These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

204 related articles for article (PubMed ID: 29402340)

  • 1. Whole-exome sequencing identifies a Novel SCN5A mutation (C335R) in a Chinese family with arrhythmia.
    Huang H; Ding DB; Fan LL; Jin JY; Li JJ; Guo S; Chen YQ; Xiang R
    Cardiol Young; 2018 May; 28(5):688-691. PubMed ID: 29402340
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Whole‑exome sequencing identifies a novel mutation (R367G) in SCN5A to be associated with familial cardiac conduction disease.
    Yu R; Fan XF; Chen C; Liu ZH
    Mol Med Rep; 2017 Jul; 16(1):410-414. PubMed ID: 28534967
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Whole exome sequencing in Brugada and long QT syndromes revealed novel rare and potential pathogenic mutations related to the dysfunction of the cardiac sodium channel.
    Chen J; Li H; Guo S; Yang Z; Sun S; Zeng J; Gou H; Chen Y; Wang F; Lin Y; Huang K; Yue H; Ma Y; Lin Y
    Orphanet J Rare Dis; 2022 Oct; 17(1):394. PubMed ID: 36303204
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical characterisation of a novel
    Kean AC; Helm BM; Vatta M; Ayers MD; Parent JJ; Darragh RK
    Cardiol Young; 2019 Oct; 29(10):1257-1263. PubMed ID: 31477192
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A Brugada syndrome proband with compound heterozygote SCN5A mutations identified from a Chinese family in Singapore.
    Tan BY; Yong RY; Barajas-Martinez H; Dumaine R; Chew YX; Wasan PS; Ching CK; Ho KL; Gan LS; Morin N; Chong AP; Yap SH; Neo JL; Yap EP; Moochhala S; Chong DT; Chow W; Seow SC; Hu D; Uttamchandani M; Teo WS
    Europace; 2016 Jun; 18(6):897-904. PubMed ID: 25829473
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family.
    Kyndt F; Probst V; Potet F; Demolombe S; Chevallier JC; Baro I; Moisan JP; Boisseau P; Schott JJ; Escande D; Le Marec H
    Circulation; 2001 Dec; 104(25):3081-6. PubMed ID: 11748104
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Multilevel analyses of SCN5A mutations in arrhythmogenic right ventricular dysplasia/cardiomyopathy suggest non-canonical mechanisms for disease pathogenesis.
    Te Riele AS; Agullo-Pascual E; James CA; Leo-Macias A; Cerrone M; Zhang M; Lin X; Lin B; Sobreira NL; Amat-Alarcon N; Marsman RF; Murray B; Tichnell C; van der Heijden JF; Dooijes D; van Veen TA; Tandri H; Fowler SJ; Hauer RN; Tomaselli G; van den Berg MP; Taylor MR; Brun F; Sinagra G; Wilde AA; Mestroni L; Bezzina CR; Calkins H; Peter van Tintelen J; Bu L; Delmar M; Judge DP
    Cardiovasc Res; 2017 Jan; 113(1):102-111. PubMed ID: 28069705
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Gain-of-function mutation in SCN5A causes ventricular arrhythmias and early onset atrial fibrillation.
    Lieve KV; Verkerk AO; Podliesna S; van der Werf C; Tanck MW; Hofman N; van Bergen PF; Beekman L; Bezzina CR; Wilde AAM; Lodder EM
    Int J Cardiol; 2017 Jun; 236():187-193. PubMed ID: 28262340
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of
    Sedaghat-Hamedani F; Rebs S; El-Battrawy I; Chasan S; Krause T; Haas J; Zhong R; Liao Z; Xu Q; Zhou X; Akin I; Zitron E; Frey N; Streckfuss-Bömeke K; Kayvanpour E
    Int J Mol Sci; 2021 Nov; 22(23):. PubMed ID: 34884792
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic analysis of cardiac SCN5A Gene in Iranian patients with hereditary cardiac arrhythmias.
    Asadi M; Foo R; Bhuiyan ZA; Samienasab MR; Salehi AR; Shahrzad S; Salehi R
    Anatol J Cardiol; 2016 Mar; 16(3):170-4. PubMed ID: 26467377
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of rare heterozygous linkage R965C-R1309H mutations in the pore-forming region of SCN5A gene associated with complex arrhythmia.
    Lin Y; Qin J; Shen Y; Huang J; Zhang Z; Zhu Z; Lu H; Huang Y; Yin Y; Wang A; Jin L; Hu Z; Lin X; Jiang B
    Mol Genet Genomic Med; 2021 May; 9(5):e1613. PubMed ID: 33764691
    [TBL] [Abstract][Full Text] [Related]  

  • 13. p.Y1449C SCN5A mutation associated with overlap disorder comprising conduction disease, Brugada syndrome, and atrial flutter.
    Hothi SS; Ara F; Timperley J
    J Cardiovasc Electrophysiol; 2015 Jan; 26(1):93-7. PubMed ID: 24903439
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Myotonic dystrophy type 1 mimics and exacerbates Brugada phenotype induced by Nav1.5 sodium channel loss-of-function mutation.
    Pambrun T; Mercier A; Chatelier A; Patri S; Schott JJ; Le Scouarnec S; Chahine M; Degand B; Bois P
    Heart Rhythm; 2014 Aug; 11(8):1393-400. PubMed ID: 24768612
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel SCN5A mutation in amiodarone-responsive multifocal ventricular ectopy-associated cardiomyopathy.
    Beckermann TM; McLeod K; Murday V; Potet F; George AL
    Heart Rhythm; 2014 Aug; 11(8):1446-53. PubMed ID: 24815523
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A balanced translocation disrupting SCN5A in a family with Brugada syndrome and sudden cardiac death.
    Yeates L; Ingles J; Gray B; Singarayar S; Sy RW; Semsarian C; Bagnall RD
    Heart Rhythm; 2019 Feb; 16(2):231-238. PubMed ID: 30170230
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Dysfunction of the Voltage-Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome.
    Portero V; Le Scouarnec S; Es-Salah-Lamoureux Z; Burel S; Gourraud JB; Bonnaud S; Lindenbaum P; Simonet F; Violleau J; Baron E; Moreau E; Scott C; Chatel S; Loussouarn G; O'Hara T; Mabo P; Dina C; Le Marec H; Schott JJ; Probst V; Baró I; Marionneau C; Charpentier F; Redon R
    J Am Heart Assoc; 2016 Jun; 5(6):. PubMed ID: 27287695
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Whole-Exome Molecular Autopsy After Exertion-Related Sudden Unexplained Death in the Young.
    Anderson JH; Tester DJ; Will ML; Ackerman MJ
    Circ Cardiovasc Genet; 2016 Jun; 9(3):259-65. PubMed ID: 27114410
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Functional Characterization of Two Novel Mutations in
    Balla C; Conte E; Selvatici R; Marsano RM; Gerbino A; Farnè M; Blunck R; Vitali F; Armaroli A; Brieda A; Liantonio A; De Luca A; Ferlini A; Rapezzi C; Bertini M; Gualandi F; Imbrici P
    Int J Mol Sci; 2021 Jun; 22(12):. PubMed ID: 34204499
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Concomitant Brugada-like and short QT electrocardiogram linked to SCN5A mutation.
    Hong K; Hu J; Yu J; Brugada R
    Eur J Hum Genet; 2012 Nov; 20(11):1189-92. PubMed ID: 22490985
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.