{"id":175,"date":"2020-03-25T21:02:11","date_gmt":"2020-03-25T12:02:11","guid":{"rendered":"https:\/\/www.bri.niigata-u.ac.jp\/~neuroscience_disease_sugie\/lab\/en\/?page_id=175"},"modified":"2024-08-02T10:16:21","modified_gmt":"2024-08-02T01:16:21","slug":"publications","status":"publish","type":"page","link":"https:\/\/www.bri.niigata-u.ac.jp\/~neuroscience_disease_sugie\/lab\/en\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"<p>&nbsp;<\/p>\n<p>Nitta Y., Osaka J., Maki R., Hakeda-Suzuki S., Suzuki E., Ueki S., Suzuki T., <span style=\"text-decoration: underline;\">Sugie A.<\/span>, (2024) <em>eLife<\/em> 10.7554\/eLife.87880.2 <em>Drosophila<\/em> model to clarify the pathological significance of OPA1 in autosomal dominant optic atrophy.<\/p>\n<p>Chauvin SD, Ando S, Holley JA, <span style=\"text-decoration: underline;\">Sugie A.<\/span>, Zhao FR, Poddar S, Kato R, Miner CA, Nitta Y, Krishnamurthy SR, Saito R, Ning Y, Hatano Y, Kitahara S, Koide S, Stinson WA, Fu J, Surve N, Kumble L, Qian W, Polishchuk O, Andhey PS, Chiang C, Liu G, Colombeau L, Rodriguez R, Manel N, Kakita A, Artyomov MN, Schultz DC, Coates PT, Roberson EDO, Belkaid Y, Greenberg RA, Cherry S, Gack MU, Hardy T, Onodera O, Kato T,corresponding author and Miner JJ,corresponding author. (2024) <em>Nat Commun.<\/em> 15: 4696. Inherited C-terminal TREX1 variants disrupt homology-directed repair to cause senescence and DNA damage phenotypes in Drosophila, mice, and humans.<\/p>\n<p>Iida T., Igarashi A., Fukunaga K., Aoki T., Hidai T., Yanagi K., Yamamori M., Satou K., Go H., Kosho T., Maki R., Suzuki T., Nitta Y., <span style=\"text-decoration: underline;\">Sugie A.<\/span>, Asaoka Y., Furutani-Seiki M., Kimura T., Matsubara Y., Kaname T. (2024) <em>Front. Genet.<\/em> 15:1383176. doi: 10.3389\/fgene.2024.1383176 Functional analysis of RRAS2 pathogenic variants with a Noonan-like phenotype.<\/p>\n<div class=\"docsum-citation full-citation\"><span class=\"docsum-authors full-authors\">Osaka J, Ishii A, Wang X, Iwanaga R, Kawamura H, Akino S, <span style=\"text-decoration: underline;\">Sugie A<\/span>, Hakeda-Suzuki S, Suzuki T. (2024)<\/span> <span class=\"docsum-journal-citation full-journal-citation\"><em>Cell Rep<\/em>. Feb 19;43(2):113798. doi: 10.1016\/j.celrep.2024.113798. Online ahead of print.<\/span> <span class=\"citation-part\">PMID: <span class=\"docsum-pmid\">38381608\u00a0 Complex formation of immunoglobulin superfamily molecules Side-IV and Beat-IIb regulates synaptic specificity.<br \/>\n<\/span><\/span><\/p>\n<div class=\"share dropdown-block\"><\/div>\n<\/div>\n<div><\/div>\n<p>Vetro et al., (2023)<em> The American Journal of Human Genetics<\/em> 110(8):1356-1376. doi: 10.1016\/j.ajhg.2023.06.008 Stretch-activated ion channel TMEM63B associates with developmental and epileptic encephalopathies and progressive neurodegeneration.<\/p>\n<p>Yamada M., Nitta Y. Uehara T., Suzuki H., Takenouchi T., Tamura M., Ayabe S., Yoshiki A., Maeno A., Saga Y., Tamio Furuse T., Yamada I., Okamoto N., <span style=\"text-decoration: underline;\">Sugie A.<\/span><sup>\u2020<\/sup>, Kosaki K.<sup>\u2020<\/sup>, (2023) <em>European Journal of Medical Genetics<\/em> 66(8):104804. doi: 10.1016\/j.ejmg.2023.104804 Heterozygous loss-of-function DHX9 variants are associated with neurodevelopmental disorders.<em>\u00a0<\/em><sup>\u2020<\/sup> Co-corresponding authors<\/p>\n<p>Nitta Y., Osaka J., Maki R., Hakeda-Suzuki S., Suzuki E., Ueki S., Suzuki T., <span style=\"text-decoration: underline;\">Sugie A.<\/span>, (2023) <em>eLife<\/em> <em>Drosophila<\/em> model to clarify the pathological significance of OPA1 in autosomal dominant optic atrophy. reviewed preprint<\/p>\n<p>Itai T., <span style=\"text-decoration: underline;\">Sugie A.<\/span>, Nitta Y., Maki R., Suzuki T., Shinkai Y., Watanabe Y., Nakano Y., Ichikawa K., Okamoto N., Utsuno Y., Koshimizu E., Fujita A., Hamanaka K., Uchiyama Y., Tsuchida N., Miyake N., Misawa K., Mizuguchi T., Miyatake S., Matsumoto N. (2023) <em>Scientific Reports,<\/em> Volume 13, Article number: 975. A novel <em>NONO<\/em> variant that causes developmental delay and cardiac phenotypes.<\/p>\n<p>Nitta Y., Kawai H., Maki R., Osaka J., Hakeda-Suzuki S., Nagai Y., Doubkov\u00e1 K., Uehara T., Watanabe K., Kosaki K., Suzuki T., Tavosanis G., <span style=\"text-decoration: underline;\">Sugie A.<\/span> (2023) <em>Human Molecular Genetics<\/em>,<em>\u00a0<\/em>Volume 32, Issue 9, Pages 1524-1528. Direct evaluation of neuroaxonal degeneration with the causative genes of neurodegenerative diseases in <em>Drosophila<\/em> using the automated axon quantification system, MeDUsA. <a href=\"https:\/\/github.com\/SugieLab\/MeDUsA\">SugieLab\/MeDUsA (github.com)<\/a><\/p>\n<p>Osaka J., Yasuda H., Watanuki Y., Kato Y., Nitta Y., <u>Sugie A.<\/u>, Sato M., Suzuki T. (2022) <em>Genes &amp; Genetic Systems<\/em>,<em>\u00a0<\/em>Volume 97, Issue 6, Pages 297-309. Identification of genes regulating stimulus-dependent synaptic assembly in <em>Drosophila<\/em> using an automated synapse quantification system.<\/p>\n<p>Nitta Y., <u>Sugie A.<\/u>. (2022) <em>Fly<\/em>,\u00a0Volume 16, Issue 1, Pages 275-298. Studies of neurodegenerative diseases using <em>Drosophila<\/em> and the development of novel approaches for their analysis.<\/p>\n<p>Richard M., Doubkov\u00e1 K., Nitta Y., Kawai H., <span style=\"text-decoration: underline;\">Sugie A.<\/span><sup>\u2020<\/sup>, Tavosanis G.<sup>\u2020<\/sup> (2022) <em>The Journal of Neuroscience<\/em>, Volume 42, Issue 24, Pages 4937-4952. A Quantitative Model of Sporadic Axonal Degeneration in the <em>Drosophila<\/em> Visual System.\u2020 Co-corresponding authors<\/p>\n<p>Utomo Y. R., <span style=\"text-decoration: underline;\">Sugie A.<\/span><sup>\u2020<\/sup>, Okada S., Miura K., Nakamura H.<sup>\u2020<\/sup> (2022) <em>Chemical Communications<\/em>, Volume 58, Issue 15, Pages 2576-2579.\u00a0Detoxification of amyloid \u03b2 fibrils by curcumin derivatives and their verification in a <em>Drosophila<\/em> Alzheimer&#8217;s model. <sup>\u2020<\/sup> Co-corresponding authors<\/p>\n<p>Kato T., Manabe R., Igarashi H., Kametani F., Hirokawa S., Sekine Y., Fujita N., Saito S., Kawashima Y., Hatano Y., Ando S., Nozaki H., Sugai A., Uemura M., Fukunaga M., Sato T., Koyama A., Saito R., <u>Sugie A.<\/u>, Toyoshima Y., Kawata H., Murayama S., Matsumoto M., Kakita A., Hasegawa M., Ihara M., Kanazawa M., Nishizawa M., Tsuji S., Onodera O. (2021) <em>Journal of Clinical Investigation<\/em>, Volume 131, Issue 22, e140555. Candesartan prevents arteriopathy progression in cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy model.<\/p>\n<p>Sakamoto M., Sasaki K., <u>Sugie A.<\/u>, Nitta Y., Kimura T., G\u00fcrsoy S., Cinleti T., Iai M., Sengoku T., Ogata K., Suzuki A, Okamoto N., Iwama K., Tsuchida N., Uchiyama Y., Koshimizu E., Fujita A., Hamanaka K., Miyatake S., Mizuguchi T., Taguri M., Ito S., Takahashi H., Miyake N., Matsumoto N. (2021) <em>Human Molecular Genetics<\/em>,\u00a0Volume 31, Issue 1, Pages 69-81. <em>De novo ARF3<\/em> variants cause neurodevelopmental disorder with brain abnormality<\/p>\n<p>Takechi H., Hakeda-Suzuki S., Nitta Y., Ishiwata Y., Iwanaga R., Sato M., <span style=\"text-decoration: underline;\">Sugie A.<\/span>, Suzuki T. (2021) <em>eLife, <\/em>Volume 10, e66718. Glial insulin regulates cooperative or antagonistic Golden goal\/Flamingo interactions during photoreceptor axon guidance.<\/p>\n<p>Nitta Y., Matsui S., Kato Y., Kaga Y., Sugimoto K., <u>Sugie A<\/u><span style=\"text-decoration: underline;\">.<\/span> (2019) <em>Scientific Reports,<\/em> Volume 9, Article number: 8857. Analysing the evolutional and functional differentiation of four types of Daphnia magna cryptochrome in Drosophila circadian clock.<\/p>\n<p><u>Sugie A<\/u><span style=\"text-decoration: underline;\">.<\/span>, Marchetti G., Tavosanis G. (2018) <em>Neural Development<\/em>, Volume\u00a013, Article number: 14. Structural aspects of plasticity in the nervous system of <em>Drosophila.<\/em><\/p>\n<p><u>Sugie A.<\/u><sup>\u2020<\/sup>, M\u00f6hl C.<sup>\u2020<\/sup>, Hakeda-Suzuki S., Matsui H., Suzuki T., Tavosanis G. (2017) <em>Journal of Visualized Experiments, <\/em>120, e55716. Analyzing synaptic modulation of Drosophila photoreceptors after exposure to prolonged light. <sup>\u2020<\/sup> Co-corresponding authors<\/p>\n<p>Nitta Y.<sup>\u2020<\/sup>\u00a0and <u>Sugie A.<\/u><sup>\u2020<\/sup> (2017) <em>Biochemical and Biophysical Research <\/em><em>Communications, <\/em>Volume 487, Issue 1, Pages 116-121. DISCO Interacting Protein 2 determines direction of axon projection under the regulation of c-Jun N-terminal kinase in the Drosophila mushroom body.\u00a0 <sup>\u2020<\/sup> Co-corresponding authors<\/p>\n<p>Nitta Y.<sup>\u2020<\/sup>\u00a0and <u>Sugie A.<\/u><sup>\u2020<\/sup> (2017) <em>Biochemical and Biophysical Research <\/em><em>Communications,<\/em>\u00a0Volume 487, Issue 4, Pages 898-902. Identification of glaikit in a genome-wide expression profiling for axonal bifurcation of the mushroom body in Drosophila.\u00a0\u00a0 <sup>\u2020<\/sup> Co-corresponding authors<\/p>\n<p>Nitta Y., Yamazaki D., <u>Sugie A.<\/u>, Hiroi M., Tabata T. (2017) <em>Developmental Biology<\/em>, Volume 421, Issue 2, Pages 233-244. DISCO Interacting Protein 2 regulates axonal bifurcation and guidance of Drosophila mushroom body neurons.<\/p>\n<p><u>Sugie A.<\/u>, Hakeda-Suzuki S., Suzuki E., Silies M., Shimozono M., M\u00f6hl C., Suzuki T. and Tavosanis G. (2015) <em>Neuron<\/em>, Volume 86, Issue 3, Pages 711-725. Molecular remodeling of the presynaptic active zone of <em>Drosophila<\/em> photoreceptors via activity-dependent feedback.<\/p>\n<p>Berger-M\u00fcller S.<sup>\u2020<\/sup>, <u>Sugie A.<\/u><sup>\u2020<\/sup>, Takahashi F., Tavosanis G., Hakeda-Suzuki S., Suzuki T. (2013) <em>PLOS ONE<\/em>, Volume 8, Issue 12, e83732. Assessing the role of cell-surface molecules in central synaptogenesis in the Drosophila visual system.<br \/>\n\u2020These authors contributed equally.<\/p>\n<p><u>Sugie A.<\/u>, Umetsu D., Yasugi T., Fischbach K-F., Tabata T. (2010) <em>Development<\/em>, Volume 137, Issue 19, Pages 3303-3313. Recognition of pre- and postsynaptic neurons via nephrin\/NEPH1 homologs is a basis for the formation of the <em>Drosophila<\/em> retinotopic map.<\/p>\n<p>Yasugi T., <u>Sugie A<\/u>., Umetsu D., Tabata T. (2010) <em>Development<\/em>, Volume 137, Issue 19, Pages 3193-3203. Coordinated sequential action of EGFR and Notch signaling pathways regulates proneural wave progression in the <em>Drosophila<\/em> optic lobe.<\/p>\n<p>Taniue K., Nishida A., Hamada F., <u>Sugie A.<\/u>, Oda T., Ui-Tei K., Tabata T., Akiyama T. (2010) <em>Development,<\/em> Volume 137, Issue 10, Pages 1755-1764. Sunspot, a link between Wingless signaling and endoreplication in <em>Drosophila<\/em>.<\/p>\n<p>Mizuno N., <u>Sugie A.<\/u>, Kobayashi F., Takumi S. (2008) <em>Journal of Plant Physiology, Urban &amp; Fischer<\/em>, Volume 165, Issue 4, Pages 462-467. Mitochondrial alternative pathway is associated with development of freezing tolerance in common wheat.<\/p>\n<p><u>Sugie A.<\/u>, Murai K., Takumi S. (2007) <em>Genes and Genetic Systems, Genetics Society Of Japan<\/em>,\u00a0Volume 82, Issue 3, Pages 231-239. Alteration of respiration capacity and transcript accumulation level of alternative oxidase genes in necrosis lines of common wheat.<\/p>\n<p><u>Sugie A.<\/u>, Naydenov N., Mizuno N., Nakamura C., Takumi S. (2006) <em>Genes and Genetic Systems, Genetics Society Of Japan<\/em>, Volume 81, Issue 5, Pages 349-354. Overexpression of wheat alternative oxidase gene Waox1a alters respiration capacity and response to reactive oxygen species under low temperature in transgenic <em>Arabidopsis<\/em>.<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"&nbsp; Nitta Y., Osaka J., Maki R., Hakeda-Suzuki S., Suzuki E., Ueki S., Suzuki T., Sugie A., (2024 [&hellip;]","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"_links":{"self":[{"href":"https:\/\/www.bri.niigata-u.ac.jp\/~neuroscience_disease_sugie\/lab\/en\/wp-json\/wp\/v2\/pages\/175"}],"collection":[{"href":"https:\/\/www.bri.niigata-u.ac.jp\/~neuroscience_disease_sugie\/lab\/en\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.bri.niigata-u.ac.jp\/~neuroscience_disease_sugie\/lab\/en\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.bri.niigata-u.ac.jp\/~neuroscience_disease_sugie\/lab\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.bri.niigata-u.ac.jp\/~neuroscience_disease_sugie\/lab\/en\/wp-json\/wp\/v2\/comments?post=175"}],"version-history":[{"count":25,"href":"https:\/\/www.bri.niigata-u.ac.jp\/~neuroscience_disease_sugie\/lab\/en\/wp-json\/wp\/v2\/pages\/175\/revisions"}],"predecessor-version":[{"id":293,"href":"https:\/\/www.bri.niigata-u.ac.jp\/~neuroscience_disease_sugie\/lab\/en\/wp-json\/wp\/v2\/pages\/175\/revisions\/293"}],"wp:attachment":[{"href":"https:\/\/www.bri.niigata-u.ac.jp\/~neuroscience_disease_sugie\/lab\/en\/wp-json\/wp\/v2\/media?parent=175"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}