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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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Gonadotrophin-releasing hormone receptor agonist-mediated down-regulation of Gq alpha/G11 alpha (pertussis toxin-insensitive) G proteins in alpha T3-1 gonadotroph cells reflects increased G protein turnover but not alterations in mRNA levels

TL;DR: These studies indicate that gonadotrophin-releasing hormone receptor agonist-mediated down-regulation of Gq alpha/G11 alpha is a reflection of enhanced proteolysis of the activated G proteins.
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Melatonin Receptors Couple Through a Cholera Toxin‐Sensitive Mechanism to Inhibit Cyclic AMP in the Ovine Pituitary

TL;DR: The nature of melatonin receptor‐G‐protein coupling in ovine pars tuberalis (PT) cells of the pituitary was addressed using cholera (CTX) and pertussis (PTX) toxins using 32P‐NAD in the presence of CTX radiolabelled several substrates including 44, 51, and 60 kD proteins.
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Antagonists of GPR35 display high species ortholog selectivity and varying modes of action

TL;DR: These studies demonstrate that marked species selectivity of ligands at GPR35 is not restricted to agonists and considerable care is required to select appropriate ligands to explore the function of G PR35 in nonhuman cells and tissues.
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The specificity and molecular basis of α1-adrenoceptor and CXCR chemokine receptor dimerization

TL;DR: It is demonstrated that CXCR1 is able to both homodimerizing and heterodimerize with the CX CR2 receptor and that the relative affinity of these interactions suggests that with coexpression of these two GPCRs a random mixture of homo- andheterodimers will be present.
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The role of palmitoylation of the guanine nucleotide binding protein G11 alpha in defining interaction with the plasma membrane.

TL;DR: The data demonstrate that the palmitoylation status of the cysteine residues at positions 9 and 10 in murine G11 alpha plays a central role in defining membrane association of this G-protein and indicate that much of the particulate fraction of the expressed palMIToylation-resistant mutants is likely to represent non-functional rather than correctly folded protein.