Shinichi Hirose

4PUBLICATIONS
25CO-AUTHORS
Developmental genetics (incl. sex determination)Epigenetics (incl. genome methylation and epigenomics)Cell and nuclear divisionSystem and network security
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Publications (4)

|Jun 18, 2025
SCN1A gain of function effects in Dravet syndrome: Insights into clinical phenotypes and therapeutic implications.

Yoko Kobayashi Takahashi, Kenshiro Tabata, Shimpei Baba

|May 17, 2022
CUX2 deficiency causes facilitation of excitatory synaptic transmission onto hippocampus and increased seizure susceptibility to kainate.

Toshimitsu Suzuki, Tetsuya Tatsukawa, Genki Sudo

|Aug 18, 2021
Genome sequencing and RNA-seq analyses of mitochondrial complex I deficiency revealed Alu insertion-mediated deletion in NDUFV2.

Yoshihito Kishita, Masaru Shimura, Masakazu Kohda

|May 21, 2021
Inhibitory synaptic transmission is impaired at higher extracellular Ca2+ concentrations in Scn1a+/- mouse model of Dravet syndrome.

Kouya Uchino, Hiroyuki Kawano, Yasuyoshi Tanaka

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Frequent Collaborators

1 joint publications

Kouya Uchino

1 joint publications

Hiroyuki Kawano

1 joint publications

Yasuyoshi Tanaka

1 joint publications

Shutaro Katsurabayashi