Kojiro Suda
Onna, 9040495, Japan
Last Updated: 09/26/2026
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Found 10 publications
Biallelic variants in FAT3 cause axonal neuropathy with multisystem neurodevelopmental features.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: July 26, 2025
Cytoplasmic zoning by protein phase transition after membrane permeabilization.
Journal: Journal of biochemistry
Published: August 30, 2023
Drosophila models to study causative genes for human rare intractable neurological diseases.
Journal: Experimental cell research
Published: February 12, 2021
Neuron-specific knockdown of solute carrier protein SLC25A46a induces locomotive defects, an abnormal neuron terminal morphology, learning disability, and shortened lifespan.
Journal: IBRO reports
Published: December 04, 2019
Reduction of Rpd3 suppresses defects in locomotive ability and neuronal morphology induced by the knockdown of Drosophila SLC25A46 via an epigenetic pathway.
Journal: Experimental cell research
Published: September 11, 2019
Neuron-specific knockdown of Drosophila HADHB induces a shortened lifespan, deficient locomotive ability, abnormal motor neuron terminal morphology and learning disability.
Journal: Experimental cell research
Published: March 01, 2019
Novel roles of Drosophila FUS and Aub responsible for piRNA biogenesis in neuronal disorders.
Journal: Brain research
Published: June 21, 2018
Novel Drosophila model for mitochondrial diseases by targeting of a solute carrier protein SLC25A46.
Novel Drosophila model for mitochondrial diseases by targeting of a solute carrier protein SLC25A46.
Journal: Brain research
Published: January 10, 2018
Genetic screening of the genes interacting with Drosophila FIG4 identified a novel link between CMT-causing gene and long noncoding RNAs.
Journal: Experimental neurology
Published: November 15, 2017
Showing 1-10 of 10
Last Updated: 09/26/2026