Subcellular patch-clamp techniques for single-bouton stimulation and simultaneous pre- and postsynaptic recording at cortical synapses
Vandael, David, Okamoto, Yuji, Borges-Merjane, Carolina, Vargas-Barroso, Victor, Suter, Benjamin A., Jonas, Peter
Published in Nature protocols (01.06.2021)
Published in Nature protocols (01.06.2021)
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Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex Neuropathy
Gonzaga-Jauregui, Claudia, Harel, Tamar, Gambin, Tomasz, Kousi, Maria, Griffin, Laurie B., Francescatto, Ludmila, Ozes, Burcak, Karaca, Ender, Jhangiani, Shalini N., Bainbridge, Matthew N., Lawson, Kim S., Pehlivan, Davut, Okamoto, Yuji, Withers, Marjorie, Mancias, Pedro, Slavotinek, Anne, Reitnauer, Pamela J., Goksungur, Meryem T., Shy, Michael, Crawford, Thomas O., Koenig, Michel, Willer, Jason, Flores, Brittany N., Pediaditrakis, Igor, Us, Onder, Wiszniewski, Wojciech, Parman, Yesim, Antonellis, Anthony, Muzny, Donna M., Katsanis, Nicholas, Battaloglu, Esra, Boerwinkle, Eric, Gibbs, Richard A., Lupski, James R.
Published in Cell reports (Cambridge) (18.08.2015)
Published in Cell reports (Cambridge) (18.08.2015)
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Elderly patients with suspected Charcot-Marie-Tooth disease should be tested for the TTR gene for effective treatments
Taniguchi, Takaki, Ando, Masahiro, Okamoto, Yuji, Yoshimura, Akiko, Higuchi, Yujiro, Hashiguchi, Akihiro, Matsuda, Nozomu, Yamamoto, Mamoru, Dohi, Eisuke, Takahashi, Makoto, Yoshino, Masanao, Nomura, Taichi, Matsushima, Masaaki, Yabe, Ichiro, Sanpei, Yui, Ishiura, Hiroyuki, Mitsui, Jun, Nakagawa, Masanori, Tsuji, Shoji, Takashima, Hiroshi
Published in Journal of human genetics (01.06.2022)
Published in Journal of human genetics (01.06.2022)
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Journal Article
Developmental changes in Ca2+ channel subtypes regulating endocytosis at the calyx of Held
Midorikawa, Mitsuharu, Okamoto, Yuji, Sakaba, Takeshi
Published in The Journal of physiology (15.08.2014)
Published in The Journal of physiology (15.08.2014)
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Journal Article
Neuron-specific knockdown of Drosophila HADHB induces a shortened lifespan, deficient locomotive ability, abnormal motor neuron terminal morphology and learning disability
Li, Jialin, Suda, Kojiro, Ueoka, Ibuki, Tanaka, Ryo, Yoshida, Hideki, Okada, Yasushi, Okamoto, Yuji, Hiramatsu, Yu, Takashima, Hiroshi, Yamaguchi, Masamitsu
Published in Experimental cell research (15.06.2019)
Published in Experimental cell research (15.06.2019)
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Mutations in MME cause an autosomal-recessive Charcot-Marie-Tooth disease type 2
Higuchi, Yujiro, Hashiguchi, Akihiro, Yuan, Junhui, Yoshimura, Akiko, Mitsui, Jun, Ishiura, Hiroyuki, Tanaka, Masaki, Ishihara, Satoshi, Tanabe, Hajime, Nozuma, Satoshi, Okamoto, Yuji, Matsuura, Eiji, Ohkubo, Ryuichi, Inamizu, Saeko, Shiraishi, Wataru, Yamasaki, Ryo, Ohyagi, Yasumasa, Kira, Jun-ichi, Oya, Yasushi, Yabe, Hayato, Nishikawa, Noriko, Tobisawa, Shinsuke, Matsuda, Nozomu, Masuda, Masayuki, Kugimoto, Chiharu, Fukushima, Kazuhiro, Yano, Satoshi, Yoshimura, Jun, Doi, Koichiro, Nakagawa, Masanori, Morishita, Shinichi, Tsuji, Shoji, Takashima, Hiroshi
Published in Annals of neurology (01.04.2016)
Published in Annals of neurology (01.04.2016)
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Journal Article
Adipose Mitochondrial Biogenesis Is Suppressed in db/db and High-Fat Diet–Fed Mice and Improved by Rosiglitazone
RONG, James X, YANG QIU, STRUM, Jay C, RYAN, Terence E, HANSEN, Michael K, LEI ZHU, ZHANG, Vivian, MI XIE, OKAMOTO, Yuji, MATTIE, Michael D, HIGASHIYAMA, Hiroyuki, ASANO, Satoshi
Published in Diabetes (New York, N.Y.) (01.07.2007)
Published in Diabetes (New York, N.Y.) (01.07.2007)
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Complex hereditary peripheral neuropathies caused by novel variants in mitochondrial-related nuclear genes
Hiramatsu, Yu, Okamoto, Yuji, Yoshimura, Akiko, Yuan, Jun-Hui, Ando, Masahiro, Higuchi, Yujiro, Hashiguchi, Akihiro, Matsuura, Eiji, Nozaki, Fumihito, Kumada, Tomohiro, Murayama, Kei, Suzuki, Mikiya, Yamamoto, Yuki, Matsui, Naoko, Miyazaki, Yoshimichi, Yamaguchi, Masamitsu, Suzuki, Youji, Mitsui, Jun, Ishiura, Hiroyuki, Tanaka, Masaki, Morishita, Shinichi, Nishino, Ichizo, Tsuji, Shoji, Takashima, Hiroshi
Published in Journal of neurology (01.08.2022)
Published in Journal of neurology (01.08.2022)
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Journal Article
An NEFH founder mutation causes broad phenotypic spectrum in multiple Japanese families
Ando, Masahiro, Higuchi, Yujiro, Okamoto, Yuji, Yuan, Junhui, Yoshimura, Akiko, Takei, Jun, Taniguchi, Takaki, Hiramatsu, Yu, Sakiyama, Yusuke, Hashiguchi, Akihiro, Matsuura, Eiji, Nakagawa, Hiroto, Sonoda, Ken, Yamashita, Toru, Tamura, Akiko, Terasawa, Hideo, Mitsui, Jun, Ishiura, Hiroyuki, Tsuji, Shoji, Takashima, Hiroshi
Published in Journal of human genetics (01.07.2022)
Published in Journal of human genetics (01.07.2022)
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The First Case of Spinocerebellar Ataxia Type 8 in Monozygotic Twins
Sawada, Jun, Katayama, Takayuki, Tokashiki, Takashi, Kikuchi, Shiori, Kano, Kohei, Takahashi, Kae, Saito, Tsukasa, Adachi, Yoshiki, Okamoto, Yuji, Yoshimura, Akiko, Takashima, Hiroshi, Hasebe, Naoyuki
Published in Internal Medicine (15.01.2020)
Published in Internal Medicine (15.01.2020)
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Nationwide survey of Alexander disease in Japan and proposed new guidelines for diagnosis
Yoshida, Tomokatsu, Sasaki, Masayuki, Yoshida, Mari, Namekawa, Michito, Okamoto, Yuji, Tsujino, Seiichi, Sasayama, Hiroshi, Mizuta, Ikuko, Nakagawa, Masanori
Published in Journal of neurology (01.11.2011)
Published in Journal of neurology (01.11.2011)
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Genetic and pathophysiological insights from autopsied patient with primary familial brain calcification: novel MYORG variants and astrocytic implications
Hobara, Takahiro, Higuchi, Yujiro, Yoshida, Mari, Suehara, Masahito, Ando, Masahiro, Yuan, Jun-Hui, Yoshimura, Akiko, Kojima, Fumikazu, Matsuura, Eiji, Okamoto, Yuji, Mitsui, Jun, Tsuji, Shoji, Takashima, Hiroshi
Published in Acta neuropathologica communications (23.08.2024)
Published in Acta neuropathologica communications (23.08.2024)
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Clinical diversity caused by novel IGHMBP2 variants
Yuan, Jun-Hui, Hashiguchi, Akihiro, Yoshimura, Akiko, Yaguchi, Hiroshi, Tsuzaki, Koji, Ikeda, Azusa, Wada-Isoe, Kenji, Ando, Masahiro, Nakamura, Tomonori, Higuchi, Yujiro, Hiramatsu, Yu, Okamoto, Yuji, Takashima, Hiroshi
Published in Journal of human genetics (01.06.2017)
Published in Journal of human genetics (01.06.2017)
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Journal Article
Genetic and clinical features of cerebellar ataxia with RFC1 biallelic repeat expansions in Japan
Ando, Masahiro, Higuchi, Yujiro, Yuan, Junhui H., Yoshimura, Akiko, Higashi, Shuntaro, Takeuchi, Mika, Hobara, Takahiro, Kojima, Fumikazu, Noguchi, Yutaka, Takei, Jun, Hiramatsu, Yu, Nozuma, Satoshi, Sakiyama, Yusuke, Hashiguchi, Akihiro, Matsuura, Eiji, Okamoto, Yuji, Nagai, Masahiro, Takashima, Hiroshi
Published in Frontiers in neurology (10.08.2022)
Published in Frontiers in neurology (10.08.2022)
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Bilateral striatal necrosis caused by a founder mitochondrial 14459G > A mutation in two independent Japanese families
Hirayanagi, Kimitoshi, Okamoto, Yuji, Takai, Eriko, Ishizawa, Kunihiko, Makioka, Kouki, Fujita, Yukio, Kaneko, Yuka, Tanaka, Makoto, Takashima, Hiroshi, Ikeda, Yoshio
Published in Journal of the neurological sciences (15.07.2017)
Published in Journal of the neurological sciences (15.07.2017)
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