Search filters

List of works by Brian P. Delisle

A KCNQ1 mutation causes a high penetrance for familial atrial fibrillation

scientific article published on 25 January 2013

A KCNQ1 mutation contributes to the concealed type 1 long QT phenotype by limiting the Kv7.1 channel conformational changes associated with protein kinase A phosphorylation

scientific article published in March 2014

A Practical ECG Criterion to Unmask Left Accessory AV Connections in Patients With Subtle Preexcitation

scientific article published on 20 May 2015

A molecular mechanism for adrenergic-induced long QT syndrome

scientific article published on 4 March 2014

A novel KCNQ1 missense mutation identified in a patient with juvenile-onset atrial fibrillation causes constitutively open IKs channels.

scientific article published in October 2013

A snapshot in time: Does exercise training impact the muscle circadian clock in patients?

scientific article

Adenosine Testing in Atrial Flutter Ablation: Unmasking of Dormant Conduction Across the Cavotricuspid Isthmus and Risk of Recurrence

scientific article published on 23 May 2013

Biology of cardiac arrhythmias: ion channel protein trafficking

scientific article published on June 2004

Circadian Regulation of Cardiac Arrhythmias and Electrophysiology

scientific article published on 15 March 2024

Coexistence of hERG current block and disruption of protein trafficking in ketoconazole-induced long QT syndrome

scientific article published on 29 October 2007

Comparison of HERG channel blocking effects of various beta-blockers-- implication for clinical strategy

scientific article published on March 2006

Digoxin and short term mortality after acute STEMI: Results from the MAGIC trial

scientific article published on 13 May 2016

Drug-induced long QT syndrome: hERG K+ channel block and disruption of protein trafficking by fluoxetine and norfluoxetine.

scientific article

Editorial: Ion Channel Trafficking and Cardiac Arrhythmias

scientific article published on 25 September 2018

Functional Neuroplasticity in the Nucleus Tractus Solitarius and Increased Risk of Sudden Death in Mice with Acquired Temporal Lobe Epilepsy

scientific article published in September 2017

Gender differences in management of patients undergoing catheter ablation of atrioventricular nodal reentry tachycardia

scientific article published on 10 June 2019

Genetic basis for the origin of cardiac arrhythmias: implications for therapy

scientific article published in September 2002

High-risk long QT syndrome mutations in the Kv7.1 (KCNQ1) pore disrupt the molecular basis for rapid K(+) permeation

scientific article published on 2 November 2012

Intragenic Suppression of Trafficking-Defective KCNH2 Channels Associated with Long QT Syndrome

scientific article published on 25 April 2005

Junctional ectopic rhythm after AVNRT ablation: An under-recognized complication

scientific article published on 20 December 2017

LUF7244 plus dofetilide rescues aberrant Kv11.1 trafficking and produces functional IKv11.1.

scientific article published on 02 April 2020

Large-scale mutational analysis of Kv11.1 reveals molecular insights into type 2 long QT syndrome

scientific article

Light phase-restricted feeding slows basal heart rate to exaggerate the type-3 long QT syndrome phenotype in mice

scientific article published on 24 October 2014

Long QT syndrome-associated mutations in intrauterine fetal death

scientific article published on April 2013

Mechanism of loss of Kv11.1 K+ current in mutant T421M-Kv11.1-expressing rat ventricular myocytes: interaction of trafficking and gating

scientific article published on 6 November 2012

Mechanistic basis for type 2 long QT syndrome caused by KCNH2 mutations that disrupt conserved arginine residues in the voltage sensor

scientific article published on 02 April 2013

Molecular and functional characterization of common polymorphisms in HERG (KCNH2) potassium channels

scientific article published on 19 February 2004

Molecular heterogeneity of calcium channel beta-subunits in canine and human heart: evidence for differential subcellular localization

scientific article (publication date: 13 April 2004)

Molecular pathogenesis of long QT syndrome type 2

scientific article

Monovalent cations contribute to T-type calcium channel (Cav3.1 and Cav3.2) selectivity

scientific article published in June 2003

Most LQT2 mutations reduce Kv11.1 (hERG) current by a class 2 (trafficking-deficient) mechanism

scientific article published on January 2006

Mutation-Specific Differences in Kv7.1 (KCNQ1) and Kv11.1 (KCNH2) Channel Dysfunction and Long QT Syndrome Phenotypes

scientific article published in 2022

Pharmacological correction of long QT-linked mutations in KCNH2 (hERG) increases the trafficking of Kv11.1 channels stored in the transitional endoplasmic reticulum

scientific article published on 17 July 2013

Properties of WT and mutant hERG K(+) channels expressed in neonatal mouse cardiomyocytes

scientific article published on 2 April 2010

R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation

scientific article published on 17 September 2010

Small GTPase Rab11b regulates degradation of surface membrane L-type Cav1.2 channels

scientific article published on 19 January 2011

Small GTPase determinants for the Golgi processing and plasmalemmal expression of human ether-a-go-go related (hERG) K+ channels

scientific article published on 24 November 2008

Tbx3-Mediated Regulation of Cardiac Conduction System Development and Function: Potential Contributions of Alternative RNA Processing

scientific article published on 01 August 2019

Thapsigargin selectively rescues the trafficking defective LQT2 channels G601S and F805C.

scientific article published in July 2003

The Promise and Peril of Precision Medicine: Phenotyping Still Matters Most.

scientific article published on 8 October 2016

The cardiomyocyte molecular clock regulates the circadian expression of Kcnh2 and contributes to ventricular repolarization

scientific article published on 19 February 2015

The cardiomyocyte molecular clock, regulation of Scn5a, and arrhythmia susceptibility

scientific article published on 30 January 2013

Trafficking-deficient hERG K⁺ channels linked to long QT syndrome are regulated by a microtubule-dependent quality control compartment in the ER.

scientific article

Paulina is supported by:

About Paulina

Help