330 related articles for article (PubMed ID: 25500882)
1. Genetically engineered SCN5A mutant pig hearts exhibit conduction defects and arrhythmias.
Park DS; Cerrone M; Morley G; Vasquez C; Fowler S; Liu N; Bernstein SA; Liu FY; Zhang J; Rogers CS; Priori SG; Chinitz LA; Fishman GI
J Clin Invest; 2015 Jan; 125(1):403-12. PubMed ID: 25500882
[TBL] [Abstract][Full Text] [Related]
2. Bringing home the bacon? The next step in cardiac sodium channelopathies.
Wilde AA; Postema PG
J Clin Invest; 2015 Jan; 125(1):99-101. PubMed ID: 25500878
[TBL] [Abstract][Full Text] [Related]
3. A heterozygous deletion mutation in the cardiac sodium channel gene SCN5A with loss- and gain-of-function characteristics manifests as isolated conduction disease, without signs of Brugada or long QT syndrome.
Zumhagen S; Veldkamp MW; Stallmeyer B; Baartscheer A; Eckardt L; Paul M; Remme CA; Bhuiyan ZA; Bezzina CR; Schulze-Bahr E
PLoS One; 2013; 8(6):e67963. PubMed ID: 23840796
[TBL] [Abstract][Full Text] [Related]
4. Arrhythmic substrate, slowed propagation and increased dispersion in conduction direction in the right ventricular outflow tract of murine Scn5a+/- hearts.
Zhang Y; Guzadhur L; Jeevaratnam K; Salvage SC; Matthews GD; Lammers WJ; Lei M; Huang CL; Fraser JA
Acta Physiol (Oxf); 2014 Aug; 211(4):559-73. PubMed ID: 24913289
[TBL] [Abstract][Full Text] [Related]
5. Genetic background determines the severity of age-dependent cardiac structural abnormalities and arrhythmia susceptibility in Scn5a-1798insD mice.
Marchal GA; Rivaud MR; Wolswinkel R; Basso C; van Veen TAB; Bezzina CR; Remme CA
Europace; 2024 Jun; 26(6):. PubMed ID: 38875491
[TBL] [Abstract][Full Text] [Related]
6. Normal interventricular differences in tissue architecture underlie right ventricular susceptibility to conduction abnormalities in a mouse model of Brugada syndrome.
Kelly A; Salerno S; Connolly A; Bishop M; Charpentier F; Stølen T; Smith GL
Cardiovasc Res; 2018 Apr; 114(5):724-736. PubMed ID: 29267949
[TBL] [Abstract][Full Text] [Related]
7. Variants in the SCN5A Promoter Associated With Various Arrhythmia Phenotypes.
Yagihara N; Watanabe H; Barnett P; Duboscq-Bidot L; Thomas AC; Yang P; Ohno S; Hasegawa K; Kuwano R; Chatel S; Redon R; Schott JJ; Probst V; Koopmann TT; Bezzina CR; Wilde AA; Nakano Y; Aiba T; Miyamoto Y; Kamakura S; Darbar D; Donahue BS; Shigemizu D; Tanaka T; Tsunoda T; Suda M; Sato A; Minamino T; Endo N; Shimizu W; Horie M; Roden DM; Makita N
J Am Heart Assoc; 2016 Sep; 5(9):. PubMed ID: 27625342
[TBL] [Abstract][Full Text] [Related]
8. Overexpression of SCN5A in mouse heart mimics human syndrome of enhanced atrioventricular nodal conduction.
Liu GX; Remme CA; Boukens BJ; Belardinelli L; Rajamani S
Heart Rhythm; 2015 May; 12(5):1036-45. PubMed ID: 25623181
[TBL] [Abstract][Full Text] [Related]
9. Variable Na(v)1.5 protein expression from the wild-type allele correlates with the penetrance of cardiac conduction disease in the Scn5a(+/-) mouse model.
Leoni AL; Gavillet B; Rougier JS; Marionneau C; Probst V; Le Scouarnec S; Schott JJ; Demolombe S; Bruneval P; Huang CL; Colledge WH; Grace AA; Le Marec H; Wilde AA; Mohler PJ; Escande D; Abriel H; Charpentier F
PLoS One; 2010 Feb; 5(2):e9298. PubMed ID: 20174578
[TBL] [Abstract][Full Text] [Related]
10. Brugada syndrome: clinical presentation and genotype-correlation with magnetic resonance imaging parameters.
Rudic B; Schimpf R; Veltmann C; Doesch C; Tülümen E; Schoenberg SO; Borggrefe M; Papavassiliu T
Europace; 2016 Sep; 18(9):1411-9. PubMed ID: 26511399
[TBL] [Abstract][Full Text] [Related]
11. A transgenic zebrafish model of a human cardiac sodium channel mutation exhibits bradycardia, conduction-system abnormalities and early death.
Huttner IG; Trivedi G; Jacoby A; Mann SA; Vandenberg JI; Fatkin D
J Mol Cell Cardiol; 2013 Aug; 61():123-32. PubMed ID: 23791817
[TBL] [Abstract][Full Text] [Related]
12. Mannitol and hyponatremia regulate cardiac ventricular conduction in the context of sodium channel loss of function.
Blair GA; Wu X; Bain C; Warren M; Hoeker GS; Poelzing S
Am J Physiol Heart Circ Physiol; 2024 Mar; 326(3):H724-H734. PubMed ID: 38214908
[TBL] [Abstract][Full Text] [Related]
13. Type of SCN5A mutation determines clinical severity and degree of conduction slowing in loss-of-function sodium channelopathies.
Meregalli PG; Tan HL; Probst V; Koopmann TT; Tanck MW; Bhuiyan ZA; Sacher F; Kyndt F; Schott JJ; Albuisson J; Mabo P; Bezzina CR; Le Marec H; Wilde AA
Heart Rhythm; 2009 Mar; 6(3):341-8. PubMed ID: 19251209
[TBL] [Abstract][Full Text] [Related]
14. Refractory dispersion promotes conduction disturbance and arrhythmias in a Scn5a (+/-) mouse model.
Martin CA; Grace AA; Huang CL
Pflugers Arch; 2011 Oct; 462(4):495-504. PubMed ID: 21779762
[TBL] [Abstract][Full Text] [Related]
15. Whole-exome sequencing identifies Y1495X of SCN5A to be associated with familial conduction disease and sudden death.
Tan ZP; Xie L; Deng Y; Chen JL; Zhang WZ; Wang J; Yang JF; Yang YF
Sci Rep; 2014 Jul; 4():5616. PubMed ID: 25010007
[TBL] [Abstract][Full Text] [Related]
16. Cardiac channelopathies associated with infantile fatal ventricular arrhythmias: from the cradle to the bench.
Kato K; Makiyama T; Wu J; Ding WG; Kimura H; Naiki N; Ohno S; Itoh H; Nakanishi T; Matsuura H; Horie M
J Cardiovasc Electrophysiol; 2014 Jan; 25(1):66-73. PubMed ID: 24112685
[TBL] [Abstract][Full Text] [Related]
17. Clinical Spectrum of
Villarreal-Molina T; García-Ordóñez GP; Reyes-Quintero ÁE; Domínguez-Pérez M; Jacobo-Albavera L; Nava S; Carnevale A; Medeiros-Domingo A; Iturralde P
Genes (Basel); 2021 Dec; 13(1):. PubMed ID: 35052356
[TBL] [Abstract][Full Text] [Related]
18. Action potential wavelength restitution predicts alternans and arrhythmia in murine Scn5a(+/-) hearts.
Matthews GD; Guzadhur L; Sabir IN; Grace AA; Huang CL
J Physiol; 2013 Sep; 591(17):4167-88. PubMed ID: 23836691
[TBL] [Abstract][Full Text] [Related]
19.
Makarawate P; Chaosuwannakit N; Vannaprasaht S; Sahasthas D; Koo SH; Lee EJD; Tassaneeyakul W; Barajas-Martinez H; Hu D; Sawanyawisuth K
J Am Heart Assoc; 2017 Jun; 6(6):. PubMed ID: 28584071
[TBL] [Abstract][Full Text] [Related]
20. Mapping of reentrant spontaneous polymorphic ventricular tachycardia in a Scn5a+/- mouse model.
Martin CA; Guzadhur L; Grace AA; Lei M; Huang CL
Am J Physiol Heart Circ Physiol; 2011 May; 300(5):H1853-62. PubMed ID: 21378142
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
