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Kazuo Ueda

Showing results (51-60 of 64) with videos related to

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Journal of Human Genetics|January 24, 2009
Role of HCN4 channel in preventing ventricular arrhythmiaKazuo Ueda, Yuji Hirano, Yasushi Higashiuesato, et al.
Journal of Human Hypertension|January 6, 2004
Impact of elevated blood pressure on mortality from all causes, cardiovascular diseases, heart disease and stroke among Japanese: 14 year follow-up of randomly selected population from Japanese -- Nippon data 80Minoru Lida, Kazuo Ueda, Akira Okayama, et al.
Biochemical and Biophysical Research Communications|December 16, 2003
Identification and functional analysis of a caveolin-3 mutation associated with familial hypertrophic cardiomyopathyTakeharu Hayashi, Takuro Arimura, Kazuo Ueda, et al.
Journal of Cardiovascular Electrophysiology|July 28, 2007
A novel mutation in KCNQ1 associated with a potent dominant negative effect as the basis for the LQT1 form of the long QT syndromeYoshiyasu Aizawa, Kazuo Ueda, Fabiana Scornik, et al.
FEBS Letters|September 11, 2004
Truncated KCNQ1 mutant, A178fs/105, forms hetero-multimer channel with wild-type causing a dominant-negative suppression due to trafficking defectYoshiyasu Aizawa, Kazuo Ueda, Long-Mei Wu, et al.
International Journal of Cardiology|March 8, 2005
A novel mutation in FKBP12.6 binding region of the human cardiac ryanodine receptor gene (R2401H) in a Japanese patient with catecholaminergic polymorphic ventricular tachycardiaYoshiyasu Aizawa, Kazuo Ueda, Satoru Komura, et al.
Journal of the American College of Cardiology|October 30, 2007
Anti-KCNH2 antibody-induced long QT syndrome: novel acquired form of long QT syndromeKazufumi Nakamura, Yusuke Katayama, Kengo F Kusano, et al.
Biochemical and Biophysical Research Communications|February 16, 2002
Titin mutations as the molecular basis for dilated cardiomyopathyManatsu Itoh-Satoh, Takeharu Hayashi, Hirofumi Nishi, et al.
The Journal of Biological Chemistry|May 5, 2004
Functional characterization of a trafficking-defective HCN4 mutation, D553N, associated with cardiac arrhythmiaKazuo Ueda, Kazufumi Nakamura, Takeharu Hayashi, et al.
Circulation|June 27, 2007
SCN4B-encoded sodium channel beta4 subunit in congenital long-QT syndromeArgelia Medeiros-Domingo, Toshihiko Kaku, David J Tester, et al.
Pageof 7

Showing results (51-60 of 64) with videos related to

Sort By:
Pageof 7
Journal of Human Genetics|January 24, 2009
Role of HCN4 channel in preventing ventricular arrhythmiaKazuo Ueda, Yuji Hirano, Yasushi Higashiuesato, et al.
Journal of Human Hypertension|January 6, 2004
Impact of elevated blood pressure on mortality from all causes, cardiovascular diseases, heart disease and stroke among Japanese: 14 year follow-up of randomly selected population from Japanese -- Nippon data 80Minoru Lida, Kazuo Ueda, Akira Okayama, et al.
Biochemical and Biophysical Research Communications|December 16, 2003
Identification and functional analysis of a caveolin-3 mutation associated with familial hypertrophic cardiomyopathyTakeharu Hayashi, Takuro Arimura, Kazuo Ueda, et al.
Journal of Cardiovascular Electrophysiology|July 28, 2007
A novel mutation in KCNQ1 associated with a potent dominant negative effect as the basis for the LQT1 form of the long QT syndromeYoshiyasu Aizawa, Kazuo Ueda, Fabiana Scornik, et al.
FEBS Letters|September 11, 2004
Truncated KCNQ1 mutant, A178fs/105, forms hetero-multimer channel with wild-type causing a dominant-negative suppression due to trafficking defectYoshiyasu Aizawa, Kazuo Ueda, Long-Mei Wu, et al.
International Journal of Cardiology|March 8, 2005
A novel mutation in FKBP12.6 binding region of the human cardiac ryanodine receptor gene (R2401H) in a Japanese patient with catecholaminergic polymorphic ventricular tachycardiaYoshiyasu Aizawa, Kazuo Ueda, Satoru Komura, et al.
Journal of the American College of Cardiology|October 30, 2007
Anti-KCNH2 antibody-induced long QT syndrome: novel acquired form of long QT syndromeKazufumi Nakamura, Yusuke Katayama, Kengo F Kusano, et al.
Biochemical and Biophysical Research Communications|February 16, 2002
Titin mutations as the molecular basis for dilated cardiomyopathyManatsu Itoh-Satoh, Takeharu Hayashi, Hirofumi Nishi, et al.
The Journal of Biological Chemistry|May 5, 2004
Functional characterization of a trafficking-defective HCN4 mutation, D553N, associated with cardiac arrhythmiaKazuo Ueda, Kazufumi Nakamura, Takeharu Hayashi, et al.
Circulation|June 27, 2007
SCN4B-encoded sodium channel beta4 subunit in congenital long-QT syndromeArgelia Medeiros-Domingo, Toshihiko Kaku, David J Tester, et al.
Pageof 7