Works matching AU Mori, Daisuke

Results: 159
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    Identification of ultra-rare disruptive variants in voltage-gated calcium channel-encoding genes in Japanese samples of schizophrenia and autism spectrum disorder.

    Published in:
    Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-01851-y
    By:
    • Wang, Chenyao;
    • Horigane, Shin-ichiro;
    • Wakamori, Minoru;
    • Ueda, Shuhei;
    • Kawabata, Takeshi;
    • Fujii, Hajime;
    • Kushima, Itaru;
    • Kimura, Hiroki;
    • Ishizuka, Kanako;
    • Nakamura, Yukako;
    • Iwayama, Yoshimi;
    • Ikeda, Masashi;
    • Iwata, Nakao;
    • Okada, Takashi;
    • Aleksic, Branko;
    • Mori, Daisuke;
    • Yoshida, Takashi;
    • Bito, Haruhiko;
    • Yoshikawa, Takeo;
    • Takemoto-Kimura, Sayaka
    Publication type:
    Article
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    Rare genetic variants in the gene encoding histone lysine demethylase 4C (KDM4C) and their contributions to susceptibility to schizophrenia and autism spectrum disorder.

    Published in:
    Translational Psychiatry, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41398-020-01107-7
    By:
    • Kato, Hidekazu;
    • Kushima, Itaru;
    • Mori, Daisuke;
    • Yoshimi, Akira;
    • Aleksic, Branko;
    • Nawa, Yoshihiro;
    • Toyama, Miho;
    • Furuta, Sho;
    • Yu, Yanjie;
    • Ishizuka, Kanako;
    • Kimura, Hiroki;
    • Arioka, Yuko;
    • Tsujimura, Keita;
    • Morikawa, Mako;
    • Okada, Takashi;
    • Inada, Toshiya;
    • Nakatochi, Masahiro;
    • Shinjo, Keiko;
    • Kondo, Yutaka;
    • Kaibuchi, Kozo
    Publication type:
    Article
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    LIS1 and NDEL1 coordinate the plus-end-directed transport of cytoplasmic dynein.

    Published in:
    EMBO Journal, 2008, v. 27, n. 19, p. 2471, doi. 10.1038/emboj.2008.182
    By:
    • Yamada, Masami;
    • Toba, Shiori;
    • Yoshida, Yuko;
    • Haratani, Koji;
    • Mori, Daisuke;
    • Yano, Yoshihisa;
    • Mimori-Kiyosue, Yuko;
    • Nakamura, Takeshi;
    • Itoh, Kyoko;
    • Fushiki, Shinji;
    • Setou, Mitsutoshi;
    • Wynshaw-Boris, Anthony;
    • Torisawa, Takayuki;
    • Toyoshima, Yoko Y;
    • Hirotsune, Shinji
    Publication type:
    Article
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    Proteinuria-associated renal magnesium wasting leads to hypomagnesemia: a common electrolyte abnormality in chronic kidney disease.

    Published in:
    Nephrology Dialysis Transplantation, 2019, v. 34, n. 7, p. 1154, doi. 10.1093/ndt/gfy119
    By:
    • Oka, Tatsufumi;
    • Hamano, Takayuki;
    • Sakaguchi, Yusuke;
    • Yamaguchi, Satoshi;
    • Kubota, Keiichi;
    • Senda, Masamitsu;
    • Yonemoto, Sayoko;
    • Shimada, Karin;
    • Matsumoto, Ayumi;
    • Hashimoto, Nobuhiro;
    • Mori, Daisuke;
    • Monden, Chikako;
    • Takahashi, Atsushi;
    • Obi, Yoshitsugu;
    • Yamamoto, Ryohei;
    • Takabatake, Yoshitsugu;
    • Kaimori, Jun-Ya;
    • Moriyama, Toshiki;
    • Horio, Masaru;
    • Matsui, Isao
    Publication type:
    Article
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    Association between Density of Coronary Artery Calcification and Serum Magnesium Levels among Patients with Chronic Kidney Disease.

    Published in:
    PLoS ONE, 2016, v. 11, n. 9, p. 1, doi. 10.1371/journal.pone.0163673
    By:
    • Sakaguchi, Yusuke;
    • Hamano, Takayuki;
    • Nakano, Chikako;
    • Obi, Yoshitsugu;
    • Matsui, Isao;
    • Kusunoki, Yasuo;
    • Mori, Daisuke;
    • Oka, Tatsufumi;
    • Hashimoto, Nobuhiro;
    • Takabatake, Yoshitsugu;
    • Takahashi, Atsushi;
    • Kaimori, Jun-Ya;
    • Moriyama, Toshiki;
    • Yamamoto, Ryohei;
    • Horio, Masaru;
    • Sugimoto, Ken;
    • Yamamoto, Koichi;
    • Rakugi, Hiromi;
    • Isaka, Yoshitaka
    Publication type:
    Article
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    Pioglitazone strengthen therapeutic effect of adipose-derived regenerative cells against ischemic cardiomyopathy through enhanced expression of adiponectin and modulation of macrophage phenotype.

    Published in:
    Cardiovascular Diabetology, 2019, v. 18, n. 1, p. N.PAG, doi. 10.1186/s12933-019-0829-x
    By:
    • Mori, Daisuke;
    • Miyagawa, Shigeru;
    • Matsuura, Ryohei;
    • Sougawa, Nagako;
    • Fukushima, Satsuki;
    • Ueno, Takayoshi;
    • Toda, Koichi;
    • Kuratani, Toru;
    • Tomita, Koichi;
    • Maeda, Norikazu;
    • Shimomura, Iichiro;
    • Sawa, Yoshiki
    Publication type:
    Article
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    A hyper-activatable CAMK2A variant associated with intellectual disability causes exaggerated long-term potentiation and learning impairments.

    Published in:
    Translational Psychiatry, 2025, v. 15, n. 1, p. 1, doi. 10.1038/s41398-025-03316-4
    By:
    • Pan, Miao;
    • Liu, Pin-Wu;
    • Ozawa, Yukihiro;
    • Arima-Yoshida, Fumiko;
    • Dong, Geyao;
    • Sawahata, Masahito;
    • Mori, Daisuke;
    • Nagase, Masashi;
    • Fujii, Hajime;
    • Ueda, Shuhei;
    • Yabuuchi, Yurie;
    • Liu, Xinzi;
    • Narita, Hajime;
    • Konno, Ayumu;
    • Hirai, Hirokazu;
    • Ozaki, Norio;
    • Yamada, Kiyofumi;
    • Kidokoro, Hiroyuki;
    • Bito, Haruhiko;
    • Mizoguchi, Hiroyuki
    Publication type:
    Article
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    Excessive mechanical loading promotes osteoarthritis through the gremlin-1–NF-κB pathway.

    Published in:
    Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-09491-5
    By:
    • Chang, Song Ho;
    • Mori, Daisuke;
    • Kobayashi, Hiroshi;
    • Mori, Yoshifumi;
    • Nakamoto, Hideki;
    • Okada, Keita;
    • Taniguchi, Yuki;
    • Sugita, Shurei;
    • Yano, Fumiko;
    • Chung, Ung-il;
    • Kim-Kaneyama, Joo-ri;
    • Yanagita, Motoko;
    • Economides, Aris;
    • Canalis, Ernesto;
    • Chen, Di;
    • Tanaka, Sakae;
    • Saito, Taku
    Publication type:
    Article
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