Publications by authors named "Stuart R Hawtin"

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Systematic analysis of the entire second extracellular loop of the V(1a) vasopressin receptor: key residues, conserved throughout a G-protein-coupled receptor family, identified.
Matthew Conner, Stuart R Hawtin, John Simms, Denise Wootten, Zoe Lawson

J Biol Chem· June 2007

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Charged extracellular residues, conserved throughout a G-protein-coupled receptor family, are required for ligand binding, receptor activation, and cell-surface expression.
Stuart R Hawtin, John Simms, Matthew Conner, Zoe Lawson, Rosemary A Parslow

J Biol Chem· December 2006

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Pharmacological chaperone activity of SR49059 to functionally recover misfolded mutations of the vasopressin V1a receptor.
Stuart R Hawtin

J Biol Chem· May 2006

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The N-terminal juxtamembrane segment of the V1a vasopressin receptor provides two independent epitopes required for high-affinity agonist binding and signaling.
Stuart R Hawtin, Victoria J Wesley, John Simms, Cymone C H Argent, Khalid Latif

Mol Endocrinol· November 2005

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Charged residues of the conserved DRY triplet of the vasopressin V1a receptor provide molecular determinants for cell surface delivery and internalization.
Stuart R Hawtin

Mol Pharmacol· October 2005

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A Gly/Ala switch contributes to high affinity binding of benzoxazinone-based non-peptide oxytocin receptor antagonists.
Stuart R Hawtin, Sookhee N Ha, Douglas J Pettibone, Mark Wheatley

FEBS Lett· January 2005

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An arginyl in the N-terminus of the V1a vasopressin receptor is part of the conformational switch controlling activation by agonist.
Stuart R Hawtin, Victoria J Wesley, John Simms, Rosemary A Parslow, Alice Miles

Eur J Biochem· December 2003

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Agonist-specific, high-affinity binding epitopes are contributed by an arginine in the N-terminus of the human oxytocin receptor.
Victoria J Wesley, Stuart R Hawtin, Helen C Howard, Mark Wheatley

Biochemistry· April 2002

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A single residue (arg46) located within the N-terminus of the V1a vasopressin receptor is critical for binding vasopressin but not peptide or nonpeptide antagonists.
Stuart R Hawtin, Victoria J Wesley, Rosemary A Parslow, John Simms, Alice Miles

Mol Endocrinol· March 2002

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