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Neurobiology of Disease|January 17, 2018
Impairments in social novelty recognition and spatial memory in mice with conditional deletion of Scn1a in parvalbumin-expressing cellsTetsuya Tatsukawa, Ikuo Ogiwara, Emi Mazaki, et al.Neurobiology of Disease|December 11, 2017
DYRK1A-haploinsufficiency in mice causes autistic-like features and febrile seizuresMatthieu Raveau, Atsushi Shimohata, Kenji Amano, et al.Molecular and Cellular Neurosciences|June 23, 2023
The intracellular C-terminal domain of mGluR6 contains ER retention motifsAtsushi Shimohata, Dilip Rai, Takumi Akagi, et al.Journal of Molecular Neuroscience : MN|May 27, 2026
N-Glycosylation of mGluR6 Modulates Receptor Cell-Surface Transport, G-Protein Coupling, and Interactions With Synaptic Adhesion MoleculesTakumi Akagi, Ikuo Ogiwara, Atsushi Shimohata, et al.Cerebral Cortex (New York, N.Y. : 1991)|August 28, 2009
Enlarged brain ventricles and impaired neurogenesis in the Ts1Cje and Ts2Cje mouse models of Down syndromeKeiichi Ishihara, Kenji Amano, Eiichi Takaki, et al.Human Molecular Genetics|January 11, 2017
Brain ventriculomegaly in Down syndrome mice is caused by Pcp4 dose-dependent cilia dysfunctionMatthieu Raveau, Takashi Nakahari, Sachie Asada, et al.Journal of Neurochemistry|October 17, 2020
Involvement of the C-terminal domain in cell surface localization and G-protein coupling of mGluR6Dilip Rai, Takumi Akagi, Atsushi Shimohata, et al.Human Molecular Genetics|October 18, 2017
Potentiation of excitatory synaptic transmission ameliorates aggression in mice with Stxbp1 haploinsufficiencyHiroyuki Miyamoto, Atsushi Shimohata, Manabu Abe, et al.Molecular and Cellular Neurosciences|April 18, 2026
Myoclonin1 haploinsufficiency in motile ciliated cells partially recapitulates epileptic features of Efhc1-deficient mice in adult ageToshimitsu Suzuki, Tetsuya Tatsukawa, Genki Sudo, et al.Journal of Neurochemistry|August 4, 2009
Increased lipid peroxidation in Down's syndrome mouse modelsKeiichi Ishihara, Kenji Amano, Eiichi Takaki, et al.Pageof 2