NARUSE Ichiro 成瀬一郎

Researcher Number	20113326
Other IDs
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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

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

NARUSE Ichiro 成瀬 一郎

Research Projects

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Co-Researchers

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

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Molecular mechanism of gender dependent difference in the neural tube defect manifestation.Principal Investigator

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Prevention of the neural tube defects by folic acid in the genetic polydactyly/arhinencephaly mouse, Pdn/Pdn

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Molecular mechanisms of arhinencephaly and polydactyly manifestations in the mouse homolog of GCPS.Principal Investigator

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Abnormal gene expressions in the Gli3 and Shh of the mouse homolog of GCPS, PdnPrincipal Investigator

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Developmental Brain Disorders due to Physical Agents

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Developmental and molecular cell biological study of the mechanisms of limb differentiation

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Genetic polydactyly / arhinencephaly mouse (Pdn / Pdn) is a homologue of Greig cephalopolysyndactyly syndrome.Principal Investigator

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Arhinencephaly induced by fetal laser surgery exo utero in mice.Principal Investigator

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Experimental Research for Mechanism of Brain Abnormalities Induced by Intrauterine Infection with Cytomegalovirus.

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Fetal surgical prevention of genetic limb anomalies in mice.Principal Investigator

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Im uitro発生毒性の一次スクリーニング法の開発

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[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)

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Publisher

NARUSE Ichiro 成瀬一郎