Canlyniadau Chwilio - Okamoto, Yuji

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

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Transsynaptic modulation of presynaptic short-term plasticity in hippocampal mossy fiber synapses gan 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 gan 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 gan Tokuhisa, Atsushi, Akinaga, Yoshinobu, Terayama, Kei, Okamoto, Yuji, Okuno, Yasushi

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Receptor‐activated Smad localisation in Bleomycin‐induced pulmonary fibrosis gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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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