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Items: 1 to 20 of 94

1.

KCNQ potassium channel mutations cause cardiac arrhythmias in Drosophila that mimic the effects of aging.

Ocorr K, Reeves NL, Wessells RJ, Fink M, Chen HS, Akasaka T, Yasuda S, Metzger JM, Giles W, Posakony JW, Bodmer R.

Proc Natl Acad Sci U S A. 2007 Mar 6;104(10):3943-8. Epub 2007 Feb 28.

2.

Evidence for a cardiac ion channel mutation underlying drug-induced QT prolongation and life-threatening arrhythmias.

Napolitano C, Schwartz PJ, Brown AM, Ronchetti E, Bianchi L, Pinnavaia A, Acquaro G, Priori SG.

J Cardiovasc Electrophysiol. 2000 Jun;11(6):691-6.

PMID:
10868744
3.

Dysfunction of delayed rectifier potassium channels in an inherited cardiac arrhythmia.

Sanguinetti MC.

Ann N Y Acad Sci. 1999 Apr 30;868:406-13. Review.

PMID:
10414310
4.

C-terminal HERG mutations: the role of hypokalemia and a KCNQ1-associated mutation in cardiac event occurrence.

Berthet M, Denjoy I, Donger C, Demay L, Hammoude H, Klug D, Schulze-Bahr E, Richard P, Funke H, Schwartz K, Coumel P, Hainque B, Guicheney P.

Circulation. 1999 Mar 23;99(11):1464-70.

5.

KCNE2 confers background current characteristics to the cardiac KCNQ1 potassium channel.

Tinel N, Diochot S, Borsotto M, Lazdunski M, Barhanin J.

EMBO J. 2000 Dec 1;19(23):6326-30.

6.
7.

Hypokalemia-induced long QT syndrome with an underlying novel missense mutation in S4-S5 linker of KCNQ1.

Kubota T, Shimizu W, Kamakura S, Horie M.

J Cardiovasc Electrophysiol. 2000 Sep;11(9):1048-54.

PMID:
11021476
8.

Pharmacological activation of normal and arrhythmia-associated mutant KCNQ1 potassium channels.

Seebohm G, Pusch M, Chen J, Sanguinetti MC.

Circ Res. 2003 Nov 14;93(10):941-7. Epub 2003 Oct 23.

9.

Evidence for a single nucleotide polymorphism in the KCNQ1 potassium channel that underlies susceptibility to life-threatening arrhythmias.

Kubota T, Horie M, Takano M, Yoshida H, Takenaka K, Watanabe E, Tsuchiya T, Otani H, Sasayama S.

J Cardiovasc Electrophysiol. 2001 Nov;12(11):1223-9.

PMID:
11761407
10.

Genetic control of heart function and aging in Drosophila.

Ocorr K, Perrin L, Lim HY, Qian L, Wu X, Bodmer R.

Trends Cardiovasc Med. 2007 Jul;17(5):177-82. Review.

11.

Coordinated down-regulation of KCNQ1 and KCNE1 expression contributes to reduction of I(Ks) in canine hypertrophied hearts.

Ramakers C, Vos MA, Doevendans PA, Schoenmakers M, Wu YS, Scicchitano S, Iodice A, Thomas GP, Antzelevitch C, Dumaine R.

Cardiovasc Res. 2003 Feb;57(2):486-96.

12.

QT interval prolongation and cardiac risk assessment for novel drugs.

Picard S, Lacroix P.

Curr Opin Investig Drugs. 2003 Mar;4(3):303-8. Review.

PMID:
12735231
13.

Long QT syndrome-associated mutations in the S4-S5 linker of KvLQT1 potassium channels modify gating and interaction with minK subunits.

Franqueza L, Lin M, Shen J, Splawski I, Keating MT, Sanguinetti MC.

J Biol Chem. 1999 Jul 23;274(30):21063-70. Erratum in: J Biol Chem 1999 Aug 27;274(35):25188.

14.

Identification and characterisation of a novel KCNQ1 mutation in a family with Romano-Ward syndrome.

Zehelein J, Thomas D, Khalil M, Wimmer AB, Koenen M, Licka M, Wu K, Kiehn J, Brockmeier K, Kreye VA, Karle CA, Katus HA, Ulmer HE, Schoels W.

Biochim Biophys Acta. 2004 Nov 5;1690(3):185-92.

15.

The long QT syndromes: genetic basis and clinical implications.

Chiang CE, Roden DM.

J Am Coll Cardiol. 2000 Jul;36(1):1-12. Review.

16.

Biophysical characteristics of a new mutation on the KCNQ1 potassium channel (L251P) causing long QT syndrome.

Deschênes D, Acharfi S, Pouliot V, Hegele R, Krahn A, Daleau P, Chahine M.

Can J Physiol Pharmacol. 2003 Feb;81(2):129-34.

PMID:
12710526
17.

Long QT syndrome: ionic basis and arrhythmia mechanism in long QT syndrome type 1.

Sanguinetti MC.

J Cardiovasc Electrophysiol. 2000 Jun;11(6):710-2.

PMID:
10868746
18.

Mutations in a dominant-negative isoform correlate with phenotype in inherited cardiac arrhythmias.

Mohammad-Panah R, Demolombe S, Neyroud N, Guicheney P, Kyndt F, van den Hoff M, Baró I, Escande D.

Am J Hum Genet. 1999 Apr;64(4):1015-23.

19.

Expression and coassociation of ERG1, KCNQ1, and KCNE1 potassium channel proteins in horse heart.

Finley MR, Li Y, Hua F, Lillich J, Mitchell KE, Ganta S, Gilmour RF Jr, Freeman LC.

Am J Physiol Heart Circ Physiol. 2002 Jul;283(1):H126-38.

20.

Identification of specific pore residues mediating KCNQ1 inactivation. A novel mechanism for long QT syndrome.

Seebohm G, Scherer CR, Busch AE, Lerche C.

J Biol Chem. 2001 Apr 27;276(17):13600-5. Epub 2001 Jan 17.

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