96 related articles for article (PubMed ID: 15845383)
1. Differential Ca2+ sensitivity of RyR2 mutations reveals distinct mechanisms of channel dysfunction in sudden cardiac death.
Thomas NL; Lai FA; George CH
Biochem Biophys Res Commun; 2005 May; 331(1):231-8. PubMed ID: 15845383
[TBL] [Abstract][Full Text] [Related]
2. Functional heterogeneity of ryanodine receptor mutations associated with sudden cardiac death.
Thomas NL; George CH; Lai FA
Cardiovasc Res; 2004 Oct; 64(1):52-60. PubMed ID: 15364613
[TBL] [Abstract][Full Text] [Related]
3. Arrhythmogenic mutation-linked defects in ryanodine receptor autoregulation reveal a novel mechanism of Ca2+ release channel dysfunction.
George CH; Jundi H; Walters N; Thomas NL; West RR; Lai FA
Circ Res; 2006 Jan; 98(1):88-97. PubMed ID: 16339485
[TBL] [Abstract][Full Text] [Related]
4. Endoplasmic reticulum Ca2+ measurements reveal that the cardiac ryanodine receptor mutations linked to cardiac arrhythmia and sudden death alter the threshold for store-overload-induced Ca2+ release.
Jones PP; Jiang D; Bolstad J; Hunt DJ; Zhang L; Demaurex N; Chen SR
Biochem J; 2008 May; 412(1):171-8. PubMed ID: 18092949
[TBL] [Abstract][Full Text] [Related]
5. Enhanced store overload-induced Ca2+ release and channel sensitivity to luminal Ca2+ activation are common defects of RyR2 mutations linked to ventricular tachycardia and sudden death.
Jiang D; Wang R; Xiao B; Kong H; Hunt DJ; Choi P; Zhang L; Chen SR
Circ Res; 2005 Nov; 97(11):1173-81. PubMed ID: 16239587
[TBL] [Abstract][Full Text] [Related]
6. Ryanodine receptor mutations in arrhythmias: advances in understanding the mechanisms of channel dysfunction.
Thomas NL; George CH; Williams AJ; Lai FA
Biochem Soc Trans; 2007 Nov; 35(Pt 5):946-51. PubMed ID: 17956252
[TBL] [Abstract][Full Text] [Related]
7. Ryanodine receptor mutations associated with stress-induced ventricular tachycardia mediate increased calcium release in stimulated cardiomyocytes.
George CH; Higgs GV; Lai FA
Circ Res; 2003 Sep; 93(6):531-40. PubMed ID: 12919952
[TBL] [Abstract][Full Text] [Related]
8. Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia.
Marks AR; Priori S; Memmi M; Kontula K; Laitinen PJ
J Cell Physiol; 2002 Jan; 190(1):1-6. PubMed ID: 11807805
[TBL] [Abstract][Full Text] [Related]
9. Role of ryanodine receptor mutations in cardiac pathology: more questions than answers?
Thomas NL; George CH; Lai FA
Biochem Soc Trans; 2006 Nov; 34(Pt 5):913-8. PubMed ID: 17052226
[TBL] [Abstract][Full Text] [Related]
10. Calstabin deficiency, ryanodine receptors, and sudden cardiac death.
Lehnart SE; Wehrens XH; Marks AR
Biochem Biophys Res Commun; 2004 Oct; 322(4):1267-79. PubMed ID: 15336974
[TBL] [Abstract][Full Text] [Related]
11. Sarcoplasmic reticulum calcium leak and cardiac arrhythmias.
Chelu MG; Wehrens XH
Biochem Soc Trans; 2007 Nov; 35(Pt 5):952-6. PubMed ID: 17956253
[TBL] [Abstract][Full Text] [Related]
12. Ryanodine receptors and ventricular arrhythmias: emerging trends in mutations, mechanisms and therapies.
George CH; Jundi H; Thomas NL; Fry DL; Lai FA
J Mol Cell Cardiol; 2007 Jan; 42(1):34-50. PubMed ID: 17081562
[TBL] [Abstract][Full Text] [Related]
13. Mutant ryanodine receptors in catecholaminergic polymorphic ventricular tachycardia generate delayed afterdepolarizations due to increased propensity to Ca2+ waves.
Paavola J; Viitasalo M; Laitinen-Forsblom PJ; Pasternack M; Swan H; Tikkanen I; Toivonen L; Kontula K; Laine M
Eur Heart J; 2007 May; 28(9):1135-42. PubMed ID: 17347175
[TBL] [Abstract][Full Text] [Related]
14. Ca2+/calmodulin-dependent protein kinase modulates cardiac ryanodine receptor phosphorylation and sarcoplasmic reticulum Ca2+ leak in heart failure.
Ai X; Curran JW; Shannon TR; Bers DM; Pogwizd SM
Circ Res; 2005 Dec; 97(12):1314-22. PubMed ID: 16269653
[TBL] [Abstract][Full Text] [Related]
15. The RyR2 central domain peptide DPc10 lowers the threshold for spontaneous Ca2+ release in permeabilized cardiomyocytes.
Yang Z; Ikemoto N; Lamb GD; Steele DS
Cardiovasc Res; 2006 Jun; 70(3):475-85. PubMed ID: 16624262
[TBL] [Abstract][Full Text] [Related]
16. Alternative splicing of ryanodine receptors modulates cardiomyocyte Ca2+ signaling and susceptibility to apoptosis.
George CH; Rogers SA; Bertrand BM; Tunwell RE; Thomas NL; Steele DS; Cox EV; Pepper C; Hazeel CJ; Claycomb WC; Lai FA
Circ Res; 2007 Mar; 100(6):874-83. PubMed ID: 17322175
[TBL] [Abstract][Full Text] [Related]
17. Mechanisms of abnormal calcium homeostasis in mutations responsible for catecholaminergic polymorphic ventricular tachycardia.
Iyer V; Hajjar RJ; Armoundas AA
Circ Res; 2007 Feb; 100(2):e22-31. PubMed ID: 17234962
[TBL] [Abstract][Full Text] [Related]
18. The CPVT-associated RyR2 mutation G230C enhances store overload-induced Ca2+ release and destabilizes the N-terminal domains.
Liu Y; Kimlicka L; Hiess F; Tian X; Wang R; Zhang L; Jones PP; Van Petegem F; Chen SR
Biochem J; 2013 Aug; 454(1):123-31. PubMed ID: 23746327
[TBL] [Abstract][Full Text] [Related]
19. Catecholaminergic polymorphic ventricular tachycardia: recent mechanistic insights.
Kontula K; Laitinen PJ; Lehtonen A; Toivonen L; Viitasalo M; Swan H
Cardiovasc Res; 2005 Aug; 67(3):379-87. PubMed ID: 15913575
[TBL] [Abstract][Full Text] [Related]
20. The arrhythmogenic human HRC point mutation S96A leads to spontaneous Ca(2+) release due to an impaired ability to buffer store Ca(2+).
Zhang JZ; McLay JC; Jones PP
J Mol Cell Cardiol; 2014 Sep; 74():22-31. PubMed ID: 24805197
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
