Pharmacogenetics and cardiac ion channels (Q36339192)

13 August 2017

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title

Pharmacogenetics and cardiac ion channels (English)

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13 August 2017

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13 August 2017

Torsten K Roepke

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13 August 2017

publication date

15 December 2005

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13 August 2017

published in

Vascular Pharmacology

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13 August 2017

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13 August 2017

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13 August 2017

page(s)

90-106

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MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia

13 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Differential control of the hyperpolarization-activated current (i(f)) by cAMP gating and phosphatase inhibition in rabbit sino-atrial node myocytes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Ethnic differences in cardiac potassium channel variants: implications for genetic susceptibility to sudden cardiac death and genetic testing for congenital long QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Molecular biology and cellular mechanisms of Brugada and long QT syndromes in infants and young children

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

A neutral amino acid change in segment IIS4 dramatically alters the gating properties of the voltage-dependent sodium channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

The cardiac sodium channel: gating function and molecular pharmacology

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

The anatomical substrates of wolff-parkinson-white syndrome. A clinicopathologic correlation in seven patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Mutation in the KCNQ1 gene leading to the short QT-interval syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

A common antitussive drug, clobutinol, precipitates the long QT syndrome 2

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Molecular mechanism for an inherited cardiac arrhythmia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Macromolecular complexes regulating cardiac ryanodine receptor function.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Expression of voltage-gated K+ channels in human atrium.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

C-terminal HERG mutations: the role of hypokalemia and a KCNQ1-associated mutation in cardiac event occurrence

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Blockers of the Kv1.5 channel for the treatment of atrial arrhythmias

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Further characterization of the syndrome of right bundle branch block, ST segment elevation, and sudden cardiac death

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Identification of a genetic locus for familial atrial fibrillation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Sudden death associated with short-QT syndrome linked to mutations in HERG.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Ion channel remodeling is related to intraoperative atrial effective refractory periods in patients with paroxysmal and persistent atrial fibrillation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

The incorporation of an ion channel gene mutation associated with the long QT syndrome (Q9E-hMiRP1) in a plasmid vector for site-specific arrhythmia gene therapy: in vitro and in vivo feasibility studies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

From ionic currents to molecular mechanisms: the structure and function of voltage-gated sodium channels

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Charybdotoxin Binding in the IKs Pore Demonstrates Two MinK Subunits in Each Channel Complex

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

KCNQ1 gain-of-function mutation in familial atrial fibrillation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Pentamidine reduces hERG expression to prolong the QT interval

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Analysis of the cyclic nucleotide binding domain of the HERG potassium channel and interactions with KCNE2

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Rate vs rhythm control in patients with atrial fibrillation: a meta-analysis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Unusual effects of a QT-prolonging drug, arsenic trioxide, on cardiac potassium currents

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Multiple mechanisms of Na+ channel--linked long-QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Protein trafficking abnormalities: a new mechanism in drug-induced long QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Mutations in the long QT gene, KCNQ1, are an uncommon cause of atrial fibrillation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Antisense oligodeoxynucleotides directed against Kv1.5 mRNA specifically inhibit ultrarapid delayed rectifier K+ current in cultured adult human atrial myocytes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Retention in the endoplasmic reticulum as a mechanism of dominant-negative current suppression in human long QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

The binding site for channel blockers that rescue misprocessed human long QT syndrome type 2 ether-a-gogo-related gene (HERG) mutations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Role of the cytosolic chaperones Hsp70 and Hsp90 in maturation of the cardiac potassium channel HERG.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Expression and coassociation of ERG1, KCNQ1, and KCNE1 potassium channel proteins in horse heart

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Association of human connexin40 gene polymorphisms with atrial vulnerability as a risk factor for idiopathic atrial fibrillation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Novel mechanism associated with an inherited cardiac arrhythmia: defective protein trafficking by the mutant HERG (G601S) potassium channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Short QT Syndrome: a familial cause of sudden death

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

A targeting motif involved in sodium channel clustering at the axonal initial segment

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Primary structure and functional expression of the human cardiac tetrodotoxin-insensitive voltage-dependent sodium channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Molecular genetics of ion channel diseases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Ryanodine receptor mutations associated with stress-induced ventricular tachycardia mediate increased calcium release in stimulated cardiomyocytes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Prevalence of diagnosed atrial fibrillation in adults: national implications for rhythm management and stroke prevention: the AnTicoagulation and Risk Factors in Atrial Fibrillation (ATRIA) Study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Potassium leak channels and the KCNK family of two-P-domain subunits

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Identification of a gene responsible for familial Wolff-Parkinson-White syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Novel PRKAG2 mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Pharmacological rescue of trafficking defective HERG channels formed by coassembly of wild-type and long QT mutant N470D subunits

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

The Brugada syndrome: clinical, electrophysiologic and genetic aspects.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Idiopathic short QT interval: a new clinical syndrome?

7 January 2021

2 references

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

7 January 2021

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

inferred from DOI database lookup

7 January 2021

based on heuristic

Conduction disturbances and increased atrial vulnerability in Connexin40-deficient mice analyzed by transesophageal stimulation

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Probucol aggravates long QT syndrome associated with a novel missense mutation M124T in the N-terminus of HERG.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

KCR1, a membrane protein that facilitates functional expression of non-inactivating K+ currents associates with rat EAG voltage-dependent K+ channels

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Reconstitution of IKATP: an inward rectifier subunit plus the sulfonylurea receptor

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Identification and functional characterization of a novel KCNE2 (MiRP1) mutation that alters HERG channel kinetics

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

KCNE2 protein is expressed in ventricles of different species, and changes in its expression contribute to electrical remodeling in diseased hearts

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Molecular basis of transient outward potassium current downregulation in human heart failure: a decrease in Kv4.3 mRNA correlates with a reduction in current density

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Phenotypic Characterization of a Novel Long-QT Syndrome Mutation (R1623Q) in the Cardiac Sodium Channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Channel structure and drug-induced cardiac arrhythmias

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

A new family of outwardly rectifying potassium channel proteins with two pore domains in tandem.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Additional gene variants reduce effectiveness of beta-blockers in the LQT1 form of long QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

The natural history of lone atrial fibrillation. A population-based study over three decades

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

An LQT mutant minK alters KvLQT1 trafficking

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Cardiac-enriched LIM domain protein fhl2 is required to generate I(Ks) in a heterologous system

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

I Kr drug response is modulated by KCR1 in transfected cardiac and noncardiac cell lines

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Pentamidine-induced long QT syndrome and block of hERG trafficking

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Autosomal recessive catecholamine- or exercise-induced polymorphic ventricular tachycardia: clinical features and assignment of the disease gene to chromosome 1p13-21.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Association of the human minK gene 38G allele with atrial fibrillation: evidence of possible genetic control on the pathogenesis of atrial fibrillation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Andersen mutations of KCNJ2 suppress the native inward rectifier current IK1 in a dominant-negative fashion

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Catecholaminergic polymorphic ventricular tachycardia in children. A 7-year follow-up of 21 patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Voltage-gated ion channels and hereditary disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Identification of a Conserved Ankyrin-binding Motif in the Family of Sodium Channel α Subunits

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Factors Predisposing to the Development of Atrial Fibrillation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Block of Kcnk3 by protons. Evidence that 2-P-domain potassium channel subunits function as homodimers.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Hydrophobic substitution mutations in the S4 sequence alter voltage-dependent gating in Shaker K+ channels

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Determination of the subunit stoichiometry of a voltage-activated potassium channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Pore loops: an emerging theme in ion channel structure

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Drug-induced long-QT syndrome associated with a subclinical SCN5A mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Requirement of a macromolecular signaling complex for beta adrenergic receptor modulation of the KCNQ1-KCNE1 potassium channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Familial Wolff-Parkinson-White syndrome with cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

A minK-HERG complex regulates the cardiac potassium current I(Kr)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Recurrent third-trimester fetal loss and maternal mosaicism for long-QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

A structural basis for drug-induced long QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Nav1.5 E1053K mutation causing Brugada syndrome blocks binding to ankyrin-G and expression of Nav1.5 on the surface of cardiomyocytes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Crystal structure and functional analysis of the HERG potassium channel N terminus: a eukaryotic PAS domain

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Evidence for a cardiac ion channel mutation underlying drug-induced QT prolongation and life-threatening arrhythmias

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

New ideas about atrial fibrillation 50 years on.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Molecular basis of functional voltage-gated K+ channel diversity in the mammalian myocardium

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Genetic manipulation of cardiac K(+) channel function in mice: what have we learned, and where do we go from here?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Inward rectifier potassium channels

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

KCNQ1/KCNE1 potassium channels in mammalian vestibular dark cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Pre-excitation syndrome in Leber's hereditary optic neuropathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Structure and function of sodium channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Primary structure of Electrophorus electricus sodium channel deduced from cDNA sequence

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Alteration of voltage-dependence of Shaker potassium channel by mutations in the S4 sequence

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

N ‐glycosylation‐dependent block is a novel mechanism for drug‐induced cardiac arrhythmia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

S4 mutations alter gating currents of Shaker K channels

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Association between HERG K897T polymorphism and QT interval in middle-aged Finnish women

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Mutations in an S4 segment of the adult skeletal muscle sodium channel cause paramyotonia congenita

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Acid alpha-glucosidase deficiency (glycogenosis type II, Pompe disease).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Pharmacological rescue of human K(+) channel long-QT2 mutations: human ether-a-go-go-related gene rescue without block

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Bidirectional tachycardia in a child. A study using His bundle electrography

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Pharmacogenetics and drug-induced arrhythmias

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Regulation of KChIP2 potassium channel beta subunit gene expression underlies the gradient of transient outward current in canine and human ventricle

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Interaction with GM130 during HERG ion channel trafficking. Disruption by type 2 congenital long QT syndrome mutations. Human Ether-à-go-go-Related Gene.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

The HCN gene family: molecular basis of the hyperpolarization-activated pacemaker channels

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Identification of a gene encoding a hyperpolarization-activated pacemaker channel of brain

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Pacemaker channel dysfunction in a patient with sinus node disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Primary structure of a beta subunit of alpha-dendrotoxin-sensitive K+ channels from bovine brain.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Single-channel characteristics of wild-type IKs channels and channels formed with two minK mutants that cause long QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

A common polymorphism associated with antibiotic-induced cardiac arrhythmia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

A fundamental role for KChIPs in determining the molecular properties and trafficking of Kv4.2 potassium channels

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Potassium channel mechanics

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Polymorphism screening in the cardiac K+ channel gene KCNA5.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

The inward rectification mechanism of the HERG cardiac potassium channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Molecular basis of the long-QT syndrome associated with deafness

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Mutations in the hminK gene cause long QT syndrome and suppress lKs function

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Structural parts involved in activation and inactivation of the sodium channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Role of a KCNH2 polymorphism (R1047 L) in dofetilide-induced Torsades de Pointes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

The long QT interval is not only inherited but is also linked to cardiac hypertrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Cloning of a membrane protein that induces a slow voltage-gated potassium current

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

A sodium-channel mutation causes isolated cardiac conduction disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Calsequestrin determines the functional size and stability of cardiac intracellular calcium stores: Mechanism for hereditary arrhythmia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Renin-angiotensin system gene polymorphisms and atrial fibrillation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

IsK and KvLQT1: Mutation in Either of the Two Subunits of the Slow Component of the Delayed Rectifier Potassium Channel Can Cause Jervell and Lange-Nielsen Syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-Nielsen

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Functional characterization of a trafficking-defective HCN4 mutation, D553N, associated with cardiac arrhythmia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

A trafficking defective, Brugada syndrome-causing SCN5A mutation rescued by drugs

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Novel mutations in domain I of SCN5A cause Brugada syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Molecular genetic analysis of PRKAG2 in sporadic Wolff-Parkinson-White syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Cardiac conduction abnormalities in mice lacking the gap junction protein connexin40

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Molecular mechanism of cAMP modulation of HCN pacemaker channels.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

K(+)-induced stimulation of K+ secretion involves activation of the IsK channel in vestibular dark cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

FKBP12.6 deficiency and defective calcium release channel (ryanodine receptor) function linked to exercise-induced sudden cardiac death

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Clinical and molecular heterogeneity in the Brugada syndrome: a novel gene locus on chromosome 3.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

Correction of defective protein trafficking of a mutant HERG potassium channel in human long QT syndrome. Pharmacological and temperature effects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VPH.2005.07.013

10.1016/J.VPH.2005.07.013

7 January 2021

Identifiers

DOI

1 reference

13 August 2017

1 reference