Two distinct α1-adrenergic receptor sites in rat liver: Differential binding of (−)-[3H]norepinephrine, [3H]prazosin and [3H]dihydroergocryptine
- 1 June 1981
- journal article
- research article
- Published by Elsevier in Biochemical Pharmacology
- Vol. 30 (12) , 1665-1675
- https://doi.org/10.1016/0006-2952(81)90395-6
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- The α-adrenergic mediated effect in rat liverBiochemical Pharmacology, 1980
- Subclassification fo two types of α-adrenergic binding sites in rat liverEuropean Journal of Pharmacology, 1980
- Adrenergic receptor of the alpha1-subtype mediates the activation of the glycogen phosphorylase in normal rat liverBiochemical Pharmacology, 1980
- (3H)-Vasopressin Binding to Isolated Rat Hepatocytes and Liver Membranes: Regulation by GTP and Relation to Glycogen Phosphorylase ActivationJournal of Receptor Research, 1980
- Alpha-adrenergic receptor subtypes: Quantitative assessment by ligand bindingLife Sciences, 1979
- Binding characteristics of 3H-prazosin to rat brain α-adrenergic receptorsEuropean Journal of Pharmacology, 1979
- Multiple receptors for dopamineNature, 1979
- Proteolytic activation of adenylate cyclase from rat‐liver plasma membranesFEBS Letters, 1977
- Relationship between the inhibition constant (KI) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reactionBiochemical Pharmacology, 1973
- Isolation of an organ specific protein antigen from cell-surface membrane rat liverBiochimica et Biophysica Acta (BBA) - Protein Structure, 1968