Kinetic and pharmacological characterization of vasopressin membrane receptors from human kidney medulla: Relation to adenylate cyclase activation
- 1 December 1982
- journal article
- research article
- Published by Elsevier in European Journal of Pharmacology
- Vol. 85 (3-4), 291-304
- https://doi.org/10.1016/0014-2999(82)90216-3
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Adenylate cyclase responsiveness to hormones in various portions of the human nephron.Journal of Clinical Investigation, 1980
- (3H)-Vasopressin Binding to Isolated Rat Hepatocytes and Liver Membranes: Regulation by GTP and Relation to Glycogen Phosphorylase ActivationJournal of Receptor Research, 1980
- Design of potent antagonists of the vasopressor response to arginine-vasopressinJournal of Medicinal Chemistry, 1978
- [1-(.beta.-Mercapto-.beta.,.beta.-cyclopentamethylenepropionic acid),4-valine, 8-D-arginine]vasopressin, a potent and selective inhibitor of the vasopressor response to arginine-vasopressinJournal of Medicinal Chemistry, 1978
- Interaction of Lithium with Vasopressin-Sensitive Cyclic AMP System of Human Renal MedullaEndocrinology, 1974
- Synthesis and some biological activities of analogues of deamino-vasopressin with the disulphide bridge altered to a thioether bridgeCollection of Czechoslovak Chemical Communications, 1974
- De-glycinamide9-vasopressin and de-lysine8, glycinamide9-vasopressin: Some pharmacological propertiesCollection of Czechoslovak Chemical Communications, 1974
- Specific Binding of [3H]Lysine-Vasopressin to Pig Kidney Plasma MembranesPublished by Elsevier ,1973
- Hormonal Interactions at the Molecular LevelEuropean Journal of Biochemistry, 1973
- Synthèse de la désamino1‐Arg8‐vasopressine et de la désamino1‐Phe2‐Arg8‐vasopressine, deux analogues possédant une activité antidiurétique plus élevée et plus sélective que celle des vasopressines naturellesHelvetica Chimica Acta, 1966