Søgeresultater - Okamoto, Yuji

Developmental changes in Ca(2+) channel subtypes regulating endocytosis at the calyx of Held af Midorikawa, Mitsuharu, Okamoto, Yuji, Sakaba, Takeshi

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Transsynaptic modulation of presynaptic short-term plasticity in hippocampal mossy fiber synapses af Vandael, David, Okamoto, Yuji, Jonas, Peter

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Effective silicon production from SiCl(4) source using hydrogen radicals generated and transported at atmospheric pressure af Okamoto, Yuji, Sumiya, Masatomo, Nakamura, Yuya, Suzuki, Yoshikazu

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Single-Image Super-Resolution Improvement of X-ray Single-Particle Diffraction Images Using a Convolutional Neural Network af Tokuhisa, Atsushi, Akinaga, Yoshinobu, Terayama, Kei, Okamoto, Yuji, Okuno, Yasushi

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Receptor‐activated Smad localisation in Bleomycin‐induced pulmonary fibrosis af Higashiyama, Hiroyuki, Yoshimoto, Daisuke, Okamoto, Yuji, Kikkawa, Hideo, Asano, Satoshi, Kinoshita, Mine

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Distinct modes of endocytotic presynaptic membrane and protein uptake at the calyx of Held terminal of rats and mice af Okamoto, Yuji, Lipstein, Noa, Hua, Yunfeng, Lin, Kun-Han, Brose, Nils, Sakaba, Takeshi, Midorikawa, Mitsuharu

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Toxocara canis myelitis involving the lumbosacral region: a case report af Hiramatsu, Yu, Yoshimura, Michiyoshi, Saigo, Ryuji, Arata, Hitoshi, Okamoto, Yuji, Matsuura, Eiji, Maruyama, Haruhiko, Takashima, Hiroshi

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A case of adult-onset Wolfram syndrome with compound heterozygous mutations of the WFS1 gene af Lee, Jinhee, Iwasaki, Takuya, Kaida, Tomoko, Chuman, Hideki, Yoshimura, Akiko, Okamoto, Yuji, Takashima, Hiroshi, Miyata, Kazunori

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Curcumin facilitates a transitory cellular stress response in Trembler-J mice af Okamoto, Yuji, Pehlivan, Davut, Wiszniewski, Wojciech, Beck, Christine R., Snipes, G. Jackson, Lupski, James R., Khajavi, Mehrdad

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Stenotic changes of the posterior cerebral artery are a major contributing factor for cerebral infarction in moyamoya disease af Ohkura, Akira, Negoto, Tetsuya, Aoki, Takachika, Noguchi, Kei, Okamoto, Yuji, Komatani, Hideki, Kawano, Takayuki, Mukasa, Akitake, Morioka, Motohiro

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Genetic profile and onset features of 1005 patients with Charcot-Marie-Tooth disease in Japan af Yoshimura, Akiko, Yuan, Jun-Hui, Hashiguchi, Akihiro, Ando, Masahiro, Higuchi, Yujiro, Nakamura, Tomonori, Okamoto, Yuji, Nakagawa, Masanori, Takashima, Hiroshi

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Combinatorial screening of halide perovskite thin films and solar cells by mask-defined IR laser molecular beam epitaxy af Kawashima, Kazuhiro, Okamoto, Yuji, Annayev, Orazmuhammet, Toyokura, Nobuo, Takahashi, Ryota, Lippmaa, Mikk, Itaka, Kenji, Suzuki, Yoshikazu, Matsuki, Nobuyuki, Koinuma, Hideomi

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A new phenotype of mitochondrial disease characterized by familial late-onset predominant axial myopathy and encephalopathy af Sakiyama, Yusuke, Okamoto, Yuji, Higuchi, Itsuro, Inamori, Yukie, Sangatsuda, Yoko, Michizono, Kumiko, Watanabe, Osamu, Hatakeyama, Hideyuki, Goto, Yu-ichi, Arimura, Kimiyoshi, Takashima, Hiroshi

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The First Case of Spinocerebellar Ataxia Type 8 in Monozygotic Twins af Sawada, Jun, Katayama, Takayuki, Tokashiki, Takashi, Kikuchi, Shiori, Kano, Kohei, Takahashi, Kae, Saito, Tsukasa, Adachi, Yoshiki, Okamoto, Yuji, Yoshimura, Akiko, Takashima, Hiroshi, Hasebe, Naoyuki

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Clinical and genetic diversities of Charcot‐Marie‐Tooth disease with MFN2 mutations in a large case study af Ando, Masahiro, Hashiguchi, Akihiro, Okamoto, Yuji, Yoshimura, Akiko, Hiramatsu, Yu, Yuan, Junhui, Higuchi, Yujiro, Mitsui, Jun, Ishiura, Hiroyuki, Umemura, Ayako, Maruyama, Koichi, Matsushige, Takeshi, Morishita, Shinichi, Nakagawa, Masanori, Tsuji, Shoji, Takashima, Hiroshi

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Genetic spectrum of Charcot–Marie–Tooth disease associated with myelin protein zero gene variants in Japan af Taniguchi, Takaki, Ando, Masahiro, Okamoto, Yuji, Yoshimura, Akiko, Higuchi, Yujiro, Hashiguchi, Akihiro, Shiga, Kensuke, Hayashida, Arisa, Hatano, Taku, Ishiura, Hiroyuki, Mitsui, Jun, Hattori, Nobutaka, Mizuno, Toshiki, Nakagawa, Masanori, Tsuji, Shoji, Takashima, Hiroshi

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Novel de novo POLR3B mutations responsible for demyelinating Charcot–Marie–Tooth disease in Japan af Ando, Masahiro, Higuchi, Yujiro, Yuan, Jun‐Hui, Yoshimura, Akiko, Kitao, Ruriko, Morimoto, Takehiko, Taniguchi, Takaki, Takeuchi, Mika, Takei, Jun, Hiramatsu, Yu, Sakiyama, Yusuke, Hashiguchi, Akihiro, Okamoto, Yuji, Mitsui, Jun, Ishiura, Hiroyuki, Tsuji, Shoji, Takashima, Hiroshi

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Comprehensive Genetic Analyses of Inherited Peripheral Neuropathies in Japan: Making Early Diagnosis Possible af Ando, Masahiro, Higuchi, Yujiro, Yuan, Junhui, Yoshimura, Akiko, Taniguchi, Takaki, Kojima, Fumikazu, Noguchi, Yutaka, Hobara, Takahiro, Takeuchi, Mika, Takei, Jun, Hiramatsu, Yu, Sakiyama, Yusuke, Hashiguchi, Akihiro, Okamoto, Yuji, Mitsui, Jun, Ishiura, Hiroyuki, Tsuji, Shoji, Takashima, Hiroshi

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Exonic duplication CNV of NDRG1 associated with autosomal-recessive HMSN-Lom/CMT4D af Okamoto, Yuji, Goksungur, Meryem Tuba, Pehlivan, Davut, Beck, Christine R., Gonzaga-Jauregui, Claudia, Muzny, Donna M., Atik, Mehmed M., Carvalho, Claudia M.B., Matur, Zeliha, Bayraktar, Serife, Boone, Philip M., Akyuz, Kaya, Gibbs, Richard A., Battaloglu, Esra, Parman, Yesim, Lupski, James R.

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Novel heterozygous variants of SLC12A6 in Japanese families with Charcot–Marie–Tooth disease af Ando, Masahiro, Higuchi, Yujiro, Yuan, Junhui, Yoshimura, Akiko, Taniguchi, Takaki, Takei, Jun, Takeuchi, Mika, Hiramatsu, Yu, Shimizu, Fumitaka, Kubota, Masaya, Takeshima, Akari, Ueda, Takehiro, Koh, Kishin, Nagaoka, Utako, Tokashiki, Takashi, Sawai, Setsu, Sakiyama, Yusuke, Hashiguchi, Akihiro, Sato, Ryota, Kanda, Takashi, Okamoto, Yuji, Takashima, Hiroshi

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