A plethora of mechanisms in the HERG-related long QT syndrome. Genetics meets electrophysiology

scientific article published on 01 November 1999

A plethora of mechanisms in the HERG-related long QT syndrome. Genetics meets electrophysiology is …
instance of (P31):
scholarly articleQ13442814
editorialQ871232
review articleQ7318358

External links are
P356DOI10.1016/S0008-6363(99)00224-2
P698PubMed publication ID10690299

P2093author name stringD M Roden
J R Balser
P433issue2
P921main subjectelectrophysiologyQ1154774
P304page(s)242-246
P577publication date1999-11-01
P1433published inCardiovascular ResearchQ4642329
P1476titleA plethora of mechanisms in the HERG-related long QT syndrome. Genetics meets electrophysiology
P478volume44

Reverse relations

cites work (P2860)
Q2429435314-3-3 amplifies and prolongs adrenergic stimulation of HERG K+ channel activity
Q33154577A missense mutation (G604S) in the S5/pore region of HERG causes long QT syndrome in a Chinese family with a high incidence of sudden unexpected death
Q35064579A novel approach to identifying antiarrhythmic drug targets
Q34181088BeKm-1 Is a HERG-Specific Toxin that Shares the Structure with ChTx but the Mechanism of Action with ErgTx1
Q33157691Characterization of novel KCNH2 mutations in type 2 long QT syndrome manifesting as seizures
Q36015209Computational biology in the study of cardiac ion channels and cell electrophysiology.
Q57945041Computational biology of propagation in excitable media models of cardiac tissue
Q84920028Expression and immunolocalization of ERG1 potassium channels in the rat kidney
Q36436477Extracellular sodium interacts with the HERG channel at an outer pore site
Q47414764Functional interaction between extracellular sodium, potassium and inactivation gating in HERG channels
Q33150817Mechanisms of genetic arrhythmias: from DNA to ECG.
Q35783131Modelling and imaging cardiac repolarization abnormalities
Q92025079R534C mutation in hERG causes a trafficking defect in iPSC-derived cardiomyocytes from patients with type 2 long QT syndrome
Q37193903Recurrent intrauterine fetal loss due to near absence of HERG: clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation
Q34201433The impact of drug-induced QT interval prolongation on drug discovery and development

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