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Seiko Ohno

Showing results (11-20 of 222) with videos related to

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Molecular Genetics & Genomic Medicine|November 28, 2017
Unique genetic background and outcome of non-Caucasian Japanese probands with arrhythmogenic right ventricular dysplasia/cardiomyopathyYuko Wada, Seiko Ohno, Takeshi Aiba, et al.
Mobile DNA|February 15, 2018
Association of zygotic piRNAs derived from paternal <i>P</i> elements with hybrid dysgenesis in <i>Drosophila melanogaster</i>Keiko Tsuji Wakisaka, Kenji Ichiyanagi, Seiko Ohno, et al.
Mobile DNA|October 28, 2017
Diversity of <i>P-</i>element piRNA production among M' and Q strains and its association with P-M hybrid dysgenesis in <i>Drosophila melanogaster</i>Keiko Tsuji Wakisaka, Kenji Ichiyanagi, Seiko Ohno, et al.
International Heart Journal|July 17, 2019
Cardiac Arrest Associated with Both an Anomalous Left Coronary Artery and KCNE1 PolymorphismHideki Kawai, Eiichi Watanabe, Seiko Ohno, et al.
Journal of Arrhythmia|April 6, 2023
Computerized misinterpretation of QT interval in 12-lead electrocardiogram and its clinical consequences: A case of recurrent syncopeKanae Hasegawa, Yoshitomo Fukuoka, Seiko Ohno, et al.
BMC Cardiovascular Disorders|July 4, 2020
Postoperative supraventricular tachycardia and polymorphic ventricular tachycardia due to a novel SCN5A variant: a case report of a rare comorbidity that is difficult to diagnoseKoichi Kato, Tomoya Ozawa, Seiko Ohno, et al.
Journal of Arrhythmia|February 21, 2017
Cardiac conduction defects and Brugada syndrome: A family with overlap syndrome carrying a nonsense SCN5A mutationHisaaki Aoki, Yoshihide Nakamura, Seiko Ohno, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|June 4, 2021
Early diagnosis of infantile Danon disease complicated by tetralogy of FallotTsubasa Shimozono, Kentaro Ueno, Naohiro Shiokawa, et al.
Journal of Human Genetics|July 19, 2020
An NGS-based genotyping in LQTS; minor genes are no longer minorSeiko Ohno, Junichi Ozawa, Megumi Fukuyama, et al.
Circulation. Genomic and Precision Medicine|August 13, 2021
Long-Read Sequence Confirmed a Large Deletion Including <i>MYH6</i> and <i>MYH7</i> in an Infant of Atrial Septal Defect and Atrial ArrhythmiasKeiko Sonoda, Haruko Ishihara, Hisanori Sakazaki, et al.
Pageof 23

Showing results (11-20 of 222) with videos related to

Sort By:
Pageof 23
Molecular Genetics & Genomic Medicine|November 28, 2017
Unique genetic background and outcome of non-Caucasian Japanese probands with arrhythmogenic right ventricular dysplasia/cardiomyopathyYuko Wada, Seiko Ohno, Takeshi Aiba, et al.
Mobile DNA|February 15, 2018
Association of zygotic piRNAs derived from paternal <i>P</i> elements with hybrid dysgenesis in <i>Drosophila melanogaster</i>Keiko Tsuji Wakisaka, Kenji Ichiyanagi, Seiko Ohno, et al.
Mobile DNA|October 28, 2017
Diversity of <i>P-</i>element piRNA production among M' and Q strains and its association with P-M hybrid dysgenesis in <i>Drosophila melanogaster</i>Keiko Tsuji Wakisaka, Kenji Ichiyanagi, Seiko Ohno, et al.
International Heart Journal|July 17, 2019
Cardiac Arrest Associated with Both an Anomalous Left Coronary Artery and KCNE1 PolymorphismHideki Kawai, Eiichi Watanabe, Seiko Ohno, et al.
Journal of Arrhythmia|April 6, 2023
Computerized misinterpretation of QT interval in 12-lead electrocardiogram and its clinical consequences: A case of recurrent syncopeKanae Hasegawa, Yoshitomo Fukuoka, Seiko Ohno, et al.
BMC Cardiovascular Disorders|July 4, 2020
Postoperative supraventricular tachycardia and polymorphic ventricular tachycardia due to a novel SCN5A variant: a case report of a rare comorbidity that is difficult to diagnoseKoichi Kato, Tomoya Ozawa, Seiko Ohno, et al.
Journal of Arrhythmia|February 21, 2017
Cardiac conduction defects and Brugada syndrome: A family with overlap syndrome carrying a nonsense SCN5A mutationHisaaki Aoki, Yoshihide Nakamura, Seiko Ohno, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|June 4, 2021
Early diagnosis of infantile Danon disease complicated by tetralogy of FallotTsubasa Shimozono, Kentaro Ueno, Naohiro Shiokawa, et al.
Journal of Human Genetics|July 19, 2020
An NGS-based genotyping in LQTS; minor genes are no longer minorSeiko Ohno, Junichi Ozawa, Megumi Fukuyama, et al.
Circulation. Genomic and Precision Medicine|August 13, 2021
Long-Read Sequence Confirmed a Large Deletion Including <i>MYH6</i> and <i>MYH7</i> in an Infant of Atrial Septal Defect and Atrial ArrhythmiasKeiko Sonoda, Haruko Ishihara, Hisanori Sakazaki, et al.
Pageof 23