G
Graeme Milligan
Researcher at University of Glasgow
Publications - 570
Citations - 32250
Graeme Milligan is an academic researcher from University of Glasgow. The author has contributed to research in topics: Receptor & G protein. The author has an hindex of 88, co-authored 556 publications receiving 30032 citations. Previous affiliations of Graeme Milligan include University of Leicester & Autonomous University of Barcelona.
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Journal ArticleDOI
Palmitoylation Regulates Regulator of G-protein Signaling (RGS) 16 Function II. PALMITOYLATION OF A CYSTEINE RESIDUE IN THE RGS BOX IS CRITICAL FOR RGS16 GTPase ACCELERATING ACTIVITY AND REGULATION OF Gi-COUPLED SIGNALING*
James L. Osterhout,Abdul A. Waheed,Abel Hiol,Richard J. Ward,Penelope C. Davey,Lylia Nini,Jiun Wang,Graeme Milligan,Teresa L.Z. Jones,Kirk M. Druey +9 more
TL;DR: The results suggest that palmitoylation of a Cys residue in the RGS box is critical for RGS16 and RGS4 GAP activity and their ability to regulate Gi-coupled signaling in mammalian cells.
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Distribution of G-proteins in rat liver plasma-membrane domains and endocytic pathways.
TL;DR: The presence of high levels of the G-protein inhibitory alpha-subunit in bile-canalicular plasma membranes was confirmed by demonstration of its co-fractionation with marker enzymes in Nycodenz gradients and by free-flow electrophoresis.
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Gi3 does not contribute to the inhibition of adenylate cyclase when stimulation of an alpha 2-adrenergic receptor causes activation of both Gi2 and Gi3.
TL;DR: Calculations indicated that essentially all of the cellular Gi3, but only 15% of the available Gi2, can be activated by the alpha 2-C10 adrenergic receptor in these cells, and results demonstrate that, although Gi3 is activated byalpha 2-adrenergic agonists in membranes of clone 1C cells, it does not contribute to the transduction of receptor-mediated inhibition of adenylate cyclase.
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Regulation of Spontaneous Activity of the δ‐Opioid Receptor: Studies of Inverse Agonism in Intact Cells
TL;DR: Using two distinct experimental strategies, ICI174864 was shown to function in a manner anticipated for an inverse agonist, demonstrating that such effects can be observed in intact cells and are not restricted to assays performed on membrane preparations.
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Lymphocyte trafficking through the blood–brain barrier is dependent on endothelial cell heterotrimeric G-protein signaling
Peter Adamson,Barry Wilbourn,Sandrine Etienne-Manneville,Sandrine Etienne-Manneville,Virginia L. Calder,Evelyne Beraud,Graeme Milligan,Graeme Milligan,Pierre-Olivier Couraud,Pierre-Olivier Couraud,John Greenwood +10 more
TL;DR: It is concluded that a heterotrimeric G‐protein‐mediated signaling pathway in brain EC is essential for efficient transendothelial migration of T lymphocytes into the brain.