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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2005 11
2006 20
2007 20
2008 30
2009 32
2010 31
2011 33
2012 43
2013 53
2014 45
2015 45
2016 27
2017 33
2018 28
2019 16
2020 0
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396 results
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Page 1
Genetics of long QT syndrome.
Tester DJ, Ackerman MJ. Tester DJ, et al. Methodist Debakey Cardiovasc J. 2014 Jan-Mar;10(1):29-33. doi: 10.14797/mdcj-10-1-29. Methodist Debakey Cardiovasc J. 2014. PMID: 24932360 Free PMC article. Review.
KCNE1 and KCNE3 modulate KCNQ1 channels by affecting different gating transitions.
Barro-Soria R, Ramentol R, Liin SI, Perez ME, Kass RS, Larsson HP. Barro-Soria R, et al. Proc Natl Acad Sci U S A. 2017 Aug 29;114(35):E7367-E7376. doi: 10.1073/pnas.1710335114. Epub 2017 Aug 14. Proc Natl Acad Sci U S A. 2017. PMID: 28808020 Free PMC article.
Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test.
Kapplinger JD, Tester DJ, Salisbury BA, Carr JL, Harris-Kerr C, Pollevick GD, Wilde AA, Ackerman MJ. Kapplinger JD, et al. Heart Rhythm. 2009 Sep;6(9):1297-303. doi: 10.1016/j.hrthm.2009.05.021. Epub 2009 Jun 23. Heart Rhythm. 2009. PMID: 19716085 Free PMC article.
A double-point mutation in the selectivity filter site of the KCNQ1 potassium channel results in a severe phenotype, LQT1, of long QT syndrome.
Ikrar T, Hanawa H, Watanabe H, Okada S, Aizawa Y, Ramadan MM, Komura S, Yamashita F, Chinushi M, Aizawa Y. Ikrar T, et al. J Cardiovasc Electrophysiol. 2008 May;19(5):541-9. doi: 10.1111/j.1540-8167.2007.01076.x. Epub 2008 Feb 4. J Cardiovasc Electrophysiol. 2008. PMID: 18266681
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