Jimbo Eriko 神保恵理子 (藤田恵理子)

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… Alternative Names

神保恵理子ジンボエリコ

藤田恵理子

神保恵理子(藤田恵理子) ジンボエリコ

JINBO Eriko 神保恵理子

藤田恵理子

FUJITA Eriko 藤田恵理子

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Researcher Number	20291651
Other IDs
Affiliation (Current)	2025: 自治医科大学, 医学部, 講師
Affiliation (based on the past Project Information) *help	2020 – 2023: 自治医科大学, 医学部, 講師 2010 – 2018: 自治医科大学, 医学部, 講師 2009 – 2010: 自治医科大学, 医学部, 助教 2009: 自治医科大学, 小児科学教室, 研究員 2008: National Center of Neurology and Psychiatry, 疾病研究第5部, 流動研究員 … More 2008: National Center of Neurology and Psychiatry, 神経研究所・疾病研究第5部, 流動研究員 2008: 国立精神・神経センター, 神経研究所・疾病第5部, 流動研究員 2008: 国立精神・神経センター, 神経研究所疾病研究第5部, 流動研究員 2007: 神経研究所, 疾病研究第5部, 研究員 2006 – 2007: 国立精神・神経センター, 神経研究所疾病研究第五部, 研究員 1997: 共立女子大学家政学部, 助手 Less
Review Section/Research Field	Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related / Neuroscience in general / Neurophysiology / General neuroscience / Neuroscience in general Except Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related / Embryonic/Neonatal medicine / Nerve anatomy/Neuropathology / Fisheries chemistry / Pediatrics / Physical anthropology / Nerve anatomy/Neuropathology
Keywords	Principal Investigator Autism / シナプス接着因子 / Foxp2 / シグナル伝達 / 神経分化 / Neuron / 自閉症スペクトラム障害 / GPCR / シナプス接着蛋白遺伝子 / 自閉性障害 … More / CADM1 / GPR37 / 自閉性スペクトラム障害 / 変異 / Cadm1 / シナプス接着分子 / 言語障害 / 脳 / マウス / 超音波音声 / 機能シナプス / SynCAM / 脳・神経 … More Except Principal Investigator メチル化 / 自閉性障害 / 自閉症スペクトラム障害 / シナプス / 腎疾患 / 心血管系疾患 / 早産低出生体重児 / 妊娠高血圧症候群 / 発達障害 / 早産児 / グルココルチコイド / ストレス反応 / 低出生体重児 / ASD / j自閉性障害 / スパイン / セレトニン / PDZ / CNTNAP2 / スパイン形成 / CADM1 / MUPP1 / Taste active component / Sensory analysis / Umami / Free amino acids / Peptide / Extract / Fish sauce / 旨味 / D-アラニン / 塩辛 / 発酵食品 / 呈味成分 / 官能検査 / うま味 / 遊離アミノ酸 / ペプチド / エキス成分 / 魚醤油 / セクレチン受容体 / モデルマウス / 候補遺伝子解析 / CNV / 病因遺伝子 / シナプス足場蛋白 / コピー数多型（CNV) / マイクロアレーCGH / G蛋白結合型受容体 / セクレチン / LIN7 / 足場蛋白 / 遺伝子変異 / コピー数多型 / FOXP2 / Broca / 言語障害 / 言語 / 進化 / SynGAM1 / Par-3 / Neuroligin / 接着蛋白 / SynCAM1 / RA175 / 自閉症 / Cadm1 Less

Foxp2による消化管・腸管神経系形成の分子機構と転写活性欠失変異の影響Principal Investigator
- Principal Investigator
  
  神保恵理子 (藤田恵理子)
- Project Period (FY)
  2023 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Jichi Medical University
Methylation of genes related to cardiovascular and chronic kidney diseases in preterm low birth weight infants born to mothers with hypertensive disorders of pregnancy
- Principal Investigator
  
  河野由美
- Project Period (FY)
  2021 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Jichi Medical University
自閉症スペクトラム障害の分子病態に関連するGPR85のシグナル伝達機構の解析Principal Investigator
- Principal Investigator
  
  神保恵理子 (藤田恵理子)
- Project Period (FY)
  2020 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Jichi Medical University
The effects of the GPR37-mutation in autism spectrum disorder on the signal transduction by prosaponinPrincipal Investigator
- Principal Investigator
  
  Jimbo Eriko
- Project Period (FY)
  2015 – 2018
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurophysiology / General neuroscience
- Research Institution
  Jichi Medical University
Molecular Pathogenesis of the abnormal spine morphology and 5-HTR complex induced by ASD-related mutated Mupp1
- Principal Investigator
  
  MOMOI TAKASHI
- Project Period (FY)
  2015 – 2018
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Nerve anatomy/Neuropathology
- Research Institution
  Tokyo Medical University
DNA methylation of human glucocorticoid receptor gene (NR3C1) and stress response in low birth weight infants
- Principal Investigator
  
  Kono Yumi
- Project Period (FY)
  2014 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Embryonic/Neonatal medicine
- Research Institution
  Jichi Medical University
Studies on the influence of brain and neurons of mutation of synaptic cell adhesion molecule protein, Cadm1 using autism mouse models.Principal Investigator
- Principal Investigator
  
  Jimbo Eriko
- Project Period (FY)
  2012 – 2015
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neuroscience in general
- Research Institution
  Jichi Medical University
Analysis for the pathogenesis and the target molecules of treatment for autism focusing on G-protein coupled receptors and synaptic molecules
- Principal Investigator
  
  YAMAGATA Takanori
- Project Period (FY)
  2011 – 2013
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- 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
  
  Physical anthropology
- Research Institution
  International University of Health and Welfare
The regulation of mouse ultrasonic vocalization and behavior by Foxp2Principal Investigator
- Principal Investigator
  
  JIMBO Eriko
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Neuroscience in general
- Research Institution
  Jichi Medical University
The molecular system of the selective transport of Synaptic adhesion molecules to the pre-and post-synaptic membrane.
- Principal Investigator
  
  MOMOI Takashi
- Project Period (FY)
  2007 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Nerve anatomy/Neuropathology
- Research Institution
  National Center of Neurology and Psychiatry
Loss of the functional-synapse in RA175(SynCAM)-deficient micePrincipal Investigator
- Principal Investigator
  
  FUJITA Eriko
- Project Period (FY)
  2006 – 2008
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Neuroscience in general
- Research Institution
  National Center of Neurology and Psychiatry
Taste active components of fish sauces
- Principal Investigator
  
  ABE Hiroki
- Project Period (FY)
  1997 – 1999
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Fisheries chemistry
- Research Institution
  The University of Tokyo

[Journal Article] Aggregate formation analysis of GFAPR416W found in one case of Alexander disease.2019
- Author(s)
  Tulyeu J, Tamaura M, Jimbo E, Shimbo H, Takano K, Iai M, Yamashita S, Goto T, Aida N, Tokuhiro E, Yamagata T, Osaka H.
- Journal Title
  
  Brain Dev.
  
  Volume: 41 Issue: 2 Pages: 195-200
- DOI
  10.1016/j.braindev.2018.08.009
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K06716
[Journal Article] Role of a circadian-relevant gene NR1D1 in brain development: possible involvement in the pathophysiology of autism spectrum disorders.2017
- Author(s)
  Goto, M., Mizuno, M., Matsumoto, A., Yang, Z., Jimbo, E.F., Tabata, H., Yamagata, T., Nagata, K.-I.
- Journal Title
  
  Sci Rep.
  
  Volume: 7 Issue: 1 Pages: 43945-43945
- DOI
  10.1038/srep43945
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-25430046, KAKENHI-PROJECT-15K06716, KAKENHI-PROJECT-16K07037, KAKENHI-PROJECT-16K09995, KAKENHI-PROJECT-15K15399, KAKENHI-PROJECT-16H05363
[Journal Article] Negative feedback loop of bone resorption by NFATc1-dependent induction of Cadm1.2017
- Author(s)
  Nakamura S, Koyama T, Izawa N, Nomura S, Fujita T, Omata Y, Minami T, Matsumoto M, Nakamura M, Fujita-Jimbo E, Momoi T, Miyamoto T, Aburatani H, Tanaka S.
- Journal Title
  
  PLoS One.
  
  Volume: 12
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K06716
[Journal Article] Foxp2 Regulates Identities and Projection Patterns of Thalamic Nuclei During Development.2016
- Author(s)
  Ebisu H, Iwai-Takekoshi L, Fujita-Jimbo E, Momoi T, Kawasaki H.
- Journal Title
  
  Cereb Cortex
  
  Volume: 印刷中
- NAID
  120006334915
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K06744
[Journal Article] The association of GPR85 with PSD-95-neuroligin complex and autism spectrum disorder: a molecular analysis.2015
- Author(s)
  Fujita-Jimbo E, Tanabe Y, Yu Z, Kojima K, Mori M, Li H, Iwamoto S, Yamagata T, Momoi MY, Momoi T.
- Journal Title
  
  Mol Autism.
  
  Volume: 6 Issue: 1 Pages: 17-17
- DOI
  10.1186/s13229-015-0012-5
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-25461377, KAKENHI-PROJECT-26830030, KAKENHI-PROJECT-24500386
[Journal Article] The association of GPR85 with PSD-95-neuroligin complex and autism spectrum disorder: a molecular analysis.2015
- Author(s)
  Fujita-Jimbo E, Tanabe Y, Yu Z, Kojima K, Mori M, Li H, Iwamoto S, Yamagata T, Momoi MY, Momoi T.
- Journal Title
  
  Mol Autism.
  
  Volume: 6 Pages: 17-17
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-24500386
[Journal Article] Role of an adaptor protein Lin-7B in brain development: possible involvement in autism spectrum disorders.2015
- Author(s)
  Mizuno M, Matsumoto A, Hamada N, Ito H, Miyauchi A, Jimbo EF, Momoi MY, Tabata H, Yamagata T, Nagata K.
- Journal Title
  
  J Neurochem
  
  Volume: 132 Issue: 1 Pages: 61-69
- DOI
  10.1111/jnc.12943
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-23590124, KAKENHI-PROJECT-24500386, KAKENHI-PUBLICLY-25123727, KAKENHI-PROJECT-25430046, KAKENHI-PROJECT-26893252, KAKENHI-PUBLICLY-25122722, KAKENHI-PROJECT-24590314, KAKENHI-PROJECT-24390271
[Journal Article] CASPR2 forms a complex with GPR37 via MUPP1 but not with GPR37(R558Q), an autism spectrum disorder-related mutation.2015
- Author(s)
  Tanabe Y et al.
- Journal Title
  
  J Neurochem.
  
  Volume: 134 Issue: 4 Pages: 783-793
- DOI
  10.1111/jnc.13168
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-15K06716, KAKENHI-PROJECT-15K06744, KAKENHI-PROJECT-24500386
[Journal Article] Specific expression of FOXP2 in cerebellum improves ultrasonic vocalization in heterozygous but not in homozygous Foxp2 (R552H) knock-in pups.2014
- Author(s)
  Fujita-Jimbo E, Momoi T.
- Journal Title
  
  Neurosci Lett.
  
  Volume: 566 Pages: 162-166
- DOI
  10.1016/j.neulet.2014.02.062
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24500386
[Journal Article] LIN7A depletion disrupts cerebral cortex development, contributing to intellectual disability in 12q21-deletion syndrome.2014
- Author(s)
  Matsumoto A, Mizuno M, Hamada N, Nozaki Y, Jimbo E, Momoi M, Nagata K, Yamagata T
- Journal Title
  
  PLOS ONE
  
  Volume: 9 Issue: 3 Pages: e92695-e92695
- DOI
  10.1371/journal.pone.0092695
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-13J40147, KAKENHI-PROJECT-23390275, KAKENHI-PROJECT-24390271, KAKENHI-PROJECT-24500386, KAKENHI-PROJECT-25670488
[Journal Article] MAOA/B deletion syndrome in male siblings with severe developmental delay and sudden loss of muscle tonus2014
- Author(s)
  Saito M, Yamagata T, Shiba Y, Nagashima M, Taniguchi S, Jimbo E, Momoi MY
- Journal Title
  
  Brain Dev
  
  Volume: 36 Issue: 1 Pages: 64-69
- DOI
  10.1016/j.braindev.2013.01.004
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23390275
[Journal Article] An Xp22.12 microduplication including RPS6KA3 identified in a family with variably affected intellectual and behavioral disabilities2013
- Author(s)
  Matsumoto A, Kuwajima M, Miyake K, Kojima K, Nakashima N, Jimbo EF, Kubota T, Momoi MY, Yamagata T
- Journal Title
  
  J Hum Genet
  
  Volume: 58 Issue: 11 Pages: 755-757
- DOI
  10.1038/jhg.2013.88
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23390275
[Journal Article] MAOA/B deletion syndrome in male siblings with severe developmental delay and sudden loss of muscle tonus.2013
- Author(s)
  Saito M, Yamagata T, Matsumoto A, Shiba Y, Nagashima M, Taniguchi S, Jimbo E, Momoi MY.
- Journal Title
  
  Brain Dev
  
  Volume: 35
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23390275
[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] Cntnap2 expression in the cerebellum of Foxp2(R552H) mice, with a mutation related to speech-language disorder.2012
- Author(s)
  Fujita E, et al.
- Journal Title
  
  NeurosciLett.
  
  Volume: 506 Issue: 2 Pages: 277-280
- DOI
  10.1016/j.neulet.2011.11.022
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21200011
[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, M. Y., and Momoi, T.
- Journal Title
  
  Neurosci Lett
  
  Volume: 506 Pages: 277-280
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21700377
[Journal Article] Mutation in Parkinson disease-associated, G-protein coupled receptor 37 (GPR37/PaelR) is related to Autism spectrum disorder2012
- Author(s)
  Fujita-Jimbo E, Yu ZL, Li H, Yamagata T, Mori M, Momoi T, Momoi MY
- Journal Title
  
  PLoS One
  
  Volume: 7
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23390275
[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] 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] Mutation in Parkinson disease-associated, G-protein-coupled receptor 37 (GPR37/PaelR) is related to Autism spectrum disorder.2012
- Author(s)
  2. Fujita-Jimbo E, Yu ZL, Li H, Yamagata T, Mori M, Momoi T, Momoi MY
- Journal Title
  
  PLoS One
  
  Volume: 7 Issue: 12 Pages: e51155-e51155
- DOI
  10.1371/journal.pone.0051155
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23390275
[Journal Article] A complex of synaptic adhesion molecule CADM1, a molecule related to autism spectrum disorder, with MUPP1 in the cerebellum.2012
- Author(s)
  Fujita E, et al.
- Journal Title
  
  J Neurochem.
  
  Volume: 123 Issue: 5 Pages: 886-894
- DOI
  10.1111/jnc.12022
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21200011, KAKENHI-PROJECT-21500334, KAKENHI-PROJECT-24500386
[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] 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., and Momoi, T
- Journal Title
  
  Biochem Biophys Res Commun
  
  Volume: 410 Pages: 593-596
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21700377
[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] 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] 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] Genetic factors and epigenetic factors for autism : endoplasmic reticulum stress and impaired synaptic function2009
- Author(s)
  Momoi, T., Fujita, E., Senoo, H., and Momoi, M
- Journal Title
  
  Cell Biol. Int
  
  Volume: 34 Pages: 13-19
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21700377
[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] 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
- Data Source
  KAKENHI-PROJECT-18700333
[Journal Article] Neuronal RA175/SynCAM1 isoforms are processed by tumor necrosis factor-alpha-converting enzyme (TACE)/ADAM17-like proteases.2008
- Author(s)
  Tanabe Y, Kasahara T, Momoi T, Fujita E.
- Journal Title
  
  Neurosci .Lett. 444(1)
  
  Pages: 16-21
- Data Source
  KAKENHI-PROJECT-19500305
[Journal Article] Mutations in the gene encoding CADM1 are associated with autism spectrum disorder2008
- 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-19500305
[Journal Article] Mutations in the gene encoding CADMI are associated with autism spectrum disorder2008
- 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-19500305
[Journal Article] Ultrasonic vocalization impairment of Foxp2 (R552H) 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 Sci USA. 105(8)
  
  Pages: 3117-22
- Data Source
  KAKENHI-PROJECT-19500305
[Journal Article] Mutations in the gene encoding CADM1 are associated with autism spectrum disorder2008
- 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-18700333
[Journal Article] Neuronal RA175/SynCAM1 isoforms are processed by tumor necrosis factor-alpha-converting enzyme (TACE)/ADAM17-like proteases2008
- Author(s)
  Tanabe Y, Kasahara T, Momoi T, Fujita E.
- Journal Title
  
  Neurosci Lett 444
  
  Pages: 16-21
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19500305
[Journal Article] Neuronal RA175/SynCAM1 isoforms are processed by tumor necrosis factor-alphaーconverting enzyme(TACE)/ADAM17-like proteases2008
- Author(s)
  Tanabe Y, Kasahara T, Momoi T, Fujita E.
- Journal Title
  
  Neurosci Lett. 44
  
  Pages: 6-21
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18700333
[Journal Article] Neuronal RA175/SynCAMI isoforms are processed by tumor necrosis factor-alpha-converting enzyme (TACE)/ADAM17-like proteases2008
- Author(s)
  anabe Y, Kasahara T, Momoi T, Fujita E.
- Journal Title
  
  Neurosci Lett. 444
  
  Pages: 16-21
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19500305
[Journal Article] Neuronal RA175/SynCAM1 isoforms are processed by tumor necrosis factor-alpha-converting enzyme (TACE)/ADAM17-like proteases.2008
- Author(s)
  Tanabe Y, Kasahara T, Momoi T, Fujita E
- Journal Title
  
  Neurosci Lett 444
  
  Pages: 16-21
- Data Source
  KAKENHI-PROJECT-18700333
[Journal Article] Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells2008
- Author(s)
  Fujita E, Tanabe Y, Shiota A, Ueda M, Suwa K, Momoi MY, Momoi T.
- Journal Title
  
  Proc Natl Acad Sci USA 16105
  
  Pages: 3117-3122
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19500305
[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(3)
  
  Pages: 926-9
- Data Source
  KAKENHI-PROJECT-19500305
[Journal Article] Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinije cells2008
- Author(s)
  Fujita E, Tanabe Y, Shiota A, Ueda M, Suwa K, Momoi MY, Momoi T.
- Journal Title
  
  Proc Natl Acad Sci USA 16105
  
  Pages: 3117-3122
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19500305
[Journal Article] Endoplasmic reticulum stress caused by aggregate-prone proteins containing homopolymeric amino acids.2007
- Author(s)
  Uchio N, Oma Y, Toriumi K, Sasagawa N, Tanida I, Fujita E, Kouroku Y, Kuroda R, Momoi T, Ishiura S.
- Journal Title
  
  FEBS J. 274(21)
  
  Pages: 5619-27
- Data Source
  KAKENHI-PROJECT-19500305
[Journal Article] Loss of partitioning-defective-3/isotype-specific interacting protein (par-3/ASIP) in the elongating spermatid of RA175 (IGSF4A/SynCAM)-deficient mice.2007
- Author(s)
  Fujita E, Tanabe Y, Hirose T, Aurrand-Lions M, Kasahara T, Imhof BA, Ohno S, Momoi T
- Journal Title
  
  Am J Pathol 171
  
  Pages: 1800-1810
- Data Source
  KAKENHI-PROJECT-18700333
[Journal Article] Lose of partirioning defective -3/isotype specific interacting protein (par-3/ASIP)in the elongating spermatid of RA175 (IGSF4A/SynCAM)-deficient mice2007
- Author(s)
  Fujita E, Tanabe Y, Hirose T, Aurrand-Lions M, Kasahara T, Imhof BA, Ohno S, Momoi T.
- Journal Title
  
  Am J Pathol. 171
  
  Pages: 1800-1810
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18700333
[Journal Article] Two endoplasmic reticulum-associated degradation (ERAD) systems for the novel variant of the mutant dysferlin: ubiquitin/proteasome ERAD(I) and autophagy/lysosome ERAD(II).2007
- Author(s)
  Fujita E, Kouroku Y, Isoai A, Kumagai H, Misutani A, Matsuda C, Hayashi YK, Momoi T.
- Journal Title
  
  Hum Mol Genet. 16(6)
  
  Pages: 618-29
- Data Source
  KAKENHI-PROJECT-19500305
[Journal Article] Loss of artitioning-defective-3/isotype-specific interacting protein (par-3/ASIP) in the elongating spermatid of RA175 (IGSF4A/SynCAM)-deficient mice.2007
- Author(s)
  Fujita E, Tanabe Y, Hirose T, Aurrand-Lions M, Kasahara T, Imhof BA, Ohno S, Momoi T.
- Journal Title
  
  Am J Pathol. 171(6)
  
  Pages: 1800-10
- Data Source
  KAKENHI-PROJECT-19500305
[Journal Article] Two endoplasmic reticulum-associated degradation (ERAD) systems for the novel variant of the mutant dysferlin : ubiquitin/proteasome ERAD(I) and autophagy/lysosome ERAD(II).2007
- Author(s)
  Fujita E, Kouroku Y, Isoai A, Kumagai H, Misutani A, Matsuda C, Hayashi YK, Momoi T.
- Journal Title
  
  Hum Mol Genet. 16・6
  
  Pages: 618-629
- Data Source
  KAKENHI-PROJECT-18700333
[Journal Article] Oligo-astheno-teratozoospermia in mice lacking RA175/TSLC1/SynCAM/IGSF4A, a cell adhesion molecule in the immunoglobulin superfamily.2006
- Author(s)
  Fujita E, Kouroku Y, Ozeki S, Tanabe Y, Toyama Y, Maekawa M, Kojima N, Senoo H, Toshimori K, Momoi T
- Journal Title
  
  Mol Cell Biol. 26・2
  
  Pages: 718-726
- Data Source
  KAKENHI-PROJECT-18700333
[Journal Article] Oligo-astheno-teratozoospermia in mice lacking RA175/TSLC1/SynCAM/IGSF4A, a cell adhesion molecule in the immunoglobulin superfamily.2006
- Author(s)
  Fujita E, Kouroku Y, Ozeki S, Tanabe Y, Toyama Y, Maekawa M, Kojima N, Senoo H, Toshimori K, Momoi T
- Journal Title
  
  Mol Cell Biol 26
  
  Pages: 718-726
- Data Source
  KAKENHI-PROJECT-18700333
[Presentation] GPCR and risk for schizophrenia and autism-spectrum disorders2021
- Author(s)
  Jimbo　E, Hayashi Y, Yamagata T, Momoi T.
- Organizer
  第44回日本神経科学大会/第1回 CJK 国際会議
- Data Source
  KAKENHI-PROJECT-20K08166
[Presentation] GPR85変異は自閉症スペクトラム障害に関与する2020
- Author(s)
  神保恵理子, 林由起子, 山形崇倫, 桃井隆
- Organizer
  日本神経科学学会
- Data Source
  KAKENHI-PROJECT-20K08166
[Presentation] Alterated migration of the neurons with Foxp2(R552H), mutation related to the human speech-language2018
- Author(s)
  Fujita-jimbo E, Momoi T.
- Organizer
  Neuroscience2018
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K06716
[Presentation] Alterated migration of the neurons with Foxp2(R552H), mutation related to the human speech-language2018
- Author(s)
  Fujita-jimbo E, Momoi T.
- Organizer
  Neuroscience2018
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K06744
[Presentation] CADM1 Mutation Knock-in Mice As Mice Model of ASD Showing Abnormal Excitatory-Inhibitory Synaptic Balance2017
- Author(s)
  Kojima K, Jimbo EF, Yamagata T, Momoi M, Momoi T.
- Organizer
  International Society for Autism Research (INSAR) 2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K06744
[Presentation] Gene therapy for a mouse model of glucose transporter deficiency syndrome.2016
- Author(s)
  Nakamura S，Osaka H，Muramatsu S，Takino N，Aoki S， Jimbo E，Shimazaki K，Onaka T，Ohtsuki S，Terasaki T，Yamagata T.
- Organizer
  第58回　日本小児神経学会学術大会
- Place of Presentation
  京王プラザホテル（東京都新宿区）
- Data Source
  KAKENHI-PROJECT-15K06716
[Presentation] CASPR2 forms a complex with GPR37 via MUPP1 but not with GPR37(R558Q), an autism spectrum disorder-related mutation2015
- Author(s)
  Tanabe Y, Fujita-Jimbo E, Momoi MY, Momoi T.
- Organizer
  第38回日本神経科学大会
- Place of Presentation
  神戸国際会議場、神戸国際展示場（神戸）
- Year and Date
  2015-07-28
- Data Source
  KAKENHI-PROJECT-15K06716
[Presentation] CASPR2はMUPP1を介してGPR37と複合体形成するが自閉性障害変異GPR37(R558Q)とは複合体形成しない2015
- Author(s)
  田辺裕子、神保恵理子、桃井眞里子、桃井隆
- Organizer
  第38回日本神経科学学会大会
- Place of Presentation
  神戸国際会議場、神戸国際展示場
- Year and Date
  2015-07-28
- Data Source
  KAKENHI-PROJECT-15K06744
[Presentation] The Foxp2 promoter-mediated mcherry-visulalized thalamocortical pathway and its alteration in the Foxp2(R552H)-KI mice.2015
- Author(s)
  Jimbo E et al.
- Organizer
  第38回日本神経科学会
- Place of Presentation
  神戸国際会議場、神戸国際展示場（神戸）
- Year and Date
  2015-07-30
- Data Source
  KAKENHI-PROJECT-24500386
[Presentation] 自閉性障害原因遺伝子CADM1に結合する足場タンパクMUPP1の遺伝子変異解析2014
- Author(s)
  楊志亮、小島華林、神保恵理子、山形崇倫、桃井隆、桃井眞里子
- Organizer
  第56回日本小児神経学会学術集会
- Place of Presentation
  静岡
- Year and Date
  2014-05-30
- Data Source
  KAKENHI-PROJECT-24500386
[Presentation] Trappc5, a constituent of TRAPP complex, is up-regulated in cerebellum expressing FOXP2 and involved in synaptogenesis2014
- Author(s)
  Jimbo Eriko, Tanabe Yuko, Imhof Beat, Momoi Takashi
- Organizer
  第37回日本神経科学大会
- Place of Presentation
  横浜
- Year and Date
  2014-09-13
- Data Source
  KAKENHI-PROJECT-24500386
[Presentation] 発達障害はいつ形成されるか？先天性？後天性？あるいは両方か～発症および病態修飾のメカニズムについて　（発達障害における遺伝性要因(先天的素因)について）～2014
- Author(s)
  神保恵理子、桃井眞里子
- Organizer
  第56回日本小児神経学会学術集会
- Place of Presentation
  静岡
- Year and Date
  2014-05-30
- Invited
- Data Source
  KAKENHI-PROJECT-24500386
[Presentation] 自閉性障害患者における時計関連遺伝子の変異解析2014
- Author(s)
  松本歩, 楊志亮, 小島華林, 中山一大, 神保恵理子, 岩本禎彦, 永田浩一, 山形崇倫
- Organizer
  第56回日本小児神経学会
- Place of Presentation
  浜松
- Data Source
  KAKENHI-PROJECT-23390275
[Presentation] 自閉性障害原因遺伝子 CADM1 に結合する足場タンパク MUPP1 の遺伝子変異解析2014
- Author(s)
  楊志亮, 小島華林, 神保恵理子, 山形崇倫, 桃井隆, 桃井真里子
- Organizer
  第56回日本小児神経学会
- Place of Presentation
  浜松
- Data Source
  KAKENHI-PROJECT-23390275
[Presentation] 自閉性障害原因遺伝子変異と小胞体ストレスの関与2014
- Author(s)
  小島華林, 神保恵理子, 松本歩, 山形崇倫, 桃井隆, 桃井真里子
- Organizer
  第56回日本小児神経学会
- Place of Presentation
  浜松
- Data Source
  KAKENHI-PROJECT-23390275
[Presentation] 欠損マウスにおける超音波異常と自閉性障害2014
- Author(s)
  神保恵理子、インホフベアト、桃井隆
- Organizer
  第37回日本分子生物学会年会
- Place of Presentation
  横浜
- Year and Date
  2014-11-27
- Data Source
  KAKENHI-PROJECT-24500386
[Presentation] 自閉性障害原因遺伝子変異と小胞体ストレスの関与2014
- Author(s)
  小島華林、神保恵理子、松本歩、楊志亮、山形崇倫、桃井隆、桃井眞里子
- Organizer
  第56回日本小児神経学会学術集会
- Place of Presentation
  静岡
- Year and Date
  2014-05-29
- Data Source
  KAKENHI-PROJECT-24500386
[Presentation] 発達障害患者CNV領域におけるシナプス関連分子の解析.2013
- Author(s)
  松本歩、山形崇倫、野崎靖之、神保恵理子、永田浩一、桃井真里子
- Organizer
  第55回日本小児神経学会
- Place of Presentation
  大分
- Data Source
  KAKENHI-PROJECT-23390275
[Presentation] Contribution of Scaffold proteins to developmental disorder2013
- Author(s)
  Matsumoto A, Mizuno M, Hamada N, Jimbo EF, Kojima K, Momoi MY, Nagata K, Yamagata T
- Organizer
  The 63rd Annual Meeting for the American Society of Human Genetics
- Place of Presentation
  Boston
- Data Source
  KAKENHI-PROJECT-23390275
[Presentation] Mutations in Secretin receptor may be related to autism spectrum disorder2013
- Author(s)
  Kojima K, Yamagata T, Matsumoto A, Jimbo EF, Momoi MY
- Organizer
  The 63rd Annual Meeting for the American Society of Human Genetics
- Place of Presentation
  Boston
- Data Source
  KAKENHI-PROJECT-23390275
[Presentation] Mutations in Secretin receptor may be related to autism spectrum disorder.2013
- Author(s)
  Kojima K, Yamagata T, Matsumoto A, Jimbo EF, Momoi MY
- Organizer
  The 63rd Annual Meeting for the American Society of Human Genetics.
- Place of Presentation
  Boston
- Data Source
  KAKENHI-PROJECT-23390275
[Presentation] Contribution of Scaffold proteins to developmental disorder.2013
- Author(s)
  Matsumoto A, Mizuno M, Hamada N, Jimbo EF, Kojima K, Momoi MY, Nagata K, Yamagata T.
- Organizer
  The 63rd Annual Meeting for the American Society of Human Genetics.
- Place of Presentation
  Boston
- Data Source
  KAKENHI-PROJECT-23390275
[Presentation] 自閉性障害患者に見出したGPR85変異についての解析2013
- Author(s)
  神保恵理子、ゆじりん、山形崇倫、小島華林、松本歩、田辺裕子、桃井隆、桃井真里子
- Organizer
  第36回　日本神経科学大会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-24500386
[Presentation] マウス脳における自閉性障害に関係するCadm1とCntnap2の分子複合体の解析2013
- Author(s)
  田辺裕子、藤田恵理子、桃井隆
- Organizer
  第36回　日本神経科学大会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-24500386
[Presentation] 発達障害患者 CNV領域におけるシナプス関連分子の解析2013
- Author(s)
  松本歩, 山形崇倫, 野崎靖之, 神保恵理子, 永田浩一, 桃井真里子
- Organizer
  第55回日本小児神経学会
- Place of Presentation
  大分
- Data Source
  KAKENHI-PROJECT-23390275
[Presentation] Cadm1 変異を持つ自閉性障害患者のリンパ芽球を用いた小胞体ストレス感受性についての検討2012
- Author(s)
  小島華林, 松本歩, 楊志亮, 神保恵理子, 山形崇倫, 桃井真里子
- Organizer
  第57回日本人類遺伝学会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-23390275
[Presentation] Interstitial Deletion 12(q21.2-q21.33) in a Boy with Facial Dysmorphism and Mental Retardation2012
- Author(s)
  Matsumoto A, Yamagata T, Nozaki Y, Jimbo EF, Momoi MY
- Organizer
  The 62rd Annual Meeting for the American Society of Human Genetics
- Place of Presentation
  San Francisco
- Data Source
  KAKENHI-PROJECT-23390275
[Presentation] Cadm1遺伝子変異をもつ自閉性障害患者のリンパ芽球を用いた小胞体ストレス感受性についての検討2012
- Author(s)
  小島華林、松本歩、楊志亮、神保恵理子、山形崇倫、桃井眞里子
- Organizer
  日本人類遺伝学会　第57回大会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-23390275
[Presentation] 自閉性障害に関与するシナプス接着因子Cadm1とMultiple PDZ domain protein(Mupp1)の関与2012
- Author(s)
  神保恵理子、小島華林、田辺裕子、山形崇倫、桃井真里子、桃井隆
- Organizer
  第35回日本神経科学大会
- Place of Presentation
  名古屋
- Data Source
  KAKENHI-PROJECT-24500386
[Presentation] RPS6KA3 の重複を認めた軽度知的障害男児例2012
- Author(s)
  松本歩, 山形崇倫, 桑島真理, 神保恵理子, 桃井真里子
- Organizer
  第57回日本人類遺伝学会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-23390275
[Presentation] RPS6KA3の重複を認めた軽度知的障害男児例2012
- Author(s)
  松本歩、山形崇倫、桑島真理、神保恵理子、桃井真里子
- Organizer
  日本人類遺伝学会　第57回大会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-23390275
[Presentation] Mutation in Secretin receptor gene in Autism spectrum disorder and genes regulated by secretin in the brain2012
- Author(s)
  Kojima K, Yamagata T, Matsumoto A, Saito M, Jimbo EF, Momoi MY
- Organizer
  The 62rd Annual Meeting for the American Society of Human Genetics
- Place of Presentation
  San Francisco
- Data Source
  KAKENHI-PROJECT-23390275
[Presentation] Mutation in the gene encoding Secretin Recepor is associated with autism spectrum disorder2012
- Author(s)
  Kojima K, Yamagata T, Matsumoto A, Jimbo E, Momoi MY
- Organizer
  The 62th Annual Meeting of the American Society of Human Genetics
- Place of Presentation
  San Francisco
- Data Source
  KAKENHI-PROJECT-23390275
[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] Secretin receptor and the associated molecular processes relevant to autism spectrum disorder．2012
- Author(s)
  Kojima K, Yamagata T, Saito M, Matsumoto A, Jimbo EF, Momoi MY
- Organizer
  American Society of Human Genetics (ASHG) 62nd annual meeting
- Place of Presentation
  San Francisco
- Data Source
  KAKENHI-PROJECT-24500386
[Presentation] CADM1遺伝子変異をもつ自閉性障害患者のリンパ芽球を用いた小胞体ストレス感受性についての検討2012
- Author(s)
  小島華林、松本歩、楊志亮、神保恵理子、山形崇倫、桃井眞里子
- Organizer
  日本人類遺伝学会第57回大会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-24500386
[Presentation] Interstitial Deletion 12(q21.2-q21.33) in a Boy with Facial Dysmorphism and Menta Retardation2012
- Author(s)
  Matsumoto A, Yamagata T, Nozaki Y, Jimbo E, Momoi MY
- Organizer
  The 62th Annual Meeting of the American Society of Human Genetics
- Place of Presentation
  San Francisco
- Data Source
  KAKENHI-PROJECT-23390275
[Presentation] Deletion of MAOA and MAOB in male siblings with severe mental retardation and autistic phenotype2011
- Author(s)
  Saito M, Yamagata T, Shiba Y, Nakashima N, Nagashima M, Jimbo E, Momoi MY
- Organizer
  The 61st Annual Meeting of the American Society of Human Genetics
- Place of Presentation
  Montreal, Canada
- Year and Date
  2011-11-13
- Data Source
  KAKENHI-PROJECT-23390275
[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-21700377
[Presentation] Deletion of MAOA and MAOB in male siblings with severe mental retardation and autistic phenotype2011
- Author(s)
  Saito M, Yamagata T, Shiba Y, Nakashima N, Nagashima M, Jimbo E, Momoi MY
- Organizer
  The 62rd Annual Meeting for the American Society of Human Genetics
- Place of Presentation
  Montreal
- Data Source
  KAKENHI-PROJECT-23390275
[Presentation] Cntnap2 expression in the cerebellum of the Foxp2(R552H) mice, with mutation related to the speech-language disorder2011
- Author(s)
  藤田恵理子
- Organizer
  第34回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜(横浜)
- Year and Date
  2011-12-14
- Data Source
  KAKENHI-PROJECT-21700377
[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] 自閉性障害患者に見いだされた変異蛋白による小胞体ストレスと分子病態との関係2011
- Author(s)
  神保恵理子、山形崇倫、桃井真里子
- Organizer
  第53回日本小児神経学会総会
- Place of Presentation
  横浜
- Year and Date
  2011-05-27
- Data Source
  KAKENHI-PROJECT-23390275
[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
- Organizer
  第34回日本神経科学大会
- Place of Presentation
  パシフィコ横浜(横浜)
- Year and Date
  2011-09-15
- Data Source
  KAKENHI-PROJECT-21700377
[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、桃井真里子
- 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-21700377
[Presentation] 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新規Foxp2アイソフォームの発現の解析2010
- 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33回日本神経科学大会・第53回日本神経科学会大会・第20回日本神経回路学会大会合同学術集会抄録集
- Place of Presentation
  神戸
- Year and Date
  2010-09-04
- Data Source
  KAKENHI-PROJECT-21700377
[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] 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] 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、Mariko Momoi、Takashi Momoi
- Organizer
  Neuroscience2009
- Place of Presentation
  名古屋
- Year and Date
  2009-09-18
- Data Source
  KAKENHI-PROJECT-21700377
[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] メタロプロテアーゼによるRA175/SynCAM12008
- Author(s)
  田辺裕子、笠原忠、桃井隆、藤田恵理子
- Organizer
  特異的アイソフォームのプロセッシングNeuroscience 2008
- Place of Presentation
  東京
- Year and Date
  2008-07-10
- Data Source
  KAKENHI-PROJECT-18700333
[Presentation] メタロプロテアーゼによるRA175/SynCAM1特異的アイソフォームのプロセッシング2008
- Author(s)
  田辺裕子、笠原忠、桃井隆、藤田恵理子
- Organizer
  Neuroscience 2008
- Place of Presentation
  東京
- Year and Date
  2008-07-10
- Data Source
  KAKENHI-PROJECT-19500305
[Presentation] メタロプロテアーゼによるRA175/SynCAM1特異的アイソフォームのプロセッシング2008
- Author(s)
  田辺裕子、笠原忠、桃井隆、藤田恵理子
- Organizer
  Neuroscience 2008
- Place of Presentation
  東京国際フォーラム
- Year and Date
  2008-07-10
- Data Source
  KAKENHI-PROJECT-18700333
[Presentation] The RA175/SynCAM complex on the GABAergic synapse2007
- Author(s)
  Tanabe Y, Fujita E, Giulo P, Nigro V, Momoi MY, Ishiura S, Kasahara T, Momoi T
- Organizer
  第30回日本分子生物学会年会、第80回日本生化学会大会
- Place of Presentation
  横浜
- Year and Date
  2007-12-12
- Data Source
  KAKENHI-PROJECT-18700333
[Presentation] 脳におけるRA175/SyaCAM結合蛋白の解析2007
- Author(s)
  田辺裕子、松崎鮎美、藤田恵理子、Giulo Pilus、大野茂男、石浦章一、Alaa Hussein、Vbnoenzo Mgm、桃井隆
- Organizer
  30回日本神経科学大会、第50回日本神経化学会大会、第17回日本神経回路学会大会
- Place of Presentation
  パシフィコ横浜(神奈川県横浜市)
- Year and Date
  2007-09-12
- Data Source
  KAKENHI-PROJECT-18700333
[Presentation] The RA175/SynCAM complex on the GABAergic synapse2007
- Author(s)
  Tanabe Y, Fujita E, Giulo P, Nigro V, Momoi MY, Ishiura S, Kasahara T, Momoi T
- Organizer
  第30回日本分子生物学会年会、第80回日本生化学会大会
- Place of Presentation
  横浜
- Year and Date
  2007-12-12
- Data Source
  KAKENHI-PROJECT-19500305
[Presentation] The RA175/SynCAM complex on the GABAergic synapse2007
- Author(s)
  Y. Tanabe, E. Fujita, P. Giulo, V. Nigro, M. Y. Momai, S. lshiura, T. Kasahara, T Momoi
- Organizer
  第30回日本分子生物学会年会、第80回日本生化学会大会
- Place of Presentation
  パシフィコ横浜(神奈川県横浜市)
- Year and Date
  2007-12-12
- Data Source
  KAKENHI-PROJECT-18700333
[Presentation] 脳におけるRA175/SynCAM結合蛋白の解析2007
- Author(s)
  田辺裕子、松崎鮎美、藤田恵理子、Giulo Piluso、大野茂男、石浦章一、Alaa Husseini、Vencenzo Nigro、桃井隆
- Organizer
  、第30回日本神経科学大会、第50回日本神経化学会大会、第17回日本神経回路学会大会
- Place of Presentation
  横浜
- Year and Date
  2007-09-12
- Data Source
  KAKENHI-PROJECT-19500305
[Presentation] 脳におけるRA175/SynCAM結合蛋白の解析2007
- Author(s)
  田辺裕子、松崎鮎美、藤田恵理子、Giulo Piluso、大野茂男、石浦章一、Alaa Husseini、Vencenzo Nigro、桃井隆
- Organizer
  第30回日本神経科学大会、第50回日本神経化学会大会、第17回日本神経回路学会大会
- Place of Presentation
  横浜
- Year and Date
  2007-09-12
- Data Source
  KAKENHI-PROJECT-18700333
[Presentation] IGSF4A/ RA175 Interacts with PAR-3 and Its Deficiency Causes Defect in the Spermatocytes Differentiation.2006
- Author(s)
  Fujita E, Tanabe Y, Senoo H, Toshimori K, Momoi T
- Organizer
  第20回国際生化学・分子生物学会議(第79回日本生化学会大会/第29回日本分子生物学会年会)
- Place of Presentation
  京都
- Year and Date
  2006-06-20
- Data Source
  KAKENHI-PROJECT-18700333
[Presentation] IGSF4A/ RA175 Interacts with PAR-3(IGSF4A/ RA175と結合する蛋白)2006
- Author(s)
  Fujita E, Tanabe Y, Momoi T
- Organizer
  第29回神経科学大会
- Place of Presentation
  京都
- Year and Date
  2006-07-09
- Data Source
  KAKENHI-PROJECT-18700333

1. MOMOI Takashi (40143507)

# of Collaborated Projects: 7 results

# of Collaborated Products: 50 results
2. Kono Yumi (50243390)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
3. MOMOI Mariko (90166348)

# of Collaborated Projects: 1 results

# of Collaborated Products: 14 results
4. YAMAGATA Takanori (00239857)

# of Collaborated Projects: 1 results

# of Collaborated Products: 25 results
5. NAGATA Kouichi (50252143)

# of Collaborated Projects: 1 results

# of Collaborated Products: 5 results
6. MIRI Masato (10337347)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
7. NOZAKI Yasuyuki (90281295)

# of Collaborated Projects: 1 results

# of Collaborated Products: 4 results
8. NAKASHIMA Naomi (20337330)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
9. MONDEN Yukifumi (80382951)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
10. NAGASHIMA Masako (70438662)

# of Collaborated Projects: 1 results

# of Collaborated Products: 4 results
11. ABE Hiroki (80086727)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
12. WATANABE Katsuko (30092381)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
13. SUZUKI Yume (40458302)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
14. MATANO Miyuki (90458315)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
15. 林由起子 (50238135)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
16. 大口昭英 (10306136)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
17. 岩本禎彦

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
18. 田畑秀典

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
19. 伊東秀記

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Jimbo Eriko 神保 恵理子 (藤田 恵理子)

神保 恵理子 ジンボ エリコ

藤田恵理子

神保 恵理子(藤田恵理子) ジンボ エリコ

JINBO Eriko 神保 恵理子

藤田 恵理子

FUJITA Eriko 藤田 恵理子

Research Projects

Research Products

Co-Researchers

Foxp2による消化管・腸管神経系形成の分子機構と転写活性欠失変異の影響Principal Investigator

Principal Investigator

Project Period (FY)

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Research Institution

Methylation of genes related to cardiovascular and chronic kidney diseases in preterm low birth weight infants born to mothers with hypertensive disorders of pregnancy

Principal Investigator

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Review Section

Research Institution

自閉症スペクトラム障害の分子病態に関連するGPR85のシグナル伝達機構の解析Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

The effects of the GPR37-mutation in autism spectrum disorder on the signal transduction by prosaponinPrincipal Investigator

Principal Investigator

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Research Field

Research Institution

Molecular Pathogenesis of the abnormal spine morphology and 5-HTR complex induced by ASD-related mutated Mupp1

Principal Investigator

Project Period (FY)

Research Category

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Research Institution

DNA methylation of human glucocorticoid receptor gene (NR3C1) and stress response in low birth weight infants

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Studies on the influence of brain and neurons of mutation of synaptic cell adhesion molecule protein, Cadm1 using autism mouse models.Principal Investigator

Principal Investigator

Project Period (FY)

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Research Institution

Analysis for the pathogenesis and the target molecules of treatment for autism focusing on G-protein coupled receptors and synaptic molecules

Principal Investigator

Project Period (FY)

Research Category

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Research Institution

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

Principal Investigator

Project Period (FY)

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Research Institution

The regulation of mouse ultrasonic vocalization and behavior by Foxp2Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

The molecular system of the selective transport of Synaptic adhesion molecules to the pre-and post-synaptic membrane.

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Loss of the functional-synapse in RA175(SynCAM)-deficient micePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Jimbo Eriko 神保恵理子 (藤田恵理子)

神保恵理子ジンボエリコ

神保恵理子(藤田恵理子) ジンボエリコ

JINBO Eriko 神保恵理子

藤田恵理子

FUJITA Eriko 藤田恵理子