L. Gutierrez

Kir2.1 dysfunction at the sarcolemma and the sarcoplasmic reticulum causes arrhythmias in a mouse model of Andersen–Tawil syndrome type 1

J. Jalife, J. A. Bernal, V. Andrés, 2022, Nature Cardiovascular Research.

SNTA1 gene rescues ion channel function and is antiarrhythmic in cardiomyocytes derived from induced pluripotent stem cells from muscular dystrophy patients

J. Jalife, Daniela Ponce-Balbuena, G. Guerrero-Serna, 2022, eLife.

Dual Dysfunction of Kir2.1 Underlies Conduction and Excitation-Contraction Coupling Defects Promoting Arrhythmias in a Mouse Model of Andersen-Tawil Syndrome Type 1

J. Jalife, J. A. Bernal, F. M. Cruz, 2021, bioRxiv.

Molecular stratification of arrhythmogenic mechanisms in the Andersen Tawil syndrome

J. Jalife, Isabel Carrascoso, Á. Macías, 2022, Cardiovascular research.

Kir2.1 dysfunction at the sarcolemma and the sarcoplasmic reticulum causes arrhythmias in a mouse model of Andersen–Tawil syndrome type 1

J. Jalife, J. A. Bernal, V. Andrés, 2022, Nature Cardiovascular Research.

Extracellular cysteine disulfide bond break at Cys122 disrupts PIP2-dependent Kir2.1 channel function and leads to arrhythmias in Andersen-Tawil Syndrome

M. Martín-Martínez, J. Jalife, J. A. Bernal, 2023, bioRxiv.

Extracellular Kir2.1C122Y Mutant Upsets Kir2.1-PIP2 Bonds and Is Arrhythmogenic in Andersen-Tawil Syndrome

M. Gutiérrez-Rodríguez, J. Jiménez-Jáimez, Á. Macías, 2024, Circulation research.