A specific binding site for K+ channel openers in rat aorta.
Open Access
- 1 June 1992
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 267 (17) , 11689-11692
- https://doi.org/10.1016/s0021-9258(19)49750-0
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Potassium channel openers and vascular smooth muscle relaxationPharmacology & Therapeutics, 1990
- Structure-activity relationships of K+ channel openersTrends in Pharmacological Sciences, 1990
- Potassium channel modulators: scientific applications and therapeutic promiseJournal of Medicinal Chemistry, 1990
- Ruthenium red selectively inhibits oedema formation and increased blood flow induced by capsaicin in rabbit skinBritish Journal of Pharmacology, 1990
- Moving together: K+ channel openersand ATP-sensitive K+ channelsTrends in Pharmacological Sciences, 1989
- Properties of the cromakalim‐induced potassium conductance in smooth muscle cells isolated from the rabbit portal veinBritish Journal of Pharmacology, 1989
- A Ca2+-activated K+ channel from rabbit aorta: modulation by cromakalimEuropean Journal of Pharmacology, 1989
- Hyperpolarizing Vasodilators Activate ATP-sensitive K + Channels in Arterial Smooth MuscleScience, 1989
- The Relation Between Vascular Relaxant and Cardiac Electrophysiological Effects of PinacidilJournal of Cardiovascular Pharmacology, 1988
- Comparison of the effects of BRL 34915 and verapamil on electrical and mechanical activity in rat portal veinBritish Journal of Pharmacology, 1986