Ngā hua rapu - Taisuke Ishikawa

  • E whakaatu ana i te 1 - 16 hua o te 16
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  1. 1
    Dilated Cardiomyopathy-Associated <i>FHOD3</i> Variant Impairs the Ability to Induce Activation of Transcription Factor Serum Response Factor

    Dilated Cardiomyopathy-Associated <i>FHOD3</i> Variant Impairs the Ability to Induce Activation of Transcription Factor Serum Response Factor mā Takuro Arimura, Ryu Takeya, Taisuke Ishikawa, Tetsuhiro Yamano, Akiko Matsuo, Tetsuya Tatsumi, Tetsuya Nomura, Hideki Sumimoto, Akinori Kimura

    I whakaputaina 2013
    Whiwhi kuputuhi katoa
    Artigo
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  2. 2
    The Effect of Pimobendan on Left Atrial Pressure in Dogs with Mitral Valve Regurgitation

    The Effect of Pimobendan on Left Atrial Pressure in Dogs with Mitral Valve Regurgitation mā Shuji Suzuki, Ryuji Fukushima, Taisuke Ishikawa, Lina Hamabe, Derya Aytemiz, Huai-Che Hsu, Shu Nakao, Noboru Machida, Ryou Tanaka

    I whakaputaina 2011
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  3. 3
    Novel <i>SCN3B</i> Mutation Associated With Brugada Syndrome Affects Intracellular Trafficking and Function of Nav1.5

    Novel <i>SCN3B</i> Mutation Associated With Brugada Syndrome Affects Intracellular Trafficking and Function of Nav1.5 mā Taisuke Ishikawa, Naohiko Takahashi, Seiko Ohno, Harumizu Sakurada, Kazufumi Nakamura, Young Keun On, Jeong Euy Park, Takeru Makiyama, Minoru Horie, Takuro Arimura, Naomasa Makita, Akinori Kimura

    I whakaputaina 2012
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  4. 4
    Genotype-dependent differences in age of manifestation and arrhythmia complications in short QT syndrome

    Genotype-dependent differences in age of manifestation and arrhythmia complications in short QT syndrome mā Daniel Toshio Harrell, Takashi Ashihara, Taisuke Ishikawa, Ichiko Tominaga, Andrea Mazzanti, Kazuhiro Takahashi, Yasushi Oginosawa, Haruhiko Abe, Koji Maemura, Naokata Sumitomo, Kikuya Uno, Makoto Takano, Silvia G. Priori, Naomasa Makita

    I whakaputaina 2015
    Whiwhi kuputuhi katoa
    Artigo
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  5. 5
    A Novel Disease Gene for Brugada Syndrome

    A Novel Disease Gene for Brugada Syndrome mā Taisuke Ishikawa, Akinori Sato, Cherisse A. Marcou, David J. Tester, Michael J. Ackerman, Lia Crotti, Peter J. Schwartz, Young Keun On, Jeong-Euy Park, Kazufumi Nakamura, Masayasu Hiraoka, Kiyoshi Nakazawa, Harumizu Sakurada, Takuro Arimura, Naomasa Makita, Akinori Kimura

    I whakaputaina 2012
    Whiwhi kuputuhi katoa
    Artigo
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  6. 6
    Sodium Channelopathy Underlying Familial Sick Sinus Syndrome With Early Onset and Predominantly Male Characteristics

    Sodium Channelopathy Underlying Familial Sick Sinus Syndrome With Early Onset and Predominantly Male Characteristics mā Keisuke Abé, Taku Machida, Naokata Sumitomo, Hirokazu Yamamoto, Kimie Ohkubo, Ichiro Watanabe, Takeru Makiyama, Satoki Fukae, Masaki Kohno, Daniel Toshio Harrell, Taisuke Ishikawa, Yukiomi Tsuji, Akihiko Nogami, Taichi Watabe, Yasushi Oginosawa, Haruhiko Abe, Koji Maemura, Hideki Motomura, Naomasa Makita

    I whakaputaina 2014
    Whiwhi kuputuhi katoa
    Artigo
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  7. 7
    Allele-specific ablation rescues electrophysiological abnormalities in a human iPS cell model of long-QT syndrome with a CALM2 mutation

    Allele-specific ablation rescues electrophysiological abnormalities in a human iPS cell model of long-QT syndrome with a CALM2 mutation mā Yuta Yamamoto, Takeru Makiyama, Takeshi Harita, Kenichi Sasaki, Yimin Wuriyanghai, Mamoru Hayano, Suguru Nishiuchi, Hirohiko Kohjitani, Sayako Hirose, Jia‐Rong Chen, Fumika Yokoi, Taisuke Ishikawa, Seiko Ohno, Kazuhisa Chonabayashi, Hideki Motomura, Yoshinori Yoshida, Minoru Horie, Naomasa Makita, Takeshi Kimura

    I whakaputaina 2017
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  8. 8
    Genetic defects in a His-Purkinje system transcription factor,<i>IRX3</i>, cause lethal cardiac arrhythmias

    Genetic defects in a His-Purkinje system transcription factor,<i>IRX3</i>, cause lethal cardiac arrhythmias mā Akiko Koizumi, Tetsuo Sasano, Wataru Kimura, Yoshihiro Miyamoto, Takeshi Aiba, Taisuke Ishikawa, Akihiko Nogami, Seiji Fukamizu, Harumizu Sakurada, Yoshihide Takahashi, Hiroaki Nakamura, Tomoyuki Ishikura, Haruhiko Koseki, Takuro Arimura, Akinori Kimura, Kenzo Hirao, Mitsuaki Isobe, Wataru Shimizu, Naoyuki Miura, Tetsushi Furukawa

    I whakaputaina 2015
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  9. 9
    Nuclear accumulation of androgen receptor in gender difference of dilated cardiomyopathy due to lamin A/C mutations

    Nuclear accumulation of androgen receptor in gender difference of dilated cardiomyopathy due to lamin A/C mutations mā Takuro Arimura, Kenji Onoue, Yumiko Takahashi-Tanaka, Taisuke Ishikawa, Masayoshi Kuwahara, Mitsutoshi Setou, Shuji Shigenobu, Katsushi Yamaguchi, A. Bertrand, Noboru Machida, Kazumi Takayama, Masayuki Fukusato, Ryou Tanaka, Satoshi Somekawa, Tomoya Nakano, Yoshihisa YAMANE, Keiji Kuba, Yumiko Imai, Yoshihiko Saito, Gisèle Bonne, Akinori Kimura

    I whakaputaina 2013
    Whiwhi kuputuhi katoa
    Artigo
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  10. 10
    Electrocardiographic Characteristics and <i>SCN5A</i> Mutations in Idiopathic Ventricular Fibrillation Associated With Early Repolarization

    Electrocardiographic Characteristics and <i>SCN5A</i> Mutations in Idiopathic Ventricular Fibrillation Associated With Early Repolarization mā Hiroshi Watanabe, Akihiko Nogami, Kimie Ohkubo, Hiro Kawata, Yuka Hayashi, Taisuke Ishikawa, Takeru Makiyama, Satomi Nagao, Nobue Yagihara, Naofumi Takehara, Yuichiro Kawamura, Akinori Sato, Kazuki Okamura, Yukio Hosaka, Masahito Sato, Satoki Fukae, Masaomi Chinushi, Hirotaka Oda, Masaaki Okabe, Akinori Kimura, Koji Maemura, Ichiro Watanabe, Shiro Kamakura, Minoru Horie, Yoshifusa Aizawa, Wataru Shimizu, Naomasa Makita

    I whakaputaina 2011
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  11. 11
    Gene-Based Risk Stratification for Cardiac Disorders in <i>LMNA</i> Mutation Carriers

    Gene-Based Risk Stratification for Cardiac Disorders in <i>LMNA</i> Mutation Carriers mā Suguru Nishiuchi, Takeru Makiyama, Takeshi Aiba, Kenzaburo Nakajima, Sayako Hirose, Hirohiko Kohjitani, Yuta Yamamoto, Takeshi Harita, Mamoru Hayano, Yimin Wuriyanghai, Jia‐Rong Chen, Kenichi Sasaki, Nobue Yagihara, Taisuke Ishikawa, Kenji Onoue, Nobuyuki Murakoshi, Ichiro Watanabe, Kimie Ohkubo, Hiroshi Watanabe, Seiko Ohno, Takahiro Doi, Satoshi Shizuta, Tohru Minamino, Yoshihiko Saito, Yasushi Oginosawa, Akihiko Nogami, Kazutaka Aonuma, Kengo Kusano, Naomasa Makita, Wataru Shimizu, Minoru Horie, Takeshi Kimura

    I whakaputaina 2017
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  12. 12
    Novel Calmodulin Mutations Associated With Congenital Arrhythmia Susceptibility

    Novel Calmodulin Mutations Associated With Congenital Arrhythmia Susceptibility mā Naomasa Makita, Nobue Yagihara, Lia Crotti, Christopher N. Johnson, Britt Maria Beckmann, Michelle S. Roh, Daichi Shigemizu, Peter Lichtner, Taisuke Ishikawa, Takeshi Aiba, Tessa Homfray, Elijah R. Behr, Didier Klug, Isabelle Denjoy, Elisa Mastantuono, Daniel Theisen, Tatsuhiko Tsunoda, Wataru Satake, Tatsushi Toda, Hidewaki Nakagawa, Yukiomi Tsuji, Takeshi Tsuchiya, Hirokazu Yamamoto, Yoshihiro Miyamoto, Naoto Endo, Akinori Kimura, Kouichi Ozaki, Hideki Motomura, Kenji Suda, Toshihiro Tanaka, Peter J. Schwartz, Thomas Meitinger, Stefan Kääb, Pascale Guicheney, Wataru Shimizu, Zahurul A. Bhuiyan, Hiroshi Watanabe, Walter Chazin, Alfred L. George

    I whakaputaina 2014
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  13. 13
    TAD boundary deletion causes PITX2-related cardiac electrical and structural defects

    TAD boundary deletion causes PITX2-related cardiac electrical and structural defects mā 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, A 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, C Vieyres, Takeru Makiyama, Stefan Mundlos, Vincent M. Christoffels, Vincent Probst, Jean‐Jacques Schott, Julien Barc

    I whakaputaina 2024
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  14. 14
    <i>SCN5A</i> Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in <i>SCN5A</i> Families

    <i>SCN5A</i> Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in <i>SCN5A</i> Families mā Yanushi D. Wijeyeratne, Michael W.T. Tanck, Yuka Mizusawa, Velislav N. Batchvarov, Julien Barc, Lia Crotti, J. Martijn Bos, David J. Tester, Alison Muir, Christian Veltmann, Seiko Ohno, Stephen P Page, Joseph Galvin, Rafik Tadros, Martina Muggenthaler, Hariharan Raju, Isabelle Denjoy, Jean‐Jacques Schott, Jean‐Baptiste Gourraud, Doris Škorić‐Milosavljević, Eline A. Nannenberg, Richard Redon, Michael Papadakis, Florence Kyndt, Federica Dagradi, Silvia Castelletti, Margherita Torchio, Thomas Meitinger, Peter Lichtner, Taisuke Ishikawa, Arthur A.M. Wilde, Kazuhiro Takahashi, Sanjay Sharma, Dan M. Roden, Martin Borggrefe, Pascal McKeown, Wataru Shimizu, Minoru Horie, Naomasa Makita, Takeshi Aiba, Michael J. Ackerman, Peter J. Schwartz, Vincent Probst, Connie R. Bezzina, Elijah R. Behr

    I whakaputaina 2020
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  15. 15
    Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

    Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome mā Najim Lahrouchi, Rafik Tadros, Lia Crotti, Yuka Mizusawa, Pieter G. Postema, Leander Beekman, Roddy Walsh, Kanae Hasegawa, Julien Barc, Marko Ernsting, Kari L. Turkowski, Andrea Mazzanti, Britt M. Beckmann, Keiko Shimamoto, Ulla-Britt Diamant, Yanushi D. Wijeyeratne, Yu Kucho, Tomas Robyns, Taisuke Ishikawa, Elena Arbelo, Michael Christiansen, Annika Winbo, Reza Jabbari, Steven A. Lubitz, Johannes Steinfurt, Boris Rudic, Bart Loeys, Moore B. Shoemaker, Peter Weeke, Ryan Pfeiffer, Brianna Davies, Antoine Andorin, Nynke Hofman, Federica Dagradi, Matteo Pedrazzini, David J. Tester, J. Martijn Bos, Geòrgia Sarquella-Brugada, Òscar Campuzano, Pyotr G. Platonov, Birgit Stallmeyer, Sven Zumhagen, Eline A. Nannenberg, Jan H. Veldink, Leonard H. van den Berg, Ammar Al‐Chalabi, Christopher E. Shaw, Pamela J. Shaw, Karen Morrison, Peter M. Andersen, Martina Müller‐Nurasyid, Daniele Cusi, Cristina Barlassina, Pilar Galán, Mark Lathrop, Markus Munter, Thomas Werge, Marta Ribasés, Tin Aung, Chiea Chuen Khor, Mineo Ozaki, Peter Lichtner, Thomas Meitinger, J. Peter van Tintelen, Yvonne M. Hoedemaekers, Isabelle Denjoy, Antoine Leenhardt, Carlo Napolitano, Wataru Shimizu, Jean‐Jacques Schott, Jean‐Baptiste Gourraud, Takeru Makiyama, Seiko Ohno, Hideki Itoh, Andrew D. Krahn, Charles Antzelevitch, Dan M. Roden, Johan Saenen, Martin Borggrefe, Katja E. Odening, Patrick T. Ellinor, Jacob Tfelt‐Hansen, Jonathan R. Skinner, Maarten P. van den Berg, Morten S. Olesen, Josép Brugada, Ramón Brugada, Naomasa Makita, Jeroen Breckpot, Masao Yoshinaga, Elijah R. Behr, Annika Rydberg, Takeshi Aiba, Stefan Kääb, Silvia G. Priori, Pascale Guicheney, Hanno L. Tan, Christopher Newton‐Cheh, Michael Ackerman, Peter J. Schwartz

    I whakaputaina 2020
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  16. 16
    Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

    Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls mā Roddy Walsh, Najim Lahrouchi, Rafik Tadros, Florence Kyndt, Charlotte Glinge, Pieter G. Postema, Ahmad S. Amin, Eline A. Nannenberg, James S. Ware, Nicola Whiffin, Francesco Mazzarotto, Doris Škorić‐Milosavljević, Christian Krijger, Elena Arbelo, Dominique Babuty, Hector Barajas‐Martínez, Britt Maria Beckmann, Stéphane Bézieau, J Martijn Bos, Jeroen Breckpot, Òscar Campuzano, Silvia Castelletti, Candan Celen, Sebastian Clauß, Anniek Corveleyn, Lia Crotti, Federica Dagradi, Carlo de Asmundis, Isabelle Denjoy, Sven Dittmann, Patrick T. Ellinor, Cristina Gil, Carla Giustetto, Jean‐Baptiste Gourraud, Daisuke Hazeki, Minoru Horie, Taisuke Ishikawa, Hideki Itoh, Yoshiaki Kaneko, Jørgen K. Kanters, Hiroki Kimoto, Maria‐Christina Kotta, Ingrid P.C. Krapels, Masahiko Kurabayashi, Julieta Lazarte, Antoine Leenhardt, Bart Loeys, Catarina Lundin, Takeru Makiyama, Jacques Mansourati, Raphaël P. Martins, Andrea Mazzanti, Stellan Mörner, Carlo Napolitano, Kimie Ohkubo, Michael Papadakis, Boris Rudic, María Sabater‐Molina, Fréderic Sacher, Hatice Şahin, Geòrgia Sarquella-Brugada, Regina Sebastiano, Sanjay Sharma, Mary N. Sheppard, Keiko Shimamoto, M. Benjamin Shoemaker, Birgit Stallmeyer, Johannes Steinfurt, Yuji Tanaka, David J. Tester, Keisuke Usuda, Paul A. van der Zwaag, Sonia Van Dooren, Lut Van Laer, Annika Winbo, Bo Gregers Winkel, Kenichiro Yamagata, Sven Zumhagen, Paul G.A. Volders, Steven A. Lubitz, Charles Antzelevitch, Pyotr G. Platonov, Katja E. Odening, Dan M. Roden, Jason D. Roberts, Jonathan R. Skinner, Jacob Tfelt‐Hansen, Maarten P. van den Berg, Morten S. Olesen, Pier D. Lambiase, Martin Borggrefe, Kenshi Hayashi, Annika Rydberg, Tadashi Nakajima, Masao Yoshinaga, Johan Saenen, Stefan Kääb, Pedro Brugada, Tomas Robyns, Daniela Giachino

    I whakaputaina 2020
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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