BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

241 related articles for article (PubMed ID: 28104484)

  • 1. Sick sinus syndrome with HCN4 mutations shows early onset and frequent association with atrial fibrillation and left ventricular noncompaction.
    Ishikawa T; Ohno S; Murakami T; Yoshida K; Mishima H; Fukuoka T; Kimoto H; Sakamoto R; Ohkusa T; Aiba T; Nogami A; Sumitomo N; Shimizu W; Yoshiura KI; Horigome H; Horie M; Makita N
    Heart Rhythm; 2017 May; 14(5):717-724. PubMed ID: 28104484
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Sodium channelopathy underlying familial sick sinus syndrome with early onset and predominantly male characteristics.
    Abe K; Machida T; Sumitomo N; Yamamoto H; Ohkubo K; Watanabe I; Makiyama T; Fukae S; Kohno M; Harrell DT; Ishikawa T; Tsuji Y; Nogami A; Watabe T; Oginosawa Y; Abe H; Maemura K; Motomura H; Makita N
    Circ Arrhythm Electrophysiol; 2014 Jun; 7(3):511-7. PubMed ID: 24762805
    [TBL] [Abstract][Full Text] [Related]  

  • 3. HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathy.
    Milano A; Vermeer AM; Lodder EM; Barc J; Verkerk AO; Postma AV; van der Bilt IA; Baars MJ; van Haelst PL; Caliskan K; Hoedemaekers YM; Le Scouarnec S; Redon R; Pinto YM; Christiaans I; Wilde AA; Bezzina CR
    J Am Coll Cardiol; 2014 Aug; 64(8):745-56. PubMed ID: 25145517
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A rare HCN4 variant with combined sinus bradycardia, left atrial dilatation, and hypertrabeculation/left ventricular noncompaction phenotype.
    Alonso-Fernández-Gatta M; Gallego-Delgado M; Caballero R; Villacorta E; Díaz-Peláez E; García-BerrocaL B; Crespo-García T; Plata-Izquierdo B; Marcos-Vadillo E; García-Cuenllas L; Barreiro-Pérez M; Isidoro-García M; Tamargo-Menéndez J; Delpón E; Sánchez PL
    Rev Esp Cardiol (Engl Ed); 2021 Sep; 74(9):781-789. PubMed ID: 33008772
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A truncating SCN5A mutation combined with genetic variability causes sick sinus syndrome and early atrial fibrillation.
    Ziyadeh-Isleem A; Clatot J; Duchatelet S; Gandjbakhch E; Denjoy I; Hidden-Lucet F; Hatem S; Deschênes I; Coulombe A; Neyroud N; Guicheney P
    Heart Rhythm; 2014 Jun; 11(6):1015-1023. PubMed ID: 24582607
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The symptom complex of familial sinus node dysfunction and myocardial noncompaction is associated with mutations in the HCN4 channel.
    Schweizer PA; Schröter J; Greiner S; Haas J; Yampolsky P; Mereles D; Buss SJ; Seyler C; Bruehl C; Draguhn A; Koenen M; Meder B; Katus HA; Thomas D
    J Am Coll Cardiol; 2014 Aug; 64(8):757-67. PubMed ID: 25145518
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Cardiac Emerinopathy: A Nonsyndromic Nuclear Envelopathy With Increased Risk of Thromboembolic Stroke Due to Progressive Atrial Standstill and Left Ventricular Noncompaction.
    Ishikawa T; Mishima H; Barc J; Takahashi MP; Hirono K; Terada S; Kowase S; Sato T; Mukai Y; Yui Y; Ohkubo K; Kimoto H; Watanabe H; Hata Y; Aiba T; Ohno S; Chishaki A; Shimizu W; Horie M; Ichida F; Nogami A; Yoshiura KI; Schott JJ; Makita N
    Circ Arrhythm Electrophysiol; 2020 Oct; 13(10):e008712. PubMed ID: 32755394
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Loss-of-Function SCN5A Mutations Associated With Sinus Node Dysfunction, Atrial Arrhythmias, and Poor Pacemaker Capture.
    Chiang DY; Kim JJ; Valdes SO; de la Uz C; Fan Y; Orcutt J; Domino M; Smith M; Wehrens XH; Miyake CY
    Circ Arrhythm Electrophysiol; 2015 Oct; 8(5):1105-12. PubMed ID: 26111534
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel homozygous SCN5A variant detected in sick sinus syndrome.
    Alkorashy M; Al-Ghamdi B; Tulbah S; Al-Numair NS; Alhadeq F; A Takroni S; Al-Hassnan ZN
    Pacing Clin Electrophysiol; 2021 Feb; 44(2):380-384. PubMed ID: 32965045
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Rare Compound Heterozygous Missense Mutation of the SCN5A Gene with Childhood-Onset Sick Sinus Syndrome in Two Chinese Sisters.
    Wang Y; Long S; Wei C; Wang X
    Int Heart J; 2023 Mar; 64(2):299-305. PubMed ID: 36927930
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical Spectrum of
    Villarreal-Molina T; García-Ordóñez GP; Reyes-Quintero ÁE; Domínguez-Pérez M; Jacobo-Albavera L; Nava S; Carnevale A; Medeiros-Domingo A; Iturralde P
    Genes (Basel); 2021 Dec; 13(1):. PubMed ID: 35052356
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Relationship between two arrhythmias: sinus node dysfunction and atrial fibrillation.
    Zhao J; Liu T; Li G
    Arch Med Res; 2014 May; 45(4):351-5. PubMed ID: 24825742
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel trafficking-defective HCN4 mutation is associated with early-onset atrial fibrillation.
    Macri V; Mahida SN; Zhang ML; Sinner MF; Dolmatova EV; Tucker NR; McLellan M; Shea MA; Milan DJ; Lunetta KL; Benjamin EJ; Ellinor PT
    Heart Rhythm; 2014 Jun; 11(6):1055-1062. PubMed ID: 24607718
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Altered HCN4 channel C-linker interaction is associated with familial tachycardia-bradycardia syndrome and atrial fibrillation.
    Duhme N; Schweizer PA; Thomas D; Becker R; Schröter J; Barends TR; Schlichting I; Draguhn A; Bruehl C; Katus HA; Koenen M
    Eur Heart J; 2013 Sep; 34(35):2768-75. PubMed ID: 23178648
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical Presentation of Left Ventricular Noncompaction Cardiomyopathy and Bradycardia in Three Families Carrying
    Paszkowska A; Piekutowska-Abramczuk D; Ciara E; Mirecka-Rola A; Brzezinska M; Wicher D; Kostrzewa G; Sarnecki J; Ziółkowska L
    Genes (Basel); 2022 Mar; 13(3):. PubMed ID: 35328031
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Phenotype/Genotype Relationship in Left Ventricular Noncompaction: Ion Channel Gene Mutations Are Associated With Preserved Left Ventricular Systolic Function and Biventricular Noncompaction: Phenotype/Genotype of Noncompaction.
    Cambon-Viala M; Gerard H; Nguyen K; Richard P; Ader F; Pruny JF; Donal E; Eicher JC; Huttin O; Selton-Suty C; Raud-Raynier P; Jondeau G; Mansencal N; Sawka C; Casalta AC; Michel N; Donghi V; Martel H; Faivre L; Charron P; Habib G
    J Card Fail; 2021 Jun; 27(6):677-681. PubMed ID: 34088380
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A Functional Assay for Sick Sinus Syndrome Genetic Variants.
    Jou CJ; Arrington CB; Barnett S; Shen J; Cho S; Sheng X; McCullagh PC; Bowles NE; Pribble CM; Saarel EV; Pilcher TA; Etheridge SP; Tristani-Firouzi M
    Cell Physiol Biochem; 2017; 42(5):2021-2029. PubMed ID: 28803248
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel 'splice site' HCN4 Gene mutation, c.1737+1 G>T, causes familial bradycardia, reduced heart rate response, impaired chronotropic competence and increased short-term heart rate variability.
    Hategan L; Csányi B; Ördög B; Kákonyi K; Tringer A; Kiss O; Orosz A; Sághy L; Nagy I; Hegedűs Z; Rudas L; Széll M; Varró A; Forster T; Sepp R
    Int J Cardiol; 2017 Aug; 241():364-372. PubMed ID: 28465117
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 13.