Brugada syndrome trafficking–defective Nav1. 5 channels can trap cardiac Kir2. 1/2.2 channels M Pérez-Hernández, M Matamoros, S Alfayate, P Nieto-Marín, RG Utrilla, ... JCI insight 3 (18), 2018 | 48 | 2018 |
Kir2. 1-Nav1. 5 channel complexes are differently regulated than Kir2. 1 and Nav1. 5 channels alone RG Utrilla, P Nieto-Marín, S Alfayate, D Tinaquero, M Matamoros, ... Frontiers in physiology 8, 903, 2017 | 45 | 2017 |
Tbx20 controls the expression of the KCNH2 gene and of hERG channels R Caballero, RG Utrilla, I Amorós, M Matamoros, M Pérez-Hernández, ... Proceedings of the National Academy of Sciences 114 (3), E416-E425, 2017 | 41 | 2017 |
Probiotic Lactobacillus plantarum IS 10506 supplementation increase SCFA of women with functional constipation PD Kusumo, H Maulahela, AP Utari, IS Surono, A Soebandrio, ... Iranian Journal of Microbiology 11 (5), 389, 2019 | 27 | 2019 |
Tbx5 variants disrupt Nav1. 5 function differently in patients diagnosed with Brugada or Long QT Syndrome P Nieto-Marín, D Tinaquero, RG Utrilla, J Cebrián, A González-Guerra, ... Cardiovascular research 118 (4), 1046-1060, 2022 | 18 | 2022 |
Digenic heterozigosity in SCN5A and CACNA1C explains the variable expressivity of the long QT phenotype in a Spanish family P Nieto-Marin, J Jimenez-Jaimez, D Tinaquero, S Alfayate, RG Utrilla, ... Revista Española de Cardiología (English Edition) 72 (4), 324-332, 2019 | 13 | 2019 |
Zfhx3 Transcription Factor Represses the Expression of SCN5A Gene and Decreases Sodium Current Density (INa) M Rubio-Alarcón, A Cámara-Checa, M Dago, T Crespo-García, ... International Journal of Molecular Sciences 22 (23), 13031, 2021 | 10 | 2021 |
The p.P888L SAP97 polymorphism increases the transient outward current (Ito,f) and abbreviates the action potential duration and the QT interval D Tinaquero, T Crespo-García, RG Utrilla, P Nieto-Marín, ... Scientific Reports 10 (1), 10707, 2020 | 7 | 2020 |
Kir2. 1-Nav1. 5 channel complexes are differently regulated than Kir2. 1 and Nav1. 5 channels alone. Front Physiol 8: 903 RG Utrilla, P Nieto-Marín, S Alfayate, D Tinaquero, M Matamoros, ... | 6 | 2017 |
Cholinergic regulation of proliferation of the urothelium in response to E. coli lipopolysaccharide exposition L Podmolikova, MF Mukanyangezi, P Nieto-Marin, D Giglio International Immunopharmacology 56, 222-229, 2018 | 5 | 2018 |
A Cantú syndrome mutation produces dual effects on KATP channels by disrupting ankyrin B regulation T Crespo-García, M Rubio-Alarcón, A Cámara-Checa, M Dago, J Rapún, ... Journal of General Physiology 155 (1), e202112995, 2022 | 3 | 2022 |
La expresividad variable del síndrome de QT largo de una familia española se explica por la heterocigosis digénica en SCN5A y CACNA1C P Nieto-Marín, J Jiménez-Jáimez, D Tinaquero, S Alfayate, RG Utrilla, ... Revista Española de Cardiología 72 (4), 324-332, 2019 | 2 | 2019 |
P6281 A DLG1 polymorphism shortens the action potential duration and the QT interval E Delpon, D Tinaquero, S Alfayate, P Nieto-Marin, RG Utrilla, ... European Heart Journal 38 (suppl_1), ehx493. P6281, 2017 | 1 | 2017 |
Tbx5 variants disrupt Nav1. 5 function differently in patients diagnosed with Brugada or Long QT Syndrome. D Tinaquero, RG Utrilla, D Filgueiras-Rama, R Peinado, J Jalife, ... Oxford University Press, 2022 | | 2022 |
Zfhx3 Transcription Factor Represses the Expression of SCN5A Gene and Decreases Sodium Current Density (INa). J Toquero, M Rubio Alarcón, A Cámara Checa, M Dago Requena, ... MPDI, 2021 | | 2021 |
Factores condicionantes de la variabilidad fenotípica de los síndromes arritmogénicos hereditarios: análisis funcional de mutaciones asociadas a los síndromes de Brugada y de … P Nieto Marín Universidad Complutense de Madrid, 2021 | | 2021 |
Zfhx3 decreases expression of cardiac Nav1. 5 channels and inhibits sodium current R Caballero, A Camara-Checa, M Rubio-Alarcon, T Crespo-Garcia, ... European Heart Journal 42 (Supplement_1), ehab724. 3209, 2021 | | 2021 |
A missense mutation in the Tbx5 transcription factor causes long QT syndrome R Caballero, P Nieto-Marin, R Garcia-Utrilla, S Alfayate, D Tinaquero, ... EUROPEAN JOURNAL OF CLINICAL INVESTIGATION 48, 59-60, 2018 | | 2018 |
A mutation in the gene encoding the tbx5 transcription factor is associated with the Brugada Syndrome R Caballero, S Alfayate, RG Utrilla, P Nieto-Marin, D Tinaquero, ... EUROPEAN HEART JOURNAL 38, 1235-1235, 2017 | | 2017 |
A DLG1 polymorphism shortens the action potential duration and the QT interval E Delpon, D Tinaquero, S Alfayate, P Nieto-Marin, RG Utrilla, ... EUROPEAN HEART JOURNAL 38, 1342-1342, 2017 | | 2017 |