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by Kawamura, Seiji and Ando, Masaki and Seto, Naoki and Sato, Shuichi and Nakamura, Takashi and Tsubono, Kimio and Kanda, Nobuyuki and Tanaka, Takahiro and Yokoyama, Jun'ichi and Funaki, Ikkoh and Numata, Kenji and Ioka, Kunihito and Takashima, Takeshi and Agatsuma, Kazuhiro and Akutsu, Tomotada and Aoyanagi, Koh-suke and Arai, Koji and Araya, Akito and Asada, Hideki and Aso, Yoichi and Chen, Dan and Chiba, Takeshi and Ebisuzaki, Toshikazu and Ejiri, Yumiko and Enoki, Motohiro and Eriguchi, Yoshiharu and Fujimoto, Masa-Katsu and Fujita, Ryuichi and Fukushima, Mitsuhiro and Futamase, Toshifumi and Harada, Tomohiro and Hashimoto, Tatsuaki and Hayama, Kazuhiro and Hikida, Wataru and Himemoto, Yoshiaki and Hirabayashi, Hisashi and Hiramatsu, Takashi and Hong, Feng-Lei and Horisawa, Hideyuki and Hosokawa, Mizuhiko and Ichiki, Kiyotomo and Ikegami, Takeshi and Inoue, Kaiki T and Ishidoshiro, Koji and Ishihara, Hideki and Ishikawa, Takehiko and Ishizaki, Hideharu and Ito, Hiroyuki and Itoh, Yousuke and Izumi, Kiwamu and Kawano, Isao and Kawashima, Nobuki and Kawazoe, Fumiko and Kishimoto, Naoko and Kiuchi, Kenta and Kobayashi, Shiho and Kohri, Kazunori and Koizumi, Hiroyuki and Kojima, Yasufumi and Kokeyama, Keiko and Kokuyama, Wataru and Kotake, Kei and Kozai, Yoshihide and Kunimori, Hiroo and Kuninaka, Hitoshi and Kuroda, Kazuaki and Kuroyanagi, Sachiko and Maeda, Kei-ichi and Matsuhara, Hideo and Matsumoto, Nobuyuki and Michimura, Yuta and Miyakawa, Osamu and Miyamoto, Umpei and Miyoki, Shinji and Morimoto, Mutsuko Y and Morisawa, Toshiyuki and Moriwaki, Shigenori and Mukohyama, Shinji and Musha, Mitsuru and Nagano, Shigeo and Naito, Isao and Nakamura, Kouji and Nakano, Hiroyuki and Nakao, Kenichi and Nakasuka, Shinichi and Nakayama, Yoshinori and Nakazawa, Kazuhiro and Nishida, Erina and Nishiyama, Kazutaka and Nishizawa, Atsushi and Niwa, Yoshito and Noumi, Taiga and Obuchi, Yoshiyuki and Ohashi, Masatake and Ohishi, Naoko and Ohkawa, Masashi and Okada, Kenshi and Okada, Norio and Oohara, Kenichi and Sago, Norichika and ...
Classical and Quantum Gravity, ISSN 0264-9381, 05/2011, Volume 28, Issue 9, p. 094011
The objectives of the DECi-hertz Interferometer Gravitational Wave Observatory (DECIGO) are to open a new window of observation for gravitational wave... 
PHYSICS, MULTIDISCIPLINARY | COMPACT BINARIES | ASTRONOMY & ASTROPHYSICS | PHYSICS, PARTICLES & FIELDS
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 03/2019, Volume 27, Issue 3, pp. 378 - 383
Journal Article
Congenital Anomalies, ISSN 0914-3505, 06/2012, Volume 52, Issue 2, pp. 67 - 71
Journal Article
Human Mutation, ISSN 1059-7794, 07/2010, Volume 31, Issue 7, pp. 820 - 829
Journal Article
Neurobiology of Disease, ISSN 0969-9961, 04/2018, Volume 112, pp. 24 - 34
Loss of function mutations in the gene, which encodes the voltage-gated sodium channel Nav1.1, have been described in the majority of Dravet syndrome patients... 
Hyperactivity | Epilepsy | Dravet syndrome | Conditional knockout mouse model | Somatostatin | Parvalbumin | Autism spectrum disorder | Scn1a | Interneuron
Journal Article
Nature communications, ISSN 2041-1723, 2014, Volume 5, Issue 1, pp. 3393 - 3393
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2013, Volume 8, Issue 10, pp. e77843 - e77843
Objective: Dravet syndrome is a severe form of intractable pediatric epilepsy with a high incidence of SUDEP: Sudden Unexpected Death in epilepsy. Cardiac... 
PLURIPOTENT STEM-CELLS | INHIBITORY INTERNEURONS | NA+ CHANNEL | MULTIDISCIPLINARY SCIENCES | MOUSE MODEL | SEVERE MYOCLONIC EPILEPSY | LONG-QT SYNDROME | SUDDEN UNEXPECTED DEATH | NEURONAL SODIUM-CHANNEL | RAT VENTRICULAR MYOCYTES | SINOATRIAL NODE | Transcription, Genetic - drug effects | Humans | Mice, Inbred C57BL | Epilepsies, Myoclonic - physiopathology | NAV1.5 Voltage-Gated Sodium Channel - metabolism | Mutation - genetics | Telemetry | Death, Sudden, Cardiac | Arrhythmias, Cardiac - physiopathology | Epilepsies, Myoclonic - complications | Heart Rate - drug effects | Myocytes, Cardiac - pathology | Animals | Myocytes, Cardiac - metabolism | Protein Biosynthesis - drug effects | Arrhythmias, Cardiac - complications | Mice | Pentylenetetrazole | Cardiac Electrophysiology | NAV1.5 Voltage-Gated Sodium Channel - genetics | Tetrodotoxin - pharmacology | Action Potentials - drug effects | Disease Models, Animal | Ion Channel Gating - drug effects | Animal experimentation | Heart | Medical research | Arrhythmia | Marine toxins | Epilepsy | Electrocardiogram | Medicine, Experimental | Electrocardiography | Genetic aspects | Electric properties | Tetrodotoxin | Cardiac arrhythmia | Electrophysiology | Action potential | Myocytes | Ventricular fibrillation | Fibrillation | Risk assessment | Rodents | Long QT syndrome | Sodium channels (voltage-gated) | Heart diseases | Euthanasia | EKG | Phenotypes | Cardiac muscle | Excitability | Pharmacology | Patients | Haploinsufficiency | Heart rate | Neurology | Bradycardia | Mutation | Ventricle | Laboratory animals | Prolongation | Index Medicus
Journal Article
PLoS ONE, 01/2012, Volume 7, Issue 1
Journal Article