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NaV1.1 and NaV1.6 selective compounds reduce the behavior phenotype and epileptiform activity in a novel zebrafish model for Dravet Syndrome

PloS one, 2020-03, Vol.15 (3), p.e0219106

2020

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Arabidopsis Sterol Endocytosis Involves Actin-Mediated Trafficking via ARA6-Positive Early Endosomes

Current biology, 2003-08, Vol.13 (16), p.1378-1387

2003

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Structure–Affinity Relationships (SARs) and Structure–Kinetics Relationships (SKRs) of Kv11.1 Blockers

Journal of medicinal chemistry, 2015-08, Vol.58 (15), p.5916

2015

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A Cardiac Sodium Channel Mutation Cosegregates With a Rare Connexin40 Genotype in Familial Atrial Standstill

Circulation research, 2003-01, Vol.92 (1), p.14-22

2003

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Efficient and specific cardiac IK₁ inhibition by a new pentamidine analogue

Cardiovascular research, 2013-07, Vol.99 (1), p.203-214

2013

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A Single Na+ Channel Mutation Causing Both Long-QT and Brugada Syndromes

Circulation research, 1999-12, Vol.85 (12), p.1206-1206

1999

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Compound Heterozygosity for Mutations (W156X and R225W) in SCN5A Associated With Severe Cardiac Conduction Disturbances and Degenerative Changes in the Conduction System

Circulation research, 2003-02, Vol.92 (2), p.159-168

2003

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Fever-induced QTc prolongation and ventricular arrhythmias in individuals with type 2 congenital long QT syndrome

The Journal of clinical investigation, 2008-07, Vol.118 (7), p.2552-2561

2008

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Gap junctional remodeling in relation to stabilization of atrial fibrillation in the goat

Cardiovascular research, 2000-06, Vol.46 (3), p.476-486

2000

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Febrile temperatures unmask biophysical defects in Nav1.1 epilepsy mutations supportive of seizure initiation

The Journal of general physiology, 2013-12, Vol.142 (6), p.641-653

2013

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Inhibition of lysosomal degradation rescues pentamidine-mediated decreases of KIR2.1 ion channel expression but not that of Kᵥ11.1

European journal of pharmacology, 2011-02, Vol.652 (1-3), p.96-103

2011

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Inhibition of lysosomal degradation rescues pentamidine-mediated decreases of K(IR)2.1 ion channel expression but not that of K(v)11.1

European journal of pharmacology, 2011-02, Vol.652 (1-3), p.96-103

2011

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Physiologic function of IK1 requires a combination of Kir2 isoforms

Heart rhythm, 2007-04, Vol.4 (4), p.497-498

Rook, Martin B., PhD

2007

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Biology of cardiac sodium channel Nav1.5 expression

Cardiovascular research, 2012-01, Vol.93 (1), p.12-23

2012

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Exploring Chemical Substructures Essential for hERG K+ Channel Blockade by Synthesis and Biological Evaluation of Dofetilide Analogues

ChemMedChem, 2009-10, Vol.4 (10), p.1722-1732

2009

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Ragged spiking of free calcium in ADP-stimulated human platelets: regulation of puff-like calcium signals in vitro and ex vivo

The Journal of physiology, 2001-09, Vol.535 (3), p.625-635

2001

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Functional analysis of novel KCNQ2 mutations found in patients with Benign Familial Neonatal Convulsions

Neuroscience letters, 2009-10, Vol.462 (1), p.24-29

2009

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Trafficking and functional expression of cardiac Na + channels

Journal of Molecular and Cellular Cardiology, 2004-02, Vol.36 (2), p.185-193

2004

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P19 embryonal carcinoma cells: a suitable model system for cardiac electrophysiological differentiation at the molecular and functional level

Cardiovascular research, 2003-05, Vol.58 (2), p.410-422

2003

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Gap junctions in the rabbit sinoatrial node

American journal of physiology. Heart and circulatory physiology, 2001-05, Vol.280 (5), p.H2103-H2115

2001

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Pro-arrhythmogenic potential of immature cardiomyocytes is triggered by low coupling and cluster size

Cardiovascular research, 2006-09, Vol.71 (4), p.704-714

2006

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Connexin43 repression following epithelium-to-mesenchyme transition in embryonal carcinoma cells requires Snail1 transcription factor

Differentiation (London), 2007-03, Vol.75 (3), p.208-218

2007

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Cloning, embryonic expression, and functional characterization of two novel connexins from Xenopus laevis

Biochemical and biophysical research communications, 2006-10, Vol.349 (2), p.855-862

2006

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NaV1.1 and NaV1.6 selective compounds reduce the behavior phenotype and epileptiform activity in a novel zebrafish model for Dravet Syndrome

Dominant missense mutations in ABCC9 cause Cantú syndrome

Arabidopsis Sterol Endocytosis Involves Actin-Mediated Trafficking via ARA6-Positive Early Endosomes

Structure–Affinity Relationships (SARs) and Structure–Kinetics Relationships (SKRs) of Kv11.1 Blockers

A Cardiac Sodium Channel Mutation Cosegregates With a Rare Connexin40 Genotype in Familial Atrial Standstill

Efficient and specific cardiac IK₁ inhibition by a new pentamidine analogue

A Single Na+ Channel Mutation Causing Both Long-QT and Brugada Syndromes

Compound Heterozygosity for Mutations (W156X and R225W) in SCN5A Associated With Severe Cardiac Conduction Disturbances and Degenerative Changes in the Conduction System

Fever-induced QTc prolongation and ventricular arrhythmias in individuals with type 2 congenital long QT syndrome

Gap junctional remodeling in relation to stabilization of atrial fibrillation in the goat

Febrile temperatures unmask biophysical defects in Nav1.1 epilepsy mutations supportive of seizure initiation

Inhibition of lysosomal degradation rescues pentamidine-mediated decreases of KIR2.1 ion channel expression but not that of Kᵥ11.1

Inhibition of lysosomal degradation rescues pentamidine-mediated decreases of K(IR)2.1 ion channel expression but not that of K(v)11.1

Physiologic function of IK1 requires a combination of Kir2 isoforms

Biology of cardiac sodium channel Nav1.5 expression

Exploring Chemical Substructures Essential for hERG K+ Channel Blockade by Synthesis and Biological Evaluation of Dofetilide Analogues

Ragged spiking of free calcium in ADP-stimulated human platelets: regulation of puff-like calcium signals in vitro and ex vivo

Functional analysis of novel KCNQ2 mutations found in patients with Benign Familial Neonatal Convulsions

Trafficking and functional expression of cardiac Na + channels

P19 embryonal carcinoma cells: a suitable model system for cardiac electrophysiological differentiation at the molecular and functional level

Gap junctions in the rabbit sinoatrial node

Pro-arrhythmogenic potential of immature cardiomyocytes is triggered by low coupling and cluster size

Neurodevelopmental Disorders Caused by De Novo Variants in KCNB1 Genotypes and Phenotypes

Connexin43 repression following epithelium-to-mesenchyme transition in embryonal carcinoma cells requires Snail1 transcription factor

Cloning, embryonic expression, and functional characterization of two novel connexins from Xenopus laevis

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