hiroyuki miyamoto
hiroyuki miyamoto
IRCN, university of Tokyo
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Nav1. 1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation
I Ogiwara, H Miyamoto, N Morita, N Atapour, E Mazaki, I Inoue, ...
Journal of Neuroscience 27 (22), 5903-5914, 2007
Selective control of inhibitory synapse development by Slitrk3-PTPδ trans-synaptic interaction
H Takahashi, K Katayama, K Sohya, H Miyamoto, T Prasad, Y Matsumoto, ...
Nature neuroscience 15 (3), 389-398, 2012
Separable features of visual cortical plasticity revealed by N-methyl-d-aspartate receptor 2A signaling
M Fagiolini, H Katagiri, H Miyamoto, H Mori, SGN Grant, M Mishina, ...
Proceedings of the National Academy of Sciences 100 (5), 2854-2859, 2003
Nav1. 1 haploinsufficiency in excitatory neurons ameliorates seizure-associated sudden death in a mouse model of Dravet syndrome
I Ogiwara, T Iwasato, H Miyamoto, R Iwata, T Yamagata, E Mazaki, ...
Human molecular genetics 22 (23), 4784-4804, 2013
A theory of the transition to critical period plasticity: inhibition selectively suppresses spontaneous activity
T Toyoizumi, H Miyamoto, Y Yazaki-Sugiyama, N Atapour, TK Hensch, ...
Neuron 80 (1), 51-63, 2013
Experience-dependent slow-wave sleep development
H Miyamoto, H Katagiri, T Hensch
Nature neuroscience 6 (6), 553-554, 2003
Mouse with Nav1. 1 haploinsufficiency, a model for Dravet syndrome, exhibits lowered sociability and learning impairment
S Ito, I Ogiwara, K Yamada, H Miyamoto, TK Hensch, M Osawa, ...
Neurobiology of disease 49, 29-40, 2013
Elfn1 recruits presynaptic mGluR7 in trans and its loss results in seizures
NH Tomioka, H Yasuda, H Miyamoto, M Hatayama, N Morimura, ...
Nature communications 5 (1), 4501, 2014
Nav1. 2 haplodeficiency in excitatory neurons causes absence-like seizures in mice
I Ogiwara, H Miyamoto, T Tatsukawa, T Yamagata, T Nakayama, ...
Communications biology 1 (1), 96, 2018
Impaired cortico-striatal excitatory transmission triggers epilepsy
H Miyamoto, T Tatsukawa, A Shimohata, T Yamagata, T Suzuki, K Amano, ...
Nature communications 10 (1), 1917, 2019
CRISPR/dCas9-based Scn1a gene activation in inhibitory neurons ameliorates epileptic and behavioral phenotypes of Dravet syndrome model mice
T Yamagata, M Raveau, K Kobayashi, H Miyamoto, T Tatsukawa, ...
Neurobiology of Disease 141, 104954, 2020
Efhc1 deficiency causes spontaneous myoclonus and increased seizure susceptibility
T Suzuki, H Miyamoto, T Nakahari, I Inoue, T Suemoto, B Jiang, Y Hirota, ...
Human molecular genetics 18 (6), 1099-1109, 2009
Scn2a haploinsufficient mice display a spectrum of phenotypes affecting anxiety, sociability, memory flexibility and ampakine CX516 rescues their hyperactivity
T Tatsukawa, M Raveau, I Ogiwara, S Hattori, H Miyamoto, E Mazaki, ...
Molecular Autism 10, 1-15, 2019
Serotonergic integration of circadian clock and ultradian sleep–wake cycles
H Miyamoto, E Nakamaru-Ogiso, K Hamada, TK Hensch
Journal of Neuroscience 32 (42), 14794-14803, 2012
Novel biochemical manipulation of brain serotonin reveals a role of serotonin in the circadian rhythm of sleep–wake cycles
E Nakamaru‐Ogiso, H Miyamoto, K Hamada, K Tsukada, K Takai
European Journal of Neuroscience 35 (11), 1762-1770, 2012
IP3R1 deficiency in the cerebellum/brainstem causes basal ganglia-independent dystonia by triggering tonic Purkinje cell firings in mice
C Hisatsune, H Miyamoto, M Hirono, N Yamaguchi, T Sugawara, ...
Frontiers in neural circuits 7, 156, 2013
Variant intestinal-cell kinase in juvenile myoclonic epilepsy
JN Bailey, L de Nijs, D Bai, T Suzuki, H Miyamoto, M Tanaka, C Patterson, ...
New England Journal of Medicine 378 (11), 1018-1028, 2018
DYRK1A-haploinsufficiency in mice causes autistic-like features and febrile seizures
M Raveau, A Shimohata, K Amano, H Miyamoto, K Yamakawa
Neurobiology of Disease 110, 180-191, 2018
Reciprocal interaction of sleep and synaptic plasticity
H Miyamoto, TK Hensch
Molecular Interventions 3 (7), 404, 2003
Potentiation of excitatory synaptic transmission ameliorates aggression in mice with Stxbp1 haploinsufficiency
H Miyamoto, A Shimohata, M Abe, T Abe, E Mazaki, K Amano, T Suzuki, ...
Human Molecular Genetics 26 (24), 4961-4974, 2017
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