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Results: 16

1.

Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias.

Chouabe C, Neyroud N, Guicheney P, Lazdunski M, Romey G, Barhanin J.

EMBO J. 1997 Sep 1;16(17):5472-9.

PMID:
9312006
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

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
[PubMed - indexed for MEDLINE]
3.

The long QT syndromes: genetic basis and clinical implications.

Chiang CE, Roden DM.

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

PMID:
10898405
[PubMed - indexed for MEDLINE]
Free Article
4.

KCNQ1 gene mutations and the respective genotype-phenotype correlations in the long QT syndrome.

Herbert E, Trusz-Gluza M, Moric E, Smiłowska-Dzielicka E, Mazurek U, Wilczok T.

Med Sci Monit. 2002 Oct;8(10):RA240-8. Review.

PMID:
12388934
[PubMed - indexed for MEDLINE]
5.

[Clinical aspects and molecular genetics of the Jervell- and Lange-Nielsen Syndrome].

Mönnig G, Schulze-Bahr E, Wedekind H, Eckardt L, Kirchhof P, Funke H, Kotthoff S, Vogt J, Assmann G, Breithardt G, Haverkamp W.

Z Kardiol. 2002 May;91(5):380-8. Review. German.

PMID:
12132284
[PubMed - indexed for MEDLINE]
6.

[Molecular genetics of the long QT syndrome: clinical aspects].

Sepp R, Csanády M.

Orv Hetil. 1999 Nov 21;140(47):2633-8. Review. Hungarian.

PMID:
10613047
[PubMed - indexed for MEDLINE]
7.

KCNQ potassium channels: physiology, pathophysiology, and pharmacology.

Robbins J.

Pharmacol Ther. 2001 Apr;90(1):1-19. Review.

PMID:
11448722
[PubMed - indexed for MEDLINE]
8.

Two components of delayed rectifier K+ current in heart: molecular basis, functional diversity, and contribution to repolarization.

Cheng JH, Kodama I.

Acta Pharmacol Sin. 2004 Feb;25(2):137-45. Review.

PMID:
14769199
[PubMed - indexed for MEDLINE]
Free Article
9.

The molecular basis of long QT syndrome and prospects for therapy.

Wang Q, Bowles NE, Towbin JA.

Mol Med Today. 1998 Sep;4(9):382-8. Review.

PMID:
9791861
[PubMed - indexed for MEDLINE]
10.

[Molecular genetics in the hereditary form of long QT syndrome].

Georgijević Milić L.

Med Pregl. 2000 Jan-Feb;53(1-2):51-4. Review. Croatian.

PMID:
10953551
[PubMed - indexed for MEDLINE]
11.

Genetics and molecular biology of the inherited long QT syndrome.

Vincent GM.

Ann Med. 1994 Dec;26(6):419-25. Review.

PMID:
7695867
[PubMed - indexed for MEDLINE]
12.

Role of the ISK protein in the IminK channel complex.

Busch AE, Suessbrich H.

Trends Pharmacol Sci. 1997 Jan;18(1):26-9. Review.

PMID:
9114727
[PubMed - indexed for MEDLINE]
13.

The rate-dependent biophysical properties of the LQT1 H258R mutant are counteracted by a dominant negative effect on channel trafficking.

Labro AJ, Boulet IR, Timmermans JP, Ottschytsch N, Snyders DJ.

J Mol Cell Cardiol. 2010 Jun;48(6):1096-104. doi: 10.1016/j.yjmcc.2009.10.027. Epub 2009 Nov 11. Review.

PMID:
19913547
[PubMed - indexed for MEDLINE]
14.

The KCNQ1 potassium channel: from gene to physiological function.

Jespersen T, Grunnet M, Olesen SP.

Physiology (Bethesda). 2005 Dec;20:408-16. Review.

PMID:
16287990
[PubMed - indexed for MEDLINE]
Free Article
15.

Gain of function mutants: ion channels and G protein-coupled receptors.

Lester HA, Karschin A.

Annu Rev Neurosci. 2000;23:89-125. Review.

PMID:
10845060
[PubMed - indexed for MEDLINE]
16.

[Jervell and Lange-Nielsen syndrome].

Aoki T.

Ryoikibetsu Shokogun Shirizu. 1996;(12):188-91. Review. Japanese. No abstract available.

PMID:
9047439
[PubMed - indexed for MEDLINE]

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