• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

NARUSE Ichiro  成瀬 一郎

ORCIDConnect your ORCID iD *help
Researcher Number 20113326
Other IDs
External Links
Affiliation (based on the past Project Information) *help 2005 – 2012: 鳥取大学, 医学部, 教授
2004: 国立大学法人 鳥取大学, 医学部, 教授
2000 – 2002: 鳥取大学, 医学部, 教授
1999: 京都大学, 大学院・医学研究科, 助教授
1996 – 1999: 京都大学, 医学研究科, 助教授 … More
1998: 京都大学, 医学研究科, 教授
1995: 愛知県心身障害者コロニー発達障害研究所, 発達障害研究所・形態学部, 室長
1994 – 1995: 愛知県心身障害者コロニー発達障害研究所, 形態学部, 室長
1993: 愛知県心身障害者コロニー発達障害研究所, 室長
1990: 研究員
1989: 愛知県心身障害者コロニー, 発達障害研究所・発生学部, 研究員
1989: Inst. Develop. Res. Aichi Colony, 研究員(主任)
1988: 愛知県コロニー, 発達障害研究所, 研究員
1987: 愛知県心身障害者コロニー, 発達障害研究所・発生学部, 研究員 Less
Review Section/Research Field
Principal Investigator
Embryonic/Neonatal medicine / Orthopaedic surgery / General anatomy (including Histology/Embryology) / Embryonic/Neonatal medicine / Obstetrics and gynecology
Except Principal Investigator
General anatomy (including Histology/Embryology) / Embryonic/Neonatal medicine / Virology / Experimental pathology
Keywords
Principal Investigator
Gli3 / GCPS / Pdn / 無嗅脳症 / Shh / 多指症 / arhinencephaly / NTD / polydactyly / Pdn mouse … More / laser / fetal surgery / 子宮切開法 / Pdnマウス / レーザー / 胎児外科 / genetic anomaly / mouse / fetal therapy / exo utero / limb anomaly / 四肢奇形 / 胎仔手術 / 胎仔外科 / プログラム細胞死 / 奇形 / レ-ザ- / 胎児手術 / 胎児治療 / Fgf8 / suckling behavior / GLI3 / Greig cephalopolysyndactyly syndrome (GCPS) / apoptosis / TRPM-2遺伝子 / レーザーサージェリー / アポトーシス / マイクロアレイ / オクラトキシン / 性差 / 催奇形性 / 脳神経疾患 / 先天異常 … More
Except Principal Investigator
形態形成 / Gli3 / 葉酸 / 先天異常学 / Mouse fetus / Limb anomalies / Matrix metalloproteinase / Vascular remodelling / Programmed cell death / Limb bud / リモデリング / アポトーシス / 指奇形 / 分化 / Hammer-toe / マウス / カスパーゼ / メタロプロテアーゼ / 細胞死 / マウス胎児 / 四肢奇形 / マトリックス分解酵素 / 血管リモデリング / プログラム細胞死 / 四肢原基 / Folic acid / Neurulation / Central nervous system / Hox genes / Embryos / Developmental abnormalities / Hyperthermia / Physical agents / 先天異常 / 熱ショック蛋白 / 遺伝子発現 / 脳発生異常 / トランスフォーメーション / 脊柱 / ニューロン / 胎児脳 / 熱ショック / 神経管形成 / 中枢神経系 / Hox遺伝子 / 胚子 / 発生異常 / 高温 / 物理的要因 / brain abnormalities / intrauterine infection / cytomegalovirus / サイトメガロウィルス / 脳発達障害 / 胎内感染 / サイトメガロウイルス / カドミウム / ビングラスチン / 発生毒性スクリーニング法 / in vitro / 組織再構成 / 細胞認識機構 / 解離細胞 / ラット胎仔脳 / オクラトキシンA / オクラトキシンA / 神経管閉鎖障害 / 外脳症 Less
  • Research Projects

    (12 results)
  • Research Products

    (49 results)
  • Co-Researchers

    (16 People)
  •  Neural tube defect manifestation due to the interaction of genetic mutation and Ochratoxin A in the genetic polydactyly/ arhinencephaly mouse embryo, Pdn/Pdn

    • Principal Investigator
      UETA Etsuko
    • Project Period (FY)
      2010 – 2012
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Embryonic/Neonatal medicine
    • Research Institution
      Tottori University
  •  Molecular mechanism of gender dependent difference in the neural tube defect manifestation.Principal Investigator

    • Principal Investigator
      NARUSE Ichiro
    • Project Period (FY)
      2008 – 2010
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Embryonic/Neonatal medicine
    • Research Institution
      Tottori University
  •  Prevention of the neural tube defects by folic acid in the genetic polydactyly/arhinencephaly mouse, Pdn/Pdn

    • Principal Investigator
      UETA Etsuko
    • Project Period (FY)
      2006 – 2008
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Embryonic/Neonatal medicine
    • Research Institution
      Tottori University
  •  Molecular mechanisms of arhinencephaly and polydactyly manifestations in the mouse homolog of GCPS.Principal Investigator

    • Principal Investigator
      NARUSE Ichiro
    • Project Period (FY)
      2004 – 2006
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Embryonic/Neonatal medicine
    • Research Institution
      Tottori University
  •  Abnormal gene expressions in the Gli3 and Shh of the mouse homolog of GCPS, PdnPrincipal Investigator

    • Principal Investigator
      NARUSE Ichiro
    • Project Period (FY)
      2000 – 2002
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      General anatomy (including Histology/Embryology)
    • Research Institution
      Tottori University
  •  Developmental Brain Disorders due to Physical Agents

    • Principal Investigator
      SHIOTA Kohei
    • Project Period (FY)
      1998 – 1999
    • Research Category
      Grant-in-Aid for Scientific Research (B).
    • Research Field
      General anatomy (including Histology/Embryology)
    • Research Institution
      KYOTO UNIVERSITY
  •  Developmental and molecular cell biological study of the mechanisms of limb differentiation

    • Principal Investigator
      SHIOTA Kohei
    • Project Period (FY)
      1998 – 2000
    • Research Category
      Grant-in-Aid for Scientific Research (B).
    • Research Field
      General anatomy (including Histology/Embryology)
    • Research Institution
      KYOTO UNIVERSITY
  •  Genetic polydactyly / arhinencephaly mouse (Pdn / Pdn) is a homologue of Greig cephalopolysyndactyly syndrome.Principal Investigator

    • Principal Investigator
      NARUSE Ichiro
    • Project Period (FY)
      1996 – 1998
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Embryonic/Neonatal medicine
    • Research Institution
      KYOTO UNIVERSITY
  •  Arhinencephaly induced by fetal laser surgery exo utero in mice.Principal Investigator

    • Principal Investigator
      NARUSE Ichiro
    • Project Period (FY)
      1993 – 1995
    • Research Category
      Grant-in-Aid for General Scientific Research (C)
    • Research Field
      Obstetrics and gynecology
    • Research Institution
      Institute for Developmental Research, Aichi Prefectural Colony
  •  Experimental Research for Mechanism of Brain Abnormalities Induced by Intrauterine Infection with Cytomegalovirus.

    • Principal Investigator
      TSUTSUI Yoshihiro
    • Project Period (FY)
      1989 – 1990
    • Research Category
      Grant-in-Aid for General Scientific Research (C)
    • Research Field
      Virology
    • Research Institution
      Institute for Developmental Research, Aichi Prefectural Colony.
  •  Fetal surgical prevention of genetic limb anomalies in mice.Principal Investigator

    • Principal Investigator
      NARUSE Ichiro
    • Project Period (FY)
      1988 – 1989
    • Research Category
      Grant-in-Aid for General Scientific Research (C)
    • Research Field
      Orthopaedic surgery
    • Research Institution
      Institute for Developmental Research, Aichi Prefectural Colony
  •  Im uitro発生毒性の一次スクリーニング法の開発

    • Principal Investigator
      東海林 隆次郎
    • Project Period (FY)
      1987
    • Research Category
      Grant-in-Aid for General Scientific Research (C)
    • Research Field
      Experimental pathology
    • Research Institution
      Institute for Developmental Research, Aichi Human Service Center

All 2012 2011 2010 2009 2008 2007 2006 2005 2004

All Journal Article Presentation Book

  • [Book] 形の科学百科事典-嗅球欠損と生殖器低形成の連鎖発現-2004

    • Author(s)
      成瀬一郎
    • Total Pages
      924
    • Publisher
      朝倉書店
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-16591075
  • [Book] 形の科学百科事典2004

    • Author(s)
      成瀬一郎
    • Total Pages
      924
    • Publisher
      形の科学会編、朝倉書店
    • Data Source
      KAKENHI-PROJECT-16591075
  • [Journal Article] Normal location of thumb/big toe may be related to programmed cell death (PCD) in the preaxial area of embryonic limb.2011

    • Author(s)
      Kimura S, Yamada S, Naruse I.
    • Journal Title

      The Anatomical Record 293:(in press)

    • Data Source
      KAKENHI-PROJECT-20591297
  • [Journal Article] Birth defects caused by the mutations in human GLI3 and mouse Gli3 genes.2010

    • Author(s)
      Naruse I., et al
    • Journal Title

      Congenital Anomalies

      Volume: 50 Pages: 1-7

    • NAID

      10029577246

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22591200
  • [Journal Article] Birth defects caused by the mutations in human GLI3 and mouse Gli3 genes.2010

    • Author(s)
      Naruse I., et al.
    • Journal Title

      Congenital Anomalies 50

      Pages: 1-7

    • NAID

      10029577246

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591297
  • [Journal Article] Syndromes caused by the mutations in GLI3 gene.2010

    • Author(s)
      Naruse, et al.
    • Journal Title

      Current Pediatric Reviews

      Volume: 6 Pages: 219-225

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591297
  • [Journal Article] et al Syndromes Caused by the Mutations in GLI3 Gene2010

    • Author(s)
      Naruse I.
    • Journal Title

      Current Pediatric Reviews

      Volume: 6 Pages: 219-225

    • Data Source
      KAKENHI-PROJECT-22591200
  • [Journal Article] et al Birth defects caused by the mutations in human GLI3 and mouse Gli3 genes2010

    • Author(s)
      Naruse I
    • Journal Title

      Congenital Anomalies

      Volume: 50 Pages: 1-7

    • Data Source
      KAKENHI-PROJECT-22591200
  • [Journal Article] Birth defects caused by the mutations in human GLI3 and mouse Gli3 genes.2010

    • Author(s)
      Naruse I., et al.
    • Journal Title

      Congenital Anomalies

      Volume: 50 Pages: 1-7

    • NAID

      10029577246

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591297
  • [Journal Article] Syndromes Caused by the Mutations in GLI3 Gene.2010

    • Author(s)
      Naruse I., et al
    • Journal Title

      Current Pediatric Reviews

      Volume: 6 Pages: 219-225

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22591200
  • [Journal Article] Birth defects caused by the mutations in human Gli3 and mouse Gli3 genes.2010

    • Author(s)
      Naruse I, Ueta E, Sumino Y, Ogawa M, Ishikiriyama S.
    • Journal Title

      Congenit.Anom. 50(1)

      Pages: 1-7

    • NAID

      10029577246

    • Data Source
      KAKENHI-PROJECT-20591297
  • [Journal Article] Syndromes caused by the mutations in Gli3 gene.2010

    • Author(s)
      Naruse I, Ueta E, Sumino Y, Ogawa M.
    • Journal Title

      Current Pediatric Reviews 6(4)

      Pages: 219-225

    • Data Source
      KAKENHI-PROJECT-20591297
  • [Journal Article] Gender-dependent differences in the incidence of ochratoxin A-induced neural tube defects in Pdn/Pdn mouse.2010

    • Author(s)
      Ueta E, Kodama M, Sumino Y, Kurome M, Ohta K, Katagiri R, Naruse I.
    • Journal Title

      Congenit Anom. 50(1)

      Pages: 29-39

    • NAID

      10029577445

    • Data Source
      KAKENHI-PROJECT-20591297
  • [Journal Article] 1 Altered signaling pathway in the dysmorphogeof telencephalon in the Gli3 depressed mousembryo, Pdn/Pdn2008

    • Author(s)
      Ueta E., Kurome M, Teshima Y, Kodama M, Otsuka Y, and Naruse I.
    • Journal Title

      Congenital Anomalies 48(2)

      Pages: 74-80

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18591219
  • [Journal Article] Altered signaling pathway in the dysmorphogenesis of telencephalon in the Gli3 depressed mouse embryo, Pdn/Pdn.2008

    • Author(s)
      Ueta E, Kurome M, Teshima Y, Kodama M, Otsuka Y, Naruse I.
    • Journal Title

      Congenit.Anom. 48(2)

      Pages: 74-80

    • NAID

      10027387234

    • Data Source
      KAKENHI-PROJECT-20591297
  • [Journal Article] Prevention of ochratoxin A-induced neural tube defects by folinic acid in the genetic polydactyly/arhinencephaly mouse, Pdn/Pdn.2007

    • Author(s)
      Katagiri R., Kurome M., Teshima Y., Ueta E., Naruse, I.
    • Journal Title

      Congenital Anomalies 47(3)(in press)

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-16591075
  • [Journal Article] Genetic susceptibility in the neural tube defects induced by ochratoxin A in the genetic arhinencephaly mouse, Pdn/Pdn2007

    • Author(s)
      Ohta K, Maekawa M, Katagiri R, Ueta E, and Naruse I.
    • Journal Title

      Congenital Anomalies 46(3)

      Pages: 144-148

    • NAID

      10027385677

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18591219
  • [Journal Article] Prevention of ochratoxin A-induced neural tube defects by folinic acid in the genetic polydactyly/arhinencephaly mouse, Pdn/Pdn.2007

    • Author(s)
      Katagiri R., Kurome M., Teshima Y., Ueta E., Naruse, I.
    • Journal Title

      Congenital Anomalies 47・3(in press)

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-16591075
  • [Journal Article] Prevention of ochratoxin A-induced neural tube defects by folic acid in the genetic polydactyly/arhinencephaly mouse, Pdn/Pdn2007

    • Author(s)
      Katagiri R, Kurome M, Teshima Y, Ueta E, and Naruse I.
    • Journal Title

      Congenital Anomalies 47(3)

      Pages: 90-96

    • NAID

      10027386489

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18591219
  • [Journal Article] Genetic susceptibility in the neural tube defects induced by ochratoxin A in the genetic arhinencephaly mouse Pdn/Pdn.2006

    • Author(s)
      Ohta K., Maekawa M., Katagiri R., Ueta E., Naruse I.
    • Journal Title

      Congenital Anomalies 46・3

      Pages: 144-148

    • NAID

      10027385677

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-16591075
  • [Journal Article] Genetic susceptibility in the neural tube defects induced by ochratoxin A in the genetic arhinencephaly mouse Pdn/Pdn.2006

    • Author(s)
      Ohta K., Maekawa M., Katagiri R., Ueta E., Naruse I.
    • Journal Title

      Congenital Anomalies 46(3)

      Pages: 144-148

    • NAID

      10027385677

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-16591075
  • [Journal Article] Molecular analyses in the mouse homolog of Greig Cephalopolysyndactyly syndrome (GCPS).2005

    • Author(s)
      Naruse I., Ueta E., Maekawa, M., Ohta K.
    • Journal Title

      Trend of Developmental Biology 1

      Pages: 83-87

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-16591075
  • [Journal Article] Molecular analyses in the mouse homolog of Greig cephalopolysyndactyly syndrome (GCPS).2005

    • Author(s)
      Naruse I., Ueta E., Maekawa, M., Ohta K.
    • Journal Title

      Trend of Developmental Biology 1

      Pages: 83-87

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-16591075
  • [Journal Article] Molecular analyses in the mouse homolog of Greig cephalopolysyndactyly syndrome (GCPS)2005

    • Author(s)
      Naruse I., Ueta E., Maekawa M., Ohta K.
    • Journal Title

      Trends in Developmental Biology 1

      Pages: 1-5

    • Data Source
      KAKENHI-PROJECT-16591075
  • [Journal Article] Exencephaly induction by valproic acid in the genetic polydactyly/arhinencephaly mouse, Pdn/Pdn.2005

    • Author(s)
      Maekawa M., Ohta K., Katagiri R., Ueta E., Naruse I.
    • Journal Title

      Congenital Anomalies 45(4)

      Pages: 132-136

    • NAID

      10027384537

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-16591075
  • [Journal Article] Molecular analyses in the mouse homolog of Greig cephalopolysyndactyly syndrome (GCPS).2005

    • Author(s)
      Naruse I. et al.
    • Journal Title

      Trend Dev Biol 1

      Pages: 83-87

    • Data Source
      KAKENHI-PROJECT-16591075
  • [Journal Article] Exencephaly induction by valproic acid in the genetic polydactyly/arhinencephaly mouse, Pdn/Pdn.2005

    • Author(s)
      Maekawa M., Ohta K., Katagiri R., Ueta E., Naruse I.
    • Journal Title

      Congenital Anomalies 45・4

      Pages: 132-136

    • NAID

      10027384537

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-16591075
  • [Journal Article] Correlation between absence of the olfactory bulb and defect of the reproductive organ.2004

    • Author(s)
      Naruse I.
    • Journal Title

      Encyclopedia of Science on Form (Asakura Shoten)

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-16591075
  • [Journal Article] Sonic hedgehog expression in Gli3 depressed mouse embryo, Pdn/Pdn.2004

    • Author(s)
      Ueta E., Maekawa M., Morimoto I., Nanba E., Naruse I.
    • Journal Title

      Congenital Anomalies 44・1

      Pages: 27-32

    • NAID

      10018085451

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-16591075
  • [Journal Article] Sonic hedgehog expression in Gli3 depressed mouse embryo, Pdn/Pdn.2004

    • Author(s)
      Ueta E., Maekawa M., Morimoto I., Nanba E., Naruse I.
    • Journal Title

      Congenital Anomalies 44

      Pages: 27-32

    • NAID

      10018085451

    • Data Source
      KAKENHI-PROJECT-16591075
  • [Journal Article] Sonic hedgehog expression in Gli3 depressed mouse embryo, Pdn/Pdn.2004

    • Author(s)
      Ueta E., Maekawa M., Morimoto I., Nanba E., Naruse I.
    • Journal Title

      Congenital Anomalies 44(1)

      Pages: 27-32

    • NAID

      10018085451

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-16591075
  • [Presentation] 神経管閉鎖期におけるOchratoxin A曝露による遺伝子の発現変化2012

    • Author(s)
      上田悦子、鳥谷裕太郎、成瀬一郎、曽根保子、大塚譲
    • Organizer
      日本先天異常学会学術集会
    • Place of Presentation
      東京都新宿区 東京女子医科大学
    • Year and Date
      2012-07-06
    • Data Source
      KAKENHI-PROJECT-22591200
  • [Presentation] 遺伝性多指症/無嗅脳症マウス胚におけるOchratoxin Aによる遺伝子発現の変動2012

    • Author(s)
      鳥谷裕太郎、上田悦子、成瀬一郎
    • Organizer
      第52回日本先天異常学会学術集会
    • Place of Presentation
      東京都新宿区 東京女子医科大学
    • Year and Date
      2012-07-08
    • Data Source
      KAKENHI-PROJECT-22591200
  • [Presentation] オクラトキシンAと転写因子Gli3による神経管閉鎖障害発症と脳形態形成関連遺伝子の発現変化2011

    • Author(s)
      上田悦子、曽根保子 大塚譲、成瀬一郎
    • Organizer
      日本栄養食糧学会
    • Place of Presentation
      東京都文京区 お茶の水女子大学
    • Year and Date
      2011-05-13
    • Data Source
      KAKENHI-PROJECT-22591200
  • [Presentation] Gli3変異とオクラトキシンA曝露による神経管閉鎖障害発症における遺伝子発現の変動2011

    • Author(s)
      上田悦子、鳥谷裕太郎、成瀬一郎
    • Organizer
      日本先天異常学会学術集会
    • Place of Presentation
      東京都千代田区 シェーンバッハサボー
    • Year and Date
      2011-07-22
    • Data Source
      KAKENHI-PROJECT-22591200
  • [Presentation] 遺伝性多指症/無嗅脳症マウスにおけるOchratoxin Aによる神経管閉鎖障害発症の性差 -第3報-2010

    • Author(s)
      角野良紀、上田悦子、小川将也、成瀬一郎
    • Organizer
      日本先天異常学会学術集会
    • Place of Presentation
      淡路市 淡路夢舞台国際会議場
    • Year and Date
      2010-07-08
    • Data Source
      KAKENHI-PROJECT-22591200
  • [Presentation] オクラトキシンA曝露による神経管閉鎖障害と性関連遺伝子の変動2010

    • Author(s)
      上田悦子、角野良紀、小川将也、成瀬一郎
    • Organizer
      日本先天異常学会学術集会
    • Place of Presentation
      淡路市 淡路夢舞台国際会議場
    • Year and Date
      2010-07-08
    • Data Source
      KAKENHI-PROJECT-22591200
  • [Presentation] オクラトキシンA曝露による神経管閉鎖障害と性関連遺伝子の変動2010

    • Author(s)
      上田悦子、角野良紀、小川将也、成瀬一郎
    • Organizer
      第50回日本先天異常学会学術集会
    • Place of Presentation
      淡路
    • Data Source
      KAKENHI-PROJECT-20591297
  • [Presentation] 遺伝性多指症/無嗅脳症マウスにおけるOchratoxin Aによる神経管閉鎖障害発症の性差2010

    • Author(s)
      角野良紀、上田悦子、小川将也、成瀬一郎
    • Organizer
      第50回日本先天異常学会学術集会
    • Place of Presentation
      淡路
    • Data Source
      KAKENHI-PROJECT-20591297
  • [Presentation] オクラトキシンAによる神経管閉鎖障害-Gli3発現抑制と性差との関連-2009

    • Author(s)
      上田悦子、見玉真実、角野良紀、成瀬一郎
    • Organizer
      第49回日本先天異常学会学術集会
    • Place of Presentation
      鹿児島
    • Data Source
      KAKENHI-PROJECT-20591297
  • [Presentation] 遺伝性多指症/無嗅脳症マウスにおいてGli3発現抑制を受ける遺伝子群の探索2008

    • Author(s)
      上田悦子、児玉真実、黒目万帆、手嶋優子、大塚譲、成瀬一郎
    • Organizer
      日本先天異常学会学術集会
    • Place of Presentation
      東京
    • Year and Date
      2008-06-29
    • Data Source
      KAKENHI-PROJECT-18591219
  • [Presentation] 遺伝性多指症/無嗅脳症マウスにおけるOchratoxin Aによる神経管閉鎖障害発症の性差)第2報-2008

    • Author(s)
      児玉真実、上田悦子、成瀬一郎
    • Organizer
      日本先天異常学会学術集会
    • Place of Presentation
      東京
    • Year and Date
      2008-06-29
    • Data Source
      KAKENHI-PROJECT-18591219
  • [Presentation] 遺伝性多指症/無嗅脳症マウスにおけるOchratoxin Aによる神経管閉鎖障害発症の性差-第2報-2008

    • Author(s)
      見玉真実、上田悦子、成瀬一郎
    • Organizer
      第48回日本先天異常学会学術集会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-20591297
  • [Presentation] 遺伝性多指症/無嗅脳症マウスにおいてGli3発現抑制を受ける遺伝子群の探索2008

    • Author(s)
      上田悦子、見玉真実、黒目万帆、手嶋優子、大塚譲、成瀬一郎
    • Organizer
      第48回日本先天異常学会学術集会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-20591297
  • [Presentation] バルプロ酸に対する遺伝性多指症/無嗅脳症マウスの感受性の差2007

    • Author(s)
      手嶋優子、黒目万帆、上田悦子、成瀬一郎
    • Organizer
      日本先天異常学会学術集会
    • Place of Presentation
      名古屋
    • Year and Date
      2007-07-08
    • Data Source
      KAKENHI-PROJECT-18591219
  • [Presentation] 遺伝性多指症/無嗅脳症マウスにおけるOchratoxin Aによる神経管閉鎖異常発症の性差2007

    • Author(s)
      黒目万帆、手嶋優子、上田悦子、成瀬一郎
    • Organizer
      日本先天異常学会学術集会
    • Place of Presentation
      名古屋
    • Year and Date
      2007-07-08
    • Data Source
      KAKENHI-PROJECT-18591219
  • [Presentation] 遺伝性多指症/無嗅脳症マウスにおいてオクラトキシンA処理で起きる神経管閉鎖異常を葉酸で防御する試み2007

    • Author(s)
      上田悦子、片桐龍一、黒目万帆、手嶋優子、成瀬一郎
    • Organizer
      日本先天異常学会学術集会
    • Place of Presentation
      名古屋
    • Year and Date
      2007-07-08
    • Data Source
      KAKENHI-PROJECT-18591219
  • [Presentation] 遺伝性多指症/無嗅脳症マウス(Pdn/Pdn)においてOchratoxinAで惹起される神経管閉鎖異常の葉酸による防御2006

    • Author(s)
      片桐龍一、太田健一、上田悦子、成瀬一郎
    • Organizer
      日本先天異常学会学術集会
    • Place of Presentation
      山形
    • Year and Date
      2006-06-30
    • Data Source
      KAKENHI-PROJECT-18591219
  • [Presentation] 遺伝性多指症/無嗅脳症マウス(Pdnの責任遺伝子Gli3へのトランスポゾンの挿入2006

    • Author(s)
      上田悦子、片桐龍一、難波栄二、成瀬一郎
    • Organizer
      日本先天異常学会学術集会
    • Place of Presentation
      山形
    • Year and Date
      2006-06-30
    • Data Source
      KAKENHI-PROJECT-18591219
  • 1.  UETA Etsuko (40335526)
    # of Collaborated Projects: 4 results
    # of Collaborated Products: 37 results
  • 2.  SHIOTA Kohei (80109529)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 0 results
  • 3.  TAKIGAWA Toshiya (90263095)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 0 results
  • 4.  MIURA Takashi (10324617)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 0 results
  • 5.  TSUTSUI Yoshihiro (50073135)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 6.  KADOTA Chika (80214419)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 7.  HATAYAMA Takumi (10094484)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 8.  MORIMOTO Takeshi (00311746)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 9.  ISHIBASHI Makoto (30232341)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 10.  東海林 隆次郎 (30090418)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 11.  松田 素子 (40165832)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 12.  大平 敦彦 (20101074)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 13.  竹内 郁夫 (20090433)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 14.  李 忠連 (80319532)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 15.  森 千里 (90174375)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 16.  KEINO Hiromi
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results

URL: 

Are you sure that you want to link your ORCID iD to your KAKEN Researcher profile?
* This action can be performed only by the researcher himself/herself who is listed on the KAKEN Researcher’s page. Are you sure that this KAKEN Researcher’s page is your page?

この研究者とORCID iDの連携を行いますか?
※ この処理は、研究者本人だけが実行できます。

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi