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W B Im

Showing results (51-60 of 96) with videos related to

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Molecular Pharmacology|March 1, 1990
Studies on the mechanism of interactions between anesthetic steroids and gamma-aminobutyric acidA receptorsW B Im, D P Blakeman, J P Davis, et al.
British Journal of Pharmacology|March 1, 1995
Interaction of beta-carboline inverse agonists for the benzodiazepine site with another site on GABAA receptorsH K Im, W B Im, D B Carter, et al.
The Journal of Biological Chemistry|April 25, 1985
Omeprazole, a specific inhibitor of gastric (H+-K+)-ATPase, is a H+-activated oxidizing agent of sulfhydryl groupsW B Im, J C Sih, D P Blakeman, et al.
Biochimica Et Biophysica Acta|May 29, 1987
Gastric antisecretory activity of cycloheximide due to inhibition of protein synthesisW B Im, J P Davis, D P Blakeman, et al.
General and Comparative Endocrinology|February 3, 1998
Seasonal fluctuations in pituitary gland and plasma levels of gonadotropic hormones in RanaJ W Kim, W B Im, H H Choi, et al.
Journal of Medicinal Chemistry|March 1, 1991
Studies on (H(+)-K+)-ATPase inhibitors of gastric acid secretion. Prodrugs of 2-[(2-pyridinylmethyl)sulfinyl]benzimidazole proton-pump inhibitorsJ C Sih, W B Im, A Robert, et al.
The Journal of Biological Chemistry|November 3, 1995
Chloride channel expression with the tandem construct of alpha 6-beta 2 GABAA receptor subunit requires a monomeric subunit of alpha 6 or gamma 2W B Im, J F Pregenzer, J A Binder, et al.
Journal of Medicinal Chemistry|March 18, 1994
Antagonist, partial agonist, and full agonist imidazo[1,5-a]quinoxaline amides and carbamates acting through the GABAA/benzodiazepine receptorR E TenBrink, W B Im, V H Sethy, et al.
British Journal of Pharmacology|February 1, 1997
Alterations of the benzodiazepine site of rat alpha 6 beta 2 gamma 2-GABAA receptor by replacement of several divergent amino-terminal regions with the alpha 1 counterpartsW B Im, J F Pregenzer, J A Binder, et al.
Neuroscience Letters|December 24, 1997
Characterization of ligand binding properties of the 5-HT1D receptors cloned from chimpanzee, gorilla and rhesus monkey in comparison with those from the human and guinea pig receptorsJ F Pregenzer, G L Alberts, J H Bock, et al.
Pageof 10

Showing results (51-60 of 96) with videos related to

Sort By:
Pageof 10
Molecular Pharmacology|March 1, 1990
Studies on the mechanism of interactions between anesthetic steroids and gamma-aminobutyric acidA receptorsW B Im, D P Blakeman, J P Davis, et al.
British Journal of Pharmacology|March 1, 1995
Interaction of beta-carboline inverse agonists for the benzodiazepine site with another site on GABAA receptorsH K Im, W B Im, D B Carter, et al.
The Journal of Biological Chemistry|April 25, 1985
Omeprazole, a specific inhibitor of gastric (H+-K+)-ATPase, is a H+-activated oxidizing agent of sulfhydryl groupsW B Im, J C Sih, D P Blakeman, et al.
Biochimica Et Biophysica Acta|May 29, 1987
Gastric antisecretory activity of cycloheximide due to inhibition of protein synthesisW B Im, J P Davis, D P Blakeman, et al.
General and Comparative Endocrinology|February 3, 1998
Seasonal fluctuations in pituitary gland and plasma levels of gonadotropic hormones in RanaJ W Kim, W B Im, H H Choi, et al.
Journal of Medicinal Chemistry|March 1, 1991
Studies on (H(+)-K+)-ATPase inhibitors of gastric acid secretion. Prodrugs of 2-[(2-pyridinylmethyl)sulfinyl]benzimidazole proton-pump inhibitorsJ C Sih, W B Im, A Robert, et al.
The Journal of Biological Chemistry|November 3, 1995
Chloride channel expression with the tandem construct of alpha 6-beta 2 GABAA receptor subunit requires a monomeric subunit of alpha 6 or gamma 2W B Im, J F Pregenzer, J A Binder, et al.
Journal of Medicinal Chemistry|March 18, 1994
Antagonist, partial agonist, and full agonist imidazo[1,5-a]quinoxaline amides and carbamates acting through the GABAA/benzodiazepine receptorR E TenBrink, W B Im, V H Sethy, et al.
British Journal of Pharmacology|February 1, 1997
Alterations of the benzodiazepine site of rat alpha 6 beta 2 gamma 2-GABAA receptor by replacement of several divergent amino-terminal regions with the alpha 1 counterpartsW B Im, J F Pregenzer, J A Binder, et al.
Neuroscience Letters|December 24, 1997
Characterization of ligand binding properties of the 5-HT1D receptors cloned from chimpanzee, gorilla and rhesus monkey in comparison with those from the human and guinea pig receptorsJ F Pregenzer, G L Alberts, J H Bock, et al.
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