116 related articles for article (PubMed ID: 31437535)
1. A novel homozygous mutation in the TRDN gene causes a severe form of pediatric malignant ventricular arrhythmia.
Rossi D; Gigli L; Gamberucci A; Bordoni R; Pietrelli A; Lorenzini S; Pierantozzi E; Peretto G; De Bellis G; Della Bella P; Ferrari M; Sorrentino V; Benedetti S; Sala S; Di Resta C
Heart Rhythm; 2020 Feb; 17(2):296-304. PubMed ID: 31437535
[TBL] [Abstract][Full Text] [Related]
2. Homozygous/Compound Heterozygous Triadin Mutations Associated With Autosomal-Recessive Long-QT Syndrome and Pediatric Sudden Cardiac Arrest: Elucidation of the Triadin Knockout Syndrome.
Altmann HM; Tester DJ; Will ML; Middha S; Evans JM; Eckloff BW; Ackerman MJ
Circulation; 2015 Jun; 131(23):2051-60. PubMed ID: 25922419
[TBL] [Abstract][Full Text] [Related]
3. Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human.
Roux-Buisson N; Cacheux M; Fourest-Lieuvin A; Fauconnier J; Brocard J; Denjoy I; Durand P; Guicheney P; Kyndt F; Leenhardt A; Le Marec H; Lucet V; Mabo P; Probst V; Monnier N; Ray PF; Santoni E; Trémeaux P; Lacampagne A; Fauré J; Lunardi J; Marty I
Hum Mol Genet; 2012 Jun; 21(12):2759-67. PubMed ID: 22422768
[TBL] [Abstract][Full Text] [Related]
4. Novel cases of pediatric sudden cardiac death secondary to TRDN mutations presenting as long QT syndrome at rest and catecholaminergic polymorphic ventricular tachycardia during exercise: The TRDN arrhythmia syndrome.
Rabbani B; Khorgami M; Dalili M; Zamani N; Mahdieh N; Gollob MH
Am J Med Genet A; 2021 Nov; 185(11):3433-3445. PubMed ID: 34415104
[TBL] [Abstract][Full Text] [Related]
5. Phenotype-guided whole genome analysis in a patient with genetically elusive long QT syndrome yields a novel TRDN-encoded triadin pathogenetic substrate for triadin knockout syndrome and reveals a novel primate-specific cardiac TRDN transcript.
Clemens DJ; Tester DJ; Marty I; Ackerman MJ
Heart Rhythm; 2020 Jun; 17(6):1017-1024. PubMed ID: 32402482
[TBL] [Abstract][Full Text] [Related]
6. Cardiomyocyte-Specific Long Noncoding RNA Regulates Alternative Splicing of the Triadin Gene in the Heart.
Zhao Y; Riching AS; Knight WE; Chi C; Broadwell LJ; Du Y; Abdel-Hafiz M; Ambardekar AV; Irwin DC; Proenza C; Xu H; Leinwand LA; Walker LA; Woulfe KC; Bristow MR; Buttrick PM; Song K
Circulation; 2022 Aug; 146(9):699-714. PubMed ID: 35862102
[TBL] [Abstract][Full Text] [Related]
7. International Triadin Knockout Syndrome Registry.
Clemens DJ; Tester DJ; Giudicessi JR; Bos JM; Rohatgi RK; Abrams DJ; Balaji S; Crotti L; Faure J; Napolitano C; Priori SG; Probst V; Rooryck-Thambo C; Roux-Buisson N; Sacher F; Schwartz PJ; Silka MJ; Walsh MA; Ackerman MJ
Circ Genom Precis Med; 2019 Feb; 12(2):e002419. PubMed ID: 30649896
[TBL] [Abstract][Full Text] [Related]
8. A novel heterozygous mutation in cardiac calsequestrin causes autosomal dominant catecholaminergic polymorphic ventricular tachycardia.
Gray B; Bagnall RD; Lam L; Ingles J; Turner C; Haan E; Davis A; Yang PC; Clancy CE; Sy RW; Semsarian C
Heart Rhythm; 2016 Aug; 13(8):1652-60. PubMed ID: 27157848
[TBL] [Abstract][Full Text] [Related]
9. New Family With Catecholaminergic Polymorphic Ventricular Tachycardia Linked to the Triadin Gene.
Rooryck C; Kyndt F; Bozon D; Roux-Buisson N; Sacher F; Probst V; Thambo JB
J Cardiovasc Electrophysiol; 2015 Oct; 26(10):1146-50. PubMed ID: 26200674
[TBL] [Abstract][Full Text] [Related]
10. Triadin regulates cardiac muscle couplon structure and microdomain Ca(2+) signalling: a path towards ventricular arrhythmias.
Chopra N; Knollmann BC
Cardiovasc Res; 2013 May; 98(2):187-91. PubMed ID: 23396608
[TBL] [Abstract][Full Text] [Related]
11. Compound Heterozygous Triadin Mutation Causing Cardiac Arrest in Two Siblings.
Walsh MA; Stuart AG; Schlecht HB; James AF; Hancox JC; Newbury-Ecob RA
Pacing Clin Electrophysiol; 2016 May; 39(5):497-501. PubMed ID: 26768964
[TBL] [Abstract][Full Text] [Related]
12. A very rare cause of sudden cardiac arrest in children: triadin knockout syndrome.
Sulu A; Karacan M; Ergul Y
Cardiol Young; 2022 Apr; ():1-3. PubMed ID: 35481495
[TBL] [Abstract][Full Text] [Related]
13. Cellular and electrophysiological characterization of triadin knockout syndrome using induced pluripotent stem cell-derived cardiomyocytes.
Clemens DJ; Ye D; Wang L; Kim CSJ; Zhou W; Dotzler SM; Tester DJ; Marty I; Knollmann BC; Ackerman MJ
Stem Cell Reports; 2023 May; 18(5):1075-1089. PubMed ID: 37163978
[TBL] [Abstract][Full Text] [Related]
14. Generation of a Triadin KnockOut Syndrome Zebrafish Model.
Vecchi VM; Spreafico M; Brix A; Santoni A; Sala S; Pistocchi A; Marozzi A; Di Resta C
Int J Mol Sci; 2021 Sep; 22(18):. PubMed ID: 34575879
[TBL] [Abstract][Full Text] [Related]
15. Pediatric Malignant Arrhythmias Caused by Rare Homozygous Genetic Variants in
Sarquella-Brugada G; Fernandez-Falgueras A; Cesar S; Arbelo E; Jordà P; García-Álvarez A; Cruzalegui JC; Merchan EF; Fiol V; Brugada J; Brugada R; Campuzano O
Front Pediatr; 2020; 8():601708. PubMed ID: 33692971
[No Abstract] [Full Text] [Related]
16. Triadin Knockout Syndrome Is Absent in a Multi-Center Molecular Autopsy Cohort of Sudden Infant Death Syndrome and Sudden Unexplained Death in the Young and Is Extremely Rare in the General Population.
Clemens DJ; Gray B; Bagnall RD; Tester DJ; Dotzler SM; Giudicessi JR; Matthews E; Semsarian C; Behr ER; Ackerman MJ
Circ Genom Precis Med; 2020 Apr; 13(2):e002731. PubMed ID: 32167373
[TBL] [Abstract][Full Text] [Related]
17. Identification of a Novel Homozygous Multi-Exon Duplication in RYR2 Among Children With Exertion-Related Unexplained Sudden Deaths in the Amish Community.
Tester DJ; Bombei HM; Fitzgerald KK; Giudicessi JR; Pitel BA; Thorland EC; Russell BG; Hamrick SK; Kim CSJ; Haglund-Turnquist CM; Johnsrude CL; Atkins DL; Ochoa Nunez LA; Law I; Temple J; Ackerman MJ
JAMA Cardiol; 2020 Mar; 5(3):13-18. PubMed ID: 31913406
[TBL] [Abstract][Full Text] [Related]
18. A homozygous SCN5A mutation in a severe, recessive type of cardiac conduction disease.
Neu A; Eiselt M; Paul M; Sauter K; Stallmeyer B; Isbrandt D; Schulze-Bahr E
Hum Mutat; 2010 Aug; 31(8):E1609-21. PubMed ID: 20564468
[TBL] [Abstract][Full Text] [Related]
19. Interplay between Triadin and Calsequestrin in the Pathogenesis of CPVT in the Mouse.
Cacheux M; Fauconnier J; Thireau J; Osseni A; Brocard J; Roux-Buisson N; Brocard J; Fauré J; Lacampagne A; Marty I
Mol Ther; 2020 Jan; 28(1):171-179. PubMed ID: 31607542
[TBL] [Abstract][Full Text] [Related]
20. A mutation in CALM1 encoding calmodulin in familial idiopathic ventricular fibrillation in childhood and adolescence.
Marsman RF; Barc J; Beekman L; Alders M; Dooijes D; van den Wijngaard A; Ratbi I; Sefiani A; Bhuiyan ZA; Wilde AA; Bezzina CR
J Am Coll Cardiol; 2014 Jan; 63(3):259-66. PubMed ID: 24076290
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
