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Published in Neuromuscular disorders : NMD (01.03.2009)
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Fukutin gene mutations cause dilated cardiomyopathy with minimal muscle weakness
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Published in Annals of neurology (01.11.2006)
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Mutant BIN1-Dynamin 2 complexes dysregulate membrane remodeling in the pathogenesis of centronuclear myopathy
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Published in The Journal of biological chemistry (21.11.2020)
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Published in The Journal of biological chemistry (21.11.2020)
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A Gne knockout mouse expressing human GNE D176V mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy
Malicdan, May Christine V., Noguchi, Satoru, Nonaka, Ikuya, Hayashi, Yukiko K., Nishino, Ichizo
Published in Human molecular genetics (15.11.2007)
Published in Human molecular genetics (15.11.2007)
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Necklace cytoplasmic bodies in hereditary myopathy with early respiratory failure
Uruha, Akinori, Hayashi, Yukiko K, Oya, Yasushi, Mori-Yoshimura, Madoka, Kanai, Masahiro, Murata, Miho, Kawamura, Mayumi, Ogata, Katsuhisa, Matsumura, Tsuyoshi, Suzuki, Shigeaki, Takahashi, Yukako, Kondo, Takayuki, Kawarabayashi, Takeshi, Ishii, Yuko, Kokubun, Norito, Yokoi, Satoshi, Yasuda, Rei, Kira, Jun-ichi, Mitsuhashi, Satomi, Noguchi, Satoru, Nonaka, Ikuya, Nishino, Ichizo
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Published in Journal of neurology, neurosurgery and psychiatry (01.05.2015)
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Correction: Corrigendum: Genetic diagnosis of Duchenne/Becker muscular dystrophy using next-generation sequencing: validation analysis of DMD mutations
Okubo, Mariko, Minami, Narihiro, Goto, Kanako, Goto, Yuichi, Noguchi, Satoru, Mitsuhashi, Satomi, Nishino, Ichizo
Published in Journal of human genetics (01.01.2017)
Published in Journal of human genetics (01.01.2017)
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Vehicle clustering algorithm for sharing information on traffic congestion
Kanemaru, Yohei, Matsuura, Satoshi, Kakiuchi, Masatoshi, Noguchi, Satoru, Inomata, Atsuo, Fujikawa, Kazutoshi
Published in 2013 13th International Conference on ITS Telecommunications (ITST) (01.11.2013)
Published in 2013 13th International Conference on ITS Telecommunications (ITST) (01.11.2013)
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Conference Proceeding
GAME MACHINE
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Year of Publication 06.01.2022
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Year of Publication 06.01.2022
Patent
GAME MACHINE
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Year of Publication 06.01.2022
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Year of Publication 06.01.2022
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カテコラミン誘発性多型性心室頻拍(CPVT)モデルマウスの不整脈に対する新規RyR2特異的阻害薬の効果
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Published in 日本薬理学会年会要旨集 (2023)
Published in 日本薬理学会年会要旨集 (2023)
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Central core disease is due to RYR1 mutations in more than 90% of patients
Wu, Shiwen, Ibarra, M Carlos A., Malicdan, May Christine V., Murayama, Kumiko, Ichihara, Yasuko, Kikuchi, Hirosato, Nonaka, Ikuya, Noguchi, Satoru, Hayashi, Yukiko K., Nishino, Ichizo
Published in Brain (London, England : 1878) (01.06.2006)
Published in Brain (London, England : 1878) (01.06.2006)
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Central core disease is due to RYRI mutations in more than 90% of patients
SHIWEN WU, IBARRA M, Carlos A, MALICDAN, May Christine V, MURAYAMA, Kumiko, ICHIHARA, Yasuko, KIKUCHI, Hirosato, NONAKA, Ikuya, NOGUCHI, Satoru, HAYASHI, Yukiko K, NISHINO, Ichizo
Published in Brain (London, England : 1878) (01.06.2006)
Published in Brain (London, England : 1878) (01.06.2006)
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OIKAWA SEIJI, NOGUCHI SATORU, ODA NAOKI, IGARI KIMINORI, SASAKI KOTA, SAITO KIYOSHI, FUKANO AKIRA, OGURA TOSHIO
Year of Publication 01.11.2021
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Year of Publication 01.11.2021
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DNAJB6 myopathy in an Asian cohort and cytoplasmic/nuclear inclusions
Sato, Takatoshi, Hayashi, Yukiko K, Oya, Yasushi, Kondo, Tomoyoshi, Sugie, Kazuma, Kaneda, Daita, Houzen, Hideki, Yabe, Ichiro, Sasaki, Hidenao, Noguchi, Satoru, Nonaka, Ikuya, Osawa, Makiko, Nishino, Ichizo
Published in Neuromuscular disorders : NMD (01.03.2013)
Published in Neuromuscular disorders : NMD (01.03.2013)
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