Emi Mazaki
Wako, Japan
Last Updated: 09/26/2026
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Found 13 publications
Myoclonin1 haploinsufficiency in motile ciliated cells partially recapitulates epileptic features of Efhc1-deficient mice in adult age.
Journal: Molecular and cellular neurosciences
Published: January 28, 2026
Rapid and cumulative adult plasticity in the mouse visual cortex.
Journal: Frontiers in neural circuits
Published: November 30, 2024
A recurrent PJA1 variant in trigonocephaly and neurodevelopmental disorders.
Journal: Annals of clinical and translational neurology
Published: April 25, 2020
Scn2a haploinsufficient mice display a spectrum of phenotypes affecting anxiety, sociability, memory flexibility and ampakine CX516 rescues their hyperactivity.
Journal: Molecular autism
Published: December 06, 2018
Impaired cortico-striatal excitatory transmission triggers epilepsy.
Journal: Nature communications
Published: September 18, 2018
Nav1.2 haplodeficiency in excitatory neurons causes absence-like seizures in mice.
Journal: Communications biology
Published: September 04, 2018
Impairments in social novelty recognition and spatial memory in mice with conditional deletion of Scn1a in parvalbumin-expressing cells.
Journal: Neurobiology of disease
Published: September 19, 2017
Nav1.2 is expressed in caudal ganglionic eminence-derived disinhibitory interneurons: Mutually exclusive distributions of Nav1.1 and Nav1.2.
Journal: Biochemical and biophysical research communications
Published: July 26, 2017
Potentiation of excitatory synaptic transmission ameliorates aggression in mice with Stxbp1 haploinsufficiency.
Journal: Human molecular genetics
Published: June 29, 2017
Nav1.1 haploinsufficiency in excitatory neurons ameliorates seizure-associated sudden death in a mouse model of Dravet syndrome.
Journal: Human molecular genetics
Published: August 08, 2013
Last Updated: 09/26/2026