Argyrophilic grain disease in a 46-year-old male suicide victim von Yoshida, Koji, Hata, Yukiko, Kinoshita, Koshi, Nishida, Naoki

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MicroRNA-145-5p and microRNA-320a encapsulated in endothelial microparticles contribute to the progression of vasculitis in acute Kawasaki Disease von Nakaoka, Hideyuki, Hirono, Keiichi, Yamamoto, Seiji, Takasaki, Ichiro, Takahashi, Kei, Kinoshita, Koshi, Takasaki, Asami, Nishida, Naonori, Okabe, Mako, Ce, Wang, Miyao, Nariaki, Saito, Kazuyoshi, Ibuki, Keijiro, Ozawa, Sayaka, Adachi, Yuichi, Ichida, Fukiko

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Lack of modulatory effect of the SCN5A R1193Q polymorphism on cardiac fast Na+ current at body temperature von Abe, Masayoshi, Kinoshita, Koshi, Matsuoka, Kenta, Nakada, Takahito, Miura, Kimiaki, Hata, Yukiko, Nishida, Naoki, Tabata, Toshihide

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MicroRNA-93 may control vascular endothelial growth factor A in circulating peripheral blood mononuclear cells in acute Kawasaki disease von Saito, Kazuyoshi, Nakaoka, Hideyuki, Takasaki, Ichiro, Hirono, Keiichi, Yamamoto, Seiji, Kinoshita, Koshi, Miyao, Nariaki, Ibuki, Keijiro, Ozawa, Sayaka, Watanabe, Kazuhiro, Bowles, Neil E., Ichida, Fukiko

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A functional neuron maturation device provides convenient application on microelectrode array for neural network measurement von Han, Xiaobo, Matsuda, Naoki, Ishibashi, Yuto, Odawara, Aoi, Takahashi, Sayuri, Tooi, Norie, Kinoshita, Koshi, Suzuki, Ikuro

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An Autopsy Case of Sudden Unexpected Death of a Young Adult in a Hot Bath: Molecular Analysis Using Next-Generation DNA Sequencing von Hata, Yukiko, Kinoshita, Koshi, Nishida, Naoki

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A mutant HCN4 channel in a family with bradycardia, left bundle branch block, and left ventricular noncompaction von Yokoyama, Ryosuke, Kinoshita, Koshi, Hata, Yukiko, Abe, Masayoshi, Matsuoka, Kenta, Hirono, Keiichi, Kano, Masanobu, Nakazawa, Makoto, Ichida, Fukiko, Nishida, Naoki, Tabata, Toshihide

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The Susceptibilities of Human Ether-à-Go-Go-Related Gene Channel with the G487R Mutation to Arrhythmogenic Factors von Hisajima, Nozomi, Hata, Yukiko, Kinoshita, Koshi, Fukushima, Toshiki, Nishida, Naoki, Kano, Masanobu, Tabata, Toshihide

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Glycine/Serine Polymorphism at Position 38 Influences KCNE1 Subunit’s Modulatory Actions on Rapid and Slow Delayed Rectifier K+ Currents von Yamaguchi, Yoshiaki, Nishide, Kohki, Kato, Mario, Hata, Yukiko, Mizumaki, Koichi, Kinoshita, Koshi, Nonobe, Yuki, Tabata, Toshihide, Sakamoto, Tamotsu, Kataoka, Naoya, Nakatani, Yosuke, Ichida, Fukiko, Mori, Hisashi, Fukurotani, Kenkichi, Inoue, Hiroshi, Nishida, Naoki

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Sudden unexpected death owing to unilateral medial medullary infarction with early involvement of the respiratory center von Hata, Yukiko, Yoshida, Koji, Kinoshita, Koshi, Nishida, Naoki

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A Novel Missense Mutation Causing a G487R Substitution in the S2-S3 Loop of Human ether-à-go-go-Related Gene Channel von KINOSHITA, KOSHI, YAMAGUCHI, YOSHIAKI, NISHIDE, KOHKI, KIMOTO, KATSUYA, NONOBE, YUKI, FUJITA, AKIRA, ASANO, KENTA, TABATA, TOSHIHIDE, MORI, HISASHI, INOUE, HIROSHI, HATA, YUKIKO, FUKUROTANI, KENKICHI, NISHIDA, NAOKI

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Cell‐microarray analysis of antigen‐specific B‐cells: Single cell analysis of antigen receptor expression and specificity von Tajiri, Kazuto, Kishi, Hiroyuki, Tokimitsu, Yoshiharu, Kondo, Sachiko, Ozawa, Tatsuhiko, Kinoshita, Koshi, Jin, Aishun, Kadowaki, Shinichi, Sugiyama, Toshiro, Muraguchi, Atsushi

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Pathological features of preclinical or early clinical stages of corticobasal degeneration: a comparison with advanced cases von Nishida, Naoki, Yoshida, Koji, Hata, Yukiko, Arai, Yuichi, Kinoshita, Koshi

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SCN5A(K817E), a novel Brugada syndrome–associated mutation that alters the activation gating of NaV1.5 channel von Kinoshita, Koshi, Takahashi, Hiroyuki, Hata, Yukiko, Nishide, Kohki, Kato, Mario, Fujita, Hiroki, Yoshida, Sho, Murai, Kazutaka, Mizumaki, Koichi, Nishida, Kunihiro, Yamaguchi, Yoshiaki, Kano, Masanobu, Tabata, Toshihide, Nishida, Naoki

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An Autopsy Case of Acute and Nonalcoholic Thiamine-Deficient Encephalopathy von Hata, Yukiko, Takeuchi, Yui, Kinoshita, Koshi, Nishida, Naoki

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Identification and characterization of a novel genetic mutation with prolonged QT syndrome in an unexplained postoperative death von Hata, Yukiko, Mori, Hisashi, Tanaka, Ayumi, Fujita, Yosuke, Shimomura, Takeshi, Tabata, Toshihide, Kinoshita, Koshi, Yamaguchi, Yoshiaki, Ichida, Fukiko, Kominato, Yoshihiko, Ikeda, Noriaki, Nishida, Naoki

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SCN5A(K817E), a novel Brugada syndrome–associated mutation that alters the activation gating of NaV 1.5 channel von Kinoshita, Koshi, PhD, Takahashi, Hiroyuki, BE, Hata, Yukiko, PhD, Nishide, Kohki, ME, Kato, Mario, ME, Fujita, Hiroki, PhD, Yoshida, Sho, BE, Murai, Kazutaka, BE, Mizumaki, Koichi, MD, PhD, Nishida, Kunihiro, MD, PhD, FHRS, Yamaguchi, Yoshiaki, MD, PhD, Kano, Masanobu, PhD, Tabata, Toshihide, PhD, Nishida, Naoki, MD, PhD

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Ternary complex formation of pVHL, elongin B and elongin C visualized in living cells by a fluorescence resonance energy transfer-fluorescence lifetime imaging microscopy technique von Kinoshita, Koshi, Goryo, Kenji, Takada, Mamiko, Tomokuni, Yosuke, Aso, Teijiro, Okuda, Heiwa, Shuin, Taro, Fukumura, Hiroshi, Sogawa, Kazuhiro

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Altered DNA binding specificity of Arnt by selection of partner bHLH–PAS proteins von Kinoshita, Koshi, Kikuchi, Yasuo, Sasakura, Yukie, Suzuki, Masashi, Fujii‐Kuriyama, Yoshiaki, Sogawa, Kazuhiro

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A case of esophageal perforation due to esd for which treatment selection was difficult von IRIE, Tomoko, KINOSHITA, Koshi

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