BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

279 related articles for article (PubMed ID: 19666841)

  • 1. 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]  

  • 2. Cardiac Na+ current regulation by pyridine nucleotides.
    Liu M; Sanyal S; Gao G; Gurung IS; Zhu X; Gaconnet G; Kerchner LJ; Shang LL; Huang CL; Grace A; London B; Dudley SC
    Circ Res; 2009 Oct; 105(8):737-45. PubMed ID: 19745168
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na+ current and causes inherited arrhythmias.
    London B; Michalec M; Mehdi H; Zhu X; Kerchner L; Sanyal S; Viswanathan PC; Pfahnl AE; Shang LL; Madhusudanan M; Baty CJ; Lagana S; Aleong R; Gutmann R; Ackerman MJ; McNamara DM; Weiss R; Dudley SC
    Circulation; 2007 Nov; 116(20):2260-8. PubMed ID: 17967977
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cardiac metabolic state and Brugada syndrome: a link revealed.
    Chahine M
    Circ Res; 2009 Oct; 105(8):721-3. PubMed ID: 19815826
    [No Abstract]   [Full Text] [Related]  

  • 5. GPD1L-A306del modifies sodium current in a family carrying the dysfunctional SCN5A-G1661R mutation associated with Brugada syndrome.
    Semino F; Darche FF; Bruehl C; Koenen M; Skladny H; Katus HA; Frey N; Draguhn A; Schweizer PA
    Pflugers Arch; 2024 Feb; 476(2):229-242. PubMed ID: 38036776
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Alpha1-syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium current.
    Cheng J; Van Norstrand DW; Medeiros-Domingo A; Valdivia C; Tan BH; Ye B; Kroboth S; Vatta M; Tester DJ; January CT; Makielski JC; Ackerman MJ
    Circ Arrhythm Electrophysiol; 2009 Dec; 2(6):667-76. PubMed ID: 20009079
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Cardiac ion channel gene mutations in sudden infant death syndrome.
    Otagiri T; Kijima K; Osawa M; Ishii K; Makita N; Matoba R; Umetsu K; Hayasaka K
    Pediatr Res; 2008 Nov; 64(5):482-7. PubMed ID: 18596570
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na(v)1.5 and K(v)4.3 channel currents.
    Hu D; Barajas-Martínez H; Medeiros-Domingo A; Crotti L; Veltmann C; Schimpf R; Urrutia J; Alday A; Casis O; Pfeiffer R; Burashnikov E; Caceres G; Tester DJ; Wolpert C; Borggrefe M; Schwartz P; Ackerman MJ; Antzelevitch C
    Heart Rhythm; 2012 May; 9(5):760-9. PubMed ID: 22155597
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Readthrough of nonsense mutation W822X in the SCN5A gene can effectively restore expression of cardiac Na+ channels.
    Teng S; Gao L; Paajanen V; Pu J; Fan Z
    Cardiovasc Res; 2009 Aug; 83(3):473-80. PubMed ID: 19377070
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Ca2+/calmodulin-dependent protein kinase II (CaMKII) regulates cardiac sodium channel NaV1.5 gating by multiple phosphorylation sites.
    Ashpole NM; Herren AW; Ginsburg KS; Brogan JD; Johnson DE; Cummins TR; Bers DM; Hudmon A
    J Biol Chem; 2012 Jun; 287(24):19856-69. PubMed ID: 22514276
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Analyses of a novel SCN5A mutation (C1850S): conduction vs. repolarization disorder hypotheses in the Brugada syndrome.
    Petitprez S; Jespersen T; Pruvot E; Keller DI; Corbaz C; Schläpfer J; Abriel H; Kucera JP
    Cardiovasc Res; 2008 Jun; 78(3):494-504. PubMed ID: 18252757
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Sudden infant death syndrome-associated mutations in the sodium channel beta subunits.
    Tan BH; Pundi KN; Van Norstrand DW; Valdivia CR; Tester DJ; Medeiros-Domingo A; Makielski JC; Ackerman MJ
    Heart Rhythm; 2010 Jun; 7(6):771-8. PubMed ID: 20226894
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Brugada syndrome and fever: genetic and molecular characterization of patients carrying SCN5A mutations.
    Keller DI; Rougier JS; Kucera JP; Benammar N; Fressart V; Guicheney P; Madle A; Fromer M; Schläpfer J; Abriel H
    Cardiovasc Res; 2005 Aug; 67(3):510-9. PubMed ID: 15890323
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A sodium channel pore mutation causing Brugada syndrome.
    Pfahnl AE; Viswanathan PC; Weiss R; Shang LL; Sanyal S; Shusterman V; Kornblit C; London B; Dudley SC
    Heart Rhythm; 2007 Jan; 4(1):46-53. PubMed ID: 17198989
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The genetic basis of Brugada syndrome: a mutation update.
    Hedley PL; Jørgensen P; Schlamowitz S; Moolman-Smook J; Kanters JK; Corfield VA; Christiansen M
    Hum Mutat; 2009 Sep; 30(9):1256-66. PubMed ID: 19606473
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Single-cell transcriptomics trajectory and molecular convergence of clinically relevant mutations in Brugada syndrome.
    Tambi R; Abdel Hameid R; Bankapur A; Nassir N; Begum G; Alsheikh-Ali A; Uddin M; Berdiev BK
    Am J Physiol Heart Circ Physiol; 2021 May; 320(5):H1935-H1948. PubMed ID: 33797273
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome.
    Ackerman MJ; Siu BL; Sturner WQ; Tester DJ; Valdivia CR; Makielski JC; Towbin JA
    JAMA; 2001 Nov; 286(18):2264-9. PubMed ID: 11710892
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.