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 *

226 related articles for article (PubMed ID: 16415376)

  • 1. Common sodium channel promoter haplotype in asian subjects underlies variability in cardiac conduction.
    Bezzina CR; Shimizu W; Yang P; Koopmann TT; Tanck MW; Miyamoto Y; Kamakura S; Roden DM; Wilde AA
    Circulation; 2006 Jan; 113(3):338-44. PubMed ID: 16415376
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. A common SCN5A polymorphism attenuates a severe cardiac phenotype caused by a nonsense SCN5A mutation in a Chinese family with an inherited cardiac conduction defect.
    Niu DM; Hwang B; Hwang HW; Wang NH; Wu JY; Lee PC; Chien JC; Shieh RC; Chen YT
    J Med Genet; 2006 Oct; 43(10):817-21. PubMed ID: 16707561
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel pore mutation in SCN5A manifests as a spectrum of phenotypes ranging from atrial flutter, conduction disease, and Brugada syndrome to sudden cardiac death.
    Rossenbacker T; Carroll SJ; Liu H; Kuipéri C; de Ravel TJ; Devriendt K; Carmeliet P; Kass RS; Heidbüchel H
    Heart Rhythm; 2004 Nov; 1(5):610-5. PubMed ID: 15851228
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Polymorphisms in the cardiac sodium channel promoter displaying variant in vitro expression activity.
    Yang P; Koopmann TT; Pfeufer A; Jalilzadeh S; Schulze-Bahr E; Kääb S; Wilde AA; Roden DM; Bezzina CR
    Eur J Hum Genet; 2008 Mar; 16(3):350-7. PubMed ID: 18059420
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical and molecular heterogeneity in the Brugada syndrome: a novel gene locus on chromosome 3.
    Weiss R; Barmada MM; Nguyen T; Seibel JS; Cavlovich D; Kornblit CA; Angelilli A; Villanueva F; McNamara DM; London B
    Circulation; 2002 Feb; 105(6):707-13. PubMed ID: 11839626
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Critical Roles of Xirp Proteins in Cardiac Conduction and Their Rare Variants Identified in Sudden Unexplained Nocturnal Death Syndrome and Brugada Syndrome in Chinese Han Population.
    Huang L; Wu KH; Zhang L; Wang Q; Tang S; Wu Q; Jiang PH; Lin JJ; Guo J; Wang L; Loh SH; Cheng J
    J Am Heart Assoc; 2018 Jan; 7(1):. PubMed ID: 29306897
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 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. Electrocardiographic characteristics and SCN5A mutations in idiopathic ventricular fibrillation associated with early repolarization.
    Watanabe H; Nogami A; Ohkubo K; Kawata H; Hayashi Y; Ishikawa T; Makiyama T; Nagao S; Yagihara N; Takehara N; Kawamura Y; Sato A; Okamura K; Hosaka Y; Sato M; Fukae S; Chinushi M; Oda H; Okabe M; Kimura A; Maemura K; Watanabe I; Kamakura S; Horie M; Aizawa Y; Shimizu W; Makita N
    Circ Arrhythm Electrophysiol; 2011 Dec; 4(6):874-81. PubMed ID: 22028457
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Variant Intronic Enhancer Controls
    Man JCK; Bosada FM; Scholman KT; Offerhaus JA; Walsh R; van Duijvenboden K; van Eif VWW; Bezzina CR; Verkerk AO; Boukens BJ; Barnett P; Christoffels VM
    Circulation; 2021 Jul; 144(3):229-242. PubMed ID: 33910361
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. SCN5A promoter haplotype affects the therapeutic range for serum flecainide concentration in Asian patients.
    Doki K; Homma M; Kuga K; Aonuma K; Kohda Y
    Pharmacogenet Genomics; 2013 Jul; 23(7):349-54. PubMed ID: 23635804
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cardiac histological substrate in patients with clinical phenotype of Brugada syndrome.
    Frustaci A; Priori SG; Pieroni M; Chimenti C; Napolitano C; Rivolta I; Sanna T; Bellocci F; Russo MA
    Circulation; 2005 Dec; 112(24):3680-7. PubMed ID: 16344400
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing.
    Ackerman MJ; Splawski I; Makielski JC; Tester DJ; Will ML; Timothy KW; Keating MT; Jones G; Chadha M; Burrow CR; Stephens JC; Xu C; Judson R; Curran ME
    Heart Rhythm; 2004 Nov; 1(5):600-7. PubMed ID: 15851227
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic variation in SCN10A influences cardiac conduction.
    Chambers JC; Zhao J; Terracciano CM; Bezzina CR; Zhang W; Kaba R; Navaratnarajah M; Lotlikar A; Sehmi JS; Kooner MK; Deng G; Siedlecka U; Parasramka S; El-Hamamsy I; Wass MN; Dekker LR; de Jong JS; Sternberg MJ; McKenna W; Severs NJ; de Silva R; Wilde AA; Anand P; Yacoub M; Scott J; Elliott P; Wood JN; Kooner JS
    Nat Genet; 2010 Feb; 42(2):149-52. PubMed ID: 20062061
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Elevated oxidative stress is associated with ventricular fibrillation episodes in patients with Brugada-type electrocardiogram without SCN5A mutation.
    Tanaka M; Nakamura K; Kusano KF; Morita H; Ohta-Ogo K; Miura D; Miura A; Nakagawa K; Tada T; Murakami M; Nishii N; Nagase S; Hata Y; Kohno K; Ouchida M; Shimizu K; Yutani C; Ohe T; Ito H
    Cardiovasc Pathol; 2011; 20(1):e37-42. PubMed ID: 20219395
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic mutation in Korean patients of sudden cardiac arrest as a surrogating marker of idiopathic ventricular arrhythmia.
    Son MK; Ki CS; Park SJ; Huh J; Kim JS; On YK
    J Korean Med Sci; 2013 Jul; 28(7):1021-6. PubMed ID: 23853484
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Loss of function associated with novel mutations of the SCN5A gene in patients with Brugada syndrome.
    Baroudi G; Napolitano C; Priori SG; Del Bufalo A; Chahine M
    Can J Cardiol; 2004 Mar; 20(4):425-30. PubMed ID: 15057319
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.