Ana I. Manuel-Moreno
Madrid, MD, Spain
Last Updated: 09/26/2026
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Found 10 publications
MOG1L18F-mediated increase in late sodium current produces Long QT Syndrome.
Journal: medRxiv : the preprint server for health sciences
Published: December 25, 2025
Repurposing polyamines to prevent life-threatening arrhythmias in Short QT Syndrome type 3.
Journal: Nature communications
Published: November 27, 2025
Kir2.1 mutations differentially increase the risk of flecainide proarrhythmia in Andersen Tawil Syndrome.
Journal: medRxiv : the preprint server for health sciences
Published: December 23, 2024
Ion channel traffic jams: the significance of trafficking deficiency in long QT syndrome.
Journal: Cell discovery
Published: May 07, 2024
Extracellular Kir2.1C122Y Mutant Upsets Kir2.1-PIP2 Bonds and Is Arrhythmogenic in Andersen-Tawil Syndrome.
Journal: Circulation research
Published: March 18, 2024
Kir2.1-NaV1.5 channelosome and its role in arrhythmias in inheritable cardiac diseases.
Journal: Heart rhythm
Published: November 20, 2023
The Kir2.1E299V mutation increases atrial fibrillation vulnerability while protecting the ventricles against arrhythmias in a mouse model of short QT syndrome type 3.
Journal: Cardiovascular research
Published: July 04, 2023
Extracellular cysteine disulfide bond break at Cys122 disrupts PIP2-dependent Kir2.1 channel function and leads to arrhythmias in Andersen-Tawil Syndrome.
Journal: bioRxiv : the preprint server for biology
Published: June 19, 2023
Kir2.1 dysfunction at the sarcolemma and the sarcoplasmic reticulum causes arrhythmias in a mouse model of Andersen-Tawil syndrome type 1.
Journal: Nature cardiovascular research
Published: March 28, 2022
Molecular stratification of arrhythmogenic mechanisms in the Andersen Tawil syndrome.
Journal: Cardiovascular research
Published: March 18, 2022
Showing 1-10 of 10
Last Updated: 09/26/2026