175 related articles for article (PubMed ID: 9600240)
1. Genomic organization and mutational analysis of HERG, a gene responsible for familial long QT syndrome.
Itoh T; Tanaka T; Nagai R; Kamiya T; Sawayama T; Nakayama T; Tomoike H; Sakurada H; Yazaki Y; Nakamura Y
Hum Genet; 1998 Apr; 102(4):435-9. PubMed ID: 9600240
[TBL] [Abstract][Full Text] [Related]
2. Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome.
Tanaka T; Nagai R; Tomoike H; Takata S; Yano K; Yabuta K; Haneda N; Nakano O; Shibata A; Sawayama T; Kasai H; Yazaki Y; Nakamura Y
Circulation; 1997 Feb; 95(3):565-7. PubMed ID: 9024139
[TBL] [Abstract][Full Text] [Related]
3. Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1.
Splawski I; Shen J; Timothy KW; Vincent GM; Lehmann MH; Keating MT
Genomics; 1998 Jul; 51(1):86-97. PubMed ID: 9693036
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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; 99(11):1464-70. PubMed ID: 10086971
[TBL] [Abstract][Full Text] [Related]
6. Multiple different missense mutations in the pore region of HERG in patients with long QT syndrome.
Satler CA; Vesely MR; Duggal P; Ginsburg GS; Beggs AH
Hum Genet; 1998 Mar; 102(3):265-72. PubMed ID: 9544837
[TBL] [Abstract][Full Text] [Related]
7. Genomic organization and mutational analysis of KVLQT1, a gene responsible for familial long QT syndrome.
Itoh T; Tanaka T; Nagai R; Kikuchi K; Ogawa S; Okada S; Yamagata S; Yano K; Yazaki Y; Nakamura Y
Hum Genet; 1998 Sep; 103(3):290-4. PubMed ID: 9799083
[TBL] [Abstract][Full Text] [Related]
8. A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome.
Curran ME; Splawski I; Timothy KW; Vincent GM; Green ED; Keating MT
Cell; 1995 Mar; 80(5):795-803. PubMed ID: 7889573
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Romano-Ward long QT syndrome: identification of a HERG mutation in a Taiwanese kindred.
Lee-Chen GJ; Tai DY; Chu CH; Teng YN
J Formos Med Assoc; 1999 Sep; 98(9):649-52. PubMed ID: 10560244
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Characterization of a novel missense mutation in the pore of HERG in a patient with long QT syndrome.
Yoshida H; Horie M; Otani H; Takano M; Tsuji K; Kubota T; Fukunami M; Sasayama S
J Cardiovasc Electrophysiol; 1999 Sep; 10(9):1262-70. PubMed ID: 10517660
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndrome.
Larsen LA; Andersen PS; Kanters J; Svendsen IH; Jacobsen JR; Vuust J; Wettrell G; Tranebjaerg L; Bathen J; Christiansen M
Clin Chem; 2001 Aug; 47(8):1390-5. PubMed ID: 11468227
[TBL] [Abstract][Full Text] [Related]
15. Molecular biology and cellular mechanisms of Brugada and long QT syndromes in infants and young children.
Antzelevitch C
J Electrocardiol; 2001; 34 Suppl():177-81. PubMed ID: 11781953
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Survey of the coding region of the HERG gene in long QT syndrome reveals six novel mutations and an amino acid polymorphism with possible phenotypic effects.
Laitinen P; Fodstad H; Piippo K; Swan H; Toivonen L; Viitasalo M; Kaprio J; Kontula K
Hum Mutat; 2000 Jun; 15(6):580-1. PubMed ID: 10862094
[TBL] [Abstract][Full Text] [Related]
19. Sinus node function and ventricular repolarization during exercise stress test in long QT syndrome patients with KvLQT1 and HERG potassium channel defects.
Swan H; Viitasalo M; Piippo K; Laitinen P; Kontula K; Toivonen L
J Am Coll Cardiol; 1999 Sep; 34(3):823-9. PubMed ID: 10483966
[TBL] [Abstract][Full Text] [Related]
20. KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population.
Liu W; Yang J; Hu D; Kang C; Li C; Zhang S; Li P; Chen Z; Qin X; Ying K; Li Y; Li Y; Li Z; Cheng X; Li L; Qi Y; Chen S; Wang Q
Hum Mutat; 2002 Dec; 20(6):475-6. PubMed ID: 12442276
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]