Publicaciones en colaboración con investigadores/as de University of Michigan–Ann Arbor (10)

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

2021

  1. New Mechanistic Insights, Novel Treatment Paradigms, and Clinical Progress in Cerebrovascular Diseases

    Frontiers in Aging Neuroscience, Vol. 13

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. Nav1.5 N-terminal domain binding to α1-syntrophin increases membrane density of human Kir2.1, Kir2.2 and Nav1.5 channels

    Cardiovascular Research, Vol. 110, Núm. 2, pp. 279-290

2008

  1. Timing of preovulatory LH surge and ovulation in superovulated sheep are affected by follicular status at start of the FSH treatment

    Reproduction in Domestic Animals, Vol. 43, Núm. 1, pp. 92-98