Resultados da pesquisa - Makito Hirano

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  1. 1
    ALADIN <sup>I482S</sup> causes selective failure of nuclear protein import and hypersensitivity to oxidative stress in triple A syndrome

    ALADIN <sup>I482S</sup> causes selective failure of nuclear protein import and hypersensitivity to oxidative stress in triple A syndrome Por Makito Hirano, Yoshiko Furiya, Hirohide Asai, Akira Yasui, Satoshi Ueno

    Publicado em 2006
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  2. 2
    Biometric Study of the Bifurcations of the Popliteal Artery and the Tibiofibular Trunk

    Biometric Study of the Bifurcations of the Popliteal Artery and the Tibiofibular Trunk Por Makito Hirano, H. R. Teles, Thanila A. Macedo, Emerson Alexandre Sgrott, H. Stuker, E Olave, Romina Moreira

    Publicado em 2014
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  3. 3
    Molecular dissection of ALS-associated toxicity of SOD1 in transgenic mice using an exon-fusion approach

    Molecular dissection of ALS-associated toxicity of SOD1 in transgenic mice using an exon-fusion approach Por Han-Xiang, Deng, Hujun, Jiang, Ronggen, Fu, Hong, Zhai, Yong, Shi, Erdong, Liu, Makito, Hirano, Mauro, C. Dal Canto, Teepu, Siddique

    Publicado em 2008
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  4. 4
    Expanding the Genetic and Clinical Spectrum of SCN1A-Related Hemiplegic Migraine: Analysis of Mutations in Japanese

    Expanding the Genetic and Clinical Spectrum of SCN1A-Related Hemiplegic Migraine: Analysis of Mutations in Japanese Por Daisuke Danno, Haruka Tada, Itsuki Oda, Norihito Kawashita, Makito Hirano, Shigekazu Kitamura, Shoji Kikui, Makoto Samukawa, Koji Yoshikawa, Yoshiyuki Mitsui, Yoshitaka Nagai, Takao Takeshima, Kazumasa Saigoh

    Publicado em 2025
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  5. 5
    DNA single‐strand break repair is impaired in aprataxin‐related ataxia

    DNA single‐strand break repair is impaired in aprataxin‐related ataxia Por Makito Hirano, Aya Yamamoto, Toshio Mori, Li Lan, Takaaki Iwamoto, Masashi Aoki, Keiji Shimada, Yoshiko Furiya, Shingo Kariya, Hirohide Asai, Akira Yasui, Tomohisa Nishiwaki, Kyoko Imoto, Nobuhiko Kobayashi, Takao Kiriyama, Tetsuya Nagata, Noboru Konishi, Yasuto Itoyama, Satoshi Ueno

    Publicado em 2007
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  6. 6
    Overlapping demyelinating syndromes and anti–N‐methyl‐D‐aspartate receptor encephalitis

    Overlapping demyelinating syndromes and anti–N‐methyl‐D‐aspartate receptor encephalitis Por Maarten J. Titulaer, Romana Höftberger, Takahiro Iizuka, Frank Leypoldt, Lindsey McCracken, Tania Cellucci, Leslie Benson, Huidy Shu, Takashi Irioka, Makito Hirano, Gagandeep Singh, Álvaro Cobo‐Calvo, Kenichi Kaida, Pamela S. Morales, Paul W. Wirtz, Tomotaka Yamamoto, Markus Reindl, Myrna R. Rosenfeld, Francesc Graus, Albert Saiz, Josep Dalmau

    Publicado em 2014
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  7. 7
    Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia

    Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia Por Han‐Xiang Deng, Wenjie Chen, Seong‐Tshool Hong, Kym M. Boycott, George Gorrie, Nailah Siddique, Yi Yang, Faisal Fecto, Yong Shi, Hong Zhai, Hu-Jun Jiang, Makito Hirano, Evadnie Rampersaud, Gerard H. Jansen, Sandra Donkervoort, Eileen H. Bigio, Benjamin Rix Brooks, Kaouther Ajroud, Robert Sufit, Jonathan L. Haines, Enrico Mugnaini, Margaret A. Pericak‐Vance, Teepu Siddique

    Publicado em 2011
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  8. 8
    Proteasome assembly defect due to a proteasome subunit beta type 8 (PSMB8) mutation causes the autoinflammatory disorder, Nakajo-Nishimura syndrome

    Proteasome assembly defect due to a proteasome subunit beta type 8 (PSMB8) mutation causes the autoinflammatory disorder, Nakajo-Nishimura syndrome Por Kazuhiko Arima, Akira Kinoshita, Hiroyuki Mishima, Nobuo Kanazawa, Takeumi Kaneko, Tsunehiro Mizushima, Kunihiro Ichinose, Hideki Nakamura, Akira Tsujino, Atsushi Kawakami, Masahiro Matsunaka, Shimpei Kasagi, Seiji Kawano, Shunichi Kumagai, Koichiro Ohmura, Tsuneyo Mimori, Makito Hirano, Satoshi Ueno, Keiko Tanaka, Masami Tanaka, Itaru Toyoshima, Hirotoshi Sugino, A. Yamakawa, Keiji Tanaka, Norio Niikawa, Fukumi Furukawa, Shigeo Murata, Katsumi Eguchi, Hiroaki Ida, Koh-ichiro Yoshiura

    Publicado em 2011
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