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245 related items for PubMed ID: 16769042

  • 1. Composite polymorphisms in the ryanodine receptor 2 gene associated with arrhythmogenic right ventricular cardiomyopathy.
    Milting H, Lukas N, Klauke B, Körfer R, Perrot A, Osterziel KJ, Vogt J, Peters S, Thieleczek R, Varsányi M.
    Cardiovasc Res; 2006 Aug 01; 71(3):496-505. PubMed ID: 16769042
    [Abstract] [Full Text] [Related]

  • 2. Enhanced store overload-induced Ca2+ release and channel sensitivity to luminal Ca2+ activation are common defects of RyR2 mutations linked to ventricular tachycardia and sudden death.
    Jiang D, Wang R, Xiao B, Kong H, Hunt DJ, Choi P, Zhang L, Chen SR.
    Circ Res; 2005 Nov 25; 97(11):1173-81. PubMed ID: 16239587
    [Abstract] [Full Text] [Related]

  • 3. Genetics of arrhythmogenic right ventricular cardiomyopathy--status quo and future perspectives.
    Paul M, Schulze-Bahr E, Breithardt G, Wichter T.
    Z Kardiol; 2003 Feb 25; 92(2):128-36. PubMed ID: 12596074
    [Abstract] [Full Text] [Related]

  • 4. Prevalence and significance of rare RYR2 variants in arrhythmogenic right ventricular cardiomyopathy/dysplasia: results of a systematic screening.
    Roux-Buisson N, Gandjbakhch E, Donal E, Probst V, Deharo JC, Chevalier P, Klug D, Mansencal N, Delacretaz E, Cosnay P, Scanu P, Extramiana F, Keller D, Hidden-Lucet F, Trapani J, Fouret P, Frank R, Fressart V, Fauré J, Lunardi J, Charron P.
    Heart Rhythm; 2014 Nov 25; 11(11):1999-2009. PubMed ID: 25041964
    [Abstract] [Full Text] [Related]

  • 5. Postmortem genetic screening of SNPs in RyR2 gene in sudden unexplained nocturnal death syndrome in the southern Chinese Han population.
    Huang L, Liu C, Tang S, Su T, Cheng J.
    Forensic Sci Int; 2014 Feb 25; 235():14-8. PubMed ID: 24447446
    [Abstract] [Full Text] [Related]

  • 6. Differential expression of the cardiac ryanodine receptor in normal and arrhythmogenic right ventricular cardiomyopathy canine hearts.
    Meurs KM, Lacombe VA, Dryburgh K, Fox PR, Reiser PR, Kittleson MD.
    Hum Genet; 2006 Aug 25; 120(1):111-8. PubMed ID: 16733711
    [Abstract] [Full Text] [Related]

  • 7. Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia.
    Marks AR, Priori S, Memmi M, Kontula K, Laitinen PJ.
    J Cell Physiol; 2002 Jan 25; 190(1):1-6. PubMed ID: 11807805
    [Abstract] [Full Text] [Related]

  • 8. Myocardial transcriptome analysis of human arrhythmogenic right ventricular cardiomyopathy.
    Gaertner A, Schwientek P, Ellinghaus P, Summer H, Golz S, Kassner A, Schulz U, Gummert J, Milting H.
    Physiol Genomics; 2012 Jan 18; 44(1):99-109. PubMed ID: 22085907
    [Abstract] [Full Text] [Related]

  • 9. Beta-blockers restore calcium release channel function and improve cardiac muscle performance in human heart failure.
    Reiken S, Wehrens XH, Vest JA, Barbone A, Klotz S, Mancini D, Burkhoff D, Marks AR.
    Circulation; 2003 May 20; 107(19):2459-66. PubMed ID: 12743001
    [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 04; 113(13):1650-8. PubMed ID: 16567567
    [Abstract] [Full Text] [Related]

  • 11. Myocardial expression profiles of candidate molecules in patients with arrhythmogenic right ventricular cardiomyopathy/dysplasia compared to those with dilated cardiomyopathy and healthy controls.
    Akdis D, Medeiros-Domingo A, Gaertner-Rommel A, Kast JI, Enseleit F, Bode P, Klingel K, Kandolf R, Renois F, Andreoletti L, Akdis CA, Milting H, Lüscher TF, Brunckhorst C, Saguner AM, Duru F.
    Heart Rhythm; 2016 Mar 04; 13(3):731-41. PubMed ID: 26569459
    [Abstract] [Full Text] [Related]

  • 12. Gene symbol: RYR2. Disease: Arrhythmogenic right ventricular cardiomyopathy type 2.
    Tiso N, Bauce B, Rampazzo A, Bagattin A, Nava A, Danieli GA.
    Hum Genet; 2004 Mar 04; 114(4):405. PubMed ID: 15046075
    [No Abstract] [Full Text] [Related]

  • 13. Desmosomal gene evaluation in Boxers with arrhythmogenic right ventricular cardiomyopathy.
    Meurs KM, Ederer MM, Stern JA.
    Am J Vet Res; 2007 Dec 04; 68(12):1338-41. PubMed ID: 18052738
    [Abstract] [Full Text] [Related]

  • 14. Arrhythmogenic mutation-linked defects in ryanodine receptor autoregulation reveal a novel mechanism of Ca2+ release channel dysfunction.
    George CH, Jundi H, Walters N, Thomas NL, West RR, Lai FA.
    Circ Res; 2006 Jan 06; 98(1):88-97. PubMed ID: 16339485
    [Abstract] [Full Text] [Related]

  • 15. Integrin β1D Deficiency-Mediated RyR2 Dysfunction Contributes to Catecholamine-Sensitive Ventricular Tachycardia in Arrhythmogenic Right Ventricular Cardiomyopathy.
    Wang Y, Li C, Shi L, Chen X, Cui C, Huang J, Chen B, Hall DD, Pan Z, Lu M, Hong J, Song LS, Zhao S.
    Circulation; 2020 May 05; 141(18):1477-1493. PubMed ID: 32122157
    [Abstract] [Full Text] [Related]

  • 16. Cardiac ryanodine receptor function and regulation in heart disease.
    Lehnart SE, Wehrens XH, Kushnir A, Marks AR.
    Ann N Y Acad Sci; 2004 May 05; 1015():144-59. PubMed ID: 15201156
    [Abstract] [Full Text] [Related]

  • 17. Maximum phosphorylation of the cardiac ryanodine receptor at serine-2809 by protein kinase a produces unique modifications to channel gating and conductance not observed at lower levels of phosphorylation.
    Carter S, Colyer J, Sitsapesan R.
    Circ Res; 2006 Jun 23; 98(12):1506-13. PubMed ID: 16709901
    [Abstract] [Full Text] [Related]

  • 18. 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 01; 19(23):4595-607. PubMed ID: 20829228
    [Abstract] [Full Text] [Related]

  • 19. 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 01; 96(16):1268-74. PubMed ID: 20525856
    [Abstract] [Full Text] [Related]

  • 20. Molecular genetics of exercise-induced polymorphic ventricular tachycardia: identification of three novel cardiac ryanodine receptor mutations and two common calsequestrin 2 amino-acid polymorphisms.
    Laitinen PJ, Swan H, Kontula K.
    Eur J Hum Genet; 2003 Nov 01; 11(11):888-91. PubMed ID: 14571276
    [Abstract] [Full Text] [Related]

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