BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

468 related articles for article (PubMed ID: 20829228)

  • 1. De novo desmin-mutation N116S is associated with arrhythmogenic right ventricular cardiomyopathy.
    Klauke B; Kossmann S; Gaertner A; Brand K; Stork I; Brodehl A; Dieding M; Walhorn V; Anselmetti D; Gerdes D; Bohms B; Schulz U; Zu Knyphausen E; Vorgerd M; Gummert J; Milting H
    Hum Mol Genet; 2010 Dec; 19(23):4595-607. PubMed ID: 20829228
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice.
    Fressart V; Duthoit G; Donal E; Probst V; Deharo JC; Chevalier P; Klug D; Dubourg O; Delacretaz E; Cosnay P; Scanu P; Extramiana F; Keller D; Hidden-Lucet F; Simon F; Bessirard V; Roux-Buisson N; Hebert JL; Azarine A; Casset-Senon D; Rouzet F; Lecarpentier Y; Fontaine G; Coirault C; Frank R; Hainque B; Charron P
    Europace; 2010 Jun; 12(6):861-8. PubMed ID: 20400443
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Lower than expected desmosomal gene mutation prevalence in endurance athletes with complex ventricular arrhythmias of right ventricular origin.
    La Gerche A; Robberecht C; Kuiperi C; Nuyens D; Willems R; de Ravel T; Matthijs G; Heidbüchel H
    Heart; 2010 Aug; 96(16):1268-74. PubMed ID: 20525856
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Comprehensive analysis of desmosomal gene mutations in Han Chinese patients with arrhythmogenic right ventricular cardiomyopathy.
    Zhou X; Chen M; Song H; Wang B; Chen H; Wang J; Wang W; Feng S; Zhang F; Ju W; Li M; Gu K; Cao K; Wang DW; Yang B
    Eur J Med Genet; 2015 Apr; 58(4):258-65. PubMed ID: 25765472
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations in the Lamin A/C gene mimic arrhythmogenic right ventricular cardiomyopathy.
    Quarta G; Syrris P; Ashworth M; Jenkins S; Zuborne Alapi K; Morgan J; Muir A; Pantazis A; McKenna WJ; Elliott PM
    Eur Heart J; 2012 May; 33(9):1128-36. PubMed ID: 22199124
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutation analysis and evaluation of the cardiac localization of TMEM43 in arrhythmogenic right ventricular cardiomyopathy.
    Christensen AH; Andersen CB; Tybjaerg-Hansen A; Haunso S; Svendsen JH
    Clin Genet; 2011 Sep; 80(3):256-64. PubMed ID: 21214875
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic testing of candidate genes in arrhythmogenic right ventricular cardiomyopathy/dysplasia.
    Campuzano O; Alcalde M; Berne P; Castro V; Guzzo G; Iglesias A; Alonso-Pulpon L; Garcia-Pavia P; Brugada J; Brugada R
    Eur J Med Genet; 2012 Apr; 55(4):225-34. PubMed ID: 22421524
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The novel desmin mutant p.A120D impairs filament formation, prevents intercalated disk localization, and causes sudden cardiac death.
    Brodehl A; Dieding M; Klauke B; Dec E; Madaan S; Huang T; Gargus J; Fatima A; Saric T; Cakar H; Walhorn V; Tönsing K; Skrzipczyk T; Cebulla R; Gerdes D; Schulz U; Gummert J; Svendsen JH; Olesen MS; Anselmetti D; Christensen AH; Kimonis V; Milting H
    Circ Cardiovasc Genet; 2013 Dec; 6(6):615-23. PubMed ID: 24200904
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Screening of genes encoding junctional candidates in arrhythmogenic right ventricular cardiomyopathy/dysplasia.
    Gandjbakhch E; Vite A; Gary F; Fressart V; Donal E; Simon F; Hidden-Lucet F; Komajda M; Charron P; Villard E
    Europace; 2013 Oct; 15(10):1522-5. PubMed ID: 23858024
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy.
    van Tintelen JP; Entius MM; Bhuiyan ZA; Jongbloed R; Wiesfeld AC; Wilde AA; van der Smagt J; Boven LG; Mannens MM; van Langen IM; Hofstra RM; Otterspoor LC; Doevendans PA; Rodriguez LM; van Gelder IC; Hauer RN
    Circulation; 2006 Apr; 113(13):1650-8. PubMed ID: 16567567
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Sudden death during exercise in a juvenile with arrhythmogenic right ventricular cardiomyopathy and desmoglein-2 gene substitution: a case report.
    Sato T; Nishio H; Suzuki K
    Leg Med (Tokyo); 2011 Nov; 13(6):298-300. PubMed ID: 22000064
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Age- and training-dependent development of arrhythmogenic right ventricular cardiomyopathy in heterozygous plakoglobin-deficient mice.
    Kirchhof P; Fabritz L; Zwiener M; Witt H; Schäfers M; Zellerhoff S; Paul M; Athai T; Hiller KH; Baba HA; Breithardt G; Ruiz P; Wichter T; Levkau B
    Circulation; 2006 Oct; 114(17):1799-806. PubMed ID: 17030684
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Multiple mutations in desmosomal proteins encoding genes in arrhythmogenic right ventricular cardiomyopathy/dysplasia.
    Bauce B; Nava A; Beffagna G; Basso C; Lorenzon A; Smaniotto G; De Bortoli M; Rigato I; Mazzotti E; Steriotis A; Marra MP; Towbin JA; Thiene G; Danieli GA; Rampazzo A
    Heart Rhythm; 2010 Jan; 7(1):22-9. PubMed ID: 20129281
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Desmoglein-2 and desmocollin-2 mutations in dutch arrhythmogenic right ventricular dysplasia/cardiomypathy patients: results from a multicenter study.
    Bhuiyan ZA; Jongbloed JD; van der Smagt J; Lombardi PM; Wiesfeld AC; Nelen M; Schouten M; Jongbloed R; Cox MG; van Wolferen M; Rodriguez LM; van Gelder IC; Bikker H; Suurmeijer AJ; van den Berg MP; Mannens MM; Hauer RN; Wilde AA; van Tintelen JP
    Circ Cardiovasc Genet; 2009 Oct; 2(5):418-27. PubMed ID: 20031616
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The changing spectrum of arrhythmogenic (right ventricular) cardiomyopathy.
    Rizzo S; Pilichou K; Thiene G; Basso C
    Cell Tissue Res; 2012 May; 348(2):319-23. PubMed ID: 22476658
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Arrhythmogenic Right Ventricular Cardiomyopathy-Associated Desmosomal Variants Are Rarely De Novo.
    van Lint FHM; Murray B; Tichnell C; Zwart R; Amat N; Lekanne Deprez RH; Dittmann S; Stallmeyer B; Calkins H; van der Smagt JJ; van den Wijngaard A; Dooijes D; van der Zwaag PA; Schulze-Bahr E; Judge DP; Jongbloed JDH; van Tintelen JP; James CA
    Circ Genom Precis Med; 2019 Aug; 12(8):e002467. PubMed ID: 31386562
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Desmin myopathy, a skeletal myopathy with cardiomyopathy caused by mutations in the desmin gene.
    Dalakas MC; Park KY; Semino-Mora C; Lee HS; Sivakumar K; Goldfarb LG
    N Engl J Med; 2000 Mar; 342(11):770-80. PubMed ID: 10717012
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel Desmin Mutation p.Glu401Asp Impairs Filament Formation, Disrupts Cell Membrane Integrity, and Causes Severe Arrhythmogenic Left Ventricular Cardiomyopathy/Dysplasia.
    Bermúdez-Jiménez FJ; Carriel V; Brodehl A; Alaminos M; Campos A; Schirmer I; Milting H; Abril BÁ; Álvarez M; López-Fernández S; García-Giustiniani D; Monserrat L; Tercedor L; Jiménez-Jáimez J
    Circulation; 2018 Apr; 137(15):1595-1610. PubMed ID: 29212896
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Desmosomal gene evaluation in Boxers with arrhythmogenic right ventricular cardiomyopathy.
    Meurs KM; Ederer MM; Stern JA
    Am J Vet Res; 2007 Dec; 68(12):1338-41. PubMed ID: 18052738
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel plakophilin2 mutation: three-generation family with arrhythmogenic right ventricular cardiomyopathy.
    Aneq MÅ; Fluur C; Rehnberg M; Söderkvist P; Engvall J; Nylander E; Gunnarsson C
    Scand Cardiovasc J; 2012 Apr; 46(2):72-5. PubMed ID: 22035158
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 24.