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Biochemical and Biophysical Research Communications|November 16, 1992
[125I]EXP985: a highly potent and specific nonpeptide radioligand antagonist for the AT1 angiotensin receptorA T Chiu, D E McCall, W A Roscoe
European Journal of Pharmacology|August 7, 1986
Pharmacological characteristics of receptor-operated and potential-operated Ca2+ channels in rat aortaA T Chiu, D E McCall, P B Timmermans
Biochemical and Biophysical Research Communications|November 15, 1990
[3H]DUP 753, a highly potent and specific radioligand for the angiotensin II-1 receptor subtypeA T Chiu, D E McCall, P E Aldrich, et al.
The Journal of Pharmacology and Experimental Therapeutics|July 1, 1986
Ca++ utilization in the constriction of rat aorta to full and partial alpha-1 adrenoceptor agonistsA T Chiu, D E McCall, M J Thoolen, et al.
Regulatory Peptides|March 19, 1993
Characterization of angiotensin AT1A receptor isoform by its ligand binding signatureA T Chiu, J H Dunscomb, D E McCall, et al.
Receptor|January 1, 1990
Angiotensin II receptor subtypes and their selective nonpeptide ligandsA T Chiu, D E McCall, R J Ardecky, et al.
Journal of Medicinal Chemistry|December 10, 1993
A novel series of selective, non-peptide inhibitors of angiotensin II binding to the AT2 siteM K VanAtten, C L Ensinger, A T Chiu, et al.
European Journal of Pharmacology|November 15, 1988
Non-peptide angiotensin II receptor antagonists. II. Pharmacology of S-8308A T Chiu, D J Carini, A L Johnson, et al.
The Journal of Pharmacology and Experimental Therapeutics|September 1, 1989
Nonpeptide angiotensin II receptor antagonists. III. Structure-function studiesA T Chiu, J V Duncia, D E McCall, et al.
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