Pharmacogenetics of antiarrhythmic therapy (Q36548713)

14 August 2017

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title

Pharmacogenetics of antiarrhythmic therapy (English)

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14 August 2017

Dawood Darbar

1

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14 August 2017

Dan M Roden

series ordinal

2

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14 August 2017

language of work or name

English

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publication date

1 August 2006

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Expert Opinion on Pharmacotherapy

14 August 2017

published in

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14 August 2017

volume

7

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14 August 2017

issue

12

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14 August 2017

page(s)

1583-1590

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Effect of acetylator phenotype on the rate at which procainamide induces antinuclear antibodies and the lupus syndrome

14 August 2017

cites work

1 reference

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Polymorphic hydroxylation of Debrisoquine in man.

21 January 2018

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Defective N-oxidation of sparteine in man: A new pharmacogenetic defect

21 January 2018

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Molecular mechanisms of genetic polymorphisms of drug metabolism

21 January 2018

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Pharmacogenetics and drug development: the path to safer and more effective drugs

21 January 2018

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Pharmacogenomics: translating functional genomics into rational therapeutics

21 January 2018

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A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

21 January 2018

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Genotyping and phenotyping the cytochrome p-450 enzymes

21 January 2018

1 reference

https://api.crossref.org/works/10.1517/14656566.7.12.1583

Association between CYP2C9 genetic variants and anticoagulation-related outcomes during warfarin therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1517/14656566.7.12.1583

Genetic variability in cytochrome P450 3A5 and in vivo cytochrome P450 3A activity: some answers but still questions

21 January 2018

1 reference

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Drug-induced prolongation of the QT interval

21 January 2018

1 reference

https://api.crossref.org/works/10.1517/14656566.7.12.1583

Functional characterization of human N-acetyltransferase 2 (NAT2) single nucleotide polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1517/14656566.7.12.1583

Impact of genetic polymorphisms in transmembrane carrier-systems on drug and xenobiotic distribution

21 January 2018

1 reference

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Functional polymorphisms of the human multidrug-resistance gene: multiple sequence variations and correlation of one allele with P-glycoprotein expression and activity in vivo

21 January 2018

1 reference

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Drugs as P-glycoprotein substrates, inhibitors, and inducers

21 January 2018

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Inhibition of P-glycoprotein-mediated drug transport: A unifying mechanism to explain the interaction between digoxin and quinidine [seecomments]

21 January 2018

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A common polymorphism associated with antibiotic-induced cardiac arrhythmia

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517/14656566.7.12.1583

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

21 January 2018

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Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia.

21 January 2018

1 reference

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

21 January 2018

1 reference

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Electrocardiographic and Clinical Predictors of Torsades de Pointes Induced by Almokalant Infusion in Patients with Chronic Atrial Fibrillation or Flutter: A Prospective Study

21 January 2018

1 reference

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Rapid inactivation determines the rectification and [K ]o dependence of the rapid component of the delayed rectifier K current in cardiac cells.

21 January 2018

1 reference

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Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia

21 January 2018

1 reference

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SNP S1103Y in the cardiac sodium channel gene SCN5A is associated with cardiac arrhythmias and sudden death in a white family

21 January 2018

1 reference

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Congenital long-QT syndrome caused by a novel mutation in a conserved acidic domain of the cardiac Na channel

21 January 2018

1 reference

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Sodium channel blockers identify risk for sudden death in patients with ST-segment elevation and right bundle branch block but structurally normal hearts

21 January 2018

1 reference

https://api.crossref.org/works/10.1517/14656566.7.12.1583

A ubiquitous splice variant and a common polymorphism affect heterologous expression of recombinant human SCN5A heart sodium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1517/14656566.7.12.1583

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517/14656566.7.12.1583

How Really Rare Are Rare Diseases?:

21 January 2018

1 reference

https://api.crossref.org/works/10.1517/14656566.7.12.1583

10.1517/14656566.7.12.1583

21 January 2018

Identifiers

DOI

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release_rlc5nlclbfacdlsunzujmlobwq

14 August 2017

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/rlc5nlclbfacdlsunzujmlobwq

mapped directly with Wikidata item

24 November 2022

based on heuristic

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