Richard G. W. Proudman

The affinity and selectivity of α‐adrenoceptor antagonists, antidepressants, and antipsychotics for the human α1A, α1B, and α1D‐adrenoceptors

Richard G. W. Proudman, André Sampaio Pupo, Jillian G. Baker · Pharmacology Research & Perspectives · 2020 · 49 citations · Full text

Human α1A, Psychotropic Medication, Psychopharmacology +22

The pharmacological effects of the thermostabilising (m23) mutations and intra and extracellular (β36) deletions essential for crystallisation of the turkey β-adrenoceptor

Jillian G. Baker, Richard G. W. Proudman, Christopher G. Tate · Naunyn-Schmiedeberg s Archives of Pharmacology · 2011 · 26 citations · Full text

Salmeterol’s Extreme β2 Selectivity Is Due to Residues in Both Extracellular Loops and Transmembrane Domains

Jillian G. Baker, Richard G. W. Proudman, Stephen J. Hill · Molecular Pharmacology · 2014 · 25 citations · Full text

The signaling and selectivity of α‐adrenoceptor agonists for the human <scp>α2A</scp>, <scp>α2B</scp> and <scp>α2C</scp>‐adrenoceptors and comparison with human α1 and β‐adrenoceptors

Richard G. W. Proudman, Juliana Akinaga, Jillian G. Baker · Pharmacology Research & Perspectives · 2022 · 25 citations · Full text

Role of Key Transmembrane Residues in Agonist and Antagonist Actions at the Two Conformations of the Human β1-Adrenoceptor

Jillian G. Baker, Richard G. W. Proudman, Nicola C. Hawley et al. · Molecular Pharmacology · 2008 · 21 citations