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JAMA Cardiology|September 8, 2021
Early-Onset Atrial Fibrillation and the Prevalence of Rare Variants in Cardiomyopathy and Arrhythmia GenesZachary T Yoneda, Katherine C Anderson, Joseph A Quintana, et al.
Circulation. Genomic and Precision Medicine|November 3, 2020
<i>KCNQ1</i> and Long QT Syndrome in 1/45 Amish: The Road From Identification to Implementation of Culturally Appropriate Precision MedicineElizabeth A Streeten, Vincent Y See, Linda B J Jeng, et al.
Circulation. Genomic and Precision Medicine|July 2, 2024
Multisite Validation of a Functional Assay to Adjudicate <i>SCN5A</i> Brugada Syndrome-Associated VariantsJoanne G Ma, Matthew J O'Neill, Ebony Richardson, et al.
Medrxiv : the Preprint Server for Health Sciences|January 10, 2024
Multi-site validation of a functional assay to adjudicate <i>SCN5A</i> Brugada Syndrome-associated variantsJoanne G Ma, Matthew J O'Neill, Ebony Richardson, et al.
Nature Communications|October 27, 2016
In vivo correction of anaemia in β-thalassemic mice by γPNA-mediated gene editing with nanoparticle deliveryRaman Bahal, Nicole Ali McNeer, Elias Quijano, et al.
Science Translational Medicine|February 3, 2017
2-Hydroxyglutarate produced by neomorphic IDH mutations suppresses homologous recombination and induces PARP inhibitor sensitivityParker L Sulkowski, Christopher D Corso, Nathaniel D Robinson, et al.
Biorxiv : the Preprint Server for Biology|June 12, 2025
Scaled multidimensional assays of variant effect identify sequence-function relationships in hypertrophic cardiomyopathyYuta Yamamoto, Kaiser Chua, Alexis Ferrasse, et al.
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