Yohei Nitta

4PUBLICATIONS
25CO-AUTHORS
NeurogeneticsVision scienceMolecular targets
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Publications (4)

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|Jun 23, 2026
Hemizygous loss-of-function variants of EIF1AX are associated with a syndromic neurodevelopmental disorder.

|Aug 23, 2024
<i>Drosophila</i> model to clarify the pathological significance of OPA1 in autosomal dominant optic atrophy.

Yohei Nitta, Jiro Osaka, Ryuto Maki

|Jun 01, 2024
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

|Mar 05, 2021
Glial insulin regulates cooperative or antagonistic Golden goal/Flamingo interactions during photoreceptor axon guidance.

Hiroki Takechi, Satoko Hakeda-Suzuki, Yohei Nitta

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Frequent Collaborators

3 joint publications

Atsushi Sugie

2 joint publications

Takashi Suzuki

1 joint publications

Satoko Hakeda-Suzuki

1 joint publications

Makoto Sato

1 joint publications

Samuel D Chauvin

1 joint publications

Fang R Zhao

1 joint publications

Rie Saito

1 joint publications

Shin Koide

1 joint publications

Guanqun Liu

1 joint publications

Raphaël Rodriguez

Frequent Collaborators

3 joint publications

Atsushi Sugie

2 joint publications

Takashi Suzuki

1 joint publications

Satoko Hakeda-Suzuki

1 joint publications

Makoto Sato

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