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The Journal of General Physiology|October 26, 2022
A Cantú syndrome mutation produces dual effects on KATP channels by disrupting ankyrin B regulationTeresa Crespo-García, Marcos Rubio-Alarcón, Anabel Cámara-Checa, et al.
Journal of Inherited Metabolic Disease|April 30, 2025
Propionic Acidemia-Induced Proarrhythmic Electrophysiological Alterations in Human iPSC-Derived CardiomyocytesAnabel Cámara-Checa, Mar Álvarez, Josu Rapún, 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.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|March 18, 2025
Two concurrent mechanisms are responsible for the I<sub>Na</sub> increase produced by dapagliflozin and empagliflozin in healthy and heart failure cardiomyocytesJosu Rapún, Sara Pérez-Martín, Anabel Cámara-Checa, 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.
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