Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M H Antoine

Showing results (11-20 of 31) with videos related to

Pageof 4
Sort By:
European Journal of Pharmacology|October 17, 1996
Hydroxylamine, a nitric oxide donor, inhibits insulin release and activates K+ATP channelsM H Antoine, R Ouedraogo, J Sergooris, et al.
Biochemical Pharmacology|April 25, 1997
3-Morpholinosydnonimine as instigator of a glibenclamide-sensitive reduction in the insulin secretory rateM H Antoine, R Ouedraogo, M Hermann, et al.
Current Medicinal Chemistry|May 12, 2004
Recent developments in the chemistry of potassium channel activators: the cromakalim analogsS Sebille, P De Tullio, S Boverie, et al.
European Journal of Pharmacology|June 5, 1992
Mechanical and ionic response of rat aorta to diazoxideM H Antoine, G Berkenboom, Z Y Fang, et al.
Diabetologia|July 25, 2000
A potent diazoxide analogue activating ATP-sensitive K+ channels and inhibiting insulin releaseP Lebrun, P Arkhammar, M H Antoine, et al.
Experientia|September 15, 1994
Cationic and secretory effects of BPDZ 44 and diazoxide in rat pancreatic isletsM H Antoine, B Pirotte, M Hermann, et al.
Pflugers Archiv : European Journal of Physiology|January 1, 1996
Dynamics of the cationic, bioelectrical and secretory responses to formycin A in pancreatic islet cellsP Lebrun, E Renström, M H Antoine, et al.
Advances in Experimental Medicine and Biology|January 1, 1997
Pyridothiadiazines as potent inhibitors of glucose-induced insulin releaseP Lebrun, M H Antoine, R Ouedraogo, et al.
Pharmacology|January 1, 1990
Hypoglycemic sulfonylureas antagonize the effects of cromakalim and pinacidil on 86Rb fluxes and contractile activity in the rat aortaP Lebrun, Z Y Fang, M H Antoine, et al.
Biochemical Pharmacology|April 20, 1994
A pyridothiadiazine (BPDZ 44) as a new and potent activator of ATP-sensitive K+ channelsB Pirotte, M H Antoine, P de Tullio, et al.
Pageof 4

Showing results (11-20 of 31) with videos related to

Sort By:
Pageof 4
European Journal of Pharmacology|October 17, 1996
Hydroxylamine, a nitric oxide donor, inhibits insulin release and activates K+ATP channelsM H Antoine, R Ouedraogo, J Sergooris, et al.
Biochemical Pharmacology|April 25, 1997
3-Morpholinosydnonimine as instigator of a glibenclamide-sensitive reduction in the insulin secretory rateM H Antoine, R Ouedraogo, M Hermann, et al.
Current Medicinal Chemistry|May 12, 2004
Recent developments in the chemistry of potassium channel activators: the cromakalim analogsS Sebille, P De Tullio, S Boverie, et al.
European Journal of Pharmacology|June 5, 1992
Mechanical and ionic response of rat aorta to diazoxideM H Antoine, G Berkenboom, Z Y Fang, et al.
Diabetologia|July 25, 2000
A potent diazoxide analogue activating ATP-sensitive K+ channels and inhibiting insulin releaseP Lebrun, P Arkhammar, M H Antoine, et al.
Experientia|September 15, 1994
Cationic and secretory effects of BPDZ 44 and diazoxide in rat pancreatic isletsM H Antoine, B Pirotte, M Hermann, et al.
Pflugers Archiv : European Journal of Physiology|January 1, 1996
Dynamics of the cationic, bioelectrical and secretory responses to formycin A in pancreatic islet cellsP Lebrun, E Renström, M H Antoine, et al.
Advances in Experimental Medicine and Biology|January 1, 1997
Pyridothiadiazines as potent inhibitors of glucose-induced insulin releaseP Lebrun, M H Antoine, R Ouedraogo, et al.
Pharmacology|January 1, 1990
Hypoglycemic sulfonylureas antagonize the effects of cromakalim and pinacidil on 86Rb fluxes and contractile activity in the rat aortaP Lebrun, Z Y Fang, M H Antoine, et al.
Biochemical Pharmacology|April 20, 1994
A pyridothiadiazine (BPDZ 44) as a new and potent activator of ATP-sensitive K+ channelsB Pirotte, M H Antoine, P de Tullio, et al.
Pageof 4