α1-Adrenoceptor-induced contractility in rat aorta is mediated by the α1D subtype

Author:

Buckner Steven A.,Oheim K.W.,Morse P.A.,Knepper S.M.,Hancock A.A.

Publisher

Elsevier BV

Subject

Pharmacology

Reference26 articles.

1. Investigation of the subtypes of α1-adrenoceptor mediating contractions of the rat aorta, vas deferens, and spleen;Aboud;Br. J. Pharmacol.,1993

2. Some quantitative uses of drug antagonists;Arunlakshana;Br. J. Pharmacol.,1959

3. Calcium antagonists inhibit contractions to norepinephrine in the rat aorta in the absence but not in the presence of the endothelium;Auch-Schwelk;Gen. Pharmacol.,1991

4. International Union of Pharmacology nomenclature of adrenoceptors;Bylund;Pharmacol. Rev.,1994

5. Simultaneous analysis of families of sigmoidal curves: application to bioassay, radioligand assay, and physiological dose-response curves;DeLean;Am. J. Physiol.,1980

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