Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

72,107 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
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.
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.
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
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
A novel HCN4 mutation, G1097W, is associated with atrioventricular block.
Zhou J, Ding WG, Makiyama T, Miyamoto A, Matsumoto Y, Kimura H, Tarutani Y, Zhao J, Wu J, Zang WJ, Matsuura H, Horie M. Zhou J, et al. Among authors: wu j. Circ J. 2014;78(4):938-42. doi: 10.1253/circj.cj-13-0996. Epub 2014 Jan 31. Circ J. 2014. PMID: 24492017 Free article. Clinical Trial.
The genetics underlying acquired long QT syndrome: impact for genetic screening.
Itoh H, Crotti L, Aiba T, Spazzolini C, Denjoy I, Fressart V, Hayashi K, Nakajima T, Ohno S, Makiyama T, Wu J, Hasegawa K, Mastantuono E, Dagradi F, Pedrazzini M, Yamagishi M, Berthet M, Murakami Y, Shimizu W, Guicheney P, Schwartz PJ, Horie M. Itoh H, et al. Among authors: wu j. Eur Heart J. 2016 May 7;37(18):1456-64. doi: 10.1093/eurheartj/ehv695. Epub 2015 Dec 28. Eur Heart J. 2016. PMID: 26715165 Free PMC article.
72,107 results
You have reached the last available page of results. Please see the User Guide for more information.