Human D2 and D4 dopamine receptors couple through βγ G-protein subunits to inwardly rectifying K+ channels (GIRK1) in a Xenopus oocyte expression system: selective antagonism by L-741,626 and L-745,870 respectively

This publication has 14 references indexed in Scilit:

• Antagonism of the effects of (+)‐PD 128907 on midbrain dopamine neurones in rat brain slices by a selective D₂ receptor antagonist L‐741,626
  British Journal of Pharmacology, 1996
• Cloning of a Xenopus laevis Inwardly Rectifying K+ Channel Subunit That Permits GIRK1 Expression of IKACh Currents in Oocytes
  Published by Elsevier ,1996
• The K⁺ channel inward rectifier subunits form a channel similar to neuronal G protein‐gated K⁺ channel
  FEBS Letters, 1996
• 3-[[4-(4-Chlorophenyl)piperazin-1-yl]methyl]-1H-pyrrolo[2,3-b]pyridine: An Antagonist with High Affinity and Selectivity for the Human Dopamine D₄ Receptor
  Journal of Medicinal Chemistry, 1996
• Molecular Cloning of a Mouse G-Protein-Activated K+ Channel (mGIRK1) and Distinct Distributions of 3 GIRK (GIRK1, 2 and 3) mRNAs in Mouse Brain
  Biochemical and Biophysical Research Communications, 1995
• The G-protein-gated atrial K+ channel IKAch is a heteromultimer of two inwardly rectifying K+-channel proteins
  Nature, 1995
• A region of the muscarinic-gated atrial K+ channel critical for activation by G protein βγ subunits
  Neuron, 1994
• Comparison between the pharmacology of dopamine receptors mediating the inhibition of cell firing in rat brain slices through the substantia nigra pars compacta and ventral tegmental area
  British Journal of Pharmacology, 1994
• Activation of the cloned muscarinic potassium channel by G protein βγ subunits
  Nature, 1994
• Primary structure and functional expression of a rat G-protein-coupled muscarinic potassium channel
  Nature, 1993