BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

228 related articles for article (PubMed ID: 32248749)

  • 21. Long-range
    Zhang M; Hill MC; Kadow ZA; Suh JH; Tucker NR; Hall AW; Tran TT; Swinton PS; Leach JP; Margulies KB; Ellinor PT; Li N; Martin JF
    Proc Natl Acad Sci U S A; 2019 Nov; 116(45):22692-22698. PubMed ID: 31636200
    [TBL] [Abstract][Full Text] [Related]  

  • 22. In Vitro Analyses of Novel HCN4 Gene Mutations.
    Möller M; Silbernagel N; Wrobel E; Stallmayer B; Amedonu E; Rinné S; Peischard S; Meuth SG; Wünsch B; Strutz-Seebohm N; Decher N; Schulze-Bahr E; Seebohm G
    Cell Physiol Biochem; 2018; 49(3):1197-1207. PubMed ID: 30196304
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Next-generation sequencing of nine atrial fibrillation candidate genes identified novel de novo mutations in patients with extreme trait of atrial fibrillation.
    Tsai CT; Hsieh CS; Chang SN; Chuang EY; Juang JM; Lin LY; Lai LP; Hwang JJ; Chiang FT; Lin JL
    J Med Genet; 2015 Jan; 52(1):28-36. PubMed ID: 25391453
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genetic Control of Left Atrial Gene Expression Yields Insights into the Genetic Susceptibility for Atrial Fibrillation.
    Hsu J; Gore-Panter S; Tchou G; Castel L; Lovano B; Moravec CS; Pettersson GB; Roselli EE; Gillinov AM; McCurry KR; Smedira NG; Barnard J; Van Wagoner DR; Chung MK; Smith JD
    Circ Genom Precis Med; 2018 Mar; 11(3):e002107. PubMed ID: 29545482
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Targeted sequencing in candidate genes for atrial fibrillation: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Targeted Sequencing Study.
    Lin H; Sinner MF; Brody JA; Arking DE; Lunetta KL; Rienstra M; Lubitz SA; Magnani JW; Sotoodehnia N; McKnight B; McManus DD; Boerwinkle E; Psaty BM; Rotter JI; Bis JC; Gibbs RA; Muzny D; Kovar CL; Morrison AC; Gupta M; Folsom AR; Kääb S; Heckbert SR; Alonso A; Ellinor PT; Benjamin EJ;
    Heart Rhythm; 2014 Mar; 11(3):452-7. PubMed ID: 24239840
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Common and rare variants in SCN10A modulate the risk of atrial fibrillation.
    Jabbari J; Olesen MS; Yuan L; Nielsen JB; Liang B; Macri V; Christophersen IE; Nielsen N; Sajadieh A; Ellinor PT; Grunnet M; Haunsø S; Holst AG; Svendsen JH; Jespersen T
    Circ Cardiovasc Genet; 2015 Feb; 8(1):64-73. PubMed ID: 25691686
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. 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]  

  • 29. Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development.
    Nielsen JB; Fritsche LG; Zhou W; Teslovich TM; Holmen OL; Gustafsson S; Gabrielsen ME; Schmidt EM; Beaumont R; Wolford BN; Lin M; Brummett CM; Preuss MH; Refsgaard L; Bottinger EP; Graham SE; Surakka I; Chu Y; Skogholt AH; Dalen H; Boyle AP; Oral H; Herron TJ; Kitzman J; Jalife J; Svendsen JH; Olesen MS; Njølstad I; Løchen ML; Baras A; Gottesman O; Marcketta A; O'Dushlaine C; Ritchie MD; Wilsgaard T; Loos RJF; Frayling TM; Boehnke M; Ingelsson E; Carey DJ; Dewey FE; Kang HM; Abecasis GR; Hveem K; Willer CJ
    Am J Hum Genet; 2018 Jan; 102(1):103-115. PubMed ID: 29290336
    [TBL] [Abstract][Full Text] [Related]  

  • 30. HCN4 mutation as a molecular explanation on patients with bradycardia and non-compaction cardiomyopathy.
    Millat G; Janin A; de Tauriac O; Roux A; Dauphin C
    Eur J Med Genet; 2015 Sep; 58(9):439-42. PubMed ID: 26206080
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Diminished
    Tucker NR; Dolmatova EV; Lin H; Cooper RR; Ye J; Hucker WJ; Jameson HS; Parsons VA; Weng LC; Mills RW; Sinner MF; Imakaev M; Leyton-Mange J; Vlahakes G; Benjamin EJ; Lunetta KL; Lubitz SA; Mirny L; Milan DJ; Ellinor PT
    Circ Cardiovasc Genet; 2017 Oct; 10(5):. PubMed ID: 28974514
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Pacemaker channel dysfunction in a patient with sinus node disease.
    Schulze-Bahr E; Neu A; Friederich P; Kaupp UB; Breithardt G; Pongs O; Isbrandt D
    J Clin Invest; 2003 May; 111(10):1537-45. PubMed ID: 12750403
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Candidate gene approach to identifying rare genetic variants associated with lone atrial fibrillation.
    Weeke P; Parvez B; Blair M; Short L; Ingram C; Kucera G; Stubblefield T; Roden DM; Darbar D
    Heart Rhythm; 2014 Jan; 11(1):46-52. PubMed ID: 24120998
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Identification of atrial fibrillation associated genes and functional non-coding variants.
    van Ouwerkerk AF; Bosada FM; van Duijvenboden K; Hill MC; Montefiori LE; Scholman KT; Liu J; de Vries AAF; Boukens BJ; Ellinor PT; Goumans MJTH; Efimov IR; Nobrega MA; Barnett P; Martin JF; Christoffels VM
    Nat Commun; 2019 Oct; 10(1):4755. PubMed ID: 31628324
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A genetic model of ivabradine recapitulates results from randomized clinical trials.
    Legault MA; Sandoval J; Provost S; Barhdadi A; Lemieux Perreault LP; Shah S; Lumbers RT; de Denus S; Tyl B; Tardif JC; Dubé MP
    PLoS One; 2020; 15(7):e0236193. PubMed ID: 32692755
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Transcriptional control of pacemaker channel genes HCN2 and HCN4 by Sp1 and implications in re-expression of these genes in hypertrophied myocytes.
    Lin H; Xiao J; Luo X; Chen G; Wang Z
    Cell Physiol Biochem; 2009; 23(4-6):317-26. PubMed ID: 19471099
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Cohesin-protein Shugoshin-1 controls cardiac automaticity via HCN4 pacemaker channel.
    Liu D; Song AT; Qi X; van Vliet PP; Xiao J; Xiong F; Andelfinger G; Nattel S
    Nat Commun; 2021 May; 12(1):2551. PubMed ID: 33953173
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.