about
Usefulness of Genetic Testing in Hypertrophic Cardiomyopathy: an Analysis Using Real-World Data.Clonal analysis in mice underlines the importance of rhombomeric boundaries in cell movement restriction during hindbrain segmentation.Clonal analysis identifies hemogenic endothelium as the source of the blood-endothelial common lineage in the mouse embryo.Animal models of arrhythmogenic right ventricular cardiomyopathy: what have we learned and where do we go? Insight for therapeutics.Leukocyte Elastase Inhibitor, the precursor of L-DNase II, inhibits apoptosis by interfering with caspase-8 activation.Conformational modification of serpins transforms leukocyte elastase inhibitor into an endonuclease involved in apoptosis.Lung ultrasound as a translational approach for non-invasive assessment of heart failure with reduced or preserved ejection fraction in mice.Genetic basis of familial dilated cardiomyopathy patients undergoing heart transplantation.Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies.[Lineage tracing of epicardial cells during development and regeneration].Idiopathic Restrictive Cardiomyopathy Is Primarily a Genetic Disease
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description
researcher ORCID ID = 0000-0002-7726-7761
@en
wetenschapper
@nl
name
Laura Padrón-Barthe
@ast
Laura Padrón-Barthe
@en
Laura Padrón-Barthe
@es
Laura Padrón-Barthe
@nl
type
label
Laura Padrón-Barthe
@ast
Laura Padrón-Barthe
@en
Laura Padrón-Barthe
@es
Laura Padrón-Barthe
@nl
prefLabel
Laura Padrón-Barthe
@ast
Laura Padrón-Barthe
@en
Laura Padrón-Barthe
@es
Laura Padrón-Barthe
@nl
P106
P21
P31
P496
0000-0002-7726-7761