Lista de obras -

'Mature' resting membrane potentials in human-induced pluripotent stem cell-derived cardiomyocytes: fact or artefact?

artículo científico publicado en 2019

A Heterozygous Deletion Mutation in the Cardiac Sodium Channel Gene SCN5A with Loss- and Gain-of-Function Characteristics Manifests as Isolated Conduction Disease, without Signs of Brugada or Long QT Syndrome ⬇️

artículo científico publicado el 28 de junio de 2013

Animal models and animal-free innovations for cardiovascular research: current status and routes to be explored. Consensus document of the ESC Working Group on Myocardial Function and the ESC Working Group on Cellular Biology of the Heart

artículo científico publicado en 2022

CDNA arrays: the ups and downs

artículo científico publicado el 1 de marzo de 2001

Cardiac sodium channelopathy associated with SCN5A mutations: electrophysiological, molecular and genetic aspects ⬇️

artículo científico publicado el 1 de septiembre de 2013

Cardiomyocytes derived from pluripotent stem cells recapitulate electrophysiological characteristics of an overlap syndrome of cardiac sodium channel disease

artículo científico publicado en 2012

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

artículo científico publicado en 2013

Coxsackie and adenovirus receptor is a modifier of cardiac conduction and arrhythmia vulnerability in the setting of myocardial ischemia

artículo científico publicado en 2014

Early repolarization in mice causes overestimation of ventricular activation time by the QRS duration

scientific article published on 20 September 2012

Erratum: Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

scholarly article published in Nature Genetics

Functional Consequences of the SCN5A-p.Y1977N Mutation within the PY Ubiquitylation Motif: Discrepancy between HEK293 Cells and Transgenic Mice

scientific article published on 11 October 2019

Genetically determined differences in sodium current characteristics modulate conduction disease severity in mice with cardiac sodium channelopathy

artículo científico publicado en 2009

Getting to the heart of rhythm: a century of progress

artículo científico publicado en 2022

Human iPSC-Derived Cardiomyocytes for Investigation of Disease Mechanisms and Therapeutic Strategies in Inherited Arrhythmia Syndromes: Strengths and Limitations.

artículo científico publicado en 2017

Intercalated disc abnormalities, reduced Na(+) current density, and conduction slowing in desmoglein-2 mutant mice prior to cardiomyopathic changes

artículo científico publicado en 2012

Late Sodium Current Inhibition in Acquired and Inherited Ventricular (dys)function and Arrhythmias ⬇️

artículo científico publicado el 1 de febrero de 2013

Neurokinin-3 receptor activation selectively prolongs atrial refractoriness by inhibition of a background K channel

scientific article published in Nature Communications

Overlap syndrome of cardiac sodium channel disease in mice carrying the equivalent mutation of human SCN5A-1795insD

artículo científico publicado en 2006

Reduced sodium channel function unmasks residual embryonic slow conduction in the adult right ventricular outflow tract.