Fumihito Saitow
Tokyo, 1138602, Japan
Last Updated: 09/26/2026
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Found 21 publications
GPR17+ Oligodendrocyte Lineage Cells Regulate the Critical Period of Brain Development Through Novel Chondroitin Sulfate-Rich Structures.
Journal: Glia
Published: April 18, 2025
Q241R mutation of Braf causes neurological abnormalities in a mouse model of cardio-facio-cutaneous syndrome, independent of developmental malformations.
Journal: Human molecular genetics
Published: July 10, 2024
Cesarean section delivery is a risk factor of autism-related behaviors in mice.
Journal: Scientific reports
Published: November 28, 2020
Upregulated 5-HT1A receptor-mediated currents in the prefrontal cortex layer 5 neurons in the 15q11-13 duplication mouse model of autism.
Journal: Molecular brain
Published: June 03, 2020
Genetic dissection identifies Necdin as a driver gene in a mouse model of paternal 15q duplications.
Genetic dissection identifies Necdin as a driver gene in a mouse model of paternal 15q duplications.
Journal: Nature communications
Published: November 22, 2019
Change in serotonergic modulation contributes to the synaptic imbalance of neuronal circuit at the prefrontal cortex in the 15q11-13 duplication mouse model of autism.
Journal: Neuropharmacology
Published: August 13, 2019
Downregulation of Dopamine D1-like Receptor Pathways of GABAergic Interneurons in the Anterior Cingulate Cortex of Spontaneously Hypertensive Rats.
Journal: Neuroscience
Published: June 09, 2018
Developmental Changes in Serotonergic Modulation of GABAergic Synaptic Transmission and Postsynaptic GABAA Receptor Composition in the Cerebellar Nuclei.
Journal: Cerebellum (London, England)
Published: January 20, 2018
Ant1 mutant mice bridge the mitochondrial and serotonergic dysfunctions in bipolar disorder.
Journal: Molecular psychiatry
Published: January 16, 2018
Serotonin rebalances cortical tuning and behavior linked to autism symptoms in 15q11-13 CNV mice.
Journal: Science advances
Published: November 30, 2016
Last Updated: 09/26/2026