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Professor Jules Hancox

Professor Jules Hancox

Professor Jules Hancox
DSc (Bristol), B.Sc.(Leeds), Ph.D.(St.And.)

Professor of Cardiac Electrophysiology

Office C39A
Biomedical Sciences Building,
University Walk, Bristol BS8 1TD
(See a map)

+44 (0) 117 331 2292
+44 (0) 117 331 2295


I am interested in elucidating the function of small membrane proteins (ion channels and exchangers) responsible for generating electrical activity of cells in the heart. I have a long-standing interest is the basis of the activity of a key part of the heart's electrical conducting system called the atrioventricular (AV) node, which co-ordinates the normal sequence of beating of the heart's upper and lower chambers (the atria and ventricles). We study single AV node cells using electrophysiological and imaging techniques. Recent work in collaboration with Clive Orchard , Andrew James and Prof Godfrey Smith (Glasgow) has been focused on the effects of acidosis, endothelin-1 and calcium-cycling on AV node cellular electrophysiology. Collaborative work with colleagues in Manchester (Prof Mark Boyett, Prof Henggui Zhang) and Kings College London (Dr Oleg Aslanidi) is focused on producing biophysically accurate models of the AV node and atrium.

I also have a long-standing interest in the electrophysiology and pharmacology of the hERG potassium channel, which plays an important role in drug-induced arrhythmias and in the congenital 'Short QT syndrome'. Using a combination of molecular and electrophysiological methods, we have studied mechanisms of hERG blockade by a range of drugs and identified in vitro the antiarrhythmic disopyramide as an effective inhibitor of the hERG mutant K+ channel responsible for one form of Short QT syndrome. We are also investigating different K+ channel mutations involved in other forms of this syndrome and are focused both on identifying pharmacological agents that can inhibit Short QT mutant channels and on identifying arrhythmia substrates in the syndrome (in collaboration with Prof Henggui Zhang and colleagues, Manchester).

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Activities / Findings

  • Disruption of hERG function by extracellular acidosis reduces protection against a premature cardiac action potential Read more >


  • cardio


  • Hypertension

Processes and functions

  • Molecular microbiology


  • Electrophysiological recording

Selected publications

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Recent publications

View complete publications list in the University of Bristol publications system

Networks & contacts

  • Dave Bates - Bristol
  • Mark Boyett - Manchester
  • Massimo Caputo - Bristol Heart Institute
  • Chris Dempsey - Biochemistry
  • Bristol Andrew James - Bristol
  • John Vann Jones
  • Cardiology
  • BRI
  • Bristol Clive Orchard - Bristol
  • Godfrey - Glasgow
  • Saadeh Suleiman - Bristol Heart Institute
  • Harry Witchel - Sussex
  • Henggui Zhang - Manchester

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