟野宏之, 李知子, 八木麻理子, 竹島泰弘, 西尾久英, 松尾雅文.
    • Organizer
      第251回日本小児科学会兵庫県地方会
    • Place of Presentation
      姫路
    • Year and Date
      2010-09-25
    • Data Source
      KAKENHI-PROJECT-22591127
  • [Presentation] Chemical treatment of muscular dystrophy that enhances skiping of the mutated exon in the dystrophin gene2010

    • Author(s)
      Nishida A, Kataoka N, Takeshima Y, Yagi M, Awano H, Ota M, Itoh K, Hagiwara M, Matsuo M
    • Organizer
      The American Society of Human Genetics60th Anual Meeting
    • Place of Presentation
      Washigton, DC
    • Data Source
      KAKENHI-PROJECT-21390311
  • [Presentation] Duchenne 型筋ジストロフィー分子治療の適応に関する検討2009

    • Author(s)
      竹島泰弘
    • Organizer
      第51回日本小児神経学会総会
    • Place of Presentation
      米子コンベンションセンター(鳥取県)
    • Year and Date
      2009-05-29
    • Data Source
      KAKENHI-PROJECT-20591223
  • [Presentation] High incidence of outlier from the reading-frame rule in dystrophinopathy patients with duplication mutations in the dystrophin gene.2009

    • Author(s)
      Yagi M, Awano H, Okizuka Y, Takeshima Y, Matsuo M.
    • Organizer
      Pediatric Academic Societies' 2009 Annual Meeting.
    • Place of Presentation
      Baltimore.
    • Data Source
      KAKENHI-PROJECT-20591223
  • [Presentation] In vitro splicing analysis reveals that availability of a cryptic splice site is not a determinant for alternative splicing patterns caused by +1G>A mutations in introns of the dystrophin gene.2009

    • Author(s)
      Matsuo M, Habara Y, Takeshima Y, Awano H, Okizuka Y, Zhang Z, Yagi M.
    • Organizer
      14th International Congress of The World Muscle Society.
    • Place of Presentation
      Geneva.
    • Data Source
      KAKENHI-PROJECT-20591223
  • [Presentation] Antisense RNA/ethylene-bridged nucleic acids chimera induces exon skipping and restores dystrophin expression in myocytes of Duchenne muscular dystrophy.2009

    • Author(s)
      Yagi M, Yamauchi Y, Awano H, Takeshima Y, Matsuo M.
    • Organizer
      The American Society of Human Genetics 59th Annual Meeting.
    • Place of Presentation
      Hawaii.
    • Data Source
      KAKENHI-PROJECT-20591223
  • [Presentation] Splicing errors casued by small mutations in the dystrophin gene are different between lymphocytes and muscle tissues.2008

    • Author(s)
      Okizuka Y, Awano H, Yagi M, Takeshima Y, Matsuo M.
    • Organizer
      Pediatric Academic Societies' 2008 Annual Meeting.
    • Place of Presentation
      Hawaii.
    • Data Source
      KAKENHI-PROJECT-20591223
  • [Presentation] Mutation spectrum of the dystrophin gene in 433 Japanese dystrophinopathy cases.2008

    • Author(s)
      Takeshima Y
    • Organizer
      The American Society of Human Genetics 58th Annual Meeting
    • Place of Presentation
      Philadelphia, USA
    • Data Source
      KAKENHI-PROJECT-20591223
  • [Presentation] Mutation spectrum of the dystrophin gene in 433 Japanese dystrophinopathy cases.2008

    • Author(s)
      Takeshima, Y. Yagi, M. Okizuka, Y. Awano, H. Zang, Z. Saiki, K. Matsuo, M.
    • Organizer
      The American Society of Human Genetics 58th Annual Meeting.
    • Year and Date
      2008-11-14
    • Data Source
      KAKENHI-PROJECT-19390284
  • [Presentation] A novel retrotransposon that was recently inserted into exon 67 of the dystrophin gene.2008

    • Author(s)
      Awano H, Yagi M, Okizuka Y, Zhang Z, Takeshima Y, Matsuo M.
    • Organizer
      Joint 7th Human Genome Organization (HUGO)-Pacific Meeting and the 8th Asia-Pacific Conference on Human Genetics.
    • Place of Presentation
      Cebu.
    • Data Source
      KAKENHI-PROJECT-20591223
  • [Presentation] Mutation spectrum of the dystrophin gene in 433 Japanese dystrophinopathy cases.2008

    • Author(s)
      Takeshima Y, Yagi M, Okizuka Y, Awano H, Zang Z, Saiki K, Matsuo M.
    • Organizer
      The American Society of Human Genetics 58th Annual Meeting.
    • Place of Presentation
      Philadelphia.
    • Data Source
      KAKENHI-PROJECT-20591223
  • [Presentation] Intravenous infusion of antisense oligonucleotide induces dystrophin protein expression in the muscle of a Dchenne muscular dystrophy patient2007

    • Author(s)
      Takeshima, Y
    • Organizer
      25th International Congress of Pediatrics
    • Place of Presentation
      Athens
    • Year and Date
      2007-08-25
    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-18591152
  • [Presentation] Chronological changes of serum creatine kinase(CK)levels in molecularly confirmed Duchenne muscular dystrophy cases and examination of the cases with deviated CK levels.2007

    • Author(s)
      Okizuka,Y. Takeshima,Y. Yagi,M. Oyazato,Y. Awano,H. Zhang,Z. Matsuo,M.
    • Organizer
      57th The American Society of Human Genetics.
    • Year and Date
      2007-10-26
    • Data Source
      KAKENHI-PROJECT-19390284
  • [Presentation] The Xq28 inversion breakpoint interrupted a novel noncoding gene in a patient with Duchenne muscular dystrophy with severe mental retardation.2007

    • Author(s)
      Yagi,M. Tran Thi,H.T. Zhang,Z. Nishiyama,A. Oyazato,Y. Okinaga,T. Takeshima,Y. Matsuo,M.
    • Organizer
      57th The American Society of Human Genetics.
    • Year and Date
      2007-10-24
    • Data Source
      KAKENHI-PROJECT-19390284
  • [Presentation] A complex insertion event produced a chimeric dystrophin-IL1RAPL1 transcript in the dystrophin gene.2007

    • Author(s)
      Zhang,Z. Takeshima,Y. Yagi,M. Nishiyama,A. Okizuka,Y. Awano,H. Matsuo,M.
    • Organizer
      57th The American Society of Human Genetics.
    • Year and Date
      2007-10-26
    • Data Source
      KAKENHI-PROJECT-19390284
  • [Presentation] Intravenous infusion of antisense oligonucleotide induces dystrophin protein expression in the muscle of a Dchenne muscular dystrophy patient.2007

    • Author(s)
      Takeshima Y
    • Organizer
      25th International Congress of Pediatrics
    • Place of Presentation
      Athens
    • Year and Date
      2007-08-25
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-18591152
  • [Presentation] A novel retrotransposon that was recently inserted into exon 67 of the dystrophin gene.2007

    • Author(s)
      Awano,H. Yagi,M. Okizuka,Y. Zhang,Z. Takeshima,Y. Matsuo,M.
    • Organizer
      57th The American Society of Human Genetics.
    • Year and Date
      2007-10-26
    • Data Source
      KAKENHI-PROJECT-19390284
  • [Presentation] Evolutionary acquired alternative splicing in the 5'-UTR of retinal dystrophin transcript is a default pathway with weaker translational activity than nonspliced retina specific form

    • Author(s)
      Kubokawa I, Yagi M, Awano H, Ota M, Nishida A, Dwianingsih EK, Malueka RG, Takeshima Y, Matsuo M
    • Data Source
      KAKENHI-PROJECT-21390311
  • 1.  MATSUO Masafumi (10157266)
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    # of Collaborated Products: 50 results
  • 2.  YAGI Mariko (60362787)
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    # of Collaborated Products: 92 results
  • 3.  NISHIO Hisahide (80189258)
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    # of Collaborated Products: 16 results
  • 4.  李 知子 (10596042)
    # of Collaborated Projects: 6 results
    # of Collaborated Products: 18 results
  • 5.  下村 英毅 (30441273)
    # of Collaborated Projects: 6 results
    # of Collaborated Products: 15 results
  • 6.  SHIRAKAWA Taku (30171044)
    # of Collaborated Projects: 4 results
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  • 7.  NISHIYAMA Kaoru (00150061)
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    # of Collaborated Products: 0 results
  • 8.  YOKOYAMA Naoki (20314487)
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    # of Collaborated Products: 0 results
  • 9.  KAWASAKI Keiichiro (30359864)
    # of Collaborated Projects: 4 results
    # of Collaborated Products: 2 results
  • 10.  TSUNEISHI Syuichi (10271040)
    # of Collaborated Projects: 3 results
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  • 11.  NAKAMURA Hajime (40030978)
    # of Collaborated Projects: 3 results
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  • 12.  OHASHI Tamaki (60362779)
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  • 13.  LEE Miyojin (20273766)
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  • 14.  AWANO Hiroyuki (30437470)
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  • 15.  UETANI Yoshiyuki (40168620)
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    # of Collaborated Products: 0 results
  • 16.  OKUMURA Katsuhiko (60025707)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 0 results
  • 17.  SAKAEDA Toshiyuki (00304098)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 0 results
  • 18.  AYAKI Hitosi (80222701)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 0 results
  • 19.  北山 真次 (10346257)
    # of Collaborated Projects: 2 results
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  • 20.  NISHIMURA Noriyuki (00322719)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 10 results
  • 21.  MORIOKA Ichiro (80437467)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 3 results
  • 22.  MORI Yasuko (50343257)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 3 results
  • 23.  DEGUCHI Masashi (50403291)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 24.  KOSAKI Kenjiro (30234743)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 25.  HAYAKAWA Akira (40379376)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 26.  OKAMURA Noboru (60379401)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 27.  NAKAMURA Tsutomu (80379411)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 28.  小椋 たみ子 (60031720)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 29.  松嶋 隆二 (80025072)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 30.  池田 真理子 (00410738)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 31.  野津 寛大 (70362796)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 1 results
  • 32.  森沢 猛 (30379375)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 33.  三崎 真生子 (50595048)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 3 results
  • 34.  田中 靖彦 (20595045)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 35.  奥野 美佐子 (60646553)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 36.  TANIGUCHI Mariko
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 4 results
  • 37.  HAGIWARA Masatoshi
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 2 results
  • 38.  戸田 達史
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 2 results
  • 39.  原田 理沙
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 40.  中川 卓
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 41.  森川 悟
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 42.  片岡 直行
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 43.  高岡 裕
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 44.  飯島 一誠
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 45.  倉橋 浩樹
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 46.  李 明鎭
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 2 results

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