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 *

290 related articles for article (PubMed ID: 24704780)

  • 21. Sodium current deficit and arrhythmogenesis in a murine model of plakophilin-2 haploinsufficiency.
    Cerrone M; Noorman M; Lin X; Chkourko H; Liang FX; van der Nagel R; Hund T; Birchmeier W; Mohler P; van Veen TA; van Rijen HV; Delmar M
    Cardiovasc Res; 2012 Sep; 95(4):460-8. PubMed ID: 22764151
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Missense variants in plakophilin-2 in arrhythmogenic right ventricular cardiomyopathy patients--disease-causing or innocent bystanders?
    Christensen AH; Benn M; Tybjaerg-Hansen A; Haunso S; Svendsen JH
    Cardiology; 2010; 115(2):148-54. PubMed ID: 19955750
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Correlation of ventricular arrhythmias with genotype in arrhythmogenic right ventricular cardiomyopathy.
    Bao J; Wang J; Yao Y; Wang Y; Fan X; Sun K; He DS; Marcus FI; Zhang S; Hui R; Song L
    Circ Cardiovasc Genet; 2013 Dec; 6(6):552-6. PubMed ID: 24125834
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy.
    Gerull B; Heuser A; Wichter T; Paul M; Basson CT; McDermott DA; Lerman BB; Markowitz SM; Ellinor PT; MacRae CA; Peters S; Grossmann KS; Drenckhahn J; Michely B; Sasse-Klaassen S; Birchmeier W; Dietz R; Breithardt G; Schulze-Bahr E; Thierfelder L
    Nat Genet; 2004 Nov; 36(11):1162-4. PubMed ID: 15489853
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Contribution of exome sequencing for genetic diagnostic in arrhythmogenic right ventricular cardiomyopathy/dysplasia.
    Fedida J; Fressart V; Charron P; Surget E; Hery T; Richard P; Donal E; Keren B; Duthoit G; Hidden-Lucet F; Villard E; Gandjbakhch E
    PLoS One; 2017; 12(8):e0181840. PubMed ID: 28767663
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Characterization of the molecular phenotype of two arrhythmogenic right ventricular cardiomyopathy (ARVC)-related plakophilin-2 (PKP2) mutations.
    Joshi-Mukherjee R; Coombs W; Musa H; Oxford E; Taffet S; Delmar M
    Heart Rhythm; 2008 Dec; 5(12):1715-23. PubMed ID: 19084810
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Unique genetic background and outcome of non-Caucasian Japanese probands with arrhythmogenic right ventricular dysplasia/cardiomyopathy.
    Wada Y; Ohno S; Aiba T; Horie M
    Mol Genet Genomic Med; 2017 Nov; 5(6):639-651. PubMed ID: 29178656
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. 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]  

  • 31. Molecular disturbance underlies to arrhythmogenic cardiomyopathy induced by transgene content, age and exercise in a truncated PKP2 mouse model.
    Moncayo-Arlandi J; Guasch E; Sanz-de la Garza M; Casado M; Garcia NA; Mont L; Sitges M; Knöll R; Buyandelger B; Campuzano O; Diez-Juan A; Brugada R
    Hum Mol Genet; 2016 Sep; 25(17):3676-3688. PubMed ID: 27412010
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Pathogenic variants in plakophilin-2 gene (PKP2) are associated with better survival in arrhythmogenic right ventricular cardiomyopathy.
    Biernacka EK; Borowiec K; Franaszczyk M; Szperl M; Rampazzo A; Woźniak O; Roszczynko M; Śmigielski W; Lutyńska A; Hoffman P
    J Appl Genet; 2021 Dec; 62(4):613-620. PubMed ID: 34191271
    [TBL] [Abstract][Full Text] [Related]  

  • 33. PKP2 mutations in sudden death from arrhythmogenic right ventricular cardiomyopathy (ARVC) and sudden unexpected death with negative autopsy (SUDNA).
    Zhang M; Tavora F; Oliveira JB; Li L; Franco M; Fowler D; Zhao Z; Burke A
    Circ J; 2012; 76(1):189-94. PubMed ID: 22019812
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Characterizing the Molecular Pathology of Arrhythmogenic Cardiomyopathy in Patient Buccal Mucosa Cells.
    Asimaki A; Protonotarios A; James CA; Chelko SP; Tichnell C; Murray B; Tsatsopoulou A; Anastasakis A; te Riele A; Kléber AG; Judge DP; Calkins H; Saffitz JE
    Circ Arrhythm Electrophysiol; 2016 Feb; 9(2):e003688. PubMed ID: 26850880
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Detection of genomic deletions of PKP2 in arrhythmogenic right ventricular cardiomyopathy.
    Roberts JD; Herkert JC; Rutberg J; Nikkel SM; Wiesfeld AC; Dooijes D; Gow RM; van Tintelen JP; Gollob MH
    Clin Genet; 2013 May; 83(5):452-6. PubMed ID: 22889254
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Disruption of Ca
    Kim JC; Pérez-Hernández M; Alvarado FJ; Maurya SR; Montnach J; Yin Y; Zhang M; Lin X; Vasquez C; Heguy A; Liang FX; Woo SH; Morley GE; Rothenberg E; Lundby A; Valdivia HH; Cerrone M; Delmar M
    Circulation; 2019 Sep; 140(12):1015-1030. PubMed ID: 31315456
    [TBL] [Abstract][Full Text] [Related]  

  • 37. AAV-Mediated Delivery of Plakophilin-2a Arrests Progression of Arrhythmogenic Right Ventricular Cardiomyopathy in Murine Hearts: Preclinical Evidence Supporting Gene Therapy in Humans.
    van Opbergen CJM; Narayanan B; Sacramento CB; Stiles KM; Mishra V; Frenk E; Ricks D; Chen G; Zhang M; Yarabe P; Schwartz J; Delmar M; Herzog CD; Cerrone M
    Circ Genom Precis Med; 2024 Feb; 17(1):e004305. PubMed ID: 38288614
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Recessive arrhythmogenic right ventricular dysplasia due to novel cryptic splice mutation in PKP2.
    Awad MM; Dalal D; Tichnell C; James C; Tucker A; Abraham T; Spevak PJ; Calkins H; Judge DP
    Hum Mutat; 2006 Nov; 27(11):1157. PubMed ID: 17041889
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Generation of iPSC line from patient with arrhythmogenic right ventricular cardiomyopathy carrying mutations in PKP2 gene.
    Khudiakov A; Kostina D; Zlotina A; Yany N; Sergushichev A; Pervunina T; Tomilin A; Kostareva A; Malashicheva A
    Stem Cell Res; 2017 Oct; 24():85-88. PubMed ID: 29034900
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Stop-gain mutations in PKP2 are associated with a later age of onset of arrhythmogenic right ventricular cardiomyopathy.
    Alcalde M; Campuzano O; Berne P; García-Pavía P; Doltra A; Arbelo E; Sarquella-Brugada G; Iglesias A; Alonso-Pulpon L; Brugada J; Brugada R
    PLoS One; 2014; 9(6):e100560. PubMed ID: 24967631
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.