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MOMOI Mariko  桃井 真理子

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… Alternative Names

桃井 真理子  モモイ マリコ

MOMOI Mariko Y.  桃井 真里子

桃井 真里子  モモイ マリコ

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Researcher Number 90166348
Other IDs
Affiliation (based on the past Project Information) *help 2010 – 2011: 自治医科大学, 医学部, 教授
2009: 自治医科大学, 小児科学教室, 教授
1994 – 2008: 自治医科大学, 医学部, 教授
1989 – 1993: 自治医科大学, 医学部, 助教授
1987: 自治医科大学, 医学部, 助教授
1986: 自治医大, 医学部, 講師
Review Section/Research Field
Principal Investigator
Pediatrics / Pediatrics
Except Principal Investigator
Neuroscience in general / Physical anthropology
Keywords
Principal Investigator
MELAS / 脆弱X症候群 / MBD1 / 精神遅滞 / 家族性精神遅滞 / FOXP2 / 自閉症 / WNT / (CAG / CTG)n … More / ミトコンドリア異常症 / ミトコンドリアDNA / 細胞死 / 自閉性障害 / CADM1 / 遺伝子導入 / ミトコンドリア遺伝子 / 母系遺伝 / 不安定DNA / unstable DNA / fragile X syndrome A / fragile X syndrome E / fragile X syndrome / 筋強直性ジストロフィー / WNT2 / autism / Fas抗原 / レチノイン酸 / P19EC細胞 / トリプレットリピート / トリプレットリピート伸展疾患 / シナプス形成 / secretin受容体 / ノックインマウス / 遺伝子発現解析 / 発現アレイ解析 / 内科系臨床医学 / 小児科学 / 自閉性障害関連遺伝子 / ERストレス / Duchenne型筋ジストロフィー症 / 骨格筋細胞 / 起始部欠損SV40 / 形質転換 / 起始部欠損SV40・DNA / 筋ジストロフィー症 / クローン化培養筋細胞 / ミトコンドリア脳筋症 / ミトコンドリアtRNAーLeu(UUR) / ミトコンドリア遺伝子点変異 / ミトコンドリア・ミオパチ- / チトクロ-ムc酸化酵素 / 筋細胞 / 電子伝達系酵素 / mitochondrial myopathy / mitochondrial DNA / point mutation in mitochondrial gene / mitochondrial tRNA-LEU (UUR) / Maternal inheritance / ヘテロプラスミ- / ニトコンドリア異常症 / ヘテロプラスミー / ミトコンドリアtRNAーLeu / mitochondrial disease / mitochondrial gene / maternal transmission / heteroplasmy / 脆弱X症候群A / 脆弱X症候群E / 三塩基対反復配列 / トリプレットリピート配列 / DRPLA / 脆弱x症候群 / 不安定DNA配列 / 筋強直性ジストロフィー症 / トリプレットリピート疾患 / 片麻痺性片頭痛 / 脊髄小脳失調症 / 遅発性小脳失調症 / カスパーゼ8 / カスパーゼ12 / 先天性筋ジストロフィー / caspase-3 / 三塩基対リピート疾患 / Pfu polymerase ポリメラーゼ / 毛根 / 遺伝子診断 / MT-PK遺伝子 / DMAHP遺伝子 / myotonic dystrophy / trinucleotide repeat disorder / hemiplegic migraine / spinocerebellar degeneration / late-onset cerebellar ataxia / caspase-8 / caspase-12 / 染色体7q / セクレチン / セクレチン受容体 / EXT! / forkhead遺伝子ファミリー / MBD遺伝子ファミリ / MECP2 / MBD / chromosome 7q / メチル化部位結合蛋白 / WNTシグナル / 自閉症障害 / 7q31-34 / WNT16 / 広汎性発達障害 / 染色体7q31 / GPR85 / methyl-CpG binding protein / WNT signal … More
Except Principal Investigator
進化 / 言語 / 言語障害 / Broca / FOXP2 Less
  • Research Projects

    (15 results)
  • Research Products

    (49 results)
  • Co-Researchers

    (21 People)
  •  Activation of ER stress as the major molecular pathology in autism spectrum disorder and the animal model for intervention studyPrincipal Investigator

    • Principal Investigator
      MOMOI Mariko
    • Project Period (FY)
      2010 – 2011
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Jichi Medical University
  •  The mechanisms of language acquisition and evolution of mouse brain in Foxp2-KI mice

    • Principal Investigator
      MOMOI Takashi
    • Project Period (FY)
      2009 – 2011
    • Research Category
      Grant-in-Aid for Scientific Research on Innovative Areas (Research a proposed research project)
    • Research Field
      Neuroscience in general
      Physical anthropology
    • Research Institution
      International University of Health and Welfare
  •  Research on the common molecular pathology for autismPrincipal Investigator

    • Principal Investigator
      MOMOI Mariko
    • Project Period (FY)
      2006 – 2008
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Pediatrics
    • Research Institution
      Jichi Medical University
  •  Molecular and genetic analysis for autismPrincipal Investigator

    • Principal Investigator
      MOMOI Mariko Y.
    • Project Period (FY)
      2003 – 2005
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Pediatrics
    • Research Institution
      JICHI MEDICAL UNIVERSITY
  •  GENE ANALYSES OF AUTISM : INVESTIGATIONS OF GENES FOR SIGNAL TRANSMISSION IN THE BRAINPrincipal Investigator

    • Principal Investigator
      MOMOI Mariko
    • Project Period (FY)
      2000 – 2002
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Pediatrics
    • Research Institution
      JICHI MEDICAL SCHOOL
  •  Studies on the molecular genetics and diagnostic and therapeutic procedures for myotonic dystrophy and allied disordersPrincipal Investigator

    • Principal Investigator
      MOMOI Mariko
    • Project Period (FY)
      1998 – 2000
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Pediatrics
    • Research Institution
      JICHI MEDICAL SCHOOL
  •  トリプレットリピート伸展疾患の遺伝子診断法の確立、病態解析、新たな疾患遺伝子同定Principal Investigator

    • Principal Investigator
      桃井 真里子
    • Project Period (FY)
      1996 – 1997
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Pediatrics
    • Research Institution
      Jichi Medical University
  •  心筋発生過程における細胞死関連抗原FASの発現とレチノイン酸による制御機構の解析Principal Investigator

    • Principal Investigator
      桃井 真里子
    • Project Period (FY)
      1994
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      Jichi Medical University
  •  Analysie of unstable suquences of genes in mental disorders.Principal Investigator

    • Principal Investigator
      MOMOI Mariko
    • Project Period (FY)
      1994 – 1995
    • Research Category
      Grant-in-Aid for General Scientific Research (B)
    • Research Field
      Pediatrics
    • Research Institution
      Jichi Medical School
  •  Development of the methods of the detection of unstable DNA sequences of genes in pediatric neurological disorders.Principal Investigator

    • Principal Investigator
      MOMOI Mariko
    • Project Period (FY)
      1994 – 1995
    • Research Category
      Grant-in-Aid for Developmental Scientific Research (B)
    • Research Field
      Pediatrics
    • Research Institution
      Jichi Medical School
  •  ミトコンドリア異常症における患者形成機構の細胞遺伝学的解析Principal Investigator

    • Principal Investigator
      桃井 真里子
    • Project Period (FY)
      1992
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      Jichi Medical University
  •  Molecular biological studies of mitochondrial diseasesPrincipal Investigator

    • Principal Investigator
      MOMOI Mariko
    • Project Period (FY)
      1991 – 1993
    • Research Category
      Grant-in-Aid for General Scientific Research (B)
    • Research Field
      Pediatrics
    • Research Institution
      Jichi Medical School
  •  Molecular Genetic Analyses of Mitochondrial MyopathyPrincipal Investigator

    • Principal Investigator
      MOMOI Mariko Y.
    • Project Period (FY)
      1989 – 1990
    • Research Category
      Grant-in-Aid for General Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Jichi Medical School, Department of Medicine
  •  起始部欠損SV40・DNS導入によりクローン化された筋ジストロフィー細胞の変異形質Principal Investigator

    • Principal Investigator
      桃井 真理子
    • Project Period (FY)
      1987
    • Research Category
      Grant-in-Aid for General Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Jichi Medical University
  •  起始部欠損SV40・DNA導入によるジストロフィー筋細胞株の樹立と変異形質の検出Principal Investigator

    • Principal Investigator
      桃井 真里子
    • Project Period (FY)
      1986
    • Research Category
      Grant-in-Aid for General Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Jichi Medical University

All 2012 2011 2010 2009 2008 2007 2006 2005 2004 Other

All Journal Article Presentation

  • [Journal Article] Cntnap2 expression in the cerebellum of Foxp2(R552H) mice, with a mutation related to speech-language disorder2012

    • Author(s)
      Fujita E, Tanabe Y, Momoi MY, and Momoi T
    • Journal Title

      Neurosci Lett

      Volume: 506 Pages: 277-280

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21200011
  • [Journal Article] Cadm1-expressing synapses on Purkinje cell dendrites are involved in mouse ultrasonic vocalization activity2012

    • Author(s)
      Fujita E, Tanabe Y, Imhof BA, Momoi MY, Momoi T
    • Journal Title

      PLoS One

      Volume: 7

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21200011
  • [Journal Article] A complex of synaptic adhesion molecule CADM1, a molecule related to autism spectrum disorder, with MUPP1 in the cerebellum2012

    • Author(s)
      Fujita E, Tanabe Y, Imhof BA, Momoi MY, Momoi T
    • Journal Title

      J Neurochem

      Volume: 123 Pages: 886-894

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21200011
  • [Journal Article] FOXP2 promotes the nuclear translocation of POT1, but FOXP2(R553H), mutation related to speech-language disorder, partially prevents it2011

    • Author(s)
      Tanabe Y, Fujita E, Momoi T
    • Journal Title

      Biochem Biophys Res Commun

      Volume: 410 Pages: 593-596

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21200011
  • [Journal Article] Autism spectrum disorder ; shared molecular pathology2011

    • Author(s)
      Momoi MY
    • Journal Title

      Medical Science Digest

      Volume: 37 Pages: 410-413

    • Data Source
      KAKENHI-PROJECT-22591135
  • [Journal Article] Impairment of social and emotional behaviors in Cadml-knockout mice.2010

    • Author(s)
      Takayanagi Y, Fujita E, Yu Z, Yamagata T, Momoi MY, Momoi T, Onaka
    • Journal Title

      Biochem.Biophys.Res.Commun.

      Volume: 396(3) Pages: 703-708

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21200011
  • [Journal Article] Endoplasmic reticulum stress induced by synaptic adhesion molecules, CADM1, with mutation related to the Autism Spectrum Discorders.2010

    • Author(s)
      Fujita E., Dai, H., Tanabe, Y., Zhiling Y., Yamagata, T., Miyakawa, T., Tanokura, M., Momoi, MY., Momoi, T.
    • Journal Title

      Cell Death and Disease

      Volume: 1(6)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21200011
  • [Journal Article] Expression analysis and mutation detection of DLX5 and DLX6 in autism.2009

    • Author(s)
      Nakashima, N, Yamagata, T, Mori M, Kuwajima M, Suwa K, MOMOI MY.
    • Journal Title

      Brain & Development Feb3 (E-pub)

    • NAID

      10027212757

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18390301
  • [Journal Article] Genetic factors and epigenetic factors for autism: endoplasmic reticulum stress and impaired synaptic function2009

    • Author(s)
      Momoi T, Fujita E, Senoo H, Momoi MY
    • Journal Title

      Cell Biol. Int

      Volume: 34 Pages: 13-19

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21200011
  • [Journal Article] Expression analysis and mutation detection of DLX5 and DLX6 in autism.2009

    • Author(s)
      Nakajima N, Yamagata T, MoriM, Kuwajima M, Suwa K, Momoi MY.
    • Journal Title

      Brain Dev doi:10

      Pages: 1016-1016

    • NAID

      10027212757

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18390301
  • [Journal Article] Genetic factors and epidemic factors for autism : endoplasmic reticulum stress and impaired synaptic function.2009

    • Author(s)
      Momoi T, Fujita E, Senoo H, Momoi MY.
    • Journal Title

      Cell Biol.Int.

      Volume: 34 Pages: 13-19

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21200011
  • [Journal Article] Ultrasonic vocalization impairment of Foxp2(R552)knockin mice related to speech-language disorder and abnormality of Purkinje cells.2008

    • Author(s)
      Fujita E, Tanabe Y, Shiota A, Ueda M, Suwa K, Momoi MY, Momoi T.
    • Journal Title

      Proc Natl Acad Soi USA 105

      Pages: 3117-22

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18390301
  • [Journal Article] Mutations in the gene encoding CADM1 are associated with autism spectrum disorder.2008

    • Author(s)
      Zhiling Y, Fujita E, Tmomoi anabe Y, Yamagata T, k, Momoi T, Momoi MY.
    • Journal Title

      Biochem Biophys, Res Commun. 377

      Pages: 926-9

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18390301
  • [Journal Article] Ultrasonic vocaliz ation impairment of FOXP2 (R552H) knockin mice related to speech-language disorder and abnormality of Pukinje cells.2008

    • Author(s)
      Fijita E, Tanabe Y, Shiota A, Ueda M, Suwa K, Momoi MY, Momoi T.
    • Journal Title

      Proc Natl Acad Sci USA 105

      Pages: 3117-3122

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18390301
  • [Journal Article] Mutations in the gene encoding CADM1 are associated with autism spectrum disorder.2008

    • Author(s)
      Zhiling Y, Fujita E, Tanabe Y, Yamagata T, Momoi T, Momoi MY.
    • Journal Title

      Biochem Biophys Res Commun 377

      Pages: 926-929

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18390301
  • [Journal Article] Intracellular distribution of a speech/language disorder associated FOXP2 mutant.2007

    • Author(s)
      Mizutani A, Matsuzaki A, F, Momoi MY, Ujita E, Tanabe Y, Momoi T.
    • Journal Title

      Biochem Biophys Res Commun 353

      Pages: 869-874

    • Data Source
      KAKENHI-PROJECT-18390301
  • [Journal Article] Intracellular dist ribution of a speech/language disorder associated FOXP2 mutant.2007

    • Author(s)
      Mizutani A, Matsuzaki A, Momoi MY,Fujita E, Tanabe Y, Momoi T.
    • Journal Title

      Biochem Biopys Res Commun 353

      Pages: 869-874

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18390301
  • [Journal Article] Intracellular distribution of a speech/language disorder associated with FOXP2 mutant.2007

    • Author(s)
      Mizutani A, Matsuzaki A, Momoi MY, Fujita E, et al.
    • Journal Title

      Biochem Biophys Res Commun 353(4)

      Pages: 869-874

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-15390326
  • [Journal Article] A. Secretin receptor-deficient mice exhibit impaired synaptic plasticity and social behavior.2006

    • Author(s)
      Nishijima I, Yamagata T, Soencer CM, Weber EJ, Alekseyenko O, Seat JD, Momoi MY, Ito M, Armstrong DL, Nelson DL, Oaylor R, Bradley A.
    • Journal Title

      Hum Mol Genet 15

      Pages: 3241-3250

    • Data Source
      KAKENHI-PROJECT-18390301
  • [Journal Article] Evidence supporting WNT16 as autism susceptible gene.2006

    • Author(s)
      Imai M, Yamagata T, Mori M, Momoi MY.
    • Journal Title

      Am J Genet (In press)

    • Data Source
      KAKENHI-PROJECT-15390326
  • [Journal Article] Secretin receptor deficient mice exh ibited impaired synaptic plasticity and social behavior2006

    • Author(s)
      Nishijima I, Yamagata T, Spencer Cm,Weeber EJ, Alekseyenko O, Sweatt JD, Momoi MY, et al.
    • Journal Title

      Hum mol Genet 15

      Pages: 3241-3250

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18390301
  • [Journal Article] Secretin receptor-deficient mice exhibit impaired synaptic plasticity and social behavior.2006

    • Author(s)
      Nishijima I, Yamagata T, Spencer CM, Wevber EJ, Alekseyenko O, Seat JD, Momoi MY, et al.
    • Journal Title

      Hum Mol Genet 15

      Pages: 3241-3250

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-15390326
  • [Journal Article] Secretin receptor-deficient mice exhibit impaired synaptic plasticity and social behavior.2006

    • Author(s)
      Nishijima I, Yamagata T, Spencer CM, Weber EJ, Alekseyenko 0, Seat JD, Momoi MY, Ito M, Armstrong DL, Nelson DL, Paylor R, Bradley A.
    • Journal Title

      Hum Mol Genet 15

      Pages: 3241-3241

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15390326
  • [Journal Article] Two new XPD patients compound heterozygotes for the same mutation demonstrate diverse clinical features.2005

    • Author(s)
      Fujimoto M, Leech SN, Theron T, Mori M, Fawcett H, Botta E, Nozaki Y, Yamagata T, Moriwaki S, StefaniniM, Momoi MY, Nakagawa H, Shuster S, Moss C, Lehmann AR.
    • Journal Title

      J Invest Dermatol 25:86-92-3250 (BBRC-06-6032)

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15390326
  • [Journal Article] Mutation analysis of methyl-CpG binding protein family genes in autistic patients.2005

    • Author(s)
      Li H, Yamagata T, Mori M, Momoi MY
    • Journal Title

      Brain & Dev 27

      Pages: 321-325

    • NAID

      10019356605

    • Data Source
      KAKENHI-PROJECT-15390326
  • [Journal Article] Absence of causative mutation and presence of autism-related allele in FOXP in Japanese autistic population2005

    • Author(s)
      Li H, Yamagata T, Mori M, Momoi MY
    • Journal Title

      Brain & Dev 27

      Pages: 207-210

    • Data Source
      KAKENHI-PROJECT-15390326
  • [Journal Article] RSK2 gene mutations in Coffin-Lowry syndrome with drop episodes.2005

    • Author(s)
      Nakamura M, Yamagata T, Mori M, Momoi MY.
    • Journal Title

      Brain Dev 27

      Pages: 114-117

    • NAID

      10015453219

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15390326
  • [Journal Article] Mutation analysis of methyl-CpG binding protein family genes I autistic spectrum disorders.2005

    • Author(s)
      Li H, Yamagata T, Mori M, Momoi MY.
    • Journal Title

      Brain & Development (In press)

    • Data Source
      KAKENHI-PROJECT-15390326
  • [Journal Article] Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients.2005

    • Author(s)
      Li H, Yamagata T, Mori M, Momoi MY.
    • Journal Title

      Brain & Development 27

      Pages: 207-210

    • NAID

      10015453725

    • Data Source
      KAKENHI-PROJECT-15390326
  • [Journal Article] Absence of caisative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients.2005

    • Author(s)
      Li H, Yamagta T, Mori M, Momoi MY.
    • Journal Title

      Brain & Dev 27

      Pages: 207-210

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-15390326
  • [Journal Article] RSK2 gene mutation in Coffinn-Lowy syndrome with erop episodes.2005

    • Author(s)
      Nakamura M, Yamagata T, Mori M, Momoi MY.
    • Journal Title

      Brain & Dev 27

      Pages: 114-117

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-15390326
  • [Journal Article] Two new XPD patients counopund heterozygotes for the same mutation demonstrate diverse clinical features.2005

    • Author(s)
      Fijimoto M, Leech SN, Theron T, Mori M, _nozaki Y, Momoi MY. et al.
    • Journal Title

      J Invest Dermatol 25

      Pages: 86-92

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-15390326
  • [Journal Article] Mutation analysis of methyl-CpG binding protein family genes in auistic patients.2005

    • Author(s)
      Li H, Yamagta T, Mori M, Yasuhara A, Momoi MY.
    • Journal Title

      Brain & Dev 27

      Pages: 321-325

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-15390326
  • [Journal Article] Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese aitistic patients.2005

    • Author(s)
      Li H, Yaqmagata T, Mori M, Momoi MY.
    • Journal Title

      Brain Dev 27

      Pages: 207-210

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15390326
  • [Journal Article] Mutation analysis of methyl-CpG binding protein family genes in autistic patients.2005

    • Author(s)
      Li H, Yamagata T, Mori M, Yasuhara A, Momoi MY.
    • Journal Title

      Brain Dev 27

      Pages: 321-325

    • NAID

      10019356605

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15390326
  • [Journal Article] Non-invasive screening of fragile X syndrome A using urine and hail roots.2004

    • Author(s)
      Suwa K, Momoi MY.
    • Journal Title

      Brain Dev 26

      Pages: 380-383

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15390326
  • [Journal Article] RSK gene mutations in Coffin-Lowry syndrome with drop episodes.2004

    • Author(s)
      Nakamura M, Yamagata T, Mori M, Momoi MY.
    • Journal Title

      Brain & Development 26

      Pages: 453-458

    • Data Source
      KAKENHI-PROJECT-15390326
  • [Journal Article] Non-invasive screening of fragile X syndrme A using urine and hair roots.2004

    • Author(s)
      Suwa K, Yamagata T, goto T, Saito S, Momoi MY.
    • Journal Title

      Brain & Dev 26

      Pages: 380-383

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-15390326
  • [Journal Article] Dichloroacetate treatment for mitochondrial vytopathy : ling-term egffets in MELAS.2004

    • Author(s)
      Mori M, Yamagata T, Saito S, Gotou, Momoi MY.
    • Journal Title

      Brain $ Development 26

      Pages: 453-458

    • Data Source
      KAKENHI-PROJECT-15390326
  • [Journal Article] Non-invasive screening of fragile X syndrome using urine and hair roots.2004

    • Author(s)
      Suwa T, Tamagata T, Mori M, Momoi MY.
    • Journal Title

      Brain & Development 26

      Pages: 380-383

    • NAID

      10020552348

    • Data Source
      KAKENHI-PROJECT-15390326
  • [Journal Article] Intracellular distribution of a speech/language disorder associated FOXP2 mutant.

    • Author(s)
      Mizutani A, Matsuzaki A, F, Momoi MY ujita E, Tanabe Y, Momoi T.
    • Journal Title

      Biochem Biophys Res Commun 2006 Dec. Online

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15390326
  • [Presentation] マウス小脳発達過程におけるフォークヘッドドメインを欠いたFoxp2アイソフォームの発現と局在の解析2012

    • Author(s)
      田辺裕子、藤原裕士、松崎鮎美、笠原忠、湯浅茂樹、桃井隆、藤田恵理子
    • Organizer
      第35回日本分子生物学会
    • Place of Presentation
      福岡
    • Year and Date
      2012-12-12
    • Data Source
      KAKENHI-PROJECT-21200011
  • [Presentation] 自閉性障害候補遺伝子CADM1ノックアウトマウスにおける超音波音声2011

    • Author(s)
      藤田恵理子、田辺裕子、桃井隆、桃井真里子
    • Organizer
      第34回日本神経科学大会
    • Place of Presentation
      横浜
    • Year and Date
      2011-09-15
    • Data Source
      KAKENHI-PROJECT-21200011
  • [Presentation] Catnap2 expression in the cerebellum of the Foxp2(R552H) mice, with mutation related to the speech-language disorder2011

    • Author(s)
      藤田恵理子、田辺裕子、桃井隆、桃井真子
    • Organizer
      第34回日本分子生物学会年会
    • Place of Presentation
      横浜
    • Year and Date
      2011-12-14
    • Data Source
      KAKENHI-PROJECT-21200011
  • [Presentation] Future Trends in the Biology of Language2011

    • Author(s)
      Momoi T
    • Organizer
      The impaired Purkinje cell development in the Foxp2(R552H) -KI mice, linkage to autism spectrum disorder, 2011
    • Place of Presentation
      慶應義塾大学グローバルCOE プログラム
    • Year and Date
      2011-03-09
    • Data Source
      KAKENHI-PROJECT-21200011
  • [Presentation] ER stress and degradation of the misfolded proteins neurodegeneratinve disorders and brain developmental disorders.2009

    • Author(s)
      Momoi T, Saegusa C, Fujita E, Momoi MY.
    • Organizer
      17 th ECDO Euroconference cell death control in cancer and neurodegeneration.
    • Place of Presentation
      Paris
    • Data Source
      KAKENHI-PROJECT-21200011
  • [Presentation] Impaired Social Interaction and ultrasonic vocalization of the RA175/SynCAM1(Cadm1)-deficient mice and the down-regulation of Mupp1 in the brain2009

    • Author(s)
      Momoi T, Fujita E, Takayanagi Y, Tanabe Y, Saegusa C, Onaka T, Momoi MY.
    • Organizer
      Neuroscience2009
    • Place of Presentation
      名古屋国際会議場(名古屋)
    • Year and Date
      2009-09-18
    • Data Source
      KAKENHI-PROJECT-21200011
  • [Presentation] Ultrasonic vocalization of the knock-in mice with mutated Foxp2 related to speech-language disorder and normal Foxp2 expressed in Purkinje cells2009

    • Author(s)
      Fujita E、Tababe Y、Fujiwara Y、Momoi MY、Momoi T
    • Organizer
      Neuroscience2009
    • Place of Presentation
      名古屋
    • Year and Date
      2009-09-18
    • Data Source
      KAKENHI-PROJECT-21200011
  • [Presentation] 小児期の広汎性発達障害:遺伝子と環境

    • Author(s)
      桃井真里子
    • Organizer
      第28回日本医学会総会
    • Data Source
      KAKENHI-PROJECT-22591135
  • 1.  YAMAGATA Takanori (00239857)
    # of Collaborated Projects: 7 results
    # of Collaborated Products: 22 results
  • 2.  OGURO Noriko (10214107)
    # of Collaborated Projects: 7 results
    # of Collaborated Products: 0 results
  • 3.  SAITO Sugiko (00260836)
    # of Collaborated Projects: 5 results
    # of Collaborated Products: 0 results
  • 4.  ICHIHASI Kou (70213006)
    # of Collaborated Projects: 5 results
    # of Collaborated Products: 0 results
  • 5.  SHIMOIZUMI Hideo (30196547)
    # of Collaborated Projects: 4 results
    # of Collaborated Products: 0 results
  • 6.  KOBAYASHI Yoko (20245046)
    # of Collaborated Projects: 3 results
    # of Collaborated Products: 0 results
  • 7.  NOZAKI Yasuyuki (90281295)
    # of Collaborated Projects: 3 results
    # of Collaborated Products: 0 results
  • 8.  MORI Masato (10337347)
    # of Collaborated Projects: 3 results
    # of Collaborated Products: 18 results
  • 9.  TSURU Tomohiko (90296111)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 0 results
  • 10.  SUWA Kiyotaka (30285796)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 3 results
  • 11.  中三川 晃利
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 0 results
  • 12.  GOTO Tamako (40364509)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 13.  KUWAJIMA Mari (30398515)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 2 results
  • 14.  MOMOI Takashi (40143507)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 15 results
  • 15.  JINBO Eriko (20291651)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 16.  SAITO Mari (10424011)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 17.  KAGAWA Yasuo (30048962)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 18.  NAKAMURA Miki (20296114)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 19.  五十嵐 浩 (80260834)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 20.  岡本 範子 (00103747)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 21.  FUJITA Eriko
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 14 results

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