Pharmacologic characterization of cloned α1-adrenoceptor subtypes: selective antagonists suggest the existence of a fourth subtype-Reference-Cited by-同舟云学术

Pharmacologic characterization of cloned α1-adrenoceptor subtypes: selective antagonists suggest the existence of a fourth subtype

Published:1992-12 Issue:4 Volume:227 Page:433-436
ISSN:0922-4106
Container-title:European Journal of Pharmacology: Molecular Pharmacology
language:en
Short-container-title:European Journal of Pharmacology: Molecular Pharmacology

Author:

Schwinn Debra A,Lomasney Jon W

Publisher

Elsevier BV

Subject

Pharmacology

Reference13 articles.

1. (+)-Niguldipine binds with very high affinity to Ca2+-channels and to a subtype of α1-adrenoceptors;Boer;Eur. J. Pharmacol.,1989

2. Molecular cloning and expression of the cDNA for the hamster α1-adrenoceptor;Cotecchia,1988

3. Validation and statistical analysis of a computer modelling method for quantitative analysis of radioligand binding data for mixtures of pharmacological receptor subtypes;DeLean;Mol. Pharmacol.,1982

4. 5-Methyl-urapidil discriminates between subtypes of the α1-adrenoceptor;Gross;Eur. J. Pharmacol.,1988

5. Interaction of subtype-selective antagonists with α1-adrenoceptor binding sites in rat tissues;Han;Mol. Pharmacol.,1991

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