Indications for selective coupling to phosphoinositide hydrolysis or to adenylate cyclase inhibition by endogenous muscarinic receptor subtypes M3 and M4 but not by M2 in tumor cell lines
- 1 January 1990
- journal article
- research article
- Published by Elsevier in Neuroscience Letters
- Vol. 108 (3) , 335-340
- https://doi.org/10.1016/0304-3940(90)90663-t
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Functionally distinct G proteins selectively couple different receptors to PI hydrolysis in the same cellCell, 1989
- Tissue distribution of mRNAs encoding muscarinic acetylcholine receptor subtypesFEBS Letters, 1988
- Second-messenger generation in PC12 cells. Interactions between cyclic AMP and Ca2+ signalsBiochemical Journal, 1988
- Selective coupling with K+ currents of muscarinic acetylcholine receptor subtypes in NG108-15 cellsNature, 1988
- Muscarinic receptor-mediated increase in cAMP levels in SK-N-SH human neuroblastoma cellsBiochemical and Biophysical Research Communications, 1988
- Cloning and expression of the human and rat m5 muscarinic acetylcholine receptor genesNeuron, 1988
- A Putative M3 Muscarinic Cholinergic Receptor of High Molecular Weight Couples to Phosphoinositide Hydrolysis in Human SK‐N‐SH Neuroblastoma CellsJournal of Neurochemistry, 1988
- Identification of a Family of Muscarinic Acetylcholine Receptor GenesScience, 1987
- Primary structure of porcine cardiac muscarinic acetylcholine receptor deduced from the cDNA sequenceFEBS Letters, 1986
- Pharmacological Characterization of Cholinergic Receptors in a Human Neuroblastoma Cell LineJournal of Neurochemistry, 1986