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HARADA Eimei  原田 英明

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… Alternative Names

原田 英明  ハラダ エイメイ

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Researcher Number 90309790
External Links
Affiliation (Current) 2025: 久留米大学, 医学部, 助教
Affiliation (based on the past Project Information) *help 2007: Kurume University, School of medicine, Assistant
2000 – 2006: 久留米大学, 医学部, 助手
Review Section/Research Field
Except Principal Investigator
Pediatrics / Pediatrics
Keywords
Except Principal Investigator
MALDI-TOF-MS / screening / 発症予防 / スクリーニング / オルニチントランスカルバミラーゼ欠損症 / Wilson disease / hypoceruloplasminemia / proteome analysis / Cerulonlasmin / 質量分析 … More / ウィルソン病 / 低セルロプラスミン血症 / ペプチド解析 / セルロプラスミン / male patients / late-onset presentation / ornithine transcarbamylase deficiency / オルチニントランスカルバミラーゼ欠損症 / 予後因子 / 遺伝疫学 / 遅発男子例 / prevention / orinithine transcarbamylase / オルニチントランスカルパミラーゼ / 一塩基置換 / オルニチントランスカルバミラーゼ Less
  • Research Projects

    (3 results)
  • Research Products

    (20 results)
  • Co-Researchers

    (3 People)
  •  Structural Analysis of Serum Ceruloplasmin Peptides From The Patients With Wilson disease and Familial Hypoccerulosminemia

    • Principal Investigator
      WATANABE Yoriko
    • Project Period (FY)
      2005 – 2007
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Kurume University
  •  A study on Presymptomatic recognition and prevention of late-onset ornithine transcarbamylase deficiency in male

    • Principal Investigator
      YOSHINO Makoto
    • Project Period (FY)
      2003 – 2005
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Kurume University
  •  A Study on Molecular Epidemiology and Prevention of Onset of Late-onset Ornithine Transcarbamylase Deficiency in Male Patients

    • Principal Investigator
      YOSHINO Makoto
    • Project Period (FY)
      2000 – 2002
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      KURUME UNIVERSITY

All 2008 2007 2006 2005 Other

All Journal Article

  • [Journal Article] Paternal transmission and slow elimination of mutant allelesassociated with late-onset ornithine transcarbamylase deficiencyin male patients2008

    • Author(s)
      Numata S, Harada E, Maeno Y, Ueki I, Watanabe Y, Fujii C, Yanagawa T, Takenaka S, Inoue T, Inoue S, Goushi T, Yasutake T, Mizuta T, Ybshino M
    • Journal Title

      J Hum Genet 53

      Pages: 10-17

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17591125
  • [Journal Article] Paternal transmission and slow elimination of mutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients2008

    • Author(s)
      Numata S, Harada E, Maeno Y, Ueki I, Watanabe Y, Fujii C, Yanagawa T, Takenaka S, Inoue T, Inoue S, Goushi T, Yasutake T, Mizuta T, Yoshino M
    • Journal Title

      J Hum Genet 53

      Pages: 10-17

    • NAID

      10021247384

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17591125
  • [Journal Article] Paternal transmission and slow elimination of mutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients.2008

    • Author(s)
      Numata S, Harada E, Maeno Y, Ueki I, Watanabe Y, Fujii C, Yanagawa T, Takenaka S, Inoue T, Inoue S, Goushi T, Yasutake T, Mizuta T, Yoshino M.
    • Journal Title

      J Hum Genet 53(doi ; 10.1007/s10038-007-0212-8)

      Pages: 10-17

    • NAID

      10021247384

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-17591125
  • [Journal Article] Roles of some cytokines in bone remodeling and hematopoiesis in Gaucher disease.2007

    • Author(s)
      Yoshino M, Watanabe Y, Thkunaga Y, Harada E, Fujii C, Numata S, Harada M, Tajima A, Ida H.
    • Journal Title

      Pediatr Int 49(doi : 10.1111/j.1442-200x.2007.02502.x)

      Pages: 959-956

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-17591125
  • [Journal Article] Roles of specific cytokines in bone remodeling and hematopoiesis in Gaucher disease2007

    • Author(s)
      Yoshino M, Watanabe Y, Tokunaga Y, Harada E, Fujii C, Numata S, Harada M, Tajima A, Ida H
    • Journal Title

      Pediatr Int 49

      Pages: 959-965

    • NAID

      10024152088

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17591125
  • [Journal Article] Late-onset ornithine transcarbamylase deficiency in male patients : Prognostic factors and characteristics of plasma amino acid profile.2006

    • Author(s)
      Harada E, Nishiyori A, Tokunaga Y, Watanabe Y, Kuriya N, Kumashiro R, Kuno T, Kuromaru R, Hirose S, Ichikawa K, Yoshino M.
    • Journal Title

      Pediatr Int 48

      Pages: 105-111

    • NAID

      10018195131

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15591148
  • [Journal Article] Late-onset ornithine transcarbamylase deficiency in male patients:Prognostic factors and characteristics of plasma amino acid profile2006

    • Author(s)
      Harada E, Nishiyori A, Tokunaga Y, Watanabe Y, Kuriya N, Kumashiro R, Kuno T, Kuromaru R, Hirose S, Ichikawa K, Yoshino M
    • Journal Title

      Pediatr Int 48

      Pages: 105-111

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17591125
  • [Journal Article] Comprehensive genetic analysis of relevant four genes in 49 patients with Marfan syndrome or Marfan-related phenotypes2006

    • Author(s)
      Sakai H, Visser R, Ikegawa S, Ito E, Numabe H, Watanabe Y, Mikami H, Kondoh T, Kitoh H, Sugiyama R, Okamoto N, Ogata T, Fodde R, Mizuno S, Takamura K, Egashira M, Sasaki N, Watanabe S, Nishimaki S, Takada F, Nagai T, Okada Y, Aoka Y, Yasuda K, Iwasa M, Kogaki S, Harada N, Mizuguchi T, Matsumoto N
    • Journal Title

      Am J Med Genet A 140・16

      Pages: 1719-1725

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17591125
  • [Journal Article] Late-onset Ornithine Transcarbamylase Deficiency in Male Patients : Prognostic Factors and Characteristics of Plasma Amino Acid Profile2006

    • Author(s)
      Harada E, Nishiyori A, Tokunaga Y, Watanabe Y, Kuriya N, Kumashiro R, Kuno T, Kuromaru R, Hirose S, Ichikawa K, Yoshino M
    • Journal Title

      Pediatrics International 48

      Pages: 105-111

    • NAID

      10018195131

    • Data Source
      KAKENHI-PROJECT-15591148
  • [Journal Article] Late-onset ornithine transcarbamylase deficiency inmale patients:Prognostic factors and characteristics of plasma amino acid profile.2006

    • Author(s)
      Harada E, Nishiyori A, Tokunaga Y, Watanabe Y, Kuriya N,Kumasbiro R, Kuno T, Kuromaru R, Hirose 5, Ichikawa K,Yoshino M.
    • Journal Title

      Pediatr Int 48(doi : 10.1111/j.1442-200x.02181.x)

      Pages: 105-111

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-17591125
  • [Journal Article] Comprehensive genetic analysis of relevant four genes in 49 patients with Marfan syndrome or Marfan-related phenotypes.2006

    • Author(s)
      Sakai H, Visser R, Ikegawa S, Ito E, Numabe H, Watanabe Y, Mikami H, Kondoh T, Kitoh H, Sugiyama R, Okamoto N, Ogata T, Fodde R, Mizuno S, Takamura K, Egashira M, Sasaki N, Watanabe S, Nishimaki S, Takada F, Nagai T, Okada Y, Aoka Y, Yasuda K, Iwasa M, Kogaki S, Harada N, Mizuguchi T, Matsumoto N
    • Journal Title

      Am J Med Genet A 140・16

      Pages: 1719-1725

    • Data Source
      KAKENHI-PROJECT-17591125
  • [Journal Article] Comprehensive genetic analysis of relevant fourgenes in 49 patients with Marfan syndrome or Marfan-related phenotypes.2006

    • Author(s)
      Sakai H, Visser R, Ikegawa S, Ito E, Numabe H, Watanabe Y, Mikami H, Kondoh T, Kitoh H, Sugiyama R, Okamoto N, Ogata T, Fodde R, Mizuno S, Takamura K, Egashira M, Sasaki N,Watanabe S, Nishimaki S, Takada F, Nagai T, Okada Y, Aoka Y, Yasuda K, Iwasa M, Kogaki S, Harada N, Mizuguchi T, Matsumoto N.
    • Journal Title

      Am J Med GenetA. 140(16)(doi : 10.1002/ajmg.a.31353)

      Pages: 1719-25

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-17591125
  • [Journal Article] Late-onset ornithine transcarbamylase deficiency in male patients : Prognostic factors and characteristics of plasma amino acid profile.2006

    • Author(s)
      Harada E, Nishiyori A, Tokunaga Y, Watanabe Y, Kuriya N, Kumashiro R, Kuno T, Kuromaru R, Hirose S, Ichikawa K, Yoshino M
    • Journal Title

      Pediatr Int 48

      Pages: 105-111

    • NAID

      10018195131

    • Data Source
      KAKENHI-PROJECT-17591125
  • [Journal Article] Late-onset ornithine transcarbamylase deficiency in male patients : Prognostic factors and characteristics of plasma amino acid profile.2006

    • Author(s)
      Harada E, Nishiyori A, Tokunaga Y, Watanabe Y, Kuriya N, Kumashiro R, Kuno T, Kuromaru R, Hirose S, Ichikawa K, Yoshino M
    • Journal Title

      Pediatr Int 48

      Pages: 105-111

    • NAID

      10018195131

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-15591148
  • [Journal Article] Ornithine transcarbamylase deficiency : recurrence of mutations associated with late-onset disease in maple patients in unrelated families and phenotypic variability2005

    • Author(s)
      Watanabe Y, Harada E, Yoshino M
    • Journal Title

      Journal of Inherited Metabolic Disease 28・suppl.

      Pages: 67-67

    • Data Source
      KAKENHI-PROJECT-15591148
  • [Journal Article] 男子OTC欠損症:新生児例と遅発例の変異の対比2005

    • Author(s)
      首藤紳介, 渡辺順子, 原田英明, 西依 淳, 前野泰樹, 竹中 聡, 井上敏郎, 井上真改, 合志光史
    • Journal Title

      日本先天代謝異常学会雑誌 21

      Pages: 74-74

    • NAID

      10016759792

    • Data Source
      KAKENHI-PROJECT-15591148
  • [Journal Article] Ornithine transcarbamylase deficiency : recurrence of mutations associated with late-onset disease in maple patients in unrelated families and phenotypic variability2005

    • Author(s)
      Watanabe Y, Harada H, Yoshino M
    • Journal Title

      J Inherit Metab Dis 28 - suppl.

      Pages: 67-67

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-15591148
  • [Journal Article] Omithine transcarbamylase deficiency : recurrence of mutations associated with late-onset disease in maple patients in unrelated families and phenotypic variability.2005

    • Author(s)
      Watanabe Y, Harada H, Yoshino M.
    • Journal Title

      J Inherit Metab Dis 28 suppl

      Pages: 67-67

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15591148
  • [Journal Article] 男子OTC欠損症 : 新生児例と遅発例の変異の対比2005

    • Author(s)
      首藤紳介, 渡辺順子, 原田英明, 西依 淳, 前野泰樹, 竹中 聡, 井上敏郎, 井上真改, 合志光史
    • Journal Title

      日本先天代謝異常学会雑誌 21

      Pages: 74-74

    • NAID

      10016759792

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-15591148
  • [Journal Article] OTC deficiency in male : a comparison of mutations in the neonatal onset with those in the late-onset presentations.

    • Author(s)
      Shuto S, Watanabe Y, Harada E, Nishiyori A, Maeno Y, Takenaka S, Inoue T, Inoue S, Goshi T.
    • Journal Title

      J Jpn Soc Inher Metab Dis 21

      Pages: 74-74

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15591148
  • 1.  WATANABE Yoriko (40258489)
    # of Collaborated Projects: 3 results
    # of Collaborated Products: 20 results
  • 2.  YOSHINO Makoto (40080569)
    # of Collaborated Projects: 3 results
    # of Collaborated Products: 13 results
  • 3.  徳永 泰幸 (60227585)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results

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