Publications by authors named "Yohei Nitta"

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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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Inherited C-terminal TREX1 variants disrupt homology-directed repair to cause senescence and DNA damage phenotypes in Drosophila, mice, and humans.
Samuel D Chauvin, Shoichiro Ando, Joe A Holley, Atsushi Sugie, Fang R Zhao, Yohei Nitta

Nat Commun· June 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, Yohei Nitta

Front Genet· March 2024

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Heterozygous loss-of-function DHX9 variants are associated with neurodevelopmental disorders: Human genetic and experimental evidences.
Mamiko Yamada, Yohei Nitta, Tomoko Uehara, Hisato Suzuki, Fuyuki Miya

Eur J Med Genet· August 2023

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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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Identification of genes regulating stimulus-dependent synaptic assembly in Drosophila using an automated synapse quantification system.
Jiro Osaka, Haruka Yasuda, Yusuke Watanuki, Yuya Kato, Yohei Nitta

Genes Genet Syst· 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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Studies of neurodegenerative diseases using and the development of novel approaches for their analysis.
Yohei Nitta, Atsushi Sugie

Fly (Austin)· December 2022

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A Quantitative Model of Sporadic Axonal Degeneration in the Visual System.
Mélisande Richard, Karolína Doubková, Yohei Nitta, Hiroki Kawai, Atsushi Sugie

J Neurosci· June 2022

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De novo ARF3 variants cause neurodevelopmental disorder with brain abnormality.
Masamune Sakamoto, Kazunori Sasaki, Atsushi Sugie, Yohei Nitta, Tetsuaki Kimura

Hum Mol Genet· December 2021

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Glial insulin regulates cooperative or antagonistic Golden goal/Flamingo interactions during photoreceptor axon guidance.
Hiroki Takechi, Satoko Hakeda-Suzuki, Yohei Nitta, Yuichi Ishiwata, Riku Iwanaga

Elife· March 2021

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Degeneration of dopaminergic neurons and impaired intracellular trafficking in Atp13a2 deficient zebrafish.
Hiromi Nyuzuki, Shinji Ito, Keisuke Nagasaki, Yohei Nitta, Noriko Matsui

IBRO Rep· December 2020

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Analysing the evolutional and functional differentiation of four types of Daphnia magna cryptochrome in Drosophila circadian clock.
Yohei Nitta, Sayaka Matsui, Yukine Kato, Yosuke Kaga, Kenkichi Sugimoto

Sci Rep· June 2019

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Identification of glaikit in a genome-wide expression profiling for axonal bifurcation of the mushroom body in Drosophila.
Yohei Nitta, Atsushi Sugie

Biochem Biophys Res Commun· June 2017

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DISCO interacting protein 2 determines direction of axon projection under the regulation of c-Jun N-terminal kinase in the Drosophila mushroom body.
Yohei Nitta, Atsushi Sugie

Biochem Biophys Res Commun· May 2017

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DISCO Interacting Protein 2 regulates axonal bifurcation and guidance of Drosophila mushroom body neurons.
Yohei Nitta, Daisuke Yamazaki, Atsushi Sugie, Makoto Hiroi, Tetsuya Tabata

Dev Biol· January 2017

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Correction: the NAV2 homolog Sickie regulates F-actin-mediated axonal growth in Drosophila mushroom body neurons via the non-canonical Rac-Cofilin pathway.
Takashi Abe, Daisuke Yamazaki, Satoshi Murakami, Makoto Hiroi, Yohei Nitta

Development· March 2015

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The NAV2 homolog Sickie regulates F-actin-mediated axonal growth in Drosophila mushroom body neurons via the non-canonical Rac-Cofilin pathway.
Takashi Abe, Daisuke Yamazaki, Satoshi Murakami, Makoto Hiroi, Yohei Nitta

Development· December 2014

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