Select Publications
Journal articles
2023, 'Gene expression analyses of TAS1R taste receptors relevant to the treatment of cardiometabolic disease', Chemical Senses, 48, http://dx.doi.org/10.1093/chemse/bjad027
,2022, 'Orphan GPR146: an alternative therapeutic pathway to achieve cholesterol homeostasis?', Trends in Endocrinology and Metabolism, 33, pp. 481 - 492, http://dx.doi.org/10.1016/j.tem.2022.04.008
,2022, 'Characterisation of bis(4-aminoquinoline)s as α
2021, 'Critically evaluating sweet taste receptor expression and signaling through a molecular pharmacology lens', FEBS Journal, 288, pp. 2660 - 2672, http://dx.doi.org/10.1111/febs.15768
,2021, 'Orphan receptor GPR37L1 remains unliganded', Nature Chemical Biology, 17, pp. 383 - 386, http://dx.doi.org/10.1038/s41589-021-00748-z
,2020, 'Vicinal difluorination as a C=C surrogate: An analog of piperine with enhanced solubility, photostability, and acetylcholinesterase inhibitory activity', Beilstein Journal of Organic Chemistry, 16, pp. 2663 - 2670, http://dx.doi.org/10.3762/BJOC.16.216
,2020, 'Orphan G protein-coupled receptor, GPR37L1: pharmacological toolbox empty once again', , http://dx.doi.org/10.1101/2020.09.11.290486
,2020, 'Vicinal difluorination as a C=C surrogate: an analog of piperine with enhanced solubility, photostability, and acetylcholinesterase inhibitory activity', , http://dx.doi.org/10.3762/bxiv.2020.93.v1
,2018, 'Design, Synthesis, and Evaluation of N- and C-Terminal Protein Bioconjugates as G Protein-Coupled Receptor Agonists', Bioconjugate Chemistry, 29, pp. 403 - 409, http://dx.doi.org/10.1021/acs.bioconjchem.7b00716
,2017, 'Template selection and refinement considerations for modelling aminergic GPCR-ligand complexes', Journal of Molecular Graphics and Modelling, 76, pp. 488 - 503, http://dx.doi.org/10.1016/j.jmgm.2017.07.030
,2017, 'Homobivalent conjugation increases the allosteric effect of 9-aminoacridine at the α
2014, 'Human α
2014, 'An aspartate in the second extracellular loop of the α
2014, 'Expression of adrenoceptor subtypes in preterm piglet heart is different to term heart', PLoS ONE, 9, http://dx.doi.org/10.1371/journal.pone.0092167
,2013, '5-HT1A receptor pharmacophores to screen for off-target activity of á1-adrenoceptor antagonists', Journal of Computer - Aided Molecular Design, 27, pp. 305 - 319, http://dx.doi.org/10.1007/s10822-013-9647-5
,2013, 'a1-Adrenoceptor and serotonin 5-HT1A receptor affinity of homobivalent 4-aminoquinoline compounds: An investigation of the effect of linker length', Biochemical Pharmacology, 85, pp. 1534 - 1541, http://dx.doi.org/10.1016/j.bcp.2013.03.010
,2011, 'A novel structural framework for á1a/d-adrenoceptor selective antagonists identified using subtype selective pharmacophores', PLoS One, 6, pp. e19695, http://dx.doi.org/10.1371/journal.pone.0019695
,2008, 'Effect of controlled alterations in maternal dietary retinol on foetal and neonatal retinol status and pregnancy outcome in pigs', Livestock Science, 118, pp. 247 - 254
,2008, 'Peripheral changes above and below injury level lead to prolonged vascular responses following high spinal cord injury', American Journal of Physiology - Heart and Circulatory Physiology, 294, pp. H785 - H792, http://dx.doi.org/10.1152/ajpheart.01002.2007
,2008, 'Wide turn diversity in protein transmembrane helices implications for G-protein-coupled receptor and other polytopic membrane protein structure and function', Molecular Pharmacology, 73, pp. 1092 - 1104, http://dx.doi.org/10.1124/mol.107.043042
,2007, 'Glucocorticoid exposure and tissue gene expression of 11â HSD-1, 11 â HSD-2, and glucocorticoid receptor in a porcine model of differential fetal growth', Reproduction, 133, pp. 653 - 661
,2006, 'The α
2006, 'Cardiac overexpression of the alpha(1A)-adrenergic receptor limits post-infarct ventricular remodeling and dysfunction, and improves survival', Journal of Molecular and Cellular Cardiology, 41, pp. 735 - 735
,2006, 'The alpha(1D)-adrenergic receptor: Cinderella or ugly stepsister', Molecular Pharmacology, 69, pp. 1 - 4
,2006, 'Transgenic alpha(1A)-adrenergic activation limits post-infarct ventricular remodeling and dysfunction and improves survival', Cardiovascular Research, 71, pp. 735 - 743
,2005, 'The effect of fetal pig size and stage of gestation on tissue fatty acid metabolism and profile', Reproduction, 129, pp. 757 - 763
,2004, 'Genetic enhancement of ventricular contractility protects against pressure-overload-induced cardiac dysfunction', Journal of Molecular and Cellular Cardiology, 37, pp. 979 - 987
,2004, 'Placental transport of leucine in a porcine model of low birth weight', Reproduction, 128, pp. 229 - 235
,2004, 'Synthesis and biological evaluation of bicyclic and tricyclic substituted nortropan derivatives: discovery of a novel selective Ą1D-adrenergic receptor ligand', Bioorganic and Medicinal Chemistry, 12, pp. 5639 - 5650
,2003, 'Sodium transport across the chorioallantoic membrane of porcine placenta involves the epithelial sodium channel (ENaC)', The Journal of Physiology, 547, pp. 849 - 857, http://dx.doi.org/10.1113/jphysiol.2002.031153
,2002, 'Patterns of fetal growth within Large White x Landrace and Chinese Meishan gilt litters at three stages of gestation', Reproduction, Fertility and Development, 14, pp. 419 - 425, http://dx.doi.org/10.1071/RD01131
,2001, 'Causes and consequences of fetal growth retardation in pigs.', Reproduction (Cambridge, England) Supplement, 58, pp. 233 - 246
,2001, 'The effect of feeding salmon oil to sows throughout pregnancy on pre-weaning mortality of piglets', Animal Science, 73, pp. 489 - 500, http://dx.doi.org/10.1017/s135772980005846x
,1999, 'Low-molecular-weight peptidic and cyclic antagonists of the receptor for the complement factor C5a', Journal of Medicinal Chemistry, 42, pp. 1965 - 1974, http://dx.doi.org/10.1021/jm9806594
,1999, 'Effects of a new C5a receptor antagonist on C5a- and endotoxin-induced neutropenia in the rat', British Journal of Pharmacology, 126, pp. 551 - 554, http://dx.doi.org/10.1038/sj.bjp.0702338
,1999, 'Pharmacological characterization of antagonists of the C5a receptor', British Journal of Pharmacology, 128, pp. 1461 - 1466, http://dx.doi.org/10.1038/sj.bjp.0702938
,1999, 'The influence of Lys68 in decapeptide agonists of C5a on C5a receptor binding, activation and selectivity', Journal of Peptide Research, 53, pp. 8 - 17, http://dx.doi.org/10.1111/j.1399-3011.1999.tb01612.x
,1998, 'Small molecular probes for G-protein-coupled C5a receptors: Conformationally constrained antagonists derived from the C terminus of the human plasma protein C5a', Journal of Medicinal Chemistry, 41, pp. 3417 - 3425, http://dx.doi.org/10.1021/jm9800651
,1997, 'Biologically active conformer of the effector region of human C5a and modulatory effects of N-terminal receptor binding determinants on activity', Journal of Medicinal Chemistry, 40, pp. 877 - 884, http://dx.doi.org/10.1021/jm960727r
,1997, 'Molecular Adjuvant Effects of a Conformationally Biased Agonist of Human C5a Anaphylatoxin', Journal of Immunology, 158, pp. 1377 - 1382
,1996, 'Conformationally biased analogs of human C5a mediate changes in vascular permeability', Journal of Pharmacology and Experimental Therapeutics, 278, pp. 432 - 440
,1995, 'Decapeptide Agonists of Human C5a: The Relationship between Conformation and Neutrophil Response', Journal of Medicinal Chemistry, 38, pp. 3669 - 3675, http://dx.doi.org/10.1021/jm00018a028
,1995, 'The effect of C5a and U46619 on the isolated, perfused human placental lobule: Development of a method for the online estimation of tissue fluid accumulation', Journal of Pharmacological and Toxicological Methods, 34, pp. 133 - 141, http://dx.doi.org/10.1016/1056-8719(95)00046-3
,1994, 'Reversibility of tachyphylaxis to C5a in guinea pig tissues, perfused human placental lobule, and umbilical artery', Inflammation, 18, pp. 645 - 657, http://dx.doi.org/10.1007/BF01535262
,1994, 'Decapeptide Agonists of Human C5a: The Relationship between Conformation and Spasmogenic and Platelet Aggregatory Activities', Journal of Medicinal Chemistry, 37, pp. 3171 - 3180, http://dx.doi.org/10.1021/jm00045a023
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