Dopamine Agonist Therapy in Advanced Parkinson’s Disease [PDF]
Heinz Reichmann
doaj +1 more source
Effects of the dopamine D2 agonist, quinpirole, on time and number processing in rats [PDF]
Angelo Santi, Romina Coppa, Lori E. Ross
openalex +1 more source
Differential Effects of Direct and Indirect Dopamine Agonists on Prepulse Inhibition: A Study in D1 and D2 Receptor Knock-Out Mice [PDF]
Rebecca J. Ralph-Williams+4 more
openalex +1 more source
Differential G protein activation by the long and short isoforms of the dopamine D2 receptor
Background and Purpose The dopamine D2 receptor is expressed as a short (D2S) and a long (D2L) isoform with 29 additional amino acids in the third intracellular loop. The D2S isoform shows higher presynaptic expression than the D2L isoform, and decreased D2S expression has recently been linked to an increased risk for schizophrenia.
David Reiner‐Link+4 more
wiley +1 more source
Dopamine Agonist-Associated Hiccup in Parkinson's Disease: A Case Report. [PDF]
Emekli AS, Hanagasi HA.
europepmc +1 more source
ERNEST COST action overview on the (patho)physiology of GPCRs and orphan GPCRs in the nervous system
G protein‐coupled receptors (GPCRs) are a large family of cell surface receptors that play a critical role in nervous system function by transmitting signals between cells and their environment. They are involved in many, if not all, nervous system processes, and their dysfunction has been linked to various neurological disorders representing important
Necla Birgül Iyison+15 more
wiley +1 more source
The Comparative Efficacy of Non-ergot Dopamine Agonist and Potential Risk Factors for Motor Complications and Side Effects From NEDA Use in Early Parkinson's Disease: Evidence From Clinical Trials. [PDF]
Wu C+7 more
europepmc +1 more source
Distinct Residues in the Carboxyl Tail Mediate Agonist-induced Desensitization and Internalization of the Human Dopamine D1 Receptor [PDF]
Michael Lamey+6 more
openalex +1 more source
Abstract G protein‐coupled receptors (GPCRs) are one of the major drug targets. In recent years, computational drug design for GPCRs has mainly focused on static structures obtained through X‐ray crystallography, cryogenic electron microscopy (cryo‐EM) or in silico modelling as a starting point for virtual screening campaigns. However, GPCRs are highly
Marta Lopez‐Balastegui+6 more
wiley +1 more source