Kazuo Nakajima

Itabashi, 1738605, Japan

Last Updated: 09/26/2026

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Found 17 publications

Author Correction: Utility of a commercial antibody against NTRK1 for western blotting and potential application to immunohistochemistry in adult mouse brain.

Author Correction: Utility of a commercial antibody against NTRK1 for western blotting and potential application to immunohistochemistry in adult mouse brain.

Journal: Scientific reports
Published: April 24, 2025

Possible role of mosaic mutations of neurodevelopmental disorder-related genes in bipolar disorder: Lessons from Kmt2c chimeric heterozygous knockout mice.

Possible role of mosaic mutations of neurodevelopmental disorder-related genes in bipolar disorder: Lessons from Kmt2c chimeric heterozygous knockout mice.

Journal: Neuroscience research
Published: February 17, 2025

Utility of a commercial antibody against NTRK1 for western blotting and potential application to immunohistochemistry in adult mouse brain.

Utility of a commercial antibody against NTRK1 for western blotting and potential application to immunohistochemistry in adult mouse brain.

Journal: Scientific reports
Published: February 07, 2024

Transcriptomic dysregulation and autistic-like behaviors in Kmt2c haploinsufficient mice rescued by an LSD1 inhibitor.

Transcriptomic dysregulation and autistic-like behaviors in Kmt2c haploinsufficient mice rescued by an LSD1 inhibitor.

Journal: Molecular psychiatry
Published: January 05, 2024

Functional and behavioral effects of de novo mutations in calcium-related genes in patients with bipolar disorder.

Functional and behavioral effects of de novo mutations in calcium-related genes in patients with bipolar disorder.

Journal: Human molecular genetics
Published: May 09, 2021

Brain-specific heterozygous loss-of-function of ATP2A2, endoplasmic reticulum Ca2+ pump responsible for Darier's disease, causes behavioral abnormalities and a hyper-dopaminergic state.

Brain-specific heterozygous loss-of-function of ATP2A2, endoplasmic reticulum Ca2+ pump responsible for Darier's disease, causes behavioral abnormalities and a hyper-dopaminergic state.

Journal: Human molecular genetics
Published: March 23, 2021

Development of x-ray mirror foils using a hot plastic deformation process.

Development of x-ray mirror foils using a hot plastic deformation process.

Journal: Applied optics
Published: October 26, 2020

Ntrk1 mutation co-segregating with bipolar disorder and inherited kidney disease in a multiplex family causes defects in neuronal growth and depression-like behavior in mice.

Ntrk1 mutation co-segregating with bipolar disorder and inherited kidney disease in a multiplex family causes defects in neuronal growth and depression-like behavior in mice.

Journal: Translational psychiatry
Published: February 17, 2020

Glutamine-induced signaling pathways via amino acid receptors in enteroendocrine L cell lines.

Glutamine-induced signaling pathways via amino acid receptors in enteroendocrine L cell lines.

Journal: Journal of molecular endocrinology
Published: December 22, 2019

De novo UNC13B mutation identified in a bipolar disorder patient increases a rare exon-skipping variant.

De novo UNC13B mutation identified in a bipolar disorder patient increases a rare exon-skipping variant.

Journal: Neuropsychopharmacology reports
Published: June 26, 2018

Quantitative evaluation of incomplete preweaning lethality in mice by using the CRISPR/Cas9 system.

Quantitative evaluation of incomplete preweaning lethality in mice by using the CRISPR/Cas9 system.

Journal: Scientific reports
Published: June 08, 2018

Loss of function mutations in ATP2A2 and psychoses: A case report and literature survey.

Loss of function mutations in ATP2A2 and psychoses: A case report and literature survey.

Journal: Psychiatry and clinical neurosciences
Published: March 06, 2016
Showing 1-12 of 17

Last Updated: 09/26/2026