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1.

Extracellular Kir2.1^C122Y Mutant Upsets Kir2.1-PIP₂ Bonds and Is Arrhythmogenic in Andersen-Tawil Syndrome.

Cruz, Francisco M; Macías, Álvaro; Moreno-Manuel, Ana I; Gutiérrez, Lilian K; Vera-Pedrosa, María Linarejos; Martínez-Carrascoso, Isabel; Sánchez Pérez, Patricia; Ruiz Robles, Juan Manuel; Bermúdez-Jiménez, Francisco J; Díaz-Agustín, Aitor; Martínez de Benito, Fernando; Arias-Santiago, Salvador; Braza-Boils, Aitana; Martín-Martínez, Mercedes; Gutierrez-Rodríguez, Marta; Bernal, Juan A; Zorio, Esther; Jiménez-Jaimez, Juan; Jalife, José.

Circ Res ; 134(8): e52-e71, 2024 Apr 12.

Artículo en Inglés | MEDLINE | ID: mdl-38497220

2.

Kir2.1-Na_V1.5 channelosome and its role in arrhythmias in inheritable cardiac diseases.

Gutiérrez, Lilian K; Moreno-Manuel, Ana I; Jalife, José.

Heart Rhythm ; 2024 Jan 18.

Artículo en Inglés | MEDLINE | ID: mdl-38244712

3.

The Kir2.1E299V mutation increases atrial fibrillation vulnerability while protecting the ventricles against arrhythmias in a mouse model of Short QT Syndrome type 3.

Moreno-Manuel, Ana I; Macías, Álvaro; Cruz, Francisco M; Gutiérrez, Lilian K; Martínez, Fernando; González-Guerra, Andrés; Martínez Carrascoso, Isabel; Bermúdez-Jimenez, Francisco José; Sánchez-Pérez, Patricia; Vera-Pedrosa, María Linarejos; Ruiz, Juan Manuel; Bernal, Juan A; Jalife, José.

Cardiovasc Res ; 2024 Jan 23.

Artículo en Inglés | MEDLINE | ID: mdl-38261726

4.

Molecular stratification of arrhythmogenic mechanisms in the Andersen Tawil syndrome.

Moreno-Manuel, Ana Isabel; Gutiérrez, Lilian K; Vera-Pedrosa, María Linarejos; Cruz, Francisco Miguel; Bermúdez-Jiménez, Francisco José; Martínez-Carrascoso, Isabel; Sánchez-Pérez, Patricia; Macías, Álvaro; Jalife, José.

Cardiovasc Res ; 119(4): 919-932, 2023 05 02.

Artículo en Inglés | MEDLINE | ID: mdl-35892314

5.

Extracellular cysteine disulfide bond break at Cys122 disrupts PIP₂-dependent Kir2.1 channel function and leads to arrhythmias in Andersen-Tawil Syndrome.

Cruz, Francisco M; Macías, Álvaro; Moreno-Manuel, Ana I; Gutiérrez, Lilian K; Vera-Pedrosa, María Linarejos; Martínez-Carrascoso, Isabel; Pérez, Patricia Sánchez; Robles, Juan Manuel Ruiz; Bermúdez-Jiménez, Francisco J; Díaz-Agustín, Aitor; de Benito, Fernando Martínez; Santiago, Salvador Arias; Braza-Boils, Aitana; Martín-Martínez, Mercedes; Gutierrez-Rodríguez, Marta; Bernal, Juan A; Zorio, Esther; Jiménez-Jaimez, Juan; Jalife, José.

bioRxiv ; 2023 Jun 08.

Artículo en Inglés | MEDLINE | ID: mdl-37333254

6.

SNTA1 gene rescues ion channel function and is antiarrhythmic in cardiomyocytes derived from induced pluripotent stem cells from muscular dystrophy patients.

Jimenez-Vazquez, Eric N; Arad, Michael; Macías, Álvaro; Vera-Pedrosa, Maria L; Cruz, Francisco Miguel; Gutierrez, Lilian K; Cuttitta, Ashley J; Monteiro da Rocha, André; Herron, Todd J; Ponce-Balbuena, Daniela; Guerrero-Serna, Guadalupe; Binah, Ofer; Michele, Daniel E; Jalife, José.

Elife ; 112022 06 28.

Artículo en Inglés | MEDLINE | ID: mdl-35762211

7.

Time-efficient three-dimensional transmural scar assessment provides relevant substrate characterization for ventricular tachycardia features and long-term recurrences in ischemic cardiomyopathy.

Merino-Caviedes, Susana; Gutierrez, Lilian K; Alfonso-Almazán, José Manuel; Sanz-Estébanez, Santiago; Cordero-Grande, Lucilio; Quintanilla, Jorge G; Sánchez-González, Javier; Marina-Breysse, Manuel; Galán-Arriola, Carlos; Enríquez-Vázquez, Daniel; Torres, Carlos; Pizarro, Gonzalo; Ibáñez, Borja; Peinado, Rafael; Merino, Jose Luis; Pérez-Villacastín, Julián; Jalife, José; López-Yunta, Mariña; Vázquez, Mariano; Aguado-Sierra, Jazmín; González-Ferrer, Juan José; Pérez-Castellano, Nicasio; Martín-Fernández, Marcos; Alberola-López, Carlos; Filgueiras-Rama, David.

Sci Rep ; 11(1): 18722, 2021 09 28.

Artículo en Inglés | MEDLINE | ID: mdl-34580343

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Extracellular Kir2.1^C122Y Mutant Upsets Kir2.1-PIP₂ Bonds and Is Arrhythmogenic in Andersen-Tawil Syndrome.

Kir2.1-Na_V1.5 channelosome and its role in arrhythmias in inheritable cardiac diseases.

The Kir2.1E299V mutation increases atrial fibrillation vulnerability while protecting the ventricles against arrhythmias in a mouse model of Short QT Syndrome type 3.

Molecular stratification of arrhythmogenic mechanisms in the Andersen Tawil syndrome.

Extracellular cysteine disulfide bond break at Cys122 disrupts PIP₂-dependent Kir2.1 channel function and leads to arrhythmias in Andersen-Tawil Syndrome.

SNTA1 gene rescues ion channel function and is antiarrhythmic in cardiomyocytes derived from induced pluripotent stem cells from muscular dystrophy patients.

Time-efficient three-dimensional transmural scar assessment provides relevant substrate characterization for ventricular tachycardia features and long-term recurrences in ischemic cardiomyopathy.

OPS/OMS Uruguay

Biblioteca Virtual en Salud

Configurar filtros

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Formato de exportación:

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Extracellular Kir2.1C122Y Mutant Upsets Kir2.1-PIP2 Bonds and Is Arrhythmogenic in Andersen-Tawil Syndrome.

Kir2.1-NaV1.5 channelosome and its role in arrhythmias in inheritable cardiac diseases.

The Kir2.1E299V mutation increases atrial fibrillation vulnerability while protecting the ventricles against arrhythmias in a mouse model of Short QT Syndrome type 3.

Molecular stratification of arrhythmogenic mechanisms in the Andersen Tawil syndrome.

Extracellular cysteine disulfide bond break at Cys122 disrupts PIP2-dependent Kir2.1 channel function and leads to arrhythmias in Andersen-Tawil Syndrome.

SNTA1 gene rescues ion channel function and is antiarrhythmic in cardiomyocytes derived from induced pluripotent stem cells from muscular dystrophy patients.

Time-efficient three-dimensional transmural scar assessment provides relevant substrate characterization for ventricular tachycardia features and long-term recurrences in ischemic cardiomyopathy.

Extracellular Kir2.1^C122Y Mutant Upsets Kir2.1-PIP₂ Bonds and Is Arrhythmogenic in Andersen-Tawil Syndrome.

Kir2.1-Na_V1.5 channelosome and its role in arrhythmias in inheritable cardiac diseases.

Extracellular cysteine disulfide bond break at Cys122 disrupts PIP₂-dependent Kir2.1 channel function and leads to arrhythmias in Andersen-Tawil Syndrome.