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A useful irrigated tip to cannulate distal coronary sinus

Europace (London, England), 2016-09, Vol.18 (9), p.1327-1327

2016

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The role of mental health home hospitalization care during the COVID‐19 pandemic

Acta psychiatrica Scandinavica, 2020-05, Vol.141 (5), p.479-480

2020

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Scaling up of highly active antiretroviral therapy in a rural district of Malawi: an effectiveness assessment

The Lancet (British edition), 2006-04, Vol.367 (9519), p.1335-1342

2006

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The new antiarrhythmic drug vernakalant: ex vivo study of human atrial tissue from sinus rhythm and chronic atrial fibrillation

Cardiovascular research, 2013-04, Vol.98 (1), p.145-154

2013

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Heterogeneous expression of repolarizing, voltage-gated K+ currents in adult mouse ventricles

The Journal of physiology, 2004-08, Vol.559 (1), p.103-120

2004

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Sequence of Gating Charge Movement and Pore Gating in hERG Activation and Deactivation Pathways

Biophysical journal, 2015-03, Vol.108 (6), p.1435-1447

2015

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RSD1235 blocks late INa and suppresses early afterdepolarizations and torsades de pointes induced by class III agents

Cardiovascular research, 2006-06, Vol.70 (3), p.486-496

2006

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External Ba(2+) block of Kv4.2 channels is enhanced in the closed-inactivated state

American Journal of Physiology: Cell Physiology, 2013-02, Vol.304 (4), p.C370-C381

2013

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Modeling of high-affinity binding of the novel atrial anti-arrhythmic agent, vernakalant, to Kv1.5 channels

Journal of molecular graphics & modelling, 2009-10, Vol.28 (3), p.226-235

2009

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The Ca(v)1.4 calcium channel is a critical regulator of T cell receptor signaling and naive T cell homeostasis

Immunity (Cambridge, Mass.), 2011-09, Vol.35 (3), p.349-360

2011

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Allosteric coupling of the inner activation gate to the outer pore of a potassium channel

Scientific reports, 2013-10, Vol.3 (1), p.3025, Article 3025

2013

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Risk of sural nerve injury during lateral distal Achilles tendinoscopy: A Cadaver Study

Orthopaedics & traumatology, surgery & research, 2015-02, Vol.101 (1), p.93-96

2015

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Cardiac Ryanodine Receptor (Ryr2)-mediated Calcium Signals Specifically Promote Glucose Oxidation via Pyruvate Dehydrogenase

The Journal of biological chemistry, 2016-11, Vol.291 (45), p.23490-23505

2016

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Gating charge movement precedes ionic current activation in hERG channels

Channels (Austin, Tex.), 2014-01, Vol.8 (1), p.84-89

2014

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Modulation of human ether-Ã -go-go-related K+ (HERG) channel inactivation by Cs+ and K

The Journal of physiology, 2003-05, Vol.548 (3), p.691-702

2003

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Kv1.5 Is an Important Component of Repolarizing K+ Current in Canine Atrial Myocytes

Circulation research, 2003-10, Vol.93 (8), p.744-751

2003

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Basis for allosteric open-state stabilization of voltage-gated potassium channels by intracellular cations

The Journal of general physiology, 2012-11, Vol.140 (5), p.495-511

2012

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Rb+ flux through hERG channels affects the potency of channel blocking drugs: correlation with data obtained using a high-throughput Rb+ efflux assay

Journal of biomolecular screening, 2004-10, Vol.9 (7), p.588-597

2004

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An Activation Gating Switch in Kv1.2 Is Localized to a Threonine Residue in the S2-S3 Linker

Biophysical journal, 2007-12, Vol.93 (12), p.4173-4186

2007

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The neutral, hydrophobic isoleucine at position I521 in the extracellular S4 domain of hERG contributes to channel gating equilibrium

American Journal of Physiology: Cell Physiology, 2013-08, Vol.305 (4), p.C468-C478

2013

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ShakerIR and Kv1.5 mutant channels with enhanced slow inactivation also exhibit K+o-dependent resting inactivation

Pflügers Archiv, 2013-11, Vol.465 (11), p.1545-1555

2013

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A novel mechanism for LQT3 with 2:1 block: A pore-lining mutation in Nav1.5 significantly affects voltage-dependence of activation

Heart rhythm, 2011-05, Vol.8 (5), p.770-777

2011

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Kinetic analysis of the effects of H+ or Ni2+ on Kv1.5 current shows that both ions enhance slow inactivation and induce resting inactivation

The Journal of physiology, 2010-08, Vol.588 (16), p.3011-3030

2010

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Use of voltage clamp fluorimetry in understanding potassium channel gating: a review of Shaker fluorescence data

Canadian journal of physiology and pharmacology, 2009-06, Vol.87 (6), p.411-418

2009

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4-aminopyridine prevents the conformational changes associated with p/c-type inactivation in shaker channels

The Journal of pharmacology and experimental therapeutics, 2007-01, Vol.320 (1), p.162-172

2007

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A useful irrigated tip to cannulate distal coronary sinus

The role of mental health home hospitalization care during the COVID‐19 pandemic

Scaling up of highly active antiretroviral therapy in a rural district of Malawi: an effectiveness assessment

The new antiarrhythmic drug vernakalant: ex vivo study of human atrial tissue from sinus rhythm and chronic atrial fibrillation

Heterogeneous expression of repolarizing, voltage-gated K+ currents in adult mouse ventricles

Sequence of Gating Charge Movement and Pore Gating in hERG Activation and Deactivation Pathways

RSD1235 blocks late INa and suppresses early afterdepolarizations and torsades de pointes induced by class III agents

External Ba(2+) block of Kv4.2 channels is enhanced in the closed-inactivated state

Modeling of high-affinity binding of the novel atrial anti-arrhythmic agent, vernakalant, to Kv1.5 channels

The Ca(v)1.4 calcium channel is a critical regulator of T cell receptor signaling and naive T cell homeostasis

Allosteric coupling of the inner activation gate to the outer pore of a potassium channel

Risk of sural nerve injury during lateral distal Achilles tendinoscopy: A Cadaver Study

Cardiac Ryanodine Receptor (Ryr2)-mediated Calcium Signals Specifically Promote Glucose Oxidation via Pyruvate Dehydrogenase

Gating charge movement precedes ionic current activation in hERG channels

Modulation of human ether-Ã -go-go-related K+ (HERG) channel inactivation by Cs+ and K

Kv1.5 Is an Important Component of Repolarizing K+ Current in Canine Atrial Myocytes

Basis for allosteric open-state stabilization of voltage-gated potassium channels by intracellular cations

Rb+ flux through hERG channels affects the potency of channel blocking drugs: correlation with data obtained using a high-throughput Rb+ efflux assay

An Activation Gating Switch in Kv1.2 Is Localized to a Threonine Residue in the S2-S3 Linker

The neutral, hydrophobic isoleucine at position I521 in the extracellular S4 domain of hERG contributes to channel gating equilibrium

ShakerIR and Kv1.5 mutant channels with enhanced slow inactivation also exhibit K+o-dependent resting inactivation

A novel mechanism for LQT3 with 2:1 block: A pore-lining mutation in Nav1.5 significantly affects voltage-dependence of activation

Kinetic analysis of the effects of H+ or Ni2+ on Kv1.5 current shows that both ions enhance slow inactivation and induce resting inactivation

Use of voltage clamp fluorimetry in understanding potassium channel gating: a review of Shaker fluorescence data

4-aminopyridine prevents the conformational changes associated with p/c-type inactivation in shaker channels

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