Publications by authors named "Ryuto Maki"

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model to clarify the pathological significance of OPA1 in autosomal dominant optic atrophy.
Yohei Nitta, Jiro Osaka, Ryuto Maki, Satoko Hakeda-Suzuki, Emiko Suzuki

Elife· August 2024

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Functional analysis of pathogenic variants with a Noonan-like phenotype.
Takaya Iida, Arisa Igarashi, Kae Fukunaga, Taiga Aoki, Tomomi Hidai, Ryuto Maki

Front Genet· March 2024

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Direct evaluation of neuroaxonal degeneration with the causative genes of neurodegenerative diseases in Drosophila using the automated axon quantification system, MeDUsA.
Yohei Nitta, Hiroki Kawai, Ryuto Maki, Jiro Osaka, Satoko Hakeda-Suzuki

Hum Mol Genet· April 2023

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Publisher Correction: A novel NONO variant that causes developmental delay and cardiac phenotypes.
Toshiyuki Itai, Atsushi Sugie, Yohei Nitta, Ryuto Maki, Takashi Suzuki

Sci Rep· March 2023

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A novel NONO variant that causes developmental delay and cardiac phenotypes.
Toshiyuki Itai, Atsushi Sugie, Yohei Nitta, Ryuto Maki, Takashi Suzuki

Sci Rep· January 2023

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