Shin-ichiro Horigane
Nagoya, Japan
Last Updated: 09/26/2026
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Found 17 publications
A hypofunctional PREX1 variant (p.Y191C) leads to neurodevelopmental abnormalities and epilepsy by attenuating RAC1 signaling.
Journal: Scientific reports
Published: November 04, 2025
A hyper-activatable CAMK2A variant associated with intellectual disability causes exaggerated long-term potentiation and learning impairments.
Journal: Translational psychiatry
Published: October 04, 2024
Ca2+ Imaging in Immature Cortical Neurons.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: April 17, 2024
Förster resonance energy transfer-based kinase mutation phenotyping reveals an aberrant facilitation of Ca2+/calmodulin-dependent CaMKIIα activity in de novo mutations related to intellectual disability.
Journal: Frontiers in molecular neuroscience
Published: June 15, 2022
Author Correction: Remote control of neural function by X-ray-induced scintillation.
Journal: Nature communications
Published: April 07, 2022
Identification of ultra-rare disruptive variants in voltage-gated calcium channel-encoding genes in Japanese samples of schizophrenia and autism spectrum disorder.
Journal: Translational psychiatry
Published: January 20, 2022
A Flp-dependent G-CaMP9a transgenic mouse for neuronal imaging in vivo.
Journal: Cell reports methods
Published: September 02, 2021
Distinctive Regulation of Emotional Behaviors and Fear-Related Gene Expression Responses in Two Extended Amygdala Subnuclei With Similar Molecular Profiles.
Journal: Frontiers in molecular neuroscience
Published: July 15, 2021
Remote control of neural function by X-ray-induced scintillation.
Journal: Nature communications
Published: May 10, 2021
Last Updated: 09/26/2026