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Items: 13


Effects of BKCa and Kir2.1 Channels on Cell Cycling Progression and Migration in Human Cardiac c-kit+ Progenitor Cells.

Zhang YY, Li G, Che H, Sun HY, Xiao GS, Wang Y, Li GR.

PLoS One. 2015 Sep 21;10(9):e0138581. doi: 10.1371/journal.pone.0138581. eCollection 2015.


Protein assemblies of sodium and inward rectifier potassium channels control cardiac excitability and arrhythmogenesis.

Willis BC, Ponce-Balbuena D, Jalife J.

Am J Physiol Heart Circ Physiol. 2015 Jun 15;308(12):H1463-73. doi: 10.1152/ajpheart.00176.2015. Epub 2015 Apr 10. Review.


Saccadic oscillations - membrane, model, and medicine.

Shaikh AG.

Expert Rev Ophthalmol. 2012 Oct;7(5):481-486.


Electrocardiogram in Andersen-Tawil syndrome. New electrocardiographic criteria for diagnosis of type-1 Andersen-Tawil syndrome.

Kukla P, Biernacka EK, Baranchuk A, Jastrzebski M, Jagodzinska M.

Curr Cardiol Rev. 2014 Aug;10(3):222-8. Review.


KCNJ2 mutation causes an adrenergic-dependent rectification abnormality with calcium sensitivity and ventricular arrhythmia.

Kalscheur MM, Vaidyanathan R, Orland KM, Abozeid S, Fabry N, Maginot KR, January CT, Makielski JC, Eckhardt LL.

Heart Rhythm. 2014 May;11(5):885-94. doi: 10.1016/j.hrthm.2014.02.015. Epub 2014 Feb 21.


Prevalence study of genetically defined skeletal muscle channelopathies in England.

Horga A, Raja Rayan DL, Matthews E, Sud R, Fialho D, Durran SC, Burge JA, Portaro S, Davis MB, Haworth A, Hanna MG.

Neurology. 2013 Apr 16;80(16):1472-5. doi: 10.1212/WNL.0b013e31828cf8d0. Epub 2013 Mar 20.


Genetic defects in the hotspot of inwardly rectifying K(+) (Kir) channels and their metabolic consequences: a review.

Pattnaik BR, Asuma MP, Spott R, Pillers DA.

Mol Genet Metab. 2012 Jan;105(1):64-72. doi: 10.1016/j.ymgme.2011.10.004. Epub 2011 Oct 19. Review.


Golgi export of the Kir2.1 channel is driven by a trafficking signal located within its tertiary structure.

Ma D, Taneja TK, Hagen BM, Kim BY, Ortega B, Lederer WJ, Welling PA.

Cell. 2011 Jun 24;145(7):1102-15. doi: 10.1016/j.cell.2011.06.007.


Biophysical and molecular characterization of a novel de novo KCNJ2 mutation associated with Andersen-Tawil syndrome and catecholaminergic polymorphic ventricular tachycardia mimicry.

Barajas-Martinez H, Hu D, Ontiveros G, Caceres G, Desai M, Burashnikov E, Scaglione J, Antzelevitch C.

Circ Cardiovasc Genet. 2011 Feb;4(1):51-7. doi: 10.1161/CIRCGENETICS.110.957696. Epub 2010 Dec 10.


Protein kinase A-dependent biophysical phenotype for V227F-KCNJ2 mutation in catecholaminergic polymorphic ventricular tachycardia.

Vega AL, Tester DJ, Ackerman MJ, Makielski JC.

Circ Arrhythm Electrophysiol. 2009 Oct;2(5):540-7. doi: 10.1161/CIRCEP.109.872309. Epub 2009 Aug 25.


KCNJ2 mutations in arrhythmia patients referred for LQT testing: a mutation T305A with novel effect on rectification properties.

Eckhardt LL, Farley AL, Rodriguez E, Ruwaldt K, Hammill D, Tester DJ, Ackerman MJ, Makielski JC.

Heart Rhythm. 2007 Mar;4(3):323-9. Epub 2006 Nov 10.


Andersen-Tawil syndrome.

Smith AH, Fish FA, Kannankeril PJ.

Indian Pacing Electrophysiol J. 2006 Jan 1;6(1):32-43.


Long QT syndrome: from channels to cardiac arrhythmias.

Moss AJ, Kass RS.

J Clin Invest. 2005 Aug;115(8):2018-24.

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