MOMOI Mariko 桃井真理子

… 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

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

MOMOI Mariko 桃井 真理子

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

Research Projects

Research Products

Co-Researchers

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

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The mechanisms of language acquisition and evolution of mouse brain in Foxp2-KI mice

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Research on the common molecular pathology for autismPrincipal Investigator

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Molecular and genetic analysis for autismPrincipal Investigator

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GENE ANALYSES OF AUTISM : INVESTIGATIONS OF GENES FOR SIGNAL TRANSMISSION IN THE BRAINPrincipal Investigator

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Studies on the molecular genetics and diagnostic and therapeutic procedures for myotonic dystrophy and allied disordersPrincipal Investigator

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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

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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

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Analysie of unstable suquences of genes in mental disorders.Principal Investigator

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Development of the methods of the detection of unstable DNA sequences of genes in pediatric neurological disorders.Principal Investigator

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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

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Molecular biological studies of mitochondrial diseasesPrincipal Investigator

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Molecular Genetic Analyses of Mitochondrial MyopathyPrincipal Investigator

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MOMOI Mariko 桃井真理子

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