Yoshitsugu Aoki
Kodaira, 1878502, Japan
Last Updated: 09/26/2026
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Found 113 publications
DMD-Null mice exhibit severe muscle weakness, impaired regeneration, and deficient satellite cell function.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: June 16, 2026
Systemic regeneration medicines for muscular dystrophy: progress and challenges in pro-regenerative drug development.
Journal: Cell regeneration (London, England)
Published: March 04, 2026
Making brain health routine in Duchenne muscular dystrophy: What the BIND screener adds-and what it is not designed to do.
Journal: Developmental medicine and child neurology
Published: January 11, 2026
RNA Therapeutics for Duchenne Muscular Dystrophy: Exon Skipping, RNA Editing, and Translational Insights from Genome-Edited Microminipig Models.
Journal: International journal of molecular sciences
Published: December 08, 2025
Tppp3 determines basal body positioning and identity of respiratory cilia via microtubule assembly and sphingolipid homeostasis.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: December 01, 2025
Dystrophin-gene mutation location influences severity of electroretinogram defects in mouse models of Duchenne muscular dystrophy.
Journal: BMC medicine
Published: November 28, 2025
Glutamine Promotes Myogenesis in Myoblasts Through Glutaminolysis-Mediated Histone H3 Acetylation That Enhances Myogenin Transcription.
Journal: Nutrients
Published: October 18, 2025
Splice Modulation Studies Using Urine-Derived Cells.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: October 01, 2025
Digital Outcome Measures for Gait and Spontaneous Locomotor Activity in Dystrophic Dogs.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: October 01, 2025
Splice Modulation Studies Using Reporter Mice.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: October 01, 2025
Neurological Behavioral Assessment of Exon-Skipping Therapy for Neuromuscular Disorders Using Displaced Object Recognition Test, Open Field Test, and Three-Chamber Social Approach Test.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: October 01, 2025
In Vivo Evaluation of CTG Repeat-Affected Muscle Pathology in a Myotonic Dystrophy Model Mouse Using Electromyography and Fluorescence In Situ Hybridization.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: October 01, 2025
Last Updated: 09/26/2026