Hasil Pencarian - Taisuke Ishikawa

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  1. 1
    Letter regarding “SCN9A variant in a family of mixed breed dogs with congenital insensitivity to pain”—Navigating the pathogenicity of candidate gene mutations: Spotlight on paralog Nav genes

    Letter regarding “SCN9A variant in a family of mixed breed dogs with congenital insensitivity to pain”—Navigating the pathogenicity of candidate gene mutations: Spotlight on paralo... oleh Taisuke Ishikawa, Hiroshi Aoki

    Diterbitkan 2023-05-01
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  2. 2
    Catalytic trifluoromethylation of iodoarenes by use of 2-trifluoromethylated benzimidazoline as trifluoromethylating reagent

    Catalytic trifluoromethylation of iodoarenes by use of 2-trifluoromethylated benzimidazoline as trifluoromethylating reagent oleh Tatsuhiro Uchikura, Nanami Kamiyama, Taisuke Ishikawa, Takahiko Akiyama

    Diterbitkan 2020-09-01
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  3. 3
    Arrhythmogenic right ventricular cardiomyopathy in a Japanese patient with a homozygous founder variant of DSG2 in the East Asian population

    Arrhythmogenic right ventricular cardiomyopathy in a Japanese patient with a homozygous founder variant of DSG2 in the East Asian population oleh Haruka Murakami, Yoko Tanimoto, Kojiro Tanimoto, Satomi Inoue, Taisuke Ishikawa, Naomasa Makita, Kazuki Yamazawa

    Diterbitkan 2022-08-01
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  4. 4
    Molecular mechanisms of heart failure progression associated with implantable cardioverter-defibrillator shocks for ventricular tachyarrhythmias

    Molecular mechanisms of heart failure progression associated with implantable cardioverter-defibrillator shocks for ventricular tachyarrhythmias oleh Yukiomi Tsuji, MD, PhD, Taisuke Ishikawa, DVM, PhD, Naomasa Makita, MD, PhD

    Diterbitkan 2014-08-01
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  5. 5
    Inherited bradyarrhythmia: A diverse genetic background

    Inherited bradyarrhythmia: A diverse genetic background oleh Taisuke Ishikawa, DVM, PhD, Yukiomi Tsuji, MD, PhD, Naomasa Makita, MD, PhD

    Diterbitkan 2016-10-01
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  6. 6
    A novel de novo calmodulin mutation in a 6-year-old boy who experienced an aborted cardiac arrest

    A novel de novo calmodulin mutation in a 6-year-old boy who experienced an aborted cardiac arrest oleh Kazuhiro Takahashi, MD, PhD, Taisuke Ishikawa, DVM, PhD, Naomasa Makita, MD, PhD, Kiyotaka Takefuta, MD, Taisuke Nabeshima, MD, Mami Nakayashiro, MD

    Diterbitkan 2017-01-01
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  7. 7
    Desmin‐related myopathy characterized by non‐compaction cardiomyopathy, cardiac conduction defect, and coronary artery dissection

    Desmin‐related myopathy characterized by non‐compaction cardiomyopathy, cardiac conduction defect, and coronary artery dissection oleh Ran Tamiya, Yuki Saito, Daisuke Fukamachi, Koichi Nagashima, Yoshihiro Aizawa, Kimie Ohkubo, Takumi Hatta, Akira Sezai, Masashi Tanaka, Taisuke Ishikawa, Naomasa Makita, Naokata Sumitomo, Yasuo Okumura

    Diterbitkan 2020-06-01
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  8. 8
    TBX5 R264K acts as a modifier to develop dilated cardiomyopathy in mice independently of T-box pathway.

    TBX5 R264K acts as a modifier to develop dilated cardiomyopathy in mice independently of T-box pathway. oleh Nariaki Miyao, Yukiko Hata, Hironori Izumi, Ryo Nagaoka, Yuko Oku, Ichiro Takasaki, Taisuke Ishikawa, Shinya Takarada, Mako Okabe, Hideyuki Nakaoka, Keijiro Ibuki, Sayaka Ozawa, Tomoyuki Yoshida, Hideyuki Hasegawa, Naomasa Makita, Naoki Nishida, Hisashi Mori, Fukiko Ichida, Keiichi Hirono

    Diterbitkan 2020-01-01
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  9. 9
    Targeted deep sequencing analyses of long QT syndrome in a Japanese population

    Targeted deep sequencing analyses of long QT syndrome in a Japanese population oleh Yuki Nagata, Ryo Watanabe, Christian Eichhorn, Seiko Ohno, Takeshi Aiba, Taisuke Ishikawa, Yukiko Nakano, Yoshiyasu Aizawa, Kenshi Hayashi, Nobuyuki Murakoshi, Tadashi Nakajima, Nobue Yagihara, Hiroyuki Mishima, Takeaki Sudo, Chihiro Higuchi, Atsushi Takahashi, Akihiro Sekine, Takeru Makiyama, Yoshihiro Tanaka, Atsuyuki Watanabe, Motomi Tachibana, Hiroshi Morita, Koh-ichiro Yoshiura, Tatsuhiko Tsunoda, Hiroshi Watanabe, Masahiko Kurabayashi, Akihiko Nogami, Yasuki Kihara, Minoru Horie, Wataru Shimizu, Naomasa Makita, Toshihiro Tanaka

    Diterbitkan 2022-01-01
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  10. 10
    Targeted deep sequencing analyses of long QT syndrome in a Japanese population.

    Targeted deep sequencing analyses of long QT syndrome in a Japanese population. oleh Yuki Nagata, Ryo Watanabe, Christian Eichhorn, Seiko Ohno, Takeshi Aiba, Taisuke Ishikawa, Yukiko Nakano, Yoshiyasu Aizawa, Kenshi Hayashi, Nobuyuki Murakoshi, Tadashi Nakajima, Nobue Yagihara, Hiroyuki Mishima, Takeaki Sudo, Chihiro Higuchi, Atsushi Takahashi, Akihiro Sekine, Takeru Makiyama, Yoshihiro Tanaka, Atsuyuki Watanabe, Motomi Tachibana, Hiroshi Morita, Koh-Ichiro Yoshiura, Tatsuhiko Tsunoda, Hiroshi Watanabe, Masahiko Kurabayashi, Akihiko Nogami, Yasuki Kihara, Minoru Horie, Wataru Shimizu, Naomasa Makita, Toshihiro Tanaka

    Diterbitkan 2022-01-01
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  11. 11
    TAD boundary deletion causes PITX2-related cardiac electrical and structural defects

    TAD boundary deletion causes PITX2-related cardiac electrical and structural defects oleh Manon Baudic, Hiroshige Murata, Fernanda M. Bosada, Uirá Souto Melo, Takanori Aizawa, Pierre Lindenbaum, Lieve E. van der Maarel, Amaury Guedon, Estelle Baron, Enora Fremy, Adrien Foucal, Taisuke Ishikawa, Hiroya Ushinohama, Sean J. Jurgens, Seung Hoan Choi, Florence Kyndt, Solena Le Scouarnec, Vincent Wakker, Aurélie Thollet, Annabelle Rajalu, Tadashi Takaki, Seiko Ohno, Wataru Shimizu, Minoru Horie, Takeshi Kimura, Patrick T. Ellinor, Florence Petit, Yves Dulac, Paul Bru, Anne Boland, Jean-François Deleuze, Richard Redon, Hervé Le Marec, Thierry Le Tourneau, Jean-Baptiste Gourraud, Yoshinori Yoshida, Naomasa Makita, Claude Vieyres, Takeru Makiyama, Stephan Mundlos, Vincent M. Christoffels, Vincent Probst, Jean-Jacques Schott, Julien Barc

    Diterbitkan 2024-04-01
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