“PAR2 induces ovarian cancer cell motility by merging three signalling pathways to transactivate EGFR”. British Journal of Pharmacology178 (4): 913–932. (November 2020). doi:10.1111/bph.15332. PMID33226635.
“Proteinase-activated receptor-2 in the skin: receptor expression, activation and function during health and disease”. Drug News & Perspectives21 (7): 369–81. (September 2008). doi:10.1358/dnp.2008.21.7.1255294. PMID19259550.
“Protease-activated receptors and their biological role - focused on skin inflammation”. The Journal of Pharmacy and Pharmacology67 (12): 1623–33. (December 2015). doi:10.1111/jphp.12447. PMID26709036.
“Potent and metabolically stable agonists for protease-activated receptor-2: evaluation of activity in multiple assay systems in vitro and in vivo”. The Journal of Pharmacology and Experimental Therapeutics309 (3): 1098–107. (June 2004). doi:10.1124/jpet.103.061010. PMID14976227.
“Thrombin-Mediated Direct Activation of Proteinase-Activated Receptor-2: Another Target for Thrombin Signaling”. Molecular Pharmacology89 (5): 606–14. (May 2016). doi:10.1124/mol.115.102723. PMID26957205.
“Mast cell tryptase stimulates human lung fibroblast proliferation via protease-activated receptor-2”. American Journal of Physiology. Lung Cellular and Molecular Physiology278 (1): L193-201. (January 2000). doi:10.1152/ajplung.2000.278.1.l193. PMID10645907.
“Kallikrein protease activated receptor (PAR) axis: an attractive target for drug development”. Journal of Medicinal Chemistry55 (15): 6669–86. (August 2012). doi:10.1021/jm300407t. PMID22607152.
“PAR2 induces ovarian cancer cell motility by merging three signalling pathways to transactivate EGFR”. British Journal of Pharmacology178 (4): 913–932. (November 2020). doi:10.1111/bph.15332. PMID33226635.
“Protease-activated receptors and their biological role - focused on skin inflammation”. The Journal of Pharmacy and Pharmacology67 (12): 1623–33. (December 2015). doi:10.1111/jphp.12447. PMID26709036.
“Mast cell tryptase stimulates human lung fibroblast proliferation via protease-activated receptor-2”. American Journal of Physiology. Lung Cellular and Molecular Physiology278 (1): L193-201. (January 2000). doi:10.1152/ajplung.2000.278.1.l193. PMID10645907.
“Activation of protease-activated receptor (PAR)-1, PAR-2, and PAR-4 stimulates IL-6, IL-8, and prostaglandin E2 release from human respiratory epithelial cells”. Journal of Immunology168 (7): 3577–85. (April 2002). doi:10.4049/jimmunol.168.7.3577. PMID11907122.
“Protease-activated receptors (PARs) in cancer: Novel biased signaling and targets for therapy”. Methods in Cell Biology132: 341–58. (2016). doi:10.1016/bs.mcb.2015.11.006. PMID26928551.
“Identification and characterization of novel small-molecule protease-activated receptor 2 agonists”. The Journal of Pharmacology and Experimental Therapeutics327 (3): 799–808. (December 2008). doi:10.1124/jpet.108.142570. PMID18768780.
“Novel agonists and antagonists for human protease activated receptor 2”. Journal of Medicinal Chemistry53 (20): 7428–40. (October 2010). doi:10.1021/jm100984y. PMID20873792.
“PAR2 induces ovarian cancer cell motility by merging three signalling pathways to transactivate EGFR”. British Journal of Pharmacology178 (4): 913–932. (November 2020). doi:10.1111/bph.15332. PMID33226635.
“Proteinase-activated receptor-2 in the skin: receptor expression, activation and function during health and disease”. Drug News & Perspectives21 (7): 369–81. (September 2008). doi:10.1358/dnp.2008.21.7.1255294. PMID19259550.
“Protease-activated receptors and their biological role - focused on skin inflammation”. The Journal of Pharmacy and Pharmacology67 (12): 1623–33. (December 2015). doi:10.1111/jphp.12447. PMID26709036.
“Potent and metabolically stable agonists for protease-activated receptor-2: evaluation of activity in multiple assay systems in vitro and in vivo”. The Journal of Pharmacology and Experimental Therapeutics309 (3): 1098–107. (June 2004). doi:10.1124/jpet.103.061010. PMID14976227.
“Thrombin-Mediated Direct Activation of Proteinase-Activated Receptor-2: Another Target for Thrombin Signaling”. Molecular Pharmacology89 (5): 606–14. (May 2016). doi:10.1124/mol.115.102723. PMID26957205.
“Mast cell tryptase stimulates human lung fibroblast proliferation via protease-activated receptor-2”. American Journal of Physiology. Lung Cellular and Molecular Physiology278 (1): L193-201. (January 2000). doi:10.1152/ajplung.2000.278.1.l193. PMID10645907.
“Kallikrein protease activated receptor (PAR) axis: an attractive target for drug development”. Journal of Medicinal Chemistry55 (15): 6669–86. (August 2012). doi:10.1021/jm300407t. PMID22607152.
“PAR2 induces ovarian cancer cell motility by merging three signalling pathways to transactivate EGFR”. British Journal of Pharmacology178 (4): 913–932. (November 2020). doi:10.1111/bph.15332. PMID33226635.
“Protease-activated receptors and their biological role - focused on skin inflammation”. The Journal of Pharmacy and Pharmacology67 (12): 1623–33. (December 2015). doi:10.1111/jphp.12447. PMID26709036.
“Mast cell tryptase stimulates human lung fibroblast proliferation via protease-activated receptor-2”. American Journal of Physiology. Lung Cellular and Molecular Physiology278 (1): L193-201. (January 2000). doi:10.1152/ajplung.2000.278.1.l193. PMID10645907.
“Activation of protease-activated receptor (PAR)-1, PAR-2, and PAR-4 stimulates IL-6, IL-8, and prostaglandin E2 release from human respiratory epithelial cells”. Journal of Immunology168 (7): 3577–85. (April 2002). doi:10.4049/jimmunol.168.7.3577. PMID11907122.
“Protease-activated receptors (PARs) in cancer: Novel biased signaling and targets for therapy”. Methods in Cell Biology132: 341–58. (2016). doi:10.1016/bs.mcb.2015.11.006. PMID26928551.
“Identification and characterization of novel small-molecule protease-activated receptor 2 agonists”. The Journal of Pharmacology and Experimental Therapeutics327 (3): 799–808. (December 2008). doi:10.1124/jpet.108.142570. PMID18768780.
“Novel agonists and antagonists for human protease activated receptor 2”. Journal of Medicinal Chemistry53 (20): 7428–40. (October 2010). doi:10.1021/jm100984y. PMID20873792.