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Items: 1 to 20 of 63

1.

Multifactorial impact of channel beta-subunit gene mutation on automaticity.

Difrancesco D, Nawathe PA, Robinson RB.

J Cardiovasc Electrophysiol. 2013 Dec;24(12):E26-7. doi: 10.1111/jce.12235. Epub 2013 Sep 9. No abstract available.

PMID:
24015862
2.

Pacemaker gene mutations, bradycardia, arrhythmias and the coupled clock theory.

Yaniv Y, Lakatta EG.

J Cardiovasc Electrophysiol. 2013 Dec;24(12):E28-9. doi: 10.1111/jce.12236. Epub 2013 Sep 9. No abstract available.

3.

An LQTS6 MiRP1 mutation suppresses pacemaker current and is associated with sinus bradycardia.

Nawathe PA, Kryukova Y, Oren RV, Milanesi R, Clancy CE, Lu JT, Moss AJ, Difrancesco D, Robinson RB.

J Cardiovasc Electrophysiol. 2013 Sep;24(9):1021-7. doi: 10.1111/jce.12163. Epub 2013 Apr 30.

4.

Long QT syndrome in neonates: conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations.

Lupoglazoff JM, Denjoy I, Villain E, Fressart V, Simon F, Bozio A, Berthet M, Benammar N, Hainque B, Guicheney P.

J Am Coll Cardiol. 2004 Mar 3;43(5):826-30.

5.

Enzymatic activation of voltage-gated potassium channels.

Ramu Y, Xu Y, Lu Z.

Nature. 2006 Aug 10;442(7103):696-9. Epub 2006 Jun 21.

PMID:
16799569
6.

Mutations in the long QT gene, KCNQ1, are an uncommon cause of atrial fibrillation.

Ellinor PT, Moore RK, Patton KK, Ruskin JN, Pollak MR, Macrae CA.

Heart. 2004 Dec;90(12):1487-8. No abstract available.

7.

Up-regulation of the Kv3.4 potassium channel subunit in early stages of Alzheimer's disease.

Angulo E, Noé V, Casadó V, Mallol J, Gomez-Isla T, Lluis C, Ferrer I, Ciudad CJ, Franco R.

J Neurochem. 2004 Nov;91(3):547-57.

8.

Altered HCN4 channel C-linker interaction is associated with familial tachycardia-bradycardia syndrome and atrial fibrillation.

Duhme N, Schweizer PA, Thomas D, Becker R, Schröter J, Barends TR, Schlichting I, Draguhn A, Bruehl C, Katus HA, Koenen M.

Eur Heart J. 2013 Sep;34(35):2768-75. doi: 10.1093/eurheartj/ehs391. Epub 2012 Nov 23.

PMID:
23178648
9.

Long-term outcomes of pediatric sinus bradycardia.

Chiu SN, Lin LY, Wang JK, Lu CW, Chang CW, Lin MT, Hua YC, Lue HC, Wu MH.

J Pediatr. 2013 Sep;163(3):885-9.e1. doi: 10.1016/j.jpeds.2013.03.054. Epub 2013 Apr 25.

PMID:
23623512
10.

Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation.

Olesen MS, Bentzen BH, Nielsen JB, Steffensen AB, David JP, Jabbari J, Jensen HK, Haunsø S, Svendsen JH, Schmitt N.

BMC Med Genet. 2012 Apr 3;13:24. doi: 10.1186/1471-2350-13-24.

11.

Ancillary subunits associated with voltage-dependent K+ channels.

Pongs O, Schwarz JR.

Physiol Rev. 2010 Apr;90(2):755-96. doi: 10.1152/physrev.00020.2009. Review.

12.

Genetic variation in KCNA5: impact on the atrial-specific potassium current IKur in patients with lone atrial fibrillation.

Christophersen IE, Olesen MS, Liang B, Andersen MN, Larsen AP, Nielsen JB, Haunsø S, Olesen SP, Tveit A, Svendsen JH, Schmitt N.

Eur Heart J. 2013 May;34(20):1517-25. doi: 10.1093/eurheartj/ehs442. Epub 2012 Dec 21.

PMID:
23264583
13.

Contribution of sodium channel mutations to bradycardia and sinus node dysfunction in LQT3 families.

Veldkamp MW, Wilders R, Baartscheer A, Zegers JG, Bezzina CR, Wilde AA.

Circ Res. 2003 May 16;92(9):976-83. Epub 2003 Apr 3.

14.

Amiodarone-associated macroscopic T-wave alternans and torsade de pointes unmasking the inherited long QT syndrome.

Wegener FT, Ehrlich JR, Hohnloser SH.

Europace. 2008 Jan;10(1):112-3. Epub 2007 Nov 15. No abstract available.

PMID:
18006559
15.

T-type calcium current contributes to escape automaticity and governs the occurrence of lethal arrhythmias after atrioventricular block in mice.

Le Quang K, Benito B, Naud P, Qi XY, Shi YF, Tardif JC, Gillis MA, Dobrev D, Charpentier F, Nattel S.

Circ Arrhythm Electrophysiol. 2013 Aug;6(4):799-808. doi: 10.1161/CIRCEP.113.000407. Epub 2013 Jul 24.

16.

Genetic manipulation of cardiac K(+) channel function in mice: what have we learned, and where do we go from here?

Nerbonne JM, Nichols CG, Schwarz TL, Escande D.

Circ Res. 2001 Nov 23;89(11):944-56. Review.

17.

The alpha1 subunit EGL-19, the alpha2/delta subunit UNC-36, and the beta subunit CCB-1 underlie voltage-dependent calcium currents in Caenorhabditis elegans striated muscle.

Lainé V, Frøkjær-Jensen C, Couchoux H, Jospin M.

J Biol Chem. 2011 Oct 21;286(42):36180-7. doi: 10.1074/jbc.M111.256149. Epub 2011 Aug 30.

18.

Loss of the potassium channel beta-subunit gene, KCNAB2, is associated with epilepsy in patients with 1p36 deletion syndrome.

Heilstedt HA, Burgess DL, Anderson AE, Chedrawi A, Tharp B, Lee O, Kashork CD, Starkey DE, Wu YQ, Noebels JL, Shaffer LG, Shapira SK.

Epilepsia. 2001 Sep;42(9):1103-11.

19.

Point mutation in the HCN4 cardiac ion channel pore affecting synthesis, trafficking, and functional expression is associated with familial asymptomatic sinus bradycardia.

Nof E, Luria D, Brass D, Marek D, Lahat H, Reznik-Wolf H, Pras E, Dascal N, Eldar M, Glikson M.

Circulation. 2007 Jul 31;116(5):463-70. Epub 2007 Jul 23.

20.

Targeted deletion of Kcne2 impairs HCN channel function in mouse thalamocortical circuits.

Ying SW, Kanda VA, Hu Z, Purtell K, King EC, Abbott GW, Goldstein PA.

PLoS One. 2012;7(8):e42756. doi: 10.1371/journal.pone.0042756. Epub 2012 Aug 3.

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