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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.
Published in:
Journal of Veterinary Internal Medicine, 2023, v. 37, n. 3, p. 791, doi. 10.1111/jvim.16708
By:
- Ishikawa, Taisuke;
- Aoki, Hiroshi
Publication type:
Article
Comparative effects of amlodipine and benazepril on Left Atrial Pressure in Dogs with experimentally-induced Mitral Valve Regurgitation.
Published in:
BMC Veterinary Research, 2012, v. 8, n. 1, p. 166, doi. 10.1186/1746-6148-8-166
By:
- Shuji Suzuki;
- Ryuji Fukushima;
- Taisuke Ishikawa;
- Yuta Yamamoto;
- Hamabe, Lina;
- Soomin Kim;
- Rieko Yoshiyuki;
- Noboru Machida;
- Ryou Tanaka
Publication type:
Article
TAD boundary deletion causes PITX2-related cardiac electrical and structural defects.
Published in:
Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-47739-x
By:
- Baudic, Manon;
- Murata, Hiroshige;
- Bosada, Fernanda M.;
- Melo, Uirá Souto;
- Aizawa, Takanori;
- Lindenbaum, Pierre;
- van der Maarel, Lieve E.;
- Guedon, Amaury;
- Baron, Estelle;
- Fremy, Enora;
- Foucal, Adrien;
- Ishikawa, Taisuke;
- Ushinohama, Hiroya;
- Jurgens, Sean J.;
- Choi, Seung Hoan;
- Kyndt, Florence;
- Le Scouarnec, Solena;
- Wakker, Vincent;
- Thollet, Aurélie;
- Rajalu, Annabelle
Publication type:
Article
Brugada syndrome in Japan and Europe: a genome-wide association study reveals shared genetic architecture and new risk loci.
Published in:
European Heart Journal, 2024, v. 45, n. 26, p. 2320, doi. 10.1093/eurheartj/ehae251
By:
- Ishikawa, Taisuke;
- Masuda, Tatsuo;
- Hachiya, Tsuyoshi;
- Dina, Christian;
- Simonet, Floriane;
- Nagata, Yuki;
- Tanck, Michael W T;
- Sonehara, Kyuto;
- Glinge, Charlotte;
- Tadros, Rafik;
- Khongphatthanayothin, Apichai;
- Lu, Tzu-Pin;
- Higuchi, Chihiro;
- Nakajima, Tadashi;
- Hayashi, Kenshi;
- Aizawa, Yoshiyasu;
- Nakano, Yukiko;
- Nogami, Akihiko;
- Morita, Hiroshi;
- Ohno, Seiko
Publication type:
Article
Functionally validated SCN5A variants allow interpretation of pathogenicity and prediction of lethal events in Brugada syndrome.
Published in:
European Heart Journal, 2021, v. 49, n. 29, p. 2854, doi. 10.1093/eurheartj/ehab254
By:
- Ishikawa, Taisuke;
- Kimoto, Hiroki;
- Mishima, Hiroyuki;
- Yamagata, Kenichiro;
- Ogata, Soshiro;
- Aizawa, Yoshiyasu;
- Hayashi, Kenshi;
- Morita, Hiroshi;
- Nakajima, Tadashi;
- Nakano, Yukiko;
- Nagase, Satoshi;
- Murakoshi, Nobuyuki;
- Kowase, Shinya;
- Ohkubo, Kimie;
- Aiba, Takeshi;
- Morimoto, Shimpei;
- Ohno, Seiko;
- Kamakura, Shiro;
- Nogami, Akihiko;
- Takagi, Masahiko
Publication type:
Article
Inherited bradyarrhythmia: A diverse genetic background.
Published in:
Journal of Arrhythmia, 2016, v. 32, n. 5, p. 352, doi. 10.1016/j.joa.2015.09.009
By:
- Ishikawa, Taisuke;
- Tsuji, Yukiomi;
- Makita, Naomasa
Publication type:
Article
Molecular mechanisms of heart failure progression associated with implantable cardioverter-defibrillator shocks for ventricular tachyarrhythmias.
Published in:
Journal of Arrhythmia, 2014, v. 30, n. 4, p. 235, doi. 10.1016/j.joa.2014.04.003
By:
- Tsuji, Yukiomi;
- Ishikawa, Taisuke;
- Makita, Naomasa
Publication type:
Article
Nuclear accumulation of androgen receptor in gender difference of dilated cardiomyopathy due to lamin A/C mutations.
Published in:
Cardiovascular Research, 2013, v. 99, n. 3, p. 382, doi. 10.1093/cvr/cvt106
By:
- Arimura, Takuro;
- Onoue, Kenji;
- Takahashi-Tanaka, Yumiko;
- Ishikawa, Taisuke;
- Kuwahara, Masayoshi;
- Setou, Mitsutoshi;
- Shigenobu, Shuji;
- Yamaguchi, Katsushi;
- Bertrand, Anne T.;
- Machida, Noboru;
- Takayama, Kazumi;
- Fukusato, Masayuki;
- Tanaka, Ryo;
- Somekawa, Satoshi;
- Nakano, Tomoya;
- Yamane, Yoshihisa;
- Kuba, Keiji;
- Imai, Yumiko;
- Saito, Yoshihiko;
- Bonne, Gisèle
Publication type:
Article
TBX5 R264K acts as a modifier to develop dilated cardiomyopathy in mice independently of T-box pathway.
Published in:
PLoS ONE, 2020, v. 15, n. 4, p. 1, doi. 10.1371/journal.pone.0227393
By:
- Miyao, Nariaki;
- Hata, Yukiko;
- Izumi, Hironori;
- Nagaoka, Ryo;
- Oku, Yuko;
- Takasaki, Ichiro;
- Ishikawa, Taisuke;
- Takarada, Shinya;
- Okabe, Mako;
- Nakaoka, Hideyuki;
- Ibuki, Keijiro;
- Ozawa, Sayaka;
- Yoshida, Tomoyuki;
- Hasegawa, Hideyuki;
- Makita, Naomasa;
- Nishida, Naoki;
- Mori, Hisashi;
- Ichida, Fukiko;
- Hirono, Keiichi
Publication type:
Article
Identification of transmembrane protein 168 mutation in familial Brugada syndrome.
Published in:
FASEB Journal, 2020, v. 34, n. 5, p. 6399, doi. 10.1096/fj.201902991R
By:
- Shimizu, Akio;
- Zankov, Dimitar P.;
- Sato, Akira;
- Komeno, Masahiro;
- Toyoda, Futoshi;
- Yamazaki, Satoru;
- Makita, Toshinori;
- Noda, Taichi;
- Ikawa, Masahito;
- Asano, Yoshihiro;
- Miyashita, Yohei;
- Takashima, Seiji;
- Morita, Hiroshi;
- Ishikawa, Taisuke;
- Makita, Naomasa;
- Hitosugi, Masahito;
- Matsuura, Hiroshi;
- Ohno, Seiko;
- Horie, Minoru;
- Ogita, Hisakazu
Publication type:
Article
Desmin‐related myopathy characterized by non‐compaction cardiomyopathy, cardiac conduction defect, and coronary artery dissection.
Published in:
ESC Heart Failure, 2020, v. 7, n. 3, p. 1338, doi. 10.1002/ehf2.12667
By:
- Tamiya, Ran;
- Saito, Yuki;
- Fukamachi, Daisuke;
- Nagashima, Koichi;
- Aizawa, Yoshihiro;
- Ohkubo, Kimie;
- Hatta, Takumi;
- Sezai, Akira;
- Tanaka, Masashi;
- Ishikawa, Taisuke;
- Makita, Naomasa;
- Sumitomo, Naokata;
- Okumura, Yasuo
Publication type:
Article
Arrhythmogenic right ventricular cardiomyopathy in a Japanese patient with a homozygous founder variant of DSG2 in the East Asian population.
Published in:
Human Genome Variation, 2022, v. 9, n. 1, p. 1, doi. 10.1038/s41439-022-00206-9
By:
- Murakami, Haruka;
- Tanimoto, Yoko;
- Tanimoto, Kojiro;
- Inoue, Satomi;
- Ishikawa, Taisuke;
- Makita, Naomasa;
- Yamazawa, Kazuki
Publication type:
Article
Allele-specific ablation rescues electrophysiological abnormalities in a human iPS cell model of long-QT syndrome with a CALM2 mutation.
Published in:
Human Molecular Genetics, 2017, v. 26, n. 9, p. 1670, doi. 10.1093/hmg/ddx073
By:
- Yamamoto, Yuta;
- Makiyama, Takeru;
- Harita, Takeshi;
- Sasaki, Kenichi;
- Wuriyanghai, Yimin;
- Hayano, Mamoru;
- Nishiuchi, Suguru;
- Kohjitani, Hirohiko;
- Hirose, Sayako;
- Chen, Jiarong;
- Yokoi, Fumika;
- Ishikawa, Taisuke;
- Ohno, Seiko;
- Chonabayashi, Kazuhisa;
- Motomura, Hideki;
- Yoshida, Yoshinori;
- Horie, Minoru;
- Makita, Naomasa;
- Kimura, Takeshi
Publication type:
Article
HCN4 pacemaker channels attenuate the parasympathetic response and stabilize the spontaneous firing of the sinoatrial node.
Published in:
Journal of Physiology, 2018, v. 596, n. 5, p. 809, doi. 10.1113/JP275303
By:
- Kozasa, Yuko;
- Nakashima, Noriyuki;
- Ito, Masayuki;
- Ishikawa, Taisuke;
- Kimoto, Hiroki;
- Ushijima, Kazuo;
- Makita, Naomasa;
- Takano, Makoto
Publication type:
Article
Targeted deep sequencing analyses of long QT syndrome in a Japanese population.
Published in:
PLoS ONE, 2022, v. 17, n. 12, p. 1, doi. 10.1371/journal.pone.0277242
By:
- Nagata, Yuki;
- Watanabe, Ryo;
- Eichhorn, Christian;
- Ohno, Seiko;
- Aiba, Takeshi;
- Ishikawa, Taisuke;
- Nakano, Yukiko;
- Aizawa, Yoshiyasu;
- Hayashi, Kenshi;
- Murakoshi, Nobuyuki;
- Nakajima, Tadashi;
- Yagihara, Nobue;
- Mishima, Hiroyuki;
- Sudo, Takeaki;
- Higuchi, Chihiro;
- Takahashi, Atsushi;
- Sekine, Akihiro;
- Makiyama, Takeru;
- Tanaka, Yoshihiro;
- Watanabe, Atsuyuki
Publication type:
Article
Dilated cardiomyopathy-associated BAG3 mutations impair Z-disc assembly and enhance sensitivity to apoptosis in cardiomyocytes.
Published in:
Human Mutation, 2011, v. 32, n. 12, p. 1481, doi. 10.1002/humu.21603
By:
- Arimura, Takuro;
- Ishikawa, Taisuke;
- Nunoda, Shinichi;
- Kawai, Sachio;
- Kimura, Akinori
Publication type:
Article
Genetic defects in a His-Purkinje system transcription factor, IRX3, cause lethal cardiac arrhythmias.
Published in:
European Heart Journal, 2016, v. 37, n. 18, p. 1469, doi. 10.1093/eurheartj/ehv449
By:
- Koizumi, Akiko;
- Sasano, Tetsuo;
- Kimura, Wataru;
- Miyamoto, Yoshihiro;
- Aiba, Takeshi;
- Ishikawa, Taisuke;
- Nogami, Akihiko;
- Fukamizu, Seiji;
- Sakurada, Harumizu;
- Takahashi, Yoshihide;
- Nakamura, Hiroaki;
- Ishikura, Tomoyuki;
- Koseki, Haruhiko;
- Arimura, Takuro;
- Kimura, Akinori;
- Hirao, Kenzo;
- Isobe, Mitsuaki;
- Shimizu, Wataru;
- Miura, Naoyuki;
- Furukawa, Tetsushi
Publication type:
Article
Pathological findings of myocardium in a patient with cardiac conduction defect associated with an SCN5A mutation.
Published in:
Medical Molecular Morphology, 2021, v. 54, n. 3, p. 259, doi. 10.1007/s00795-021-00283-9
By:
- Kawano, Hiroaki;
- Kawamura, Koichi;
- Kohno, Masaki;
- Ishijima, Mitsuaki;
- Fukae, Satoki;
- Ishikawa, Taisuke;
- Makita, Naomasa;
- Maemura, Koji
Publication type:
Article

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