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MATSUO MASAFUMI  松尾 雅文

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MATSUO Masafumi  松尾 雅文

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Researcher Number 10157266
Other IDs
External Links
Affiliation (Current) 2023: 神戸常盤大学, 保健科学部, 特命教授
Affiliation (based on the past Project Information) *help 2018 – 2021: 神戸学院大学, 総合リハビリテーション学部, 特命教授
2011 – 2017: 神戸学院大学, 総合リハビリテーション学部, 教授
2013: 神戸学院大学, 大学院総合リハビリテーション学部, 教授
2012: 神戸大学, 医学研究科, 教授
2008 – 2010: Kobe University, 医学研究科, 教授 … More
2008: Kobe University, 大学院医学研究科, 教授
2004 – 2007: 神戸大学, 医学系研究科, 教授
2006: kobe University, Graduate School of Medicine, protessor, 大学院医学系研究科, 教授
2002 – 2005: Kobe University Graduate School of medicine Professor, 大学院・医学系研究科, 教授
1992 – 2003: 神戸大学, 医学部, 教授
1997: 神戸大学, 医学部・付属病院, 教授
1989 – 1990: 神戸大学, 医学部, 講師 Less
Review Section/Research Field
Principal Investigator
Pediatrics / Pediatrics / Basic Section 52050:Embryonic medicine and pediatrics-related / Human genetics
Except Principal Investigator
Pediatrics / Pediatrics / Hygiene / Experimental psychology / Medical sociology / Experimental pathology … More / Human genetics / Metabolomics / Laboratory medicine / 応用薬理学・医療系薬学 / Urology / Embryonic/Neonatal medicine / Rehabilitation science/Welfare engineering / Medical genome science / Basic Section 52050:Embryonic medicine and pediatrics-related Less
Keywords
Principal Investigator
ジストロフィン / スプライシング / エクソンスキッピング / Duchenne型筋ジストロフィー / dystrophin / 筋ジストロフィー / 点突然変異 / クローニング / 治療 / ジストロフィン遺伝子 … More / エクソン / exon skipping / メッセンジャーRNA / Duchenne型 / 分子種 / スキッピング / Duchenne / がん遺伝子 / 遺伝子異常 / マイクロサテライト / アイソフォーム / 精神発達遅滞 / ゲノム / mRNA / 心筋 / isoform / スプライシング促進配列 / splicing / splicing enhancer sequence / アンチセンス / デュシェンヌ型筋ジストロフィー / SNPs / ジストロフィンDp71 / RNA / レトロポゾン / 遺伝子診断 / 神経線椎腫症1型 / NF1 / がん抑制遺伝子 / Duchenn型筋ジストロフィー / 神経線維腫症I型 / 蛋白合成 / In vitro翻訳 / 転写 / 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 / 非コード遺伝子 / 新規遺伝子 / 逆位 / 小児神経学 / リボゾーム / 遺伝学 / 臨床 / 低分子化合物 / 筋ジス / PGD2 / 炎症 / 低分子 / 遺伝子 / 核酸 / 脳神経疾患 / 内在遺伝子 / ウェスターンブット / 転写産物 / 楕円赤血球症 / 赤血球 / バンド3蛋白 / 遺伝子欠失 / インドネシア / 遺伝性楕円赤血球症 / バンド3蛋白遺伝子 / Ovalocytosis / Erythrocyte / Band 3 protein / Deletion mutation / Indonesia / ジストロフィン神戸 / リンパ芽球 / アンチセンスオリゴヌクレオチド / 遺伝子治療 / dystrophin Kobe / lymphoblastoid cells / antisenseoligonucleotide / alternative splicing / heart / イントロン / 拡張型心筋症 / exon intron / dilated cardiomyopathy / 骨系統疾患 / 連鎖解析 / Mesomelic dysplasia / mesomedic dysplasia / 責任遺伝子 / タイ / bone disease / linkage analysis / mesomelic dysplasia / Thailand / アンチセンスオリゴオヌクレオチド / treatment / Duchenne muscular dystrophy / antisense oligonucleotide / 分子治療 / キメラRNA / DNA / 点変異 / 筋細胞 / muscular dystrophy / 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 / DMD / antisense / フィリピン / 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 / 衛生細胞 / 衛星細胞 / 筋芽細胞増殖因子 / ミニ遺伝子 … More
Except Principal Investigator
筋ジストロフィー / ジストロフィン / 遺伝子異常 / 遺伝子解析 / G6PD欠損症 / スプライシング / splicing / 遺伝子治療 / プロモーター / アンチセンスオリゴヌクレオチド / エクソンスキッピング / フィリピン / Philippines / スプライシング促進配列 / 脊髄性筋萎縮症 / spinal muscular atrophy / gene therapy / HPLC / muscular dystrophy / MSUD / mRNA / hnRNP C1 / C2 / 小児白血病 / キメラ遺伝子 / childhood leukemia / RNAi / 分散性反復配列 / リンパ球 / 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 / Duchenne型筋ジストロフィー / dp140 / シグナル伝達因子 / 筋ジストロフー / NF-κB / 医学 / 薬学教育 / 遺伝子医療 / ゲノム薬理学 / おくすり体質検査 / テーラーメイド医療 / 逆流性食道炎 / 非びらん性胃食道逆流症 / 薬物代謝酵素 / CYP2C19 / プロトンポンプ阻害薬 / テーラーメード医療 / ワルファリン / 遺伝子多型 / 薬物感受性遺伝子 / CYP2C9 / VKORC1 / iPS細胞 / 疾患再現 / デュシェンヌ型筋ジストロフィー / 細胞内カルシウムイメージング / 疾患特異的iPS細胞 / 病態再現 / 骨格筋細胞 / 創薬スクリーニング / 未熟児 / 成長因子 / ミオイノシト-ル / 細胞増殖因子 / イノシト-ル / Premature infant / Growth factor / myo-Inositol / 連鎖解析 / 疾患遺伝子座 / 中間肢短縮小人症 / Engelmann病 / 発作性運動誘発性コレオアテトーシス / 家族性白内症 / 心房中隔欠損症 / ポジショナルクローニング / 肢中部短縮型小人症 / LINKAGE ANALYSIS / DISEASE LOCUS / MESOMELIC DYSPLASIA / ENGELMANN DISEASE / Paroxysmal kinetogenic choreoathetosis / FAMILIAL CATARACT / ATRIAL SPEPTAL DEFECT / POSITIONAL CLONING / G6PD deficienc / mutation / マススクリーニング / ベトナム / スクリーニング / ホルマザン法 / 赤血球 / G6PD deficiency / Mass screening / Vietnam / Genetic analysis / マラリア / α-サラセミア / 楕円赤血球症 / ヘモグロビン異常 / G6PD / Malaria / G6PD Deficiency / α-Thalassemia / Southeast Asian Ovalocytosis / Hemoglobin Abnormality / Gene Analysis / メッセンジャーRNA前躯体 / dsx遺伝子 / ミニ遺伝子 / 抗SMN抗体 / カドミウム / メッセンジャーRNA前駆体 / SMN蛋白 / 可変スプライシング / pre-mRNA / splicing enhancer sequences / the dsx gene / mini-gene / anti-SMN antibody / cadmium / スプラシング / dystrophin / splicing enhancer sequence / アンチセンス / 血中濃度 / リアルタイムPCR / antisense / blood concentration / real time quantitative PCR / 臨床研究 / 前立腺癌 / 骨転移 / 臓器特異性プロモーター / アデノウイルス / 自殺遺伝子 / オステオカルシン / 遺伝子治療臨床研究 / 局所再発 / チミジンキナーゼ / バラシクロビル / 遺伝子治療臨床試験 / アデノウィルス / Gene Therapy / Clinical Research / Prostate cancer / Bone Metastasis / Tissue-specific promoter / Adenovirus / Suicide gene / Osteocalcin / 新生児スクリーニング / メープルシロップ尿症 / E2遺伝子 / 遺伝子欠失 / gene mutation / neonatal screeing / 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 / SMN1遺伝子 / SMN2遺伝子 / in vitroスプライシング / ペプチド核酸 / the SMN1 gene / the SMN2 gene / in vitro splicing assay / peptide nucleic acid / クローニング / chimera mRNA / cloning / chimeric gene / 分子治療 / エクソン・スキッピング / 小児神経学 / molecular therapy / antisense oligonucleotide / exon skipping / 褥瘡 / 直流パルス微弱電流刺激療法 / 無作為化試験 / 二重盲検試験 / クロスオーバー比較試験 / 電気刺激療法 / 無作為化比較試験 / クロスオーバー研究 / 創の縮小 / 直流微弱電流刺激 / 線維芽細胞 / 筋線維芽細胞 / 損傷電流 / 酸化還元電位 / 線維芽細胞増殖 / 物理療法 / Splicing、 / Intron retention, / Dystrophin, / Antisense oligo, / Rhabdomyosarcoma / splicing, / intron retention, / dystrophin, / antisense chemistry, / rhabdomyosarcoma, / tumor, / tumor suppressor gene, / Dystrophin / Intron retention / Splicing / AO therapy / アンチセンス核酸 / ミオスタチン / 横紋筋肉腫 Less
  • Research Projects

    (57 results)
  • Research Products

    (80 results)
  • Co-Researchers

    (50 People)
  •  Myostatin antisense nucleic acid therapy for rhabdomyosarcoma

    • Principal Investigator
      前田 和宏
    • 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
      Kobe Gakuin University
  •  Identification of chemicals that enhance expression of myoblast growth factor Dp71abPrincipal Investigator

    • Principal Investigator
      松尾 雅文
    • 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
      Kobe Gakuin University
  •  Study on dystrophin Dp71 to regulate satellite cell divisionPrincipal Investigator

    • Principal Investigator
      Matsuo Masafumi
    • Project Period (FY)
      2018 – 2020
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 52050:Embryonic medicine and pediatrics-related
    • Research Institution
      Kobe Gakuin University
  •  Study of personalized electrophysical therapy for stage of pressure injury healing by Monophasic Pulsed Microcurrent stimulation

    • Principal Investigator
      Sugimoto Masaharu
    • Project Period (FY)
      2016 – 2019
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Rehabilitation science/Welfare engineering
    • Research Institution
      Kobe Gakuin University
  •  Dystrophin intron retention analysis to identify new targets for Antisense Oligonucleotide mediated RNA modulation in Rhabdomyosarcoma

    • Principal Investigator
      NIBA TABE EMMA EKO
    • Project Period (FY)
      2016 – 2018
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Medical genome science
    • Research Institution
      Kobe University
      Kobe Gakuin University
  •  Fluorescent detection of dystrophin mRNA with bispyrene labeled probePrincipal Investigator

    • Principal Investigator
      Matsuo Masafumi
    • Project Period (FY)
      2015 – 2016
    • Research Category
      Grant-in-Aid for Challenging Exploratory Research
    • Research Field
      Pediatrics
    • Research Institution
      Kobe Gakuin University
  •  Cloning of non-dystrophin transcript from the dystrophin genePrincipal Investigator

    • 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
  •  Expression of dystrophin via exon skipping with a small chemicalPrincipal Investigator

    • Principal Investigator
      MATSUO Masafumi
    • Project Period (FY)
      2012 – 2014
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe Gakuin University
  •  Modeling Duchenne muscular dystrophy using patient-derived iPS cells

    • Principal Investigator
      SAKURAI Hidetoshi
    • Project Period (FY)
      2012 – 2013
    • Research Category
      Grant-in-Aid for Young Scientists (B)
    • Research Field
      Experimental pathology
    • Research Institution
      Kyoto University
  •  Dose prostaglandin-mediated inflammation commit to pathology of Duchenne muscular dystrophy?Principal Investigator

    • Principal Investigator
      MATSUO Masafumi
    • Project Period (FY)
      2011
    • Research Category
      Grant-in-Aid for Challenging Exploratory Research
    • Research Field
      Pediatrics
    • Research Institution
      Kobe Gakuin University
  •  A pharmacist's strategic practical use in promotion of gene medical treatment

    • Principal Investigator
      HIRAI Midori
    • Project Period (FY)
      2010 – 2012
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Medical sociology
    • Research Institution
      Kobe University
  •  Duchenne型筋ジストロフィーは低分子化合物により治療できるか?Principal Investigator

    • Principal Investigator
      松尾 雅文
    • Project Period (FY)
      2010
    • Research Category
      Grant-in-Aid for Challenging Exploratory Research
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  Genes responsible for mental retardation complicating to Duchenne muscular dystrophyPrincipal Investigator

    • 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 dystrophy

    • 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
  •  レトロトランスポジション能を有する新規ヒト遺伝子のクローニングPrincipal Investigator

    • Principal Investigator
      松尾 雅文
    • Project Period (FY)
      2008
    • Research Category
      Grant-in-Aid for Exploratory Research
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  Study on treatment of Duchenne muscular dystrophy by inducing exon skippingPrincipal Investigator

    • 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
  •  染色体Xq28に座位する精神発達遅滞の発症に関与する新しい遺伝子Principal Investigator

    • Principal Investigator
      松尾 雅文
    • Project Period (FY)
      2006
    • Research Category
      Grant-in-Aid for Exploratory Research
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  Research of antisense oligonucleotide therapy for muscular dystrophy using knockout mouse as a model

    • 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
  •  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 acidsPrincipal Investigator

    • 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

    • 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 RNAi

    • 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
  •  Clinical research of gene therapy using tissue-specific promoter for the treatment of metastatic prostate cancer.

    • Principal Investigator
      KAMIDONO Sadao
    • Project Period (FY)
      2002 – 2005
    • Research Category
      Grant-in-Aid for Scientific Research (A)
    • Research Field
      Urology
    • Research Institution
      Kobe University
  •  Molecular genetic study on maple syrup urine disease in Philippines

    • 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
  •  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

    • 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/DNAPrincipal Investigator

    • 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 Epidemiological Study on Human Hereditary Resistant Factors to Malaria

    • Principal Investigator
      SHIRAKAWA Taku
    • Project Period (FY)
      2001 – 2003
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Hygiene
    • Research Institution
      Kobe University
  •  Molecular genetic study of frontoethmoidal encephalocele in IndonesiaPrincipal Investigator

    • 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
  •  Screening system for chemicals attacking pre-mRNA splicing machinery in cells

    • Principal Investigator
      NISHIO Hisahide
    • Project Period (FY)
      2001 – 2002
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Hygiene
    • Research Institution
      Kobe University Graduate School of medicine
  •  Research for the exonic splicing enhancer sequences in dysttrophin gene

    • 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

    • 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 dystrophyPrincipal Investigator

    • 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
  •  The molecular epidemiological analyses of G6PD deficiency in Vietnam

    • Principal Investigator
      NISHIYAMA Kaoru
    • Project Period (FY)
      2000 – 2002
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Laboratory medicine
    • 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

    • 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
  •  Study on gene responsible for mesomelic dysplasia identified in ThailandPrincipal Investigator

    • Principal Investigator
      MATSUO Masafumi
    • Project Period (FY)
      1998 – 1999
    • Research Category
      Grant-in-Aid for Scientific Research (A).
    • Research Field
      Human genetics
    • Research Institution
      Kobe University
  •  Establishment of treatment of Duchenne muscular dystrophyPrincipal Investigator

    • 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

    • 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
  •  Study on dystrophin isoform expressed in heartPrincipal Investigator

    • 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

    • Principal Investigator
      松尾 雅文
    • Project Period (FY)
      1996
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      Kobe University
  •  リンパ球特異的に発現するL-ジストロフィンの発現制御機構に関する研究

    • Principal Investigator
      西尾 久英
    • Project Period (FY)
      1996
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  LINKAGE ANALYSIS OF UNKNOWN GENETIC DISEASES

    • Principal Investigator
      NIIKAWA Norio
    • Project Period (FY)
      1996 – 1998
    • Research Category
      Grant-in-Aid for Scientific Research (A)
    • Research Field
      Human genetics
    • Research Institution
      NAGASAKI UNIVERSITY
  •  神経線維種症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

    • Principal Investigator
      松尾 雅文
    • Project Period (FY)
      1995
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      Kobe University
  •  Cloning and study on physiological role of new dystrophin isoform.Principal Investigator

    • Principal Investigator
      MATSUO Masafumi
    • Project Period (FY)
      1995 – 1996
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  蛋白発現ベクターを応用した神経線椎腫症1型の遺伝子異常の解析Principal Investigator

    • Principal Investigator
      松尾 雅文
    • Project Period (FY)
      1994
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      Kobe University
  •  メッセンジャーRNAを標的としたジストロフィン異常の分子遺伝学的研究Principal Investigator

    • Principal Investigator
      松尾 雅文
    • Project Period (FY)
      1994
    • Research Category
      Grant-in-Aid for General Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  ゲノム内分散性反復配列の挿入を認めたジストロフィン遺伝子転写開始領域の構造の研究

    • Principal Investigator
      西尾 久英
    • Project Period (FY)
      1994
    • Research Category
      Grant-in-Aid for General Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  Molecular epidemiological study ovalocytosis in IndonesiaPrincipal Investigator

    • Principal Investigator
      MATSUO Masafumi
    • Project Period (FY)
      1994 – 1995
    • Research Category
      Grant-in-Aid for international Scientific Research
    • Research Institution
      Kobe University
  •  Molecular biological study to establish the treatment for Duchenne muscular dystrophyPrincipal Investigator

    • Principal Investigator
      MATSUO Masafumi
    • Project Period (FY)
      1994 – 1996
    • Research Category
      Grant-in-Aid for Scientific Research (A)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  MyoDの筋分化誘導作用を応用したジストロフィン異常の分子生物学的解析Principal Investigator

    • Principal Investigator
      松尾 雅文
    • Project Period (FY)
      1993
    • Research Category
      Grant-in-Aid for General Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  メッセンジャーRNA前駆体2次構造の有するプライシング部位の制御機能Principal Investigator

    • Principal Investigator
      松尾 雅文
    • Project Period (FY)
      1992
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      Kobe University
  •  筋分化誘導因子を応用したジストロフィン異常の分子生物学的解析Principal Investigator

    • Principal Investigator
      松尾 雅文
    • Project Period (FY)
      1992
    • Research Category
      Grant-in-Aid for General Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University
  •  An Application of Growth Factor for the Maturation of Premature InfantsPrincipal Investigator

    • Principal Investigator
      UETANI Yoshiyuki, 松尾 雅文
    • Project Period (FY)
      1989 – 1990
    • Research Category
      Grant-in-Aid for General Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Kobe University

All 2022 2021 2020 2019 2018 2017 2015 2013 2012 2010 2009 2008 2007 2005 2004 Other

All Journal Article Presentation Book

  • [Book] RNAiとアンチセンス法-新しいRNAの科学と応用(医療の立場からのアンチセンス法)2005

    • Author(s)
      松尾雅文
    • Publisher
      講談社
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-16390301
  • [Journal Article] An Antisense Oligonucleotide against a Splicing Enhancer Sequence within Exon 1 of the MSTN Gene Inhibits Pre-mRNA Maturation to Act as a Novel Myostatin Inhibitor2022

    • Author(s)
      Kazuhiro Maeta, Manal Farea, Hisahide Nishio, Masafumi Matsuo
    • Journal Title

      International Journal of Molecular Sciences

      Volume: 23(9) Pages: 5016-5016

    • DOI

      10.3390/ijms23095016

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-21K07762
  • [Journal Article] Human dystrophin Dp71ab enhances the proliferation of myoblasts across species but not human nonmyoblast cells.2022

    • Author(s)
      Farea M, Maeta K, Nishio H, and Matsuo M
    • Journal Title

      Front Cell Dev Biol

      Volume: 10 Pages: 877612-877612

    • DOI

      10.3389/fcell.2022.877612

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-21K07875
  • [Journal Article] Dystrophin Dp71ab is monoclonally expressed in human satellite cells and enhances proliferation of myoblast cells2020

    • Author(s)
      Manal Farea, Abdul Qawee Mahyoob Rani, Kazuhiro Maeta, Hisahide Nishio, Masafumi Matsuo
    • Journal Title

      Sci Rep

      Volume: 10 Pages: 17123-17123

    • DOI

      10.1038/s41598-020-74157-y

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-18K07861
  • [Journal Article] Skipping of an exon with a nonsense mutation in the DMD gene is induced by the conversion of a splicing enhancer to a splicing silencer.2019

    • Author(s)
      Zhu Y, Deng H, Chen X, Li H, Yang C, Li S, Pan X, Tian S, Feng S, Tan X, Matsuo M, Zhang Z
    • Journal Title

      Hum Genet

      Volume: 138 Pages: 771-785

    • DOI

      10.1007/s00439-019-02036-2

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18K07861
  • [Journal Article] Identification of the shortest splice variant of Dp71, together with five known variants, in glioblastoma cells2018

    • Author(s)
      Abdul Q Rani, Farea M, Maeta K, Kawaguchi T, Awano H, Nagai M, Nishio H, Matsuo M
    • Journal Title

      Biochem Biophy Res Commun

      Volume: 508 Pages: 640-645

    • DOI

      10.1016/j.bbrc.2018.11.168

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-18K07861
  • [Journal Article] DMD transcripts in CRL-2061 rhabdomyosarcoma cells show high levels of intron retention by intron-specific PCR amplification2017

    • Author(s)
      Niba ETE, Yamanaka R, Rani AQM, Awano H, Matsumoto M, Nishio H, Matsuo M
    • Journal Title

      Cancer Cell International

      Volume: 17 Pages: 58-73

    • DOI

      10.1186/s12935-017-0428-4

    • NAID

      120006373783

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-16K07216, KAKENHI-PROJECT-17K10077
  • [Journal Article] Tissue and case-specific retention of intron 40 in mature dystrophin mRNA2015

    • Author(s)
      Nishida.A., Minegishi.M., Takeuchi.A., Niba.ET., Awano.H., Lee.T., Iijima.K., Takeshima.Y., Matsuo.M
    • Journal Title

      J Hum Genet

      Volume: in press

    • DOI

      10.1038/jhg.2015.24

    • Peer Reviewed / Acknowledgement Compliant
    • Data Source
      KAKENHI-PROJECT-24390267
  • [Journal Article] Exon deletion patterns of the dystrophin gene in 82 vietnamese duchenne/ becker muscular dystrophy patients.2013

    • Author(s)
      Tran VK., Ta VT., Vu DC., Nguyen ST., Do HN., Ta MH., Tran TH., Matsuo M.
    • Journal Title

      Journal of Neurogenetics

      Volume: 27 Pages: 170-5

    • DOI

      10.3109/01677063.2013.830616

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24390267
  • [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] 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] A polymorphic mutation, c.-3279T>G, in theUGT1A1 promoter is a risk factor for neonatal jaundice in the Malay population.2012

    • Author(s)
      Kataoka Y, Mukohara T, Tomioka H, Funakoshi Y, Kiyota N, Fujiwara Y, Yashiro M, Hirakawa K, Hirai M, Minami H.
    • Journal Title

      Invest New Drugs

      Volume: 30(4) Pages: 1352-1360

    • DOI

      10.1007/s10637-011-9699-0

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22390105
  • [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] A polymorphic mutation, c.-3279T>G, in the UGT1A1 promoter is a risk factor for neonatal jaundice in the Malay population.2010

    • Author(s)
      Yusoff S, Takeuchi A, Ashi C, Tsukada M, Ma□amor NH, Alwi Zilfalil B, Mohd Yusoff N, Nakamura T, Hirai M, Sari Kusuma Harahap I, Gunadi, Jin Lee M, Yutaka Takaoka NN, Morikawa S, Morioka I, Yokoyama N, Matsuo M, Nishio H, van Rostenberghe H.
    • Journal Title

      Pediatr Research

      Volume: 67 Pages: 401-406

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22390105
  • [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] 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 gene2009

    • Author(s)
      Zhang Z., Matsuo, M., et al
    • Journal Title

      J Him Genet 54(8)

      Pages: 466-73

    • NAID

      10030731391

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21390311
  • [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] A Strong Exonic Splicing Enhancer in Dystrophin Exon 19 achieve proper splicing without an upstream polypyrimidine tract2008

    • Author(s)
      Habara, Y., Matsuo, M., et al
    • Journal Title

      J Biochem. 143

      Pages: 303-310

    • NAID

      10024908594

    • 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] 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] Early diagnosis of maple syrup urine disease by PCR-based mutation detection2008

    • Author(s)
      CATHERINE LYNN, T.SILAO, MD, PhD, CARMENCITA D.PADILLA, MD MASAFUMI MATSUO, MD, PhD
    • Journal Title

      Pediatric international (In press)

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-16406031
  • [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>Amutations in introns of the dystrophin gene.2008

    • Author(s)
      Habara, Y., Matsuo, M., et al
    • Journal Title

      J Med Genet. (Web)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19390284
  • [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] Multi-exon skipping leading to an artificial DMD protein lacking amino acids from exons 45 through 55 could rescue up to 63% of patients with Duchenne Muscular Dystrophy.2007

    • Author(s)
      Beroud C, Giraud TS, Matsuo M, Hamroun D., Humbertclaude V, Monnier N, Moizard MP, Voelckel MA, Calemard LM, Boisseau P, Blayau M, Philippe C, Cossee M, Pages M, Rivier F, Danos O, Garcia L, Claustres M.
    • Journal Title

      Hum Mutat. 28

      Pages: 196-202

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19390284
  • [Journal Article] Rescue of dystrophin mRNA of Duchenne muscular dystrophy by inducing exon skipping2005

    • Author(s)
      Matsuo, M
    • Journal Title

      Acta Myologica XXIV

      Pages: 110-114

    • Data Source
      KAKENHI-PROJECT-16653066
  • [Journal Article] Rescue of dystrophin mRNA of Duchenne muscular dystrophy by inducing exon skipping.2005

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

      Acta Myologica XXIV

      Pages: 110-114

    • Description
      「研究成果報告書概要(欧文)」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] Rescue of dystrophin mRNA of Duchenne muscular dystrophy by inducing exon skipping.2005

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

      Acta Myologica XXIV

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-16390301
  • [Journal Article] Rescue of dystrophin mRNA of Duchenne muscular dystrophy by inducing exon skipping.2005

    • Author(s)
      Matsuo, M.
    • Journal Title

      Acta Myologica XXIV

      Pages: 110-114

    • Data Source
      KAKENHI-PROJECT-16390301
  • [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] Duchenne型筋ジストロフィーのgentamicin治療2004

    • Author(s)
      松尾雅文
    • Journal Title

      脳と発達 36巻2号

      Pages: 125-129

    • Data Source
      KAKENHI-PROJECT-16591027
  • [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] Early diagnosis of maple syrup urine disease by PCR-based mutation detection

    • Author(s)
      CATHERINE, LYNN T.SILAO, MD, PhD, CARMENCITA D.PADILLA, MD, MASAFUMI MATSUO, MD, PhD
    • Journal Title

      Pediatric international (In press)(印刷中)

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-16406031
  • [Presentation] ミオスタチン新規アイソフォームはミオスタチンを特異的に阻害し筋芽細胞増殖を促進する2021

    • Author(s)
      前田和宏、Manal Farea、西尾久英、松尾雅文
    • Organizer
      日本分子生物学会
    • Data Source
      KAKENHI-PROJECT-21K07762
  • [Presentation] Spontaneous development of spindle cell sarcoma in mdx mice2018

    • Author(s)
      : Satoru Takafuji, Emma Niba, Khin Kyae Mon Thwin, Nobuyuki Yamamoto, Hiroyuki Awano, Suguru Uemura, Takeshi Mori, Shoji Fukushima, Kyoko Itoh, Hisahide Nishio, Masafumi Matsuo, Kazumoto Iijima, Noriyuki Nishimura
    • Organizer
      International Society of Pediatric Oncology
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-16K07216
  • [Presentation] Glioma from a DMD patient exhibits differential splicing pattern including exon 71 skipping and intron 40 retention2018

    • Author(s)
      : Emma E.T. Niba, Hiroyuki Awano, Masashi Nagai, Masaaki Taniguchi, Rani Adul Qawee, Masakazu Shinohara, Hisahide Nishio, Masafumi Matsuo
    • Organizer
      Molecular Biology Society of Japan
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-16K07216
  • [Presentation] DMD transcription profiling in spontaneously developed tumor from three mdx mice revealed extensive intron retentions and Dp71 isoform expression2018

    • Author(s)
      Emma E.T. Niba, Noriyuki Nishimura, Satoru Takafuji, Khin Kyae Mon Thwin, Nobuyuki Yamamoto, Hiroyuki Awano, Shoji Fukushima, Kyoko Itoh, Hisahide Nishio, Masafumi Matsuo
    • Organizer
      American Society of Cell Biology
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-16K07216
  • [Presentation] Dystrophin Dp427 is lost due to multiple DMD intron retentions in rhabdomyosarcoma CRL-2061 cells2017

    • Author(s)
      Emma Tabe Eko Niba1,3, Ryo Yamanaka1, Abdul Qawee Mahyoob Rani1, Hiroyuki Awano2, Masaaki Matsumoto2, Hisahide Nishio3, Masafumi Matsuo1
    • Organizer
      22nd international congress of the WORLD MUSCLE SOCIETY
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-16K07216
  • [Presentation] Multi-intron retentions in DMD transcripts in CRL-2061 rhabdomyosarcoma cells identified by intron specific RT-PCR amplification2017

    • Author(s)
      Emma Tabe Eko Niba1,2, Ryo Yamanaka2, Abdul Qawee Mahyoob Rani2, Hiroyuki Awano3, Masaaki Matsumoto3, Hisahide Nishio1, Masafumi Matsuo2
    • Organizer
      Japan Society of Human Genetics
    • Data Source
      KAKENHI-PROJECT-16K07216
  • [Presentation] 筋ジストロフィー患者の尿中プロスタグランジンD2代謝物の定量2012

    • Author(s)
      垣内涼平, 成田哲也, 竹内敦子, 鎌内慎也, 裏出良博, 松尾雅文
    • Organizer
      日本薬学会第132年会
    • Place of Presentation
      札幌
    • Data Source
      KAKENHI-PROJECT-23659521
  • [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] 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] 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, Y., Matsuo, M.
    • Organizer
      The American Society of Human Genetics 60th Annual Meeting
    • Place of Presentation
      Washington D.C.
    • Data Source
      KAKENHI-PROJECT-22659194
  • [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] 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. 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] 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] 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
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    # of Collaborated Products: 50 results
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