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Items: 1 to 20 of 73

1.

DDESC: Dragon database for exploration of sodium channels in human.

Sagar S, Kaur M, Dawe A, Seshadri SV, Christoffels A, Schaefer U, Radovanovic A, Bajic VB.

BMC Genomics. 2008 Dec 20;9:622. doi: 10.1186/1471-2164-9-622.

2.

The LQT syndromes--current status of molecular mechanisms.

Schulze-Bahr E, Wedekind H, Haverkamp W, Borggrefe M, Assmann G, Breithardt G, Funke H.

Z Kardiol. 1999 Apr;88(4):245-54. Review.

PMID:
10408028
3.

Inherited Brugada and long QT-3 syndrome mutations of a single residue of the cardiac sodium channel confer distinct channel and clinical phenotypes.

Rivolta I, Abriel H, Tateyama M, Liu H, Memmi M, Vardas P, Napolitano C, Priori SG, Kass RS.

J Biol Chem. 2001 Aug 17;276(33):30623-30. Epub 2001 Jun 15.

4.

Voltage-gated sodium channels: mutations, channelopathies and targets.

Andavan GS, Lemmens-Gruber R.

Curr Med Chem. 2011;18(3):377-97. Review.

PMID:
21143119
5.

Molecular mechanism for an inherited cardiac arrhythmia.

Bennett PB, Yazawa K, Makita N, George AL Jr.

Nature. 1995 Aug 24;376(6542):683-5.

PMID:
7651517
6.

[Inherited cardiac diseases caused by Nav1.5 sodium channel mutations].

Tfelt-Hansen J, Olesen SP, Svendsen JH, Jespersen T.

Ugeskr Laeger. 2009 Apr 6;171(15):1261-5. Review. Danish.

PMID:
19416615
7.

Single-channel properties of human NaV1.1 and mechanism of channel dysfunction in SCN1A-associated epilepsy.

Vanoye CG, Lossin C, Rhodes TH, George AL Jr.

J Gen Physiol. 2006 Jan;127(1):1-14.

8.

Biophysical defects in voltage.gated sodium channels associated with long QT and Brugada syndromes.

Jones DK, Ruben PC.

Channels (Austin). 2008 Mar-Apr;2(2):70-80. Epub 2008 Mar 18. Review.

PMID:
18849657
9.

Enhanced Na(+) channel intermediate inactivation in Brugada syndrome.

Wang DW, Makita N, Kitabatake A, Balser JR, George AL Jr.

Circ Res. 2000 Oct 13;87(8):E37-43.

10.

Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms.

Lai LP, Su YN, Hsieh FJ, Chiang FT, Juang JM, Liu YB, Ho YL, Chen WJ, Yeh SJ, Wang CC, Ko YL, Wu TJ, Ueng KC, Lei MH, Tsao HM, Chen SA, Lin TK, Wu MH, Lo HM, Huang SK, Lin JL.

J Hum Genet. 2005;50(9):490-6. Epub 2005 Sep 10. Erratum in: J Hum Genet. 2006;51(3):267. Hsieh, Fon-Jou [added].

PMID:
16155735
11.

Inherited cardiac diseases caused by mutations in the Nav1.5 sodium channel.

Tfelt-Hansen J, Winkel BG, Grunnet M, Jespersen T.

J Cardiovasc Electrophysiol. 2010 Jan;21(1):107-15. doi: 10.1111/j.1540-8167.2009.01633.x. Epub 2009 Oct 20. Review.

PMID:
19845816
13.

Brugada and long QT-3 syndromes: two phenotypes of the sodium channel disease.

Khan IA, Nair CK.

Ann Noninvasive Electrocardiol. 2004 Jul;9(3):280-9. Review.

PMID:
15245345
14.

Molecular biology of sodium channels and their role in cardiac arrhythmias.

Grant AO.

Am J Med. 2001 Mar;110(4):296-305. Review.

PMID:
11239848
15.

A novel mutation in SCN5A, delQKP 1507-1509, causing long QT syndrome: role of Q1507 residue in sodium channel inactivation.

Keller DI, Acharfi S, Delacrétaz E, Benammar N, Rotter M, Pfammatter JP, Fressart V, Guicheney P, Chahine M.

J Mol Cell Cardiol. 2003 Dec;35(12):1513-21.

PMID:
14654377
16.

Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome.

Vatta M, Dumaine R, Varghese G, Richard TA, Shimizu W, Aihara N, Nademanee K, Brugada R, Brugada J, Veerakul G, Li H, Bowles NE, Brugada P, Antzelevitch C, Towbin JA.

Hum Mol Genet. 2002 Feb 1;11(3):337-45.

PMID:
11823453
17.

Increased neuronal firing in computer simulations of sodium channel mutations that cause generalized epilepsy with febrile seizures plus.

Spampanato J, Aradi I, Soltesz I, Goldin AL.

J Neurophysiol. 2004 May;91(5):2040-50. Epub 2003 Dec 31.

18.

A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families.

Smits JP, Koopmann TT, Wilders R, Veldkamp MW, Opthof T, Bhuiyan ZA, Mannens MM, Balser JR, Tan HL, Bezzina CR, Wilde AA.

J Mol Cell Cardiol. 2005 Jun;38(6):969-81. Epub 2005 Apr 1.

PMID:
15910881
19.

Familial pain syndromes from mutations of the NaV1.7 sodium channel.

Fischer TZ, Waxman SG.

Ann N Y Acad Sci. 2010 Jan;1184:196-207. doi: 10.1111/j.1749-6632.2009.05110.x. Review.

PMID:
20146699
20.

A cardiac sodium channel mutation identified in Brugada syndrome associated with atrial standstill.

Takehara N, Makita N, Kawabe J, Sato N, Kawamura Y, Kitabatake A, Kikuchi K.

J Intern Med. 2004 Jan;255(1):137-42.

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