Nozomu Yoshioka
Niigata, Japan
Last Updated: 09/26/2026
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Found 23 publications
Disruption of afferent neural circuits leads to arrhythmia in the animal model of hereditary sensory and autonomic neuropathy 6.
Journal: Frontiers in neural circuits
Published: December 29, 2025
Sensory-motor circuit is a therapeutic target for dystonia musculorum mice, a model of hereditary sensory and autonomic neuropathy 6.
Journal: Science advances
Published: July 26, 2024
Roles of dystonin isoforms in the maintenance of neural, muscle, and cutaneous tissues.
Journal: Anatomical science international
Published: May 31, 2023
Attenuated cerebellar phenotypes in Inpp4a truncation mutants with preserved phosphatase activity.
Journal: Disease models & mechanisms
Published: March 06, 2023
Astrocytic dysfunction induced by ABCA1 deficiency causes optic neuropathy.
Journal: Science advances
Published: November 04, 2022
Lethal adulthood myelin breakdown by oligodendrocyte-specific Ddx54 knockout.
Journal: iScience
Published: February 21, 2022
Perturbation of monoamine metabolism and enhanced fear responses in mice defective in the regeneration of tetrahydrobiopterin.
Journal: Journal of neurochemistry
Published: November 03, 2021
Retrograde gene transfer into neural pathways mediated by adeno-associated virus (AAV)-AAV receptor interaction.
Journal: Journal of neuroscience methods
Published: April 11, 2020
Disruption of dystonin in Schwann cells results in late-onset neuropathy and sensory ataxia.
Journal: Glia
Published: March 13, 2020
Diverse dystonin gene mutations cause distinct patterns of Dst isoform deficiency and phenotypic heterogeneity in Dystonia musculorum mice.
Journal: Disease models & mechanisms
Published: July 23, 2019
Motoneuron degeneration in the trigeminal motor nucleus innervating the masseter muscle in Dystonia musculorum mice.
Journal: Neurochemistry international
Published: June 09, 2017
Last Updated: 09/26/2026