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Cardiovascular Research
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October 26, 1999
Structure and function of cardiac potassium channels
D J Snyders
Molecular Pharmacology
|
June 1, 1996
High affinity open channel block by dofetilide of HERG expressed in a human cell line
D J Snyders, A Chaudhary
Circulation Research
|
February 1, 1990
Effects of quinidine on the sodium current of guinea pig ventricular myocytes. Evidence for a drug-associated rested state with altered kinetics
D J Snyders, L M Hondeghem
Cardiovascular Research
|
March 1, 1997
Electrophysiological and pharmacological correspondence between Kv4.2 current and rat cardiac transient outward current
S W Yeola, D J Snyders
Proceedings of the Western Pharmacology Society
|
January 1, 1987
Drug associated sodium channels inactivate and reactivate at more negative potentials than drug-free channels
D J Snyders, L M Hondeghem
Circulation
|
February 1, 1990
Class III antiarrhythmic agents have a lot of potential but a long way to go. Reduced effectiveness and dangers of reverse use dependence
L M Hondeghem, D J Snyders
Circulation Research
|
September 1, 1995
Determinants of antiarrhythmic drug action. Electrostatic and hydrophobic components of block of the human cardiac hKv1.5 channel
D J Snyders, S W Yeola
Biophysical Journal
|
July 2, 1998
Evidence for multiple open and inactivated states of the hKv1.5 delayed rectifier
T C Rich, D J Snyders
Archives Internationales De Physiologie Et De Biochimie
|
February 1, 1978
Modification of cardiac pace-maker current by 4-aminopyridine [proceedings]
D J Snyders, P P van Bogaert
Archives Internationales De Physiologie Et De Biochimie
|
May 1, 1979
Intracellular pH transients induced by chloride substitution in cardiac Purkyne fibres [proceedings]
P P van Bogaert, D J Snyders
Page
of 5
Search research articles
Search
Showing results (1-10 of 49) with videos related to
Sort By:
Page
of 5
Cardiovascular Research
|
October 26, 1999
Structure and function of cardiac potassium channels
D J Snyders
Molecular Pharmacology
|
June 1, 1996
High affinity open channel block by dofetilide of HERG expressed in a human cell line
D J Snyders, A Chaudhary
Circulation Research
|
February 1, 1990
Effects of quinidine on the sodium current of guinea pig ventricular myocytes. Evidence for a drug-associated rested state with altered kinetics
D J Snyders, L M Hondeghem
Cardiovascular Research
|
March 1, 1997
Electrophysiological and pharmacological correspondence between Kv4.2 current and rat cardiac transient outward current
S W Yeola, D J Snyders
Proceedings of the Western Pharmacology Society
|
January 1, 1987
Drug associated sodium channels inactivate and reactivate at more negative potentials than drug-free channels
D J Snyders, L M Hondeghem
Circulation
|
February 1, 1990
Class III antiarrhythmic agents have a lot of potential but a long way to go. Reduced effectiveness and dangers of reverse use dependence
L M Hondeghem, D J Snyders
Circulation Research
|
September 1, 1995
Determinants of antiarrhythmic drug action. Electrostatic and hydrophobic components of block of the human cardiac hKv1.5 channel
D J Snyders, S W Yeola
Biophysical Journal
|
July 2, 1998
Evidence for multiple open and inactivated states of the hKv1.5 delayed rectifier
T C Rich, D J Snyders
Archives Internationales De Physiologie Et De Biochimie
|
February 1, 1978
Modification of cardiac pace-maker current by 4-aminopyridine [proceedings]
D J Snyders, P P van Bogaert
Archives Internationales De Physiologie Et De Biochimie
|
May 1, 1979
Intracellular pH transients induced by chloride substitution in cardiac Purkyne fibres [proceedings]
P P van Bogaert, D J Snyders
Page
of 5