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Biorxiv : the Preprint Server for Biology|July 29, 2026
Damaging RBM20 E-rich domain variants are not rescued by gene replacementFang Flora Bai, Kaiser Chua, Daniel Li, et al.JACC. Heart Failure|July 18, 2025
Genetic and Phenotypic Characterization of Nexilin (NEXN)-Related Cardiomyopathy: Results From a Multicentric StudyMaria Perotto, Alessia Paldino, Francesco Mazzarotto, et al.Journal of the American College of Cardiology|May 20, 2026
Sex and Age Specific Genetic Risk Across the Dilated and Arrhythmogenic Cardiomyopathy Spectrum: Insights From the SHaRe RegistrySophie L V M Stroeks, Nicole K Bart, Joseph Rossano, et al.Medrxiv : the Preprint Server for Health Sciences|August 8, 2025
The contribution of RBM20 truncating variants to human cardiomyopathyBrendan J Floyd, Joyce N Njoroge, Vikki A Krysov, et al.Medrxiv : the Preprint Server for Health Sciences|August 9, 2020
High-throughput SARS-CoV-2 and host genome sequencing from single nasopharyngeal swabsJohn E Gorzynski, Hannah N De Jong, David Amar, et al.JAMA Cardiology|April 8, 2026
RBM20 Truncating Variants and Human CardiomyopathyBrendan J Floyd, Joyce N Njoroge, Vikki A Krysov, et al.Orthopaedic Journal of Sports Medicine|March 12, 2026
Complications Leading to Reoperation After Pediatric Tibial Spine Fracture FixationBenjamin R Caruso, Suzanna M Ohlsen, Keinan Agonias, et al.Circulation. Genomic and Precision Medicine|July 8, 2026
Variant Site-Specific Natural History of Titin-Induced Cardiomyopathy: An International Multicenter RegistryMaria Perotto, Cinzia Radesich, Alessia Paldino, et al.Science Translational Medicine|January 10, 2024
Allele-specific control of rodent and human lncRNA KMT2E-AS1 promotes hypoxic endothelial pathology in pulmonary hypertensionYi-Yin Tai, Qiujun Yu, Ying Tang, et al.JAMA Cardiology|February 12, 2025
Arrhythmic Risk Stratification of Carriers of Filamin C Truncating Variants, Marta Gigli, Davide Stolfo, et al.Pageof 85