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Emerging roles of ARHGAP33 in intracellular trafficking of TrkB and pathophysiology of neuropsychiatric disorders.
Nakazawa T, Hashimoto R, Sakoori K, Sugaya Y, Tanimura A, Hashimotodani Y, Ohi K, Yamamori H, Yasuda Y, Umeda-Yano S, Kiyama Y, Konno K, Inoue T, Yokoyama K, Inoue T, Numata S, Ohnuma T, Iwata N, Ozaki N, Hashimoto H, Watanabe M, Manabe T, Yamamoto T, Takeda M, Kano M. Nakazawa T, et al. Among authors: sugaya y. Nat Commun. 2016 Feb 3;7:10594. doi: 10.1038/ncomms10594. Nat Commun. 2016. PMID: 26839058 Free PMC article.
Corrigendum: Emerging roles of ARHGAP33 in intracellular trafficking of TrkB and pathophysiology of neuropsychiatric disorders.
Nakazawa T, Hashimoto R, Sakoori K, Sugaya Y, Tanimura A, Hashimotodani Y, Ohi K, Yamamori H, Yasuda Y, Umeda-Yano S, Kiyama Y, Konno K, Inoue T, Yokoyama K, Inoue T, Numata S, Ohnuma T, Iwata N, Ozaki N, Hashimoto H, Watanabe M, Manabe T, Yamamoto T, Takeda M, Kano M. Nakazawa T, et al. Among authors: sugaya y. Nat Commun. 2016 Apr 20;7:11466. doi: 10.1038/ncomms11466. Nat Commun. 2016. PMID: 27095349 Free PMC article. No abstract available.
Transsynaptic Modulation of Kainate Receptor Functions by C1q-like Proteins.
Matsuda K, Budisantoso T, Mitakidis N, Sugaya Y, Miura E, Kakegawa W, Yamasaki M, Konno K, Uchigashima M, Abe M, Watanabe I, Kano M, Watanabe M, Sakimura K, Aricescu AR, Yuzaki M. Matsuda K, et al. Among authors: sugaya y. Neuron. 2016 May 18;90(4):752-67. doi: 10.1016/j.neuron.2016.04.001. Epub 2016 Apr 28. Neuron. 2016. PMID: 27133466 Free article.
Comprehensive analysis of a novel mouse model of the 22q11.2 deletion syndrome: a model with the most common 3.0-Mb deletion at the human 22q11.2 locus.
Saito R, Koebis M, Nagai T, Shimizu K, Liao J, Wulaer B, Sugaya Y, Nagahama K, Uesaka N, Kushima I, Mori D, Maruyama K, Nakao K, Kurihara H, Yamada K, Kano M, Fukada Y, Ozaki N, Aiba A. Saito R, et al. Among authors: sugaya y. Transl Psychiatry. 2020 Feb 5;10(1):35. doi: 10.1038/s41398-020-0723-z. Transl Psychiatry. 2020. PMID: 32066675 Free PMC article.
Combined glyoxalase 1 dysfunction and vitamin B6 deficiency in a schizophrenia model system causes mitochondrial dysfunction in the prefrontal cortex.
Toriumi K, Berto S, Koike S, Usui N, Dan T, Suzuki K, Miyashita M, Horiuchi Y, Yoshikawa A, Asakura M, Nagahama K, Lin HC, Sugaya Y, Watanabe T, Kano M, Ogasawara Y, Miyata T, Itokawa M, Konopka G, Arai M. Toriumi K, et al. Among authors: sugaya y. Redox Biol. 2021 Sep;45:102057. doi: 10.1016/j.redox.2021.102057. Epub 2021 Jun 24. Redox Biol. 2021. PMID: 34198071 Free PMC article.
A recurrent PJA1 variant in trigonocephaly and neurodevelopmental disorders.
Suzuki T, Suzuki T, Raveau M, Miyake N, Sudo G, Tsurusaki Y, Watanabe T, Sugaya Y, Tatsukawa T, Mazaki E, Shimohata A, Kushima I, Aleksic B, Shiino T, Toyota T, Iwayama Y, Nakaoka K, Ohmori I, Sasaki A, Watanabe K, Hirose S, Kaneko S, Inoue Y, Yoshikawa T, Ozaki N, Kano M, Shimoji T, Matsumoto N, Yamakawa K. Suzuki T, et al. Among authors: sugaya y. Ann Clin Transl Neurol. 2020 Jul;7(7):1117-1131. doi: 10.1002/acn3.51093. Epub 2020 Jun 12. Ann Clin Transl Neurol. 2020. PMID: 32530565 Free PMC article.
343 results