Dopamine D1 receptors characterized with [3H]SCH 23390. Solubilization of a guanine nucleotide-sensitive form of the receptor.
Open Access
- 1 June 1986
- journal article
- research article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 261 (18) , 8397-8406
- https://doi.org/10.1016/s0021-9258(19)83926-1
Abstract
No abstract availableThis publication has 35 references indexed in Scilit:
- Hyperactivity induced by stimulation of separate dopamine D-1 and D-2 receptors in rats with bilateral 6-OHDA lesionsLife Sciences, 1985
- Selective D2 dopamine receptor agonists prevent catalepsy induced by SCH 23390, a selective D1 antagonistLife Sciences, 1985
- Endogenous proteinases modulate the function of the β-adrenergic receptor-adenylate cyclase systemBiochimica et Biophysica Acta (BBA) - General Subjects, 1984
- Two dopamine receptors: Biochemistry, physiology and pharmacologyLife Sciences, 1984
- Characterization of the binding of 3H-SCH 23390, a selective D-1 receptor antagonist ligand, in rat striatumLife Sciences, 1984
- Reconstitution of solubilised brain D2 dopamine receptors into phospholipid vesiclesFEBS Letters, 1984
- Sodium Regulation of Hormone-Sensitive Adenylate CyclaseJournal of Receptor Research, 1984
- A dopamine- and cyclic AMP-regulated phosphoprotein enriched in dopamine-innervated brain regionsNature, 1983
- Solubilization of D-2 dopamine receptors from canine caudate: Agonist-occupation stabilizes guanine nucleotide sensitive receptor complexesBiochemical and Biophysical Research Communications, 1982
- Effects of neuroleptics on 3H-haloperidol and 3H-CIS (Z)-flupenthixol binding and on adenylate cyclase activity in vitroLife Sciences, 1978