BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 36927930)

  • 1. 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]  

  • 2. Errata: Rare Compound Heterozygous Missense Mutation of the SCN5A Gene with Childhood-Onset Sick Sinus Syndrome in Two Chinese Sisters: A Case Report.
    Int Heart J; 2024; 65(1):169. PubMed ID: 38296574
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Identification of rare heterozygous linkage R965C-R1309H mutations in the pore-forming region of SCN5A gene associated with complex arrhythmia.
    Lin Y; Qin J; Shen Y; Huang J; Zhang Z; Zhu Z; Lu H; Huang Y; Yin Y; Wang A; Jin L; Hu Z; Lin X; Jiang B
    Mol Genet Genomic Med; 2021 May; 9(5):e1613. PubMed ID: 33764691
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Cardiac sinus node dysfunction due to a new mutation of the SCN5A gene].
    Selly JB; Boumahni B; Edmar A; Jamal Bey K; Randrianaivo H; Clerici G; Millat G; Caillet D
    Arch Pediatr; 2012 Aug; 19(8):837-41. PubMed ID: 22795782
    [TBL] [Abstract][Full Text] [Related]  

  • 9. An Adolescent Patient with Sick Sinus Syndrome Complicated by Hypothyroidism Carrying an SCN5A Variant.
    Yamane H; Seki M; Ikeda T; Matsumoto A; Furui S; Sato T; Muramatsu K; Tajima T; Yamagata T
    Int Heart J; 2022; 63(3):627-632. PubMed ID: 35650162
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel SCN5A mutation demonstrating a variety of clinical phenotypes in familial sick sinus syndrome.
    Nakajima S; Makiyama T; Hanazawa K; Kaitani K; Amano M; Hayama Y; Onishi N; Tamaki Y; Miyake M; Tamura T; Kondo H; Motooka M; Izumi C; Nakagawa Y; Horie M
    Intern Med; 2013; 52(16):1805-8. PubMed ID: 23955615
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Autosomal recessive paediatric sick sinus syndrome associated with novel compound mutations in SCN5A.
    Kodama T; Serio A; Disertori M; Bronzetti G; Diegoli M; Narula N; Grasso M; Mazzola S; Arbustini E
    Int J Cardiol; 2013 Sep; 167(6):3078-80. PubMed ID: 23200271
    [No Abstract]   [Full Text] [Related]  

  • 12. Mechanistic links between Na+ channel (SCN5A) mutations and impaired cardiac pacemaking in sick sinus syndrome.
    Butters TD; Aslanidi OV; Inada S; Boyett MR; Hancox JC; Lei M; Zhang H
    Circ Res; 2010 Jul; 107(1):126-37. PubMed ID: 20448214
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A).
    Benson DW; Wang DW; Dyment M; Knilans TK; Fish FA; Strieper MJ; Rhodes TH; George AL
    J Clin Invest; 2003 Oct; 112(7):1019-28. PubMed ID: 14523039
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. A novel C-terminal truncation SCN5A mutation from a patient with sick sinus syndrome, conduction disorder and ventricular tachycardia.
    Tan BH; Iturralde-Torres P; Medeiros-Domingo A; Nava S; Tester DJ; Valdivia CR; Tusié-Luna T; Ackerman MJ; Makielski JC
    Cardiovasc Res; 2007 Dec; 76(3):409-17. PubMed ID: 17897635
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A Brugada syndrome proband with compound heterozygote SCN5A mutations identified from a Chinese family in Singapore.
    Tan BY; Yong RY; Barajas-Martinez H; Dumaine R; Chew YX; Wasan PS; Ching CK; Ho KL; Gan LS; Morin N; Chong AP; Yap SH; Neo JL; Yap EP; Moochhala S; Chong DT; Chow W; Seow SC; Hu D; Uttamchandani M; Teo WS
    Europace; 2016 Jun; 18(6):897-904. PubMed ID: 25829473
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Whole exome sequencing in Brugada and long QT syndromes revealed novel rare and potential pathogenic mutations related to the dysfunction of the cardiac sodium channel.
    Chen J; Li H; Guo S; Yang Z; Sun S; Zeng J; Gou H; Chen Y; Wang F; Lin Y; Huang K; Yue H; Ma Y; Lin Y
    Orphanet J Rare Dis; 2022 Oct; 17(1):394. PubMed ID: 36303204
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Case Report:
    Liang J; Luo S; Huang B
    Front Cardiovasc Med; 2023; 10():1294197. PubMed ID: 38107266
    [TBL] [Abstract][Full Text] [Related]  

  • 19. TGF-β1-mediated fibrosis and ion channel remodeling are key mechanisms in producing the sinus node dysfunction associated with SCN5A deficiency and aging.
    Hao X; Zhang Y; Zhang X; Nirmalan M; Davies L; Konstantinou D; Yin F; Dobrzynski H; Wang X; Grace A; Zhang H; Boyett M; Huang CL; Lei M
    Circ Arrhythm Electrophysiol; 2011 Jun; 4(3):397-406. PubMed ID: 21493874
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of a novel missense SCN5A mutation in a Chinese Han family with Brugada syndrome.
    Zhu J; Shen Y; Xiong H; Zha H; Zhang L; Peng H; Tian L
    Biochem Biophys Res Commun; 2023 Mar; 649():55-61. PubMed ID: 36745970
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.