A common polymorphism associated with antibiotic-induced cardiac arrhythmia (Q28138550)

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scientific article (publication date: 12 September 2000)

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English	A common polymorphism associated with antibiotic-induced cardiac arrhythmia	scientific article (publication date: 12 September 2000)

Statements

instance of

scholarly article

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title

A common polymorphism associated with antibiotic-induced cardiac arrhythmia (English)

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main subject

heart arrhythmia

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author name string

F Sesti

series ordinal

1

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G W Abbott

series ordinal

2

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J Wei

series ordinal

3

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K T Murray

series ordinal

4

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S Saksena

series ordinal

5

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P J Schwartz

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6

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S G Priori

series ordinal

7

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D M Roden

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8

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A L George

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9

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S A Goldstein

series ordinal

10

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language of work or name

English

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publication date

12 September 2000

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published in

Proceedings of the National Academy of Sciences of the United States of America

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volume

97

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issue

19

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page(s)

10613-8

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cites work

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

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

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20 March 2017

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20 March 2017

Ion channels--basic science and clinical disease

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20 March 2017

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29 September 2017

Mechanisms and management of proarrhythmia

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29 September 2017

Multiple mechanisms in the long-QT syndrome. Current knowledge, gaps, and future directions. The SADS Foundation Task Force on LQTS.

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29 September 2017

Molecular genetic insights into cardiovascular disease

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29 September 2017

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29 September 2017

Molecular mechanism for an inherited cardiac arrhythmia

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29 September 2017

QT prolongation and paroxysmal ventricular tachycardia occurring during fever following trimethoprim-sulfamethoxazole administration

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29 September 2017

Oxatomide plasma levels in man during chronic dosing

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29 September 2017

Plasma level monitoring of antiarrhythmic drugs.

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2 June 2018

QT prolongation and torsades de pointes after administration of trimethoprim-sulfamethoxazole

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2 June 2018

Clinical characteristics of patients with ventricular fibrillation during antiarrhythmic drug therapy

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2 June 2018

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

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27 November 2018

Long QT syndrome-associated mutations in the Per-Arnt-Sim (PAS) domain of HERG potassium channels accelerate channel deactivation

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27 November 2018

A prospective study of the effect of I.V. pentamidine therapy on ventricular arrhythmias and QTc prolongation in HIV-infected patients

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27 November 2018

Serum drug concentrations in patients with ischemic heart disease after administration of a sustained release procainamide preparation

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12 December 2020

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Taking the "idio" out of "idiosyncratic": predicting torsades de pointes

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10984545

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12 December 2020

based on heuristic

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A search for type 1 diabetes susceptibility genes in families from the United Kingdom

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https://pubmed.ncbi.nlm.nih.gov/10984545

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12 December 2020

based on heuristic

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Genomics and hypertension: concepts, potentials, and opportunities

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10984545

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12 December 2020

based on heuristic

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An estimate of unique DNA sequence heterozygosity in the human genome

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10984545

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variability of serum concentrations of trimethoprim and sulfamethoxazole during high dose therapy

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10984545

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sudden cardiac death in heart failure. The role of abnormal repolarization

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10984545

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12 December 2020

based on heuristic

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Positional cloning moves from perditional to traditional

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10984545

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10984545

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variations on a theme: cataloging human DNA sequence variation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10984545

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1073/PNAS.180223197

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ADS bibcode

2000PNAS...9710613S

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PMC publication ID

27073

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PubMed publication ID

10984545

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ResearchGate publication ID

12336860

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