Found: 27
Select item for more details and to access through your institution.
'Hot phase' clinical presentation in arrhythmogenic cardiomyopathy.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Phenotypic expression is a prerequisite for malignant arrhythmic events and sudden cardiac death in arrhythmogenic right ventricular cardiomyopathy.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Recent Advances in CRISPR/Cas9-Based Genome Editing Tools for Cardiac Diseases.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 20, p. 10985, doi. 10.3390/ijms222010985
- By:
- Publication type:
- Article
Modeling Cardiovascular Diseases with hiPSC-Derived Cardiomyocytes in 2D and 3D Cultures.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 9, p. 3404, doi. 10.3390/ijms21093404
- By:
- Publication type:
- Article
Arrhythmogenic cardiomyopathy: a disease of intercalated discs.
- Published in:
- Cell & Tissue Research, 2015, v. 360, n. 3, p. 491, doi. 10.1007/s00441-014-2015-5
- By:
- Publication type:
- Article
Hypertrophic Cardiomyopathy and Primary Restrictive Cardiomyopathy: Similarities, Differences and Phenocopies.
- Published in:
- Journal of Clinical Medicine, 2021, v. 10, n. 9, p. 1954, doi. 10.3390/jcm10091954
- By:
- Publication type:
- Article
Clinical and Functional Characterization of a Novel Mutation in Lamin A/C Gene in a Multigenerational Family with Arrhythmogenic Cardiac Laminopathy.
- Published in:
- PLoS ONE, 2015, v. 10, n. 4, p. 1, doi. 10.1371/journal.pone.0121723
- By:
- Publication type:
- Article
Arrhythmogenic Cardiomyopathy.
- Published in:
- European Heart Journal, 2020, v. 41, n. 47, p. 4457, doi. 10.1093/eurheartj/ehaa719
- By:
- Publication type:
- Article
Transcriptomic Characterization of a Human In Vitro Model of Arrhythmogenic Cardiomyopathy Under Topological and Mechanical Stimuli.
- Published in:
- Annals of Biomedical Engineering, 2019, v. 47, n. 3, p. 852, doi. 10.1007/s10439-018-02134-8
- By:
- Publication type:
- Article
Identification of a PKP2 gene deletion in a family with arrhythmogenic right ventricular cardiomyopathy.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 11, p. 1226, doi. 10.1038/ejhg.2013.39
- By:
- Publication type:
- Article
The p.A897KfsX4 frameshift variation in desmocollin-2 is not a causative mutation in arrhythmogenic right ventricular cardiomyopathy.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 7, p. 776, doi. 10.1038/ejhg.2010.19
- By:
- Publication type:
- Article
Arrhythmogenic right ventricular cardiomyopathy type 1 (ARVD1): confirmation of locus assignment and mutation screening of four candidate genes.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 1, p. 69, doi. 10.1038/sj.ejhg.5200914
- By:
- Publication type:
- Article
Ultrastructural evidence of intercalated disc remodelling in arrhythmogenic right ventricular cardiomyopathy: an electron microscopy investigation on endomyocardial biopsies.
- Published in:
- European Heart Journal, 2006, v. 27, n. 15, p. 1847, doi. 10.1093/eurheartj/ehl095
- By:
- Publication type:
- Article
Clinical profile of four families with arrhythmogenic right ventricular cardiomyopathy caused by dominant desmoplakin mutations.
- Published in:
- European Heart Journal, 2005, v. 26, n. 16, p. 1666, doi. 10.1093/eurheartj/ehi341
- By:
- Publication type:
- Article
A novel murine model for arrhythmogenic cardiomyopathy points to a pathogenic role of Wnt signalling and miRNA dysregulation.
- Published in:
- Cardiovascular Research, 2019, v. 115, n. 4, p. 739, doi. 10.1093/cvr/cvy253
- By:
- Publication type:
- Article
Regulatory mutations in transforming growth factor-β3 gene involved in arrhythmogenic right ventricular cardiomyopathy.
- Published in:
- Cardiovascular Research, 2012, v. 96, n. 2, p. 191, doi. 10.1093/cvr/cvs221
- By:
- Publication type:
- Article
Regulatory mutations in transforming growth factor-β3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1
- Published in:
- Cardiovascular Research, 2005, v. 65, n. 2, p. 366, doi. 10.1016/j.cardiores.2004.10.005
- By:
- Publication type:
- Article
The novel S59P mutation in the TNFRSF1A gene identified in an adult onset TNF receptor associated periodic syndrome (TRAPS) constitutively activates NF-κB pathway.
- Published in:
- Arthritis Research & Therapy, 2015, v. 17, n. 1, p. 1, doi. 10.1186/s13075-015-0604-7
- By:
- Publication type:
- Article
The novel S59P mutation in the TNFRSF1A gene identified in an adult onset TNF receptor associated periodic syndrome (TRAPS) constitutively activates NF-κB pathway
- Published in:
- Arthritis Research & Therapy, 2015, v. 17, n. 1, p. 93, doi. 10.1186/s13075-015-0604-7
- By:
- Publication type:
- Article
Evolving Diagnostic Criteria for Arrhythmogenic Cardiomyopathy.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Circulating miR-185-5p as a Potential Biomarker for Arrhythmogenic Right Ventricular Cardiomyopathy.
- Published in:
- Cells (2073-4409), 2021, v. 10, n. 10, p. 2578, doi. 10.3390/cells10102578
- By:
- Publication type:
- Article
Animal Models and Molecular Pathogenesis of Arrhythmogenic Cardiomyopathy Associated with Pathogenic Variants in Intercalated Disc Genes.
- Published in:
- International Journal of Molecular Sciences, 2024, v. 25, n. 11, p. 6208, doi. 10.3390/ijms25116208
- By:
- Publication type:
- Article
Mutations of the same sequence of the myelin P0 gene causing two different phenotypes.
- Published in:
- Human Mutation, 1998, v. 11, p. S217, doi. 10.1002/humu.1380110170
- By:
- Publication type:
- Article
Homozygous SCN5A mutation in Brugada syndrome with monomorphic ventricular tachycardia and structural heart abnormalities.
- Published in:
- 2007
- By:
- Publication type:
- journal article
A new locus for arrhythmogenic right ventricular cardiomyopathy (ARVD2) maps to chromosome 1q42–q43.
- Published in:
- Human Molecular Genetics, 1995, v. 4, n. 11, p. 2151
- By:
- Publication type:
- Article
The gene for arrhythmogenic right ventricular cardiomyopathy maps to chromosome 14q23–q24.
- Published in:
- Human Molecular Genetics, 1994, v. 3, n. 6, p. 959
- By:
- Publication type:
- Article
Missense mutations in Desmocollin-2 N-terminus, associated with arrhythmogenic right ventricular cardiomyopathy, affect intracellular localization of desmocollin-2 in vitro.
- Published in:
- BMC Medical Genetics, 2007, v. 8, p. 65, doi. 10.1186/1471-2350-8-65
- By:
- Publication type:
- Article