408 related articles for article (PubMed ID: 7651517)
1. Molecular mechanism for an inherited cardiac arrhythmia.
Bennett PB; Yazawa K; Makita N; George AL
Nature; 1995 Aug; 376(6542):683-5. PubMed ID: 7651517
[TBL] [Abstract][Full Text] [Related]
2. [Long QT syndrome].
Nakajima T; Kaneko Y; Taniguchi Y; Nagai R
Nihon Rinsho; 1996 Mar; 54(3):776-81. PubMed ID: 8904236
[TBL] [Abstract][Full Text] [Related]
3. Congenital long-QT syndrome caused by a novel mutation in a conserved acidic domain of the cardiac Na+ channel.
Wei J; Wang DW; Alings M; Fish F; Wathen M; Roden DM; George AL
Circulation; 1999 Jun; 99(24):3165-71. PubMed ID: 10377081
[TBL] [Abstract][Full Text] [Related]
4. A revised view of cardiac sodium channel "blockade" in the long-QT syndrome.
Kambouris NG; Nuss HB; Johns DC; Marbán E; Tomaselli GF; Balser JR
J Clin Invest; 2000 Apr; 105(8):1133-40. PubMed ID: 10772658
[TBL] [Abstract][Full Text] [Related]
5. Impaired stretch modulation in potentially lethal cardiac sodium channel mutants.
Banderali U; Juranka PF; Clark RB; Giles WR; Morris CE
Channels (Austin); 2010; 4(1):12-21. PubMed ID: 20090423
[TBL] [Abstract][Full Text] [Related]
6. Phenotypic characterization of a novel long-QT syndrome mutation (R1623Q) in the cardiac sodium channel.
Kambouris NG; Nuss HB; Johns DC; Tomaselli GF; Marban E; Balser JR
Circulation; 1998 Feb; 97(7):640-4. PubMed ID: 9495298
[TBL] [Abstract][Full Text] [Related]
7. Characterization of human cardiac Na+ channel mutations in the congenital long QT syndrome.
Wang DW; Yazawa K; George AL; Bennett PB
Proc Natl Acad Sci U S A; 1996 Nov; 93(23):13200-5. PubMed ID: 8917568
[TBL] [Abstract][Full Text] [Related]
8. Malignant perinatal variant of long-QT syndrome caused by a profoundly dysfunctional cardiac sodium channel.
Wang DW; Crotti L; Shimizu W; Pedrazzini M; Cantu F; De Filippo P; Kishiki K; Miyazaki A; Ikeda T; Schwartz PJ; George AL
Circ Arrhythm Electrophysiol; 2008 Dec; 1(5):370-8. PubMed ID: 19808432
[TBL] [Abstract][Full Text] [Related]
9. Substitution of a conserved alanine in the domain IIIS4-S5 linker of the cardiac sodium channel causes long QT syndrome.
Smits JP; Veldkamp MW; Bezzina CR; Bhuiyan ZA; Wedekind H; Schulze-Bahr E; Wilde AA
Cardiovasc Res; 2005 Aug; 67(3):459-66. PubMed ID: 16039271
[TBL] [Abstract][Full Text] [Related]
10. A novel LQT-3 mutation disrupts an inactivation gate complex with distinct rate-dependent phenotypic consequences.
Bankston JR; Sampson KJ; Kateriya S; Glaaser IW; Malito DL; Chung WK; Kass RS
Channels (Austin); 2007; 1(4):273-80. PubMed ID: 18708744
[TBL] [Abstract][Full Text] [Related]
11. Trafficking defects and gating abnormalities of a novel SCN5A mutation question gene-specific therapy in long QT syndrome type 3.
Ruan Y; Denegri M; Liu N; Bachetti T; Seregni M; Morotti S; Severi S; Napolitano C; Priori SG
Circ Res; 2010 Apr; 106(8):1374-83. PubMed ID: 20339117
[TBL] [Abstract][Full Text] [Related]
12. [Molecular genetics in the hereditary form of long QT syndrome].
Georgijević Milić L
Med Pregl; 2000; 53(1-2):51-4. PubMed ID: 10953551
[TBL] [Abstract][Full Text] [Related]
13. Novel arrhythmogenic mechanism revealed by a long-QT syndrome mutation in the cardiac Na(+) channel.
Abriel H; Cabo C; Wehrens XH; Rivolta I; Motoike HK; Memmi M; Napolitano C; Priori SG; Kass RS
Circ Res; 2001 Apr; 88(7):740-5. PubMed ID: 11304498
[TBL] [Abstract][Full Text] [Related]
14. A de novo missense mutation of human cardiac Na+ channel exhibiting novel molecular mechanisms of long QT syndrome.
Makita N; Shirai N; Nagashima M; Matsuoka R; Yamada Y; Tohse N; Kitabatake A
FEBS Lett; 1998 Feb; 423(1):5-9. PubMed ID: 9506831
[TBL] [Abstract][Full Text] [Related]
15. Combination of cardiac conduction disease and long QT syndrome caused by mutation T1620K in the cardiac sodium channel.
Surber R; Hensellek S; Prochnau D; Werner GS; Benndorf K; Figulla HR; Zimmer T
Cardiovasc Res; 2008 Mar; 77(4):740-8. PubMed ID: 18065446
[TBL] [Abstract][Full Text] [Related]
16. Cardiac Na(+) channel dysfunction in Brugada syndrome is aggravated by beta(1)-subunit.
Makita N; Shirai N; Wang DW; Sasaki K; George AL; Kanno M; Kitabatake A
Circulation; 2000 Jan 4-11; 101(1):54-60. PubMed ID: 10618304
[TBL] [Abstract][Full Text] [Related]
17. Biophysical characterization of a new SCN5A mutation S1333Y in a SIDS infant linked to long QT syndrome.
Huang H; Millat G; Rodriguez-Lafrasse C; Rousson R; Kugener B; Chevalier P; Chahine M
FEBS Lett; 2009 Mar; 583(5):890-6. PubMed ID: 19302788
[TBL] [Abstract][Full Text] [Related]
18. A trafficking defective, Brugada syndrome-causing SCN5A mutation rescued by drugs.
Valdivia CR; Tester DJ; Rok BA; Porter CB; Munger TM; Jahangir A; Makielski JC; Ackerman MJ
Cardiovasc Res; 2004 Apr; 62(1):53-62. PubMed ID: 15023552
[TBL] [Abstract][Full Text] [Related]
19. A sodium channel pore mutation causing Brugada syndrome.
Pfahnl AE; Viswanathan PC; Weiss R; Shang LL; Sanyal S; Shusterman V; Kornblit C; London B; Dudley SC
Heart Rhythm; 2007 Jan; 4(1):46-53. PubMed ID: 17198989
[TBL] [Abstract][Full Text] [Related]
20. Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndrome.
Rook MB; Bezzina Alshinawi C; Groenewegen WA; van Gelder IC; van Ginneken AC; Jongsma HJ; Mannens MM; Wilde AA
Cardiovasc Res; 1999 Dec; 44(3):507-17. PubMed ID: 10690282
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]