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Journal Abstract Search

154 related items for PubMed ID: 27607605

  • 1. Role of Class III phosphoinositide 3-kinase in the brain development: possible involvement in specific learning disorders.
    Inaguma Y, Matsumoto A, Noda M, Tabata H, Maeda A, Goto M, Usui D, Jimbo EF, Kikkawa K, Ohtsuki M, Momoi MY, Osaka H, Yamagata T, Nagata KI.
    J Neurochem; 2016 Oct; 139(2):245-255. PubMed ID: 27607605
    [Abstract] [Full Text] [Related]

  • 2. Morphological characterization of Class III phosphoinositide 3-kinase during mouse brain development.
    Inaguma Y, Ito H, Iwamoto I, Matsumoto A, Yamagata T, Tabata H, Nagata K.
    Med Mol Morphol; 2016 Mar; 49(1):28-33. PubMed ID: 26242203
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  • 3. Role of an adaptor protein Lin-7B in brain development: possible involvement in autism spectrum disorders.
    Mizuno M, Matsumoto A, Hamada N, Ito H, Miyauchi A, Jimbo EF, Momoi MY, Tabata H, Yamagata T, Nagata K.
    J Neurochem; 2015 Jan; 132(1):61-9. PubMed ID: 25196215
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  • 4. Role of a circadian-relevant gene NR1D1 in brain development: possible involvement in the pathophysiology of autism spectrum disorders.
    Goto M, Mizuno M, Matsumoto A, Yang Z, Jimbo EF, Tabata H, Yamagata T, Nagata KI.
    Sci Rep; 2017 Mar 06; 7():43945. PubMed ID: 28262759
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  • 5. MUNC18-1 gene abnormalities are involved in neurodevelopmental disorders through defective cortical architecture during brain development.
    Hamada N, Iwamoto I, Tabata H, Nagata KI.
    Acta Neuropathol Commun; 2017 Nov 30; 5(1):92. PubMed ID: 29191246
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  • 6. Role of a heterotrimeric G-protein, Gi2, in the corticogenesis: possible involvement in periventricular nodular heterotopia and intellectual disability.
    Hamada N, Negishi Y, Mizuno M, Miya F, Hattori A, Okamoto N, Kato M, Tsunoda T, Yamasaki M, Kanemura Y, Kosaki K, Tabata H, Saitoh S, Nagata KI.
    J Neurochem; 2017 Jan 30; 140(1):82-95. PubMed ID: 27787898
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  • 7. Role of Per3, a circadian clock gene, in embryonic development of mouse cerebral cortex.
    Noda M, Iwamoto I, Tabata H, Yamagata T, Ito H, Nagata KI.
    Sci Rep; 2019 Apr 10; 9(1):5874. PubMed ID: 30971765
    [Abstract] [Full Text] [Related]

  • 8. Heterotrimeric G-protein, Gi1, is involved in the regulation of proliferation, neuronal migration, and dendrite morphology during cortical development in vivo.
    Hamada N, Iwamoto I, Kawamura N, Nagata KI.
    J Neurochem; 2021 May 10; 157(4):1167-1181. PubMed ID: 33025585
    [Abstract] [Full Text] [Related]

  • 9. LIN7A depletion disrupts cerebral cortex development, contributing to intellectual disability in 12q21-deletion syndrome.
    Matsumoto A, Mizuno M, Hamada N, Nozaki Y, Jimbo EF, Momoi MY, Nagata K, Yamagata T.
    PLoS One; 2014 May 10; 9(3):e92695. PubMed ID: 24658322
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  • 11. Essential role of the nuclear isoform of RBFOX1, a candidate gene for autism spectrum disorders, in the brain development.
    Hamada N, Ito H, Nishijo T, Iwamoto I, Morishita R, Tabata H, Momiyama T, Nagata K.
    Sci Rep; 2016 Aug 02; 6():30805. PubMed ID: 27481563
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  • 14. In vivo knockdown of cKit impairs neuronal migration and axonal extension in the cerebral cortex.
    Guijarro P, Wang Y, Ying Y, Yao Y, Jieyi X, Yuan X.
    Dev Neurobiol; 2013 Dec 02; 73(12):871-87. PubMed ID: 23843227
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  • 18. Nitric oxide synthase 1 adaptor protein, a protein implicated in schizophrenia, controls radial migration of cortical neurons.
    Carrel D, Hernandez K, Kwon M, Mau C, Trivedi MP, Brzustowicz LM, Firestein BL.
    Biol Psychiatry; 2015 Jun 01; 77(11):969-78. PubMed ID: 25542305
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