294 related articles for article (PubMed ID: 17956282)
1. 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]
2. 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]
3. 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]
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. Functional effects of a KCNQ1 mutation associated with the long QT syndrome.
Boulet IR; Raes AL; Ottschytsch N; Snyders DJ
Cardiovasc Res; 2006 Jun; 70(3):466-74. PubMed ID: 16564513
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. [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]
10. D85N, a KCNE1 polymorphism, is a disease-causing gene variant in long QT syndrome.
Nishio Y; Makiyama T; Itoh H; Sakaguchi T; Ohno S; Gong YZ; Yamamoto S; Ozawa T; Ding WG; Toyoda F; Kawamura M; Akao M; Matsuura H; Kimura T; Kita T; Horie M
J Am Coll Cardiol; 2009 Aug; 54(9):812-9. PubMed ID: 19695459
[TBL] [Abstract][Full Text] [Related]
11. Calmodulin is essential for cardiac IKS channel gating and assembly: impaired function in long-QT mutations.
Shamgar L; Ma L; Schmitt N; Haitin Y; Peretz A; Wiener R; Hirsch J; Pongs O; Attali B
Circ Res; 2006 Apr; 98(8):1055-63. PubMed ID: 16556865
[TBL] [Abstract][Full Text] [Related]
12. Abnormal KCNQ1 trafficking influences disease pathogenesis in hereditary long QT syndromes (LQT1).
Wilson AJ; Quinn KV; Graves FM; Bitner-Glindzicz M; Tinker A
Cardiovasc Res; 2005 Aug; 67(3):476-86. PubMed ID: 15935335
[TBL] [Abstract][Full Text] [Related]
13. Action potential clamp and mefloquine sensitivity of recombinant 'I KS' channels incorporating the V307L KCNQ1 mutation.
El Harchi A; McPate MJ; Zhang YH; Zhang H; Hancox JC
J Physiol Pharmacol; 2010 Apr; 61(2):123-31. PubMed ID: 20436212
[TBL] [Abstract][Full Text] [Related]
14. Insights into Cardiac IKs (KCNQ1/KCNE1) Channels Regulation.
Wu X; Larsson HP
Int J Mol Sci; 2020 Dec; 21(24):. PubMed ID: 33322401
[TBL] [Abstract][Full Text] [Related]
15. Mechanisms of disease pathogenesis in long QT syndrome type 5.
Harmer SC; Wilson AJ; Aldridge R; Tinker A
Am J Physiol Cell Physiol; 2010 Feb; 298(2):C263-73. PubMed ID: 19907016
[TBL] [Abstract][Full Text] [Related]
16. Dysfunctional potassium channel subunit interaction as a novel mechanism of long QT syndrome.
Hoosien M; Ahearn ME; Myerburg RJ; Pham TV; Miller TE; Smets MJ; Baumbach-Reardon L; Young ML; Farooq A; Bishopric NH
Heart Rhythm; 2013 May; 10(5):728-37. PubMed ID: 23291057
[TBL] [Abstract][Full Text] [Related]
17. Long QT syndrome in neonates: conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations.
Lupoglazoff JM; Denjoy I; Villain E; Fressart V; Simon F; Bozio A; Berthet M; Benammar N; Hainque B; Guicheney P
J Am Coll Cardiol; 2004 Mar; 43(5):826-30. PubMed ID: 14998624
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Mutations in the genes KCND2 and KCND3 encoding the ion channels Kv4.2 and Kv4.3, conducting the cardiac fast transient outward current (ITO,f), are not a frequent cause of long QT syndrome.
Frank-Hansen R; Larsen LA; Andersen P; Jespersgaard C; Christiansen M
Clin Chim Acta; 2005 Jan; 351(1-2):95-100. PubMed ID: 15563876
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
