Atsu Aiba

Affiliations: 
Graduate School of Medicine, The University of Tokyo 
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"Atsu Aiba"
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Harbers M, Nakao H, Watanabe T, et al. (2022) mGluR5 Is Substitutable for mGluR1 in Cerebellar Purkinje Cells for Motor Coordination, Developmental Synapse Elimination, and Motor Learning. Cells. 11
Mori K, Koebis M, Nakao K, et al. (2022) Loss of calsyntenin paralogs disrupts interneuron stability and mouse behavior. Molecular Brain. 15: 23
Kawarada L, Fukaya M, Saito R, et al. (2021) Telencephalon-specific Alkbh1 conditional knockout mice display hippocampal atrophy and impaired learning. Febs Letters. 595: 1671-1680
Saito R, Miyoshi C, Koebis M, et al. (2021) Two novel mouse models mimicking minor deletions in 22q11.2 deletion syndrome revealed the contribution of each deleted region to psychiatric disorders. Molecular Brain. 14: 68
Arioka Y, Shishido E, Kushima I, et al. (2020) Chromosome 22q11.2 deletion causes PERK-dependent vulnerability in dopaminergic neurons. Ebiomedicine. 63: 103138
Nagahama K, Sakoori K, Watanabe T, et al. (2020) Setd1a Insufficiency in Mice Attenuates Excitatory Synaptic Function and Recapitulates Schizophrenia-Related Behavioral Abnormalities. Cell Reports. 32: 108126
Saito R, Koebis M, Nagai T, et al. (2020) Comprehensive analysis of a novel mouse model of the 22q11.2 deletion syndrome: a model with the most common 3.0-Mb deletion at the human 22q11.2 locus. Translational Psychiatry. 10: 35
Narushima M, Yagasaki Y, Takeuchi Y, et al. (2019) The metabotropic glutamate receptor subtype 1 regulates development and maintenance of lemniscal synaptic connectivity in the somatosensory thalamus. Plos One. 14: e0226820
Sakai Y, Kassai H, Nakayama H, et al. (2019) Hyperactivation of mTORC1 disrupts cellular homeostasis in cerebellar Purkinje cells. Scientific Reports. 9: 2799
Naito R, Kassai H, Sakai Y, et al. (2018) New Features on the Expression and Trafficking of mGluR1 Splice Variants Exposed by Two Novel Mutant Mouse Lines. Frontiers in Molecular Neuroscience. 11: 439
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