Результаты поиска - Takanobu Otomo

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  1. 1
    Impaired lysosomal acidity maintenance in acid lipase-deficient cells leads to defective autophagy

    Impaired lysosomal acidity maintenance in acid lipase-deficient cells leads to defective autophagy по Takahito Moriwaki, Seigo Terawaki, Takanobu Otomo

    Опубликовано 2024
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    Artigo
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  2. 2
    Autophagosome–lysosome fusion in neurons requires <scp>INPP</scp> 5E, a protein associated with Joubert syndrome

    Autophagosome–lysosome fusion in neurons requires <scp>INPP</scp> 5E, a protein associated with Joubert syndrome по Junya Hasegawa, Ryo Iwamoto, Takanobu Otomo, Akiko Nezu, Maho Hamasaki, Tamotsu Yoshimori

    Опубликовано 2016
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    Artigo
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  3. 3
    Late-onset Krabbe disease is predominant in Japan and its mutant precursor protein undergoes more effective processing than the infantile-onset form

    Late-onset Krabbe disease is predominant in Japan and its mutant precursor protein undergoes more effective processing than the infantile-onset form по Mohammad Arif Hossain, Takanobu Otomo, Seiji Saito, Kazuki Ohno, Hitoshi Sakuraba, Yusuke Hamada, Keiichi Ozono, Norio Sakai

    Опубликовано 2013
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    Artigo
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  4. 4
    Identification of CUL4A-DDB1-WDFY1 as an E3 ubiquitin ligase complex involved in initiation of lysophagy

    Identification of CUL4A-DDB1-WDFY1 as an E3 ubiquitin ligase complex involved in initiation of lysophagy по Hirofumi Teranishi, Keisuke Tabata, Marika Saeki, Tetsuo Umemoto, Tomohisa Hatta, Takanobu Otomo, K. Yamamoto, Tohru Natsume, Tamotsu Yoshimori, Maho Hamasaki

    Опубликовано 2022
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    Artigo
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  5. 5
    A brain-enriched Drp1 isoform associates with lysosomes, late endosomes, and the plasma membrane

    A brain-enriched Drp1 isoform associates with lysosomes, late endosomes, and the plasma membrane по Kie Itoh, Yoshihiro Adachi, Tatsuya Yamada, Takamichi L. Suzuki, Takanobu Otomo, Heidi M. McBride, Tamotsu Yoshimori, Miho Iijima, Hiromi Sesaki

    Опубликовано 2018
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    Artigo
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  6. 6
    Mucolipidosis II and III alpha/beta: mutation analysis of 40 Japanese patients showed genotype–phenotype correlation

    Mucolipidosis II and III alpha/beta: mutation analysis of 40 Japanese patients showed genotype–phenotype correlation по Takanobu Otomo, Takeshi Muramatsu, Tohru Yorifuji, Torayuki Okuyama, Hiroki Nakabayashi, Toshiyuki Fukao, Toshihiro Ohura, Makoto Yoshino, Akemi Tanaka, Nobuhiko Okamoto, Koji Inui, Keiichi Ozono, Norio Sakai

    Опубликовано 2009
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    Artigo
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  7. 7
    Mutation in<i>VPS33A</i>affects metabolism of glycosaminoglycans: a new type of mucopolysaccharidosis with severe systemic symptoms

    Mutation in<i>VPS33A</i>affects metabolism of glycosaminoglycans: a new type of mucopolysaccharidosis with severe systemic symptoms по H. Kondo, Н. Р. Максимова, Takanobu Otomo, Hisakazu Kato, Atsuko Imai, Yoshihiro Asano, Kaori Kobayashi, Satoshi Nojima, Akihiro Nakaya, Yusuke Hamada, K Irahara, Elizaveta Gurinova, A. L. Sukhomyasova, Anna Nogovicina, М. Т. Саввина, Tamotsu Yoshimori, Keiichi Ozono, Norio Sakai

    Опубликовано 2016
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    Artigo
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  8. 8
    Defects in autophagosome-lysosome fusion underlie Vici syndrome, a neurodevelopmental disorder with multisystem involvement

    Defects in autophagosome-lysosome fusion underlie Vici syndrome, a neurodevelopmental disorder with multisystem involvement по Ikumi Hori, Takanobu Otomo, Mitsuko Nakashima, Fuyuki Miya, Yutaka Negishi, Hideaki Shiraishi, Yutaka Nonoda, Shinichi Magara, Jun Tohyama, Nobuhiko Okamoto, Takeshi Kumagai, Konomi Shimoda, Yoshiya Yukitake, Daigo Kajikawa, Tomohiro Morio, Ayako Hattori, Motoo Nakagawa, N Ando, Ichizo Nishino, Mitsuhiro Kato, Tatsuhiko Tsunoda, Hirotomo Saitsu, Yonehiro Kanemura, Mami Yamasaki, Kenjiro Kosaki, Naomichi Matsumoto, Tamotsu Yoshimori, Shinji Saitoh

    Опубликовано 2017
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    Artigo
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