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The Canadian Journal of Cardiology|March 3, 2024
Coexistent HCN4 and GATA5 Rare Variants and Atrial Fibrillation in a Large Spanish FamilyAlfonso Fraile, Jorge Cebrián, Israel Thuissard-Vasallo, et al.International Journal of Molecular Sciences|December 10, 2021
Zfhx3 Transcription Factor Represses the Expression of SCN5A Gene and Decreases Sodium Current Density (INa)Marcos Rubio-Alarcón, Anabel Cámara-Checa, María Dago, et al.Nucleic Acids Research|November 22, 2014
Electrophoretic mobility of supercoiled, catenated and knotted DNA moleculesJorge Cebrián, Maridian J Kadomatsu-Hermosa, Alicia Castán, et al.Proceedings of the National Academy of Sciences of the United States of America|November 30, 2023
A gain-of-function HCN4 mutant in the HCN domain is responsible for inappropriate sinus tachycardia in a Spanish familyAnabel Cámara-Checa, Francesca Perin, Marcos Rubio-Alarcón, et al.Scientific Reports|July 3, 2020
The p.P888L SAP97 polymorphism increases the transient outward current (Ito,f) and abbreviates the action potential duration and the QT intervalDavid Tinaquero, Teresa Crespo-García, Raquel G Utrilla, et al.International Journal of Molecular Sciences|May 11, 2024
Variable Penetrance and Expressivity of a Rare Pore Loss-of-Function Mutation (p.L889V) of Nav1.5 Channels in Three Spanish FamiliesMaría Gallego-Delgado, Anabel Cámara-Checa, Marcos Rubio-Alarcón, et al.Cardiovascular Research|February 12, 2021
Tbx5 variants disrupt Nav1.5 function differently in patients diagnosed with Brugada or Long QT SyndromePaloma Nieto-Marín, David Tinaquero, Raquel G Utrilla, et al.Pageof 2