Position
Research Fellow
Faculty of Pharmacy and Pharmaceutical Sciences
Drug Discovery Biology
Monash Institute of Pharmaceutical Sciences
Bathgate, R., Halls, M.L., Van Der Westhuizen, E.T., Callander, G., Kocan, M., Summers, R.J., 2013, Relaxin family peptides and their receptors, Physiological Reviews [P], vol 93, issue 1, The American Physiological Society, Bethesda Maryland USA, pp. 405-480.
Van Der Westhuizen, E., Christopoulos, A., Sexton, P., Wade, J., Summers, R., 2010, H2 relaxin is a biased ligand relative to H3 relaxin at the relaxin family peptide receptor 3 (RXFP3) [S], Molecular Pharmacology [P], vol 77, issue 5, American Society for Pharmacology and Experimental Therapeutics, United States, pp. 759-772.
van der Westhuizen, E.T., Wade, J.D., Sexton, P.M., Summers, R.J., 2009, Addition of a carboxy-terminal green fluorescent protein does not alter the binding and signaling properties of relaxin family peptide receptor 3, Annals of the New York Academy of Sciences [P], vol 1160, Wiley-Blackwell Publishing, Inc., USA, pp. 105-107.
Halls, M.L., van der Westhuizen, E.T., Wade, J.D., Evans, B.A., Bathgate, R.A.D., Summers, R.J., 2009, Relaxin family peptide receptor (RXFP1) coupling to Galphai3, involves the C-terminal Arg752 and localization within membrane raft microdomains, Molecular Pharmacology [P], vol 75, issue 2, American Society for Pharmacology and Experimental Therapeutics, USA, pp. 415-428.
Summers, R.J., Bathgate, R.A.D., Wade, J.D., van der Westhuizen, E.T., Halls, M.L., 2009, Roles of the receptor, the ligand, and the cell in the signal transduction pathways utilized by the relaxin family peptide receptors 1-3, Annals of the New York Academy of Sciences [P], vol 1160, Wiley-Blackwell Publishing, Inc., USA, pp. 99-104.
Van Der Westhuizen, E.T., Halls, M.L., Samuel, C.S., Bathgate, R., Unemori, E.N., Sutton, S.W., Summers, R.J., 2008, Relaxin family peptide receptors - from orphans to therapeutic targets, Drug Discovery Today, vol 13, issue 15-16, Elsevier Ltd., United Kingdom, pp. 640-651.
Halls, M.L., Van Der Westhuizen, E.T., Bathgate, R., Summers, R.J., 2007, Relaxin family peptide receptors - Former orphans reunite with their parent ligands to activate multiple signalling pathways, British Journal of Pharmacology, vol 150, issue 6, Nature Publishing Group, London England UK, pp. 677-691.
Van Der Westhuizen, E.T., Summers, R.J., Halls, M.L., Bathgate, R., Sexton, P., 2007, Relaxin receptors - new drug targets for multiple disease states, Current Drug Targets, vol 8, issue 1, Bentham Science Ltd, Sharjah UAE, pp. 91-104.
Van Der Westhuizen, E.T., Werry, T.D., Sexton, P., Summers, R.J., 2007, The relaxin family peptide receptor 3 activates extracellular signal-regulated kinase 1/2 through a protein kinase C-dependent mechanism, Molecular Pharmacology, vol 71, issue 6, American Society of Pharmacology, Experimental Therapeutics, Bethesda MD USA, pp. 1618-1629.
Chu, S., Rushdi, S., Zumpe, E.T., Mamers, P., Healy, D.W., Jobling, T., Burger, H., Fuller, P.J., 2002, FSH-regulated gene expression profiles in ovarian tumours and normal ovaries, Molecular Human Reproduction, vol 8, issue 5, Oxford University Press, Oxford UK, pp. 426-433.
Fuller, P.J., Zumpe, E.T., Chu, S., Mamers, P., Burger, H., 2002, Inhibin-Activin Receptor Subunit Gene Expression in Ovarian Tumors, The Journal of Clinical Endocrinology and Metabolism, vol 87, The Endocrine Society, USA, pp. 1395-1401.
Van Der Westhuizen, E.T., Sexton, P.M., Bathgate, R.A.D., Summers, R.J., 2005, Responses of GPCR135 to human gene 3 (H3) relaxin in CHO-K1 cells determined by microphysiometry, Relaxin and Related Peptides: Fourth International Conference, 5 September 2004 to 10 September 2004, New York Academy of Sciences, New York USA, pp. 332-337.
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