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Current Medicinal Chemistry
|
July 23, 2002
Large-conductance, ca(2+)-activated k(+) channels: function, pharmacology and drugs
V Calderone
Journal of Pharmacological and Toxicological Methods
|
September 19, 1998
An alternative method to evaluate the nature of an antagonist and its potency: a theoretical approach
V Calderone
Journal of Pharmacological and Toxicological Methods
|
August 28, 1999
Intrinsic activity and EC50: the simplest tools for the evaluation of the dissociation constant of a partial agonist
V Calderone, E Martinotti
Journal of Pharmacological and Toxicological Methods
|
January 27, 1999
A simplified empirical approach to evaluate the dissociation constant of a full agonist by the irreversible receptor inactivation method
V Calderone, E Martinotti
Minerva Medica
|
July 3, 2002
[Ventricular arrhythmias. A potential risk associated with the use of non-cardiovascular drugs prolonging the QT interval]
V Calderone, I Cavero
Current Medicinal Chemistry
|
March 15, 2006
NO-releasing hybrids of cardiovascular drugs
A Martelli, S Rapposelli, V Calderone
Cardiovascular & Hematological Agents in Medicinal Chemistry
|
January 29, 2008
New emerging prospects in the pharmacotherapy of hypertension
A Balsamo, V Calderone, S Rapposelli
Cardiovascular & Hematological Agents in Medicinal Chemistry
|
February 3, 2007
Cardiac ATP-sensitive potassium channels: a potential target for an anti-ischaemic pharmacological strategy
L Testai, S Rapposelli, V Calderone
Journal of Biological Inorganic Chemistry : JBIC : a Publication of the Society of Biological Inorganic Chemistry
|
January 12, 2017
Solving the crystal structure of human calcium-free S100Z: the siege and conquer of one of the last S100 family strongholds
V Calderone, M Fragai, G Gallo, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology
|
November 24, 1998
Influence of depolarization on vasorelaxant potency and efficacy of Ca2+ entry blockers, K+ channel openers, nitrate derivatives, salbutamol and papaverine in rat aortic rings
M Magnon, V Calderone, A Floch, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 43) with videos related to
Sort By:
Page
of 5
Current Medicinal Chemistry
|
July 23, 2002
Large-conductance, ca(2+)-activated k(+) channels: function, pharmacology and drugs
V Calderone
Journal of Pharmacological and Toxicological Methods
|
September 19, 1998
An alternative method to evaluate the nature of an antagonist and its potency: a theoretical approach
V Calderone
Journal of Pharmacological and Toxicological Methods
|
August 28, 1999
Intrinsic activity and EC50: the simplest tools for the evaluation of the dissociation constant of a partial agonist
V Calderone, E Martinotti
Journal of Pharmacological and Toxicological Methods
|
January 27, 1999
A simplified empirical approach to evaluate the dissociation constant of a full agonist by the irreversible receptor inactivation method
V Calderone, E Martinotti
Minerva Medica
|
July 3, 2002
[Ventricular arrhythmias. A potential risk associated with the use of non-cardiovascular drugs prolonging the QT interval]
V Calderone, I Cavero
Current Medicinal Chemistry
|
March 15, 2006
NO-releasing hybrids of cardiovascular drugs
A Martelli, S Rapposelli, V Calderone
Cardiovascular & Hematological Agents in Medicinal Chemistry
|
January 29, 2008
New emerging prospects in the pharmacotherapy of hypertension
A Balsamo, V Calderone, S Rapposelli
Cardiovascular & Hematological Agents in Medicinal Chemistry
|
February 3, 2007
Cardiac ATP-sensitive potassium channels: a potential target for an anti-ischaemic pharmacological strategy
L Testai, S Rapposelli, V Calderone
Journal of Biological Inorganic Chemistry : JBIC : a Publication of the Society of Biological Inorganic Chemistry
|
January 12, 2017
Solving the crystal structure of human calcium-free S100Z: the siege and conquer of one of the last S100 family strongholds
V Calderone, M Fragai, G Gallo, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology
|
November 24, 1998
Influence of depolarization on vasorelaxant potency and efficacy of Ca2+ entry blockers, K+ channel openers, nitrate derivatives, salbutamol and papaverine in rat aortic rings
M Magnon, V Calderone, A Floch, et al.
Page
of 5