Kenichiro Nagahama
Affiliations: | Johns Hopkins University School of Medicine, Baltimore, MD, United States |
Area:
NeuroscienceGoogle:
"Kenichiro Nagahama"Mean distance: (not calculated yet)
Parents
Sign in to add mentorKatsunori Kobayashi | research assistant | 2009-2011 | Nippon Medical School |
Masanobu Kano | grad student | 2015-2020 | Graduate School of Medicine, The University of Tokyo |
Naofumi Uesaka | grad student | 2015-2020 | Tokyo Medical and Dental University Graduate School |
Hyungbae Kwon | post-doc | 2020- | Johns Hopkins Medical School |
Collaborators
Sign in to add collaboratorPaul F. Worley | collaborator | 2021- | Johns Hopkins Medical School |
Tomomi Karigo | collaborator | 2022- | Johns Hopkins School of Medicine and Kennedy Krieger Institute |
Atsu Aiba | collaborator | 2017-2020 | Graduate School of Medicine, The University of Tokyo |
Yukiko Gotoh | collaborator | 2017-2020 | Graduate School of Pharmaceutical Sciences, The University of Tokyo |
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Publications
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Son S, Nagahama K, Lee J, et al. (2024) Real-time visualization of structural dynamics of synapses in live cells in vivo. Nature Methods |
Obi-Nagata K, Suzuki N, Miyake R, et al. (2023) Distorted neurocomputation by a small number of extra-large spines in psychiatric disorders. Science Advances. 9: eade5973 |
Hyun JH, Nagahama K, Namkung H, et al. (2022) Tagging active neurons by soma-targeted Cal-Light. Nature Communications. 13: 7692 |
Toriumi K, Berto S, Koike S, et al. (2021) Combined glyoxalase 1 dysfunction and vitamin B6 deficiency in a schizophrenia model system causes mitochondrial dysfunction in the prefrontal cortex. Redox Biology. 45: 102057 |
Nagahama K, Fujino S, Watanabe T, et al. (2021) Combining electrophysiology and optogenetics for functional screening of pyramidal neurons in the mouse prefrontal cortex. Star Protocols. 2: 100469 |
Sacai H, Sakoori K, Konno K, et al. (2020) Autism spectrum disorder-like behavior caused by reduced excitatory synaptic transmission in pyramidal neurons of mouse prefrontal cortex. Nature Communications. 11: 5140 |
Nagahama K, Sakoori K, Watanabe T, et al. (2020) Setd1a Insufficiency in Mice Attenuates Excitatory Synaptic Function and Recapitulates Schizophrenia-Related Behavioral Abnormalities. Cell Reports. 32: 108126 |
Saito R, Koebis M, Nagai T, et al. (2020) Comprehensive analysis of a novel mouse model of the 22q11.2 deletion syndrome: a model with the most common 3.0-Mb deletion at the human 22q11.2 locus. Translational Psychiatry. 10: 35 |