Studies of neurodegenerative diseases using Drosophila and the development of novel approaches for their analysis by Nitta, Yohei, Sugie, Atsushi

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Drosophila model to clarify the pathological significance of OPA1 in autosomal dominant optic atrophy by Nitta, Yohei, Osaka, Jiro, Maki, Ryuto, Hakeda-Suzuki, Satoko, Suzuki, Emiko, Ueki, Satoshi, Suzuki, Takashi, Sugie, Atsushi

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

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

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Identification of genes regulating stimulus-dependent synaptic assembly in Drosophila using an automated synapse quantification system by Osaka, Jiro, Yasuda, Haruka, Watanuki, Yusuke, Kato, Yuya, Nitta, Yohei, Sugie, Atsushi, Sato, Makoto, Suzuki, Takashi

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

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A novel NONO variant that causes developmental delay and cardiac phenotypes by Itai, Toshiyuki, Sugie, Atsushi, Nitta, Yohei, Maki, Ryuto, Suzuki, Takashi, Shinkai, Yoichi, Watanabe, Yoshihiro, Nakano, Yusuke, Ichikawa, Kazushi, Okamoto, Nobuhiko, Utsuno, Yasuhiro, Koshimizu, Eriko, Fujita, Atsushi, Hamanaka, Kohei, Uchiyama, Yuri, Tsuchida, Naomi, Miyake, Noriko, Misawa, Kazuharu, Mizuguchi, Takeshi, Miyatake, Satoko, Matsumoto, Naomichi

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Publisher Correction: A novel NONO variant that causes developmental delay and cardiac phenotypes by Itai, Toshiyuki, Sugie, Atsushi, Nitta, Yohei, Maki, Ryuto, Suzuki, Takashi, Shinkai, Yoichi, Watanabe, Yoshihiro, Nakano, Yusuke, Ichikawa, Kazushi, Okamoto, Nobuhiko, Utsuno, Yasuhiro, Koshimizu, Eriko, Fujita, Atsushi, Hamanaka, Kohei, Uchiyama, Yuri, Tsuchida, Naomi, Miyake, Noriko, Misawa, Kazuharu, Mizuguchi, Takeshi, Miyatake, Satoko, Matsumoto, Naomichi

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Functional analysis of RRAS2 pathogenic variants with a Noonan-like phenotype by Iida, Takaya, Igarashi, Arisa, Fukunaga, Kae, Aoki, Taiga, Hidai, Tomomi, Yanagi, Kumiko, Yamamori, Masahiko, Satou, Kazuhito, Go, Hayato, Kosho, Tomoki, Maki, Ryuto, Suzuki, Takashi, Nitta, Yohei, Sugie, Atsushi, Asaoka, Yoichi, Furutani-Seiki, Makoto, Kimura, Tetsuaki, Matsubara, Yoichi, Kaname, Tadashi

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

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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 by Nitta, Yohei, Sugie, Atsushi

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Identification of genes regulating stimulus-dependent synaptic assembly in Drosophila using an automated synapse quantification system by Jiro Osaka, Haruka Yasuda, Yusuke Watanuki, Yuya Kato, Yohei Nitta, Atsushi Sugie, Makoto Sato, Takashi Suzuki

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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 by Nitta, Yohei, Kawai, Hiroki, Maki, Ryuto, Osaka, Jiro, Hakeda-Suzuki, Satoko, Nagai, Yoshitaka, Doubková, Karolína, Uehara, Tomoko, Watanabe, Kenji, Kosaki, Kenjiro, Suzuki, Takashi, Tavosanis, Gaia, Sugie, Atsushi

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

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

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Stretch-activated ion channel TMEM63B associates with developmental and epileptic encephalopathies and progressive neurodegeneration by Vetro, Annalisa, Pelorosso, Cristiana, Balestrini, Simona, Masi, Alessio, Hambleton, Sophie, Argilli, Emanuela, Giubbolini, Simone, Barrick, Rebekah, Bergant, Gaber, Writzl, Karin, Bijlsma, Emilia K., Cacheiro, Pilar, Mei, Davide, Devlin, Anita, Machol, Keren, Mannaioni, Guido, Sakamoto, Masamune, Menezes, Manoj P., Courtin, Thomas, Sherr, Elliott, Parra, Riccardo, Richardson, Ruth, Roscioli, Tony, Scala, Marcello, von Stülpnagel, Celina, Smedley, Damian, Pochiero, Francesca, Ramesh, Venkateswaran, Capra, Valeria, Mancardi, Margherita, Keren, Boris, Mignot, Cyiril, Lulli, Matteo, Parks, Kendall, Griffin, Helen, Nigro, Vincenzo, Hirata, Yuko, Koichihara, Reiko, Peterlin, Borut, Maki, Ryuto, Nitta, Yohei, Ambrose, John C., Arumugam, Prabhu, Bevers, Roel, Bleda, Marta, Boustred, Christopher R., Brittain, Helen, Brown, Matthew A., Caulfield, Mark J., Chan, Georgia C., Giess, Adam, Griffin, John N., Hamblin, Angela, Henderson, Shirley, Hubbard, Tim J.P., Jackson, Rob, Jones, Louise J., Kasperaviciute, Dalia, Kayikci, Melis, Kousathanas, Athanasios, Lahnstein, Lea, Lakey, Anna, Lopez, Javier F., Maleady-Crowe, Fiona, Minneci, Federico, Mueller, Michael, Murugaesu, Nirupa, Need, Anna C., O’Donovan, Peter, Odhams, Chris A., Patch, Christine, Rahim, Tahrima, Rendon, Augusto, Sawant, Kushmita, Siddiq, Afshan, Sieghart, Alexander, Smith, Samuel C., Stuckey, Alexander, Tanguy, Mélanie, Taylor Tavares, Ana Lisa, Thomas, Ellen R.A., Tucci, Arianna, Welland, Matthew J., Williams, Eleanor, Witkowska, Katarzyna, Wood, Suzanne M., Zarowiecki, Magdalena, Torella, Annalaura, Tohyama, Jun, Hamada, Keisuke, Ogata, Kazuhiro, Sugie, Atsushi, van der Smagt, Jasper J., van Gassen, Koen, Valence, Stephanie, Vittery, Emma, Malone, Stephen, Kato, Mitsuhiro, Ratto, Gian Michele, Guerrini, Renzo

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Heterozygous loss-of-function DHX9 variants are associated with neurodevelopmental disorders: Human genetic and experimental evidences by Yamada, Mamiko, Nitta, Yohei, Uehara, Tomoko, Suzuki, Hisato, Miya, Fuyuki, Takenouchi, Toshiki, Tamura, Masaru, Ayabe, Shinya, Yoshiki, Atsushi, Maeno, Akiteru, Saga, Yumiko, Furuse, Tamio, Yamada, Ikuko, Okamoto, Nobuhiko, Kosaki, Kenjiro, Sugie, Atsushi

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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 by Chauvin, Samuel D, Ando, Shoichiro, Holley, Joe A, Sugie, Atsushi, Zhao, Fang R, Poddar, Subhajit, Kato, Rei, Miner, Cathrine A, Nitta, Yohei, Krishnamurthy, Siddharth R, Saito, Rie, Ning, Yue, Hatano, Yuya, Kitahara, Sho, Koide, Shin, Stinson, W Alexander, Fu, Jiayuan, Surve, Nehalee, Kumble, Lindsay, Qian, Wei, Polishchuk, Oleksiy, Andhey, Prabhakar S, Chiang, Cindy, Liu, Guanqun, Colombeau, Ludovic, Rodriguez, Raphaël, Manel, Nicolas, Kakita, Akiyoshi, Artyomov, Maxim N, Schultz, David C, Coates, P Toby, Roberson, Elisha D O, Belkaid, Yasmine, Greenberg, Roger A, Cherry, Sara, Gack, Michaela U, Hardy, Tristan, Onodera, Osamu, Kato, Taisuke, Miner, Jonathan J

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Early arthroscopic debridement of posterior cruciate ligament calcification after symptom presentation led to immediate recovery: a case report by Matsubara, Yuki, Nitta, Yasuaki, Tanaka, Kumi, Ito, Yohei, Adachi, Nobuo

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A Simple Risk Score to Differentiate Between Coronary Artery Obstruction and Coronary Artery Spasm of Patients With Acute Coronary Syndrome Without Persistent ST-Segment Elevation by Gohbara, Masaomi, Iwahashi, Noriaki, Okada, Kozo, Ogino, Yutaka, Hanajima, Yohei, Kirigaya, Jin, Minamimoto, Yugo, Matsuzawa, Yasushi, Nitta, Manabu, Konishi, Masaaki, Hibi, Kiyoshi, Kosuge, Masami, Ebina, Toshiaki, Sugano, Teruyasu, Ishikawa, Toshiyuki, Tamura, Kouichi, Kimura, Kazuo

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