221 related articles for article (PubMed ID: 8994043)
1. The seizure locus encodes the Drosophila homolog of the HERG potassium channel.
Wang XJ; Reynolds ER; Déak P; Hall LM
J Neurosci; 1997 Feb; 17(3):882-90. PubMed ID: 8994043
[TBL] [Abstract][Full Text] [Related]
2. The eag family of K+ channels in Drosophila and mammals.
Ganetzky B; Robertson GA; Wilson GF; Trudeau MC; Titus SA
Ann N Y Acad Sci; 1999 Apr; 868():356-69. PubMed ID: 10414305
[TBL] [Abstract][Full Text] [Related]
3. The Drosophila erg K+ channel polypeptide is encoded by the seizure locus.
Titus SA; Warmke JW; Ganetzky B
J Neurosci; 1997 Feb; 17(3):875-81. PubMed ID: 8994042
[TBL] [Abstract][Full Text] [Related]
4. New missense mutation (G626V) in the predicted selectivity filter of the HERG channel associated with familial long QT syndrome.
Jahr S; Lewalter T; Hesch RD; Lüderitz B; Englisch S
Hum Mutat; 2000 Jun; 15(6):584. PubMed ID: 10862104
[No Abstract] [Full Text] [Related]
5. Is restoration of intracellular trafficking clinically feasible in the long QT syndrome?: The example of HERG mutations.
Kaufman ES; Ficker E
J Cardiovasc Electrophysiol; 2003 Mar; 14(3):320-2. PubMed ID: 12716119
[No Abstract] [Full Text] [Related]
6. Novel missense mutation in the cyclic nucleotide-binding domain of HERG causes long QT syndrome.
Satler CA; Walsh EP; Vesely MR; Plummer MH; Ginsburg GS; Jacob HJ
Am J Med Genet; 1996 Oct; 65(1):27-35. PubMed ID: 8914737
[TBL] [Abstract][Full Text] [Related]
7. Novel KCNQ1 and HERG missense mutations in Dutch long-QT families.
Jongbloed RJ; Wilde AA; Geelen JL; Doevendans P; Schaap C; Van Langen I; van Tintelen JP; Cobben JM; Beaufort-Krol GC; Geraedts JP; Smeets HJ
Hum Mutat; 1999; 13(4):301-10. PubMed ID: 10220144
[TBL] [Abstract][Full Text] [Related]
8. A plethora of mechanisms in the HERG-related long QT syndrome. Genetics meets electrophysiology.
Roden DM; Balser JR
Cardiovasc Res; 1999 Nov; 44(2):242-6. PubMed ID: 10690299
[No Abstract] [Full Text] [Related]
9. RsaI and MaeI intragenic RFLPs in the human HERG gene.
Fung D; Zhang L; French J; Bailey B; Trent RJ
Clin Genet; 1998 Jun; 53(6):504. PubMed ID: 9712545
[No Abstract] [Full Text] [Related]
10. Increased risk of arrhythmic events in long-QT syndrome with mutations in the pore region of the human ether-a-go-go-related gene potassium channel.
Moss AJ; Zareba W; Kaufman ES; Gartman E; Peterson DR; Benhorin J; Towbin JA; Keating MT; Priori SG; Schwartz PJ; Vincent GM; Robinson JL; Andrews ML; Feng C; Hall WJ; Medina A; Zhang L; Wang Z
Circulation; 2002 Feb; 105(7):794-9. PubMed ID: 11854117
[TBL] [Abstract][Full Text] [Related]
11. Long QT syndrome: cellular basis and arrhythmia mechanism in LQT2.
January CT; Gong Q; Zhou Z
J Cardiovasc Electrophysiol; 2000 Dec; 11(12):1413-8. PubMed ID: 11196567
[TBL] [Abstract][Full Text] [Related]
12. Novel missense mutation (G601S) of HERG in a Japanese long QT syndrome family.
Akimoto K; Furutani M; Imamura S; Furutani Y; Kasanuki H; Takao A; Momma K; Matsuoka R
Hum Mutat; 1998; Suppl 1():S184-6. PubMed ID: 9452080
[No Abstract] [Full Text] [Related]
13. Missense mutation in the pore region of HERG causes familial long QT syndrome.
Benson DW; MacRae CA; Vesely MR; Walsh EP; Seidman JG; Seidman CE; Satler CA
Circulation; 1996 May; 93(10):1791-5. PubMed ID: 8635257
[TBL] [Abstract][Full Text] [Related]
14. Homozygosity for a HERG potassium channel mutation causes a severe form of long QT syndrome: identification of an apparent founder mutation in the Finns.
Piippo K; Laitinen P; Swan H; Toivonen L; Viitasalo M; Pasternack M; Paavonen K; Chapman H; Wann KT; Hirvelä E; Sajantila A; Kontula K
J Am Coll Cardiol; 2000 Jun; 35(7):1919-25. PubMed ID: 10841244
[TBL] [Abstract][Full Text] [Related]
15. Long-QT syndrome-associated missense mutations in the pore helix of the HERG potassium channel.
Huang FD; Chen J; Lin M; Keating MT; Sanguinetti MC
Circulation; 2001 Aug; 104(9):1071-5. PubMed ID: 11524404
[TBL] [Abstract][Full Text] [Related]
16. The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.
Vincent GM
Annu Rev Med; 1998; 49():263-74. PubMed ID: 9509262
[TBL] [Abstract][Full Text] [Related]
17. Identical twins with long QT syndrome associated with a missense mutation in the S4 region of the HERG.
Hayashi K; Shimizu M; Ino H; Okeie K; Yamaguchi M; Yasuda T; Fujino N; Fujii H; Fujita S; Mabuchi H
Jpn Heart J; 2000 May; 41(3):399-404. PubMed ID: 10987356
[TBL] [Abstract][Full Text] [Related]
18. Two isoforms of the mouse ether-a-go-go-related gene coassemble to form channels with properties similar to the rapidly activating component of the cardiac delayed rectifier K+ current.
London B; Trudeau MC; Newton KP; Beyer AK; Copeland NG; Gilbert DJ; Jenkins NA; Satler CA; Robertson GA
Circ Res; 1997 Nov; 81(5):870-8. PubMed ID: 9351462
[TBL] [Abstract][Full Text] [Related]
19. Clinical, genetic, and biophysical characterization of a homozygous HERG mutation causing severe neonatal long QT syndrome.
Johnson WH; Yang P; Yang T; Lau YR; Mostella BA; Wolff DJ; Roden DM; Benson DW
Pediatr Res; 2003 May; 53(5):744-8. PubMed ID: 12621127
[TBL] [Abstract][Full Text] [Related]
20. The use of genotype-phenotype correlations in mutation analysis for the long QT syndrome.
Van Langen IM; Birnie E; Alders M; Jongbloed RJ; Le Marec H; Wilde AA
J Med Genet; 2003 Feb; 40(2):141-5. PubMed ID: 12566525
[No Abstract] [Full Text] [Related]
[Next] [New Search]
