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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2003 | 1 |
2013 | 2 |
2014 | 3 |
2024 | 0 |
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KCNQ1 gain-of-function mutation in familial atrial fibrillation.
Science. 2003 Jan 10;299(5604):251-4. doi: 10.1126/science.1077771.
Science. 2003.
PMID: 12522251
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.
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A KCNQ1 mutation contributes to the concealed type 1 long QT phenotype by limiting the Kv7.1 channel conformational changes associated with protein kinase A phosphorylation.
Bartos DC, Giudicessi JR, Tester DJ, Ackerman MJ, Ohno S, Horie M, Gollob MH, Burgess DE, Delisle BP.
Bartos DC, et al.
Heart Rhythm. 2014 Mar;11(3):459-68. doi: 10.1016/j.hrthm.2013.11.021. Epub 2013 Nov 21.
Heart Rhythm. 2014.
PMID: 24269949
Free PMC article.
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Long QT mutations at the interface between KCNQ1 helix C and KCNE1 disrupt I(KS) regulation by PKA and PIP₂.
Dvir M, Strulovich R, Sachyani D, Ben-Tal Cohen I, Haitin Y, Dessauer C, Pongs O, Kass R, Hirsch JA, Attali B.
Dvir M, et al.
J Cell Sci. 2014 Sep 15;127(Pt 18):3943-55. doi: 10.1242/jcs.147033. Epub 2014 Jul 18.
J Cell Sci. 2014.
PMID: 25037568
Free PMC article.
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