BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

162 related articles for article (PubMed ID: 29077258)

  • 1. Whole-exome sequencing identifies a novel mutation of GPD1L (R189X) associated with familial conduction disease and sudden death.
    Huang H; Chen YQ; Fan LL; Guo S; Li JJ; Jin JY; Xiang R
    J Cell Mol Med; 2018 Feb; 22(2):1350-1354. PubMed ID: 29077258
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Whole exome sequencing identifies a novel mutation (c.333 + 2T > C) of TNNI3K in a Chinese family with dilated cardiomyopathy and cardiac conduction disease.
    Fan LL; Huang H; Jin JY; Li JJ; Chen YQ; Zhao SP; Xiang R
    Gene; 2018 Mar; 648():63-67. PubMed ID: 29355681
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Exome sequencing identifies a novel nonsense mutation of Ring Finger Protein 207 in a Chinese family with Long QT syndrome and syncope.
    Fan LL; Chen YQ; Huang H; Yuan ZZ; Jin JY; Hu M; Xiang R
    J Hum Genet; 2019 Mar; 64(3):233-238. PubMed ID: 30542207
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. GPD1L links redox state to cardiac excitability by PKC-dependent phosphorylation of the sodium channel SCN5A.
    Valdivia CR; Ueda K; Ackerman MJ; Makielski JC
    Am J Physiol Heart Circ Physiol; 2009 Oct; 297(4):H1446-52. PubMed ID: 19666841
    [TBL] [Abstract][Full Text] [Related]  

  • 6. p.N1380del mutation in the pore-forming region of SCN5A gene is associated with cardiac conduction disturbance and ventricular tachycardia.
    Yang Z; Lu D; Zhang L; Hu J; Nie Z; Xie C; Qiu F; Cheng H; Yan Y
    Acta Biochim Biophys Sin (Shanghai); 2017 Mar; 49(3):270-276. PubMed ID: 28159958
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of a nonsense mutation in TNNI3K associated with cardiac conduction disease.
    Liu J; Liu D; Li M; Wu K; Liu N; Zhao C; Shi X; Liu Q
    J Clin Lab Anal; 2020 Sep; 34(9):e23418. PubMed ID: 32529721
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. A novel mutation in GPD1‑L associated with early repolarization syndrome via modulation of cardiomyocyte fast sodium currents.
    Fan J; Ji CC; Cheng YJ; Yao H; Chen XM; Zheng ZH; Wu SH
    Int J Mol Med; 2020 Mar; 45(3):947-955. PubMed ID: 31922248
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Novel
    Yuan M; Guo Y; Xia H; Xu H; Deng H; Yuan L
    Front Cardiovasc Med; 2021; 8():758903. PubMed ID: 34957250
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Whole exome sequencing identified a pathogenic nonsense mutation in LMNA in a family with a progressive cardiac conduction defect: A case report.
    Fan P; Zhang D; Yang KQ; Tian T; Luo F; Liu YX; Wang LP; Zhou XL
    Mol Med Rep; 2020 Jun; 21(6):2459-2465. PubMed ID: 32323820
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A nonsense SCN5A mutation associated with Brugada-type electrocardiogram and intraventricular conduction defects.
    Samani K; Ai T; Towbin JA; Brugada R; Shuraih M; Xi Y; Wu G; Cheng J; Vatta M
    Pacing Clin Electrophysiol; 2009 Sep; 32(9):1231-6. PubMed ID: 19719504
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Whole-Exome Sequencing Identifies a Novel Mutation (p.L320R) of Alpha-Actinin 2 in a Chinese Family with Dilated Cardiomyopathy and Ventricular Tachycardia.
    Fan LL; Huang H; Jin JY; Li JJ; Chen YQ; Xiang R
    Cytogenet Genome Res; 2019; 157(3):148-152. PubMed ID: 30630173
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndrome.
    Van Norstrand DW; Valdivia CR; Tester DJ; Ueda K; London B; Makielski JC; Ackerman MJ
    Circulation; 2007 Nov; 116(20):2253-9. PubMed ID: 17967976
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Gain-of-function mutation of the SCN5A gene causes exercise-induced polymorphic ventricular arrhythmias.
    Swan H; Amarouch MY; Leinonen J; Marjamaa A; Kucera JP; Laitinen-Forsblom PJ; Lahtinen AM; Palotie A; Kontula K; Toivonen L; Abriel H; Widen E
    Circ Cardiovasc Genet; 2014 Dec; 7(6):771-81. PubMed ID: 25210054
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Whole exome sequencing identified a pathogenic mutation in RYR2 in a Chinese family with unexplained sudden death.
    Lin Y; He S; Liao Z; Feng R; Liu R; Peng Y; Yu N; Qi H; Chen J; Huang Z; Lei H; Liu Y; Rao F; Deng C; Xue Y; Zhang G; Zhang B; Yao H; Wu S
    J Electrocardiol; 2018; 51(2):309-315. PubMed ID: 29132927
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel SCN5A mutations in two families with "Brugada-like" ST elevation in the inferior leads and conduction disturbances.
    Maury P; Moreau A; Hidden-Lucet F; Leenhardt A; Fressart V; Berthet M; Denjoy I; Bennamar N; Rollin A; Cardin C; Guicheney P; Chahine M
    J Interv Card Electrophysiol; 2013 Aug; 37(2):131-40. PubMed ID: 23612926
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Complex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutations.
    Béziau DM; Barc J; O'Hara T; Le Gloan L; Amarouch MY; Solnon A; Pavin D; Lecointe S; Bouillet P; Gourraud JB; Guicheney P; Denjoy I; Redon R; Mabo P; le Marec H; Loussouarn G; Kyndt F; Schott JJ; Probst V; Baró I
    Basic Res Cardiol; 2014; 109(6):446. PubMed ID: 25341504
    [TBL] [Abstract][Full Text] [Related]  

  • 20. GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death.
    Juang JJ; Binda A; Lee SJ; Hwang JJ; Chen WJ; Liu YB; Lin LY; Yu CC; Ho LT; Huang HC; Chen CJ; Lu TP; Lai LC; Yeh SS; Lai LP; Chuang EY; Rivolta I; Antzelevitch C
    EBioMedicine; 2020 Jul; 57():102843. PubMed ID: 32645615
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.