未登录Novel KCNQ1 Q234K variant, identified in patients with long QT syndrome and epileptiform activity, induces both gain- and loss-of-function of slowly activating delayed rectifier potassium currents
Nakajima, Tadashi; Tamura, Shuntaro; Kawabata-Iwakawa, Reika; Itoh, Hideki; Hasegawa, Hiroshi; Kobari, Takashi; Harasawa, Shun; Sekine, Akiko; Nishiyama, Masahiko; Kurabayashi, Masahiko; Imoto, Keiji; Kaneko, Yoshiaki; Nakatani, Yosuke; Horie, Minoru; Ishii, Hideki .png)
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收藏分享 收藏 分享 收藏 分享 收藏 Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophySCN5A的剪接失调导致强直性肌营养不良的心脏传导延迟和心律失常Freyermuth, Fernande; Rau, Frederique; Kokunai, Yosuke; Linke, Thomas; Sellier, Chantal; Nakamori, Masayuki; Kino, Yoshihiro; Arandel, Ludovic; Jollet, Arnaud; Thibault, Christelle; Philipps, Muriel; Vicaire, Serge; Jost, Bernard; Udd, Bjarne; Day, John W.; Duboc, Denis; Wahbi, Karim; Matsumura, Tsuyoshi; Fujimura, Harutoshi; Mochizuki, Hideki; Deryckere, Francois; Kimura, Takashi; Nukina, Nobuyuki; Ishiura, Shoichi; Lacroix, Vincent; Campan-Fournier, Amandine; Navratil, Vincent; Chautard, Emilie; Auboeuf, Didier; Horie, Minoru; Imoto, Keiji; Lee, Kuang-Yung; Swanson, Maurice S.; Lopez de Munain, Adolfo; Inada, Shin; Itoh, Hideki; Nakazawa, Kazuo; Ashihara, Takashi; Wang, Eric; Zimmer, Thomas; Furling, Denis; Takahashi, Masanori P.; Charlet-Berguerand, Nicolas 分享 收藏 Chemical corrector treatment ameliorates increased seizure susceptibility in a mouse model of familial epilepsyYokoi, Norihiko; Fukata, Yuko; Kase, Daisuke; Miyazaki, Taisuke; Jaegle, Martine; Ohkawa, Toshika; Takahashi, Naoki; Iwanari, Hiroko; Mochizuki, Yasuhiro; Hamakubo, Takao; Imoto, Keiji; Meijer, Dies; Watanabe, Masahiko; Fukata, Masaki 分享 收藏 分享 收藏 CCL-1 in the spinal cord contributes to neuropathic pain induced by nerve injuryAkimoto, N.; Honda, K.; Uta, D.; Beppu, K.; Ushijima, Y.; Matsuzaki, Y.; Nakashima, S.; Kido, M. A.; Imoto, K.; Takano, Y.; Noda, M. 分享 收藏 Hyperpolarization-activated cyclic nucleotide gated channels: a potential molecular link between epileptic seizures and Aβ generation in Alzheimer's diseaseSaito, Yuhki; Inoue, Tsuyoshi; Zhu, Gang; Kimura, Naoki; Okada, Motohiro; Nishimura, Masaki; Kimura, Nobuyuki; Murayama, Shigeo; Kaneko, Sunao; Shigemoto, Ryuichi; Imoto, Keiji; Suzuki, Toshiharu 分享 收藏 Hypothalamic Orexin Stimulates Feeding-Associated Glucose Utilization in Skeletal Muscle via Sympathetic Nervous SystemShiuchi, Tetsuya; Haque, Mohammad Shahidul; Okamoto, Shiki; Inoue, Tsuyoshi; Kageyama, Haruaki; Lee, Suni; Toda, Chitoku; Suzuki, Atsushi; Bachman, Eric S.; Kim, Young-Bum; Sakurai, Takashi; Yanagisawa, Masashi; Shioda, Seiji; Imoto, Keiji; Minokoshi, Yasuhiko 分享 收藏 Latent Genetic Backgrounds and Molecular Pathogenesis in Drug-Induced Long-QT SyndromeItoh, Hideki; Sakaguchi, Tomoko; Ding, Wei-Guang; Watanabe, Eiichi; Watanabe, Ichiro; Nishio, Yukiko; Makiyama, Takeru; Ohno, Seiko; Akao, Masaharu; Higashi, Yukei; Zenda, Naoko; Kubota, Tomoki; Mori, Chikara; Okajima, Katsunori; Haruna, Tetsuya; Miyamoto, Akashi; Kawamura, Mihoko; Ishida, Katsuya; Nagaoka, Iori; Oka, Yuko; Nakazawa, Yuko; Yao, Takenori; Jo, Hikari; Sugimoto, Yoshihisa; Ashihara, Takashi; Hayashi, Hideki; Ito, Makoto; Imoto, Keiji; Matsuura, Hiroshi; Horie, Minoru 分享 收藏 A paradoxical effect of lidocaine for the N406S mutation of SCN5A associated with Brugada syndromeItoh, Hideki; Tsuji, Keiko; Sakaguchi, Tomoko; Nagaoka, Lori; Oka, Yuko; Nakazawa, Yuko; Yao, Takenori; Jo, Hikari; Ashihara, Takashi; Ito, Makoto; Horie, Minoru; Imoto, Keiji 分享 收藏 Imaging cellular signals in the heart in vivo:: Cardiac expression of the high-signal Ca2+ indicator GCaMP2Tallini, YN; Ohkura, M; Choi, BR; Ji, GJ; Imoto, K; Doran, R; Lee, J; Plan, P; Wilson, J; Xin, HB; Sanbe, A; Gulick, J; Mathai, J; Robbins, J; Salama, G; Nakai, J; Kotlikoff, MI 分享 收藏 分享 收藏 分享 收藏 分享 收藏 分享 收藏 分享 收藏 LTRPC2 Ca2+-permeable channel activated by changes in redox status confers susceptibility to cell deathHara, Y; Wakamori, M; Ishii, M; Maeno, E; Nishida, M; Yoshida, T; Yamada, H; Shimizu, S; Mori, E; Kudoh, J; Shimizu, N; Kurose, H; Okada, Y; Imoto, K; Mori, Y 分享 收藏 A missense mutation of the Na+ channel αII subunit gene Nav1.2 in a patient with febrile and afebrile seizures causes channel dysfunctionSugawara, T; Tsurubuchi, Y; Agarwala, KL; Ito, M; Fukuma, G; Mazaki-Miyazaki, E; Nagafuji, H; Noda, M; Imoto, K; Wada, K; Mitsudome, A; Kaneko, S; Montal, M; Nagata, K; Hirose, S; Yamakawa, K 分享 收藏 
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