Publicaciones en colaboración con investigadores/as de Centro Nacional de Investigaciones Cardiovasculares Carlos III (10)

2023

  1. A gain-of-function HCN4 mutant in the HCN domain is responsible for inappropriate sinus tachycardia in a Spanish family

    Proceedings of the National Academy of Sciences of the United States of America, Vol. 120

2022

  1. Tbx5 variants disrupt Nav1.5 function differently in patients diagnosed with Brugada or Long QT Syndrome

    Cardiovascular research, Vol. 118, Núm. 4, pp. 1046-1060

2020

  1. The p.P888L SAP97 polymorphism increases the transient outward current (Ito,f) and abbreviates the action potential duration and the QT interval

    Scientific Reports, Vol. 10, Núm. 1

2018

  1. Brugada syndrome trafficking-defective Nav1.5 channels can trap cardiac Kir2.1/2.2 channels

    JCI insight, Vol. 3, Núm. 18

  2. Cardiac Kir2.1 and NaV1.5 Channels Traffic Together to the Sarcolemma to Control Excitability

    Circulation Research, Vol. 122, Núm. 11, pp. 1501-1516

  3. Reciprocity of Cardiac Sodium and Potassium Channels in the Control of Excitability and Arrhythmias

    Cardiac Electrophysiology: From Cell to Bedside: Seventh Edition (Elsevier), pp. 187-197

2017

  1. Tbx20 controls the expression of the KCNH2 gene and of hERG channels

    Proceedings of the National Academy of Sciences of the United States of America, Vol. 114, Núm. 3, pp. E416-E425

2016

  1. Cardiac electrical defects in progeroid mice and Hutchinson-Gilford progeria syndrome patients with nuclear lamina alterations

    Proceedings of the National Academy of Sciences of the United States of America, Vol. 113, Núm. 46, pp. E7250-E7259

  2. miR-208b upregulation interferes with calcium handling in HL-1 atrial myocytes: Implications in human chronic atrial fibrillation

    Journal of Molecular and Cellular Cardiology, Vol. 99, pp. 162-173

2009

  1. Nitric oxide increases cardiac ik1 by nitrosylation of cysteine 76 of Kir2.1 Channels

    Circulation Research, Vol. 105, Núm. 4, pp. 383-392