492 related articles for article (PubMed ID: 18266681)
1. A double-point mutation in the selectivity filter site of the KCNQ1 potassium channel results in a severe phenotype, LQT1, of long QT syndrome.
Ikrar T; Hanawa H; Watanabe H; Okada S; Aizawa Y; Ramadan MM; Komura S; Yamashita F; Chinushi M; Aizawa Y
J Cardiovasc Electrophysiol; 2008 May; 19(5):541-9. PubMed ID: 18266681
[TBL] [Abstract][Full Text] [Related]
2. [The mutation scanning of KCNQ1 gene for 31 long QT syndrome families].
Li P; Li CL; Hu DY; Liu WL; Qin XG; Li YT; Li ZM; Li L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Jun; 21(3):236-9. PubMed ID: 15192825
[TBL] [Abstract][Full Text] [Related]
3. Dominant-negative I(Ks) suppression by KCNQ1-deltaF339 potassium channels linked to Romano-Ward syndrome.
Thomas D; Wimmer AB; Karle CA; Licka M; Alter M; Khalil M; Ulmer HE; Kathöfer S; Kiehn J; Katus HA; Schoels W; Koenen M; Zehelein J
Cardiovasc Res; 2005 Aug; 67(3):487-97. PubMed ID: 15950200
[TBL] [Abstract][Full Text] [Related]
4. Biophysical characterization of KCNQ1 P320 mutations linked to long QT syndrome 1.
Thomas D; Khalil M; Alter M; Schweizer PA; Karle CA; Wimmer AB; Licka M; Katus HA; Koenen M; Ulmer HE; Zehelein J
J Mol Cell Cardiol; 2010 Jan; 48(1):230-7. PubMed ID: 19540844
[TBL] [Abstract][Full Text] [Related]
5. Biophysical characteristics of a new mutation on the KCNQ1 potassium channel (L251P) causing long QT syndrome.
Deschênes D; Acharfi S; Pouliot V; Hegele R; Krahn A; Daleau P; Chahine M
Can J Physiol Pharmacol; 2003 Feb; 81(2):129-34. PubMed ID: 12710526
[TBL] [Abstract][Full Text] [Related]
6. Clinical and electrophysiological characterization of a novel mutation (F193L) in the KCNQ1 gene associated with long QT syndrome.
Yamaguchi M; Shimizu M; Ino H; Terai H; Hayashi K; Mabuchi H; Hoshi N; Higashida H
Clin Sci (Lond); 2003 Apr; 104(4):377-82. PubMed ID: 12653681
[TBL] [Abstract][Full Text] [Related]
7. Characterization and subcellular localization of KCNQ1 with a heterozygous mutation in the C terminus.
Yamashita F; Horie M; Kubota T; Yoshida H; Yumoto Y; Kobori A; Ninomiya T; Kono Y; Haruna T; Tsuji K; Washizuka T; Takano M; Otani H; Sasayama S; Aizawa Y
J Mol Cell Cardiol; 2001 Feb; 33(2):197-207. PubMed ID: 11162126
[TBL] [Abstract][Full Text] [Related]
8. Novel KCNE3 mutation reduces repolarizing potassium current and associated with long QT syndrome.
Ohno S; Toyoda F; Zankov DP; Yoshida H; Makiyama T; Tsuji K; Honda T; Obayashi K; Ueyama H; Shimizu W; Miyamoto Y; Kamakura S; Matsuura H; Kita T; Horie M
Hum Mutat; 2009 Apr; 30(4):557-63. PubMed ID: 19306396
[TBL] [Abstract][Full Text] [Related]
9. The G314S KCNQ1 mutation exerts a dominant-negative effect on expression of KCNQ1 channels in oocytes.
Li W; Du R; Wang QF; Tian L; Yang JG; Song ZF
Biochem Biophys Res Commun; 2009 May; 383(2):206-9. PubMed ID: 19348785
[TBL] [Abstract][Full Text] [Related]
10. New KCNQ1 mutations leading to haploinsufficiency in a general population; Defective trafficking of a KvLQT1 mutant.
Gouas L; Bellocq C; Berthet M; Potet F; Demolombe S; Forhan A; Lescasse R; Simon F; Balkau B; Denjoy I; Hainque B; Baró I; Guicheney P;
Cardiovasc Res; 2004 Jul; 63(1):60-8. PubMed ID: 15194462
[TBL] [Abstract][Full Text] [Related]
11. 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. PubMed ID: 12388934
[TBL] [Abstract][Full Text] [Related]
12. Additional gene variants reduce effectiveness of beta-blockers in the LQT1 form of long QT syndrome.
Kobori A; Sarai N; Shimizu W; Nakamura Y; Murakami Y; Makiyama T; Ohno S; Takenaka K; Ninomiya T; Fujiwara Y; Matsuoka S; Takano M; Noma A; Kita T; Horie M
J Cardiovasc Electrophysiol; 2004 Feb; 15(2):190-9. PubMed ID: 15028050
[TBL] [Abstract][Full Text] [Related]
13. Mechanistic basis for the pathogenesis of long QT syndrome associated with a common splicing mutation in KCNQ1 gene.
Tsuji K; Akao M; Ishii TM; Ohno S; Makiyama T; Takenaka K; Doi T; Haruna Y; Yoshida H; Nakashima T; Kita T; Horie M
J Mol Cell Cardiol; 2007 Mar; 42(3):662-9. PubMed ID: 17292394
[TBL] [Abstract][Full Text] [Related]
14. Mutation site-specific differences in arrhythmic risk and sensitivity to sympathetic stimulation in the LQT1 form of congenital long QT syndrome: multicenter study in Japan.
Shimizu W; Horie M; Ohno S; Takenaka K; Yamaguchi M; Shimizu M; Washizuka T; Aizawa Y; Nakamura K; Ohe T; Aiba T; Miyamoto Y; Yoshimasa Y; Towbin JA; Priori SG; Kamakura S
J Am Coll Cardiol; 2004 Jul; 44(1):117-25. PubMed ID: 15234419
[TBL] [Abstract][Full Text] [Related]
15. DHPLC analysis of potassium ion channel genes in congenital long QT syndrome.
Jongbloed R; Marcelis C; Velter C; Doevendans P; Geraedts J; Smeets H
Hum Mutat; 2002 Nov; 20(5):382-91. PubMed ID: 12402336
[TBL] [Abstract][Full Text] [Related]
16. Phenotypic variability and unusual clinical severity of congenital long-QT syndrome in a founder population.
Brink PA; Crotti L; Corfield V; Goosen A; Durrheim G; Hedley P; Heradien M; Geldenhuys G; Vanoli E; Bacchini S; Spazzolini C; Lundquist AL; Roden DM; George AL; Schwartz PJ
Circulation; 2005 Oct; 112(17):2602-10. PubMed ID: 16246960
[TBL] [Abstract][Full Text] [Related]
17. Isoproterenol exacerbates a long QT phenotype in Kcnq1-deficient neonatal mice: possible roles for human-like Kcnq1 isoform 1 and slow delayed rectifier K+ current.
Knollmann BC; Casimiro MC; Katchman AN; Sirenko SG; Schober T; Rong Q; Pfeifer K; Ebert SN
J Pharmacol Exp Ther; 2004 Jul; 310(1):311-8. PubMed ID: 15004216
[TBL] [Abstract][Full Text] [Related]
18. A hydrophobicity-dependent motif responsible for surface expression of cardiac potassium channel.
Pan N; Sun J; Lv C; Li H; Ding J
Cell Signal; 2009 Feb; 21(2):349-55. PubMed ID: 19041715
[TBL] [Abstract][Full Text] [Related]
19. The role of abnormal trafficking of KCNE1 in long QT syndrome 5.
Harmer SC; Tinker A
Biochem Soc Trans; 2007 Nov; 35(Pt 5):1074-6. PubMed ID: 17956282
[TBL] [Abstract][Full Text] [Related]
20. Dominant-negative control of cAMP-dependent IKs upregulation in human long-QT syndrome type 1.
Heijman J; Spätjens RL; Seyen SR; Lentink V; Kuijpers HJ; Boulet IR; de Windt LJ; David M; Volders PG
Circ Res; 2012 Jan; 110(2):211-9. PubMed ID: 22095730
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]