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MATSUMOTO Tadashi  松本 正

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… Alternative Names

松本 正  マツモト タダシ

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Researcher Number 70190535
External Links
Affiliation (based on the past Project Information) *help 2010: Nagasaki University, 医歯(薬)学総合研究科, 教授
2009: 長崎大学, 大学院・医歯薬学総合研究科, 教授
2008: 長崎大学, 医歯薬学総合研究科, 教授
2007: 長崎大学, 大学院・医歯薬学総合研究科, 教授
2005: NAGASAKI UNIVERSITY, GRADUATE SCHOOL OF BIOMEDICAL SCIENCES, DEPARTMENT OF BASIC NURSING, PROFESSOR, 大学院・医歯薬学総合研究科, 教授 … More
2001 – 2005: 長崎大学, 医学部, 教授
1998 – 1999: 長崎大学, 医学部, 講師
1997: 長崎大学, 医学部附属病院, 講師
1994: 長崎大学, 医学部, 講師
1991: 長崎大学, 医学部, 講師
1988: 長崎大学, 医学部, 助手
1986: Nagasaki University School of Medicine, Assistant, 医学部, 助手 Less
Review Section/Research Field
Principal Investigator
Pediatrics / Human genetics
Except Principal Investigator
Human genetics / 医学一般 / Clinical nursing / Pediatrics
Keywords
Principal Investigator
ウエスタンブロッティング / ジストロフィン / 遺伝子欠失 / X連鎖性遺伝 / 遺伝形質 / 女性筋ジストロフィー症患者 / デュシャンヌ筋ジストロフィー症 / 過成長症候群 / H19 / IGF2 … More / ゲノム刷り込み現象 / EMG症候群 / グリセロ-ルキナ-ゼ / マイクロクロ-ニング / マイクロディセクション … More
Except Principal Investigator
染色体異常 / 心房中隔欠損症 / 疾患遺伝子座 / 連鎖解析 / PCR / molecular genetics / gene dose effect / nondisjunction / restriction fragment length polymorphism / parental origin / mechanism of formation / chromosome abnormality / サザンハイブリダイゼーション / 親起源 / 分子遺伝学 / 遺伝子量効果 / 染色体不分離 / RFLP / 制限酵素断片長多型 / 親起原 / 発生機構 / Prader-Willi syndrome / Gene deletion / Micro-deletion of chromosome / Origin of chromosome abnormality / Chromosome abnormality / 乳児型グリセロールキナーゼ欠損症 / プラダー・ウィリー症候群 / 遺伝子欠失 / 微細染色体欠失 / 染色体異常の起源 / familial cases of genetic diseases / disease genes / gene mapping / single-gene disorders / linkage analysis / ITGA3B遺伝子 / 遺伝性難聴 / WFS1遺伝子 / 疾病遺伝子 / 変異解析 / マイクロサテライトマーカー / 単一遺伝子疾患 / 緊張性四肢麻痺 / 無臭覚症 / 家族性側索硬化症 / ハプロタイプ解析 / 無嗅覚症 / 下顎前突症 / 多汗症 / 家族性心房中核欠損症 / 遺伝病家系 / 疾患遺伝子 / 遺伝子マッピング / 遺伝子病 / POSITIONAL CLONING / ATRIAL SPEPTAL DEFECT / FAMILIAL CATARACT / Paroxysmal kinetogenic choreoathetosis / ENGELMANN DISEASE / MESOMELIC DYSPLASIA / DISEASE LOCUS / LINKAGE ANALYSIS / 肢中部短縮型小人症 / ポジショナルクローニング / 家族性白内症 / 発作性運動誘発性コレオアテトーシス / Engelmann病 / 中間肢短縮小人症 / 発達障害児 / 性発達 / 認識 / 母親 / ピア・エデュケーション / 自閉症 / 性教育 / 性行動 / 発達障害 / 子宮内感染 / 母乳感染 / 母子感染 / HTLV-1 / ATL / 家系診断 / SSCP / DGGE / 21ー水酸化酵素欠損症 Less
  • Research Projects

    (11 results)
  • Research Products

    (20 results)
  • Co-Researchers

    (19 People)
  •  小中学生のための遺伝教育プログラムの開発研究Principal Investigator

    • Principal Investigator
      松本 正
    • Project Period (FY)
      2010
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Human genetics
    • Research Institution
      Nagasaki University
  •  発達障害児の性行動の実態と性教育の有用性に関する研究

    • Principal Investigator
      宮原 春美
    • Project Period (FY)
      2007 – 2009
    • Research Category
      Grant-in-Aid for Challenging Exploratory Research
    • Research Field
      Clinical nursing
    • Research Institution
      Nagasaki University
  •  CONSORTIUM-BACED LINKAGE ANALYSIS AND IDENTIFICATION OF GENES FOR SINGEL-GENE DISEASES

    • Principal Investigator
      NIIKAWA Norio
    • Project Period (FY)
      2001 – 2005
    • Research Category
      Grant-in-Aid for Scientific Research (S)
    • Research Field
      Human genetics
    • Research Institution
      NAGASAKI UNIVERSITY
  •  長崎県を対象としたHTLV-1母乳感染防止長期介入試験

    • Principal Investigator
      日野 茂男
    • Project Period (FY)
      1999
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas (A)
    • Research Institution
      Tottori 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
  •  EMG症候群発症におけるゲノム刷り込み現象の意義に関する研究Principal Investigator

    • Principal Investigator
      松本 正
    • Project Period (FY)
      1994
    • Research Category
      Grant-in-Aid for General Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Nagasaki University
  •  21ー水酸化酵素欠損症のPCR法及びDGGE法を用いた家系診断法の確立

    • Principal Investigator
      吉本 雅昭
    • Project Period (FY)
      1991
    • Research Category
      Grant-in-Aid for General Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Nagasaki University
  •  染色体マイクロディセクション法を用いたグリセロ-ルキナ-ゼ遺伝子の単離Principal Investigator

    • Principal Investigator
      松本 正
    • Project Period (FY)
      1991
    • Research Category
      Grant-in-Aid for General Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Nagasaki University
  •  女性Duchenns筋ジストロフィー症の分子遺伝学的研究Principal Investigator

    • Principal Investigator
      松本 正
    • Project Period (FY)
      1988
    • Research Category
      Grant-in-Aid for General Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Nagasaki University
  •  Parental Origin of de novo chromosome abnormalities.

    • Principal Investigator
      NIIKAWA Norio
    • Project Period (FY)
      1988 – 1989
    • Research Category
      Grant-in-Aid for General Scientific Research (B)
    • Research Field
      Human genetics
    • Research Institution
      Nagasaki University
  •  A Study on the Etiology of Congenital Anomaly Syndromes of Unknown Cause: Cytogenetic Study with High-Resolution Banding and Origin of Abnormal Chromosomes.

    • Principal Investigator
      NIIKAWA Norio
    • Project Period (FY)
      1985 – 1986
    • Research Category
      Grant-in-Aid for General Scientific Research (B)
    • Research Field
      医学一般
    • Research Institution
      Nagasaki University

All 2006 2005 2004 2003 2002 2001 Other

All Journal Article

  • [Journal Article] No detectable genomic aberrations by BAC array CGH in Kabuki make-up syndrome patients.2006

    • Author(s)
      Miyake N, Shimokawa O, Harada N, Sosonkina N, Okubo A, Kawara H, Okamoto N, Ohashi H, Kurosawa K, Naritomi K, Kaname T, Nagai T, Shotelersuk V, Hou J-W, Fukushima Y, Kondoh T, Matsumoto T, Shinoki T, Kato M, Tonoki H, Nomura M, Yoshiura K, Kishino T, Ohta T, Niikawa N, Matsumoto N.
    • Journal Title

      Am J Med Genet 140A

      Pages: 291-293

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] BAC array CGH reveals genomic aberrations in idiopathic mental retardation.2006

    • Author(s)
      Miyake N, Shimokawa O, Harada N, Sosonkina N, Okubo A, Kawara H, Okamoto N, Kurosawa K, Kawame H, Iwakoshi M, Kosho T, Fukushima Y, Makita Y, Yokoyama Y, Yamagata T, Kato M, Hiraki Y, Nomura M, Yoshiura K, Kishino T, Ohta T, Mizuguchi T, Niikawa N, Matsumoto N.
    • Journal Title

      Am J Med Genet 140A

      Pages: 205-211

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] Non-hotspot-related breakpoints of common deletions in Sotos syndrome are located within destabilized DNA regions.2006

    • Author(s)
      Visser R, Shimokawa O, Harada N, Niikawa N, Matsumoto N
    • Journal Title

      J Med Genet 42(11)

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] Four novel NIPBL mutations in Japanese patients with Cornelia de Lange syndrome.2005

    • Author(s)
      Miyake N, Visser R, Kinoshita A, Yoshiura K, Harada N, Okamoto N, Sonoda T, Kaname T, Chinen Y, Naritomi K, Tonoki H, Kondoh T, Kurosawa K, Niikawa N, Matsumoto N
    • Journal Title

      Am J Med Genet 135A

      Pages: 103-105

    • NAID

      120006981060

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] Novel deletion spanning RCC1-like domain of RPGR in Japanese X-linked retinitis pigmentosa family.2005

    • Author(s)
      Jin Z-B, Liu X-Q, Uchida A, Vervoot R, Morishita K, Hayakawa M, Murakami A, Matsumoto N, Niikawa N, Nao-I N
    • Journal Title

      Mol Vis 11

      Pages: 535-541

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] X-linked adrenoleukodystrophy with partial deletion of ALD due to fusion with the neighbor gene, PLXNB.2005

    • Author(s)
      Matsumoto T, Miyake N, Watanabe Y, Yamanaka G, Oana S, Ogiwara M, Hoshika A, Miyahara H, Niikawa N
    • Journal Title

      Am J Med Genet 138A

      Pages: 300-302

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] X-linked adrenoleukodystrophy with partial deletion of ALD due to fusion with the neighbor gene,2005

    • Author(s)
      Matsumoto T, Niikawa N, et al.
    • Journal Title

      Am J Med Genet 138A

      Pages: 300-302

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] Eight novel microsatellite markers in the 3'region of the dystrophin gene useful for diagnosis of Duchenne muscular dystrophy.2004

    • Author(s)
      Matsumoto T, Niikawa N
    • Journal Title

      Prenat Diagn 24(12)

      Pages: 1014-1015

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] A rapid diagnostic method for a retrotransposal insertional mutation into the FCMD gene in Japanese patients with Fukuyama congenital muscular dystrophy.2004

    • Author(s)
      Kato R, Kawamura J, Sugawara H, Niikawa N, Matsumoto N
    • Journal Title

      Am J Med Genet 127A

      Pages: 54-57

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] Heterozygous TGFBR2 mutations in Marfan syndrome.2004

    • Author(s)
      Mizuguchi T, Collod-Beroud G, Abifadel M, Akiyama T, Harada N, Morisaki T, Allard D, Varret M, Claustres M, Morisaki H, Ihara M, Kinoshita A, Yoshiura K, Junien C, Kajii T, Jondeau G, Ohta T, Kishino T, Fukukawa Y, Nakamura Y, Niikawa N, Boileau C, Matsumoto N
    • Journal Title

      Nat Genet 36(8)

      Pages: 855-860

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] A novel GATA4 mutation completely segregated with atrial septal defect in a large Japanese family.2004

    • Author(s)
      Okubo A, Miyoshi O, Baba K, Takagi M, Tsukamoto K, Kinoshita A, Yoshiura K, Kishino T, Ohta T, Niikawa N, Matsumoto N
    • Journal Title

      J Med Genet 41(7)

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] Eight novel microsatellite markers in the 3' region of the dystrophin gene useful for diagnosis of Duchenne muscular dystrophy.2004

    • Author(s)
      Matsumoto T, Niikawa N
    • Journal Title

      Prenat Diagn 24

      Pages: 1014-1015

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] A rapid diagnostic method for a retrotransposal insertiona mutation into the FCMD gene in Japanese patients with Fukuyam● congenital muscular dystrophy.2004

    • Author(s)
      Kato R, Kawamura J, Sugawara H, Niikawa N, Matsumoto N
    • Journal Title

      Am J Med Genet 127A

      Pages: 54-57

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] Fifty microdeletions among 112 cases of Sotos syndrome : Low copy repeats possibly mediate the common deletion.2003

    • Author(s)
      Kurotaki N, Harada N, Shimokawa O, Miyake N, Kawame H, Uetake K, Makita Y, Kondoh T, Ogata T, Hasegawa T, Nagai T, Ozaki T, Touyama M, Shenhav R, Ohashi H, Medne L, Shiihara T, Ohtsu S, Kato Z, Okamoto N, Nishimoto J, Lev D, Miyoshi Y, Ishikiriyama S, Sonoda T, Sakazume S, Fukushima Y, Kurosawa K, Cheng J-F, Yoshiura K, Ohta T, Kishino T, Niikawa N, Matsumoto N
    • Journal Title

      Hum Mut 22(5)

      Pages: 378-387

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] Sotos syndrome and haploinsufficiency of NSD1 : Clinical features of intragenic mutations and submicroscopic deletions.2003

    • Author(s)
      Nagai T, Matsumoto N, Kurotaki N, Harada N, Niikawa N, Ogata T, Imaizumi K, Kurosawa K, Kondoh T, Ohashi H, Tsukahara M, Makita Y, Sugimoto T, Sonoda T, Yokoyama T, Uetake K, Sakazume S, Fukushima Y, Naritomi K
    • Journal Title

      J Med Genet 40(4)

      Pages: 285-289

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] Confirmation of genetic homogeneity of non-syndromic low frequency sensorineural hearing loss by linkage analysis and DFNA6/14 mutations in a Japanese family.2002

    • Author(s)
      Komatsu K, Nakamura N, Ghadami M, Matsumoto N, Kishino K, Ohta T, Niikawa N, Yoshiura K
    • Journal Title

      J Hum Genet 47

      Pages: 395-399

    • NAID

      50000580507

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] Haploinsufficiency of the NSD1 gene causes Sotos syndrome.2002

    • Author(s)
      Kurotaki N, Imaizumi K, Harada N, Masuno M, Kondoh T, Nagai T, Ohashi H, Naritomi K, Tsukahara M, Makita Y, Sugimoto T, Sonoda T, Hasegawa T, Chinen Y, Tomita H-A, Kinoshita A, Mizuguchi T, Yoshiura K, Ohta T, Kishino T, Fukushima Y, Niikawa N, Matsumoto N
    • Journal Title

      Nat Genet 30(April)

      Pages: 365-366

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] Molecular characterization of NSD1, a human homologue of the mouse Nsd1 gene.2001

    • Author(s)
      Kurotaki N, Harada N, Yoshiura K, Sugano S, Niikawa N, Matsumoto N
    • Journal Title

      Gene 279

      Pages: 197-204

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] Molecular characterization of NSD1, a human homologue of the mouse Nsdl gene.2001

    • Author(s)
      Kurotaki N, Harada N, YoshiurK, Sugano S, NiikawaN, Matsumoto N
    • Journal Title

      Gene 279

      Pages: 197-204

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • [Journal Article] Polymorphic alleles of the human MEI1 gene are associated with human azoospermia by meiotic arrest.

    • Author(s)
      Sato H, Miyamoto T, Yogev L, Namiki M, Koh E, Hayashi H, Sasaki Y, Ishikawa M, Lamb DJ, Matsumoto N, Niikawa N, Sengoku K
    • Journal Title

      J Hum Genet (in press)

    • NAID

      10017608347

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-13854024
  • 1.  NIIKAWA Norio (00111170)
    # of Collaborated Projects: 7 results
    # of Collaborated Products: 20 results
  • 2.  TSUJI Yoshiro (30039812)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 0 results
  • 3.  FUKUSHIMA Yoshimitsu (70273084)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 5 results
  • 4.  SHIDA Takafumi (20184533)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 5.  MATSUO Masafumi (10157266)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 6.  SONTA Shinichi (00100165)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 7.  IKEGAWA Shiro (30272496)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 8.  YOSHIURA Koh-ichiro (00304931)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 9 results
  • 9.  KISHINO Tatsuya (70315232)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 10.  TSUKAMOTO Kazuhiro (30253305)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 1 results
  • 11.  NARITOMI Kenji (20101446)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 4 results
  • 12.  JINNO Yoshihiro (20179097)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 13.  吉本 雅昭 (70167021)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 14.  日野 茂男 (70012763)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 15.  片峰 茂 (40161062)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 16.  宮原 春美 (00209933)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 17.  中尾 優子 (40325725)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 18.  辻田 高宏 (40304919)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 19.  木住野 達也
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 7 results

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