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<li>[[file:Vikas_Cell_Rep_2025.pdf|50px|border|right]]<pubmed>40199325</pubmed>
<li>[[file:Vikas_Cell_Rep_2025.pdf|50px|border|right]]<pubmed>40199325</pubmed>
[[https://scholar.google.co.jp/citations?view_op=view_citation&hl=ja&user=jK4VsLQAAAAJ&sortby=pubdate&citation_for_view=jK4VsLQAAAAJ:lK9BDNCuzFgC Google Scholar]]</li>
[[https://scholar.google.co.jp/citations?view_op=view_citation&hl=ja&user=jK4VsLQAAAAJ&sortby=pubdate&citation_for_view=jK4VsLQAAAAJ:lK9BDNCuzFgC Google Scholar]]</li>
</ul>
===2024===
<ul>
<li>[[file:Kaizuka_PLoS_Biol_2024.pdf|50px|border|right]]<pubmed>38452102</pubmed>
[[https://scholar.google.co.jp/citations?view_op=view_citation&hl=ja&user=jK4VsLQAAAAJ&sortby=pubdate&citation_for_view=jK4VsLQAAAAJ:gV6rEsy15s0C Google Scholar]]</li>
</ul>
===2023===
<ul>
<li>[[file:Ripoli_Sci_Adv_2023.pdf|50px|border|right]]<pubmed>37967196</pubmed>
[[https://scholar.google.co.jp/citations?view_op=view_citation&hl=ja&user=jK4VsLQAAAAJ&sortby=pubdate&citation_for_view=jK4VsLQAAAAJ:bXQfdp6S9ecC Google Scholar]]</li>
</ul>
===2022===
<ul>
<li>[[file:Ozden_Cell_Rep_2022.pdf|50px|border|right]]<pubmed>35830796</pubmed>
[[https://scholar.google.co.jp/citations?view_op=view_citation&hl=ja&user=jK4VsLQAAAAJ&sortby=pubdate&citation_for_view=jK4VsLQAAAAJ:Ej9njvOgR2oC Google Scholar]]</li>
</ul>
===2021===
<ul>
<li>[[file:Goto_Science_2021.pdf|50px|border|right]]<pubmed>34762472</pubmed>
[[https://scholar.google.co.jp/citations?view_op=view_citation&hl=ja&user=jK4VsLQAAAAJ&sortby=pubdate&citation_for_view=jK4VsLQAAAAJ:X4-KO54GjGYC Google Scholar]]</li>
<li>[[file:Cid_Cell_Rep_2021.pdf|50px|border|right]]<pubmed>34107264</pubmed>
[[https://scholar.google.co.jp/citations?view_op=view_citation&hl=ja&user=jK4VsLQAAAAJ&sortby=pubdate&citation_for_view=jK4VsLQAAAAJ:as0KMg8qHbkC Google Scholar]]</li>
<li>[[file:Takamura_J_Neurosci_2021.pdf|50px|border|right]]<pubmed>33980545</pubmed>
[[https://scholar.google.co.jp/citations?view_op=view_citation&hl=ja&user=jK4VsLQAAAAJ&sortby=pubdate&citation_for_view=jK4VsLQAAAAJ:sbeIDTyQOFgC Google Scholar]]</li>
<li>[[file:Hosokawa_Nat_Neurosci_2021.pdf|50px|border|right]]<pubmed>33927400</pubmed>
[[https://scholar.google.co.jp/citations?view_op=view_citation&hl=ja&user=jK4VsLQAAAAJ&sortby=pubdate&citation_for_view=jK4VsLQAAAAJ:QaSi33NTfwYC Google Scholar]]</li>
<li>[[file:Kastian_Cell_Rep_2021.pdf|50px|border|right]]<pubmed>34010643</pubmed>
[[https://scholar.google.co.jp/citations?view_op=view_citation&hl=ja&user=jK4VsLQAAAAJ&sortby=pubdate&citation_for_view=jK4VsLQAAAAJ:vVJNg6_NJEsC Google Scholar]]</li>
<li>[[file:Mizuta_Hippocampus_2021.pdf|50px|border|right]]<pubmed>33452849</pubmed>
[[https://scholar.google.co.jp/citations?view_op=view_citation&hl=ja&user=jK4VsLQAAAAJ&sortby=pubdate&citation_for_view=jK4VsLQAAAAJ:TGkaJS32XoUC Google Scholar]]</li>
</ul>
===2020===
<ul>
<li>[[file:Eriksen_FEBS_J_2020.pdf|50px|border|right]]<pubmed>33175445</pubmed>
[[https://scholar.google.co.jp/citations?view_op=view_citation&hl=ja&user=jK4VsLQAAAAJ&sortby=pubdate&citation_for_view=jK4VsLQAAAAJ:6ZzL7HXColQC Google Scholar]]</li>
<li>[[file:Sato_Cell_Rep_2020.pdf|50px|border|right]]<pubmed>32640229</pubmed>
[[https://scholar.google.co.jp/citations?view_op=view_citation&hl=ja&user=jK4VsLQAAAAJ&sortby=pubdate&citation_for_view=jK4VsLQAAAAJ:kUhpeDhEZMUC Google Scholar]]</li>
<li>[[file:Luchetti_J_Neurosci_2020.pdf|50px|border|right]]<pubmed>32414785</pubmed>
[[https://scholar.google.co.jp/citations?view_op=view_citation&hl=ja&user=jK4VsLQAAAAJ&sortby=pubdate&citation_for_view=jK4VsLQAAAAJ:bVQMTfhMCi4C Google Scholar]]</li>
<li>[[file:Cai_Structure_2020.pdf|50px|border|right]]<pubmed>31879129</pubmed>
[[https://scholar.google.co.jp/citations?view_op=view_citation&hl=ja&user=jK4VsLQAAAAJ&sortby=pubdate&citation_for_view=jK4VsLQAAAAJ:QoJ_w57xiyAC Google Scholar]]</li>
</ul>
===2019===
<ul>
<li>[[file:Kojima_Neurobiol_Learn_Mem_2019.pdf|50px|border|right]]<pubmed>31445077</pubmed>
[[https://scholar.google.co.jp/citations?view_op=view_citation&hl=ja&user=jK4VsLQAAAAJ&sortby=pubdate&citation_for_view=jK4VsLQAAAAJ:1r-w4gtu6w8C Google Scholar]]</li>
<li>[[file:Saneyoshi_Neuron_2019.pdf|50px|border|right]]<pubmed>31078368</pubmed>
[[https://scholar.google.co.jp/citations?view_op=view_citation&hl=ja&user=jK4VsLQAAAAJ&sortby=pubdate&citation_for_view=jK4VsLQAAAAJ:BmWJbWwHJAwC Google Scholar]]</li>
<li>[[file:Ghandour_Nat_Commun_2019.pdf|50px|border|right]]<pubmed>31201332</pubmed></li>
<li>[[file:Kobayashi_Sci_Rep_2019.pdf|50px|border|right]]<pubmed>31182818</pubmed></li>
<li>[[File:Kim_Neurobiol_Learn_Mem_2019.pdf|50px|border|right]]<pubmed>30528771</pubmed></li>
</ul>
</ul>


Latest revision as of 15:29, 12 April 2026

2025

  • Saneyoshi, T., Suematsu, C., & Hayashi, Y. (2025).
    Transient Photoactivation of Rac1 Induces Persistent Structural LTP Independent of CaMKII in Hippocampal Dendritic Spines. eNeuro, 12(11). [PubMed:41249054] [PMC] [WorldCat] [DOI]     [Google Scholar]
  • Kuo, L.M.S., Liu, P.W., Arizono, M., & Hayashi, Y. (2025).
    CaMKII Drives Synaptic Maturation by Coordinating Spine Remodeling and Receptor Segregation via Liquid-Liquid Phase Separation. The Journal of neuroscience : the official journal of the Society for Neuroscience, 45(48). [PubMed:41102003] [PMC] [WorldCat] [DOI]     [Google Scholar]
  • Liu, J., Goto, A., & Hayashi, Y. (2025).
    Time-window of offline long-term potentiation in anterior cingulate cortex during memory consolidation and recall. Neuroscience research, 212, 75-83. [PubMed:40440255] [WorldCat] [DOI]     [Google Scholar]
  • Pandey, V., Hosokawa, T., Hayashi, Y., & Urakubo, H. (2025).
    Multiphasic protein condensation governed by shape and valency. Cell reports, 44(4), 115504. [PubMed:40199325] [WorldCat] [DOI]     [Google Scholar]

2024

  • Kaizuka, T., Hirouchi, T., Saneyoshi, T., Shirafuji, T., Collins, M.O., Grant, S.G.N., ..., & Takumi, T. (2024).
    FAM81A is a postsynaptic protein that regulates the condensation of postsynaptic proteins via liquid-liquid phase separation. PLoS biology, 22(3), e3002006. [PubMed:38452102] [PMC] [WorldCat] [DOI]     [Google Scholar]

2023

  • Ripoli, C., Dagliyan, O., Renna, P., Pastore, F., Paciello, F., Sollazzo, R., ..., & Grassi, C. (2023).
    Engineering memory with an extrinsically disordered kinase. Science advances, 9(46), eadh1110. [PubMed:37967196] [PMC] [WorldCat] [DOI]     [Google Scholar]

2022

  • Özden, C., Sloutsky, R., Mitsugi, T., Santos, N., Agnello, E., Gaubitz, C., ..., & Stratton, M.M. (2022).
    CaMKII binds both substrates and activators at the active site. Cell reports, 40(2), 111064. [PubMed:35830796] [PMC] [WorldCat] [DOI]     [Google Scholar]

2021

  • Goto, A., Bota, A., Miya, K., Wang, J., Tsukamoto, S., Jiang, X., ..., & Hayashi, Y. (2021).
    Stepwise synaptic plasticity events drive the early phase of memory consolidation. Science (New York, N.Y.), 374(6569), 857-863. [PubMed:34762472] [WorldCat] [DOI]     [Google Scholar]
  • Cid, E., Marquez-Galera, A., Valero, M., Gal, B., Medeiros, D.C., Navarron, C.M., ..., & de la Prida, L.M. (2021).
    Sublayer- and cell-type-specific neurodegenerative transcriptional trajectories in hippocampal sclerosis. Cell reports, 35(10), 109229. [PubMed:34107264] [WorldCat] [DOI]     [Google Scholar]
  • Takamura, R., Mizuta, K., Sekine, Y., Islam, T., Saito, T., Sato, M., ..., & Hayashi, Y. (2021).
    Modality-Specific Impairment of Hippocampal CA1 Neurons of Alzheimer's Disease Model Mice. The Journal of neuroscience : the official journal of the Society for Neuroscience, 41(24), 5315-5329. [PubMed:33980545] [PMC] [WorldCat] [DOI]     [Google Scholar]
  • Hosokawa, T., Liu, P.W., Cai, Q., Ferreira, J.S., Levet, F., Butler, C., ..., & Hayashi, Y. (2021).
    CaMKII activation persistently segregates postsynaptic proteins via liquid phase separation. Nature neuroscience, 24(6), 777-785. [PubMed:33927400] [WorldCat] [DOI]     [Google Scholar]
  • File:Kastian Cell Rep 2021.pdf
    Kastian, R.F., Minegishi, T., Baba, K., Saneyoshi, T., Katsuno-Kambe, H., Saranpal, S., ..., & Inagaki, N. (2021).
    Shootin1a-mediated actin-adhesion coupling generates force to trigger structural plasticity of dendritic spines. Cell reports, 35(7), 109130. [PubMed:34010643] [WorldCat] [DOI]     [Google Scholar]
  • Mizuta, K., Nakai, J., Hayashi, Y., & Sato, M. (2021).
    Multiple coordinated cellular dynamics mediate CA1 map plasticity. Hippocampus, 31(3), 235-243. [PubMed:33452849] [PMC] [WorldCat] [DOI]     [Google Scholar]

2020

  • Eriksen, M.S., Nikolaienko, O., Hallin, E.I., Grødem, S., Bustad, H.J., Flydal, M.I., ..., & Bramham, C.R. (2021).
    Arc self-association and formation of virus-like capsids are mediated by an N-terminal helical coil motif. The FEBS journal, 288(9), 2930-2955. [PubMed:33175445] [WorldCat] [DOI]     [Google Scholar]
  • Sato, M., Mizuta, K., Islam, T., Kawano, M., Sekine, Y., Takekawa, T., ..., & Hayashi, Y. (2020).
    Distinct Mechanisms of Over-Representation of Landmarks and Rewards in the Hippocampus. Cell reports, 32(1), 107864. [PubMed:32640229] [PMC] [WorldCat] [DOI]     [Google Scholar]
  • Luchetti, A., Bota, A., Weitemier, A., Mizuta, K., Sato, M., Islam, T., ..., & Hayashi, Y. (2020).
    Two Functionally Distinct Serotonergic Projections into Hippocampus. The Journal of neuroscience : the official journal of the Society for Neuroscience, 40(25), 4936-4944. [PubMed:32414785] [PMC] [WorldCat] [DOI]     [Google Scholar]
  • Cai, Q., Hosokawa, T., Zeng, M., Hayashi, Y., & Zhang, M. (2020).
    Shank3 Binds to and Stabilizes the Active Form of Rap1 and HRas GTPases via Its NTD-ANK Tandem with Distinct Mechanisms. Structure (London, England : 1993), 28(3), 290-300.e4. [PubMed:31879129] [WorldCat] [DOI]     [Google Scholar]

2019

  • Kojima, H., Rosendale, M., Sugiyama, Y., Hayashi, M., Horiguchi, Y., Yoshihara, T., ..., & Hayashi, Y. (2019).
    The role of CaMKII-Tiam1 complex on learning and memory. Neurobiology of learning and memory, 166, 107070. [PubMed:31445077] [WorldCat] [DOI]     [Google Scholar]
  • Saneyoshi, T., Matsuno, H., Suzuki, A., Murakoshi, H., Hedrick, N.G., Agnello, E., ..., & Hayashi, Y. (2019).
    Reciprocal Activation within a Kinase-Effector Complex Underlying Persistence of Structural LTP. Neuron, 102(6), 1199-1210.e6. [PubMed:31078368] [PMC] [WorldCat] [DOI]     [Google Scholar]
  • Ghandour, K., Ohkawa, N., Fung, C.C.A., Asai, H., Saitoh, Y., Takekawa, T., ..., & Inokuchi, K. (2019).
    Orchestrated ensemble activities constitute a hippocampal memory engram. Nature communications, 10(1), 2637. [PubMed:31201332] [PMC] [WorldCat] [DOI]
  • Kobayashi, T., Islam, T., Sato, M., Ohkura, M., Nakai, J., Hayashi, Y., & Okamoto, H. (2019).
    Wide and Deep Imaging of Neuronal Activities by a Wearable NeuroImager Reveals Premotor Activity in the Whole Motor Cortex. Scientific reports, 9(1), 8366. [PubMed:31182818] [PMC] [WorldCat] [DOI]
  • Kim, K., Suzuki, A., Kojima, H., Kawamura, M., Miya, K., Abe, M., ..., & Hayashi, Y. (2019).
    Autophosphorylation of F-actin binding domain of CaMKIIβ is required for fear learning. Neurobiology of learning and memory, 157, 86-95. [PubMed:30528771] [WorldCat] [DOI]

2024

  • Kaizuka, T., Hirouchi, T., Saneyoshi, T., Shirafuji, T., Collins, M.O., Grant, S.G.N., ..., & Takumi, T. (2024).
    FAM81A is a postsynaptic protein that regulates the condensation of postsynaptic proteins via liquid-liquid phase separation. PLoS biology, 22(3), e3002006. [PubMed:38452102] [PMC] [WorldCat] [DOI]     [Google Scholar]

2023

  • Ripoli, C., Dagliyan, O., Renna, P., Pastore, F., Paciello, F., Sollazzo, R., ..., & Grassi, C. (2023).
    Engineering memory with an extrinsically disordered kinase. Science advances, 9(46), eadh1110. [PubMed:37967196] [PMC] [WorldCat] [DOI]     [Google Scholar]

2022

  • Özden, C., Sloutsky, R., Mitsugi, T., Santos, N., Agnello, E., Gaubitz, C., ..., & Stratton, M.M. (2022).
    CaMKII binds both substrates and activators at the active site. Cell reports, 40(2), 111064. [PubMed:35830796] [PMC] [WorldCat] [DOI]     [Google Scholar]

2021

  • Goto, A., Bota, A., Miya, K., Wang, J., Tsukamoto, S., Jiang, X., ..., & Hayashi, Y. (2021).
    Stepwise synaptic plasticity events drive the early phase of memory consolidation. Science (New York, N.Y.), 374(6569), 857-863. [PubMed:34762472] [WorldCat] [DOI]     [Google Scholar]
  • Cid, E., Marquez-Galera, A., Valero, M., Gal, B., Medeiros, D.C., Navarron, C.M., ..., & de la Prida, L.M. (2021).
    Sublayer- and cell-type-specific neurodegenerative transcriptional trajectories in hippocampal sclerosis. Cell reports, 35(10), 109229. [PubMed:34107264] [WorldCat] [DOI]     [Google Scholar]
  • Takamura, R., Mizuta, K., Sekine, Y., Islam, T., Saito, T., Sato, M., ..., & Hayashi, Y. (2021).
    Modality-Specific Impairment of Hippocampal CA1 Neurons of Alzheimer's Disease Model Mice. The Journal of neuroscience : the official journal of the Society for Neuroscience, 41(24), 5315-5329. [PubMed:33980545] [PMC] [WorldCat] [DOI]     [Google Scholar]
  • Hosokawa, T., Liu, P.W., Cai, Q., Ferreira, J.S., Levet, F., Butler, C., ..., & Hayashi, Y. (2021).
    CaMKII activation persistently segregates postsynaptic proteins via liquid phase separation. Nature neuroscience, 24(6), 777-785. [PubMed:33927400] [WorldCat] [DOI]     [Google Scholar]
  • File:Kastian Cell Rep 2021.pdf
    Kastian, R.F., Minegishi, T., Baba, K., Saneyoshi, T., Katsuno-Kambe, H., Saranpal, S., ..., & Inagaki, N. (2021).
    Shootin1a-mediated actin-adhesion coupling generates force to trigger structural plasticity of dendritic spines. Cell reports, 35(7), 109130. [PubMed:34010643] [WorldCat] [DOI]     [Google Scholar]
  • Mizuta, K., Nakai, J., Hayashi, Y., & Sato, M. (2021).
    Multiple coordinated cellular dynamics mediate CA1 map plasticity. Hippocampus, 31(3), 235-243. [PubMed:33452849] [PMC] [WorldCat] [DOI]     [Google Scholar]

2020

  • Eriksen, M.S., Nikolaienko, O., Hallin, E.I., Grødem, S., Bustad, H.J., Flydal, M.I., ..., & Bramham, C.R. (2021).
    Arc self-association and formation of virus-like capsids are mediated by an N-terminal helical coil motif. The FEBS journal, 288(9), 2930-2955. [PubMed:33175445] [WorldCat] [DOI]     [Google Scholar]
  • Sato, M., Mizuta, K., Islam, T., Kawano, M., Sekine, Y., Takekawa, T., ..., & Hayashi, Y. (2020).
    Distinct Mechanisms of Over-Representation of Landmarks and Rewards in the Hippocampus. Cell reports, 32(1), 107864. [PubMed:32640229] [PMC] [WorldCat] [DOI]     [Google Scholar]
  • Luchetti, A., Bota, A., Weitemier, A., Mizuta, K., Sato, M., Islam, T., ..., & Hayashi, Y. (2020).
    Two Functionally Distinct Serotonergic Projections into Hippocampus. The Journal of neuroscience : the official journal of the Society for Neuroscience, 40(25), 4936-4944. [PubMed:32414785] [PMC] [WorldCat] [DOI]     [Google Scholar]
  • Cai, Q., Hosokawa, T., Zeng, M., Hayashi, Y., & Zhang, M. (2020).
    Shank3 Binds to and Stabilizes the Active Form of Rap1 and HRas GTPases via Its NTD-ANK Tandem with Distinct Mechanisms. Structure (London, England : 1993), 28(3), 290-300.e4. [PubMed:31879129] [WorldCat] [DOI]     [Google Scholar]

2019

  • Kojima, H., Rosendale, M., Sugiyama, Y., Hayashi, M., Horiguchi, Y., Yoshihara, T., ..., & Hayashi, Y. (2019).
    The role of CaMKII-Tiam1 complex on learning and memory. Neurobiology of learning and memory, 166, 107070. [PubMed:31445077] [WorldCat] [DOI]     [Google Scholar]
  • Saneyoshi, T., Matsuno, H., Suzuki, A., Murakoshi, H., Hedrick, N.G., Agnello, E., ..., & Hayashi, Y. (2019).
    Reciprocal Activation within a Kinase-Effector Complex Underlying Persistence of Structural LTP. Neuron, 102(6), 1199-1210.e6. [PubMed:31078368] [PMC] [WorldCat] [DOI]     [Google Scholar]
  • Ghandour, K., Ohkawa, N., Fung, C.C.A., Asai, H., Saitoh, Y., Takekawa, T., ..., & Inokuchi, K. (2019).
    Orchestrated ensemble activities constitute a hippocampal memory engram. Nature communications, 10(1), 2637. [PubMed:31201332] [PMC] [WorldCat] [DOI]
  • Kobayashi, T., Islam, T., Sato, M., Ohkura, M., Nakai, J., Hayashi, Y., & Okamoto, H. (2019).
    Wide and Deep Imaging of Neuronal Activities by a Wearable NeuroImager Reveals Premotor Activity in the Whole Motor Cortex. Scientific reports, 9(1), 8366. [PubMed:31182818] [PMC] [WorldCat] [DOI]
  • Kim, K., Suzuki, A., Kojima, H., Kawamura, M., Miya, K., Abe, M., ..., & Hayashi, Y. (2019).
    Autophosphorylation of F-actin binding domain of CaMKIIβ is required for fear learning. Neurobiology of learning and memory, 157, 86-95. [PubMed:30528771] [WorldCat] [DOI]
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