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Proceedings of the National Academy of Sciences of the United States of America|August 7, 2023
Astrocyte-targeting therapy rescues cognitive impairment caused by neuroinflammation via the Nrf2 pathwayAkiko Nakano-Kobayashi, Andres Canela, Toru Yoshihara, et al.
Neuron|October 25, 2011
Rapid synthesis of the X-linked mental retardation protein OPHN1 mediates mGluR-dependent LTD through interaction with the endocytic machineryNael Nadif Kasri, Akiko Nakano-Kobayashi, Linda Van Aelst
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 27, 2014
The X-linked mental retardation protein OPHN1 interacts with Homer1b/c to control spine endocytic zone positioning and expression of synaptic potentiationAkiko Nakano-Kobayashi, Yilin Tai, Nael Nadif Kasri, et al.
Current Biology : CB|June 2, 2009
The Rho-linked mental retardation protein OPHN1 controls synaptic vesicle endocytosis via endophilin A1Akiko Nakano-Kobayashi, Nael Nadif Kasri, Sarah E Newey, et al.
Pharmacology & Therapeutics|October 1, 2018
DYRK1A and cognition: A lifelong relationshipMaria L Arbones, Aurore Thomazeau, Akiko Nakano-Kobayashi, et al.
Genes & Development|June 3, 2009
The Rho-linked mental retardation protein oligophrenin-1 controls synapse maturation and plasticity by stabilizing AMPA receptorsNael Nadif Kasri, Akiko Nakano-Kobayashi, Roberto Malinow, et al.
BMC Biology|March 2, 2025
Switching of OAS1 splicing isoforms overcomes SNP-derived vulnerability to SARS-CoV-2 infectionKei Iida, Masahiko Ajiro, Akiko Nakano-Kobayashi, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 7, 2017
Prenatal neurogenesis induction therapy normalizes brain structure and function in Down syndrome miceAkiko Nakano-Kobayashi, Tomonari Awaya, Isao Kii, et al.
The EMBO Journal|February 10, 2007
Role of activation of PIP5Kgamma661 by AP-2 complex in synaptic vesicle endocytosisAkiko Nakano-Kobayashi, Masakazu Yamazaki, Takamitsu Unoki, et al.
RNA (New York, N.Y.)|June 9, 2017
RBM24 promotes U1 snRNP recognition of the mutated 5' splice site in the <i>IKBKAP</i> gene of familial dysautonomiaKenji Ohe, Mayumi Yoshida, Akiko Nakano-Kobayashi, et al.
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