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For: Gerull B, Brodehl A. Genetic Animal Models for Arrhythmogenic Cardiomyopathy. Front Physiol 2020;11:624. [PMID: 32670084 DOI: 10.3389/fphys.2020.00624] [Cited by in Crossref: 15] [Cited by in F6Publishing: 15] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 Shoykhet M, Dervishi O, Menauer P, Hiermaier M, Moztarzadeh S, Osterloh C, Ludwig RJ, Williams T, Gerull B, Kääb S, Clauss S, Schüttler D, Waschke J, Yeruva S. EGFR inhibition leads to enhanced desmosome assembly and cardiomyocyte cohesion via ROCK activation. JCI Insight 2023;8:e163763. [PMID: 36795511 DOI: 10.1172/jci.insight.163763] [Reference Citation Analysis]
2 Niu Y, Sun Y, Liu Y, Du K, Xu X, Ding Y. Using Zebrafish Animal Model to Study the Genetic Underpinning and Mechanism of Arrhythmogenic Cardiomyopathy. Int J Mol Sci 2023;24. [PMID: 36835518 DOI: 10.3390/ijms24044106] [Reference Citation Analysis]
3 Ponzoni M, Coles JG, Maynes JT. Rodent Models of Dilated Cardiomyopathy and Heart Failure for Translational Investigations and Therapeutic Discovery. Int J Mol Sci 2023;24. [PMID: 36834573 DOI: 10.3390/ijms24043162] [Reference Citation Analysis]
4 Vallverdú-Prats M, Carreras D, Pérez GJ, Campuzano O, Brugada R, Alcalde M. Alterations in Calcium Handling Are a Common Feature in an Arrhythmogenic Cardiomyopathy Cell Model Triggered by Desmosome Genes Loss. Int J Mol Sci 2023;24. [PMID: 36768439 DOI: 10.3390/ijms24032109] [Reference Citation Analysis]
5 Spindler V, Gerull B, Green KJ, Kowalczyk AP, Leube R, Marian AJ, Milting H, Müller EJ, Niessen C, Payne AS, Schlegel N, Schmidt E, Strnad P, Tikkanen R, Vielmuth F, Waschke J. Meeting report - Desmosome dysfunction and disease: Alpine desmosome disease meeting. J Cell Sci 2023;136:jcs260832. [PMID: 36594662 DOI: 10.1242/jcs.260832] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 De Bortoli M, Meraviglia V, Mackova K, Frommelt LS, König E, Rainer J, Volani C, Benzoni P, Schlittler M, Cattelan G, Motta BM, Volpato C, Rauhe W, Barbuti A, Zacchigna S, Pramstaller PP, Rossini A. Modeling incomplete penetrance in arrhythmogenic cardiomyopathy by human induced pluripotent stem cell derived cardiomyocytes. Comput Struct Biotechnol J 2023;21:1759-73. [PMID: 36915380 DOI: 10.1016/j.csbj.2023.02.029] [Reference Citation Analysis]
7 Vaka R, Remortel SV, Ly V, Davis DR. Extracellular vesicle therapy for non-ischemic heart failure: A systematic review of preclinical studies. Extracellular Vesicle 2022;1:100009. [DOI: 10.1016/j.vesic.2022.100009] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Schinner C, Xu L, Franz H, Zimmermann A, Wanuske MT, Rathod M, Hanns P, Geier F, Pelczar P, Liang Y, Lorenz V, Stüdle C, Maly PI, Kauferstein S, Beckmann BM, Sheikh F, Kuster GM, Spindler V. Defective Desmosomal Adhesion Causes Arrhythmogenic Cardiomyopathy by Involving an Integrin-αVβ6/TGF-β Signaling Cascade. Circulation 2022;146:1610-26. [PMID: 36268721 DOI: 10.1161/CIRCULATIONAHA.121.057329] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
9 Volani C, Pagliaro A, Rainer J, Paglia G, Porro B, Stadiotti I, Foco L, Cogliati E, Paolin A, Lagrasta C, Frati C, Corradini E, Falco A, Matzinger T, Picard A, Ermon B, Piazza S, De Bortoli M, Tondo C, Philippe R, Medici A, Lavdas AA, Blumer MJF, Pompilio G, Sommariva E, Pramstaller PP, Troppmair J, Meraviglia V, Rossini A. GCN5 contributes to intracellular lipid accumulation in human primary cardiac stromal cells from patients affected by Arrhythmogenic cardiomyopathy. J Cell Mol Med 2022. [PMID: 35712781 DOI: 10.1111/jcmm.17396] [Reference Citation Analysis]
10 Shoykhet M, Dervishi O, Menauer P, Hiermaier M, Osterloh C, Ludwig RJ, Waschke J, Yeruva S. EGFR inhibition led ROCK activation enhances desmosome assembly and cohesion in cardiomyocytes.. [DOI: 10.1101/2022.04.27.489705] [Reference Citation Analysis]
11 Vallverdú-Prats M, Brugada R, Alcalde M. Premature Termination Codon in 5' Region of Desmoplakin and Plakoglobin Genes May Escape Nonsense-Mediated Decay through the Reinitiation of Translation. Int J Mol Sci 2022;23:656. [PMID: 35054841 DOI: 10.3390/ijms23020656] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Kohela A, van Rooij E. Fibro-fatty remodelling in arrhythmogenic cardiomyopathy. Basic Res Cardiol 2022;117:22. [PMID: 35441328 DOI: 10.1007/s00395-022-00929-4] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
13 Müller L, Hatzfeld M, Keil R. Desmosomes as Signaling Hubs in the Regulation of Cell Behavior. Front Cell Dev Biol 2021;9:745670. [PMID: 34631720 DOI: 10.3389/fcell.2021.745670] [Cited by in Crossref: 8] [Cited by in F6Publishing: 11] [Article Influence: 4.0] [Reference Citation Analysis]
14 Kohela A, van Kampen SJ, Moens T, Wehrens M, Molenaar B, Boogerd CJ, Monshouwer-Kloots J, Perini I, Goumans MJ, Smits AM, van Tintelen JP, van Rooij E. Epicardial differentiation drives fibro-fatty remodeling in arrhythmogenic cardiomyopathy. Sci Transl Med 2021;13:eabf2750. [PMID: 34550725 DOI: 10.1126/scitranslmed.abf2750] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
15 Schinner C, Franz H, Zimmermann A, Wanuske M, Geier F, Pelczar P, Lorenz V, Xu L, Stüdle C, Maly PI, Kauferstein S, Beckmann BM, Kuster GM, Spindler V. Defective Desmosomal Adhesion Causes Arrhythmogenic Cardiomyopathy by involving an Integrin-αVβ6/TGF-β Signaling Cascade.. [DOI: 10.1101/2021.09.02.458734] [Reference Citation Analysis]
16 Gerull B, Brodehl A. Insights Into Genetics and Pathophysiology of Arrhythmogenic Cardiomyopathy. Curr Heart Fail Rep 2021. [PMID: 34478111 DOI: 10.1007/s11897-021-00532-z] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 2.5] [Reference Citation Analysis]
17 Narumanchi S, Wang H, Perttunen S, Tikkanen I, Lakkisto P, Paavola J. Zebrafish Heart Failure Models. Front Cell Dev Biol 2021;9:662583. [PMID: 34095129 DOI: 10.3389/fcell.2021.662583] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 5.0] [Reference Citation Analysis]
18 Brodehl A, Meshkov A, Myasnikov R, Kiseleva A, Kulikova O, Klauke B, Sotnikova E, Stanasiuk C, Divashuk M, Pohl GM, Kudryavtseva M, Klingel K, Gerull B, Zharikova A, Gummert J, Koretskiy S, Schubert S, Mershina E, Gärtner A, Pilus P, Laser KT, Sinitsyn V, Boytsov S, Drapkina O, Milting H. Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset. Int J Mol Sci 2021;22:3786. [PMID: 33917638 DOI: 10.3390/ijms22073786] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
19 Yokota T, Wang Y. Damage control in broken heart-DNA damage response as a common path in arrhythmogenic cardiomyopathy. Cardiovasc Res 2021:cvab064. [PMID: 33693630 DOI: 10.1093/cvr/cvab064] [Reference Citation Analysis]
20 Iop L. Toward the Effective Bioengineering of a Pathological Tissue for Cardiovascular Disease Modeling: Old Strategies and New Frontiers for Prevention, Diagnosis, and Therapy. Front Cardiovasc Med 2020;7:591583. [PMID: 33748193 DOI: 10.3389/fcvm.2020.591583] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
21 Beffagna G, Sommariva E, Bellin M. Mechanotransduction and Adrenergic Stimulation in Arrhythmogenic Cardiomyopathy: An Overview of in vitro and in vivo Models. Front Physiol 2020;11:568535. [PMID: 33281612 DOI: 10.3389/fphys.2020.568535] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
22 Tharp C, Mestroni L, Taylor M. Modifications of Titin Contribute to the Progression of Cardiomyopathy and Represent a Therapeutic Target for Treatment of Heart Failure. J Clin Med 2020;9:E2770. [PMID: 32859027 DOI: 10.3390/jcm9092770] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 3.3] [Reference Citation Analysis]