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Neuron-specific knockdown of solute carrier protein SLC25A46a induces locomotive defects, an abnormal neuron terminal morphology, learning disability, and shortened lifespan.
IBRO Rep. 2020 Feb 19;8:65-75. doi: 10.1016/j.ibror.2020.02.001. eCollection 2020 Jun.
IBRO Rep. 2020.
PMID: 32140609
Free PMC article.
Identification of Rpd3 as a novel epigenetic regulator of Drosophila FIG 4, a Charcot-Marie-Tooth disease-causing gene.
Muraoka Y, Nikaido A, Kowada R, Kimura H, Yamaguchi M, Yoshida H.
Muraoka Y, et al. Among authors: kowada r.
Neuroreport. 2021 May 5;32(7):562-568. doi: 10.1097/WNR.0000000000001636.
Neuroreport. 2021.
PMID: 33850086
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The function of Scox in glial cells is essential for locomotive ability in Drosophila.
Kowada R, Kodani A, Ida H, Yamaguchi M, Lee IS, Okada Y, Yoshida H.
Kowada R, et al.
Sci Rep. 2021 Oct 27;11(1):21207. doi: 10.1038/s41598-021-00663-2.
Sci Rep. 2021.
PMID: 34707123
Free PMC article.
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Drosophila transcription factor NF-Y suppresses transcription of the lipase 4 gene, a key gene for lipid storage.
Yoshioka Y, Anzai K, Kowada R, Hiratsuka K, Hirayabu T, Yasuda M, Ohkawa Y, Sato T, Suyama M, Yoshida H, Yamaguchi M.
Yoshioka Y, et al. Among authors: kowada r.
Exp Cell Res. 2022 Nov 1;420(1):113307. doi: 10.1016/j.yexcr.2022.113307. Epub 2022 Aug 24.
Exp Cell Res. 2022.
PMID: 36028059
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