I. Martínez-Carrascoso

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.

The CoQH2/CoQ Ratio Serves as a Sensor of Respiratory Chain Efficiency.

P. Navas, J. Enríquez, E. Calvo, 2016, Cell reports.

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.

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.