Search Results - Yoshihide Sunada
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Dystrophin-glycoprotein complex by Yoshihide Sunada, Kevin P. Campbell
Published 1995Artigo -
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Taurine Ameliorates Impaired the Mitochondrial Function and Prevents Stroke-like Episodes in Patients with MELAS by Mitsue Rikimaru, Yutaka Ohsawa, Alexander M. Wolf, Kiyomi Nishimaki, Harumi Ichimiya, Naomi Kamimura, Shin‐ichiro Nishimatsu, Shigeo Ohta, Yoshihide Sunada
Published 2012Artigo -
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Effect of Neurofeedback Facilitation on Poststroke Gait and Balance Recovery by Masahito Mihara, Hiroaki Fujimoto, Noriaki Hattori, Hironori Otomune, Yuta Kajiyama, Kuni Konaka, Yoshiyuki Watanabe, Yuichi Hiramatsu, Yoshihide Sunada, Ichiro Miyai, Hideki Mochizuki
Published 2021Artigo -
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Dystroglycan Is Essential for Early Embryonic Development: Disruption of Reichert's Membrane in Dag1-Null Mice by Roger A. Williamson, Michael D. Henry, Karla J. Daniels, Ronald F. Hrstka, Jane C. Lee, Yoshihide Sunada, Oxana Ibraghimov‐Beskrovnaya, Kevin P. Campbell
Published 1997Artigo -
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Taurine supplementation for prevention of stroke-like episodes in MELAS: a multicentre, open-label, 52-week phase III trial by Yutaka Ohsawa, Hiroki Hagiwara, Shin‐ichiro Nishimatsu, Akihiro Hirakawa, Naomi Kamimura, Hideaki Ohtsubo, Yuta Fukai, T. Murakami, Yasutoshi Koga, Yu‐ichi Goto, Shigeo Ohta, Yoshihide Sunada
Published 2018Artigo -
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iPSC Screening identifies α2δ2 as a Potential Therapeutic Target for FTLD-Tau by Keiko Imamura, Ayako Nagahashi, Aya Okusa, Tomoki Sakasai, Kayoko Tsukita, Yumiko Kutoku, Yutaka Ohsawa, Yoshihide Sunada, Naruhiko Sahara, Nicholas M. Kanaan, Makoto Higuchi, Kohji Mori, Manabu Ikeda, Haruhisa Inoue
Published 2025Artigo -
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Mild Congenital Muscular Dystrophy in Two Patients with an Internally Deleted Laminin 2-Chain by Valérie Allamand, Yoshihide Sunada, Mustafa A. Salih, Volker Straub, O. Ozo, Muath Al-Turaiki, Muhammad Akbar, T. Kolo, Holly Colognato, X Zhang, Lydia Sorokin, Peter D. Yurchenco, Karl Tryggvason, Kevin P. Campbell
Published 1997Artigo -
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SLC25A13 Gene Analysis in Citrin Deficiency: Sixteen Novel Mutations in East Asian Patients, and the Mutation Distribution in a Large Pediatric Cohort in China by Yuan‐Zong Song, Zhan‐Hui Zhang, Wei‐Xia Lin, Xin-Jing Zhao, Mei Deng, Yanli Ma, Guo Li, Fengping Chen, Xiaoling Long, Xiangling He, Yoshihide Sunada, Shun Soneda, Akiko Nakatomi, Sumito Dateki, Lock Hock Ngu, Keiko Kobayashi, Takeyori Saheki
Published 2013Artigo -
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Calcium dysregulation contributes to neurodegeneration in FTLD patient iPSC-derived neurons by Keiko Imamura, Naruhiko Sahara, Nicholas M. Kanaan, Kayoko Tsukita, Takayuki Kondo, Yumiko Kutoku, Yutaka Ohsawa, Yoshihide Sunada, Koichi Kawakami, Akitsu Hotta, Satoshi Yawata, Dai Watanabe, Masato Hasegawa, John Q. Trojanowski, Virginia M.‐Y. Lee, Tetsuya Suhara, Makoto Higuchi, Haruhisa Inoue
Published 2016Artigo -
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Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D). by Alain Carrié, F. Piccolo, France Leturcq, Claudia de Toma, K. Azibi, C. Beldjord, Jean‐Michel Vallat, Luciano Merlini, Thomas Voit, Caroline A. Sewry, J.A. Urtizberea, Norma B. Romero, F.M.S. Tomé, Michel Fardeau, Yoshihide Sunada, Kevin P. Campbell, J.‐C. Kaplan, Marc Jeanpierre
Published 1997Artigo -
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Modeling Alzheimer’s Disease with iPSCs Reveals Stress Phenotypes Associated with Intracellular Aβ and Differential Drug Responsiveness by Takayuki Kondo, Masashi Asai, Kayoko Tsukita, Yumiko Kutoku, Yutaka Ohsawa, Yoshihide Sunada, Keiko Imamura, Naohiro Egawa, Naoki Yahata, Keisuke Okita, Kazutoshi Takahashi, Isao Asaka, Takashi Aoi, Akira Watanabe, Kaori Watanabe, Chie Kadoya, Rie Nakano, Dai Watanabe, Kei Maruyama, Osamu Hori, Satoshi Hibino, Tominari Choshi, Tatsutoshi Nakahata, Hiroyuki Hioki, Takeshi Kaneko, Motoko Naitoh, Katsuhiro Yoshikawa, Satoko Yamawaki, Shigehiko Suzuki, Ryuji Hata, Shu-ichi Ueno, Tsuneyoshi Seki, Kazuhiro Kobayashi, Tatsushi Toda, Kazuma Murakami, Kazuhiro Irie, William L. Klein, Hiroshi Mori, Takashi Asada, Ryōsuke Takahashi, Nobuhisa Iwata, Shinya Yamanaka, Haruhisa Inoue
Published 2013Artigo
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MELAS syndrome