Brian E. Marron
Argyll and Bute Hospital(GB)
Publications by Year
Research Areas
Ion channel regulation and function, Pain Mechanisms and Treatments, Asymmetric Synthesis and Catalysis, Neuroscience and Neuropharmacology Research, Cardiac electrophysiology and arrhythmias
Most-Cited Works
- → A-803467, a potent and selective Na v 1.8 sodium channel blocker, attenuates neuropathic and inflammatory pain in the rat(2007)520 cited
- → Voltage sensor interaction site for selective small molecule inhibitors of voltage-gated sodium channels(2013)241 cited
- → Subtype-Selective Small Molecule Inhibitors Reveal a Fundamental Role for Nav1.7 in Nociceptor Electrogenesis, Axonal Conduction and Presynaptic Release(2016)188 cited
- → Recent progress in sodium channel modulators for pain(2014)169 cited
- → Voltage gated sodium channels as drug discovery targets(2015)133 cited
- → Identification of Lipoxin A 4 and Its Relationship to the Sulfidopeptide Leukotrienes C 4 , D 4 , and E 4 in the Bronchoalveolar Lavage Fluids Obtained from Patients with Selected Pulmonary Diseases(1990)132 cited
- → Bridging of macrodithionolactones to bicyclic systems. Synthesis and modeling of oxapolycyclic frameworks(1990)113 cited
- → Inhibition of cartilage and bone destruction in adjuvant arthritis in the rat by a matrix metalloproteinase inhibitor.(1995)108 cited
- → Discovery and Biological Evaluation of 5-Aryl-2-furfuramides, Potent and Selective Blockers of the Nav1.8 Sodium Channel with Efficacy in Models of Neuropathic and Inflammatory Pain(2008)84 cited
- → Discovery of Clinical Candidate 4-[2-(5-Amino-1H-pyrazol-4-yl)-4-chlorophenoxy]-5-chloro-2-fluoro-N-1,3-thiazol-4-ylbenzenesulfonamide (PF-05089771): Design and Optimization of Diaryl Ether Aryl Sulfonamides as Selective Inhibitors of NaV1.7(2017)83 cited