BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

189 related articles for article (PubMed ID: 34300226)

  • 1. Altered Electrical, Biomolecular, and Immunologic Phenotypes in a Novel Patient-Derived Stem Cell Model of Desmoglein-2 Mutant ARVC.
    Hawthorne RN; Blazeski A; Lowenthal J; Kannan S; Teuben R; DiSilvestre D; Morrissette-McAlmon J; Saffitz JE; Boheler KR; James CA; Chelko SP; Tomaselli G; Tung L
    J Clin Med; 2021 Jul; 10(14):. PubMed ID: 34300226
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Electrical dysfunctions in human-induced pluripotent stem cell-derived cardiomyocytes from a patient with an arrhythmogenic right ventricular cardiomyopathy.
    El-Battrawy I; Zhao Z; Lan H; Cyganek L; Tombers C; Li X; Buljubasic F; Lang S; Tiburcy M; Zimmermann WH; Utikal J; Wieland T; Borggrefe M; Zhou XB; Akin I
    Europace; 2018 Jun; 20(FI1):f46-f56. PubMed ID: 29566126
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Desmoglein-2 mutations in propeptide cleavage-site causes arrhythmogenic right ventricular cardiomyopathy/dysplasia by impairing extracellular 1-dependent desmosomal interactions upon cellular stress.
    Vite A; Gandjbakhch E; Hery T; Fressart V; Gary F; Simon F; Varnous S; Hidden Lucet F; Charron P; Villard E
    Europace; 2020 Feb; 22(2):320-329. PubMed ID: 31845994
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Distal myopathy induced arrhythmogenic right ventricular cardiomyopathy in a pedigree carrying novel DSG2 null variant.
    Chen P; Li Z; Yu B; Ma F; Li X; Wang DW
    Int J Cardiol; 2020 Jan; 298():25-31. PubMed ID: 31653443
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Modeling of arrhythmogenic right ventricular cardiomyopathy with human induced pluripotent stem cells.
    Caspi O; Huber I; Gepstein A; Arbel G; Maizels L; Boulos M; Gepstein L
    Circ Cardiovasc Genet; 2013 Dec; 6(6):557-68. PubMed ID: 24200905
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Rare non-coding Desmoglein-2 variant contributes to Arrhythmogenic right ventricular cardiomyopathy.
    Christensen AH; Andersen CB; Wassilew K; Svendsen JH; Bundgaard H; Brand SM; Schmitz B
    J Mol Cell Cardiol; 2019 Jun; 131():164-170. PubMed ID: 31051180
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An autoantibody identifies arrhythmogenic right ventricular cardiomyopathy and participates in its pathogenesis.
    Chatterjee D; Fatah M; Akdis D; Spears DA; Koopmann TT; Mittal K; Rafiq MA; Cattanach BM; Zhao Q; Healey JS; Ackerman MJ; Bos JM; Sun Y; Maynes JT; Brunckhorst C; Medeiros-Domingo A; Duru F; Saguner AM; Hamilton RM
    Eur Heart J; 2018 Nov; 39(44):3932-3944. PubMed ID: 30239670
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutated desmoglein-2 proteins are incorporated into desmosomes and exhibit dominant-negative effects in arrhythmogenic right ventricular cardiomyopathy.
    Rasmussen TB; Palmfeldt J; Nissen PH; Magnoni R; Dalager S; Jensen UB; Kim WY; Heickendorff L; Mølgaard H; Jensen HK; Baandrup UT; Bross P; Mogensen J
    Hum Mutat; 2013 May; 34(5):697-705. PubMed ID: 23381804
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Endurance Training Provokes Arrhythmogenic Right Ventricular Cardiomyopathy Phenotype in Heterozygous Desmoglein-2 Mutants: Alleviation by Preload Reduction.
    Fabritz L; Fortmueller L; Gehmlich K; Kant S; Kemper M; Kucerova D; Syeda F; Faber C; Leube RE; Kirchhof P; Krusche CA
    Biomedicines; 2024 Apr; 12(5):. PubMed ID: 38790949
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Phenotypic recapitulation and correction of desmoglein-2-deficient cardiomyopathy using human-induced pluripotent stem cell-derived cardiomyocytes.
    Shiba M; Higo S; Kondo T; Li J; Liu L; Ikeda Y; Kohama Y; Kameda S; Tabata T; Inoue H; Nakamura S; Takeda M; Ito E; Takashima S; Miyagawa S; Sawa Y; Hikoso S; Sakata Y
    Hum Mol Genet; 2021 Jul; 30(15):1384-1397. PubMed ID: 33949662
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutations of desmoglein-2 in sudden death from arrhythmogenic right ventricular cardiomyopathy and sudden unexplained death.
    Zhang M; Xue A; Shen Y; Oliveira JB; Li L; Zhao Z; Burke A
    Forensic Sci Int; 2015 Oct; 255():85-8. PubMed ID: 26296472
    [TBL] [Abstract][Full Text] [Related]  

  • 12. In vitro analysis of arrhythmogenic cardiomyopathy associated desmoglein-2 (DSG2) mutations reveals diverse glycosylation patterns.
    Debus JD; Milting H; Brodehl A; Kassner A; Anselmetti D; Gummert J; Gaertner-Rommel A
    J Mol Cell Cardiol; 2019 Apr; 129():303-313. PubMed ID: 30885746
    [TBL] [Abstract][Full Text] [Related]  

  • 13. High risk of heart failure associated with desmoglein-2 mutations compared to plakophilin-2 mutations in arrhythmogenic right ventricular cardiomyopathy/dysplasia.
    Hermida A; Fressart V; Hidden-Lucet F; Donal E; Probst V; Deharo JC; Chevalier P; Klug D; Mansencal N; Delacretaz E; Cosnay P; Scanu P; Extramiana F; Keller DI; Rouanet S; Charron P; Gandjbakhch E
    Eur J Heart Fail; 2019 Jun; 21(6):792-800. PubMed ID: 30790397
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Desmoglein 2-Dependent Arrhythmogenic Cardiomyopathy Is Caused by a Loss of Adhesive Function.
    Kant S; Holthöfer B; Magin TM; Krusche CA; Leube RE
    Circ Cardiovasc Genet; 2015 Aug; 8(4):553-63. PubMed ID: 26085008
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Case report of familial sudden cardiac death caused by a DSG2 p.F531C mutation as genetic background when carrying with heterozygous KCNE5 p.D92E/E93X mutation.
    Lin Y; Huang J; He S; Feng R; Zhong Z; Liu Y; Ye W; Li X; Liao H; Fei H; Rao F; Shan Z; Deng C; Zhan X; Xue Y; Liu H; Zhang B; Wang K; Zhang Q; Wu S; Lin X
    BMC Med Genet; 2018 Aug; 19(1):148. PubMed ID: 30129429
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Single-cell RNA sequencing in donor and end-stage heart failure patients identifies NLRP3 as a therapeutic target for arrhythmogenic right ventricular cardiomyopathy.
    Fu M; Hua X; Shu S; Xu X; Zhang H; Peng Z; Mo H; Liu Y; Chen X; Yang Y; Zhang N; Wang X; Liu Z; Yue G; Hu S; Song J
    BMC Med; 2024 Jan; 22(1):11. PubMed ID: 38185631
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) Probably Caused by DSG2 p.Val149Ile Mutation as Genetic Background When Carrying with Heterozygous PRRT2 p.Arg217ProfsTer8 Mutation: A Case Report.
    Huang R; Luo Y; Zhao J; Su K; Lei Y; Li Y
    Int Med Case Rep J; 2021; 14():307-313. PubMed ID: 34012299
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Case reports of two pedigrees with recessive arrhythmogenic right ventricular cardiomyopathy associated with homozygous Thr335Ala variant in DSG2.
    Qadri S; Anttonen O; Viikilä J; Seppälä EH; Myllykangas S; Alastalo TP; Holmström M; Heliö T; Koskenvuo JW
    BMC Med Genet; 2017 Aug; 18(1):86. PubMed ID: 28818065
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Exercise triggers CAPN1-mediated AIF truncation, inducing myocyte cell death in arrhythmogenic cardiomyopathy.
    Chelko SP; Keceli G; Carpi A; Doti N; Agrimi J; Asimaki A; Beti CB; Miyamoto M; Amat-Codina N; Bedja D; Wei AC; Murray B; Tichnell C; Kwon C; Calkins H; James CA; O'Rourke B; Halushka MK; Melloni E; Saffitz JE; Judge DP; Ruvo M; Kitsis RN; Andersen P; Di Lisa F; Paolocci N
    Sci Transl Med; 2021 Feb; 13(581):. PubMed ID: 33597260
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.