Analysis of ankyrin-B gene mutations in patients with long QT syndrome.
Xiang Zhou(Hubei University of Medicine), Hiroshi Mabuchi(Koto Hospital), Tomoya Kaneda(Tokyo Medical and Dental University), Hiromasa Kato(Iwate University), Katsuharu Uchiyama(Kouseiren Takaoka Hospital), Takashi Fujita(Gifu Prefectural Tajimi Hospital), Hidekazu Ino(Kanazawa University), Ei-ichi Masuda, Tetsuo Konno(Kanazawa University), Masami Shimizu(Kanazawa University), Noboru Fujino(Kanazawa University), Tomohito Mabuchi(Fukui CardioVascular Center), Akira Funada(National Cerebral and Cardiovascular Center)
PubMed
July 1, 2006
Cited by 5
Related Papers
Runx2 and Runx3 are essential for chondrocyte maturation, and Runx2 regulates limb growth through induction of <i>Indian hedgehog</i>
|Genes & Development|2004|583
Negative regulation of the RIG-I signaling by the ubiquitin ligase RNF125
|Proceedings of the National Academy of Sciences|2007|474
Cardiac fibrosis in mice with hypertrophic cardiomyopathy is mediated by non-myocyte proliferation and requires Tgf-β
|Journal of Clinical Investigation|2010|440
T wave peak-to-end interval and QT dispersion in acquired long QT syndrome: a new index for arrhythmogenicity
|Clinical Science|2003|313
Core-binding factor β interacts with Runx2 and is required for skeletal development
|Nature Genetics|2002|285