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Phenotype variability in patients carrying KCNJ2 mutations.
Kimura H, Zhou J, Kawamura M, Itoh H, Mizusawa Y, Ding WG, Wu J, Ohno S, Makiyama T, Miyamoto A, Naiki N, Wang Q, Xie Y, Suzuki T, Tateno S, Nakamura Y, Zang WJ, Ito M, Matsuura H, Horie M. Kimura H, et al. Among authors: wu j. Circ Cardiovasc Genet. 2012 Jun;5(3):344-53. doi: 10.1161/CIRCGENETICS.111.962316. Epub 2012 May 15. Circ Cardiovasc Genet. 2012. PMID: 22589293
A molecular mechanism for adrenergic-induced long QT syndrome.
Wu J, Naiki N, Ding WG, Ohno S, Kato K, Zang WJ, Delisle BP, Matsuura H, Horie M. Wu J, et al. J Am Coll Cardiol. 2014 Mar 4;63(8):819-27. doi: 10.1016/j.jacc.2013.08.1648. Epub 2013 Oct 30. J Am Coll Cardiol. 2014. PMID: 24184248 Free article.
Gain-of-function KCNH2 mutations in patients with Brugada syndrome.
Wang QI, Ohno S, Ding WG, Fukuyama M, Miyamoto A, Itoh H, Makiyama T, Wu J, Bai J, Hasegawa K, Shinohara T, Takahashi N, Shimizu A, Matsuura H, Horie M. Wang QI, et al. Among authors: wu j. J Cardiovasc Electrophysiol. 2014 May;25(5):522-530. doi: 10.1111/jce.12361. Epub 2014 Jan 30. J Cardiovasc Electrophysiol. 2014. PMID: 24400717
Molecular pathogenesis of long QT syndrome type 1.
Wu J, Ding WG, Horie M. Wu J, et al. J Arrhythm. 2016 Oct;32(5):381-388. doi: 10.1016/j.joa.2015.12.006. Epub 2016 Jan 27. J Arrhythm. 2016. PMID: 27761162 Free PMC article. Review.
KCNE3 T4A as the genetic basis of Brugada-pattern electrocardiogram.
Nakajima T, Wu J, Kaneko Y, Ashihara T, Ohno S, Irie T, Ding WG, Matsuura H, Kurabayashi M, Horie M. Nakajima T, et al. Among authors: wu j. Circ J. 2012;76(12):2763-72. doi: 10.1253/circj.cj-12-0551. Epub 2012 Sep 13. Circ J. 2012. PMID: 22987075 Free article.
72,144 results
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