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 *

133 related articles for article (PubMed ID: 38933375)

  • 21. Targeted deep sequencing reveals no definitive evidence for somatic mosaicism in atrial fibrillation.
    Roberts JD; Longoria J; Poon A; Gollob MH; Dewland TA; Kwok PY; Olgin JE; Deo RC; Marcus GM
    Circ Cardiovasc Genet; 2015 Feb; 8(1):50-7. PubMed ID: 25406240
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Very early-onset lone atrial fibrillation patients have a high prevalence of rare variants in genes previously associated with atrial fibrillation.
    Olesen MS; Andreasen L; Jabbari J; Refsgaard L; Haunsø S; Olesen SP; Nielsen JB; Schmitt N; Svendsen JH
    Heart Rhythm; 2014 Feb; 11(2):246-51. PubMed ID: 24144883
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Gain-of-function mutations in GATA6 lead to atrial fibrillation.
    Tucker NR; Mahida S; Ye J; Abraham EJ; Mina JA; Parsons VA; McLellan MA; Shea MA; Hanley A; Benjamin EJ; Milan DJ; Lin H; Ellinor PT
    Heart Rhythm; 2017 Feb; 14(2):284-291. PubMed ID: 27756709
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genetics of atrial fibrillation-practical applications for clinical management: if not now, when and how?
    Kany S; Reissmann B; Metzner A; Kirchhof P; Darbar D; Schnabel RB
    Cardiovasc Res; 2021 Jun; 117(7):1718-1731. PubMed ID: 33982075
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Whole-Exome Sequencing Implicates Neuronal Calcium Channel with Familial Atrial Fibrillation.
    Vad OB; Yan Y; Denti F; Ahlberg G; Refsgaard L; Bomholtz SH; Santos JL; Rasmussen S; Haunsø S; Svendsen JH; Christophersen IE; Schmitt N; Olesen MS; Bentzen BH
    Front Genet; 2022; 13():806429. PubMed ID: 35154276
    [No Abstract]   [Full Text] [Related]  

  • 26. Design and Production of Heart Chamber-Specific AAV9 Vectors.
    Bilal AS; Thuerauf DJ; Blackwood EA; Glembotski CC
    Methods Mol Biol; 2022; 2573():89-113. PubMed ID: 36040589
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Enhanced Cardiomyocyte NLRP3 Inflammasome Signaling Promotes Atrial Fibrillation.
    Yao C; Veleva T; Scott L; Cao S; Li L; Chen G; Jeyabal P; Pan X; Alsina KM; Abu-Taha I; Ghezelbash S; Reynolds CL; Shen YH; LeMaire SA; Schmitz W; Müller FU; El-Armouche A; Tony Eissa N; Beeton C; Nattel S; Wehrens XHT; Dobrev D; Li N
    Circulation; 2018 Nov; 138(20):2227-2242. PubMed ID: 29802206
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Characteristics of atrial fibrillation and comorbidities in familial atrial fibrillation.
    Jurkko R; Palojoki E; Huttunen H; Holm C; Lehto M; Heliö T; Swan H; Toivonen L
    J Cardiovasc Electrophysiol; 2013 Jul; 24(7):768-74. PubMed ID: 23551519
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Atrial Fibrillation and Ventricular Arrhythmias: Sex Differences in Electrophysiology, Epidemiology, Clinical Presentation, and Clinical Outcomes.
    Gillis AM
    Circulation; 2017 Feb; 135(6):593-608. PubMed ID: 28153995
    [TBL] [Abstract][Full Text] [Related]  

  • 30. KLF15 Loss-of-Function Mutation Underlying Atrial Fibrillation as well as Ventricular Arrhythmias and Cardiomyopathy.
    Li N; Xu YJ; Shi HY; Yang CX; Guo YH; Li RG; Qiu XB; Yang YQ; Zhang M
    Genes (Basel); 2021 Mar; 12(3):. PubMed ID: 33809104
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Shensong Yangxin attenuates metabolic syndrome-induced atrial fibrillation via inhibition of ferroportin-mediated intracellular iron overload.
    Yang HJ; Kong B; Shuai W; Zhang JJ; Huang H
    Phytomedicine; 2022 Jul; 101():154086. PubMed ID: 35421806
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Loss-of-Function Variants in Cytoskeletal Genes Are Associated with Early-Onset Atrial Fibrillation.
    Vad OB; Paludan-Müller C; Ahlberg G; Kalstø SM; Ghouse J; Andreasen L; Haunsø S; Tveit A; Sajadieh A; Christophersen IE; Svendsen JH; Olesen MS
    J Clin Med; 2020 Jan; 9(2):. PubMed ID: 32013268
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Genetics of atrial fibrillation: rare mutations, common variants and clinical relevance?].
    Sinner MF; Pfeufer A; Kääb S
    Herzschrittmacherther Elektrophysiol; 2006 Jun; 17(2):95-105. PubMed ID: 16786468
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Connexin45 (GJC1) loss-of-function mutation contributes to familial atrial fibrillation and conduction disease.
    Li RG; Xu YJ; Ye WG; Li YJ; Chen H; Qiu XB; Yang YQ; Bai D
    Heart Rhythm; 2021 May; 18(5):684-693. PubMed ID: 33429106
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Loss of the Atrial Fibrillation-Related Gene,
    Jameson HS; Hanley A; Hill MC; Xiao L; Ye J; Bapat A; Ronzier E; Hall AW; Hucker WJ; Clauss S; Barazza M; Silber E; Mina JA; Tucker NR; Mills RW; Dong JT; Milan DJ; Ellinor PT
    Circ Res; 2023 Aug; 133(4):313-329. PubMed ID: 37449401
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The Cumulative Incidence of Stroke, Myocardial infarction, Heart Failure and Sudden Cardiac Death in Patients with Atrial Fibrillation.
    Naser N; Kulic M; Dilic M; Dzubur A; Durak A; Pepic E; Smajic E; Kusljugic Z
    Med Arch; 2017 Oct; 71(5):316-319. PubMed ID: 29284897
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Association Between Atrial Fibrillation and Sudden Cardiac Death: Pathophysiological and Epidemiological Insights.
    Waldmann V; Jouven X; Narayanan K; Piot O; Chugh SS; Albert CM; Marijon E
    Circ Res; 2020 Jul; 127(2):301-309. PubMed ID: 32833581
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Human iPSC modelling of a familial form of atrial fibrillation reveals a gain of function of If and ICaL in patient-derived cardiomyocytes.
    Benzoni P; Campostrini G; Landi S; Bertini V; Marchina E; Iascone M; Ahlberg G; Olesen MS; Crescini E; Mora C; Bisleri G; Muneretto C; Ronca R; Presta M; Poliani PL; Piovani G; Verardi R; Di Pasquale E; Consiglio A; Raya A; Torre E; Lodrini AM; Milanesi R; Rocchetti M; Baruscotti M; DiFrancesco D; Memo M; Barbuti A; Dell'Era P
    Cardiovasc Res; 2020 May; 116(6):1147-1160. PubMed ID: 31504264
    [TBL] [Abstract][Full Text] [Related]  

  • 39. ISL1 loss-of-function variation causes familial atrial fibrillation.
    Wu SH; Wang XH; Xu YJ; Gu JN; Yang CX; Qiao Q; Guo XJ; Guo YH; Qiu XB; Jiang WF; Yang YQ
    Eur J Med Genet; 2020 Nov; 63(11):104029. PubMed ID: 32771629
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Association between familial atrial fibrillation and risk of new-onset atrial fibrillation.
    Lubitz SA; Yin X; Fontes JD; Magnani JW; Rienstra M; Pai M; Villalon ML; Vasan RS; Pencina MJ; Levy D; Larson MG; Ellinor PT; Benjamin EJ
    JAMA; 2010 Nov; 304(20):2263-9. PubMed ID: 21076174
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.