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渡邊 順子  ワタナベ ヨリコ

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WATANABE Yoriko  渡辺 順子

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Researcher Number 40258489
External Links
Affiliation *help 2018 : 久留米大学, 医学部, 准教授
2016 – 2017 : 久留米大学, 医学部, 講師
2005 – 2007 : Kurume University School of Medicine, Department of Pediatrics & Child Health, Lecturer, 医学部, 講師
2002 – 2004 : Department of Pediatrics and Child Health, Kurume University School of Medicine Research Associate, 医学部, 助手
1997 – 1998 : 久留米大学, 医学部, 助手
1994 : 久留米大学, 医学部, 助手
Review Section/Research Field
Principal Investigator
Pediatrics / Pediatrics
Except Principal Investigator
Pediatrics / Pediatrics
Keywords
Principal Investigator
MALDI-TOF-MS / 刺激伝導系障害 / 心房中隔欠損症 / BOR / 8q11-q13 / Cerulonlasmin / 家族性心房中隔欠損症 / 刺激伝導障害 / ウィルソン病 / 連鎖解析 … More / proteome analysis / STS / Wilson disease / YAC / hypoceruloplasminemia / ペプチド解析 / HYRC gene / セルロプラスミン / 質量分析 / 低セルロプラスミン血症 / SCID / 内臓錯位 … More
Except Principal Investigator
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 / RNA 19 / screening / MELAS / 発症予防 / late-onset presentation / mitochondrial DNA / 電子伝達系酵素 / 一塩基置換 / 点変異 / 臓器特異性 / orinithine transcarbamylase / プロセッシング / mitochondrial RNA / 予後因子 / オルニチントランスカルバミラーゼ / ミトコンドリアDNA / processing / male patients / respiratory chain enzymes / ミトコンドリア脳筋症 / ミトコンドリア DNA / point mutation / オルチニントランスカルバミラーゼ欠損症 / オルニチントランスカルパミラーゼ / RNAプロセッシング / RNA19 / ミトコンドリアtRNA / 遺伝疫学 / 遅発男子例 / 母性遺伝 / ミトコンドリアRNA / ornithine transcarbamylase deficiency / prevention / tissue specificity Less
  • Research Projects

    (6results)
  • Research Products

    (30results)
  • Co-Researchers

    (5People)
  •  Structural Analysis of Serum Ceruloplasmin Peptides From The Patients With Wilson disease and Familial HypoccerulosminemiaPrincipal Investigator

    • 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
  •  先天性心疾患発症におけるNeurotrophin-3の発現Principal Investigator

    • Principal Investigator
      渡辺 順子
    • Project Period (FY)
      1997 – 1998
    • Research Category
      Grant-in-Aid for Encouragement of Young Scientists (A)
    • Research Field
      Pediatrics
    • Research Institution
      Kurume University
  •  MOLECULAR BASIS OF MITOCHONDRIAL RNA PROCESSING SYSTEM IN DEVELOPMENTAL TISSUES AND IN MITOCHONDRIAL MYOPATHY.

    • Principal Investigator
      KOGA Yasutoshi
    • Project Period (FY)
      1997 – 1998
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      KURUME UNIVERSITY SCHOOL OF MEDICINE
  •  鰓、耳、腎症候群(BOR)座領域のDNA多型マーカーの作製と連鎖解析Principal Investigator

    • Principal Investigator
      渡辺 順子
    • Project Period (FY)
      1994
    • Research Category
      Grant-in-Aid for Encouragement of Young Scientists (A)
    • Research Field
      Pediatrics
    • Research Institution
      Kurume University

All 2008 2007 2006 2005 2003 Other

All Journal Article Book

  • [Book] 小児救急学習用テキスト原著第4版2006

    • Author(s)
      渡辺順子
    • Total Pages
      759
    • Publisher
      診断と治療社
    • 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

    • 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

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-17591125
  • [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] Screening for Alagille syndrome mutations in the JAG1 and NOTCH2 genes using denaturing high-performance liquid chromatography2007

    • Author(s)
      Samejima H, Torii C, Kosaki R, Kurosawa K, Yoshihashi H, Muroya K, Okamoto N, Watanabe Y, Kosho T, Kubota M, Matsuda O, Goto M, Izumi K, Takahashi T, Kosaki K
    • Journal Title

      Genet Test 11

      Pages : 216-227

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
    • 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

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17591125
  • [Journal Article] Novel mutations in five Japanese patients with 3-methylcrotonyl-CoA carboxylase deficiency2007

    • Author(s)
      Uematsu M, Sakamoto O, Sugawara N, Kumagai N, Morimoto T, Yamaguchi S, Hasegawa Y, Kobayashi H, Ihara K, Yoshino M, Watanabe Y, Inokuchi T, Yokoyama T, Kiwaki K, Nakamura K, Endo F, Tsuchiya S, Ohura T
    • Journal Title

      J Hum Genet 52

      Pages : 1040-1043

    • Description
      「研究成果報告書概要(和文)」より
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-17591125
  • [Journal Article] Novel mutations in five Japanese patients with 3-methylcrotonyl-CoAcarboxylase deficiency2007

    • Author(s)
      Uematsu M, Sakamoto O, Sugawara N, Kumagai N, Morimoto T, Yamaguchi S, Hasegawa Y, Kobayashi H, Ihara K, Yoshino M, Watanabe Y, Inokuchi T, Yokoyama T, Kiwaki K, Nakamura K, Endo F, Tsuchja S, Ohura T
    • Journal Title

      J Hum Genet 52

      Pages : 1040-1043

    • Peer Reviewed
    • 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] Novel mutations in five Japanese patients with 3-methylcrotonyl-C0A carboxylase deficiency.2007

    • Author(s)
      Uematsu M, Sakamoto O, Sugawara N, Kumagai N, Morimoto T,Yamaguchi S, Hasegawa Y, Kobayashi H, Ihara K, Yoshino M,Watanabe Y, Inokuchi T, Yokoyama T. Kiwaki K, Nakamura K, Endo F, Tsuchiya S, Ohura T.
    • Journal Title

      J Hum Genet. 52(doi : 10.1007/s10038-007-0211-9)

      Pages : 1040-1043

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-17591125
  • [Journal Article] Screening for Alagille syndrome mutations in the JAG1 and NOTCH2 genes using denaturing high-performance liquid chromatography.2007

    • Author(s)
      Samejima H,'Ibrii C, Kosaki R, Kurosawa K, Yoshihashi H,Muroya K, Okamoto N, Watanabe Y, Kosho T, Kubota M, Matsuda O, Goto M, Izumi K, Takahashi'F, Kosaki K.
    • Journal Title

      Genet Test 11(doi : 10.1089/gte.2006.0519)

      Pages : 216-227

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-17591125
  • [Journal Article] Screening for Alagille syndrome mutations in the JAGl andNOTCH2 genes using denaturing high-performance liquidchromatography2007

    • Author(s)
      Samejima H, Torii C, Kosaki R, Kurosawa K, Yoshihashi H, Muroya K, Okamoto N, Watanabe Y, Kosho T, Kubota M, Matsuda O, Goto M, Izumi K, Takahashi T, Kosaki K
    • Journal Title

      Genet Test 11

      Pages : 216-227

    • 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

      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

    • Data Source
      KAKENHI-PROJECT-15591148
  • [Journal Article] 栄養療法で急性期治療を行ったメープルシロップ尿症の1例2006

    • Author(s)
      岡田純一郎, 渡辺順子, 平井裕子, 神戸太郎, 廣瀬彰子, 藤野 浩, 前野泰樹, 芳野 信
    • Journal Title

      日本マススクリーニング学会雑誌 16

      Pages : 63-67

    • 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

    • 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] 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 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

    • 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 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

    • Description
      「研究成果報告書概要(和文)」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

    • 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

    • 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] 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] Effect of supplementation with L-carnitine at a small dose on acylcarnitine profiles in serum and urine and the renal handling of acylcarnitines in a patient with multiple acyl-coenzyme A dehydrogenation defect.2003

    • Author(s)
      Yoshino M, Tokunaga Y, Watanabe Y, Yoshida I, Sakaguchi M, Hata I, Shigematsu Y, Kimura M, Yamaguchi S
    • Journal Title

      J Chromatogr B 792

      Pages : 73-82

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-15591148
  • [Journal Article] Effect of supplementation with L-carnitine at a small dose on acycarnitine profiles in serum and urine andthe renal handling of acylcarnitines in a patient withmultiple acylcoenzyme A dehydrogenation defect.2003

    • Author(s)
      Yoshino M, Tokunaga Y, Watanabe Y, Yoshida I, Sakaguchi M, Hata I, Shigematsu Y, Kimura M, Yamaguchi S.
    • Journal Title

      J Chromatogr B 792

      Pages : 73-82

    • Description
      「研究成果報告書概要(欧文)」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.  YOSHINO Makoto (40080569)
    # of Collaborated Projects : 3results
    # of Collaborated Products : 19results
  • 2.  HARADA Eimei (90309790)
    # of Collaborated Projects : 3results
    # of Collaborated Products : 20results
  • 3.  KOGA Yasutoshi (00225400)
    # of Collaborated Projects : 1results
    # of Collaborated Products : 0results
  • 4.  YANO Shoji (00220202)
    # of Collaborated Projects : 1results
    # of Collaborated Products : 0results
  • 5.  徳永 泰幸 (60227585)
    # of Collaborated Projects : 1results
    # of Collaborated Products : 0results

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