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Masakazu Yamagishi
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Articles

Long QT syndrome and associated gene mutation carriers in Japanese children: results from ECG screening examinations

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Kenshi Hayashi, Noboru Fujino, Katsuharu Uchiyama, Hidekazu Ino, Kenji Sakata, Tetsuo Konno, Eiichi Masuta, Akira Funada, Yuichiro Sakamoto, Toshinari Tsubokawa, Keisuke Nakashima, Li Liu, Haruhiro Higashida, Yoshitake Hiramaru, Masami Shimizu, Masakazu Yamagishi
Journal: Clinical Science
Clin Sci (Lond) (2009) 117 (12): 415–424.
https://doi.org/10.1042/CS20080528
Published: 21 September 2009
View articletitled, Long QT syndrome and associated gene mutation carriers in Japanese children: results from ECG screening examinations
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Articles

Expression and function of ephrin-B1 and its cognate receptor EphB2 in human atherosclerosis: from an aspect of chemotaxis

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Aiji Sakamoto, Hatsue Ishibashi-Ueda, Yuka Sugamoto, Takeo Higashikata, Susumu Miyamoto, Masa-aki Kawashiri, Kunimasa Yagi, Tetsuo Konno, Kenshi Hayashi, Noboru Fujino, Hidekazu Ino, Yoshiyu Takeda, Masakazu Yamagishi
Journal: Clinical Science
Clin Sci (Lond) (2008) 114 (10): 643–650.
https://doi.org/10.1042/CS20070339
Published: 14 April 2008
View articletitled, Expression and function of ephrin-B1 and its cognate receptor EphB2 in human atherosclerosis: from an aspect of chemotaxis
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Includes: Supplementary data
Articles

A novel β-myosin heavy chain gene mutation, p.Met531Arg, identified in isolated left ventricular non-compaction in humans, results in left ventricular hypertrophy that progresses to dilation in a mouse model

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Tomoya Kaneda, Chie Naruse, Atsuhiro Kawashima, Noboru Fujino, Toru Oshima, Masanobu Namura, Shinichi Nunoda, Sumio Mori, Tetsuo Konno, Hidekazu Ino, Masakazu Yamagishi, Masahide Asano
Journal: Clinical Science
Clin Sci (Lond) (2008) 114 (6): 431–440.
https://doi.org/10.1042/CS20070179
Published: 12 February 2008
View articletitled, A novel β-myosin heavy chain gene mutation, p.Met531Arg, identified in isolated left ventricular non-compaction in humans, results in left ventricular hypertrophy that progresses to dilation in a mouse model
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Articles

Differences in the diagnostic value of various criteria of negative T waves for hypertrophic cardiomyopathy based on a molecular genetic diagnosis

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Tetsuo Konno, Noboru Fujino, Kenshi Hayashi, Katsuharu Uchiyama, Eiichi Masuta, Hiromasa Katoh, Yuichiro Sakamoto, Toshinari Tsubokawa, Hidekazu Ino, Masakazu Yamagishi
Journal: Clinical Science
Clin Sci (Lond) (2007) 112 (11): 577–582.
https://doi.org/10.1042/CS20060293
Published: 01 May 2007
View articletitled, Differences in the diagnostic value of various criteria of negative T waves for hypertrophic cardiomyopathy based on a molecular genetic diagnosis
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Articles

CETP (cholesteryl ester transfer protein) promoter −1337 C>T polymorphism protects against coronary atherosclerosis in Japanese patients with heterozygous familial hypercholesterolaemia

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Mutsuko Takata, Akihiro Inazu, Shoji Katsuda, Kenji Miwa, Masa-aki Kawashiri, Atsushi Nohara, Toshinori Higashikata, Junji Kobayashi, Hiroshi Mabuchi, Masakazu Yamagishi
Journal: Clinical Science
Clin Sci (Lond) (2006) 111 (5): 325–331.
https://doi.org/10.1042/CS20060088
Published: 13 October 2006
View articletitled, CETP (cholesteryl ester transfer protein) promoter −1337 C>T polymorphism protects against coronary atherosclerosis in Japanese patients with heterozygous familial hypercholesterolaemia
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