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Journal Abstract Search

146 related items for PubMed ID: 35320795

  • 1. Reentry in cardiac ventricular epicardial tissue due to SCN5A L812Q gene mutation: a computational study.
    Satish H, Reddy MR.
    Biomed Phys Eng Express; 2022 Apr 14; 8(3):. PubMed ID: 35320795
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  • 2. A Simulation Study on Electrical Activity of Ventricular Endocardial Tissue due to SCN5A L812Q Mutation.
    Satish H, Reddy M R.
    Annu Int Conf IEEE Eng Med Biol Soc; 2021 Nov 14; 2021():5543-5546. PubMed ID: 34892380
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  • 3. 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 Nov 14; 20(1):e37-42. PubMed ID: 20219395
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  • 4. 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 Nov 14; 36(6):2250-62. PubMed ID: 26279430
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  • 5. 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 13; 5(9):. PubMed ID: 27625342
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  • 6. Brugada syndrome genetics is associated with phenotype severity.
    Ciconte G, Monasky MM, Santinelli V, Micaglio E, Vicedomini G, Anastasia L, Negro G, Borrelli V, Giannelli L, Santini F, de Innocentiis C, Rondine R, Locati ET, Bernardini A, Mazza BC, Mecarocci V, Ćalović Ž, Ghiroldi A, D'Imperio S, Benedetti S, Di Resta C, Rivolta I, Casari G, Petretto E, Pappone C.
    Eur Heart J; 2021 Mar 14; 42(11):1082-1090. PubMed ID: 33221895
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  • 7. Role of SCN5A coding and non-coding sequences in Brugada syndrome onset: What's behind the scenes?
    Daimi H, Khelil AH, Neji A, Ben Hamda K, Maaoui S, Aranega A, Be Chibani J, Franco D.
    Biomed J; 2019 Aug 14; 42(4):252-260. PubMed ID: 31627867
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  • 9. Molecular biology and cellular mechanisms of Brugada and long QT syndromes in infants and young children.
    Antzelevitch C.
    J Electrocardiol; 2001 Aug 14; 34 Suppl():177-81. PubMed ID: 11781953
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  • 15. Pilsicainide Administration Unmasks a Phenotype of Brugada Syndrome in a Patient with Overlap Syndrome due to the E1784K SCN5A Mutation.
    Hasebe H, Yokoya T, Murakoshi N, Kurebayashi N.
    Intern Med; 2020 Jan 01; 59(1):83-87. PubMed ID: 31484910
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  • 19. Transcriptional profiles of genes related to electrophysiological function in Scn5a+/- murine hearts.
    Takla M, Edling CE, Zhang K, Saadeh K, Tse G, Salvage SC, Huang CL, Jeevaratnam K.
    Physiol Rep; 2021 Oct 01; 9(19):e15043. PubMed ID: 34617689
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  • 20. Idiopathic ventricular fibrillation and the V1764fsX1786 frameshift mutation of the SCN5A gene in a myotonic dystrophy type 1 patient.
    Shimoyama T, Hayashi H, Suzuki F, Nishiyama Y, Miyamoto Y, Aiba T, Shimizu W, Kimura K.
    J Clin Neurosci; 2020 Apr 01; 74():242-244. PubMed ID: 32063450
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