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 *

125 related articles for article (PubMed ID: 32192759)

  • 1. Brugada Syndrome Caused by Sodium Channel Dysfunction Associated with a SCN1B Variant A197V.
    Wang L; Han Z; Dai J; Cao K
    Arch Med Res; 2020 Apr; 51(3):245-253. PubMed ID: 32192759
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. SCN5A(K817E), a novel Brugada syndrome-associated mutation that alters the activation gating of NaV1.5 channel.
    Kinoshita K; Takahashi H; Hata Y; Nishide K; Kato M; Fujita H; Yoshida S; Murai K; Mizumaki K; Nishida K; Yamaguchi Y; Kano M; Tabata T; Nishida N
    Heart Rhythm; 2016 May; 13(5):1113-1120. PubMed ID: 26776555
    [TBL] [Abstract][Full Text] [Related]  

  • 4. SCN1B gene variants in Brugada Syndrome: a study of 145 SCN5A-negative patients.
    Ricci MT; Menegon S; Vatrano S; Mandrile G; Cerrato N; Carvalho P; De Marchi M; Gaita F; Giustetto C; Giachino DF
    Sci Rep; 2014 Sep; 4():6470. PubMed ID: 25253298
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotype.
    Hu D; Barajas-Martinez H; Burashnikov E; Springer M; Wu Y; Varro A; Pfeiffer R; Koopmann TT; Cordeiro JM; Guerchicoff A; Pollevick GD; Antzelevitch C
    Circ Cardiovasc Genet; 2009 Jun; 2(3):270-8. PubMed ID: 20031595
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Investigations of the Navβ1b sodium channel subunit in human ventricle; functional characterization of the H162P Brugada syndrome mutant.
    Yuan L; Koivumäki JT; Liang B; Lorentzen LG; Tang C; Andersen MN; Svendsen JH; Tfelt-Hansen J; Maleckar M; Schmitt N; Olesen MS; Jespersen T
    Am J Physiol Heart Circ Physiol; 2014 Apr; 306(8):H1204-12. PubMed ID: 24561865
    [TBL] [Abstract][Full Text] [Related]  

  • 7. De Novo Mutation in the SCN5A Gene Associated with Brugada Syndrome.
    Wang L; Meng X; Yuchi Z; Zhao Z; Xu D; Fedida D; Wang Z; Huang C
    Cell Physiol Biochem; 2015; 36(6):2250-62. PubMed ID: 26279430
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel missense mutation, I890T, in the pore region of cardiac sodium channel causes Brugada syndrome.
    Tarradas A; Selga E; Beltran-Alvarez P; Pérez-Serra A; Riuró H; Picó F; Iglesias A; Campuzano O; Castro-Urda V; Fernández-Lozano I; Pérez GJ; Scornik FS; Brugada R
    PLoS One; 2013; 8(1):e53220. PubMed ID: 23308164
    [TBL] [Abstract][Full Text] [Related]  

  • 9. High prevalence of concealed Brugada syndrome in patients with atrioventricular nodal reentrant tachycardia.
    Hasdemir C; Payzin S; Kocabas U; Sahin H; Yildirim N; Alp A; Aydin M; Pfeiffer R; Burashnikov E; Wu Y; Antzelevitch C
    Heart Rhythm; 2015 Jul; 12(7):1584-94. PubMed ID: 25998140
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Reduced current density, partially rescued by mexiletine, and depolarizing shift in activation of SCN5A W374G channels as a cause of severe form of Brugada syndrome.
    Nakajima T; Dharmawan T; Kawabata-Iwakawa R; Tamura S; Hasegawa H; Kobari T; Ota M; Tange S; Nishiyama M; Kaneko Y; Kurabayashi M
    Ann Noninvasive Electrocardiol; 2021 May; 26(3):e12828. PubMed ID: 33463855
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Frequency of Irritable Bowel Syndrome in Patients with Brugada Syndrome and Drug-Induced Type 1 Brugada Pattern.
    Sarica AS; Bor S; Orman MN; Barajas-Martinez H; Juang JJ; Antzelevitch C; Hasdemir C
    Am J Cardiol; 2021 Jul; 151():51-56. PubMed ID: 34034907
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Electrophysiological characteristics of a SCN5A voltage sensors mutation R1629Q associated with Brugada syndrome.
    Zeng Z; Zhou J; Hou Y; Liang X; Zhang Z; Xu X; Xie Q; Li W; Huang Z
    PLoS One; 2013; 8(10):e78382. PubMed ID: 24167619
    [TBL] [Abstract][Full Text] [Related]  

  • 15. p.D1690N sodium voltage-gated channel α subunit 5 mutation reduced sodium current density and is associated with Brugada syndrome.
    Zeng Z; Xie Q; Huang Y; Zhao Y; Li W; Huang Z
    Mol Med Rep; 2016 Jun; 13(6):5216-22. PubMed ID: 27108952
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel microsatellite polymorphism of sodium channel beta1-subunit gene (SCN1B) may underlie abnormal cardiac excitation manifested by coved-type ST-elevation compatible with Brugada syndrome in Japanese.
    Ogawa R; Kishi R; Takagi A; Sakaue I; Takahashi H; Matsumoto N; Masuhara K; Nakazawa K; Kobayashi S; Miyake F; Echizen H
    Int J Clin Pharmacol Ther; 2010 Feb; 48(2):109-19. PubMed ID: 20137763
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Brugada syndrome disease phenotype explained in apparently benign sodium channel mutations.
    Hoshi M; Du XX; Shinlapawittayatorn K; Liu H; Chai S; Wan X; Ficker E; Deschênes I
    Circ Cardiovasc Genet; 2014 Apr; 7(2):123-31. PubMed ID: 24573164
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Electrophysiological and trafficking defects of the SCN5A T353I mutation in Brugada syndrome are rescued by alpha-allocryptopine.
    Zhang J; Chen Y; Yang J; Xu B; Wen Y; Xiang G; Wei G; Zhu C; Xing Y; Li Y
    Eur J Pharmacol; 2015 Jan; 746():333-43. PubMed ID: 25261036
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A mutation causing Brugada syndrome identifies a mechanism for altered autonomic and oxidant regulation of cardiac sodium currents.
    Aiba T; Farinelli F; Kostecki G; Hesketh GG; Edwards D; Biswas S; Tung L; Tomaselli GF
    Circ Cardiovasc Genet; 2014 Jun; 7(3):249-56. PubMed ID: 24795344
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterization of a novel Nav1.5 channel mutation, A551T, associated with Brugada syndrome.
    Chiang KC; Lai LP; Shieh RC
    J Biomed Sci; 2009 Aug; 16(1):76. PubMed ID: 19706159
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.