171 related articles for article (PubMed ID: 30967788)
21. Cardiac sodium channel mutation associated with epinephrine-induced QT prolongation and sinus node dysfunction.
Chen J; Makiyama T; Wuriyanghai Y; Ohno S; Sasaki K; Hayano M; Harita T; Nishiuchi S; Yuta Yamamoto ; Ueyama T; Shimizu A; Horie M; Kimura T
Heart Rhythm; 2016 Jan; 13(1):289-98. PubMed ID: 26282245
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. 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]
24. A KCNQ1 mutation contributes to the concealed type 1 long QT phenotype by limiting the Kv7.1 channel conformational changes associated with protein kinase A phosphorylation.
Bartos DC; Giudicessi JR; Tester DJ; Ackerman MJ; Ohno S; Horie M; Gollob MH; Burgess DE; Delisle BP
Heart Rhythm; 2014 Mar; 11(3):459-68. PubMed ID: 24269949
[TBL] [Abstract][Full Text] [Related]
25. Biophysical properties of mutant KCNQ1 S277L channels linked to hereditary long QT syndrome with phenotypic variability.
Aidery P; Kisselbach J; Schweizer PA; Becker R; Katus HA; Thomas D
Biochim Biophys Acta; 2011 Apr; 1812(4):488-94. PubMed ID: 21241800
[TBL] [Abstract][Full Text] [Related]
26. Suppression-Replacement
Dotzler SM; Kim CSJ; Gendron WAC; Zhou W; Ye D; Bos JM; Tester DJ; Barry MA; Ackerman MJ
Circulation; 2021 Apr; 143(14):1411-1425. PubMed ID: 33504163
[TBL] [Abstract][Full Text] [Related]
27. Complex aberrant splicing in the induced pluripotent stem cell-derived cardiomyocytes from a patient with long QT syndrome carrying KCNQ1-A344Aspl mutation.
Wuriyanghai Y; Makiyama T; Sasaki K; Kamakura T; Yamamoto Y; Hayano M; Harita T; Nishiuchi S; Chen J; Kohjitani H; Hirose S; Yokoi F; Gao J; Chonabayashi K; Watanabe K; Ohno S; Yoshida Y; Kimura T; Horie M
Heart Rhythm; 2018 Oct; 15(10):1566-1574. PubMed ID: 29857160
[TBL] [Abstract][Full Text] [Related]
28. A KCNQ1 mutation causes a high penetrance for familial atrial fibrillation.
Bartos DC; Anderson JB; Bastiaenen R; Johnson JN; Gollob MH; Tester DJ; Burgess DE; Homfray T; Behr ER; Ackerman MJ; Guicheney P; Delisle BP
J Cardiovasc Electrophysiol; 2013 May; 24(5):562-9. PubMed ID: 23350853
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. Differential conditions for early after-depolarizations and triggered activity in cardiomyocytes derived from transgenic LQT1 and LQT2 rabbits.
Liu GX; Choi BR; Ziv O; Li W; de Lange E; Qu Z; Koren G
J Physiol; 2012 Mar; 590(5):1171-80. PubMed ID: 22183728
[TBL] [Abstract][Full Text] [Related]
31. [Novel mutations of potassium channel KCNQ1 S145L and KCNH2 Y475C genes in Chinese pedigrees of long QT syndrome].
Liu WL; Hu DY; Li P; Li CL; Qin XG; Li YT; Li L; Li ZM; Dong W; Qi Y; Wang Q
Zhonghua Nei Ke Za Zhi; 2006 Jun; 45(6):463-6. PubMed ID: 16831322
[TBL] [Abstract][Full Text] [Related]
32. Functional Characterization of a Spectrum of Novel Romano-Ward Syndrome
Rinné S; Oertli A; Nagel C; Tomsits P; Jenewein T; Kääb S; Kauferstein S; Loewe A; Beckmann BM; Decher N
Int J Mol Sci; 2023 Jan; 24(2):. PubMed ID: 36674868
[TBL] [Abstract][Full Text] [Related]
33. IKs Gain- and Loss-of-Function in Early-Onset Lone Atrial Fibrillation.
Steffensen AB; Refsgaard L; Andersen MN; Vallet C; Mujezinovic A; Haunsø S; Svendsen JH; Olesen SP; Olesen MS; Schmitt N
J Cardiovasc Electrophysiol; 2015 Jul; 26(7):715-23. PubMed ID: 25786344
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Electrophysiological phenotype in the LQTS mutations Y111C and R518X in the KCNQ1 gene.
Diamant UB; Vahedi F; Winbo A; Rydberg A; Stattin EL; Jensen SM; Bergfeldt L
J Appl Physiol (1985); 2013 Nov; 115(10):1423-32. PubMed ID: 24052033
[TBL] [Abstract][Full Text] [Related]
36. Congenital long QT syndrome.
Crotti L; Celano G; Dagradi F; Schwartz PJ
Orphanet J Rare Dis; 2008 Jul; 3():18. PubMed ID: 18606002
[TBL] [Abstract][Full Text] [Related]
37. Mutation of an A-kinase-anchoring protein causes long-QT syndrome.
Chen L; Marquardt ML; Tester DJ; Sampson KJ; Ackerman MJ; Kass RS
Proc Natl Acad Sci U S A; 2007 Dec; 104(52):20990-5. PubMed ID: 18093912
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. 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]
40. Pharmacological rescue of specific long QT variants of KCNQ1/KCNE1 channels.
Zou X; Wu X; Sampson KJ; Colecraft HM; Larsson HP; Kass RS
Front Physiol; 2022; 13():902224. PubMed ID: 36505078
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
