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CIRCULATION RESEARCH
Rivista
Codice:
E037296
ISSN:
0009-7330
Dati Generali
Dati Generali
Pubblicazioni (51)
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Ordina Pubblicazioni:
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A cardiocardiac sympathovagal reflex in the cat.
Articolo
A mutant tropomyosin that causes hypertrophic cardiomyopathy is expressed in vivo and associated with an increased calcium sensitivity
Articolo
A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene.
Articolo
Abnormal Calcium Signalling and Sudden Cardiac Death Associated With Mutation of Calsequestrin.
Articolo
Abnormal Interactions of Calsequestrin With the Ryanodine Receptor Calcium Release Channel Complex Linked to Exercise-Induced Sudden Cardiac Death
Articolo
Abnormal Propagation of Calcium Waves and Ultrastructural Remodeling in Recessive Catecholaminergic Polymorphic Ventricular Tachycardia.
Articolo
Abstract P1075: Igf-1 Signaling And Nuclear Localization Of Pdgfralpha Tyrosine Kinase Activity Control The Fibrotic Response Of Mesenchymal Stromal Cells To Myocardial Ischemia
Abstract
Adenosine mediates sustained adrenergic desensitization in the rat heart via activation of protein kinase C.
Articolo
Allele-Specific Silencing of Mutant mRNA Rescues Ultrastructural and Arrhythmic Phenotype in Mice Carriers of the R4496C Mutation in the Ryanodine Receptor Gene (RYR2).
Articolo
Arrhythmogenesis in Catecholaminergic Polymorphic Ventricular Tachycardia: insights from a RyR2 R4496C knock-in mouse model
Articolo
Arrhythmogenesis in catecholaminergic polymorphic ventricular tachycardia: insights from a RyR2 R4496C knock-in mouse model
Articolo
Arrhythmogenic Cardiomyopathy: Pathophysiology Beyond Cardiac Myocytes.
Articolo
Arrhythmogenic mechanisms in a mouse model of Catecholaminergic Polymorphic Ventricular Tachycardia.
Articolo
Bidirectional Ventricular Tachycardia and Fibrillation Elicited in a Knock-In Mouse Model Carrier of a Mutation in the Cardiac Ryanodine Receptor (RyR2)
Articolo
Cardiac hypertrophy is inhibited by a local pool of cAMP regulated by phosphodiesterase 2
Articolo
Characterization of SEMA3A-encoded semaphorin as a naturally cccurring Kv4.3 protein inhibitor and its contribution to Brugada Syndrome
Articolo
Differential response to Na+ channel blockade, ß-adrenergic stimulation, and rapid pacing in a cellular model mimicking the SCN5A and HERG defects present in the long QT syndrome
Articolo
Effect of stellectomy and vagotomy on ventricular refractoriness in dogs.
Articolo
Effects of thyroid state on mechanical restitution of myocardium.
Articolo
Effects of unilateral stellectomy upon cardiac performance during exercise in dogs.
Articolo
Enhancing repair of the mammalian heart
Articolo
Genetic determinants of cardiac (electric) conduction.
Articolo
Genetics of sudden cardiac death
Articolo
In the RyR2R4496C Mouse Model of CPVT, {beta}-Adrenergic Stimulation Induces Ca Waves by Increasing SR Ca Content and Not by Decreasing the Threshold for Ca Waves.
Articolo
Increased Ca2+ Sensitivity of the Ryanodine Receptor Mutant RyR2R4496C Underlies Catecholaminergic Polymorphic Ventricular Tachycardia.
Articolo
Induced Pluripotent Stem Cell Derived Cardiomyocytes and Long QT Syndrome: Is Personalized Medicine Ready for Prime Time?
Articolo
Inherited arrhythmogenic diseases: the complexity beyond monogenic disorders.
Articolo
Inherited dysfunction of sarcoplasmic reticulum Ca2+handling and arrhythmogenesis
Articolo
Intracellular calcium handling dysfunction and arrhythmogenesis: a new challenge for the electrophysiologist
Articolo
Multiple mechanisms of Na+ channel--linked long-QT syndrome.
Articolo
Novel Arrhythmogenic mechanism revealed by Long-QT Syndrome mutation in the Cardiac NA+ Channel
Articolo
Origin of cardiomyocytes in the adult heart
Recensione
Paracrine mechanisms in adult stem cell signaling and therapy
Articolo
Predicting Patient Response to the Antiarrhythmic Mexiletine Based on Genetic Variation: Personalized Medicine for Long QT Syndrome
Articolo
Protective effect of vagal stimulation on reperfusion arrhythmias in cats.
Articolo
Purkinje cells from RyR2 mutant mice are highly arrhythmogenic but responsive to targeted therapy
Articolo
Reduction of Cardiac Fibrosis by Interference With YAP-Dependent Transactivation
Articolo
Reflex hemodynamic responses initiated from the thoracic aorta.
Articolo
Short communication: flecainide exerts an antiarrhythmic effect in a mouse model of catecholaminergic polymorphic ventricular tachycardia by increasing the threshold for triggered activity
Articolo
Shortening velocity and myosin and myofibrillar ATPase activity related to myosin isoenzyme composition during postnatal development in rat myocardium
Articolo
Single cardiac vagal fiber activity, acute myocardial ischemia, and risk for sudden death.
Articolo
Sympathetic modulation of the relation between ventricular repolarization and cycle length.
Articolo
Systems Biology Approach to Elucidate Fundamental Mechanisms of Heart Growthand Maturation
Abstract
The fifteen years of discoveries that shaped molecular electrophysiology: time for appraisal
Articolo
Tonic influence of the sympathetic nervous system on myocardial reactive hyperemia and on coronary blood flow distribution.
Articolo
Trafficking defects and gating abnormalities of a novel SCN5A mutation question gene-specific therapy in long QT syndrome type 3
Articolo
Unexpected structural and functional consequences of the R33Q homozygous mutation in cardiac calsequestrin: a complex arrhythmogenic cascade in a knock in mouse model.
Articolo
Unilateral stellectomy and dysrhythmias.
Articolo
Vagal stimulation and prevention of sudden death in conscious dogs with a healed myocardial infarction
Articolo
Vagal stimulation and prevention of sudden death in conscious dogs with a healed myocardial infarction.
Articolo
Viral Gene Transfer Rescues Arrhythmogenic Phenotype and Ultrastructural Abnormalities in Adult Calsequestrin-Null Mice With Inherited Arrhythmias
Articolo
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