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Acta Virologica|November 5, 2020
Variability of nonpathogenic influenza virus H5N3 under immune pressureT A Timofeeva, I A Rudneva, G K Sadykova, et al.
JACC. Heart Failure|September 16, 2023
Predicted Deleterious Variants in Cardiomyopathy Genes Prognosticate Mortality and Composite Outcomes in the UK BiobankBabken Asatryan, Ravi A Shah, Ghaith Sharaf Dabbagh, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 24, 2006
An efficient rapid system for profiling the cellular activities of molecular librariesJonathan S Melnick, Jeff Janes, Sungjoon Kim, et al.
Medrxiv : the Preprint Server for Health Sciences|August 12, 2024
ClinGen Hereditary Cardiovascular Disease Gene Curation Expert Panel: Reappraisal of Genes associated with Hypertrophic CardiomyopathySophie Hespe, Amber Waddell, Babken Asatryan, et al.
Journal of the American College of Cardiology|February 19, 2025
Genes Associated With Hypertrophic Cardiomyopathy: A Reappraisal by the ClinGen Hereditary Cardiovascular Disease Gene Curation Expert PanelSophie Hespe, Amber Waddell, Babken Asatryan, et al.
JACC. Clinical Electrophysiology|April 17, 2025
Long-Term Follow-Up Data on Flecainide Use as an Antiarrhythmic in Arrhythmogenic Right Ventricular Cardiomyopathy: A Multicenter StudySean Gaine, Thomas Rolland, Babken Asatryan, et al.
Circulation|May 5, 2021
Evidence-Based Assessment of Genes in Dilated CardiomyopathyElizabeth Jordan, Laiken Peterson, Tomohiko Ai, et al.
Molecular Therapy. Methods & Clinical Development|September 16, 2024
Lentiviral vector packaging and producer cell lines yield titers equivalent to the industry-standard four-plasmid processMatthew Tridgett, Marie Mulet, Sherin Parokkaran Johny, et al.
Medrxiv : the Preprint Server for Health Sciences|April 17, 2023
Beyond gene-disease validity: capturing structured data on inheritance, allelic-requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditionsKatherine S Josephs, Angharad M Roberts, Pantazis Theotokis, et al.
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