Publications by authors named "Emi Mazaki"

Claim this Profile
R
Rapid and cumulative adult plasticity in the mouse visual cortex.
Hiroyuki Miyamoto, Emi Mazaki, Yuichi Makino, Qi Fang, Tomohito Hamada

Front Neural Circuits· May 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
-
-GFP transgenic mouse revealed Nav1.1 expression in neocortical pyramidal tract projection neurons.
Tetsushi Yamagata, Ikuo Ogiwara, Tetsuya Tatsukawa, Toshimitsu Suzuki, Yuka Otsuka, Emi Mazaki

Elife· May 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A recurrent PJA1 variant in trigonocephaly and neurodevelopmental disorders.
Toshimitsu Suzuki, Toshifumi Suzuki, Matthieu Raveau, Noriko Miyake, Genki Sudo, Emi Mazaki

Ann Clin Transl Neurol· July 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
haploinsufficient mice display a spectrum of phenotypes affecting anxiety, sociability, memory flexibility and ampakine CX516 rescues their hyperactivity.
Tetsuya Tatsukawa, Matthieu Raveau, Ikuo Ogiwara, Satoko Hattori, Hiroyuki Miyamoto, Emi Mazaki

Mol Autism· May 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Impaired cortico-striatal excitatory transmission triggers epilepsy.
Hiroyuki Miyamoto, Tetsuya Tatsukawa, Atsushi Shimohata, Tetsushi Yamagata, Toshimitsu Suzuki, Emi Mazaki

Nat Commun· April 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
[
[F]fluorodeoxyglucose-positron emission tomography study of genetically confirmed patients with Dravet syndrome.
Kazuhiro Haginoya, Noriko Togashi, Tomohiro Kaneta, Naomi Hino-Fukuyo, Mamiko Ishitobi, Emi Mazaki

Epilepsy Res· November 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Nav1.2 haplodeficiency in excitatory neurons causes absence-like seizures in mice.
Ikuo Ogiwara, Hiroyuki Miyamoto, Tetsuya Tatsukawa, Tetsushi Yamagata, Tojo Nakayama, Emi Mazaki

Commun Biol· July 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Impairments in social novelty recognition and spatial memory in mice with conditional deletion of Scn1a in parvalbumin-expressing cells.
Tetsuya Tatsukawa, Ikuo Ogiwara, Emi Mazaki, Atsushi Shimohata, Kazuhiro Yamakawa

Neurobiol Dis· April 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Potentiation of excitatory synaptic transmission ameliorates aggression in mice with Stxbp1 haploinsufficiency.
Hiroyuki Miyamoto, Atsushi Shimohata, Manabu Abe, Teruo Abe, Emi Mazaki

Hum Mol Genet· December 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Nav1.2 is expressed in caudal ganglionic eminence-derived disinhibitory interneurons: Mutually exclusive distributions of Nav1.1 and Nav1.2.
Tetsushi Yamagata, Ikuo Ogiwara, Emi Mazaki, Yuchio Yanagawa, Kazuhiro Yamakawa

Biochem Biophys Res Commun· September 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Nav1.1 haploinsufficiency in excitatory neurons ameliorates seizure-associated sudden death in a mouse model of Dravet syndrome.
Ikuo Ogiwara, Takuji Iwasato, Hiroyuki Miyamoto, Ryohei Iwata, Tetsushi Yamagata, Emi Mazaki

Hum Mol Genet· December 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A homozygous mutation of voltage-gated sodium channel β(I) gene SCN1B in a patient with Dravet syndrome.
Ikuo Ogiwara, Tojo Nakayama, Tetsushi Yamagata, Hideyuki Ohtani, Emi Mazaki

Epilepsia· December 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Acute encephalopathy with a truncation mutation in the SCN1A gene: a case report.
Masaru Takayanagi, Kazuhiro Haginoya, Naoki Umehara, Taro Kitamura, Yurika Numata, Emi Mazaki

Epilepsia· September 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Deletions of SCN1A 5' genomic region with promoter activity in Dravet syndrome.
Tojo Nakayama, Ikuo Ogiwara, Koichi Ito, Makoto Kaneda, Emi Mazaki

Hum Mutat· July 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Patients with a sodium channel alpha 1 gene mutation show wide phenotypic variation.
Hitoshi Osaka, Ikuo Ogiwara, Emi Mazaki, Nami Okamura, Sumimasa Yamashita

Epilepsy Res· June 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation.
Ikuo Ogiwara, Hiroyuki Miyamoto, Noriyuki Morita, Nafiseh Atapour, Emi Mazaki

J Neurosci· May 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A Kv4.2 truncation mutation in a patient with temporal lobe epilepsy.
Baljinder Singh, Ikuo Ogiwara, Makoto Kaneda, Natsuko Tokonami, Emi Mazaki

Neurobiol Dis· November 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
SCN1A mutation mosaicism in a family with severe myoclonic epilepsy in infancy.
Masafumi Morimoto, Emi Mazaki, Akira Nishimura, Tomohiro Chiyonobu, Yasuko Sawai

Epilepsia· October 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A nonsense mutation of the sodium channel gene SCN2A in a patient with intractable epilepsy and mental decline.
Kazusaku Kamiya, Makoto Kaneda, Takashi Sugawara, Emi Mazaki, Nami Okamura

J Neurosci· March 2004

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis